| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs212331554 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91792884 | GTAGCGGCTTCCAGT[A/G]CAGATCTCAGGGTTT | 16443 |
| rs212335472 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91739822 | TCTCTGAGAGCCCCC[A/G]AGAGTCCAGGTTAAT | 16443 |
| rs212344611 | in-del | -/C | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914678 | CTCTGAGGACAGAAG[-/C]CCCTGACTGGGCTTC | 16443 |
| rs212344771 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91787361 | CCTTCCCGCTCCTTT[C/T]TGAGAGGGATTTCTA | 16443 |
| rs212346918 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91733940 | TTATTAGACATTAGT[A/G]TAGTGTGTCATGACA | 16443 |
| rs212363715 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91824071 | TTGTTGCAGGACTTG[-/T]TAATTGAAAACCCAT | 16443 |
| rs212364519 | in-del | -/CCCC | | | intron-variant | Itsn1 | Mm_Celera | 16:91838258 | TGAGCCATCTCCCTG[-/CCCC]CCCCCCCCCCAGTTG | 16443 |
| rs212370881 | snp | C/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830357 | AGATGCACTCCTCCC[C/G]TTCCCAGAGAGGTGC | 16443 |
| rs212391291 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91800857 | CTCTCTCTGTATCGA[A/G]GGTGACTTGAATTTC | 16443 |
| rs212392987 | in-del | -/TTTTTTTTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91897443 | TATGATAACTAAGCC[-/TTTTTTTTTT]TTTTTTTTTTTAGAT | 16443 |
| rs212393033 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91792274 | TCATATCACCTGGAG[C/T]TGTTTCAACAAAGCT | 16443 |
| rs212393081 | in-del | -/CCCT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872518 | GGAGGGGAGGGATGG[-/CCCT]GCTGTTTCCCATCCA | 16443 |
| rs212400523 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91755184 | TGTGAAGCCTGGCAT[C/T]AGCCTGGTACCTCGC | 16443 |
| rs212402921 | snp | C/G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91800286 | CCGCCCTGGAGAAGC[C/G/T]GTGCTGCCCAGAGAA | 16443 |
| rs212408771 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91899258 | CAGAGTTTGTGCTGG[A/G]ACATTCAAGGGTTTG | 16443 |
| rs212422127 | in-del | -/GGTGGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91799197 | AGACGGGAGAGAGGG[-/GGTGGT]GGGTGGGTGGGGGCA | 16443 |
| rs212423403 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746483 | TTCAATAAAGGACAG[A/G]AGTGTAACATGATGC | 16443 |
| rs212431033 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91890159 | AGGCACGGGCTCTCC[C/T]CCCTCTGTGCCAGGC | 16443 |
| rs212444570 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91850318 | TGGAAAGGGAGAGCT[C/T]AAGGAATCACAAGGT | 16443 |
| rs212450455 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904486 | TTCCAAACTAGTAAC[A/G]GGGTTCGATTAAGCA | 16443 |
| rs212459557 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91836306 | TATTTCTTGGGGGGC[A/G]GGGTTGCTATAAAAT | 16443 |
| rs212463040 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917387 | AACATTAGTGTTTAT[C/T]TCCACCAAACAACTA | 16443 |
| rs212477084 | in-del | -/CTGGGGGAAAATACCAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91751390 | ATTTACTAGCACCGC[-/CTGGGGGAAAATACCAA]CCCCTAACCTCCAAG | 16443 |
| rs212503994 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91849516 | TGTTAGTAAACTCCA[G/T]AAGAGCAGTCAGAAG | 16443 |
| rs212517286 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91857050 | TAGCCAAACCTGACA[C/T]CTCAGTGTGATCCCC | 16443 |
| rs212518522 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91793311 | ATCCAATTTTAGAAC[-/T]TTTTTTTAATTTAAA | 16443 |
| rs212522865 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91866722 | ATTTTTATTTTATGT[G/T]TATGGGCATTCAGCC | 16443 |
| rs212563754 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91783792 | CCACCACCACAATGA[-/T]TTTTTTTTTTTAATG | 16443 |
| rs212574555 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91769761 | CAGTTGGCTCAGTTA[C/T]TTATTTTATGTATAT | 16443 |
| rs212579242 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91910843 | AAAAGGTATCTGTGT[A/G]TTTGCTCACATGAGT | 16443 |
| rs212580625 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91856110 | AGGCAGGTTCCCATC[A/G]TCAGTGGCTTCTGCT | 16443 |
| rs212589393 | in-del | -/TGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91772562 | TGTGGGAAGCTACGC[-/TGG]AGGGTTGCCAGTTAG | 16443 |
| rs212612501 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91770312 | GAGTTTTCACAAAAC[-/A]AAAACAAAACAAAAC | 16443 |
| rs212615595 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91916728 | CTGATACCTAGAAAG[C/T]AGCTGAGCTAGAGGA | 16443 |
| rs212627029 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91903643 | GTCCCAATTTTTCTG[A/T]CTTAGTTTAGGGTTT | 16443 |
| rs212639461 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91874864 | CACACACTTGGCAGC[A/G]AGGGCACTGAGGAGC | 16443 |
| rs212643083 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91767183 | GACTCTTGCCTGCCC[-/T]TACTCTTTCTGTGTT | 16443 |
| rs212644852 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91889007 | GTGCTAAACAAACCC[A/G]AGTATGCACGTAGTT | 16443 |
| rs212647859 | in-del | -/GTGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91872285 | CCACATAAGCATAGA[-/GTGT]GTGTGTGTGTGTGTG | 16443 |
| rs212659598 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91820932 | GTTGTGTCCTTGCCT[G/T]AAAGGGGCCTTTCAA | 16443 |
| rs212663037 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91778782 | ATAATTTTTAGGAAG[A/G]TAGATAGATCCCTTT | 16443 |
| rs212663200 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91769145 | AATGCTTTGAACTTT[A/C]GTTCTAAACCTTTCA | 16443 |
| rs212665762 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91808363 | CTGAACAGCAGGCCA[A/G]TGACTTAGAGGAGTA | 16443 |
| rs212671267 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91827995 | TGTTCTGTTGGTACA[C/T]ATCCCGAATGCTGGA | 16443 |
| rs212675809 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91755692 | GCAATTTCTAACCCA[A/G]ACAGACAAGCATGAA | 16443 |
| rs212697396 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91777823 | GCCACAGATTGCCCA[A/G]GCATTGGAAGATGTG | 16443 |
| rs212699777 | snp | C/G | | | missense | Itsn1 | GRCm38.p3 | 16:91841574 | TGAATCCAGAAGTCA[C/G]GATGAGATCACCATC | 16443 |
| rs212710966 | in-del | -/TTAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91807285 | ATTGCTTTGTATTGC[-/TTAT]TTATGATCATAATTT | 16443 |
| rs212712526 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91784615 | TCCCTGGAAGTCCCT[C/T]GTGTACCTGTCTGTG | 16443 |
| rs212717800 | in-del | -/TTAATT | | | intron-variant | Itsn1 | Mm_Celera | 16:91738435 | TTCCTTTTCATTCCG[-/TTAATT]TTAAATCACAGTCAT | 16443 |
| rs212728320 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91731061 | CTTTCTGTAGGAGAT[A/G]TGTAAAGAACTCAGG | 16443 |
| rs212736508 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91827136 | CAGGCCTAGCACAGT[G/T]CATTCTGCAAATGCC | 16443 |
| rs212741402 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91882085 | CATGGCCTTTTCTAT[G/T]CCCTGTGTCTCCCAC | 16443 |
| rs212754596 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91881628 | AACACAGCTGTGGTA[C/T]AGAGATAAAGCCAGA | 16443 |
| rs212773882 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91791508 | ACGATTGTTAAAAAT[C/T]CTGCAAAGGAGAGAT | 16443 |
| rs212785968 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91834399 | TCTGAAACTCCAAAA[C/T]CCAAAGGGAACATTC | 16443 |
| rs212797250 | in-del | -/CTCGGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91735070 | GGTGCTCCTGCCACC[-/CTCGGG]CTCTAGCAGTCAGTC | 16443 |
| rs212805572 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91738643 | CACCTTCCAGTGCTG[C/T]CTGTAGCTAACCCAG | 16443 |
| rs212815822 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91881052 | CGTGCTGCTCACTGC[A/G]TGCGTTGTCACAGCA | 16443 |
| rs212817990 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91888299 | TGTTATGGGAGTTTC[A/G]GGCTAAAAATGCTAG | 16443 |
| rs212848145 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91840610 | TTCCTGAGGTCCTAT[A/G]GCTGCAGGGAGAACT | 16443 |
| rs212857343 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91826547 | TTGCTCCTCCTGTGC[A/G]TTGGCGCTCTGCCTT | 16443 |
| rs212876598 | in-del | -/TTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91762354 | AAATTGTAGCATGTA[-/TTT]TTTAAGTTTTTCACA | 16443 |
| rs212885488 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91737878 | GCATTTCCCACTTTG[A/G]ATATTTCCAGTTTAT | 16443 |
| rs212892007 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91762896 | AGACCCCACTGGCCC[C/T]GTATTTCTCTCGTGT | 16443 |
| rs212894630 | snp | A/C | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745879 | ACTGCCTTTTCCTTT[A/C]AGCTTGGAAGAAAGA | 16443 |
| rs212901783 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91847840 | ACTTTTAGAGAGATG[A/G]CCCAGCAGTTAGGAG | 16443 |
| rs212924184 | snp | C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745563 | TGTTACCATTTCAAG[C/G]TCAAAAGGTGTGAGA | 16443 |
| rs212930401 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91887816 | CTTGAGTTTTAGCTC[A/G]GCCACCAACTGATTG | 16443 |
| rs212940689 | in-del | -/TG | | | intron-variant | Itsn1 | Mm_Celera | 16:91751496 | GTGTGTGTGTATGTA[-/TG]TATGTATGTATGTAT | 16443 |
| rs212946175 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798867 | GAAGACCTGAGAGAT[C/T]TGGAACAGTCTGCTT | 16443 |
| rs212971921 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91753574 | CTTGCAATATATTTT[A/C]ATATCATGTAATTTT | 16443 |
| rs212978732 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91813986 | GCAGTAGGACTAGTG[A/G]TATAGAGCGTGTACG | 16443 |
| rs213004706 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910408 | AGAATATGATTTTTT[A/T]AAAATTTAAGTACAC | 16443 |
| rs213011998 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91897574 | GCTGGGATTTGAACT[C/T]GGGACCTTCGGAAGA | 16443 |
| rs213025557 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91865821 | CCTGGTCCATGTGTC[C/T]CTCTGCTGTCCAGAG | 16443 |
| rs213029242 | in-del | -/CACACACACACA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890916 | ATACACACACACACT[-/CACACACACACA]CACACACACACACAC | 16443 |
| rs213030012 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91805621 | ATTATTAAATAATAT[A/G]TAGAATATGAGACGG | 16443 |
| rs213030147 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91797184 | ATGCTGGGATCACAC[C/T]CTGGATGCTGCTGCC | 16443 |
| rs213032639 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91847231 | AGGGAGTTCCAGGAC[A/G]GCCATGGCTACACAG | 16443 |
| rs213040520 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916209 | TGCCACGTACTCCCC[A/G]TGGGGGTTTAGGGGA | 16443 |
| rs213071161 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91864383 | AGAGCACATAGATGG[C/T]GGCTGGACTGGGTGT | 16443 |
| rs213075879 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91902707 | ACAGTGTCATCAACT[A/G]TCTGTTTTGTTATAC | 16443 |
| rs213093076 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91804815 | ACAGCGAAAACTTCA[G/T]TCTGTGCCTAAATCT | 16443 |
| rs213095697 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91846494 | TCGTTAAAATGAGCT[A/G]ACCCCACAAGAGTAA | 16443 |
| rs213104765 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91874543 | CCCATCATGCTGCAG[A/G]GCACGGAAAAGATGT | 16443 |
| rs213109856 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91854144 | TTTGGACTCTTTATG[C/T]CCAGTATGGTACCAA | 16443 |
| rs213122206 | in-del | -/CAGGTCCCTGTGCACATGTGCAGCAGCTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91890048 | CTGCCACGGTCTAAC[lengthTooLong]CAGGTCCCTCGGTCT | 16443 |
| rs213129661 | in-del | -/AATA | | | intron-variant | Itsn1 | Mm_Celera | 16:91763809 | ACAAAGTTAGGAGCT[-/AATA]AATAGGTCATTTCTT | 16443 |
| rs213139876 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91819628 | CTGGAGATGTTGTCT[C/T]AGGGTTTTTATCACT | 16443 |
| rs213141086 | in-del | -/TG | | | intron-variant | Itsn1 | Mm_Celera | 16:91805697 | GTTTTAAAGATTTCC[-/TG]TGTGTGTGTCTGTGT | 16443 |
| rs213156385 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91865512 | CTTTTCTTTTCTTTT[-/C]TTTTTTTTTTTCTTT | 16443 |
| rs213163500 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768537 | CGCTCCAGTTGTTGC[A/G]GGACCCTCCTGGAGA | 16443 |
| rs213189523 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783972 | CATGCTTACAGCACA[A/G]CAACAGAACTTTAGA | 16443 |
| rs213199322 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91768044 | ACAAACCTACTTGAA[A/G]GTAGAATTCTAGATA | 16443 |
| rs213206662 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91902353 | GTTAATAGGGCCAAG[A/G]AGGATGTGGACCTGT | 16443 |
| rs213234804 | snp | C/G | | | missense | Itsn1 | Mm_Celera | 16:91818452 | TTCGAGCGAGGCAGT[C/G]TGGAGCTGGAGAAGC | 16443 |
| rs213238792 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91908618 | AAGGATGAAGGGCAG[A/G]TTCCAGGGGCAAGAG | 16443 |
| rs213247409 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91833612 | AATAGGACCCTGAAA[C/T]CCCCCATTTCTGAGT | 16443 |
| rs213252703 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91825726 | TAGTCCTTATAAATA[G/T]ATTGAGACTTTGGAT | 16443 |
| rs213266704 | snp | C/T | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91727925 | TGCAAAACTCAGCTA[C/T]TGTGGACTGGCTATA | 16443 |
| rs213275220 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91767319 | ATGGTTCTGTGGTAA[A/C]GGAGCCAGCTGTCAT | 16443 |
| rs213277204 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91775931 | GAGTGTTTATGAAAA[A/G]CTCTTCTGAATCCAT | 16443 |
| rs213282438 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91850363 | TGAGACTGAGGTTGA[A/G]GGTGCCCAAGACTCC | 16443 |
| rs213305977 | in-del | -/GGGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91856427 | CCACAGCCGTGTGCA[-/GGGC]GGGCGGGCGGGCGGC | 16443 |
| rs213323299 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91755802 | TAGAAATGGAGGGCA[A/C]ACCTGTGGTCCAGGT | 16443 |
| rs213323983 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91800913 | TAGTTCCCTGGAGTT[A/C]TGGGGTTGTGAGCAT | 16443 |
| rs213325260 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91840078 | TTGCTTACATTAATC[A/G]AGCTGAGATGTCTGT | 16443 |
| rs213326091 | in-del | -/AAAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91770314 | AGTTTTCACAAAACA[-/AAAC]AAAACAAAACAAATC | 16443 |
| rs213385580 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91892989 | ACACCTTCATAGGCC[A/T]TCTCCATAGGGACAC | 16443 |
| rs213387609 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91763168 | CAAGGACTCCTCTTT[-/A]TACAGGGTGGTTTTT | 16443 |
| rs213388052 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899354 | CTGAGCCTGAGGCTG[C/T]TCACTGCTGCCAACA | 16443 |
| rs213397001 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91815575 | GAAAGAATTATGCAT[C/G]CATTCCAAACCTAGC | 16443 |
| rs213401182 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91808530 | AGGAATTTTTTATGT[A/G]TTTATGTAACATACA | 16443 |
| rs213415512 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91755224 | CTCTCTTACTATGTG[A/G]GAGTAGCACAGGTTA | 16443 |
| rs213448145 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91763880 | AAAATCATTTCTTTT[C/T]GCTTTAGCGTTTAAT | 16443 |
| rs213457252 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91814825 | GATGATCATTGGATT[A/G]TTAGAATGAGGTGGG | 16443 |
| rs213457316 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91821845 | CTCTGGGGATATCTG[A/G]GGAGCGAGCTCAAGA | 16443 |
| rs213463833 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91867396 | GTAACTTTTCAAGGT[C/T]GGTTTAGCCATCTCA | 16443 |
| rs213467223 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91753057 | TATGAAGAGGACACT[G/T]TGCTTAGGGGAAGAA | 16443 |
| rs213493557 | snp | A/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91917259 | TAGCTGTAGTACCAG[A/T]GCTGGGGATGTGGAG | 16443 |
| rs213525651 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91875780 | CAGGTTGTTGGCAGG[C/T]CCTTGCAGGCAATAA | 16443 |
| rs213525658 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91866833 | ACAGTGGTTAGTACT[A/G]AGGGCTAGACTTAGA | 16443 |
| rs213534417 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91874950 | CCTCTCCTAGAGCCT[C/T]GCCCTCAAGCTGCAA | 16443 |
| rs213552818 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91821218 | TGTCTTACATGAATG[A/G]CCTGAAAATAATTTT | 16443 |
| rs213579567 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91731890 | TACTGCTGGCATTAG[A/G]TCCTGGGGCCTTGTG | 16443 |
| rs213585021 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91760797 | CCTCTGGAGCCCCAC[C/T]GACGCCTCCTGTGGA | 16443 |
| rs213613093 | snp | A/C | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916885 | CACAGGAAAATACAA[A/C]CCGTGAGAAAGATGG | 16443 |
| rs213616152 | snp | A/G | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91863411 | CATTTAAAGTTCTCT[A/G]TCTAAGCATGAACAC | 16443 |
| rs213617588 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91769852 | GCTCCAGTCAACCCC[C/G]CTTGCTCTGGCCCAA | 16443 |
| rs213626762 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91812339 | AACTTACTTGTTTTC[A/G]TTTCATGTGCATCGG | 16443 |
| rs213634503 | in-del | -/CCTTGGAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91834601 | CTACGAGCTCTGTTT[-/CCTTGGAG]CCAGTTGAGGCTGCA | 16443 |
| rs213648835 | in-del | -/GATGCAGCCCTTG | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91918380 | AGTGGCAAATGGTTT[-/GATGCAGCCCTTG]GATGCCCGGAGTGTG | 16443 |
| rs213665205 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91731165 | TTTAAGTGGCTGCAG[A/T]AAGGCACCTCTCAGA | 16443 |
| rs213665246 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91739634 | CTAGGTTCATCCATG[C/G]CCCTGAGGCCAGACA | 16443 |
| rs213695553 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91882261 | TGTAGTTCCTGAGAC[C/T]GTGTTTCTCAGAGAC | 16443 |
| rs213696372 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91841302 | AGTCCTGGCGGCTTG[C/T]TTGTGGGATCTGCTG | 16443 |
| rs213699152 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91818948 | TGTCTTGTCTGAGTG[C/T]ATTGCTACAAAAGCA | 16443 |
| rs213702622 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91738675 | GAAGGTTGCTGCAGG[C/T]GCCCAGTGTGCTGTT | 16443 |
| rs213704676 | in-del | -/GTACTCACAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91787135 | ATGCTGCACACATAA[-/GTACTCACAT]GTGCCCCTCGTACCC | 16443 |
| rs213708789 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91792095 | GAACTACAGACAGTT[G/T]TAAGCAGGTGCTGGG | 16443 |
| rs213719027 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91828138 | AAACATGAAAGTTGA[A/C]CATGTTCCACACTGT | 16443 |
| rs213724666 | snp | G/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914652 | GTCACCCCTGAGAAT[G/T]ATCCCGAGAGCTCTG | 16443 |
| rs213726142 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91791581 | CACGCTTAGAAGTTC[C/G]GTAATACAATTAAGT | 16443 |
| rs213741470 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91834860 | AATATAGAGAGGAAA[C/T]TGCGTAATTCTTTGG | 16443 |
| rs213747200 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91872748 | TCTTCAGTTTGTGTG[C/G]CCTGCAGAGAATCCA | 16443 |
| rs213754453 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91893989 | AAGTAAGGGTGACCC[A/T]GGGGACTCTCTCCAG | 16443 |
| rs213791106 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91893349 | GCAGAAGGGATACTT[C/T]ACATGATCATTTTTA | 16443 |
| rs213808383 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91840757 | AAGCCCCTGTGACTC[G/T]TCAGTGTGAACTAGG | 16443 |
| rs213828278 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91839557 | GGGTGAAGGGGTGAT[-/G]GGGGGGCGACTGTTG | 16443 |
| rs213839893 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91888758 | GACCCATGGCTTGTC[A/G]GGTTGTAAAGAAGGT | 16443 |
| rs213864902 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91847943 | CAGGTCACATGTATA[A/G]ACGTAAGAATAGGAC | 16443 |
| rs213878778 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91847407 | CTACACGCATAGCCC[C/T]GTTTTTCATCAGACT | 16443 |
| rs213897235 | in-del | -/TCTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91754623 | GAATGTCTCTCTGTC[-/TCTG]TCTCTGTCTCTCTCT | 16443 |
| rs213899385 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91762763 | ATTCATCCCGTTAAT[C/G]TTAAGTTTCAAGAGG | 16443 |
| rs213933657 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798941 | CTGGGTTTGATCTCT[G/T]GTGTCACAGGGGAAA | 16443 |
| rs213936088 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91761573 | GTTTGGAGTTCTTTG[C/G]CTGTGCCTCATCTGA | 16443 |
| rs213940342 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745902 | AAGAAAGAAGAGGGC[C/T]AGCTAGCTGCATGAT | 16443 |
| rs213953979 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91813858 | TCTTCAGCTCATTAA[C/T]TGATATATTTTAAAA | 16443 |
| rs213964828 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91904267 | GCCTTGAAGATCAGA[C/T]ACTTCCTGGTTTCTT | 16443 |
| rs213968017 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91857155 | GAATACTGTGAATGT[A/C]AAATTGGCCAATGGA | 16443 |
| rs213994623 | in-del | -/GCGTGATAGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91862341 | TCAGATTTCAGGACA[-/GCGTGATAGG]GCTGCTTAAAGGAAC | 16443 |
| rs214002840 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91910907 | GGCCCAGAAGAAAGT[A/G]TTGGATCCCCTGGAA | 16443 |
| rs214007175 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768579 | ATCTGCTACATTCAC[A/G]CGGGCGGCCTAGGTC | 16443 |
| rs214011104 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91819657 | CTACAACAGAACAGC[A/G]TGACCAAAAAAGCAA | 16443 |
| rs214029554 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91754326 | GACGTCACTGCAGCT[C/T]TTGGGACCAAACACA | 16443 |
| rs214034473 | in-del | -/AGGAAACACTTCCG | | | intron-variant | Itsn1 | Mm_Celera | 16:91844176 | TCCCTGAAATGGTCT[-/AGGAAACACTTCCG]AGTCCCAGGACTTCT | 16443 |
| rs214052476 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915234 | CTGGAAAGGGTGATC[A/G]CAGGTTGGTCTTCCA | 16443 |
| rs214069506 | in-del | -/AAACAAAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91765765 | AAACCCTGTCTCGGA[-/AAACAAAC]AAACAAACAAACAAA | 16443 |
| rs214084024 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873701 | CCCTAAAATATTCCA[A/G]GAGAATAGTTCTAGA | 16443 |
| rs214086168 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768133 | TGATTGGTTATGAGG[A/G]AATTTTGAACCTTTC | 16443 |
| rs214091560 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91873040 | CATTCTGTAAGCTCG[C/T]CTCCTGTGTCTGTGG | 16443 |
| rs214093967 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91855874 | AATGTCCAACTTCCT[A/C]ATTTTCCTTATTCCC | 16443 |
| rs214095322 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91880702 | TTGAGGAACATGTCA[A/G]CAACAACAAAATTAG | 16443 |
| rs214100462 | snp | A/G | | | upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91729061 | GAAACCTCTAGTTAC[A/G]CCTTCAAGGGACGAG | 16443 |
| rs214115045 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91818993 | GAACCAAATATCAAG[A/G]CAAGGTTTTCCTTAT | 16443 |
| rs214138734 | snp | A/G | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91728069 | TGGGATAATTCTTTA[A/G]TATGGCTCAAGTATG | 16443 |
| rs214152365 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91880158 | TGTTGTTTCTTAACC[G/T]GGGCTTTATCAAGCT | 16443 |
| rs214170052 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91865513 | CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTCTTTT | 16443 |
| rs214178349 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91827361 | TTGGCACATTACCAC[A/T]GAAATTCCAAATAGT | 16443 |
| rs214181111 | snp | C/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914662 | AGAATTATCCCGAGA[C/G]CTCTGAGGACAGAAG | 16443 |
| rs214199392 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91903369 | AAAATAAATCTTTTT[A/T]AAAAAACCAGTAAAA | 16443 |
| rs214220372 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91737145 | GGGAAGTAGCACTTA[C/T]TTTTGTGCCTGTTCA | 16443 |
| rs214221799 | in-del | -/A | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830708 | AAGACTGAGGATTTT[-/A]TAGTCTTTCTATACA | 16443 |
| rs214243833 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91910133 | GTGGAGCAAGAAGGA[C/T]ATTGGCTAACAGCAG | 16443 |
| rs214249853 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91839445 | CTTCATTTTGCTCAG[C/T]CAGAGCTCGGAGAAC | 16443 |
| rs214257069 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91834548 | CAGGCTGCCACGGCC[G/T]CCTGTTAATGTTCTT | 16443 |
| rs214258660 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91736389 | AGTGCTTCTTACCTA[A/C]CCCTGAGTGGTAGAA | 16443 |
| rs214267097 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91790197 | GGGTTTACCATACAC[G/T]TGTCCTTCTGACGTA | 16443 |
| rs214273221 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91881720 | TGCCTGTGATGTTGA[C/G]TGGTTCCTAATAGAA | 16443 |
| rs214275406 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911228 | TGAAGAGAGCAATGG[C/T]GGTGTACTCATATAA | 16443 |
| rs214280943 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91796638 | CACTACCAGTGAAAA[C/T]TGAGCATGGATGGGA | 16443 |
| rs214332011 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91888355 | TGTCTCAAGACGTCT[A/G]CCTGCTATTACATGT | 16443 |
| rs214333035 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91776792 | TGTTTTTTAGAGTTT[A/G]TTGTATTTGACGAAA | 16443 |
| rs214341707 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91795970 | GTAGGCTCCTTCCTG[C/T]GACTTCTCACCTTAT | 16443 |
| rs214344891 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91897359 | TAGTATCGTTAGAGC[A/G]CAGTTCTTGCTCCAT | 16443 |
| rs214350102 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91768167 | AAGGTATGAAATTGG[-/A]AAAAAAAATGAGTTT | 16443 |
| rs214362320 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91838935 | TGTGCTCTCAGGCCA[A/G]GAGAGGGCAGTGAAC | 16443 |
| rs214363865 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91846231 | GCCTGAGACTCCCTC[A/T]TAAAAGCCACAGTGG | 16443 |
| rs214382303 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91896922 | TCTGAGCCTTAGAAC[A/T]AAAGACAAAAGTGTG | 16443 |
| rs214401447 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783604 | GCGTACGTACTTTGG[C/T]CATTAGTTTTATCAG | 16443 |
| rs214411002 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745642 | AACTGTGCGGTGTCC[C/T]TGCCTCACCAACAGG | 16443 |
| rs214423304 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91826417 | TGACTGAACACATTT[A/G]GTACCAAACACAAGA | 16443 |
| rs214424163 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91845684 | GATGGCTGGATAATG[C/T]ACCCCAGGGTAGGAG | 16443 |
| rs214456213 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91759775 | TACTTTGATTTCCTC[A/T]GCAGTATTAGTGTTT | 16443 |
| rs214465492 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91887676 | AGAGGACATGCTCAC[A/G]TTTTTTTCCCACACA | 16443 |
| rs214493111 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91833476 | CTCAGCCTCTGTTGC[C/T]GGTCCTCTTCCTCTT | 16443 |
| rs214495457 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91767137 | TTATGTGGCGGACGT[A/G]ACCTATTCTATGATG | 16443 |
| rs214511779 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91901696 | AAGTACCGGTAACTC[C/T]GGTTCCAGGGGACCT | 16443 |
| rs214513364 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91753658 | TATCACGTTTTAGGT[A/G]GTTAACCTTTTTTGT | 16443 |
| rs214526371 | in-del | -/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91887886 | GTTGGCTCCTGAGGA[-/C]AACAGCTAGCTGCAC | 16443 |
| rs214550282 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91855327 | TTGGAACAGTTACTT[C/T]AGTGGAGGCAGCAGA | 16443 |
| rs214567996 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91805888 | TCCAGCCCCTAATTT[A/C]CTTCTTGAAAGATGT | 16443 |
| rs214578243 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91766374 | TTAGATGGTGCTTGG[C/T]GCCTGTTTTTAAGTG | 16443 |
| rs214595897 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91824735 | CTCCCTCCCCAGCCT[C/T]CCTGCTCTCTCCCTC | 16443 |
| rs214595952 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91817687 | AAAATCTTGGTATGT[G/T]ACTCAAGCTAGCCGA | 16443 |
| rs214596788 | snp | C/T | | | utr-variant-3-prime, intron-variant | Itsn1 | GRCm38.p3 | 16:91871280 | ATGGCGCTCCTGGTC[C/T]GTGTGTGTGTTAACT | 16443 |
| rs214599626 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91744496 | TTGAACTCAGTTCCT[C/T]TGGAAAACAATCAGT | 16443 |
| rs214616611 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91902837 | GAAAAACATCCTCTC[A/G]TAAGACAGAGTCCAG | 16443 |
| rs214657706 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91878881 | CCAGACCCCTCTGAA[A/G]CCATTGCCTCAGGGT | 16443 |
| rs214663346 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91909456 | CTTTGGCCCCGCCCT[C/T]GGGGCAGCTTGGCAC | 16443 |
| rs214671527 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91878585 | TGGCAGAGAACCCAG[C/T]ACAGAGCCTGTGCTG | 16443 |
| rs214682497 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91864553 | GCCTCTTAGGAGTTA[C/T]TGCTCACTGATGTTA | 16443 |
| rs214683993 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91891966 | CTTCGGGAACATTAA[G/T]GGATGCTAGGACTCT | 16443 |
| rs214693706 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91752924 | CCATCCGCTGGACCT[A/G]TAATGGGACCCAAGA | 16443 |
| rs214694893 | in-del | -/CACACACACA | | | intron-variant | Itsn1 | Mm_Celera | 16:91890917 | ATACACACACACACT[-/CACACACACA]CACACACACACACTC | 16443 |
| rs214696182 | snp | G/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91804537 | ACACTCTGGAAGAGC[G/T]AAGAGTGTCTCTGTG | 16443 |
| rs214703019 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91823892 | ATGCACATTCATGGA[A/G]ATTGATTGGCCATTT | 16443 |
| rs214711149 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91735151 | TCACTTATTCTTAGC[A/G]CCCTGGTCAGTTTTG | 16443 |
| rs214749808 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91788796 | TCTCTATTCCAGGGG[C/G]CCTAGAGAATGCCGA | 16443 |
| rs214756928 | in-del | -/CCTCCATAGGACA | | | intron-variant | Itsn1 | Mm_Celera | 16:91892951 | GACACTGTAGGGATG[-/CCTCCATAGGACA]CCTCCATAGGACACC | 16443 |
| rs214773682 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919984 | GTCCTTGGCAGCCCA[C/T]AAGCTAAAGTCTCCT | 16443 |
| rs214789184 | snp | A/T | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91853621 | GCGTGCATGCGCGCG[A/T]GCTCGGCACTCGCTG | 16443 |
| rs214796580 | in-del | -/TT | | | intron-variant | Itsn1 | Mm_Celera | 16:91896296 | GATTTCTGAACCACA[-/TT]TTAAAAAAAAATACC | 16443 |
| rs214799164 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734709 | ATTGTCCTCCCTGGT[C/T]TCCTTGTTCCTCATC | 16443 |
| rs214800505 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91776127 | TGGGTTTTGTGTTAG[A/C]GACAGGAGATGAATA | 16443 |
| rs214800781 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91743485 | CGTTCACATGATACT[A/G]TAGAAGAAAAACTAC | 16443 |
| rs214809481 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91844285 | GCCTCCTCCTCCCCA[-/G]CACTGGGGTCACAGG | 16443 |
| rs214849569 | in-del | -/TTTTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91879150 | TTTTGTTTGCTTGGT[-/TTTTG]TTTTGTTTTGTTTTG | 16443 |
| rs214859731 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91825876 | CTTACAGATCTGTGC[C/G]TTCTGCAGCGGTGGC | 16443 |
| rs214867089 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91865675 | AAATCCTCCAGCCTC[A/G]AGTGGTAGGGTTGCA | 16443 |
| rs214874126 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91759049 | GGAATTACAGGCGTG[C/T]GCCACCACTGCCCGG | 16443 |
| rs214876746 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91833004 | ATCATAAAACTCAAG[A/G]GGGCCAGCAAGTTGG | 16443 |
| rs214885300 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91864682 | TGGCCTGCTGGCTCT[C/T]GAGCAAGAAGTGCCT | 16443 |
| rs214896220 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91813313 | GATTTGCCTTGTGCT[C/G]TGGCAGGGGTGTGAT | 16443 |
| rs214902164 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910364 | AGAGCAGTCAGTGCT[C/T]TTAGCCACTGAGTCA | 16443 |
| rs214903461 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91736841 | TTTTGTTTTGGGAAA[-/G]GATTTCACTGTAGCA | 16443 |
| rs214906271 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91782965 | CTCAACCCAGACTCT[A/G]TAACAGAGCAAAGCC | 16443 |
| rs214941653 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91909555 | CGTCGTCATCCCAGT[C/T]GAGCAGGGTGCATGC | 16443 |
| rs214944754 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916134 | GGGAGACAGGGCAGG[C/T]GGTCAAAGAGAACGT | 16443 |
| rs214968564 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91887049 | TCCGTGCTTCTGATG[C/G]AGCATGTGTTTGCTA | 16443 |
| rs214968923 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91775040 | TTTAAACTCTCGGTG[A/G]TCCTTCTGTTTCTGT | 16443 |
| rs214971031 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91874242 | AAAGAAAGAAAGAAA[-/G]AAAAAAGTATGGATT | 16443 |
| rs214973669 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91906959 | ACTGCAGTGGTATCA[C/T]CTCTGTGTGGAAGGA | 16443 |
| rs214976761 | in-del | -/CA | | | intron-variant | Itsn1 | Mm_Celera | 16:91764159 | AGTCTACAGGGAATC[-/CA]CACAGAGAGCACAGG | 16443 |
| rs214981425 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915418 | ACCTGAGCCAGCTGA[A/G]ACCGCAGGGAGGATT | 16443 |
| rs214995880 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91860516 | ATTTAATTTACTACA[A/C]GGGTAGGCACTCAAG | 16443 |
| rs215004475 | snp | C/T | | | upstream-variant-2KB | Itsn1, Cryzl1 | GRCm38.p3 | 16:91729192 | TTGGCTCCTTTCTTC[C/T]TTTTTGCCCACCTAG | 16443 |
| rs215021031 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91803168 | TTTTAAATTTATTTA[-/T]TTTTTTGTATATGAA | 16443 |
| rs215022061 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91845124 | CGATGCCTTGAGGGA[-/G]GGGGCTAGCAGGACG | 16443 |
| rs215025614 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913674 | TGAAGATAGTGTTGA[C/T]TTTTGTATCAAGAAC | 16443 |
| rs215029657 | in-del | -/GG | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890780 | GGGCAGCTGTAGAGT[-/GG]GGGGGGGGGGGGGGG | 16443 |
| rs215044290 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91833495 | CCTCTTCCTCTTCCT[C/T]CTCCTCCTCCTCCTC | 16443 |
| rs215044520 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892259 | AATTGAACCTAGCAG[A/G]TAGTAAGTCAGGCCA | 16443 |
| rs215056373 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783900 | GACTGTTAGTTTTCT[A/G]TAAATAATTACTGAC | 16443 |
| rs215068558 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91783078 | GCAGTTGCAAAGAGA[G/T]TGAGAAGGCACCGTG | 16443 |
| rs215071938 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743968 | TAAGAAACCACTGAG[C/T]CCTGTTACTGGTGCT | 16443 |
| rs215080617 | in-del | -/CACACACA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890965 | ACATACACACACACT[-/CACACACA]CACACACACACACAC | 16443 |
| rs215088826 | snp | G/T | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91728131 | CAAGGCCCCATTACT[G/T]CGAACACCCACCCTT | 16443 |
| rs215107750 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91887148 | AGAAAGTCCGAAGTC[A/G]GGGTGCGAGCAGAAT | 16443 |
| rs215109103 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91892873 | TAGTGGAACCTCCTC[A/G]AAATTGCTTAGCCTT | 16443 |
| rs215117265 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91752186 | TAACTAATGCACCTG[C/T]TCCTGTCTGCAAGTG | 16443 |
| rs215129332 | in-del | -/TTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91794388 | CCCTTACAGTTTGCA[-/TTG]TTGTTGTTGTTGTCC | 16443 |
| rs215141818 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91839967 | GGTTTGGGGAAAGTT[C/T]TCACTCTGTAGACCA | 16443 |
| rs215149035 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91833049 | AGTTCAGTCCTTGGA[A/G]CCCAAGTGACAGAAA | 16443 |
| rs215160218 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91780947 | GGCAGAGGGGAGGAG[C/T]GGTGGCTGGCACAGG | 16443 |
| rs215190289 | snp | G/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830840 | TTATCTGATAAGCTA[G/T]GGAAAGTCTTGAGTT | 16443 |
| rs215195203 | snp | A/G | | | intron-variant, synonymous-codon | Itsn1 | GRCm38.p3 | 16:91853198 | GTTCCTTGCACACAA[A/G]GTTCCTCACTAGAGA | 16443 |
| rs215212985 | snp | A/C | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803866 | GTGCTCAGCAGCAGC[A/C]CCAGAAAAGAAACAC | 16443 |
| rs215219119 | in-del | -/TTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91758920 | TTTGTTTCTTTGTTT[-/TTG]GTTTTTTCGAGACAG | 16443 |
| rs215244944 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91752946 | GACCCAAGAGTTTGC[A/G]CTTCTGGAAAGTTCT | 16443 |
| rs215245234 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91826224 | TTGTTTGTTTGTTTG[-/T]GAGTCTCACTCTAGC | 16443 |
| rs215252396 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91801329 | GTTGAGTGTTGAAGC[-/T]AGATCCGAGTGTATT | 16443 |
| rs215266074 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91861528 | GAAAGTCCTTGCTGG[C/T]GCCTGTTAGCACATA | 16443 |
| rs215278119 | in-del | -/AAAAAAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91738245 | CTTTGTGAAAAAAAA[-/AAAAAAC]TCTTTAAAAGCACAG | 16443 |
| rs215286772 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91811762 | GGTTTCTCTGTAACT[C/G]TTCTATACCCATTTT | 16443 |
| rs215294747 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91768986 | CCTGCTGCTGACAGC[A/C]GCTGTGCTTCAGCTT | 16443 |
| rs215300554 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91874463 | AGGGTGCAGCTGGAA[G/T]CGGATAGTGCTGTAT | 16443 |
| rs215302237 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91804746 | AATCTGTTGACTCTC[A/G]GGGACTTTACATTGT | 16443 |
| rs215313378 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91812318 | CTAACAGTTCTTTCT[C/T]TTAATAACTTACTTG | 16443 |
| rs215313482 | snp | A/G | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803890 | GAAACACAACTGGAC[A/G]GACTAGAACAGTCTC | 16443 |
| rs215323950 | in-del | -/ACACACACACAGAC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91807586 | CACACACACACACAT[-/ACACACACACAGAC]ACACACACACAGACA | 16443 |
| rs215324991 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91760711 | CGGAACCAGGTGTTC[A/T]GCTACCCGAGTCTCT | 16443 |
| rs215337577 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91820240 | ATGTTTACTTAGCGC[A/G]CTGTGATTTCTGGGA | 16443 |
| rs215344473 | in-del | -/AGAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91779417 | ATGTGAGGCAAGGAC[-/AGAG]AGAGATAGGAGCTTC | 16443 |
| rs215345122 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907736 | GCAGAATTCTGGGTT[C/T]GATGCCTAGCACCAC | 16443 |
| rs215362705 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91759933 | TATGTCCATTAGTAA[A/G]GTTAACTCACAGGGC | 16443 |
| rs215369448 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91881486 | AGAGAAACCAGTCCA[G/T]GATGCCAGGGTCTCC | 16443 |
| rs215377785 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91863025 | GGGCAGGCAGGATGG[C/T]GGGGAGCTGCTGAGT | 16443 |
| rs215380321 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91757803 | TACAGAGTGCTTCCT[-/G]TAATAAGTATCTATG | 16443 |
| rs215380647 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91908584 | AAGTGGGGCTAGGTG[C/T]AAGGCAGGGCGCAGT | 16443 |
| rs215392331 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914066 | GATGTTGAACATCAG[C/T]GTTCCTGTAGGAAGG | 16443 |
| rs215412883 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914592 | TCTGACCTCCTCTCA[C/T]TCAGGAAGGCACTTT | 16443 |
| rs215412944 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907859 | GAGTTTATCACCAGC[C/T]TGGACTACAGTATAT | 16443 |
| rs215415033 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91827092 | TAAGAGGTCCCTGAA[C/T]CCCTCTATTGAGTTA | 16443 |
| rs215434757 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91861661 | TACCAAATGATAATC[A/G]TGCTTCAGAGTCTAG | 16443 |
| rs215440872 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872666 | ACTTTCAACCCTCCG[A/G]TCCCCTCTCATGGTT | 16443 |
| rs215451648 | snp | A/C | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91871488 | TGCTGACAGTGTGTC[A/C]CGGTGCTGAGGACAG | 16443 |
| rs215493128 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91731193 | AGAGAGTATGTGTTT[-/A]AAAAAAAAGTGTCTG | 16443 |
| rs215507612 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91781360 | TTTTAGAAGAGCTTC[A/T]CGAAGCTCAGTCTGG | 16443 |
| rs215543998 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91791010 | ATTCATTCAGGACCA[C/T]GAGATTCTGTCAACA | 16443 |
| rs215544819 | snp | C/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91832332 | AAACATTTAATAAAA[C/G]GTTATGAGAGAAAGG | 16443 |
| rs215545245 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91843870 | CCTGACCCTCCCTGT[-/C]TGATTCCTGTAACCA | 16443 |
| rs215547834 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914151 | CCCCATGATTGTAGT[A/G]TGTGAATGCAGTCTG | 16443 |
| rs215572108 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91737709 | CCTTGACTGTGTGGT[A/G]CAGGAGCAATGTGTG | 16443 |
| rs215579374 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91838886 | CTGTGCACTAGCTTT[C/T]CTGGCGCTGTGTCGC | 16443 |
| rs215588132 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831702 | CTATTTAGCATCTTC[A/G]TTCAGTGACCAAATT | 16443 |
| rs215599957 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91885731 | GACTCTCTCAGTCCT[C/G]AACCCAGACAAGCCC | 16443 |
| rs215619828 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91781423 | TAAACTCTTGCCTTC[A/G]CCTTCTAAATGCTGT | 16443 |
| rs215620493 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91789414 | TTAATATATCCTCCT[C/G]GTTTTCTCCTCAGCA | 16443 |
| rs215622724 | snp | A/C | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831439 | AACTTTAAGAATTAA[A/C]CTCTGGATGGGGTCA | 16443 |
| rs215623434 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91735257 | TGTATAAAGTTTAAA[A/G]AGCAGCAGTGTGTAC | 16443 |
| rs215629524 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91788885 | TACTCGGCACCACCC[A/G]TACTAATCTGATTTG | 16443 |
| rs215629689 | in-del | -/AAAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91903174 | GACCCTTATCTTAAA[-/AAAC]AAACAGTGGGCTGGA | 16443 |
| rs215637740 | in-del | -/AG | | | intron-variant | Itsn1 | Mm_Celera | 16:91810148 | GGCTCCTGGGTAGAT[-/AG]AGTCAGTTCTCCACG | 16443 |
| rs215654452 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91837940 | GCTTGCTTTGTGTTT[A/G]TATGTTTTTATTTTT | 16443 |
| rs215655410 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745536 | CCTAATTTCAAGTGA[C/T]GGGGCAAGGCATGTT | 16443 |
| rs215656086 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91891902 | CAGCTTGAACCCTGA[A/G]CCCTGTGAGCTACAA | 16443 |
| rs215665391 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91797469 | GTCCTAAGTTCAAAT[C/T]CCAGCAACCAAGTGG | 16443 |
| rs215671077 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91838041 | GGCACACTGTATGTA[C/T]TGACTGCAGCAACTC | 16443 |
| rs215697046 | in-del | -/TT | | | downstream-variant-500B | Itsn1 | Mm_Celera | 16:91920909 | TTCTTTTTTTCTTTC[-/TT]TTTTTTTTTTTTATT | 16443 |
| rs215722678 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91896201 | CAACTCCAGGCAGCT[C/T]AGCCACTCTCCAGGT | 16443 |
| rs215727290 | in-del | -/GGCCCG | | | intron-variant | Itsn1 | Mm_Celera | 16:91851664 | AGGGGAGACGGAGCA[-/GGCCCG]GGCCCTCGGGTCAGA | 16443 |
| rs215740319 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91903284 | ACAAGCATCTGTAAT[-/G]GGATCTGATGCCCTC | 16443 |
| rs215744227 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91844331 | CTGGCTTTTATGTGG[A/G]CTGTAGGGACCCAAA | 16443 |
| rs215757064 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91751434 | AAGCCATTGTAAAAG[C/T]ATCGTTCCTACTTGC | 16443 |
| rs215772483 | in-del | -/CCCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91883087 | TTTAGTTTTGAGTCA[-/CCCT]CCATCCCTGCTCCGT | 16443 |
| rs215792425 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91758978 | CCTGGAACTCACTCT[A/G]TAGATCAGGCTGGCC | 16443 |
| rs215795826 | in-del | -/ATCTATCTATCT | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745386 | GGAGATCGATCATCC[-/ATCTATCTATCT]ATCTATCTATCTATC | 16443 |
| rs215808981 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91768593 | CACGGGCGGCCTAGG[G/T]CCAGCCTGTGGACCA | 16443 |
| rs215813866 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91892239 | CATTCTAGAAAGAGA[-/T]TCTCAATTGAACCTA | 16443 |
| rs215843461 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91873763 | CAGAGAGAGAGAGAA[C/T]GCATAGGAAAATAAA | 16443 |
| rs215877195 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91758063 | GGAAGAGCAGTCAGT[A/G]CTCTTAAATGCCGAG | 16443 |
| rs215893200 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91819716 | CTTGTTTCCACATTG[C/T]TCTTTATCTCCAAAG | 16443 |
| rs215897466 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91816770 | AGCAAGCTTGTGAGA[C/T]AGATAGTCAGCCCTT | 16443 |
| rs215911167 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91765593 | CGGTAGGCGTAGTTG[A/C]GAGGAAGGCTTGCTT | 16443 |
| rs215911975 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91826466 | TGCAGGTCCTGGATT[A/C]CTGGTGAGGTGACCG | 16443 |
| rs215938279 | in-del | -/AAAAAATGACTTTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91807320 | TACTTCCAGATGAGA[-/AAAAAATGACTTTTT]AAAAAATGACTTTTT | 16443 |
| rs215944190 | in-del | -/CAAAAAACAAACAAACAAAC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892773 | AGAAAAAAAAAAAAA[-/CAAAAAACAAACAAACAAAC]AAAAAAAAACAATGT | 16443 |
| rs215945242 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91767918 | GTGAGCCTTTCTACC[C/T]TTTAGTGACAATAAT | 16443 |
| rs215950561 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91818875 | CTGTCTTTATTCGCC[A/T]CTTAACAGAAGGGGT | 16443 |
| rs215960216 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91849959 | AGCTCAGATTTTGTT[-/G]GGGGGGTAACTTGGA | 16443 |
| rs215962903 | snp | A/G | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91853476 | GACAGGGCTCTGGGA[A/G]TGGCGACCGGTTTTT | 16443 |
| rs215992115 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91869153 | GGAGCATGAGAAGAT[C/T]AGGTGACAGCTGCAC | 16443 |
| rs215996493 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91765006 | TAATCTTCATGTGGT[A/G]AGCACAGTAATCGAT | 16443 |
| rs216002513 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91780870 | TTAGACATCATCACC[A/G]AGGCAGCTTATAGAA | 16443 |
| rs216004771 | in-del | -/T | | | downstream-variant-500B | Itsn1 | Mm_Celera | 16:91920606 | ATTCAAACGTGTGGA[-/T]TTTTTTTTTCTGCCT | 16443 |
| rs216005127 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91868444 | TGAGAGCCGTGGGGG[C/T]CTGCTGATCATAATA | 16443 |
| rs216013890 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91816295 | CACTCTGTAGTCCTG[A/G]CTGTCCTAGAACTCA | 16443 |
| rs216059724 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91876825 | TCTCCTCCTTGGGCT[C/T]CCATGTGCCACCTTG | 16443 |
| rs216075424 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919130 | TTCTGGTGTCACAGA[A/G]GAGATTCTAAACTAC | 16443 |
| rs216077528 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91912199 | TCTCTTTTCCTTTGC[C/T]CTCCCTATGGTCTCA | 16443 |
| rs216088967 | in-del | -/CG | | | intron-variant | Itsn1 | Mm_Celera | 16:91825483 | TATCAGATTTCATTA[-/CG]TGGGTGGTTGTGAGC | 16443 |
| rs216092734 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91737172 | TTCAAATGTTCTTTT[A/G]CTATTCTTTTAGTGA | 16443 |
| rs216107585 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91790306 | GCATGGCTGCTGTTA[A/C]GGAGCAGCAGCTGGA | 16443 |
| rs216109986 | snp | A/C | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91918306 | CCTGCGAGACAGGGT[A/C]GCCCTACTTGGTAGG | 16443 |
| rs216111482 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91762413 | GCATCCCATTTTCTG[-/T]TTTTGACACTAGAAA | 16443 |
| rs216130817 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91734107 | AGAAAAGGGCACTGG[A/C]TCCCCTGGAACTGGA | 16443 |
| rs216162308 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91836381 | TCATAAAGGGATTTG[G/T]GAGAATAAAGGCTCT | 16443 |
| rs216167849 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91732966 | CTAGTTCACACTGAC[A/G]GGAAGAATTGGAGTG | 16443 |
| rs216169345 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91787464 | CTTTCCGTAGTCACA[A/G]TCTTCACTGGAAATC | 16443 |
| rs216184804 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91823916 | GCCATTTTCTTGTGA[A/G]TGCCCTCATATAGTT | 16443 |
| rs216186312 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91793491 | GCTTCACTTTGCTTC[A/G]TTCTCCACAGCGGGA | 16443 |
| rs216188218 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91786457 | AAGTGCCAACATTAC[A/G]TAAAATCATGTTCTG | 16443 |
| rs216191896 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91744613 | CCCCAGGGCATATGA[A/G]CTCTGAGCTGTGGGC | 16443 |
| rs216198751 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91774494 | CACCAGCTGGGAGAC[C/T]ACACTGAGTTCCTCC | 16443 |
| rs216200027 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91846411 | CGTGTTCATGTTGAC[A/G]CTCTGTTTTCCAAGT | 16443 |
| rs216212155 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91736169 | CTCTCAACCTCTTCC[C/T]GGTAGATTCAATGAT | 16443 |
| rs216228230 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91890218 | GTGGGGTACCAGACT[C/T]TTGGGCTCTCATCTC | 16443 |
| rs216231245 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91920021 | TCCGTCTGCCGCGGT[A/G]CACACAGGGGCGCAG | 16443 |
| rs216232057 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91796948 | AGGTGACAGCATCCA[A/G]ACCCAGCCTCCAGTG | 16443 |
| rs216255857 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91792953 | CAGATTGCACTTGTC[A/C]ATGGATGCTTGAGAG | 16443 |
| rs216261745 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91843825 | TCCCAGAAAGTAAGC[A/G]GCGGCTTAGGGAAGG | 16443 |
| rs216262023 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91835738 | TACAAATTTCTGTGG[A/G]AGCCAGCGTGGCTGG | 16443 |
| rs216265075 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878661 | CTAAACCAGGAAGAG[C/T]TCTCCATTCTTGTGA | 16443 |
| rs216270718 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91854120 | AAGAATCCCTGAACT[G/T]TTTGAGAGTTTGGAC | 16443 |
| rs216290069 | in-del | -/AA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798420 | AGGAAGGAAGGGAGG[-/AA]GGAAGGAAGGAAGGA | 16443 |
| rs216294517 | in-del | -/TGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91823161 | ATGTAGACAGACGCT[-/TGG]TGGCACCATTGTCTG | 16443 |
| rs216309020 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91843106 | TGGGAACGGTGGAGC[C/T]CAACAGGCTGACTGT | 16443 |
| rs216319169 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91897476 | ATTTATTTATTATAT[A/G]TAAGTACACTGTAGC | 16443 |
| rs216319285 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91823360 | TTAGTCTGACAAGAC[-/G]AGTCATTTTAACACT | 16443 |
| rs216321859 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91775273 | TTGTTTTGTTTTAGA[C/T]AGCCTCTCACCTATG | 16443 |
| rs216339617 | in-del | -/TG | | | intron-variant | Itsn1 | Mm_Celera | 16:91882155 | GACTGGCCCATTCTT[-/TG]TGTGTGTGAGTGTGC | 16443 |
| rs216340961 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91885887 | GAAAGGCTACTTGGC[A/G]AAGTTCTGGTCATTT | 16443 |
| rs216354618 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91825112 | AAGGTGTGTGTGTGC[C/T]ACCATCTCTGGCTTT | 16443 |
| rs216355961 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91832854 | CGTCCATTTTCTTTG[A/G]CTTTGTACTTTTTTT | 16443 |
| rs216364692 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91902276 | TCTACTTTAATAAGT[A/G]TACTTAATTGTTTTA | 16443 |
| rs216365635 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91880045 | TCAAGCCACCCCGTC[C/T]GTGATTGGTCCTGGC | 16443 |
| rs216378111 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91886979 | CAGCGGTCAGCTCCC[C/G]AAACAGTGGCTGGCG | 16443 |
| rs216379798 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91879022 | GATGGTGCCTGTAGA[G/T]ATCAGAAGAAGGCAT | 16443 |
| rs216431254 | in-del | -/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915929 | CACAGTCTCCTTTAA[-/G]AGGGGGGTCAGCACC | 16443 |
| rs216436136 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91886673 | CAGCGTCCTCGCCTG[A/G]AGAGTCTTCCCGGTC | 16443 |
| rs216452784 | in-del | -/AAAACAAAAAACAAACAAACAAACAAAAAAAAAC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892769 | TAGCAGAAAAAAAAA[lengthTooLong]AATGTGGGAGAAAGA | 16443 |
| rs216458624 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91832380 | GAAAGTTTTTTTTTC[A/C]TCCTCTGTATCATTT | 16443 |
| rs216464111 | in-del | -/TTAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91731931 | TAGACTCTCATCCTT[-/TTAA]TTTGCTCAACCTGTG | 16443 |
| rs216467911 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91743087 | CCCTCCCTCTCCCTC[C/T]CCCTTTCTCCCTCCC | 16443 |
| rs216507575 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743951 | ATCCTCACATTTGTA[G/T]ATAAGAAACCACTGA | 16443 |
| rs216508983 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91767170 | GAACGTATAACCAGA[C/T]TCTTGCCTGCCCTTA | 16443 |
| rs216514131 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91794637 | CATGAAGTGTGTAAT[A/C]GTCTTCCTCTGTTGC | 16443 |
| rs216519510 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91749496 | AGAATAAGCTAGGAC[C/T]TTAGCAGTAAATCAG | 16443 |
| rs216542905 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91752121 | TGCACGACAGCTAAA[A/C]TCTCACGGAGAGATG | 16443 |
| rs216544299 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743620 | CTATGGCATTAAATG[A/C]CCATGGCATTAAAAA | 16443 |
| rs216549921 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91818394 | TCCCATCGCTGGTGT[C/G]TCCTTTGTTTAAGTG | 16443 |
| rs216551577 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91852055 | GAGTGACAAAGTGAC[C/T]ATCAGTCTGTGGGTG | 16443 |
| rs216554439 | in-del | -/TT | | | intron-variant | Itsn1 | Mm_Celera | 16:91779015 | TAAATAAAATAAATC[-/TT]TTTTTTTTTTTAAGA | 16443 |
| rs216556491 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91766721 | TTCATCCCCCCCACA[-/C]ACTTATGTTCTTTAT | 16443 |
| rs216558456 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91775211 | CTGTTTAGCTCTTCA[C/G]TTTTTCTTAGCAGTG | 16443 |
| rs216567413 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91881822 | TAACGTCCTGGAGAA[-/C]CCCTACTTTCCACAT | 16443 |
| rs216573565 | snp | C/T | | | intron-variant, missense | Itsn1 | Mm_Celera | 16:91853166 | CCACCCAATGATACA[C/T]GCGGCTGTTTCTATC | 16443 |
| rs216581457 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91802494 | ATGTAAGGCTGCACA[C/T]GATAGCAGCCAACAT | 16443 |
| rs216595509 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91878974 | TAGATTTTATTTCTA[G/T]TTATGTGTATGTGTG | 16443 |
| rs216614965 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803789 | TTTTACAAACAGAAT[C/T]ATGGTAGTACCGGCT | 16443 |
| rs216615004 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795103 | ACTATATGCCTTTCT[C/T]TTAGGGACCGTTGGC | 16443 |
| rs216624802 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91751453 | GTTCCTACTTGCGGG[C/T]GCCATGCGTGTGTGT | 16443 |
| rs216625712 | snp | A/G | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91803472 | CCTACATATACACAT[A/G]TATGTATGTGTACCA | 16443 |
| rs216632080 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91900443 | GGCGGTCACGGGGTC[A/G]GGGCAGCATATTTGC | 16443 |
| rs216633452 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91901460 | GACAACCTTTCCTTG[A/G]CTGGCTCATTCGCTC | 16443 |
| rs216637624 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91825026 | TTTGGCTGTTCCAGG[G/T]ACTGGCTCTATAGCT | 16443 |
| rs216674037 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91905797 | AGGACTGTCCATGTC[C/T]CACACCTTGGTTCCC | 16443 |
| rs216677994 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91852704 | TACTGGCCAGTTATG[C/T]TCCGGCAAGTGCAGG | 16443 |
| rs216686705 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91779561 | TGCTTTGCAGTAAAC[-/G]GGGGAAGGACCGAGC | 16443 |
| rs216730203 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91860493 | CTTTGTCTCATTTCA[A/G]TTGAAATATTTAATT | 16443 |
| rs216751291 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91886649 | TGCTCAGCTTCCACG[A/G]GTACCCCACAGCGTC | 16443 |
| rs216756577 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91860212 | GCCTTGGGAATCGTC[A/C]CACGCTTATGTGCAT | 16443 |
| rs216765704 | in-del | -/C | | | downstream-variant-500B | Itsn1 | Mm_Celera | 16:91920858 | CTGGCTTCAGCCTCT[-/C]ACCGTTTGGAAGCAC | 16443 |
| rs216780433 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91810782 | AGTAATAGAAATGGT[A/G]CCCATCACCTGCTGG | 16443 |
| rs216780536 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91774240 | CCATCCAAGAAGCAA[A/G]CGCTTTTGATTTATC | 16443 |
| rs216785381 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91906742 | TCCTTAATGCCCTTG[C/T]ATTATGACTTTGCAG | 16443 |
| rs216838375 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823235 | GAACGTTATCTTACG[C/T]AATCCTTTACATTTC | 16443 |
| rs216850211 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743565 | CCATTTATGATAAAA[A/C]CTCATCAAACTTGGT | 16443 |
| rs216856605 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91773772 | TAGCAATGCTCTCTG[C/T]CCAGAAATTTGAAGC | 16443 |
| rs216856617 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91740682 | GAAGAGGTAGTGACT[-/G]GACTACCCAAGGGCT | 16443 |
| rs216863658 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91794975 | GCAGGACCGTTGGCT[C/G]TTTTCCTTCTTTGGA | 16443 |
| rs216873347 | in-del | -/TA | | | intron-variant | Itsn1 | Mm_Celera | 16:91838035 | ACACTGGGCACACTG[-/TA]TGTATTGACTGCAGC | 16443 |
| rs216896509 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830791 | TAAAGGTCTTACCCA[C/T]TTTCTTTACCCTGGG | 16443 |
| rs216905556 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91822723 | TCCTATCAGCAAGCC[A/G]GATGACTTGTTTCAC | 16443 |
| rs216922490 | in-del | -/GTGTGTGTGC | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91829386 | TGTGTGCGTGTGTGT[-/GTGTGTGTGC]GTGTGTCGTATCAGT | 16443 |
| rs216922765 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91780923 | TTCCAGAGGGATAAG[A/G]GTAGTGATGGCAGAG | 16443 |
| rs216925614 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830394 | GGCGCGGTCACCCAC[A/G]GGTGCACAGCTGCTC | 16443 |
| rs216935558 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91780341 | CCAGCCTACCGCCTC[A/G]CTGTTAATGTAAAGG | 16443 |
| rs216938567 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91885031 | TTCTCCTATCCCTGC[A/G]GGCAGGAGAACACTG | 16443 |
| rs216940565 | in-del | -/GT | | | upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91729098 | TGGGAGGGGAAAAAA[-/GT]GTGTGTGTGTGTGGG | 16443 |
| rs216941796 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91844966 | ATGTCCCTGTACAAA[C/T]GTGAAAGTCATCATA | 16443 |
| rs216961902 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91852622 | GGAGGAGTCCATGTT[A/C]TAGGCATAAGGAGGT | 16443 |
| rs216962668 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91846978 | CCGGAGCAGAGAACC[-/A]AAGCTTGTTTAGAGT | 16443 |
| rs216982386 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91742731 | AAAGTTAAATGTCTG[C/T]TATAGTGACAGACAG | 16443 |
| rs216991006 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91803351 | CTCTCCAGCAAGACT[A/G]CTTGTTTTTAATGCA | 16443 |
| rs216993562 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830464 | ATTCATTTCATGTTC[A/G]TGGAGGTTATGCACT | 16443 |
| rs216994377 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91884425 | CACTACCTGGGGAGC[A/G]GAGAGAAATAGCAGT | 16443 |
| rs217044351 | in-del | -/GG | | | intron-variant | Itsn1 | Mm_Celera | 16:91799189 | GAGGAGGAGACGGGA[-/GG]GAGAGGGGGTGGTGG | 16443 |
| rs217044896 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91836450 | TGTATGTTGGGGCTG[A/G]GCAAGCTCACAGAGA | 16443 |
| rs217065578 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91884266 | CAGCCTGGGGGGGAA[C/G]GACAGAGTACTATCT | 16443 |
| rs217082289 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91748531 | CACTGTCCTAGACAC[A/G]TCTGGGAAGAGGATG | 16443 |
| rs217085948 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91890251 | TGTTACTGTCTAGCT[A/G]GGTCGTTTTTTGGGG | 16443 |
| rs217106205 | in-del | -/TTCAGGGTATT | | | intron-variant | Itsn1 | Mm_Celera | 16:91844068 | CTTAGGCCATAGACA[-/TTCAGGGTATT]TTCAATTCTGATACA | 16443 |
| rs217115358 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91906650 | TTACTGGGTTGCACG[C/T]ACGCGCGCGCGCGCG | 16443 |
| rs217115831 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91851294 | CCAGTCCATTTGGCT[A/G]CCCCATCAGTCTGTA | 16443 |
| rs217133825 | snp | G/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91801933 | CCAATAAGAGCAGCA[G/T]CGATGGGCAGTATTT | 16443 |
| rs217140936 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91800973 | GGTTGCACTCAGGAC[A/C]TCCTGGGTAGTAGGA | 16443 |
| rs217142898 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91809674 | GTGTGTGCGTGTGCT[G/T]CCACAGAGACTGTCT | 16443 |
| rs217167297 | in-del | -/TCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91769291 | TGGGATCCGACACCC[-/TCT]TCTGGTGTGTCTGAA | 16443 |
| rs217167398 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904951 | GTGCGCCACCATGCC[A/C]GGCTATTCTCATACA | 16443 |
| rs217172790 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91756907 | CTTGAGCTTCCACAT[G/T]CCCAGAGTTCAGCAA | 16443 |
| rs217176854 | snp | A/G | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91747778 | TCGGGCAATGTTTGC[A/G]TGGCATTTCTACTTG | 16443 |
| rs217180681 | in-del | -/AGGGGAGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91905740 | AGCCAGGATAGAGTA[-/AGGGGAGG]AGCTAAAATAGAGTA | 16443 |
| rs217211096 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91755926 | GAAAGCTTCGGCCCA[A/G]GCAAGGTAGTACACA | 16443 |
| rs217212145 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91740830 | AGGACAGGACTGACA[A/G]GGTCCCTGTCCTTAC | 16443 |
| rs217232799 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91858844 | CGGTCCTCATAGGTT[A/G]GAAATGGCTCCTTAG | 16443 |
| rs217250839 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91773475 | AGTGTAAATACCAGA[A/G]CTCATAGATCAGTAT | 16443 |
| rs217261717 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904534 | CTTTGAGGGGGTCAA[A/G]TGCACCACCGAATTC | 16443 |
| rs217262248 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91877320 | CAGGGACATGTGGCA[G/T]GGCAGGCTCGGTTAC | 16443 |
| rs217285732 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911304 | CAACAACAAAAAAAC[G/T]TATGTCCATGAGCCT | 16443 |
| rs217286515 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91857781 | GAACCGTATTTGAAA[A/G]TCTTCTAAACTGTAG | 16443 |
| rs217289903 | in-del | -/TT | | | intron-variant | Itsn1 | Mm_Celera | 16:91906991 | GTAGTATATATACTG[-/TT]TTTTTTTTTAAAGAA | 16443 |
| rs217290307 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91823133 | TGAAGATGAGGGTTG[A/G]GACTGATCTTTCCAT | 16443 |
| rs217296969 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867511 | ATTAACTAGAGCATC[A/G]GCATCACCCGAGTCT | 16443 |
| rs217314148 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91779380 | GAGTGTCAACAGTCA[C/T]AGGTGCTTCGGACAC | 16443 |
| rs217339881 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91884882 | GGTATTTCGTATAGT[A/G]CATAGGGCTTTTTAT | 16443 |
| rs217340249 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91779053 | CTTGTCTGCATTGTG[A/T]TTACTACAGTAAAGG | 16443 |
| rs217353580 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91883725 | AGGGCAAGGTGTACC[A/G]CAGCCCTCAAGTGCA | 16443 |
| rs217359575 | in-del | -/AAAAC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890389 | GACTATAACAAAAAA[-/AAAAC]CCCTGAGGCTACCCT | 16443 |
| rs217366702 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91786284 | AAGCCAGCAAACAAA[C/T]CCCAGGAAGGTAGGG | 16443 |
| rs217370206 | snp | G/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830774 | TAGACTCATTCTTCC[G/T]CTAAAGGTCTTACCC | 16443 |
| rs217375410 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91855882 | ACTTCCTCATTTTCC[-/T]TATTCCCTTGCTTAC | 16443 |
| rs217398220 | snp | A/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91829341 | GCCGACGTGTGTTTC[A/T]TTTCACATTGCTTTC | 16443 |
| rs217398935 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889594 | GAGAGTGTGAGAGTG[C/T]GGGATGACTCTCCAC | 16443 |
| rs217407993 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91888926 | CCTCCTCAGAGGTTC[G/T]CCTGGACTCCCCTTG | 16443 |
| rs217429319 | in-del | -/CT | | | intron-variant | Itsn1 | Mm_Celera | 16:91870036 | CCTCCTTCCCCTCCC[-/CT]TCCTCCTTTTTCTTT | 16443 |
| rs217437162 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914201 | ACCCTACTAGACACC[C/T]CTGGGTTGTCCTGAG | 16443 |
| rs217438215 | in-del | -/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91869976 | AACTATCTCGTGGGG[-/T]TTTTGGTTTTGTTTT | 16443 |
| rs217446984 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91894049 | CAAAAGTCCACAGGC[A/G]TCTTTCCACTAGTGG | 16443 |
| rs217447199 | in-del | -/TT | | | intron-variant | Itsn1 | Mm_Celera | 16:91870061 | TCTTTTCCTGGTTTG[-/TT]TTTTTTTTTGTTTTT | 16443 |
| rs217457173 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91835586 | TTAGTGTCCCTCCCA[A/G]TTACTCCTGTGTTCA | 16443 |
| rs217463143 | snp | C/T | | | intron-variant, synonymous-codon | Itsn1 | GRCm38.p3 | 16:91828354 | TCCTGGGTGCTGGGC[C/T]GCCTCCCCTTTGCTT | 16443 |
| rs217466555 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91741551 | TTCCCCACCCATACC[G/T]TATCTGGTGCAGTGG | 16443 |
| rs217468101 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746454 | TGGTGAGTTTTATGT[A/G]TGCTACATCGTTATT | 16443 |
| rs217496196 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91755087 | CTAGTCGTCCACCTT[G/T]TTATCATATCTGTTC | 16443 |
| rs217496463 | in-del | -/GGGGGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91875576 | CCTCCTCTCTGGCAT[-/GGGGGG]CAGGGGGCTCACCTG | 16443 |
| rs217499559 | snp | G/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745969 | ACACAGTGCTTGCAA[G/T]TCAACATTAAAAGGA | 16443 |
| rs217524247 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91856839 | AGCTGTGAGGCCAGC[A/G]GTCAGTGTTGGGTGG | 16443 |
| rs217530814 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91893489 | GGCTCAATGCTCAGA[C/T]TGAGCCAGCCTTGGA | 16443 |
| rs217535746 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91782929 | GCCCAGCTGAGCACG[A/C]TAGGCAAGCACTGGG | 16443 |
| rs217539012 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91792056 | AGCAGGCCAGAAGCA[-/G]GTGTCAGAGCCCCCC | 16443 |
| rs217541497 | snp | C/G | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91871840 | TGCCTAGCATGGAAG[C/G]CTACCGGCCAGCTTA | 16443 |
| rs217547647 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889792 | TTGGACTATAAATGG[A/G]CCGCAAAGATCTCCT | 16443 |
| rs217551940 | in-del | -/AC | | | intron-variant | Itsn1 | Mm_Celera | 16:91807666 | CACACACACATACAT[-/AC]ACACACACACACACA | 16443 |
| rs217553942 | in-del | -/AACA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911293 | ACCGCCAACAACAAC[-/AACA]AAAAAACGTATGTCC | 16443 |
| rs217562990 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91754522 | GCATCTTGACCTCCA[A/G]ATCCTCCTGCTTCAG | 16443 |
| rs217563634 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91748436 | AAGCTCTTGATGTAC[C/T]AGCATGTGTTTGGGT | 16443 |
| rs217566381 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91834902 | ATCTCGGTTTGATAG[A/C]TACATTGGGACGTCA | 16443 |
| rs217575984 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91737127 | CAGTTAGCATTGGCC[A/G]ATGGGAAGTAGCACT | 16443 |
| rs217618917 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91856071 | TCGGTGGCTTCTGCT[C/T]TGACATGAGCAGCAG | 16443 |
| rs217631958 | in-del | -/CTC | | | intron-variant | Itsn1 | Mm_Celera | 16:91832504 | GTATTAGGTGGCATG[-/CTC]CTCTATGATGGCATA | 16443 |
| rs217638544 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91851143 | CCAGAGTTCAGAGGG[C/T]TTAAACTCTCCTGCC | 16443 |
| rs217659131 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91918749 | GGCTGCGCGGAGCTG[A/G]GATGGAAACACATCG | 16443 |
| rs217670879 | in-del | -/GG | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919038 | CTCTGGATATCAAGT[-/GG]GGCCTTTGAGTCTTC | 16443 |
| rs217685143 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917697 | GCCCAGCGTCCCTCC[A/G]GGATTTCTGGGGAGC | 16443 |
| rs217729130 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91807247 | TCTGTTACACAGAAC[C/G]TTTTAATTGTGGTTC | 16443 |
| rs217737733 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91793888 | CCTTCAGAAAGATAG[C/T]GCTGTCTCCCATGAA | 16443 |
| rs217738399 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91806619 | CTTTGGATATCATTT[C/T]TTTGTCTATGAAAGG | 16443 |
| rs217741346 | snp | G/T | | | intron-variant, upstream-variant-2KB | Cryzl1, Itsn1 | GRCm38.p3 | 16:91727364 | ATTGTACATTGCAGT[G/T]GCTGATGCCTAAGAT | 16443 |
| rs217745053 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91903996 | TCTCAAAGCCCCGCC[C/T]CCACAGTGACGTACT | 16443 |
| rs217762105 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91838365 | GAAAATACTTTTCTA[C/T]AAATAGAATATGTGA | 16443 |
| rs217781286 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91736327 | TGACCATCAAACCCT[A/G]TCTCACAGTTGCGCA | 16443 |
| rs217799312 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91813905 | GTCCTGGTTGGCAAC[C/T]CAGCGTGTGTGCCTC | 16443 |
| rs217809104 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91788909 | TGATTTGTTCTAAAC[A/T]AAAAGGTAGAGACCG | 16443 |
| rs217849532 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734170 | CTAGGAATTGAACCC[C/T]GGGTCACCCTGAAGA | 16443 |
| rs217852030 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91876975 | ACACACTTCCTGGAA[C/T]TTTTGCCTTAAGTTT | 16443 |
| rs217870432 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91844997 | AAAACAAAGCTGTGG[A/C]GGGCGCGAGCTGTGT | 16443 |
| rs217877781 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91838896 | GCTTTCCTGGCGCTG[C/T]GTCGCTCTGTACACC | 16443 |
| rs217888109 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91801137 | CAGGAAACGTCAATG[C/T]TGACAGTGGCCACGT | 16443 |
| rs217895789 | in-del | -/AG | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878088 | GGAAGGAAAGAAGAA[-/AG]AGAGGGAGGGAGGAA | 16443 |
| rs217898440 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91800584 | TTGGTTACTCCCCGC[C/T]ATCATATATTTTGGA | 16443 |
| rs217902332 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91845581 | ACGGATTTCTGAGTT[C/G]GAGGCCAGCCTGGTC | 16443 |
| rs217903068 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91884610 | CGACTCAGCACAGCC[A/T]TGGCGAAGATCACAA | 16443 |
| rs217907670 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91891568 | CACAACAGGCTGGCC[A/C]CACCCACAATGGCGC | 16443 |
| rs217911926 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91883965 | AGGGCTCTCTGTCCT[A/G]TGTATTTTAGTCCAT | 16443 |
| rs217914648 | in-del | -/TGGGGG | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91730200 | ATTGCGGTCCCTTCT[-/TGGGGG]TGGGGGGGGGCACCA | 16443 |
| rs217923573 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91733205 | ACTTTAGAATTAGTC[A/T]TAACCAATTTAGAGT | 16443 |
| rs217923977 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91741942 | TTGCATGTGATCTTG[A/G]TTGTGTATGTGCCAC | 16443 |
| rs217929460 | in-del | -/ATC | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830825 | ATTAGCTTTTTATCT[-/ATC]TATCTGATAAGCTAG | 16443 |
| rs217934478 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91759726 | AGGGACCGCTGTGAG[C/T]CCCGCATTAGTTTGT | 16443 |
| rs217935110 | in-del | -/GTTTGAAAGAGGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91826985 | TTCCTCCTGATGGGG[-/GTTTGAAAGAGGC]CTTGAAAGCACTGAG | 16443 |
| rs217942867 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91891928 | TACAATAACGGCTGG[C/T]CTGAGAAGGAGAGTG | 16443 |
| rs217955480 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91764383 | AGTGTTTCTGTGAAC[A/T]CTATGCTTTTTTTTC | 16443 |
| rs217958254 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91741098 | GAAGAAAGGCCGCCA[G/T]CACTGATGGGAGGCT | 16443 |
| rs217961173 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899041 | CCGGAGAAGAGCAGC[C/T]GCTGGCTGCCAGCAG | 16443 |
| rs217963883 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91904578 | GTCCTGGGGCCTGGA[C/T]GCTGCACCTGGGAAA | 16443 |
| rs217985887 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91764045 | AGGGGTGGCCACATG[C/G]CTCACTCAGGACTTT | 16443 |
| rs217992815 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91843941 | CTGCAGCTTCCACAC[A/G]CTCCCTGCCACCCCC | 16443 |
| rs217993396 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904372 | CTCGGATGAGCTGAC[C/T]TGACATGACAGCCCC | 16443 |
| rs218005862 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91843373 | CTTTCTTGTGTGTCG[C/T]CATATTCTGATGTTT | 16443 |
| rs218057331 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91770078 | GGCTGTACTCTCCTT[A/G]CCTTTTACTGTGCTC | 16443 |
| rs218066329 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91841986 | AACCACATGGTGGCT[C/T]ACAACCACCTGTAAT | 16443 |
| rs218067907 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91850634 | GTCGCTGGAGACAGA[G/T]TCTAGGGCTTTGTGC | 16443 |
| rs218073940 | in-del | -/TGCTGTGG | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746218 | GTGTCAGTGTTCGAC[-/TGCTGTGG]AAAGCAAGCAGAAAG | 16443 |
| rs218087506 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91875307 | CTTTGTGGTCTTGGG[C/T]ACATTACATTTAGAG | 16443 |
| rs218090574 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91769428 | ATTACATATTCATTG[C/T]ATAGCCTCACTCTAA | 16443 |
| rs218116069 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91758100 | CTCCAGCCTCTCTCT[C/G]TTTTCTTTTCTTTCT | 16443 |
| rs218167058 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91850016 | GTTCAAACTTAGGTC[A/G]AGTTCTCTAAAATGG | 16443 |
| rs218185100 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91765684 | GAGGCAGAGGCAGGC[A/G]GATTTCTGAGTTCGA | 16443 |
| rs218187867 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91766236 | TAGTCAAAGGAAGGA[A/T]ATGAAAAATGGGATT | 16443 |
| rs218188219 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91882603 | TTCGACTTCCTAGAA[A/G]CGTAATAGTCATTGA | 16443 |
| rs218190009 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91874707 | TCCCCTCCCCCAACG[C/T]CCCATGCTGCCTCCT | 16443 |
| rs218199604 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91869534 | TATCTCATTTTCCCC[A/C]GTTCTGAAGGGAAAA | 16443 |
| rs218239177 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91881867 | ACAACACCTGTTGTA[C/T]AGACAGGAACTCCAG | 16443 |
| rs218247009 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91817437 | GGCTCTCTGTTCTGA[C/G]TACGTCCTTGCCAGT | 16443 |
| rs218248257 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91869525 | CCCCCATCTATCTCA[-/T]TTTTCCCCCGTTCTG | 16443 |
| rs218256990 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91738947 | CTGAAAGTGTTGTCC[C/G]CTTCTGTGGCAAAAG | 16443 |
| rs218257138 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91878372 | GTGATGGTGCCCTCC[-/T]TTATAGAGCTGACAT | 16443 |
| rs218271039 | snp | C/G | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91816866 | TCGCTCCGGCAGTGG[C/G]ATGTCCGTCATAAGC | 16443 |
| rs218276886 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91751409 | GGAAAATACCAACCC[-/T]CTAACCTCCAAGCCA | 16443 |
| rs218284628 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878416 | CATCTCTTACTGCTT[A/G]TAAGCCACATTTGCA | 16443 |
| rs218287419 | in-del | -/CTGTTACC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890806 | GGGGGGGCGATGTGT[-/CTGTTACC]CTCAAGTATCCCTTA | 16443 |
| rs218289645 | snp | G/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746097 | GATGGAAACAAGATT[G/T]CACTTCTCACTAGGA | 16443 |
| rs218289755 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91738447 | CCGTTAATTTTAAAT[C/T]ACAGTCATTGTGTGT | 16443 |
| rs218290674 | in-del | -/ATTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91758900 | TTGACTGGTATGGTA[-/ATTT]GTTTGTTTCTTTGTT | 16443 |
| rs218291754 | in-del | -/CATA | | | intron-variant | Itsn1 | Mm_Celera | 16:91844676 | ACACCAATAAGCATG[-/CATA]CATACATACAGTATT | 16443 |
| rs218301174 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912883 | TTGTGAGAAGTAACA[A/G]CAACAATCCTTAGTG | 16443 |
| rs218304620 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91821600 | CACTTCCTGGGCCAA[C/G]CATATGCAAACCATC | 16443 |
| rs218317855 | snp | C/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91828421 | GCTGTCGTGGTGCCC[C/G]CTGCCCCTCCAGTTG | 16443 |
| rs218319847 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91820409 | AAAGCAACATTGCAC[C/G]GTGTCAGAATTAAGG | 16443 |
| rs218323590 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91869174 | ACAGCTGCACACCAT[C/G]TATAGAAGGGCCAGG | 16443 |
| rs218340274 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91848113 | GCAGAACTAAGGACG[A/G]ACACAAGCACTGGCT | 16443 |
| rs218346623 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919923 | AAGACATGCATTTAA[C/T]TGAGCATTTGTTGTC | 16443 |
| rs218347459 | snp | C/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919420 | GGAGGCCAGAAGTTA[C/G]GAAGCCGCTCCTCAA | 16443 |
| rs218368339 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91827709 | GTGGGAGTTTCTTTC[A/G]TTTCATGTATGTCAC | 16443 |
| rs218369388 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745703 | GGGTGGTCAGGCAGT[C/T]AGCACAGAGCCTCTG | 16443 |
| rs218390066 | in-del | -/TTTTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91800788 | TACTGTTTTGTTTTG[-/TTTTA]TTTTATTTTATTTTA | 16443 |
| rs218397912 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91847603 | GCATGAACCAGGAGT[A/T]CAGAGCAGCACCAAA | 16443 |
| rs218419032 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91877382 | AGGACAGGGACCAGG[A/T]AAGGCATGCCTCTAG | 16443 |
| rs218453556 | snp | A/C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91791832 | GTTTTTTTATTTTTT[A/C/T]TTTATGTGTATGTAT | 16443 |
| rs218457434 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91788044 | ACACTGGTGTTTATG[A/T]CCATGCTTAGATGCA | 16443 |
| rs218476634 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91734568 | CACACATACAACAGC[A/C]ATTTCTTACAAGGCC | 16443 |
| rs218494309 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91855471 | CCACAGAACTATTAT[G/T]ATTTATTTTTATATG | 16443 |
| rs218510237 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799348 | TTTCAATCAAGCCAC[A/G]GGGTGCTGTGGACCT | 16443 |
| rs218510336 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91791382 | AGGACAAGTTACTGA[A/G]CAGACCTCCCGACTA | 16443 |
| rs218519456 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734159 | CCACGTGGGTGCTAG[G/T]AATTGAACCCTGGGT | 16443 |
| rs218521921 | in-del | -/AAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91875483 | GCTACTGCTTTACCA[-/AAG]GAGAGATTTCAGAGA | 16443 |
| rs218536238 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91794521 | CTCATACAGTCTTTC[C/T]GCCTCCCCCTCCACA | 16443 |
| rs218546495 | snp | A/G | | | synonymous-codon | Itsn1 | GRCm38.p3 | 16:91837120 | GTCCCTGGAGGCAGC[A/G]CGACTGAAGCAGAAA | 16443 |
| rs218549223 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91854665 | GAGAAGGTAAGGGCC[G/T]GGGTGTGTGGCCTCC | 16443 |
| rs218577003 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91819846 | TTTTTATAGAACCCA[A/G]GACCACCAGCCCAGG | 16443 |
| rs218584410 | in-del | -/CC | | | intron-variant | Itsn1 | Mm_Celera | 16:91791874 | TGTGAGTGAATGCCT[-/CC]CGTGTGTGTGTGTCT | 16443 |
| rs218605353 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798465 | CCCAGGGTAAGCCAG[A/G]TACAGCCCGCAAGCA | 16443 |
| rs218611338 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898590 | AGGTGGGAGCAGGAC[A/G]GCATCCAGGCAGGCA | 16443 |
| rs218621590 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91844135 | CATTAAGGAATGTAG[C/T]CCCGCCCCTCTGTCC | 16443 |
| rs218630377 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91819102 | AGTTGCCAGCACCCC[C/T]ATGGGCAGTTCACAG | 16443 |
| rs218630829 | in-del | -/CTCCTC | | | intron-variant | Itsn1 | Mm_Celera | 16:91814137 | CCCCCTCCCCCTTCT[-/CTCCTC]CTCCTCCTCCTCCTC | 16443 |
| rs218644462 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91826026 | AGAGGTTCCCTTCCC[A/G]TCTGTCTGTTGTGGT | 16443 |
| rs218662561 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91741768 | CACACTAGCTCTGAT[A/G]GGTGGGTCACAACTA | 16443 |
| rs218667822 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91843869 | AGCCTGACCCTCCCT[G/T]TTGATTCCTGTAACC | 16443 |
| rs218673031 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91895601 | ACTCTTATCCACTAG[A/G]GGCATTAATACAGTT | 16443 |
| rs218680652 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91902961 | CAGGCGGTGGTGGCT[A/C]ATGCCTTTAATCCCA | 16443 |
| rs218702990 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91825484 | TATCAGATTTCATTA[C/T]GGGTGGTTGTGAGCC | 16443 |
| rs218703769 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91793532 | CGATTTGCTTAGTGC[C/T]GAGGAAGTGGTGCTG | 16443 |
| rs218708394 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91768657 | CCCCAAGGGTCCAGG[C/T]TAGTTGACTCTCTTG | 16443 |
| rs218711297 | snp | A/G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91902491 | TGAATCAGCAGAAGA[A/G/T]TTCCAGAAGAAATGC | 16443 |
| rs218763336 | in-del | -/TT | | | intron-variant | Itsn1 | Mm_Celera | 16:91832862 | TCTTTGACTTTGTAC[-/TT]TTTTTTTTTTATATC | 16443 |
| rs218763426 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91895040 | TGCCACAGTGGGTTA[A/G]GCATCTTTTGCTAAG | 16443 |
| rs218771899 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91754387 | CTAATCCGTGCCCCC[-/T]AGGAAGTGGGCTGCC | 16443 |
| rs218790417 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91768295 | TTTTCTCCATTAATT[C/T]ATGTATTTATCCCGA | 16443 |
| rs218797801 | in-del | -/TT | | | intron-variant | Itsn1 | Mm_Celera | 16:91850162 | GTGGGAAGGGTTTTC[-/TT]TTTTTTTTTTTTTTT | 16443 |
| rs218800884 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91832695 | TGAGTATTGACTTCG[A/G]TTTTCAAAGAATGAT | 16443 |
| rs218818843 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91899435 | AGAACACTGTGGTTT[C/T]CATGACAACGGGCCC | 16443 |
| rs218824653 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91764769 | CTTGTTCAGTCTGAG[C/T]GGCCTCCTCACCACC | 16443 |
| rs218827090 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91776579 | CTTCATTTAATGATG[C/T]TGCGTCATATTTCTA | 16443 |
| rs218839428 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91816146 | TGAGTATCTGCTTCG[C/T]GTGGCGCTGGGAGCA | 16443 |
| rs218840398 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91796119 | TGTCTTAGGGAGGAC[C/T]ACAACAGTCTCGTCA | 16443 |
| rs218846710 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91850439 | AGTCGCACCACCCCT[A/G]CTTGCCTTGGTCTTT | 16443 |
| rs218915317 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91880377 | CATCCTCTTTGTCCA[G/T]GAGTCTTAGTGCATG | 16443 |
| rs218926319 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91868248 | CTGTCTGTGGCCTCT[C/T]TTTGCTGAGCACCAC | 16443 |
| rs218943207 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795320 | CACTGGATACTGGAA[A/C]GTACTTGCAGCTAAT | 16443 |
| rs218943400 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91804087 | GCGCCATTCAGATGA[C/T]TGTCCCCGGTCACAT | 16443 |
| rs218972308 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91879534 | TAGCTGTTGTAGCTG[C/T]CGAGACATTTTGAAT | 16443 |
| rs218975114 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91887252 | GGGCTGTGCCACTCC[A/T]GTTTCTACAACTCAA | 16443 |
| rs218985520 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91886887 | AGGAGGACCAGGGGC[G/T]AGCTGGCCTCTCTGA | 16443 |
| rs218987214 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91901992 | CTCTGGTAAGGAGTG[C/T]GGATGAACAATAGGC | 16443 |
| rs218991622 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91744639 | TGGGCTTTGGACCAG[A/G]CCTGCCTGAATTTGT | 16443 |
| rs218995706 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91764322 | GCTTGTCCACCACTC[G/T]GACTGTCAAAGGGTG | 16443 |
| rs219003557 | snp | A/C | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803618 | GCAGCAGTGCTCTAA[A/C]GCACTGGACCGTCTG | 16443 |
| rs219020119 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91907961 | AAACTAACAACAATG[A/G]CTGCAGCGATGGTTT | 16443 |
| rs219021692 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91901345 | CTCCCCTCCCCTCCC[C/T]ACCTCCTACCTGCTT | 16443 |
| rs219022473 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91744268 | GAGATGCTTTTCTGG[C/T]GAGTGTTGCAGGCAC | 16443 |
| rs219050882 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91770818 | CCCCTGACAGGCACA[C/T]ATTCTGGGGAGAAGG | 16443 |
| rs219054671 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91841680 | CAATTAGGAAACCTC[A/C]AGCAAGCATGCATAT | 16443 |
| rs219064940 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91834693 | GTGTGAATGGCACCG[A/G]GCTGTGGTAAAGCTG | 16443 |
| rs219076929 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91845871 | TCAGTCGAGGTCATT[A/C]AAGAGCCAAATGTAA | 16443 |
| rs219082234 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91744986 | TGACTGACACTGAGA[-/T]TTTTTATATAATAAT | 16443 |
| rs219095310 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91732596 | GATGATAATCCCAAC[A/G]TAAAGAATCATTTTT | 16443 |
| rs219100674 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91743801 | TGCTGGGATTAAAGG[C/T]GTGCACCACCACCCC | 16443 |
| rs219104250 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91752417 | CTCAGCAGACCTAGC[C/T]CTAAGTGGGCTCACT | 16443 |
| rs219107147 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91841087 | GCTGCGTAGACCGAC[A/C]TTTGCCTGTTTATAG | 16443 |
| rs219108809 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91875876 | CCTGCCAGCAAAGAG[C/T]GGTATGTTTGCTCCC | 16443 |
| rs219126724 | snp | A/G | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91853535 | GAGAAGCCACAAGGT[A/G]ACTAGCACTCCTGAG | 16443 |
| rs219127974 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917000 | AGTGAGCAATGCTGA[C/T]AGGATGCTGTTCCTT | 16443 |
| rs219133263 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91751820 | ACGTGCTTTAGAGAA[A/T]CAGTATCTGCTGTAG | 16443 |
| rs219154600 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91875118 | TTTTCATTCCCGGCT[A/T]TAGCCAGAAGACCAT | 16443 |
| rs219156012 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91821993 | TTCCTCAGTGGGATG[C/T]TGGCCTTACTTTGAT | 16443 |
| rs219189432 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91917328 | TCACAGGGGTTGGGA[C/T]TGGGGATGTCTTGAA | 16443 |
| rs219226295 | snp | C/T | | | intron-variant, missense | Itsn1 | Mm_Celera | 16:91852864 | GCCTGCCTTTGCAGC[C/T]ATGTCTCCTGCTCCG | 16443 |
| rs219233619 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91882467 | ACCATTCCCAGCCCC[A/G]CACCCCCCTCCTTCA | 16443 |
| rs219268862 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91784979 | CTTTTAAAATCTCGA[C/T]TCTTCTCAGTAGCAT | 16443 |
| rs219271247 | in-del | -/AGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91819264 | CAGTATGTAGTTGTT[-/AGC]AGCTTTTTGTTCAAG | 16443 |
| rs219297830 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91814047 | GCACAATAACTTCTA[A/G]TAGGCATTGATGAGT | 16443 |
| rs219301822 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91850607 | GTGTGCACTGCCACA[-/C]CTACCATGCATGTCG | 16443 |
| rs219322059 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91791955 | AGAATAGGGTGTCAG[G/T]TTCCTTGGAACTGGA | 16443 |
| rs219326338 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91894136 | GTAGAGGAATGTGCT[C/T]GGACAGGAGAGCCAT | 16443 |
| rs219336761 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91732026 | CCTCCTGAATGGCTC[C/T]ACTTACTGGCTCCAT | 16443 |
| rs219344698 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91820337 | CCAGTGTTGGGTGAG[C/T]CCTGCAATGGGAGAT | 16443 |
| rs219345675 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91813460 | GTTACGTAGTCATAC[A/G]CAAAGAAGAAACAAC | 16443 |
| rs219354932 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91893734 | TCTGCAACCTGAAAG[G/T]GTGAGGTATCACCAG | 16443 |
| rs219354933 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91898872 | GCATCAGTGGCTCTG[C/T]GTGCTCTCAGGGCAC | 16443 |
| rs219356417 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91819996 | TGAATGTAAAATGCC[C/G]CAGATTCAAAACTCC | 16443 |
| rs219379876 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91754748 | CCTAGGCACCACAGT[A/G]GCATCTATCTGCTGA | 16443 |
| rs219383713 | in-del | -/GAGTGTCACCATGCGAGTGTCACCATGCGAGT | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91801460 | CGAGTGTCACCATGC[lengthTooLong]GACTGGCTGAGTTTG | 16443 |
| rs219384583 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91840837 | TACAGAGACAACAGT[A/C]TACCTCACGCTCTTC | 16443 |
| rs219389731 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898632 | GAGCTGAGAGTTCTA[C/T]ATCTTCATCTGAAGG | 16443 |
| rs219393858 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91739708 | TTTAGGGACAGCCAC[A/T]GCTCCAGTTGTTTGG | 16443 |
| rs219409289 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91792214 | GTCTATTCTCTCCAG[C/T]CCCAAAACCAATTCC | 16443 |
| rs219415344 | snp | A/C | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915516 | CTGATGGATTCTTTT[A/C]CTCTTTTAGACCCTG | 16443 |
| rs219415925 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91791742 | GCATGAATATAGGTG[C/T]ACAAGTGTGTGCGTG | 16443 |
| rs219442505 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91784001 | GAGAGCTGTGGACAC[C/T]GCGTGCCTGACCCCT | 16443 |
| rs219447809 | in-del | -/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916147 | GTGGTCAAAGAGAAC[-/G]GTTAAAGAGGCTTCC | 16443 |
| rs219454222 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91762919 | TCTCGTGTGATTTTG[A/G]TGGTGTTGTCTCTTT | 16443 |
| rs219460778 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91865959 | TGTTTGTCTGAGACA[A/G]CCAATCTCCTGGGCC | 16443 |
| rs219490744 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91761963 | TTCCTGTTTCTGAGT[A/G]TGGGAAGTAAATTTC | 16443 |
| rs219491335 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91791248 | TAGCATTTCACAGTC[C/T]GTAGTCCTAACACTT | 16443 |
| rs219500068 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799177 | AAGGCCCTGAGGGGA[A/G]GAGGAGACGGGAGAG | 16443 |
| rs219512201 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91865100 | AGGGGTGGTGTGAGA[A/G]ACAGATAAGTCTAAG | 16443 |
| rs219513966 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91874652 | GAACATGGTATTGTG[A/G]CCTACCTGTGTGCAT | 16443 |
| rs219528504 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898586 | ATCAAGGTGGGAGCA[G/T]GACAGCATCCAGGCA | 16443 |
| rs219541023 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91849080 | AGGGTTATTGGCTTC[G/T]CAACTAGATTTAGTA | 16443 |
| rs219553907 | in-del | -/CAGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91801077 | TCCAAGCTGAGTGTA[-/CAGT]CAGTCTTCTTGCTAT | 16443 |
| rs219574716 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91903521 | CACTCACAGGAATTC[A/G]AAGGGAGCATGCTGG | 16443 |
| rs219584287 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91790552 | TTCTCCGTGCCTGCC[A/G]GAAGAAGTGCAGAGT | 16443 |
| rs219584890 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91800013 | ACCTGTCCATGTGTT[C/T]TGTCTATTCATCTTT | 16443 |
| rs219615120 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873914 | GGCAGCTCACAGCTG[C/T]CTGCAACTCAGTCCA | 16443 |
| rs219615344 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | Itsn1, Cryzl1 | GRCm38.p3 | 16:91729525 | CGCGGCTGCGGACTC[G/T]GCGTTCCTCCGCGCG | 16443 |
| rs219616559 | in-del | -/AGCTTCATTGGGA | | | intron-variant | Itsn1 | Mm_Celera | 16:91763076 | TCAATCCAGTTTTCC[-/AGCTTCATTGGGA]AGCTTCATTGAGCGC | 16443 |
| rs219628067 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91892547 | AACTACCAGTGGCTA[A/G]TACTAGAACAAAGTT | 16443 |
| rs219656289 | snp | C/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830501 | CAAGAAGACAGAGCT[C/G]TTGGCCGGCCTTAGC | 16443 |
| rs219657614 | in-del | -/TC | | | intron-variant | Itsn1 | Mm_Celera | 16:91900109 | CATCTGTGTGTTGTT[-/TC]TGTTAGCTCACACCC | 16443 |
| rs219659462 | in-del | -/ACTTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91761744 | AGGTACAAATTAGAC[-/ACTTA]AAGTTTATCATTTAC | 16443 |
| rs219671699 | in-del | -/AAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91753130 | GCTTTGGAATCTGAA[-/AAG]AAGGAATTCCTTTTG | 16443 |
| rs219676759 | in-del | -/AA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892792 | AACAAACAAACAAAC[-/AA]AAAAAAAAACAATGT | 16443 |
| rs219677701 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91866403 | GAGGTGAGGGAGAAG[-/C]GCTGCTGGGAGCCAC | 16443 |
| rs219680915 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91780449 | TGGCTAAGTCAGAAG[G/T]CTGGTGGTGTTATCA | 16443 |
| rs219682773 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91898812 | TGGACGAAACACACA[C/T]ATGTGAGCAGGGGAG | 16443 |
| rs219689525 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91737972 | AAATAGCAGTCTAAG[A/G]TGGTATACAGCTATT | 16443 |
| rs219700344 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91787663 | GAAGCAGAACTCTGT[C/T]CCTCCTCAGCCCCCT | 16443 |
| rs219707455 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91760867 | CATTGCCTCTAGGAT[C/G]AACATTATTTGGAGT | 16443 |
| rs219729399 | in-del | -/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911229 | GAAGAGAGCAATGGC[-/G]GTGTACTCATATAAA | 16443 |
| rs219755296 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91840139 | CCAGGTGTGCACAGG[A/T]AGCCCCTCGGATACC | 16443 |
| rs219767048 | snp | G/T | | | missense | Itsn1 | GRCm38.p3 | 16:91839777 | TGCAAGACAAGCAGA[G/T]TCGGCTTTTCCATCC | 16443 |
| rs219769155 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91890276 | TTGGGGGGGGGGGGG[A/G]ATGGCTTTATAGCCA | 16443 |
| rs219769415 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91762837 | GGATTGTTCATGCCC[C/T]GGGGCAGGCATTGGA | 16443 |
| rs219800925 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91836662 | TCATAAAACTAGTTA[C/T]CTTCCAGTACTTATT | 16443 |
| rs219816551 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91767371 | CCTTGGCACCTATCA[G/T]GTAGAAGGAGAGAAC | 16443 |
| rs219822899 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91760926 | TCTTTTGGAAAGAAA[-/G]GTATTGATCCCTCAT | 16443 |
| rs219824125 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91846718 | GCTGGCAGGCTGGGT[A/G]GGGTGGGGCTAGACC | 16443 |
| rs219824633 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91895092 | AGACTTTTGGGGGTG[A/G]CCATGCTCACCTCAG | 16443 |
| rs219841196 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91872188 | AGTCTGCAGATGGTT[C/T]GGGGGAAGGGGGTGA | 16443 |
| rs219901365 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91812524 | TAACCCAAGGCCAGA[C/G]TCCTTTCTCCCAAAG | 16443 |
| rs219908459 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91845899 | TAATAGCACCTCCCC[A/G]GGAACCAAGTTGGAA | 16443 |
| rs219935712 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91747920 | AGGGTGAGCTATAGG[C/T]GTCAGTCAGACCTCG | 16443 |
| rs219938344 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91879115 | GCTGCTGGGCTACCT[C/T]TCTAGCCCCAGGGGT | 16443 |
| rs219938352 | snp | C/T | | | utr-variant-3-prime, intron-variant | Itsn1 | GRCm38.p3 | 16:91870827 | TGTCTGTGACCATCA[C/T]GTGTACCTGTCGCGC | 16443 |
| rs219955797 | in-del | -/AAAAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91844480 | AATAACAACAACAAC[-/AAAAA]AAAAAAAACCAAACC | 16443 |
| rs219982368 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878746 | CCTCCGCAAGTGTGG[C/G]GGCCTCACAGAAGCA | 16443 |
| rs219987177 | in-del | -/TA | | | intron-variant | Itsn1 | Mm_Celera | 16:91909032 | TAATCATATATATAC[-/TA]TATATATATACACGG | 16443 |
| rs220018694 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91905030 | ACTTCTCAATAAATG[-/A]AAGGGGGAGACATAC | 16443 |
| rs220022042 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91734990 | ACCAGTCTTGTGCAA[A/G]CAACTTCTATTGCTG | 16443 |
| rs220023488 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91743705 | ACAGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTCC | 16443 |
| rs220035801 | in-del | -/CAAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91835157 | GCTGGCTCGTATTTG[-/CAAT]CAAAGACATGCACAT | 16443 |
| rs220042563 | in-del | -/GT | | | intron-variant | Itsn1 | Mm_Celera | 16:91889036 | TGTGTGTGTGTGTGA[-/GT]GTGTGTGTGTGTGTG | 16443 |
| rs220053723 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91845051 | CCTGGGACCTTCAGC[C/T]CTGCTTGTTCCTCCT | 16443 |
| rs220054936 | snp | C/G | | | missense | Itsn1 | Mm_Celera | 16:91818527 | TTGGCTCAGCTGGAG[C/G]GCGCCGAGCAGGAGA | 16443 |
| rs220059187 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91894345 | GGTCCCATTACAGAT[A/G]GTTGTGAGCCACCAT | 16443 |
| rs220066364 | snp | A/C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91817935 | GGGATTAAAGGCATG[A/C/T]GCCACCACACCCGGC | 16443 |
| rs220075738 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830006 | ATCATAGCTGTGTTG[C/T]TGATCCTTTAACGTC | 16443 |
| rs220083801 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91743157 | ATTTCGGGTTTGCAC[A/G]TGCTCTGTCATGAGT | 16443 |
| rs220105150 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914275 | ATTTCTGGATGAGCT[A/G]GGCTGACCCTCAGAC | 16443 |
| rs220116665 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91844676 | AACACCAATAAGCAT[A/G]CATACATACAGTATT | 16443 |
| rs220119634 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91889986 | CCTCTGACGGAGCAT[C/T]CTGGACAGGATCCAG | 16443 |
| rs220128918 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823995 | TTCTTCTTCCTACAT[C/T]CTAGAAATGTTGATG | 16443 |
| rs220144266 | in-del | -/CCGA | | | intron-variant | Itsn1 | Mm_Celera | 16:91805148 | CCCAGCAGGAAATAT[-/CCGA]CTTTATTAAGAAGTG | 16443 |
| rs220155059 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91835981 | GAGATGGCCCAGTCT[A/G]TACCTAGCCCAGCTC | 16443 |
| rs220194811 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867559 | AGGGTTTCTATCTTT[A/T]AAAAAAATAATTGTT | 16443 |
| rs220215561 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852175 | TCTCTAGCAGTACTG[C/T]CCACTGGAGACCAGA | 16443 |
| rs220224583 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91789047 | TGGTGGTGGTAGTGT[A/T]AATGAATGAATTTCC | 16443 |
| rs220254591 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91763122 | TTGTAGCATTTGAAG[A/G]TGTAAGGATTTGAGC | 16443 |
| rs220268475 | in-del | -/CA | | | intron-variant | Itsn1 | Mm_Celera | 16:91742756 | GACAGTGGCCACAAG[-/CA]CAGTTTGGCCTTCTG | 16443 |
| rs220287226 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91866380 | TGATCTGCCCTTGTA[A/G]AGCAGCAGAGGTGAG | 16443 |
| rs220290517 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91894797 | CTCAGACTCAGCCAC[C/T]TTTCTTAGTTCCCAC | 16443 |
| rs220303913 | snp | A/C | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91816923 | TGAGGAGCCGTCGTC[A/C]GAGGATGAGCAGCAG | 16443 |
| rs220304895 | in-del | -/CCC | | | intron-variant | Itsn1 | Mm_Celera | 16:91838259 | TGAGCCATCTCCCTG[-/CCC]CCCCCCCAGTTGTCA | 16443 |
| rs220311383 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91814338 | CCTCTCTTCTTCCCT[C/T]CTGTGTAGTAGAGTC | 16443 |
| rs220326266 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91795206 | AGAGGACACACAAAG[C/T]TATGCATGAGCAAAG | 16443 |
| rs220328793 | in-del | -/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91739599 | TATCTCCCCCACCCC[-/G]GGATATCAAGTATGC | 16443 |
| rs220340686 | in-del | -/CCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91755205 | GGTACCTCGCCAGCA[-/CCT]CCTCTCTTACTATGT | 16443 |
| rs220358277 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91910663 | GTGTTGGGGTTACAC[A/G]TCTGTGCCACCACAC | 16443 |
| rs220359658 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91816588 | TGGGGAAGCTGAGAG[G/T]TACTTCAGCACTGAT | 16443 |
| rs220365033 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91732208 | CTTTTCTCTCTTACC[A/G]AGTGTCTCCTAAGAC | 16443 |
| rs220369987 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91822782 | TCACTTTCGCTCTTC[A/G]CTTGTGCTGTTTTGG | 16443 |
| rs220387588 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91794778 | TCCGAGATCCGTGAC[A/G]TTACTAGCTTTGGGT | 16443 |
| rs220392517 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91834930 | TCATAGCCAGTGTCT[A/G]TCCTGGTTTCACAGC | 16443 |
| rs220393412 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91896441 | GTAAGTGTGGCCCCC[C/T]TGTGCCTTCACCAGC | 16443 |
| rs220397523 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916513 | TGAGCCATCTCTCCA[A/G]CCCCCACCATCACGG | 16443 |
| rs220397807 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91755581 | AACTCACTCTGTACT[C/T]TGTAGACCAGACTGG | 16443 |
| rs220402378 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91808166 | TAAATCCTTTTAAAA[A/T]CTATAGCAAAGCATA | 16443 |
| rs220404429 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919531 | GAGGCTCTGTTTGCC[A/G]TTTGCAGATGTGGAC | 16443 |
| rs220430111 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91901120 | TCAACCTCCACTCTC[C/T]TCTTTTCTGCCTGTT | 16443 |
| rs220452665 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91855373 | GACTCACAGGAATAG[A/G]GTTCCATTCTCAAGA | 16443 |
| rs220454349 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91753291 | TGTTGAAAGGACCCT[A/G]AGTGTGTTCTGCACG | 16443 |
| rs220460937 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91854498 | CTGCAGCTGTGCACT[C/T]GTAGCTTTCAGAGAA | 16443 |
| rs220478279 | in-del | -/TGTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91910509 | GTGTGTGTGTGTGTG[-/TGTA]TGTGTGTGTGTGTGT | 16443 |
| rs220489025 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91761021 | ATATCGAGGTCCAGG[C/T]AGTACATCAACGTTG | 16443 |
| rs220496444 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91765785 | AAACAAACAAACAAA[C/G]AAAGGCCTGGCTAAA | 16443 |
| rs220502456 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91900341 | AGCGGATTGCTACCC[A/G]GGCCACTCCAAATTA | 16443 |
| rs220506204 | snp | C/G | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91729971 | CCGGCCTCGAGTCCC[C/G]GGCTCATCCTTTTTC | 16443 |
| rs220508543 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91857254 | GTTACAGTGTGACAG[G/T]ACAGTGTCTGTTCTG | 16443 |
| rs220516174 | in-del | -/GAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91779739 | AAGCTGCTGGGAAAA[-/GAT]GATGACACGTGCAGG | 16443 |
| rs220519526 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91867152 | TAAAAATGCTCAGTA[C/T]CTTGGGTCAAATCAG | 16443 |
| rs220521694 | snp | A/G | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91863655 | CATGGCCTGGCAAAC[A/G]GAATCAGCGCTTCGT | 16443 |
| rs220522594 | in-del | -/AG | | | intron-variant | Itsn1 | Mm_Celera | 16:91854832 | CCTCTCAAACAGTGC[-/AG]ATCATCCCAATCTGG | 16443 |
| rs220545117 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91814932 | GAACCTGTCTGCTCC[C/T]ATTTTTGTAGAGGTT | 16443 |
| rs220564330 | in-del | -/TGTGTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91742119 | GTGTGCGTGTGTCTC[-/TGTGTG]TGTGTATTTTTAATT | 16443 |
| rs220570354 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91760444 | TCCCTTAAGCAGTAG[A/G]GTCTTATCCTGTTAA | 16443 |
| rs220578522 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91773906 | TCTCCTCAGGTCTCT[A/G]GACTCATTGCTGTTA | 16443 |
| rs220578916 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91888107 | AGAGAAGTAACCTTT[G/T]AACCCACACGCAGTG | 16443 |
| rs220579912 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91765204 | TCCCAGCAAGCACTC[A/C]AGAGGCAGAGGCAGG | 16443 |
| rs220586872 | in-del | -/GGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91891778 | AACACATAACATCAC[-/GGG]GGGGTGGGGGCCAAT | 16443 |
| rs220602061 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91834110 | ACATAGTGAATTTGA[A/G]GCTACCTTGCTTCAA | 16443 |
| rs220609463 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91877527 | CCTATCCGGGATTGG[C/G]CACGCCAGTTGGAGA | 16443 |
| rs220612802 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91772655 | GTGGATGAGTGCTTC[A/G]CTGGCTTGCTCCAAG | 16443 |
| rs220623138 | snp | C/G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91862548 | TGGATCGCTCCCCCC[C/G/T]CCCCCCGCCCCCCTG | 16443 |
| rs220625780 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91840477 | TTTCAAAATTCTTAA[C/G]CACAGTGGTAGACAG | 16443 |
| rs220635231 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91911017 | TTTTAACTGCTGAGC[C/T]ATTTCTCCAGCCCCA | 16443 |
| rs220663172 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91754680 | CAATGCTACCATGCA[C/T]GTAAGCAGTCTTGCA | 16443 |
| rs220679950 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91872252 | GTCGTTCTAAGGAGC[A/G]GACAGGTGAAGACAA | 16443 |
| rs220692207 | in-del | -/ATG | | | intron-variant | Itsn1 | Mm_Celera | 16:91867133 | CTTATAACTTCTGAT[-/ATG]ATAAAAATGCTCAGT | 16443 |
| rs220695424 | snp | A/C | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | GRCm38.p3 | 16:91727469 | CGCACACATTACGGA[A/C]GTTGGCTTTTTAATA | 16443 |
| rs220702826 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917017 | GGATGCTGTTCCTTC[A/G]GGGGGGCTCTATCCT | 16443 |
| rs220719784 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91806782 | TAATAATATCTAAAG[C/T]ATATTATTCTTATCT | 16443 |
| rs220727312 | in-del | -/GTGTGC | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746860 | TGCTGGTGTGTGTGT[-/GTGTGC]GTGTGTGTGTGTGTC | 16443 |
| rs220737724 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91778171 | TCATCTTACATGCTG[A/T]TTTGGGGGAGAGAAC | 16443 |
| rs220754214 | snp | C/G | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91747302 | TGTGTGTGTGTCTGT[C/G]TGTGTGTGTGTGTGT | 16443 |
| rs220754361 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91804872 | GTAAGCATGGAAGGA[C/G]AAGACATGTGGAGCC | 16443 |
| rs220756891 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91731506 | TAGCTGTTCTGATGG[C/T]TGTGAGCCACCGTGT | 16443 |
| rs220760208 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91748598 | TGTGGGGGGCATTTT[-/C]TTGGTTGCTAATCAA | 16443 |
| rs220772954 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91832632 | AGCTTGCTGTGCAGA[A/G]AGGATAGGGTCAGAC | 16443 |
| rs220776845 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91838997 | CTTCCATGTCAGTGC[A/T]GGGAGCCAAGAGTAC | 16443 |
| rs220778333 | in-del | -/GGATTCTGTGGGATTCCAGAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91783116 | TCTGAGCACACTGAC[-/GGATTCTGTGGGATTCCAGAG]ACACCTGCTGACTTT | 16443 |
| rs220784222 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91832036 | CCATAAGGGACAAAT[A/G]TCTGTCTGCTTCAAG | 16443 |
| rs220812548 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91753362 | GTACTTTTCAGTTAC[A/C]TTTTGGGTGATTTTC | 16443 |
| rs220817941 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91812617 | TAACCATTATGTCAC[C/G]AGTTCACCTAAATAT | 16443 |
| rs220830337 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91908699 | TGAGCGTGCTGGAAA[A/G]AGAAGGGCATCAAGG | 16443 |
| rs220839650 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91838528 | GGAACTCACTGTGTC[A/G]ACCAGGTAGGCCTTG | 16443 |
| rs220843900 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91784897 | GTGATATACCCTAGA[C/T]AATCAGGTATTAAAA | 16443 |
| rs220854641 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91888497 | TCAGCCACAAACAGG[C/T]CACGTTCCTGTGCCC | 16443 |
| rs220858450 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91761124 | CAGGATATCTTAAAA[A/T]TTTTCTTTTATTATC | 16443 |
| rs220864059 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91908350 | AATTTGAGCAGACCC[A/G]AAGCCTGCTCTGTGC | 16443 |
| rs220867041 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914708 | CCTTCATGGGCCACT[C/T]GATCCAAAGGGTCAG | 16443 |
| rs220868587 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91776330 | CCTTGTGTACACACA[A/G]TGGCTGTAATTAACT | 16443 |
| rs220869111 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91892431 | CATTTAAAGAGGAGG[-/A]AAGCCGGTAATAGAC | 16443 |
| rs220887360 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91834677 | AGGTTTCGAGCTTAC[A/G]GTGTGAATGGCACCG | 16443 |
| rs220922682 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91893642 | AGTACTGGACTCATG[C/T]CTTTCTCTGTCCCTC | 16443 |
| rs220930400 | snp | C/T | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91863668 | ACGGAATCAGCGCTT[C/T]GTTGGAGGTGTTTGG | 16443 |
| rs220956306 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91812811 | TGTCTACATATATGT[C/T]TGTGTACCAAGTACA | 16443 |
| rs220966884 | in-del | -/AAGACAAATTGGCA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91895833 | CGAGAGCCACTGGCG[-/AAGACAAATTGGCA]GAGACTGGAGCTTTA | 16443 |
| rs220968312 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91782387 | TTCAATCTTCATTAC[C/T]ACAAAACCAAGCCAA | 16443 |
| rs221002345 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91873221 | TTAATTTTTATTTTT[A/G]CATTTACTCGTGTGT | 16443 |
| rs221003362 | in-del | -/GC | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746850 | TGGTTTAGGTGCTGG[-/GC]TGTGTGTGTGTGTGC | 16443 |
| rs221010249 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91886819 | CATAGGGTCTAGAGA[A/C]CATGCACGGCCTCTG | 16443 |
| rs221036568 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91811440 | CCTGCCTCTGCCTCC[C/T]GAGTGCTTGGATTAA | 16443 |
| rs221038182 | in-del | -/TGTTTTTTTTTTTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91835352 | TTTTTTTTTTTTTTT[-/TGTTTTTTTTTTTA]ACCTCTTTGCCTCCT | 16443 |
| rs221039416 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91908871 | GCCCATGAATTCCAC[C/T]CAAGCACTCTAGAAT | 16443 |
| rs221070127 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91781653 | TTAGCCACAGAGACA[C/T]CCTGACTGCCTGTCC | 16443 |
| rs221087237 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810919 | CAGGCCCTCAGCAGC[C/T]GGGCCTGCAGCATCT | 16443 |
| rs221087397 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91817700 | GTGACTCAAGCTAGC[C/T]GATCTCACAGCAATC | 16443 |
| rs221093789 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91811763 | GTTTCTCTGTAACTC[-/T]TCTATACCCATTTTG | 16443 |
| rs221094612 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91754033 | TCCAAGATTTTATAG[A/T]TATTATTAACCTGGA | 16443 |
| rs221121064 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91789188 | GTTCTGAAAGCAGCA[A/G]TGCATTCTGGGTGTG | 16443 |
| rs221133973 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91891638 | CAGGCTTGCTTACAG[C/T]CCGATCTTATGGAGG | 16443 |
| rs221134747 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91754779 | GTCTCCTCGGGGATT[-/C]CCCCCAGCTCCTCTT | 16443 |
| rs221135587 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91806231 | TCATTGCTTTAAGTA[C/G]AGCTCGTTTCTAGAT | 16443 |
| rs221156032 | snp | A/T | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91727560 | CCCATGTACTGAAGC[A/T]GCAAAGGGATGTCGC | 16443 |
| rs221164529 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91896510 | GCACCTGGGAGCTGA[A/C]GTGTGGAAGTCATGT | 16443 |
| rs221179894 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91781029 | CTTGACAGACTTGGC[A/G]AACCACAAGGGTAGA | 16443 |
| rs221202062 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91864758 | GGACTGCAGACTCCA[-/C]CTGGCCAGCTTCATT | 16443 |
| rs221206308 | in-del | -/TCCC | | | intron-variant | Itsn1 | Mm_Celera | 16:91824941 | GTCTTATTGTTTTCT[-/TCCC]TCCCTCCCTCCCTTT | 16443 |
| rs221222482 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91813424 | CCCCTGAAAGGGGTG[A/G]TGGGTTACTGTTTGC | 16443 |
| rs221237948 | in-del | -/CCTCT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91901319 | TGGAGAGCACCTGGC[-/CCTCT]CCTCTCCTCCCCTCC | 16443 |
| rs221255807 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91750963 | TGCTGACAGGTCCCA[C/T]GAGTCAGTCTATCCT | 16443 |
| rs221255902 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91759246 | TCACTTGGACCTTCA[A/C]GGTGCTGGGTGTCCC | 16443 |
| rs221256588 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91789778 | AACAATTACTTTCCT[A/G]TTTCTGTGATAAAAT | 16443 |
| rs221260731 | snp | A/C | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919689 | TCTTTCAAAACTAGA[A/C]ACACAGAAACTGAGA | 16443 |
| rs221261054 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91736689 | GTGTACTAAGGAAGA[C/T]ATTGACTTAGAATAA | 16443 |
| rs221266791 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91860588 | GCATGCTGGCCCCTG[G/T]CCTGGCTCCCGTGGT | 16443 |
| rs221275293 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91889749 | TTTGAACCTCAGTTT[-/C]CCCCAAGTATACCCT | 16443 |
| rs221284692 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890828 | TATCCCTTAGAAGGC[C/T]AATGTCTCCCAACAG | 16443 |
| rs221298013 | in-del | -/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890556 | TCGGGATCTGACTTG[-/T]TTTTTTTTTTTTGTT | 16443 |
| rs221299215 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91918844 | TCAAAGCCAGGGCCT[C/T]GTGCATTCTTAGAAA | 16443 |
| rs221300720 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758477 | ATACGCTGTTAGAGC[A/G]TTGTCTACATTTATG | 16443 |
| rs221315411 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91892066 | GCGATCTGTGACTGC[C/T]CTTAGCTGGTTCCTC | 16443 |
| rs221320438 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91864841 | AGACGTTTCTTAGGG[A/G]CCTGCCAGAGGGCTA | 16443 |
| rs221328419 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873840 | TGGAGAGATGGCTCC[A/G]CAGTAAGGGCACTGG | 16443 |
| rs221333416 | snp | C/T | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91870667 | CCGTAAACTGAGACT[C/T]GCTGTACCTTTGCCG | 16443 |
| rs221344101 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91839030 | GCTGCACCATCTCGC[C/T]AGCCCCAGATGTCTG | 16443 |
| rs221344417 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91787691 | CCTGCCACAGGGGTG[A/G]CCTGTGTCAGAGCCC | 16443 |
| rs221354374 | in-del | -/CCCAGCTCTCCAGGCTCGCGCCCTGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91835989 | CCAGTCTGTACCTAG[-/CCCAGCTCTCCAGGCTCGCGCCCTGC]CCAGGTCTCCGAAGT | 16443 |
| rs221369949 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890485 | GCAGATACCATGACA[A/T]CAAACATAGGGGGCG | 16443 |
| rs221399556 | in-del | -/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91870029 | ATGTTCCCCCTCCTT[-/C]CCCTCCCTCCTCCTT | 16443 |
| rs221408865 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91895176 | AAGTGCAGTGCTCTG[G/T]GTGAAGCTCAGGTGT | 16443 |
| rs221424857 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91757141 | CATGGCCTCTCATTG[A/G]CTCTCCATGCTTTTT | 16443 |
| rs221433586 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91894962 | GCTTAGACATCATAA[C/T]GCCTTTCCCAACGGA | 16443 |
| rs221463733 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91869305 | GTGCTGTGGCCCCTG[C/G]CTGTGTGCTATGCTG | 16443 |
| rs221486044 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91756436 | AATTCCAAGGCAGCA[C/T]ATCTGTGTACCTATA | 16443 |
| rs221509685 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91764467 | GTGTGTGTCTATAGA[A/G]CTTTGAAGCTGCCAC | 16443 |
| rs221533110 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91867813 | AGGGTATTCTGAATA[C/T]GCGAGCTAGAATCCA | 16443 |
| rs221544519 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91734760 | CCTTCCAGCTTTCAC[C/G]GATGTTTTTCTTTGT | 16443 |
| rs221550771 | snp | G/T | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91728190 | ATGCAAAGAGAAGGA[G/T]AAGAAGGGTGACAAG | 16443 |
| rs221568376 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91764075 | TATTCAGCACACAGC[G/T]TCCTAGCCCCGTGAC | 16443 |
| rs221569053 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91811468 | TAAAGGCGTGCGCCA[C/T]CACGCCCGGCTAGCT | 16443 |
| rs221596589 | in-del | -/CT | | | intron-variant | Itsn1 | Mm_Celera | 16:91833492 | GTCCTCTTCCTCTTC[-/CT]CTTCTCCTCCTCCTC | 16443 |
| rs221609722 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91876131 | GCTGTCTGGGGCATT[A/G]CCTTGGAATCCCATA | 16443 |
| rs221610243 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91833078 | AACAGAAAACCAGCC[A/C]CCAAAAGTTGTACAC | 16443 |
| rs221622515 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91837533 | AAGCTTCCCCAGAGC[A/T]CCCCAAACGCCTCTC | 16443 |
| rs221623079 | in-del | -/GTGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91782873 | GTAAAATCGTTATTT[-/GTGC]GTGCCTTGTATTTTC | 16443 |
| rs221624096 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91737264 | AAGGAGCACCACTGG[C/T]GTTGCTCTTGGACTT | 16443 |
| rs221627521 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91734184 | CTGGGTCACCCTGAA[A/G]AGTAGTCAGCCTCTC | 16443 |
| rs221638847 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91836789 | TGCCTAGTGTGTGCA[A/G]GGTCTCAGACTCAAT | 16443 |
| rs221643802 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91875432 | GGTCAGTAAGCATCG[A/C]GGAAGCTCATCCGGG | 16443 |
| rs221647615 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91894559 | GCCTTTCACACACAG[-/A]AGGGTCACCATAGCC | 16443 |
| rs221661123 | in-del | -/TT | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91829172 | AAGTATAGTTGAGGG[-/TT]TTTTTTTTTTGTTGC | 16443 |
| rs221682437 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746520 | CTAGCTTACTGTAGC[A/G]CTGAGTTTCCTAAAA | 16443 |
| rs221708885 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91843964 | CCACCCCCACCATCG[A/C]GGACCACCCCATATA | 16443 |
| rs221712006 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91834960 | CGCCTGCCGTTAAGT[A/G]TTTTGAATGTTATCC | 16443 |
| rs221716217 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91731590 | GCTAAGCCATCTCTC[C/T]AGCCCACATCCATCC | 16443 |
| rs221721898 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91849624 | GGAGGGGAACCTAGA[A/C]CATCTGTGGGGCAAG | 16443 |
| rs221722613 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91907534 | AGACCCTTCTGTCTT[A/C]CTGGGTCCTCCAAGT | 16443 |
| rs221732486 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91790424 | GTTTTAATAGTCATG[C/T]TTGTTAATTCAGGGG | 16443 |
| rs221734093 | in-del | -/TGTTTGTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91826702 | AGATTTGTGTCTGTG[-/TGTTTGTT]TGTCTCTGTATCTGT | 16443 |
| rs221741968 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91888614 | GTGATCAGCTTTGAG[C/T]TATATGCTCACCCAC | 16443 |
| rs221764482 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91800404 | TAGGATTACAGGCAT[A/G]TACCACTACTGTTGG | 16443 |
| rs221772913 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91851244 | AAAACTGACACGGGG[-/A]AGAGCCAGGAAGTGT | 16443 |
| rs221777301 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91774789 | AATTAATCTTTGTGC[G/T]AGATGATTTGGGTTA | 16443 |
| rs221784176 | snp | C/T | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91839688 | ACGCCCCCGGAAACC[C/T]CACGAGGAGGACAGA | 16443 |
| rs221798084 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91781550 | GGGTCAGAGGAGCTC[A/G]GTGAGATTGTTTCCC | 16443 |
| rs221800458 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878733 | TGGTATTTAGTCTCC[C/T]CCGCAAGTGTGGCGG | 16443 |
| rs221802702 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91774066 | TCACTCTGTAGATCA[A/G]GCTGACCTTGAACTC | 16443 |
| rs221836032 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810049 | CCGTCATCTGCCAGC[A/C]GGTTTTGGTTACAAT | 16443 |
| rs221850470 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91843568 | TGAGGCTGCCTAGCT[A/G]ATCATCTCCATGTCT | 16443 |
| rs221865221 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91781055 | GTAGAAATGGGGAGA[A/G]CCTTTAAACTCTGAA | 16443 |
| rs221866063 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91886236 | TTCAGACACTCCAGA[A/T]GATAGCATCAGATTT | 16443 |
| rs221884735 | in-del | -/TTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91755501 | TAATGTGGCAATTTC[-/TTTT]TTTTTTTTTTTTTTT | 16443 |
| rs221900680 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91755902 | ATCCAGATTGAAGCA[-/G]GTTGCCATGAAAGCT | 16443 |
| rs221901901 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91885384 | GCGCCATAGCAGGCT[A/G]AGCCATCTGTGTGAC | 16443 |
| rs221909568 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91891025 | CCTGAAGAGACTCTA[C/G]TCCTTGCGAGGGCCG | 16443 |
| rs221911362 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91849743 | GGCAAGCACCCAGGT[-/G]GAGAGGTATACTTTA | 16443 |
| rs221914198 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91743143 | GCACAGGGTATTGAA[C/T]TTCGGGTTTGCACGT | 16443 |
| rs221935755 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91742295 | GCCAGGCAGTTTGAT[C/T]AGATGTTAAGTGAAT | 16443 |
| rs221936769 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91750805 | TTCTACCCTGTGTGT[G/T]CAGTGCCATGGAATG | 16443 |
| rs221959112 | in-del | -/TTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91906990 | GTAGTATATATACTG[-/TTT]TTTTTTTTTTTAAAG | 16443 |
| rs221960901 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91754088 | CTTCGTTTTTTCTCC[C/T]AATGAAATCTTTAAG | 16443 |
| rs221961227 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91855594 | GTCAAAACTCTTTAG[A/C]TATAACATGCCTTCA | 16443 |
| rs221975134 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852157 | GGAAACTGAATTCAG[C/T]GGTCTCTAGCAGTAC | 16443 |
| rs221993011 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91806413 | TGTTGGTAAACTAGA[A/G]AACAGGCCTGAACCC | 16443 |
| rs222000551 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91769231 | CTTCCAGAGGTTCTG[A/C]GTTCAATTCCCAGCA | 16443 |
| rs222003996 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91748661 | ATCCCTAGGCAGATC[A/G]TGGGGAGCAAGCCAG | 16443 |
| rs222011239 | in-del | -/C | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831533 | TGCTATTATTTCTCT[-/C]CCCCTCCCCTCGTTT | 16443 |
| rs222013893 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91845250 | GCATGATGAGGGTTA[C/T]CCAGATGAAGGATGC | 16443 |
| rs222026276 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91851657 | ACAGAAGAGGGGAGA[C/T]GGAGCAGGCCCGGGC | 16443 |
| rs222036001 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91815829 | CAGAGATCACACCTG[A/C]AAATCACACACAGTC | 16443 |
| rs222059031 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91815253 | TCCTTCCAGTAGTCT[A/G]AAACAGAACTGGTTC | 16443 |
| rs222059301 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91791149 | CTAGTGACTGTGGGG[-/A]GCTCAGCACCAGAGC | 16443 |
| rs222078372 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91903137 | TTGCTGTGAGCCAGA[A/G]GATCGCCTATGCTAC | 16443 |
| rs222079328 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91911733 | ATGGAAGTGCTGGTG[C/T]TGGACTTAGTACCAG | 16443 |
| rs222092762 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91896632 | GCAACCAAGTGGCTT[C/T]GAAGCCAGGGAATGA | 16443 |
| rs222095317 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91911039 | CCAGCCCCACCCCTG[A/G]TTTTCATTTTAAATG | 16443 |
| rs222112254 | snp | A/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917451 | AGTAAAAGGAGCTAA[A/T]AGTTTATATTTTGGC | 16443 |
| rs222112796 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91811901 | GTGCTTGCTGGTCAT[C/T]TGCTCAGCAGAGTCT | 16443 |
| rs222128213 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91736367 | CCTGGAGACAGGAAG[-/T]GGGACCAGTGCTTCT | 16443 |
| rs222128583 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91859237 | TTGTAGTACATTTGC[A/C]GTTGACCTTCTCACT | 16443 |
| rs222129439 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91909902 | GGGAAACCGACTCCT[A/G]TAAGTTGTCCTCCAC | 16443 |
| rs222136791 | in-del | -/CG | | | intron-variant | Itsn1 | Mm_Celera | 16:91907585 | GAGGGCAGGAAGCCA[-/CG]CGCGCTCCTCCCTCC | 16443 |
| rs222159890 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91862091 | GTCCTTTGAGGAGCA[A/G]AAACAGCTGGTGCCA | 16443 |
| rs222183193 | snp | A/G | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91858570 | AAACTCCAGGGTTAA[A/G]TGGAGGCTGCACTCA | 16443 |
| rs222194731 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91785724 | TGTCAGATACGGTTT[G/T]GGGTTTTAGGTTCCC | 16443 |
| rs222216864 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917066 | GGGCTGGGAGGCAGA[A/G]AAGGGACCTCCTTTG | 16443 |
| rs222218290 | in-del | -/TTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91870065 | TTCCTGGTTTGTTTT[-/TTG]TTTTTGTTTTTGTTT | 16443 |
| rs222259586 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91880520 | TCATGCATCACCCCA[C/T]TTCAGATGGATGGAA | 16443 |
| rs222261304 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91739214 | GTCTCTTGCTGAGCC[G/T]AGAGCTCCACTGGTG | 16443 |
| rs222272556 | in-del | -/TGTGTGTGTGTGTGTGTG | | | intron-variant, cds-indel | Itsn1 | GRCm38.p3 | 16:91829784 | GCGGTCTTGTGACTC[-/TGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 16443 |
| rs222302359 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799416 | TAAATAACCCAGAAG[C/G]TTCAATTGGCCAGAA | 16443 |
| rs222303122 | in-del | -/GG | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890333 | TAAAATGGCAGTTGT[-/GG]GTTTTTTTTTTTTTT | 16443 |
| rs222312147 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91898919 | GGCACCTGTCCTGCT[-/C]CACCCAAAGGTACCC | 16443 |
| rs222312436 | snp | A/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746257 | TGCTTGTCAGTAGTT[A/T]AATACGGAGTTATCA | 16443 |
| rs222328682 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91829853 | GCTGCTGCGTGTGGT[A/G]TCAGAAGTTCTTAGC | 16443 |
| rs222334486 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91860683 | TGTTTCTGGAACACT[C/T]AGTTGTTGGGAAAAA | 16443 |
| rs222336502 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91835832 | ATTCTTCTCCCCCAC[C/T]GAGAGGGGACAGGGG | 16443 |
| rs222336861 | snp | C/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91828722 | GGGTCATGGCTCTGT[C/G]TCTGGCACAGCTGGT | 16443 |
| rs222355269 | snp | C/G | | | missense | Itsn1 | Mm_Celera | 16:91887433 | TCTTAGATATGCTGA[C/G]CCCGACTGAGAGGAA | 16443 |
| rs222361815 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91806800 | ATTATTCTTATCTGT[C/G]AAAAGAGTAGAGAAG | 16443 |
| rs222384441 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91833194 | TAAAGGACAAATATA[A/C]AAATAAAACAAATAC | 16443 |
| rs222393393 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91835130 | AGCATCCCCATGAAA[A/C]GCTTGGTGAGATGCT | 16443 |
| rs222404767 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91903783 | TACATGGTGGTGTCC[A/C]GACAAGCATAATGCT | 16443 |
| rs222413822 | in-del | -/ATGTTGTTAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91789584 | CTAGCCATGTGTTTT[-/ATGTTGTTAA]ATGTACCTTCAGAGT | 16443 |
| rs222418198 | in-del | -/AAGAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91765484 | GGTGAGAGAATTACT[-/AAGAG]AAGACACTGAGGGTA | 16443 |
| rs222429951 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91823960 | AATACAGGCCTCAGA[A/G]CATAAATTGGTACTG | 16443 |
| rs222435103 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91856149 | ATTGAGGCAGAAGAA[A/G]CCCCAGGGAAGACTG | 16443 |
| rs222452444 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91823466 | TCTTCCTTCTCTAGC[C/T]GGGATATCTTCCTTT | 16443 |
| rs222467457 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91741446 | AATAGTGAGGTTCCA[-/G]GTGGACACACTGAGG | 16443 |
| rs222472396 | in-del | -/CT | | | intron-variant | Itsn1 | Mm_Celera | 16:91752367 | CTAGGATAACTCACC[-/CT]GTGTAAAGAACTATG | 16443 |
| rs222480289 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91800535 | TTTGTTGGTTGGAAC[A/G]CATTCATAAAGATTT | 16443 |
| rs222486911 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831866 | GTTTCAGCTTTTTTC[A/G]ACAAGCTGAGTTGTC | 16443 |
| rs222510055 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91831021 | ATAAATAATAAGTTA[A/G]CATACTTAGAATCAC | 16443 |
| rs222549272 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910601 | TCTCTCCCTGGCCTG[G/T]CGCTCACCAACTGGT | 16443 |
| rs222571578 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768721 | CCTCAATTCTACCCC[A/G]ACTCTTCCACAAGAC | 16443 |
| rs222586202 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91807942 | TATAAGTACACTGTA[A/G]CTGTCTTCAGACACA | 16443 |
| rs222593144 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91744367 | TGTTTTGCTTGTGTG[A/G]ATGTTTGTGCACTGC | 16443 |
| rs222593672 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91799562 | AATAGAAGAAATGAA[A/G]CAGTAGATATAAAAA | 16443 |
| rs222607947 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91777279 | TAGTTGTATGCCACC[C/T]CAATTGTCTTGTAAG | 16443 |
| rs222609605 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91826624 | AACTTGAAGCTAAAG[G/T]TTTTTTAAAGATTTA | 16443 |
| rs222624262 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91887623 | AGCCTTGGGCAGACT[-/C]CTGGTGTATGGGGAA | 16443 |
| rs222634812 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904317 | GCCCCCTGCCTTCCT[G/T]CCTACTGTCAAAAGT | 16443 |
| rs222646032 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91804171 | CATAGTTTCATGTTG[C/T]CTGTCATATGTTTCT | 16443 |
| rs222662195 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91806912 | GAAGGTGATTAGAGA[C/G]CTCTCGTGAGCCATC | 16443 |
| rs222671623 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91802586 | GGCAAGGTCGAGGGG[A/G]GAGGCTATGGCTAGG | 16443 |
| rs222675938 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91910956 | TGTGAGCCACCGTGC[A/G]GATGCTGGGACCTGA | 16443 |
| rs222680091 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91903884 | ATATATATGAGACCT[C/T]AAAGCCCCGCCTCCA | 16443 |
| rs222687133 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91838479 | TTGGTGGGGTGGGTA[-/T]TTGAGACAGTTTCTC | 16443 |
| rs222688548 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91881112 | ATTTCTACACTGCTC[C/T]ATGGCAAGCCAGGTA | 16443 |
| rs222694262 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91902032 | TAGGGTAGAGGGCGA[C/T]CACGCTGGATGAGGC | 16443 |
| rs222698710 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91887977 | TGGACATGAAGACAT[A/G]TTCCCCGGGGCTCTG | 16443 |
| rs222717798 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91833750 | AATGGAAAAATAACT[C/G]AGTCTCCCTAGATAT | 16443 |
| rs222723143 | in-del | -/CCCCCTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91910693 | TTGCCTTTTTTCCCC[-/CCCCCTTT]ATTTTTAAAAGATTG | 16443 |
| rs222724088 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91910609 | TGGCCTGGCGCTCAC[A/C]AACTGGTCCCACTTG | 16443 |
| rs222731005 | snp | C/G | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91853580 | TCTATGGCTGTGTGT[C/G]TGTGTCTGTGTGTGT | 16443 |
| rs222747893 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91862366 | GCTGCTTAAAGGAAC[C/T]GCCTCTTACTTCTGC | 16443 |
| rs222751595 | in-del | -/CA | | | intron-variant | Itsn1 | Mm_Celera | 16:91873922 | CAGCTGTCTGCAACT[-/CA]CAGTCCAGAGAATCT | 16443 |
| rs222774233 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91811934 | CCCCGCTGTGCTTTC[C/T]TCCCTTGAGCTGTAG | 16443 |
| rs222785136 | in-del | -/GGAAGTCTTGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91777016 | ACCTAGGATGGGTCT[-/GGAAGTCTTGG]TTAATCTAGCCTAGA | 16443 |
| rs222786641 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802313 | TTCTTTCTAAAAAGC[C/T]CTTTGGATATCTGAG | 16443 |
| rs222828840 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91744717 | GCATAGCTCTCTAGC[C/G]ACCATTGCATCAGTG | 16443 |
| rs222830000 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91846249 | AAAGCCACAGTGGGT[-/G]AGCATGCTCTGTCTG | 16443 |
| rs222841174 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91784747 | TCCTGACTGGCAGAA[C/T]TCATTTATGCATTCT | 16443 |
| rs222842135 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91857803 | AAACTGTAGCATGCT[-/C]CCCTCAAAACTGAAA | 16443 |
| rs222852709 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91810249 | GCCCCCTCAGACTTC[C/G]CTGTTTTCATGGTGC | 16443 |
| rs222853431 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91777312 | TGAGAGTAGTGTGGT[A/G]CATTCACAGACTTGG | 16443 |
| rs222857621 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91753199 | CCTGGCCATGGAGAC[A/G]TCAGATTTAGAGACA | 16443 |
| rs222866428 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91809490 | TGAGAGCCAGTGCTA[A/T]GTCTCTCTCCGTTGG | 16443 |
| rs222869184 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91797218 | GGCACCGTTCTGCCT[C/T]CCGTCTCAGTAAGGC | 16443 |
| rs222872169 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907988 | GTTTAGCGGTTAAGA[A/G]CACTGGCTGCTCTTC | 16443 |
| rs222876454 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91905215 | TACTAAGGGCCCAAC[A/C]TTTGACTCTGATGAA | 16443 |
| rs222881038 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91804826 | TTCATTCTGTGCCTA[A/C]ATCTTGATTTGGTGT | 16443 |
| rs222946925 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91902402 | AGAAAATCCAGTCTG[C/T]GTTGTCAGGATATCA | 16443 |
| rs222947611 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91774834 | AGTGTTCTCTCCTTT[A/G]TTCTTCAGAGAGACC | 16443 |
| rs222961673 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91854300 | ACATTTAAAGATGTC[C/G]AGAACCACCTGGGGA | 16443 |
| rs222964411 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91888458 | ATCAGATTGGCAACT[C/T]GTGCAGAACAAGGCT | 16443 |
| rs222989129 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91908650 | CAGGAGGGGGCCTTG[A/C]TTTCAAGTGCGGACA | 16443 |
| rs222989552 | in-del | -/TT | | | intron-variant | Itsn1 | Mm_Celera | 16:91786018 | CATTTGTGGGTTTTG[-/TT]TTTTTGTTTGTTTGT | 16443 |
| rs222991448 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91888328 | AGTCCACAAGGGTTT[-/C]CCCAATTATGTTGTC | 16443 |
| rs222993627 | in-del | -/TGTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91875809 | AACCTGTCACAGATG[-/TGTA]TGTAAGTCGCTGGTC | 16443 |
| rs222996466 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91781591 | TTATGCAGATGCGGG[A/C]ATCAAGCTCAGTCTG | 16443 |
| rs223010665 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91771711 | CCCTCTGCCCAGTAT[C/T]CTCCGAACCTCTATG | 16443 |
| rs223020081 | snp | A/C | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91863544 | TGAGAGCTGCGGACC[A/C]GCTGAACGTGTATCC | 16443 |
| rs223034630 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91887998 | CGGGGCTCTGTCAGG[C/T]TGCTGGCCTGGGATG | 16443 |
| rs223051916 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91893117 | CCTTGCCATGGGGAA[A/G]CTGAGCTATATGCTG | 16443 |
| rs223056568 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91911770 | TAGAAGAGCTCGAGA[A/G]CGGCCAGTCATAGGA | 16443 |
| rs223061103 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91886294 | TGGTTGCTGGGATTT[G/T]AACTCAGGACCTTTG | 16443 |
| rs223062423 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745667 | AACAGGACTGATGGC[A/G]TTCTGGTCATGCTGT | 16443 |
| rs223083044 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91832015 | TTGTCCTTGGCAGTG[A/G]TGGCCCCATAAGGGA | 16443 |
| rs223095201 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91753800 | ATGTGCCTGTTTCCC[A/C]AGCTGTGTGGGAGGC | 16443 |
| rs223108134 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91742383 | TGTGTGTGTGTGTGT[-/G]GTGTGCGTGTGTGTG | 16443 |
| rs223111253 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91892690 | GAAAATCAGTGCTCA[C/T]TTATGTGACTGACTG | 16443 |
| rs223129252 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91825335 | ATTTAAATATTTTGA[A/G]TTATAAATATCATTG | 16443 |
| rs223130513 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91779137 | GAAGGTGGAGTAGGA[C/T]ACTAACTTGCTTAGC | 16443 |
| rs223141383 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91891595 | GCGCGGGGCCTCCCC[A/G]TGGATCACTAATTAA | 16443 |
| rs223150183 | snp | A/G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91883955 | GCAGGTGGTGAGGGC[A/G/T]CTCTGTCCTGTGTAT | 16443 |
| rs223151511 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91822454 | CGTTTGGAAATGTTT[A/T]GTTGCCCTTGGGCAA | 16443 |
| rs223160315 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91789523 | TTCCGTGTACTGTGA[-/T]TTTTTGATGATATGG | 16443 |
| rs223161412 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91775322 | CATTCGACACATCCT[A/G]CCCTAGGCTCCTTAG | 16443 |
| rs223172992 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91838421 | TAGTACCCAAAACTT[A/C]AGAAATCTTTTTTAC | 16443 |
| rs223180891 | snp | C/T | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91727415 | GACCCCGCAATAGGA[C/T]GCAGGCTGCTGCAAG | 16443 |
| rs223204849 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91832458 | GGCTGACAGGCTGTA[A/G]TAGGTGGCACACTAG | 16443 |
| rs223214014 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889855 | CACGGATTCTGTCAC[A/G]AGGCCCTAAGTGTGA | 16443 |
| rs223216015 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91913956 | AAAGGACATGCTCCC[A/G]TACTGTGAAACACAG | 16443 |
| rs223226809 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91889341 | TCTTTCTTTCCCCAC[C/G]TCACTCCCACCTGCT | 16443 |
| rs223228890 | in-del | -/TC | | | intron-variant | Itsn1 | Mm_Celera | 16:91754906 | TGTGTTTGTCTGGCT[-/TC]TCTCTGCAGCCCCTT | 16443 |
| rs223232774 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91782150 | ACTCACGTTTTGCGT[C/T]TTAATTACAGGCGTC | 16443 |
| rs223255376 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750867 | GGAAACACTCCATTA[A/G]TATCTAAAACAGGCA | 16443 |
| rs223261288 | in-del | -/TTGGTGCAGTGAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91767558 | ATGGGTGATGAATCA[-/TTGGTGCAGTGAC]TTTCTACTTTTGCTT | 16443 |
| rs223268926 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91821781 | TGGTGACAGGCGGAG[G/T]GATCTTGGTAACATT | 16443 |
| rs223273443 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746598 | TTCAATGAAATATTT[C/T]ATCATTCTTGTCTTA | 16443 |
| rs223289792 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802873 | AATCTAGGAGTGTTT[C/T]ATTTTGGCAAGAAGA | 16443 |
| rs223292527 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91886768 | CTAAAAGCTGGTCTC[A/C]GGATAACCACATACC | 16443 |
| rs223327057 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91821048 | TGCCTTTTGGGAGCT[A/G]CTCTCGGCAGGCCAG | 16443 |
| rs223329162 | snp | G/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917217 | TGATCCCCAGCCCTT[G/T]CGTAAAGAAACCAGA | 16443 |
| rs223335483 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91828022 | TGGAAGAGGTGACTT[C/T]TGTTCAGGCATTTGT | 16443 |
| rs223348063 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746274 | ATACGGAGTTATCAT[A/G]TGGCCCTGCAAATTC | 16443 |
| rs223354307 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91755449 | AGAGCATTTTTAATT[G/T]GAGTGCCGTCAATAC | 16443 |
| rs223361217 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91857223 | GCATTGTGGGGTTTT[A/G]TCATTTGTAATGTGT | 16443 |
| rs223366050 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91810871 | TCAGAGCCCGGACAT[A/G]AGCAGGCCTGGGAGG | 16443 |
| rs223368069 | snp | C/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91916736 | TAGAAAGTAGCTGAG[C/G]TAGAGGAAGAGAAAG | 16443 |
| rs223383296 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91754807 | CTTGTCAATAGAGCA[A/G]CTTCTGCACTGTAAA | 16443 |
| rs223401890 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91905980 | CTGAAACATCTATAC[C/T]CTTCCCTTCCGCCAC | 16443 |
| rs223403488 | in-del | -/TTT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91897444 | TATGATAACTAAGCC[-/TTT]TTTTTTTTAGATTTA | 16443 |
| rs223414558 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91867108 | TCTGTCTTCACCATG[G/T]ACCCCATGTCTTATA | 16443 |
| rs223427469 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91792627 | GGAAAGCAAAGCAAA[A/G]CTCAAAGGAGCCGAG | 16443 |
| rs223441666 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91792027 | GCGTCATGCATCACA[C/T]GCGCACAGCACCTGA | 16443 |
| rs223449167 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91860244 | CAAGCACTCTCTCAT[C/T]GCTGTTCTTCATTTG | 16443 |
| rs223457941 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91837716 | TGGGAATCTGTTTGC[G/T]ACCTTGTACTTTGTG | 16443 |
| rs223466331 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91869242 | TAGTGTACCGGCCCT[A/G]GGCTCAGTCTTCACC | 16443 |
| rs223471608 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91856314 | ACAGATTCAGATAGC[C/T]CTAAGTAGTGGCTCG | 16443 |
| rs223491350 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91751572 | ACTATATAGCCTTCT[C/T]TGGCCTTGAAATCAC | 16443 |
| rs223497732 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91799650 | AGGGAGCAGAGCAAC[G/T]GTACAGCAAATTCAG | 16443 |
| rs223499762 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91791559 | TTAGAAACTACAGCA[G/T]TAGTGTCACGCTTAG | 16443 |
| rs223521657 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91865995 | CCTTAGCGCCATGGG[C/T]CATGACACTCCTTCC | 16443 |
| rs223531194 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852717 | TGCTCCGGCAAGTGC[A/T]GGCAGCTACAGACCA | 16443 |
| rs223534656 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898759 | ATAGTTCCACTCCCT[A/G]GCACAAGCAAATACA | 16443 |
| rs223548875 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91891106 | GAGAACTGTGAATAA[C/T]ATTGACAGCTGGAGC | 16443 |
| rs223560616 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803497 | GTACCACATTCCTGA[C/T]GCCCATGGAGGTCAG | 16443 |
| rs223571796 | in-del | -/CT | | | intron-variant | Itsn1 | Mm_Celera | 16:91758045 | AACTGAACTCAGGAC[-/CT]CTGGAAGAGCAGTCA | 16443 |
| rs223588151 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798887 | ACAGTCTGCTTTCCA[C/G]AGCCCCCTGCTCCCA | 16443 |
| rs223596935 | in-del | -/TT | | | intron-variant | Itsn1 | Mm_Celera | 16:91883131 | AATCATTCACTACAC[-/TT]TGTCCTTCATCTTTC | 16443 |
| rs223600425 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91827572 | CATGCAGTCAGCCTC[A/G]GTTGAAGCTAGTGAG | 16443 |
| rs223603221 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913026 | TCCATTACTGGTTTG[A/G]GGGAAAGACCTTTGG | 16443 |
| rs223638615 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91903913 | CACAGTGGCACACTT[C/T]CGCTAACTAGGGTAC | 16443 |
| rs223665656 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91903319 | GGTTGGTGTGTCTGA[A/G]GAGAGCAACAGTGTA | 16443 |
| rs223668026 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91834614 | TTTCCAGTTGAGGCT[C/G]CAGATAAGTTCTGCC | 16443 |
| rs223668109 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91826776 | GTTTGTGTGTGTCTG[G/T]GTGTTTGTAACTCTC | 16443 |
| rs223668800 | snp | A/T | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | GRCm38.p3 | 16:91729807 | TGGGCGTCCGCAGCC[A/T]CGGCCGGCGCTCCCG | 16443 |
| rs223676754 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91833875 | AAGTGATTTATCCCT[C/T]TTGGACATAGGGAAG | 16443 |
| rs223688282 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91768881 | GGTTCTTGCCCGTGG[G/T]ATGGGTCTCGCAGTT | 16443 |
| rs223709836 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91757381 | TGCTTTTTCTAGTAC[C/T]GTGCGGAAGAACTTC | 16443 |
| rs223725660 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91777353 | CTGGTTTCTTCTTTC[A/T]TGTCTTCCCCACACT | 16443 |
| rs223768973 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91859294 | ATAAAACAAAACTGT[A/T]GTTTGGGAGAGTTTT | 16443 |
| rs223779544 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91810362 | CATAAAAATTATTTA[A/G]CACTTAAATACTCCC | 16443 |
| rs223779794 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91874190 | CCAGTCTGTTGCTTC[C/T]TGAAGGTTCTATTCA | 16443 |
| rs223780748 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91902090 | GGCCCTGTAGAGCCT[-/C]CAAGCCAACAAAGCA | 16443 |
| rs223786813 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768553 | GGACCCTCCTGGAGA[G/T]CAAGCTGCACATCTG | 16443 |
| rs223799286 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91881320 | TCTTTGATGCCCTTC[A/T]TGGCATCTCCAACCT | 16443 |
| rs223801599 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91868665 | TAGGCCTCTGTACTC[A/G]GTGACATCTGTGGAG | 16443 |
| rs223814400 | snp | C/T | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91905370 | CAAGGCCAAGAGCAA[C/T]AAAGAACTGTATGGC | 16443 |
| rs223833505 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91897744 | TTGGATGCCCTGGAA[C/G]TGGAGTGTCAGATGG | 16443 |
| rs223837369 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91776719 | TCATGGGAAGAATGG[C/G]GGGCACTTCCTCCAA | 16443 |
| rs223839017 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91806001 | ACCAGGAGAGAAAAG[G/T]CAACACCGCCAACCT | 16443 |
| rs223840984 | in-del | -/TG | | | intron-variant | Itsn1 | Mm_Celera | 16:91759121 | TGTCTGTGGAGGGCC[-/TG]TGTGGGTTTGTCATT | 16443 |
| rs223845095 | snp | G/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912488 | GATGGGGCCCTAGAT[G/T]GAATGGCTCTGGAGC | 16443 |
| rs223850344 | snp | A/G | | | synonymous-codon | Itsn1 | GRCm38.p3 | 16:91839805 | TCCGCATCAGGAGCC[A/G]GCTAAGCTGGCCACC | 16443 |
| rs223868975 | in-del | -/AGGAGGAAGGA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878137 | GGGAAGGAGGGAGGG[-/AGGAGGAAGGA]AGGAAGGAAGGAAGG | 16443 |
| rs223876622 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91764194 | GAAGGGTTCTTCTAG[A/C]CGTCACCCAGGGTGG | 16443 |
| rs223879429 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91902452 | TCAACAGCAGTAGCT[C/T]GATCCACTCGCAAAC | 16443 |
| rs223880807 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91771881 | TTGTTTGTGGGTGTA[A/G]ATTTTGATGATGTTT | 16443 |
| rs223889080 | in-del | -/TGTC | | | intron-variant | Itsn1 | Mm_Celera | 16:91838097 | ATGTGTGTGTGTCTG[-/TGTC]TGTGTCTGTGTGTGT | 16443 |
| rs223891674 | in-del | -/AATA | | | intron-variant | Itsn1 | Mm_Celera | 16:91876518 | GTGAAGTCCAGCTTG[-/AATA]AATAAAACAGGACAG | 16443 |
| rs223928600 | in-del | -/TCCCTCCC | | | intron-variant | Itsn1 | Mm_Celera | 16:91824940 | GTCTTATTGTTTTCT[-/TCCCTCCC]TCCCTCCCTCCCTCC | 16443 |
| rs223936804 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91902950 | GGAAGGGCAGCCAGG[C/T]GGTGGTGGCTCATGC | 16443 |
| rs223967599 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91875745 | GAATGTGTGAGGCTT[A/T]TAAATACCACAAGCA | 16443 |
| rs223973075 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91737598 | CTGACTCTTGGATCT[C/T]AGGTTGTGGGACATA | 16443 |
| rs223990484 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91767664 | GGGGGCTCTCCTTAG[C/T]ATCAGAAATCTCTAT | 16443 |
| rs223997591 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91819041 | GAGTTGGAGAGATGG[C/T]TCAGTGGTTAAGAGC | 16443 |
| rs223999052 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91769831 | CTGGTTGTTGGACCT[C/T]TGCTCGCTCCAGTCA | 16443 |
| rs224004071 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91768204 | TTTGAATTACATTGT[C/T]ATTGTGAAACTTTTT | 16443 |
| rs224012088 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91887644 | GTATGGGGAATAACA[C/G]AGGGGGTTTTACCCT | 16443 |
| rs224012220 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91745118 | TTCTATAGTTTTTTA[A/C]AAATGTGTTTTTATT | 16443 |
| rs224012227 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91737136 | TTGGCCAATGGGAAG[C/T]AGCACTTATTTTTGT | 16443 |
| rs224035380 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91874902 | CTGTGCCCACCCTCT[G/T]TCTAGTAGTTCCATT | 16443 |
| rs224035522 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91883474 | GAAAGAAAGAATGAA[A/T]GAATCTAAAGCCAAT | 16443 |
| rs224049321 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91825910 | GCTGGGGCCACACAC[A/G]GGCCTTCCTTCTGCC | 16443 |
| rs224052704 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873096 | TTTTCAAACTGTCTT[A/G]GTTATCCTCTATGTT | 16443 |
| rs224084708 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91887010 | TGGGAGCTCTGGTGG[A/G]TGTTAGCGGGTCATT | 16443 |
| rs224093144 | in-del | -/GT | | | intron-variant | Itsn1 | Mm_Celera | 16:91892859 | ATGGAGACCTGCATA[-/GT]GTGGAACCTCCTCGA | 16443 |
| rs224100884 | in-del | -/ATTCC | | | intron-variant | Itsn1 | Mm_Celera | 16:91881921 | TCACTTAGAAAAGGG[-/ATTCC]ATTCCGGATGAATGT | 16443 |
| rs224101320 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91740131 | CACGTTTTCAGATGG[A/G]CATGAGCCTGGTTGA | 16443 |
| rs224101533 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91775414 | AGTTAGATTTTGTGG[G/T]GCAACTCAAAATAAG | 16443 |
| rs224106777 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91879276 | CTTATAGGAAGTGGT[A/G]GAAGAAAAGATGTTG | 16443 |
| rs224120868 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91882111 | CCCACGAGTGTCTGT[A/G]TTCACCTAGCTGCTT | 16443 |
| rs224121458 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91739532 | CTCATTCTCCCCTCA[C/T]ACTGTCCCTCTCCCC | 16443 |
| rs224125788 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91744491 | GGGAATTGAACTCAG[G/T]TCCTCTGGAAAACAA | 16443 |
| rs224136550 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91880233 | GGAACGGTAGCTAGT[C/T]CACAGGATTGTTGGT | 16443 |
| rs224143787 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91869567 | CATGCAGGAGTAGCT[-/C]CTGCGCATGCCCCCC | 16443 |
| rs224146482 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91847004 | AGAGTAAACTAGGTT[A/G]AAATGAGGTACCAGA | 16443 |
| rs224151120 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91825445 | AAGTACACTGTAGCT[A/G]TCTTCAGACACACCA | 16443 |
| rs224204676 | snp | C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746335 | AGCAGGTGTTCACAT[C/G]AAAGTGAGCGTTCAC | 16443 |
| rs224205912 | in-del | -/TTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91882624 | TAGTCATTGACTAAC[-/TTA]TTATATTCTTTGGCT | 16443 |
| rs224206279 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91738650 | CAGTGCTGCCTGTAG[A/C]TAACCCAGCGAAGGT | 16443 |
| rs224217254 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91846050 | ACGCCCAGCAGGCAC[A/G]ATACTCAGTGTGTAG | 16443 |
| rs224224450 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91841270 | AAGGTTCTCTGGGCT[G/T]TCTGCCCACCGCATT | 16443 |
| rs224229258 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91736485 | AAGGTCATAGCAAGC[C/G]GCCAAGTTTTATCCT | 16443 |
| rs224235454 | snp | A/C | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91853617 | GTGCGCGTGCATGCG[A/C]GCGTGCTCGGCACTC | 16443 |
| rs224240432 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91795053 | GTCAAGTTTCCAAGT[-/C]GCCTATGAGGAACAT | 16443 |
| rs224241770 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745885 | TTTTCCTTTAAGCTT[A/G]GAAGAAAGAAGAGGG | 16443 |
| rs224243061 | in-del | -/A | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91853328 | GGACTTATGGGAAAT[-/A]AAAAAAGCACAGTCC | 16443 |
| rs224265201 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91744097 | GCATTTCATGGTATT[C/T]CCCCCATCCTATGGC | 16443 |
| rs224276244 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91735760 | GCTGTCCAGGTAAGC[A/G]GGCTCTGTGTAAGCA | 16443 |
| rs224297281 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91845759 | ATACCCCAAGCCTAA[A/T]GCTCTCTCGCTGGGC | 16443 |
| rs224307854 | in-del | -/GA | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802429 | GTGTGTGTTCCCAGT[-/GA]GAGGAGGAGTCTAAT | 16443 |
| rs224324126 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91796004 | TACCCTGAGTCAAAT[C/T]ACTCGAAGACCCAGT | 16443 |
| rs224330230 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91886356 | CATCTCACCAGCCCC[C/T]GGGGGGACCACTTTT | 16443 |
| rs224344045 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91885950 | AAGGGCGAATGTGGT[-/C]GGGGGTGGGGGGTGG | 16443 |
| rs224358887 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91855745 | ATTACATAAGAGTAA[C/G]TAATTGCCTTAACTT | 16443 |
| rs224363598 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795262 | GTAGCAATGGCACAG[A/G]TGACCTAGCCTGAAG | 16443 |
| rs224375922 | in-del | -/TGA | | | intron-variant | Itsn1 | Mm_Celera | 16:91814515 | GTACTTACTTCCACT[-/TGA]TTTCATTGATGATTT | 16443 |
| rs224378222 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91743739 | AACTCACTCTGTAGA[A/C]AAAGCTGGCCTCAAA | 16443 |
| rs224443607 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91820084 | GTCTCCGTCATCATC[A/G]TGACAAGGAACCTTC | 16443 |
| rs224448211 | snp | A/G | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803547 | TGGACTTGACGTACC[A/G]ACACAGTTATGAACC | 16443 |
| rs224468604 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91852322 | CTGAAAAATCTCTCA[A/G]TTGCTTAAGTGTCAT | 16443 |
| rs224540153 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900729 | CAAAGGGTTTTATAT[C/T]TTACTCCTTTTTTTC | 16443 |
| rs224550982 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91819632 | AGATGTTGTCTTAGG[G/T]TTTTTATCACTACAA | 16443 |
| rs224554881 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91826852 | GAGTGCTGAATCCTT[G/T]GCTGGTCCTTTGTGA | 16443 |
| rs224559569 | in-del | -/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91895523 | CGGCTTTAAACAGGA[-/C]CCCCACTCTTTGCTG | 16443 |
| rs224578959 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91906078 | GTTTGTGTGTTGCCA[C/T]GCCATGTGAGATTTT | 16443 |
| rs224591966 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91901183 | ACAGATGTGAACACA[C/T]ATGCATGCATGTCTA | 16443 |
| rs224605300 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91826363 | ATTGAGAGTAAAGAT[C/T]GTGTGCTCAGTATGC | 16443 |
| rs224616807 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91856993 | TCTTCACATTAGCCA[-/G]TGGGAGGAGCTGGCA | 16443 |
| rs224634253 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823872 | TGTTTTATCAGGGGT[C/T]TATCATGCACATTCA | 16443 |
| rs224634266 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91832134 | TAACTGACTCCTTGT[A/G]GTTCTGGGAACTTCA | 16443 |
| rs224650595 | snp | A/C | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831359 | CCTGACATAGAGGCT[A/C]CTTCCTGTGCTGGAG | 16443 |
| rs224684842 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91765870 | TGTGTTTAATTCTTG[C/T]AGCTCCTGCAGTTTA | 16443 |
| rs224713397 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91877029 | CACATGTCCTGCCCT[A/G]CCCTGCCCCCCACCC | 16443 |
| rs224718455 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91797365 | TTTTTTGCCCAAGTG[A/G]CAAAATTATAATATA | 16443 |
| rs224750293 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823439 | CTTTGAGTACCCATG[A/T]AATCTTTAAGGTCTT | 16443 |
| rs224765964 | in-del | -/GCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91790296 | CTGAGTAGTGGCATG[-/GCT]GCTGTTAAGGAGCAG | 16443 |
| rs224770190 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91884716 | GTGTAGCCCTGGCTG[C/T]CCTGGAACTCACTCT | 16443 |
| rs224776719 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91796551 | AGTGTTGGCATGGTC[A/G]CGGTGTCTGTTCACA | 16443 |
| rs224780698 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91897793 | ACTGGGAACCCAGGG[C/T]TCGTTACCATGGCAC | 16443 |
| rs224784434 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91733372 | TACAGCTTTTGGTAC[-/A]AAAAATGGGATCTTG | 16443 |
| rs224804037 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830557 | GCCTGGGACGCCACG[C/T]CCACGTGAAGCAGCT | 16443 |
| rs224814239 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91794940 | CTGTCACGGTTGTGG[C/T]TTGTGAGTGCTATAG | 16443 |
| rs224828552 | snp | G/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91803152 | ACTGCTTGGTTTTTA[G/T]TTTTAAATTTATTTA | 16443 |
| rs224830841 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91877575 | TTTGGTGTGTGCATG[C/T]GGAGGGGACATGCAA | 16443 |
| rs224833751 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91794555 | GTCCTGGAGTTGCCC[A/G]TAATGGACAGAACTC | 16443 |
| rs224850152 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91885313 | ACCCGGCTGCTGGGG[A/G]ACTTTTGGATCTGGC | 16443 |
| rs224858729 | in-del | -/GGAGGGAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91878005 | GGGGGAAGAGGGGAA[-/GGAGGGAG]GGAGGGAGGGAGGGA | 16443 |
| rs224869663 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91876123 | GGATCTTGGCTGTCT[-/G]GGGCATTGCCTTGGA | 16443 |
| rs224890006 | snp | A/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830877 | TAAAATGAGGACAGA[A/T]TCTTGCTGTAGGCAG | 16443 |
| rs224907321 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91793254 | CCACGTGTAACTCGA[C/T]GGTTTGTAGAACTGT | 16443 |
| rs224912085 | snp | G/T | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91730120 | GGGCGTGCGTCCCCT[G/T]CTCGGCCGCTTCGCC | 16443 |
| rs224923848 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91741174 | GTAAGCTCAACTGCG[A/G]TGATGCTCATCTTTG | 16443 |
| rs224934425 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91767819 | GTGAGATCATTTTAA[C/T]TCTCAGCCATGTAAG | 16443 |
| rs224944361 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803813 | ACCGGCTGGGTGTAC[C/T]GCTGAGAGGCAGAAA | 16443 |
| rs224945294 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91814576 | CTATTAGAATGATAT[-/A]ATTTTTTTTCCACAC | 16443 |
| rs224948393 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91902184 | GGCCTTGGGGACCTA[C/G]GTCTCCATCTTAAGA | 16443 |
| rs224957709 | in-del | -/GTGTGTGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91867013 | TGTGTGTGTGTGTGT[-/GTGTGTGC]GTGTGCGTGTGTGAA | 16443 |
| rs224958160 | snp | C/G | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91747986 | CTTTCCCGCTGAAGA[C/G]TGCCCTTGTGCACGG | 16443 |
| rs224963408 | in-del | -/TTTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91886186 | TTGTTTAAATATTTA[-/TTTA]TTTATTTATTATATG | 16443 |
| rs224983500 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91908362 | CCCGAAGCCTGCTCT[A/G]TGCGTTCTGTTTGGC | 16443 |
| rs224983564 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91901464 | ACCTTTCCTTGGCTG[C/G]CTCATTCGCTCATAC | 16443 |
| rs225004673 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91738503 | AGCTGAGATGATATT[A/G]TAGTTGTGGTTTGGC | 16443 |
| rs225006782 | snp | C/T | | | upstream-variant-2KB | Itsn1, Cryzl1 | GRCm38.p3 | 16:91729130 | GGGTGCTATCCAAAC[C/T]ACTTCATTGGTGTAT | 16443 |
| rs225012630 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91767131 | TTTTGATTATGTGGC[A/G]GACGTAACCTATTCT | 16443 |
| rs225017989 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91742062 | CTTGTGCAGCAGGTT[C/T]GCCACCATCTCTGTG | 16443 |
| rs225018467 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907700 | GCTGTTACTCAGGTA[A/T]TGAGTGCCTGCCTCA | 16443 |
| rs225040118 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91850787 | TCTTACTGCTTACGG[C/T]GCGTGCCTTTCCTTC | 16443 |
| rs225048021 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91774957 | TGGGCAGCAGTTCGA[A/G]GGTTCCTGACTCTTT | 16443 |
| rs225050462 | snp | A/G | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91858485 | CTGCTGAGTTCTGGA[A/G]TATGGTGGTAACTAA | 16443 |
| rs225051610 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91737631 | TGGGTTGTGTATGTT[C/G]TTTGAAGTTCTGTGA | 16443 |
| rs225071680 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91840485 | TTCTTAAGCACAGTG[A/G]TAGACAGAAAGCAAC | 16443 |
| rs225076419 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91732305 | AAGAGCAGAATTGGT[-/G]GTGGCCTGCCTAGAA | 16443 |
| rs225095674 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91793971 | GACACGCTCGCACTC[A/G]GCTGCTGCAGCTCTG | 16443 |
| rs225102440 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91878812 | GGAGCTGTCCGGGGT[C/T]GGAGGTGTTTTTTGT | 16443 |
| rs225110450 | snp | A/C | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802246 | AAGCATCAACTATAA[A/C]TATAGATAGCCTTGG | 16443 |
| rs225112243 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91753894 | CCATTTCAGAACAAC[-/A]AAAACCCCCTTACTT | 16443 |
| rs225130547 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91774253 | AAACGCTTTTGATTT[A/T]TCAGTCGGTTATTCT | 16443 |
| rs225136646 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91748641 | CAGCGGACTGGGGGT[A/G]TTCTATCCCTAGGCA | 16443 |
| rs225140719 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91839900 | TCTGTATGTATGTAA[A/G]ACAGACAGTCATCTC | 16443 |
| rs225143701 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91904604 | GGAAAGTAACATTTG[A/T]ACAGGAGTCCTGCCT | 16443 |
| rs225158215 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91886449 | GCATCTGCGGCAGGG[G/T]GTCTGCACTGATAAG | 16443 |
| rs225161385 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91878457 | GGCCCTTCATCTTGG[A/G]GCTGCAGAGGAGGTG | 16443 |
| rs225200350 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91770179 | GTCTGAGTGTCCCAG[C/T]GTCACCGTGCACACA | 16443 |
| rs225208263 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91851636 | CTGAGTCCCTGTGTC[C/T]ACACCACAGAAGAGG | 16443 |
| rs225251081 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91905160 | AAGCTGCTGCCAGGG[C/T]TCTTTAGAGCCGTTC | 16443 |
| rs225259785 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91743362 | GCTTATATTTGCAGT[C/T]CTGTAATTCCATCAC | 16443 |
| rs225260539 | in-del | -/TC | | | intron-variant | Itsn1 | Mm_Celera | 16:91731431 | CTCTTTCTCTCTCTC[-/TC]TTTCTTTCTTTCTTT | 16443 |
| rs225267287 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91885682 | ATACCACGATTCCCT[A/T]GACGGATAATTCTCG | 16443 |
| rs225270275 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91812917 | GAATATGGTTGTCTT[A/G]GTTAGGGTTTTACTG | 16443 |
| rs225283964 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91779124 | CAGTGGTGTTGGAGA[A/T]GGTGGAGTAGGATAC | 16443 |
| rs225287960 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91882744 | AGAGAGGAGAGTCTT[C/T]CCCCCCCTCCCTAAG | 16443 |
| rs225305680 | in-del | -/TCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894207 | TCCATGTATTTGTGG[lengthTooLong]TCTTTCTTTCTTTCT | 16443 |
| rs225319137 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91828559 | ATCCAAAGCCAGGCC[C/T]AACGTGCTCTCTTCT | 16443 |
| rs225329941 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91883300 | TTTTCTAAATACTAC[-/T]TTTTTTTCAAACAAA | 16443 |
| rs225343271 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91812298 | CTAAGGACTTGACGT[A/T]TAACCTAACAGTTCT | 16443 |
| rs225349524 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91889249 | TCCCCTCTAACCAAG[A/G]ATGCTGCCCCTCTGT | 16443 |
| rs225350302 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742803 | GTAGTTACAATCAGC[A/G]TTGGCTTCTTTTCTT | 16443 |
| rs225350322 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91751022 | TGTATTGGCAACCCT[C/G]ACTTCCCTGTAGAGT | 16443 |
| rs225378107 | in-del | -/CTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91814710 | GCCTGTGCTGTTGAC[-/CTT]CTTCTGAGTAAATGT | 16443 |
| rs225389728 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91915098 | GAATTTCAAGTGTGT[C/T]CCGCTGGGCTCAGCT | 16443 |
| rs225394999 | snp | G/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916093 | AAGGAAGGATGGATG[G/T]AAGGATAGAAGGGAT | 16443 |
| rs225408229 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91832863 | TCTTTGACTTTGTAC[-/T]TTTTTTTTTATATCT | 16443 |
| rs225420010 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91822278 | GAGTTAAAAACATTT[A/T]CCTACATTTTTACTT | 16443 |
| rs225474283 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91818841 | CTCCCACTCTTCCCC[A/G]GGAGAGCTACCGTAT | 16443 |
| rs225479572 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91784262 | TCATCCATTTTGCCC[C/T]AATTCAGAACCTGTA | 16443 |
| rs225485629 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91765937 | GACACTCGGTCACTG[A/G]TAATGTTAAGCTGCT | 16443 |
| rs225492585 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91783694 | GTTTGGTGATCATCA[A/G]TACATTTGCAAAGTT | 16443 |
| rs225492828 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91791414 | AATCATTCTAAGCAG[C/T]GAAACACTCGGTCCC | 16443 |
| rs225510626 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91869330 | ATGCTGTGGGAACTG[A/G]GTGGTACAGCACTCT | 16443 |
| rs225518530 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91817101 | GCTGATGAGTGTTGT[A/G]ATGCACCTGTAGTCC | 16443 |
| rs225523879 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914504 | GCACCACCTGGCACC[C/T]TGATGCCAGCTGTTC | 16443 |
| rs225551696 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91833910 | TAAAAGCAAGCTGAC[-/T]TTTTTTATCTTTAGT | 16443 |
| rs225551862 | in-del | -/TTTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91800658 | CACCTTTTTCTTTTC[-/TTTTT]TTTTTTTTTGTGAAA | 16443 |
| rs225554859 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91790930 | AGCCCCAAAACAAGC[A/C]GACTTTCACAGTGTG | 16443 |
| rs225558987 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91893176 | AGTCCACCCTGGCCG[C/T]GTGGCTCTGCACACT | 16443 |
| rs225562700 | snp | A/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913322 | GCCTTTGCATGTCTC[A/T]GGCTCCTGGGCTCAG | 16443 |
| rs225563499 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914103 | CATGCATGGTGACCC[C/T]ATAGGTTCTGGGTTA | 16443 |
| rs225583918 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91883857 | AACAGGACCTCATTC[C/T]AGTTTCTCAGTCATC | 16443 |
| rs225597857 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91898319 | AGGGAATCCTAGCTA[C/T]CCTCACCTGATTGGT | 16443 |
| rs225598163 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91892826 | AGAAAGAAAAACAAA[C/T]GGCCTGAAGATTTTA | 16443 |
| rs225602209 | snp | C/T | | | downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91920901 | AGCTTGGGTTTCTTT[C/T]TTTCTTTCTTTTTTT | 16443 |
| rs225604103 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919723 | GAAAACCCACAGAAG[A/G]CTCACCTGCCTCAGC | 16443 |
| rs225613416 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91877710 | TGTAATCCCAGCACT[A/G]GAGAGTCTGAGGCAG | 16443 |
| rs225641686 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91864477 | CTTTTCAGTAAGTTT[-/A]CTTTTTGTTTTTTGG | 16443 |
| rs225654528 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91789376 | TACACTATAAACCTA[C/G]TTTAATTTTTTGCCT | 16443 |
| rs225692438 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91787756 | GGCCTGGGGACAGGA[C/G]TGTGAGACTGGGAAG | 16443 |
| rs225695252 | in-del | -/TCTGGGGAGGCCAG | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919400 | CTGGAAGCCCACAGC[-/TCTGGGGAGGCCAG]AAGTTAGGAAGCCGC | 16443 |
| rs225696582 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91734312 | AGGAACTGAGTTTGG[A/G]TCCCCAGAGCCTACA | 16443 |
| rs225710813 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91739963 | ACACATTGCTAGCAT[C/T]ATCTTGGCCCTTATT | 16443 |
| rs225719771 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91766739 | TTATGTTCTTTATGC[A/G]AGGCGTGGGGCTGTG | 16443 |
| rs225722976 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91795628 | CCCAAGTGCTGGGAT[C/T]AAAGGTGTGCGCCAC | 16443 |
| rs225741967 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91817862 | GTCCTGGAACTCACT[C/T]TGTAGACCAGGCTGG | 16443 |
| rs225755851 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91794023 | CAGTTCTCAGAGTCT[G/T]TGTTTCTCATTGTGT | 16443 |
| rs225763179 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91761334 | GAAGTGGCTGTGCGC[C/T]TGTAATGCTGGCAGT | 16443 |
| rs225766040 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91896714 | ATTTGGAGCAACACA[C/T]GCACACACAAAGAGA | 16443 |
| rs225775959 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91836912 | TCATGTCAAAATGCA[A/G]CGAGTTCGATTTCTG | 16443 |
| rs225786886 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91843982 | ACCACCCCATATACC[A/G]CCACACTCTTATGTA | 16443 |
| rs225793368 | in-del | -/AAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91840240 | TGACATCTTGGGGGG[-/AAA]AATCACGTAACTTGT | 16443 |
| rs225793380 | snp | A/G | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91870733 | GGGCTGTTCCCTGCC[A/G]TAGAGCACAGAGGAG | 16443 |
| rs225800581 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91760669 | AGTGAGGCTGCGCCA[A/C]CCAGGCCTCCCCGAC | 16443 |
| rs225803591 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91768341 | TCCTCCCAGATCCCT[C/T]ACCCCTCACCCTTCT | 16443 |
| rs225837154 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91794953 | GGCTTGTGAGTGCTA[C/T]AGTTGAGCAGGACCG | 16443 |
| rs225872715 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91842073 | AATAAATAAATCTTT[-/A]AAAAAAAAAAGAAGA | 16443 |
| rs225882564 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91901375 | TCAGTGAGGGTGTGT[A/G]CAAGCTAAGCTCTGA | 16443 |
| rs225883475 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91896150 | TCCCTCTACATACCG[C/T]CTCAGCCTGGATTAT | 16443 |
| rs225892954 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91873386 | CCAAACTGCCCATTG[G/T]ATGGACAGATCAAAC | 16443 |
| rs225895081 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91767863 | AAGAGGAGACGAAGG[G/T]TTAGTTTTCTAATGT | 16443 |
| rs225897326 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758900 | TTGACTGGTATGGTA[A/G]TTTGTTTGTTTCTTT | 16443 |
| rs225897883 | in-del | -/ACCGTCC | | | intron-variant | Itsn1 | Mm_Celera | 16:91893035 | GAAATCATGTAGTAT[-/ACCGTCC]ACCCACACACCTGCC | 16443 |
| rs225902612 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872482 | TCAGAACAGAAAAGA[C/G]CCTGGAGGGAGGGAG | 16443 |
| rs225903779 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900938 | AGGGCGTCAGATCCC[A/T]TTACAGGGGGTTGTG | 16443 |
| rs225915892 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91766047 | GCTGTTGCCAGCACC[A/G]GTGCCATTGCAAAGG | 16443 |
| rs225923344 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913830 | TCAAAACACTACACA[C/T]TCATGTTTCTGTTGT | 16443 |
| rs225930017 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900266 | TTTGTTTTACCGTAA[G/T]TGTTTTTTGAAGCTC | 16443 |
| rs225950675 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91908145 | TAAATCTTAAAAAAA[-/G]AAAAAAGAAAAAAGA | 16443 |
| rs225961757 | snp | A/C | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91920066 | GTGCTGTACTGTCTT[A/C]GCTCTTCTGCTCTGC | 16443 |
| rs225968050 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91879851 | ATCCTACTCTGAGGT[A/G]TATGAAGCAGAATGG | 16443 |
| rs225974425 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91756515 | CCCTAGGCTGCATGC[A/C]TGTGTTTTCACATTG | 16443 |
| rs226002426 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91869430 | TACAACATTTAAGAC[A/G]GTGTAAAAATATTGC | 16443 |
| rs226007343 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91765557 | CTTGGGCATAGACTG[A/G]ACACCTTAAGCAGCA | 16443 |
| rs226013069 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734901 | ACTCTGAGTTCCTTT[C/T]CCTCTTTCAGCCACT | 16443 |
| rs226015066 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91869127 | CGCTGGCTTAACTTC[C/T]CCCTGAGGCAGGAGC | 16443 |
| rs226015500 | in-del | -/GTGTGTGTGG | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745322 | TGAGCTCTGCTGTGT[-/GTGTGTGTGG]GTGTGTGTGTGTGTG | 16443 |
| rs226015695 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91877899 | TTGTACCTCAGTATT[C/T]GGGATGTGGAGGCAG | 16443 |
| rs226026502 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91764558 | TTTAGTCATTTTGAC[C/T]TCCACTCCTCCCCGC | 16443 |
| rs226033500 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91736935 | AACTACAAGCCTGGC[C/T]ACAGCATAAATTTCC | 16443 |
| rs226040189 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91815954 | GAGCACCCCAAGATA[C/T]AGTCAGGAGACGCCT | 16443 |
| rs226065621 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91839104 | CTCGTCCTGCTCAGG[C/G]AGGACCTGTGAGAAT | 16443 |
| rs226074972 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91877186 | ACAGGGCCCTAAGGA[A/G]GACCTCACAAGGAAG | 16443 |
| rs226076607 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91878919 | TGCACTTCCCCACCA[C/T]GCAGCCTCTTGTGGG | 16443 |
| rs226085715 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91867996 | GGCTTTGATGTTCAT[A/C]AAACATTGTTATTTT | 16443 |
| rs226116781 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91794701 | CACTTACCTATGGGT[A/T]TAAGGACAAACATTT | 16443 |
| rs226121644 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91736106 | ATACAGTTTGTAGCC[A/T]CCTAACGAGCTGAAT | 16443 |
| rs226125362 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91894778 | TTACTGGCTGGCCCT[-/C]GGGCTCAGACTCAGC | 16443 |
| rs226144668 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91837629 | CTGCCTGGAAGACAA[A/T]CACTCTGTCTGTTCT | 16443 |
| rs226145764 | in-del | -/GAGGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91840658 | GGAGTCCAGGGGGAC[-/GAGGG]GGGGGAGAGATGAAC | 16443 |
| rs226147963 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734467 | CTATCTCACAACTTA[C/T]ATGGCAGAAGAGCAA | 16443 |
| rs226155957 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91876265 | TCTGCCTGCCAATAT[C/G]CCCCCTTCTCCCTCT | 16443 |
| rs226164934 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91822398 | TTCACCAGCTGAGCC[A/G]TTCTGCTGGCTCCAG | 16443 |
| rs226172657 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91895782 | ACATAAACACCAAAT[A/G]CATGCTTACTTCAAA | 16443 |
| rs226173655 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91838729 | CCCTGTGGCAGCTCA[G/T]AACTGTCTATACTGT | 16443 |
| rs226182719 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742490 | GCTCAGCCTTGAGAG[C/T]ACTGAATGCACATGC | 16443 |
| rs226201419 | in-del | -/TTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91811729 | CGCTCTAGTCTTTGG[-/TTTT]TTTTTTTTTTGAGAC | 16443 |
| rs226216697 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91844575 | AGCGCAGGTTGAGTT[C/T]CCAGCACCCACATGG | 16443 |
| rs226219106 | snp | A/C | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917554 | ATGCTATATTTTAAT[A/C]GGATCTGTTCTGTTT | 16443 |
| rs226225967 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91733993 | TTTTAACTTATTTTT[A/G]AAATTTTACTAATTT | 16443 |
| rs226236063 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91845457 | CGAGTGCATGCATGC[C/T]TGTGCTCAAGTAGAC | 16443 |
| rs226236414 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91837974 | GCCAGGGATCTTATA[C/T]AAGTTTATTGGACCG | 16443 |
| rs226240979 | in-del | -/A | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917059 | CTGTTGGGGGCTGGG[-/A]GGCAGAGAAGGGACC | 16443 |
| rs226285583 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91732356 | ACCGTTGCAGGGTGG[A/G]TGGGTGAGCCACACT | 16443 |
| rs226302023 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91757203 | GGCAAATCATATGAT[A/C]GCACACGTGCCCCAC | 16443 |
| rs226342406 | in-del | -/TGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91759195 | TGTTCTTTTGTCATT[-/TGC]TGTCTTTGTCCCCAA | 16443 |
| rs226347344 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91896568 | GGTAACTGGGAGGGG[-/A]AAAAAATGTTTTGCG | 16443 |
| rs226350689 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91785878 | AGTAAATAAAAGCAC[A/G]GAATGTGTAGTCCTG | 16443 |
| rs226360199 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91851730 | TGTGCAGTGAGGGCG[C/T]GTGGGAGGACAACTC | 16443 |
| rs226362086 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91851090 | CTGGGTCGGCTGGCT[A/G]AACCTAGTTCAGAAA | 16443 |
| rs226363477 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91792462 | ACACAGAATCAGTAG[A/G]CTAAATTTTGAAAAC | 16443 |
| rs226379729 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91740056 | GAAGGCTGCTGAGAG[A/C]CGTTCCATCCAGTGT | 16443 |
| rs226386225 | in-del | -/TCTTGTAGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91765865 | CCACTTGTGTTTAAT[-/TCTTGTAGC]TCCTGCAGTTTATAG | 16443 |
| rs226397735 | in-del | -/TTTTTTGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91748172 | TAAACTTTTTTTTTT[-/TTTTTTGG]TTTTTCGAGACAGGG | 16443 |
| rs226402802 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91816544 | AGAGGGAAGCCTCTG[A/C]CCCCAGTCAGCTGCG | 16443 |
| rs226406868 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91817128 | GTCCATCCTTGAAGT[A/G]GGATCTGATTGCTTC | 16443 |
| rs226407423 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91766905 | TTAGCCAGGATGGAT[-/C]CCCCCAGTGGGCCTT | 16443 |
| rs226413638 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91850319 | GGAAAGGGAGAGCTC[A/G]AGGAATCACAAGGTC | 16443 |
| rs226415611 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91765048 | TCTGTCAGTTTGAGG[G/T]TTTTTGTTACAATTG | 16443 |
| rs226435790 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91826981 | CAGGTTCCTCCTGAT[-/G]GGGGCTTGAAAGCAC | 16443 |
| rs226442764 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91816004 | CCCACATGGTAGTGT[A/G]TAAACCCATCATCCC | 16443 |
| rs226472500 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91841797 | AAGTTGACTGATTGT[A/G]TCTAAAGCTAGCACT | 16443 |
| rs226511612 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91823516 | CTTCTTTTGTTTTCA[A/G]TCTTACTACATTGAA | 16443 |
| rs226513138 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91816725 | CGCACATGCGCCAGC[A/G]CTGAGCTGCATCTCT | 16443 |
| rs226516728 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91868538 | TGAGGGTGGGCAAAG[A/G]CAGAGCCTGCCATTG | 16443 |
| rs226529509 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91876921 | CTGTCTGTACTTAAC[A/G]AGCCCCAAATCTTGC | 16443 |
| rs226532454 | in-del | -/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91828795 | CACAAGCCTCTTTCT[-/G]GTATGGTGTTCCATT | 16443 |
| rs226552990 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91849763 | GGTATACTTTAGCAT[A/T]CTTGGCTGGTGCTGG | 16443 |
| rs226563457 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91752654 | CCTGAAGCCATGGCT[C/G]TAGGACGCACTGGCT | 16443 |
| rs226564789 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91892124 | TGATCTTTCTGTGAG[A/G]TGGCAGCTCATCAGA | 16443 |
| rs226569944 | in-del | -/GGGGGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91876060 | TTTGCTGAATCAGAT[-/GGGGGG]GGGGGGGGGGGGGCA | 16443 |
| rs226581150 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919736 | AGGCTCACCTGCCTC[A/G]GCTTTAAATCACCTT | 16443 |
| rs226617899 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919109 | TTCAAGGGTTGGTCT[C/T]CCGGTTTCTGGTGTC | 16443 |
| rs226629151 | snp | C/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91918648 | TTGGAGGGGCTCCAA[C/G]ACCCTGGGGCTGGCC | 16443 |
| rs226649013 | in-del | -/AT | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91727972 | AAATGCCATATATAG[-/AT]ATATATATATAATTT | 16443 |
| rs226649686 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91752028 | AGTTCCGGGACGCTG[A/G]TCTGCCACAAGTGAA | 16443 |
| rs226668299 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91787846 | CTCAGTAAAGGTACT[A/G]GAGCTGGGTCTTGGA | 16443 |
| rs226680584 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91794341 | AATTCCTTAGTTGCC[A/T]TAGTTATTTAGGATC | 16443 |
| rs226683416 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91814204 | GCATGCCTCTTTTAG[C/T]TGTATGTTGCTGGCA | 16443 |
| rs226684989 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91759687 | GGTGGGAAGGAGCTA[C/T]GGGCAGCGCCTGGAG | 16443 |
| rs226695957 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91763015 | ATGCTTCATGTGGGT[C/T]TTACAGATGTTTAGT | 16443 |
| rs226707444 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91733037 | CTGTGCTGCCATACT[G/T]TGTGGTCACTTTGTG | 16443 |
| rs226737853 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91769339 | CTCACATACATAAGC[C/G]TTAGACAGAGCAGCA | 16443 |
| rs226744097 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91793441 | CATAAACCGTGCTGG[A/G]CTTTACTCTCCCCTG | 16443 |
| rs226753264 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91786692 | GACACTGTTGCAGTT[C/G]TAACTGCTGGTCGAT | 16443 |
| rs226753540 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91740937 | AAGAGATGCTCAACA[A/G]AACCTAATGTTGGAG | 16443 |
| rs226755663 | in-del | -/CTGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91865207 | GACTGCGGCTCCCTG[-/CTGC]CTGCACAAAGTTCCC | 16443 |
| rs226756700 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91820386 | AGGGCTTACTAGGCA[C/T]TTTTTAAAAAGCAAC | 16443 |
| rs226757501 | in-del | -/AGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91792633 | CAAAGCAAAACTCAA[-/AGG]AGCCGAGGAACTTGG | 16443 |
| rs226766291 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91861056 | CCTGAGCCCCCAGCA[A/G]CCCAGTTGTCACGTG | 16443 |
| rs226768061 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91758983 | AACTCACTCTATAGA[C/T]CAGGCTGGCCTTGAA | 16443 |
| rs226792143 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91843225 | ACAGCAAGCTTACAC[C/T]TTAGTCACCGTGTTT | 16443 |
| rs226796849 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91860480 | GGCTTATTAAACCCT[C/T]TGTCTCATTTCAATT | 16443 |
| rs226798688 | snp | C/T | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91870954 | GTGACCTTGTAGCCA[C/T]CTGAGGAAGCACCCA | 16443 |
| rs226801227 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91874691 | CTGCTTTCCTCCCTT[C/T]TCCCCTCCCCCAACG | 16443 |
| rs226823617 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91793001 | GCACACTCCTAAGCA[C/G]AGTTTCAGTGCTGAA | 16443 |
| rs226837215 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91894695 | TCGCAGAGGGGAATG[C/G]GGCAGGAGCTCAAGG | 16443 |
| rs226888978 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91881795 | AAGTGTAGCTCACGT[A/G]GCAAGAGAGACTAAC | 16443 |
| rs226907003 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916420 | GTCAAATCTCATTAC[A/G]GATGGTTGTGAGCCA | 16443 |
| rs226915457 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831162 | TTTCCATGCATTTAT[C/T]AGATGGAGACAACTA | 16443 |
| rs226940301 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91800875 | TGACTTGAATTTCCA[C/T]GAATCCTCTGGATCA | 16443 |
| rs226946368 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899893 | TTTCTTTTGTGTATC[C/T]TGTTCAAATGTTCAT | 16443 |
| rs227019562 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91738079 | TTAAACAAACAAACA[A/G]AAATTAAAATGAACA | 16443 |
| rs227020386 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91848431 | TCAAATTATCTTTAC[G/T]AATTGCATGACTTCC | 16443 |
| rs227022257 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830782 | TTCTTCCGCTAAAGG[C/T]CTTACCCATTTTCTT | 16443 |
| rs227034024 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91763947 | CTATAGATGTTTGCT[A/G]TAGGAGGAATCAGAC | 16443 |
| rs227048508 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91838890 | GCACTAGCTTTCCTG[A/G]CGCTGTGTCGCTCTG | 16443 |
| rs227051924 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91840418 | CTGACCTTCACTAAC[A/G]CAAGCTGTCCCTTAG | 16443 |
| rs227080237 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91837049 | CCCATAAACTATCCT[G/T]ACTCCGTCTAGGAAC | 16443 |
| rs227085168 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91791300 | TACAGTCATTCTCTC[C/T]ATAGCAAGTTCCAGG | 16443 |
| rs227086383 | in-del | -/AA | | | intron-variant | Itsn1 | Mm_Celera | 16:91874240 | TTTAAAGAAAGAAAG[-/AA]AAAAAAAGTATGGAT | 16443 |
| rs227096701 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91898695 | GGATGAGGGTCTCAA[A/G]GCCCACGCCCACTGT | 16443 |
| rs227126497 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91814889 | ACTAGAGAGATCAAC[C/T]CCTAGATACGTGAAT | 16443 |
| rs227126809 | snp | G/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91804333 | TTTATAATGCTAGGA[G/T]GACTAACAGATGGTC | 16443 |
| rs227138356 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803713 | TTCTACATAATGTTA[C/T]TATAACTCATCATTT | 16443 |
| rs227161770 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898286 | GTGGTCTACTTCAGC[A/G]CTGGACAGCAGAGAT | 16443 |
| rs227188996 | in-del | -/CT | | | intron-variant | Itsn1 | Mm_Celera | 16:91752209 | GCAAGTGGCCGCAGA[-/CT]CTGAGGCAAGCATGC | 16443 |
| rs227225685 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91815560 | TAACGTTTTATTCTT[A/G]AAAGAATTATGCATG | 16443 |
| rs227238479 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904493 | CTAGTAACGGGGTTC[C/G]ATTAAGCATGCACTG | 16443 |
| rs227246988 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91809668 | CACTCTGTGTGTGCG[C/T]GTGCTGCCACAGAGA | 16443 |
| rs227247133 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91816673 | TGATGGCTTGCAGAG[C/T]GCTGGGGATCAGAGC | 16443 |
| rs227269545 | in-del | -/GAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91857307 | AATACACAGAGGCCT[-/GAC]GACAAAATGGATGAA | 16443 |
| rs227290137 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911199 | TGGGATCCGATGCCT[C/T]CTTCTGGTGTGTCTG | 16443 |
| rs227293176 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91904496 | GTAACGGGGTTCGAT[G/T]AAGCATGCACTGTTG | 16443 |
| rs227305583 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91811148 | ACACTGTGACTGTTT[A/G]CGCTTCCCTGACACT | 16443 |
| rs227306172 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91768761 | TTCTTCCAATGTTTG[C/G]CTCTCGGCCTCTGCA | 16443 |
| rs227314710 | in-del | -/TTAAAAATTTACCAACTA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758324 | GCCCAGCTGTTTTCT[-/TTAAAAATTTACCAACTA]TAGATAATTGGGAAA | 16443 |
| rs227328436 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91731430 | TCTCTTTCTCTCTCT[C/T]TCTTTCTTTCTTTCT | 16443 |
| rs227335467 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91886375 | GGGACCACTTTTATG[-/T]AAAAAAAAAAAAAGG | 16443 |
| rs227341324 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867348 | GTGCATCTTAGCTAA[A/G]CATCAGCCAGTCTGT | 16443 |
| rs227343111 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91874061 | AAAAATATATAGACT[A/G]GTGATAAATTCCAAG | 16443 |
| rs227343935 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91906651 | TACTGGGTTGCACGC[A/G]CGCGCGCGCGCGCGC | 16443 |
| rs227346432 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91816087 | GGAGTCCTCAAGATT[C/T]CACGTGAGGCTTGGG | 16443 |
| rs227348373 | snp | C/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912585 | CTGTACCATTCCCCT[C/G]TAGACTTCCTTAGTG | 16443 |
| rs227355589 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91820032 | AATAGTTAAATAGGG[C/T]GGTTACCCTGTGATG | 16443 |
| rs227384760 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91911838 | AACTCTTTCTGATCA[C/T]CCTCTGCTTTTCCTC | 16443 |
| rs227402532 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91763907 | TAATTGTTGCTTCAA[-/G]GGGGAAAAACTGGTT | 16443 |
| rs227406646 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915881 | TCCTAAGATGCCACC[C/T]CCTCCTCCCCTGTAT | 16443 |
| rs227421297 | snp | G/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917842 | CTATACTCTTTTGTC[G/T]TTCTTGTCTTATCTC | 16443 |
| rs227434754 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91779943 | CTCATGAATGATCAA[A/G]GAAAATAAAGATTAG | 16443 |
| rs227442411 | in-del | -/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91815361 | AGTAAGATCTCTGCA[-/T]TTTTTGTGAACTGGA | 16443 |
| rs227456312 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917268 | TACCAGAGCTGGGGA[C/T]GTGGAGACAGGGGGA | 16443 |
| rs227467967 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91781215 | GTATTTGGGGAAGAG[A/G]TCTTGGTCTCCTGTT | 16443 |
| rs227482039 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91881223 | AGGAGGTTGGGTGCA[C/T]ACTCTCAGACAGACC | 16443 |
| rs227482797 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91780872 | AGACATCATCACCGA[A/G]GCAGCTTATAGAAGA | 16443 |
| rs227492094 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91787047 | TAGAGGCCATGTGAG[C/T]TACAGCTGTGACCCT | 16443 |
| rs227502831 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91731852 | TAGCTACATCTGCAG[C/T]CTCACGTTGTCTTTG | 16443 |
| rs227505675 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91786174 | GCATGCACCACCACG[C/T]CCGGCTGGGTGTTTT | 16443 |
| rs227530167 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91834813 | AGTTTACGCATTAAC[A/C]AGTTTCAATCAGAAC | 16443 |
| rs227533220 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91890039 | TCTGGGAAGCTGCCA[C/T]GGTCTAACCAGGTCC | 16443 |
| rs227543123 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823187 | GTCTGAAAACTCCCC[-/T]TGAAGTTCCTTGGTA | 16443 |
| rs227546113 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91785220 | AATGATGTGGTTCTG[A/C]TGTACAGGGATTTCT | 16443 |
| rs227549844 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91787903 | TTACCACCAGCTCTC[C/T]TGGTCATGAAATCTC | 16443 |
| rs227554614 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91891161 | CCTCAAGTCCTCTGG[C/G]CATGGCGCCCGGACT | 16443 |
| rs227562400 | in-del | -/AG | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91920366 | TTGCATAAACTTAAC[-/AG]AGTCTCTAGTCTGAA | 16443 |
| rs227568022 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889572 | CAGCAGTGGCTCTCT[A/G]TCTCTTGAGAGTGTG | 16443 |
| rs227573019 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91790726 | CTCTGTTTAACCATA[G/T]ATAGCGCATGCGTGT | 16443 |
| rs227587758 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91737548 | CTTTAGTTACCTTTC[A/G]CCTTGTCTTTATCTT | 16443 |
| rs227599381 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91888696 | CATTGTCCTCTCAGG[A/G]CCCACCTGCTTCAAG | 16443 |
| rs227628471 | snp | A/G | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91893873 | GAGCGCCCAGCTGCC[A/G]CACATGCAGCCTTAC | 16443 |
| rs227630125 | in-del | -/CGAGTGTCACCATG | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91801445 | TTCCTCTAGCTGTAC[-/CGAGTGTCACCATG]CGAGTGTCACCATGC | 16443 |
| rs227633171 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91744798 | GTGGATGGCTTCCCA[C/G]AAAGGCTAGTCAGCA | 16443 |
| rs227641628 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91797242 | GTAAGGCCGAAACAC[C/G]TGAGCTGGGAATGGC | 16443 |
| rs227659186 | in-del | -/CTGTCTGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91826768 | TCTCTGTGTTTGTGT[-/CTGTCTGG]GTGTCTGTGTGTTTG | 16443 |
| rs227661688 | in-del | -/AAAAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91886375 | GGACCACTTTTATGT[-/AAAAA]AAAAAAAAAAAAAGG | 16443 |
| rs227670196 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91755623 | GATATCCACCTGCCT[C/T]TGCCTCCTGCATGCT | 16443 |
| rs227670279 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91792140 | CTAGAGCAGCTAACA[A/G]TCTAAGCAGCCGAGC | 16443 |
| rs227671658 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91749016 | TGTACATATGTACAT[A/G]CATACATTCATACAT | 16443 |
| rs227674618 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890630 | ATGTAGACCCAGGCA[A/G]GCCTCGAACTCACCG | 16443 |
| rs227708978 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91894007 | GGACTCTCTCCAGAG[G/T]GTTGTCTTGAGGTGT | 16443 |
| rs227709947 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91911800 | ACAGTCCCAGTGTCA[C/T]GAGTGCGTGTCCTGG | 16443 |
| rs227712473 | snp | A/G | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91868112 | CACCCCAACTGAGCT[A/G]CCCAAGACCGCAGTG | 16443 |
| rs227743331 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890335 | AAAATGGCAGTTGTG[G/T]TTTTTTTTTTTTTTG | 16443 |
| rs227750957 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91757595 | ACTCAGGCCTTGGGC[C/G]AGGACAGTACTCAAT | 16443 |
| rs227779760 | in-del | -/TGGTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91817788 | TTCTATTAAGGTGTT[-/TGGTT]TGGTTTGGTTTGGTT | 16443 |
| rs227781532 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91763188 | GGGTGGTTTTTAAAA[A/T]TTTGTTTGTTTTGGT | 16443 |
| rs227782585 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91756797 | TAGATGAGACTGTCG[C/T]ACTCTGGGCAGCGCT | 16443 |
| rs227793670 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91754250 | AGTAAGCTCTAAGGG[A/G]TGCTGGGAATCCTGA | 16443 |
| rs227803835 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91859460 | CCCTTCCCCAGGCCA[G/T]CGAGTTGGCTCCATT | 16443 |
| rs227831923 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802725 | ACTAATATTTTAGCT[-/C]CTTTGATGGTAAGAA | 16443 |
| rs227841922 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91779189 | CCCAGCACCAAAAGA[A/T]AAAAGAAAAGTCCAG | 16443 |
| rs227851572 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91866464 | CTGGCAGATTCACAG[A/T]GCAGTGGCTGGCAGT | 16443 |
| rs227857298 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91868878 | GCAGAGCCCTCTCCT[A/G]TCAGCCCATAAGCCC | 16443 |
| rs227858765 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91874804 | AGTGAGGGACAGAGA[C/T]GTCCCCTGAAGAACA | 16443 |
| rs227859556 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91858800 | AAAACATCAAGTTCT[C/T]GTAGGCTGGTATGCT | 16443 |
| rs227860124 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91865539 | CTTTTTTTAAGACAT[A/G]GCCTTGACTGGCCTG | 16443 |
| rs227860792 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91732492 | ATGTACAGCCCTTCT[A/G]GGTGATGTGCTAGAA | 16443 |
| rs227866440 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91868159 | TGCTCGCAGGCCGTC[C/T]GCTCGCGCTCGCTCG | 16443 |
| rs227876744 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91806530 | CTGTTCCCTCGGTCA[G/T]ACATGGAGGCTGGAT | 16443 |
| rs227881118 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91857671 | TTGGCTCTTAAATTG[-/C]CCCCCTACCATTTGT | 16443 |
| rs227897839 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91813690 | AAGGTGGAAAAAAGA[A/G]GAACCCGCAAAATAG | 16443 |
| rs227913751 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91828868 | CTTAAATCCCAGCGC[C/T]TGGTAGGCTGAAGCA | 16443 |
| rs227916849 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91874289 | GTGTTTCTTCGATGC[A/G]ACCATTGGTTTTAAG | 16443 |
| rs227917758 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91784525 | CACACTGTTTAAATT[-/A]GGGTAGGAAGGGTGC | 16443 |
| rs227934096 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91855442 | ATCACCACAAAAAAA[-/G]ATTCCAACCTTTTCC | 16443 |
| rs227941824 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91835475 | ATGCCCTTTGATAGG[G/T]TCTCTGCATTGGGCC | 16443 |
| rs227962832 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91786101 | TCACTTTGTAGACCA[G/T]GCTGGCCTCGAACTC | 16443 |
| rs227976829 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910046 | GTCATCCCAGCATCT[A/G]GGAGGCTGATCCTGG | 16443 |
| rs227979059 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91753552 | AGGATTAGAGCATCA[-/T]TTTTTTCTTGCAATA | 16443 |
| rs227983525 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91733354 | TGCTTATGGCTCTTC[A/G]TGTACAGCTTTTGGT | 16443 |
| rs227992168 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91865382 | GGGGCAGGAGAGCCC[A/G]TCCAGAGGTGCTGGC | 16443 |
| rs228020237 | in-del | -/T/TT | | | intron-variant | Itsn1 | Mm_Celera | 16:91730957 | TACCATTTTTGTTAC[-/T/TT]TTTTTTTTTTTTACA | 16443 |
| rs228024432 | snp | C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91802413 | CCTGCACTTAGCATG[C/G]GTGTGTGTTCCCAGT | 16443 |
| rs228025990 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915985 | GCCTACCTGCCAAGG[A/G]ACCCTGTTCTGCAGG | 16443 |
| rs228029501 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91889421 | GTGGATTTCTCACAG[C/T]GGAGAGTGAACTGCG | 16443 |
| rs228043802 | in-del | -/GGGGT | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91730202 | TGCGGTCCCTTCTTG[-/GGGGT]GGGGGGGGGCACCAG | 16443 |
| rs228066470 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91732557 | AATTTAATGTAGAGT[C/T]TAATCACGTATCATT | 16443 |
| rs228096820 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91835506 | AGTGAGGGATTAGCC[C/T]GCCTCTGGCTGTGTG | 16443 |
| rs228098688 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91906347 | GAATATAGCCTGATA[C/T]AGAAGTCAGTATCAC | 16443 |
| rs228101490 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900423 | GTCTTGTATGAGAGC[C/T]ACCTGGCGGTCACGG | 16443 |
| rs228130153 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91842280 | AATTGAAACATATAA[A/G]AGTTAGTTTTAAGAA | 16443 |
| rs228137743 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91841309 | GCGGCTTGCTTGTGG[A/G]ATCTGCTGATGAACT | 16443 |
| rs228154987 | snp | G/T | | | upstream-variant-2KB | Itsn1, Cryzl1 | GRCm38.p3 | 16:91728971 | CAATTTAGTTGAATG[G/T]ATCCTAGCTACTGTC | 16443 |
| rs228156732 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91905639 | AAGGAAAAGGGGAGG[A/G]CCAAGATAGAATAAG | 16443 |
| rs228215961 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91893336 | AATGATGCCGTGAGC[A/G]GAAGGGATACTTCAC | 16443 |
| rs228230893 | in-del | -/A | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742509 | GAATGCACATGCAAG[-/A]CTGAGATTTAATAAG | 16443 |
| rs228232337 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91833340 | TTACAGTCAGTGGTC[C/T]GAGTATGTTTTTGCC | 16443 |
| rs228269330 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783591 | TACATACATCTATGC[A/G]TACGTACTTTGGCCA | 16443 |
| rs228284025 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91840615 | GAGGTCCTATGGCTG[C/G]AGGGAGAACTTGGAC | 16443 |
| rs228301241 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91856635 | CAGCAGTGGCAGGTG[A/G]GAGTGGGCAGTGGAG | 16443 |
| rs228306181 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91910714 | TAAAAGATTGGGTTT[C/T]ATGTAGCCCAGGCTG | 16443 |
| rs228306836 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91780776 | AAGATTTTAATGAAT[A/C]CTTCTCCTCCTCTTG | 16443 |
| rs228322436 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91884740 | TCACTCTGTAGACCA[A/G]GCTGGCCTCGAACTC | 16443 |
| rs228326920 | snp | A/C | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916597 | TGACTCCTATTAATG[A/C]ACATTGTCCTTTGAA | 16443 |
| rs228334854 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91839869 | GGCTGAGGTGCCAGG[C/T]TCTGCCACTGTCTCC | 16443 |
| rs228339098 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91820201 | ATAAAAATTCCCTTC[C/T]TCCTTGAGTCTGCAA | 16443 |
| rs228360695 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91790815 | AGACACTTTGCAGAA[A/G]AAGGAAAGATCACCA | 16443 |
| rs228363748 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91852541 | AGGCATAATCTCTGC[A/G]GACAGGGCGGTGGGG | 16443 |
| rs228372414 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91851898 | AACCCACTTAGGGCA[A/G]AGAGACCCCTGTGGA | 16443 |
| rs228385821 | in-del | -/AGGGGTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91774680 | TAAGAAACTAGCCCA[-/AGGGGTG]AGGTGTGAGCATATC | 16443 |
| rs228404968 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91859848 | CATTGTGGCTTTAAA[A/G]GCCAACTGACCTATG | 16443 |
| rs228413356 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91884070 | GGATGCAGTAACTTC[C/T]CGATGTACTATGAGG | 16443 |
| rs228414605 | in-del | -/TTGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91755391 | AGTTCAGAAGTTCAT[-/TTGC]TTACACTCAAAGCCT | 16443 |
| rs228434955 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91785150 | GTGCTGAGTCAGAGG[-/C]CCTTGGCCTTTCCTG | 16443 |
| rs228441361 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91892758 | GAACCCTTCTTTAGC[A/T]GAAAAAAAAAAAAAC | 16443 |
| rs228477393 | in-del | -/TA | | | intron-variant | Itsn1 | Mm_Celera | 16:91910511 | GTGTGTGTGTGTGTG[-/TA]TGTGTGTGTGTGTGT | 16443 |
| rs228489702 | in-del | -/CT | | | intron-variant | Itsn1 | Mm_Celera | 16:91901130 | TCTCTTCTTTTCTGC[-/CT]CTGTTTTCTCTGTAC | 16443 |
| rs228512941 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91741313 | AGCGCCTAGTGCCTC[C/T]CACTGAAGGCTGATT | 16443 |
| rs228513196 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91797625 | TTTGCCAGTTGGTGA[-/T]TTTTTTTTTAAACCG | 16443 |
| rs228521732 | in-del | -/GC | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91853589 | TGTGTCTGTGTCTGT[-/GC]GTGTGTGTGTGTGTG | 16443 |
| rs228521960 | snp | C/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830593 | TGGGCGTGCATGGAT[C/G]CGGTGAGGATCGCTG | 16443 |
| rs228521996 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91822630 | GTTTGCCGTTTTCCG[G/T]GTGTTTTGTTGAAGG | 16443 |
| rs228526175 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91752780 | CCTCTTTGAATGAAT[G/T]ACCGTGTTATTGTTG | 16443 |
| rs228540428 | in-del | -/CCCTGC | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91828478 | TAGCCTGTGTTAGGG[-/CCCTGC]CCCTGCCCCTGCCCC | 16443 |
| rs228554773 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830244 | TTCAATAGCAAGCAA[A/G]ATTTCTGTAGGAACT | 16443 |
| rs228557748 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91761521 | GGAGCATGTTTACAA[A/C]GGTCTTTCCTACCTG | 16443 |
| rs228559861 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91813060 | TAGGCAGGCATGGTG[C/T]AGGAAGAACTGAGAG | 16443 |
| rs228566192 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91748093 | CCCATTTGAGCCTTC[C/T]TAGGCGTTTTGCTAC | 16443 |
| rs228573056 | in-del | -/TTCC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91801241 | GTGTTTCAGTAATAT[-/TTCC]TTCCTTCCTTCCTTC | 16443 |
| rs228589132 | in-del | -/GAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91881149 | TGGCCCTTCTTGGAA[-/GAT]GATGATATTAATTAA | 16443 |
| rs228598515 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91835595 | CTCCCAGTTACTCCT[C/G]TGTTCATGGACTCTT | 16443 |
| rs228634676 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91909438 | GCTCTACCTTCCGGG[C/G]ACCTTTGGCCCCGCC | 16443 |
| rs228648593 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91760631 | ACCTGAGAGCCAGTG[C/T]GCATCAGTGTTGTAA | 16443 |
| rs228650914 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91889652 | TCCTTACAATTGCCT[A/G]AGGCCATGTATGCCT | 16443 |
| rs228660544 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91801404 | TGTTTTATGTGGGGA[C/T]ATATTGCAGCAGAGA | 16443 |
| rs228666695 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91864453 | CTGGGCACTGTTCCC[A/G]TTAGTGCTACTTTTC | 16443 |
| rs228671837 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91800853 | CAGCCTCTCTCTGTA[G/T]CGAGGGTGACTTGAA | 16443 |
| rs228674427 | in-del | -/CGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91818719 | GGGCCGAGATTCAGG[-/CGC]CGCCCTGCCCTTGTG | 16443 |
| rs228682491 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91873527 | CCCTGGTGCCCTGGT[A/G]TCCACCCCATGTGTG | 16443 |
| rs228687969 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91851020 | AACGTTCACACCAAC[A/G]GTCCCAGCAGACATT | 16443 |
| rs228692159 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91862703 | TAAAGTTCTCATAGC[C/T]CTGTGTTCCTCTTGT | 16443 |
| rs228707803 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91755651 | GCTGGGATTAAAGGC[A/G]TGCGCCACTACGCCC | 16443 |
| rs228715214 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91812217 | GGTGGGTTTCCTCAT[C/T]GGCTTTGAGATTCAG | 16443 |
| rs228727475 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91818796 | AGAATGTGTCAGGAC[C/T]CAGTGACCAGCTCTT | 16443 |
| rs228731941 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91808347 | GTAGTGGTCTTATGT[C/T]CTGAACAGCAGGCCA | 16443 |
| rs228743789 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91850303 | GGAAGGAAGACGTGG[A/T]GGAAAGGGAGAGCTC | 16443 |
| rs228757699 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91857465 | GAGCACACACCTCCT[A/G]CTCGCACCACTAGGA | 16443 |
| rs228762598 | in-del | -/TT/TTTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91783791 | CCACCACCACAATGA[-/TT/TTTTT]TTTTTTTTTTTTAAT | 16443 |
| rs228774902 | in-del | -/TTTTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91835422 | GCTGTTGATAATTGA[-/TTTTTT]TTTTTTTTTTTTAAC | 16443 |
| rs228775726 | in-del | -/GTTTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91906009 | ACCAATGTGTGGAGG[-/GTTTTT]GTTTTTGTTTTTTTA | 16443 |
| rs228789709 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91915174 | CTGTTATCTTCACTC[A/G]GTGCCAACGTGTGTT | 16443 |
| rs228791696 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91755118 | TTTGCATTAGTTCTC[C/T]GTATGTCACATGATC | 16443 |
| rs228801322 | in-del | -/TG | | | intron-variant | Itsn1 | Mm_Celera | 16:91839075 | TGGGAGCCAGACGTA[-/TG]TGTGTGAGTGTAGCT | 16443 |
| rs228813865 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91856894 | TGCTTTTGAAGGAAG[A/C]CCCTTGAGGTTAGGG | 16443 |
| rs228839111 | snp | C/T | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91728022 | CCACCAGGCCCAAAT[C/T]CAGAATCAGTATCTG | 16443 |
| rs228842554 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872426 | TACTGAAGTGGAGAC[C/G]TAAGGGGTCAACAAG | 16443 |
| rs228843942 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91904439 | ATGCCCTCGCTGTTG[A/G]TGAGTGGTGGGAGAG | 16443 |
| rs228862476 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91832963 | TCTTTTGTTTGTTGT[A/G]TCACTTAATTGGGAA | 16443 |
| rs228865656 | in-del | -/CTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91748724 | CCTGCCTCCACAGTC[-/CTG]CTCTGGCTTCCCATA | 16443 |
| rs228877778 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911146 | GAATCCTGAGTTCAA[A/T]TCCCAGCAACCACAT | 16443 |
| rs228877788 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91904069 | TAATAGTGTCCCTTC[C/T]CATGGGCCAAGCATT | 16443 |
| rs228911584 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91910835 | TAGCTTTAAAAAGGT[A/G]TCTGTGTGTTTGCTC | 16443 |
| rs228924602 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91866575 | AACTTGATGGGTAGA[A/G]GTGTGATGTGGCTCA | 16443 |
| rs228948650 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91781723 | GGGCACGGCTGTGGC[A/G]TTTGTTGCCCTGTTC | 16443 |
| rs228954227 | snp | A/G | | | missense | Itsn1 | Mm_Celera | 16:91827883 | AGCAAATGCTTGGAA[A/G]ACTTATTCCAGAGAA | 16443 |
| rs228990287 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91882076 | CCCCCATAACATGGC[C/T]TTTTCTATGCCCTGT | 16443 |
| rs229000002 | in-del | -/TT | | | intron-variant | Itsn1 | Mm_Celera | 16:91751471 | ATGCGTGTGTGTGTG[-/TT]TGTGTGTATGTGTGT | 16443 |
| rs229008697 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91839253 | TCATTAATCTCAATT[A/G]AGATGTACTTTTTCT | 16443 |
| rs229013442 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91735923 | GGAGCCAACCATCTC[C/T]CCGCTGGCCAGATCT | 16443 |
| rs229016453 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91777742 | AAAGGGTACCTGGTG[C/T]TGTACTTGCTTGTAG | 16443 |
| rs229032028 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91897294 | CCAACAGGGAGAAAA[A/C]GAAAAATCAAGAACC | 16443 |
| rs229045305 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91789278 | GTTATTTTTATTGTT[A/G]TTTATTCTTGTGATT | 16443 |
| rs229046009 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91784331 | CATCATGGTGTGTGC[A/G]TTTAGGTGGCGAGGG | 16443 |
| rs229046079 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91888626 | GAGCTATATGCTCAC[C/G]CACCCAGAGCTTGGG | 16443 |
| rs229048224 | in-del | -/CCCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91885856 | CGCAGTGCCCTGGGC[-/CCCT]CCCTCTCCCAGAGAA | 16443 |
| rs229052667 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91760006 | AAATTGTCCCCCTTT[-/A]AAAAAAATTAGTTAA | 16443 |
| rs229059520 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91834731 | GGTGTGACTGTCTTC[C/T]GTTGGCTCTTTCTAT | 16443 |
| rs229068238 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91827108 | CCCTCTATTGAGTTA[A/G]CCTCCTACCGTGCAG | 16443 |
| rs229080340 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91834359 | CTCACAATTAGGAAT[A/G]CTCTGCTTTTATTGT | 16443 |
| rs229093350 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91838633 | TGCTTTTTATAAAAC[A/G]TTGTTTGGGGCTGGA | 16443 |
| rs229096043 | in-del | -/AGA | | | intron-variant | Itsn1 | Mm_Celera | 16:91758796 | TGGAAGCCGGAATGG[-/AGA]AGAAGGCAGCCATGT | 16443 |
| rs229125618 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91752128 | CAGCTAAACTCTCAC[A/G]GAGAGATGCTTCTGT | 16443 |
| rs229135717 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919971 | AGCCTCAGCTCTGGT[C/T]CTTGGCAGCCCACAA | 16443 |
| rs229140553 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745859 | GTTGTTCGTTATCTG[A/G]AAGAACTGCCTTTTC | 16443 |
| rs229147235 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91840843 | ACAACAGTCTACCTC[-/G]ACGCTCTTCAGATAC | 16443 |
| rs229171885 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91898909 | ACGTGGCGTAGGGCA[C/T]CTGTCCTGCTCACCC | 16443 |
| rs229176376 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91759744 | CGCATTAGTTTGTGT[C/T]TTCTCTTCTAGGATT | 16443 |
| rs229182777 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91893212 | CAGCAGGTAGGCCCA[C/G]GATCAGACACTGCCT | 16443 |
| rs229195047 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91891720 | CATAGATCTTGCCAG[C/T]ACGGTTATTGTCCAG | 16443 |
| rs229209532 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91811693 | AAAAGAAATAATCTG[A/G]CCAAAGGGGCAGTCT | 16443 |
| rs229216749 | snp | A/C | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745546 | AGTGATGGGGCAAGG[A/C]ATGTTACCATTTCAA | 16443 |
| rs229218220 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91754167 | ATATAGCTTACATGT[C/T]TCAGTGTTCCATTAT | 16443 |
| rs229224485 | in-del | -/GAAGCTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91762201 | AGACTTGTGTCTGTG[-/GAAGCTT]GAGATACTGGGCTGA | 16443 |
| rs229224757 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91806472 | GAGAAGGAGCTGTGC[A/C]CAGGGCGTCCCGAGT | 16443 |
| rs229247962 | in-del | -/TGTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91836576 | GTGTGTGTGTGTGTG[-/TGTT]TGTTTTCAAAGCTAT | 16443 |
| rs229258823 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91903193 | CAGTGGGCTGGAGAG[A/T]TGGCTCAGAGGTTAT | 16443 |
| rs229272107 | in-del | -/AT | | | intron-variant | Itsn1 | Mm_Celera | 16:91768513 | GCAGCCAGGTCAGGG[-/AT]ATAGCCCCGCTCCAG | 16443 |
| rs229272912 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91813603 | TTCAGAGATCTCTTT[C/T]CTTTCTTCTCTATCC | 16443 |
| rs229274806 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91805457 | TTGTTGTAGAGAAAG[A/G]TAAATATTTTGAAGT | 16443 |
| rs229290421 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91855689 | TCTGCAATCAGGTCT[A/C]ACTAGTGGGGGAGAA | 16443 |
| rs229304195 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91865309 | GCTCTTGGCCCAAAC[A/G]AGAGCCGCAGCATGC | 16443 |
| rs229304299 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91855025 | CATAATCCAAGATAT[C/T]ACTCACCAGGCTATG | 16443 |
| rs229305015 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91861395 | CTGTTAATTAAATGT[A/C]CTTGGCTCTCAAGTG | 16443 |
| rs229317794 | in-del | -/CTTTGGTACGTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91902560 | ACACCACCAGAAGTC[-/CTTTGGTACGTTT]CTCTCTACAAAGTCA | 16443 |
| rs229330880 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914037 | CCTCCCCCTTCCAAG[C/T]TGAACATGAACATGA | 16443 |
| rs229355524 | in-del | -/CTGTAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91840107 | GTCTCTGTCTGGATA[-/CTGTAG]CTCTTTACCACCCAG | 16443 |
| rs229358992 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91864137 | TTAATTAAGACCTGA[A/G]GTAGGCTTTCAGTGC | 16443 |
| rs229370598 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91813036 | TCAAGGTGGGAGAAT[A/G]GCAATGTCTAGGCAG | 16443 |
| rs229378319 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91909958 | CGGATGTACATATAT[A/G]CATACGAAACTATGC | 16443 |
| rs229382703 | snp | G/T | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91871021 | CGTGTTTTGTTTTGA[G/T]TTTTCAATCTGGCAT | 16443 |
| rs229386671 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91827004 | GAAAGCACTGAGTAG[C/G]CTTTGCTTTCCAGGA | 16443 |
| rs229400581 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91777543 | CCCTCATAACCCGTC[C/T]TGTCTTGGGGAGCCA | 16443 |
| rs229409071 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91755360 | TCTGCTTTCAGACCG[-/T]TTTTCTTGGTTGACA | 16443 |
| rs229412936 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91909142 | TCCACTTGTGAATCT[C/T]GAAGGTGTAGGGGGA | 16443 |
| rs229443281 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915148 | GTGGATCAATGGGCC[A/G]CTCATACTGCCTGTT | 16443 |
| rs229446267 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91776671 | CACATGAATCTTCCC[A/G]TCCCGCTTGCCTCAC | 16443 |
| rs229462028 | snp | A/G | | | upstream-variant-2KB | Itsn1, Cryzl1 | GRCm38.p3 | 16:91728826 | GTTGGGCGTTGCCAA[A/G]ATGGGTTCCGTTTTA | 16443 |
| rs229478947 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91775906 | TTTTTAAAAATTATT[A/C]GTAAATGTTGAGTGT | 16443 |
| rs229478968 | snp | G/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914593 | CTGACCTCCTCTCAC[G/T]CAGGAAGGCACTTTC | 16443 |
| rs229479380 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91834220 | AAACACAGCTATTTA[C/T]AGTTTATAAAGTAGC | 16443 |
| rs229481234 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91781333 | GTATGTAAATTTTTC[C/T]TGAGGTTTTGTTTTT | 16443 |
| rs229481460 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91881398 | CCCTGAGAATTTACA[A/G]CTCTCCTGTCCTGGG | 16443 |
| rs229490258 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91833325 | GTCAAGTTCAGGAAA[A/T]TACAGTCAGTGGTCT | 16443 |
| rs229528604 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91887558 | TGGGGTTGGGCCTGC[A/G]GGGATGGCAAGAGGT | 16443 |
| rs229538928 | snp | A/G | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91727812 | TGGTTTAAGAGAAAC[A/G]TAAAATTAATTTCAC | 16443 |
| rs229563784 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91735064 | TTTTACGGTGCTCCT[G/T]CCACCCTCGGGCTCT | 16443 |
| rs229574240 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91848094 | TTGGATGCATCCTTT[-/G]GGGGCAGAACTAAGG | 16443 |
| rs229577521 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91888222 | AAACTGGTACCCTCA[C/T]GAATGCCATGAAACT | 16443 |
| rs229581409 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91886976 | AGGCAGCGGTCAGCT[C/T]CCGAAACAGTGGCTG | 16443 |
| rs229589420 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91832826 | AACTTTATAATTGCA[A/G]TTAAATATAGAACGT | 16443 |
| rs229601519 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91837872 | GGTGTCCTAGGGCAA[C/T]GGACCCTGCAGACCT | 16443 |
| rs229629584 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91799378 | TGATCCAGGGCTTCA[A/G]AGACCAACTTAAACC | 16443 |
| rs229632167 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91849613 | GCGGCTTTGGTGGAG[A/G]GGAACCTAGACCATC | 16443 |
| rs229635356 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91898866 | GCACAGGCATCAGTG[A/G]CTCTGCGTGCTCTCA | 16443 |
| rs229663017 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91890262 | AGCTGGGTCGTTTTT[G/T]GGGGGGGGGGGGGAA | 16443 |
| rs229669437 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91891330 | CGAGATCCGCCATGA[C/T]CAAAGCAACTCGGGG | 16443 |
| rs229679226 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91898592 | GTGGGAGCAGGACAG[C/T]ATCCAGGCAGGCATG | 16443 |
| rs229702089 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91896107 | TATGCAGGCAGGCTG[C/T]GGGTAGGTCCTATCC | 16443 |
| rs229708511 | in-del | -/TTGCAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91783067 | AGATGTGAAAGGCAG[-/TTGCAA]AGAGAGTGAGAAGGC | 16443 |
| rs229712237 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91763612 | TTATGGAATACACTA[C/T]CTAGTTTCTTTAAAA | 16443 |
| rs229716545 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91844892 | GGCTTGCTTAGTTAC[A/C]CTGAAGGGAAAAGTC | 16443 |
| rs229735487 | snp | A/C | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745487 | AAAGACTTGTACAGT[A/C]AGCAGTATGGCTATT | 16443 |
| rs229739035 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91762897 | GACCCCACTGGCCCT[A/G]TATTTCTCTCGTGTG | 16443 |
| rs229767820 | in-del | -/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91829173 | AAGTATAGTTGAGGG[-/T]TTTTTTTTTGTTGCC | 16443 |
| rs229776284 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91903716 | AAGGACAACATTTAA[C/T]TGGGGCTGACTTACA | 16443 |
| rs229791044 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91769161 | GTTCTAAACCTTTCA[A/G]GAAGAGATAAATCAG | 16443 |
| rs229808918 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91820294 | GGCAGGGCTCTGTCA[A/G]TGCTCACCTGTGTAA | 16443 |
| rs229810205 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91797439 | CAGTTAAGAGCACTG[A/G]CTGTTCTTCTGAAGG | 16443 |
| rs229813498 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91768692 | TCTTGTGGAGTTCCT[A/G]TCTGCTCCAGATCCC | 16443 |
| rs229820978 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91753454 | TGAGGGCATCAGCAT[A/G]GGCGGCGCCATTTCC | 16443 |
| rs229826798 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91874548 | CATGCTGCAGGGCAC[A/G]GAAAAGATGTGTCCC | 16443 |
| rs229853646 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91854933 | TGGATAACCAGGCTA[C/G]ATTATTTATGCCTGA | 16443 |
| rs229864947 | in-del | -/GT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91751523 | GTATGGGTTTTTTGG[-/GT]TTTTTTTTGGTTTTT | 16443 |
| rs229866733 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91873884 | TGACCCAGGTTTGAT[A/T]CCCAGAACCCACGTG | 16443 |
| rs229873428 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91881055 | GCTGCTCACTGCGTG[C/T]GTTGTCACAGCAAAG | 16443 |
| rs229891140 | in-del | -/TCAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91779676 | AAAGTGTGTGACCTG[-/TCAC]TCACACAAGCCTAGT | 16443 |
| rs229891326 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91827140 | CCTAGCACAGTTCAT[A/T]CTGCAAATGCCAATG | 16443 |
| rs229908014 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91737884 | CCCACTTTGGATATT[G/T]CCAGTTTATGATGAA | 16443 |
| rs229938669 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91887683 | ATGCTCACGTTTTTT[A/T]CCCACACAGCCACCA | 16443 |
| rs229948368 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745750 | CTCACCATCACCTTA[A/G]TACATGCCTGGAGTG | 16443 |
| rs229953425 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91902567 | CAGAAGTCCTTTGGT[A/G]CGTTTCTCTCTACAA | 16443 |
| rs229956784 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798765 | AAGAGAGGAAACAAA[G/T]TAGTCCGTCACCATT | 16443 |
| rs229959317 | in-del | -/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91739497 | TTCCCTTCCCTTCCC[-/T]TCCCTCATTGCTGGC | 16443 |
| rs229970525 | in-del | -/GGATCTGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91827185 | GGTGCCAGAGAGACT[-/GGATCTGG]GCCTCTACAGGAAAT | 16443 |
| rs229977803 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91737294 | TGTCTCCATGTCCCA[C/G]ATAGTCCACCACACG | 16443 |
| rs229979519 | snp | C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745589 | TGAGAGGTGGCAGAG[C/G]GAAGAAACTGCAGCT | 16443 |
| rs229980226 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91833477 | TCAGCCTCTGTTGCC[G/T]GTCCTCTTCCTCTTC | 16443 |
| rs229993710 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91826552 | CCTCCTGTGCATTGG[C/T]GCTCTGCCTTTGTAG | 16443 |
| rs230004943 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91847275 | AAAACAAAACAACAA[A/C]GATGTATCCATACAA | 16443 |
| rs230014163 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91909023 | TGTAGGTATATAATC[A/G]TATATATACTATATA | 16443 |
| rs230020692 | snp | A/G | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91863813 | AGTTCTCACTTCCAG[A/G]CACAAAGATGCTGCA | 16443 |
| rs230047015 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91847671 | GCTGGCACTGCCTGG[A/C]GAAGGGAAGAAGCAG | 16443 |
| rs230057956 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799009 | AAGGAAGGAAGGAAG[A/G]AAGAAAGAAAGAAAG | 16443 |
| rs230058303 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91744653 | GGCCTGCCTGAATTT[A/G]TTTCTGTGGAACAGG | 16443 |
| rs230087668 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91791212 | CTAATACCTAGTCAG[C/T]GAACCAAGAAACACA | 16443 |
| rs230102470 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91846522 | TAAGTTCACATTCCT[A/G]AGACCATGTCTGGGC | 16443 |
| rs230104904 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91855168 | AGCACCCATGCAGTG[C/T]GGCAGGCTCTGCTTC | 16443 |
| rs230120487 | in-del | -/TGA | | | intron-variant | Itsn1 | Mm_Celera | 16:91764729 | CATGGCTCTGGCCCT[-/TGA]AAATGTAAATCTGCC | 16443 |
| rs230141835 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91790476 | GACTTGAGGTTCAGC[A/G]TAGCAGACCTGTGCT | 16443 |
| rs230153610 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91797198 | CTCTGGATGCTGCTG[C/T]CCTAGGCACCGTTCT | 16443 |
| rs230169370 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91775867 | TTTGAAGAGGCTTCC[C/T]ACTAATTCTGTTTCA | 16443 |
| rs230183805 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91898174 | TTAAAAACAAACAAA[A/C]AACAGAACACACAGA | 16443 |
| rs230184861 | snp | A/T | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91804639 | CCAAGCATCAGTGAG[A/T]CAGAATGAGAGAAGT | 16443 |
| rs230205851 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91752927 | TCCGCTGGACCTATA[A/T]TGGGACCCAAGAGTT | 16443 |
| rs230218670 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91897622 | CCACTGAGCCATCTC[A/G]CCAGCCCATAACTAA | 16443 |
| rs230242685 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91902245 | ATACCTGTCTGTGGG[C/T]ATCTATTCTTTAAAA | 16443 |
| rs230245657 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91818966 | TGCTACAAAAGCACC[A/G]CCCTTCTATGTGAAC | 16443 |
| rs230246955 | in-del | -/TAAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91826310 | TGTAGCTTTTAGAAT[-/TAAC]TGTTACTCAGAAATC | 16443 |
| rs230258052 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91902381 | TGTTTAGAAATAGTT[C/T]TTTGGAGAAAATCCA | 16443 |
| rs230259859 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91825809 | CTTTTTCACCTTAGC[A/G]TGTCCAATTAGCCAG | 16443 |
| rs230263227 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91825536 | GAACTCAGGACCTTC[A/G]GAAGAGCAGTCAATG | 16443 |
| rs230273553 | snp | A/C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890799 | GGGGGGGGGGGGGGG[A/C/G]GATGTGTCTCAAGTA | 16443 |
| rs230275380 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91854019 | AAACTAGACTGTATG[A/T]ATGAAATGCAGAAAG | 16443 |
| rs230280958 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91832709 | GGTTTTCAAAGAATG[A/T]TTTGAACATGTTTTG | 16443 |
| rs230308264 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91782724 | CGGTCCTTGCTCTTA[G/T]GTGGTGTGCCCCTCC | 16443 |
| rs230316796 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91825178 | ATTTTTCTCTGTGAT[A/G]TGTTTTTGTTATATT | 16443 |
| rs230326307 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91768045 | CAAACCTACTTGAAG[A/G]TAGAATTCTAGATAC | 16443 |
| rs230336420 | in-del | -/GT | | | intron-variant | Itsn1 | Mm_Celera | 16:91770010 | TCAGAAGAGCAGTCA[-/GT]GTGCTCTTACCTGCT | 16443 |
| rs230354888 | in-del | -/CC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91862542 | CAGTTCTGGATCGCT[-/CC]CCCCCCCCCCCGCCC | 16443 |
| rs230357033 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91862997 | GTGGGAGGTTCTTTG[A/G]CAGGACGCATGGGGG | 16443 |
| rs230359407 | in-del | -/GGATG | | | intron-variant | Itsn1 | Mm_Celera | 16:91859674 | GATGGATGGATGGAT[-/GGATG]GGGTGGGTGGGTGGA | 16443 |
| rs230400114 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91776053 | ATTTAAATTGTGTTT[C/T]GTGAGTGGCTTTGCA | 16443 |
| rs230400328 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91767320 | TGGTTCTGTGGTAAC[A/G]GAGCCAGCTGTCATG | 16443 |
| rs230411739 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91908562 | CCGGGGCTGAAACTC[A/G]AGCCAGAAGTGGGGC | 16443 |
| rs230433128 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91775318 | TTAACATTCGACACA[A/T]CCTGCCCTAGGCTCC | 16443 |
| rs230442182 | in-del | -/CT | | | intron-variant | Itsn1 | Mm_Celera | 16:91764747 | AATGTAAATCTGCCC[-/CT]GAGGATCTTGTTCAG | 16443 |
| rs230448497 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91880064 | ATTGGTCCTGGCCAC[C/T]GGGACACACAAAAAC | 16443 |
| rs230470890 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831901 | GGGCACATGGGGCAG[A/G]CTGTAGTCCCTGGGG | 16443 |
| rs230471240 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91892106 | ATCATGGCTTCTCAT[A/G]TGTGATCTTTCTGTG | 16443 |
| rs230494377 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91743916 | CCAAGCATCCCAACA[C/T]ACACACCTTCCTACT | 16443 |
| rs230495478 | in-del | -/GACGGAGCATTCTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91889976 | AGCCACCCTTCCTCT[-/GACGGAGCATTCTG]GACAGGATCCAGATG | 16443 |
| rs230496818 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91824828 | CTCTCTCCCTCCTCC[A/T]GCCTCCCTGCTCTCT | 16443 |
| rs230505258 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91879049 | GCATTGGATCCCCTG[C/G]AGTTACAGGTGGTCA | 16443 |
| rs230505738 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91775041 | TTAAACTCTCGGTGA[C/T]CCTTCTGTTTCTGTA | 16443 |
| rs230516335 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91886676 | CGTCCTCGCCTGAAG[A/T]GTCTTCCCGGTCATG | 16443 |
| rs230526666 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91736350 | GTTGCGCAGCACGGG[C/G]TTCCTGGAGACAGGA | 16443 |
| rs230539842 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91810620 | AGGAAAGATGCGCTT[-/G]CTTGCATTCCAGGCA | 16443 |
| rs230558906 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743952 | TCCTCACATTTGTAG[A/T]TAAGAAACCACTGAG | 16443 |
| rs230560349 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91795125 | ACCGTTGGCCACAAG[A/G]CTGGTTTTCTAAGGG | 16443 |
| rs230568860 | snp | G/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91832255 | ATTTGGTTGGTTTGG[G/T]GTTTGTTTGTTTTTT | 16443 |
| rs230570252 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91886266 | TTGTTATAGATGGTT[G/T]TGAACCACCATGTGG | 16443 |
| rs230572851 | snp | G/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803483 | ACATGTATGTATGTG[G/T]ACCACATTCCTGACG | 16443 |
| rs230587059 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91891453 | CAGGGAGCTGATGCA[C/G]AGGCCGTGCAGGGGT | 16443 |
| rs230590211 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91865407 | CTGGCCAGGAGCAGT[-/G]GGCTTGTTGAGGAAT | 16443 |
| rs230591926 | in-del | -/GG | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890554 | TTCGGGATCTGACTT[-/GG]GTTTTTTTTTTTTTG | 16443 |
| rs230608710 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91845639 | GCTACACAGAGAAAC[C/T]CTGTCTCGGAAAAAG | 16443 |
| rs230625150 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802631 | GATGGGAATCACACA[C/T]AGATCTGCTCCTCCC | 16443 |
| rs230632943 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743622 | ATGGCATTAAATGCC[C/T]ATGGCATTAAAAAGA | 16443 |
| rs230634511 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91751962 | TTAGGAGGTGGGGGA[C/T]CTCACTCTAATACAC | 16443 |
| rs230635975 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91901073 | CTTCTCCCACCCAGG[A/G]GTCTTTGTTGGTCTT | 16443 |
| rs230639021 | snp | G/T | | | intron-variant, missense | Itsn1 | GRCm38.p3 | 16:91853011 | GAGCGCCCTTCTGCC[G/T]CCCTAGCTCTCCAAA | 16443 |
| rs230651605 | in-del | -/TTTTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91833217 | ACAAATACCTAGAAT[-/TTTTG]TTTTGTTTTGTTTTT | 16443 |
| rs230654465 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803667 | TTTTACCTTGTTTAA[C/T]TTTATAGAGTGCTAA | 16443 |
| rs230659985 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91886535 | CTAGCCTAGCTCAGG[G/T]CAGCTAAGGGCCTTC | 16443 |
| rs230672414 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91891887 | ATCGATAATCTTACC[C/T]AGCTTGAACCCTGAG | 16443 |
| rs230673223 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91845004 | AGCTGTGGCGGGCGC[G/T]AGCTGTGTGTCCTCC | 16443 |
| rs230677270 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91751524 | GTATGGGTTTTTTGG[G/T]TTTTTTTGGTTTTTT | 16443 |
| rs230686921 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91811535 | TATTTGTAGTGGTAC[C/T]GTTAGAGGACCTGCT | 16443 |
| rs230714463 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91766246 | AAGGAAATGAAAAAT[A/G]GGATTTCAGATGTTC | 16443 |
| rs230720835 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91906893 | AGGTAAGCCCCAACC[C/G]CTCCCAGGCACTGGG | 16443 |
| rs230724296 | in-del | -/TTGTTGTTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91780613 | GCATTTCTCTACACT[-/TTGTTGTTG]TTGTTGTTGTTGTTG | 16443 |
| rs230724483 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91907567 | ATGATGCTTTGCAGT[A/G]TGGGAGGGCAGGAAG | 16443 |
| rs230759490 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91750838 | ACTGGAATAATCTAG[G/T]CGCTATTCAAGAAGG | 16443 |
| rs230773900 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91743522 | ATATCAGCTCTTTCA[A/G]ACTATTATTTTTAAG | 16443 |
| rs230777037 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852705 | ACTGGCCAGTTATGC[G/T]CCGGCAAGTGCAGGC | 16443 |
| rs230786138 | in-del | -/CGACCTCA | | | intron-variant | Itsn1 | Mm_Celera | 16:91891272 | CCTTCATCACAGCAG[-/CGACCTCA]CGACCTCACGCTGCT | 16443 |
| rs230786984 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91736590 | CTTGCTTGCTCTTGA[-/G]GGTTTTTTTTTCCCT | 16443 |
| rs230793053 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91905757 | GGGAGGAGCTAAAAT[A/T]GAGTAACCCGAACAG | 16443 |
| rs230816277 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91860043 | GACCCACAGGTCTGC[A/G]GGCAGCCCTTCCTGC | 16443 |
| rs230818938 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91751381 | GCCCTGCTCATTTAC[C/T]AGCACCGCCTGGGGG | 16443 |
| rs230832354 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852158 | GAAACTGAATTCAGT[A/G]GTCTCTAGCAGTACT | 16443 |
| rs230841462 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91781165 | TTCAAACCCACCACA[C/G]ACCAGAAGAAAAATA | 16443 |
| rs230843065 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91860215 | TTGGGAATCGTCCCA[A/C]GCTTATGTGCATGCA | 16443 |
| rs230859693 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852578 | GGGGGAGGGGGGTGG[A/G]CAGAGAATAGCAATG | 16443 |
| rs230899206 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91862410 | GCAGTGTTGGAATGT[-/G]GGGGCCCCCACCCCC | 16443 |
| rs230905082 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91811090 | AATCTTCCTGTTCCT[C/T]GGTTCATGAGTGTTC | 16443 |
| rs230911655 | snp | A/C | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91831078 | CACATGACCTCAAAT[A/C]CGCGACCTTCACCCT | 16443 |
| rs230918530 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912673 | GTGAGCTTGGAGGAT[C/T]CTCCAAAAGCTCATT | 16443 |
| rs230919070 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91905905 | TGGCCAGTCCAAGCA[A/C]CCAAGCACCACTGCT | 16443 |
| rs230955653 | in-del | -/AT/GT | | | intron-variant | Itsn1 | Mm_Celera | 16:91786497 | GCTTACACTGGAAAC[-/AT/GT]AGCACGCTCGTGCAC | 16443 |
| rs230960081 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91773787 | CCCAGAAATTTGAAG[C/T]TTGCATGTTTACGGT | 16443 |
| rs230976636 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830804 | CATTTTCTTTACCCT[A/G]GGAAGAATTAGCTTT | 16443 |
| rs230990036 | snp | A/C | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830373 | TTCCCAGAGAGGTGC[A/C]GTGCCGGCGCGGTCA | 16443 |
| rs230997872 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91906471 | CATCTGTAACTCCAT[C/T]CTCTGGGACCCCCTC | 16443 |
| rs230998114 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91841760 | AGTGTTTCTATTGCT[-/C]CCGTAGCCTGCTTTT | 16443 |
| rs231000354 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91860375 | CTTCCTCTTCTCTAA[A/T]AGCCATTCAGTCCCA | 16443 |
| rs231004355 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91732531 | AGTAGATGTTGCCCC[-/T]GAGGGCTCAAAATTT | 16443 |
| rs231011964 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91772644 | GACATAGCTCAGTGG[A/G]TGAGTGCTTCGCTGG | 16443 |
| rs231014473 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91780135 | AATCAAAGGGCCACT[A/C]TGTGACTACACGTTC | 16443 |
| rs231026282 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91787371 | CCTTTCTGAGAGGGA[C/T]TTCTAGGAGCTGTGT | 16443 |
| rs231031700 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91877385 | ACAGGGACCAGGTAA[A/G]GCATGCCTCTAGACA | 16443 |
| rs231040450 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91780926 | CAGAGGGATAAGAGT[A/C]GTGATGGCAGAGGGG | 16443 |
| rs231042591 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913395 | TCCTGGGCTCAGGCT[C/T]TCCTGTGTTGGGTGG | 16443 |
| rs231063323 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91780397 | CACTCACAGCAGCCA[A/G]GCAGCCAGTGACAGA | 16443 |
| rs231065586 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91884264 | TTCAGCCTGGGGGGG[A/G]ACGACAGAGTACTAT | 16443 |
| rs231067399 | in-del | -/CTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91868222 | ACATGCTCGTTAGCA[-/CTT]CTTCTACTTGCTGTC | 16443 |
| rs231069827 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830490 | GCACTCCCAGGCAAG[A/G]AGACAGAGCTGTTGG | 16443 |
| rs231077395 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91890178 | TCTGTGCCAGGCTCA[C/T]GCTCTGGAAGCTGTC | 16443 |
| rs231087922 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802363 | AGCATAGGCTTTACC[A/G]TTAGATCTGTGTCAC | 16443 |
| rs231089004 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91748748 | CTTCCCATAGGGATG[A/G]ACTATAACCTGCAAG | 16443 |
| rs231097350 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91836346 | AGATCTGGAGAGATC[A/G]CTAGGAAGAGCTGGC | 16443 |
| rs231106402 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91760947 | GATCCCTCATGATTT[C/T]AATCTTAGCAAGATT | 16443 |
| rs231107292 | in-del | -/AGGA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878061 | GAGAGAGAGGAAGGG[-/AGGA]AGGAAGGAAGGAAGG | 16443 |
| rs231123192 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91773198 | TATGGTTTAAAAGGT[G/T]GTAATTACACCAGTG | 16443 |
| rs231125542 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91885169 | GGACAATGGATTAAA[A/T]TAGGGCAGGGACTGA | 16443 |
| rs231142278 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91884487 | GTGTGTTCAGCAGGG[G/T]AACCTTTCACTAGAG | 16443 |
| rs231154874 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873733 | GCTACATTGAAAGTC[A/G]GTGACACAAACACAC | 16443 |
| rs231198574 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91747571 | TTCTAGATAATTCTG[C/T]GGGTAGTTGTCCCCC | 16443 |
| rs231204947 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830763 | ATTCTTTTCCCTAGA[C/T]TCATTCTTCCGCTAA | 16443 |
| rs231217792 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91819675 | ACCAAAAAAGCAAGT[C/T]GGGGAGGAAAAGTGT | 16443 |
| rs231227154 | snp | A/T | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91728072 | GATAATTCTTTAGTA[A/T]GGCTCAAGTATGGCC | 16443 |
| rs231237770 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91780827 | GAATTAGATGAGGTG[C/T]GCATCAGTTACTTTG | 16443 |
| rs231259505 | in-del | -/AAGTGTCCTAAGGAGGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91780267 | GATGCTGACATTTGG[-/AAGTGTCCTAAGGAGGC]AAGTCAGTCTACCTG | 16443 |
| rs231275953 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915354 | CCTAGAATCCATTAA[C/T]CAAGGACACATGGAC | 16443 |
| rs231285041 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91755694 | AATTTCTAACCCAAA[C/T]AGACAAGCATGAATA | 16443 |
| rs231293326 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91836976 | CAAACGCCCAGGGCT[C/T]GGCCACTGTGAAATG | 16443 |
| rs231299136 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91884784 | CCTCTGCCTCCCGAG[A/T]GCTGGGATTAAAGGT | 16443 |
| rs231304360 | in-del | -/TTACA | | | intron-variant | Itsn1 | Mm_Celera | 16:91867909 | CAATTTCTGTGACAG[-/TTACA]TCCTTTGTCTCTCAG | 16443 |
| rs231306490 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91737160 | TTTTTGTGCCTGTTC[A/G]AATGTTCTTTTACTA | 16443 |
| rs231309286 | snp | A/G | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91727445 | GGACTGAGTGAGTAT[A/G]GTACACAGCGCACAC | 16443 |
| rs231312640 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91839510 | CCCACATTCCCTTGA[C/T]GTTTAGCAGCTCTGC | 16443 |
| rs231335772 | in-del | -/CTTTCTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91731625 | TTCCTTCCTTTTTTC[-/CTTTCTTT]CTTTCTTTCTTTTGC | 16443 |
| rs231343107 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91736412 | TGGTAGAATCAGGTG[C/T]TGAACTCAAGGATGT | 16443 |
| rs231358841 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91744420 | TTGGAAGCTAGCAGA[A/G]GGTGTTGGATCCTCT | 16443 |
| rs231360427 | in-del | -/GGGGGGTAGA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872363 | CCAACACTGGGGGGG[-/GGGGGGTAGA]GGGTTGGGGGGTGCT | 16443 |
| rs231363786 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91846009 | TGATTTCAATCTGAA[C/G]TGACCGCTCTGCACA | 16443 |
| rs231364244 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91846262 | GTGAGCATGCTCTGT[C/G]TGAAAGTCCGTCATA | 16443 |
| rs231366177 | snp | A/G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91838984 | AGATGGTTGGGAGCT[A/G/T]CCATGTCAGTGCAGG | 16443 |
| rs231370105 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890600 | TTTTTCATGAGGCAG[G/T]GTCTCACTGTTACCA | 16443 |
| rs231389414 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91796376 | AGGCATTAAGGTCTT[A/G]TATGCTCAAGCTACA | 16443 |
| rs231390337 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91883412 | GGTCAGTTTAAAGAA[-/T]TAAAAAGAAAGAAAG | 16443 |
| rs231399729 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91822853 | TGTATCCCTGGCTGG[-/T]TCTGAAACTCTGTAG | 16443 |
| rs231418472 | snp | C/T | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91853595 | CTGTGTCTGTGTGTG[C/T]GTGTGTGTGCGCGTG | 16443 |
| rs231429111 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91897156 | TCAGCCCGACCCAGC[C/T]CCACCCAACACCATA | 16443 |
| rs231460819 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91902162 | AAGTCTGATTCTTCA[A/G]TCAGCAGGCCTTGGG | 16443 |
| rs231469734 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914682 | GAGGACAGAAGCCCC[C/T]GACTGGGCTTCCTTC | 16443 |
| rs231493562 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91748410 | AGAGACTGAGGAGAG[C/T]CCAGTGGATAAAGCT | 16443 |
| rs231523539 | in-del | -/GC | | | intron-variant | Itsn1 | Mm_Celera | 16:91838459 | TAAATGTACTTGGAT[-/GC]TTTTTTGGTGGGGTG | 16443 |
| rs231530724 | in-del | -/AG | | | intron-variant | Itsn1 | Mm_Celera | 16:91791663 | TGAACATCTAAAAAT[-/AG]ATATGCAGGGAATAT | 16443 |
| rs231535674 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91801799 | ATTTGAGTTCTCCTT[C/T]CCACCCAGCGTATGA | 16443 |
| rs231540817 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91756700 | TGAAATTCATCTCAG[C/T]TGTACACCTCGAACC | 16443 |
| rs231548538 | in-del | -/TTTTC | | | intron-variant | Itsn1 | Mm_Celera | 16:91907083 | GCTGGAGGCTTTTTT[-/TTTTC]TTTTTCTTTTTCTTT | 16443 |
| rs231575528 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91766834 | CCCCACCTCGCTGCC[C/T]TGCGCTCCCAGCCCC | 16443 |
| rs231600600 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91809647 | CGGCACTGTAATACC[A/G]ATGCCCACTCTGTGT | 16443 |
| rs231607612 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91790216 | CCTTCTGACGTAAAT[C/T]TGGTGTCAGTATTGT | 16443 |
| rs231611786 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91774875 | GTCTTGCTGTGTTGA[A/C]AAGGCTTGTTTTAAG | 16443 |
| rs231615107 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91818318 | ATCCTAGGAACCTGG[C/G]CAGTTCTGGGTTTGG | 16443 |
| rs231627020 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91817689 | AATCTTGGTATGTGA[C/T]TCAAGCTAGCCGATC | 16443 |
| rs231658825 | in-del | -/AGAG | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745354 | GTGTGTGTGTGTGTA[-/AGAG]AGAGAGAGAGAGAGA | 16443 |
| rs231664820 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91913740 | ACTCTTCAGGTAGCA[A/G]CTTTCAGCTGAACAT | 16443 |
| rs231665052 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91895774 | ATGTACACACATAAA[C/T]ACCAAATACATGCTT | 16443 |
| rs231672011 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91824150 | GAGGCAGGTTGGAGG[C/T]CAGCCTGGTCTACAG | 16443 |
| rs231683120 | snp | G/T | | | missense | Itsn1 | Mm_Celera | 16:91816929 | GCCGTCGTCAGAGGA[G/T]GAGCAGCAGCCAGAG | 16443 |
| rs231707642 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91878791 | CTGGAGCTGCTGACA[C/G]GGACAGGAGCTGTCC | 16443 |
| rs231710740 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91891972 | GAACATTAAGGGATG[C/T]TAGGACTCTATGACT | 16443 |
| rs231713091 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91775171 | AACAAATTGAACCTT[-/A]AGAGTTCTTGGTGGC | 16443 |
| rs231738887 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91736187 | TAGATTCAATGATGA[A/G]TAACTTGTCTTACTA | 16443 |
| rs231743360 | in-del | -/TAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91896299 | TCTGAACCACATTTT[-/TAA]AAAAAAAAATACCAT | 16443 |
| rs231760729 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91896924 | TGAGCCTTAGAACAA[A/G]AGACAAAAGTGTGCT | 16443 |
| rs231767534 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91788855 | AAGCTCCCGCCCTTC[A/T]CTCTGGTCATAGCAT | 16443 |
| rs231783321 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91823394 | AGATTATATGACCTC[A/G]TCTTGGGTTACTTCA | 16443 |
| rs231785065 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91789434 | TCTCCTCAGCACATA[A/G]CTCCTGTCATGGTAG | 16443 |
| rs231786311 | snp | C/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91913047 | AGACCTTTGGGAACC[C/G]GTGAGCCCCACATGT | 16443 |
| rs231789178 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919990 | GGCAGCCCACAAGCT[A/G]AAGTCTCCTTGCCCC | 16443 |
| rs231790053 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91735041 | CCAAGTCATACCCAC[A/G]GGAAGCCTTTTACGG | 16443 |
| rs231819106 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91845548 | CCTTTAATCCCAGCA[C/G]TTGGGAGGCAGAGGC | 16443 |
| rs231821693 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91743223 | GTACCACTTCCTTTG[A/G]CTGTTCCTACACTGC | 16443 |
| rs231825395 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919536 | TCTGTTTGCCGTTTG[C/T]AGATGTGGACCCATG | 16443 |
| rs231830049 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91794923 | GGTTATTGTGCCAGT[C/T]CCTGTCACGGTTGTG | 16443 |
| rs231831367 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91884955 | GGGACCGTGATGTAA[C/T]GGGACATTTGTGAGA | 16443 |
| rs231833391 | in-del | -/TCTCCCTCCTCC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899966 | TCTCCCTCCTTCTCT[-/TCTCCCTCCTCC]TCTCCCTCCTCCTCT | 16443 |
| rs231856237 | in-del | -/GAGTAAGTTATACCAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91809306 | AAGAAGAGTACTTAA[-/GAGTAAGTTATACCAT]GAGTAAGTTATACCA | 16443 |
| rs231873304 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91788163 | CCTGTGCTACATGAG[A/G]TCAGCTTCAAAAATG | 16443 |
| rs231891855 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899979 | CTTCTCCCTCCTCCT[C/G]TCCCTCCTCCTCTCC | 16443 |
| rs231896025 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91844786 | TCACTGCCAGTGTGA[G/T]AGCCTGGTGTGCACA | 16443 |
| rs231899445 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91759896 | TTACTTATCTAATCT[A/G]ACAGGAATATCCTTT | 16443 |
| rs231920129 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91901417 | AGAAGCTGAGGTGCC[A/G]GCTATGGCTTCTCAG | 16443 |
| rs231923522 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91794601 | TCTTAGGACTAGACT[C/G]CACAACTCTGCATTT | 16443 |
| rs231925466 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91787674 | CTGTCCCTCCTCAGC[C/T]CCCTGCCACAGGGGT | 16443 |
| rs231953528 | snp | C/T | | | intron-variant, synonymous-codon | Itsn1 | Mm_Celera | 16:91853147 | TTGTATAGTGTGTTT[C/T]ACTCCACCCAATGAT | 16443 |
| rs231955173 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91767142 | TGGCGGACGTAACCT[A/G]TTCTATGATGTTGAA | 16443 |
| rs231962591 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91895632 | GGTAAAAGTGGTTGG[A/G]AAGCTGGGTGGTTGG | 16443 |
| rs231963272 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91896473 | AAGGGAGGCTGGAGG[C/T]GGGACAGAGTCCCTA | 16443 |
| rs231996251 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900430 | ATGAGAGCCACCTGG[C/T]GGTCACGGGGTCGGG | 16443 |
| rs231998848 | snp | A/C | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91871342 | TATTAGTTGGAAGCT[A/C]TCAATAATAAAAAGA | 16443 |
| rs232002097 | snp | A/C | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91801822 | GCGTATGACATGACG[A/C]GTGCTAAGACTGAAA | 16443 |
| rs232014235 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91748465 | GTCTCTAGCTCTTAT[A/G]TAAAATCTGGCAGGC | 16443 |
| rs232031124 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91900166 | GTGATTTCTGTTTCT[A/G]GATTAGCCACCGAAC | 16443 |
| rs232045571 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91765304 | TCCAACAGACAAAAG[C/T]CTCTCACTCAGTTAC | 16443 |
| rs232065662 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91851156 | GGCTTAAACTCTCCT[A/G]CCTGTGTCTATCTGA | 16443 |
| rs232069979 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91766145 | TCTGCACCGGTCGGG[A/G]TCCGGTTCTGTTCCC | 16443 |
| rs232082150 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91766412 | TTGATTTTCTGAGAG[A/G]AATAAAAGGGAGTGG | 16443 |
| rs232084671 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91774216 | CAGTTTCTGAAAGTG[-/C]CCCCATCCCCATCCA | 16443 |
| rs232097242 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91764858 | CTCTATGTAGAAAGC[A/G]GCTTGGCTGGTGCCC | 16443 |
| rs232099841 | in-del | -/GAAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91735539 | TATGCTTTGGAAACT[-/GAAG]TTAGATGCCTTAGCC | 16443 |
| rs232125132 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91765817 | TTTGGTCAGAAGAGA[C/T]TTTGTCAGGACTAGG | 16443 |
| rs232128006 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91868366 | ATTGGGATTTGGACC[A/G]TTGGGTTAGGCAACA | 16443 |
| rs232133978 | in-del | -/GA | | | intron-variant | Itsn1 | Mm_Celera | 16:91894714 | GGAGCTCAAGGCCAG[-/GA]GATCTAGAGGCAGAG | 16443 |
| rs232153359 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91869908 | GTTTGCAGAACTGAA[C/T]GCAGACCACTGCTGC | 16443 |
| rs232163255 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904939 | GGGATTAAAGGTGTG[C/T]GCCACCATGCCCGGC | 16443 |
| rs232172960 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823635 | ATATGTTATATAAAA[A/T]GTAAGGGCTCATCTT | 16443 |
| rs232177091 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91772296 | GTGCTCTTTATCACT[C/G]ACCCATAACCTCAGC | 16443 |
| rs232184842 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91774237 | TCCCCATCCAAGAAG[C/T]AAACGCTTTTGATTT | 16443 |
| rs232221985 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91876786 | TGGACATGGCGACAT[C/T]CCAGGTTCACACCTT | 16443 |
| rs232223648 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91821850 | GGGATATCTGGGGAG[C/T]GAGCTCAAGACAAGG | 16443 |
| rs232225975 | snp | A/C | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919829 | GAAGATTTTGGATAC[A/C]CTTCATCAATTAACA | 16443 |
| rs232232636 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91770750 | TGACAGTGATGCTGG[A/G]CAGCGGACCTTCCTG | 16443 |
| rs232242665 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878626 | CACAGTTGGAAAAGG[C/T]TCATTTTTGTGGAAA | 16443 |
| rs232245057 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91869249 | CCGGCCCTGGGCTCA[A/G]TCTTCACCATCACAA | 16443 |
| rs232263007 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91877552 | TGGAGACTGAGCACA[C/T]GTGAGCCTTTGGTGT | 16443 |
| rs232264272 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91779322 | GGGAGTTCAGAGAGA[C/T]CACTGAAATATAAAG | 16443 |
| rs232265109 | in-del | -/ATA | | | intron-variant | Itsn1 | Mm_Celera | 16:91776597 | GTCATATTTCTAGCT[-/ATA]ATGCTGCTGTGCAGA | 16443 |
| rs232270963 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91735216 | CTTCTCTGTCCAAGA[C/T]AGAGGCGATACTTAC | 16443 |
| rs232276018 | in-del | -/A | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91832231 | GATTTCATGTCACAC[-/A]GGAGACAGATTTGGT | 16443 |
| rs232277906 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91875997 | CCAGCACCCTGCTGC[C/G]TGCACCCAGACACCC | 16443 |
| rs232278218 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91829189 | TTTTTTTTTGTTGCC[C/T]TTTGGATTAAGAGTC | 16443 |
| rs232281937 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91875818 | ACAGATGTGTAAGTC[A/G]CTGGTCCTGGGTTTC | 16443 |
| rs232286600 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878381 | GCCCTCCTTATAGAG[C/T]TGACATATGGGAGGG | 16443 |
| rs232290563 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91883828 | AGAATCCCAAAGAGG[A/C]AGGCATCTCTCCCAA | 16443 |
| rs232294533 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91732862 | GTGGACTTTGCATAC[C/T]TCTATGTTGCCCAGG | 16443 |
| rs232298046 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91832887 | TATATCTTGAAATAA[-/T]TTTTTTCTAGATTAC | 16443 |
| rs232305122 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91885614 | GGAGGGAGCAAAACC[A/T]ACCACTGTAACTCTA | 16443 |
| rs232312723 | in-del | -/GAGGCGGGGACCTGGGCAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91764212 | TCACCCAGGGTGGAG[-/GAGGCGGGGACCTGGGCAT]GAGGCGGGGAACCTG | 16443 |
| rs232335968 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91883557 | GGGTTCTAGGTCCAG[A/G]GGCCAGCGTGGCCAT | 16443 |
| rs232344573 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91882620 | GTAATAGTCATTGAC[C/T]AACTTATTATATTCT | 16443 |
| rs232362930 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734518 | TGCCAGCCACGTACA[C/T]CCACTCGAGCAAATG | 16443 |
| rs232372120 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91732256 | GCAAGCTTTTCAAGT[A/G]GCAGAGGTTTTACAT | 16443 |
| rs232374310 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91740792 | CCTGCTTGACTGCCG[A/C]GTGCCAGGTGGTGTG | 16443 |
| rs232378265 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91842936 | TGCAACTTTTACAAG[A/C]GATCAGAATGATTTC | 16443 |
| rs232386678 | in-del | -/TGTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91866972 | AAAGGCGCGTGTGTG[-/TGTT]CGTGTGTGTGTGTGT | 16443 |
| rs232398496 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734740 | CCTTTATTCCTAACA[A/T]TTCCCCTTCCAGCTT | 16443 |
| rs232398633 | in-del | -/TCTG | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91739454 | TTTGTTTTGTTTTTT[-/TCTG]TCTGTCTGCCCGCCC | 16443 |
| rs232405925 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91739932 | TCCAATGTTTGCCCA[A/T]CTCTCAGTTTTAAAC | 16443 |
| rs232422596 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91808160 | GAATGTAAATCCTTT[-/A]TAAAAACTATAGCAA | 16443 |
| rs232447247 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742692 | ACCTCCTCCCCCCCA[A/C]AAAAAAAGATTGTTC | 16443 |
| rs232447814 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734179 | GAACCCTGGGTCACC[C/T]TGAAGAGTAGTCAGC | 16443 |
| rs232450973 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91844114 | TAGAATTCTCTGTAG[A/G]CCTTCCATTAAGGAA | 16443 |
| rs232451414 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91739689 | TCCACAGATAGGGAA[C/T]AGCTTTAGGGACAGC | 16443 |
| rs232478898 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91844246 | TTGTCTGAAAGCTGT[C/T]CCGTGTAAGTGCTGC | 16443 |
| rs232488499 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746375 | GTGTTGGGGCTCCCT[C/T]CCAGGTTCTGGAAGT | 16443 |
| rs232490053 | in-del | -/TGTGTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91742309 | CAGATGTTAAGTGAA[-/TGTGTG]TGTGTGTGTGTGTGT | 16443 |
| rs232491864 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91794503 | AACTCCCTGACCCTC[C/T]GACTCATACAGTCTT | 16443 |
| rs232518995 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91849061 | TAGCTGGCCTACTGA[C/T]AACAGGGTTATTGGC | 16443 |
| rs232534648 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91741994 | ACAGCTTTTAAGAGT[A/C]GCTTCTCTCCTTGAG | 16443 |
| rs232536596 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91851754 | ACAACTCAGCAGCAG[C/T]GCCTCTCCTCTGCCT | 16443 |
| rs232546115 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799967 | GGGTCTCAAGGGGTA[A/C]CTGTTATTTCTACTG | 16443 |
| rs232549980 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913828 | TATCAAAACACTACA[C/T]ATTCATGTTTCTGTT | 16443 |
| rs232554302 | in-del | -/GTGTGTGTGTGTGTGT | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913545 | AGAAGGTCCCTCTCC[-/GTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 16443 |
| rs232556698 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91807123 | GAGAAATCACTGTCT[A/G]TACACAGCTAAGCTT | 16443 |
| rs232560863 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91898803 | TCTCACACATGGACG[A/C]AACACACATATGTGA | 16443 |
| rs232575925 | snp | A/C | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802389 | GTCACTATTGCTGTA[A/C]CTGAGCAGCCTGCAC | 16443 |
| rs232593181 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91903948 | TCTTAAAGCCCCGCC[C/T]CCACAGTGACATACT | 16443 |
| rs232601355 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900393 | GTCACATCGCATGAG[G/T]GAATTACAGCGGTGG | 16443 |
| rs232616077 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91856816 | ACCCACTTGGGTGCC[C/T]TTGTGTCAGCTGTGA | 16443 |
| rs232649682 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91905544 | GGTCTCTAAAAGATG[C/T]CCGTTACAGAAGGGT | 16443 |
| rs232652197 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91885958 | ATGTGGTCGGGGGTG[A/G]GGGGTGGGGGAGGGA | 16443 |
| rs232664489 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91891544 | CACCAGCCCAGGGAT[A/G]ACCCCACCCACAACA | 16443 |
| rs232664630 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91788259 | CAATGTTTAAGAGCA[C/T]TCTGCTTTTTTAAGA | 16443 |
| rs232664652 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91891440 | AGGAACCTGGAGGCA[-/G]GGAGCTGATGCACAG | 16443 |
| rs232690008 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91851474 | AATGCCCGTCCTGGA[A/G]GCCCCAGGAAATCAC | 16443 |
| rs232704245 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91751437 | CCATTGTAAAAGCAT[C/T]GTTCCTACTTGCGGG | 16443 |
| rs232706697 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768963 | TTCTTAAAGAAGAGC[A/G]TGCGGCCCCTGCTGC | 16443 |
| rs232719566 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890846 | TGTCTCCCAACAGGA[C/T]GTTAATGAGGGCTGG | 16443 |
| rs232752787 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91764686 | GTGGACCGCAGACAT[A/C]TTGTCAGTGACTACA | 16443 |
| rs232779581 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758643 | GCCTCCCACAATACT[G/T]GCCTTTATCAACAAC | 16443 |
| rs232780016 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91749625 | CTGGAAACTGTAGAC[A/G]AGAGCTTCATCCCTC | 16443 |
| rs232792345 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91772004 | AGTCCTGAATCCTAA[C/T]TGGGAACAGTTGGTT | 16443 |
| rs232794700 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810970 | TTCATTTGGGGACAT[C/T]GCAGCCTCTGCTCCT | 16443 |
| rs232811261 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91758075 | AGTGCTCTTAAATGC[C/T]GAGCCATCTCTCCAG | 16443 |
| rs232852825 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91816260 | AGAATTTTTTGCTTC[C/T]CTTCGTTGAGACAGG | 16443 |
| rs232853393 | in-del | -/GTCTC | | | intron-variant | Itsn1 | Mm_Celera | 16:91816106 | TGAGGCTTGGGCACA[-/GTCTC]GTTAAATGACGAGCC | 16443 |
| rs232880353 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91815806 | GAGTGAGCAGACAGG[C/T]AGGAAATCAGAGATC | 16443 |
| rs232885284 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91801276 | CTTCCTTCCTTCCTT[-/C]CATTCATTCATTCAT | 16443 |
| rs232889235 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830038 | ATTCACGGGGGTCCA[C/T]TGAAGGGGCTGTGTT | 16443 |
| rs232932681 | in-del | -/GGGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91864348 | GGGAGGAAGTGGTGG[-/GGGT]GGGTTAGGAAGGGCA | 16443 |
| rs232937951 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91866310 | CATGCCCAGCATTGT[-/C]CCTGTATGGAGAGTC | 16443 |
| rs232944816 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91918291 | AAGTAGGCCTCTGTC[C/T]CTGCGAGACAGGGTA | 16443 |
| rs232960629 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91859213 | TTTGGCGAGGGTGAG[A/C]CTTAAGACTTGTAGT | 16443 |
| rs232965091 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91884041 | GAACAGGAATACACT[C/G]AGCCTTGCGGGTGGG | 16443 |
| rs232970348 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91764773 | TTCAGTCTGAGTGGC[C/T]TCCTCACCACCGAGA | 16443 |
| rs232972214 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91822129 | TGCTGCCTTCCTGTT[A/G]GATGCTGGCACTGTC | 16443 |
| rs232977805 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91868456 | GGGTCTGCTGATCAT[A/T]ATAGTTCTGTGTCAG | 16443 |
| rs232995518 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91837505 | GAAAGCAAAGCCCCC[-/A]GTCTACTGCCACAAG | 16443 |
| rs233010611 | snp | A/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912033 | CGATGATCGTAGATG[A/T]CTTCCTCCTCAAGGC | 16443 |
| rs233044673 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91868252 | CTGTGGCCTCTCTTT[G/T]CTGAGCACCACAGAG | 16443 |
| rs233051957 | in-del | -/CCTGCCTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91904306 | GCACAGCTGCGGCCC[-/CCTGCCTT]CCTGCCTACTGTCAA | 16443 |
| rs233054667 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91876761 | CATCAGGGGAAAGTG[A/G]CAGGTGGGGTGGACA | 16443 |
| rs233076361 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91844733 | GTTCCCACAGTCTTA[-/C]CCTCAGAGCTCAGCA | 16443 |
| rs233081721 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91740280 | GACCACCAAGCCCAT[A/G]TGGGCCGCTGGCATC | 16443 |
| rs233084909 | in-del | -/GA | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919228 | AGATACTGCTTTCTG[-/GA]GAGAGAGTGGGCGGA | 16443 |
| rs233092228 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91792673 | CTCGAGGGTCACGGC[A/G]ACAGGACCCAGGCTG | 16443 |
| rs233098992 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734111 | AAGGGCACTGGATCC[C/T]CTGGAACTGGAGTTA | 16443 |
| rs233104172 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91836389 | GGATTTGTGAGAATA[A/G]AGGCTCTGCAATAGT | 16443 |
| rs233124647 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917396 | GTTTATCTCCACCAA[A/G]CAACTAACTCAGTTC | 16443 |
| rs233132986 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91732991 | GGAGTGTGTGAGATA[G/T]AAAGTTTGCAAGCTG | 16443 |
| rs233139117 | snp | C/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91918091 | ACTGTAGTGCTCCCC[C/G]ACTCTCCCAGCTGAG | 16443 |
| rs233155075 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91733830 | AAAACAAACAAAAAA[-/C]ACAAAAACCAAAAAC | 16443 |
| rs233160977 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91835784 | CTATTAGGCTGTCAC[A/G]GTATTCCAGTTAGGA | 16443 |
| rs233163405 | in-del | -/GTC | | | intron-variant | Itsn1 | Mm_Celera | 16:91906594 | CTATATTCTGGTATA[-/GTC]GTGTGTGCTAAGCTA | 16443 |
| rs233176055 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91732626 | TAGAAAATATGGACA[A/G]TACATATGCTTTCCA | 16443 |
| rs233203068 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91850145 | TGGGCAGTGAGTGTA[G/T]GAGTGGGAAGGGTTT | 16443 |
| rs233207764 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91740465 | AGTCAGCTGGAGAAA[A/G]CCACACCACAGCCTA | 16443 |
| rs233237045 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91800696 | TGTTTTAAGAACTTG[C/T]AAATAAAATAGCATG | 16443 |
| rs233237397 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91845830 | CCTGATGAAGAAGAC[-/G]GTAGTGCATGGGAAT | 16443 |
| rs233274890 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91792873 | CAGTTGGGTGGGTAG[C/T]GGCTTCCAGTGCAGA | 16443 |
| rs233278210 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91857395 | TGGTCTGAGCCTCAG[C/G]CTCAGTTCAAAGCAA | 16443 |
| rs233294594 | in-del | -/GAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91766898 | CTCCTTTTTAGCCAG[-/GAT]GGATCCCCCCAGTGG | 16443 |
| rs233294646 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894506 | TCACACACAGAGGAG[C/T]CCACCTCTTCATGTA | 16443 |
| rs233309159 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91842667 | CCCTGTCAGGAAGTC[C/T]GCCTCCCACTCCGTG | 16443 |
| rs233320396 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91792286 | GAGTTGTTTCAACAA[A/C]GCTAATCTGGTAATG | 16443 |
| rs233329863 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91899222 | CATGCTAGAAGCCAC[A/C]ATTCTGAAGGACAGG | 16443 |
| rs233330529 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91894529 | TTCATGTAGCATCAA[C/T]GTTGCCCCAGCCTCT | 16443 |
| rs233332592 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904389 | GACATGACAGCCCCC[A/G]GGTAGATGTTGGAAC | 16443 |
| rs233338629 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91800287 | CGCCCTGGAGAAGCT[A/G]TGCTGCCCAGAGAAG | 16443 |
| rs233362591 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91808569 | CACACATAAACATAT[A/G]TAACAACAATTAGGG | 16443 |
| rs233396328 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91904096 | ATTATTCAAACCACC[-/G]ACGGACATGAGTTGA | 16443 |
| rs233420982 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91815601 | CTAGCTGTTTCCTTT[G/T]CTGGCATGAAGGTCA | 16443 |
| rs233422153 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91807744 | GTCTTAGTTAATGTC[A/G]TTCTGAGAGGGCATG | 16443 |
| rs233427537 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91814826 | ATGATCATTGGATTG[C/T]TAGAATGAGGTGGGA | 16443 |
| rs233433324 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911230 | AAGAGAGCAATGGCG[A/G]TGTACTCATATAAAT | 16443 |
| rs233453490 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91832340 | AATAAAAGGTTATGA[A/G]AGAAAGGGGCAAAGA | 16443 |
| rs233466679 | in-del | -/AT | | | intron-variant | Itsn1 | Mm_Celera | 16:91874049 | AAAGAAATAATAAAA[-/AT]ATATATAGACTGGTG | 16443 |
| rs233469424 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91910920 | GTATTGGATCCCCTG[A/G]AATCAGAGTTACAAG | 16443 |
| rs233489824 | in-del | -/AG | | | intron-variant | Itsn1 | Mm_Celera | 16:91908144 | ATAAATCTTAAAAAA[-/AG]AAAAAAGAAAAAAGA | 16443 |
| rs233490599 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831747 | TTGTTTATAAAATGT[A/G]TCTTACATACAACCA | 16443 |
| rs233496719 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91769471 | CCGACTTCCCTAAGG[C/T]CCATATAATTTGAGG | 16443 |
| rs233508717 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91814660 | GGGGGAGAATGGGAG[C/T]TTTGAAAACCATTCC | 16443 |
| rs233518902 | snp | A/G | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91820777 | GAACAAGTCTAGAGA[A/G]CTAAGAATTGCTGAA | 16443 |
| rs233524633 | in-del | -/TCTCTCTCTTTC | | | intron-variant | Itsn1 | Mm_Celera | 16:91839317 | ATCTCTCTCTCTCTT[-/TCTCTCTCTTTC]TCTCTCTCTTTCTCT | 16443 |
| rs233541048 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91778317 | AAGAAGCTGTGAAAT[A/G]TTTAAAGTAAGGTAT | 16443 |
| rs233551720 | in-del | -/TTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91884661 | GGCAGCACACAGGCA[-/TTT]TTTGTTTGTTTGTTT | 16443 |
| rs233561836 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916701 | GGACTCCTCTTTCCA[A/G]TTCCCTGTTTCCTGA | 16443 |
| rs233569259 | in-del | -/GA | | | intron-variant | Itsn1 | Mm_Celera | 16:91843694 | AATTGGATGAGCAAT[-/GA]GAGAGACTTCACTCA | 16443 |
| rs233575040 | in-del | -/A | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913915 | CTTGGTTCTGGAACC[-/A]GGGGGGCTTTGTTCG | 16443 |
| rs233577368 | in-del | -/TC | | | intron-variant | Itsn1 | Mm_Celera | 16:91894248 | CTTTCTTTCTTTCTT[-/TC]AATAAAAAAGATTCA | 16443 |
| rs233579841 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91882004 | AGGCCTCCACTCCAC[A/G]GCTCTCCTGCCGTTC | 16443 |
| rs233589570 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91910602 | CTCTCCCTGGCCTGG[C/G]GCTCACCAACTGGTC | 16443 |
| rs233604961 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91874833 | CAGTTTGACAGTACT[C/G]GGTTCTTAGAGCCTG | 16443 |
| rs233619969 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91916331 | CCTAGAACCATCACG[A/G]CTTCCTTTCTTTTTT | 16443 |
| rs233622472 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91827758 | AACCAAAGGCGTGGC[A/G]GGGCAATGTGCAAAA | 16443 |
| rs233647466 | in-del | -/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830817 | CTGGGAAGAATTAGC[-/T]TTTTATCTTATCTGA | 16443 |
| rs233654773 | snp | A/T | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91730684 | GGGAACAAATGCCCG[A/T]GGAAAATATCAGTTC | 16443 |
| rs233657935 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91838236 | TGGATGCAAGTGCCT[C/T]CATCAGCTGAGCCAT | 16443 |
| rs233669583 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91784676 | TCCGGACAGAAAGAG[C/G]GCATCTGGGCTTCCC | 16443 |
| rs233716607 | in-del | -/AGA | | | intron-variant | Itsn1 | Mm_Celera | 16:91807316 | TTTTACTTCCAGATG[-/AGA]AGAAAAAAATGACTT | 16443 |
| rs233722306 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91803392 | GCATTATTTGATTTT[C/T]TTTAAATGAATTTTG | 16443 |
| rs233724317 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91791602 | ACAATTAAGTGTAGC[A/G]TGAATGACTAATAAA | 16443 |
| rs233728554 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91757726 | GACAAAGATTCCTAC[A/G]AATAGCAAGGAAGGA | 16443 |
| rs233732299 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91738550 | CGGTTTTCTTACTAC[A/G]AAAACAGTGCATGCT | 16443 |
| rs233737581 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91791279 | AGAGCAGGAGGAGCA[A/G]GAGTTTACAGTCATT | 16443 |
| rs233740814 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91893430 | CTTGCCTTTCTTTCC[A/G]TTGCTGGCATAACTT | 16443 |
| rs233753063 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91837607 | CAAAAGGTGGAGATC[A/G]CCGCTACTGCCTGGA | 16443 |
| rs233760778 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91840536 | ATAAACCATTTGTTT[C/T]CTCCCTGGGCACACA | 16443 |
| rs233769396 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91765458 | TTTATAGCTGTGTGC[A/G]GAGTAAGTAGGGTGA | 16443 |
| rs233774432 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91898524 | GTCTTACAAAGGACA[A/G]CATTTAATTGGGGCA | 16443 |
| rs233775014 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91791477 | TCAGGAGCATCTTCA[G/T]CTAAAGAGACTGGGG | 16443 |
| rs233776828 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91893096 | CTGAACACTTGGTCT[C/T]GCTCTCCTTGCCATG | 16443 |
| rs233781871 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91754455 | GTTTGGTTTGTTTTT[G/T]GGAAACTTTATCTAG | 16443 |
| rs233789030 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810500 | ACGAGCTGTGCAGCA[C/G]TGAGGGCTCTGCTCG | 16443 |
| rs233801761 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91816709 | CAGGCCCTGACACGT[A/G]CGCACATGCGCCAGC | 16443 |
| rs233846245 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798821 | TGAGCACTGTGTGCC[A/T]GAAAGACAGGTACTG | 16443 |
| rs233863024 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91898347 | GGTGAGCCCTGCGTG[C/G]CATTAAAACATTCTG | 16443 |
| rs233871369 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91910407 | AGAATATGATTTTTT[-/A]TAAAATTTAAGTACA | 16443 |
| rs233875680 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91847784 | CGCCCTTGACCGCAC[A/G]TGACCCGAGGGCCCG | 16443 |
| rs233880231 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912626 | GAAACACGGTGGTGG[C/T]ATGCTACAGGGTGAT | 16443 |
| rs233892769 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91761582 | TCTTTGCCTGTGCCT[C/T]ATCTGATTGTATTGA | 16443 |
| rs233893267 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91869002 | AAACAATGATAAGAC[A/G]CCAGGCAGTAAGGGT | 16443 |
| rs233893843 | in-del | -/TG | | | intron-variant | Itsn1 | Mm_Celera | 16:91808527 | TTTAGGAATTTTTTA[-/TG]TGTTTATGTAACATA | 16443 |
| rs233920460 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91864608 | CTTCATGTTCTGGAA[C/T]CTTCAGGGATCCTAG | 16443 |
| rs233930364 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91918956 | GCTAACACCTGGAAG[C/T]GCCCTGGATGGACGG | 16443 |
| rs233960370 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91810099 | AGGTAACTTGTTTCA[A/C]TAATGTCAGGCAAAG | 16443 |
| rs233978206 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91877095 | GCCATGAAGCCCTTT[C/T]ATACAAAATGACAAA | 16443 |
| rs233979986 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91761478 | TGAGATGCTTGTGTG[C/T]GGTCAGGGCGCGCCT | 16443 |
| rs233992251 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91740205 | AAAGGTTGCATTTGG[-/T]TTTTTTTCCTTTATA | 16443 |
| rs234016873 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91768379 | TTTCAAGAAGGGAGA[G/T]GCCCCACCTGGTACC | 16443 |
| rs234017272 | in-del | -/ACACACACACACACAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91833089 | GCCACCAAAAGTTGT[-/ACACACACACACACAC]ACACACACACACACA | 16443 |
| rs234040188 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91816310 | GCTGTCCTAGAACTC[A/G]CTGTGTGGATCGAGC | 16443 |
| rs234046559 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91733444 | CTTTCTTCTTCAAAG[C/T]CCTATCTAGCCTTGG | 16443 |
| rs234074375 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91787187 | TCAAATTTTTATTTC[A/G]ATGCAGAGTCCTGCT | 16443 |
| rs234075063 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91801934 | CAATAAGAGCAGCAG[C/T]GATGGGCAGTATTTG | 16443 |
| rs234078731 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91819486 | GCTTCGTGAGAGGTA[G/T]ACACACTAAGTGCCA | 16443 |
| rs234084764 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91801005 | AACACTTTACTGACT[A/G]AGCCTCATCTCTGAC | 16443 |
| rs234088243 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91809675 | TGTGTGCGTGTGCTG[C/T]CACAGAGACTGTCTG | 16443 |
| rs234093000 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91826336 | AAATCTGGGCAAATA[A/C]TACCCAAAGAGATTG | 16443 |
| rs234093855 | in-del | -/TTCCAGGAAAGTACTC | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91829288 | TGCTCAATTGTACAA[-/TTCCAGGAAAGTACTC]TCCCTTAGGGGAGTG | 16443 |
| rs234110751 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900135 | CACCCTCATCCATTC[C/T]TTTTCTGTATGAGCA | 16443 |
| rs234117909 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91836188 | ACACCCCAGCCTAAC[A/T]GCCTAACACAGTTTT | 16443 |
| rs234118142 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873422 | TAGAATACACCTGAT[C/T]CCAGGTTCTTGACAC | 16443 |
| rs234144209 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91808851 | CAGACGTCTTGGTGT[A/C]TTCAAATTCTGGCTC | 16443 |
| rs234147348 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904952 | TGCGCCACCATGCCC[G/T]GCTATTCTCATACAT | 16443 |
| rs234175330 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91780192 | GGCAGCATGAAGGTG[A/G]ATGGTGCCACACCCT | 16443 |
| rs234175790 | in-del | -/C | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919088 | TGAAATGAAACCTTT[-/C]CCCTATTCAAGGGTT | 16443 |
| rs234177671 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91880588 | CACACGTTCATATCC[A/G]TATCCCAGCCCTTAG | 16443 |
| rs234182297 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91904551 | GCACCACCGAATTCT[A/G]CAGCCCCTCTTGTCC | 16443 |
| rs234187963 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91843645 | GTGGCCATCCCCAGG[A/G]GATGGAGTTGACTCG | 16443 |
| rs234200471 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912223 | GGTCTCATCATGGCT[C/T]CTAGAGTCTCTGAAA | 16443 |
| rs234209673 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91793404 | GGGTAAAGAGTAACA[G/T]ATGCAAGATACCATG | 16443 |
| rs234227138 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91795374 | ATGTTTGGTTTGTTT[-/G]TCTTTCTTTCTTTCT | 16443 |
| rs234238017 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91737120 | CAGATTGCAGTTAGC[A/C]TTGGCCAATGGGAAG | 16443 |
| rs234248899 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91790026 | GCAAGGCCACACTTA[A/C]GCCTCCTTAAACAGG | 16443 |
| rs234266227 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91894986 | CAACGGAAGATCGTG[A/G]GCGTGAACTCTGGCC | 16443 |
| rs234271998 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91770877 | ATGGCTCTAATCGCC[G/T]CGTCCCTACCCCTTT | 16443 |
| rs234283793 | snp | G/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746157 | TGCCAAGTGCTGGCC[G/T]GGATGCTAGCCAAGC | 16443 |
| rs234293547 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91779641 | ATCCAGAGCTGAGCG[G/T]TTTTGGAAAGATGGC | 16443 |
| rs234293601 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91787482 | TTCACTGGAAATCCG[A/G]TCGGGGCACAAGCAG | 16443 |
| rs234310683 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91899793 | CCAGCAGGGCTCTCT[C/T]CCGCTCGTTAATACA | 16443 |
| rs234311788 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91779460 | AACAGATCTAGTAAA[C/T]CTAAGATGTTTGCAA | 16443 |
| rs234319611 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91892488 | TTTTGGGCCAACAAT[-/A]GAACTGAGGGGCTTA | 16443 |
| rs234332022 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911311 | AAAAAAACGTATGTC[C/T]ATGAGCCTGGAAGGC | 16443 |
| rs234349613 | in-del | -/TTGTTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91780614 | GCATTTCTCTACACT[-/TTGTTG]TTGTTGTTGTTGTTA | 16443 |
| rs234362443 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91890223 | GTACCAGACTCTTGG[G/T]CTCTCATCTCACTGT | 16443 |
| rs234368412 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91754738 | AGACATCGGTCCTAG[A/G]CACCACAGTAGCATC | 16443 |
| rs234371274 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91856126 | TCAGTGGCTTCTGCT[C/T]TGAAATGATTGAGGC | 16443 |
| rs234374599 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889799 | ATAAATGGGCCGCAA[A/T]GATCTCCTCAGTTCA | 16443 |
| rs234378755 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91910980 | GACCTGAATTCAGGT[C/T]CTCTGGAGGAGAAGC | 16443 |
| rs234380492 | in-del | -/TTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91794073 | TGTGATAACTCAGCC[-/TTT]TTTTTTTTTTTTTGA | 16443 |
| rs234380590 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91895026 | GATTCGGTATGAGAT[A/G]CCACAGTGGGTTAAG | 16443 |
| rs234395463 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91806789 | ATCTAAAGCATATTA[C/T]TCTTATCTGTGAAAA | 16443 |
| rs234405878 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91840965 | TGAATGCATCTTCAA[-/T]TTTTTTTAATTTGAT | 16443 |
| rs234419164 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91767284 | GTGTGTGCCTCTGTG[-/C]CTGACTTCAAGAGCT | 16443 |
| rs234422670 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91764142 | GGAAGTTGGTGAGCC[A/G]CAGTCTACAGGGAAT | 16443 |
| rs234439939 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91779075 | CAGTAAAGGTCTAGA[A/G]TAACTTAATAGTAGC | 16443 |
| rs234452344 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867308 | CTGGGCATTGTCTGA[C/T]ATCACACAGAGCTCA | 16443 |
| rs234464038 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91865918 | CCTGCCTTTGCAGCA[A/G]CATGTCTCGTCCAGC | 16443 |
| rs234513785 | in-del | -/GT | | | intron-variant | Itsn1 | Mm_Celera | 16:91775679 | GTGCCTGTGTGTGGG[-/GT]GTGTGTGTGTGTGTG | 16443 |
| rs234528223 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91882468 | CCATTCCCAGCCCCG[C/T]ACCCCCCTCCTTCAA | 16443 |
| rs234530161 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91821724 | TCAGATCAGGAATCA[A/G]CTTGGCACCAGTAGG | 16443 |
| rs234531810 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91755276 | TTAATCAGCACTTGC[C/T]GGGCAAGCCTTCCAC | 16443 |
| rs234534896 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91910422 | TTAAAATTTAAGTAC[A/G]CATATATTATGTGTT | 16443 |
| rs234536029 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91764278 | GGAAACGTTCTCTCT[C/G]AGGCTACTTCTGCAA | 16443 |
| rs234541619 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91888931 | TCAGAGGTTCGCCTG[A/G]ACTCCCCTTGTCAAG | 16443 |
| rs234544556 | in-del | -/TGTCTG | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91739453 | TTTGTTTTGTTTTTT[-/TGTCTG]TCTGTCTGTCTGCCC | 16443 |
| rs234551887 | snp | A/C | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917193 | CCGGCAAACCTGAGG[A/C]CCTGAGTTTGATCCC | 16443 |
| rs234556121 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91787068 | CTGTGACCCTATCCC[-/A]AGGGAAGAAAACACA | 16443 |
| rs234568668 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91867494 | TTAGTGAGCCCTCTG[C/G]CATTAACTAGAGCAT | 16443 |
| rs234572384 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91916240 | CCGCATCTCTGGAGA[A/G]GAGACTCGCAAACTG | 16443 |
| rs234580820 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91875530 | TGGAGCCTTCACATG[C/T]ACCCCTGCAGCTTTG | 16443 |
| rs234590308 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746464 | TATGTGTGCTACATC[A/G]TTATTCAATAAAGGA | 16443 |
| rs234600927 | in-del | -/CTCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91834737 | ACTGTCTTCCGTTGG[-/CTCT]TTCTATCACTTTGTG | 16443 |
| rs234609343 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91888472 | TTGTGCAGAACAAGG[C/G]TCCCAAGGATCAGCC | 16443 |
| rs234610626 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91806556 | TGGATGCAGGGTACC[-/G]GGTGTGGAAGGAGTG | 16443 |
| rs234620651 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91763889 | TCTTTTTGCTTTAGC[A/G]TTTAATTGTTGCTTC | 16443 |
| rs234664208 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91783977 | TTACAGCACAACAAC[A/G]GAACTTTAGAGAGCT | 16443 |
| rs234666325 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91729488 | CCGGGAGGCAGGCAG[C/G]CGGGCGGGCGGGGAT | 16443 |
| rs234687856 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746064 | ATGGACAACAAACTC[A/C/G]TGAAAGATGCTCTAC | 16443 |
| rs234688908 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91731602 | CTCCAGCCCACATCC[A/T]TCCTTCCTTCCTTCC | 16443 |
| rs234700450 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91866855 | AGACTTAGAGATGCT[A/G]GGATCTGAACTCAGG | 16443 |
| rs234713086 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91874989 | AATTGTTGGTGGCTG[A/T]CCTTCCTCACCAGGA | 16443 |
| rs234717124 | in-del | -/CTT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91740525 | TCTTCATGAAGGAAG[-/CTT]CTTCAGGCCTTCCTC | 16443 |
| rs234717690 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91887843 | ATTGGTGTCATCTAG[C/T]TAGTCACATGACACC | 16443 |
| rs234721048 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91754605 | ATGGCTATCCCTTCT[C/T]TCTGAATGTCTCTCT | 16443 |
| rs234733751 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91739338 | GAACTCAGCTCTTTA[A/T]GCTTGCAGAGTAAGT | 16443 |
| rs234738156 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91833636 | TCTGAGTCTCTTTAC[G/T]ACCCCGTGAAGGAGA | 16443 |
| rs234744565 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91792000 | GACTGTCTTCCTAGT[A/G]TGTGTATCAGTGCGT | 16443 |
| rs234746180 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91881533 | GATGTCTCATCCATC[G/T]CTGCCTTCGGTTCCA | 16443 |
| rs234761626 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91731955 | TCAACCTGTGACTTA[A/T]AGAAAATTAATTAAT | 16443 |
| rs234762959 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91840105 | CTGTCTCTGTCTGGA[C/T]ACTGTAGCTCTTTAC | 16443 |
| rs234774471 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91874684 | CTAGCCACTGCTTTC[C/T]TCCCTTCTCCCCTCC | 16443 |
| rs234814123 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91753833 | ATGCAGGAGGTCGAC[A/G]TGGGTTTACTTAAGT | 16443 |
| rs234838167 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91856085 | TTTGACATGAGCAGC[A/G]GAGCAGAGCAGGCAG | 16443 |
| rs234844984 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91834892 | AAGATGAACCATCTC[A/G]GTTTGATAGCTACAT | 16443 |
| rs234851079 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91731385 | TTCCCTGAAATGTTT[G/T]TTCCTCAGCATTTTC | 16443 |
| rs234851386 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91893006 | CTCCATAGGGACACC[A/T]TGCAGCCTTGTCCTG | 16443 |
| rs234853154 | in-del | -/AC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899242 | TGAAGGACAGGTTAT[-/AC]AGAGTTTGTGCTGGG | 16443 |
| rs234862720 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91834569 | TAATGTTCTTTGGCA[C/T]CTGTTATTTTATGGC | 16443 |
| rs234891629 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91893761 | CCAGGGCAGTGACAG[C/T]GGGCGACTCACCTCC | 16443 |
| rs234891875 | in-del | -/TG | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91900288 | TGAAGCTCTCCCCCT[-/TG]GTGAGTCTTTGCTGT | 16443 |
| rs234895184 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91865700 | GTTGCAGACTTGTGT[C/T]GCCAGTCCTGGCTTC | 16443 |
| rs234901325 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91855397 | CTCAAGAAGATGATT[G/T]AAAGTAATTATCCTT | 16443 |
| rs234912009 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91753060 | GAAGAGGACACTGTG[A/C]TTAGGGGAAGAATCT | 16443 |
| rs234913596 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91864726 | CACCTTCCTCTTAAT[A/G]TAGTGAGCCCCAGTT | 16443 |
| rs234923157 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91840759 | GCCCCTGTGACTCTT[C/T]AGTGTGAACTAGGAT | 16443 |
| rs234930367 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91780887 | GGCAGCTTATAGAAG[-/A]AAACCTTTATTTATT | 16443 |
| rs234972510 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91797561 | CAGTGTACTTACATA[G/T]AATAAATAAGTCTTA | 16443 |
| rs234987354 | in-del | -/GTTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91845245 | GTCCGCATGATGAGG[-/GTTA]GTTACCCAGATGAAG | 16443 |
| rs234997053 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91760823 | GTGGAGATGTCCCAC[A/G]CTGGAACTGGGGCTT | 16443 |
| rs235001122 | in-del | -/AG | | | intron-variant | Itsn1 | Mm_Celera | 16:91852039 | AGAGAGAACTGACAC[-/AG]AGTGACAAAGTGACC | 16443 |
| rs235018593 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91826505 | CTCTGAGGAAGAGAA[A/G]CACACAGACAGTGAG | 16443 |
| rs235019910 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91812421 | GACAGTTGTGAGTTG[C/T]CATGTAGGTGCTGGG | 16443 |
| rs235021342 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91762278 | AGTAGCCAAGAGAAG[G/T]AAGGATATTTACATT | 16443 |
| rs235049313 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91847166 | AATCCCAGCATTTGG[A/G]AGGCAGTGGCAGGCA | 16443 |
| rs235052202 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91840147 | GCACAGGAAGCCCCT[C/T]GGATACCCAGGAGCC | 16443 |
| rs235068453 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872859 | CAGCACAGTTCACAC[A/G]ACACTGTGGTCCATT | 16443 |
| rs235089249 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91833499 | TTCCTCTTCCTTCTC[C/T]TCCTCCTCCTCCTCC | 16443 |
| rs235117573 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91908636 | CCAGGGGCAAGAGAC[A/T]GGAGGGGGCCTTGCT | 16443 |
| rs235124319 | in-del | -/ATGA | | | intron-variant | Itsn1 | Mm_Celera | 16:91879894 | AAGAAGAAACCTCAC[-/ATGA]ATGGACACCATGGGT | 16443 |
| rs235147357 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91902653 | ATCAGCAAAGCCCAA[C/T]GAAGACCAGCAAAGA | 16443 |
| rs235152649 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914654 | CACCCCTGAGAATTA[C/T]CCCGAGAGCTCTGAG | 16443 |
| rs235195223 | snp | C/G | | | intron-variant, upstream-variant-2KB | Cryzl1, Itsn1 | GRCm38.p3 | 16:91727365 | TTGTACATTGCAGTG[C/G]CTGATGCCTAAGATT | 16443 |
| rs235198016 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91833055 | GTCCTTGGAACCCAA[A/G]TGACAGAAACAGAAA | 16443 |
| rs235224911 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91741852 | GTACACATGTACACA[C/G]TTATGCTTGTGAGCA | 16443 |
| rs235235106 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91890256 | CTGTCTAGCTGGGTC[G/T]TTTTTTGGGGGGGGG | 16443 |
| rs235279095 | in-del | -/AG | | | intron-variant | Itsn1 | Mm_Celera | 16:91874238 | CATTTAAAGAAAGAA[-/AG]AAAAAAAAAGTATGG | 16443 |
| rs235293848 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91832387 | TTTTTTTCATCCTCT[C/G]TATCATTTACCCAAC | 16443 |
| rs235298017 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91748545 | CGTCTGGGAAGAGGA[C/T]GTCTCAACTGAGGAA | 16443 |
| rs235301275 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91741010 | TAGGCCTTAATCAGG[A/G]AAGCGGAAGTTGTTT | 16443 |
| rs235325464 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91891944 | CTGAGAAGGAGAGTG[C/T]TCAGTGCTTCGGGAA | 16443 |
| rs235326579 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91851315 | TCAGTCTGTACTGGA[A/G]AAGGAAGGCTGATTT | 16443 |
| rs235330562 | snp | A/G | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91747780 | GGGCAATGTTTGCGT[A/G]GCATTTCTACTTGCA | 16443 |
| rs235337581 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91804768 | TTACATTGTGAGTGT[A/G]ACCACATGGACACCA | 16443 |
| rs235351666 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91838897 | CTTTCCTGGCGCTGT[G/T]TCGCTCTGTACACCG | 16443 |
| rs235388100 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91812330 | TCTCTTAATAACTTA[C/T]TTGTTTTCATTTCAT | 16443 |
| rs235389664 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91804073 | GATTGTGGTGAACTG[C/T]GCCATTCAGATGACT | 16443 |
| rs235398087 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91770358 | AGTATAGAGAGTGCC[-/T]TTTGAATGTTCCCTT | 16443 |
| rs235398820 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91811888 | TCATGTCTTCAGTGT[G/T]CTTGCTGGTCATCTG | 16443 |
| rs235402622 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91908594 | AGGTGTAAGGCAGGG[C/T]GCAGTATAAAGGATG | 16443 |
| rs235416197 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91850527 | CTGTGCTTGTTGGTT[G/T]AAATGGAGTCTCCTA | 16443 |
| rs235429972 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91896890 | GTGTTTCCATATCCA[C/T]GCCGGCTCAGCTGCC | 16443 |
| rs235434283 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91907937 | AACATACACACAAAA[C/T]GAAGCAAAAAACTAA | 16443 |
| rs235443495 | in-del | -/AAAAAAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91814592 | TTTTTTTTCCACACT[-/AAAAAAA]AAAAAAAAAAAAAAA | 16443 |
| rs235469191 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91857851 | CAAGCCTTCATGTGA[A/G]CAAATCCTACCCCAT | 16443 |
| rs235473226 | in-del | -/AAA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890784 | GCTGTAGAGTGGGGG[-/AAA]GGGGGGGGGGGGGGC | 16443 |
| rs235474606 | in-del | -/AGTTGAATGTTGTTCTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91781688 | CAGTCCTCATGAAGC[-/AGTTGAATGTTGTTCTT]AGTGGGCACGGCTGT | 16443 |
| rs235481943 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91759045 | TGCTGGAATTACAGG[C/T]GTGTGCCACCACTGC | 16443 |
| rs235502468 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91775241 | GTTTCGATAATTTCA[A/T]TGTAGAGGACTAATG | 16443 |
| rs235527607 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91781869 | CTCAGTGAGAATCCT[G/T]TAGTGGTGGGGTATA | 16443 |
| rs235540906 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914155 | ATGATTGTAGTATGT[A/G]AATGCAGTCTGTGAG | 16443 |
| rs235557476 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91738448 | CGTTAATTTTAAATC[A/G]CAGTCATTGTGTGTT | 16443 |
| rs235558184 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91869593 | CCCCCCGGGTGGCCA[G/T]GTGCTCACCAGCCTG | 16443 |
| rs235558995 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91829342 | CCGACGTGTGTTTCA[C/T]TTCACATTGCTTTCC | 16443 |
| rs235568825 | in-del | -/TTTGTTTGTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91826213 | TTATTTGTTTGTTTG[-/TTTGTTTGTTT]GGAGTCTCACTCTAG | 16443 |
| rs235573402 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91841073 | CAGGTCATGAGGACG[C/T]TGCGTAGACCGACCT | 16443 |
| rs235584178 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91825649 | ACTTATATTGTTTAA[C/T]TTTTAAGTACTTATT | 16443 |
| rs235613961 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91828412 | TGTGTGAAGGCTGTC[A/G]TGGTGCCCGCTGCCC | 16443 |
| rs235621661 | snp | C/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913669 | TTTATTGAAGATAGT[C/G]TTGACTTTTGTATCA | 16443 |
| rs235632323 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91840481 | AAAATTCTTAAGCAC[A/G]GTGGTAGACAGAAAG | 16443 |
| rs235635475 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745709 | TCAGGCAGTTAGCAC[A/G]GAGCCTCTGCATAGG | 16443 |
| rs235642058 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91847644 | GCAGAAGAACACAGC[A/T]GTTTATAAATAGCTG | 16443 |
| rs235669179 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872680 | GATCCCCTCTCATGG[C/T]TTCTCCAGTCTTCCT | 16443 |
| rs235674564 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91745159 | TGTGTACCTACTTGT[C/T]TATATGTGTGCAGGA | 16443 |
| rs235685848 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91879989 | TGACTTGATCTTGGA[C/T]GGCCGCCCTCCTGGG | 16443 |
| rs235701112 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734670 | CATTTTCAGACACAT[A/T]CATAGTATGTCTGAT | 16443 |
| rs235706471 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91847010 | AACTAGGTTAAAATG[A/G]GGTACCAGAACCAAT | 16443 |
| rs235709376 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91805489 | ACTTTTAAAAAGTCA[-/C]GTTGTTAGCATTGCT | 16443 |
| rs235728618 | in-del | -/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91832065 | AGTTTGCCACCTCAC[-/T]TTGCTCAACATGAAA | 16443 |
| rs235729417 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91834912 | GATAGCTACATTGGG[A/G]CGTCATAGCCAGTGT | 16443 |
| rs235733047 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91918657 | CTCCAACACCCTGGG[A/G]CTGGCCTTGACTACA | 16443 |
| rs235746536 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91903768 | ATCAGCAAGGCAAGA[-/T]ACATGGTGGTGTCCC | 16443 |
| rs235777307 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91854782 | CTCCCGAGCACTGAG[A/G]TAAAACAGAGATTGA | 16443 |
| rs235783105 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91876924 | TCTGTACTTAACAAG[C/T]CCCAAATCTTGCTTT | 16443 |
| rs235790655 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91800263 | ACAGTAGAACAGTAA[C/T]GGACAGACCGCCCTG | 16443 |
| rs235794342 | in-del | -/CACCC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91740557 | AGCCCCACACACCTT[-/CACCC]CACCCTCAGGATGTA | 16443 |
| rs235800627 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890663 | ATCCTTCTGAGTCCG[C/T]CTCCCGAGTACTGGG | 16443 |
| rs235812785 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91834643 | CCTGAGCTGTGATGC[C/T]GTTGTCCTCAAAAGA | 16443 |
| rs235813984 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91755193 | TGGCATCAGCCTGGT[A/T]CCTCGCCAGCACCTC | 16443 |
| rs235828894 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91837219 | AGCCCAGGGCCTGTG[A/G]CATTCATTCGCCCTG | 16443 |
| rs235856992 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91909476 | CAGCTTGGCACCTCA[C/T]GCTTTGCCCTCCGGG | 16443 |
| rs235870490 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91819289 | TTCAAGCAAATATAT[A/G]CAGATACTAACAGCA | 16443 |
| rs235876553 | in-del | -/GG | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91730207 | TCCCTTCTTGGGGGT[-/GG]GGGGGGGCACCAGAA | 16443 |
| rs235881269 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91768142 | ATGAGGGAATTTTGA[A/G]CCTTTCTCAAAAGGT | 16443 |
| rs235917889 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91857096 | GAGGGAGAGAACCAA[C/G]TCCTGGGACTAGTCA | 16443 |
| rs235924435 | in-del | -/CTCC | | | intron-variant | Itsn1 | Mm_Celera | 16:91754644 | TCTCTCTCTCTCTCT[-/CTCC]CCCTCCCTCTCACAC | 16443 |
| rs235933045 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91866745 | ATTCAGCCTACATGC[A/T]TGTCTATGCACCATG | 16443 |
| rs235933419 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91799235 | GAAAGCAGGGCCCAA[A/G]TACAAACAAGCAACA | 16443 |
| rs235944556 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91818814 | GTGACCAGCTCTTCC[A/C]CAGCCACTCTCCTCC | 16443 |
| rs235948111 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91806650 | AAAGGCTAAGAATTA[A/T]TTTCCAGGATCTCAG | 16443 |
| rs235955933 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91776141 | GCGACAGGAGATGAA[C/T]AGCAAGTGATGCCTC | 16443 |
| rs235958449 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91814747 | CAACGACATCTCCTG[A/G]TTGTGATTGAAAGAC | 16443 |
| rs235960863 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91825495 | ATTATGGGTGGTTGT[A/G]AGCCACCATGTGGTT | 16443 |
| rs235964252 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91880186 | GCTGTTTATCCTCTC[C/T]GTGTCTCTGACTCCT | 16443 |
| rs235998337 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91825877 | TTACAGATCTGTGCG[C/T]TCTGCAGCGGTGGCT | 16443 |
| rs235998906 | in-del | -/TGTGTGTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91775683 | TGTGTGTGGGGTGTG[-/TGTGTGTA]TGTGTGTGTGTGTGT | 16443 |
| rs236003755 | in-del | -/GCCGAG | | | intron-variant, cds-indel | Itsn1 | Mm_Celera | 16:91852891 | TCCGCCCCTTCCTGA[-/GCCGAG]GCTGCCCACAGCCCC | 16443 |
| rs236025782 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910850 | ATCTGTGTGTTTGCT[C/T]ACATGAGTTTATGGG | 16443 |
| rs236038850 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91806002 | CCAGGAGAGAAAAGT[A/C]AACACCGCCAACCTT | 16443 |
| rs236041602 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91887062 | TGGAGCATGTGTTTG[A/C]TACTTGGATTTATGA | 16443 |
| rs236044505 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91903609 | GTTTCAGATAAACGA[C/T]TCAATAACCCAGTCT | 16443 |
| rs236054256 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91883527 | ACAAACCTCACAAAA[-/T]CTTTGCCTTTAACTG | 16443 |
| rs236060157 | in-del | -/TTTTT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890335 | AAAATGGCAGTTGTG[-/TTTTT]TTTTTTTTTTGTTGT | 16443 |
| rs236067316 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91902959 | GCCAGGCGGTGGTGG[C/T]TCATGCCTTTAATCC | 16443 |
| rs236067362 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91910391 | GTCATCTCTCTAGCC[C/G]TAGAATATGATTTTT | 16443 |
| rs236076306 | in-del | -/CT | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912414 | TTGGCCTATAATATC[-/CT]GTGTGTGTGTGTCCA | 16443 |
| rs236088323 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91833009 | AAAACTCAAGGGGGC[C/T]AGCAAGTTGGCTCAG | 16443 |
| rs236104434 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91731062 | TTTCTGTAGGAGATA[G/T]GTAAAGAACTCAGGA | 16443 |
| rs236114427 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91797347 | TGGTCTCAAAACTTC[-/T]TTTTTTTTGCCCAAG | 16443 |
| rs236119307 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91796141 | GTCTCGTCACAGTCT[C/G]AATAAGTGCAGCTGG | 16443 |
| rs236122964 | in-del | -/TTATG | | | intron-variant | Itsn1 | Mm_Celera | 16:91825679 | TTGTTTCTTGTTTAC[-/TTATG]TTATCTGAAAAATAT | 16443 |
| rs236136199 | in-del | -/CTCCTCCTC | | | intron-variant | Itsn1 | Mm_Celera | 16:91814136 | CCCCCTCCCCCTTCT[-/CTCCTCCTC]CTCCTCCTCCTCCTC | 16443 |
| rs236140680 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91784620 | GGAAGTCCCTCGTGT[A/G]CCTGTCTGTGACCTT | 16443 |
| rs236147450 | snp | G/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915483 | ACCTGGCCTGATTCC[G/T]AGGAAGAAGCCAAAC | 16443 |
| rs236162205 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91897079 | ACACACACATGTACA[C/T]ACAAACTGCACAAAT | 16443 |
| rs236183299 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91776958 | TTGTGCTCACCTCAC[C/T]TCCCTTTTACCCTAG | 16443 |
| rs236198173 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91796001 | TCTTACCCTGAGTCA[A/G]ATTACTCGAAGACCC | 16443 |
| rs236202910 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91909570 | TGAGCAGGGTGCATG[C/T]TTCCCCACCTGAGAA | 16443 |
| rs236214312 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91743984 | CCTGTTACTGGTGCT[G/T]ATTGGAATCCTGACT | 16443 |
| rs236226014 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91834406 | CTCCAAAACCCAAAG[A/G]GAACATTCAGAATTT | 16443 |
| rs236234124 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91882745 | GAGAGGAGAGTCTTT[-/C]CCCCCCTCCCTAAGA | 16443 |
| rs236234969 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91795321 | ACTGGATACTGGAAC[A/G]TACTTGCAGCTAATT | 16443 |
| rs236244146 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91752191 | AATGCACCTGTTCCT[A/G]TCTGCAAGTGGCCGC | 16443 |
| rs236256776 | snp | A/G | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803869 | CTCAGCAGCAGCACC[A/G]GAAAAGAAACACAAC | 16443 |
| rs236272274 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91776524 | GTTTATATTTTTATT[A/C]TTTGTTCTACTTCTG | 16443 |
| rs236296073 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91783924 | TACTGACTTCCTAGG[C/T]TTTCATATGAGGCTA | 16443 |
| rs236304208 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91902007 | TGGATGAACAATAGG[C/G]CACAAGGCATAGGGT | 16443 |
| rs236306413 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91743037 | TTAATATCTGCACTT[-/A]AAAAAAATGCCCTTT | 16443 |
| rs236319490 | snp | G/T | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91853278 | TGGAGAGAGCAGAAA[G/T]GACGTTTTCTTCATT | 16443 |
| rs236328672 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91861568 | TGACATAGCAGTGGA[A/G]GTCAGAGGCAAGGTG | 16443 |
| rs236343031 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91901363 | CTCCTACCTGCTTCA[A/G]TGAGGGTGTGTGCAA | 16443 |
| rs236355144 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91887726 | AGGCAGTTCTTACCG[G/T]AGCCGAGGCCAAGAG | 16443 |
| rs236358363 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783119 | TGAGCACACTGACAC[A/G]CCTGCTGACTTTTCC | 16443 |
| rs236359859 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91901783 | AGGCAAAACCAAAAC[C/T]GTCATACACATAAAA | 16443 |
| rs236365906 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91766767 | GTGGGGCTTTACCTG[C/T]CACACCTGATTGACA | 16443 |
| rs236366077 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91887232 | ATGTGTGGGGTCTCT[A/G]CGCCGGGCTGTGCCA | 16443 |
| rs236366423 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91892891 | ATTGCTTAGCCTTAC[C/T]CACACCTCATGGTTT | 16443 |
| rs236366527 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91887008 | CGTGGGAGCTCTGGT[-/G]GGTGTTAGCGGGTCA | 16443 |
| rs236378349 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91907557 | CTCCAAGTATATGAT[A/G]CTTTGCAGTATGGGA | 16443 |
| rs236379911 | in-del | -/AAGAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91793459 | TTACTCTCCCCTGTA[-/AAGAT]GCCGGTAAAGATGCT | 16443 |
| rs236393708 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91748800 | AAGTTGATTTAGTCA[-/G]TGTTTAATCATAGCA | 16443 |
| rs236394498 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907746 | GGGTTCGATGCCTAG[C/T]ACCACGTAAACAAGT | 16443 |
| rs236410465 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91744632 | TGAGCTGTGGGCTTT[A/G]GACCAGGCCTGCCTG | 16443 |
| rs236416816 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91906428 | GGATCTGGGTTCAGT[G/T]CCCAAAACTCACATG | 16443 |
| rs236455212 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91765951 | GGTAATGTTAAGCTG[C/T]TGCCGCTGTCACCTG | 16443 |
| rs236455321 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91774815 | GGTTAGTTAGGTTTG[C/G]GTCAGTGTTCTCTCC | 16443 |
| rs236463422 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91878737 | ATTTAGTCTCCTCCG[A/C]AAGTGTGGCGGCCTC | 16443 |
| rs236472798 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91774394 | TTGTATTAGTGTCCC[C/T]GGCAGCACATGGCTC | 16443 |
| rs236484530 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91805663 | GTTGTTTTTCTTTAT[A/T]AAAAAAAGTTTAGCT | 16443 |
| rs236487377 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823898 | ATTCATGGAAATTGA[G/T]TGGCCATTTTCTTGT | 16443 |
| rs236494213 | in-del | -/TCAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91738967 | TGTGGCAAAAGCTTG[-/TCAC]TCACTCACTTGTTGC | 16443 |
| rs236496680 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91774118 | TCCTGAGTGCTGAAC[C/T]TAAAGGCGTGCGCCA | 16443 |
| rs236503058 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91753595 | ATGTAATTTTGAAAC[C/T]TCCCCCCAACTCCTG | 16443 |
| rs236506197 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91752960 | CACTTCTGGAAAGTT[C/G]TCTATTAACATTAGT | 16443 |
| rs236514648 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91781388 | TGGCTTTAAACTCAC[C/T]ATGTACCTGGGTGTG | 16443 |
| rs236531420 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91877733 | TGAGGCAGGAGGATC[A/G]TGATTTTGGGGTCAG | 16443 |
| rs236535912 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91854129 | TGAACTGTTTGAGAG[G/T]TTGGACTCTTTATGC | 16443 |
| rs236547621 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91752278 | AAACAAATGTGACAC[A/G]TTTGCGGTTGGCATT | 16443 |
| rs236563147 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91885766 | TGCGAGGGAGGAATC[C/T]CTGAGGAGCCCTTGG | 16443 |
| rs236586507 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915564 | GAGAGTTAGAGACAG[C/T]TCCTCCTCCTCTTCC | 16443 |
| rs236597661 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91831458 | TGGATGGGGTCAAGC[A/G]AACCATCTAACCAGT | 16443 |
| rs236625460 | in-del | -/CCCAAGTACCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91760042 | TAGTTGACTCTTTCA[-/CCCAAGTACCT]CACGTGTACTAATTT | 16443 |
| rs236646338 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91743144 | CACAGGGTATTGAAT[C/T]TCGGGTTTGCACGTG | 16443 |
| rs236652030 | in-del | -/TAAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91791634 | ATTTGTACACATGTT[-/TAAA]TAAGGGTCTTATGAA | 16443 |
| rs236652722 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91863056 | CACAGGACAGTGAGG[A/G]CCGCACAAGTCTGAG | 16443 |
| rs236652771 | snp | C/T | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91853527 | CAGTTGCTGAGAAGC[C/T]ACAAGGTGACTAGCA | 16443 |
| rs236671423 | in-del | -/ATATTAGAAGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91773008 | TAGCCCTCTTTGAAC[-/ATATTAGAAGT]ATAGTGATTATATGA | 16443 |
| rs236680048 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91907090 | GGCTTTTTTTTTTTC[-/T]TTTTCTTTTTCTTTT | 16443 |
| rs236707925 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91884763 | TCGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 16443 |
| rs236713509 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91861707 | TAAACAAAATCACAC[A/G]TTCTATTAATAGTGG | 16443 |
| rs236727510 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742439 | TTTGCTCAAAGCACC[A/G]TAGTTCTGTTTGCCT | 16443 |
| rs236731892 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91836703 | CACTGCCCCTCACAA[A/G]CAAGGGCCTTTCAAA | 16443 |
| rs236735286 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91862101 | GAGCAAAAACAGCTG[A/G]TGCCAAATAGGACAC | 16443 |
| rs236760987 | in-del | -/TAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91764382 | AGTGTTTCTGTGAAC[-/TAT]ACTATGCTTTTTTTT | 16443 |
| rs236767666 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91811910 | GGTCATCTGCTCAGC[A/C]GAGTCTGACCCCGCT | 16443 |
| rs236784360 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91812207 | CGCGCTTAGGGTGGG[-/T]TTTCCTCATCGGCTT | 16443 |
| rs236793783 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91749429 | AAAAATCATCAGCTT[C/T]TCTGGGGGTCCTGTG | 16443 |
| rs236807285 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890364 | TGTTGTTGTTTTTTT[G/T]TTTTTCTGTGACTAT | 16443 |
| rs236817187 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91748689 | CAGTAAGCTGCATTC[C/T]TTCATAGTCTGCTGC | 16443 |
| rs236823142 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91851669 | AGACGGAGCAGGCCC[A/G]GGCCCTCGGGTCAGA | 16443 |
| rs236824690 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91907967 | ACAACAATGGCTGCA[A/G]CGATGGTTTAGCGGT | 16443 |
| rs236831408 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91757947 | GTATACGAGTACACT[A/G]TTGCTATCTTCAGAC | 16443 |
| rs236836492 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91791393 | CTGAACAGACCTCCC[A/G]ACTAAAATCATTCTA | 16443 |
| rs236846611 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91851962 | GTTGGAAGTGAGGTC[A/G]GTCCAGATGGCAGTG | 16443 |
| rs236853914 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91748200 | CGAGACAGGGTTTCT[A/C]TGTATAGCCCTGGCT | 16443 |
| rs236863924 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91792055 | GAGCAGGCCAGAAGC[-/A]AGTGTCAGAGCCCCC | 16443 |
| rs236873518 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914212 | CACCCCTGGGTTGTC[C/T]TGAGGGGTGACAGAT | 16443 |
| rs236881272 | snp | A/G | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91871851 | GAAGCCTACCGGCCA[A/G]CTTAGCTGTCAACTC | 16443 |
| rs236886903 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91851054 | GGCAATGTCATTTAC[A/G]AGCAGGCTCCTCCTA | 16443 |
| rs236887048 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91859238 | TGTAGTACATTTGCC[A/G]TTGACCTTCTCACTC | 16443 |
| rs236946920 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798499 | CTGCCTCAGTAAAGT[A/G]GAGAGTGATCTGCAA | 16443 |
| rs236952492 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91779016 | TAAATAAAATAAATC[-/T]TTTTTTTTTTAAGAA | 16443 |
| rs236953084 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91756160 | ACAACCAGCCTTGTG[A/G]GACTGAGCAACTACT | 16443 |
| rs236953656 | in-del | -/TTGTTGTTGTTTTTTTG | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890348 | TGTTTTTTTTTTTTT[-/TTGTTGTTGTTTTTTTG]TTTTTCTGTGACTAT | 16443 |
| rs236990668 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91858028 | GTCCTCACAGCAGCC[A/G]TCTCCGAGTGCACTG | 16443 |
| rs236996352 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91781581 | CCTTCCACCTTTATG[C/T]AGATGCGGGCATCAA | 16443 |
| rs237000547 | snp | C/T | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91858584 | AGTGGAGGCTGCACT[C/T]AGGGGCCTGCTCTTC | 16443 |
| rs237015180 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91797434 | CTTAGCAGTTAAGAG[C/T]ACTGACTGTTCTTCT | 16443 |
| rs237019070 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91898304 | GGACAGCAGAGATGG[A/C]GGGAATCCTAGCTAC | 16443 |
| rs237032594 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91897796 | GGGAACCCAGGGCTC[A/G]TTACCATGGCACACA | 16443 |
| rs237038110 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91904579 | TCCTGGGGCCTGGAC[A/G]CTGCACCTGGGAAAG | 16443 |
| rs237043105 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91761887 | GGCGAGTGTGTCTCT[C/G]TATGTCCAGCCTTGC | 16443 |
| rs237046983 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91735482 | AGTCCTTCTGCAGCA[A/T]TTCTGTGTGTTAACT | 16443 |
| rs237054560 | in-del | -/CCCTGCGCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91766832 | TGCCCCACCTCGCTG[-/CCCTGCGCT]CCCAGCCCCTCTCTG | 16443 |
| rs237055500 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91902963 | GGCGGTGGTGGCTCA[C/T]GCCTTTAATCCCAGC | 16443 |
| rs237070429 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91902506 | TTTCCAGAAGAAATG[C/T]AAGGCTCGGCCAGTC | 16443 |
| rs237075714 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91911625 | ATATATATATATATA[A/T]AATTGGGAATATTAA | 16443 |
| rs237098894 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91867685 | ACTGCATTGCAGACC[A/T]TTGTCAGCTGCCTTT | 16443 |
| rs237104198 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91822401 | ACCAGCTGAGCCATT[C/G]TGCTGGCTCCAGTTT | 16443 |
| rs237126484 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91838387 | AATATGTGATACATA[G/T]TCTAAGTGTATAGGT | 16443 |
| rs237150949 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91788927 | AAGGTAGAGACCGAC[C/T]AGGTCTATTCTTAAT | 16443 |
| rs237164059 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768308 | TTCATGTATTTATCC[C/T]GATCACAGCTGCCTT | 16443 |
| rs237169829 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91873348 | TCATATGGCTTACCT[A/G]ACATGTGATAGGTTT | 16443 |
| rs237184468 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91760362 | ACTTTGAAAGCTAGA[A/C]ACCAGGGAGGAAGTT | 16443 |
| rs237206769 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91779104 | GCTAGCACGTTACTG[C/T]AATTCAGTGGTGTTG | 16443 |
| rs237216933 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91891581 | CCCCACCCACAATGG[C/T]GCGGGGCCTCCCCAT | 16443 |
| rs237228583 | in-del | -/AG | | | intron-variant | Itsn1 | Mm_Celera | 16:91852266 | TTTACTGAACATCAC[-/AG]TGTCTTCAGGAGAGT | 16443 |
| rs237233610 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91880499 | CTGTGTATGGTATAG[C/T]CTTCCTCATGCATCA | 16443 |
| rs237233998 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91874019 | AAAGCACCCACACAC[-/A]TAAAATATTCTTTAA | 16443 |
| rs237275175 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91759531 | AGAATTCCTGTATTT[C/T]ACTTTTGTAGTGGCT | 16443 |
| rs237276739 | snp | A/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91828434 | CCGCTGCCCCTCCAG[A/T]TGTGCTTGCTTTCTC | 16443 |
| rs237278971 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91834946 | TCCTGGTTTCACAGC[A/G]CCTGCCGTTAAGTGT | 16443 |
| rs237285440 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91775823 | CTCTTGCAAGCCCTG[A/C]TGAACTTTTCATAGA | 16443 |
| rs237306323 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91872191 | CTGCAGATGGTTCGG[A/G]GGAAGGGGGTGATAA | 16443 |
| rs237307722 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91785695 | GTTTGGCCACAATCT[C/T]GAGTAAAACAGGCTG | 16443 |
| rs237315664 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91766808 | TCCGGGCACACAGGG[C/T]TAACAGTGTGCCCCA | 16443 |
| rs237341263 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91758297 | GCTGGGATTAAAGGC[A/G]TGCACCACCACGCCC | 16443 |
| rs237353661 | in-del | -/A | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91871057 | ACACCATAAACTAGT[-/A]AAGACGCCAACTGCC | 16443 |
| rs237358354 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91879573 | ATGTGGCAGCCCTGA[G/T]CTGCCTTCAGCTGAG | 16443 |
| rs237377213 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91889069 | TGTGTGTGTGGTATG[C/T]TGAGCTAACTGTCTG | 16443 |
| rs237398246 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91765693 | GCAGGCAGATTTCTG[A/G]GTTCGAGGCCAGCCT | 16443 |
| rs237417268 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91869182 | ACACCATCTATAGAA[A/G]GGCCAGGTCCAGGGC | 16443 |
| rs237419553 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91736726 | TGAAACAAAATCCTC[A/G]GGAGCCATTCAGTGT | 16443 |
| rs237422860 | in-del | -/ATAAAATAAAATAAAATAAAATAAA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91901792 | AAAACCGTCATACAC[-/ATAAAATAAAATAAAATAAAATAAA]ATAAAATAAAATAAA | 16443 |
| rs237445021 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91886893 | ACCAGGGGCGAGCTG[A/G]CCTCTCTGAGCCCTG | 16443 |
| rs237463556 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912905 | TCCTTAGTGGTCACC[A/G]CACCCCCAAACCCCA | 16443 |
| rs237465404 | snp | A/G | | | utr-variant-3-prime, intron-variant | Itsn1 | GRCm38.p3 | 16:91870839 | TCACGTGTACCTGTC[A/G]CGCATGTACCATCTG | 16443 |
| rs237467137 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91736008 | GCAGGACGTTATGGG[C/T]CCACTCAGAAAGCCT | 16443 |
| rs237470110 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91744274 | CTTTTCTGGCGAGTG[C/T]TGCAGGCACCAGTAA | 16443 |
| rs237484638 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919509 | TGTTGGATGCTCCAA[A/G]CCCTTTGAGGCTCTG | 16443 |
| rs237545950 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91787631 | GAAAGAGTGGGACAG[G/T]ACAGTTAGCTGCTGC | 16443 |
| rs237547992 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91734160 | CACGTGGGTGCTAGG[A/G]ATTGAACCCTGGGTC | 16443 |
| rs237552405 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878756 | TGTGGCGGCCTCACA[A/G]AAGCATCCCTGGGTG | 16443 |
| rs237568077 | in-del | -/AAAAAA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91844479 | AATAACAACAACAAC[-/AAAAAA]AAAAAAAAAAAAACC | 16443 |
| rs237568532 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91877902 | TACCTCAGTATTTGG[A/G]ATGTGGAGGCAGAGG | 16443 |
| rs237576087 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91845876 | CGAGGTCATTAAAGA[A/G]CCAAATGTAATAGCA | 16443 |
| rs237581490 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743807 | GATTAAAGGCGTGCA[A/C]CACCACCCCAGCTTA | 16443 |
| rs237582170 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91735642 | AATGTACCCATGAAT[C/G]TACTTCTTTATATCT | 16443 |
| rs237588637 | snp | A/T | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91853536 | AGAAGCCACAAGGTG[A/T]CTAGCACTCCTGAGC | 16443 |
| rs237588773 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91845353 | TTAAGAGCACTCCCT[A/C]CTCTTCCAGAAGACC | 16443 |
| rs237603721 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91902403 | GAAAATCCAGTCTGC[A/G]TTGTCAGGATATCAG | 16443 |
| rs237607984 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91768580 | TCTGCTACATTCACA[C/G]GGGCGGCCTAGGTCC | 16443 |
| rs237616948 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91735017 | GCTGGGAGTTTGTGG[A/G]TGCAACAGCCAAGTC | 16443 |
| rs237635608 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91838424 | TACCCAAAACTTCAG[A/G]AATCTTTTTTACCCT | 16443 |
| rs237648356 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91788906 | ATCTGATTTGTTCTA[A/T]ACAAAAAGGTAGAGA | 16443 |
| rs237651145 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91908667 | TTCAAGTGCGGACAG[A/T]TGCCTCGCATAGATT | 16443 |
| rs237651770 | snp | A/G | | | intron-variant, missense | Itsn1 | Mm_Celera | 16:91852912 | GCTGCCCACAGCCCC[A/G]GAGCCTGCTCCTCCT | 16443 |
| rs237661482 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91776803 | GTTTATTGTATTTGA[C/T]GAAACATTTTCTCAT | 16443 |
| rs237662359 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91795087 | AAACTCAAGTCATAG[C/T]ACTATATGCCTTTCT | 16443 |
| rs237665760 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743586 | CAAACTTGGTAGAAC[A/T]TTTCAGTCTGATAAT | 16443 |
| rs237681640 | in-del | -/AGCCCCGTTTTTCATC | | | intron-variant | Itsn1 | Mm_Celera | 16:91847402 | GCACTCTACACGCAT[-/AGCCCCGTTTTTCATC]AGACTCAGCAGTGCT | 16443 |
| rs237681755 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91826450 | GTTCGTCATTGGTAG[A/G]TGCAGGTCCTGGATT | 16443 |
| rs237712019 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91844711 | ACCTCTTCTTCCACC[A/T]TCTTTAGGTTCCCAC | 16443 |
| rs237736581 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91880011 | CCTCCTGGGCTGTGA[-/G]GAAGGAAACTTGTGC | 16443 |
| rs237746282 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91844978 | AAACGTGAAAGTCAT[C/T]ATAAAAACAAAGCTG | 16443 |
| rs237752464 | in-del | -/CC | | | intron-variant | Itsn1 | Mm_Celera | 16:91766339 | GAATTATCAAGTAAG[-/CC]CTATGAATCAGCTGT | 16443 |
| rs237760533 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852647 | GGAGGTAAGGGTCCG[C/T]GCAGAGCAAGGGTCA | 16443 |
| rs237763836 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91880783 | ACTGCCTCCTTCATC[C/T]GATCCCCATAGGAAT | 16443 |
| rs237771446 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91892624 | GCTGCTGCCTTTCTC[-/A]AACCCCAGATGGCCA | 16443 |
| rs237777289 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91844064 | CTTCCTTAGGCCATA[A/G]ACATTCAGGGTATTT | 16443 |
| rs237806437 | in-del | -/TC | | | intron-variant | Itsn1 | Mm_Celera | 16:91800012 | CACCTGTCCATGTGT[-/TC]TGTCTATTCATCTTT | 16443 |
| rs237865186 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91823965 | AGGCCTCAGAACATA[A/C]ATTGGTACTGAATTT | 16443 |
| rs237869604 | in-del | -/GTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91760272 | AGGAGGTTTGCTTGT[-/GTG]GTGGTGTTGGTGCCT | 16443 |
| rs237887652 | in-del | -/GTGTGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91775678 | GTGCCTGTGTGTGGG[-/GTGTGT]GTGTGTGTGTGTGTG | 16443 |
| rs237896273 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91825353 | ATAAATATCATTGCC[A/C]CAGCCATAGCTACAT | 16443 |
| rs237901617 | in-del | -/TT | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830703 | AATAAAGACTGAGGA[-/TT]TTTTATAGTCTTTCT | 16443 |
| rs237914458 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91832472 | AATAGGTGGCACACT[A/G]GAGTAGTCGGCATGC | 16443 |
| rs237924499 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91765630 | AGAGGCCTGGCTAGC[C/T]GGGCGTGGTGGCGCA | 16443 |
| rs237928749 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91823470 | CCTTCTCTAGCCGGG[A/G]TATCTTCCTTTTTGG | 16443 |
| rs237940246 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831037 | CATACTTAGAATCAC[A/G]GCACTGCTGGCAACT | 16443 |
| rs237945091 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91744510 | TCTGGAAAACAATCA[A/G]TGCTCTTAACTGCTG | 16443 |
| rs237949256 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91879220 | TTGCAGCCAGCTCCT[A/G]GAAGTCTGAACTCCA | 16443 |
| rs237953191 | in-del | -/TTTTTTTTTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91818267 | ATATTTTGGCTTTGC[-/TTTTTTTTTTT]TTTTTTTTCTGCAGT | 16443 |
| rs237961934 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91905171 | AGGGCTCTTTAGAGC[A/C]GTTCTTGTTTGTATG | 16443 |
| rs237962292 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91773578 | ATATTCTAGAAATGG[C/T]TTAATAATTTTAACG | 16443 |
| rs237968030 | in-del | -/A | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917238 | GAAACCAGATTCAGC[-/A]ATGCGTAGCTGTAGT | 16443 |
| rs237970665 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91897456 | GCCttttttttttta[A/G]atttatttatttatt | 16443 |
| rs237994324 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91816598 | GAGAGTTACTTCAGC[A/G]CTGATTGGTCCCATG | 16443 |
| rs238013137 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830634 | CTCGCCGGCCTCACC[A/G]CACTACACACGGCTT | 16443 |
| rs238024913 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91796719 | TGAGGCAAGAACAGG[A/G]CAGGGAAATAGTGAC | 16443 |
| rs238037738 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91794748 | ATTTTAATAAGAGGC[A/C]GTTATGGCTTCTCCT | 16443 |
| rs238038547 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91886770 | AAAAGCTGGTCTCCG[A/G]ATAACCACATACCTG | 16443 |
| rs238055002 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91816019 | GTAAACCCATCATCC[C/T]AGAATGTTCCGTTTC | 16443 |
| rs238056827 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91822892 | TGCTTTGTGCCCGGG[A/G]CCTCTGCTCTCCAAG | 16443 |
| rs238078256 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91918763 | GAGATGGAAACACAT[C/T]GTCCCTTCTCCCTCT | 16443 |
| rs238093602 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919190 | GGGTCCCTGTCTGAC[A/G]TCGAGAGGTCCTTTG | 16443 |
| rs238106619 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91794135 | CCTTCTTCTCTCATA[C/T]ACCTCTCCTTGCTCT | 16443 |
| rs238108640 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91917708 | CTCCGGGATTTCTGG[A/G]GAGCTGGCCAGTGAC | 16443 |
| rs238122888 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91799191 | GGAGGAGACGGGAGA[-/G]GAGGGGGTGGTGGGT | 16443 |
| rs238162075 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91829761 | AGCACCATCAGATGG[A/G]CTGAGTCGCGGTCTT | 16443 |
| rs238189315 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91741608 | CTGAGTTCTGTGATT[C/T]TTGTAGTGAGTCACT | 16443 |
| rs238222178 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802337 | ATCTGAGCAAATTCA[A/G]TAGTACCAGCAGCAT | 16443 |
| rs238225468 | in-del | -/GAGT | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91801488 | CGAGTGTCACCATGC[-/GAGT]GACTGGCTGAGTTTG | 16443 |
| rs238231062 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91786144 | GCCTCTGCCTCCCAA[A/G]TACTGGAACTAAAAG | 16443 |
| rs238232685 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91793124 | TGGACGAGGAACACC[A/G]CAGACTAAGTGGAAT | 16443 |
| rs238234301 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91852733 | GGCAGCTACAGACCA[A/G]TTGTCCTTGGGCATT | 16443 |
| rs238240560 | in-del | -/CA | | | intron-variant | Itsn1 | Mm_Celera | 16:91856983 | TAGAACAAAGCTCTT[-/CA]CATTAGCCATGGGAG | 16443 |
| rs238241289 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91812491 | GATCCATCTCTCCAG[-/C]CCCTGGCTAACAATT | 16443 |
| rs238250431 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91883914 | TGTTGTAGAAAGCAG[C/T]TGGCATTTCTCAGCA | 16443 |
| rs238276457 | snp | A/G | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803498 | TACCACATTCCTGAC[A/G]CCCATGGAGGTCAGT | 16443 |
| rs238282963 | snp | A/G | | | missense, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91801664 | CCCCTGGCTAACGGG[A/G]CTCCTCCCGTCATAC | 16443 |
| rs238288925 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900268 | TGTTTTACCGTAAGT[G/T]TTTTTTGAAGCTCTC | 16443 |
| rs238325809 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91860527 | TACAAGGGTAGGCAC[C/T]CAAGGGAAGCATTAA | 16443 |
| rs238328258 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91792632 | GCAAAGCAAAACTCA[A/G]AGGAGCCGAGGAACT | 16443 |
| rs238330365 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91899795 | AGCAGGGCTCTCTCC[C/T]GCTCGTTAATACAAC | 16443 |
| rs238331840 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91905256 | GAAACAAACACATCT[C/T]GCCTTCTTCCTGTCT | 16443 |
| rs238371380 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904712 | TGCAGTGCCCCACAT[A/G]GAACAGATAGCTAAG | 16443 |
| rs238371735 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91894371 | ACCATGTGGTTGCTG[A/G]GAATTGAATCAAGAC | 16443 |
| rs238388452 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91907210 | TTGAGACTAATCCCC[A/G]CCCCTCCGCCCCCAC | 16443 |
| rs238397793 | snp | G/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746536 | CTGAGTTTCCTAAAA[G/T]AACTTACTTTAACCT | 16443 |
| rs238407037 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899042 | CGGAGAAGAGCAGCT[A/G]CTGGCTGCCAGCAGG | 16443 |
| rs238410288 | in-del | -/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91885979 | GGGGAGGGAGGGGAT[-/G]GAGTGGGAGGGGGGA | 16443 |
| rs238426533 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91849632 | ACCTAGACCATCTGT[A/G]GGGCAAGGTTTTATA | 16443 |
| rs238441383 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91800408 | ATTACAGGCATGTAC[C/T]ACTACTGTTGGCTAT | 16443 |
| rs238445370 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91771755 | TTACCTAGGTTTGAG[C/T]CCCCAACCATTCTTT | 16443 |
| rs238476693 | in-del | -/GTG | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91730047 | GCCGTTTGGGCCGAA[-/GTG]GTGCGGCCGGGGCTG | 16443 |
| rs238479127 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91770255 | AGGCACTGTGCTCCC[A/C]GTTTCTGCAGCTAAG | 16443 |
| rs238481668 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91898895 | CAGGGCACACGAGCA[C/T]GTGGCGTAGGGCACC | 16443 |
| rs238484881 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91757280 | TCATAACACTGTCTG[-/C]TTGTAGTTGCATTTG | 16443 |
| rs238519239 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904300 | GCCTGTGCACAGCTG[C/T]GGCCCCCTGCCTTCC | 16443 |
| rs238519440 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91845959 | AATGGCGGTCAGTGC[A/C]CATAGACCTGTTAGA | 16443 |
| rs238541413 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91857189 | CTGTATACCAAAGTT[C/G]TAGCTGCAAGCCAAC | 16443 |
| rs238546601 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91811964 | GCTTCCTTTCCTTCC[C/T]GAGTGCTCCTGGGTA | 16443 |
| rs238552634 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91770094 | CCTTTTACTGTGCTC[C/T]GTCAGCCTGTGTGCA | 16443 |
| rs238552750 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91763152 | CTGGTGGATTTCAGG[A/G]CAAGGACTCCTCTTT | 16443 |
| rs238556315 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91875385 | AGAACAGAAGGGACG[A/G]GCTGTTCTTGGGAAA | 16443 |
| rs238565863 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91773909 | CCTCAGGTCTCTAGA[C/T]TCATTGCTGTTATCT | 16443 |
| rs238588178 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91769443 | CATAGCCTCACTCTA[A/G]TCCCAGTGACTACCG | 16443 |
| rs238593754 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91780988 | GTGCAGGTGTGATGC[A/T]GGAACAGGAAGTGGA | 16443 |
| rs238621291 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91874749 | ATTCTTGCACACTGA[A/G]CCAGGCCACATGCTA | 16443 |
| rs238653341 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91769267 | ATGGTGGCTCACAAC[C/T]ATCTGCAATGGGATC | 16443 |
| rs238654685 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91811536 | ATTTGTAGTGGTACC[C/G]TTAGAGGACCTGCTA | 16443 |
| rs238656456 | snp | C/T | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91818667 | GGAGATCGAGAGGCG[C/T]GAGGTGAGTGAGCAG | 16443 |
| rs238674334 | in-del | -/GAACTAGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91863983 | TGATAACAGAGTTGA[-/GAACTAGG]GTACCACCTCATCAG | 16443 |
| rs238693539 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91731517 | ATGGCTGTGAGCCAC[C/T]GTGTGGTTGCTGGGA | 16443 |
| rs238695641 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830847 | ATAAGCTAGGGAAAG[C/T]CTTGAGTTTTCATCT | 16443 |
| rs238698164 | snp | A/C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91837322 | ATCTCTGCATATGCG[A/C/T]GTACACGCCCCCTGA | 16443 |
| rs238699562 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91820892 | CCATCATTAGGTGCT[-/G]GGGGGGCAAGCAGGA | 16443 |
| rs238708619 | in-del | -/GAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91886387 | TGTAAAAAAAAAAAA[-/GAG]AGGGGGGGGGACCAG | 16443 |
| rs238723449 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91817973 | AAGGTTTAAGGCACA[A/G]AAAAACAAGTCACTC | 16443 |
| rs238738218 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91881868 | CAACACCTGTTGTAT[A/C]GACAGGAACTCCAGG | 16443 |
| rs238747954 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91827450 | CAGAAAAAGAGGGTA[A/G]TTCAGGACTCTTAAG | 16443 |
| rs238781502 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91738998 | TGCAGGTAAAATCAG[C/T]TTGCTTTTTAATAAA | 16443 |
| rs238784703 | snp | A/G | | | downstream-variant-500B | Itsn1 | Mm_Celera | 16:91920643 | GGATATGTGGTCGAT[A/G]AGATGGGTGGAGCCA | 16443 |
| rs238786083 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91881745 | ATAGAATCAGGATCC[G/T]AGGAGGATCAAACCC | 16443 |
| rs238801068 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91881363 | CTCACACTTGCTCCT[A/G]CTTTCTTATCAAAAG | 16443 |
| rs238841600 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91888402 | GTATGAGTGTCACCT[A/G]CTTCCATGTGGCAGC | 16443 |
| rs238842705 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91789057 | AGTGTTAATGAATGA[A/T]TTTCCAAACTGGTTT | 16443 |
| rs238862142 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91737983 | TAAGGTGGTATACAG[C/T]TATTATCCCAGTACT | 16443 |
| rs238886620 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91913124 | GTCATAGGAACACAC[A/G]CACTTTTTGCGAGAA | 16443 |
| rs238886670 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91768254 | TTTCTTTGCTGTGCT[-/G]TTTTAAAAAAACTTT | 16443 |
| rs238886714 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91739880 | CCTGTCCTCTTTGGG[-/C]CCTTTATCCTTTCTT | 16443 |
| rs238892834 | in-del | -/TGCCTTC | | | intron-variant | Itsn1 | Mm_Celera | 16:91795001 | TGGAAGCTTGCACAG[-/TGCCTTC]TGGCACCTGAAGGTT | 16443 |
| rs238894038 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91748612 | TCTTGGTTGCTAATC[A/G]ATGTAGGAGGACTCA | 16443 |
| rs238896032 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802060 | GGAAAACCGAGCAGT[A/G]TTGAACAGGTAGAAC | 16443 |
| rs238902211 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745643 | ACTGTGCGGTGTCCC[C/T]GCCTCACCAACAGGA | 16443 |
| rs238916406 | in-del | -/AAAACA | | | intron-variant | Itsn1 | Mm_Celera | 16:91770307 | GGTCTGAGTTTTCAC[-/AAAACA]AAAACAAAACAAAAC | 16443 |
| rs238920162 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91788518 | CTTTTGCTTTGTCTC[A/G]TTTCCTCTTTGCTGT | 16443 |
| rs238935957 | in-del | -/TTTGTTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91884673 | GCATTTGTTTGTTTG[-/TTTGTTTT]TTTGTTTTTTTGAGA | 16443 |
| rs238936815 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91912601 | TAGACTTCCTTAGTG[C/T]CCATCAGTGGAAACA | 16443 |
| rs238942649 | snp | C/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919790 | GACCTGACCACTACT[C/G]TGCCAGCATCCATTT | 16443 |
| rs238947090 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91757125 | CCAGAGCACAGGATG[A/G]CATGGCCTCTCATTG | 16443 |
| rs238947448 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91859135 | AGTGGCCAGGCACTC[A/G]TTGTCATTTAAATGC | 16443 |
| rs238963366 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91809868 | TCGTCGGCCACTCAC[A/G]AGTCCTCAGATAAGC | 16443 |
| rs238985734 | in-del | -/CG | | | intron-variant | Itsn1 | Mm_Celera | 16:91862554 | GCTCCCCCCCCCCCC[-/CG]CCCCCCTGGCCTGAG | 16443 |
| rs238992341 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91781033 | ACAGACTTGGCAAAC[C/G]ACAAGGGTAGAAATG | 16443 |
| rs239008068 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91847444 | TGCTTTGTTGTTTGA[G/T]AGACACTCCTGACTC | 16443 |
| rs239012769 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91905075 | GAAGCAGAGTCCCAG[A/G]AGAAAGGCTTGAGAA | 16443 |
| rs239017937 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91855363 | GGCTAGTCCAGACTC[A/C]CAGGAATAGGGTTCC | 16443 |
| rs239044791 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91805906 | TCTTGAAAGATGTCT[A/G]TACTGATGTGTAGAG | 16443 |
| rs239056235 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91794824 | CAGTACCAGCCATGA[C/T]TTTCCTCCAGTTTCG | 16443 |
| rs239075558 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91787723 | TCCGAATCCTCTCTG[G/T]AATGACAAGCACACT | 16443 |
| rs239087804 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91902871 | AGCATCACATGACAC[A/G]ACTGAGTCTCCAAAG | 16443 |
| rs239103280 | in-del | -/CTGACTGACTGACTGACTGA | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91828946 | TTCAGAAGTAAACGG[-/CTGACTGACTGACTGACTGA]CTGACTGACTGACTG | 16443 |
| rs239144720 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91895509 | TACCTGTGCCTAAAC[C/T]GGCTTTAAACAGGAC | 16443 |
| rs239150935 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758453 | TTGTCTATTATCTCT[C/T]TTTTCTTCATACGCT | 16443 |
| rs239183255 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91748646 | GACTGGGGGTGTTCT[A/G]TCCCTAGGCAGATCA | 16443 |
| rs239183997 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91779524 | TGCAGTCTCTGGACA[C/T]GAAGGGGTTAATAAT | 16443 |
| rs239185470 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890540 | CCAGGAAACCAGAGA[C/T]TCGGGATCTGACTTG | 16443 |
| rs239189273 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91757385 | TTTTCTAGTACTGTG[A/C]GGAAGAACTTCACTA | 16443 |
| rs239212996 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91786412 | CCACCTGTGGCTTTC[C/T]GACTCCAGACCTCAG | 16443 |
| rs239234633 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91829479 | CACTGTAACTTACTG[C/T]TGTATTAAGCAGAAA | 16443 |
| rs239234932 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91895199 | TCAGGTGTTTCTCTG[A/G]GTTGAGGGATTTTCT | 16443 |
| rs239238293 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91756967 | GTGTAAGCCCATTAC[C/T]TGGGGACTTCAGAGT | 16443 |
| rs239250203 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890078 | ATGTGCAGCAGCTTC[A/G]GGTCCCTCGGTCTGC | 16443 |
| rs239253616 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91793075 | ACAGCATAGTAGTGT[C/T]CCAGTATAGGATAGC | 16443 |
| rs239268246 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91747989 | TCCCGCTGAAGAGTG[C/T]CCTTGTGCACGGCTT | 16443 |
| rs239268481 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889684 | GTACCTGTTTAGTCT[G/T]CAGAGGGTCTGCAGG | 16443 |
| rs239277757 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91765224 | GCAGAGGCAGGCGGA[C/T]CTCAGTGACTTCCGG | 16443 |
| rs239285383 | in-del | -/TATT | | | intron-variant | Itsn1 | Mm_Celera | 16:91886180 | TAAAATTTGTTTAAA[-/TATT]TATTTATTTATTTAT | 16443 |
| rs239285507 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91868791 | GTCAGGACCTATGAA[A/T]GTGACCGACCTCTGA | 16443 |
| rs239292717 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91753596 | GTAATTTTGAAACTT[-/C]CCCCCCAACTCCTGT | 16443 |
| rs239293798 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91835629 | TTCCAGCAGGAGAGA[A/G]TGAATCAATCTCTTC | 16443 |
| rs239298122 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91894738 | GGCAGAGAGACTGAA[A/G]CAGAGATCTTAGAGG | 16443 |
| rs239313179 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91764651 | TAGTCACTCTCTTTG[A/G]TGTGGGAGAAGCTTA | 16443 |
| rs239347444 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91876994 | TGCCTTAAGTTTAAG[C/T]CATTGGTGCACTCCA | 16443 |
| rs239363117 | snp | A/G | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91858487 | GCTGAGTTCTGGAAT[A/G]TGGTGGTAACTAACG | 16443 |
| rs239389275 | in-del | -/TT | | | intron-variant | Itsn1 | Mm_Celera | 16:91835423 | GCTGTTGATAATTGA[-/TT]TTTTTTTTTTAACTG | 16443 |
| rs239400990 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91755636 | CTTTGCCTCCTGCAT[C/G]CTGGGATTAAAGGCG | 16443 |
| rs239418311 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91868149 | GCAGGTAAGATGCTC[G/T]CAGGCCGTCTGCTCG | 16443 |
| rs239424775 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91857396 | GGTCTGAGCCTCAGG[C/G]TCAGTTCAAAGCAAA | 16443 |
| rs239430181 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867815 | GGTATTCTGAATACG[C/T]GAGCTAGAATCCAGC | 16443 |
| rs239453917 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91763983 | AAGAACCCTTGCTTA[C/G]TTCTGAGTGTAGGTG | 16443 |
| rs239461632 | in-del | -/AAAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91792417 | GACCAAAATTTGATA[-/AAAT]AAATAATGTCTACAC | 16443 |
| rs239466095 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746501 | TGTAACATGATGCTT[A/G]TTCCTAGCTTACTGT | 16443 |
| rs239481219 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91876574 | GCAGGGTATGCCCTG[A/G]GAGTCCTCTCCAAAG | 16443 |
| rs239486550 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91854992 | AATAGTTAATTCCTT[-/G]TTTTTCCTCTGATAT | 16443 |
| rs239486734 | snp | A/C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91867145 | GATATGATAAAAATG[A/C/T]TCAGTATCTTGGGTC | 16443 |
| rs239506838 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91733303 | AATACCCATAAATCC[A/G]TGGCCCAAGCATATA | 16443 |
| rs239508109 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91814924 | CCTGGGTGGAACCTG[A/T]CTGCTCCTATTTTTG | 16443 |
| rs239510771 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91823937 | TCATATAGTTTTGGT[A/G]TCAGGTTAATACAGG | 16443 |
| rs239520035 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91821562 | CACACTTCCTCCAGC[A/G]AGGCCACACCTTCTA | 16443 |
| rs239536720 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867205 | GGCAGTAGAAAGTGT[A/G]GCCAGTGCTCTGAAA | 16443 |
| rs239546105 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91732526 | TGTCTAGTAGATGTT[A/G]CCCCTGAGGGCTCAA | 16443 |
| rs239547523 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91741113 | GCACTGATGGGAGGC[A/T]CAGGGCCTGACTGTG | 16443 |
| rs239590861 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91917001 | GTGAGCAATGCTGAC[A/G]GGATGCTGTTCCTTC | 16443 |
| rs239596235 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91920028 | GCCGCGGTGCACACA[A/G]GGGCGCAGGCTACCA | 16443 |
| rs239600366 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91875277 | GTTTGAACCCCAGCT[C/T]TGCTACTTCACCTAC | 16443 |
| rs239608639 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91878678 | CTCCATTCTTGTGAT[C/G]ACTTAACTCGTGTTC | 16443 |
| rs239613893 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91732339 | AAGCCAGTGCCTTTC[A/G]GACCGTTGCAGGGTG | 16443 |
| rs239630838 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91843548 | CGTGATGTGGGATCT[C/G]TGACTGAGGCTGCCT | 16443 |
| rs239639124 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91740226 | TTCCTTTATAAATCT[A/G]TAAGGTCATTTACTC | 16443 |
| rs239643037 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91842096 | AAAGAAGAAGAAGAG[C/T]GTTTATACCTTTGAG | 16443 |
| rs239643495 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91850747 | TGTGGCTGTGGGTGT[A/C]CCGCGATGCGCGACA | 16443 |
| rs239653273 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91731596 | CCATCTCTCCAGCCC[A/C]CATCCATCCTTCCTT | 16443 |
| rs239680782 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91784810 | AGCTTTTGCTAAAGT[A/C]TGGCTTATCTATCAG | 16443 |
| rs239682640 | snp | A/C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91731448 | TTTCTTTCTTTCTTT[A/C/T]TAATTTTTAAAAAAA | 16443 |
| rs239684128 | in-del | -/CCT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91895380 | CAGGGGCTTGCGGTC[-/CCT]CCTCCTCCTTCTCAC | 16443 |
| rs239694940 | in-del | -/TCCC | | | intron-variant | Itsn1 | Mm_Celera | 16:91862184 | CATGCCAGAGGAGCG[-/TCCC]TCCCTACACATTCCC | 16443 |
| rs239695273 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91834963 | CTGCCGTTAAGTGTT[G/T]TGAATGTTATCCTCC | 16443 |
| rs239706587 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91834694 | TGTGAATGGCACCGG[A/G]CTGTGGTAAAGCTGT | 16443 |
| rs239708455 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91850025 | TAGGTCAAGTTCTCT[A/G]AAATGGAGTCTGAAC | 16443 |
| rs239728177 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91738892 | TGCCTGTTTGTAATC[C/T]CTAGAACGGAAAGGT | 16443 |
| rs239757264 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743104 | CCTTTCTCCCTCCCT[A/C]CCTTTCTGTTGTTGT | 16443 |
| rs239761256 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91750938 | ACCTTTCCTCGCAGA[-/G]GCTTTCCTGTGCTGA | 16443 |
| rs239766815 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91841101 | CCTTTGCCTGTTTAT[A/G]GGGAAGGTTGTGTTT | 16443 |
| rs239787230 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91794655 | CTTCCTCTGTTGCAG[A/G]GAGAAGTTGCCTTGA | 16443 |
| rs239800649 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91791805 | GTTTGTTTCTTAGGA[A/G]CTGTCCACCTTGTTT | 16443 |
| rs239812872 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91815092 | TTGTCAGCCCTTTGT[C/G]TAGCAGGTAGAATTT | 16443 |
| rs239825514 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91844427 | CTTCCAGGACAGCCA[G/T]GGCTACACAGAGAAA | 16443 |
| rs239847801 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91848041 | GGTGCTCCTAAGCCA[A/G]GGAGGTAACTGTAGG | 16443 |
| rs239852435 | in-del | -/CCATAGTTTCATGTTGTCTG | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91804155 | CTTATATGTGACCAA[-/CCATAGTTTCATGTTGTCTG]TCATATGTTTCTTTT | 16443 |
| rs239859517 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91806864 | GTACTTAAAACTACC[G/T]AATTGAATGCTATAA | 16443 |
| rs239864989 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91839882 | GGCTCTGCCACTGTC[-/T]CCTCTGTATGTATGT | 16443 |
| rs239880258 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91840488 | TTAAGCACAGTGGTA[G/T]ACAGAAAGCAACAAG | 16443 |
| rs239905318 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91852086 | ATGAGCAAGCCCTCG[C/T]GACCTTGTTGGAAGA | 16443 |
| rs239909904 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91898588 | CAAGGTGGGAGCAGG[A/G]CAGCATCCAGGCAGG | 16443 |
| rs239921587 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91814053 | TAACTTCTAATAGGC[A/C]TTGATGAGTGTGGCT | 16443 |
| rs239928750 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91895661 | GGGAGGATGATTCGG[A/G]GTAAGGCACTTTCCA | 16443 |
| rs239929783 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91814440 | GTCCAACCAGCACCC[C/T]AGGGCCCTCTGAGAC | 16443 |
| rs239929920 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91821607 | TGGGCCAAGCATATG[C/T]AAACCATCACAGTGA | 16443 |
| rs239942615 | in-del | -/TTCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91800816 | ATTTTAAACACAATC[-/TTCT]TTCTGTAGCCCAGGC | 16443 |
| rs239974330 | snp | C/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917022 | CTGTTCCTTCAGGGG[C/G]GCTCTATCCTGTCCA | 16443 |
| rs239983034 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91761781 | TAGCCTGTGACAACC[C/T]AATTCCTTTGAGTCA | 16443 |
| rs240005106 | in-del | -/GTGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91873230 | TTTTTACATTTACTC[-/GTGT]GTGTGTGTGTGTGTG | 16443 |
| rs240013586 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916527 | AGCCCCCACCATCAC[A/G]GCTTTCTGAGTGGCA | 16443 |
| rs240035048 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91813533 | GCCCCAAGGAACTTG[C/T]TGCCCCTGGTCAGCA | 16443 |
| rs240068968 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91826853 | AGTGCTGAATCCTTT[A/G]CTGGTCCTTTGTGAA | 16443 |
| rs240070511 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91765008 | ATCTTCATGTGGTGA[A/G]CACAGTAATCGATTA | 16443 |
| rs240071783 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768610 | CAGCCTGTGGACCAG[C/T]CTCTTTGGTTGGTGG | 16443 |
| rs240080954 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91909930 | CACGAGTGCCATGAC[A/G]TGTACACATGCACGG | 16443 |
| rs240102367 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91873765 | GAGAGAGAGAGAATG[C/T]ATAGGAAAATAAAAA | 16443 |
| rs240103660 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91791856 | TATGTATGTATACAT[A/C]GGTGTGAGTGAATGC | 16443 |
| rs240121140 | snp | A/C | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915739 | AAAGACACATTGAAG[A/C]TGACATTTCAGGGAA | 16443 |
| rs240126042 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91819754 | GGACAGGACCTCAAA[C/G]AGGACAGGAACCTGG | 16443 |
| rs240160376 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915101 | TTTCAAGTGTGTCCC[A/G]CTGGGCTCAGCTGTC | 16443 |
| rs240170759 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915430 | TGAGACCGCAGGGAG[A/G]ATTTGCACCCCCAAG | 16443 |
| rs240175235 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91772389 | GAGCCCCTGCATTTT[C/T]GAGCCAGCCAGCCCT | 16443 |
| rs240204348 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91784003 | GAGCTGTGGACACCG[C/T]GTGCCTGACCCCTTG | 16443 |
| rs240214409 | snp | A/C | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91728163 | TTTGCTTTAGGAAAC[A/C]GCTTACTGGAAATGC | 16443 |
| rs240217554 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91783326 | AGAGGTGTCTGTGTC[A/G]GGCACCTTTCCAAGC | 16443 |
| rs240218095 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91880947 | AAGCATGTGTGGAGA[C/T]ACAAATGCAGCCAAG | 16443 |
| rs240220060 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91876837 | GCTCCCATGTGCCAC[C/T]TTGTAGTTGGGAGGG | 16443 |
| rs240228588 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91822730 | AGCAAGCCAGATGAC[C/T]TGTTTCACTGATGTA | 16443 |
| rs240278543 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91790613 | ATTCTTATTTAAAGG[C/T]CTCTTCTTCCTTAAC | 16443 |
| rs240285789 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91918329 | TTGGTAGGATAGCAG[A/G]GTGTCTACCTGAAGA | 16443 |
| rs240296103 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91868898 | CCCATAAGCCCCTCA[C/T]GATGGTGGACGCCCC | 16443 |
| rs240300925 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91790364 | GGTGAGCCTTGTGAG[A/G]AGCTGTGCTTTCAGA | 16443 |
| rs240301011 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91737175 | AAATGTTCTTTTACT[A/G]TTCTTTTAGTGATTA | 16443 |
| rs240308395 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830452 | AGGGTTCAGCAGATT[C/T]ATTTCATGTTCGTGG | 16443 |
| rs240311517 | in-del | -/GAGCAGGCCTGGGAGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91810871 | TCAGAGCCCGGACAT[-/GAGCAGGCCTGGGAGG]GAGCAGCTCCCCTGC | 16443 |
| rs240329935 | snp | C/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830890 | GAATCTTGCTGTAGG[C/G]AGACAGCAGGCCTTT | 16443 |
| rs240360861 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91884341 | GGTGCAGCACCACCT[C/T]CAGCTTGGGGTGCAG | 16443 |
| rs240361781 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91797091 | GGCTGCTCAGAGACT[C/T]CCAGAGACCTAGTCT | 16443 |
| rs240372160 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91907002 | ACTGTTTTTTTTTTT[-/A]AAGAACTTTTCAAAA | 16443 |
| rs240387230 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91839606 | GGCAATCAAGCATCT[C/T]TGTTGGCAGACGAGT | 16443 |
| rs240393768 | snp | C/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830586 | CTGACTGTGGGCGTG[C/G]ATGGATCCGGTGAGG | 16443 |
| rs240394499 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91892626 | TGCTGCCTTTCTCAA[A/G]CCCCAGATGGCCATT | 16443 |
| rs240401521 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91846460 | AATTCCTGCTGCCTG[C/T]TGTGGTCCTTAATCA | 16443 |
| rs240405593 | in-del | -/GA | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91804117 | ATGTGGCTCACGTTG[-/GA]GAGAGTCTCTACAGT | 16443 |
| rs240410070 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91836834 | ATAAGTAAGTGTCCT[A/G]GGAAATGACATATTG | 16443 |
| rs240431647 | in-del | -/TTTAAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91825249 | TTTACTTATTTAGAG[-/TTTAAT]TTTATTTTTCACAAT | 16443 |
| rs240438622 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91897684 | TGGAATTTTGCCTGC[A/G]TGTGTGTCTGGATAC | 16443 |
| rs240458495 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91892114 | TTCTCATGTGTGATC[G/T]TTCTGTGAGGTGGCA | 16443 |
| rs240468267 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91740837 | GACTGACAGGGTCCC[C/T]GTCCTTACTCTATTT | 16443 |
| rs240474465 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91836075 | CCAGCTCTCTACCAC[C/T]CAATTTCCAGTTAAA | 16443 |
| rs240500592 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91821730 | CAGGAATCAACTTGG[C/T]ACCAGTAGGATATGG | 16443 |
| rs240502646 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91829871 | AGAAGTTCTTAGCTT[C/T]CCCCACACACACTGG | 16443 |
| rs240514355 | snp | A/C | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91828752 | TGATGGCTTTGTCAC[A/C]CTGCACAGTAATTCA | 16443 |
| rs240521954 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91747680 | GGCTGGTAGGTGGCA[C/T]ATATGGCCTTTGGAC | 16443 |
| rs240527093 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91902287 | AAGTATACTTAATTG[C/T]TTTAACCTCCCTTCT | 16443 |
| rs240533742 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91800923 | GAGTTATGGGGTTGT[A/G]AGCATGTAACTCCAC | 16443 |
| rs240564325 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91759988 | TCCCATTATTATGAA[A/G]TCTAAATTGTCCCCC | 16443 |
| rs240595418 | in-del | -/AGAAAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91896724 | CACACGCACACACAA[-/AGAAAG]AGAGAGAGAGAGAGA | 16443 |
| rs240603616 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91767182 | AGACTCTTGCCTGCC[C/G]TTACTCTTTCTGTGT | 16443 |
| rs240615342 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91809422 | CCTTTTAATGCTTTC[A/T]CTTCCTCTTAGAGAT | 16443 |
| rs240635260 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91850397 | CTGTGGAGGGAGCCT[A/G]CTTCAGAGACAGCCT | 16443 |
| rs240650686 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91739633 | CTAGGTTCATCCATG[-/C]GCCCTGAGGCCAGAC | 16443 |
| rs240651759 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91857730 | ACTGGGGCACTTAAA[C/T]GGTGACAGGTATATC | 16443 |
| rs240666536 | snp | A/G | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91871727 | CACAGACAGATGTTA[A/G]CCACTGACCTGCCTG | 16443 |
| rs240678978 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91800543 | TTGGAACGCATTCAT[A/G]AAGATTTATTTCTCT | 16443 |
| rs240722676 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91815852 | ACACAGTCAGGAAGT[A/G]ACAAAAATGCTGGTC | 16443 |
| rs240724529 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91808271 | TCATTGGTATGCTTG[A/G]ACATAAGAACAGACA | 16443 |
| rs240731635 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91878981 | TATTTCTAGTTATGT[A/G]TATGTGTGTATGCCC | 16443 |
| rs240739040 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91825050 | TATAGCTCAGGCTGG[C/T]CTCAAACTCGAGATC | 16443 |
| rs240754839 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91904512 | AAGCATGCACTGTTG[C/T]GTAGGGCTTTGAGGG | 16443 |
| rs240757920 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91888111 | AAGTAACCTTTGAAC[A/C]CACACGCAGTGAGAG | 16443 |
| rs240768468 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91911737 | AAGTGCTGGTGTTGG[A/T]CTTAGTACCAGCGGT | 16443 |
| rs240784417 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91815270 | AACAGAACTGGTTCT[A/C]TAAGCTGGCACGCTG | 16443 |
| rs240788463 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91808087 | CTCTAACCCCAGGAT[A/G]TATTTTTTATGAGTG | 16443 |
| rs240788514 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799582 | AGATATAAAAAGGCT[A/G]GAGAAAGTGACAGAT | 16443 |
| rs240792781 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91834114 | AGTGAATTTGAGGCT[A/G]CCTTGCTTCAACCCC | 16443 |
| rs240801258 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917459 | GAGCTAATAGTTTAT[A/G]TTTTGGCAAATAATT | 16443 |
| rs240803078 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91911082 | CTCAAACTTATGTCC[A/G]TGGGCTGGAGAGATG | 16443 |
| rs240804319 | in-del | -/TATAATATAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91733861 | AAACCCTTCCATGTC[-/TATAATATAA]TATAATATAAATTTA | 16443 |
| rs240823673 | in-del | -/AA | | | intron-variant | Itsn1 | Mm_Celera | 16:91757908 | CCATTCTCCTTTTTT[-/AA]AAAAAAAGATTTATT | 16443 |
| rs240848132 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91806925 | GACCTCTCGTGAGCC[A/G]TCCCGTCCTGGCAAG | 16443 |
| rs240866067 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91755275 | TTTAATCAGCACTTG[-/C]TGGGCAAGCCTTCCA | 16443 |
| rs240869016 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91769888 | TATTTATTTATTATA[C/T]GTAACTACACTGTAG | 16443 |
| rs240890742 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91903892 | GAGACCTCAAAGCCC[C/T]GCCTCCACAGTGGCA | 16443 |
| rs240892242 | in-del | -/TATTAGAAGTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91773009 | AGCCCTCTTTGAACA[-/TATTAGAAGTG]TAGTGATTATATGAA | 16443 |
| rs240892324 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91821382 | TCATTATCATTAATT[C/T]AGTCCATTATCATCA | 16443 |
| rs240897515 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91785766 | GCAGTGCTGAATTCT[A/C]CTGATCTGAAAGAAG | 16443 |
| rs240919382 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91769354 | CTTAGACAGAGCAGC[A/C]CATCTGTGAAGAATC | 16443 |
| rs240925084 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910610 | GGCCTGGCGCTCACC[A/G]ACTGGTCCCACTTGC | 16443 |
| rs240928744 | in-del | -/AAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91773076 | TATTGTATAATTTTC[-/AAA]AAAAAAACTTAAAAG | 16443 |
| rs240953703 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91778021 | AGAAAGCCTTATATC[A/G]CAGATGTTGGATGCA | 16443 |
| rs240960131 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91889278 | GTGGCATGTGTGCCA[G/T]CACCTCTGTGTGGTC | 16443 |
| rs240963875 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91758149 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTGT | 16443 |
| rs240965335 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91804931 | CACTTTCCTGTCTTC[A/G]TTGTGTTGATGGAGC | 16443 |
| rs240966544 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91909967 | ATATATACATACGAA[A/T]CTATGCAAAATAAAT | 16443 |
| rs240975127 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91753389 | TTTCACCCTGTATGT[C/T]ATGTTAGAAAATGAA | 16443 |
| rs240986107 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916601 | TCCTATTAATGAACA[C/T]TGTCCTTTGAAGGGC | 16443 |
| rs241000023 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91778951 | TGTAATGAGATCTGA[C/T]GCCCTCTTATGGAGT | 16443 |
| rs241005663 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91881859 | CCACTCTAACAACAC[C/T]TGTTGTATAGACAGG | 16443 |
| rs241024761 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91761199 | CTTTTAAATTAGCCT[C/T]AATTGTAGTGACTCA | 16443 |
| rs241031754 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91777325 | GTACATTCACAGACT[G/T]GGGTGCTCTTGTCTG | 16443 |
| rs241042520 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91812852 | CCTTGGAGATCAGAA[A/G]AGTATAGTGAGAATT | 16443 |
| rs241045635 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91882299 | CTTGCCAAATGCTAA[A/G]CCAGGCTGGCTGGCC | 16443 |
| rs241054221 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91881256 | GCTAACATGCCTCAC[A/C]ATGAGTCCCTTACAC | 16443 |
| rs241064736 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91828179 | TCTCCTAACTTGTGT[C/G]CTCTTCTGAAATAGG | 16443 |
| rs241070329 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91894273 | AGATTCATTTTATTT[A/G]TTTAATGTATATGAG | 16443 |
| rs241081097 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91840559 | GCACACAGTGGGGTG[-/A]GGGAGTGAGGTGCAG | 16443 |
| rs241120003 | in-del | -/TATGTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91751490 | GTGTATGTGTGTGTG[-/TATGTA]TGTATGTATGTATGT | 16443 |
| rs241127780 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91754767 | TCTATCTGCTGAGGT[C/T]TCCTCGGGGATTCCC | 16443 |
| rs241127831 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91893197 | TCTGCACACTGCACA[A/C]AGCAGGTAGGCCCAG | 16443 |
| rs241149592 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745668 | ACAGGACTGATGGCG[C/T]TCTGGTCATGCTGTT | 16443 |
| rs241149678 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91888046 | GCCAGTAAAGGTCTT[A/G]ACACTCTGTCTGAAA | 16443 |
| rs241157193 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91783465 | ATGGCCATCGGATGT[C/T]CCCACCTCAGGGACA | 16443 |
| rs241158013 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91754098 | TCTCCCAATGAAATC[A/T]TTAAGCCATCTCTAA | 16443 |
| rs241164618 | in-del | -/CATTATCATTAAGTTAATTAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91821347 | TATAATTGGGCTGGC[-/CATTATCATTAAGTTAATTAT]CATTATCATTAATTC | 16443 |
| rs241166813 | in-del | -/TT | | | intron-variant | Itsn1 | Mm_Celera | 16:91822771 | AGCCCCAGATTTCAC[-/TT]TCGCTCTTCGCTTGT | 16443 |
| rs241169732 | in-del | -/GCTC | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91747321 | TGTGTGTGTGTGTGT[-/GCTC]GCTCTTTGGGATCTC | 16443 |
| rs241201514 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91908914 | CTGCCCTCCCCCACA[C/T]ACTCTTTACCAATTT | 16443 |
| rs241206042 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91887585 | AGGTGGAGGCCCTGC[C/T]GAGGGCGCCATGCCC | 16443 |
| rs241208040 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91865963 | TGTCTGAGACAACCA[A/G]TCTCCTGGGCCTTGG | 16443 |
| rs241217894 | in-del | -/GAGGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91865119 | GATAAGTCTAAGACA[-/GAGGG]TGGGTGTGACCATGG | 16443 |
| rs241225793 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91744919 | GTTCTGGCCACAAGG[A/G]TGGGTAGCCTGTGGG | 16443 |
| rs241227002 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91738702 | TGTTGCCCAGCCTGG[A/G]AGACTGAACACCTGT | 16443 |
| rs241230254 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91888895 | ATCCTAGCTTCCTGT[C/T]GGTGGAGCCAAGCTT | 16443 |
| rs241235250 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91762049 | CAATCTGCTACTAAG[A/G]AAGAGCAGATTCCCT | 16443 |
| rs241252227 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914913 | TGCTGGAGAAACTGG[A/G]CAAGGGTGCTGGGTT | 16443 |
| rs241257244 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91865143 | TGTGACCATGGAGTG[G/T]CGAGAACAGGGTGGT | 16443 |
| rs241262888 | in-del | -/GGCTAGCCGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91791314 | CCATAGCAAGTTCCA[-/GGCTAGCCGG]GGCTACCTGCAACCC | 16443 |
| rs241304065 | in-del | -/GTGTGTTCTGCACGAGAGGAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91753293 | TTGAAAGGACCCTGA[-/GTGTGTTCTGCACGAGAGGAT]GTGGCTCCTCTAAAC | 16443 |
| rs241308929 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91854499 | TGCAGCTGTGCACTC[A/G]TAGCTTTCAGAGAAG | 16443 |
| rs241315053 | in-del | -/CCCATGCGCTCAGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91765975 | CACCTGCCCTTGCTG[-/CCCATGCGCTCAGT]TCATCCTAACTGTTG | 16443 |
| rs241320032 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799117 | TTCTGGGCACAAGCC[A/C]ATAGCAAGGTGAAGT | 16443 |
| rs241322502 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91887983 | TGAAGACATGTTCCC[C/T]GGGGCTCTGTCAGGT | 16443 |
| rs241325530 | snp | A/C | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91727573 | GCAGCAAAGGGATGT[A/C]GCTGGCAATCACATG | 16443 |
| rs241335861 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91752684 | TCTAACTCTCCGACA[C/T]CACTGAGGTATGATG | 16443 |
| rs241361292 | snp | C/T | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91853605 | GTGTGTGTGTGTGTG[C/T]GCGTGCATGCGCGCG | 16443 |
| rs241363747 | snp | G/T | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91863659 | GCCTGGCAAACGGAA[G/T]CAGCGCTTCGTTGGA | 16443 |
| rs241366706 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91863978 | TACAGTGATAACAGA[G/T]TTGAGAACTAGGGTA | 16443 |
| rs241370473 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91874050 | AAAGAAATAATAAAA[A/C]TATATAGACTGGTGA | 16443 |
| rs241370677 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91729607 | GAGATGAGGTGAGGA[A/G]CTGACGCGGGCGGCC | 16443 |
| rs241387137 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91832698 | GTATTGACTTCGGTT[C/T]TCAAAGAATGATTTG | 16443 |
| rs241397836 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91833845 | GGCTCAAAAACCTTA[A/G]TTATTTGGGGAAAGA | 16443 |
| rs241398902 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91806582 | GAGTGACTCTGCTGT[A/C]CTCATTGCCTGCTGC | 16443 |
| rs241407753 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91847944 | AGGTCACATGTATAG[A/G]CGTAAGAATAGGACT | 16443 |
| rs241419769 | in-del | -/AAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91874237 | GCATTTAAAGAAAGA[-/AAG]AAAAAAAAAGTATGG | 16443 |
| rs241423750 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91789807 | ATACCATGACCGAGG[A/C]AACTTACAGATGGCC | 16443 |
| rs241435695 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | Itsn1, Cryzl1 | GRCm38.p3 | 16:91728757 | ATCTCCCAGCATGCT[C/G]CTTCCCGTAGAGAGA | 16443 |
| rs241475425 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91862553 | CGCTCCCCCCCCCCC[C/T]CGCCCCCCTGGCCTG | 16443 |
| rs241484144 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892071 | CTGTGACTGCCCTTA[C/G]CTGGTTCCTCCCCAT | 16443 |
| rs241497885 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91855923 | ACTTAGAGCAGTGAG[C/T]GTTTCATCACTGCTC | 16443 |
| rs241521330 | in-del | -/GGAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91890274 | TTTTGGGGGGGGGGG[-/GGAA]TGGCTTTATAGCCAG | 16443 |
| rs241550973 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91903376 | ATCTTTTTTAAAAAA[A/C]CAGTAAAATACTAAG | 16443 |
| rs241551967 | snp | A/G | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91727523 | TGTAAGCTCAGTATC[A/G]TATTGTGAAAGTAGT | 16443 |
| rs241555092 | snp | A/C | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91839779 | CAAGACAAGCAGAGT[A/C]GGCTTTTCCATCCGC | 16443 |
| rs241559343 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91737036 | ATTCCTATAAATCAT[A/G]AGGGCTTATGCACCG | 16443 |
| rs241564927 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91839127 | GTGAGAATCTCTACT[C/T]GTGCTCTACTCACGC | 16443 |
| rs241566035 | in-del | -/AT | | | intron-variant | Itsn1 | Mm_Celera | 16:91839294 | GCCACTTTGTGAAAG[-/AT]ATCACAATCTCTCTC | 16443 |
| rs241569346 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91753756 | AAAATTTTATTTTTT[-/A]AAATTCGTGAATCAC | 16443 |
| rs241579112 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91739667 | CAGCCCAGTTAGGAG[-/A]CCGGATTCCACAGAT | 16443 |
| rs241590491 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91854315 | CAGAACCACCTGGGG[A/G]CTGTGAGAGGTTACA | 16443 |
| rs241623477 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91832660 | GACTGCCCAGAGGCT[G/T]GCTGTGTAGTGCTAC | 16443 |
| rs241631014 | in-del | -/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91740534 | AGGAAGCTTCAGGCC[-/T]TTCCTCAAGCCCCAC | 16443 |
| rs241635376 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91832040 | AAGGGACAAATATCT[A/G]TCTGCTTCAAGTTTG | 16443 |
| rs241666935 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91841385 | AGAAATTCCCTGAAT[-/G]GGTGGAAATATTTCC | 16443 |
| rs241669652 | in-del | -/TTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91895553 | GATGGGAGAGAAGGA[-/TTTT]TTTTTTTTTTTTTTT | 16443 |
| rs241672170 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91883956 | CAGGTGGTGAGGGCT[A/C]TCTGTCCTGTGTATT | 16443 |
| rs241696757 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91836504 | CTCAAAGAGCCAAGT[A/T]TTTATCAGTGGCTGT | 16443 |
| rs241702106 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91838552 | GGCCTTGAAATTGCA[C/G]AGATCCTCCTGCCTC | 16443 |
| rs241710200 | in-del | -/TG | | | intron-variant | Itsn1 | Mm_Celera | 16:91910464 | TGTATGTCAAATATA[-/TG]TGTGTGTATGTTGTG | 16443 |
| rs241711662 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91843870 | GCCTGACCCTCCCTG[C/T]TGATTCCTGTAACCA | 16443 |
| rs241715790 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91811502 | CACATCTTAATGCAT[A/G]TGTAGTGACATGGTT | 16443 |
| rs241725644 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91736592 | TGCTTGCTCTTGAGG[-/T]TTTTTTTTTCCCTTT | 16443 |
| rs241726054 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91779154 | CTAACTTGCTTAGCA[C/T]ATGAGGCTCAGATTC | 16443 |
| rs241731108 | snp | A/G | | | synonymous-codon | Itsn1 | GRCm38.p3 | 16:91793763 | TTCCAGTGCACCAGC[A/G]TTTGGTAAGTGCTTG | 16443 |
| rs241741613 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91759480 | CCTATATAGACTCAG[A/G]CTACTCTGTGAGTAG | 16443 |
| rs241776994 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91740071 | CCGTTCCATCCAGTG[C/T]TGTCTGTTTCTCTCC | 16443 |
| rs241777063 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91883152 | CTTCATCTTTCCCTG[A/G]GCCAAGCTTCCTGCA | 16443 |
| rs241777431 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889900 | AGACTAAGATCTGGC[C/G]CCCAAGGCACAGCAG | 16443 |
| rs241783997 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803598 | CAAACCCGAGTCCTG[C/T]AAGAGCAGCAGTGCT | 16443 |
| rs241808737 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91895067 | TAAGTAAACAGCATG[A/G]CTGTGCCTCAGACTT | 16443 |
| rs241810549 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91864950 | CTGCTGCATACCACA[-/G]GGGGGTCCCCAAGTG | 16443 |
| rs241823368 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91817899 | ACTCAGAAATCCGCC[A/T]GCCTCTGCCTCCCGA | 16443 |
| rs241827091 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889353 | CACCTCACTCCCACC[C/T]GCTCTTCATCGCCAT | 16443 |
| rs241840960 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91860684 | GTTTCTGGAACACTC[A/G]GTTGTTGGGAAAAAA | 16443 |
| rs241848910 | snp | A/C | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746620 | CTTGTCTTATAACCC[A/C]TAGAAAAGGTGAGAA | 16443 |
| rs241864239 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91845081 | GTGCTGGTTGTAGAA[-/C]CTAGGAAACAGTGGG | 16443 |
| rs241880646 | snp | A/C | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913851 | TTTCTGTTGTTGTTA[A/C]GAAACTGTTTTAAAT | 16443 |
| rs241885803 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746298 | CAAATTCATTCCTAC[A/G]CACACAGGCAGCAAA | 16443 |
| rs241923170 | snp | A/G | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91870804 | CTGACTATGGAAGGG[A/G]TTATGCTTGTCTGTG | 16443 |
| rs241926253 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91849806 | AAACTTAACTTCTGC[C/T]TCCCACTGCATTGGT | 16443 |
| rs241933698 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91764327 | TCCACCACTCTGACT[C/G]TCAAAGGGTGACATA | 16443 |
| rs241938930 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91848465 | GTAATGAGACCTGTC[A/T]GGTGGACGCTGTGAG | 16443 |
| rs241940495 | snp | A/G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91857233 | GTTTTATCATTTGTA[A/G/T]TGTGTGTTACAGTGT | 16443 |
| rs241953908 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91907366 | AAGCATCCCCAAGAA[C/T]GTTCCTGCCAGGCAA | 16443 |
| rs241958975 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91880682 | TGCAGGATAGTATGA[A/G]AACATTGAGGAACAT | 16443 |
| rs241977026 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91813239 | CACTACAATGGTTTT[-/C]TTTTAATCCCAGGTG | 16443 |
| rs241989732 | in-del | -/GT | | | intron-variant | Itsn1 | Mm_Celera | 16:91739107 | AAAAGAAATTTTGAA[-/GT]GTGTGTGTGTTGTGT | 16443 |
| rs241998309 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91856420 | TGGCTTTCCCACAGC[C/T]GTGTGCAGGGCGGGC | 16443 |
| rs242000523 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867544 | CAGCAGAATGCTAAC[A/T]GGGTTTCTATCTTTA | 16443 |
| rs242025797 | in-del | -/CCCCCA | | | intron-variant | Itsn1 | Mm_Celera | 16:91862415 | TGTTGGAATGTGGGG[-/CCCCCA]CCCCCACCCCTTCTT | 16443 |
| rs242032071 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91815746 | TTGTGCCCTCCTGTT[A/G]CCAAAGCTCACCAGA | 16443 |
| rs242054800 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91737608 | GATCTCAGGTTGTGG[A/G]ACATAAATGGGTTGT | 16443 |
| rs242055188 | in-del | -/CT | | | intron-variant | Itsn1 | Mm_Celera | 16:91890947 | ACACACACTCTCACA[-/CT]CACATACACACACAC | 16443 |
| rs242057665 | in-del | -/ATT | | | intron-variant | Itsn1 | Mm_Celera | 16:91825386 | CATTAGATTTTAGAC[-/ATT]ATGTTTTCTTTTTTT | 16443 |
| rs242077501 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91781063 | GGGGAGAACCTTTAA[A/G]CTCTGAAGTCCTGTC | 16443 |
| rs242091218 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91880126 | GCTAAGAATGTGGAC[A/G]TAGGTCCTACTTCCT | 16443 |
| rs242093040 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91737144 | TGGGAAGTAGCACTT[A/G]TTTTTGTGCCTGTTC | 16443 |
| rs242093388 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734902 | CTCTGAGTTCCTTTT[C/T]CTCTTTCAGCCACTA | 16443 |
| rs242102325 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91822040 | TGGATCAAGTGTTTC[C/T]GTAGGTGTGTGAGAG | 16443 |
| rs242149940 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91788463 | TCATTGAGACAAAAT[A/C]CAAAGCTGTCACCAA | 16443 |
| rs242165130 | in-del | -/AGAAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91866346 | ATGGGAGCACAGTGG[-/AGAAT]AGCGAGGAGGTCTGT | 16443 |
| rs242166408 | snp | A/C/G/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917363 | AAGGTACAGAAAACT[A/C/G/T]AGTACGGAAACATTA | 16443 |
| rs242171140 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91744493 | GAATTGAACTCAGTT[C/T]CTCTGGAAAACAATC | 16443 |
| rs242206028 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743964 | TAGATAAGAAACCAC[G/T]GAGCCCTGTTACTGG | 16443 |
| rs242206817 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91891039 | AGTCCTTGCGAGGGC[C/T]GGTCTGTGTGCCCTC | 16443 |
| rs242214530 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91732057 | CTAAGTCTGGCATTC[A/G]GATATCTTTACATCA | 16443 |
| rs242222382 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91846217 | TTGTTCATTAAAAAG[A/C]CTGAGACTCCCTCAT | 16443 |
| rs242239321 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91895851 | ACAAATTGGCAGAGA[C/T]TGGAGCTTTAGCCCT | 16443 |
| rs242240241 | in-del | -/ACACACACACACACAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91807496 | ATTTTAGGCATAAAT[-/ACACACACACACACAC]ACACACACACACACA | 16443 |
| rs242254126 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91826783 | TGTGTCTGTGTGTTT[C/G]TAACTCTCTGTGTCT | 16443 |
| rs242255034 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91844604 | GGCTGCTCACGCCTG[C/T]CTGTAACTCCAGTTC | 16443 |
| rs242267764 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91833936 | TTAGTTTGGTGCCAA[C/T]CAGGGCTACACAGAG | 16443 |
| rs242280701 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91845649 | GAAACCCTGTCTCGG[A/G]AAAAGTAAGAGTTTG | 16443 |
| rs242284513 | snp | C/T | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91853619 | GCGCGTGCATGCGCG[C/T]GTGCTCGGCACTCGC | 16443 |
| rs242306781 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91906990 | AGTAGTATATATACT[-/G]TTTTTTTTTTTAAAG | 16443 |
| rs242321046 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91792230 | CCCAAAACCAATTCC[C/T]TTAAAAAGGAAAAAC | 16443 |
| rs242324261 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91739765 | TACATGTGTGCAGGG[A/G]AAAGGGCCTAGTCTG | 16443 |
| rs242327623 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91833327 | CAAGTTCAGGAAATT[A/G]CAGTCAGTGGTCTGA | 16443 |
| rs242352997 | in-del | -/AT | | | intron-variant | Itsn1 | Mm_Celera | 16:91765155 | CTTCTGTTAAAACTC[-/AT]AGTTAGCTGGGTGTA | 16443 |
| rs242360926 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91894083 | CCAGGGATGGATGGA[A/C]GTTTTCAGTGGTACT | 16443 |
| rs242367225 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798139 | AGGAGTGACAGATAA[C/T]GATTGAAAATGCCAA | 16443 |
| rs242374196 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91757217 | TCGCACACGTGCCCC[A/C]CAGACAAGAATTTAA | 16443 |
| rs242395993 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91818239 | ATTTTAAACAGGATA[A/G]GACACTGTCAGGATA | 16443 |
| rs242411298 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91841338 | CTGCACGTGGTCTGA[A/G]TCTGCTCTCCTCTGG | 16443 |
| rs242425660 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91849467 | AACAGCATGTAAGCA[A/G]TTGATGGGTGAAGCC | 16443 |
| rs242433774 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810269 | TTTCATGGTGCAAGT[A/G]AGTAGTGCTACACAC | 16443 |
| rs242447411 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91816559 | CCCCCAGTCAGCTGC[A/G]CCAGTGCCTGCCTTG | 16443 |
| rs242453931 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91824713 | TCCCTCCTCCTGCCT[C/T]CCTGCTCTCCCTCCC | 16443 |
| rs242453952 | in-del | -/AC | | | intron-variant | Itsn1 | Mm_Celera | 16:91823302 | ATTAAGCACACACAT[-/AC]ACACACACACACTTA | 16443 |
| rs242456601 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91817595 | AGGCTGTATGTTAAG[C/T]ATACTGAGAAATTTA | 16443 |
| rs242472268 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91765051 | GTCAGTTTGAGGGTT[C/T]TTGTTACAATTGCAG | 16443 |
| rs242519474 | in-del | -/TGTTTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91884664 | CAGCACACAGGCATT[-/TGTTTG]TTTGTTTGTTTTTTT | 16443 |
| rs242531441 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898823 | CACATATGTGAGCAG[G/T]GGAGCCATCCTAATT | 16443 |
| rs242532923 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912246 | CTCTGAAATCTGTGA[C/T]CTTTAACTAGGTTCC | 16443 |
| rs242534332 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91804874 | AAGCATGGAAGGAGA[A/T]GACATGTGGAGCCTT | 16443 |
| rs242536623 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91868544 | TGGGCAAAGGCAGAG[A/C]CTGCCATTGCCTGGC | 16443 |
| rs242560811 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91823874 | TTTTATCAGGGGTTT[A/C]TCATGCACATTCATG | 16443 |
| rs242568487 | snp | C/T | | | downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91920822 | GTCAGAGAATTCAGG[C/T]GCATTTGGGGAGGCC | 16443 |
| rs242589067 | snp | A/G | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91804362 | TCAGCAAATATTAAA[A/G]TCTTTAGATGGTTGA | 16443 |
| rs242594659 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91902474 | CTCGCAAACACCATT[C/T]GTGAATCAGCAGAAG | 16443 |
| rs242604213 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91812167 | TGGTAAGGAAGCACA[A/C]GTTCCGTGGTTTGTA | 16443 |
| rs242605193 | snp | G/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919979 | CTCTGGTCCTTGGCA[G/T]CCCACAAGCTAAAGT | 16443 |
| rs242621860 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91762846 | ATGCCCCGGGGCAGG[C/T]ATTGGAGAACCAGAA | 16443 |
| rs242623979 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91813910 | GGTTGGCAACTCAGC[A/G]TGTGTGCCTCCTGAG | 16443 |
| rs242660717 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91908351 | ATTTGAGCAGACCCG[A/C]AGCCTGCTCTGTGCG | 16443 |
| rs242670062 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91769010 | TCAGCTTTTCTCTTA[C/T]TTTCCCAACGCCAAA | 16443 |
| rs242674076 | in-del | -/TTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91851114 | TCAGAAAGTTGAGAC[-/TTA]TTATAAACCTCCCAG | 16443 |
| rs242690214 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91775428 | GGGCAACTCAAAATA[A/C]GATTATTTTTCTTTA | 16443 |
| rs242706857 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91794950 | TGTGGCTTGTGAGTG[C/T]TATAGTTGAGCAGGA | 16443 |
| rs242707234 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91752617 | GCCAGATGTGTTGGG[A/G]TGCCTCCGGAGCTGC | 16443 |
| rs242717078 | snp | C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91803215 | TCAGACACACCAGAA[C/G]AGGGCATCAGATCCT | 16443 |
| rs242718928 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91794570 | GTAATGGACAGAACT[C/T]TACAGGAGATGGCTG | 16443 |
| rs242735639 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91874527 | CTTCATAGCTGGTTG[A/G]CCCATCATGCTGCAG | 16443 |
| rs242746618 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91782517 | CTCTAAGACATCTTA[A/G]CCTCTCATTGCTGAA | 16443 |
| rs242753244 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91902047 | CCACGCTGGATGAGG[C/T]TATGTATGCTCTGAA | 16443 |
| rs242761335 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91820251 | GCGCACTGTGATTTC[C/T]GGGAGGCGTGAGGAA | 16443 |
| rs242778795 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802439 | CCAGTGAGAGGAGGA[A/G]TCTAATACGCCTCAT | 16443 |
| rs242786425 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900936 | AGAGGGCGTCAGATC[C/T]CTTTACAGGGGGTTG | 16443 |
| rs242796943 | snp | C/G | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91853586 | GCTGTGTGTCTGTGT[C/G]TGTGTGTGTGTGTGT | 16443 |
| rs242804305 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91886826 | TCTAGAGACCATGCA[C/T]GGCCTCTGGACTCTC | 16443 |
| rs242809576 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91862480 | TTGCCATCCTTCCTT[C/T]CTTTCTGTCCTTTCG | 16443 |
| rs242816846 | in-del | -/AA | | | intron-variant | Itsn1 | Mm_Celera | 16:91844394 | TCTATTTGTGGAGAC[-/AA]AAAAAAAAAATACAG | 16443 |
| rs242844495 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916199 | GCTCACTCAGTGCCA[C/T]GTACTCCCCGTGGGG | 16443 |
| rs242888377 | snp | A/G | | | upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91729297 | ATGGGTGGGGCGGAG[A/G]GCAGGCTGTGGGCGG | 16443 |
| rs242890704 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91765542 | TACTGTACCAGTCTG[C/T]TTGGGCATAGACTGG | 16443 |
| rs242896356 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91900424 | TCTTGTATGAGAGCC[A/G]CCTGGCGGTCACGGG | 16443 |
| rs242908667 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91908096 | TCTGGTGTGTCCGAG[A/G]AGAACCACAATGTAC | 16443 |
| rs242919570 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91886357 | ATCTCACCAGCCCCC[A/G]GGGGGACCACTTTTA | 16443 |
| rs242935740 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91905671 | GGAGGGGCTAAGATA[A/G]GGCAAGGGGAGGAGC | 16443 |
| rs242936019 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91737736 | TGTGTTCCGTAGCAA[C/T]GGTAGTCTGGCAGTC | 16443 |
| rs242975897 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91905032 | TTCTCAATAAATGAA[A/G]GGGGGAGACATACCA | 16443 |
| rs242977954 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91891686 | TACCTCTCTGATGCC[C/T]TCATCTGTGCCAAGT | 16443 |
| rs242980695 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91773117 | TTTCAGGAAGATTAT[C/G]AAATCAGTAAGATTA | 16443 |
| rs242996004 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91824108 | TGGGCAATGGCACAG[G/T]CCTTTAATCTCAGCA | 16443 |
| rs242998295 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91751776 | GAAAAAGTGGCCGGG[C/T]CATTCAAAGCCTTAA | 16443 |
| rs243000833 | in-del | -/CTCCGA | | | intron-variant | Itsn1 | Mm_Celera | 16:91774096 | CAGAGATCCACCTGC[-/CTCCGA]CTCCTGAGTGCTGAA | 16443 |
| rs243010986 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91774848 | TATTCTTCAGAGAGA[C/G]CTGCATGGTTGGTCT | 16443 |
| rs243013147 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91880259 | TTGGTGAGGATGGAG[C/T]TGTTATCTACAAGGG | 16443 |
| rs243013228 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91791037 | AACATTGGTATTTAT[C/T]TCAGTAGATGAAGGC | 16443 |
| rs243023686 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91750986 | TCTATCCTGAGCTCT[A/G]TGTTGGGTTCACAGC | 16443 |
| rs243024870 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91759273 | TCCCTCTTCTGAGGT[A/G]GATGGGACATTTTTG | 16443 |
| rs243027413 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91877137 | CCAATACATACACAC[A/G]TGGACACTGGGTAAG | 16443 |
| rs243041050 | in-del | -/TC | | | intron-variant | Itsn1 | Mm_Celera | 16:91758113 | TGTTTTCTTTTCTTT[-/TC]CTTTCTTTCTTTCTT | 16443 |
| rs243057357 | in-del | -/GGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91827424 | GTGCTAAATTAAAAA[-/GGG]GGGGGGAGGACAGAA | 16443 |
| rs243062284 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91839973 | GGGAAAGTTCTCACT[C/G]TGTAGACCAGGCTGG | 16443 |
| rs243074860 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91832020 | CTTGGCAGTGGTGGC[C/T]CCATAAGGGACAAAT | 16443 |
| rs243081105 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91860626 | GGCTGACTCAGCTGG[A/G]TTAAAGTTCCATGGG | 16443 |
| rs243084139 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91876763 | TCAGGGGAAAGTGAC[A/C]GGTGGGGTGGACATG | 16443 |
| rs243097313 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91884071 | GATGCAGTAACTTCC[C/T]GATGTACTATGAGGA | 16443 |
| rs243103167 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91778412 | TTAATACCCATATAT[-/A]ATAGCAAATATTAAG | 16443 |
| rs243123055 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91886302 | GGGATTTTAACTCAG[C/G]ACCTTTGGAAGAGCA | 16443 |
| rs243123495 | in-del | -/AAAAAAAAAAAAAACAAAAAACAAACAAACAAACAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91892759 | ACCCTTCTTTAGCAG[lengthTooLong]AAAAAAAAAAAAACA | 16443 |
| rs243129453 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91779472 | AAATCTAAGATGTTT[G/T]CAAAAGAAAGGAAAT | 16443 |
| rs243140150 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91860287 | TGAAAATAACAAGAA[A/C]ATTAATAGATTAAAT | 16443 |
| rs243160704 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91883807 | CTTGTACCCAGAGGA[A/G]CCTCCAGAATCCCAA | 16443 |
| rs243186025 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91741363 | GCCAGGGGCCAGTGG[C/G]GCTGAAACTGTCACC | 16443 |
| rs243188465 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91744199 | CCACTTAGGACCAAG[C/T]ACTCTAAACAGACAA | 16443 |
| rs243195591 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91826396 | TTATTGTGACTGAGT[A/G]TTTTATGACTGAACA | 16443 |
| rs243209008 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91891617 | ACTAATTAAGAAAAT[A/G]CCCGGCAGGCTTGCT | 16443 |
| rs243218964 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91740488 | ACAGCCTAAGACCTC[C/T]GCCCTTCAGTTAGAT | 16443 |
| rs243228921 | in-del | -/GTGGTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91789027 | GTGTATGTGTGTGTG[-/GTGGTT]GTGGTGGTGGTGGTA | 16443 |
| rs243241688 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91760718 | AGGTGTTCAGCTACC[C/T]GAGTCTCTCCTGGGG | 16443 |
| rs243285453 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91743162 | GGGTTTGCACGTGCT[C/T]TGTCATGAGTTGTGT | 16443 |
| rs243291528 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912741 | GTGGGTCACTGCGGG[C/T]CACTGGGATGACCTT | 16443 |
| rs243298289 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91790834 | GAAAGATCACCACCT[C/T]ACTTATGTCTTTAAT | 16443 |
| rs243303079 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91747534 | ACAACTAATATTTAC[C/T]ATTTCTCATGCCTAG | 16443 |
| rs243325109 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750891 | ACAGGCACTGGAGTT[C/T]TTTCCCTCTACAATA | 16443 |
| rs243338570 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746476 | ATCGTTATTCAATAA[A/G]GGACAGGAGTGTAAC | 16443 |
| rs243350057 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91901923 | AGAATCATGAGGTGT[G/T]TCCAGAACAGAATCA | 16443 |
| rs243354092 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91850314 | GTGGTGGAAAGGGAG[A/G]GCTCAAGGAATCACA | 16443 |
| rs243369045 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91796552 | GTGTTGGCATGGTCA[C/T]GGTGTCTGTTCACAG | 16443 |
| rs243374558 | in-del | -/ATAAAATAAAATAAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91901793 | AAAACCGTCATACAC[-/ATAAAATAAAATAAA]ATAAAATAAAATAAA | 16443 |
| rs243397167 | snp | G/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91802901 | AGACAGGGTATGGGG[G/T]AGTGGCTGTGACTCC | 16443 |
| rs243410838 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91766565 | TCTTATCTCCCCTCT[-/C]TCTGCTGCAGGGGTG | 16443 |
| rs243411690 | in-del | -/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91828515 | CCTTTCACACCTTTC[-/T]TTTTTTTGCCTATTT | 16443 |
| rs243413481 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91897357 | ACTAGTATCGTTAGA[A/G]CACAGTTCTTGCTCC | 16443 |
| rs243414681 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91849508 | CAAGGAAGTGTTAGT[A/G]AACTCCAGAAGAGCA | 16443 |
| rs243416318 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91857481 | CTCGCACCACTAGGA[A/G]CACCAGCTCTACTCC | 16443 |
| rs243433590 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91795907 | CTTGCACTGCTACCT[A/C]GAAACCCTGGCTGCC | 16443 |
| rs243434876 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91768258 | TTGCTGTGCTGTTTT[-/A]AAAAAAACTTTTCAA | 16443 |
| rs243476617 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91906044 | AACAGAATGCTAAAT[C/T]CCGTGTGAGCAGGGT | 16443 |
| rs243477679 | in-del | -/AG | | | intron-variant | Itsn1 | Mm_Celera | 16:91809362 | CGGCACACAATCGAC[-/AG]AGAGCACGTGTGTGC | 16443 |
| rs243479172 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91891889 | CGATAATCTTACCCA[A/G]CTTGAACCCTGAGCC | 16443 |
| rs243479420 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91788858 | CTCCCGCCCTTCACT[C/T]TGGTCATAGCATACT | 16443 |
| rs243490068 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91766667 | GCACTCACCTTTAAT[C/T]TCTGAAAACCAAAAT | 16443 |
| rs243522835 | snp | A/C | | | utr-variant-3-prime, intron-variant | Itsn1 | GRCm38.p3 | 16:91870669 | GTAAACTGAGACTTG[A/C]TGTACCTTTGCCGTT | 16443 |
| rs243532688 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91774503 | GGAGACCACACTGAG[C/T]TCCTCCTTCTTCCGG | 16443 |
| rs243537013 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91891480 | GGGTGCTGCTTACCA[A/G]CCTGCTCCCCATGGC | 16443 |
| rs243538792 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91902215 | TGTTAAGAACAGTTG[A/G]TGGTGTGATAGCTCA | 16443 |
| rs243540431 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91896920 | CCTCTGAGCCTTAGA[A/G]CAAAAGACAAAAGTG | 16443 |
| rs243549149 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91817748 | GTGCATGCTGGGATT[G/T]CAGGTGCATGCTACC | 16443 |
| rs243578868 | in-del | -/CTATTTCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91911016 | TTTTTAACTGCTGAG[-/CTATTTCT]CCAGCCCCACCCCTG | 16443 |
| rs243584897 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91893693 | AGCGGCTCTCCCATC[C/T]GTGTCTCTCCCACCC | 16443 |
| rs243635829 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758941 | TTTTCGAGACAGGGT[G/T]TCTCTGTGTAGCCCT | 16443 |
| rs243648952 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91766310 | TTTTCATGAAAAATT[A/G]TTTAACTATGGGTGA | 16443 |
| rs243653636 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91772664 | TGCTTCGCTGGCTTG[C/T]TCCAAGCCTGTAAGC | 16443 |
| rs243693708 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91818118 | ATCTGTCCTGTGTGT[-/A]GAGACTGCCACACTC | 16443 |
| rs243721771 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91754083 | AATAGCTTCGTTTTT[A/T]CTCCCAATGAAATCT | 16443 |
| rs243722190 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91757986 | AGAGGGCATCGAATC[A/C]CATTCCAGATGGTTG | 16443 |
| rs243730215 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91878845 | TCTGCAGGAGTCAGT[A/G]TGTCAGGGACCAGGG | 16443 |
| rs243734521 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91774275 | GGTTATTCTAATGAT[C/G]TTACATTGCCTCTTC | 16443 |
| rs243737800 | in-del | -/AA | | | intron-variant | Itsn1 | Mm_Celera | 16:91760553 | AGTCTAACATGAAAC[-/AA]AAGAGTCTGTCCTGG | 16443 |
| rs243740075 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91886465 | GTCTGCACTGATAAG[C/T]CACAAAGGTCCTGTG | 16443 |
| rs243742169 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91878485 | GTGTGGTGTTGGTGG[C/T]GGCCTTTGCCTCTCC | 16443 |
| rs243743154 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830510 | AGAGCTGTTGGCCGG[C/T]CTTAGCTGCTAACAA | 16443 |
| rs243751809 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91855510 | TATTTATTATTATAT[A/G]AACTCCTATAATGAT | 16443 |
| rs243761505 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91816436 | GTTGACAAGGGTTAA[-/G]GGTATAATGTGACAC | 16443 |
| rs243766988 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91845162 | TATGAAAGTATGGTA[-/G]GGGGTGCAGGGGAGT | 16443 |
| rs243771856 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91780481 | TATACAGGGGCCGAG[C/T]ACTAGGAATAGGTGG | 16443 |
| rs243777077 | snp | A/G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91806262 | ACCGAGTCAAGAAAG[A/G/T]GTATTTTCCTGATGC | 16443 |
| rs243778752 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91896020 | TTGACTCTTCTGGAT[-/T]CCTGGCATATCATGA | 16443 |
| rs243798926 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91885721 | CTGTATGTAAGACTC[C/T]CTCAGTCCTCAACCC | 16443 |
| rs243804675 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91869439 | TAAGACGGTGTAAAA[A/T]TATTGCTATCGTCTT | 16443 |
| rs243816533 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91869143 | CCCTGAGGCAGGAGC[A/G]TGAGAAGATCAGGTG | 16443 |
| rs243828015 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91884611 | GACTCAGCACAGCCA[C/T]GGCGAAGATCACAAA | 16443 |
| rs243828694 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91735073 | GCTCCTGCCACCCTC[A/G]GGCTCTAGCAGTCAG | 16443 |
| rs243832371 | in-del | -/TT | | | intron-variant | Itsn1 | Mm_Celera | 16:91745059 | CTGTTTCTAAACTCA[-/TT]TTTTTTTCAGTTATG | 16443 |
| rs243860817 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91743471 | AACGCGATATACCAC[A/G]TTCACATGATACTGT | 16443 |
| rs243876097 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91877251 | TTGTCATACAGGGTG[C/T]GTTCAGCTTGCTCCA | 16443 |
| rs243882374 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91909688 | GAAGTGCTTGGGCTC[C/G]TTGGTTCACTGAACT | 16443 |
| rs243884739 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91864921 | TCCTCCTTTAGACCC[A/T]AGTGCTGGGGCCTGC | 16443 |
| rs243891973 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91844900 | TAGTTACACTGAAGG[A/G]AAAAGTCCCCGTCCT | 16443 |
| rs243946911 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91742869 | CTCAGCAGTATTGTC[A/G]TAATAACCCTGCCCT | 16443 |
| rs243947489 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91734494 | GCAATTGAGGAAAAG[A/G]CATCTCAATGCCAGC | 16443 |
| rs243983782 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91876808 | TCACACCTTGGTCAC[C/T]ATCTCCTCCTTGGGC | 16443 |
| rs243983827 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734012 | TTTTACTAATTTTCA[A/T]AAAATTTTAAGTAGG | 16443 |
| rs243984426 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91749257 | GGACCATCCCTTCAG[C/G]ACACACCCAAGTCCC | 16443 |
| rs243991467 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91885336 | ATCTGGCTTCCTTCT[-/G]GGGGGGCATTGCTAA | 16443 |
| rs243996828 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852567 | TGGGGGGCTTGGGGG[A/G]AGGGGGGTGGACAGA | 16443 |
| rs243996999 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91844210 | CAGGACTTCTTTCAC[A/T]GTTACCAGCTACCTA | 16443 |
| rs244009897 | in-del | -/TA | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91804357 | ATGGTCAGCAAATAT[-/TA]TAAAGTCTTTAGATG | 16443 |
| rs244021702 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91835484 | GATAGGTTCTCTGCA[C/T]TGGGCCAGTGAGGGA | 16443 |
| rs244030482 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91889816 | TCTCCTCAGTTCATT[-/A]AAAAAAAATCAAAGC | 16443 |
| rs244052184 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91851952 | ACTTGAAGGGGTTGG[A/G]AGTGAGGTCAGTCCA | 16443 |
| rs244059357 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91741514 | AGGTGCACCCGTGTT[C/T]CCAGAGGGCGGATGG | 16443 |
| rs244068837 | in-del | -/GTCAACCCCCCTTGCTCTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91769843 | CCTTTGCTCGCTCCA[-/GTCAACCCCCCTTGCTCTG]GCCCAAAGTTTTATT | 16443 |
| rs244069415 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872449 | TCAACAAGGAGCCAG[A/G]TGAGGTGAACCTAGA | 16443 |
| rs244077689 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91801217 | TTCCAACTGTTTAAC[C/G]TAAGGGTGTGTGTTT | 16443 |
| rs244080325 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91889435 | GCGGAGAGTGAACTG[A/C]GCGTGGACACAGGTT | 16443 |
| rs244088020 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91740820 | GTGGCAGTCAAGGAC[A/G]GGACTGACAGGGTCC | 16443 |
| rs244109539 | snp | C/G | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91728311 | CTTTGCCTCCATAAA[C/G]GCGGAGGAAGAAGCA | 16443 |
| rs244112770 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91843824 | GTCCCAGAAAGTAAG[C/T]AGCGGCTTAGGGAAG | 16443 |
| rs244128718 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91833140 | CACACACAGAGGCAC[G/T]CACATGTGCACATAC | 16443 |
| rs244131123 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914476 | GTCTGCTTTGTAAAT[A/G]CTTGCCCAGGCTGCA | 16443 |
| rs244141468 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91842980 | CCTTCTTACTTACCT[A/G]CTGACTGACACAAGG | 16443 |
| rs244150727 | snp | A/C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783200 | TCTTAACTAATGATA[A/C/T]CATTTTTATTTGTTT | 16443 |
| rs244167006 | in-del | -/AA | | | intron-variant | Itsn1 | Mm_Celera | 16:91743453 | AATATTTGGAAAACC[-/AA]TCAACGCGATATACC | 16443 |
| rs244170025 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823071 | CTGCCTTTGAGCTGT[C/T]ATTGTGCTTGGGTCC | 16443 |
| rs244198510 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91850320 | GAAAGGGAGAGCTCA[A/T]GGAATCACAAGGTCT | 16443 |
| rs244212656 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91887263 | CTCCTGTTTCTACAA[C/T]TCAACCCACAACCCC | 16443 |
| rs244229817 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91822668 | CAGACCTTTGGTCCA[C/T]TTTGATTGGGTTGAA | 16443 |
| rs244237262 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91806993 | TATGCAGAGAACATG[C/G]AGCAGCCTCTAAGGT | 16443 |
| rs244306231 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91751619 | TGTCTCCCAAGTGTT[-/G]GGGGGCAAAGGTGTG | 16443 |
| rs244322382 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91856657 | GCAGTGGAGGGACAG[A/G]TGTGACTAGTCAGTG | 16443 |
| rs244332774 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91866387 | CCCTTGTAAAGCAGC[A/T]GAGGTGAGGGAGAAG | 16443 |
| rs244339046 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91821802 | TGGTAACATTTGAGC[A/G]GAGATCTGAAAGTAA | 16443 |
| rs244339395 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830325 | AGTGCTTCCGGGGCA[C/T]CTGCACAAATGCTGT | 16443 |
| rs244342544 | in-del | -/A | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91832109 | TCCACCTAGAATAAT[-/A]AAAATCCTTTAACTG | 16443 |
| rs244343560 | in-del | -/CTTACTTGTTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91812326 | TCTTTCTCTTAATAA[-/CTTACTTGTTTT]CATTTCATGTGCATC | 16443 |
| rs244376660 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91903916 | AGTGGCACACTTCCG[A/C]TAACTAGGGTACACC | 16443 |
| rs244382671 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91891752 | ATTTGGTAAGATTCT[A/C]TTACTGAAGACAACA | 16443 |
| rs244400636 | snp | C/G/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91829464 | GTTCTCGCTTGCTCT[C/G/T]ACTGTAACTTACTGC | 16443 |
| rs244412536 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91838645 | AACGTTGTTTGGGGC[A/T]GGAGAGATGGCCCAG | 16443 |
| rs244423872 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91793405 | GGTAAAGAGTAACAG[A/T]TGCAAGATACCATGT | 16443 |
| rs244428593 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91752487 | GATTGTTGTACTTCT[C/T]CCTAGATACAGCCGG | 16443 |
| rs244430523 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910694 | TTGCCTTTTTTCCCC[A/T]TTTTTAAAAGATTGG | 16443 |
| rs244438914 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91821117 | GTTAGAATTTCAGGG[G/T]TTTTTGTTGTTTTGT | 16443 |
| rs244445231 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917221 | CCCCAGCCCTTTCGT[A/G]AAGAAACCAGATTCA | 16443 |
| rs244489131 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91777706 | ATAACTTACAGATTA[-/T]TTTTTTCAGATCCAA | 16443 |
| rs244498907 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91800854 | AGCCTCTCTCTGTAT[C/T]GAGGGTGACTTGAAT | 16443 |
| rs244537289 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91777363 | CTTTCTTGTCTTCCC[C/T]ACACTCTGCAGGCTC | 16443 |
| rs244552293 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91800275 | TAATGGACAGACCGC[A/C]CTGGAGAAGCTGTGC | 16443 |
| rs244558267 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91899231 | AGCCACCATTCTGAA[G/T]GACAGGTTATACAGA | 16443 |
| rs244576561 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91792070 | CAGTGTCAGAGCCCC[C/T]CAAGAACTGGAACTA | 16443 |
| rs244587130 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799653 | GAGCAGAGCAACTGT[A/C]CAGCAAATTCAGGAC | 16443 |
| rs244588719 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91791568 | ACAGCATTAGTGTCA[C/T]GCTTAGAAGTTCCGT | 16443 |
| rs244594188 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91893982 | TTCGTCAAAGTAAGG[A/G]TGACCCTGGGGACTC | 16443 |
| rs244615110 | in-del | -/ATC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783199 | TTCTTAACTAATGAT[-/ATC]ATTTTTATTTGTTTA | 16443 |
| rs244622501 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91784205 | AGCGGCAGGAAATCC[A/G]TTAGGCAGAGTGGAA | 16443 |
| rs244629475 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91898778 | CAAGCAAATACAAAC[C/G]GTCGCATGCTCTCAC | 16443 |
| rs244643133 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91807380 | GAGGCCTTCAGGCTG[C/T]TGTGCTCTTGAACCC | 16443 |
| rs244643516 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798940 | TCTGGGTTTGATCTC[C/T]GGTGTCACAGGGGAA | 16443 |
| rs244650125 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91810979 | GGACATCGCAGCCTC[C/T]GCTCCTAGCTATGCA | 16443 |
| rs244651556 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | GRCm38.p3 | 16:91729994 | CCTTTTTCTCTAGCG[C/T]CTGCTTGGAATACCC | 16443 |
| rs244671880 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91735240 | TACTTACTGTGTATA[A/G]GTGTATAAAGTTTAA | 16443 |
| rs244685391 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91838871 | AAGACATTCTATGTT[A/C]TGTGCACTAGCTTTC | 16443 |
| rs244697265 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91817066 | TTGGCCAGAAGGCGG[A/G]CACAGGTGCTTTTGG | 16443 |
| rs244698674 | in-del | -/GT | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91829379 | TGTGTGTGTGTGTGC[-/GT]GTGTGTGTGTGTCGT | 16443 |
| rs244715363 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91894880 | TAGTGATGTAAAACA[-/C]TTGTCCCACAGACCA | 16443 |
| rs244739048 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91837988 | ACAAGTTTATTGGAC[C/T]GGGTATTTATTTTAT | 16443 |
| rs244741937 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91762757 | TCTACTATTCATCCC[G/T]TTAATCTTAAGTTTC | 16443 |
| rs244743124 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91860373 | GCCTTCCTCTTCTCT[A/T]ATAGCCATTCAGTCC | 16443 |
| rs244747368 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91898448 | CCACACACTTACATA[C/T]GCATGTGTCCTGTCT | 16443 |
| rs244749279 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91844960 | GGCAAAATGTCCCTG[C/T]ACAAACGTGAAAGTC | 16443 |
| rs244755196 | in-del | -/ATGTGT | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91853605 | TGTGTGTGTGTGTGC[-/ATGTGT]GCGTGCATGCGCGCG | 16443 |
| rs244765894 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91869379 | CTGGGTGAGGACCCT[C/G]TGGTTTTTCTGACGA | 16443 |
| rs244767048 | in-del | -/GCATAGA | | | upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91729036 | ACAAAATCTCCGCAC[-/GCATAGA]GCAGAAACCTCTAGT | 16443 |
| rs244781325 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91903330 | CTGAAGAGAGCAACA[C/G]TGTACTCATATATAT | 16443 |
| rs244790228 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91817107 | GAGTGTTGTGATGCA[C/T]CTGTAGTCCATCCTT | 16443 |
| rs244794062 | in-del | -/CT | | | intron-variant | Itsn1 | Mm_Celera | 16:91775931 | AGTGTTTATGAAAAA[-/CT]CTCTTCTGAATCCAT | 16443 |
| rs244799984 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91823440 | TTTGAGTACCCATGT[A/G]ATCTTTAAGGTCTTC | 16443 |
| rs244813525 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91902752 | AACATCACGTGGGGT[C/G]TGCTCTAGCAAAACG | 16443 |
| rs244819336 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768927 | TGGCCATTCCTTCAG[G/T]CTCTCATATCTTTCC | 16443 |
| rs244819428 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91761528 | GTTTACAACGGTCTT[C/T]CCTACCTGGAAACTC | 16443 |
| rs244846849 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91811725 | TTTGACGCTCTAGTC[-/T]TTGGTTTTTTTTTTG | 16443 |
| rs244855931 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91768564 | GAGATCAAGCTGCAC[A/T]TCTGCTACATTCACA | 16443 |
| rs244866690 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919691 | TTTCAAAACTAGAAA[C/T]ACAGAAACTGAGAAG | 16443 |
| rs244881004 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913341 | TCCTGGGCTCAGGCT[C/T]TCCTGTGTTGGGTGG | 16443 |
| rs244881644 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91817168 | AAAACTTTTATAGGC[A/G]TTTTCTATGGAATAG | 16443 |
| rs244884146 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91810719 | TGTACATTAATGTAC[A/G]CTTTTCTGCCAATAC | 16443 |
| rs244900885 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91861679 | CTTCAGAGTCTAGAA[-/T]TTTCAGTTTATTTAA | 16443 |
| rs244905676 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91877592 | GAGGGGACATGCAAA[C/T]TGTAAGATAAACTCA | 16443 |
| rs244923084 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91873669 | GAGAGACAAAATTAT[A/T]ATTTATTCTTTTTAG | 16443 |
| rs244923545 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919727 | ACCCACAGAAGGCTC[A/G]CCTGCCTCAGCTTTA | 16443 |
| rs244924947 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91885363 | CTAAGACAGATGTTT[A/G]AGAAGGCGCCATAGC | 16443 |
| rs244937861 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91913412 | CCTGTGTTGGGTGGT[A/G]TTCCTTTTTATGGTA | 16443 |
| rs244938238 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810480 | TGTGACACAGTCCCA[C/T]GGTAACGAGCTGTGC | 16443 |
| rs244954032 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91816768 | AGAGCAAGCTTGTGA[C/G]ACAGATAGTCAGCCC | 16443 |
| rs244983342 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91810893 | CTGGGAGGGAGCAGC[-/T]TCCCCTGCCCCAGGC | 16443 |
| rs244987037 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91780780 | TTTTAATGAATACTT[C/T]TCCTCCTCTTGACTG | 16443 |
| rs244993335 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91809673 | TGTGTGTGCGTGTGC[C/T]GCCACAGAGACTGTC | 16443 |
| rs244996959 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91905572 | GGTTTGGGACTGCAG[G/T]GTGGAGAGAGCAAAG | 16443 |
| rs245003857 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91787764 | GACAGGACTGTGAGA[C/T]TGGGAAGCTGCCCTT | 16443 |
| rs245020652 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734347 | GCTGGGATGGTGACA[C/T]GGGGAAGAAACATTA | 16443 |
| rs245031284 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91904947 | AGGTGTGCGCCACCA[C/T]GCCCGGCTATTCTCA | 16443 |
| rs245057849 | in-del | -/TG | | | intron-variant | Itsn1 | Mm_Celera | 16:91846188 | TAGTTAGATAATTAA[-/TG]ACTAAGACTAAGCTT | 16443 |
| rs245059388 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912725 | TGAGTTAGGTCCTGC[C/T]GTGGGTCACTGCGGG | 16443 |
| rs245068475 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890597 | GTTTTTTTCATGAGG[C/G]AGTGTCTCACTGTTA | 16443 |
| rs245088683 | snp | C/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919112 | AAGGGTTGGTCTCCC[C/G]GTTTCTGGTGTCACA | 16443 |
| rs245097648 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91836914 | ATGTCAAAATGCAGC[A/G]AGTTCGATTTCTGAG | 16443 |
| rs245109239 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91822722 | TTCCTATCAGCAAGC[C/T]AGATGACTTGTTTCA | 16443 |
| rs245120762 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91742063 | TTGTGCAGCAGGTTC[A/G]CCACCATCTCTGTGT | 16443 |
| rs245124296 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91918293 | GTAGGCCTCTGTCCC[C/T]GCGAGACAGGGTAGC | 16443 |
| rs245134693 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91780023 | GGGTCCCACAGGCCG[A/C]AGTTCAAATTGGGAA | 16443 |
| rs245134787 | in-del | -/GA | | | intron-variant | Itsn1 | Mm_Celera | 16:91860143 | ACAGAGAACACACTG[-/GA]GCCCTGTGACCTCTG | 16443 |
| rs245137133 | in-del | -/GTTT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91751523 | TGTATGGGTTTTTTG[-/GTTT]TTTTTGGTTTTTTTT | 16443 |
| rs245146866 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91787860 | TGGAGCTGGGTCTTG[A/G]AGGCAGCTTACACAG | 16443 |
| rs245152063 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91911841 | TCTTTCTGATCATCC[C/T]CTGCTTTTCCTCCTT | 16443 |
| rs245155729 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91843985 | ACCCCATATACCACC[A/G]CACTCTTATGTACAT | 16443 |
| rs245165277 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91843966 | ACCCCCACCATCGCG[A/G]ACCACCCCATATACC | 16443 |
| rs245173650 | in-del | -/AC | | | intron-variant | Itsn1 | Mm_Celera | 16:91765274 | GAGCTCCGGAGCTAA[-/AC]ACGGAGACCCTGACT | 16443 |
| rs245181048 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91793978 | TCGCACTCGGCTGCT[A/G]CAGCTCTGTCTCCTG | 16443 |
| rs245182543 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911302 | AACAACAACAAAAAA[A/T]CGTATGTCCATGAGC | 16443 |
| rs245208725 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91787462 | AGCTTTCCGTAGTCA[C/T]AGTCTTCACTGGAAA | 16443 |
| rs245210893 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91779372 | AGCCACTAGAGTGTC[A/T]ACAGTCATAGGTGCT | 16443 |
| rs245261280 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91895015 | CCTTTCCATTGGATT[C/T]GGTATGAGATGCCAC | 16443 |
| rs245275528 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91869126 | GCGCTGGCTTAACTT[-/C]CCCCTGAGGCAGGAG | 16443 |
| rs245280543 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91792930 | CCTTTTCCACTGAAA[A/G]CTCAGTACAGATTGC | 16443 |
| rs245287229 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91786223 | GAGTGGATTAGCAAA[C/G]AAATTATACATGAAG | 16443 |
| rs245292942 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91809517 | TTGGACACAAAGCAT[C/T]GGACTCCATATAATT | 16443 |
| rs245296310 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91889593 | TGAGAGTGTGAGAGT[A/G]CGGGATGACTCTCCA | 16443 |
| rs245300599 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900230 | GCCACACTCTCAGCT[C/T]CTGCCTTAGGATTTT | 16443 |
| rs245305009 | in-del | -/AGA | | | intron-variant | Itsn1 | Mm_Celera | 16:91846948 | CTGGCAAGATTAACC[-/AGA]AGTGACAGGCATCCG | 16443 |
| rs245307616 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91790266 | AGGGATGGAAGTTCA[-/C]TGGAGAAGAAATCCC | 16443 |
| rs245316856 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91851639 | AGTCCCTGTGTCCAC[A/G]CCACAGAAGAGGGGA | 16443 |
| rs245335931 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91750699 | TTCATCCTTCTACCC[-/T]TATGTGTGAACTGGG | 16443 |
| rs245342767 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91894460 | GTATTTCTGAGAATC[G/T]TGTCTAAATCCTTGA | 16443 |
| rs245345658 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91756795 | GGTAGATGAGACTGT[C/T]GCACTCTGGGCAGCG | 16443 |
| rs245352145 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91888921 | AGCTTCCTCCTCAGA[A/G]GTTCGCCTGGACTCC | 16443 |
| rs245362854 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91764599 | ACCCTTTTCAACAGT[C/T]CTTCTCCTCCGACCC | 16443 |
| rs245366783 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91815966 | ATACAGTCAGGAGAC[A/G]CCTCCAGTGACTGTC | 16443 |
| rs245373477 | in-del | -/ACACAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91873742 | AAGTCGGTGACACAA[-/ACACAC]ACACACAGAGAGAGA | 16443 |
| rs245411663 | in-del | -/TGTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91872302 | GTGTGTGTGTGTGTG[-/TGTA]TGTGTGTGTTCCACG | 16443 |
| rs245424918 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91911771 | AGAAGAGCTCGAGAG[C/T]GGCCAGTCATAGGAC | 16443 |
| rs245433433 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91838059 | CTGCAGCAACTCGCC[-/T]TTTTTTTTTTTAACT | 16443 |
| rs245448372 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91755023 | ACATCTCAGAAACTA[C/T]TCCTAACGTCTTCTC | 16443 |
| rs245453167 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91764268 | CTTCTCAAGGGGAAA[C/T]GTTCTCTCTGAGGCT | 16443 |
| rs245461304 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91868004 | TGTTCATAAAACATT[A/G]TTATTTTCTTCCTAG | 16443 |
| rs245464547 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91894046 | CATCAAAAGTCCACA[A/G]GCATCTTTCCACTAG | 16443 |
| rs245474280 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91876321 | TGCCCTGCCCCAGTT[A/T]CCCCTCTCCTTTTAC | 16443 |
| rs245481393 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91764527 | TTTGACATTTTCATA[A/T]ATTTTTATAATGAAG | 16443 |
| rs245486250 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91770504 | TCCTGAGCAGACACT[A/C]CTGGGTCTCTTTCTG | 16443 |
| rs245488565 | in-del | -/CTCCCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91743073 | TTTTCCTCCCCTCCC[-/CTCCCT]CTCCCTCTCCCTCTC | 16443 |
| rs245507529 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890564 | TGACTTGTTTTTTTT[G/T]TTTTGTTTTTGTTTT | 16443 |
| rs245522661 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91867388 | ACTGCCATGTAACTT[C/T]TCAAGGTCGGTTTAG | 16443 |
| rs245531520 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91763263 | AACATTTAGAACAAA[C/G]GAGATGACACACAGC | 16443 |
| rs245531624 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91754508 | TGTGCAGCTGAAGAG[C/G]ATCTTGACCTCCAGA | 16443 |
| rs245532377 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91875768 | CACAAGCACAGACAG[A/G]TTGTTGGCAGGCCCT | 16443 |
| rs245535664 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91894086 | GGGATGGATGGAAGT[C/T]TTCAGTGGTACTGAA | 16443 |
| rs245536097 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91771297 | TTCACTGTGTGTTCC[G/T]GACCCCTCCTTCACT | 16443 |
| rs245556944 | in-del | -/CGTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91807701 | ACACACACACACACA[-/CGTG]CGCGCCTTTGCAGGC | 16443 |
| rs245557066 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91899180 | GCTACCTAAGATCTG[A/G]GATGTCTCTGTGTGT | 16443 |
| rs245561952 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91769838 | TTGGACCTTTGCTCG[C/T]TCCAGTCAACCCCCC | 16443 |
| rs245563250 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91762833 | AACTGGATTGTTCAT[G/T]CCCCGGGGCAGGCAT | 16443 |
| rs245587926 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91874938 | GGAGCATTCCTGCCT[C/G]TCCTAGAGCCTTGCC | 16443 |
| rs245590392 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91751975 | GATCTCACTCTAATA[C/T]ACTAGGAAGGGTGGG | 16443 |
| rs245599174 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91866505 | AGAACGGGAGTCCTG[G/T]CTGGACAACCAAAAG | 16443 |
| rs245607462 | in-del | -/AGCA | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914128 | GGGTTACCTACTCAT[-/AGCA]AGCACCCCATGATTG | 16443 |
| rs245609801 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91865615 | GAGATTAAAGGCCTT[C/T]CTTTGAGGGTCTTAC | 16443 |
| rs245611829 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91904410 | ATGTTGGAACCACAT[A/G]TCAGCATTCACAGAT | 16443 |
| rs245634346 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91822309 | TTTATGTAGGGAACA[C/T]GCATGTAAAGGTGAA | 16443 |
| rs245654453 | snp | C/T | | | intron-variant, missense | Itsn1 | GRCm38.p3 | 16:91853079 | AAACTGTCCCTGGCG[C/T]CCCGAGGCAGGGGTT | 16443 |
| rs245660811 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91874376 | TGTGGTCTGTGCATG[G/T]GACAGACATAGGTAG | 16443 |
| rs245664156 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91731876 | GTCTTTGTGTGTGGT[A/G]CTGCTGGCATTAGAT | 16443 |
| rs245691815 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91835353 | TTTTTTTTTTTTTTT[-/G]TTTTTTTTTTTAACC | 16443 |
| rs245699660 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91731124 | GCCACTGATTTGGTG[A/G]CAGGGCATAGATATT | 16443 |
| rs245699723 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91739632 | GGCTAGGTTCATCCA[G/T]GGCCCTGAGGCCAGA | 16443 |
| rs245699856 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91882171 | GTGTGTGTGAGTGTG[A/C]AGGTGTGATTGTGAG | 16443 |
| rs245702673 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91876147 | CCTTGGAATCCCATA[A/G]CCCCATGGGAAGGCC | 16443 |
| rs245723863 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91841281 | GGCTGTCTGCCCACC[A/G]CATTCAGTCCTGGCG | 16443 |
| rs245724772 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91860911 | GACTCAGATGTCTGT[A/G]GTATCTCTACACTGT | 16443 |
| rs245735636 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91775354 | GCTAAGATTGCAGGT[A/G]TGTACACCACGAGTC | 16443 |
| rs245747859 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91834225 | CAGCTATTTACAGTT[C/T]ATAAAGTAGCAAAAT | 16443 |
| rs245748277 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91901415 | GCAGAAGCTGAGGTG[A/C]CAGCTATGGCTTCTC | 16443 |
| rs245756112 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91766488 | GCTAGCTTGTGGGCA[-/G]GGGCCTGCTCTCCCA | 16443 |
| rs245758712 | snp | G/T | | | upstream-variant-2KB | Itsn1, Cryzl1 | GRCm38.p3 | 16:91729142 | AACTACTTCATTGGT[G/T]TATCTCGTTGTCACT | 16443 |
| rs245764884 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91873748 | GGTGACACAAACACA[C/G]AGAGAGAGAGAGAAT | 16443 |
| rs245774950 | in-del | -/CT | | | intron-variant | Itsn1 | Mm_Celera | 16:91824508 | CCTCCTGCCTCCCTG[-/CT]CTCTCCCTCCTCCTG | 16443 |
| rs245775079 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91738659 | CTGTAGCTAACCCAG[C/G]GAAGGTTGCTGCAGG | 16443 |
| rs245794726 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907612 | CTCCTCCAGCCTGGC[A/G]TTTATCAGGCTTTCT | 16443 |
| rs245804876 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734226 | GGCATTTCTTAAGGA[-/T]TTTTTTCCCCCTTTT | 16443 |
| rs245813807 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91874820 | GTCCCCTGAAGAACA[A/G]TTTGACAGTACTGGG | 16443 |
| rs245821777 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91840745 | CAGGGGTCATCGAAG[C/T]CCCTGTGACTCTTCA | 16443 |
| rs245829078 | in-del | -/A | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911381 | AATATATTTTAAAAT[-/A]TACACAGAATATATT | 16443 |
| rs245845800 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91848252 | GTGATAGCTCTGAAT[-/A]ATGCTGTGTGTTCAT | 16443 |
| rs245850221 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91833493 | GTCCTCTTCCTCTTC[C/T]TTCTCCTCCTCCTCC | 16443 |
| rs245863409 | in-del | -/AG | | | intron-variant | Itsn1 | Mm_Celera | 16:91789958 | AAACAGAGACTGCTT[-/AG]AGAGGAGTCTTTTAA | 16443 |
| rs245873939 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91778434 | AATATTAAGAGTATA[C/T]TGAGTGGGGCAGTGG | 16443 |
| rs245878482 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91847940 | CTACAGGTCACATGT[A/G]TAGACGTAAGAATAG | 16443 |
| rs245880453 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91774180 | GAACAAGACATCTAG[C/T]TTCCATATATCAAAT | 16443 |
| rs245897072 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823566 | ATTGTTATATACATA[C/T]GATATGTATATTTTA | 16443 |
| rs245897718 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91740016 | TCTTTCTGGAACTGC[C/T]GGAAAACCATGAGTT | 16443 |
| rs245908142 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91839963 | GCTCGGTTTGGGGAA[A/G]GTTCTCACTCTGTAG | 16443 |
| rs245919515 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91882016 | CACGGCTCTCCTGCC[A/G]TTCCTCGTTGTATCT | 16443 |
| rs245921468 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91839591 | CAGAGTTGCTTCCTC[A/G]GCAATCAAGCATCTT | 16443 |
| rs245922626 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91792362 | GAGATAGTTAATGTG[C/G]ATTGAAAGTGTAGTG | 16443 |
| rs245941084 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91781168 | AAACCCACCACAGAC[A/C]AGAAGAAAAATAGCC | 16443 |
| rs245946011 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91827854 | TGTTTCCTTCCCTCT[C/G]CCCTAGGAATCTCAG | 16443 |
| rs245968820 | in-del | -/CTTTCTTCCTTTC | | | intron-variant | Itsn1 | Mm_Celera | 16:91795484 | TTTCTTTCTTTCTTT[-/CTTTCTTCCTTTC]TTTTTTTTTTTTGTT | 16443 |
| rs245982913 | in-del | -/TCTTTCTTTCTTTCTTTCTTTCTT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894208 | TCCATGTATTTGTGG[-/TCTTTCTTTCTTTCTTTCTTTCTT]TCTTTCTTTCTTTCT | 16443 |
| rs246001038 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91765893 | CAGTTTATAGATCAA[-/T]TATGTGAAGCTTAGA | 16443 |
| rs246001682 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91743711 | TTTCTCTGTATAGCC[C/T]TGGCTGTCCTGGAAC | 16443 |
| rs246011447 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91885506 | AGAGCGTTTCTATAA[C/G]GATAGCTTAATTCCC | 16443 |
| rs246021263 | snp | A/C | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831081 | ATGACCTCAAATCCG[A/C]GACCTTCACCCTTCA | 16443 |
| rs246032951 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915998 | GGGACCCTGTTCTGC[A/G]GGGACGTGGGGGTGT | 16443 |
| rs246059613 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91780971 | CACAGGAAGCAGGCA[-/G]GGTGCAGGTGTGATG | 16443 |
| rs246061460 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91812304 | ACTTGACGTATAACC[C/T]AACAGTTCTTTCTCT | 16443 |
| rs246113768 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91818863 | CTACCGTATATACTG[C/T]CTTTATTCGCCACTT | 16443 |
| rs246151720 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91891109 | AACTGTGAATAATAT[C/T]GACAGCTGGAGCATC | 16443 |
| rs246151760 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742629 | CCAGCCTGGTCTACA[A/G]AGTGAGTTCTAGGAC | 16443 |
| rs246173460 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91756846 | TGTTCCCCTTGGGGC[C/T]ATGAGTCCAGGGTTT | 16443 |
| rs246193163 | snp | A/C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798771 | GGAAACAAATTAGTC[A/C/T]GTCACCATTCCTAAG | 16443 |
| rs246197478 | in-del | -/TAACA | | | intron-variant | Itsn1 | Mm_Celera | 16:91887094 | ACAAACTTTATGGTG[-/TAACA]TAACACAAGGGGGAT | 16443 |
| rs246197924 | snp | A/C | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745781 | TGGGCTTTAAGACAA[A/C]AATGGGAGGTATTGT | 16443 |
| rs246220759 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914515 | CACCTTGATGCCAGC[C/T]GTTCAGATACCCCCT | 16443 |
| rs246221114 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91818347 | GGGTTTGTATTCCAT[C/T]ATGCACCTGAGTTTT | 16443 |
| rs246227955 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91749494 | AAGAATAAGCTAGGA[-/C]CTTTAGCAGTAAATC | 16443 |
| rs246231879 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91802369 | GGCTTTACCGTTAGA[C/T]CTGTGTCACTATTGC | 16443 |
| rs246244453 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91858839 | TCCCACGGTCCTCAT[A/T]GGTTGGAAATGGCTC | 16443 |
| rs246247046 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91748866 | TACTAGTGTTCAGGA[A/G]GTAGAAGTGAGATTC | 16443 |
| rs246254860 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91868170 | CGTCTGCTCGCGCTC[A/G]CTCGGGTCTCTCATC | 16443 |
| rs246255761 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91857734 | GGGCACTTAAACGGT[A/G]ACAGGTATATCATTT | 16443 |
| rs246256368 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914104 | ATGCATGGTGACCCC[A/G]TAGGTTCTGGGTTAC | 16443 |
| rs246260345 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91898324 | ATCCTAGCTACCCTC[A/G]CCTGATTGGTGAGCC | 16443 |
| rs246284868 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91806438 | GAACCCTCTTGCACC[A/G]GTCAGTGGGACAGCG | 16443 |
| rs246291210 | snp | C/T | | | downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91920903 | CTTGGGTTTCTTTTT[C/T]TCTTTCTTTTTTTTT | 16443 |
| rs246309023 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91847755 | ACAGTGACCAAATTG[A/T]AAAGCAAAGCCAGCG | 16443 |
| rs246314187 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91851731 | GTGCAGTGAGGGCGC[A/G]TGGGAGGACAACTCA | 16443 |
| rs246321411 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867502 | CCCTCTGGCATTAAC[C/T]AGAGCATCAGCATCA | 16443 |
| rs246332334 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91855675 | ACGTGAGTGTACTAT[A/C]TGCAATCAGGTCTCA | 16443 |
| rs246352135 | snp | A/C | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830106 | CTGCGGAAACCAAAA[A/C]AGAAATGAGACAACT | 16443 |
| rs246355987 | in-del | -/GTTGCTT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899090 | TGCTCTCTGGCTGAG[-/GTTGCTT]TTCTGTGAAATAGGA | 16443 |
| rs246357013 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91781400 | CACCATGTACCTGGG[G/T]GTGACCTTAAACTCT | 16443 |
| rs246359186 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91789404 | CCTTTCTTACTTAAT[A/G]TATCCTCCTGGTTTT | 16443 |
| rs246377842 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91767522 | ACATCATTTAGCTTT[-/G]GGTTTTTTTTAGGCA | 16443 |
| rs246384224 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91859325 | GTTTGCTGCAGTGTT[A/G]GAAGCAGTGTGCTAA | 16443 |
| rs246426141 | in-del | -/TGTC | | | intron-variant | Itsn1 | Mm_Celera | 16:91769587 | GTGTCTTTTCATGTT[-/TGTC]TGTGCACACGTGCTC | 16443 |
| rs246428009 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91901683 | CATGGTGGGTCTCAA[-/G]TACCGGTAACTCTGG | 16443 |
| rs246434852 | in-del | -/GTTTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91817785 | GGTTTCTATTAAGGT[-/GTTTG]GTTTGGTTTGGTTTG | 16443 |
| rs246437435 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91905521 | TTTATGTAGCTCGTG[A/G]AAAGAGGGGTCTCTA | 16443 |
| rs246444561 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91903142 | GTGAGCCAGAAGATC[A/G]CCTATGCTACAGTGT | 16443 |
| rs246451266 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91765664 | CTTTAATCCCAGCAC[-/T]TTGGGAGGCAGAGGC | 16443 |
| rs246466173 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91827990 | TTGTTTGTTCTGTTG[A/G]TACACATCCCGAATG | 16443 |
| rs246506112 | in-del | -/TTTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91811569 | CCTCTTCCTCTTTTC[-/TTTG]TTTGTTTGATGACAG | 16443 |
| rs246523135 | in-del | -/TC | | | intron-variant | Itsn1 | Mm_Celera | 16:91791921 | GTGTCTGTGTGTCTG[-/TC]TGTGTGTCTTGAGAG | 16443 |
| rs246533721 | in-del | -/TG | | | intron-variant | Itsn1 | Mm_Celera | 16:91890262 | AGCTGGGTCGTTTTT[-/TG]GGGGGGGGGGGGAAT | 16443 |
| rs246537078 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91768348 | AGATCCCTCACCCCT[C/T]ACCCTTCTCCTTCTC | 16443 |
| rs246546455 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91835553 | GCCCCTTCCTTCCTG[A/G]GGACACTAGAGCTTG | 16443 |
| rs246572636 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91827135 | GCAGGCCTAGCACAG[C/T]TCATTCTGCAAATGC | 16443 |
| rs246574938 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830012 | GCTGTGTTGTTGATC[C/T]TTTAACGTCCATTCA | 16443 |
| rs246592994 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91826261 | TGGCCTTGAACTCAA[A/G]GAGATCCACTTGCCT | 16443 |
| rs246602385 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91779848 | CCTTAATCGGAATCA[A/G]CGTGTCACTCATTCA | 16443 |
| rs246613046 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91834893 | AGATGAACCATCTCG[A/G]TTTGATAGCTACATT | 16443 |
| rs246620712 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91883977 | CCTGTGTATTTTAGT[C/T]CATTACTCCTGGGCC | 16443 |
| rs246627346 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91841314 | TTGCTTGTGGGATCT[A/G]CTGATGAACTGCACG | 16443 |
| rs246633875 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91834360 | TCACAATTAGGAATA[C/T]TCTGCTTTTATTGTT | 16443 |
| rs246636538 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91880554 | TTAAAGAACACACAC[A/C]AAAGAGCAGAGTGTC | 16443 |
| rs246700144 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91890007 | CAGGATCCAGATGCT[C/G]GCATTTGCTCCCGAG | 16443 |
| rs246703721 | snp | C/T | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91887504 | AACTACGTGAACGAC[C/T]TGCAGCTGGTCACAG | 16443 |
| rs246704319 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91835991 | AGTCTGTACCTAGCC[A/C]AGCTCTCCAGGCTCG | 16443 |
| rs246712090 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91833301 | AATCAAGCTCTTTAG[A/G]TTTGTGGCGTCAAGT | 16443 |
| rs246716395 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798865 | CAGAAGACCTGAGAG[A/C]TCTGGAACAGTCTGC | 16443 |
| rs246720034 | in-del | -/CTTGTTTG | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91728144 | CTGCGAACACCCACC[-/CTTGTTTG]CTTTAGGAAACCGCT | 16443 |
| rs246727847 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91807230 | TAGCCTGTGTGGGTT[C/G]ATCTGTTACACAGAA | 16443 |
| rs246729139 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91806525 | AGAGGCTGTTCCCTC[G/T]GTCAGACATGGAGGC | 16443 |
| rs246743685 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91818083 | ATGAGTCGGAAGAGT[-/G]GGGCTGAGGGAACAG | 16443 |
| rs246782915 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91805552 | GCAAAAACCTGGGCA[A/G]TATATAATGCCTCAG | 16443 |
| rs246785091 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91806586 | GACTCTGCTGTCCTC[A/G]TTGCCTGCTGCTCAT | 16443 |
| rs246788112 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91903268 | AACCACATGGTGGCT[C/T]ACAAGCATCTGTAAT | 16443 |
| rs246811025 | in-del | -/GAGAGAGA | | | intron-variant | Itsn1 | Mm_Celera | 16:91778562 | AACAAAGACAAAAAC[-/GAGAGAGA]GAGAGAGAGAGAGAG | 16443 |
| rs246823260 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91902685 | TGGCAAGGTGAACCA[A/G]TGCCACACAGTGTCA | 16443 |
| rs246825971 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91910729 | CATGTAGCCCAGGCT[A/G]GCCTGGAGCCAGTTT | 16443 |
| rs246827752 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746747 | CGGGCTCGCCTTGCT[C/T]TATACATAACAGTGC | 16443 |
| rs246853111 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91744386 | TTTGTGCACTGCACT[C/G]TGTGTAGGCTTGGTA | 16443 |
| rs246863883 | in-del | -/GTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91816490 | TTTTCAGAATGACAA[-/GTG]TATGTTGTGCTTAGG | 16443 |
| rs246887338 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91813880 | ATTTTAAAAATCCGC[C/T]TTAATCTCTGTCCTG | 16443 |
| rs246897972 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91800585 | TGGTTACTCCCCGCT[A/G]TCATATATTTTGGAG | 16443 |
| rs246914389 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91808167 | AAATCCTTTTAAAAA[A/C]TATAGCAAAGCATAA | 16443 |
| rs246924796 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91869577 | GTAGCTCTGCGCATG[-/C]CCCCCCGGGTGGCCA | 16443 |
| rs246929181 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91755601 | GACCAGACTGGCCTC[A/G]AACTCAGATATCCAC | 16443 |
| rs246938300 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91733134 | TAATAAACTACCAAG[A/G]ATTATACATATGATT | 16443 |
| rs246949278 | snp | C/T | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91909276 | ACAATCCAGGACACG[C/T]TAAACCCCAAGTGGA | 16443 |
| rs246953504 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91875533 | AGCCTTCACATGCAC[C/T]CCTGCAGCTTTGCAA | 16443 |
| rs246954422 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91910349 | CTCAGGACCTCTGGA[A/G]GAGCAGTCAGTGCTC | 16443 |
| rs246962738 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904376 | GATGAGCTGACTTGA[C/G]ATGACAGCCCCCGGG | 16443 |
| rs246974380 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91776697 | CTCACTTAGGTCTCC[C/T]TTTGTCTCATGGGAA | 16443 |
| rs246974522 | in-del | -/CCAAAGCACTTCCTGTCTGTGTGACTGGGAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91785895 | AATGTGTAGTCCTGG[lengthTooLong]CCAAAGCACTTCCTG | 16443 |
| rs246985904 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91908616 | TAAAGGATGAAGGGC[A/G]GATTCCAGGGGCAAG | 16443 |
| rs246996188 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91835845 | ACCGAGAGGGGACAG[A/G]GGAGCTGCTTCATTA | 16443 |
| rs246996391 | snp | A/C | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916100 | GATGGATGTAAGGAT[A/C]GAAGGGATGGAGGAA | 16443 |
| rs247011427 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91775914 | AATTATTAGTAAATG[C/T]TGAGTGTTTATGAAA | 16443 |
| rs247011813 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91786717 | GTCGATTAGAGAGAG[A/T]GGAAGCCCATGAGCA | 16443 |
| rs247018281 | snp | A/C | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917206 | GGCCCTGAGTTTGAT[A/C]CCCAGCCCTTTCGTA | 16443 |
| rs247037766 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915371 | AAGGACACATGGACG[A/G]GCCCCTCTGGCTTTC | 16443 |
| rs247047482 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91784279 | ATTCAGAACCTGTAT[A/T]TTTGTTGTTACTTCT | 16443 |
| rs247061201 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91867155 | AAATGCTCAGTATCT[A/T]GGGTCAAATCAGATC | 16443 |
| rs247085565 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745355 | GTGTGTGTGTGTGTA[-/AG]AGAGAGAGAGAGAGG | 16443 |
| rs247092147 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91886978 | GCAGCGGTCAGCTCC[C/T]GAAACAGTGGCTGGC | 16443 |
| rs247109697 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91790933 | CCCAAAACAAGCAGA[C/G]TTTCACAGTGTGTGA | 16443 |
| rs247122476 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91911025 | GCTGAGCTATTTCTC[C/T]AGCCCCACCCCTGGT | 16443 |
| rs247134211 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91744421 | TGGAAGCTAGCAGAG[C/G]GTGTTGGATCCTCTG | 16443 |
| rs247145299 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91886667 | ACCCCACAGCGTCCT[C/T]GCCTGAAGAGTCTTC | 16443 |
| rs247158321 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91892866 | ACCTGCATAGTGGAA[C/T]CTCCTCGAAATTGCT | 16443 |
| rs247162044 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91790226 | TAAATTTGGTGTCAG[C/T]ATTGTCCAGACTGAA | 16443 |
| rs247203113 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91827733 | ATGTCACACCCACCC[A/T]CGTAAGCAGAACCAA | 16443 |
| rs247212938 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91778214 | AAATTCATTTCTGTG[A/G]TAAACAGCAATTATT | 16443 |
| rs247215901 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91753464 | AGCATGGGCGGCGCC[A/G]TTTCCCTCCCGTAGT | 16443 |
| rs247216740 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743950 | CATCCTCACATTTGT[A/T]GATAAGAAACCACTG | 16443 |
| rs247239056 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91844481 | TAACAACAACAACAA[-/C]AAAAAAAAAAACCAA | 16443 |
| rs247245473 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91792004 | GTCTTCCTAGTGTGT[A/G]TATCAGTGCGTCATG | 16443 |
| rs247247639 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91739352 | ATGCTTGCAGAGTAA[C/G]TGCGCTTACCTCCAT | 16443 |
| rs247248965 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91752047 | GCCACAAGTGAAGAC[A/C]CGCCCACCACTTGGT | 16443 |
| rs247250143 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91752945 | GGACCCAAGAGTTTG[C/T]ACTTCTGGAAAGTTC | 16443 |
| rs247250189 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91761434 | AGTGGAAGGAGACAG[A/T]GCTGTAAAGAAGACA | 16443 |
| rs247250391 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91891921 | TGTGAGCTACAATAA[C/T]GGCTGGCCTGAGAAG | 16443 |
| rs247251528 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892272 | AGGTAGTAAGTCAGG[C/T]CATGACTTCAAGCTG | 16443 |
| rs247257951 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91897965 | TAGAGTTATAACAAT[A/C]TAAAAGAAAAATTTA | 16443 |
| rs247272257 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91834684 | GAGCTTACGGTGTGA[A/T]TGGCACCGGGCTGTG | 16443 |
| rs247293332 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91897401 | GGAAAGAACCGAGGG[C/T]GGGCAACTGAACACA | 16443 |
| rs247296691 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91755485 | TTCATAAGTCCATTG[A/G]TAATGTGGCAATTTC | 16443 |
| rs247307332 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91893775 | GCGGGCGACTCACCT[C/T]CCATGTTTCTGTGCA | 16443 |
| rs247324001 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91751449 | CATCGTTCCTACTTG[C/T]GGGCGCCATGCGTGT | 16443 |
| rs247326220 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91760691 | CTCCCCGACAGCACC[A/G]CACCCGGAACCAGGT | 16443 |
| rs247346918 | snp | C/T | | | intron-variant, missense | Itsn1 | Mm_Celera | 16:91853151 | ATAGTGTGTTTCACT[C/T]CACCCAATGATACAC | 16443 |
| rs247354424 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91759899 | CTTATCTAATCTAAC[A/G]GGAATATCCTTTGAG | 16443 |
| rs247367957 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91841185 | CTCTGAGCAGCACCC[A/T]GGGTGGGGAGCAGAG | 16443 |
| rs247402505 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852670 | AAGGGTCAGGGGTCA[A/T]GAGCACACTCATGGG | 16443 |
| rs247402826 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91863003 | GGTTCTTTGACAGGA[C/T]GCATGGGGGCAGGCA | 16443 |
| rs247410689 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91861163 | GATGAACTCTTCAGC[G/T]TGCCAATGAGACCTT | 16443 |
| rs247416680 | in-del | -/CCG | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91818687 | GAGTGAGCAGTGTGC[-/CCG]CCGCCCGCCCGCGGC | 16443 |
| rs247421948 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872660 | CTCCTCACTTTCAAC[C/T]CTCCGATCCCCTCTC | 16443 |
| rs247423569 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91861582 | AGGTCAGAGGCAAGG[C/T]GACAGCATCAGGTGA | 16443 |
| rs247423851 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899996 | ccctcctcctctccc[C/T]cctcctctccctcct | 16443 |
| rs247427744 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91765398 | CTATTGAAAGGAGAA[A/G]GAGAAAGCAGCCTCT | 16443 |
| rs247427983 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91816674 | GATGGCTTGCAGAGC[A/G]CTGGGGATCAGAGCA | 16443 |
| rs247457953 | in-del | -/AAA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91886124 | TAAAGATCATCTAAT[-/AAA]AAAAAAAAAGTATAT | 16443 |
| rs247473477 | snp | A/G | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | GRCm38.p3 | 16:91727683 | CCGCACGTGAGTGGC[A/G]TGCCCTTAGGATGAG | 16443 |
| rs247480724 | snp | C/T | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91871458 | TCCCTCCGTGCTGCT[C/T]CTGGGGAGAGGCCAT | 16443 |
| rs247496744 | in-del | -/CT | | | intron-variant | Itsn1 | Mm_Celera | 16:91890963 | TCACATACACACACA[-/CT]CACACACACACACAC | 16443 |
| rs247536578 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91762610 | AAGTGCTCGCCTGAA[C/T]ATCCTCTGGCTTCTC | 16443 |
| rs247538228 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91813609 | GATCTCTTTCCTTTC[C/T]TCTCTATCCTTTTTT | 16443 |
| rs247538831 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91877033 | TGTCCTGCCCTGCCC[G/T]GCCCCCCACCCCCTG | 16443 |
| rs247544788 | in-del | -/TG | | | intron-variant | Itsn1 | Mm_Celera | 16:91784845 | AGCTGAGGCATCTGC[-/TG]TGTGTGTGCCTGGTT | 16443 |
| rs247555936 | in-del | -/CGCGCGCGCG | | | intron-variant | Itsn1 | Mm_Celera | 16:91906652 | ACTGGGTTGCACGCA[-/CGCGCGCGCG]CGCGCGCGCACACAC | 16443 |
| rs247567176 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823045 | ATTATGAGATAAGTG[C/T]ATCCTCTGTGCTGCC | 16443 |
| rs247583655 | snp | C/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831304 | GTTACACTTTGCTAT[C/G]GTCTCATAAAGGAAA | 16443 |
| rs247591539 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91736160 | ATTCATCCTCTCTCA[A/G]CCTCTTCCCGGTAGA | 16443 |
| rs247594135 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91905619 | CTAATGGGAGGAGCT[-/A]AAAAAAGGAAAAGGG | 16443 |
| rs247616648 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91865316 | GCCCAAACGAGAGCC[A/G]CAGCATGCAGTGTAA | 16443 |
| rs247622649 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91884726 | GGCTGCCCTGGAACT[C/T]ACTCTGTAGACCAGG | 16443 |
| rs247628093 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91768873 | CAGGGATTGGTTCTT[G/T]CCCGTGGGATGGGTC | 16443 |
| rs247632969 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91874112 | AGGTTTCTCCTTGTC[C/T]TCTGTTTCCTTGAAC | 16443 |
| rs247640954 | in-del | -/CCGGCCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91862239 | CAGACTAGCTGGGAG[-/CCGGCCT]CCGGCCTCCGGGCTT | 16443 |
| rs247683332 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91859748 | ATAAGCTGTTACCCA[-/G]GAAAACCAAAAGCTC | 16443 |
| rs247688867 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830783 | TCTTCCGCTAAAGGT[C/T]TTACCCATTTTCTTT | 16443 |
| rs247695219 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91837859 | GGGCTAGGGACTAGG[C/T]GTCCTAGGGCAATGG | 16443 |
| rs247696097 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91733417 | TTTCCTCCTTCTCTT[C/T]CTCCTTCTCTTCTTT | 16443 |
| rs247718814 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91769660 | GTTAGAGGCAATTGT[A/G]AGCCACTGATGTGGA | 16443 |
| rs247745383 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91808721 | CAAGGACTGTGCACA[-/T]TCCTGCATCCTAACT | 16443 |
| rs247746716 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91837055 | AACTATCCTGACTCC[G/T]TCTAGGAACTGAGAG | 16443 |
| rs247749001 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91778631 | CACCTCAGTTTTCCT[C/G]TCTGAAGTGGTTTTA | 16443 |
| rs247750657 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91769020 | TCTTACTTTCCCAAC[G/T]CCAAATTGATTGATG | 16443 |
| rs247768276 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892802 | acaaacaaaaaaaaa[A/C]AATGTGGGAGAAAGA | 16443 |
| rs247789130 | in-del | -/AAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91886376 | GGACCACTTTTATGT[-/AAA]AAAAAAAAAAGGGGG | 16443 |
| rs247799160 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915896 | CCCTCCTCCCCTGTA[C/T]CTCCCCGCTCCTCCC | 16443 |
| rs247824046 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91882081 | ATAACATGGCCTTTT[A/C]TATGCCCTGTGTCTC | 16443 |
| rs247828915 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91777815 | GAGGTACAGCCACAG[A/G]TTGCCCAGGCATTGG | 16443 |
| rs247832811 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91881542 | TCCATCGCTGCCTTC[A/G]GTTCCAAGCACAGAT | 16443 |
| rs247834603 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91793351 | CTTCAAAAGTAAGGA[A/C]TCTTCAAATTCGACT | 16443 |
| rs247835305 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91888670 | TTTAACAGAGCCCAG[A/G]AAGAGGGAAGCATTG | 16443 |
| rs247843453 | in-del | -/TCAGATCGT | | | cds-indel | Itsn1 | Mm_Celera | 16:91919876 | TGCTGAATATTGCTG[-/TCAGATCGT]TCTCTCAAATGATGC | 16443 |
| rs247850029 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872878 | CTGTGGTCCATTCCC[A/G]TGTAGCCAGTGCTGA | 16443 |
| rs247859951 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91767339 | CCAGCTGTCATGCGC[A/G]ATGACCTGAATTCAG | 16443 |
| rs247860883 | snp | A/G | | | upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91728853 | TTTATGCAAATTAGA[A/G]TAAAAGGCCACACCC | 16443 |
| rs247890965 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91888282 | AGTGATTGCCTCTTT[G/T]GTGTTATGGGAGTTT | 16443 |
| rs247904366 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91899689 | TAGCCACCTACTGGG[C/T]GGGACCTGGACCCCT | 16443 |
| rs247921120 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91737565 | CTTGTCTTTATCTTT[C/T]TGATGAGGATGATGA | 16443 |
| rs247932643 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91775320 | AACATTCGACACATC[C/T]TGCCCTAGGCTCCTT | 16443 |
| rs247937587 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91850789 | TTACTGCTTACGGTG[C/T]GTGCCTTTCCTTCCA | 16443 |
| rs247951472 | snp | G/T | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91872005 | TGGATAAAGGCAGAC[G/T]TGCATATTTCCTTGT | 16443 |
| rs247953538 | in-del | -/ACCCCGACTCTTCCACA | | | intron-variant | Itsn1 | Mm_Celera | 16:91768716 | AGATCCCTCAATTCT[-/ACCCCGACTCTTCCACA]AGACTCCCTGAGCTT | 16443 |
| rs247963627 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745865 | CGTTATCTGGAAGAA[C/T]TGCCTTTTCCTTTAA | 16443 |
| rs247968543 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91774820 | GTTAGGTTTGGGTCA[A/G]TGTTCTCTCCTTTAT | 16443 |
| rs247986991 | in-del | -/TCCAGCCTGGGCTGCAGACATGGTCTCAAAACT | | | intron-variant | Itsn1 | Mm_Celera | 16:91797313 | GATTGTAGGTTCAAG[lengthTooLong]TCTTTTTTTTGCCCA | 16443 |
| rs248013353 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91879095 | GGATGCTAGGAACCA[A/T]CTTAGCTGCTGGGCT | 16443 |
| rs248015117 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91797248 | CCGAAACACGTGAGC[C/T]GGGAATGGCAGCATA | 16443 |
| rs248027927 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91878742 | GTCTCCTCCGCAAGT[A/G]TGGCGGCCTCACAGA | 16443 |
| rs248034470 | snp | C/T | | | missense | Itsn1 | Mm_Celera | 16:91839813 | AGGAGCCAGCTAAGC[C/T]GGCCACCCAGGCACC | 16443 |
| rs248045656 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91736388 | CAGTGCTTCTTACCT[A/T]ACCCTGAGTGGTAGA | 16443 |
| rs248049119 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91764079 | CAGCACACAGCTTCC[C/T]AGCCCCGTGACAGAT | 16443 |
| rs248063229 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745547 | GTGATGGGGCAAGGC[A/G]TGTTACCATTTCAAG | 16443 |
| rs248064163 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91754185 | AGTGTTCCATTATCT[G/T]TAATTTATCAAGCTC | 16443 |
| rs248086856 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91846968 | TGACAGGCATCCGGA[A/G]CAGAGAACCAAAGCT | 16443 |
| rs248113966 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91855691 | TGCAATCAGGTCTCA[C/G]TAGTGGGGGAGAATT | 16443 |
| rs248130555 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91767402 | GACTGGTGCACTCTG[-/C]CCCCCCACATATGTG | 16443 |
| rs248147427 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91743674 | TTTGTTTTGTTTTTG[A/T]TTTTTGTTTTTTGAG | 16443 |
| rs248153715 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91845006 | CTGTGGCGGGCGCGA[A/G]CTGTGTGTCCTCCTG | 16443 |
| rs248164350 | in-del | -/CAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91783650 | GAGGCACAATTGAGA[-/CAT]CATACAGGTGACTCA | 16443 |
| rs248171212 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91855027 | TAATCCAAGATATTA[C/T]TCACCAGGCTATGAA | 16443 |
| rs248176104 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91743146 | CAGGGTATTGAATTT[A/C]GGGTTTGCACGTGCT | 16443 |
| rs248181859 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91864346 | GGGGGGAGGAAGTGG[G/T]GGGGGTTAGGAAGGG | 16443 |
| rs248195328 | in-del | -/GT | | | intron-variant | Itsn1 | Mm_Celera | 16:91872286 | CCACATAAGCATAGA[-/GT]GTGTGTGTGTGTGTG | 16443 |
| rs248202349 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852707 | TGGCCAGTTATGCTC[C/T]GGCAAGTGCAGGCAG | 16443 |
| rs248202761 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91844648 | ACCATCACACAGACA[C/T]ACATGCCAGCAAAAC | 16443 |
| rs248222592 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91818722 | CCGAGATTCAGGCGC[C/T]GCCCTGCCCTTGTGA | 16443 |
| rs248235437 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91863168 | CTGCAGAGTTCCATG[A/G]CGTTGGTGTCTGATC | 16443 |
| rs248263793 | snp | C/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914406 | TTTTTGACCAGCTAG[C/G]CTTCAGTTCCTACAA | 16443 |
| rs248275340 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91821653 | CTGAATTCCCCACTT[C/G]AGGCTTCATGTCAAT | 16443 |
| rs248277987 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91826347 | AATAATACCCAAAGA[G/T]ATTGAGAGTAAAGAT | 16443 |
| rs248286823 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91770186 | TGTCCCAGCGTCACC[A/G]TGCACACATGGTGTC | 16443 |
| rs248305413 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872253 | TCGTTCTAAGGAGCA[A/G]ACAGGTGAAGACAAT | 16443 |
| rs248309629 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852159 | AAACTGAATTCAGTG[G/T]TCTCTAGCAGTACTG | 16443 |
| rs248321354 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91879289 | GTAGAAGAAAAGATG[G/T]TGGGCCCCCTGGGAA | 16443 |
| rs248339976 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91825455 | TAGCTATCTTCAGAC[A/G]CACCAGAAGAGGTTA | 16443 |
| rs248340406 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91825659 | TTTAATTTTTAAGTA[C/T]TTATTTGTTTCTTGT | 16443 |
| rs248402937 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91875483 | GCTACTGCTTTACCA[A/G]AGGAGAGATTTCAGA | 16443 |
| rs248414040 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91882746 | AGAGGAGAGTCTTTC[C/T]CCCCCTCCCTAAGAA | 16443 |
| rs248439959 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91828590 | CTGTGTTCACTGAGG[A/G]TTACCCAGGTGCTTT | 16443 |
| rs248449152 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91832836 | TTGCAGTTAAATATA[C/G]AACGTCCATTTTCTT | 16443 |
| rs248454631 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91735768 | GGTAAGCGGGCTCTG[G/T]GTAAGCAGCTGCCTG | 16443 |
| rs248475493 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91823256 | TTTACATTTCCAAAT[C/G]TAGGAATAGCTTCTC | 16443 |
| rs248475818 | in-del | -/TCTCTC | | | intron-variant | Itsn1 | Mm_Celera | 16:91754629 | CTCTCTGTCTCTCTG[-/TCTCTC]TCTCTCTCTCTCTCT | 16443 |
| rs248484230 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91822781 | TTCACTTTCGCTCTT[C/T]GCTTGTGCTGTTTTG | 16443 |
| rs248486727 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91827732 | ATGTCACACCCACCC[-/T]TCGTAAGCAGAACCA | 16443 |
| rs248494664 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91743740 | ACTCACTCTGTAGAC[A/C]AAGCTGGCCTCAAAC | 16443 |
| rs248495118 | snp | A/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919514 | GATGCTCCAAGCCCT[A/T]TGAGGCTCTGTTTGC | 16443 |
| rs248512013 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91832349 | TTATGAGAGAAAGGG[A/G]CAAAGACAGTCTCCT | 16443 |
| rs248549303 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830500 | GCAAGAAGACAGAGC[C/T]GTTGGCCGGCCTTAG | 16443 |
| rs248567984 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91739218 | CTTGCTGAGCCTAGA[A/G]CTCCACTGGTGACCA | 16443 |
| rs248577224 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795263 | TAGCAATGGCACAGG[C/T]GACCTAGCCTGAAGC | 16443 |
| rs248615167 | in-del | -/CCAGGACGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91743419 | CAAAGTGAAGCCATT[-/CCAGGACGC]AAGACTGGTTCAATA | 16443 |
| rs248615945 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746261 | TGTCAGTAGTTAAAT[A/G]CGGAGTTATCATATG | 16443 |
| rs248618102 | snp | G/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803771 | ATGCCATTGTCCTAA[G/T]TTTTTTACAAACAGA | 16443 |
| rs248621955 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91845208 | TTGTCAGGGATCGGG[A/G]CGTAGGGTGGGAAAG | 16443 |
| rs248628824 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91791982 | TGGAATTTTTACCTG[C/T]GGGACTGTCTTCCTA | 16443 |
| rs248637060 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91793858 | TTTTCGGCTAGTGTT[A/G]CTAAATATTGGCAGC | 16443 |
| rs248650975 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91901267 | CTTTCTTCCCTGTGG[A/T]TTTCCCCTCTTCTAA | 16443 |
| rs248694965 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91811622 | TATCTGAGGCAGAAG[A/T]TATTCAATCTATAGG | 16443 |
| rs248695074 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91803425 | CTTCTTAATTTTCTT[A/G]AAGGTTTATTTTATG | 16443 |
| rs248696419 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852844 | AAGCAGATAATAAGC[A/G]CCTCGCCTGCCTTTG | 16443 |
| rs248726866 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91793077 | AGCATAGTAGTGTCC[C/T]AGTATAGGATAGCAT | 16443 |
| rs248726908 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91801998 | ATTCTTTAACTTCCA[C/T]GAGTTAGTTGCTAAT | 16443 |
| rs248731782 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91799465 | GCAAAGAATGAACAT[A/C]AAACTTTTATTCTAA | 16443 |
| rs248735656 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907677 | TGTGTTCATTACTTA[C/T]GGGCAGAGCTGTTAC | 16443 |
| rs248748309 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898633 | AGCTGAGAGTTCTAC[A/G]TCTTCATCTGAAGGC | 16443 |
| rs248761262 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91910890 | TACATAGGAGCCAGC[-/G]GGGCCCAGAAGAAAG | 16443 |
| rs248767854 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91900148 | TCCTTTTCTGTATGA[A/G]CAGTGATTTCTGTTT | 16443 |
| rs248781447 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91765922 | GAGAACAGGAGCTGG[A/G]ACACTCGGTCACTGG | 16443 |
| rs248789417 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91801007 | CACTTTACTGACTGA[A/G]CCTCATCTCTGACCC | 16443 |
| rs248793924 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91903793 | TGTCCCGACAAGCAT[A/G]ATGCTGGAGAAGGAG | 16443 |
| rs248833906 | in-del | -/GAG | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802431 | GTGTGTTCCCAGTGA[-/GAG]GAGGAGTCTAATACG | 16443 |
| rs248838105 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91856177 | CTGCCGGCCTCGAGG[A/G]AGGAACAGTGGTAGG | 16443 |
| rs248840240 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91776070 | TGAGTGGCTTTGCAT[C/T]TGTACTCTCGGGATC | 16443 |
| rs248848593 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91904554 | CCACCGAATTCTGCA[A/G]CCCCTCTTGTCCTGG | 16443 |
| rs248853883 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915182 | TTCACTCAGTGCCAA[C/T]GTGTGTTCTAGACGT | 16443 |
| rs248862451 | in-del | -/GCGAGCTGTGTGTCCTCCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91845002 | AAAGCTGTGGCGGGC[-/GCGAGCTGTGTGTCCTCCT]GCAGTGTGGGTCCTG | 16443 |
| rs248866142 | in-del | -/GGGGGTGG | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91730201 | TTGCGGTCCCTTCTT[-/GGGGGTGG]GGGGGGGCACCAGAA | 16443 |
| rs248877866 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914007 | CAGTATAGGGTCACC[A/G]TTACAATCCCTTCCC | 16443 |
| rs248882296 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91906734 | TGCCTTGTTCCTTAA[C/T]GCCCTTGTATTATGA | 16443 |
| rs248895362 | in-del | -/AG | | | intron-variant | Itsn1 | Mm_Celera | 16:91886388 | TGTAAAAAAAAAAAA[-/AG]GGGGGGGGACCAGCC | 16443 |
| rs248908504 | snp | A/G | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | GRCm38.p3 | 16:91728039 | AGAATCAGTATCTGC[A/G]CCTCCTCACGACCCT | 16443 |
| rs248909588 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91774238 | CCCCATCCAAGAAGC[A/T]AACGCTTTTGATTTA | 16443 |
| rs248916424 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91832992 | AAATATTATTGTATC[A/G]TAAAACTCAAGGGGG | 16443 |
| rs248919122 | snp | G/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913532 | CTCCATGTGACCCCA[G/T]AAGGTCCCTCTCCGT | 16443 |
| rs248937429 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91770878 | TGGCTCTAATCGCCG[C/G]GTCCCTACCCCTTTT | 16443 |
| rs248951407 | in-del | -/CGGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91766001 | TGTTGTGAAATGGAG[-/CGGT]CGGTGTGTGCCACTG | 16443 |
| rs248964802 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768727 | TTCTACCCCGACTCT[C/T]CCACAAGACTCCCTG | 16443 |
| rs248966806 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91781216 | TATTTGGGGAAGAGG[A/T]CTTGGTCTCCTGTTG | 16443 |
| rs248971869 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91770074 | TAAAGGCTGTACTCT[A/C]CTTGCCTTTTACTGT | 16443 |
| rs248973078 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91839416 | TGTGTGTGGGGTTTT[G/T]GTAAGTCATGTGACT | 16443 |
| rs248979023 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91780917 | TTACGTTTCCAGAGG[A/G]ATAAGAGTAGTGATG | 16443 |
| rs249001151 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91887017 | TCTGGTGGGTGTTAG[C/T]GGGTCATTTAACCCT | 16443 |
| rs249010170 | in-del | -/TGGA | | | intron-variant | Itsn1 | Mm_Celera | 16:91859625 | CCTAAGTTTTCTGTG[-/TGGA]TGGATGGATGGATGG | 16443 |
| rs249012542 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91885617 | GGGAGCAAAACCTAC[C/G]ACTGTAACTCTAGGA | 16443 |
| rs249023180 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91891184 | CCCGGACTCAGAAGG[A/G]ACTTTCACTCTGATC | 16443 |
| rs249023342 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91884973 | GACATTTGTGAGACT[C/T]GCTGGCCCACTGTTG | 16443 |
| rs249055003 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91875223 | TGGTCCTTGGTAGCG[-/T]TTAAAGCTAGTGTTC | 16443 |
| rs249072800 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890644 | AAGCCTCGAACTCAC[A/C]GAGATCCTTCTGAGT | 16443 |
| rs249077052 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91778135 | TATGAATTTAATCTA[A/G]CATTGGTCACTACTT | 16443 |
| rs249091244 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91882565 | CTTAAGAAAAGAACA[G/T]TCTCTGCTCACTTCT | 16443 |
| rs249120549 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91752134 | AACTCTCACGGAGAG[A/T]TGCTTCTGTCGGGTG | 16443 |
| rs249125763 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91739782 | AAGGGCCTAGTCTGT[A/G]TGTGCTCTTTGGTTG | 16443 |
| rs249139086 | in-del | -/AGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91810217 | GCTCTGAGTGGAGAG[-/AGC]TGTAACAAGGAGCTG | 16443 |
| rs249141662 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91759757 | GTTTTCTCTTCTAGG[A/T]TTTACTTTGATTTCC | 16443 |
| rs249142571 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803854 | CATGTGAGAGCTGTG[C/T]TCAGCAGCAGCACCA | 16443 |
| rs249143242 | in-del | -/ACACAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91823301 | ATTAAGCACACACAT[-/ACACAC]ACACACACACACACT | 16443 |
| rs249147303 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91881865 | TAACAACACCTGTTG[C/T]ATAGACAGGAACTCC | 16443 |
| rs249147410 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91888932 | CAGAGGTTCGCCTGG[A/G]CTCCCCTTGTCAAGC | 16443 |
| rs249158730 | in-del | -/AT | | | intron-variant | Itsn1 | Mm_Celera | 16:91890902 | CCTTCACACACACAC[-/AT]ACACACACACACTCA | 16443 |
| rs249159771 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91749071 | ACACATGGACAAAAG[A/G]AAATAGAAGAATGAG | 16443 |
| rs249161398 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91861398 | TTAATTAAATGTCCT[G/T]GGCTCTCAAGTGTGC | 16443 |
| rs249161680 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91888474 | GTGCAGAACAAGGCT[C/T]CCAAGGATCAGCCAC | 16443 |
| rs249169575 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91738932 | TTTAGTTAACAGGTG[C/T]TGAAAGTGTTGTCCG | 16443 |
| rs249179295 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91811701 | TAATCTGACCAAAGG[C/G]GCAGTCTGTTTGACG | 16443 |
| rs249185425 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91751406 | GGGGGAAAATACCAA[-/C]CCCCTAACCTCCAAG | 16443 |
| rs249189118 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907720 | TGCCTGCCTCAAATG[C/T]GCAGAATTCTGGGTT | 16443 |
| rs249190775 | in-del | -/A | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878191 | AGGAAGGAAGGAAGG[-/A]AGGAAGGAAGGAAGG | 16443 |
| rs249200001 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91819998 | AATGTAAAATGCCGC[A/G]GATTCAAAACTCCAC | 16443 |
| rs249210553 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914065 | TGATGTTGAACATCA[A/G]TGTTCCTGTAGGAAG | 16443 |
| rs249212336 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91826656 | TTTACTTCTTCTGTG[G/T]GTCTGTGTGTCTCTG | 16443 |
| rs249213050 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91757672 | TGCAGACACGGGATC[C/T]AGAGCATGGTAGCTG | 16443 |
| rs249217134 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91890224 | TACCAGACTCTTGGG[C/T]TCTCATCTCACTGTT | 16443 |
| rs249217223 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91748482 | AAAATCTGGCAGGCA[C/T]GGCAGTTGTACTGCT | 16443 |
| rs249223459 | in-del | -/CTAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91756578 | CACCATGACTCAGTG[-/CTAC]CTACCTCTTTTACTG | 16443 |
| rs249223619 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91777280 | AGTTGTATGCCACCC[C/T]AATTGTCTTGTAAGC | 16443 |
| rs249223680 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91909061 | GGGGTCTGAAATTGA[A/G]TCCCACTAATGGATT | 16443 |
| rs249240969 | snp | A/G | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91871214 | CTGCAATTAATTTCC[A/G]GTGTTTACATTTTTT | 16443 |
| rs249268748 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91818975 | AGCACCGCCCTTCTA[C/T]GTGAACCAAATATCA | 16443 |
| rs249272758 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746085 | GATGCTCTACATGAT[A/G]GAAACAAGATTGCAC | 16443 |
| rs249294371 | in-del | -/AG | | | intron-variant | Itsn1 | Mm_Celera | 16:91822351 | GTTTTCTCTCCTACC[-/AG]ATGTGAGTTCAGGTC | 16443 |
| rs249316661 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745690 | CATGCTGTTGTAAGG[A/G]TGGTCAGGCAGTTAG | 16443 |
| rs249326594 | snp | C/G | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91818478 | GAAGCGCCGCCAAGC[C/G]CTCTTGGAGCAGCAG | 16443 |
| rs249332401 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91881168 | GATATTAATTAAAAA[C/T]TATGGCTGCTTTTGA | 16443 |
| rs249334921 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91781342 | TTTTTCTTGAGGTTT[C/T]GTTTTTAGAAGAGCT | 16443 |
| rs249343869 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91825236 | GTTTTTGTTTCCATT[A/T]ACTTATTTAGAGTTT | 16443 |
| rs249378449 | in-del | -/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830752 | AATCTACTTTTATTC[-/T]TTTCCCTAGACTCAT | 16443 |
| rs249399176 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823981 | ATTGGTACTGAATTT[C/T]CTTCTTCCTACATCC | 16443 |
| rs249413292 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831360 | CTGACATAGAGGCTC[C/T]TTCCTGTGCTGGAGA | 16443 |
| rs249416346 | in-del | -/CTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91774848 | ATTCTTCAGAGAGAC[-/CTG]CTGCATGGTTGGTCT | 16443 |
| rs249419614 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91837896 | CAGACCTGGCAGCCC[A/G]CTGCTGCTGGGCACA | 16443 |
| rs249420491 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919537 | CTGTTTGCCGTTTGC[A/G]GATGTGGACCCATGT | 16443 |
| rs249438991 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91789500 | TTCTGCCCATCCACA[C/T]TAGGTTGTTTCCGTG | 16443 |
| rs249446810 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91788744 | CCTAAGTTCACCTAG[A/T]TACTCCTCTCCCATC | 16443 |
| rs249478896 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91774347 | CTGGGGGTCTTTTTT[-/C]CCCCTCCATTCTGTT | 16443 |
| rs249492303 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91891342 | TGACCAAAGCAACTC[C/G]GGGAGGAAAGGGTTT | 16443 |
| rs249505695 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890805 | GGGGGGGGGCGATGT[C/G]TCTCAAGTATCCCTT | 16443 |
| rs249507691 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91794610 | TAGACTCCACAACTC[G/T]GCATTTGATTGCATG | 16443 |
| rs249509650 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91787690 | CCCTGCCACAGGGGT[C/G]GCCTGTGTCAGAGCC | 16443 |
| rs249532375 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91832741 | AAACATTAATCTGAA[C/T]CTTCTTAGAATTTAG | 16443 |
| rs249537247 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91744730 | GCCACCATTGCATCA[A/G]TGGGCACATCCTGCC | 16443 |
| rs249552014 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91895638 | AGTGGTTGGGAAGCT[A/G]GGTGGTTGGGAGGAT | 16443 |
| rs249554826 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91896131 | CCTATCCAGGGTCCC[A/G]TCCTCCCTCTACATA | 16443 |
| rs249568369 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91793966 | TCAAGGACACGCTCG[C/T]ACTCGGCTGCTGCAG | 16443 |
| rs249586053 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91895163 | CAGAGCCTCCCATAA[G/T]TGCAGTGCTCTGTGT | 16443 |
| rs249593441 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91797229 | GCCTCCCGTCTCAGT[A/G]AGGCCGAAACACGTG | 16443 |
| rs249593694 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91753257 | CTAGATTAGAGGGAA[A/G]GAAGGGCTGTATGCG | 16443 |
| rs249595631 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91886968 | ACCACTCAAGGCAGC[A/G]GTCAGCTCCCGAAAC | 16443 |
| rs249616729 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91795178 | TGTTAGGTTAGTAGG[A/T]CAAGGGTCTATGAGA | 16443 |
| rs249620259 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91900178 | TCTAGATTAGCCACC[A/G]AACCTCCTGCATGCT | 16443 |
| rs249620266 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91757132 | ACAGGATGGCATGGC[C/T]TCTCATTGGCTCTCC | 16443 |
| rs249663814 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91757748 | AAGGAAGGAAGTTAA[A/G]TATTTTCATATTTGG | 16443 |
| rs249673418 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91804855 | GTGTGACATGATTCT[C/T]TGTAAGCATGGAAGG | 16443 |
| rs249680259 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91794754 | ATAAGAGGCCGTTAT[A/G]GCTTCTCCTCCGAGA | 16443 |
| rs249700468 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91901108 | TCTTCCTGTCTCTCA[A/G]CCTCCACTCTCTTCT | 16443 |
| rs249703146 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810552 | GCAGAGCTAGCCAGG[A/G]CTAACAGAAGCATTA | 16443 |
| rs249708791 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91764963 | GACCTGAGCATGACC[A/G]TTCTTTGGATCTTTA | 16443 |
| rs249730088 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91869039 | ACCAGTCGTGCAGTC[A/G]AAAGAAAAGGAGAAA | 16443 |
| rs249739527 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91900531 | CAGCGTCTCAGCCTG[A/G]GATTCATCTGTCTTT | 16443 |
| rs249742694 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917659 | TCATTCAGAAGCGGG[C/T]TTATTCCGTCAGCCT | 16443 |
| rs249744065 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91868430 | CAGTAGGTCAAGAGT[G/T]AGAGCCGTGGGGGTC | 16443 |
| rs249746139 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91764463 | TGCAGTGTGTGTCTA[G/T]AGAACTTTGAAGCTG | 16443 |
| rs249761688 | snp | A/G | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91899552 | CCACAGCCACCTGAA[A/G]CATGCCCTGGAAAAG | 16443 |
| rs249764506 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91816710 | AGGCCCTGACACGTG[C/T]GCACATGCGCCAGCA | 16443 |
| rs249779840 | snp | A/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91912632 | CGGTGGTGGCATGCT[A/T]CAGGGTGATTCCGTT | 16443 |
| rs249792241 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91811730 | CGCTCTAGTCTTTGG[-/T]TTTTTTTTTGAGACA | 16443 |
| rs249795869 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91732364 | AGGGTGGATGGGTGA[A/G]CCACACTGCCTCCAT | 16443 |
| rs249832556 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91835395 | TTAGCATGGCAAAGC[A/G]GGGGAGGGCTGTGCT | 16443 |
| rs249834394 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91765764 | AGAAACCCTGTCTCG[A/G]AAAACAAACAAACAA | 16443 |
| rs249849034 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91785998 | GTATTTAATCATAAT[A/G]ATTGGCATTTGTGGG | 16443 |
| rs249858529 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91867705 | CAGCTGCCTTTTGGG[A/G]CTGGGAATTGAAATC | 16443 |
| rs249864258 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91792521 | TTTCTATGTATAGAG[A/G]ATCCTTCTAAACTGA | 16443 |
| rs249871414 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91765122 | TACTCTGCATAAAGT[A/T]GGGGTCCAGGTGTTT | 16443 |
| rs249873944 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91773871 | TTGTTTTCTTTGGCC[A/G]TTAATAGGGCTCCCC | 16443 |
| rs249875582 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91780073 | CGTGTTGGGACCATC[C/T]CACAGCTAGGTCTCT | 16443 |
| rs249911717 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91877473 | GATTATGTCTCCACC[A/G]TGACTTAAGAGATGG | 16443 |
| rs249916225 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91876104 | AGCAGGCAAAGCCAA[G/T]CAGGGATCTTGGCTG | 16443 |
| rs249926946 | in-del | -/GA | | | intron-variant | Itsn1 | Mm_Celera | 16:91757338 | TGAAGGGTAGTCAAC[-/GA]GAGGTGTGGCTTGGT | 16443 |
| rs249928558 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91875399 | GAGCTGTTCTTGGGA[A/G]ACAAGTGATTTATGC | 16443 |
| rs249932102 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91733710 | TTGTGACCAGGCTAG[C/T]GTCAGTCTTATCGAG | 16443 |
| rs249936433 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91787214 | TGCTTACATCACCTA[C/T]AATTTCCTTGAATTT | 16443 |
| rs249937747 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91732897 | CCTCCAAGTGCTGGG[A/G]TTTCAAGCATGTGTC | 16443 |
| rs249950471 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894334 | AGAGGGCATCAGGTC[C/T]CATTACAGATGGTTG | 16443 |
| rs249979362 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91732272 | GCAGAGGTTTTACAT[A/G]CTGTGATGAGGGTTT | 16443 |
| rs249980556 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890150 | GGAAGCAGTAGGCAC[A/G]GGCTCTCCTCCCTCT | 16443 |
| rs250005776 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91836304 | ATTATTTCTTGGGGG[A/G]CAGGGTTGCTATAAA | 16443 |
| rs250018045 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91843660 | GGATGGAGTTGACTC[G/T]GCCATGCATTGCCCA | 16443 |
| rs250028016 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91885189 | GCAGGGACTGAATAT[G/T]CCTTCCACAGCTCAA | 16443 |
| rs250052257 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91876932 | TAACAAGCCCCAAAT[A/C]TTGCTTTGCCCCCAT | 16443 |
| rs250057943 | in-del | -/TTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91896295 | GATTTCTGAACCACA[-/TTTT]TTTTAAAAAAAAATA | 16443 |
| rs250067049 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91884599 | GCAGTGCAGCACGAC[G/T]CAGCACAGCCATGGC | 16443 |
| rs250068854 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91739948 | CTCTCAGTTTTAAAC[A/G]CACATTGCTAGCATT | 16443 |
| rs250081142 | in-del | -/GTTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91758919 | TTTGTTTCTTTGTTT[-/GTTG]TTGGTTTTTTCGAGA | 16443 |
| rs250088974 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91754833 | GTAAATGGTGGTGGC[A/G]TTCCCTTCTTAAATC | 16443 |
| rs250107433 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91739180 | GTATCGCTCTTCCAC[A/G]TTATTCTCTTTTGTC | 16443 |
| rs250114915 | in-del | -/CCC | | | intron-variant | Itsn1 | Mm_Celera | 16:91892081 | CCTTAGCTGGTTCCT[-/CCC]CATGTTGATCATGGC | 16443 |
| rs250116071 | in-del | -/GAGCAGTTGC | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91853509 | CTCCACTTTTGAAAT[-/GAGCAGTTGC]TGAGAAGCCACAAGG | 16443 |
| rs250120929 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91741937 | TCTGTTTGCATGTGA[C/T]CTTGATTGTGTATGT | 16443 |
| rs250121129 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91894989 | CGGAAGATCGTGGGC[A/G]TGAACTCTGGCCTTT | 16443 |
| rs250167302 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91763055 | TTTGGCAGAGGCTCA[C/T]AAGGCCTCAATCCAG | 16443 |
| rs250171143 | in-del | -/AA | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91828613 | GTGCTTTTCTGTTTT[-/AA]AACTGAAATTTCCCT | 16443 |
| rs250174237 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91755660 | AAAGGCGTGCGCCAC[C/T]ACGCCCAGCCCATGT | 16443 |
| rs250194229 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91748589 | ATTTGCCTGTGTGGG[A/G]GGCATTTTCTTGGTT | 16443 |
| rs250198719 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91741087 | GTCTTTGCCTTGAAG[A/G]AAGGCCGCCAGCACT | 16443 |
| rs250205294 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91851388 | ACACAGGGGTTGTTA[C/T]TGTGAACATTTCTCC | 16443 |
| rs250205708 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91841076 | GTCATGAGGACGCTG[C/T]GTAGACCGACCTTTG | 16443 |
| rs250205833 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91849620 | TGGTGGAGGGGAACC[C/T]AGACCATCTGTGGGG | 16443 |
| rs250240746 | snp | A/G | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91747901 | AGGGGTTGGCTGAGA[A/G]GTGAGGGTGAGCTAT | 16443 |
| rs250259639 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91848172 | AACATTTTCAACAGA[A/G]GGCTCTATTCTTGTG | 16443 |
| rs250267002 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91764162 | CTACAGGGAATCCAC[A/G]CAGAGAGCACAGGAG | 16443 |
| rs250272304 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91850529 | GTGCTTGTTGGTTGA[A/G]ATGGAGTCTCCTATA | 16443 |
| rs250272980 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867321 | GACATCACACAGAGC[A/T]CAGGCATGGCAGTGC | 16443 |
| rs250276881 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91910408 | GAATATGATTTTTTT[-/A]AAAATTTAAGTACAC | 16443 |
| rs250285417 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91820391 | TTACTAGGCATTTTT[A/T]AAAAAGCAACATTGC | 16443 |
| rs250295136 | snp | C/T | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91815537 | CATCCCTCCTTCCTT[C/T]AGGTAAGTAACGTTT | 16443 |
| rs250305211 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91866044 | CAGGGGTTAGCCACA[C/T]CTCACTTCTCCCAAA | 16443 |
| rs250324165 | in-del | -/TGTGTGTGTGTGTGTGTGTGTGAGTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91889021 | AAGTATGCACGTAGT[-/TGTGTGTGTGTGTGTGTGTGTGAGTG]TGTGTGTGTGTGTGA | 16443 |
| rs250336269 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91916436 | GATGGTTGTGAGCCA[C/T]CATGTGGTTGCTGGG | 16443 |
| rs250350330 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91814035 | GCCCCTGCTAATGCA[C/T]AATAACTTCTAATAG | 16443 |
| rs250356083 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91821641 | GCTGGTCAGGTGCTG[-/A]ATTCCCCACTTCAGG | 16443 |
| rs250371774 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91874696 | TTCCTCCCTTCTCCC[C/T]TCCCCCAACGTCCCA | 16443 |
| rs250373097 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91743524 | ATCAGCTCTTTCAGA[C/T]TATTATTTTTAAGAA | 16443 |
| rs250392918 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91857893 | AGTAGACACTCACTC[A/G]GCATCAACTAAAGGT | 16443 |
| rs250398065 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91794964 | GCTATAGTTGAGCAG[A/G]ACCGTTGGCTGTTTT | 16443 |
| rs250410721 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91820296 | CAGGGCTCTGTCAAT[C/G]CTCACCTGTGTAAGG | 16443 |
| rs250410815 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91813442 | GGTTACTGTTTGCAA[C/T]TTGTTACGTAGTCAT | 16443 |
| rs250427800 | snp | A/C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91916247 | TCTGGAGAAGAGACT[A/C/T]GCAAACTGAAGATGG | 16443 |
| rs250442963 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91729960 | CGCGGGTGCCCCCGG[C/T]CTCGAGTCCCCGGCT | 16443 |
| rs250453202 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91857241 | ATTTGTAATGTGTGT[G/T]ACAGTGTGACAGTAC | 16443 |
| rs250464505 | snp | A/C | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915511 | AACCTCTGATGGATT[A/C]TTTTCCTCTTTTAGA | 16443 |
| rs250474284 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91751389 | CATTTACTAGCACCG[C/T]CTGGGGGAAAATACC | 16443 |
| rs250486189 | in-del | -/AACATCAACAAAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91908181 | GAGAGTAAAACCAAC[-/AACATCAACAAAA]AACAACAAAAAAGCC | 16443 |
| rs250503184 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91822077 | CTAGCTGACTAGGTG[A/G]GTACAGGGGAGCACT | 16443 |
| rs250506573 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852607 | TGCTAGGGCTAAAAT[A/G]GAGGAGTCCATGTTC | 16443 |
| rs250520850 | snp | G/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91803255 | GGTTCTGAGCCACCA[G/T]GTGGTTGCTGGGACC | 16443 |
| rs250536434 | in-del | -/TCTGTGTGTGTG | | | intron-variant, cds-indel | Itsn1 | GRCm38.p3 | 16:91829782 | TCGCGGTCTTGTGAC[-/TCTGTGTGTGTG]TGTGTGTGTGTGTGT | 16443 |
| rs250536647 | snp | C/T | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91784109 | GGAAAGGGCCAAGCA[C/T]GACCAGCAGTTCCTT | 16443 |
| rs250545470 | in-del | -/AAAAAAAAAAAAACAAAAAACAAACAAACAAACAA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892760 | ACCCTTCTTTAGCAG[lengthTooLong]AAAAAAACAATGTGG | 16443 |
| rs250555551 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91738162 | TCAGTAATTATTTAA[C/T]ACCATAAATGTTACA | 16443 |
| rs250566036 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91821564 | CACTTCCTCCAGCAA[A/G]GCCACACCTTCTAAT | 16443 |
| rs250576684 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91791234 | AGAAACACACTGTGT[A/G]GCATTTCACAGTCTG | 16443 |
| rs250578746 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91828414 | TGTGAAGGCTGTCGT[A/G]GTGCCCGCTGCCCCT | 16443 |
| rs250602897 | snp | A/C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91906645 | CTAGATTACTGGGTT[A/C/G]CACGCACGCGCGCGC | 16443 |
| rs250615525 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91860387 | TAATAGCCATTCAGT[C/T]CCAGTACTGGGATAT | 16443 |
| rs250632230 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91791322 | AGTTCCAGGCTAGCC[G/T]GGGCTACCTGCAACC | 16443 |
| rs250634183 | in-del | -/AG | | | intron-variant | Itsn1 | Mm_Celera | 16:91884218 | TGTATGTGTGTGTGT[-/AG]GTGTGTGTGTGTGTG | 16443 |
| rs250636756 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91827669 | CAGCTTGTGGCCTTT[A/G]TGCTGCATCTCTGCA | 16443 |
| rs250647119 | in-del | -/AGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91755860 | CCCGGATCTTGACAT[-/AGG]AGGATGGCACATGCT | 16443 |
| rs250678323 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91797813 | GTCTTAGAAGATTGA[G/T]ATTGAGTGTAGTTTA | 16443 |
| rs250682318 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91790503 | TGCTTGGTGCCTGCA[G/T]GTGAAGCCCCAGAGG | 16443 |
| rs250685263 | in-del | -/TTTGTTTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91786020 | TTTGTGGGTTTTGTT[-/TTTGTTTG]TTTGTTTGTTTGTTT | 16443 |
| rs250720882 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91898182 | AAACAAACAACAGAA[C/T]ACACAGAAAAACGTA | 16443 |
| rs250733154 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898289 | GTCTACTTCAGCGCT[A/G]GACAGCAGAGATGGA | 16443 |
| rs250744029 | snp | A/G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91797206 | GCTGCTGCCCTAGGC[A/G/T]CCGTTCTGCCTCCCG | 16443 |
| rs250754065 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91780864 | TTCTGATTAGACATC[A/G]TCACCGAGGCAGCTT | 16443 |
| rs250766667 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91823115 | GTTGACAGTCCTTGC[A/G]GGTGAAGATGAGGGT | 16443 |
| rs250798612 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91902397 | TTTGGAGAAAATCCA[A/G]TCTGCGTTGTCAGGA | 16443 |
| rs250816021 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91890257 | TGTCTAGCTGGGTCG[-/T]TTTTTGGGGGGGGGG | 16443 |
| rs250822433 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91865509 | TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTTTTC | 16443 |
| rs250828098 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830771 | CCCTAGACTCATTCT[C/T]CCGCTAAAGGTCTTA | 16443 |
| rs250853645 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91799255 | AACAAGCAACAGAGC[A/G]TCATCCCACACCAAG | 16443 |
| rs250855182 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91790264 | GGAGGGATGGAAGTT[-/C]CATGGAGAAGAAATC | 16443 |
| rs250864418 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91884879 | GTGGGTATTTCGTAT[A/G]GTGCATAGGGCTTTT | 16443 |
| rs250881633 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768120 | AGCTCATACAAAATG[A/G]TTGGTTATGAGGGAA | 16443 |
| rs250882105 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91877553 | GGAGACTGAGCACAT[A/G]TGAGCCTTTGGTGTG | 16443 |
| rs250919203 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734747 | TCCTAACAATTCCCC[C/T]TCCAGCTTTCACCGA | 16443 |
| rs250926250 | snp | A/C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890615 | TGTCTCACTGTTACC[A/C/G]TGTAGACCCAGGCAA | 16443 |
| rs250944436 | in-del | -/GC | | | intron-variant | Itsn1 | Mm_Celera | 16:91798012 | TCTGTTGTACTGTGA[-/GC]GCTGTAAACATTGTT | 16443 |
| rs250953055 | in-del | -/TCTGAGCTCAGGGCCCCTCC | | | intron-variant | Itsn1 | Mm_Celera | 16:91846634 | GTTGGAGACGCTGGA[-/TCTGAGCTCAGGGCCCCTCC]TCTAGCTCTTGACGC | 16443 |
| rs250965636 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91834976 | TTTTGAATGTTATCC[C/T]CCTAAAGTTAAATTT | 16443 |
| rs250976891 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91768269 | GTTTTAAAAAAACTT[A/T]TCAATTCTTTTTTTC | 16443 |
| rs250978048 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91839937 | GCAATATCTATGCCT[-/A]ATCACGATTTGCTCG | 16443 |
| rs250989651 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91748431 | GGATAAAGCTCTTGA[C/T]GTACCAGCATGTGTT | 16443 |
| rs250998959 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91801809 | TCCTTTCCACCCAGC[A/G]TATGACATGACGCGT | 16443 |
| rs251000918 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91812691 | GCCTTACATCAGCTA[A/G]TAGTTTTATTTGTTC | 16443 |
| rs251002420 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734180 | AACCCTGGGTCACCC[G/T]GAAGAGTAGTCAGCC | 16443 |
| rs251017987 | in-del | -/AAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91751692 | CTGTAGAACAAACAA[-/AAG]AAAAACTGTGGTGCT | 16443 |
| rs251025107 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91819097 | GGTTCAGTTGCCAGC[A/T]CCCCTATGGGCAGTT | 16443 |
| rs251033710 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91844255 | AGCTGTTCCGTGTAA[C/G]TGCTGCCCTTACCCT | 16443 |
| rs251033730 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91836766 | GCATAGCTCAGTCTT[A/G]GAACACTTGCCTAGT | 16443 |
| rs251050632 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91846552 | CGTTGCTGAGGGCAG[-/T]TAAGTTTCCTCCGCT | 16443 |
| rs251068616 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91851124 | GAGACTTATTATAAA[C/T]CTCCCAGAGTTCAGA | 16443 |
| rs251077948 | snp | G/T | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91858746 | GGTGATACTGACCCC[G/T]AGTAGTGGGCGATAG | 16443 |
| rs251080019 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91902179 | CAGCAGGCCTTGGGG[A/G]CCTACGTCTCCATCT | 16443 |
| rs251105874 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91807889 | TTTTAAGTTGTTTCT[A/C]TTTTAAAGCTTTTTT | 16443 |
| rs251110921 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91809657 | ATACCGATGCCCACT[A/C]TGTGTGTGCGTGTGC | 16443 |
| rs251118673 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91814857 | GAAATGCCCCCAACT[C/T]CAGAGGTGGACTGGA | 16443 |
| rs251123099 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91806891 | ATAAAAAGCGTAATC[G/T]TTAATGAAGGTGATT | 16443 |
| rs251135827 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914723 | TGATCCAAAGGGTCA[A/G]TCCTTGTCTCTGGGG | 16443 |
| rs251139805 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91843961 | CTGCCACCCCCACCA[C/T]CGCGGACCACCCCAT | 16443 |
| rs251150138 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873140 | GTTGGACAGTAGAGC[A/G]TCACTCAGATTTTAA | 16443 |
| rs251155037 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91904851 | TGTATAGCCCTGGCT[A/G]TCCTGGAACTCACTC | 16443 |
| rs251176403 | in-del | -/GCCATCAAACCACACCCCA | | | intron-variant | Itsn1 | Mm_Celera | 16:91836143 | ATGCTGGGCAGCTGT[-/GCCATCAAACCACACCCCA]GCCATCAAACCACAC | 16443 |
| rs251180876 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91910921 | TATTGGATCCCCTGG[A/G]ATCAGAGTTACAAGG | 16443 |
| rs251213573 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91910603 | TCTCCCTGGCCTGGC[A/G]CTCACCAACTGGTCC | 16443 |
| rs251217360 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91805751 | CAGATGCTCTCAGAA[-/C]ACCAGGAGAAGGTGT | 16443 |
| rs251269077 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91816282 | TGAGACAGGCTCTCA[A/C]TCTGTAGTCCTGGCT | 16443 |
| rs251283086 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91777972 | GATCAATGACCGTCA[A/G]AGCCCCAAGCTGTAG | 16443 |
| rs251290007 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91815807 | AGTGAGCAGACAGGC[A/T]GGAAATCAGAGATCA | 16443 |
| rs251302134 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91866822 | GAGAGTTGCAGACAG[C/T]GGTTAGTACTGAGGG | 16443 |
| rs251309905 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912174 | CATGTCTCATTTTAT[A/G]AATCCAAATTCTCTT | 16443 |
| rs251330035 | in-del | -/GTGTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91855269 | GTGCATTGCCATAAA[-/GTGTT]GTGTTCCTTAGAGAC | 16443 |
| rs251334180 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91779243 | GTGATTGCTTCATTA[A/G]TGACTAAGAAAAAAA | 16443 |
| rs251338649 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91736533 | TGCCCTCTTCTTACA[A/G]CTGCAGGGCAGCACT | 16443 |
| rs251345945 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91916398 | AACAGACACACCAGA[A/G]GAGGGTGTCAAATCT | 16443 |
| rs251346220 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91822262 | CATTTACCCAGTTTT[A/G]GAGTTAAAAACATTT | 16443 |
| rs251364394 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91883478 | GAAAGAATGAATGAA[C/T]CTAAAGCCAATGTGG | 16443 |
| rs251371093 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91777304 | TGTAAGCCTGAGAGT[A/G]GTGTGGTACATTCAC | 16443 |
| rs251372751 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91878806 | GGGACAGGAGCTGTC[C/T]GGGGTTGGAGGTGTT | 16443 |
| rs251375834 | snp | C/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91828887 | TAGGCTGAAGCAGGC[C/G]GACCTCTGAGTCAGG | 16443 |
| rs251384243 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910854 | GTGTGTTTGCTCACA[C/T]GAGTTTATGGGCACC | 16443 |
| rs251384549 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917397 | TTTATCTCCACCAAA[C/T]AACTAACTCAGTTCT | 16443 |
| rs251393803 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91739765 | ACATGTGTGCAGGGG[-/A]AAAGGGCCTAGTCTG | 16443 |
| rs251393941 | in-del | -/ATCAGCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91766289 | TAATTGTAACCATTA[-/ATCAGCT]ATCTGTTTTCATGAA | 16443 |
| rs251399892 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91845493 | ACATTTTTTAAGTTT[-/A]AAAAAAATAATAATA | 16443 |
| rs251403707 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91784732 | GAAAGATCTCCAGTT[-/G]CCTGACTGGCAGAAC | 16443 |
| rs251405812 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91824341 | TCTGTAACATCTGTA[C/G]TGTTGTGTCTGTCTT | 16443 |
| rs251418917 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91888419 | TTCCATGTGGCAGCC[G/T]GGGCAGACATTACCC | 16443 |
| rs251425902 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91784026 | ACCCCTTGCTTCCCT[C/T]GGTGAACAGTTGTGT | 16443 |
| rs251450614 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91821620 | TGCAAACCATCACAG[A/T]GATTAGCTGGTCAGG | 16443 |
| rs251465562 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91893482 | AGAAATGGGCTCAAT[G/T]CTCAGACTGAGCCAG | 16443 |
| rs251475076 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91887986 | AGACATGTTCCCCGG[A/G]GCTCTGTCAGGTTGC | 16443 |
| rs251489602 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91785710 | CGAGTAAAACAGGCT[A/G]TCAGATACGGTTTTG | 16443 |
| rs251509430 | snp | G/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917061 | GTTGGGGGCTGGGAG[G/T]CAGAGAAGGGACCTC | 16443 |
| rs251510267 | snp | A/G | | | downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91920780 | CTGCTGCCACAGACA[A/G]TGGGCTCTAGTCAGG | 16443 |
| rs251511843 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91834465 | CTTAAAGTTTCTTGC[A/G]GATCTCAGCAGTGTT | 16443 |
| rs251522635 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91753760 | TTTTATTTTTTAAAA[C/T]TCGTGAATCACTCAC | 16443 |
| rs251550107 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91888350 | TATGTTGTCTCAAGA[C/T]GTCTGCCTGCTATTA | 16443 |
| rs251563309 | snp | A/C | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746336 | GCAGGTGTTCACATG[A/C]AAGTGAGCGTTCACA | 16443 |
| rs251593454 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91792290 | TGTTTCAACAAAGCT[A/G]ATCTGGTAATGTCTC | 16443 |
| rs251635603 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91761005 | GGTGTAATTTATGAG[A/C]ATATCGAGGTCCAGG | 16443 |
| rs251637829 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91868996 | TTGGTAAACAATGAT[-/A]AAGACGCCAGGCAGT | 16443 |
| rs251639014 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91894104 | CAGTGGTACTGAACT[A/G]GCAGGTGTGGGTCTC | 16443 |
| rs251664991 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91791948 | AGAGTACAGAATAGG[G/T]TGTCAGGTTCCTTGG | 16443 |
| rs251687550 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91893717 | CCCACCCATTCTGTT[A/T]CTCTGCAACCTGAAA | 16443 |
| rs251688505 | in-del | -/TCCTCT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899999 | TCCTCCTCTCCCTCC[-/TCCTCT]CCCTCCTCCTCTTCC | 16443 |
| rs251710548 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91849398 | AGAAGTGTACCTCCC[-/A]CTTGCCCACTCTGAG | 16443 |
| rs251713009 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91753653 | GCTCTTATCACGTTT[C/T]AGGTAGTTAACCTTT | 16443 |
| rs251719103 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745688 | GTCATGCTGTTGTAA[-/G]GGTGGTCAGGCAGTT | 16443 |
| rs251736036 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91898613 | GGCAGGCATGGTGCA[A/G]GAGGAGCTGAGAGTT | 16443 |
| rs251739383 | snp | A/G | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91863568 | TGTATCCAGTTGTCC[A/G]ACAAGCTCAGATAGG | 16443 |
| rs251742574 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91855249 | GTGAGGACAGGGGGT[A/G]CTCAGTGCATTGCCA | 16443 |
| rs251749065 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91896069 | GAAGAAATTCTGAAA[C/T]CAGAATGTCCTTTCA | 16443 |
| rs251770202 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91805828 | GGGTGCTGGCAGCTG[A/G]ACCTCTGTCCTGGAA | 16443 |
| rs251776516 | snp | C/G | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91747298 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT | 16443 |
| rs251795502 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873071 | TGCAGAGTCTCCCAC[A/G]ACTGCTCGTTTTTCA | 16443 |
| rs251797920 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91844864 | CTGCAGCCTCTCACA[A/C]ACTACCTCTGCAGGC | 16443 |
| rs251798707 | in-del | -/TTTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91811577 | TCTTTTCTTTGTTTG[-/TTTA]ATGACAGCCATGATG | 16443 |
| rs251806428 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872200 | GTTCGGGGGAAGGGG[A/G]TGATAAATCGACCAT | 16443 |
| rs251809895 | snp | A/G | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91728112 | AAGCAGGCAATTCCT[A/G]ACCCAAGGCCCCATT | 16443 |
| rs251817734 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91852438 | GAAAGGTGTTGGGAC[A/G]CATCCCAAAAGCTGT | 16443 |
| rs251822513 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91909450 | GGGCACCTTTGGCCC[C/T]GCCCTCGGGGCAGCT | 16443 |
| rs251839734 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91762908 | CCCTGTATTTCTCTC[A/G]TGTGATTTTGATGGT | 16443 |
| rs251849678 | snp | A/G | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91727450 | GAGTGAGTATAGTAC[A/G]CAGCGCACACATTAC | 16443 |
| rs251851887 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91864508 | AAACTGGTTCTATAG[C/T]GACTACAGTTGACTC | 16443 |
| rs251880972 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91833041 | GATAAAAGAGTTCAG[C/T]CCTTGGAACCCAAGT | 16443 |
| rs251882968 | in-del | -/GTGT | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913546 | AGAAGGTCCCTCTCC[-/GTGT]GTGTGTGTGTGTGTG | 16443 |
| rs251889550 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91769230 | TCTTCCAGAGGTTCT[G/T]AGTTCAATTCCCAGC | 16443 |
| rs251898332 | in-del | -/CT | | | intron-variant | Itsn1 | Mm_Celera | 16:91784426 | ACCTTGACCCAGAGC[-/CT]CTCTCAAACCTGGCA | 16443 |
| rs251935862 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900856 | GACCTTTGCTCACTC[C/T]GGCCCAAAGATTTAT | 16443 |
| rs251939835 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900409 | GAATTACAGCGGTGG[C/T]CTTGTATGAGAGCCA | 16443 |
| rs251940615 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91838986 | ATGGTTGGGAGCTTC[A/C]ATGTCAGTGCAGGGA | 16443 |
| rs251947326 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91735696 | GTTAACAAGCAATGA[C/T]GTGTGGGAGTTAGGT | 16443 |
| rs251948449 | in-del | -/TATATA | | | intron-variant | Itsn1 | Mm_Celera | 16:91823592 | TTTTATATATGTGTG[-/TATATA]TATATATATATTCTT | 16443 |
| rs251952721 | snp | A/C | | | upstream-variant-2KB | Itsn1, Cryzl1 | GRCm38.p3 | 16:91728979 | TTGAATGTATCCTAG[A/C]TACTGTCGCGCATAG | 16443 |
| rs251971744 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783594 | ATACATCTATGCGTA[C/T]GTACTTTGGCCATTA | 16443 |
| rs251988283 | in-del | -/GACTCTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91835604 | ACTCCTGTGTTCATG[-/GACTCTTT]GCTTCCAGCAGGAGA | 16443 |
| rs251996177 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91768711 | GCTCCAGATCCCTCA[A/G]TTCTACCCCGACTCT | 16443 |
| rs252007687 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91764699 | ATCTTGTCAGTGACT[A/G]CAGCACTAGCCACAC | 16443 |
| rs252014330 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91874557 | GGGCACGGAAAAGAT[A/G]TGTCCCTTCCTTCAC | 16443 |
| rs252039054 | in-del | -/TTGTTTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91826218 | TGTTTGTTTGTTTGT[-/TTGTTTG]GAGTCTCACTCTAGC | 16443 |
| rs252041778 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91838527 | TGGAACTCACTGTGT[C/T]GACCAGGTAGGCCTT | 16443 |
| rs252076289 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91881702 | ACCACCGCACATGCA[C/T]TCTGCCTGTGATGTT | 16443 |
| rs252078468 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873892 | GTTTGATTCCCAGAA[C/T]CCACGTGGCAGCTCA | 16443 |
| rs252081222 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91816134 | GCCATGGAGCCATGA[A/G]TATCTGCTTCGCGTG | 16443 |
| rs252088203 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91881102 | GAGGAATTCCATTTC[C/T]ACACTGCTCCATGGC | 16443 |
| rs252094407 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915576 | CAGTTCCTCCTCCTC[C/T]TCCTCCTCCCCCTCC | 16443 |
| rs252096943 | in-del | -/CTCTCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91897036 | GCATGTGACTGTCTG[-/CTCTCT]CTCTCTCTCTCTCTC | 16443 |
| rs252098776 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91729512 | CGGGGATGGTGTGCG[C/T]GGCTGCGGACTCGGC | 16443 |
| rs252100414 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91845083 | TGCTGGTTGTAGAAC[C/T]AGGAAACAGTGGGGT | 16443 |
| rs252111188 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91833341 | TACAGTCAGTGGTCT[A/G]AGTATGTTTTTGCCG | 16443 |
| rs252123874 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91876720 | AGCCAAGAGTCAGAA[C/T]TTCATGTGTCAGCAT | 16443 |
| rs252127378 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91839882 | GGCTCTGCCACTGTC[A/T]CCTCTGTATGTATGT | 16443 |
| rs252131527 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91737935 | TTTTCACTTCAGGAA[C/T]ATCTGTACTGTTGGT | 16443 |
| rs252140692 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91822609 | GGACGTAGCACTGTG[A/G]CTTTGGTTTGCCGTT | 16443 |
| rs252144698 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91904526 | GTGTAGGGCTTTGAG[C/G]GGGTCAAATGCACCA | 16443 |
| rs252150598 | in-del | -/AC | | | intron-variant | Itsn1 | Mm_Celera | 16:91809146 | GTTGACGAGCCTGAA[-/AC]ACATATACAAACAAT | 16443 |
| rs252162485 | in-del | -/CACACA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91895737 | ACACACCCACATGTG[-/CACACA]CACACACACACGTGT | 16443 |
| rs252180668 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91887659 | CAGGGGGTTTTACCC[C/T]GAGAGGACATGCTCA | 16443 |
| rs252184069 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91811348 | TTTTGGTTTTTTGAG[A/G]CAGGGTTTCACTGTG | 16443 |
| rs252196911 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91817697 | TATGTGACTCAAGCT[A/G]GCCGATCTCACAGCA | 16443 |
| rs252197217 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91810909 | TCCCCTGCCCCAGGC[C/T]CTCAGCAGCCGGGCC | 16443 |
| rs252210149 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91737295 | GTCTCCATGTCCCAG[A/G]TAGTCCACCACACGG | 16443 |
| rs252213306 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91840130 | CTTTACCACCCAGGT[A/G]TGCACAGGAAGCCCC | 16443 |
| rs252225534 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91847383 | ATCCTGCATTAAATT[C/T]GAGGCACTCTACACG | 16443 |
| rs252228259 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91884050 | TACACTCAGCCTTGC[A/G]GGTGGGATGCAGTAA | 16443 |
| rs252241684 | snp | A/G | | | missense | Itsn1 | Mm_Celera | 16:91839737 | GTCAGGAAGAAGGAG[A/G]CGGAAGAGAGAGCCA | 16443 |
| rs252249440 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91744692 | CTGATCCAAAAGGAG[C/T]AGGTTTTATGCATAG | 16443 |
| rs252251426 | snp | A/G | | | missense | Itsn1 | Mm_Celera | 16:91816949 | AGCAGCCAGAGAAGA[A/G]ACTGCCTGGTGAGTG | 16443 |
| rs252257357 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913762 | GCTGAACATGAGGTA[A/G]ACTTTAACTTCGAGC | 16443 |
| rs252291472 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913079 | GGGTGGGAAAATGGG[C/T]GATGCTCCTGGGCAT | 16443 |
| rs252299644 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91882325 | TGGCCAGCAAGCCCC[A/G]TAAATCTGCCCATTT | 16443 |
| rs252306542 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91740286 | CAAGCCCATATGGGC[C/T]GCTGGCATCCTATGA | 16443 |
| rs252319575 | snp | A/G | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91828297 | AGAGACCAGGTCAAA[A/G]CTGCAGGAGATTGAT | 16443 |
| rs252334649 | in-del | -/CAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91768418 | CTGGTTGGTGCATCA[-/CAT]CACTGCAGGATTGGG | 16443 |
| rs252339969 | snp | A/C | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91747370 | CCAGATGACTTTGTT[A/C]CTGCTCAGGAGTGAC | 16443 |
| rs252341034 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91856102 | AGCAGAGCAGGCAGG[C/T]TCCCATCGTCAGTGG | 16443 |
| rs252344567 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91847602 | AGCATGAACCAGGAG[G/T]TCAGAGCAGCACCAA | 16443 |
| rs252346585 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91846595 | CATGATGATTTCATC[G/T]TTGCCTTGGAGATGG | 16443 |
| rs252360732 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91800834 | CTGTAGCCCAGGCTG[A/G]CCTCAGCCTCTCTCT | 16443 |
| rs252386329 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91842530 | GGCTAGCTGACCCCT[C/T]GTTTCATTTGATGAG | 16443 |
| rs252402741 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91850179 | TTTTTTTTTTTTTTC[C/T]AAGTTGAATAAATAA | 16443 |
| rs252439989 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91855405 | GATGATTTAAAGTAA[C/T]TATCCTTTACGCATA | 16443 |
| rs252454459 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91782117 | ATACACAGACCTGAA[-/G]TTTTCTTAAACGCAT | 16443 |
| rs252497724 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889811 | CAAAGATCTCCTCAG[C/T]TCATTAAAAAAAATC | 16443 |
| rs252511601 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91889322 | CATGCATGCCACCCA[C/T]GTGTCTTTCTTTCCC | 16443 |
| rs252518814 | in-del | -/TTTTGTTTTGTTTTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91736806 | GTGAAAACTTACTCT[-/TTTTGTTTTGTTTTG]TTTTGTTTTGTTTTG | 16443 |
| rs252519581 | snp | A/G | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91747701 | GCCTTTGGACTCACA[A/G]TGTCTGCCCTGTTAG | 16443 |
| rs252543611 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91862707 | GTTCTCATAGCTCTG[C/T]GTTCCTCTTGTAACT | 16443 |
| rs252555894 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91755849 | ACAGGTTTGTGACCC[A/G]GATCTTGACATAGGA | 16443 |
| rs252555942 | snp | G/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746554 | CTTACTTTAACCTTA[G/T]TTTGGGTCATTTTAG | 16443 |
| rs252580041 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91826507 | CTGAGGAAGAGAAGC[A/G]CACAGACAGTGAGGC | 16443 |
| rs252588103 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898583 | ATCATCAAGGTGGGA[A/G]CAGGACAGCATCCAG | 16443 |
| rs252588657 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91825975 | CCTCCCCCTGTGACC[A/G]CTGCGGTCACCCAGA | 16443 |
| rs252588680 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91833528 | CCTCTTTCTGTTGTT[A/T]CAGGCATCTTTATGG | 16443 |
| rs252619624 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91812288 | ACAACAAGCCCTAAG[A/G]ACTTGACGTATAACC | 16443 |
| rs252622071 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91847945 | GGTCACATGTATAGA[C/T]GTAAGAATAGGACTC | 16443 |
| rs252628113 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91833072 | GACAGAAACAGAAAA[C/G]CAGCCACCAAAAGTT | 16443 |
| rs252645000 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91769482 | AAGGCCCATATAATT[C/T]GAGGGACTGTTCTCA | 16443 |
| rs252651052 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91903512 | TCTTCATGGCACTCA[C/T]AGGAATTCGAAGGGA | 16443 |
| rs252659235 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91857221 | TTGCATTGTGGGGTT[C/T]TATCATTTGTAATGT | 16443 |
| rs252692797 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91797142 | CGTTTGATGAGGGGA[A/G]GGTGGTTTTGCTTTT | 16443 |
| rs252693216 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91908494 | TACCTGGGTATGTGC[C/T]GCAGGGCCGGAGACC | 16443 |
| rs252699375 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91855940 | TTTCATCACTGCTCA[C/T]AGCAGTGTGCAAAAA | 16443 |
| rs252703368 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91857279 | TTCTGAAATGCTTCA[-/T]TTTTGTTACTTAAAA | 16443 |
| rs252715786 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91754777 | GAGGTCTCCTCGGGG[A/T]TTCCCCCAGCTCCTC | 16443 |
| rs252729276 | snp | A/G | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91820579 | AAGGAGGAAGACTCT[A/G]GAGTTTGAGTTAGAA | 16443 |
| rs252741049 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91737216 | GAAGAAGATACTCGC[-/G]GGGTGTTATTAGGAT | 16443 |
| rs252747464 | in-del | -/C | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91870658 | CCGGGCGTCCGTAAA[-/C]CTGAGACTTGCTGTA | 16443 |
| rs252771178 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91804786 | CACATGGACACCACA[G/T]GTGTTAATGAATGAC | 16443 |
| rs252779148 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91856256 | GGCCTCTTATTAATA[A/T]TACATTAAACATCAT | 16443 |
| rs252779224 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91867048 | GAAAGTGTGCATTCA[A/T]GTGGTAGTCTTTTCT | 16443 |
| rs252781694 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768581 | CTGCTACATTCACAC[A/G]GGCGGCCTAGGTCCA | 16443 |
| rs252811702 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91819707 | TGCTCAGCTCTTGTT[C/T]CCACATTGCTCTTTA | 16443 |
| rs252813206 | snp | G/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91804085 | CTGCGCCATTCAGAT[G/T]ACTGTCCCCGGTCAC | 16443 |
| rs252824042 | in-del | -/CC | | | intron-variant | Itsn1 | Mm_Celera | 16:91743681 | GTTTTTGTTTTTTGT[-/CC]TTTTTGAGACAGGGT | 16443 |
| rs252837419 | in-del | -/GGGGGTA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872364 | CAACACTGGGGGGGG[-/GGGGGTA]GAGGGTTGGGGGGTG | 16443 |
| rs252842273 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91901924 | GAATCATGAGGTGTG[C/T]CCAGAACAGAATCAG | 16443 |
| rs252849720 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91865966 | CTGAGACAACCAATC[C/T]CCTGGGCCTTGGGCC | 16443 |
| rs252859484 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91811464 | GGATTAAAGGCGTGC[A/G]CCACCACGCCCGGCT | 16443 |
| rs252864306 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91907941 | TACACACAAAATGAA[A/G]CAAAAAACTAACAAC | 16443 |
| rs252876496 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91736995 | GACATTTGATAAGTT[-/A]GGGGCAGTGAATGTG | 16443 |
| rs252876537 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91771955 | GATTGACCCAGGTTT[-/A]ACAGTACGAGGTGTG | 16443 |
| rs252876610 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91776878 | TTTGCAGTTGGGCGT[A/G]GCCGCCAGAGTATGG | 16443 |
| rs252879707 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91826452 | TCGTCATTGGTAGGT[A/G]CAGGTCCTGGATTAC | 16443 |
| rs252887900 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91738509 | GATGATATTATAGTT[A/G]TGGTTTGGCAATTTA | 16443 |
| rs252892876 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91907495 | AGTGCGAAGCCTTCT[C/T]TCCTTGGGTGATTTT | 16443 |
| rs252899849 | in-del | -/CATAGGACACCTCCATAGGACACCTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91892955 | CTGTAGGGATGCCTC[-/CATAGGACACCTCCATAGGACACCTT]CATAGGCCATCTCCA | 16443 |
| rs252914712 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91775263 | GGACTAATGTTTGTT[C/T]TGTTTTAGACAGCCT | 16443 |
| rs252919613 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91731387 | CCCTGAAATGTTTGT[C/T]CCTCAGCATTTTCTT | 16443 |
| rs252939885 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91774703 | AGCATATCTTCCCAT[G/T]TTTAAAACCTTTGTT | 16443 |
| rs252941975 | in-del | -/AAAAAAAAAAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91844393 | TCTATTTGTGGAGAC[-/AAAAAAAAAAA]AAAAAAAAAAAATAC | 16443 |
| rs252958975 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91781740 | TTGTTGCCCTGTTCT[A/T]ATCACTCCCCTCTTT | 16443 |
| rs252975503 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91834590 | ATTTTATGGCTCCTA[C/T]GAGCTCTGTTTCCAG | 16443 |
| rs252991248 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91887690 | CGTTTTTTTCCCACA[C/G]AGCCACCATGTGAGA | 16443 |
| rs252992614 | in-del | -/TTCCCGGGCACGGGCAAGAA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91895320 | CCGGGCTGCCAGCAG[-/TTCCCGGGCACGGGCAAGAA]TCCTTCCCTGTTTCA | 16443 |
| rs252996226 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91781513 | GTGCATACGGGCAGA[A/G]TGTGTGAGTTTGTGA | 16443 |
| rs253017987 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | GRCm38.p3 | 16:91729733 | TTTCTCATCCTCCCC[A/G]GGGGCAGCGGGGCGG | 16443 |
| rs253032459 | snp | A/C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91886074 | CCCCCACCTCTCAGC[A/C/G]TATGTATTTTACAAA | 16443 |
| rs253040149 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91781039 | TTGGCAAACCACAAG[A/G]GTAGAAATGGGGAGA | 16443 |
| rs253041471 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91737161 | TTTTGTGCCTGTTCA[A/C]ATGTTCTTTTACTAT | 16443 |
| rs253048602 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91840789 | TTGATTTTCCCCTCA[A/G]TAGGAACCTTTGCTT | 16443 |
| rs253049512 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91869855 | TCTCTGGTTCCTCCC[A/G]TAAGACATGCAGCAT | 16443 |
| rs253056976 | in-del | -/GA | | | intron-variant | Itsn1 | Mm_Celera | 16:91842030 | TCTTCTGGGGTGTCT[-/GA]GAAGTCAGCTACAAT | 16443 |
| rs253072835 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91885375 | TTTGAGAAGGCGCCA[G/T]AGCAGGCTGAGCCAT | 16443 |
| rs253074322 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91891551 | CCAGGGATGACCCCA[C/T]CCACAACAGGCTGGC | 16443 |
| rs253083038 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890864 | TAATGAGGGCTGGCC[A/G]CTGGCTTTCCCAACT | 16443 |
| rs253135043 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91832171 | ATCCTTGAGTATGGA[C/T]CTACTACTACCCAGA | 16443 |
| rs253136168 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91744582 | TCCTTTATCAAAGTA[A/G]TAGTAGTAGGTTCAT | 16443 |
| rs253159517 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750790 | AAGAGAGCTTCATCC[C/T]TCTACCCTGTGTGTG | 16443 |
| rs253163795 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91840374 | TTTCAATACAACTTG[C/G]CTCTTTTAAAAAGTA | 16443 |
| rs253180735 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91796855 | AGGAGGAGGGAAGGC[C/T]GCTGAGACACTGCAG | 16443 |
| rs253194130 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91748657 | TTCTATCCCTAGGCA[A/G]ATCATGGGGAGCAAG | 16443 |
| rs253194158 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91758079 | CTCTTAAATGCCGAG[C/T]CATCTCTCCAGCCTC | 16443 |
| rs253213074 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91743876 | ACCTGATCCTAGTCT[-/C]CCCAGCTCTTCCTCC | 16443 |
| rs253216949 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91827798 | AGGTGGGAAGTGACA[-/G]GGGAAGGACCCTGGG | 16443 |
| rs253221452 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91860211 | AGCCTTGGGAATCGT[C/T]CCACGCTTATGTGCA | 16443 |
| rs253236888 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91804745 | GAATCTGTTGACTCT[C/T]AGGGACTTTACATTG | 16443 |
| rs253248046 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91805914 | GATGTCTATACTGAT[A/G]TGTAGAGGCACAATG | 16443 |
| rs253257399 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91902256 | TGGGCATCTATTCTT[C/T]AAAATCTACTTTAAT | 16443 |
| rs253272119 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91854038 | AAATGCAGAAAGTGA[A/G]CCTTCTCGTGAGCTG | 16443 |
| rs253273880 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91757169 | TTTTTGCCTTTCTCC[A/G]CATACTTCCTGAGCT | 16443 |
| rs253289166 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91908563 | CGGGGCTGAAACTCG[A/C]GCCAGAAGTGGGGCT | 16443 |
| rs253297331 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91804868 | CTTTGTAAGCATGGA[A/T]GGAGAAGACATGTGG | 16443 |
| rs253301756 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91883338 | GGGGAGGTTAGAATA[-/T]CTTTTTTCAAGTCTT | 16443 |
| rs253312995 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91812558 | TCAGACCAAACCTCT[A/G]TATTGTTTTACTTAC | 16443 |
| rs253324193 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91859233 | AGACTTGTAGTACAT[G/T]TGCCGTTGACCTTCT | 16443 |
| rs253330295 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802879 | GGAGTGTTTTATTTT[-/G]GCAAGAAGACAGGGT | 16443 |
| rs253338730 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91909522 | TGCTCTACCATCCCA[A/G]CACTCTTGGTCCCAC | 16443 |
| rs253345614 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734691 | TATGTCTGATTATCC[C/T]CCATTGTCCTCCCTG | 16443 |
| rs253382367 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91868471 | AATAGTTCTGTGTCA[G/T]TTGCTGGGGACAGAG | 16443 |
| rs253394087 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867848 | TTGGAAACATCCCAG[A/G]CTCTGCAGACCAATG | 16443 |
| rs253403485 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91775059 | TTCTGTTTCTGTACA[A/G]TTATCAATGCCAGCT | 16443 |
| rs253407489 | in-del | -/TGTGTGTCTGTGTC | | | intron-variant | Itsn1 | Mm_Celera | 16:91805701 | TAAAGATTTCCTGTG[-/TGTGTGTCTGTGTC]TGTGTCTGTGTCCTG | 16443 |
| rs253408229 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914684 | GGACAGAAGCCCCTG[A/G]CTGGGCTTCCTTCAT | 16443 |
| rs253429354 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91824974 | TCTTCTTTTGGTTTG[G/T]TTTGGTTTGGTTCTA | 16443 |
| rs253461820 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91783027 | GGGACACAGCGCAAG[C/T]CCCCAGCATTGCTAA | 16443 |
| rs253462519 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91788101 | CTGTTTATATTCACA[A/G]CACTTTGAAGGTAGA | 16443 |
| rs253464968 | in-del | -/GA | | | intron-variant | Itsn1 | Mm_Celera | 16:91888164 | TACAGAGCAAGACCT[-/GA]GAGAGTCACCTTCAA | 16443 |
| rs253467949 | in-del | -/ACTTACATTATCA/ACTTACGGTATCA | | | intron-variant | Itsn1 | Mm_Celera | 16:91784780 | CCGTTCTGTGTCAGT[-/ACTTACATTATCA/ACTTACGGTATCA]ACATTCAGAGTAAAA | 16443 |
| rs253469327 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830463 | GATTCATTTCATGTT[C/T]GTGGAGGTTATGCAC | 16443 |
| rs253476179 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91818697 | GTGTGCCCGCCCGCC[C/T]GCGGCAGGGCCGAGA | 16443 |
| rs253477914 | snp | G/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91829769 | CAGATGGACTGAGTC[G/T]CGGTCTTGTGACTCT | 16443 |
| rs253485630 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91836397 | GAGAATAAAGGCTCT[C/G]CAATAGTTGTGATTT | 16443 |
| rs253507616 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91878923 | CTTCCCCACCATGCA[G/T]CCTCTTGTGGGCTGG | 16443 |
| rs253517227 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91782341 | GTAGCTTAGGGGTAG[A/C]GCTCTTGCCTAACAT | 16443 |
| rs253526450 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91854092 | AAATCATGTTCTGCA[-/T]ATTGGCTTGTAGAAG | 16443 |
| rs253541589 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91835809 | TTAGGAAGGCAATGA[A/G]AAATGGAATTCTTCT | 16443 |
| rs253565881 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890668 | TCTGAGTCCGCCTCC[C/T]GAGTACTGGGATAAA | 16443 |
| rs253570649 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91886564 | TCCCTTCCAGCAGCC[G/T]CGGCCTCTACAAAGG | 16443 |
| rs253581128 | in-del | -/AGCAGCCAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91761435 | TGGAAGGAGACAGTG[-/AGCAGCCAC]CTGTAAAGAAGACAG | 16443 |
| rs253617287 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91789579 | AGCTCCTAGCCATGT[A/G]TTTTATGTTGTTAAA | 16443 |
| rs253622426 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911171 | CCACATGGTGGCTCA[C/T]AACCATCTGTAATGG | 16443 |
| rs253636450 | in-del | -/TTTTTTTTT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91895552 | GATGGGAGAGAAGGA[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 16443 |
| rs253640784 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91901374 | TTCAGTGAGGGTGTG[C/T]GCAAGCTAAGCTCTG | 16443 |
| rs253659818 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91799760 | CACTTTAAACGTATC[-/G]GAGCACATGGAAGAA | 16443 |
| rs253671760 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91766774 | TTTACCTGCCACACC[C/T]GATTGACACTGATTG | 16443 |
| rs253673856 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91891990 | GGACTCTATGACTGT[C/T]GATGTCCGCTCAGCC | 16443 |
| rs253674404 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900937 | GAGGGCGTCAGATCC[C/T]TTTACAGGGGGTTGT | 16443 |
| rs253677595 | in-del | -/AG | | | intron-variant | Itsn1 | Mm_Celera | 16:91910182 | GTCCCTGGGAAGCAC[-/AG]AGAGCTTCGTGTTGG | 16443 |
| rs253683213 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91891621 | ATTAAGAAAATGCCC[G/T]GCAGGCTTGCTTACA | 16443 |
| rs253689679 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91752227 | GAGGCAAGCATGCAC[A/G]TCTATCTCAGTTGCT | 16443 |
| rs253690803 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91820253 | GCACTGTGATTTCTG[G/T]GAGGCGTGAGGAATG | 16443 |
| rs253695510 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91896937 | AAAAGACAAAAGTGT[A/G]CTGGGAAGTAGAAAT | 16443 |
| rs253715194 | in-del | -/AGTTCCCGGGCACGGGCAAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91895318 | TGCCGGGCTGCCAGC[-/AGTTCCCGGGCACGGGCAAG]AGTCCTTCCCTGTTT | 16443 |
| rs253717830 | in-del | -/AAGCGCTGCTGGTCTAT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783288 | CTTCACCTTTTCAGC[-/AAGCGCTGCTGGTCTAT]GAGGGAAGAGGTGTC | 16443 |
| rs253726746 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916203 | ACTCAGTGCCACGTA[C/T]TCCCCGTGGGGGTTT | 16443 |
| rs253732436 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91896475 | GGGAGGCTGGAGGCG[A/G]GACAGAGTCCCTAGC | 16443 |
| rs253746065 | in-del | -/TTTC | | | intron-variant | Itsn1 | Mm_Celera | 16:91731621 | TTCCTTCCTTCCTTT[-/TTTC]CTTTCTTTCTTTCTT | 16443 |
| rs253746186 | in-del | -/CACCCCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91834131 | CTTGCTTCAACCCCC[-/CACCCCT]CACCCCCAAAACAAA | 16443 |
| rs253753621 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91874535 | CTGGTTGGCCCATCA[C/T]GCTGCAGGGCACGGA | 16443 |
| rs253784140 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91774145 | GCCAGCACCACCTGG[A/C]CAGTAGAATTACTGT | 16443 |
| rs253793952 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91834737 | ACTGTCTTCCGTTGG[C/T]TCTTTCTATCACTTT | 16443 |
| rs253804116 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91759235 | GGTGGCTTGAGTCAC[C/T]TGGACCTTCACGGTG | 16443 |
| rs253811631 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91877862 | GTTCAATCCTCAGCA[C/G]CACAGAAGCAGGTGT | 16443 |
| rs253814771 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91773154 | TAACATACCTGTTTT[A/T]AAAACTATTTAGAAT | 16443 |
| rs253839188 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758465 | TCTCTTTTCTTCATA[C/T]GCTGTTAGAGCATTG | 16443 |
| rs253841233 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91766590 | GGGGTGGTGGCTTAT[A/G]GCAGGACTTCCCTAG | 16443 |
| rs253873634 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734904 | CTGAGTTCCTTTTCC[C/T]CTTTCAGCCACTAGC | 16443 |
| rs253875299 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91737802 | CAGGCAGGACAGCTA[A/T]TAACTCTCCAGTGTG | 16443 |
| rs253884333 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91757122 | ACTCCAGAGCACAGG[A/G]TGGCATGGCCTCTCA | 16443 |
| rs253905940 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91840043 | GCTGGGATTAAAGGC[A/G]TGTGCTACCACGGGC | 16443 |
| rs253908252 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91885481 | CTCAGTGGTGGATGG[A/G]AAGGCGTGGAGAGCG | 16443 |
| rs253908477 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91877181 | CTCTGACAGGGCCCT[A/G]AGGAAGACCTCACAA | 16443 |
| rs253915896 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91765828 | GAGACTTTGTCAGGA[C/T]TAGGAACCCCTGGGT | 16443 |
| rs253934743 | snp | C/T | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91870500 | GGCCCCGCCTTCACA[C/T]GGGCGCTTTCAATAG | 16443 |
| rs253953464 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91858935 | GGAGGGTGGTTTAGA[A/G]CGGCCAAGTTCAAGT | 16443 |
| rs253964868 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91884781 | CTGCCTCTGCCTCCC[A/G]AGTGCTGGGATTAAA | 16443 |
| rs253977756 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91892931 | GACCATGAAATTAGC[C/T]ACGGGACACTGTAGG | 16443 |
| rs253978179 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91874082 | AATTCCAAGGTTCTG[-/A]ATACAACTATGTGAA | 16443 |
| rs253983188 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742461 | TGTTTGCCTTGTATG[A/T]ATGCTTTCCAAATGC | 16443 |
| rs253992792 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91869256 | TGGGCTCAGTCTTCA[A/C]CATCACAAAAAGAAA | 16443 |
| rs254008886 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91741370 | GCCAGTGGGGCTGAA[A/G]CTGTCACCCTCCAGC | 16443 |
| rs254011926 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91847200 | TTCTTGAGTTCCATG[C/G]TAGCCTGGTCTACAG | 16443 |
| rs254017487 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91809846 | TAAGGTAATCCACAG[C/T]GTAGGCTCGTCGGCC | 16443 |
| rs254033244 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91816231 | AACTTTCAGGATGGC[A/G]GTAAAAGAATGTGAG | 16443 |
| rs254034057 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91806690 | TAAAGCATATTGATA[A/C]TGTTATCCTAATAAT | 16443 |
| rs254039581 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798448 | AGGAAGGAGGGCGGA[A/T]CCCCAGGGTAAGCCA | 16443 |
| rs254048576 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91806007 | AGAGAAAAGTCAACA[C/T]CGCCAACCTTAGACA | 16443 |
| rs254051067 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91844029 | TTGCTCTGTCTGTCT[A/G]CTCTTTCTTTCATCT | 16443 |
| rs254055905 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91764810 | GGAGGTCTGTCTCCA[C/T]GATGTCAGCACCTTT | 16443 |
| rs254060596 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91843708 | TGAGAGAGACTTCAC[C/T]CATGGCCATTTTTGT | 16443 |
| rs254060755 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91851699 | AGGCTCACGTGAGAC[A/G]GCAGGAGCCCAGGAG | 16443 |
| rs254114600 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910393 | CATCTCTCTAGCCCT[A/G]GAATATGATTTTTTT | 16443 |
| rs254121651 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91851081 | CCTACGAGGCTGGGT[C/T]GGCTGGCTGAACCTA | 16443 |
| rs254127501 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91760784 | TGGCTAAGTGGGACC[C/T]CTGGAGCCCCACTGA | 16443 |
| rs254128656 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91868288 | ACTGGACTCTGCTGG[A/G]GCAGTTGGAAATGCG | 16443 |
| rs254175861 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91812333 | CTTAATAACTTACTT[A/G]TTTTCATTTCATGTG | 16443 |
| rs254182802 | in-del | -/TT | | | downstream-variant-500B | Itsn1 | Mm_Celera | 16:91920605 | ATTCAAACGTGTGGA[-/TT]TTTTTTTTTTCTGCC | 16443 |
| rs254187131 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768645 | GTCTCTGAAAGCCCC[C/T]AAGGGTCCAGGTTAG | 16443 |
| rs254189605 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91818939 | GTTCTTGTCTGTCTT[A/G]TCTGAGTGCATTGCT | 16443 |
| rs254208609 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91767964 | TGTTTAGTCTTGGAA[C/T]CTTGAAACTTAGCAG | 16443 |
| rs254232111 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91776983 | CCCTAGACGCCAGCC[A/C]TGGGGTGCTCTAAGC | 16443 |
| rs254239440 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91909589 | CCCACCTGAGAACCT[A/G]ACCCCGGCAGTCCCT | 16443 |
| rs254258651 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91808128 | TACCTATATTCCGAA[-/G]ATATGGCCTATACAC | 16443 |
| rs254258704 | snp | G/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914648 | CTCAGTCACCCCTGA[G/T]AATTATCCCGAGAGC | 16443 |
| rs254260219 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91822440 | TTGTGTGCAGGTCTC[C/G]TTTGGAAATGTTTTG | 16443 |
| rs254264179 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872738 | CCCTCACATCTCTTC[A/T]GTTTGTGTGGCCTGC | 16443 |
| rs254278248 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91880966 | AATGCAGCCAAGAAC[A/G]AAGGAAAATTCCAGA | 16443 |
| rs254292691 | snp | C/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91918097 | GTGCTCCCCGACTCT[C/G]CCAGCTGAGCCGTGA | 16443 |
| rs254325024 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91880041 | CTTCTCAAGCCACCC[A/C]GTCTGTGATTGGTCC | 16443 |
| rs254341898 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91776576 | CTGCTTCATTTAATG[A/G]TGTTGCGTCATATTT | 16443 |
| rs254353028 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91732645 | ATATGCTTTCCAATT[C/T]GACTCTTATGATATA | 16443 |
| rs254360701 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91835598 | CCAGTTACTCCTGTG[C/T]TCATGGACTCTTTGC | 16443 |
| rs254363523 | snp | A/C | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91829876 | TTCTTAGCTTTCCCC[A/C]CACACACTGGCCCTT | 16443 |
| rs254365966 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91821767 | CCATAGAGGCTGGGT[A/G]GTGACAGGCGGAGTG | 16443 |
| rs254378681 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91786309 | GTAGGGCTTAGCATC[A/C]GAGATGGCCCTTCCA | 16443 |
| rs254392674 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91736306 | AGCCAGGGTTTAGTT[C/T]TTAGCTGACCATCAA | 16443 |
| rs254405296 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802494 | ATGTAAGGCTGCACA[-/T]GATAGCAGCCAACAT | 16443 |
| rs254406189 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91842776 | GTACCACAGAGTTGT[A/G]TTGAAAAGAAAAGTC | 16443 |
| rs254412084 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91887731 | GTTCTTACCGGAGCC[A/G]AGGCCAAGAGCTCAC | 16443 |
| rs254424193 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889666 | TGAGGCCATGTATGC[A/C]TCGTACCTGTTTAGT | 16443 |
| rs254429127 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91828831 | AATCACGTTAACTCA[A/G]GCTTGCCATAGTGGC | 16443 |
| rs254430363 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91737376 | GCTTTGAGATGGGAG[-/A]AAGGTGGGAGAGAGG | 16443 |
| rs254445267 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91836416 | AGTTGTGATTTGAGG[-/A]AAAAAATAAACCCCA | 16443 |
| rs254446137 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91792876 | TTGGGTGGGTAGCGG[C/T]TTCCAGTGCAGATCT | 16443 |
| rs254453621 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91838893 | CTAGCTTTCCTGGCG[C/G]TGTGTCGCTCTGTAC | 16443 |
| rs254459146 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91771497 | AGGCTCTGTTGTTTG[-/C]CTGATACATCAGCAG | 16443 |
| rs254466613 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91789436 | TCCTCAGCACATAGC[A/T]CCTGTCATGGTAGCA | 16443 |
| rs254479593 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91887233 | TGTGTGGGGTCTCTA[C/T]GCCGGGCTGTGCCAC | 16443 |
| rs254496909 | in-del | -/TG | | | intron-variant | Itsn1 | Mm_Celera | 16:91775668 | GTTAAATTGTGTGCC[-/TG]TGTGTGTGGGGTGTG | 16443 |
| rs254498802 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91744637 | TGTGGGCTTTGGACC[A/T]GGCCTGCCTGAATTT | 16443 |
| rs254510030 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91792618 | GAAATGTAAGGAAAG[C/T]AAAGCAAAACTCAAA | 16443 |
| rs254518011 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91845566 | GGGAGGCAGAGGCAG[A/G]CGGATTTCTGAGTTG | 16443 |
| rs254519366 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91800582 | ATTTGGTTACTCCCC[A/G]CTATCATATATTTTG | 16443 |
| rs254533083 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91795651 | TGCGCCACCACGCCC[A/G]GCTGCATGTTTGGTT | 16443 |
| rs254560061 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91899028 | TCGGGTAAGTGAGCC[G/T]GAGAAGAGCAGCTGC | 16443 |
| rs254576068 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91799612 | TAAAGAGTTGGACTG[C/G]AATTCATGAAGAATC | 16443 |
| rs254576880 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91896883 | AGAACGAGTGTTTCC[A/G]TATCCACGCCGGCTC | 16443 |
| rs254596596 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91744255 | GAGTCACTGCAGAGA[G/T]ATGCTTTTCTGGCGA | 16443 |
| rs254598944 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91753056 | ATATGAAGAGGACAC[C/T]GTGCTTAGGGGAAGA | 16443 |
| rs254605236 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91854132 | ACTGTTTGAGAGTTT[G/T]GACTCTTTATGCCCA | 16443 |
| rs254612732 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91901425 | AGGTGCCAGCTATGG[C/T]TTCTCAGTTTAGAAC | 16443 |
| rs254642003 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91752412 | CAAACCTCAGCAGAC[A/C]TAGCCCTAAGTGGGC | 16443 |
| rs254669474 | snp | A/G | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91853528 | AGTTGCTGAGAAGCC[A/G]CAAGGTGACTAGCAC | 16443 |
| rs254684671 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898737 | TCCAACAAGGCCACA[A/C]CTCCAAATAGTTCCA | 16443 |
| rs254686741 | in-del | -/GGGGTGACTTTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91818886 | CGCCACTTAACAGAA[-/GGGGTGACTTTG]GTGTCAGACCCGGAT | 16443 |
| rs254688114 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91897778 | AGCCCACATGTGAGT[A/G]CTGGGAACCCAGGGC | 16443 |
| rs254712275 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91903893 | AGACCTCAAAGCCCC[A/G]CCTCCACAGTGGCAC | 16443 |
| rs254717704 | in-del | -/TGTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91812771 | CTTTTAATGATTATT[-/TGTG]TGTGTGTGTGTTTGT | 16443 |
| rs254722787 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91766206 | TGCGAGATTTCTGTG[G/T]GTTGCCTCTTATAGT | 16443 |
| rs254727208 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91806526 | GAGGCTGTTCCCTCG[A/G]TCAGACATGGAGGCT | 16443 |
| rs254744773 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91903316 | TCTGGTTGGTGTGTC[C/T]GAAGAGAGCAACAGT | 16443 |
| rs254749468 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91769408 | AACTTCTCCATTATG[A/T]ATCTATTACATATTC | 16443 |
| rs254777915 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91823642 | ATATAAAATGTAAGG[A/G]CTCATCTTGGGCTTT | 16443 |
| rs254780272 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768877 | GATTGGTTCTTGCCC[A/G]TGGGATGGGTCTCGC | 16443 |
| rs254785320 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91885814 | CTCACTGAGGATTCA[C/T]TGGAGGGCGTGGAGG | 16443 |
| rs254787461 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795634 | TGCTGGGATCAAAGG[C/T]GTGCGCCACCACGCC | 16443 |
| rs254792602 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91743920 | GCATCCCAACACACA[A/C]ACCTTCCTACTTTAC | 16443 |
| rs254794905 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91861730 | AATAGTGGCATAAAA[A/G]AGAGAAGGAGGCAGC | 16443 |
| rs254814807 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831617 | GATTGTCCTAGAACT[C/T]ACTCTGCCCTGCCTC | 16443 |
| rs254842344 | snp | C/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919830 | AAGATTTTGGATACC[C/G]TTCATCAATTAACAT | 16443 |
| rs254852701 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91878392 | AGAGCTGACATATGG[A/G]AGGGTCCCCATCTCT | 16443 |
| rs254861918 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91777341 | GGGTGCTCTTGTCTG[C/G]TTTCTTCTTTCTTGT | 16443 |
| rs254864385 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91860662 | GGGAGGAATTCAGCC[A/C]CACACTGTTTCTGGA | 16443 |
| rs254867272 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91857421 | AGCAAAGCAGAGTTC[-/T]ACTTTCAGTTACAGG | 16443 |
| rs254892834 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91881287 | AGGCCAGAGTGAGAT[A/G]CTCAAGGCTCAGCCA | 16443 |
| rs254898334 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91776715 | TGTCTCATGGGAAGA[A/G]TGGGGGGCACTTCCT | 16443 |
| rs254898722 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91789761 | AGCACACCATTGGTG[-/T]TAACAATTACTTTCC | 16443 |
| rs254904079 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91825075 | GAGATCTGCCTGCCC[C/T]GCCTCCAGAGTGCTG | 16443 |
| rs254941021 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734551 | TTTCACACACAGGTG[C/T]ACACACATACAACAG | 16443 |
| rs254945034 | in-del | -/AA | | | intron-variant | Itsn1 | Mm_Celera | 16:91842072 | AATAAATAAATCTTT[-/AA]AAAAAAAAAAAGAAG | 16443 |
| rs254964627 | in-del | -/TGGATTTCTGTTGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91777417 | CTCATCCTGAAACAC[-/TGGATTTCTGTTGG]AGTTTTGATCTCTGC | 16443 |
| rs254979334 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742696 | CCTCCCCCCCAAAAA[A/G]AAAGATTGTTCTCAT | 16443 |
| rs254984979 | in-del | -/TTA | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91747484 | TAGCCCCTCAAACTT[-/TTA]TTAAAGTGTGTAATA | 16443 |
| rs254996813 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91749462 | GTCACACTGAAGTCT[G/T]GGTGGGATTGTGTCA | 16443 |
| rs255003572 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91880616 | TAGATAACAGCACCG[C/T]TCTATCCATGAGTAT | 16443 |
| rs255049816 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91809667 | CCACTCTGTGTGTGC[A/G]TGTGCTGCCACAGAG | 16443 |
| rs255049981 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91816654 | CCATTGGCTTTGGGG[A/T]GCATGATGGCTTGCA | 16443 |
| rs255050494 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91794504 | ACTCCCTGACCCTCT[A/G]ACTCATACAGTCTTT | 16443 |
| rs255058031 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830986 | CATGAATGAGACCAT[A/G]GGTTTAATCCCACTG | 16443 |
| rs255085511 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91802465 | CTCATCTGTCTGTCC[A/G]TTGCAAGTTCTAAAT | 16443 |
| rs255102381 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91851783 | CTGACTCAACACTTA[A/T]GCACAGTGACCAAGG | 16443 |
| rs255106274 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912563 | ACACTCCCATGTGTC[A/G]TTAGAGCTGTACCAT | 16443 |
| rs255128193 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91895593 | GTAGAAGGACTCTTA[C/T]CCACTAGAGGCATTA | 16443 |
| rs255128450 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91911835 | AGAAACTCTTTCTGA[G/T]CATCCTCTGCTTTTC | 16443 |
| rs255131630 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91918778 | CGTCCCTTCTCCCTC[C/T]CTCCCCCCTCCCTCC | 16443 |
| rs255134826 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91851999 | GAGGAAGCTGAGCCC[C/T]GAGAGGCCTGCTGGT | 16443 |
| rs255151974 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91862283 | GCTTTCTGAAGCACA[A/G]GCAGGCAGGCTGCTT | 16443 |
| rs255162740 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91811926 | GAGTCTGACCCCGCT[A/G]TGCTTTCCTCCCTTG | 16443 |
| rs255167896 | snp | G/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917803 | CTGTGCGAGAGCTGC[G/T]CCTGTGGTTTTCTGC | 16443 |
| rs255172369 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91905767 | AAAATAGAGTAACCC[A/G]AACAGGCAGAGTAGA | 16443 |
| rs255186462 | in-del | -/TGTATCCACGTGCAGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91770110 | TCAGCCTGTGTGCAT[-/TGTATCCACGTGCAGC]TGGCACACTGCTGTA | 16443 |
| rs255190848 | in-del | -/ACCACC | | | intron-variant | Itsn1 | Mm_Celera | 16:91783772 | CTCTAATTGTGCTGT[-/ACCACC]ACCACCACCACCACA | 16443 |
| rs255209312 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907974 | TGGCTGCAGCGATGG[C/T]TTAGCGGTTAAGAAC | 16443 |
| rs255231539 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91860075 | GTCCTCTGGGGCACC[C/T]GTTCTGTAGACTCAG | 16443 |
| rs255242519 | in-del | -/ACAAAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91778549 | ACCCTGTCTAGAAAA[-/ACAAAG]ACAAAAACGAGAGAG | 16443 |
| rs255243862 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91786980 | TAGCACTAGGCATGC[A/T]AGCGCTGGGCTGTAG | 16443 |
| rs255262846 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91793251 | TTACCACGTGTAACT[C/T]GACGGTTTGTAGAAC | 16443 |
| rs255265457 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91786151 | CCTCCCAAGTACTGG[A/G]ACTAAAAGCATGCAC | 16443 |
| rs255276940 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91802533 | TAACTGTCCCAGTGG[C/T]GTGAGCAAACCCACA | 16443 |
| rs255310630 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91772305 | ATCACTGACCCATAA[C/G]CTCAGCCTCTTATCA | 16443 |
| rs255332525 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91824469 | TCCCTGCTCTCTCCC[-/T]CCTCCTGCCTCCCTG | 16443 |
| rs255334027 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810750 | GTTATATGTAAATAA[C/T]AGTTAAAAATATTTC | 16443 |
| rs255335930 | in-del | -/AGATAATG | | | intron-variant | Itsn1 | Mm_Celera | 16:91892368 | GACTGAACACCTTCA[-/AGATAATG]AGCTTTGTGTCCCAG | 16443 |
| rs255338332 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802304 | AGAATGGGATTCTTT[C/T]TAAAAAGCTCTTTGG | 16443 |
| rs255348771 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91810168 | AGTTCTCCACGGTCG[A/C]TGTGCGTTGTGTGTC | 16443 |
| rs255372821 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91847148 | GTGGTGACACACATC[-/T]TTAATCCCAGCATTT | 16443 |
| rs255380788 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91905882 | TCCATACAAGTGAGC[A/C]GACATCATGGCCAGT | 16443 |
| rs255386725 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91792670 | GTCCTCGAGGGTCAC[A/G]GCAACAGGACCCAGG | 16443 |
| rs255393528 | in-del | -/ATAT | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91727971 | AAATGCCATATATAG[-/ATAT]ATATATATATATAAT | 16443 |
| rs255402964 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91789042 | GGTGGTGGTGGTGGT[A/G]GTGTTAATGAATGAA | 16443 |
| rs255404373 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91886270 | TATAGATGGTTGTGA[A/G]CCACCATGTGGTTGC | 16443 |
| rs255411054 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91905195 | TTGTATGTAGGATTC[A/G]GTCCTACTAAGGGCC | 16443 |
| rs255413728 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831944 | CAGGGCTGAGAGATG[C/T]CAACGTTGTGCAGAG | 16443 |
| rs255421560 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830378 | AGAGAGGTGCCGTGC[C/T]GGCGCGGTCACCCAC | 16443 |
| rs255443418 | snp | A/C | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912224 | GTCTCATCATGGCTT[A/C]TAGAGTCTCTGAAAT | 16443 |
| rs255449827 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91823484 | GATATCTTCCTTTTT[-/G]GTGTGTGCTTTCCTT | 16443 |
| rs255451546 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91835926 | CTAGCCCAGGCAGCC[-/T]TCCTTAACCTAGCGT | 16443 |
| rs255462556 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91838416 | GTAAATAGTACCCAA[A/G]ACTTCAGAAATCTTT | 16443 |
| rs255465230 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91755610 | GGCCTCGAACTCAGA[A/T]ATCCACCTGCCTTTG | 16443 |
| rs255488530 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91780193 | GCAGCATGAAGGTGG[A/G]TGGTGCCACACCCTT | 16443 |
| rs255502694 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91891584 | CACCCACAATGGCGC[C/G]GGGCCTCCCCATGGA | 16443 |
| rs255524524 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91899051 | GCAGCTGCTGGCTGC[C/T]AGCAGGGCGCCTGGC | 16443 |
| rs255546447 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91884265 | TCAGCCTGGGGGGGA[A/G]CGACAGAGTACTATC | 16443 |
| rs255556790 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91764063 | CACTCAGGACTTTAT[C/T]CAGCACACAGCTTCC | 16443 |
| rs255557585 | in-del | -/A | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872506 | GAGGGAGGGAGGGGG[-/A]GGGGAGGGATGGGCT | 16443 |
| rs255558278 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91890208 | CTGTGCCTCTGTGGG[C/G]TACCAGACTCTTGGG | 16443 |
| rs255561742 | in-del | -/CC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91900004 | TCTCCCTCCTCCTCT[-/CC]CCCTCCTCCTCTTCC | 16443 |
| rs255573278 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91911750 | GGACTTAGTACCAGC[A/G]GTTTTAGAAGAGCTC | 16443 |
| rs255578912 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91881699 | AGACCACCGCACATG[-/C]CATTCTGCCTGTGAT | 16443 |
| rs255586809 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91750840 | TGGAATAATCTAGGC[A/G]CTATTCAAGAAGGAA | 16443 |
| rs255597822 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91763153 | TGGTGGATTTCAGGG[C/G]AAGGACTCCTCTTTA | 16443 |
| rs255600357 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91787518 | AAACACCAATAGTTA[G/T]AGATCAAGAGTCCTG | 16443 |
| rs255612184 | in-del | -/GGGG | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91876061 | TTTGCTGAATCAGAT[-/GGGG]GGGGGGGGGCACCAG | 16443 |
| rs255620534 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758301 | GGATTAAAGGCATGC[A/G]CCACCACGCCCAGCT | 16443 |
| rs255635663 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91810864 | GATGTGCTCAGAGCC[C/G]GGACATGAGCAGGCC | 16443 |
| rs255644292 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91867193 | AGGGATAAAGAGGGC[A/G]GTAGAAAGTGTAGCC | 16443 |
| rs255658561 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91866448 | GCAAAGGCAGTAGTT[A/C]CTGGCAGATTCACAG | 16443 |
| rs255693838 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91769457 | AATCCCAGTGACTAC[C/T]GACTTCCCTAAGGCC | 16443 |
| rs255698932 | snp | A/G | | | intron-variant, missense | Itsn1 | Mm_Celera | 16:91852936 | TCCTCCTCCTGGACC[A/G]CGTGCTGTGCACTCA | 16443 |
| rs255712586 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91869203 | GGTCCAGGGCTGCAC[G/T]CTCAGTGCCACAGCA | 16443 |
| rs255724255 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91874773 | CATGCTAAGGAAGCA[A/G]AGGACAAGGTGTGGG | 16443 |
| rs255725720 | in-del | -/CTC | | | cds-indel | Itsn1 | Mm_Celera | 16:91914373 | TCAAACCTTGATTCT[-/CTC]CTCCTTGACTCTACT | 16443 |
| rs255745964 | snp | A/G | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91816917 | GCTGCCTGAGGAGCC[A/G]TCGTCAGAGGATGAG | 16443 |
| rs255747150 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91905914 | CAAGCACCCAAGCAC[C/T]ACTGCTCCTTCCACT | 16443 |
| rs255748740 | in-del | -/GA | | | intron-variant | Itsn1 | Mm_Celera | 16:91813071 | GGTGCAGGAAGAACT[-/GA]GAGTTCTACATCTTC | 16443 |
| rs255751756 | in-del | -/CA | | | intron-variant | Itsn1 | Mm_Celera | 16:91866975 | GCGCGTGTGTGTGTT[-/CA]CGTGTGTGTGTGTGT | 16443 |
| rs255762169 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91788766 | CTCCCATCATGTCCA[-/C]CTCTCAGTGGGGGGT | 16443 |
| rs255768368 | in-del | -/GTGAGCTTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91892029 | TCCGGTGGAGCCACT[-/GTGAGCTTA]GTGAGCTTAGTGAGC | 16443 |
| rs255770608 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91755754 | GACTGTTCTTGGTTG[C/T]CAACTTGACTACAAG | 16443 |
| rs255781300 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91817932 | GCTGGGATTAAAGGC[A/G]TGTGCCACCACACCC | 16443 |
| rs255782202 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91800876 | GACTTGAATTTCCAC[A/G]AATCCTCTGGATCAA | 16443 |
| rs255786895 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912933 | CCACCACACCAGGAA[A/G]TCATGCCTTAGATGG | 16443 |
| rs255797856 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91731518 | TGGCTGTGAGCCACC[A/G]TGTGGTTGCTGGGAT | 16443 |
| rs255802161 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852576 | TGGGGGGAGGGGGGT[A/G]GACAGAGAATAGCAA | 16443 |
| rs255843893 | snp | A/C | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | GRCm38.p3 | 16:91730094 | TAACAGAAAGCGGCT[A/C]CCCTTGCAGCGGGCG | 16443 |
| rs255851798 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91874217 | TTCATATAGCAAGCT[A/G]CCAGGCATTTAAAGA | 16443 |
| rs255908539 | in-del | -/TA | | | intron-variant | Itsn1 | Mm_Celera | 16:91813940 | GGCACTGCAGCAGCG[-/TA]AACGACTGAGAGAGT | 16443 |
| rs255910357 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91787647 | ACAGTTAGCTGCTGC[A/C]GAAGCAGAACTCTGT | 16443 |
| rs255915895 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91881384 | TTATCAAAAGCAAAC[C/T]CTGAGAATTTACAGC | 16443 |
| rs255919545 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91857670 | GTTTGGCTCTTAAAT[C/T]GCCCCCTACCATTTG | 16443 |
| rs255927346 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91734167 | GTGCTAGGAATTGAA[C/T]CCTGGGTCACCCTGA | 16443 |
| rs255941039 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91823484 | GATATCTTCCTTTTT[G/T]GTGTGTGCTTTCCTT | 16443 |
| rs255942334 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91738474 | GTGTTATCTGTAGTT[A/G]TTTTGATTGCATCAG | 16443 |
| rs255943899 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911216 | TTCTGGTGTGTCTGA[A/G]GAGAGCAATGGCGGT | 16443 |
| rs255974458 | in-del | -/AAAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91903395 | TAAAATACTAAGAAT[-/AAAG]AAATTCTTGTCACTT | 16443 |
| rs255978219 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91836550 | GCATGCAGGTGCACG[A/C]GTGTTCTTTGTGTGT | 16443 |
| rs255981000 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919735 | AAGGCTCACCTGCCT[C/T]AGCTTTAAATCACCT | 16443 |
| rs255991431 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91737629 | AATGGGTTGTGTATG[C/T]TCTTTGAAGTTCTGT | 16443 |
| rs255997391 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91823078 | TGAGCTGTCATTGTG[C/G]TTGGGTCCGAATCCA | 16443 |
| rs256015963 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919009 | GGTTTCTCAAGTCTC[C/T]GTCCAGGGTGTGTCT | 16443 |
| rs256037814 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91840482 | AAATTCTTAAGCACA[A/G]TGGTAGACAGAAAGC | 16443 |
| rs256042399 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91843887 | GATTCCTGTAACCAC[G/T]GGAAGCTGGAGGGAG | 16443 |
| rs256050512 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91847662 | TTATAAATAGCTGGC[A/G]CTGCCTGGCGAAGGG | 16443 |
| rs256050578 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91839892 | CTGTCTCCTCTGTAT[G/T]TATGTAAAACAGACA | 16443 |
| rs256096045 | in-del | -/CCTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91899311 | CAAGGCCACTCACTG[-/CCTT]CCTTCCCACAGCAAA | 16443 |
| rs256110966 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91794155 | CTCCTTGCTCTCTTT[C/G]AAAATCATGGCTTCT | 16443 |
| rs256159386 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91808903 | AGCTGGCCCATCTGT[A/C]GAGTGACCCTCTCTT | 16443 |
| rs256164668 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91793427 | ATACCATGTAGTCAC[A/G]TAAACCGTGCTGGAC | 16443 |
| rs256169077 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91756055 | CTGCTGGAGGCCTGC[A/G]TAAGGGCTTTGGAAG | 16443 |
| rs256178461 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91828122 | CAAGAATTCCCTTCA[G/T]AAACATGAAAGTTGA | 16443 |
| rs256192551 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91834824 | TAACAAGTTTCAATC[A/T]GAACCTGACTTCTTG | 16443 |
| rs256205293 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91842410 | ATGTGTTTTTCATTC[-/T]TAGGGTATTAAACAG | 16443 |
| rs256207679 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91764347 | AGGGTGACATAGAAA[C/T]TATGAACACATTTTT | 16443 |
| rs256225793 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91815752 | CCTCCTGTTGCCAAA[G/T]CTCACCAGAAATTGT | 16443 |
| rs256271048 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91801693 | ACAGCCTCTGCCTGC[A/G]TTTGCGCATCCTGGT | 16443 |
| rs256274304 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91900329 | GCATTTTCCCTGAGC[A/G]GATTGCTACCCGGGC | 16443 |
| rs256286170 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91867553 | GCTAACAGGGTTTCT[A/C]TCTTTAAAAAAAATA | 16443 |
| rs256299474 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91875968 | CCACTTATGGCTCCC[A/G]AAAGCACATTGCCCC | 16443 |
| rs256305263 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91888735 | TAGCTTTGTGGTTGC[C/T]TCCCTCAGACCCATG | 16443 |
| rs256306474 | in-del | -/TTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91799987 | TATTTCTACTGTCTA[-/TTT]ATCTGTCCACCTGTC | 16443 |
| rs256308518 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91819368 | TGCTGGGGATTGAAC[A/G]CAGCAGGGCTGAGCA | 16443 |
| rs256313309 | snp | C/T | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91905290 | TGTCTTTTCTAGCAA[C/T]TGGTGTTCAATTCAG | 16443 |
| rs256342841 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911312 | AAAAAACGTATGTCC[A/G]TGAGCCTGGAAGGCA | 16443 |
| rs256349064 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91764603 | TTTTCAACAGTCCTT[C/T]TCCTCCGACCCTGGC | 16443 |
| rs256349914 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91904742 | GAGGGGAGCTAGCAG[G/T]CTCCTTAATTCCTAA | 16443 |
| rs256381538 | in-del | -/ACAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91781792 | TGCAGGGTGTAATGC[-/ACAG]ACAGGGCTGTGCGTG | 16443 |
| rs256382935 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917384 | GGAAACATTAGTGTT[C/T]ATCTCCACCAAACAA | 16443 |
| rs256383493 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91771827 | TTATTCTCTGCTAGG[A/T]GAGGCATTTCTATAT | 16443 |
| rs256431482 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91876433 | CTGGTGGCTACCTGG[G/T]GGCTGTGAGCATTGG | 16443 |
| rs256437029 | in-del | -/TCTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91731426 | CTCTCTCTTTCTCTC[-/TCTT]TCTCTCTTTCTTTCT | 16443 |
| rs256439136 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91732098 | TTTCTGTCTCTCCAG[C/T]TCAGTCAGACAATGG | 16443 |
| rs256443489 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915016 | CTTATTTTCAGACAG[A/G]ACCTGACTCCATAGC | 16443 |
| rs256444837 | in-del | -/CTGACTGA | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91828947 | TTCAGAAGTAAACGG[-/CTGACTGA]CTGACTGACTGACTG | 16443 |
| rs256445794 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91818836 | CTCTCCTCCCACTCT[C/T]CCCCAGGAGAGCTAC | 16443 |
| rs256446100 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91826118 | GATGAGAAGTTCATG[A/G]CCAGAAGTCGTTTTC | 16443 |
| rs256460613 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91825520 | GTGGTTGCTGGGATT[A/T]GAACTCAGGACCTTC | 16443 |
| rs256471605 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91834914 | TAGCTACATTGGGAC[A/G]TCATAGCCAGTGTCT | 16443 |
| rs256488561 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91875694 | CAAGCTGCCTCCTTC[A/G]CAGGGCTGCCAGTGG | 16443 |
| rs256490557 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91883962 | GTGAGGGCTCTCTGT[C/T]CTGTGTATTTTAGTC | 16443 |
| rs256494096 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91754301 | AGGACGGAGAGAGGG[A/C]AAGTGTAGGGACGTC | 16443 |
| rs256502195 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91855847 | TTGAAGCTTTTAGAA[C/T]GAAAGCCAGTCAATG | 16443 |
| rs256511492 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91792249 | AAAAGGAAAAACAGA[A/G]CATGCCACATCATAT | 16443 |
| rs256526799 | in-del | -/GTGTGGGG | | | upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91729110 | AAAGTGTGTGTGTGT[-/GTGTGGGG]GGGGGGGTGCTATCC | 16443 |
| rs256530723 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91806532 | GTTCCCTCGGTCAGA[C/T]ATGGAGGCTGGATGC | 16443 |
| rs256555142 | in-del | -/TC | | | intron-variant | Itsn1 | Mm_Celera | 16:91776502 | TTCCTTTTTAAAACG[-/TC]TTTTCTGTTTATATT | 16443 |
| rs256562329 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91865437 | TCCAGTCCTAAGTCC[C/T]CGAAATGCATTCTAC | 16443 |
| rs256577930 | in-del | -/GAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91890275 | TTTGGGGGGGGGGGG[-/GAA]TGGCTTTATAGCCAG | 16443 |
| rs256588267 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91894084 | CAGGGATGGATGGAA[A/G]TTTTCAGTGGTACTG | 16443 |
| rs256593917 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91883227 | GAAAACTTTTAAATC[C/G]AATGACTTTTCCAGT | 16443 |
| rs256595605 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91740097 | TCTCCTGGAGTCAGT[C/T]GGGGTGGGAGGGGTG | 16443 |
| rs256602450 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91813731 | GCTACAGAGGAGGGC[A/G]GCAGATCCTCTGGAT | 16443 |
| rs256620312 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910082 | AGAGTTTGAAGCCAC[A/G]GGGGCTTTGTAAGGA | 16443 |
| rs256626089 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91789818 | GAGGCAACTTACAGA[A/T]GGCCTGGTGCATTGT | 16443 |
| rs256640561 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91796160 | AAGTGCAGCTGGTTT[C/T]GGTGTCAGGAAGGTG | 16443 |
| rs256672662 | in-del | -/GA | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913262 | TGAGAAGTGCAGGCT[-/GA]GTTTTGGTCCCTCGT | 16443 |
| rs256683125 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91739414 | TCCATAATTGTGAGC[G/T]TTCTTAGCTACTCCC | 16443 |
| rs256684392 | snp | A/C | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746728 | GCTAGCCGGAAGCAG[A/C]CTGCGGGCTCGCCTT | 16443 |
| rs256714785 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91795565 | GTCCTGGAACTCACT[C/T]TGTAGACCAGGCTGG | 16443 |
| rs256720880 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746312 | CGCACACAGGCAGCA[A/G]AATAGAAAGCAGGTG | 16443 |
| rs256728921 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91781007 | ACAGGAAGTGGAGCA[C/T]TTACATCTTGACAGA | 16443 |
| rs256735978 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91849851 | GGCAGGCTTGCAGCC[G/T]AAGGGTGCAGATTTG | 16443 |
| rs256770275 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91776769 | TTTGGCACATGTCGA[C/T]TTTATTTTGTTTTTT | 16443 |
| rs256773829 | in-del | -/ATAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91769167 | ACCTTTCAGGAAGAG[-/ATAA]ATAAATCAGGCTGGA | 16443 |
| rs256776162 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91801854 | GAAAGAAAATAAATG[C/T]CATTGTGGAACAGAC | 16443 |
| rs256794184 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91848518 | TGAGGTGCTTCAGCT[C/T]ATCCCATTAGGAGCT | 16443 |
| rs256806555 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91856537 | TTTCCTATTTTGAAG[A/G]CTACTCCAAGATTTT | 16443 |
| rs256809579 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830863 | CTTGAGTTTTCATCT[A/G]AAATGAGGACAGAAT | 16443 |
| rs256815490 | in-del | -/AAAAAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91814593 | TTTTTTTTCCACACT[-/AAAAAA]AAAAAAAAAAACTTT | 16443 |
| rs256864716 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91855736 | GTCATAGTAATTACA[C/T]AAGAGTAAGTAATTG | 16443 |
| rs256869942 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91731598 | ATCTCTCCAGCCCAC[A/T]TCCATCCTTCCTTCC | 16443 |
| rs256874629 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900083 | CCAGTACCTGAGGTC[G/T]CGGGTCATAGTCATC | 16443 |
| rs256889712 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91742025 | CCTTAGGGGTCGTCG[G/T]CACTGAGCTCAAGTC | 16443 |
| rs256889879 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91851285 | CTGGGACAGCCAGTC[C/G]ATTTGGCTGCCCCAT | 16443 |
| rs256901575 | snp | A/G | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91827863 | CCCTCTCCCCTAGGA[A/G]TCTCAGCAAATGCTT | 16443 |
| rs256906199 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91820406 | TAAAAAGCAACATTG[A/C]ACGGTGTCAGAATTA | 16443 |
| rs256964394 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91737955 | TACTGTTGGTCAAAT[-/A]AAAATAGCAGTCTAA | 16443 |
| rs256965957 | snp | A/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Itsn1, Cryzl1 | Mm_Celera | 16:91730312 | CCCTTCACTTCTGTT[A/T]GCCTTTGCTTTGGAA | 16443 |
| rs256970432 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91834713 | TGGTAAAGCTGTTTC[A/G]TCGGTGTGACTGTCT | 16443 |
| rs256974957 | in-del | -/ACACAC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91835221 | TTTGAGAGTCAGTCT[-/ACACAC]ACACACACACACACA | 16443 |
| rs256979819 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91748638 | ACTCAGCGGACTGGG[A/G]GTGTTCTATCCCTAG | 16443 |
| rs256984856 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91834354 | ACTGTCTCACAATTA[A/G]GAATACTCTGCTTTT | 16443 |
| rs257022297 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91764293 | GAGGCTACTTCTGCA[A/G]CCTTGTCTGTGGTGC | 16443 |
| rs257034551 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91756744 | ACCCTTCCTTCCTAA[-/G]GTTGCTTTTGTGGAC | 16443 |
| rs257045263 | in-del | -/TG | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91877168 | CAGACATTTTGTCTC[-/TG]TGACAGGGCCCTAAG | 16443 |
| rs257051819 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91851619 | TGGAAGCCTAGACCC[C/T]GCTGAGTCCCTGTGT | 16443 |
| rs257067743 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91770800 | AGACTCCTCCCCCAA[A/G]CCCCCCTGACAGGCA | 16443 |
| rs257070041 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91826840 | ATGGCTATGGAGGAG[G/T]GCTGAATCCTTTGCT | 16443 |
| rs257103690 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91821926 | GTTATAGCACCAAGA[A/G]CCAAGACTACTGGCT | 16443 |
| rs257131811 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91826351 | ATACCCAAAGAGATT[G/T]AGAGTAAAGATCGTG | 16443 |
| rs257146095 | in-del | -/AAGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91821475 | TCAGCTGAAGGAAGG[-/AAGC]AAGCCAGAAACATAC | 16443 |
| rs257153823 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91895555 | GGGAGAGAAGGATTT[-/A]TTTTTTTTTTTTTTT | 16443 |
| rs257161778 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91806441 | CCCTCTTGCACCGGT[C/G]AGTGGGACAGCGGTA | 16443 |
| rs257185543 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91829321 | CCTTAGGGGAGTGCT[A/G]TGTAGCCGACGTGTG | 16443 |
| rs257190433 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91868863 | GGCTGAGGAGATGTA[A/G]CAGAGCCCTCTCCTG | 16443 |
| rs257194989 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91917307 | CTTGTTTCTTGGTGC[C/T]GTGGCTCACAGGGGT | 16443 |
| rs257205924 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91875852 | GCACAGTGTCCTGTG[C/G]CCTTGTGTCCTGCCA | 16443 |
| rs257212126 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91784979 | CTTTTAAAATCTCGA[-/C]TCTTCTCAGTAGCAT | 16443 |
| rs257223469 | in-del | -/TTTTGTTTTGTTTTGTTTTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91736805 | GTGAAAACTTACTCT[-/TTTTGTTTTGTTTTGTTTTG]TTTTGTTTTGTTTTG | 16443 |
| rs257248823 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91877028 | ACACATGTCCTGCCC[C/T]GCCCTGCCCCCCACC | 16443 |
| rs257248848 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91868151 | AGGTAAGATGCTCGC[A/G]GGCCGTCTGCTCGCG | 16443 |
| rs257253314 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91779525 | GCAGTCTCTGGACAC[A/G]AAGGGGTTAATAATT | 16443 |
| rs257273904 | in-del | -/TTTTGTTTTTTTTTTTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91835349 | TTTTTTTTTTTTTTT[-/TTTTGTTTTTTTTTTTA]ACCTCTTTGCCTCCT | 16443 |
| rs257277598 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91883686 | TCGGTTGGGTGCTGT[A/G]TACATCCAAAGGCTG | 16443 |
| rs257287775 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91813544 | CTTGCTGCCCCTGGT[C/T]AGCAGAAGTAGTCTA | 16443 |
| rs257310382 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91883829 | GAATCCCAAAGAGGC[A/C]GGCATCTCTCCCAAC | 16443 |
| rs257313067 | in-del | -/GGGGG | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872356 | GAGCCATCCAACACT[-/GGGGG]GGGGGGGGTAGAGGG | 16443 |
| rs257314455 | in-del | -/AA | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830612 | GAGGATCGCTGCCCC[-/AA]GTGTCACTCGCCGGC | 16443 |
| rs257321065 | in-del | -/GCCC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91818686 | GTGAGTGAGCAGTGT[-/GCCC]GCCCGCCCGCGGCAG | 16443 |
| rs257332364 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91829488 | TTACTGCTGTATTAA[A/G]CAGAAAGGATTTAAC | 16443 |
| rs257348502 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91739704 | CAGCTTTAGGGACAG[C/G]CACAGCTCCAGTTGT | 16443 |
| rs257367434 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91909947 | GTACACATGCACGGA[G/T]GTACATATATACATA | 16443 |
| rs257371282 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889785 | GATTGAATTGGACTA[C/T]AAATGGGCCGCAAAG | 16443 |
| rs257392712 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91835636 | AGGAGAGAATGAATC[A/G]ATCTCTTCGGCTTGT | 16443 |
| rs257404057 | snp | A/C | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915879 | GGTCCTAAGATGCCA[A/C]CCCCTCCTCCCCTGT | 16443 |
| rs257406369 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91909108 | GTGATACCAAACTAC[A/G]GGAGGGTCCACCAGA | 16443 |
| rs257438700 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91787630 | GGAAAGAGTGGGACA[-/G]GACAGTTAGCTGCTG | 16443 |
| rs257441170 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91732553 | TCAAAATTTAATGTA[C/G]AGTCTAATCACGTAT | 16443 |
| rs257445537 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915140 | TATAAAAGGTGGATC[A/G]ATGGGCCGCTCATAC | 16443 |
| rs257447186 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91792181 | GCCTCTGCATTCTGT[C/T]TCTGCTCCAAAGACA | 16443 |
| rs257454631 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91836007 | AGCTCTCCAGGCTCG[A/C]GCCCTGCCCAGGTCT | 16443 |
| rs257469764 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746438 | TGTCACTGAGCTAGA[A/G]TGGTGAGTTTTATGT | 16443 |
| rs257471966 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746519 | CCTAGCTTACTGTAG[C/T]GCTGAGTTTCCTAAA | 16443 |
| rs257474402 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91740265 | ATTGTAGCAGTTTCT[A/G]ACCACCAAGCCCATA | 16443 |
| rs257480690 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91808922 | GACCCTCTCTTCCTC[-/T]TGAGTATGTCCCGGT | 16443 |
| rs257481268 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91783427 | ATCACTGTCAGGCAC[-/A]CCCTACCCTGCATGT | 16443 |
| rs257484613 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783368 | GTGCTTGGCAGAGTT[A/C]GTGTTCAGTAAATGT | 16443 |
| rs257505960 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91849068 | CCTACTGACAACAGG[A/G]TTATTGGCTTCTCAA | 16443 |
| rs257515379 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91835503 | GCCAGTGAGGGATTA[A/G]CCCGCCTCTGGCTGT | 16443 |
| rs257525983 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91799986 | TTATTTCTACTGTCT[A/T]TTTATCTGTCCACCT | 16443 |
| rs257528096 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91842155 | GTTTTTTAAGTAATG[A/G]ATTAAATATGAGGAA | 16443 |
| rs257541985 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91887557 | CTGGGGTTGGGCCTG[C/T]GGGGATGGCAAGAGG | 16443 |
| rs257542713 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91800387 | TGCCTCTAACCGTGC[C/G]CTAGGATTACAGGCA | 16443 |
| rs257552951 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91807446 | TAATCAGCTCTCTGC[A/G]CGCCACACTTTTCCA | 16443 |
| rs257555768 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91790681 | CAGGAGGAGAAGTGT[G/T]GGGGATGGAGGGTGG | 16443 |
| rs257559067 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91755214 | CCAGCACCTCCTCTC[C/T]TACTATGTGAGAGTA | 16443 |
| rs257570766 | in-del | -/ACATACAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91907923 | ACAACATCAACAAAA[-/ACATACAC]ACAAAATGAAGCAAA | 16443 |
| rs257578929 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91898808 | CACATGGACGAAACA[C/T]ACATATGTGAGCAGG | 16443 |
| rs257597828 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91904241 | AAGGGCAGCTGTGTG[G/T]GCAGTTGGAGGCCTT | 16443 |
| rs257604184 | in-del | -/CAAACCAT | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831457 | CTGGATGGGGTCAAG[-/CAAACCAT]CTAACCAGTATACTA | 16443 |
| rs257610546 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91892640 | AACCCCAGATGGCCA[C/T]TGCCAACCTGCCCCA | 16443 |
| rs257627686 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91903959 | CGCCTCCACAGTGAC[A/G]TACTTCTGCTAACTA | 16443 |
| rs257638432 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91857127 | TCTGACCTTCACACA[C/T]GAGCTACACGCAGAA | 16443 |
| rs257647929 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91856835 | TGTCAGCTGTGAGGC[C/T]AGCAGTCAGTGTTGG | 16443 |
| rs257658280 | in-del | -/GTAGAGGACTGTCCAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91905778 | ACCCGAACAGGCAGA[-/GTAGAGGACTGTCCAT]GTCCCACACCTTGGT | 16443 |
| rs257675033 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91789940 | TCTTTAACCACAAGC[A/G]GGAAACAGAGACTGC | 16443 |
| rs257681973 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91815143 | TATAATATGGTTTAA[A/G]TGGTCTTGCAAGGAT | 16443 |
| rs257684309 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91900004 | ctctccctcctcctc[C/T]ccctcctcctcttcc | 16443 |
| rs257685284 | in-del | -/CTATGCACCACGTAAAAATTTGCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91767079 | CTGTGTTTTCTAAAA[-/CTATGCACCACGTAAAAATTTGCT]CTTGGTGAGCACTTT | 16443 |
| rs257702153 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91848594 | CACTTCATGGGCACT[A/G]AGACTAAGACGGGAA | 16443 |
| rs257709385 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91837592 | AAATTAAACTGGATA[-/C]AAAAGGTGGAGATCG | 16443 |
| rs257721568 | in-del | -/CT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91897037 | GCATGTGACTGTCTG[-/CT]CTCTCTCTCTCTCTC | 16443 |
| rs257727027 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91752626 | GTTGGGATGCCTCCG[A/G]AGCTGCTGAAGGCCT | 16443 |
| rs257727157 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91892119 | ATGTGTGATCTTTCT[A/G]TGAGGTGGCAGCTCA | 16443 |
| rs257769793 | in-del | -/CAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91880361 | CGCCCATGCTCCTAC[-/CAT]CATCCTCTTTGTCCA | 16443 |
| rs257785740 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91897147 | ACATAAGCCTCAGCC[C/T]GACCCAGCTCCACCC | 16443 |
| rs257786813 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91768975 | AGCGTGCGGCCCCTG[C/G]TGCTGACAGCCGCTG | 16443 |
| rs257796959 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91827152 | CATTCTGCAAATGCC[A/G]ATGTGTGTCTACAAG | 16443 |
| rs257804945 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91909777 | AACCTCGATGTAGTG[C/T]GATTTTTCTGTCCTT | 16443 |
| rs257806812 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91777834 | CCCAGGCATTGGAAG[A/G]TGTGCGGGAGGCTTC | 16443 |
| rs257812956 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91751984 | CTAATACACTAGGAA[G/T]GGTGGGCCTCTGAAG | 16443 |
| rs257822518 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91865032 | GTGAGCCCATGATAA[C/T]TGCTGTCATGTGCCT | 16443 |
| rs257824371 | in-del | -/GTGT | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919438 | AGCCGCTCCTCAAAG[-/GTGT]GTGTGTGTGTGTGTG | 16443 |
| rs257825008 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91777580 | TGTGCTTTGAACAGA[C/G]GCCTGGGCTTGATGA | 16443 |
| rs257841133 | in-del | -/ACCA | | | intron-variant | Itsn1 | Mm_Celera | 16:91806060 | CTGTGCTCACAGTGC[-/ACCA]ACCACCCTCTCCTTC | 16443 |
| rs257843066 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91820238 | ACATGTTTACTTAGC[C/G]CACTGTGATTTCTGG | 16443 |
| rs257858778 | snp | C/G | | | synonymous-codon | Itsn1 | Mm_Celera | 16:91820453 | TCTGTAACCACAGGC[C/G]GCAAAACGGGAACTG | 16443 |
| rs257860277 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91827063 | GAAAGTCTGCTGTGG[G/T]TCACTCAGAGGCCTA | 16443 |
| rs257901533 | snp | A/C | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91916574 | TGGGCATAGCATTCT[A/C]TTTTGAATGACTCCT | 16443 |
| rs257903047 | in-del | -/TC | | | intron-variant | Itsn1 | Mm_Celera | 16:91754630 | CTCTCTGTCTCTCTG[-/TC]TCTCTCTCTCTCTCC | 16443 |
| rs257906088 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91862538 | AGAACAGTTCTGGAT[C/T]GCTCCCCCCCCCCCC | 16443 |
| rs257907848 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91759665 | GTGATCCCACCAAAG[C/T]GGAGGCGGTGGGAAG | 16443 |
| rs257914375 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91860999 | ACAGTGCTCCTGGCC[C/T]GGAGCCTTCTCTTCT | 16443 |
| rs257941954 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91881401 | TGAGAATTTACAGCT[C/T]TCCTGTCCTGGGAAC | 16443 |
| rs257942534 | snp | A/C | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91728325 | ACGCGGAGGAAGAAG[A/C]AAAGATCAGTCTACA | 16443 |
| rs257947205 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916007 | TTCTGCAGGGACGTG[A/G]GGGTGTGAGGGTCAC | 16443 |
| rs257958903 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91784948 | CATGGTTTCAGTTCT[C/T]GACAATTGTCTATGT | 16443 |
| rs257961763 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91783255 | GATTGTGAAGCTCAG[C/T]GGGGGCAGTAAAAGT | 16443 |
| rs257979686 | snp | A/G | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91870896 | GGCAAACCCACCACC[A/G]TGTACAGTGCTCTCA | 16443 |
| rs257996156 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91833173 | CCCCCTCCCCCAGTA[C/G]ATAAATAAAGGACAA | 16443 |
| rs258018078 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91888228 | GTACCCTCACGAATG[C/T]CATGAAACTGTAATG | 16443 |
| rs258037659 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91791397 | ACAGACCTCCCGACT[A/C]AAATCATTCTAAGCA | 16443 |
| rs258041316 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91737683 | TGGTTTAGGGTGAGT[C/T]CAGTTGAATGCCTTG | 16443 |
| rs258064982 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91887321 | CATAGTCACAAGGAC[C/T]TTCGGGAGTCTTCGC | 16443 |
| rs258079192 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91893174 | CCAGTCCACCCTGGC[C/T]GTGTGGCTCTGCACA | 16443 |
| rs258092416 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745535 | ACCTAATTTCAAGTG[A/G]TGGGGCAAGGCATGT | 16443 |
| rs258094828 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798618 | ACACACGCCCGCACA[C/G]GTTCACACTTTCCAC | 16443 |
| rs258103147 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91869470 | AGAATTCAGTCCTTC[A/G]TCTTCCTCTAGTGCC | 16443 |
| rs258121590 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91797443 | TAAGAGCACTGACTG[C/T]TCTTCTGAAGGTCCT | 16443 |
| rs258181126 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91752511 | CAGCCGGCACCTTGT[C/T]ATTAGTCAGGAATCT | 16443 |
| rs258200047 | snp | A/G | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91804170 | CCATAGTTTCATGTT[A/G]TCTGTCATATGTTTC | 16443 |
| rs258201880 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91735036 | AACAGCCAAGTCATA[C/T]CCACGGGAAGCCTTT | 16443 |
| rs258202672 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91797437 | AGCAGTTAAGAGCAC[C/T]GACTGTTCTTCTGAA | 16443 |
| rs258233593 | snp | C/T | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91853560 | CCTGAGCTGGGGCAG[C/T]GTCCTCTATGGCTGT | 16443 |
| rs258244325 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91897867 | TCTCCTCCACCATGG[A/G]TCCCATGGGTTGAAC | 16443 |
| rs258245085 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91854992 | AATAGTTAATTCCTT[G/T]TTTTTCCTCTGATAT | 16443 |
| rs258250452 | in-del | -/AAAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91842081 | AATCTTTAAAAAAAA[-/AAAG]AAGAAGAAGAGCGTT | 16443 |
| rs258263172 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91805215 | AGAGTGTCTGCCTCT[A/G]AGTCTGAGGACCTGG | 16443 |
| rs258263832 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91760278 | TTTGCTTGTGTGGTG[G/T]TGTTGGTGCCTGGGG | 16443 |
| rs258271234 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91740970 | CCCACCCCCACCCCC[-/T]CACCCCGGCCTTCTG | 16443 |
| rs258275138 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91792997 | GCAAGCACACTCCTA[A/T]GCAGAGTTTCAGTGC | 16443 |
| rs258280189 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91761240 | GAGACATCAGCTTCC[C/T]GGCTGAACCTGTGAA | 16443 |
| rs258288346 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91837731 | GACCTTGTACTTTGT[A/G]GCTTTGTGCTATTTG | 16443 |
| rs258300614 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91844712 | CCTCTTCTTCCACCT[C/T]CTTTAGGTTCCCACA | 16443 |
| rs258302470 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91837032 | TCCATCTGCTCTGAC[C/T]ACCCATAAACTATCC | 16443 |
| rs258310716 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91760668 | CAGTGAGGCTGCGCC[A/G]ACCAGGCCTCCCCGA | 16443 |
| rs258314502 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91768330 | AGCTGCCTTTCTCCT[C/T]CCAGATCCCTCACCC | 16443 |
| rs258317191 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91902568 | AGAAGTCCTTTGGTA[C/T]GTTTCTCTCTACAAA | 16443 |
| rs258340557 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91800957 | TGGTTGTGTCCTACT[A/G]GGTTGCACTCAGGAC | 16443 |
| rs258367768 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91844111 | GTTTAGAATTCTCTG[C/T]AGGCCTTCCATTAAG | 16443 |
| rs258368651 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873377 | TTATGCACTCCAAAC[A/T]GCCCATTGTATGGAC | 16443 |
| rs258371121 | in-del | -/AA | | | intron-variant | Itsn1 | Mm_Celera | 16:91761619 | AAGAATTATTTCACC[-/AA]GAGTTGCTTTGCAGA | 16443 |
| rs258373578 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91817059 | CTGATGCTTGGCCAG[-/A]AGGCGGGCACAGGTG | 16443 |
| rs258396456 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91767852 | AAGCTTGGTTGAAGA[A/G]GAGACGAAGGGTTAG | 16443 |
| rs258423171 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91850425 | CCTGCCTGAGCTCCA[C/G]TCGCACCACCCCTAC | 16443 |
| rs258423623 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872465 | TGAGGTGAACCTAGA[A/T]GTCAGAACAGAAAAG | 16443 |
| rs258425439 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91880505 | ATGGTATAGTCTTCC[C/T]CATGCATCACCCCAT | 16443 |
| rs258432410 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91752013 | GATTTGGCCACCCCA[-/G]GTTCCGGGACGCTGG | 16443 |
| rs258450454 | in-del | -/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91828093 | GTCCCTCCCTCCCCA[-/C]CCCCCCTTATCAGCA | 16443 |
| rs258464589 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91810434 | CCCTGTCTGGAAGCC[C/G]CCTGAATGTCACTGA | 16443 |
| rs258499287 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91805354 | CTCTCTCTCTCTCTC[-/T]TCTCTCTCTCTCTCT | 16443 |
| rs258501378 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91763932 | CTGGTTCTGCACCAT[C/T]TATAGATGTTTGCTA | 16443 |
| rs258524131 | in-del | -/CTCCC | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831531 | ATTGCTATTATTTCT[-/CTCCC]CTCCCCTCCCCTCGT | 16443 |
| rs258527130 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91775869 | TGAAGAGGCTTCCTA[C/G]TAATTCTGTTTCACT | 16443 |
| rs258528897 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91736925 | AAAGTGCTGGAACTA[C/G]AAGCCTGGCCACAGC | 16443 |
| rs258534837 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91879789 | TGAATTTGGAGATAG[C/T]GTCTTCAAAGATGTA | 16443 |
| rs258568956 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91879935 | AAGAGAGGCAAGCTT[C/T]TGTGGGACACATGAA | 16443 |
| rs258579484 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91825581 | GCCATCTCACCAGCC[C/T]GACATTATGTTTTCA | 16443 |
| rs258586389 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91817372 | GAATACATGGCTCTG[-/A]ATCAATAATGAGATG | 16443 |
| rs258587038 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91821418 | GGAGCAGGGCAGCAT[C/T]CAGGCAGGCATGGTG | 16443 |
| rs258595267 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91903822 | AGCTGAGAGTTCTAC[A/C]TTCTGAAGAGAACCA | 16443 |
| rs258599913 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907847 | CAACTACGTAGTGAG[C/T]TTATCACCAGCCTGG | 16443 |
| rs258610672 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91744363 | TAGGTGTTTTGCTTG[C/T]GTGAATGTTTGTGCA | 16443 |
| rs258611015 | snp | C/G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91887591 | AGGCCCTGCTGAGGG[C/G/T]GCCATGCCCTGTCTC | 16443 |
| rs258612053 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91736035 | GCCTTAAAAAATGAA[C/T]CGCAAATCTTGTGTT | 16443 |
| rs258636270 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91745117 | CTTCTATAGTTTTTT[A/T]AAAATGTGTTTTTAT | 16443 |
| rs258661349 | snp | A/C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91875011 | TCACCAGGACTGGGG[A/C/G]CTCCACCCTAGCCTA | 16443 |
| rs258673431 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91753338 | CTAAACACACTGTAT[A/G]TCTTGGCAGTACTTT | 16443 |
| rs258676984 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91744459 | AATTACAAATTGTGA[A/G]CTTCCATGTAGGTGC | 16443 |
| rs258700495 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91845379 | AGACCCAAATTCAGT[G/T]GTAAAGAGGCAATTC | 16443 |
| rs258768362 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91826745 | GGTGTGTGTCTGTGC[A/G]TTTGTAAGTCTCTGT | 16443 |
| rs258775979 | snp | C/T | | | synonymous-codon, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91854648 | CAAGCCAGCCATTCC[C/T]GGAGAAGGTAAGGGC | 16443 |
| rs258788926 | snp | C/T | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91853607 | GTGTGTGTGTGTGCG[C/T]GTGCATGCGCGCGTG | 16443 |
| rs258799616 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91785075 | GTGCTGGGTAGCTCA[C/T]CTTGTTAAACCGCAG | 16443 |
| rs258807833 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91738707 | CCCAGCCTGGGAGAC[A/T]GAACACCTGTTGTCT | 16443 |
| rs258811499 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91866640 | ATGCGATTTAAGTTA[C/G]CAAAAAGCCTTCCTC | 16443 |
| rs258820017 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91789263 | GACCGCCGTTTCTTG[-/T]TTATTTTTATTGTTG | 16443 |
| rs258834392 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91814675 | TTTTGAAAACCATTC[C/T]GTCTGACTTACCCTA | 16443 |
| rs258841054 | in-del | -/AT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890687 | ACTGGGATAAAAGGC[-/AT]GTGTCCAGCGCCCAG | 16443 |
| rs258841567 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91820878 | AGGCTCACCATCTAG[C/T]CATCATTAGGTGCTG | 16443 |
| rs258844617 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91881182 | ACTATGGCTGCTTTT[A/G]AGTTTCTTGGGTTTG | 16443 |
| rs258851574 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91888619 | CAGCTTTGAGCTATA[C/T]GCTCACCCACCCAGA | 16443 |
| rs258853399 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91791628 | ATAAAAATTTGTACA[C/T]ATGTTTAAATAAGGG | 16443 |
| rs258864662 | in-del | -/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91896734 | ACACAAAGAGAGAGA[-/G]AGAGAGAGAGAGAGA | 16443 |
| rs258869152 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91862554 | GCTCCCCCCCCCCCC[A/C]GCCCCCCTGGCCTGA | 16443 |
| rs258881382 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91910837 | GCTTTAAAAAGGTAT[C/T]TGTGTGTTTGCTCAC | 16443 |
| rs258897003 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91757281 | CATAACACTGTCTGC[-/T]TGTAGTTGCATTTGG | 16443 |
| rs258911174 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91746262 | GTCAGTAGTTAAATA[C/T]GGAGTTATCATATGG | 16443 |
| rs258922826 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91916711 | TTCCAGTTCCCTGTT[C/T]CCTGATACCTAGAAA | 16443 |
| rs258932197 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91874841 | CAGTACTGGGTTCTT[A/T]GAGCCTGCACACACT | 16443 |
| rs258933647 | in-del | -/A | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Itsn1, Cryzl1 | Mm_Celera | 16:91730247 | CGGATTCCCAGAAAG[-/A]AAAAAAAAGAAAAGA | 16443 |
| rs258949719 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91888240 | ATGCCATGAAACTGT[A/G]ATGTCGCCTACACAC | 16443 |
| rs258964955 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91744783 | GCGTGCAGGGATAAT[A/G]TGGATGGCTTCCCAC | 16443 |
| rs258973317 | in-del | -/TTTTTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91904790 | TCTCTTTTTTTTGGG[-/TTTTTTT]TTTTTTTTTTTTTTT | 16443 |
| rs259005121 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91825466 | AGACACACCAGAAGA[A/G]GTTATCAGATTTCAT | 16443 |
| rs259013561 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91861352 | GAGGCAAAGGGATCT[C/T]CCTGACAGTGCCCGG | 16443 |
| rs259027677 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91754158 | TAGGAGTGAATATAG[C/T]TTACATGTTTCAGTG | 16443 |
| rs259030669 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91730715 | TATTTTCAGGGAGGC[C/T]GGTTTACTAATCCCG | 16443 |
| rs259033693 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91797234 | CCGTCTCAGTAAGGC[C/T]GAAACACGTGAGCTG | 16443 |
| rs259047367 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91784381 | GTCCTCTCCTTCTGT[C/T]TTCCCATGGCTGTCA | 16443 |
| rs259070668 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91854447 | CCTGGTGGCTGCTGG[C/T]ACCCTCCTGTGTTCT | 16443 |
| rs259092943 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91897733 | AGAAGAGGGCATTGG[A/G]TGCCCTGGAACTGGA | 16443 |
| rs259105984 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91855678 | TGAGTGTACTATCTG[C/T]AATCAGGTCTCACTA | 16443 |
| rs259113893 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91762240 | TAAACCAGAATCTAA[C/T]GAGCAACGTGATTAA | 16443 |
| rs259115949 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91753468 | TGGGCGGCGCCATTT[C/T]CCTCCCGTAGTCCAT | 16443 |
| rs259117240 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91865291 | ACACATGAGGACAGA[C/T]GTGCTCTTGGCCCAA | 16443 |
| rs259125464 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91824382 | GGCTACCATTGCCTC[G/T]TACTCTCTTCCACTG | 16443 |
| rs259125507 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91832666 | CCAGAGGCTGGCTGT[A/G]TAGTGCTACTTGGTG | 16443 |
| rs259126776 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91902433 | GCAGTTTAGTTCACA[C/T]GAATCAACAGCAGTA | 16443 |
| rs259153683 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91792066 | GAAGCAGTGTCAGAG[-/C]CCCCCAAGAACTGGA | 16443 |
| rs259166937 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91738635 | GAAAATCTCACCTTC[C/T]AGTGCTGCCTGTAGC | 16443 |
| rs259167282 | in-del | -/TCC | | | intron-variant | Itsn1 | Mm_Celera | 16:91841445 | TCCGCCTTGGCATTG[-/TCC]GTCAGTGCTTCCTGT | 16443 |
| rs259171342 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91840560 | GCACACAGTGGGGTG[A/G]GGAGTGAGGTGCAGT | 16443 |
| rs259177759 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91864088 | TTTGTCAACAGACTG[A/G]GACCCATGATTAGGG | 16443 |
| rs259192743 | snp | A/C | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91832088 | ACATGAAATTTTATT[A/C]TTATTTCCACCTAGA | 16443 |
| rs259204069 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91791493 | CTAAAGAGACTGGGG[A/G]CGATTGTTAAAAATC | 16443 |
| rs259204870 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91761439 | AGGAGACAGTGCTGT[-/A]AAAGAAGACAGCTGT | 16443 |
| rs259213241 | snp | A/C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91847790 | TGACCGCACATGACC[A/C/T]GAGGGCCCGCCTTTC | 16443 |
| rs259222214 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91893279 | AATTGTCTTATTTTA[C/T]TTCATAATCGTTTAC | 16443 |
| rs259237481 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831305 | TTACACTTTGCTATC[A/G]TCTCATAAAGGAAAG | 16443 |
| rs259311950 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91775365 | AGGTGTGTACACCAC[A/G]AGTCATTTCTTTCAT | 16443 |
| rs259324966 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91873409 | GATCAAACAACTGTA[A/G]AATACACCTGATTCC | 16443 |
| rs259326789 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | Itsn1, Cryzl1 | Mm_Celera | 16:91728796 | CGCCCCAGGGACCAC[A/C]AATAAATGGGAGAAG | 16443 |
| rs259335551 | snp | A/G | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803616 | GAGCAGCAGTGCTCT[A/G]ACGCACTGGACCGTC | 16443 |
| rs259360169 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91879249 | CAAGACCAAGATTGT[A/C]CTCAAATAGACCTTA | 16443 |
| rs259362411 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91766974 | TTGGTTTATGTAGTG[-/C]ACATGGAAGCAGAAA | 16443 |
| rs259364747 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91761488 | GTGTGCGGTCAGGGC[G/T]CGCCTATCTCTTACA | 16443 |
| rs259377038 | in-del | -/A | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911266 | AAATAAATAAATCTT[-/A]AAAAAACTACTACCG | 16443 |
| rs259382318 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91825373 | CATAGCTACATTCCA[C/T]TAGATTTTAGACATT | 16443 |
| rs259398075 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91813040 | GGTGGGAGAATGGCA[A/G]TGTCTAGGCAGGCAT | 16443 |
| rs259401511 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91803151 | GACTGCTTGGTTTTT[A/G]TTTTTAAATTTATTT | 16443 |
| rs259409292 | snp | C/T | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | GRCm38.p3 | 16:91727796 | TAATATTTGGATAAG[C/T]TGGTTTAAGAGAAAC | 16443 |
| rs259415326 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91768436 | CACTGCAGGATTGGG[C/T]ACATTCTCTCCCACG | 16443 |
| rs259418874 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91833310 | CTTTAGATTTGTGGC[A/G]TCAAGTTCAGGAAAT | 16443 |
| rs259426783 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91834125 | GCTACCTTGCTTCAA[-/C]CCCCCCACCCCTCAC | 16443 |
| rs259453884 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873462 | CCCTTCGGAGCAACC[A/G]AGATGTTACCCTACT | 16443 |
| rs259474418 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91819531 | CAGTCAGTATAGACT[A/G]GGTTGATACTTTGAA | 16443 |
| rs259482748 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91832804 | CGTTTAGTATATCAC[A/G]TGAATAAACTTTATA | 16443 |
| rs259484893 | in-del | -/GAGAGA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91778563 | AACAAAGACAAAAAC[-/GAGAGA]GAGAGAGAGAGAGAG | 16443 |
| rs259490235 | snp | G/T | | | missense | Itsn1 | GRCm38.p3 | 16:91839802 | CCATCCGCATCAGGA[G/T]CCAGCTAAGCTGGCC | 16443 |
| rs259501059 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91839128 | TGAGAATCTCTACTC[C/G]TGCTCTACTCACGCT | 16443 |
| rs259517348 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91802409 | GCAGCCTGCACTTAG[C/T]ATGCGTGTGTGTTCC | 16443 |
| rs259518767 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91810952 | CTGGTTAGGATGCTT[C/T]CCTTCATTTGGGGAC | 16443 |
| rs259544066 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915153 | TCAATGGGCCGCTCA[C/T]ACTGCCTGTTATCTT | 16443 |
| rs259554942 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91795255 | AAACAGTGTAGCAAT[A/G]GCACAGGTGACCTAG | 16443 |
| rs259558589 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91743717 | TGTATAGCCCTGGCT[A/G]TCCTGGAACTCACTC | 16443 |
| rs259564443 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91906282 | TTTAGGACGTAATAC[A/G]GGGAAGTGGAGCAGT | 16443 |
| rs259590867 | in-del | -/TTGCTCCTCC | | | intron-variant | Itsn1 | Mm_Celera | 16:91826531 | TGAGGCTGGCTGCTG[-/TTGCTCCTCC]TTGCTCCTCCTGTGC | 16443 |
| rs259602693 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91905595 | GAGCAAAGGGGAGGA[A/G]CTGAGAGACTAATGG | 16443 |
| rs259606580 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91880614 | CTTAGATAACAGCAC[C/T]GCTCTATCCATGAGT | 16443 |
| rs259612200 | snp | A/G | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91727874 | AGGAAATCTAAAAGC[A/G]TCTGGGTGCCTAGAA | 16443 |
| rs259638511 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912604 | ACTTCCTTAGTGCCC[A/G]TCAGTGGAAACACGG | 16443 |
| rs259643226 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91772896 | TAAAAGGATATGTAA[C/T]TACTAAGATTTCTTT | 16443 |
| rs259652092 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91811985 | CTCCTGGGTAATCTG[G/T]GCAGTATTGTGGCTG | 16443 |
| rs259659139 | snp | A/C/G | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91803542 | GCCTCTGGACTTGAC[A/C/G]TACCGACACAGTTAT | 16443 |
| rs259689165 | in-del | -/CTTCCAGTCTTGTGCGCCGTC | | | intron-variant | Itsn1 | Mm_Celera | 16:91741204 | GTGTTTTCTTTCTGT[-/CTTCCAGTCTTGTGCGCCGTC]CTTGTCCTTGGCTCA | 16443 |
| rs259692204 | in-del | -/TCTGAGTTCAAGGCTCG | | | intron-variant | Itsn1 | Mm_Celera | 16:91755974 | TAAGGCAAACCAGCC[-/TCTGAGTTCAAGGCTCG]TCTAGGACAAAGCAA | 16443 |
| rs259693754 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91908106 | CCGAGGAGAACCACA[A/G]TGTACTCACATACAT | 16443 |
| rs259728629 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91772081 | TATTATTGTTGTTTC[C/T]GAAGCTGCCTCTCAG | 16443 |
| rs259731853 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91901179 | AGATACAGATGTGAA[C/T]ACACATGCATGCATG | 16443 |
| rs259735297 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91790110 | ATATAAGCCCTACCC[C/T]GTGTCTGACACCTGC | 16443 |
| rs259735314 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91737121 | AGATTGCAGTTAGCA[G/T]TGGCCAATGGGAAGT | 16443 |
| rs259739402 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91884736 | GAACTCACTCTGTAG[A/G]CCAGGCTGGCCTCGA | 16443 |
| rs259752008 | in-del | -/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783534 | GATTACTTTAGTGGA[-/T]TTTTTTAGGAGACCA | 16443 |
| rs259755159 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91780041 | TTCAAATTGGGAATT[C/T]TTTCTATTTCCCTGT | 16443 |
| rs259766459 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91811543 | GTGGTACCGTTAGAG[A/G]ACCTGCTAAGGCCTC | 16443 |
| rs259766866 | in-del | -/CTAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91761492 | GCGGTCAGGGCGCGC[-/CTAT]CTCTTACACAGGAGC | 16443 |
| rs259771904 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91907224 | CGCCCCTCCGCCCCC[A/G]CCCTCCCCCAGGACG | 16443 |
| rs259787005 | in-del | -/CC | | | intron-variant | Itsn1 | Mm_Celera | 16:91882744 | GAGAGGAGAGTCTTT[-/CC]CCCCCCCTCCCTAAG | 16443 |
| rs259803139 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91884053 | ACTCAGCCTTGCGGG[G/T]GGGATGCAGTAACTT | 16443 |
| rs259803464 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890542 | AGGAAACCAGAGATT[C/G]GGGATCTGACTTGTT | 16443 |
| rs259816314 | in-del | -/TCTGAGTGAGTCCC | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830294 | CTGACCCTTGGCGTT[-/TCTGAGTGAGTCCC]TCTGCAGCAGACAGC | 16443 |
| rs259833496 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91817997 | GTCACTCCGGAGACC[C/T]TTGTGTGCATGCTAA | 16443 |
| rs259838569 | in-del | -/TCCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91862471 | ACTTCTTTCTTGCCA[-/TCCT]TCCTTCCTTTCTGTC | 16443 |
| rs259838761 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91773911 | TCAGGTCTCTAGACT[C/T]ATTGCTGTTATCTCC | 16443 |
| rs259850336 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91846036 | CACATCTGACTTTCA[C/T]GCCCAGCAGGCACGA | 16443 |
| rs259884033 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913969 | CCATACTGTGAAACA[C/T]AGACATTCTGTGTGC | 16443 |
| rs259893677 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91744046 | AACAGCTGCAGAGAC[-/T]TCAGGGTTCAGTGGC | 16443 |
| rs259905282 | in-del | -/GTGTGTGTGTGTGTGTGTGTATGTGTGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91910492 | GTGTATGTGTATGCC[-/GTGTGTGTGTGTGTGTGTGTATGTGTGT]GTGTGTGTGTGTGTG | 16443 |
| rs259917642 | snp | C/T | | | downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91920692 | CTTGTAGCCATGACC[C/T]GGGGTGAGACCATGT | 16443 |
| rs259920250 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890101 | CGGTCTGCAGCAGGC[A/G]TAGGCAAGGGCGTGG | 16443 |
| rs259937588 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91781650 | CTTTTAGCCACAGAG[A/C]CACCCTGACTGCCTG | 16443 |
| rs259942936 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91813973 | TGCTTTGCTCTTTGC[A/G]GTAGGACTAGTGGTA | 16443 |
| rs259949798 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91781214 | TGTATTTGGGGAAGA[A/G]GTCTTGGTCTCCTGT | 16443 |
| rs259953638 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898291 | CTACTTCAGCGCTGG[A/G]CAGCAGAGATGGAGG | 16443 |
| rs259955556 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919793 | CTGACCACTACTCTG[C/T]CAGCATCCATTTTAA | 16443 |
| rs259955942 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91897179 | ACACCATACAGTGAC[A/G]GATTCCCTGATTTCA | 16443 |
| rs259963557 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91762866 | GAGAACCAGAACTGA[A/T]GTACCGCAGATCTGA | 16443 |
| rs259966760 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91748062 | AACTCTGTAAGTATT[C/T]GAATCAGGCATTTAT | 16443 |
| rs260006147 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91747422 | TTTTCAGGACATCAT[C/T]ATTTCTTGTTTAGGC | 16443 |
| rs260010519 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91788590 | ACTCTCTGTTCCTCA[C/T]CAGGGCAGGTCTCCC | 16443 |
| rs260019082 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91865739 | TTTGGAACGTGGCCA[C/T]GATGGATATGGAGAC | 16443 |
| rs260041423 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91759695 | GGAGCTATGGGCAGC[A/G]CCTGGAGCATCTGTC | 16443 |
| rs260099146 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91755649 | ATGCTGGGATTAAAG[A/G]CGTGCGCCACTACGC | 16443 |
| rs260099287 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91857431 | AGTTCTACTTTCAGT[A/T]ACAGGGACGTGCTCC | 16443 |
| rs260105972 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91901010 | GAAGAGCAGTCAGTC[C/T]CCAGCCCCATTTTAC | 16443 |
| rs260122993 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91787874 | GGAGGCAGCTTACAC[A/T]GTAGCCCGAGGTCTT | 16443 |
| rs260124769 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91768288 | ATTCTTTTTTTCTCC[A/G]TTAATTCATGTATTT | 16443 |
| rs260128929 | in-del | -/TG | | | intron-variant | Itsn1 | Mm_Celera | 16:91745141 | TTTTATTTATGTATA[-/TG]TGTGTGTACCTACTT | 16443 |
| rs260153997 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91873166 | TTTAAAGATGCTACA[C/G]TTGGGGTTGATTGGG | 16443 |
| rs260166279 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867291 | TCTGCGTTCTGTAGA[C/T]GCTGGGCATTGTCTG | 16443 |
| rs260170436 | snp | A/G/T | | | utr-variant-3-prime, intron-variant | Itsn1 | GRCm38.p3 | 16:91871007 | TACCTAGTTGTGCCC[A/G/T]TGTTTTGTTTTGAGT | 16443 |
| rs260173641 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890629 | CATGTAGACCCAGGC[A/T]AGCCTCGAACTCACC | 16443 |
| rs260186265 | snp | A/G | | | upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91729322 | GGGCGGAGGGGCGGC[A/G]GCGGAGGGAGATGAG | 16443 |
| rs260188524 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91819100 | TCAGTTGCCAGCACC[C/T]CTATGGGCAGTTCAC | 16443 |
| rs260199581 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91818072 | ATCTCCAAAGAATGA[A/G]TCGGAAGAGTGGGGC | 16443 |
| rs260206879 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914737 | AGTCCTTGTCTCTGG[A/G]GAAGCGTCCATGTTT | 16443 |
| rs260218175 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783970 | GACATGCTTACAGCA[C/T]AACAACAGAACTTTA | 16443 |
| rs260219964 | in-del | -/GTGCTGCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91847518 | CCACCAACCTACTCA[-/GTGCTGCT]GTGCTTAGGAGGATA | 16443 |
| rs260255947 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91757589 | AACCAAACTCAGGCC[C/T]TGGGCCAGGACAGTA | 16443 |
| rs260270843 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91866528 | ACCAAAAGCTGAGCT[A/G]TGTCTAGAAGTAACC | 16443 |
| rs260277823 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91895833 | CGAGAGCCACTGGCG[A/G]AGACAAATTGGCAGA | 16443 |
| rs260291774 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91765277 | GCTCCGGAGCTAAAC[A/G]GAGACCCTGACTCCA | 16443 |
| rs260293931 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91756796 | GTAGATGAGACTGTC[A/G]CACTCTGGGCAGCGC | 16443 |
| rs260335636 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91736644 | TGTAAGACACAGATG[C/T]GATGCATGGGGTCAC | 16443 |
| rs260346806 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91773593 | CTTAATAATTTTAAC[A/G]TCATCCAAACTTTGA | 16443 |
| rs260347249 | in-del | -/TTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91896298 | TTTCTGAACCACATT[-/TTA]AAAAAAAATACCATC | 16443 |
| rs260349981 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823223 | TGAAAGTTAATTGAA[C/T]GTTATCTTACGCAAT | 16443 |
| rs260362154 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91735056 | GGGAAGCCTTTTACG[A/G]TGCTCCTGCCACCCT | 16443 |
| rs260378047 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91797362 | CTTTTTTTTGCCCAA[C/G]TGGCAAAATTATAAT | 16443 |
| rs260380487 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91891998 | TGACTGTCGATGTCC[A/G]CTCAGCCCGAGGACG | 16443 |
| rs260382955 | snp | C/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919387 | TAACCTCTGCATTCT[C/G]GAAGCCCACAGCTCT | 16443 |
| rs260401623 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91839014 | GGAGCCAAGAGTACT[A/G]GCTGCACCATCTCGC | 16443 |
| rs260411235 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91845859 | ATGACAGGAATGTCA[G/T]TCGAGGTCATTAAAG | 16443 |
| rs260411688 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91877361 | CTTAGAAACAGTGAT[A/G]GGAAGAGGACAGGGA | 16443 |
| rs260420277 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91835033 | TTAAATGTATAACTA[-/G]GGGGGCTGAAAAGAT | 16443 |
| rs260423773 | in-del | -/TG | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912095 | TCAGAGCAACGGGGA[-/TG]AAGCAAAGACGAAGC | 16443 |
| rs260425630 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91804879 | TGGAAGGAGAAGACA[C/T]GTGGAGCCTTACTTA | 16443 |
| rs260498675 | in-del | -/AT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799185 | AGGGGAGGAGGAGAC[-/AT]GGGAGAGAGGGGGTG | 16443 |
| rs260513581 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91902475 | TCGCAAACACCATTC[A/G]TGAATCAGCAGAAGA | 16443 |
| rs260528672 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91759335 | AGTAAGGCATAAAGT[G/T]AATTCCTTATGAGTC | 16443 |
| rs260540320 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91741685 | TGGGGACTTGGGCAT[A/C]CATGTGACTGGGGGC | 16443 |
| rs260560066 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91902183 | AGGCCTTGGGGACCT[A/G]CGTCTCCATCTTAAG | 16443 |
| rs260562354 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91843845 | CTTAGGGAAGGATCG[C/T]GCCATGCAAGCCTGA | 16443 |
| rs260599718 | snp | C/T | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91870688 | ACCTTTGCCGTTTGT[C/T]CAGTGTTCCCAACCA | 16443 |
| rs260615967 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907684 | ATTACTTACGGGCAG[A/G]GCTGTTACTCAGGTA | 16443 |
| rs260616629 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91817750 | GCATGCTGGGATTGC[A/G]GGTGCATGCTACCAC | 16443 |
| rs260617096 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91908649 | ACAGGAGGGGGCCTT[A/G]CTTTCAAGTGCGGAC | 16443 |
| rs260647719 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914661 | GAGAATTATCCCGAG[A/G]GCTCTGAGGACAGAA | 16443 |
| rs260648646 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878679 | TCCATTCTTGTGATC[A/G]CTTAACTCGTGTTCA | 16443 |
| rs260659089 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91782581 | ACTGAAGTATAATAC[C/T]ATTACCAAACCTCTA | 16443 |
| rs260665620 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823947 | TTGGTATCAGGTTAA[C/T]ACAGGCCTCAGAACA | 16443 |
| rs260671931 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913829 | ATCAAAACACTACAC[A/G]TTCATGTTTCTGTTG | 16443 |
| rs260690553 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91774927 | AAATCAGTTGGCAAA[C/T]AGGTATGGCTGCCCT | 16443 |
| rs260693800 | snp | A/G | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | GRCm38.p3 | 16:91727377 | GTGGCTGATGCCTAA[A/G]ATTTACAACTCCCAA | 16443 |
| rs260695403 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91886856 | CTTGGACTCTCCGTT[C/T]CTTACCACTGTGGAC | 16443 |
| rs260699294 | snp | G/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91920055 | ACCATTCCCCTGTGC[G/T]GTACTGTCTTCGCTC | 16443 |
| rs260722653 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91832412 | CCCAACAACTTTCTG[C/T]TTTAGAGGCGGCATG | 16443 |
| rs260740476 | in-del | -/CTGTAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91769898 | TTATATGTAACTACA[-/CTGTAG]CTGTCTTCAGACACA | 16443 |
| rs260740524 | in-del | -/AAA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742691 | AACCTCCTCCCCCCC[-/AAA]AAAAAAGATTGTTCT | 16443 |
| rs260742518 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91782072 | TAGCTCAGGTGTTGG[C/G]GTTAAGATTAAAGAC | 16443 |
| rs260746728 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91886425 | CATGGACTGTTACTG[A/G]AAATCTGAGCATCTG | 16443 |
| rs260755151 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91886743 | AGCCTTGGCACAGTT[A/G]CTGTAGACTCTAAAA | 16443 |
| rs260755209 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91788270 | AGCACTCTGCTTTTT[A/T]AAGAGGTCCTGGGTT | 16443 |
| rs260767566 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734858 | GTGGGGGGCAATGGG[C/T]AGCTTACCAGTGGCT | 16443 |
| rs260797110 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91743140 | GCTGCACAGGGTATT[G/T]AATTTCGGGTTTGCA | 16443 |
| rs260800112 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91781306 | TTTTTGGCAGGCATT[A/G]CTGAATGTGTAGTAT | 16443 |
| rs260800709 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91743742 | TCACTCTGTAGACAA[A/G]GCTGGCCTCAAACTC | 16443 |
| rs260802834 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91794678 | TGCCTTGATGAGGGT[A/G]AGGACTACACTTACC | 16443 |
| rs260808457 | snp | A/C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91891955 | AGTGCTCAGTGCTTC[A/C/G]GGAACATTAAGGGAT | 16443 |
| rs260812964 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91838900 | TCCTGGCGCTGTGTC[A/G]CTCTGTACACCGTGA | 16443 |
| rs260823613 | in-del | -/GT | | | intron-variant | Itsn1 | Mm_Celera | 16:91809370 | ATCGACAGAGAGCAC[-/GT]GTGTGTGCGTGTGCT | 16443 |
| rs260836198 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91891719 | ACATAGATCTTGCCA[A/G]CACGGTTATTGTCCA | 16443 |
| rs260857829 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91844563 | GTTCTTCCAGAGAGC[A/G]CAGGTTGAGTTCCCA | 16443 |
| rs260862394 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91766089 | CTGCGGCATGCACTT[-/A]AGTGCGAGCCACTTG | 16443 |
| rs260864413 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91891227 | CAGAAAGTGTCAGGA[A/G]GCACAGTTCCTGTTT | 16443 |
| rs260874394 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91751795 | TCAAAGCCTTAATTA[C/T]TCTCTTGTCACGTGC | 16443 |
| rs260896632 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91846335 | TGTTGTACACTTACA[-/T]TTTTTCCAAAATTAG | 16443 |
| rs260899691 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91751534 | TTTGGTTTTTTTTGG[G/T]TTTTTTTTGAGCACA | 16443 |
| rs260899872 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91751010 | TCACAGCAGCACTGT[A/G]TTGGCAACCCTGACT | 16443 |
| rs260914872 | in-del | -/CCTGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91742392 | TGTGTGGTGTGCGTG[-/CCTGT]TGTGTGTGTGTGTGT | 16443 |
| rs260915533 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852853 | ATAAGCGCCTCGCCT[A/G]CCTTTGCAGCCATGT | 16443 |
| rs260941434 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91900493 | TCCTTGCTTTTCTTT[C/G]TGGAGAGTCACCCTG | 16443 |
| rs260949776 | snp | C/G/T | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91803492 | TATGTGTACCACATT[C/G/T]CTGACGCCCATGGAG | 16443 |
| rs260962303 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91811321 | TCACATCTTTTTTTG[G/T]TTTGGTTTGGTTTTT | 16443 |
| rs260965366 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91895868 | GGAGCTTTAGCCCTC[A/G]GGTCTCTGCTCCACG | 16443 |
| rs260970558 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91749133 | TGTTAGTATAGCAGT[A/G]TGGGTTTTGGAGGAT | 16443 |
| rs260979679 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91851821 | ATACGCGAGGCACAA[A/G]AAGCGTGGGGACAAG | 16443 |
| rs260979784 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91860349 | TAATTAGAGTCAATT[C/T]TACTTTAAGCCTTCC | 16443 |
| rs260992497 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91906908 | GCTCCCAGGCACTGG[A/G]TGAGGACCACTGGTC | 16443 |
| rs260992953 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91765036 | TTAAAGCTGAGATCT[C/G]TCAGTTTGAGGGTTT | 16443 |
| rs260993197 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91816455 | ATAATGTGACACTTA[C/T]ACATAAATGAGTTGA | 16443 |
| rs261017129 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91860507 | AATTGAAATATTTAA[C/T]TTACTACAAGGGTAG | 16443 |
| rs261022600 | in-del | -/AG | | | intron-variant | Itsn1 | Mm_Celera | 16:91867481 | GGTGCCTTGCTCTTA[-/AG]GTGAGCCCTCTGGCA | 16443 |
| rs261027795 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91859503 | ATGACATTTCAGGAG[G/T]AGGGAATGTCAGTTC | 16443 |
| rs261063912 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91876894 | ATCTTCAATCTTCTG[A/G]CTCTACCATGCCTGT | 16443 |
| rs261083122 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91822734 | AGCCAGATGACTTGT[C/T]TCACTGATGTATGGC | 16443 |
| rs261099307 | in-del | -/CT | | | intron-variant | Itsn1 | Mm_Celera | 16:91788446 | GTAAGTTAATTAAGA[-/CT]CTCATTGAGACAAAA | 16443 |
| rs261111346 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91884406 | CTTCAGCCTGAAGGG[A/C]CAGCACTACCTGGGG | 16443 |
| rs261125357 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91783810 | TTTTTTTTTAATGCT[-/C]CTCTTAGATTTTTGT | 16443 |
| rs261150251 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91816562 | CCAGTCAGCTGCGCC[A/G]GTGCCTGCCTTGGGG | 16443 |
| rs261161937 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830811 | TTTACCCTGGGAAGA[A/G]TTAGCTTTTTATCTT | 16443 |
| rs261169335 | snp | G/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91912334 | GATTTATAAACACAG[G/T]GACTGTATTTTGGAG | 16443 |
| rs261171729 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91733032 | GGTTTCTGTGCTGCC[A/G]TACTGTGTGGTCACT | 16443 |
| rs261181679 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91868633 | CAGGGTAGGAGCAGA[G/T]TTCTGGTTTAGTTCT | 16443 |
| rs261185672 | in-del | -/ACCCCTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91813575 | ATGATAACATCGTCC[-/ACCCCTG]ACTTTATTCAGAGAT | 16443 |
| rs261199344 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91740869 | TACTCCAGTGGGGCA[A/G]ATAAACAAGCAAACA | 16443 |
| rs261202268 | snp | A/C | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91830587 | TGACTGTGGGCGTGC[A/C]TGGATCCGGTGAGGA | 16443 |
| rs261224844 | in-del | -/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915370 | CAAGGACACATGGAC[-/G]GGCCCCTCTGGCTTT | 16443 |
| rs261236475 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91751369 | TATACATATAAGGCC[C/T]TGCTCATTTACTAGC | 16443 |
| rs261242745 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91836860 | TATTGTGTTGTGGCC[C/T]GCTAGAATATAATCT | 16443 |
| rs261248270 | snp | A/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830243 | GTTCAATAGCAAGCA[A/T]AATTTCTGTAGGAAC | 16443 |
| rs261252399 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91836102 | TAAACTTTGTATCTT[C/G]TTGTTACCTCTCAAG | 16443 |
| rs261274641 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91891764 | TCTATTACTGAAGAC[-/A]ACACATAACATCACG | 16443 |
| rs261288344 | snp | C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91803244 | CTATTACAGATGGTT[C/G]TGAGCCACCATGTGG | 16443 |
| rs261290283 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91733167 | AAAATAAATTTCATG[C/T]TCACTTTCATCTTAA | 16443 |
| rs261296027 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91810980 | GACATCGCAGCCTCT[G/T]CTCCTAGCTATGCAG | 16443 |
| rs261297288 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91786839 | GGCTTCTCTTGGGCT[A/G]CAGCCTGGTGTGTTG | 16443 |
| rs261303854 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758891 | CCATCTTTTTTGACT[A/G]GTATGGTAATTTGTT | 16443 |
| rs261328455 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91906455 | CATGGCTGCCCACAA[A/C]CATCTGTAACTCCAT | 16443 |
| rs261330690 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91801389 | TCTGAATCCTCTGAC[C/T]GTTTTATGTGGGGAC | 16443 |
| rs261360255 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91835869 | TTCATTACTTCCCAG[G/T]GGCCATTCTTGGATG | 16443 |
| rs261362546 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91860374 | CCTTCCTCTTCTCTA[A/T]TAGCCATTCAGTCCC | 16443 |
| rs261370912 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91843314 | TTTTGCTTTTAAACC[A/G]ATTTGCTCCCAAACG | 16443 |
| rs261374665 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91869382 | GGTGAGGACCCTCTG[A/G]TTTTTCTGACGAGTA | 16443 |
| rs261377233 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91809456 | TTTCAGTGCTGTGTG[A/G]TTATACACCAGTTAA | 16443 |
| rs261377561 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91800849 | GCCTCAGCCTCTCTC[A/T]GTATCGAGGGTGACT | 16443 |
| rs261396823 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889937 | GCTTGTCCCAGGGCA[C/T]AGAGCGAGGCAGCTG | 16443 |
| rs261400995 | in-del | -/TTCATGTATT | | | intron-variant | Itsn1 | Mm_Celera | 16:91768293 | TTTTTTCTCCATTAA[-/TTCATGTATT]TATCCCGATCACAGC | 16443 |
| rs261413421 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91904636 | TTTCCAGAAGCACCG[A/T]CGACTACCGAGTCTT | 16443 |
| rs261428342 | in-del | -/AT | | | intron-variant | Itsn1 | Mm_Celera | 16:91788388 | CAACCGTGTACATGC[-/AT]ATATATACATGCAGC | 16443 |
| rs261429865 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91894779 | TACTGGCTGGCCCTC[A/G]GGCTCAGACTCAGCC | 16443 |
| rs261438389 | snp | A/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91913376 | GCCTTTGCATGTCTC[A/T]GGCTCCTGGGCTCAG | 16443 |
| rs261457200 | in-del | -/TC | | | intron-variant | Itsn1 | Mm_Celera | 16:91845730 | CCCAGAGTCCCATAG[-/TC]TGCCTTCAAATCATA | 16443 |
| rs261466542 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91808273 | ATTGGTATGCTTGGA[C/T]ATAAGAACAGACACT | 16443 |
| rs261494798 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91755527 | TTTTTTTTTGGTTTT[G/T]CGAGACAGGGTTTCT | 16443 |
| rs261503997 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91808132 | TATATTCCGAAGATA[G/T]GGCCTATACACTTGA | 16443 |
| rs261511140 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91780826 | AGAATTAGATGAGGT[C/G]TGCATCAGTTACTTT | 16443 |
| rs261519140 | in-del | -/A | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91900356 | GGGCCACTCCAAATT[-/A]ATATTTAGAGAGAGT | 16443 |
| rs261532182 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91814630 | CTTTTCGTGGCTCTT[C/T]CTTAGCCAGTTTATG | 16443 |
| rs261538143 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91836920 | AAATGCAGCGAGTTC[A/G]ATTTCTGAGTGAGCA | 16443 |
| rs261550878 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91911084 | CAAACTTATGTCCAT[A/G]GGCTGGAGAGATGGC | 16443 |
| rs261556402 | in-del | -/TT | | | intron-variant | Itsn1 | Mm_Celera | 16:91748162 | ATTAAAAAGATAAAC[-/TT]TTTTTTTTTTTTTTG | 16443 |
| rs261563328 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91910731 | TGTAGCCCAGGCTGG[C/T]CTGGAGCCAGTTTGT | 16443 |
| rs261568258 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91779133 | TGGAGAAGGTGGAGT[A/C]GGATACTAACTTGCT | 16443 |
| rs261568962 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890598 | TTTTTTTCATGAGGC[A/T]GTGTCTCACTGTTAC | 16443 |
| rs261570100 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91764029 | CTGGAGACAAAGACA[A/C]AGGGGTGGCCACATG | 16443 |
| rs261574505 | snp | C/G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91867149 | TGATAAAAATGCTCA[C/G/T]TATCTTGGGTCAAAT | 16443 |
| rs261601160 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91814926 | TGGGTGGAACCTGTC[C/T]GCTCCTATTTTTGTA | 16443 |
| rs261612701 | in-del | -/AAAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91732598 | TGATAATCCCAACAT[-/AAAG]AATCATTTTTAGAAA | 16443 |
| rs261616742 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91875295 | CTACTTCACCTACTT[C/T]GTGGTCTTGGGTACA | 16443 |
| rs261622018 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91910999 | TGGAGGAGAAGCCTG[G/T]GTTTTTAACTGCTGA | 16443 |
| rs261638994 | in-del | -/CGA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91818692 | AGCAGTGTGCCCGCC[-/CGA]CGCCCGCGGCAGGGC | 16443 |
| rs261643137 | snp | G/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917002 | TGAGCAATGCTGACA[G/T]GATGCTGTTCCTTCA | 16443 |
| rs261648006 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91748318 | TGTGCCACCACTGCC[C/T]GGCGAAAGATGGACT | 16443 |
| rs261666754 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91756630 | GCTGAGCTGTAGTGG[A/G]GTCTGGCATGAGTCC | 16443 |
| rs261690179 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91784870 | CTGGTTGTATGCTGT[A/T]CTCTTACTGTAGTGA | 16443 |
| rs261698671 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91731457 | TTCTTTTTAATTTTT[A/T]AAAAAAGATTTATTT | 16443 |
| rs261702228 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91809563 | GTTCAGGTTCCCTCC[A/G]CAGACACGGAGGCAC | 16443 |
| rs261708495 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91815984 | TCCAGTGACTGTCAC[C/T]CCTTCCCACATGGTA | 16443 |
| rs261721387 | snp | C/T | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91858635 | AGTGCTGATCCCATT[C/T]CTGCATGTAACCAGT | 16443 |
| rs261724123 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91791831 | TGTTTTTTTATTTTT[A/T]TTTTATGTGTATGTA | 16443 |
| rs261732469 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91911774 | AGAGCTCGAGAGCGG[C/G]CAGTCATAGGACAGT | 16443 |
| rs261733835 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91834668 | AAAAGAAGTAGGTTT[C/T]GAGCTTACGGTGTGA | 16443 |
| rs261748131 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91893527 | ATAGGTAATGCAGTG[A/G]GACAGCCACACAGAG | 16443 |
| rs261762558 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91840942 | AAATCCCAAGAATGT[C/G]CTCTGCCTGAATGCA | 16443 |
| rs261792758 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91779164 | TAGCATATGAGGCTC[A/C]GATTCAATACCCAGC | 16443 |
| rs261797649 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917672 | GGCTTATTCCGTCAG[C/T]CTTCAGATTGCCCAG | 16443 |
| rs261824616 | in-del | -/GCACGCACGCGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91906645 | CTAGATTACTGGGTT[-/GCACGCACGCGC]GCGCGCGCGCGCGCA | 16443 |
| rs261828222 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91732489 | TGAATGTACAGCCCT[G/T]CTGGGTGATGTGCTA | 16443 |
| rs261831034 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91835453 | TGAATAAAACTTTCC[A/C]TGACTTATGCCCTTT | 16443 |
| rs261839109 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91819829 | GCTTGCTCAGCCTGC[-/T]TTTTTTATAGAACCC | 16443 |
| rs261842677 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91780516 | GGTAAACAGGAAAGA[A/G]CTTCTGGGGCTTCAG | 16443 |
| rs261846478 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91786047 | GTTTTTGAGTTTTTC[C/G]AGACAGGTTTCTCTG | 16443 |
| rs261859554 | snp | A/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830536 | AACAACACTTTAAGG[A/T]GAGTTGCCTGGGACG | 16443 |
| rs261863562 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91841898 | AAGAACATTTATACC[A/G]GGGGCTGGAGAGATG | 16443 |
| rs261878884 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889359 | ACTCCCACCTGCTCT[C/T]CATCGCCATCCTCCT | 16443 |
| rs261879529 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91740964 | GGAGAGCCCACCCCC[-/A]CCCCCTCACCCCGGC | 16443 |
| rs261880439 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91743074 | TTTTCCTCCCCTCCC[C/T]TCCCTCTCCCTCTCC | 16443 |
| rs261887431 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91894338 | GGCATCAGGTCCCAT[G/T]ACAGATGGTTGTGAG | 16443 |
| rs261894332 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91820391 | TACTAGGCATTTTTT[-/A]AAAAAGCAACATTGC | 16443 |
| rs261904295 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91884665 | AGCACACAGGCATTT[G/T]TTTGTTTGTTTGTTT | 16443 |
| rs261932665 | in-del | -/TGTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91836559 | TGCACGAGTGTTCTT[-/TGTG]TGTGTGTGTGTGTGT | 16443 |
| rs261939184 | in-del | -/TC | | | intron-variant | Itsn1 | Mm_Celera | 16:91774824 | GGTTTGGGTCAGTGT[-/TC]TCTCCTTTATTCTTC | 16443 |
| rs261941303 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890423 | TCTCCATCAATAAAG[A/G]AAAAAATGTTTCTTT | 16443 |
| rs261955661 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91754863 | CATCTTAGAGGTTTT[C/T]GTTACACCTCAAATA | 16443 |
| rs261972433 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91806953 | AAGTGGAAGGGAAGG[A/G]GGGTGAGCTGTCTGG | 16443 |
| rs261973209 | snp | A/T | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91747967 | GTCCTGTTTGCTGGT[A/T]GGACTTTCCCGCTGA | 16443 |
| rs261986358 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91801335 | GTGTTGAAGCAGATC[C/T]GAGTGTATTAGCCAA | 16443 |
| rs261989011 | in-del | -/CTGTGGAGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91741124 | AGGCTCAGGGCCTGA[-/CTGTGGAGG]GACGACTGCACCTCC | 16443 |
| rs261989200 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91866279 | GAGAGCAGTGTGGAA[C/T]GTCTCTAGACCTCAC | 16443 |
| rs261995185 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91898376 | TGTCTCACAAACAAG[A/G]AAGATGGCTCCTGAG | 16443 |
| rs262006632 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91814281 | GCATTTGATGCAGGG[A/T]GATACGACTTCTCTA | 16443 |
| rs262007476 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91850749 | TGGCTGTGGGTGTCC[C/T]GCGATGCGCGACACT | 16443 |
| rs262035531 | snp | C/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916477 | AGGATCTTCAGAAGA[C/G]CAGTCAGTGCTCTTA | 16443 |
| rs262045163 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91858035 | CAGCAGCCGTCTCCG[A/C]GTGCACTGAGCTCAT | 16443 |
| rs262047484 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91874703 | CTTCTCCCCTCCCCC[A/C]ACGTCCCATGCTGCC | 16443 |
| rs262064172 | in-del | -/CCTCTC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91900000 | CCTCCTCTCCCTCCT[-/CCTCTC]CCTCCTCCTCTTCCT | 16443 |
| rs262078197 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91904587 | CCTGGACGCTGCACC[C/T]GGGAAAGTAACATTT | 16443 |
| rs262091129 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91729961 | GCGGGTGCCCCCGGC[C/T]TCGAGTCCCCGGCTC | 16443 |
| rs262095647 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91784179 | CGATCACCATCCATA[C/T]ATTCCTACCGAGCGG | 16443 |
| rs262096851 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91873492 | TTGTCTCTCCCTTTA[G/T]GGCCGAGCTTCCCAG | 16443 |
| rs262149265 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91833971 | TCTCAAAACCCAACA[A/G]TAACTAATAGGTTAT | 16443 |
| rs262150457 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91738388 | GTTAATTAGTGTCAC[A/T]GGAAGGATAGATAAC | 16443 |
| rs262151875 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91779106 | TAGCACGTTACTGTA[A/G]TTCAGTGGTGTTGGA | 16443 |
| rs262153306 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91840449 | ATAACCTCAGCTGCA[C/T]ACTAAAATGTATTTT | 16443 |
| rs262170568 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91791368 | ATAAACACACGAGTA[A/G]GACAAGTTACTGAAC | 16443 |
| rs262178633 | snp | G/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91828463 | TCTGAGGTCTGTAAG[G/T]TAGCCTGTGTTAGGG | 16443 |
| rs262179944 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91873188 | TGATTGGGAGAGGGG[-/C]CCGTGTTTAGGCTTT | 16443 |
| rs262187629 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91834952 | TTTCACAGCGCCTGC[C/T]GTTAAGTGTTTTGAA | 16443 |
| rs262216941 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91771916 | GTGTGTCCCTTCCAA[A/G]GGCCTAAGACCTCTG | 16443 |
| rs262230302 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91889248 | TTCCCCTCTAACCAA[A/G]GATGCTGCCCCTCTG | 16443 |
| rs262264169 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830018 | TTGTTGATCCTTTAA[C/T]GTCCATTCACGGGGG | 16443 |
| rs262273556 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799396 | ACCAACTTAAACCCA[A/G]GACTTAAATAACCCA | 16443 |
| rs262281826 | in-del | -/AAAAAC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892768 | TTAGCAGAAAAAAAA[-/AAAAAC]AAAAAACAAACAAAC | 16443 |
| rs262285581 | in-del | -/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913037 | TTTGAGGGAAAGACC[-/T]TTGGGAACCCGTGAG | 16443 |
| rs262299496 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91754745 | GGTCCTAGGCACCAC[A/G]GTAGCATCTATCTGC | 16443 |
| rs262306228 | in-del | -/TT | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831534 | GCTATTATTTCTCTC[-/TT]CCCTCCCCTCGTTTA | 16443 |
| rs262309032 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91806798 | ATATTATTCTTATCT[G/T]TGAAAAGAGTAGAGA | 16443 |
| rs262310388 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91890013 | CCAGATGCTCGCATT[G/T]GCTCCCGAGCTCTGG | 16443 |
| rs262328934 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91856130 | TGGCTTCTGCTTTGA[A/C]ATGATTGAGGCAGAA | 16443 |
| rs262369947 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91865919 | CTGCCTTTGCAGCAA[C/T]ATGTCTCGTCCAGCC | 16443 |
| rs262378330 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91903725 | ATTTAATTGGGGCTG[A/G]CTTACAGGTTCAGAG | 16443 |
| rs262383711 | in-del | -/GTGGTGTCC | | | intron-variant | Itsn1 | Mm_Celera | 16:91874361 | GCCACCTGCTGCTCT[-/GTGGTGTCC]GTGGTCTGTGCATGT | 16443 |
| rs262394613 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91850053 | AACTTAAAAGCTTTG[C/G]TGTCTTACCACCGCC | 16443 |
| rs262399330 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91910550 | TGTGTGTGTATCTTA[C/G]TACCACCACTAAGAT | 16443 |
| rs262401327 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91800682 | TGTGAAATTTATTAT[A/G]TTTTAAGAACTTGTA | 16443 |
| rs262439028 | in-del | -/AACA | | | intron-variant | Itsn1 | Mm_Celera | 16:91846091 | TTTGTAAACCAGCTC[-/AACA]GAATCTAGGGTCTGG | 16443 |
| rs262439981 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91777271 | TTCAAGACTAGTTGT[A/G]TGCCACCCCAATTGT | 16443 |
| rs262445287 | in-del | -/CT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91828099 | TCCCTCCCCACCCCC[-/CT]TATCAGCAAGAATTC | 16443 |
| rs262446960 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91826572 | TGCCTTTGTAGTCAG[G/T]CCCGGCACATTTGGT | 16443 |
| rs262466233 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91911031 | CTATTTCTCCAGCCC[C/T]ACCCCTGGTTTTCAT | 16443 |
| rs262468891 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91783979 | ACAGCACAACAACAG[A/G]ACTTTAGAGAGCTGT | 16443 |
| rs262470113 | in-del | -/CTTGCACG | | | intron-variant | Itsn1 | Mm_Celera | 16:91888855 | GGTGAGGTAGTCCCA[-/CTTGCACG]CTTGATGATCTAGTA | 16443 |
| rs262471301 | in-del | -/TC | | | intron-variant | Itsn1 | Mm_Celera | 16:91785791 | AAGAAGTCACATTTT[-/TC]TCTGTGTTGCTTCCA | 16443 |
| rs262503623 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91887954 | CTTGAAAAATCCACC[A/G]TTAGGGCTGGACATG | 16443 |
| rs262508516 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91833640 | AGTCTCTTTACGACC[A/C]CGTGAAGGAGAGGCC | 16443 |
| rs262513334 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91753898 | TTCAGAACAACAAAA[-/G]CCCCCTTACTTGTTT | 16443 |
| rs262517419 | in-del | -/AC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91895762 | CGTGTGCACACATGT[-/AC]ACACACATAAACACC | 16443 |
| rs262527368 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91778305 | TTTGATTCTCTCAAG[A/G]AGCTGTGAAATATTT | 16443 |
| rs262535837 | in-del | -/AAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91779027 | AATCTTTTTTTTTTT[-/AAG]AAAGCACGCTTGTCT | 16443 |
| rs262541683 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91827735 | GTCACACCCACCCTC[A/G]TAAGCAGAACCAAAG | 16443 |
| rs262571395 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91893081 | TTGTGACCGGGGCAG[C/T]TGAACACTTGGTCTT | 16443 |
| rs262572866 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91834691 | CGGTGTGAATGGCAC[C/T]GGGCTGTGGTAAAGC | 16443 |
| rs262581909 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91881964 | GCATTGTGCTGTCAT[C/T]CCCTTGAGATGAAAA | 16443 |
| rs262611368 | in-del | -/CA | | | intron-variant | Itsn1 | Mm_Celera | 16:91739301 | CACTGAGGCCCACCC[-/CA]GTCTGCTTCTTATGT | 16443 |
| rs262612184 | snp | A/C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91804817 | AGCGAAAACTTCATT[A/C/G]TGTGCCTAAATCTTG | 16443 |
| rs262613626 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91753111 | ATAGAACTGTAAAGA[C/G]TTGGCTTTGGAATCT | 16443 |
| rs262640410 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745737 | AGGAAATGACAGTCT[C/T]ACCATCACCTTAATA | 16443 |
| rs262644323 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91812457 | AACCTCTAAAAGAGC[C/T]GTCAGTGCTCTTGAC | 16443 |
| rs262659256 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91854251 | CTTCATCAGTGTCTG[C/T]ATGTAGCAGAGAACC | 16443 |
| rs262665871 | snp | C/T | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91863479 | AAAGAACCCTCCTTA[C/T]CTGAACCCTGAGCCT | 16443 |
| rs262687757 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91754084 | ATAGCTTCGTTTTTT[C/T]TCCCAATGAAATCTT | 16443 |
| rs262704407 | in-del | -/TG | | | intron-variant | Itsn1 | Mm_Celera | 16:91783505 | TTTCACAGAGTGTTT[-/TG]GCCATCACCTCGGAT | 16443 |
| rs262706960 | snp | A/C/G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892773 | AGAAAAAAAAAAAAA[A/C/G/T]AAAAAACAAACAAAC | 16443 |
| rs262708943 | snp | C/G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91806263 | CCGAGTCAAGAAAGA[C/G/T]TATTTTCCTGATGCC | 16443 |
| rs262718211 | in-del | -/TGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91742393 | TGTGTGGTGTGCGTG[-/TGT]GTGTGTGTGTGTGGT | 16443 |
| rs262724944 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91792379 | TTGAAAGTGTAGTGT[A/G]TGTCTGTCAAAATGT | 16443 |
| rs262726622 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91740028 | TGCTGGAAAACCATG[A/T]GTTCGCTCTGGAGAA | 16443 |
| rs262730527 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91902995 | CTTGGGAGGCAGAGG[C/T]AGGAGGATTTCTGAG | 16443 |
| rs262736068 | in-del | -/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91768945 | TCATATCTTTCCTGT[-/G]CTTTCTTAAAGAAGA | 16443 |
| rs262772583 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91841781 | GCCTGCTTTTAACCT[G/T]AAGTTGACTGATTGT | 16443 |
| rs262780317 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91849644 | TGTGGGGCAAGGTTT[C/T]ATAGAAAGCAGCCAG | 16443 |
| rs262782604 | in-del | -/TGTC | | | intron-variant | Itsn1 | Mm_Celera | 16:91826681 | CTCTGTATCTCTGTG[-/TGTC]TGTCTAGATTTGTGT | 16443 |
| rs262787904 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91800459 | CTTAGGAAAATCATG[A/C]AGCTGTTAAAGTCGA | 16443 |
| rs262795793 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91862902 | ATTTCTCCCATTAGT[A/T]TTCAGGCAGAAGGAG | 16443 |
| rs262804055 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91812290 | AACAAGCCCTAAGGA[C/T]TTGACGTATAACCTA | 16443 |
| rs262808335 | in-del | -/CG | | | intron-variant | Itsn1 | Mm_Celera | 16:91909045 | TACTATATATATACA[-/CG]GGGTCTGAAATTGAG | 16443 |
| rs262809221 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91776597 | CGTCATATTTCTAGC[C/T]ATGCTGCTGTGCAGA | 16443 |
| rs262828971 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91898901 | ACACGAGCACGTGGC[A/G]TAGGGCACCTGTCCT | 16443 |
| rs262835925 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91908548 | CCATCCCAGTGTCTC[C/T]GGGGCTGAAACTCGA | 16443 |
| rs262846387 | in-del | -/GTGTGTGTGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91788992 | AAAGGGAGGGGGAGG[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 16443 |
| rs262850517 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904310 | AGCTGCGGCCCCCTG[C/T]CTTCCTGCCTACTGT | 16443 |
| rs262854081 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91914492 | CTTGCCCAGGCTGCA[C/T]CACCTGGCACCTTGA | 16443 |
| rs262914182 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91769302 | ACCCTCTTCTGGTGT[A/G]TCTGAAGAGAGCGAC | 16443 |
| rs262917154 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91886522 | AGTGAACAGAGAGCT[A/G]GCCTAGCTCAGGGCA | 16443 |
| rs262917826 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91874687 | GCCACTGCTTTCCTC[C/T]CTTCTCCCCTCCCCC | 16443 |
| rs262921612 | in-del | -/AAT | | | intron-variant | Itsn1 | Mm_Celera | 16:91890276 | TTGGGGGGGGGGGGG[-/AAT]GGCTTTATAGCCAGT | 16443 |
| rs262927186 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91832188 | TACTACTACCCAGAT[A/G]TAAAACAGACAGCAT | 16443 |
| rs262929614 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91820372 | CACCTTTTAAAGAAA[A/G]GGCTTACTAGGCATT | 16443 |
| rs262949112 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91891823 | TTCACAGCTCCTAGC[A/G]TTTCTGGTGCCAGAA | 16443 |
| rs262952147 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91881757 | TCCTAGGAGGATCAA[A/G]CCCAGCCTGATTAGG | 16443 |
| rs262960003 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91838722 | CCAGTATCCCTGTGG[C/T]AGCTCAGAACTGTCT | 16443 |
| rs262965478 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91827516 | CATTTAGGATTCTAG[A/G]TGTGACAAATGTCCT | 16443 |
| rs263014722 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91738008 | AGTACTCTGGAGGCT[A/C]AGGCTAGGCTACATA | 16443 |
| rs263024498 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91791291 | GCAGGAGTTTACAGT[C/T]ATTCTCTCCATAGCA | 16443 |
| rs263051278 | in-del | -/GAGTGTGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91781511 | GTGTGCATACGGGCA[-/GAGTGTGT]GAGTTTGTGAGTGTG | 16443 |
| rs263063888 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91739223 | TGAGCCTAGAGCTCC[A/G]CTGGTGACCAGCAAG | 16443 |
| rs263080543 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91791991 | TACCTGCGGGACTGT[C/T]TTCCTAGTGTGTGTA | 16443 |
| rs263085357 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91898269 | GTAAAAAAGTAGACA[C/T]GGTGGTCTACTTCAG | 16443 |
| rs263091968 | in-del | -/A | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91871066 | AACTAGTAAGACGCC[-/A]ACTGCCCAGGCGGTT | 16443 |
| rs263097044 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91848321 | TGTTTTGGTTTTATC[A/C]TCCTTGTCTCTATAT | 16443 |
| rs263108581 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91847495 | CTAAGGTGGAGGTCG[A/C]GAGCCTGGCCACCAA | 16443 |
| rs263112189 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799543 | GAAATAAAACCTTTT[C/T]TAAAATAGAAGAAAT | 16443 |
| rs263115449 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91855370 | CCAGACTCACAGGAA[C/T]AGGGTTCCATTCTCA | 16443 |
| rs263132494 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91898670 | TGGAAGACTAACTTC[C/T]AGGTAGCTAGGATGA | 16443 |
| rs263162504 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91902947 | TAAGGAAGGGCAGCC[A/G]GGCGGTGGTGGCTCA | 16443 |
| rs263191777 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91855006 | TGTTTTTCCTCTGAT[A/G]TGGCATAATCCAAGA | 16443 |
| rs263197661 | in-del | -/CA | | | intron-variant | Itsn1 | Mm_Celera | 16:91766716 | TTCTTTCATCCCCCC[-/CA]CACACACTTATGTTC | 16443 |
| rs263199737 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91768180 | TGGAAAAAAAATGAG[A/T]TTTTTTCTTTTGAAT | 16443 |
| rs263202358 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91819027 | AAAATGTTTTGATGG[A/G]GTTGGAGAGATGGCT | 16443 |
| rs263210638 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768749 | GACTCCCTGAGCTTC[C/T]TCCAATGTTTGGCTC | 16443 |
| rs263220155 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91776216 | GTTTGATAGAACTCA[C/T]TAGTGACACCAGTGG | 16443 |
| rs263225751 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91874056 | ATAATAAAAATATAT[A/G]GACTGGTGATAAATT | 16443 |
| rs263232681 | in-del | -/TGTGTGTGTGTGTGAGTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91889022 | AAGTATGCACGTAGT[-/TGTGTGTGTGTGTGAGTG]TGTGTGTGTGTGTGT | 16443 |
| rs263236976 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91820002 | TAAAATGCCGCAGAT[C/T]CAAAACTCCACTCAA | 16443 |
| rs263252221 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91880222 | TCTCATTGTGAGGAA[C/T]GGTAGCTAGTCCACA | 16443 |
| rs263253798 | in-del | -/CG | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917782 | TAGAACCATCGTACC[-/CG]TATCCTGTGCGAGAG | 16443 |
| rs263263256 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91825885 | CTGTGCGTTCTGCAG[C/T]GGTGGCTGTGCTGGG | 16443 |
| rs263287723 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91887066 | GCATGTGTTTGCTAC[C/T]TGGATTTATGACCAC | 16443 |
| rs263309747 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91775878 | TTCCTACTAATTCTG[C/T]TTCACTGAGAGGTTT | 16443 |
| rs263314384 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91879976 | CCTGCCAACACCTTG[A/G]CTTGATCTTGGACGG | 16443 |
| rs263319809 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91737537 | GATCAGCACCACTTT[A/C]GTTACCTTTCACCTT | 16443 |
| rs263325110 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91825582 | CCATCTCACCAGCCT[A/G]ACATTATGTTTTCAT | 16443 |
| rs263347624 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91886974 | CAAGGCAGCGGTCAG[A/C]TCCCGAAACAGTGGC | 16443 |
| rs263352975 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743999 | GATTGGAATCCTGAC[C/T]CCTGATATTGTTGAC | 16443 |
| rs263371258 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91796002 | CTTACCCTGAGTCAA[A/G]TTACTCGAAGACCCA | 16443 |
| rs263407302 | snp | C/T | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91803881 | ACCAGAAAAGAAACA[C/T]AACTGGACGGACTAG | 16443 |
| rs263419055 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743931 | CACACACCTTCCTAC[C/T]TTACATCCTCACATT | 16443 |
| rs263426794 | in-del | -/ACCA | | | intron-variant | Itsn1 | Mm_Celera | 16:91813711 | GCAAAATAGCATAAG[-/ACCA]ACCAGCTACAGAGGA | 16443 |
| rs263429614 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91901784 | GGCAAAACCAAAACC[A/G]TCATACACATAAAAT | 16443 |
| rs263442072 | snp | A/G | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91803697 | ATAACACCTTTTAAA[A/G]TTCTACATAATGTTA | 16443 |
| rs263455947 | in-del | -/TACT | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91747820 | CTTACCTCATCGTAG[-/TACT]TACTGCACTGAGAGG | 16443 |
| rs263458834 | snp | A/G | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91853315 | ATCCCACAGTATCTG[A/G]ACTTATGGGAAATAA | 16443 |
| rs263459926 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91901416 | CAGAAGCTGAGGTGC[C/T]AGCTATGGCTTCTCA | 16443 |
| rs263474522 | snp | A/T | | | intron-variant, synonymous-codon | Itsn1 | GRCm38.p3 | 16:91853117 | TCTCTCTGGTCCTGC[A/T]GGGAAGCAGAAGTTT | 16443 |
| rs263487203 | in-del | -/TGTGTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91836558 | TGCACGAGTGTTCTT[-/TGTGTG]TGTGTGTGTGTGTGT | 16443 |
| rs263532284 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907621 | CCTGGCATTTATCAG[A/G]CTTTCTTCATGGACG | 16443 |
| rs263545505 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91766113 | CCACTTGGCTGAAAC[A/G]GAGCACAGATGGCGC | 16443 |
| rs263549077 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91774477 | TCCTGAAAGGTTTTG[A/G]TCACCAGCTGGGAGA | 16443 |
| rs263551146 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823910 | TGATTGGCCATTTTC[C/T]TGTGAATGCCCTCAT | 16443 |
| rs263552987 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91906052 | GCTAAATCCCGTGTG[A/T]GCAGGGTTGTGTTTG | 16443 |
| rs263559946 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91860271 | TTTGATATGCAGACT[A/G]TGAAAATAACAAGAA | 16443 |
| rs263565688 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91774218 | GTTTCTGAAAGTGCC[C/T]CCATCCCCATCCAAG | 16443 |
| rs263567736 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91823567 | TTGTTATATACATAT[A/G]ATATGTATATTTTAT | 16443 |
| rs263590896 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878644 | ATTTTTGTGGAAAGG[C/T]CCTAAACCAGGAAGA | 16443 |
| rs263606666 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91878346 | ATCATCACAGGACAA[A/G]CACAGTCCATAGTGA | 16443 |
| rs263613744 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91885570 | GCTGTTCCATCCCAA[A/T]GAGAAACAAACCGAA | 16443 |
| rs263622713 | snp | G/T | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91831101 | TTCACCCTTCATTCT[G/T]CGCTCTTAGAAATGT | 16443 |
| rs263628428 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91898589 | AAGGTGGGAGCAGGA[C/T]AGCATCCAGGCAGGC | 16443 |
| rs263650138 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91813377 | GACATTTTGACTTCT[A/G]AGGACTGTTTAGAGG | 16443 |
| rs263671027 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91864830 | GCTCACCACATAGAC[A/G]TTTCTTAGGGGCCTG | 16443 |
| rs263673472 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91873816 | TGGTAAGATACAGGA[G/T]AGTGGGGCTGGAGAG | 16443 |
| rs263684917 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91819758 | AGGACCTCAAACAGG[A/G]CAGGAACCTGGAGGC | 16443 |
| rs263687227 | in-del | -/CTTTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91847471 | CTCTCTCCCACCTGA[-/CTTTG]CTTTAGTCCTAAGGT | 16443 |
| rs263697549 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91915466 | TGTTTCTAGCTGTTC[A/G]GACCTGGCCTGATTC | 16443 |
| rs263724023 | snp | A/T | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91728186 | GGAAATGCAAAGAGA[A/T]GGATAAGAAGGGTGA | 16443 |
| rs263739131 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742691 | AACCTCCTCCCCCCC[A/C]AAAAAAAAGATTGTT | 16443 |
| rs263758035 | in-del | -/TGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91751531 | TTTTTTGGTTTTTTT[-/TGG]TTTTTTTTTGAGCAC | 16443 |
| rs263758690 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91748914 | GCACAGATTGCCATG[C/T]CTGAATTGAAAGAGA | 16443 |
| rs263763496 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91790381 | GCTGTGCTTTCAGAG[C/G]TTCCTGGGAGCTCTC | 16443 |
| rs263764276 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91794493 | ATCTCACAGAAACTC[C/T]CTGACCCTCTGACTC | 16443 |
| rs263775000 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91737182 | CTTTTACTATTCTTT[C/T]AGTGATTAGAGAGAC | 16443 |
| rs263779009 | in-del | -/TGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91833521 | TCCTCCTCCTCTTTC[-/TGT]TGTTACAGGCATCTT | 16443 |
| rs263805311 | snp | A/G | | | synonymous-codon | Itsn1 | GRCm38.p3 | 16:91839673 | GCAGGAGGAGCAGCC[A/G]CGCCCCCGGAAACCC | 16443 |
| rs263806836 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900373 | TATTTAGAGAGAGTT[A/T]GAGGGTCACATCGCA | 16443 |
| rs263813766 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91851742 | GCGCGTGGGAGGACA[A/G]CTCAGCAGCAGCGCC | 16443 |
| rs263822295 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91905542 | GGGGTCTCTAAAAGA[A/T]GCCCGTTACAGAAGG | 16443 |
| rs263828293 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91897527 | GAGGGCATCAGATTT[C/T]GTTACAGATGGTTGT | 16443 |
| rs263843692 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91846480 | GTCCTTAATCATAGT[C/T]GTTAAAATGAGCTAA | 16443 |
| rs263845224 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91859441 | CAAAAAGGGGAAAAT[A/C]TAACCCTTCCCCAGG | 16443 |
| rs263860660 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91893150 | AAGACTACACACTTA[A/C]AAGGATGGCCAGTCC | 16443 |
| rs263895478 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91892219 | AGTCTACCTGGGCAG[C/T]AGAACATTCTAGAAA | 16443 |
| rs263898923 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91839237 | TACTATCATCAATCT[A/T]TCATTAATCTCAATT | 16443 |
| rs263903040 | in-del | -/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917278 | GGGGATGTGGAGACA[-/G]GGGGATTGTTGGACT | 16443 |
| rs263922934 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91811891 | TGTCTTCAGTGTGCT[C/T]GCTGGTCATCTGCTC | 16443 |
| rs263928203 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91846049 | CACGCCCAGCAGGCA[C/T]GATACTCAGTGTGTA | 16443 |
| rs263930192 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91761099 | AGCCAAAATTGAGGT[A/G]CAGTTGCTCCAGGAT | 16443 |
| rs263934587 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91760111 | ATTCATGTCTGTTTG[G/T]TTTGTTTTGTGATTT | 16443 |
| rs263936157 | snp | A/G | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91863664 | GCAAACGGAATCAGC[A/G]CTTCGTTGGAGGTGT | 16443 |
| rs263951935 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91812780 | ATTATTTGTGTGTGT[C/G]TGTGTTTGTGTGTGT | 16443 |
| rs263954646 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91767249 | CAGTTCTGCCTTTAT[A/C]TGCCAAGTGCTGAGT | 16443 |
| rs263959163 | snp | A/G | | | missense | Itsn1 | Mm_Celera | 16:91818450 | ACTTCGAGCGAGGCA[A/G]TGTGGAGCTGGAGAA | 16443 |
| rs263964953 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91901272 | TTCCCTGTGGATTTC[C/T]CCTCTTCTAAATTCC | 16443 |
| rs263984849 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914182 | TGAGTCTTTCCCCCA[A/G]GTGACCCTACTAGAC | 16443 |
| rs263987222 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91811676 | AAAGCCCCACACACA[A/C]AAAAAGAAATAATCT | 16443 |
| rs264002582 | snp | C/T | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91871773 | TACAGACATAACCCC[C/T]GAGTGGGACCTCCCA | 16443 |
| rs264008990 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91879021 | GGATGGTGCCTGTAG[A/T]TATCAGAAGAAGGCA | 16443 |
| rs264011695 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91767036 | GATATTTATAACCTA[C/T]CCAACTTCTCTTAGT | 16443 |
| rs264020153 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91818197 | CTTAGCTTTGGGATT[A/G]TCTTTTTCTGTAAAG | 16443 |
| rs264043939 | snp | A/G/T | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | GRCm38.p3 | 16:91727556 | TGAACCCATGTACTG[A/G/T]AGCAGCAAAGGGATG | 16443 |
| rs264049288 | in-del | -/A | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798439 | AGGAAGGAAGGAAGG[-/A]AGGGCGGATCCCCAG | 16443 |
| rs264054664 | snp | G/T | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91871019 | CCCGTGTTTTGTTTT[G/T]AGTTTTCAATCTGGC | 16443 |
| rs264060319 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91878811 | AGGAGCTGTCCGGGG[C/T]TGGAGGTGTTTTTTG | 16443 |
| rs264067841 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823461 | TAAGGTCTTCCTTCT[C/T]TAGCCGGGATATCTT | 16443 |
| rs264078475 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914026 | CAATCCCTTCCCCTC[C/T]CCCTTCCAAGTTGAA | 16443 |
| rs264085277 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91735376 | GCCAGTAGGAAACAC[A/G]GTTTTGCTTATAGCA | 16443 |
| rs264099657 | snp | C/T | | | downstream-variant-500B | Itsn1 | Mm_Celera | 16:91920798 | GGCTCTAGTCAGGAA[C/T]ATGGCATGGTCAGAG | 16443 |
| rs264102122 | in-del | -/TTTGGG | | | intron-variant | Itsn1 | Mm_Celera | 16:91904784 | TCACTCTCTCTTTTT[-/TTTGGG]TTTTTTTTTTTTTTT | 16443 |
| rs264104815 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91838237 | GGATGCAAGTGCCTT[C/T]ATCAGCTGAGCCATC | 16443 |
| rs264105158 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91877647 | GGCAGGGATAGCCTC[A/G]CATGCCCATCAAGAA | 16443 |
| rs264113517 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91788908 | CTGATTTGTTCTAAA[C/T]AAAAAGGTAGAGACC | 16443 |
| rs264122247 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91795096 | TCATAGCACTATATG[C/T]CTTTCTTTTAGGGAC | 16443 |
| rs264127910 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91735059 | AAGCCTTTTACGGTG[C/T]TCCTGCCACCCTCGG | 16443 |
| rs264130748 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91743603 | TTCAGTCTGATAATG[A/G]ACTATGGCATTAAAT | 16443 |
| rs264143380 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91837860 | GGCTAGGGACTAGGT[A/G]TCCTAGGGCAATGGA | 16443 |
| rs264157629 | in-del | -/CAAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91756145 | GACGGCCAGCTGAAA[-/CAAC]CAACCAGCCTTGTGG | 16443 |
| rs264161126 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91844993 | CATAAAAACAAAGCT[A/G]TGGCGGGCGCGAGCT | 16443 |
| rs264165245 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91794933 | CCAGTTCCTGTCACG[A/G]TTGTGGCTTGTGAGT | 16443 |
| rs264194567 | in-del | -/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915648 | TCCTCCTCTCCCTCC[-/T]CCCTCCTCCTCCTCT | 16443 |
| rs264204579 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91843976 | TCGCGGACCACCCCA[C/T]ATACCACCACACTCT | 16443 |
| rs264221529 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91794004 | TCCTGACTTCACAGT[A/G]CTTCAGTTCTCAGAG | 16443 |
| rs264240102 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91851655 | CCACAGAAGAGGGGA[A/G]ACGGAGCAGGCCCGG | 16443 |
| rs264252736 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91757688 | AGAGCATGGTAGCTG[C/T]ATAACAAATGCTTGT | 16443 |
| rs264258256 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91895344 | TGTTTCAACTTTGGG[A/G]CAGGCTGATGGAAGC | 16443 |
| rs264260279 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91816840 | TGTCTTCCTGTCTTT[C/T]GCAGAAGAGTTCGCT | 16443 |
| rs264267144 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91825396 | AGACATTATGTTTTC[-/T]TTTTTTTTTTAAGAT | 16443 |
| rs264275587 | snp | C/G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91765683 | GGAGGCAGAGGCAGG[C/G/T]AGATTTCTGAGTTCG | 16443 |
| rs264290633 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91816685 | GAGCGCTGGGGATCA[C/G]AGCAAGCCCAGGCCC | 16443 |
| rs264295648 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91765413 | AGAGAAAGCAGCCTC[C/T]GCTCCAAATTCAGTG | 16443 |
| rs264306494 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91869168 | CAGGTGACAGCTGCA[C/T]ACCATCTATAGAAGG | 16443 |
| rs264325776 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91823050 | GAGATAAGTGTATCC[C/T]CTGTGCTGCCTTTGA | 16443 |
| rs264326775 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91868913 | CGATGGTGGACGCCC[C/T]GAGCCATGTGTGGAA | 16443 |
| rs264342726 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91755911 | AAGCAGGTTGCCATG[-/A]AAAGCTTCGGCCCAG | 16443 |
| rs264343216 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91764556 | AGTTTAGTCATTTTG[A/T]CTTCCACTCCTCCCC | 16443 |
| rs264358153 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91877055 | CACCCCCTGCTCTCT[A/G]CCATCTTCCCTCCCA | 16443 |
| rs264358710 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91815865 | GTGACAAAAATGCTG[A/G]TCATGTAGAAATTAT | 16443 |
| rs264375127 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91734144 | CATGGTTGTAAGCCA[C/G]CACGTGGGTGCTAGG | 16443 |
| rs264382182 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91876236 | CCAGCCAGGCCTCAA[A/G]AGACAGAAGAAAATC | 16443 |
| rs264385616 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91918928 | CAGAATAATTACAGC[A/G]CCCGAACCCCCGGCT | 16443 |
| rs264394555 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91822312 | ATGTAGGGAACATGC[A/G]TGTAAAGGTGAACTC | 16443 |
| rs264413228 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91733442 | TTCTTTCTTCTTCAA[A/G]GTCCTATCTAGCCTT | 16443 |
| rs264418811 | snp | C/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917482 | AAATAATTCTCCTAG[C/G]ACTGTGTGTGGCTGT | 16443 |
| rs264430700 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91787186 | TTCAAATTTTTATTT[C/T]GATGCAGAGTCCTGC | 16443 |
| rs264431501 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91741300 | TCCTTTAGTGTGTAG[C/T]GCCTAGTGCCTCCCA | 16443 |
| rs264442244 | in-del | -/ACAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91903978 | TCTGCTAACTAGGGT[-/ACAC]CTTCTCAAAGCCCCG | 16443 |
| rs264444122 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91883919 | TAGAAAGCAGTTGGC[A/G]TTTCTCAGCAGGGAC | 16443 |
| rs264444484 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91732349 | CTTTCAGACCGTTGC[A/T]GGGTGGATGGGTGAG | 16443 |
| rs264448852 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91843642 | GAGGTGGCCATCCCC[A/G]GGGGATGGAGTTGAC | 16443 |
| rs264457258 | in-del | -/CT | | | intron-variant | Itsn1 | Mm_Celera | 16:91811668 | ATAAATAAAAGCCCC[-/CT]ACACACACAAAAAGA | 16443 |
| rs264461079 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91793358 | AGTAAGGACTCTTCA[A/T]ATTCGACTGAAAGTT | 16443 |
| rs264476413 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91759515 | TATTTTTGAAGTTTC[A/G]AGAATTCCTGTATTT | 16443 |
| rs264479441 | snp | A/G | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91803633 | CGCACTGGACCGTCT[A/G]TCCAGCCCCAGCCTT | 16443 |
| rs264481098 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91894974 | TAACGCCTTTCCCAA[C/T]GGAAGATCGTGGGCG | 16443 |
| rs264498138 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91899714 | ACCCCTCCCGGTGCT[A/G]GCAGCCAGCAGAGCA | 16443 |
| rs264527354 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91907564 | TATATGATGCTTTGC[A/G]GTATGGGAGGGCAGG | 16443 |
| rs264536754 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91860838 | CAGTTCTTAAGGAGA[A/G]TTCTAGTACAAACGT | 16443 |
| rs264549341 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913855 | TGTTGTTGTTAAGAA[A/G]CTGTTTTAAATGATA | 16443 |
| rs264552334 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91764085 | ACAGCTTCCTAGCCC[C/T]GTGACAGATGCTGGG | 16443 |
| rs264573267 | snp | A/G | | | utr-variant-3-prime, intron-variant | Itsn1 | Mm_Celera | 16:91870817 | GGGTTATGCTTGTCT[A/G]TGACCATCACGTGTA | 16443 |
| rs264581989 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91821678 | GTCAATCTTCAAAGC[A/G]TTTCAGATGATCTTG | 16443 |
| rs264613979 | in-del | -/GTGTGG | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91839404 | TGTGTGTGTGTGTGT[-/GTGTGG]GGTTTTGGTAAGTCA | 16443 |
| rs264616088 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91917162 | TGGCTGGGTAGATCG[C/T]TGACAAAGTGCTAGC | 16443 |
| rs264617611 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91781140 | TAACTGGAGACTAAA[G/T]CCACTCAAATTCAAA | 16443 |
| rs264620913 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91875511 | AGAGAGAATGCGAGC[A/T]CCCTGGAGCCTTCAC | 16443 |
| rs264643582 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91831066 | CTTTGGGTTTAACAC[A/G]TGACCTCAAATCCGC | 16443 |
| rs264653847 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91788464 | CATTGAGACAAAATC[A/C]AAAGCTGTCACCAAA | 16443 |
| rs264664977 | in-del | -/AAAAGAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91779183 | TCAATACCCAGCACC[-/AAAAGAA]AAAAGAAAAGTCCAG | 16443 |
| rs264670771 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91891041 | TCCTTGCGAGGGCCG[A/G]TCTGTGTGCCCTCCT | 16443 |
| rs264675407 | in-del | -/TCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91801276 | TTCCTTCCTTCCTTC[-/TCT]CATTCATTCATTCAT | 16443 |
| rs264685405 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91748726 | TGCCTCCACAGTCCT[G/T]CTCTGGCTTCCCATA | 16443 |
| rs264708662 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91757372 | CCCTTAGCCTGCTTT[G/T]TCTAGTACTGTGCGG | 16443 |
| rs264724942 | in-del | -/ACTGCA | | | intron-variant | Itsn1 | Mm_Celera | 16:91837566 | CCTCCTCTCTTGTTT[-/ACTGCA]ACTGCAAATTAAACT | 16443 |
| rs264733927 | in-del | -/GTAGTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91744584 | TTTATCAAAGTAATA[-/GTAGTT]GTAGTAGGTTCATCC | 16443 |
| rs264751540 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91764191 | AGAGAAGGGTTCTTC[C/T]AGACGTCACCCAGGG | 16443 |
| rs264758323 | in-del | -/TC | | | intron-variant | Itsn1 | Mm_Celera | 16:91752705 | AGGTATGATGCTGCT[-/TC]TCTGTGCTTTTGTTC | 16443 |
| rs264765768 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91779820 | TTGGCCACAGGTGTG[C/T]TCTGTTTTCTTGCCT | 16443 |
| rs264766711 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867346 | CAGTGCATCTTAGCT[A/C]AGCATCAGCCAGTCT | 16443 |
| rs264787786 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911198 | ATGGGATCCGATGCC[C/T]TCTTCTGGTGTGTCT | 16443 |
| rs264796695 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917214 | GTTTGATCCCCAGCC[C/T]TTTCGTAAAGAAACC | 16443 |
| rs264812556 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91731847 | GCACCTAGCTACATC[C/T]GCAGCCTCACGTTGT | 16443 |
| rs264820601 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91834785 | TCTCTAGTTGCTTCC[A/G]TCTGTCTGGACCAGT | 16443 |
| rs264827815 | snp | A/G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91785207 | CCACCTCTTAAATAA[A/G/T]GATGTGGTTCTGATG | 16443 |
| rs264831303 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91792014 | TGTGTGTATCAGTGC[A/G]TCATGCATCACACGC | 16443 |
| rs264831849 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91888692 | GAAGCATTGTCCTCT[C/T]AGGACCCACCTGCTT | 16443 |
| rs264850209 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91841244 | CTAGAGCCCACGCCC[A/C]GAGGCAGAGAAAGGT | 16443 |
| rs264868601 | in-del | -/CGGTCCCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91740685 | GAGGTAGTGACTGAC[-/CGGTCCCT]TACCCAAGGGCTAGA | 16443 |
| rs264876863 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91754208 | TCAAGCTCTGTAAAC[C/T]AGCAGGTTCAGGTGA | 16443 |
| rs264897048 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91813657 | TAGGGGACTGAAAGG[A/G]TAGAAAAAATGTGGA | 16443 |
| rs264898356 | in-del | -/GA | | | intron-variant | Itsn1 | Mm_Celera | 16:91843900 | ACGGGAAGCTGGAGG[-/GA]GAGAGTCAGCTCCCC | 16443 |
| rs264908380 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910045 | TGTCATCCCAGCATC[C/T]GGGAGGCTGATCCTG | 16443 |
| rs264919059 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91865345 | AACTGACGGTCAGCT[G/T]AGGCAGGGAGCAGAG | 16443 |
| rs264922514 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91874168 | AAAGTCAGATGACTT[C/G]TTTCAGCCAGTCTGT | 16443 |
| rs264942775 | snp | C/T | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915910 | ATCTCCCCGCTCCTC[C/T]CCTGCACAGTCTCCT | 16443 |
| rs264958329 | snp | C/T | | | upstream-variant-2KB | Itsn1, Cryzl1 | Mm_Celera | 16:91728944 | GTGCCCACGCTCTTT[C/T]TGCAAAACCTTCAAT | 16443 |
| rs264961290 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91833611 | AATAGGACCCTGAAA[-/C]CCCCCCATTTCTGAG | 16443 |
| rs264968680 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91737568 | GTCTTTATCTTTTTG[A/G]TGAGGATGATGAGAC | 16443 |
| rs264974622 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91858799 | AAAAACATCAAGTTC[C/T]CGTAGGCTGGTATGC | 16443 |
| rs264982425 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91772744 | CTAGGTGGGAGAGCG[C/T]GTGCTTACTTGGTGT | 16443 |
| rs264996388 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91822910 | TCTGCTCTCCAAGTG[C/T]TGGTTCACAAGTGTG | 16443 |
| rs264997276 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91904872 | GAACTCACTCTGTAG[A/T]CCAGGTTAACCTCAA | 16443 |
| rs265038522 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91779264 | AAGAAAAAAACTTCT[A/G]AAAAATTAGCATCCA | 16443 |
| rs265039920 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91883553 | AACTGGGTTCTAGGT[C/T]CAGGGGCCAGCGTGG | 16443 |
| rs265042254 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91741117 | TGATGGGAGGCTCAG[A/G]GCCTGACTGTGGAGG | 16443 |
| rs265046028 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91828910 | GAGTCAGGGGCAGCT[A/G]AGGCTGCATAATGAG | 16443 |
| rs265056917 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889537 | TCCAGCCCCAGGGTC[G/T]AGCCTTGGACCTGGG | 16443 |
| rs265081391 | in-del | -/TCT | | | intron-variant, upstream-variant-2KB, cds-indel | Itsn1, Cryzl1 | Mm_Celera | 16:91730361 | CTTGCCTATGAGCAG[-/TCT]TCTATTGTTGTGATT | 16443 |
| rs265086638 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746373 | CTGTGTTGGGGCTCC[C/T]TTCCAGGTTCTGGAA | 16443 |
| rs265092580 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91799671 | GCAAATTCAGGACCA[C/T]TATCTTGAAGTGGAA | 16443 |
| rs265095333 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91763202 | ATTTGTTTGTTTTGG[-/T]TTTTTTCTTGTTCAT | 16443 |
| rs265108661 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91754977 | GGAGCTGGCTTCTTG[A/G]GGTCTTTGCATTGGC | 16443 |
| rs265120724 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91903936 | TAGGGTACACCTTCT[C/T]AAAGCCCCGCCTCCA | 16443 |
| rs265130118 | in-del | -/GT | | | intron-variant | Itsn1 | Mm_Celera | 16:91751460 | TTGCGGGCGCCATGC[-/GT]GTGTGTGTGTGTGTG | 16443 |
| rs265131164 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91856755 | TGATCTTTCTAAGCC[G/T]TGCTTGTGATGTGCG | 16443 |
| rs265156203 | in-del | -/TG | | | intron-variant | Itsn1 | Mm_Celera | 16:91766202 | GTTTTGCGAGATTTC[-/TG]TGTGTTGCCTCTTAT | 16443 |
| rs265156743 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91910709 | ATTTTTAAAAGATTG[A/G]GTTTCATGTAGCCCA | 16443 |
| rs265174659 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91777369 | TGTCTTCCCCACACT[A/C]TGCAGGCTCCATGGG | 16443 |
| rs265175348 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91826929 | GCTTTTTAAAGAGCC[A/C]TTTCCATGGGGGACA | 16443 |
| rs265180389 | in-del | -/TG | | | intron-variant | Itsn1 | Mm_Celera | 16:91755338 | ATCTTGAGCATCAGT[-/TG]GGGGGGTCTGCTTTC | 16443 |
| rs265197466 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91784233 | GAAAGGGCGCATGTG[A/G]TCAGCGGGGCATTTC | 16443 |
| rs265199870 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91888221 | TAAACTGGTACCCTC[A/G]CGAATGCCATGAAAC | 16443 |
| rs265205728 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91834187 | CCCTTTCACAAGCGG[C/T]TGCCTAAGACCATTG | 16443 |
| rs265228019 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91887683 | TGCTCACGTTTTTTT[-/A]CCCACACAGCCACCA | 16443 |
| rs265235168 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91745291 | TGCAAGAGGTCTTAA[C/T]CACTGAGGCTGCTCT | 16443 |
| rs265246874 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91753423 | TTTCCTAACTCAGCA[A/G]ATTAAAAGCAGGTGG | 16443 |
| rs265252116 | in-del | -/TTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91825838 | GTTAGAGCAAGCTGA[-/TTG]TTCATGGTAGAGTTC | 16443 |
| rs265256959 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91797579 | TAAATAAGTCTTAAA[-/C]ATTTTTCTTTTTGGA | 16443 |
| rs265265001 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91804959 | AGCTACTTGACCAGC[C/T]GTGAGACTCTCACAG | 16443 |
| rs265268180 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91812909 | TATTATGGGAATATG[G/T]TTGTCTTAGTTAGGG | 16443 |
| rs265270449 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91902521 | CAAGGCTCGGCCAGT[C/T]GGCCCAAGTCTGTTC | 16443 |
| rs265274470 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91854826 | TGAAGTCCTCTCAAA[C/T]AGTGCAGATCATCCC | 16443 |
| rs265280411 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91909006 | TCAAAGATATGCACA[A/C]ATGTAGGTATATAAT | 16443 |
| rs265291284 | snp | C/T | | | intron-variant, downstream-variant-500B | Itsn1 | Mm_Celera | 16:91863724 | TCATGCAGCCTACGT[C/T]GGTCATGATGTTGTT | 16443 |
| rs265314470 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91775852 | GACTCCATCTCTCCT[C/T]TTGAAGAGGCTTCCT | 16443 |
| rs265315809 | in-del | -/GCGTGTGTGTGTGCGTG | | | intron-variant | Itsn1 | Mm_Celera | 16:91742397 | GGTGTGCGTGTGTGT[-/GCGTGTGTGTGTGCGTG]GTGTGTGTGTGGTGT | 16443 |
| rs265331361 | snp | C/T | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | Mm_Celera | 16:91727636 | TGCATCATCTGGATT[C/T]GGAGAGCGGCGAATA | 16443 |
| rs265339476 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91832700 | ATTGACTTCGGTTTT[C/G]AAAGAATGATTTGAA | 16443 |
| rs265344113 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91782709 | GGTGGGTAGAGGCCT[C/T]GGTCCTTGCTCTTAG | 16443 |
| rs265360960 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91886903 | AGCTGGCCTCTCTGA[A/G]CCCTGGTTTCCTTGT | 16443 |
| rs265371022 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91839099 | TGTAGCTCGTCCTGC[C/T]CAGGGAGGACCTGTG | 16443 |
| rs265395252 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91884575 | AGGCCGGCACCTGCC[-/T]TTCATCCTGCAGTGC | 16443 |
| rs265401683 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91751936 | TACTAGCTTGAAGAC[C/T]TTGGAGCCCCTTAGG | 16443 |
| rs265414093 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91874831 | AACAGTTTGACAGTA[C/T]TGGGTTCTTAGAGCC | 16443 |
| rs265417745 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91882059 | ACATTGCTACCCCCT[C/T]CCCCCCATAACATGG | 16443 |
| rs265428177 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91916679 | AATAACTGGCTGGTT[A/G]CCACAGGGACTCCTC | 16443 |
| rs265452832 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91738535 | ATTTAAAAAATAACA[C/T]GGTTTTCTTACTACG | 16443 |
| rs265467978 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91791439 | GGTCCCTTCTCTAAA[C/T]TCCGACCCAAGTGCA | 16443 |
| rs265472041 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798780 | TTAGTCCGTCACCAT[C/T]CCTAAGAAACTAGAT | 16443 |
| rs265476028 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745821 | ACTTGCAGGTAGATT[A/G]TCAGGCCTCACATTG | 16443 |
| rs265489746 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91898342 | TGATTGGTGAGCCCT[G/T]CGTGCCATTAAAACA | 16443 |
| rs265490582 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91847781 | CAGCGCCCTTGACCG[A/C]ACATGACCCGAGGGC | 16443 |
| rs265495063 | in-del | -/CCA | | | intron-variant | Itsn1 | Mm_Celera | 16:91872791 | GTTTTAGGCAGAAGT[-/CCA]CCACTACCAGCATCC | 16443 |
| rs265500426 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91903154 | ATCGCCTATGCTACA[A/G]TGTGAGACCCTTATC | 16443 |
| rs265540026 | in-del | -/TCATGAGTGCA | | | intron-variant | Itsn1 | Mm_Celera | 16:91791711 | AAAAATGATAAAATT[-/TCATGAGTGCA]CATGCATGTGTGAAT | 16443 |
| rs265542923 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768369 | TCTCCTTCTCTTTCA[A/G]GAAGGGAGAGGCCCC | 16443 |
| rs265552968 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91776650 | GGTTTCTCTTTGTCT[A/G]TAGAGCACATGAATC | 16443 |
| rs265553681 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91826273 | CAAAGAGATCCACTT[C/G]CCTCTGCCTAGTGGT | 16443 |
| rs265574854 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91880560 | AACACACACCAAAGA[A/G]CAGAGTGTCTGCCAC | 16443 |
| rs265575734 | in-del | -/GTGTGTGTGTGTGT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91866977 | CGCGTGTGTGTGTTC[-/GTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 16443 |
| rs265590960 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91737059 | ATGCACCGGACATCC[A/G]ATGTTTTATAAAAAT | 16443 |
| rs265595656 | in-del | -/GTGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91788993 | AAAGGGAGGGGGAGG[-/GTGT]GTGTGTGTGTGTGTG | 16443 |
| rs265602140 | in-del | -/GTGGGGCT | | | intron-variant | Itsn1 | Mm_Celera | 16:91766744 | TTCTTTATGCGAGGC[-/GTGGGGCT]GTGGGGCTTTACCTG | 16443 |
| rs265613959 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91744396 | GCACTGTGTGTAGGC[C/T]TGGTAACTTTGGAAG | 16443 |
| rs265616997 | in-del | -/AAAC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890390 | ACTATAACAAAAAAA[-/AAAC]CCCTGAGGCTACCCT | 16443 |
| rs265622468 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91845992 | CCAAGCTTTAACCAA[A/G]CTGATTTCAATCTGA | 16443 |
| rs265629388 | snp | A/G | | | intron-variant, utr-variant-5-prime | Itsn1 | Mm_Celera | 16:91804293 | GACTTTTCTCACATG[A/G]TTTTGAATTCTGCCT | 16443 |
| rs265651592 | snp | C/T | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91853589 | GTGTGTCTGTGTCTG[C/T]GTGTGTGTGTGTGTG | 16443 |
| rs265695133 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91824126 | TTTAATCTCAGCACT[A/G]GAGAGGCAGAGGCAG | 16443 |
| rs265701138 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91774868 | ATGGTTGGTCTTGCT[A/G]TGTTGAAAAGGCTTG | 16443 |
| rs265711677 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91832033 | GCCCCATAAGGGACA[A/G]ATATCTGTCTGCTTC | 16443 |
| rs265715306 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91878761 | CGGCCTCACAGAAGC[A/T]TCCCTGGGTGGATCC | 16443 |
| rs265731685 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91886321 | TTTGGAAGAGCAGTC[A/G]GCACTCTTAACCGCT | 16443 |
| rs265747988 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91743205 | CATCCTAGCGAGTTC[A/C]CTGTACCACTTCCTT | 16443 |
| rs265767110 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91794921 | GTGGTTATTGTGCCA[A/G]TTCCTGTCACGGTTG | 16443 |
| rs265769086 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91770465 | CAAGGGCTCCAAAGA[-/C]CGAGACTGTCAAGAT | 16443 |
| rs265769980 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750923 | CACTTTGGGTTAGGG[A/G]CCTTTCCTCGCAGAG | 16443 |
| rs265779279 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852287 | TCAGGAGAGTGCCAT[C/T]TCTTTGGTAGATGTA | 16443 |
| rs265783103 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91802927 | ACTCCGTGCTAGGGG[A/G]AGGAGGGGCCACTGC | 16443 |
| rs265794073 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91900692 | TTCTTAGTTTATTAT[G/T]TTTTATATTAGCTTG | 16443 |
| rs265829309 | snp | C/T | | | missense | Itsn1 | Mm_Celera | 16:91839819 | CAGCTAAGCTGGCCA[C/T]CCAGGCACCCTGGTC | 16443 |
| rs265841212 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91892732 | ACCTTCCTTGGCTTT[C/G]CCAGGACAAGGAACC | 16443 |
| rs265859074 | snp | A/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91846969 | GACAGGCATCCGGAG[A/C]AGAGAACCAAAGCTT | 16443 |
| rs265886997 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91760630 | AACCTGAGAGCCAGT[G/T]CGCATCAGTGTTGTA | 16443 |
| rs265904383 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91812168 | GGTAAGGAAGCACAC[A/G]TTCCGTGGTTTGTAT | 16443 |
| rs265907948 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91818747 | TTGTGAGGTTTAGGG[C/T]ATCCAGAGTTGCTCA | 16443 |
| rs265925069 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872393 | GGGGGGTGCTATGGG[A/G]CAGGGGTGCAGGGGA | 16443 |
| rs265942017 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91879437 | TGGTCAGTTGAGAAA[A/G]TGTGGCCTCACATGA | 16443 |
| rs265969542 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91735790 | AGCTGCCTGGCATCT[C/T]TCAGTTTGCTAAAAG | 16443 |
| rs265971754 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91838627 | TTTTCATGCTTTTTA[A/T]AAAACGTTGTTTGGG | 16443 |
| rs265978899 | snp | A/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91789266 | CCGCCGTTTCTTGTT[A/T]TTTTTATTGTTGTTT | 16443 |
| rs265995270 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91795307 | CAGGGGGACTTTGCA[C/G]TGGATACTGGAACGT | 16443 |
| rs266017767 | in-del | -/TTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91899854 | ACTTCCTATTGCCAA[-/TTTT]TTTTTTTTCAAATGT | 16443 |
| rs266035737 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91758627 | AAATTGTTCTGTCTC[C/T]GCCTCCCACAATACT | 16443 |
| rs266046012 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91765928 | AGGAGCTGGGACACT[C/T]GGTCACTGGTAATGT | 16443 |
| rs266063561 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91817068 | GGCCAGAAGGCGGGC[A/G]CAGGTGCTTTTGGAA | 16443 |
| rs266075639 | in-del | -/A | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917500 | GTGTGTGGCTGTCCT[-/A]ATTTCAGGGTGAATT | 16443 |
| rs266105731 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91876728 | GTCAGAACTTCATGT[A/G]TCAGCATCTTGGGCC | 16443 |
| rs266107478 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91734205 | TCAGCCTCTCCAGTC[C/T]GCTACGGGCATTTCT | 16443 |
| rs266109373 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91787733 | CTCTGTAATGACAAG[C/T]ACACTCTGGCCTGGG | 16443 |
| rs266114392 | snp | G/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91822612 | CGTAGCACTGTGGCT[G/T]TGGTTTGCCGTTTTC | 16443 |
| rs266126960 | snp | A/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917975 | TAGATGGTTCTATTG[A/G]CAGGGTCAAGGTGCT | 16443 |
| rs266131189 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742117 | TATGTGTGCGTGTGT[C/G]TCTGTGTATTTTTAA | 16443 |
| rs266161279 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91792846 | AAATGTTTTTTATGT[C/T]GTGAGTATGCACAGT | 16443 |
| rs266165291 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91740399 | AACAAATGTTCATCC[C/T]TAGACCCATCCCACG | 16443 |
| rs266175422 | in-del | -/AGGATCTTGCC | | | intron-variant | Itsn1 | Mm_Celera | 16:91822816 | GTTGGTGTTTGAGAT[-/AGGATCTTGCC]AGGATCTTGCCCTGT | 16443 |
| rs266180381 | snp | C/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91894470 | GAATCGTGTCTAAAT[C/T]CTTGATTTCATTTTC | 16443 |
| rs266180974 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91842552 | TTTGATGAGTAAAGC[A/G]TAGATGTACTCTAAG | 16443 |
| rs266181854 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91824825 | CTGCTCTCTCCCTCC[-/T]CCTGCCTCCCTGCTC | 16443 |
| rs266198141 | snp | A/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91850271 | GGAACAAACAGAGGG[A/G]GTAGAGTAATGACCA | 16443 |
| rs266208927 | in-del | -/TTTA | | | intron-variant | Itsn1 | Mm_Celera | 16:91811573 | TTCCTCTTTTCTTTG[-/TTTA]TTTGATGACAGCCAT | 16443 |
| rs266217084 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91845962 | GCGGTCAGTGCCCAT[-/A]AGACCTGTTAGAACC | 16443 |
| rs266235002 | snp | C/G | | | intron-variant | Itsn1 | Mm_Celera | 16:91763301 | TTCAGAATCTGTAAT[C/G]GAGACAGTTGCCCGT | 16443 |
| rs386844261 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91898920 | GCACCTGTCCTGCTC[-/C]ACCCAAAGGTACCCT | 16443 |
| rs386885377 | in-del | -/TCCCGGACACGGGCAAGAGT | | | intron-variant | Itsn1 | Mm_Celera | 16:91895321 | CGGGCTGCCAGCAGT[-/TCCCGGACACGGGCAAGAGT]CCTTCCCTGTTTCAA | 16443 |
| rs386887756 | in-del | -/GA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91778563 | AACAAAGACAAAAAC[-/GA]GAGAGAGAGAGAGAG | 16443 |
| rs386914464 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91906700 | ACACACACACACACA[C/T]ACACACACACACAGA | 16443 |
| rs386931824 | in-del | -/AGAGAGAGAGAGAGAGAGAGAGAGAG | | | intron-variant | Itsn1 | Mm_Celera | 16:91876377 | GAGAGAGAGAGAGAG[-/AGAGAGAGAGAGAGAGAGAGAGAGAG]GACGGATATGACAGA | 16443 |
| rs386940433 | in-del | -/GT | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91919468 | TGTGTGTGTGTGTGT[-/GT]TGCTTTGTTGTGCAG | 16443 |
| rs386951532 | in-del | -/C | | | downstream-variant-500B | Itsn1 | Mm_Celera | 16:91920977 | AAAGTCCCCCCCCCC[-/C]ACTCCCCTACCCACC | 16443 |
| rs386965559 | in-del | -/TTC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91900016 | CTCTCCCTCCTCCTC[-/TTC]CTCTAACACACTTTA | 16443 |
| rs387019059 | in-del | -/C | | | intron-variant | Itsn1 | Mm_Celera | 16:91767408 | TGCACTCTGCCCCCC[-/C]ACATATGTGCTGAAG | 16443 |
| rs387069298 | in-del | -/TTCC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899317 | CACTCACTGCCTTCC[-/TTCC]CACAGCAAAGTGTAG | 16443 |
| rs387089928 | in-del | -/TTTTTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91904806 | TTTTTTTTTTTTTTT[-/TTTTTTT]GGTTTTTTGAAACAG | 16443 |
| rs387108008 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91869529 | CATCTATCTCATTTT[-/T]CCCCCGTTCTGAAGG | 16443 |
| rs387120542 | in-del | -/TCACCATGCGAGTG | | | intron-variant, upstream-variant-2KB | Itsn1 | Mm_Celera | 16:91801479 | GTCACCATGCGAGTG[-/TCACCATGCGAGTG]ACTGGCTGAGTTTGC | 16443 |
| rs387123027 | in-del | -/G | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91915372 | AGGACACATGGACGG[-/G]CCCCTCTGGCTTTCA | 16443 |
| rs387137627 | in-del | -/CA | | | intron-variant | Itsn1 | Mm_Celera | 16:91833132 | ACACACACACACACA[-/CA]GAGGCACGCACATGT | 16443 |
| rs387162929 | in-del | -/CTTTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91907087 | GAGGCTTTTTTTTTT[-/CTTTT]TCTTTTTCTTTTTCT | 16443 |
| rs387174294 | in-del | -/TGAC | | | intron-variant | Itsn1 | Mm_Celera | 16:91892700 | CTCACTTATGTGACT[-/TGAC]GTCCCCCAGGTTACC | 16443 |
| rs387240529 | in-del | -/GGAAGGAAGGA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878141 | AGGAGGGAGGGAGGA[-/GGAAGGAAGGA]AGGAAGGAAGGAAGG | 16443 |
| rs387316609 | in-del | -/GCTTGTT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899093 | CTCTCTGGCTGAGTT[-/GCTTGTT]CTGTGAAATAGGAGA | 16443 |
| rs387317658 | in-del | -/CA | | | intron-variant | Itsn1 | Mm_Celera | 16:91895769 | ACACATGTACACACA[-/CA]TAAACACCAAATACA | 16443 |
| rs387333503 | in-del | -/A | | | intron-variant | Itsn1 | Mm_Celera | 16:91899326 | GCCTTCCCACAGCAA[-/A]GTGTAGCCCTCACTG | 16443 |
| rs387344019 | in-del | -/AG | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91920368 | GCATAAACTTAACAG[-/AG]TCTCTAGTCTGAATA | 16443 |
| rs387363776 | in-del | -/AATAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91901822 | AATAAAATAAAATAA[-/AATAA]TAAAATGATGTGGCT | 16443 |
| rs387382028 | in-del | -/GA | | | intron-variant | Itsn1 | Mm_Celera | 16:91778589 | AGAGAGAGAGAGAGA[-/GA]ATACTGACTATAACT | 16443 |
| rs387401034 | in-del | -/AC | | | intron-variant | Itsn1 | Mm_Celera | 16:91835270 | CACACACACACACAC[-/AC]GTCTTCTGGCCCATA | 16443 |
| rs387417482 | in-del | -/CA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890965 | ACATACACACACACT[-/CA]CACACACACACACAC | 16443 |
| rs387440520 | in-del | -/GCGCGCGCGC | | | intron-variant | Itsn1 | Mm_Celera | 16:91906661 | CACGCACGCGCGCGC[-/GCGCGCGCGC]ACACACACACACACA | 16443 |
| rs387461869 | in-del | -/AC | | | intron-variant | Itsn1 | Mm_Celera | 16:91807700 | CACACACACACACAC[-/AC]GTGCGCGCCTTTGCA | 16443 |
| rs387519371 | in-del | -/GG | | | intron-variant | Itsn1 | Mm_Celera | 16:91876072 | AGATGGGGGGGGGGG[-/GG]CACCAGCCCCAGAAG | 16443 |
| rs387575084 | in-del | -/T | | | downstream-variant-500B | Itsn1 | Mm_Celera | 16:91920615 | TGTGGATTTTTTTTT[-/T]CTGCCTTGCAGGGGA | 16443 |
| rs387578563 | in-del | -/AA | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91886124 | TAAAGATCATCTAAT[-/AA]AAAAAAAAAAGTATA | 16443 |
| rs387622183 | in-del | -/GTT | | | intron-variant | Itsn1 | Mm_Celera | 16:91899156 | TTCTGCTGCCCTGTT[-/GTT]CTGCATGCTACCTAA | 16443 |
| rs387633461 | in-del | -/T | | | intron-variant | Itsn1 | Mm_Celera | 16:91783803 | ATGATTTTTTTTTTT[-/T]AATGCTCCTCTTAGA | 16443 |
| rs387643624 | in-del | -/GT | | | intron-variant | Itsn1 | Mm_Celera | 16:91910543 | TGTGTGTGTGTGTGT[-/GT]ATCTTAGTACCACCA | 16443 |
| rs387649660 | in-del | -/GT | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91747201 | TGTGTGTGTGTGTGT[-/GT]ATATGTGTGTGTCTG | 16443 |
| rs387673588 | in-del | -/GA | | | intron-variant | Itsn1 | Mm_Celera | 16:91894716 | AGCTCAAGGCCAGGA[-/GA]TCTAGAGGCAGAGAG | 16443 |
| rs387707729 | in-del | -/TT | | | intron-variant | Itsn1 | Mm_Celera | 16:91907000 | ATACTGTTTTTTTTT[-/TT]AAAGAACTTTTCAAA | 16443 |
| rs387715638 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795451 | CTTCCTTCCTTCCTT[C/T]CTTTCTTTCTTTCTT | 16443 |
| rs387739382 | in-del | -/A | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91917501 | TGTGTGGCTGTCCTA[-/A]TTTCAGGGTGAATTG | 16443 |
| rs387744376 | in-del | -/CTCTCTCTC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911534 | GTCTCTCTCTCTCTT[-/CTCTCTCTC]TATATATATATATAT | 16443 |
| rs387790718 | in-del | -/TT | | | intron-variant | Itsn1 | Mm_Celera | 16:91899864 | GCCAATTTTTTTTTT[-/TT]CAAATGTCCTGGTTT | 16443 |
| rs387798650 | in-del | -/TTC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91740529 | CATGAAGGAAGCTTC[-/TTC]AGGCCTTCCTCAAGC | 16443 |
| rs387849312 | in-del | -/GTGT | | | utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91913570 | TGTGTGTGTGTGTGT[-/GTGT]TTCAAGTGATTTCTC | 16443 |
| rs387876961 | in-del | -/TG | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91839407 | GTGTGTGTGTGTGTG[-/TG]GGGTTTTGGTAAGTC | 16443 |
| rs387896874 | in-del | -/TG | | | intron-variant, utr-variant-3-prime | Itsn1 | Mm_Celera | 16:91829834 | GTGTGTGTGTGTGTG[-/TG]ACGCTGCTGCGTGTG | 16443 |
| rs387902160 | in-del | -/AAAAAAAA | | | intron-variant | Itsn1 | Mm_Celera | 16:91903098 | AAAAAAAAAAAAAAA[-/AAAAAAAA]GTCTAAGGAAGGATG | 16443 |
| rs578304527 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91836554 | GCAGGTGCACGAGTG[C/T]TCTTTGTGTGTGTGT | 16443 |
| rs578306568 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91879998 | CTTGGACGGCCGCCC[A/T]CCTGGGCTGTGAGGA | 16443 |
| rs578316432 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91903060 | GGACAGCCAGGGCTA[C/T]ACAGAGAAACCTTGT | 16443 |
| rs578322389 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750359 | AAGAGAGCTTCATCC[C/T]TCTACCCTATGTGTG | 16443 |
| rs578325214 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91824546 | TGCTCTCCCTCCTCC[A/T]GCCTCCCTGCTCTCT | 16443 |
| rs578327252 | snp | A/C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91807611 | AGACACACACACACA[A/C/G]ACACACACAGACACA | 16443 |
| rs578327433 | snp | A/G | | | intron-variant, synonymous-codon | Itsn1 | GRCm38.p3 | 16:91852907 | CCGAGGCTGCCCACA[A/G]CCCCGGAGCCTGCTC | 16443 |
| rs578332048 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783489 | AGGGACAGTGGTTAG[C/T]TTTCACAGAGTGTTT | 16443 |
| rs578337881 | snp | C/T | | | downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91920911 | TCTTTTTTTCTTTCT[C/T]TTTTTTTTTTATTAC | 16443 |
| rs578345634 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91763065 | GCTCACAAGGCCTCA[A/T]TCCAGTTTTCCAGCT | 16443 |
| rs578348280 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743692 | TTTGTTTTTTGAGAC[A/G]GGGTTTCTCTGTATA | 16443 |
| rs578356545 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795475 | CTTTCTTTCTTTCTT[C/T]CTTTCTTTCTTTCTT | 16443 |
| rs578477372 | snp | A/C | | | downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91921054 | AAGTTTGCCTGTCCA[A/C]TGGGCCTCTCTTTCC | 16443 |
| rs578506734 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91816431 | TAACGGTTGACAAGG[A/G]TTAAGGGTATAATGT | 16443 |
| rs578520349 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91747000 | TCTGTGTGTGTGTGT[A/G]TGTCTGTGTGTGTGT | 16443 |
| rs578521515 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91739499 | TCCCTTCCCTTCCCT[C/T]CCTCATTGCTGGCCC | 16443 |
| rs578522316 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892627 | GCTGCCTTTCTCAAA[C/G]CCCAGATGGCCATTG | 16443 |
| rs578527472 | snp | A/C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91791899 | TGTGTCTGTGTGTGT[A/C/G]TGTGTGTGTGTCTGT | 16443 |
| rs578541082 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91754616 | TTCTTTCTGAATGTC[A/T]CTCTGTCTCTCTGTC | 16443 |
| rs578696436 | snp | A/G | | | downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91921008 | CATTCTTATTTTTTG[A/G]CCCTGGCGTTCCCCT | 16443 |
| rs578705274 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91841750 | ACTTTAAATGCAGTG[C/T]TTCTATTGCTCCGTA | 16443 |
| rs578711518 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904886 | GACCAGGTTAACCTC[A/C]AACTCAGAAATCTGC | 16443 |
| rs578720594 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91884669 | CACAGGCATTTGTTT[G/T]TTTGTTTGTTTTTTT | 16443 |
| rs578722037 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91752204 | CTGTCTGCAAGTGGC[C/T]GCAGACTGAGGCAAG | 16443 |
| rs578724904 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91747240 | TGTGTGTGTGTGTGT[A/C/G]TGTGTGTGTCTGTGT | 16443 |
| rs578732014 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91814513 | GTTGTACTTACTTCC[A/G]CTTTTCATTGATGAT | 16443 |
| rs578749158 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91739495 | CCCTTCCCTTCCCTT[C/T]CCTCCCTCATTGCTG | 16443 |
| rs578849614 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91887607 | GCCATGCCCTGTCTC[C/T]GAGCCTTGGGCAGAC | 16443 |
| rs578871433 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867923 | AGTCCTTTGTCTCTC[A/G]GCTCAGTGTGAGCAG | 16443 |
| rs578875347 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894772 | TGCTCCTTACTGGCT[A/G]GCCCTCGGGCTCAGA | 16443 |
| rs578885370 | snp | C/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919438 | AGCCGCTCCTCAAAG[C/G]TGTGTGTGTGTGTGT | 16443 |
| rs578889530 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799767 | AACGTATCGGAGCAC[A/G]TGGAAGAAGAAATGA | 16443 |
| rs578893928 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91769301 | CACCCTCTTCTGGTG[C/T]GTCTGAAGAGAGCGA | 16443 |
| rs578894439 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91755535 | TGGTTTTGCGAGACA[G/T]GGTTTCTCTGTGTAG | 16443 |
| rs578894909 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907084 | GCTGGAGGCTTTTTT[C/T]TTTTCTTTTTCTTTT | 16443 |
| rs578915750 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91845484 | AGACACACAACATTT[C/T]TTAAGTTTAAAAAAA | 16443 |
| rs578920368 | snp | A/C/G/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91747018 | TCTGTGTGTGTGTGT[A/C/G/T]TCTGTGTGTCTGTGT | 16443 |
| rs578927882 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742560 | GTGGTGGTGGCGCAC[A/G]CCTTTAATCCTAGCA | 16443 |
| rs578936031 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91792648 | AGGAGCCGAGGAACT[C/T]GGCGAGGTCCTCGAG | 16443 |
| rs578955859 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746865 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTC | 16443 |
| rs579063708 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91836140 | TGCATGCTGGGCAGC[C/T]GTGCCATCAAACCAC | 16443 |
| rs579069391 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91797309 | ACAAGATTGTAGGTT[C/T]AAGTCCAGCCTGGGC | 16443 |
| rs579080347 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91856994 | TCTTCACATTAGCCA[G/T]GGGAGGAGCTGGCAA | 16443 |
| rs579081575 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91824808 | TCCCTCCTCCTGCTT[C/T]CCTGCTCTCTCCCTC | 16443 |
| rs579103663 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745385 | GGGAGATCGATCATC[C/T]ATCTATCTATCTATC | 16443 |
| rs579111007 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878122 | AGGGAGGGGGAAGGA[A/G]GGAAGGAGGGAGGGA | 16443 |
| rs579137436 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91805690 | AGCTAGTGTTTTAAA[A/G]ATTTCCTGTGTGTGT | 16443 |
| rs579149898 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750066 | TAGACAAGAGAGCTT[C/T]ATCCCTCTACCCTAT | 16443 |
| rs579241067 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91912861 | GCCCATTCTGTGCTT[A/G]AAAGACTTGTGAGAA | 16443 |
| rs579257354 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795599 | CCAACTCAGAAATCT[A/G]CCTGCCTCTGCCTCC | 16443 |
| rs579266087 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91903279 | GGCTCACAAGCATCT[C/G]TAATGGGATCTGATG | 16443 |
| rs579269091 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91854106 | CAATTGGCTTGTAGA[A/G]GAATCCCTGAACTGT | 16443 |
| rs579279724 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890932 | CACACACACACACAC[A/T]CACACACTCTCACAC | 16443 |
| rs579287046 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91838027 | TTCTCTTTACACTGG[A/G]CACACTGTATGTATT | 16443 |
| rs579291591 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91881692 | TACAGAACAGACCAC[C/T]GCACATGCATTCTGC | 16443 |
| rs579302262 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91824592 | CCTTCTCTCCCTCCT[C/T]CTGCCTCCCTGCTCT | 16443 |
| rs579305424 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743732 | GTCCTGGAACTCACT[C/T]TGTAGACAAAGCTGG | 16443 |
| rs579333343 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91764602 | CTTTTCAACAGTCCT[C/T]CTCCTCCGACCCTGG | 16443 |
| rs579386145 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91788763 | TCCTCTCCCATCATG[C/T]CCACTCTCAGTGGGG | 16443 |
| rs579395491 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91883415 | CAGTTTAAAGAATTA[A/G]AAAGAAAGAAAGAAA | 16443 |
| rs579437854 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91765903 | GATCAATATGTGAAG[A/C]TTAGAGAACAGGAGC | 16443 |
| rs579453180 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91859685 | TGGATGGGTGGGTGG[A/G]TGGATACAGAGAAAT | 16443 |
| rs579453270 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810200 | GAAGCAGATGCACAC[A/T]AGCTCTGAGTGGAGA | 16443 |
| rs579454484 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91788827 | ACAGTGGATTGGCTT[C/G]ACCACTGAAACAAAG | 16443 |
| rs579454615 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904787 | CTCTCTCTTTTTTTT[G/T]GGTTTTTTTTTTTTT | 16443 |
| rs579462730 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892163 | TCTTCTCATGGCTGT[C/G]GCTGCGACAGCCGAC | 16443 |
| rs579463853 | snp | A/C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91915623 | CCTCCCCCTCCTCCC[A/C/T]CTCCTCCTCTTCCTC | 16443 |
| rs579466240 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91839070 | CAGGTTTGGGAGCCA[A/G]ACGTATGTGTGAGTG | 16443 |
| rs579469857 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91736802 | TCCAGTGAAAACTTA[C/T]TCTTTTTGTTTTGTT | 16443 |
| rs579484198 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91751471 | CATGCGTGTGTGTGT[A/G]TGTGTGTATGTGTGT | 16443 |
| rs579489647 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798416 | AGGAAGGAAGGAAGG[A/G]AGGAAGGAAGGAAGG | 16443 |
| rs579597425 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795372 | AGCATGTTTGGTTTG[C/T]TTTCTTTCTTTCTTT | 16443 |
| rs579610696 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91897518 | ACTCCAGAAGAGGGC[A/G]TCAGATTTCGTTACA | 16443 |
| rs579624152 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742651 | TTCTAGGACAGCCAG[A/G]GCTACACAGAGAAAC | 16443 |
| rs579646151 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873175 | GCTACACTTGGGGTT[A/G]ATTGGGAGAGGGGCC | 16443 |
| rs579646604 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758296 | TGCTGGGATTAAAGG[C/T]ATGCACCACCACGCC | 16443 |
| rs579658103 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91819131 | AGCTGTCTGTAGCTC[A/T]AATTCTAGGGCATCT | 16443 |
| rs579659984 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91774616 | TGGCTAAATACTCAT[A/G]AAGGCCAATTTACCA | 16443 |
| rs579661773 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91748181 | TTTTTTTTTTTTGGT[C/T]TTTCGAGACAGGGTT | 16443 |
| rs579694059 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91808728 | TGTGCACATTCCTGC[A/G]TCCTAACTGACCCAT | 16443 |
| rs579718210 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91847398 | CGAGGCACTCTACAC[A/G]CATAGCCCCGTTTTT | 16443 |
| rs579718626 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889036 | TTGTGTGTGTGTGTG[A/T]GTGTGTGTGTGTGTG | 16443 |
| rs579740308 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91906649 | ATTACTGGGTTGCAC[A/G]CACGCGCGCGCGCGC | 16443 |
| rs579783089 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91801294 | TTCATTCATTCATTC[A/G]TTCATTCATTTTGGT | 16443 |
| rs579784800 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907090 | GGCTTTTTTTTTTTC[C/T]TTTTCTTTTTCTTTT | 16443 |
| rs579788901 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91902083 | GTAGCCTTGGCCCTG[G/T]AGAGCCTCAAGCCAA | 16443 |
| rs579792915 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91749687 | AAGAGAGCTTTATCC[C/T]TCTACCCTATGTGTG | 16443 |
| rs579811602 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91833531 | CTTTCTGTTGTTACA[C/G]GCATCTTTATGGAGG | 16443 |
| rs579886927 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795385 | TGTTTTCTTTCTTTC[C/T]TTCTTTCTTTCTTTC | 16443 |
| rs579912558 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91888157 | GTAGGTTTACAGAGC[A/T]AGACCTGAGAGAGTC | 16443 |
| rs579938395 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91792662 | TTGGCGAGGTCCTCG[A/T]GGGTCACGGCAACAG | 16443 |
| rs579948079 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742621 | GTTCGAGGCCAGCCT[A/G]GTCTACAAAGTGAGT | 16443 |
| rs579959245 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758105 | GCCTCTCTCTGTTTT[C/G]TTTTCTTTCTTTCTT | 16443 |
| rs579959393 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890347 | GTGTTTTTTTTTTTT[G/T]TTGTTGTTGTTTTTT | 16443 |
| rs580007477 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910472 | CAAATATATGTGTGT[A/G]TGTTGTGTATGTGTA | 16443 |
| rs580035814 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91835030 | TTTTTAAATGTATAA[C/G]TAGGGGGGCTGAAAA | 16443 |
| rs580045030 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810622 | GGAAAGATGCGCTTC[G/T]TGCATTCCAGGCAAA | 16443 |
| rs580057071 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873927 | TGTCTGCAACTCAGT[C/G]CAGAGAATCTGACAC | 16443 |
| rs580077762 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91801282 | TCCTTCCTTCCATTC[A/T]TTCATTCATTCATTC | 16443 |
| rs580077907 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91777716 | GATTATTTTTTTCAG[A/C]TCCAATAGTAAAAGG | 16443 |
| rs580151655 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91903960 | GCCTCCACAGTGACA[C/T]ACTTCTGCTAACTAG | 16443 |
| rs580176115 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91838095 | AGGATGTGTGTGTGT[C/G]TGTGTGTCTGTGTGT | 16443 |
| rs580186573 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91734161 | ACGTGGGTGCTAGGA[A/G]TTGAACCCTGGGTCA | 16443 |
| rs580197803 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91788458 | AAGACTCATTGAGAC[A/C]AAATCCAAAGCTGTC | 16443 |
| rs580216840 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91807912 | GCTTTTTTTTAGATT[G/T]ATTTATTTATTATAT | 16443 |
| rs580223471 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91916419 | TGTCAAATCTCATTA[C/T]GGATGGTTGTGAGCC | 16443 |
| rs580224829 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91883120 | TGGCCATAGAAAATC[A/G]TTCACTACACTTTGT | 16443 |
| rs580242711 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750736 | TAGACAAGAGAGCTT[C/T]ATCCTTCTACCCTAT | 16443 |
| rs580243251 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91827438 | AAGGGGGGAGGACAG[A/G]AAAAGAGGGTAATTC | 16443 |
| rs580246511 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91866964 | TCTTCCAGAAAGGCG[A/C]GTGTGTGTGTTCGTG | 16443 |
| rs580248188 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892980 | CTCCATAGGACACCT[C/T]CATAGGCCATCTCCA | 16443 |
| rs580263558 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798969 | AAAAGAAAAAGGAAG[A/G]AAGGAAGGAAGGAAG | 16443 |
| rs580323841 | snp | C/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91915919 | CTCCTCCCCTGCACA[C/G]TCTCCTTTAAAGGGG | 16443 |
| rs580347615 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91865200 | GAATTGCTGACTGCG[A/G]CTCCCTGCTGCACAA | 16443 |
| rs580368754 | snp | A/G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890972 | CACACACTCACACAC[A/G/T]CACACACACACACAC | 16443 |
| rs580379845 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798596 | ACACACACACACGCA[C/T]ATACACACACACGCC | 16443 |
| rs580383853 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750502 | AAGAGAGCTTTATCC[C/T]TCTACCCTATGTGTG | 16443 |
| rs580392221 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91826781 | TGTGTGTCTGTGTGT[G/T]TGTAACTCTCTGTGT | 16443 |
| rs580396752 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892486 | TGCTTTTGGGCCAAC[A/G]ATGAACTGAGGGGCT | 16443 |
| rs580453964 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91766473 | TAGTGTATTAGAAGA[C/T]GCTAGCTTGTGGGCA | 16443 |
| rs580456801 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91807700 | CACACACACACACAC[A/G]CGTGCGCGCCTTTGC | 16443 |
| rs580474306 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894713 | CAGGAGCTCAAGGCC[A/G]GGATCTAGAGGCAGA | 16443 |
| rs580489894 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91784768 | TATGCATTCTTGCCC[A/G]TTCTGTGTCAGTACA | 16443 |
| rs580521105 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91828483 | CTGTGTTAGGGCCCT[A/G]CCCCTGCCCCTGCCC | 16443 |
| rs580576363 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799057 | AAGAAAGAAAGAAAG[A/G]AAGAAAGAAAGAAAG | 16443 |
| rs580578680 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867020 | GTGTGTGTGTGTGTG[C/T]GTGTGCGTGTGTGAA | 16443 |
| rs580592985 | snp | C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746986 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT | 16443 |
| rs580627878 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91753749 | TATTCAAAAAATTTT[A/G]TTTTTTAAAATTCGT | 16443 |
| rs580642178 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91791876 | TGAGTGAATGCCTCC[A/C]GTGTGTGTGTGTCTG | 16443 |
| rs580687576 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91801260 | CTTCCTTCCTTCCTT[C/T]CTTCCTTCCTTCCTT | 16443 |
| rs580697439 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91902348 | GAAAGGTTAATAGGG[C/T]CAAGAAGGATGTGGA | 16443 |
| rs580703419 | snp | C/T | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91853601 | CTGTGTGTGTGTGTG[C/T]GTGCGCGTGCATGCG | 16443 |
| rs580712521 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743707 | AGGGTTTCTCTGTAT[A/G]GCCCTGGCTGTCCTG | 16443 |
| rs580720759 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795479 | CTTTCTTTCTTTCTT[C/T]CTTTCTTTCTTCCTT | 16443 |
| rs580756229 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91824551 | TCCCTCCTCCTGCCT[C/T]CCTGCTCTCTCCCTC | 16443 |
| rs580758069 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91876405 | GAGAGAGAGAGAGGA[A/C]GGATATGACAGACTG | 16443 |
| rs580791116 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91763163 | CAGGGCAAGGACTCC[C/T]CTTTATACAGGGTGG | 16443 |
| rs580791847 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890697 | AAAGGCGTGTCCAGC[A/G]CCCAGCCTCTGGCTT | 16443 |
| rs580793870 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911277 | TCTTAAAAAAACTAC[C/T]ACCGCCAACAACAAC | 16443 |
| rs580849347 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91790266 | GAGGGATGGAAGTTC[A/C]TGGAGAAGAAATCCC | 16443 |
| rs580873999 | snp | C/G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91879145 | TTTTGGTTTTGTTTG[C/G/T]TTGGTTTTTGTTTTG | 16443 |
| rs580905168 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91780890 | AGCTTATAGAAGAAA[A/C]CCTTTATTTATTTAC | 16443 |
| rs580906333 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904880 | TCTGTAGACCAGGTT[A/G]ACCTCAAACTCAGAA | 16443 |
| rs580908964 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91749863 | TGAACTGGGAAACTG[G/T]ACAAGAGAGCTTCAT | 16443 |
| rs580988440 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910538 | TGTGTGTGTGTGTGT[C/G]TGTGTATCTTAGTAC | 16443 |
| rs581009127 | snp | A/C | | | synonymous-codon | Itsn1 | GRCm38.p3 | 16:91850920 | GAGATCAGCCTTTAC[A/C]CCAGCCACAGCCACT | 16443 |
| rs581011071 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91824427 | TGCTCTCCCTCCTCC[A/T]GCCTCCCTGCTCTCC | 16443 |
| rs581031057 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743050 | CTTAAAAAAATGCCC[C/T]TTTGTCTTTTTTCCT | 16443 |
| rs581033027 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795467 | CTTTCTTTCTTTCTT[C/T]CTTTCTTTCTTTCTT | 16443 |
| rs581097061 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91782129 | TGAATTTTCTTAAAC[A/G]CATAAACTCACGTTT | 16443 |
| rs581110687 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758917 | TTGTTTGTTTCTTTG[G/T]TTTTGGTTTTTTCGA | 16443 |
| rs581116911 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91823158 | TTCCATGTAGACAGA[C/T]GCTTGGCACCATTGT | 16443 |
| rs581122180 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91905683 | ATAAGGCAAGGGGAG[A/G]AGCTGGGTTAAAGGG | 16443 |
| rs581168837 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91848261 | TCTGAATATGCTGTG[C/T]GTTCATCTCCTCATC | 16443 |
| rs581194112 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91749868 | TGGGAAACTGGACAA[A/G]AGAGCTTCATCCCTC | 16443 |
| rs581194226 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795455 | CTTCCTTCCTTCCTT[C/T]CTTTCTTTCTTTCTT | 16443 |
| rs581195564 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904098 | TTATTCAAACCACCA[C/T]GGACATGAGTTGAGT | 16443 |
| rs581199262 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894196 | ACAGATACGTTGTCC[A/G]TGTATTTGTGGTCTT | 16443 |
| rs581199495 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91814706 | AAGCAGCCTGTGCTG[C/T]TGACCTTCTGAGTAA | 16443 |
| rs581201508 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919102 | TTCCCTATTCAAGGG[C/T]TGGTCTCCCGGTTTC | 16443 |
| rs581201538 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91841768 | CTATTGCTCCGTAGC[C/G]TGCTTTTAACCTTAA | 16443 |
| rs581205519 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91884673 | GGCATTTGTTTGTTT[G/T]TTTGTTTTTTTGAGA | 16443 |
| rs581263518 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91840246 | TCTTGGGGGGAATCA[C/T]GTAACTTGTTCTCTA | 16443 |
| rs581265061 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742693 | CCTCCTCCCCCCCAA[A/C]AAAAAAGATTGTTCT | 16443 |
| rs581273128 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91835937 | AGCCTTCCTTAACCT[A/T]GCGTACATACCCAGG | 16443 |
| rs581281682 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91790278 | TTCATGGAGAAGAAA[C/T]CCCTGAGTAGTGGCA | 16443 |
| rs581353650 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91884235 | TGTGTGTGTGTGTGT[A/G]TACAAATACCACCTT | 16443 |
| rs581366567 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91752019 | GGCCACCCCAGTTCC[A/G]GGACGCTGGTCTGCC | 16443 |
| rs581368677 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91813229 | ATATTCAAACCACTA[C/T]AATGGTTTTCTTTTA | 16443 |
| rs581408433 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894882 | AGTGATGTAAAACAT[C/T]GTCCCACAGACCAAT | 16443 |
| rs581433765 | snp | C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746930 | TGTCTGTGTCTGTGT[C/G]TGTGTGTGTGTCTGT | 16443 |
| rs581443291 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91737949 | ACATCTGTACTGTTG[A/G]TCAAATAAAATAGCA | 16443 |
| rs581447212 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768254 | TTTCTTTGCTGTGCT[G/T]TTTTAAAAAAACTTT | 16443 |
| rs581447948 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919422 | AGGCCAGAAGTTAGG[A/G]AGCCGCTCCTCAAAG | 16443 |
| rs581465104 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867027 | TGTGTGTGCGTGTGC[A/G]TGTGTGAAAGTGTGC | 16443 |
| rs581496617 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91751499 | TGTGTGTATGTATGT[A/G]TGTATGTATGTATGG | 16443 |
| rs581532073 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894295 | GTATATGAGTACACT[A/G]TAGCTGTCTTCAGAC | 16443 |
| rs581558900 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91828944 | CTTTTCAGAAGTAAA[C/T]GGCTGACTGACTGAC | 16443 |
| rs581563812 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91790084 | ATGCCAGAGACTGAG[G/T]GACATTTATCATATA | 16443 |
| rs581597450 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91737224 | TACTCGCGGGGTGTT[A/G]TTAGGATGCCAACTG | 16443 |
| rs581664078 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799183 | CTGAGGGGAGGAGGA[A/G]ACGGGAGAGAGGGGG | 16443 |
| rs581664406 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91883464 | AAGAAAGAAAGAAAG[A/G]AAGAATGAATGAATC | 16443 |
| rs581666335 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904839 | ACAGGGTTTCTCTGT[A/T]TAGCCCTGGCTGTCC | 16443 |
| rs581683861 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768959 | GTCTTTCTTAAAGAA[A/G]AGCGTGCGGCCCCTG | 16443 |
| rs581683996 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91839888 | GCCACTGTCTCCTCT[C/G]TATGTATGTAAAACA | 16443 |
| rs581687734 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91747002 | TGTGTGTGTGTGTGT[A/G]TCTGTGTGTGTGTGT | 16443 |
| rs581687787 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810902 | GAGCAGCTCCCCTGC[C/T]CCAGGCCCTCAGCAG | 16443 |
| rs581756293 | snp | C/G | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91747260 | TGTGTCTGTGTGTGT[C/G]TGTGTGTGTGTGTGT | 16443 |
| rs581781961 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91859754 | CTGTTACCCAGAAAA[C/T]CAAAAGCTCTTTCTT | 16443 |
| rs581812595 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91903072 | CTACACAGAGAAACC[C/T]TGTCTCAAAAAAAAA | 16443 |
| rs581838087 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878108 | GGAGGGAGGAAGGGA[A/G]GGAGGGGGAAGGAGG | 16443 |
| rs581838545 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91739496 | CCTTCCCTTCCCTTC[A/C]CTCCCTCATTGCTGG | 16443 |
| rs581850373 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91902487 | TTCGTGAATCAGCAG[A/C]AGATTTCCAGAAGAA | 16443 |
| rs581908027 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892442 | GGAGGAAGCCGGTAA[A/T]AGACCTTGTATAATC | 16443 |
| rs581924589 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91826232 | TTTGTTTGGAGTCTC[A/G]CTCTAGCTCTGGTTG | 16443 |
| rs581989612 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91880021 | TGTGAGGAAGGAAAC[G/T]TGTGCTTCTCAAGCC | 16443 |
| rs582002346 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750368 | TCATCCTTCTACCCT[A/G]TGTGTGAACTGGGAA | 16443 |
| rs582008189 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91807648 | CATACACACACACAC[A/T]GACACACACACATAC | 16443 |
| rs582010372 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783807 | TTTTTTTTTTTTAAT[A/G]CTCCTCTTAGATTTT | 16443 |
| rs582012593 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91915642 | CTCCTCTTCCTCCTC[C/T]CCCTCCCCCTCCTCC | 16443 |
| rs582026030 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750340 | GTGAACTGGGAAACT[A/G]GACAAGAGAGCTTCA | 16443 |
| rs582026491 | snp | A/G | | | upstream-variant-2KB, intron-variant | Itsn1, Cryzl1 | GRCm38.p3 | 16:91728133 | AGGCCCCATTACTGC[A/G]AACACCCACCCTTGT | 16443 |
| rs582034581 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91805745 | TGAATGCAGATGCTC[C/T]CAGAACACCAGGAGA | 16443 |
| rs582121835 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91836520 | TTTATCAGTGGCTGT[A/G]TAAGTGCTGTGTGAG | 16443 |
| rs582139006 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783276 | CAGTAAAAGTCCCTT[C/T]ACCTTTTCAGCAAGC | 16443 |
| rs582156962 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745425 | ATCTATCTATCTATC[C/T]ATCTATCTATCTAAC | 16443 |
| rs582160278 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91839563 | AGGGGTGATGGGGGG[A/G]CGACTGTTGGGTCAG | 16443 |
| rs582178936 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91897431 | AGATTGGGGAAAGTA[C/T]GATAACTAAGCCTTT | 16443 |
| rs582189147 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91771489 | CCCATTCCAGGCTCT[A/G]TTGTTTGCCTGATAC | 16443 |
| rs582198618 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892017 | AGCCCGAGGACGTCC[A/G]GTGGAGCCACTGTGA | 16443 |
| rs582204926 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91914690 | AAGCCCCTGACTGGG[C/T]TTCCTTCATGGGCCA | 16443 |
| rs582213254 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798319 | GTACAGACCCAAACA[C/T]AGAGGGAGGGAGGGA | 16443 |
| rs582230798 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91824833 | TCCCTCCTCCTGCCT[C/T]CCTGCTCTCTCCCTC | 16443 |
| rs582241473 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91765740 | TCCAGGACAGCCAGG[A/G]CTACACAGAGAAACC | 16443 |
| rs582267940 | snp | A/C | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830697 | CTGAGACAATAAAGA[A/C]TGAGGATTTTATAGT | 16443 |
| rs582313389 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872386 | GAGGGTTGGGGGGTG[C/T]TATGGGACAGGGGTG | 16443 |
| rs582341477 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91801244 | GTTTCAGTAATATTT[C/T]CTTCCTTCCTTCCTT | 16443 |
| rs582344714 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873265 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTATGT | 16443 |
| rs582352819 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907085 | CTGGAGGCTTTTTTT[C/T]TTTCTTTTTCTTTTT | 16443 |
| rs582370849 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91792658 | GAACTTGGCGAGGTC[C/T]TCGAGGGTCACGGCA | 16443 |
| rs582375542 | snp | A/C | | | downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91921047 | GCATATAAAGTTTGC[A/C]TGTCCAATGGGCCTC | 16443 |
| rs582387696 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907450 | AAAGCACCTCCTGGC[A/G]TGCGCTCCCCACCCC | 16443 |
| rs582411627 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91747020 | TGTGTGTGTGTGTAT[A/C/G]TGTGTGTCTGTGTGT | 16443 |
| rs582425226 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743746 | TCTGTAGACAAAGCT[A/G]GCCTCAAACTCAGAA | 16443 |
| rs582497103 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91887621 | CTGAGCCTTGGGCAG[A/T]CTCTGGTGTATGGGG | 16443 |
| rs582514453 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91817052 | TTAGTTTCTGATGCT[C/T]GGCCAGAAGGCGGGC | 16443 |
| rs582532565 | snp | A/G | | | downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91921080 | TTTCCAGTGATGGCC[A/G]ACTAGGCCATCTTTT | 16443 |
| rs582560548 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873277 | TGTATGTGTGTGTGT[A/G]TGTGTGTGTAAAAAT | 16443 |
| rs582574787 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91816432 | AACGGTTGACAAGGG[C/T]TAAGGGTATAATGTG | 16443 |
| rs582589949 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91895376 | CAGGCCAGGGGCTTG[C/T]GGTCCCTCCTCCTTC | 16443 |
| rs582597869 | snp | C/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919440 | CCGCTCCTCAAAGGT[C/G]TGTGTGTGTGTGTGT | 16443 |
| rs582598552 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91754659 | TCCCTCCCTCTCACA[C/T]TGTGTCAATGCTACC | 16443 |
| rs582604267 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742578 | TTTAATCCTAGCACT[C/T]GGGAGGCAGAGGCAG | 16443 |
| rs582606179 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799773 | TCGGAGCACATGGAA[A/G]AAGAAATGATGTAGT | 16443 |
| rs582612105 | snp | A/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91829834 | GTGTGTGTGTGTGTG[A/T]GACGCTGCTGCGTGT | 16443 |
| rs582613023 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91765703 | TTCTGAGTTCGAGGC[C/T]AGCCTGGTCTACAAA | 16443 |
| rs582616491 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91755588 | TCTGTACTCTGTAGA[A/C]CAGACTGGCCTCGAA | 16443 |
| rs582712357 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91897533 | ATCAGATTTCGTTAC[A/G]GATGGTTGTGAGCCA | 16443 |
| rs582736076 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91741456 | TTCCAGGTGGACACA[C/T]TGAGGCTTGGGGAAC | 16443 |
| rs582739995 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91792059 | CAGGCCAGAAGCAGT[A/G]TCAGAGCCCCCCAAG | 16443 |
| rs582760239 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91824803 | CTCTCTCCCTCCTCC[A/T]GCTTCCCTGCTCTCT | 16443 |
| rs582763886 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91731444 | TCTCTTTCTTTCTTT[C/T]TTTTTAATTTTTAAA | 16443 |
| rs582765968 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91786062 | GAGACAGGTTTCTCT[A/G]TGTAGCCCTGGCTGT | 16443 |
| rs582770879 | snp | A/C | | | intron-variant, splice-donor-variant | Itsn1 | GRCm38.p3 | 16:91832355 | GAGAAAGGGGCAAAG[A/C]CAGTCTCCTGAAAGT | 16443 |
| rs582790382 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91748251 | GACCAGGCTGGCCTC[A/G]AACTCAGAAATCTGC | 16443 |
| rs582792657 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91801256 | TTTCCTTCCTTCCTT[C/T]CTTCCTTCCTTCCTT | 16443 |
| rs582796057 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91886197 | ATTTATTTATTTATT[A/G]TATGTAAGTACACTG | 16443 |
| rs582898656 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91807703 | ACACACACACACACG[C/T]GCGCGCCTTTGCAGG | 16443 |
| rs582902769 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91913276 | CTGTTTTGGTCCCTC[A/G]TTTGCATCTCCAGTC | 16443 |
| rs582909378 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750546 | TAGACAAGAGAGCTT[C/T]ATCCTTCTACCCTAT | 16443 |
| rs582927375 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91855429 | ACGCATAGTTATCAT[C/T]ACCACAAAAAAAGAT | 16443 |
| rs582947032 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91903409 | TAAAGAAATTCTTGT[C/T]ACTTGATTTTTGTGG | 16443 |
| rs582948581 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798441 | GGAAGGAAGGAAGGA[A/G]GGCGGATCCCCAGGG | 16443 |
| rs582970043 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91838050 | TATGTATTGACTGCA[A/G]CAACTCGCCTTTTTT | 16443 |
| rs582981976 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91881810 | GGCAAGAGAGACTAA[C/T]GTCCTGGAGAACCCC | 16443 |
| rs582996359 | snp | C/T | | | downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91920913 | TTTTTTTCTTTCTTT[C/T]TTTTTTTTATTACAT | 16443 |
| rs583000759 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91796550 | AAGTGTTGGCATGGT[C/T]ACGGTGTCTGTTCAC | 16443 |
| rs583094958 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91883185 | CTGATACCCAAGGGA[A/G]CGGCCACAACCTTTA | 16443 |
| rs583105642 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91765967 | TGCCGCTGTCACCTG[C/T]CCTTGCTGTCATCCT | 16443 |
| rs583109611 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91808133 | ATATTCCGAAGATAT[A/G]GCCTATACACTTGAA | 16443 |
| rs583125506 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768522 | TCAGGGATATAGCCC[C/T]GCTCCAGTTGTTGCA | 16443 |
| rs583135290 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91883456 | AAGAAAGAAAGAAAG[A/G]AAGAAAGAAAGAATG | 16443 |
| rs583142982 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904814 | TTTTTTTTTTTTTTG[G/T]TTTTTTGAAACAGGG | 16443 |
| rs583152974 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810616 | GGAGAAGGAAAGATG[C/T]GCTTCTTGCATTCCA | 16443 |
| rs583158316 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91789747 | AATCAAACAAGAGAA[C/G]CACACCATTGGTGTT | 16443 |
| rs583164779 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91839304 | GAAAGATATCACAAT[C/T]TCTCTCTCTCTTTCT | 16443 |
| rs583166873 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91737201 | GATTAGAGAGACTGG[G/T]AAGAAGATACTCGCG | 16443 |
| rs583171737 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904881 | CTGTAGACCAGGTTA[A/G]CCTCAAACTCAGAAA | 16443 |
| rs583178598 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91751479 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTATGT | 16443 |
| rs583270608 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91903966 | ACAGTGACATACTTC[C/T]GCTAACTAGGGTCTT | 16443 |
| rs583289854 | snp | C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746942 | TGTCTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT | 16443 |
| rs583295196 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91838103 | TGTGTGTCTGTGTGT[C/G]TGTGTGTGTGTGTGT | 16443 |
| rs583298702 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91833901 | GGAAGAAAATTAAAA[G/T]CAAGCTGACTTTTTT | 16443 |
| rs583313719 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91780252 | GGGAGCAGGTTTGAG[C/G]ATGCTGACATTTGGA | 16443 |
| rs583329088 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91917064 | GGGGGCTGGGAGGCA[A/G]AGAAGGGACCTCCTT | 16443 |
| rs583347838 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91828059 | CCTGAGTAGTGCTCC[C/T]CTCCTCCCTCCCTCC | 16443 |
| rs583362490 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91866972 | AAAGGCGCGTGTGTG[C/T]GTTCGTGTGTGTGTG | 16443 |
| rs583366264 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91893046 | AGTATACCCACACAC[C/T]TGCCCACTGATTCCC | 16443 |
| rs583370840 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91735523 | TCGTAAACTCTATGA[A/G]TATGCTTTGGAAACT | 16443 |
| rs583382865 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91751461 | TTGCGGGCGCCATGC[C/G]TGTGTGTGTGTGTGT | 16443 |
| rs583383235 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798973 | GAAAAAGGAAGGAAG[A/G]AAGGAAGGAAGGAAG | 16443 |
| rs583443806 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910495 | TATGTGTATGCCGTG[C/T]GTGTGTGTGTGTGTG | 16443 |
| rs583467114 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91849476 | TAAGCAATTGATGGG[C/T]GAAGCCACTGTAGTG | 16443 |
| rs583477124 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91801323 | GTGCACTGTTGAGTG[C/T]TGAAGCAGATCCGAG | 16443 |
| rs583486913 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91876060 | GTTTGCTGAATCAGA[G/T]GGGGGGGGGGGGGCA | 16443 |
| rs583497351 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91748733 | ACAGTCCTGCTCTGG[C/T]TTCCCATAGGGATGA | 16443 |
| rs583504541 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91749736 | AAGAGAGCTTTATCC[C/T]TCTACCCTATGTGTG | 16443 |
| rs583536178 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91888336 | AGGGTTTCCCCAATT[A/G]TGTTGTCTCAAGACG | 16443 |
| rs583547791 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91846094 | GTAAACCAGCTCAAC[A/T]GAATCTAGGGTCTGG | 16443 |
| rs583555263 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91792663 | TGGCGAGGTCCTCGA[A/G]GGTCACGGCAACAGG | 16443 |
| rs583563112 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91846934 | TACAGGAGATGACCC[A/T]GGCAAGATTAACCAG | 16443 |
| rs583563252 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91817988 | AAAAAACAAGTCACT[C/T]CGGAGACCCTTGTGT | 16443 |
| rs583575509 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758129 | CTTTCTTTCTTTCTT[C/T]CTTTTTTTTTTTTTT | 16443 |
| rs583583251 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742639 | CTACAAAGTGAGTTC[C/T]AGGACAGCCAGAGCT | 16443 |
| rs583659686 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890348 | TGTTTTTTTTTTTTT[C/T]TGTTGTTGTTTTTTT | 16443 |
| rs583681421 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758317 | CCACCACGCCCAGCT[A/G]TTTTCTTTAAAAATT | 16443 |
| rs583681627 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91823321 | ACACACACACTTATG[C/T]TGAAATTTCATTGCA | 16443 |
| rs583683447 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91822089 | GTGGGTACAGGGGAG[C/T]ACTGGAGCATCTCTG | 16443 |
| rs583702968 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91778592 | GAGAGAGAGAGAGAA[A/T]ACTGACTATAACTTA | 16443 |
| rs583721480 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894717 | AGCTCAAGGCCAGGA[G/T]CTAGAGGCAGAGAGA | 16443 |
| rs583743032 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91846539 | GACCATGTCTGGGCC[A/G]TTGCTGAGGGCAGTA | 16443 |
| rs583745197 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899950 | TCCTCCTCTTCCTCT[C/T]TCTCCCTCCTTCTCT | 16443 |
| rs583765237 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91832485 | CTAGAGTAGTCGGCA[G/T]GCTGTATTAGGTGGC | 16443 |
| rs583766904 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91760048 | GACTCTTTCACACGT[A/G]TACTAATTTGAAGGG | 16443 |
| rs583769191 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91801284 | CTTCCTTCCATTCAT[C/T]CATTCATTCATTCAT | 16443 |
| rs583773815 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873931 | TGCAACTCAGTCCAG[A/G]GAATCTGACACCTTC | 16443 |
| rs583781881 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795459 | CTTCCTTCCTTTCTT[C/T]CTTTCTTTCTTTCTT | 16443 |
| rs583796129 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742707 | AAAAAAAAGATTGTT[C/T]TCATTTAAAAAGTTA | 16443 |
| rs583829519 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91839944 | TCTATGCCTATCACG[A/G]TTTGCTCGGTTTGGG | 16443 |
| rs583834623 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91902361 | GGCCAAGAAGGATGT[A/G]GACCTGTTTAGAAAT | 16443 |
| rs583845717 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91790252 | CTGAATTGCTTTGGG[A/C]GGGATGGAAGTTCAT | 16443 |
| rs583859680 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892489 | TTTTGGGCCAACAAT[A/G]AACTGAGGGGCTTAA | 16443 |
| rs583869407 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795382 | GTTTGTTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 16443 |
| rs583897994 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742656 | GGACAGCCAGAGCTA[C/T]ACAGAGAAACCCTGT | 16443 |
| rs583904283 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878028 | GGAGGGAGGGAGGGA[A/G]AGAAAGAGAGAGAGG | 16443 |
| rs583925068 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889669 | GGCCATGTATGCCTC[A/G]TACCTGTTTAGTCTG | 16443 |
| rs583933330 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91909032 | ATAATCATATATATA[A/C]TATATATATACACGG | 16443 |
| rs584017356 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919243 | GAGAGAGAGTGGGCG[A/G]AGCCAGATGCCTCTC | 16443 |
| rs584029038 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91915942 | TAAAGGGGGGTCAGC[A/G]CCTGACCTTTTCCCA | 16443 |
| rs584029830 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799061 | AAGAAAGAAAGAAAG[A/G]AAGAAAGAAAGAAAC | 16443 |
| rs584041628 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867021 | TGTGTGTGTGTGTGC[A/G]TGTGCGTGTGTGAAA | 16443 |
| rs584042863 | snp | C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746994 | TGTGTGTCTGTGTGT[C/G]TGTGTGTGTCTGTGT | 16443 |
| rs584049332 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91866319 | GCATTGTCCTGTATG[A/G]AGAGTCTCAGCATGG | 16443 |
| rs584060891 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91811715 | GGGCAGTCTGTTTGA[C/T]GCTCTAGTCTTTGGT | 16443 |
| rs584081151 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91896755 | GAGAGAGAGAGAGAG[A/G]GAGAGGCCTGGTCCC | 16443 |
| rs584122356 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91883470 | GAAAGAAAGAAAGAA[A/T]GAATGAATCTAAAGC | 16443 |
| rs584128463 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904856 | AGCCCTGGCTGTCCT[A/G]GAACTCACTCTGTAG | 16443 |
| rs584152481 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91826993 | TGATGGGGCTTGAAA[C/G]CACTGAGTAGGCTTT | 16443 |
| rs584162083 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91801264 | CTTCCTTCCTTCCTT[C/T]CTTCCTTCCTTCCAT | 16443 |
| rs584164835 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91766504 | GGGCCTGCTCTCCCA[C/G]CCCTGGGAGGCTGTG | 16443 |
| rs584172835 | snp | C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746874 | TGTGTGCGTGTGTGT[C/G]TGTGTCTGTGTGTGT | 16443 |
| rs584183322 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798608 | GCACATACACACACA[C/T]GCCCGCACAGGTTCA | 16443 |
| rs584202900 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91770023 | CAGTGTGCTCTTACC[A/T]GCTGAGCCATCTCGC | 16443 |
| rs584207152 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91884570 | CCTGGAAGGCCGGCA[C/T]CTGCCTTCATCCTGC | 16443 |
| rs584210574 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894206 | TGTCCATGTATTTGT[A/G]GTCTTTCTTTCTTTC | 16443 |
| rs584225760 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91813593 | CCTGACTTTATTCAG[A/G]GATCTCTTTCCTTTC | 16443 |
| rs584230613 | snp | C/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91828505 | CCCCTGCCCACCTTT[C/T]ACACCTTTCTTTTTT | 16443 |
| rs584235317 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91739498 | TTCCCTTCCCTTCCC[A/T]CCCTCATTGCTGGCC | 16443 |
| rs584257513 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768941 | GGCTCTCATATCTTT[C/T]CTGTCTTTCTTAAAG | 16443 |
| rs584290423 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783655 | CACAATTGAGACATA[C/T]AGGTGACTCACTTTA | 16443 |
| rs584299602 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91905702 | TGGGTTAAAGGGAGG[A/G]GCTAAGATAGGGCAA | 16443 |
| rs584318334 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91844738 | CCACAGTCTTACCTC[A/C]GAGCTCAGCATGTTT | 16443 |
| rs584331620 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91753905 | ACAACAAAACCCCCT[C/T]ACTTGTTTAAATACA | 16443 |
| rs584347970 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91791889 | CCCGTGTGTGTGTGT[C/G]TGTGTGTGTATGTGT | 16443 |
| rs584379609 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91836548 | GAGCATGCAGGTGCA[C/T]GAGTGTTCTTTGTGT | 16443 |
| rs584397227 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783283 | AGTCCCTTCACCTTT[G/T]CAGCAAGCGCTGCTG | 16443 |
| rs584410619 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91840830 | TCAAGGCTACAGAGA[C/T]AACAGTCTACCTCAC | 16443 |
| rs584418321 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743409 | GTGTGTATGCCAAAG[A/T]GAAGCCATTCCAGGA | 16443 |
| rs584439442 | snp | C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91747094 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT | 16443 |
| rs584484975 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91869571 | GCAGGAGTAGCTCTG[C/T]GCATGCCCCCCCGGG | 16443 |
| rs584497184 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91896288 | ATTTTGCGGATTTCT[A/G]AACCACATTTTAAAA | 16443 |
| rs584501108 | snp | A/G | | | downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91920927 | TTTTTTTTTTATTAC[A/G]TATTTTCCTCAATTA | 16443 |
| rs584511706 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830508 | ACAGAGCTGTTGGCC[A/G]GCCTTAGCTGCTAAC | 16443 |
| rs584539685 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91752023 | ACCCCAGTTCCGGGA[C/T]GCTGGTCTGCCACAA | 16443 |
| rs584557827 | snp | A/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91913329 | CATGTCTCAGGCTCC[A/T]GGGCTCAGGCTTTCC | 16443 |
| rs584564683 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91738229 | AGATTTTCTTTGTTT[C/T]GCTTTGTGAAAAAAA | 16443 |
| rs584581926 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91856421 | GGCTTTCCCACAGCC[C/G]TGTGCAGGGCGGGCG | 16443 |
| rs584597596 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91805330 | TCATGTCATGTGTGC[A/T]CTCTCTCTCTCTCTC | 16443 |
| rs584602666 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91879994 | TGATCTTGGACGGCC[A/G]CCCTCCTGGGCTGTG | 16443 |
| rs584610597 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750055 | CTGGGAAACTGTAGA[C/T]AAGAGAGCTTTATCC | 16443 |
| rs584627015 | snp | C/G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91807597 | ACATACACACACACA[C/G/T]ACACACACACACAGA | 16443 |
| rs584657087 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91737389 | GAGAAGGTGGGAGAG[A/G]GGGCTGCGGAGGTTT | 16443 |
| rs584703013 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910682 | GTGCCACCACACTTG[A/C]CTTTTTTCCCCATTT | 16443 |
| rs584727755 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91824432 | TCCCTCCTCCTGCCT[C/T]CCTGCTCTCCCTCCT | 16443 |
| rs584729680 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750346 | TGGGAAACTGGACAA[A/G]AGAGCTTCATCCTTC | 16443 |
| rs584741049 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890771 | CACGTTACTGGGCAG[C/T]TGTAGAGTGGGGGGG | 16443 |
| rs584742150 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91761609 | TTGAGGGAAGAAAGA[A/C]TTATTTCACCGAGTT | 16443 |
| rs584750210 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795471 | CTTTCTTTCTTTCTT[C/T]CTTTCTTTCTTTCTT | 16443 |
| rs584751427 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91805708 | TTCCTGTGTGTGTGT[C/G]TGTGTCTGTGTCTGT | 16443 |
| rs584757285 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91824580 | TCCTCCTGCCTCCCT[G/T]CTCTCCCTCCTCCTG | 16443 |
| rs584786381 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91764206 | TAGACGTCACCCAGG[A/G]TGGAGGAGGCGGGGA | 16443 |
| rs584787165 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890988 | CACACACACACACAC[A/T]CACACACGTTCCTGC | 16443 |
| rs584836185 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91783272 | GGGGCAGTAAAAGTC[C/T]CTTCACCTTTTCAGC | 16443 |
| rs584900695 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878118 | AGGGAGGGAGGGGGA[A/G]GGAGGGAAGGAGGGA | 16443 |
| rs584934953 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894770 | AATGCTCCTTACTGG[C/T]TGGCCCTCGGGCTCA | 16443 |
| rs584992507 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91737371 | ACAAGAGCTTTGAGA[C/T]GGGAGAAGGTGGGAG | 16443 |
| rs585014167 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795598 | TCCAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 16443 |
| rs585018127 | snp | A/G | | | intron-variant, downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91853612 | TGTGTGTGCGCGTGC[A/G]TGCGCGCGTGCTCGG | 16443 |
| rs585030197 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91743709 | GGTTTCTCTGTATAG[C/T]CCTGGCTGTCCTGGA | 16443 |
| rs585081551 | snp | A/T | | | downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91921048 | CATATAAAGTTTGCC[A/T]GTCCAATGGGCCTCT | 16443 |
| rs585105025 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91872510 | GAGGGAGGGGGAGGG[A/G]AGGGATGGGCTGTTT | 16443 |
| rs585105686 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91780891 | GCTTATAGAAGAAAA[A/C]CTTTATTTATTTACG | 16443 |
| rs585114466 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91911280 | TAAAAAAACTACTAC[C/T]GCCAACAACAACAAC | 16443 |
| rs585116456 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91835222 | TTGAGAGTCAGTCTA[C/T]ACACACACACACACA | 16443 |
| rs585125005 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758241 | GACCAGGCTGGCCTC[C/G]AACTCAGAAATCCGC | 16443 |
| rs585131552 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91749865 | AACTGGGAAACTGGA[C/G]AAGAGAGCTTCATCC | 16443 |
| rs585133028 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91801248 | CAGTAATATTTCCTT[C/T]CTTCCTTCCTTCCTT | 16443 |
| rs585207437 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919423 | GGCCAGAAGTTAGGA[A/G]GCCGCTCCTCAAAGG | 16443 |
| rs585260828 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91751503 | TGTATGTATGTATGT[A/G]TGTATGTATGGGTTT | 16443 |
| rs585279457 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867034 | GCGTGTGCGTGTGTG[A/T]AAGTGTGCATTCATG | 16443 |
| rs585297511 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799764 | TTAAACGTATCGGAG[A/C]ACATGGAAGAAGAAA | 16443 |
| rs585310717 | snp | C/G/T | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91829382 | GTGTGTGTGTGCGTG[C/G/T]GTGTGTGTGTCGTAT | 16443 |
| rs585324968 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768967 | TAAAGAAGAGCGTGC[A/G]GCCCCTGCTGCTGAC | 16443 |
| rs585329388 | snp | A/C | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91747004 | TGTGTGTGTGTGTGT[A/C]TGTGTGTGTGTGTAT | 16443 |
| rs585386381 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91830605 | GATCCGGTGAGGATC[A/G]CTGCCCCGTGTCACT | 16443 |
| rs585396943 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91897517 | TACTCCAGAAGAGGG[A/C]ATCAGATTTCGTTAC | 16443 |
| rs585403543 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91774615 | TTGGCTAAATACTCA[C/T]GAAGGCCAATTTACC | 16443 |
| rs585410232 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91801252 | AATATTTCCTTCCTT[C/T]CTTCCTTCCTTCCTT | 16443 |
| rs585420326 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742642 | CAAAGTGAGTTCTAG[G/T]ACAGCCAGAGCTACA | 16443 |
| rs585432408 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91847387 | TGCATTAAATTCGAG[A/G]CACTCTACACGCATA | 16443 |
| rs585436471 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91889017 | AACCCAAGTATGCAC[A/G]TAGTTGTGTGTGTGT | 16443 |
| rs585439968 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91908145 | TAAATCTTAAAAAAA[A/G]AAAAAAGAAAAAAGA | 16443 |
| rs585447568 | snp | C/G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795371 | AAGCATGTTTGGTTT[C/G/T]TTTTCTTTCTTTCTT | 16443 |
| rs585461614 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91818871 | TATACTGTCTTTATT[C/T]GCCACTTAACAGAAG | 16443 |
| rs585500323 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91745429 | ATCTATCTATCTATC[C/T]ATCTATCTAACAGAA | 16443 |
| rs585554075 | snp | A/T | | | intron-variant, utr-variant-5-prime | Itsn1 | GRCm38.p3 | 16:91747307 | GTGTGTCTGTGTGTG[A/T]GTGTGTGTGTGTGTG | 16443 |
| rs585580423 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91860793 | TCCATGCAGGAACTG[A/C]AGGGGGAGGGGAGCC | 16443 |
| rs585586847 | snp | C/T | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91915648 | TTCCTCCTCTCCCTC[C/T]CCCTCCTCCTCCTCT | 16443 |
| rs585605319 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91845726 | TGGACCCAGAGTCCC[A/G]TAGTCTGCCTTCAAA | 16443 |
| rs585643854 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91817792 | ATTAAGGTGTTTGGT[G/T]TGGTTTGGTTTGGTT | 16443 |
| rs585644108 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91792659 | AACTTGGCGAGGTCC[G/T]CGAGGGTCACGGCAA | 16443 |
| rs585652704 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91807708 | CACACACACGTGCGC[A/G]CCTTTGCAGGCACTG | 16443 |
| rs585657440 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742614 | TTTCTGAGTTCGAGG[C/T]CAGCCTGGTCTACAA | 16443 |
| rs585663982 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750551 | AAGAGAGCTTCATCC[C/T]TCTACCCTATGTGTG | 16443 |
| rs585666568 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758033 | TTCCATTGCTGGGAA[C/T]TGAACTCAGGACCTG | 16443 |
| rs585697860 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91903273 | CATGGTGGCTCACAA[C/G]CATCTGTAATGGGAT | 16443 |
| rs585761376 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91883413 | GTCAGTTTAAAGAAT[A/T]AAAAAGAAAGAAAGA | 16443 |
| rs585800986 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91765763 | GAGAAACCCTGTCTC[A/G]GAAAACAAACAAACA | 16443 |
| rs585815379 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91791911 | TGTATGTGTGTGTGT[C/G]TGTGTGTCTGTGTGT | 16443 |
| rs585820171 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91887670 | ACCCTGAGAGGACAT[G/T]CTCACGTTTTTTTCC | 16443 |
| rs585829037 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91859679 | GATGGATGGATGGGT[A/G]GGTGGGTGGATACAG | 16443 |
| rs585831277 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892019 | CCCGAGGACGTCCGG[G/T]GGAGCCACTGTGAGC | 16443 |
| rs585841236 | snp | A/C | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91915570 | TAGAGACAGTTCCTC[A/C]TCCTCTTCCTCCTCC | 16443 |
| rs585844199 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91766095 | CATGCACTTAAGTGC[G/T]AGCCACTTGGCTGAA | 16443 |
| rs585847538 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798320 | TACAGACCCAAACAC[A/G]GAGGGAGGGAGGGAG | 16443 |
| rs585850415 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91826300 | TGGTGGGCCCTTGTA[A/G]CTTTTAGAATTGTTA | 16443 |
| rs585852185 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91833081 | AGAAAACCAGCCACC[A/C]AAAGTTGTACACACA | 16443 |
| rs585853566 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91824932 | AGTTTATTGGTCTTA[C/T]TGTTTTCTTCCCTCC | 16443 |
| rs585927022 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795380 | TGGTTTGTTTTCTTT[C/T]TTTCTTTCTTTCTTT | 16443 |
| rs585993099 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91838082 | TTTTAACTGTTATAG[A/G]ATGTGTGTGTGTCTG | 16443 |
| rs586005099 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91732522 | AAGATGTCTAGTAGA[A/T]GTTGCCCCTGAGGGC | 16443 |
| rs586008000 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91788379 | CTAAAGGCAGCAACC[A/G]TGTACATGCATATAT | 16443 |
| rs586040295 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91845072 | TGTTCCTCCTGTGCT[A/G]GTTGTAGAACTAGGA | 16443 |
| rs586050927 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742559 | GGTGGTGGTGGCGCA[C/T]ACCTTTAATCCTAGC | 16443 |
| rs586059095 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91792065 | AGAAGCAGTGTCAGA[A/G]CCCCCCAAGAACTGG | 16443 |
| rs586067518 | snp | A/C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91824806 | TCTCCCTCCTCCTGC[A/C/T]TCCCTGCTCTCTCCC | 16443 |
| rs586083088 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91765698 | CAGATTTCTGAGTTC[A/G]AGGCCAGCCTGGTCT | 16443 |
| rs586086143 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91903957 | CCCGCCTCCACAGTG[A/G]CATACTTCTGCTAAC | 16443 |
| rs586087060 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91745070 | CTCATTTTTTTTTCA[A/G]TTATGCTTTTAATTA | 16443 |
| rs586120034 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91881935 | GATTCCATTCCGGAT[G/T]AATGTCCCTAGAAGC | 16443 |
| rs586175734 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91907089 | AGGCTTTTTTTTTTT[C/T]TTTTTCTTTTTCTTT | 16443 |
| rs586188513 | snp | C/T | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91801451 | TAGCTGTACCGAGTG[C/T]CACCATGCGAGTGTC | 16443 |
| rs586197531 | snp | C/G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798554 | ACACACACACACACA[C/G/T]ACACACACACACACA | 16443 |
| rs586200039 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91876364 | AGAGAGAGAGAGAGA[A/G]AGAGAGAGAGAGAGA | 16443 |
| rs586211601 | snp | C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746862 | CTGGTGTGTGTGTGT[C/G]TGCGTGTGTGTGTGT | 16443 |
| rs586268636 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91901688 | TGGGTCTCAAGTACC[G/T]GTAACTCTGGTTCCA | 16443 |
| rs586326255 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91750483 | GTGAACTGGGAAACT[A/G]GACAAGAGAGCTTTA | 16443 |
| rs586338678 | snp | C/G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91807649 | ATACACACACACACA[C/G/T]ACACACACACATACA | 16443 |
| rs586342114 | snp | C/T | | | downstream-variant-500B | Itsn1 | GRCm38.p3 | 16:91920917 | TTTCTTTCTTTTTTT[C/T]TTTTATTACATATTT | 16443 |
| rs586344491 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91784512 | TTTAGTCAGAGGATC[A/C]CACTGTTTAAATTGG | 16443 |
| rs586347876 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894219 | GTGGTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 16443 |
| rs586354954 | snp | A/G | | | intron-variant, upstream-variant-2KB | Itsn1, Cryzl1 | GRCm38.p3 | 16:91729771 | GCGGCGGTGGCGGCC[A/G]CGGGACGGGTTCGGG | 16443 |
| rs586382023 | snp | A/G | | | intron-variant, utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91828619 | TTTCTGTTTTAACTG[A/G]AATTTCCCTGCCACT | 16443 |
| rs586391323 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91816496 | GAATGACAAGTGTAT[A/G]TTGTGCTTAGGAGGG | 16443 |
| rs586396765 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91768955 | TCCTGTCTTTCTTAA[A/G]GAAGAGCGTGCGGCC | 16443 |
| rs586400881 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91909477 | AGCTTGGCACCTCAC[A/G]CTTTGCCCTCCGGGC | 16443 |
| rs586405595 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91887107 | GTGTAACACAAGGGG[A/G]ATTTATCCCCTTACA | 16443 |
| rs586427193 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91754901 | AGGTCTGTGTTTGTC[A/T]GGCTTCTCTCTGCAG | 16443 |
| rs586499140 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91832358 | AAAGGGGCAAAGACA[A/G]TCTCCTGAAAGTTTT | 16443 |
| rs586503990 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91873906 | ACCCACGTGGCAGCT[C/T]ACAGCTGTCTGCAAC | 16443 |
| rs586506222 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91897572 | TTGCTGGGATTTGAA[C/T]TCGGGACCTTCGGAA | 16443 |
| rs586514456 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91748253 | CCAGGCTGGCCTCGA[A/T]CTCAGAAATCTGCCT | 16443 |
| rs586522026 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91801278 | TCCTTCCTTCCTTCC[A/T]TTCATTCATTCATTC | 16443 |
| rs586525798 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91777003 | GTGCTCTAAGCCATA[C/T]CTAGGATGGGTCTTT | 16443 |
| rs586551164 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91902323 | ACCACCCACCAGAGG[C/T]AGTGGAAAGGAAAGG | 16443 |
| rs586573449 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91834137 | TCAACCCCCCACCCC[C/T]CACCCCCAAAACAAA | 16443 |
| rs586587146 | snp | C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746966 | TGTGTGTGTCTGTGT[C/G]TGTGTGTGTGTGTGT | 16443 |
| rs586595607 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799053 | AAGAAAGAAAGAAAG[A/G]AAGAAAGAAAGAAAG | 16443 |
| rs586610616 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91749862 | GTGAACTGGGAAACT[A/G]GACAAGAGAGCTTCA | 16443 |
| rs586617444 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904823 | TTTTTGGTTTTTTGA[A/G]ACAGGGTTTCTCTGT | 16443 |
| rs586683648 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890680 | TCCCGAGTACTGGGA[A/T]AAAAGGCGTGTCCAG | 16443 |
| rs586744623 | snp | A/G | | | utr-variant-3-prime | Itsn1 | GRCm38.p3 | 16:91919419 | GGGAGGCCAGAAGTT[A/G]GGAAGCCGCTCCTCA | 16443 |
| rs586758396 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91883460 | AAGAAAGAAAGAAAG[A/G]AAGAAAGAATGAATG | 16443 |
| rs586761133 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91751507 | TGTATGTATGTATGT[A/G]TGTATGGGTTTTTTG | 16443 |
| rs586763914 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91799065 | AAGAAAGAAAGAAAG[A/G]AAGAAAGAAACCCGA | 16443 |
| rs586770577 | snp | A/C/G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867026 | GTGTGTGTGCGTGTG[A/C/G/T]GTGTGTGAAAGTGTG | 16443 |
| rs586775768 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91789767 | CCATTGGTGTTAACA[A/G]TTACTTTCCTGTTTC | 16443 |
| rs586781405 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810892 | GCCTGGGAGGGAGCA[A/G]CTCCCCTGCCCCAGG | 16443 |
| rs586781661 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91839542 | TAGAGGGAGGCCCTT[G/T]GGTGAAGGGGTGATG | 16443 |
| rs586792952 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91749682 | TAGACAAGAGAGCTT[C/T]ATCCTTCTACCCTAT | 16443 |
| rs586877940 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91885966 | GGGGGTGGGGGGTGG[A/G]GGAGGGAGGGGATGA | 16443 |
| rs586914264 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91852267 | TTTACTGAACATCAC[C/T]GTCTTCAGGAGAGTG | 16443 |
| rs586922427 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742743 | CTGTTATAGTGACAG[A/T]CAGTGGCCACAAGCA | 16443 |
| rs586935241 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890359 | TTTTTTGTTGTTGTT[A/T]TTTTGTTTTTCTGTG | 16443 |
| rs586973617 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91737213 | TGGGAAGAAGATACT[C/T]GCGGGGTGTTATTAG | 16443 |
| rs586976621 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91788821 | TGCCGAACAGTGGAT[G/T]GGCTTGACCACTGAA | 16443 |
| rs586977368 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910894 | TAGGAGCCAGCGGGG[A/C]CCAGAAGAAAGTATT | 16443 |
| rs586993507 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91735556 | AGTTAGATGCCTTAG[C/T]CAACAAGTAGCTTGG | 16443 |
| rs587001402 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91751467 | GCGCCATGCGTGTGT[A/G]TGTGTGTGTGTATGT | 16443 |
| rs587045672 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91905766 | TAAAATAGAGTAACC[C/T]GAACAGGCAGAGTAG | 16443 |
| rs587064949 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91893047 | GTATACCCACACACC[G/T]GCCCACTGATTCCCC | 16443 |
| rs587081362 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91828060 | CTGAGTAGTGCTCCC[A/C]TCCTCCCTCCCTCCC | 16443 |
| rs587089833 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91867004 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 16443 |
| rs587146167 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91839951 | CTATCACGATTTGCT[C/G]GGTTTGGGGAAAGTT | 16443 |
| rs587146607 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910395 | TCTCTCTAGCCCTAG[A/C]ATATGATTTTTTTAA | 16443 |
| rs587158013 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91904878 | ACTCTGTAGACCAGG[C/T]TAACCTCAAACTCAG | 16443 |
| rs587166111 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91790253 | TGAATTGCTTTGGGA[A/G]GGATGGAAGTTCATG | 16443 |
| rs587176633 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91742674 | AGAGAAACCCTGTCT[C/T]AAACCTCCTCCCCCC | 16443 |
| rs587278969 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894881 | TAGTGATGTAAAACA[A/T]TGTCCCACAGACCAA | 16443 |
| rs587280945 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91866362 | GAATAGCGAGGAGGT[C/T]TGTGATCTGCCCTTG | 16443 |
| rs587282910 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91827172 | GTGTCTACAAGTGGG[C/T]GCCAGAGAGACTGGA | 16443 |
| rs587292203 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892490 | TTTGGGCCAACAATG[A/G]ACTGAGGGGCTTAAG | 16443 |
| rs587299227 | snp | C/G | | | intron-variant, upstream-variant-2KB | Itsn1 | GRCm38.p3 | 16:91746924 | TGTGTGTGTCTGTGT[C/G]TGTGTCTGTGTGTGT | 16443 |
| rs587301833 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91798965 | GGGGAAAAGAAAAAG[A/G]AAGGAAGGAAGGAAG | 16443 |
| rs587312358 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91910499 | TGTATGCCGTGTGTG[C/T]GTGTGTGTGTGTATG | 16443 |
| rs587334118 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91751491 | TGTATGTGTGTGTGT[A/G]TGTATGTATGTATGT | 16443 |
| rs587345306 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91801286 | TCCTTCCATTCATTC[A/T]TTCATTCATTCATTC | 16443 |
| rs587393571 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91810621 | AGGAAAGATGCGCTT[C/G]TTGCATTCCAGGCAA | 16443 |
| rs587426296 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91823496 | TTTGGTGTGTGCTTT[C/T]CTTTCTTCTTTTGTT | 16443 |
| rs587427586 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91849750 | CACCCAGGTGAGAGG[C/T]ATACTTTAGCATTCT | 16443 |
| rs587430903 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91878032 | GGAGGGAGGGAGAGA[A/G]AGAGAGAGAGGAAGA | 16443 |
| rs587438213 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91760286 | TGTGGTGGTGTTGGT[G/T]CCTGGGGTTCACAAA | 16443 |
| rs587445375 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91780940 | TAGTGATGGCAGAGG[A/G]GAGGAGCGGTGGCTG | 16443 |
| rs587447320 | snp | C/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91795463 | CTTCCTTTCTTTCTT[C/T]CTTTCTTTCTTTCTT | 16443 |
| rs587448663 | snp | G/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91874227 | AAGCTACCAGGCATT[G/T]AAAGAAAGAAAGAAA | 16443 |
| rs587454077 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91835271 | CACACACACACACAC[A/G]TCTTCTGGCCCATAT | 16443 |
| rs587464120 | snp | A/C | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91749867 | CTGGGAAACTGGACA[A/C]GAGAGCTTCATCCCT | 16443 |
| rs587488285 | snp | A/T | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91890337 | AATGGCAGTTGTGTT[A/T]TTTTTTTTTTTTGTT | 16443 |
| rs587497176 | snp | C/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91758912 | GTAATTTGTTTGTTT[C/G]TTTGTTTTTGGTTTT | 16443 |
| rs587501894 | snp | A/G | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91823149 | GACTGATCTTTCCAT[A/G]TAGACAGACGCTTGG | 16443 |
| rs864310064 | in-del | -/TGT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899152 | TCCCTTCTGCTGCCC[-/TGT]TGTTCTGCATGCTAC | 16443 |
| rs864311779 | in-del | -/GGAT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894072 | ACTAGTGGCCTCCAG[-/GGAT]GGATGGAAGTTTTCA | 16443 |
| rs864312291 | in-del | -/AAAGAAAGAAAG | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91883416 | AGTTTAAAGAATTAA[-/AAAGAAAGAAAG]AAAGAAAGAAAGAAA | 16443 |
| rs864314930 | in-del | -/TGT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91899155 | CCCTTCTGCTGCCCT[-/TGT]GTTCTGCATGCTACC | 16443 |
| rs864316692 | in-del | -/GGAT | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91894073 | CTAGTGGCCTCCAGG[-/GGAT]GATGGAAGTTTTCAG | 16443 |
| rs864317554 | in-del | -/TGAC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892696 | CAGTGCTCACTTATG[-/TGAC]TGACTGTCCCCCAGG | 16443 |
| rs864320937 | in-del | -/AAAGAAAGAAAG | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91883415 | AGTTTAAAGAATTAA[-/AAAGAAAGAAAG]AAAGAAAGAAAGAAA | 16443 |
| rs864321390 | in-del | -/TGAC | | | intron-variant | Itsn1 | GRCm38.p3 | 16:91892697 | AGTGCTCACTTATGT[-/TGAC]GACTGTCCCCCAGGT | 16443 |