SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6224195 | snp | A/G | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:11959570 | ATTTGCCATCAGTAG[A/G]AAACATTCAGACCCT | 75725 |
rs6238110 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Phf14 | Mm_Celera | 6:12041245 | ACAGACAGCTCAGGT[A/G]TTTGACAGTTAATTG | 75725 |
rs6239240 | snp | A/T | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:12041493 | AGAGGCCATATATCA[A/T]AAAAATGTGGTGGAG | 75725 |
rs6239757 | snp | A/G | 0.5 | 0 | intron-variant | Phf14 | GRCm38.p3 | 6:12041582 | cacacacacgcacac[A/G]cacacacacacacac | 75725 |
rs6347458 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11907145 | ACCTTTCTCCCTGAT[C/G]TCTGCCACCTTCTGC | 75725 |
rs6347510 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11907181 | GCAACCTCACCTCCA[A/C]CCCAGNTAGAGGCTT | 75725 |
rs6347522 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11907187 | TCACCTCCANCCCAG[C/G]TAGAGGCTTCAAGCA | 75725 |
rs6347574 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11907219 | TCAGGTCATCCCAAC[A/G]ACAGAATGTAACCCC | 75725 |
rs6357013 | snp | A/G | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:12094120 | CTCTGAGCTACACTC[A/G]GTGTGATGTGCTGCC | 75725 |
rs6357497 | snp | A/G | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:12094201 | TAATGAATGTTCTAA[A/G]TGGTGATAGAAGAGG | 75725 |
rs6357570 | snp | C/T | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:12094253 | CTAAATAAGCTTAGG[C/T]TTCAGGACAAGAATC | 75725 |
rs6360634 | snp | A/G | 0.5 | 0 | utr-variant-5-prime, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11907414 | AAGATTAGGACACAC[A/G]CTAAGCCGCTTCTGC | 75725 |
rs6382415 | snp | C/T | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:11914500 | ACCTAAGGGCTTATT[C/T]TCAACAAGTATGTAA | 75725 |
rs6383530 | snp | A/G | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:11914712 | ttgagaacTTCTCTA[A/G]AGACTACGAGCAAAT | 75725 |
rs6384149 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Phf14 | Mm_Celera | 6:11914812 | AGAGAAGCTGACCTC[G/T]TAAGCTGCATAGTTG | 75725 |
rs6384628 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Phf14 | Mm_Celera | 6:11914836 | ATAGTTGTGTGGTTA[A/C]ATATTTATTATTTTG | 75725 |
rs6384755 | snp | A/C | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:11914915 | GTCAGCAGAGGAGTC[A/C]GTTGGGAAAAGAAGA | 75725 |
rs29825809 | snp | G/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:11935212 | ATTCTTATCTTTAGG[G/T]AAAGGAAAACTCATT | 75725 |
rs29828062 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12026548 | CAATTCAAATGCTAC[A/G]TTCCTTGCCTTATGT | 75725 |
rs29828134 | snp | A/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12044121 | AAACTCTCTTATACA[A/T]TTCTTTTCATTGTGG | 75725 |
rs29829988 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12019894 | CTCTGAACCCTCATA[A/G]AAAAGCTGTGCATAG | 75725 |
rs29872812 | snp | A/C | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12078832 | AGTTTCAGGAAAACT[A/C]ACACCCTCTTCTGTA | 75725 |
rs29873254 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Phf14 | Mm_Celera | 6:12057793 | GTTGGCCAGTTTAGT[A/G]ACTTTATTAGTTGAG | 75725 |
rs29874037 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12055563 | GAGCCACCTGTCTTT[C/T]TCTCCTCTTCCTCTC | 75725 |
rs29876496 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Phf14 | Mm_Celera | 6:12017539 | AATAGAAGGACTTAG[C/G]TTGTTCTTAGAGATC | 75725 |
rs29876779 | snp | G/T | 0.484429 | 0.0868505 | intron-variant | Phf14 | Mm_Celera | 6:12014114 | TGGAGGATTACTGTT[G/T]TAGTAGAGGTGGGTC | 75725 |
rs29877478 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12085484 | AAGCTAGAGACAGTT[A/G]TGTGCTGTCCAACAT | 75725 |
rs29879141 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12019982 | AGCCAGTTTAGCCAA[A/C]TCAATGAGCTCCACA | 75725 |
rs29883523 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Phf14 | Mm_Celera | 6:12061028 | GTGGAGTATAATCTG[C/T]GACTGACCCTATCCA | 75725 |
rs29920988 | snp | C/T | 0.48 | 0.0979796 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12081534 | CTAAGTAGAAAAGGG[C/T]TTTGTTGTTGTCCTC | 75725 |
rs29922374 | snp | A/C | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12022746 | GTATACGTGTGTACA[A/C]ATGGATGTGTAAATG | 75725 |
rs29923961 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12054764 | AGTTACAGCTGTTTG[A/G]GGGTTTGTTGTTGTT | 75725 |
rs29923995 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12013568 | AGTCACTGTGTTATT[A/T]TTTGGTTTTACTTTA | 75725 |
rs29924927 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Phf14 | Mm_Celera | 6:12055769 | TAGCAATGGCATTGC[C/T]TCAGCTCTGGTAGAG | 75725 |
rs29925607 | snp | A/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12069807 | ATCTAAAAATAAAAA[A/T]TGGAAAGTTTCAGAA | 75725 |
rs29927002 | snp | C/G | 0.32 | 0.24 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12040118 | ATTTTACTTGTTGAA[C/G]CTAAATGTGAAGCTA | 75725 |
rs29930528 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12068810 | TATTTATGAAGTAGA[C/T]CTCTTATATCAGGAT | 75725 |
rs29961451 | snp | C/G | 0.429688 | 0.173817 | intron-variant | Phf14 | Mm_Celera | 6:12035565 | AAGATTTTTAAAAAT[C/G]TAGACGCTTATATAT | 75725 |
rs29971659 | snp | A/C | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12057417 | TTTTTTTGAGGCAGT[A/C]TGTCATTTGGCTTGG | 75725 |
rs29972325 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Phf14 | Mm_Celera | 6:12077114 | TCACTCTTTTCCACC[C/T]AGAGTACTAGACCAT | 75725 |
rs29973990 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Phf14 | Mm_Celera | 6:12051405 | CTGTACCATGCTGTG[A/G]ATGCCACATGTGACA | 75725 |
rs29975697 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Phf14 | Mm_Celera | 6:12017012 | CATCGTCTAAGAGAC[A/G]GATGCCTGTTAGCTT | 75725 |
rs29977575 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12021730 | AGTAATACGTCATAA[A/G]CTTGGTACCAGTTTA | 75725 |
rs29982279 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Phf14 | Mm_Celera | 6:12058639 | CTTTTCCTTGTCCTT[C/T]GAAGGCTATTTAAAT | 75725 |
rs30011241 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Phf14 | Mm_Celera | 6:12034792 | CCTTGCCGTGCCTCA[C/T]CAGACATGCAGTGCC | 75725 |
rs30022344 | snp | A/C | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12068662 | GCACCTTGAACTTAG[A/C]TATAATAATCCCAGC | 75725 |
rs30024040 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Phf14 | Mm_Celera | 6:12077354 | ATTAAGAGCATGCCT[A/G]TGTGCATTCCAGTAC | 75725 |
rs30060707 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12037783 | CTTAGTAGTAATGAT[G/T]CAGTAATGATTAATC | 75725 |
rs30066659 | snp | G/T | 0.444444 | 0.157135 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12040601 | ATTTATTGATTTTAT[G/T]GCACTAGAAAAAATA | 75725 |
rs30067515 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Phf14 | Mm_Celera | 6:12017210 | TATGCAATACCTAGT[G/T]GTGTGACCTGTCACA | 75725 |
rs30073446 | snp | G/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12026708 | AGAGGTTTATTTTCT[G/T]GTGTGTGGAGCAGGG | 75725 |
rs30074804 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12035711 | GTTGTTGTTGTTGTT[G/T]TTGTTTTTGTTTTGA | 75725 |
rs30113390 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12068127 | TAATTAGCTACAGGG[C/T]CCTGGGGAAATCAGT | 75725 |
rs30115135 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12078116 | GTCATAGTGATGCCT[C/T]AGCTTCCAGACGTAT | 75725 |
rs30116985 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12043278 | GTTATCAATATCCAT[C/T]TGTAATGAGGAATTT | 75725 |
rs30117474 | snp | C/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12082291 | TTATAGAAGACTGGA[C/G]TTTGGCTTCTAGCAT | 75725 |
rs30121353 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Phf14 | GRCm38.p3 | 6:12076333 | TGTATAACCACTGTA[A/C/T]AATTTCCAGAACCAG | 75725 |
rs30123599 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phf14 | GRCm38.p3 | 6:12021979 | TGTGTGTGTGTGTGC[A/G]TGTTCTACCTAGCTT | 75725 |
rs30124635 | snp | G/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12030172 | CTAGCATTACCGCAA[G/T]ATCTTTTCTATTATT | 75725 |
rs30124920 | snp | A/T | 0.492188 | 0.0620098 | intron-variant | Phf14 | Mm_Celera | 6:12014068 | GATCAAATGTCCCTC[A/T]CAAAAGTTGGTCTCT | 75725 |
rs30125234 | snp | C/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12069504 | TTCCCCTCTGAAAAC[C/G]CCCTATCCCCTCCCC | 75725 |
rs30163992 | snp | A/G | 0.455 | 0.143091 | intron-variant | Phf14 | Mm_Celera | 6:12026486 | ACATCTGCTTGAAAA[A/G]GCCCATCTTCCTTCC | 75725 |
rs30164759 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12018573 | AGATACCATAGAGAC[C/G]CACATGGAGACTGAC | 75725 |
rs30165336 | snp | G/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12034492 | AGATTGCATCTTTCT[G/T]CTGTAAGAAGAGCTC | 75725 |
rs30168601 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Phf14 | Mm_Celera | 6:12013088 | AAGTAATGAATTCAG[A/G]CTTGTACCATCTCAC | 75725 |
rs30169863 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Phf14 | Mm_Celera | 6:12053058 | ATCTGTAATCTGAGT[A/G]CCCCTACAGTCAGGT | 75725 |
rs30169896 | snp | A/T | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12081466 | CTCAAATGTTTTTTT[A/T]AAAGAAAGAAATTGT | 75725 |
rs30208393 | snp | A/C | 0.401235 | 0.199068 | intron-variant | Phf14 | Mm_Celera | 6:12062286 | CTCAGGGTTTCCAGC[A/C]ATGCACTGACGCGTT | 75725 |
rs30211786 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Phf14 | Mm_Celera | 6:12036016 | ATCGATATTTATATT[C/G]TTCATGTAGCAAAAG | 75725 |
rs30216666 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Phf14 | Mm_Celera | 6:12027162 | GGTAACTAACTCATA[G/T]TCTTCAGGTCCTGTC | 75725 |
rs30253579 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12063697 | CTGGAATAGTTATGT[A/G]TAGTTCATTGTTTTC | 75725 |
rs30263542 | snp | G/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12051999 | TCCCTCCCATTTTGG[G/T]GGGTATTTCAGCTAA | 75725 |
rs30266356 | snp | G/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12036113 | AGTTCCAATCCTCAG[G/T]TCCCATATATAAATT | 75725 |
rs30267271 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12027041 | ACCCCAGGCAGGAGG[A/G]GAGAGCTGTAAGGAG | 75725 |
rs30267463 | snp | A/G | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:12074011 | ACTGTTGAGTGTTTA[A/G]TGACTTACTAGATTG | 75725 |
rs30267608 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Phf14 | Mm_Celera | 6:12064925 | TATGCTAAAATAAAA[A/G]TTTGGTTAAATACAG | 75725 |
rs30268190 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12019938 | TAATTATGTGCTGGA[A/G]ACAGGAGAGTCCTGG | 75725 |
rs30271417 | snp | A/G | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:12065980 | ACATCTTTAATTATA[A/G]TCTCTTTAATTTTTT | 75725 |
rs30313504 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Mm_Celera | 6:12042841 | ATTGACCTCCTAGCC[A/G]TTATCTCCTTTATCT | 75725 |
rs30313724 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12068661 | TGCACCTTGAACTTA[A/G]CTATAATAATCCCAG | 75725 |
rs30314559 | snp | A/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12082382 | TATACACACATGCAC[A/T]CATGCATACACATGC | 75725 |
rs30317417 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Mm_Celera | 6:12042658 | TAAGGAATGCGAACA[A/G]AGACGGGATTTACAA | 75725 |
rs30317587 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12021168 | AACTGCTACTGAGGC[C/T]GCACCTTTACCAACC | 75725 |
rs30317897 | snp | C/G | 0.32 | 0.24 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12039736 | GCCAGTGGGACTTAC[C/G]TGCTCTGTGCTACCC | 75725 |
rs30319449 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:11918766 | ACCATGGATATATGA[A/G]AAACTGTCTCCAAAG | 75725 |
rs30326000 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12016905 | AAAGTATGATGCAGA[C/T]CACGCCTGTTTCCTG | 75725 |
rs30351621 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phf14 | Mm_Celera | 6:12015504 | GACTTCACAGATGGG[C/T]TTTTGTTTTTTCTCA | 75725 |
rs30361253 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12083362 | CCTACACTAGGACAT[C/T]GACATCGAACCGCCT | 75725 |
rs30361883 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12016797 | AATCATTGTCTTAAT[C/T]TTATTGTCCAAGTTA | 75725 |
rs30363804 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12066870 | ATGGCTGCTGGGAGT[A/G]CAAACTTGTACAGAC | 75725 |
rs30364914 | snp | C/T | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:12025242 | TTGAGGTCCTTGATC[C/T]ACTTGGACTTGAGCT | 75725 |
rs30365581 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Phf14 | Mm_Celera | 6:12038499 | TTCGTGGTCTGTGGT[C/T]GAGTTTGGCGTGGTA | 75725 |
rs30368219 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12024283 | CCAGAGGCCTCCAGT[C/T]TCTTAAGGGTTAAGT | 75725 |
rs30369567 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12055602 | CTTCTGTTTCATTCT[C/T]TTCCCTATCTCTCAC | 75725 |
rs30369777 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12050931 | ACAATAACAACGGCT[A/G]TTGTATATTGTTACT | 75725 |
rs30411749 | snp | C/T | 0.455 | 0.143091 | intron-variant | Phf14 | Mm_Celera | 6:12051496 | GCCTTTGAAAAGTTG[C/T]CAGCATCCTTCTGCC | 75725 |
rs30412208 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Phf14 | Mm_Celera | 6:12088419 | GGGTTTGGAAAGTTT[G/T]TGAGGGGAGAGCAGA | 75725 |
rs30416908 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Phf14 | Mm_Celera | 6:12072216 | TAGCCCATCATGTGG[C/T]GTTAGTCTTAATAAA | 75725 |
rs30418132 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12052136 | GTTCAATTTCCTGAC[C/T]GTCCGTGCATCTCCC | 75725 |
rs30418275 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Phf14 | Mm_Celera | 6:12075780 | AGCATAGCACGGTTA[G/T]GAAAGTAAAAGCCAC | 75725 |
rs30418411 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12086766 | GTCATCATTGGGAGG[C/T]CCAAGAGACTGGAGT | 75725 |
rs30459609 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12065676 | GAAGAATTAGGCCAG[A/G]CATGTTGATGCATGC | 75725 |
rs30462461 | snp | A/G | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:12080296 | AATCAGAAATAACAG[A/G]AAAGCAAGACTACTT | 75725 |
rs30463314 | snp | C/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12058238 | GTAACACTGAGAGTT[C/G]AGGTGACACAGTGTT | 75725 |
rs30464184 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Phf14 | Mm_Celera | 6:12064019 | AGGTAAACTTAATTT[C/T]ACCAATCACTTAAAC | 75725 |
rs30464597 | snp | A/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12078147 | TTCTGTTACATGTTA[A/T]ACACTAAACTGTTTG | 75725 |
rs30473889 | snp | A/C | 0.415225 | 0.187619 | intron-variant | Phf14 | Mm_Celera | 6:12013854 | TCTACTCTTTTAATC[A/C]TTAGTAATATTAATT | 75725 |
rs30501093 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Phf14 | Mm_Celera | 6:12053733 | TGTTTTTCTCTTTGT[C/T]TTTTTGCTTGTTGTT | 75725 |
rs30502895 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12035789 | AGACCAGGCTGGCCT[C/T]GAACTCAGAAATCCG | 75725 |
rs30508153 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12038857 | TGTATGTTCCCTTGA[A/G]TATTGTAAAATTGCC | 75725 |
rs30508590 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12031044 | TTGTTAATTTATATA[G/T]TTTCTCTTTACCTCT | 75725 |
rs30512315 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Phf14 | Mm_Celera | 6:12058247 | AGAGTTCAGGTGACA[A/C]AGTGTTTCCTGAACA | 75725 |
rs30514711 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12028076 | AGCTGTGCTGTTCTT[A/G]CTGAGCAAATTCTAG | 75725 |
rs30517086 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Phf14 | Mm_Celera | 6:12087084 | AGTCGCACAGCCTTG[C/T]TATATTCCCTGATTT | 75725 |
rs30521785 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12086504 | CTGAATTCATTTATA[C/T]TAAACACCCATTCAA | 75725 |
rs30553343 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12036370 | CCATCCTTATTTATG[C/T]GCACACACATATACA | 75725 |
rs30563856 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Phf14 | Mm_Celera | 6:12061737 | CATTGTTATTAAGAT[C/T]TATATTTTCATTTGA | 75725 |
rs30563861 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12052935 | AAGATATACTTAAGG[C/T]AATTAATTTATCAGG | 75725 |
rs30567068 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12024716 | CCAATTTTCTGAGGA[A/C]ACTCCTTATTGATTT | 75725 |
rs30570502 | snp | A/G | 0.32 | 0.24 | intron-variant, missense | Phf14 | Mm_Celera | 6:12067243 | AGGCCTCAGCCCCTC[A/G]GCCATGGAAGACTTT | 75725 |
rs30600607 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Phf14 | Mm_Celera | 6:12051799 | GCTTTAAATGCCAGT[A/G]GAAGATTTCAGGTAT | 75725 |
rs30611938 | snp | C/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12078730 | GGACTGGAGACATGG[C/G]TCAGTGGCTGAGTGC | 75725 |
rs30612496 | snp | A/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12082465 | TTGTCCATACAAACT[A/T]TTCTCAGCTATTTAA | 75725 |
rs30614916 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12018614 | CTGTTACATATGTAC[C/T]GGGAGCCTGGTTACA | 75725 |
rs30619284 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Phf14 | Mm_Celera | 6:11938452 | GAACCATTGTGGCCC[A/G]CTGTTATGGAACACT | 75725 |
rs30623522 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12081965 | ATGCCTGTGTGGTTT[A/G]TGCAGTTACTTAGTT | 75725 |
rs30623706 | snp | A/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12036361 | CACACTCACCCATCC[A/T]TATTTATGCGCACAC | 75725 |
rs30666876 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Phf14 | Mm_Celera | 6:12064119 | GAAACATGCTTTTTA[A/G]GAATTCTGAATAGCA | 75725 |
rs30668818 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12063694 | GCACTGGAATAGTTA[C/T]GTGTAGTTCATTGTT | 75725 |
rs30702431 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12081329 | TGATAGTGGGATTTA[C/T]TTTGTTTCAGTTTTT | 75725 |
rs30702894 | snp | A/C | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12040932 | CTTCTACAGTGGTTA[A/C]TATTAGAACAGTGTA | 75725 |
rs30711275 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12046336 | AAGACCCAGAGTATT[A/T]ATTCTGTGGTCTTGC | 75725 |
rs30711279 | snp | C/T | 0.32 | 0.24 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12039968 | AGCACTTGATGTCAG[C/T]ACGGACATTTTATAA | 75725 |
rs30714619 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12046287 | GATTTAGTATTTTAG[C/T]TACTGAAAGGTAAAT | 75725 |
rs30715437 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Mm_Celera | 6:12048934 | CCAAAATAGTTCTGG[A/G]TTTAGTAAGAGAGCC | 75725 |
rs30722677 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Phf14 | Mm_Celera | 6:11932999 | TGATATAAATCAGTG[C/G]TACTATGTTTAAGGT | 75725 |
rs30740374 | snp | A/G | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12040643 | TAGGAAAAGCAGTAT[A/G]CTTTCTTTGAATATA | 75725 |
rs30746476 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Phf14 | Mm_Celera | 6:12088364 | ATTTTTTTAATTCAA[A/G]TATGGCTGTGTGTTT | 75725 |
rs30755975 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Phf14 | Mm_Celera | 6:12075856 | TTATTCATAGAAATA[A/G]TTTGTACAGTCAAAC | 75725 |
rs30756058 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12066177 | CCCTCCCCTACCCAG[C/T]TCCCTCCCATCCTCC | 75725 |
rs30756225 | snp | A/G | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:12064284 | GAAACTCTTGAATAA[A/G]CTGAAACAGTTTTCT | 75725 |
rs30757065 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12087476 | TCATGTGTGAATATA[C/T]CACAGTCTGTCCATC | 75725 |
rs30758130 | snp | G/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12052098 | AGTTCCCCGTTCCCC[G/T]TCCCCCATTACTACA | 75725 |
rs30759905 | snp | C/T | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:12078059 | GAGCTACAATAGAGA[C/T]ATGACTTTATAAGCG | 75725 |
rs30763878 | snp | A/T | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12047279 | GAACTTGACAAAAAC[A/T]AGTGAGAGTAATATC | 75725 |
rs30795539 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Phf14 | Mm_Celera | 6:12051516 | ATCCTTCTGCCCTTC[A/G]TTCTGAAATAGCATT | 75725 |
rs30800717 | snp | A/G | 0.455 | 0.143091 | intron-variant | Phf14 | Mm_Celera | 6:12037419 | TATGTTAAAAGTCCC[A/G]GTGTGAATTGCTTAG | 75725 |
rs30800767 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12035803 | TCGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 75725 |
rs30802614 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12056792 | AGCTGTAGCCCACGA[A/G]TGTTTGAGTATTTAC | 75725 |
rs30816665 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Phf14 | GRCm38.p3 | 6:12026735 | AGGGAGAAGGGTTGG[A/G/T]GGACGGGTCAACCCT | 75725 |
rs30841053 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12020493 | TAGAGTTATGTCTAA[C/T]ATGACTATTCCTGTG | 75725 |
rs30852256 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12069065 | GTTGTCTGTCTCTGA[C/T]ATATAAATACATAAA | 75725 |
rs30853297 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12054318 | GTTCCTGGTTGGTAA[A/G]CTGCCAGGAAAGTTT | 75725 |
rs30853648 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12019294 | CATACATACATGCAT[A/G]CATACATACATACAT | 75725 |
rs30855027 | snp | A/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12080105 | TTCAACTATTATGTG[A/T]TTTATTTAAACTTGG | 75725 |
rs30860876 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12036134 | TATATAAATTGAGTG[C/T]GGAAGGGCATGCTTG | 75725 |
rs30866055 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Phf14 | Mm_Celera | 6:12063062 | TCAAGTCAGCCAACT[G/T]TGAGAATTACTTATC | 75725 |
rs30901252 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12057470 | ACTTGAATCAAGCTG[C/T]GTTCCCTGTCTCCAT | 75725 |
rs30904285 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Phf14 | Mm_Celera | 6:12039095 | TAGGGTGAGGATTTC[A/T]CTCTCTTTGTTATTT | 75725 |
rs30952422 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Phf14 | Mm_Celera | 6:12085978 | GCCTTCCTATTCTTG[G/T]TATCTCTTTAGTTCT | 75725 |
rs30953241 | snp | A/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:11917731 | ATGAATCCAGCCAAT[A/T]AAAGCTGGAAGAGGT | 75725 |
rs30958614 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12016909 | TATGATGCAGACCAC[A/G]CCTGTTTCCTGTGGC | 75725 |
rs30994200 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12056732 | GAAGCTGTAGCCCAC[A/G]AGTGTTTGTAGAGGA | 75725 |
rs30996289 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12015478 | ACTTCCCCAGCACTA[C/G]AATTACGAATGACTT | 75725 |
rs30997646 | snp | C/G | 0.42 | 0.183303 | intron-variant | Phf14 | Mm_Celera | 6:12061333 | TACTTCTTTCTAACA[C/G]GATTTGAAATTCTAT | 75725 |
rs31284701 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | GRCm38.p3 | 6:11984534 | AGAGACTGCCATATC[C/T]GTTGATCCATCCCAT | 75725 |
rs31528729 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:11984786 | AACTAACCAGTACCC[C/T]TGAGCTCTTGTTTCT | 75725 |
rs32084381 | snp | C/T | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:11984291 | GGGCATTATCCTGAG[C/T]GAGGTAACCCAATCA | 75725 |
rs32128956 | snp | A/T | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:11974437 | ACTCAATTCCCCAAT[A/T]AAAAGACATAGACTA | 75725 |
rs32200237 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:11984681 | GCTCACAGTCAGCTA[A/T]TGGATGGATCACAGG | 75725 |
rs33374384 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11980598 | TCCTTTTTGATTTTG[A/T]TTCAAGTCTTCCTGC | 75725 |
rs33374386 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11985612 | GATAAAGAAACATAC[A/C]TGATTTTTGTTATTG | 75725 |
rs33374387 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11985899 | AACATTTTTATCAAT[A/G]TTTTGCAATTAATAT | 75725 |
rs33374388 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11986619 | AAAACTTTAGTTAAT[A/G]AGCAGTGGTTTTTGA | 75725 |
rs33374389 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11986996 | AAACTGCCTGCATTT[C/T]TTTCTAGGCAAGGAT | 75725 |
rs33374390 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11988072 | TAAACAGCATTATAG[G/T]TCTTATTTTTTAGTT | 75725 |
rs33374392 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11988079 | CATTATAGGTCTTAT[G/T]TTTTAGTTTGTTGAA | 75725 |
rs33374476 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12027225 | CAGCTACACTGCTCC[C/T]ATTCTCTCTTTTCTG | 75725 |
rs33374478 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12027251 | TTCTGAAGGCTATAA[A/G]CTTATTCAGTATGCA | 75725 |
rs33374480 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12027618 | GTCTGCCCTCAGACT[A/G]TCATAATTTTTCCCT | 75725 |
rs33374482 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12027655 | GCCCAAGCTGAGGGC[C/T]AGTGGCTGCACTGAC | 75725 |
rs33375164 | snp | A/C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12003133 | CAAATTGTCTATGAA[A/C/T]TAAGCACAATTAAAT | 75725 |
rs33375166 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12003193 | GCCCATTTTGTCTGC[A/G]TTTCTAAGGCAGTAC | 75725 |
rs33375168 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12003818 | GATGCATCATTTGTA[C/T]CATATTAAAGATATT | 75725 |
rs33375170 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12004052 | CTGTAGAGCTCCTGT[A/G]AAGACAGCCTGGCCT | 75725 |
rs33375172 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12004220 | AATCATATTTACTTT[C/T]GGGTATACTTTCTAA | 75725 |
rs33375334 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12027781 | GTAAATTTTTGAAAA[C/G]ATTGTGAAAATATAA | 75725 |
rs33375336 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12027919 | ACCATGACACAGTTT[C/T]CTTGATACGGCCAGC | 75725 |
rs33375338 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:12028022 | ACTGGAATTTCACTG[A/G]ATCCTATTGGTTCCA | 75725 |
rs33375340 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Phf14 | Mm_Celera | 6:12028068 | TTTTTATCAGCTGTG[C/T]TGTTCTTACTGAGCA | 75725 |
rs33375343 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:12028117 | ACAATTTCATTTAAA[A/G]CAGATATCTTCCACT | 75725 |
rs33375364 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:11988213 | AATATATAAAGCACG[A/G]TCTTTCTAAAGTGTT | 75725 |
rs33375366 | snp | G/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:11988434 | CTTGGGATTTTTAGT[G/T]TTCTCATGAAAGAAG | 75725 |
rs33375368 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:11988552 | GTAGAATAAAAGAAA[A/G]TATTTCCCTTCTCTT | 75725 |
rs33375370 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11988693 | TTGCACATATAAAAG[C/T]TTCCTAATTTGATTT | 75725 |
rs33375372 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | Phf14 | Mm_Celera | 6:11988796 | AGGGATATGGGCCTT[A/G]CTTGGCCGAATTACA | 75725 |
rs33375645 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12014278 | CAGTCTTCTCTGGAG[C/T]TTATGTAAATAGACT | 75725 |
rs33375647 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12014319 | GAAGTCATAACTGCA[C/G]AGTCACATGGCATAG | 75725 |
rs33375649 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12014516 | CTGAGTCGTAGGTGT[C/G]TTGTTAGTACTGTTG | 75725 |
rs33375651 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:12014601 | ACTAAGGGACTGTCT[C/T]CTCTCCAGCTCCTCC | 75725 |
rs33375653 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Phf14 | Mm_Celera | 6:12015122 | AGTTTATTGGCACAG[C/T]CCTGTACATATAAGA | 75725 |
rs33376014 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12004463 | AAGATGTATTTGTTG[A/C]CATAGTAAATACAGT | 75725 |
rs33376016 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12004511 | ACAGTCTTTACTGAA[C/T]CCTTCTTTCTTGTAG | 75725 |
rs33376018 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12004750 | ACCGCTCCAGTGGTA[A/G]TCTTTAATTGAGAGG | 75725 |
rs33376020 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12005016 | GTGATCTAAGTGGCT[A/G]ATAAAATTGTTCATA | 75725 |
rs33376022 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12005268 | AATCTTGAGTGTTTG[A/T]ATTGCACAGTGTAGT | 75725 |
rs33376154 | snp | A/G | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:11988964 | ATGATTTCTGTCTGA[A/G]ATACTTGCAGACCAC | 75725 |
rs33376156 | snp | C/T | 0.132653 | 0.220748 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:11988994 | CTGGCAGCCGCTGCC[C/T]ACTGAGAACCTATAA | 75725 |
rs33376158 | snp | C/G | 0.336735 | 0.234472 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:11989069 | TCTTTTGCTCAAATT[C/G]ATTGACCTGTCACTT | 75725 |
rs33376160 | snp | A/T | 0.132653 | 0.220748 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:11989254 | GAAGATGAGTTGCTT[A/T]TGGACATATTAACTT | 75725 |
rs33376162 | snp | C/G | 0.132653 | 0.220748 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:11989294 | AATAAGTACTTAGTA[C/G]ATTCAGAAAAGGAAA | 75725 |
rs33376315 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12028180 | TTTCATGTGGTTCTT[C/G]TCAGTTAACCAGAAA | 75725 |
rs33376317 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:12028373 | GATATCTCTTTGATT[C/T]ATCATATTTTAAGAT | 75725 |
rs33376319 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12028524 | TTATGGTTACAGTTT[A/T]AAAAGTGGGCTAAAT | 75725 |
rs33376321 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12028535 | GTTTAAAAAGTGGGC[A/T]AAATAACAGGATACA | 75725 |
rs33376323 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12028603 | TTTGTAAATAAAAAA[A/G]ATACAGTTTTAAGGA | 75725 |
rs33376465 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Phf14 | Mm_Celera | 6:12015228 | TCTTTAAGGAATGTA[C/G]ATATTATTTCTGGAA | 75725 |
rs33376468 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Phf14 | Mm_Celera | 6:12015535 | TTTTTGTTTTGTGGA[C/T]TTTGGTTTGGGTTGT | 75725 |
rs33376470 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12015871 | CTGTTTATTAAAAAG[A/G]ACTATAGTAGAAATT | 75725 |
rs33376472 | snp | C/T | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:12015876 | TATTAAAAAGGACTA[C/T]AGTAGAAATTTGCTT | 75725 |
rs33376646 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Phf14 | Mm_Celera | 6:11951855 | TGAGGGTTTTTTGAT[A/G]TTCATGTTTTGAATG | 75725 |
rs33376648 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11953672 | TACTGGGAAGAAGCA[A/C]ATGGTAGTTCCTCAG | 75725 |
rs33376650 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Phf14 | Mm_Celera | 6:11954583 | CAGTGCCCTGCTCTA[C/G]TGATGGCAGAATCAC | 75725 |
rs33376652 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11955478 | CTTGAGAAGTGTAGT[C/T]TCAGTAGATTGCTAG | 75725 |
rs33376804 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12006151 | ATAAAACCTAAGTGG[C/T]AGCTTGTGTCTTATC | 75725 |
rs33376806 | snp | A/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12006307 | CCTTCTTTCAAATGA[A/T]ATACAAATACAATCC | 75725 |
rs33376808 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Phf14 | Mm_Celera | 6:12007101 | AGATAATGAGAATCT[C/T]GTCAGGTAAATTGAA | 75725 |
rs33376810 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12007243 | TTTAGTGAGAATGCT[A/G]CTTTGGAAATACATT | 75725 |
rs33376812 | snp | A/C | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008130 | TGAGTTGTAAAGTTA[A/C]TAGGTTTGTTTTTTT | 75725 |
rs33376864 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11989335 | CTTGCAGATCTAGCA[A/T]TTGTTTTGTCTGGGT | 75725 |
rs33376866 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11989450 | AGGATTGAAAATTGC[A/C]TTGTGTGAAGGCAAT | 75725 |
rs33376868 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11989513 | TTCCAGTTGACTGAA[C/T]AGATGTGAGCTCACC | 75725 |
rs33376870 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11989658 | ACGATAATTTCTCTA[A/T]TTAACCTATGGAACA | 75725 |
rs33376872 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Phf14 | Mm_Celera | 6:11989800 | TCAAGTGGAAGTAGT[A/G]TAATTTTCATGAAGT | 75725 |
rs33377034 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12068038 | AAATGGTACCAAATC[A/C]GTGTTGACTTAACCG | 75725 |
rs33377036 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12068325 | TGGAGTTGTCATGTG[C/T]CCAGTGCTTTTCCAT | 75725 |
rs33377038 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12068343 | AGTGCTTTTCCATAA[A/T]ACATAGAGGAAGGTG | 75725 |
rs33377040 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Phf14 | Mm_Celera | 6:12068401 | ATTCAGCAAAATACT[C/T]AATAAAATCCTCAGG | 75725 |
rs33377042 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12068712 | AACAAGCGTATTGTC[A/G]GCGTTCTATACAGCC | 75725 |
rs33377085 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Phf14 | Mm_Celera | 6:12028652 | ATTATAGTTTAATTT[G/T]CTGAAAACAGTACAG | 75725 |
rs33377087 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12028973 | CAGGCACCCATTAAC[A/G]TTAAAAAGCCTTTGG | 75725 |
rs33377089 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:12029046 | AAGGCTACAGTGGAT[A/T]CTAGTAATGTAAAAG | 75725 |
rs33377091 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12029124 | AGGGTCCTGTAGAAC[A/G]CAGATTGTCACACTA | 75725 |
rs33377093 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12029193 | TCACTATTTCAGCCA[C/T]GCTGGGAGTTGGTAA | 75725 |
rs33377284 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12039018 | AAGAGGAGGCAGCTC[A/G]GTGTTCAAAAAGTAA | 75725 |
rs33377286 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12039034 | GTGTTCAAAAAGTAA[A/C]GTATTCACTTGTAAT | 75725 |
rs33377289 | snp | A/T | 0.32 | 0.24 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12039289 | TTATAAGTGTGATTT[A/T]AAAATGTGGATAAAA | 75725 |
rs33377291 | snp | A/G | 0.375 | 0.216506 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12039854 | TGCGAGTATTCACAC[A/G]TGAGAACAACCCTAG | 75725 |
rs33377293 | snp | A/C | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12040915 | AGTGTTAACCAAAAG[A/C]CCTTCTACAGTGGTT | 75725 |
rs33377314 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Phf14 | Mm_Celera | 6:12015946 | AGCTGATTTTAAAAA[C/T]AATGAACATGACTTA | 75725 |
rs33377316 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12016079 | AACAGTTTCCAGGCA[G/T]GTAACACATTTATCC | 75725 |
rs33377318 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12016241 | ATTTTGTTCTCATTT[C/T]CTTGTGTAATCTTAC | 75725 |
rs33377320 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12016572 | TTTTTGACACAAAAT[A/G]TTGCAAAATGATTTA | 75725 |
rs33377322 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12016743 | TAAAAGTGTGTACTT[A/C]TTTTTCTCTTTTATA | 75725 |
rs33377464 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12058671 | TACTTAAATACGGTG[A/G]CTTAACTGCCATTAT | 75725 |
rs33377466 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12058876 | TTTTCCTTCTACCTC[A/G]GGCCACACAAAATTG | 75725 |
rs33377468 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12058969 | TTCCAGCCTGATTCC[A/G]AGCTTGTTTAAAGCT | 75725 |
rs33377470 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12059264 | ATTTTGCGTTTTTTC[A/G]TATTTTAAAGACATT | 75725 |
rs33377472 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Phf14 | Mm_Celera | 6:12059740 | TCTTTCTCAGATGTA[A/G]GCTGAAAGGATTTTG | 75725 |
rs33377534 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11955690 | AATAGTTTGTGCTTT[A/C]AAAATGTTTTGCCCA | 75725 |
rs33377536 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11955788 | ATAACCTCATGACTA[C/T]ACCTTAGTTTGGTAG | 75725 |
rs33377538 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11958650 | ATACCTTTTCATGGG[C/T]CATCTGAAAAATTTT | 75725 |
rs33377539 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:11960331 | TTTATCAGAGGTAAA[C/G]TCCTGTAGAGAAAGG | 75725 |
rs33377541 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Phf14 | Mm_Celera | 6:11960364 | GCGTTTAATACATCA[C/G]TGCATGAAGAGAAGA | 75725 |
rs33377543 | snp | C/G/T | 0.132653 | 0.220748 | intron-variant | Phf14 | GRCm38.p3 | 6:11960391 | AAGAGGCTACACAGA[C/G/T]TACATTGAGAAAGTT | 75725 |
rs33377584 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009306 | TACTTAATATTTGTC[A/G]GTTTGTCTGGCATCT | 75725 |
rs33377586 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009324 | TTGTCTGGCATCTCA[C/T]TTATTTTGGAATTGG | 75725 |
rs33377588 | snp | C/T | 0.32 | 0.24 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009591 | AGCTAAGTCAGCAGG[C/T]TACTTACTATACTAA | 75725 |
rs33377590 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009684 | TATAATCCCTTTGCT[A/G]TAGAGGAAGAGACAA | 75725 |
rs33377592 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009840 | AATGAGAGAGAAATA[A/G]GATTATCAAGGTTAT | 75725 |
rs33377674 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12079749 | TTCAGATGTCAGTTG[A/G]TAGAAAATAATCTAC | 75725 |
rs33377676 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12079824 | GTAGTTGTTGGAAAA[G/T]TAGTCAAAATTGTAT | 75725 |
rs33377677 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12080195 | TAAAGATACTTGAGA[A/G]TTTCTGCCTATGCTT | 75725 |
rs33377681 | snp | A/G | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12081583 | CTAAAAGAAACCTCT[A/G]GGAATATGTAATTCA | 75725 |
rs33377683 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12081704 | CCCAGTATTCTGATT[G/T]GCTTTCCTGTTCCTA | 75725 |
rs33377724 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Phf14 | Mm_Celera | 6:11990559 | TAGTGATGAATGGTA[A/G]TGTATAAAGATGATG | 75725 |
rs33377726 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11990630 | GCTTAGCTACAATTA[G/T]TTCATTTCCAGACAT | 75725 |
rs33377728 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11990738 | CTCTAAATAAAAAAG[A/G]CCTCATTTCTATATT | 75725 |
rs33377729 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11991228 | CTCTCAGACAACTTT[C/T]CTATCATTCTGTACA | 75725 |
rs33377731 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11991982 | CTTGCTGCTTTTATT[A/G]AAGTTGTGGAATTTG | 75725 |
rs33377733 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Phf14 | Mm_Celera | 6:11992462 | CCAGAAACTTTGAAA[A/G]CTTTTTTCTTTTTTA | 75725 |
rs33377894 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12068743 | TTGCAGAAATCAGCC[A/T]CTTATTAAATATTTA | 75725 |
rs33377896 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12068912 | GCTAGTTATATTTCT[A/G]CCTGAATTTTTTTAA | 75725 |
rs33377899 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12069570 | AATCATCCTTACATG[A/T]GCTTATTTTAGGCCC | 75725 |
rs33377901 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12069629 | AAAGTCATTTTACTC[A/G]GAAGCTGGTCCTTGC | 75725 |
rs33377903 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12069677 | CCTCTGCTTCTCCTA[C/T]GTGTATGTTCTCTCA | 75725 |
rs33377935 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Phf14 | GRCm38.p3 | 6:12032466 | GTTTTTCAAACTATC[A/T]AAAATTCAATACATA | 75725 |
rs33377937 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12033184 | GGATGGCCTTTCCTT[A/G]GGAGACACTTTTTAA | 75725 |
rs33377939 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12034776 | CAGGTCGGGTGTTTT[C/T]CCTTGCCGTGCCTCA | 75725 |
rs33377942 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12034850 | CAAAGCAGCCTTGAA[A/T]GCTTATTGAACATTT | 75725 |
rs33378205 | snp | C/G | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:12050396 | GCATTGGTATTTTTC[C/G]TGTATGCACGTCTGT | 75725 |
rs33378207 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Phf14 | Mm_Celera | 6:12050898 | ACATAGCAAGACTGC[A/G]TTTATCAAAATAGAC | 75725 |
rs33378209 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12050902 | AGCAAGACTGCATTT[A/T]TCAAAATAGACCAAC | 75725 |
rs33378211 | snp | A/G | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:12050912 | CATTTATCAAAATAG[A/G]CCAACAATAACAACG | 75725 |
rs33378236 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12017058 | CATTAGAAATAAATG[C/G]TTTCATCTTGTCCTA | 75725 |
rs33378239 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12017248 | TTTGAAAAAATGAGA[A/G]TGTTATATGTGCACA | 75725 |
rs33378241 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12017311 | CAGATGTGCTTGATT[A/G]TGCATCCTTTTATCT | 75725 |
rs33378243 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12017382 | CATAAGTTGGAGTAG[C/T]CCAGCCCCAATGCCA | 75725 |
rs33378284 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Phf14 | Mm_Celera | 6:12059764 | GATTTTGACTTCCTC[A/G]TGTACCTGAACTGAG | 75725 |
rs33378286 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12059934 | TCAGAATTCCAAACT[A/G]GGGACTAGACAGTGT | 75725 |
rs33378288 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12059948 | TGGGGACTAGACAGT[A/G]TAAGTAATTTACATG | 75725 |
rs33378290 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Phf14 | Mm_Celera | 6:12060182 | GTGCCACAGACTGAG[A/G]CCAGCACGAAACCAC | 75725 |
rs33378292 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12060273 | GGAAAAACTGTTAAG[C/T]ATCACTGACATAAAT | 75725 |
rs33378344 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010412 | TATTTAGATTGCCCA[C/T]TTGCTGATGCCGTTT | 75725 |
rs33378346 | snp | A/G | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011110 | GCATGCAGATAGGAA[A/G]TAATCTGTGAAGCTA | 75725 |
rs33378348 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011217 | ATACTGATCCATTTT[A/G]GATATAAGGTTAGCT | 75725 |
rs33378350 | snp | C/T | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011339 | TGCATCATTAAACTA[C/T]TAGGGATACCAGCAA | 75725 |
rs33378352 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011401 | ATTAGTCTCTAATGA[A/G]TCTGAGTATTTAGAT | 75725 |
rs33378385 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11960461 | GGACGCATAGGGGAG[A/G]TTAGATTAAAATGTT | 75725 |
rs33378387 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11960631 | AAACTAGGATAAAGC[A/G]AAAGTTGTCAGTATA | 75725 |
rs33378389 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11961008 | TTTTCTCAACCACCA[A/G]CAAAAGTTAAACTTT | 75725 |
rs33378391 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11961275 | GACCAAAGTGCAGTG[A/G]ATCTTAAGTGGAAAG | 75725 |
rs33378393 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11961321 | ATCTACAGTTTGGCT[C/T]CTTGAAAAGTAATGC | 75725 |
rs33378585 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Phf14 | Mm_Celera | 6:11992625 | GGTGTAATGACTCAA[A/T]CTGTAGAGTTTGTTG | 75725 |
rs33378587 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:11992638 | AAACTGTAGAGTTTG[C/T]TGTGTTAGTAAATAC | 75725 |
rs33378589 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11993072 | CAAGGAAGAAACAGA[C/T]ACTCAGATTTTCTTA | 75725 |
rs33378590 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11993500 | ACAGAATGTTGTGAT[A/G]ATGAGTATTAACTAC | 75725 |
rs33378592 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11994918 | CTTATTCATTTAGGA[C/G]ACAATGACATTATGT | 75725 |
rs33378715 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12071305 | TGTGGAAAACAAAAA[A/G]TTATTTAAATTACAA | 75725 |
rs33378717 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12071685 | CTGCTTAAAGAGACC[A/G]TTGGTTAAATGATGC | 75725 |
rs33378719 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12071905 | TGTTTGTTCCTGATA[A/C]TAAAGTACAACTATA | 75725 |
rs33378721 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12072035 | AGATATGTTACTTGG[A/G]AATCTAATGAGCTAT | 75725 |
rs33378785 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12082077 | GGAAATGCTCAGGCA[A/T]GCAAACACTGACAAC | 75725 |
rs33378787 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12082099 | ACTGACAACCAGCCA[A/G]TGCCACAGGAAATGC | 75725 |
rs33378789 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12082492 | TTAAAAACAAAAACA[C/G]TCTCTCTGTGTGTCC | 75725 |
rs33378791 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12082547 | CCCTTTCTGACCCTC[A/G]TGTTTATTAGTGTGT | 75725 |
rs33378792 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12082923 | AAACAAGAAGTTTAC[C/T]GAAGGGTAGCTTCTA | 75725 |
rs33378844 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12034875 | ACATTTTAGGACAGA[C/T]GAGAGCTTATAGCAC | 75725 |
rs33378846 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12034934 | CTTTCCATCACTGTT[C/T]TTAAACATTTTTCAA | 75725 |
rs33378848 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Phf14 | Mm_Celera | 6:12035277 | TGTTCACTTACCATG[A/T]CCTTTCCCTAATTTT | 75725 |
rs33378851 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:12035875 | AAATCATGTTTTCAA[A/G]TACATTTAACAGTGA | 75725 |
rs33379084 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12060311 | ATCTTGGCCATTTCT[C/T]TAATATTGCCTTATT | 75725 |
rs33379086 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12060374 | TTTGTGTTCTGTACA[A/G]CATGCACTGTGGAAT | 75725 |
rs33379088 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12060799 | TTAGTCAGAGAGCCA[A/G]AGAAAGACTATAATC | 75725 |
rs33379090 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12060894 | CTTTGACACATGCAT[A/T]CATTAAGTCCAAGCC | 75725 |
rs33379092 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12060908 | TTCATTAAGTCCAAG[C/T]CTCTATAAGCTTCCT | 75725 |
rs33379127 | snp | A/G/T | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:12051834 | GTTAAGATATGGGTA[A/G/T]TTTGTTTACTCTAGT | 75725 |
rs33379129 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12052269 | AGGGCTCAAATTTCA[C/T]GACAGTGCTGTGATC | 75725 |
rs33379131 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Phf14 | Mm_Celera | 6:12052398 | AAGCAATATCAATGT[A/G]AAACACAATTTCCTG | 75725 |
rs33379133 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12052767 | AACATTAGAGGAAAC[A/G]TACAAATCATTTTTT | 75725 |
rs33379146 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12017643 | TGACATAAGCACTTC[A/G]TTAATAATGTGTTTT | 75725 |
rs33379148 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12017940 | ATTACTCTAGTTTAG[A/G]AAACCAGACAAGTTA | 75725 |
rs33379150 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12018140 | TATTTCTATTGATTG[C/T]GTTCCGTGTGCATGG | 75725 |
rs33379152 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12018169 | GGCACTGTGTTCCAC[A/C]AGGTCATTTCCATCC | 75725 |
rs33379165 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:11961412 | TTTTTAGTTAGGCGT[C/T]TTGAGGATTTTTTAA | 75725 |
rs33379167 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11961455 | CATAGAATGCTTTCA[A/G]AACTATTTTAAGGTG | 75725 |
rs33379168 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Phf14 | Mm_Celera | 6:11961973 | GTTTCTCCAGAGGCT[A/G]ACTTATTGATTAGTC | 75725 |
rs33379169 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Phf14 | Mm_Celera | 6:11962108 | TCTTACAACTTTAAT[C/T]TTAAAATGGATTTTA | 75725 |
rs33379170 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Phf14 | Mm_Celera | 6:11962812 | TATTCCCTCATTAAC[C/G]ACTGGGTGCTGGTAA | 75725 |
rs33379171 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Phf14 | Mm_Celera | 6:11962824 | AACGACTGGGTGCTG[C/G]TAACAGTGTTCAGAA | 75725 |
rs33379173 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11962944 | ATGCCTGAGTCTGGT[C/G]AGTCTTTAGACTAGA | 75725 |
rs33379184 | snp | A/G | 0.32 | 0.24 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011535 | GTGAACCTAAATTTG[A/G]CTGTCATTTTGTTAA | 75725 |
rs33379186 | snp | A/G | 0.277778 | 0.248452 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011791 | TCTCATATCAAAATT[A/G]CTATTTTTATTGAAT | 75725 |
rs33379188 | snp | A/G | 0.152778 | 0.230321 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12012004 | ATAAAAGGCAAAGCA[A/G]AAGTGCTATAGCTAC | 75725 |
rs33379190 | snp | C/T | 0.165289 | 0.235211 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12012011 | GCAAAGCAGAAGTGC[C/T]ATAGCTACATATCTT | 75725 |
rs33379192 | snp | A/T | 0.375 | 0.216506 | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12012049 | TTTATTTCCTATAAT[A/T]CATATCCTGAAACTA | 75725 |
rs33379464 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Phf14 | Mm_Celera | 6:11996320 | GATTAAAGAGTAAAA[A/G]TAAGCTTAATCTAAG | 75725 |
rs33379466 | snp | A/G/T | 0.132653 | 0.220748 | intron-variant | Phf14 | GRCm38.p3 | 6:11996366 | TATCAAAAATAAAAA[A/G/T]TTTGATAGAATGAAT | 75725 |
rs33379468 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11996478 | AAAATAATTTAATAT[A/T]CTACAAACCAGACTT | 75725 |
rs33379470 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11996872 | ATTCTTACAAGAGTA[A/G]AGGTATCTTTCTGTT | 75725 |
rs33379472 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11997247 | AATGTAAAAACTTTA[A/C]GCAGATAAAAGGTTT | 75725 |
rs33379473 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11997299 | AAGTCAATCAAGTGT[C/T]CATATTGCTCTTAAG | 75725 |
rs33379574 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12072315 | GAAAGTGTCTGGTGC[C/T]GTAGCCCAGCTTTGT | 75725 |
rs33379576 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12072437 | AGTCGATGGAGTCCT[A/G]TCTGTACGTCCTGTC | 75725 |
rs33379578 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12072502 | TTTAGAAGGACATTT[A/G]CGACATCTTCACATA | 75725 |
rs33379580 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12072602 | CCTGATTCAGGGTAT[G/T]AAAGTAAAATGTCAT | 75725 |
rs33379582 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12072715 | CGCTTGTCATAATAC[A/C]GTTAAATCATGTTCT | 75725 |
rs33379604 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12082974 | AGGAGCTCACACTTA[C/G]AAAGCACCCTCCCTG | 75725 |
rs33379605 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12083139 | CAGATTGGTATATTA[C/T]CAGGTTTTTGGTGAT | 75725 |
rs33379606 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12084763 | GGATAGAATGGTGCT[C/T]GTAATGAACCAACTA | 75725 |
rs33379607 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12084806 | ATTGTTTGTCTGTGA[A/C]ATCCCAGAAGAGCTT | 75725 |
rs33379609 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12084990 | TTAGTCAAAAATTGT[A/G]TGATGTCTCTTTAAA | 75725 |
rs33379611 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12085805 | TTTCTTTCCCACAAC[A/G]CATTCTCTCCCTCAC | 75725 |
rs33379613 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12085847 | GTGTTAAGGATCATT[A/G]CAACAGTATCTGTGG | 75725 |
rs33379834 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Phf14 | Mm_Celera | 6:12036478 | GTTACTGTTAAAATG[A/G]ATTACCTTGAATTAA | 75725 |
rs33379836 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Phf14 | Mm_Celera | 6:12036557 | AAAACAAAACAATAT[C/G]CAAATCAGACAATAA | 75725 |
rs33379838 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Phf14 | Mm_Celera | 6:12036582 | CAATAATCTGGAAAT[G/T]CATATCTGACCATTC | 75725 |
rs33379840 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Phf14 | Mm_Celera | 6:12036676 | GAGGGATAGTCAAGT[C/T]TCTTGTGGTATGTAA | 75725 |
rs33379842 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Phf14 | Mm_Celera | 6:12036732 | TCTCTCCAAGGGCGC[C/T]ATCGTGTTTTCTCTT | 75725 |
rs33379945 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12061058 | ACAGACATAACTTAC[C/T]ACCTTTATTATCTTG | 75725 |
rs33379947 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12061382 | ACTCAAGCAACCCAT[C/T]TAGGCACAAATAAAT | 75725 |
rs33379948 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12061473 | TTCTTTTACCTTCAG[A/C]CCAAGTTTTAAAGTT | 75725 |
rs33379950 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12062158 | CTTTGAAGAACTGAG[A/G]ATGACAAGACAGGAA | 75725 |
rs33379952 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12062199 | TAACAGATGTCTCTA[A/G]GATACTACCTACTGC | 75725 |
rs33380024 | snp | C/T | 0.152778 | 0.230321 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12012129 | TATTCCAAATCTAGA[C/T]TGAATCATAAGGGAT | 75725 |
rs33380026 | snp | A/C | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12012171 | AAATGAAGGTTTATA[A/C]TTATGACCGCATAGT | 75725 |
rs33380028 | snp | C/T | 0.277778 | 0.248452 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12012462 | CAGCTGCTCTGTCTC[C/T]GATTATTCTAGGACA | 75725 |
rs33380030 | snp | G/T | 0.277778 | 0.248452 | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12012595 | AAACACCTCTGTTGA[G/T]CTGTAATTTTCATCC | 75725 |
rs33380032 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Phf14 | Mm_Celera | 6:12012883 | ATAAATGTGATGATG[C/T]AATGCCAGATTAGGT | 75725 |
rs33380054 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12019437 | AAGATTGTCTCTGGT[C/T]ACCCCAACTTATATA | 75725 |
rs33380056 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12019591 | ATCACCTATTTCAGC[A/G]TTTACAAAGAGTACT | 75725 |
rs33380058 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12019632 | TTTGGCTCAAAAATG[C/T]TGTTTTGGGGTAGGA | 75725 |
rs33380060 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12020074 | AAAAGAAAATAGAGT[A/G]ATTGAGGAAGGCACA | 75725 |
rs33380062 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12022290 | GCCCTAATTTAATAC[A/G]AAGAGACCATGGATT | 75725 |
rs33380065 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12052998 | GGTGTGCAAGCCTGA[C/T]GAAGTAGACTCTATC | 75725 |
rs33380069 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12053858 | GAGAGTGTAAAATTG[A/G]AGGAATGTGTACAAG | 75725 |
rs33380071 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12054984 | TCATATAACAAGTTG[C/T]GAGTACAGGTATTAA | 75725 |
rs33380073 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12055405 | TGTCCTTGTTTTTAT[A/C]TCAGGAAAAATGCCA | 75725 |
rs33380285 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Phf14 | Mm_Celera | 6:11997467 | GCCTCCCTCAGCAAG[C/T]TTACCTGTCGAGGTT | 75725 |
rs33380286 | snp | C/G/T | 0.132653 | 0.220748 | intron-variant | Phf14 | GRCm38.p3 | 6:11997553 | GTGTGCTGTGTGCTC[C/G/T]TGAACAGCATTTCCT | 75725 |
rs33380287 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11998681 | TGTTGTGGCTCAGGA[A/G]GTGTCAGGACCCATT | 75725 |
rs33380288 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:11998884 | GACGTTTCTGGAATG[C/T]GAACAAATGTCTGTG | 75725 |
rs33380289 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11999026 | GACCTCCCATAACTT[C/T]GTCTTGCATGTTCTA | 75725 |
rs33380290 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11999859 | TGGATAAGATATAGG[A/G]GTAAAAGCAAGTTTG | 75725 |
rs33380292 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Phf14 | GRCm38.p3 | 6:11999862 | ATAAGATATAGGGGT[A/G]AAAGCAAGTTTGGAA | 75725 |
rs33380305 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11977861 | TGTTAAAATGGAGGT[A/G]TTATTTATCCCGTTT | 75725 |
rs33380307 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11977873 | GGTGTTATTTATCCC[A/G]TTTGTACACATGTAC | 75725 |
rs33380309 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11978157 | AAGTTGGATGTCATA[C/T]TTTTATAGAGCTACT | 75725 |
rs33380311 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11979280 | AGATTAAACTGCCAG[C/T]TGATGCATTAGCTAG | 75725 |
rs33380313 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11979311 | AGGAATGACAAAGTT[G/T]CCTCCCAGACTTGCA | 75725 |
rs33380464 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12072774 | AAATACATGACATGA[A/G]CTTCATTGGTGAAAT | 75725 |
rs33380466 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12072800 | GAAATATTTCTCAAT[A/G]ACTTTAATTTTCTGG | 75725 |
rs33380468 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12072890 | AAGAGTGAAGGAGTC[A/G]AGAAGGAGTGGCCCT | 75725 |
rs33380470 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12072946 | TAAGAACGAAGTATC[A/T]TTTCTTTGGAGTGTT | 75725 |
rs33380472 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12072962 | TTTCTTTGGAGTGTT[C/T]GCTGCTCATTTGCCT | 75725 |
rs33380605 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12085932 | TATGGTCTATGAGTT[A/C]ATTTCTACAGGTTAT | 75725 |
rs33380608 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12086031 | CAGTGTTAAGTACCA[C/G]AGCGCTGAGGCAGCC | 75725 |
rs33380610 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12086111 | CATGAAAACCTAGCC[A/C]ACAATTCCTAGAAAC | 75725 |
rs33380612 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12086342 | GCTGGCAAATGGAAG[C/T]TGCTAGATACAAGTT | 75725 |
rs33380634 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12036769 | TTCAATTCTTAAAAC[C/T]CCAAGACAAATTTAA | 75725 |
rs33380637 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Phf14 | Mm_Celera | 6:12037430 | TCCCGGTGTGAATTG[C/T]TTAGTATTAAGAGTT | 75725 |
rs33380640 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:12037903 | ACTCTTTGATTTTAA[A/G]ATACTGCAGCCTTTT | 75725 |
rs33380642 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Phf14 | Mm_Celera | 6:12038138 | CATGTATTTTCATCA[C/T]ATTTCCATGGATGCA | 75725 |
rs33380844 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12022321 | TCTTTTCATGGCTCA[A/C]TTTGACTTCTTTATG | 75725 |
rs33380846 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12022357 | TATGCATTCTAAGAT[A/G]TATCCTTTTTGCATT | 75725 |
rs33380848 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12022387 | TCATCAGAGCATTCC[C/T]GAGCCTTTCTAATTT | 75725 |
rs33380850 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12022443 | TTTCTTATGTCACAA[A/G]TACCAGAAGAGACTA | 75725 |
rs33380852 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12022492 | AAAGTTTCACATAGC[A/C]GAATAGACTTAGTTG | 75725 |
rs33380864 | snp | A/G/T | 0.152778 | 0.230321 | intron-variant | Phf14 | Mm_Celera | 6:12012916 | TGATAAACATTCCCC[A/G/T]TGTACTAATTAGAAA | 75725 |
rs33380866 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12013008 | CAGGCAATGTTATTA[C/G]TACTGAGATGGTTTT | 75725 |
rs33380869 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12013217 | ATTTGTGGGTCAGGG[A/C]TAGGAGAATAATTGT | 75725 |
rs33380871 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12013248 | TAGAGACCAGTCTGA[A/G]TTACTAGTCCCATAG | 75725 |
rs33380873 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12013490 | CTACAACCTTATTCT[C/G]TTAAGCAAGCTATTT | 75725 |
rs33381045 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12055464 | GTTCCCATCAACAAG[A/G]TGTATTCCTTTTTCT | 75725 |
rs33381047 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12055625 | TCTCTCACTTTCTCT[C/T]GTCTATGCTTTGGTA | 75725 |
rs33381049 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12055626 | CTCTCACTTTCTCTC[A/G]TCTATGCTTTGGTAT | 75725 |
rs33381052 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12055807 | ATGGTAGATGACATC[A/C]TAGAGGCAGAGACTC | 75725 |
rs33381145 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:11979324 | TTTCCTCCCAGACTT[A/G]CATAGGAGTTCACAA | 75725 |
rs33381147 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11979383 | TTACTAATTTAATAA[A/C]AACTGAAAGGAAGAC | 75725 |
rs33381149 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11979675 | CAGCTTCAGGATAGA[C/G]CTCTTCATTCTCAGA | 75725 |
rs33381151 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:11979744 | TTAAGAAATCACAAC[A/G]TTAATCATGTTATTA | 75725 |
rs33381153 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:11979886 | AAAAGGTATTGTGAT[A/G]GATAACAATGTTATC | 75725 |
rs33381164 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12073024 | AGGAGTTGTACAGTG[G/T]TATAGCAAGCTTGTA | 75725 |
rs33381166 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12073266 | GATTGGCACTTGGTT[A/G]TTTTATACAGTGTCT | 75725 |
rs33381168 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12073838 | GAAAGTAAAAGAGGT[C/T]CCCATACATAATCAT | 75725 |
rs33381170 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12073898 | TTTCAGTCTGAGGTA[A/G]TTTTTGCAGTGAGTA | 75725 |
rs33381173 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12074130 | TATTAGCTATAAACA[C/T]ACATAAACCTGAGCA | 75725 |
rs33381175 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12062399 | CCTTGCTGTGTTCAG[C/T]TTTATTCTATCCTGT | 75725 |
rs33381177 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12062430 | TCTATGTCTCCTTTA[A/G]ACATTCACAACTTAC | 75725 |
rs33381179 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12062538 | TCAGTAGGTTTCCAG[A/G]TATATTAATATAGAA | 75725 |
rs33381181 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12062714 | TATATTGACTGCAGT[C/T]CACCAAAACCTAATT | 75725 |
rs33381183 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12062988 | TGTTGCCTACTAAAA[C/T]TTAAAAATGATGTTT | 75725 |
rs33381514 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11999947 | GTGGCTTCCCGATTC[C/T]CGGACATTCTGCTGT | 75725 |
rs33381516 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12000982 | CAAATAGTCACTGTT[A/G]AACTTCCCTTTTAAC | 75725 |
rs33381518 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12002509 | TATTCCTAAACTGAT[A/G]ACTTGCAGTATGTAA | 75725 |
rs33381520 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12002546 | ATTATCAGTGAAACA[C/T]TGTTGCAAGTATTCT | 75725 |
rs33381584 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12055925 | TGCCATCCCCTGCTT[C/T]TGGAAACAGTGCTGT | 75725 |
rs33381586 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12055937 | CTTTTGGAAACAGTG[C/T]TGTTAATGGCCTAAA | 75725 |
rs33381588 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12055943 | GAAACAGTGCTGTTA[A/C]TGGCCTAAAGACCTT | 75725 |
rs33381590 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12056051 | CGTAGCCTGCAGCTT[A/C]AATCCTGGTTTCTCT | 75725 |
rs33381592 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12056109 | TAGCCTGCTTCTTTT[G/T]TGAGGCCGTTCATCT | 75725 |
rs33381596 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12013795 | ATTTAATGGCACGTA[A/T]TTTATTAAAGTTGCC | 75725 |
rs33381598 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:12013808 | TAATTTATTAAAGTT[G/T]CCATTTAGGTAAAGT | 75725 |
rs33381601 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Phf14 | Mm_Celera | 6:12013910 | CTGTGGTTCTTCTGC[C/G]TTAGAAAAAGTGCAT | 75725 |
rs33381603 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12013970 | AAAGCTAAACTTTAG[A/C]GCGGCAAATAATTAA | 75725 |
rs33381614 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12022593 | TCCTTCTGTGGGATT[A/T]GTCATTTCACTCCTT | 75725 |
rs33381616 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12022601 | TGGGATTTGTCATTT[C/T]ACTCCTTCAATTTTG | 75725 |
rs33381618 | snp | A/G | 0.5 | 0 | intron-variant | Phf14 | Mm_Celera | 6:12022743 | TGTGTATACGTGTGT[A/G]CAAATGGATGTGTAA | 75725 |
rs33381620 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12023065 | GAGGAAAGAATGGAG[C/T]AAGGCATTTCAGAAG | 75725 |
rs33381622 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12023268 | TCCCCATGTTAGTTT[A/T]TTCTAATTTATTTTG | 75725 |
rs33381635 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:12086542 | AATCTGGGAACATGA[A/G]CACATCTATGTGTAT | 75725 |
rs33381636 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12087073 | TGTAGTTTTGAAGTC[A/G]CACAGCCTTGTTATA | 75725 |
rs33381637 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12087087 | CGCACAGCCTTGTTA[C/T]ATTCCCTGATTTATC | 75725 |
rs33381639 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:12087721 | TTTTGGAACTATACT[A/G]AAAGTAATAACAATA | 75725 |
rs33381641 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12087966 | CTACATCATTTCAAA[A/C]AATTAAAGGATCTTT | 75725 |
rs33381674 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12038191 | AAGTAATTCCAAAAT[C/T]CGTTTCAGTTTTCTG | 75725 |
rs33381676 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12038207 | CGTTTCAGTTTTCTG[C/T]TAGTCTCCATTACTT | 75725 |
rs33381678 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12038225 | GTCTCCATTACTTTG[C/T]ACATAATTGCAAGTG | 75725 |
rs33381680 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12038253 | GTGAAATATGCTTAC[A/T]TTATAAATGCTTACT | 75725 |
rs33381682 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12038284 | CCCTTTAGAATATGC[G/T]TTAGCTGTGTGGCTT | 75725 |
rs33381786 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12063109 | GTTATGGTTTGAATA[A/T]TTAAATAGCAGCAAT | 75725 |
rs33381788 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12063266 | TACTAATAAAGCTTA[G/T]GAAACACAAACACAG | 75725 |
rs33381790 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12063384 | TGACCTTTTCTGTTC[G/T]TACAGTAGTATACAT | 75725 |
rs33381955 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12074486 | ATTTTCACCAAGAGA[A/T]TCCAATGGTACTCCA | 75725 |
rs33381957 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12075065 | AATACTATAGAGAGT[C/T]AAAACTAATGCATGC | 75725 |
rs33381959 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12075567 | TTTAAAAGATACACA[A/G]CTTACTTCTTTAAAA | 75725 |
rs33381961 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12075631 | CAAATTTAAATTCTA[G/T]TTTAGTAACTATTCC | 75725 |
rs33382264 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12023682 | TTCGTCTTCTAACTC[C/T]GGCTAATAGATACAC | 75725 |
rs33382266 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12023709 | ACACACTTTATCTGA[C/T]TTTTGCTGGATCCTG | 75725 |
rs33382268 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12025425 | CATATAATAGAAATG[A/C]GCATTTTGTTCTGAC | 75725 |
rs33382269 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12025450 | TCTGACTTTTCATGT[A/G]AAATTTCCATGTGTT | 75725 |
rs33382270 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12025567 | ACTAGACTATAACTC[A/G]TGTTCTGTCGATTTA | 75725 |
rs33382272 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12026010 | GTCCAGCATTCCTGG[A/G]TGTGACTCTGACCTG | 75725 |
rs33382304 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Phf14 | Mm_Celera | 6:12056169 | GCATCGTTTATGCCC[A/C]AGTCATCTGTACTAA | 75725 |
rs33382306 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12056287 | GTCTACTTCTCCACA[C/G]CTAGCCTGATTCCTG | 75725 |
rs33382308 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12056391 | CTGAATTGTGCTTTA[C/T]AGGCCTTAGGCTATT | 75725 |
rs33382310 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12056478 | TGCAGAAAAGATAAA[A/G]GAGAAGAAAATACCT | 75725 |
rs33382312 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12056669 | TTTGCCTAAAAGTGT[A/T]TAGTGAATCTGGCAG | 75725 |
rs33382485 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Phf14 | GRCm38.p3 | 6:12014045 | TCATTTTGTGAATGA[A/G]CTTTGTAGATCAAAT | 75725 |
rs33382487 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Phf14 | Mm_Celera | 6:12014063 | TTGTAGATCAAATGT[A/C]CCTCACAAAAGTTGG | 75725 |
rs33382715 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12089368 | ACTTTGATATCTGCA[A/G]AGGAAGTCAAGCACT | 75725 |
rs33382717 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:12089447 | GTTTTTAGAAAACTC[C/T]TAATTTCCTAGTTAC | 75725 |
rs33382719 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12089614 | TAGACCATTGGTTTC[C/T]CAGCATGACACCTAT | 75725 |
rs33382721 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Phf14 | Mm_Celera | 6:12089776 | AGAGAATAAGCCCCT[A/G]CTTTCACCGCCACTG | 75725 |
rs33382723 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12090470 | TGTTTTGATTCTTAA[A/T]GGTGATTATATGTAA | 75725 |
rs33382795 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12064575 | TTAAAATGTTGTATC[A/G]GACCTAAGTTTATGA | 75725 |
rs33382798 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12064965 | CATTAGCGGCTGCTC[A/G]TGTATATTAGAAGTG | 75725 |
rs33382800 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12067060 | GGTTCTCAGACAAGC[C/T]AAAGTATCACAGTGG | 75725 |
rs33382802 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12067089 | GGCTTGTTAAGCTAG[C/G]CTAACATTTCACCTC | 75725 |
rs33382915 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12076857 | CCATTGCATTGAGTT[A/G]GTTTCTGCTTAAAAG | 75725 |
rs33382917 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12077241 | ATTAGGTGTTATGGG[C/T]GTTGCTGTCATAGGA | 75725 |
rs33382919 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12077294 | AGAAGTACGAGGTCA[C/G]TTGGAATCAATATGT | 75725 |
rs33382922 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12077575 | GTAGAAAGAAATGCT[A/G]TGCCGCAGCCTCCTT | 75725 |
rs33383124 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:12056715 | TGCACAACATTGTAG[A/T]GGAAGCTGTAGCCCA | 75725 |
rs33383126 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12056831 | TGTGGACATGCTCGC[A/G]CTTTCACATAATTTA | 75725 |
rs33383128 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12056876 | TACATGTTATTCATA[C/T]GCTGTGCTAAATCTT | 75725 |
rs33383130 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12057216 | CCACCAATGAACCAG[C/T]TAATGTCTAATTTGT | 75725 |
rs33383132 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:12057307 | TGTGTATGTAAAAGG[G/T]TTTTTTTTTGGTGAA | 75725 |
rs33383505 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12091060 | TCCTCTAAGAGCTTC[A/G]GCACCTCATGTATCT | 75725 |
rs33383506 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12093623 | TCAGCATTCATTCTC[A/G]CTGTACCTCCTGTAC | 75725 |
rs33383508 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12093700 | CCTGAACTATAAACC[C/T]AGCCGAGCTAATCAG | 75725 |
rs33383510 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12093985 | ATCTTGTGAATCCAC[A/C/G]CTCATTCTGAATATC | 75725 |
rs33383584 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12067370 | TCTGACAGTTTTCCC[A/G]TTGTTGCTCACTACT | 75725 |
rs33383586 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12067521 | AGATTGTTTAAAATA[A/G]AAAGTAGAAATCATT | 75725 |
rs33383588 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12067556 | CTCTGGTTATAGAAT[A/T]AAAATCACTTATCTT | 75725 |
rs33383590 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12067575 | ATCACTTATCTTCTA[A/C]CTTGTGCATCTGAGT | 75725 |
rs33383592 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12067735 | TTTGTTTTTACCATA[C/G]CTTGCACATGTTCTT | 75725 |
rs33383934 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12057636 | TTTTACTGGTACTTA[C/T]GTGGTTTAAAAAATT | 75725 |
rs33383937 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:12057873 | TATAGACATGTGGGA[C/T]CATTTTGCGAAATTC | 75725 |
rs33383940 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12058334 | GAACCCAGTTGTTGA[A/G]AAAATTGGGTAAGAA | 75725 |
rs33384044 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12078006 | ATAAGCAGAAGAAAA[A/G]CCAAGGCCAAGACTG | 75725 |
rs33384047 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12078683 | TTTGTTTGCCATGAC[C/T]TAAAGGATATGAATT | 75725 |
rs33384048 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12078996 | TTATCAGTGTTGTTA[C/T]TGTAAATCAAGATTG | 75725 |
rs33384050 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12079132 | AGAAAACATTGAGTA[C/G]ACTCCAATTCTATGC | 75725 |
rs33384052 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Phf14 | Mm_Celera | 6:12079664 | GGAAGGTAGAAAATG[A/G]AGATTTAATTTTTAA | 75725 |
rs33384464 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12067747 | ATACCTTGCACATGT[A/T]CTTGTATTTTTAGTT | 75725 |
rs33384466 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12067809 | GGTTTTTCCTCTTTG[A/T]TTTGGGTCTTACATT | 75725 |
rs33384468 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12067921 | CATAGGGTTTTTGGA[C/G]TTATTTGGAGCCAAA | 75725 |
rs33384470 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:12067950 | AAATATCATAATTGT[A/T]TTTCAGTATAATATC | 75725 |
rs33857026 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:12069193 | ATTTTACAACCTTAT[A/G]TGTTTCTTAATTATA | 75725 |
rs45656308 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11917531 | TTCAAGGCCTCAGGC[A/T]AGTTCATTCATGTGA | 75725 |
rs45665962 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11914784 | AAGGTCAGTACATCA[C/G]TTAGGGTCAAGCAGA | 75725 |
rs45759550 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11947027 | TCAGTAGTGCTCTGG[C/T]CCCTGTTTACTTAAT | 75725 |
rs45800666 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11947981 | TTTTAGAAACAACTA[A/C]AATGTCAGTCTGAAT | 75725 |
rs45819177 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11920767 | GAGAACACATGAAAA[G/T]AATCAGCTCATTCTT | 75725 |
rs45944546 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11911030 | TATAACTCAGTTCTC[C/T]ATCACTTGCTTAGTG | 75725 |
rs45982518 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11936866 | GTAACATTTTCAGAA[A/T]ACGGTTCTCAATTTC | 75725 |
rs46037569 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12041978 | GTGGGTTTAATGCCT[A/T]TAAGGGGCTCTTCCA | 75725 |
rs46187369 | snp | A/C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | GRCm38.p3 | 6:11947774 | TGTATACCTACACTT[A/C/T]TTCCTATTGTTTTGA | 75725 |
rs46216306 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11942099 | GATCTCACATGGAAG[A/G]TTTATTTGGGAGGGA | 75725 |
rs46227183 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11935288 | ACATGCTGTCTTGGC[A/G]TATTTATGGATATTT | 75725 |
rs46239067 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11919006 | ACCATTGGCTGACAG[C/G]CGTGAGAGATGCTTT | 75725 |
rs46430561 | snp | G/T | 0.375 | 0.216506 | intron-variant | Phf14 | Mm_Celera | 6:11933005 | AAATCAGTGGTACTA[G/T]GTTTAAGGTATATTC | 75725 |
rs46476322 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12048801 | GGTAAGCATGAGGAC[A/G]TAAGCACAGATCACC | 75725 |
rs46554990 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11913265 | CCCCATCAATGGCAC[C/G]CAAGATAAATTAGTG | 75725 |
rs46560321 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11936446 | ATTAAAACGTTATTG[A/C]AGACTTGGAGTATTT | 75725 |
rs46564270 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11939200 | TCACTTACCTCTGAC[A/G]TTCAAAAGAGCTCAT | 75725 |
rs46578850 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12066843 | GAGGATGTGGAACAT[A/G]GACACTCCTGCATGG | 75725 |
rs46596855 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11921791 | GAGGTGCAAAATCTA[C/G]CAGCAGCTGAGAGTC | 75725 |
rs46603032 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11929387 | AGCCATTGTGCCTAG[A/G]AGTAATCTAGCTGGA | 75725 |
rs46623056 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11940844 | TCGATATTTCTTGAC[A/G]TAAAAGTAAAGAGTA | 75725 |
rs46648624 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066679 | ACAGACTTCTCAACA[G/T]AGGGATCTCAAATAG | 75725 |
rs46668758 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11913998 | ATTCAGTCATTTGCT[C/T]ATGAGCATGTATTGG | 75725 |
rs46703867 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11910559 | TTACACCTTTGACCA[A/G]TGATGCAGGGTTCAA | 75725 |
rs46727387 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12066799 | CAGAATGGCTAAGAT[A/C]AAAAACACAAGTGAT | 75725 |
rs46754453 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11940966 | CTTGTATACTTTGGA[A/G]TCTAGAGTCTCTGAC | 75725 |
rs46773665 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12027580 | CTGATGGCAGGTTCT[A/G]TTCTCTCTATGTCTA | 75725 |
rs46811095 | snp | A/G | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12048311 | AATGTTTTTACAATT[A/G]GTGAGTAATTTAATA | 75725 |
rs46819621 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11911595 | CATTCTCCAATCCTA[C/G]AGAAAACAGACAGAC | 75725 |
rs46851388 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11940909 | TTTTCTGTTGTAGCT[G/T]ATGTGTTCAGGCTGT | 75725 |
rs47081349 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11931268 | GGTGTTACAACGTTG[A/G]GTTCTCACCAGGAAT | 75725 |
rs47096411 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11915045 | TCACAAATGACTCTA[C/T]CGCTCTTCTTACAAA | 75725 |
rs47152906 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12042118 | TAATAGAGCAACACT[A/G]CTTGCCCAAAGTGTC | 75725 |
rs47169149 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:11932004 | CTTCAAAACACTATT[A/G]AATAAGCTGATAGTC | 75725 |
rs47171754 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066728 | CATGTTTAAAGTCCC[C/T]AGTCTTCAGGGAAAT | 75725 |
rs47288184 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11916580 | AAAGGAGTATGGACT[A/G]TAGTTATCTGTGACA | 75725 |
rs47290267 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060550 | GGTTCTACATTTACT[A/G]TAAACCCTATGTAGG | 75725 |
rs47348451 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12077847 | TATCCTAGCAATTAG[C/T]CTGGAAATTTTTTTA | 75725 |
rs47424344 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11929986 | TACATGTTGTACCTG[A/C]TGTGTGACTGCCAGT | 75725 |
rs47497864 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066593 | ACTAATATCCAAAAT[G/T]TATAAAGAACACAAG | 75725 |
rs47530559 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11934559 | CATCCTTAATGAGCA[A/C]ATTTTCTGCAAAGAA | 75725 |
rs47545531 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11916472 | TGTGTTCAGTCTAAA[A/G]TACTAAAATCAACCA | 75725 |
rs47655395 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:11915578 | AAGATAAGAAGCCAC[C/T]ATAGTGTGTCTAAGA | 75725 |
rs47665926 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11911965 | GGGGAGTGTAGCATG[A/G]TGGCACTTGAGATTC | 75725 |
rs47739010 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11914965 | CCTTAGACACATAGT[C/G]AGTACAATCACATAA | 75725 |
rs47827103 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11919158 | GGGGCTTGCATGCAG[A/G]TTTTTTTAAAAGTTG | 75725 |
rs47840867 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11945874 | ATGTAGAGAGTGTGA[A/G]CAATGGAACTGTAGC | 75725 |
rs47904717 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11947416 | CCTTCAAACCGTCAT[A/C]GTCTCCTATGTTGCC | 75725 |
rs47922414 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12050562 | AAACATTTAATCTAT[C/G]ATGTATTATTCTCTC | 75725 |
rs47963360 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11953987 | CAGTCCTGAGAGTCT[C/T]TCACTTCCCAGGTCT | 75725 |
rs48001597 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Phf14 | Mm_Celera | 6:11932100 | AACACACAGGATAGT[G/T]TGATTATTAGCTGTG | 75725 |
rs48197523 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11915072 | CAAAACTAAACACAA[A/T]CTTAGTCCAGAAGAA | 75725 |
rs48219652 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11931026 | ATTCTGTGACTAAAA[C/T]GTTGGGCTAGTATTT | 75725 |
rs48278617 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11930842 | TAGCCAGTTGTGGAC[A/C]TTGTTTTCTCATTGT | 75725 |
rs48297384 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11921766 | GCTGATACTTTTTTT[A/G]GTACCATTGGAGGTG | 75725 |
rs48330779 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11910957 | ACAGACCTTCAGACC[A/G]ATCAAAAACAATCCT | 75725 |
rs48341498 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11913363 | TATTAATGCATGACA[A/G]TAAAGAAATAGCTTC | 75725 |
rs48377049 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12086548 | GGAACATGAGCACAT[C/G]TATGTGTATTACACA | 75725 |
rs48462533 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11932732 | CTTTTGTACTGATCA[A/G]ACATCTGCTACAAGT | 75725 |
rs48474643 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11930219 | TATGCTTATTTATGG[C/T]GCTAATTCTTGTTGC | 75725 |
rs48522386 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12086901 | TACCTCTGAGGAAGA[A/C]ATTTTAGTTAGTCTC | 75725 |
rs48531752 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11935627 | CATTTACATAGTCTG[C/G]TAAATAATGAGACCT | 75725 |
rs48539200 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11938586 | TAGAGCACAGTACAT[G/T]TTGAGATAATTGGCA | 75725 |
rs48544103 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11911669 | AGTAGCCAACAGGAA[A/G]GAATTCTGTCTCAAA | 75725 |
rs48544590 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11914787 | GTCAGTACATCAGTT[A/C]GGGTCAAGCAGAGAA | 75725 |
rs48588591 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11941842 | GACCACAGAATCGTC[C/T]CCTGAGTCCTAATGT | 75725 |
rs48595157 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11937111 | TAATGATAGATGTCA[C/T]TTGATGTTTGCAGTT | 75725 |
rs48634919 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11910601 | GCAGACTACATATTG[C/T]CAAAGGAACTCTTAG | 75725 |
rs48641674 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11912776 | ATGGTCACCATTTAT[C/G]TAAGTGGTCAACTCC | 75725 |
rs48691725 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11947011 | GTAAGCATTGTTCCA[A/T]TCAGTAGTGCTCTGG | 75725 |
rs48699498 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11936457 | ATTGAAGACTTGGAG[G/T]ATTTACATAGACTAC | 75725 |
rs48708854 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11915908 | CAATCAAGTCAAGCC[C/T]ATGTCTACAGTGTTG | 75725 |
rs48718681 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11910685 | TCCAGTCCTCTAGAG[G/T]AAAGAATCAGGCAGA | 75725 |
rs48740622 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11916687 | CATGCTGCTGTTCAC[A/C]TACAGTCTTGTAGCT | 75725 |
rs48797701 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066284 | GCTTCTTTGGGTACC[C/T]GTGTGTTATGGTTAA | 75725 |
rs48889761 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12066578 | TACATCTGACAAAGG[A/G]CTAATATCCAAAATT | 75725 |
rs48910560 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12066311 | TTAATGTCTATTTAT[A/G]AGTGAATAAATACCA | 75725 |
rs48943103 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12059594 | GGCCCAGTCTATATG[A/G]CAAGTCTATATGACA | 75725 |
rs48973086 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11953591 | TTGGCCATGTAGATG[A/G]ATGAGGGGAGGAAGA | 75725 |
rs48979050 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12086645 | TCAGAAAACAGCTGG[A/T]TGGAAAAACAAGCCA | 75725 |
rs49011229 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11928632 | AGTTTATAAGCTACC[C/T]GAAAAAGAGTGTATG | 75725 |
rs49061722 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11941185 | AAGTCAAATGTTAAG[C/T]AGGTAGAGCTATTTG | 75725 |
rs49135112 | snp | A/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:11914887 | TGGAAAACAACTTCC[A/T]GTGCTACCTGAGGTC | 75725 |
rs49154449 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11932718 | ATTGTCTAGCTTTGC[C/T]TTTGTACTGATCAGA | 75725 |
rs49253744 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11928106 | GTTTAAAGGACTGCT[C/T]ATGACGTTCTTCAGA | 75725 |
rs49264623 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12049345 | CTACCACAAGATGAG[C/T]TAAGCAGGGAGAATT | 75725 |
rs49271675 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12066494 | AGGGTCATTTTGGTT[A/G]TTTCCAGTTTCTGGC | 75725 |
rs49296915 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11946902 | CCAAGAAATACTACC[A/T]TTGAAAATTCAGAAG | 75725 |
rs49365905 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12086960 | AGACATGTGTCTTCC[C/T]ATTGACTCCAGACCC | 75725 |
rs49370529 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066604 | AAATTTATAAAGAAC[A/T]CAAGAAGTTAGATAC | 75725 |
rs49380524 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12013531 | ATATTTACTAAAATA[C/T]TTTATTCTTTTAAAC | 75725 |
rs49411117 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11920902 | GTTTCTCAGGCTTTC[A/C]TTCCTAGAACTAGAA | 75725 |
rs49416978 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11928201 | CTGGCAATTGTGGCA[A/C]CTAATGAGTTCACGC | 75725 |
rs49473599 | snp | A/T | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:11928712 | GACGTTATATTTGGC[A/T]AATGTTTGATCCCTA | 75725 |
rs49483713 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12044889 | ATCAACATTTGTTTC[A/G]TTTAATAAAGTGTTG | 75725 |
rs49543283 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11945707 | ATGTCATGCTATTTT[C/T]ACTCTCCAACCACCA | 75725 |
rs49680525 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11936307 | CTCTTGAACCATAAC[A/G]ATTTTCAGTTTCTTA | 75725 |
rs49698438 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11928032 | TTTGCTACAGAATCT[C/T]GTTTAACTTTATAAT | 75725 |
rs49729752 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11918951 | CAAGTGTAGTTTTTC[A/C]AACTTTGTTGTTGTT | 75725 |
rs49737136 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066842 | TGAGGATGTGGAACA[A/T]GGACACTCCTGCATG | 75725 |
rs49809758 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066289 | TTTGGGTACCCGTGT[G/T]TTATGGTTAATGTCT | 75725 |
rs49863389 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11930167 | TTTAGGATAACTCAG[A/G]ATTAACCAGCAAACT | 75725 |
rs49935852 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11911880 | CTTGTAGACCATACA[C/T]ATAAAATGTTCTTAA | 75725 |
rs49953112 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12066268 | GGGCTTGCCTTGTTT[A/G]GCTTCTTTGGGTACC | 75725 |
rs49957565 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11929370 | GGTTATTTAGTTAGT[A/G]TAGCCATTGTGCCTA | 75725 |
rs50040304 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12080828 | GAAACCTTGAAAAAT[C/T]GGTTGCTCTTAATCA | 75725 |
rs50042396 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11910679 | CATTTCTCCAGTCCT[C/G]TAGAGGAAAGAATCA | 75725 |
rs50078124 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11927504 | ATGATACAGGCTGTT[A/G]TATCTGCAAAGCATC | 75725 |
rs50129853 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11910765 | AAGGAAGAACACTGA[C/G]AAAATCATGCTCTAG | 75725 |
rs50206743 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12015334 | TTGATTACCTGTGGG[C/T]ATGGAAGTCAACTTT | 75725 |
rs50254648 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12027500 | CTGCAGGGAAAGTTA[A/C]GTTTAATCCCCTCCT | 75725 |
rs50275779 | snp | A/C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12044841 | TTGCCTTTTTACTAT[A/C/G]ATGTGCTATTGGTAT | 75725 |
rs50300968 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12049266 | TCTTGTTACTTTTCC[A/G]TCTTTTATCCTTCTT | 75725 |
rs50320690 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11938277 | TTCCTTTGAAAGATG[A/G]CACATACCTTCAGAA | 75725 |
rs50504911 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11928498 | GTTTACGTTCTGTAA[A/G]TGTTCAAAAGTGGTT | 75725 |
rs50727298 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12042236 | CATCAGTTATGTATC[A/G]CTACATCTTGTGTTT | 75725 |
rs50741636 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12063715 | GTTCATTGTTTTCTT[C/T]GTTAAGTTCTCAAAA | 75725 |
rs50789401 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11929616 | AATTATTTTAGACCA[G/T]ATTGAGAAATAGATG | 75725 |
rs50834182 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11910645 | AAACTGTGACTGTTT[A/G]AGATATGAATTGACA | 75725 |
rs50863962 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024092 | TGTAGACCAGGCTGG[C/T]CTCGAACTCAGAAAT | 75725 |
rs50883930 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11930179 | CAGGATTAACCAGCA[A/G]ACTAGTGGTGTCTGT | 75725 |
rs50900271 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950999 | TATATTTTTTCAAAA[C/T]AGTCCTTAGTATAAA | 75725 |
rs50911019 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11914054 | CCCGAGTGGGCAGGG[A/T]ATCTGCATACTTATG | 75725 |
rs50971650 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12066317 | TCTATTTATAAGTGA[A/G]TAAATACCATGCATG | 75725 |
rs51034249 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12048658 | TTTCATACATACCAA[G/T]TTTTAATAAACATAG | 75725 |
rs51038994 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11916642 | TCTAGTAGAACCTAT[C/G]TGGCTTGCTCTGTTC | 75725 |
rs51051140 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11916415 | GAAGGTGTTAAGGAT[C/G]TAGCTCAATGGTTTA | 75725 |
rs51071602 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066895 | ACAGACACTTTAGAA[A/T]TCAATTTGGCAGTTT | 75725 |
rs51086952 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11936625 | GAGCTTCCTGGGACA[C/T]ACTTTTGCCACTCTA | 75725 |
rs51122032 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12046000 | TGTCAGACAAAATAG[C/T]AGATGAATAGTATTT | 75725 |
rs51171562 | snp | A/C | 0.32 | 0.24 | intron-variant | Phf14 | Mm_Celera | 6:11939229 | ATCCCACCCTTGCCT[A/C]ATGCTTAGGTGTCAG | 75725 |
rs51273450 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11942074 | CATAGAGTCACACCA[G/T]TCAAGGACAGATCTC | 75725 |
rs51359044 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11913859 | GTGCTTGTCTTGTTT[C/G]GAATAGGACATGAAA | 75725 |
rs51372776 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12059562 | GGCCCAGTCTATATG[A/G]CAAGTCTATATGACT | 75725 |
rs51395378 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12063714 | AGTTCATTGTTTTCT[A/T]TGTTAAGTTCTCAAA | 75725 |
rs51414734 | snp | C/G | 0.124444 | 0.216185 | synonymous-codon, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11933719 | ATCCATGGAAGAACT[C/G]AATGCTATGGATGAT | 75725 |
rs51422084 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11928033 | TTGCTACAGAATCTC[C/G]TTTAACTTTATAATA | 75725 |
rs51520072 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11990542 | TTTGCTTTTGATCTA[C/G]GTAGTGATGAATGGT | 75725 |
rs51538534 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf14 | Mm_Celera | 6:11946012 | GAGGACACTGACTCC[A/G]TTTACTTCTCGCTAT | 75725 |
rs51551519 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066553 | GTTGAGCAAATGTCT[C/T]CACCAACCCTACATC | 75725 |
rs51552192 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11947446 | CAGTCACTTAATTTG[A/C]CACTCTCCTTCCTCA | 75725 |
rs51589360 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12027535 | TGTAGTACGACTTCT[A/G]ATAATGAACTCAATG | 75725 |
rs51592456 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066823 | AAGTGATAGCACATG[C/T]TGGTGAGGATGTGGA | 75725 |
rs51695838 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11911975 | GCATGGTGGCACTTG[A/G]GATTCCTAGGAAGGA | 75725 |
rs51787050 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11916739 | GTCCTCTTAGATCCA[A/G]CACAACTCAGATACT | 75725 |
rs51796868 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029791 | ATCTATCTGTCCCCA[A/T]CCCCTTAGTCCTTAC | 75725 |
rs51825885 | snp | C/T | | | upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11907490 | GAAGGACCCCTGGCG[C/T]TGAGGGCAGCCTGCA | 75725 |
rs51937815 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11911777 | ATATGCATACACACT[C/T]GGAAATATAAAAAGA | 75725 |
rs51953912 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf14 | Mm_Celera | 6:11915013 | TTTCCATATTTCCAA[C/T]TCAATGTATGGGAGT | 75725 |
rs52017691 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12076040 | AGCCAGTTTAAGAAA[A/C]CGTTTCTTTAACTAT | 75725 |
rs52075887 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11933797 | AAAGGGGCGATCAGC[A/G]TCTCAGAAGGAGGGC | 75725 |
rs52107556 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031261 | gtgctattaagtcac[C/T]aatctctctctctct | 75725 |
rs52147027 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12032299 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTCTGTGT | 75725 |
rs52200839 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12022909 | TCTCTCTCTCTCTCT[C/G]TGTGTGTGTGTGTGT | 75725 |
rs52255047 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf14 | Mm_Celera | 6:11911176 | AATAAGAGAAGAAGC[A/G]TCTACAGCATCATTT | 75725 |
rs52350164 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12032283 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT | 75725 |
rs52370531 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12022911 | TCTCTCTCTCTCTGT[C/G]TGTGTGTGTGTGTGT | 75725 |
rs52387244 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066242 | TGAGTGAGGTTCAAG[C/T]ATCCTTGCTTGGGCT | 75725 |
rs52428825 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12035748 | GTTTCTCTGTGTAGC[C/T]CTGGCTGTCCTGGAA | 75725 |
rs52475988 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066248 | AGGTTCAAGTATCCT[C/T]GCTTGGGCTTGCCTT | 75725 |
rs52502322 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066217 | CTATGACTATTTTAT[A/T]CTCCCCTTCTGAGTG | 75725 |
rs52560901 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12032541 | ACATATTTGTGTGTG[A/C]GTGTGTAGTTGTATT | 75725 |
rs52585852 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12039544 | ctctctctctctctg[C/T]ctctctctctttctc | 75725 |
rs107697932 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010925 | CTCTGCTATTAAAGT[A/G]AGAGCAAGACTGAAC | 75725 |
rs107747090 | snp | G/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010923 | TACTCTGCTATTAAA[G/T]TGAGAGCAAGACTGA | 75725 |
rs107765933 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011181 | TGGAATCTCATCTGA[A/G]TATATGGTGAGTTTA | 75725 |
rs107766040 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11981930 | TTAATAGTCTCCCAG[C/G]CAAAAAAAGCCCTTG | 75725 |
rs107972100 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11981937 | TCTCCCAGGCAAAAA[A/T]AGCCCTTGACCAGAT | 75725 |
rs108646898 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021950 | GTGTGTGTGTGTGTG[C/T]GTGTTCTACCTAGCT | 75725 |
rs108787924 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11970427 | CATACAAGACAGCTA[A/T]AACAGGGTCCCTTCA | 75725 |
rs108824472 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11982009 | AATTCCAGTTCTGCA[C/T]AAACTATTCCACAAA | 75725 |
rs108839322 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011227 | ATTTTGGATATAAGG[C/T]TAGCTTGATGCCTAA | 75725 |
rs211699743 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:11916608 | ACACTTGCTCGCCCC[-/G]ATTACTCAAGCTTTA | 75725 |
rs211708578 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055261 | AGCTGGGAGTGTGAG[G/T]CCAACCTGGTTTCCA | 75725 |
rs211709195 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12000914 | TTTTTAAGAATCTTG[C/T]CTATTTAAGTCATAT | 75725 |
rs211711834 | snp | A/C | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12048153 | ATAATAGGACAACAT[A/C]TCTCTGCTAATTTAG | 75725 |
rs211711936 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11991873 | CAGAGGACCAGAAAT[A/G]CCATAGCAGAAAACA | 75725 |
rs211730506 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12089331 | AATGTTGTCCCATTG[C/T]GAATGCAATGTGGAA | 75725 |
rs211730638 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11922704 | TTTTCTTTTCAAAGG[A/G]CATTTGGCAAAAACT | 75725 |
rs211741964 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12098839 | TAGTGAATAAAAATC[C/T]ACTGGAAGCTCCTTA | 75725 |
rs211742711 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12043298 | TGAGGAATTTTAGAC[-/T]TATCCTACCACCCAC | 75725 |
rs211766133 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12049179 | AGTGAATAGACACAT[G/T]TCCTTTAAAGTGGCT | 75725 |
rs211779920 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924117 | CAGTAGGGATTTGCT[A/G]TCAGGTTGTAGAGAT | 75725 |
rs211789332 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11923792 | TAATATCAATATAAG[A/T]TTTGCCATATTTGTA | 75725 |
rs211799076 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908746 | TTGATAGTTGGATGG[C/T]TATGGGTGAATGAGT | 75725 |
rs211799342 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11916963 | TAGGAACAGCCCTCT[A/G]TGGTACACTTGTCCC | 75725 |
rs211801353 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12044157 | CCAACCATAAAATTA[-/TT]TTTGTCACTTTCATA | 75725 |
rs211821757 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11978524 | AAAGTTATCACCTTT[C/T]CCTGCCCCCTGAAGT | 75725 |
rs211844651 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12082470 | CATACAAACTTTTCT[C/T]AGCTATTTAAAAACA | 75725 |
rs211848435 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12076441 | ggcccactgttccag[A/G]ctgcattaaatgatc | 75725 |
rs211863286 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12033832 | TATAGGTCAAGGAGT[A/G]GTATATGCAACTCAT | 75725 |
rs211874027 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12090461 | GAAGATATTTGTTTT[G/T]ATTCTTAAAGGTGAT | 75725 |
rs211894425 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11958756 | CTTTTGCTGCATTGT[A/G]ATACCAGCTTGATTT | 75725 |
rs211902346 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12040312 | ACTTAATCTCGAACT[A/G]ATTTAGAAGAGCCTG | 75725 |
rs211930435 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12075492 | AGAAAGAACTTTCAT[C/T]TCTGAGAGGCCAATC | 75725 |
rs211931574 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083114 | CTATTTCAGAAAACC[C/G]ATATTTACACAGATT | 75725 |
rs211947524 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11909398 | GAAATAAACAGATAA[C/T]TTTATATAACTATAG | 75725 |
rs211948086 | snp | C/G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11959418 | GAGGGGTCATAACCT[C/G/T]CCAGCTGAGAGCCAC | 75725 |
rs211956035 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12034353 | ATCAGATGATCAGGT[A/T]GGAAGTGGGCTCTGG | 75725 |
rs211957639 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12068615 | TCTTATTTGTCTTCA[A/C]AATAAGATTAAGTAA | 75725 |
rs211963275 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11948969 | GAAGGAAGAGGAGGG[C/T]AAGAAAGTGTGTGAT | 75725 |
rs211968382 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12075790 | GGTTATGAAAGTAAA[A/C]GCCACTGACTTCACT | 75725 |
rs212018337 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12020307 | GCTGATACAAAGGTC[A/G]TGCAGGGTGCTTTTA | 75725 |
rs212043037 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12028108 | GACACCCTAACAATT[C/T]CATTTAAAGCAGATA | 75725 |
rs212056117 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11940700 | TTTACATCCACAAAT[A/G]CAAAAGGTTTAAATT | 75725 |
rs212080408 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949581 | AAATAACTCTGGATT[C/T]TGACTTCATATTCTT | 75725 |
rs212098744 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11954752 | ATGGTCACCAACAGA[A/G]CAGTTGTCTCAGAGA | 75725 |
rs212124335 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12037727 | CACTCCACTGCATTG[G/T]ACTGACTTAACATGC | 75725 |
rs212133043 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12073470 | TGGCTCCCATGTGCA[C/T]TTTTCGCATATGTTC | 75725 |
rs212137299 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12041270 | TAATTGCTGTAGGAT[-/A]AGAAATGGAAGGAAT | 75725 |
rs212162288 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11955886 | CTTTCTTCTGAGCAG[G/T]GTTGTTCTACTTACT | 75725 |
rs212168309 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11950668 | CTTTCAGCAGCATTT[-/A]TTAAAAGTGAACCAA | 75725 |
rs212190740 | in-del | -/CACTCA | | | intron-variant | Phf14 | Mm_Celera | 6:11922932 | TGAACTTTTGCTCAT[-/CACTCA]CACTCACACTCACAC | 75725 |
rs212191931 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032353 | TGTGAGTCATGATTT[C/T]TACTTATTCATATTT | 75725 |
rs212213372 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12027138 | CTGGAGCTGTGCTCA[-/G]GGGTCTTGGGTAACT | 75725 |
rs212225126 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12020692 | ATCAAACACTTAAAA[A/G]TCCAGCCTCTTTAAA | 75725 |
rs212228852 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12069132 | ATTTATATGTAAATA[C/G]ATATGCATATGTGTA | 75725 |
rs212272959 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12026725 | TGTGTGGAGCAGGGA[A/G]AAGGGTTGGAGGAAC | 75725 |
rs212276343 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11976839 | TTTTGACCTTTATTA[G/T]TTTGTTCTACCTTTT | 75725 |
rs212277701 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11947192 | CATCATGGTGTGAGC[A/C]TGGCAGCAGGCAAGC | 75725 |
rs212291509 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11938905 | CCGGGCAGTGGTAGT[A/G]CACGCCTTTAATCCC | 75725 |
rs212310079 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12060073 | TCGTCACACCCTAAG[A/C]ACTATAAACTGAGTG | 75725 |
rs212332612 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12003677 | GTGTTCACAGGTTTT[A/G]TTTTGTTTTTTACAT | 75725 |
rs212343130 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11947761 | ATTGTCAGTGAACTG[G/T]ATACCTACACTTCTT | 75725 |
rs212370516 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Ndufa4, Phf14 | Mm_Celera | 6:11907730 | ACGGCATGCGTATAG[A/G]CCAGGGTCATCCGGC | 75725 |
rs212379647 | in-del | -/CACC | | | intron-variant | Phf14 | Mm_Celera | 6:12065090 | TAGGCTTTGAGACTT[-/CACC]CACACACATACACAC | 75725 |
rs212398293 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060508 | TGAATCAGTTTATAA[C/T]ACTTTAATGTTATGA | 75725 |
rs212432262 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010197 | TCAGTACAGGGAAAC[A/G]CCAGGGCCAAGAAGT | 75725 |
rs212434701 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12054943 | CAGACACACACACAC[A/G]TACACATACTCAGGA | 75725 |
rs212439055 | in-del | -/AAGTTA | | | intron-variant | Phf14 | Mm_Celera | 6:11920573 | TTTAGCATGGCTCAG[-/AAGTTA]AGAGCACTTGCTGCT | 75725 |
rs212447120 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12098112 | GCCCTCTTCCTCCAG[G/T]GAAGCAACAGGCCCT | 75725 |
rs212448577 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12000011 | CCATACTTCCAAGCT[A/G]TGCTTATTATGTAAG | 75725 |
rs212487887 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12074015 | TTGAGTGTTTAGTGA[C/G]TTACTAGATTGTTCC | 75725 |
rs212497793 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11945868 | AAGCAGATGTAGAGA[A/G]TGTGAACAATGGAAC | 75725 |
rs212499206 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12064498 | CCCTCTGAAAGAGCA[A/G]CCTTTACTGGTAACC | 75725 |
rs212509404 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11937161 | AAAATTTATCAAATT[A/T]TAAGTAGGAAAATAT | 75725 |
rs212523136 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12016531 | GAGCAGTAACCTTTC[C/T]CTAGATGTGTGTCTT | 75725 |
rs212568679 | in-del | -/T | | | upstream-variant-2KB, utr-variant-5-prime | Ndufa4, Phf14 | Mm_Celera | 6:11907661 | AGGTTTATTTTTTTA[-/T]TTTTTTGCATAGCAG | 75725 |
rs212577147 | in-del | -/AA | | | intron-variant | Phf14 | Mm_Celera | 6:11995309 | ATGACTGCATCAGCC[-/AA]AAAAAAAAAAAAATA | 75725 |
rs212585751 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12058526 | GAGCATAAGAACAAT[A/T]AATAAATGTTTTTCA | 75725 |
rs212586036 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12065273 | CTTCTAGAAAAGTTT[A/G]TAAGATTCCTAAAAC | 75725 |
rs212586567 | in-del | -/CTT | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099510 | CCCTTAGAAAATATG[-/CTT]CTTCTTCTTTTTTTA | 75725 |
rs212600854 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12089243 | CCATTTTCCATTACA[-/TT]TTTTTTTACAAAGCC | 75725 |
rs212602847 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11939439 | AAGCTGCAAATGAAC[C/T]CAGGATGTTCATTAG | 75725 |
rs212619436 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927785 | TTTGGAACGTCTTGC[C/T]CCTTTTCTCCGACAC | 75725 |
rs212621844 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12018819 | GCATCTGTCTCAGTC[A/G]GCTGCTGGGTAGAGC | 75725 |
rs212625041 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12059256 | TCAATTCTATTTTGC[A/G]TTTTTTCGTATTTTA | 75725 |
rs212663621 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12007516 | GTGATTATAGAGTAC[A/G]ATTGGCAACAACTTT | 75725 |
rs212666220 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12053583 | AGTAGAAAGAAGATA[A/T]CTATGTAGAAGTAAA | 75725 |
rs212686628 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12096131 | CCAGTTTTTAGGGAC[A/T]ATAGTTAAGGTTGTT | 75725 |
rs212688719 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11930231 | TGGTGCTAATTCTTG[C/T]TGCTCTGTACCTATG | 75725 |
rs212690506 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11917428 | TGTTTTCATGGGATT[-/A]AAAAAAATGTAGGAG | 75725 |
rs212704864 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12046063 | CCAGCTGTCATTTAG[C/G]CTGATGATCCTAATG | 75725 |
rs212708563 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12098940 | ATTAAGATTTCTAGG[-/T]TTTTTTTCTTCAGAC | 75725 |
rs212729451 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11920456 | ACATTCTAGGCCTAG[A/C]TATGATTCTACAGAG | 75725 |
rs212729521 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11928322 | GGTTTGGTACTTTCA[A/G]AGAAGGAAAACAAGG | 75725 |
rs212761513 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11915053 | GACTCTATCGCTCTT[C/T]TTACAAAACTAAACA | 75725 |
rs212781044 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12074698 | TGAAATAAGAATCTC[-/A]AATATGCAAAGTCAG | 75725 |
rs212783960 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11989811 | TAGTGTAATTTTCAT[A/G]AAGTTTAATGTATTT | 75725 |
rs212811006 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12086806 | TAGAGCACATCCACA[A/G]CAGCAATGGGCTCAC | 75725 |
rs212825083 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906958 | GGGGATTACACGATG[A/G]CGATCCCTTGCACTT | 75725 |
rs212846190 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11975263 | AATCTTGCATCTATA[A/G]TTCCAGATTGCTTTC | 75725 |
rs212848443 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079857 | CCAAGATGAACTAAA[A/G]TCTCACCTGATATCT | 75725 |
rs212850288 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12087512 | ACTGACATTTAAACA[A/G]ATGTAAAATAGTAGA | 75725 |
rs212853077 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12037292 | AATTAGATTTTGGTC[A/C]CAGACTCTGCCCTCT | 75725 |
rs212889403 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031732 | ATATCTGCCCATTGG[A/T]TTATGATGTCAGTTA | 75725 |
rs212925059 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12057723 | TTAGCTTAGAGATTC[A/G]TGGTAACCACAAGCT | 75725 |
rs212942270 | snp | C/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11925894 | TCACTTCCTCCTTGT[C/T]GGAGCTGTATCCGGG | 75725 |
rs212948167 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12093941 | ACTTTCTTAAGATCT[A/G]CCAGTTGTCCTTCAT | 75725 |
rs212951401 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11937973 | CCTGTACTCTGCCTG[A/G]TTCCCCTCCTCTCTT | 75725 |
rs212953610 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12052306 | GAGTGCTCCTGTTCT[A/C]TAAGGTTGAGCTTGT | 75725 |
rs212955474 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12052999 | GTGTGCAAGCCTGAC[A/G]AAGTAGACTCTATCC | 75725 |
rs212970384 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12016946 | AGTGCCCTGTGTGTG[C/T]TCTCATGTGGCCACG | 75725 |
rs212982495 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11996314 | ATCTCAGATTAAAGA[A/G]TAAAAGTAAGCTTAA | 75725 |
rs212994653 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12043640 | TTCACTGCAGTAACT[G/T]ATCACAGTTAGTTGC | 75725 |
rs213006353 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927202 | ACCACAATATTCTTG[C/T]GCAGTGTTACTCCCA | 75725 |
rs213019241 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11919124 | AGCTCTTCCACTTCT[A/G]TCTGTTTTAAGATTG | 75725 |
rs213026613 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11912993 | TTAAATGATTTAAAA[A/T]TTTAAAATCATGTAG | 75725 |
rs213039934 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12094281 | ATCTCAAAAAATAAC[A/C]CTTGAGCCTGGCTTT | 75725 |
rs213050810 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11987302 | ACTGATACATACACA[A/G]TCTCCCTGAGAATAA | 75725 |
rs213073998 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12085147 | ACTTGCACATATACA[C/T]AAACACCCAAATAAA | 75725 |
rs213080865 | in-del | -/GT | | | intron-variant | Phf14 | Mm_Celera | 6:11937674 | TTGATCACATGTTTG[-/GT]ATAGCATTTTTTTAA | 75725 |
rs213106490 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029299 | TAACAGTGTGGTTTG[-/T]TTGGGGGGTCCCATG | 75725 |
rs213118987 | in-del | -/GTTTT | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009194 | AGTTGTAACGTTATC[-/GTTTT]TTTTTTTTTTTTTTA | 75725 |
rs213125992 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036530 | CTATCATTTTTTAAA[C/T]TTAGAGATTCCAAAA | 75725 |
rs213131431 | in-del | -/TATT | | | intron-variant | Phf14 | Mm_Celera | 6:12096152 | TAAGGTTGTTATAAA[-/TATT]TATAGAAGGATCTTT | 75725 |
rs213136845 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11905657 | CATGCCTTTAATTCC[A/G]GCACTAGAGAGGCCA | 75725 |
rs213138433 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12079127 | AATTCAGAAAACATT[G/T]AGTAGACTCCAATTC | 75725 |
rs213163451 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12085833 | CACTTATTTGGATTG[C/T]GTTAAGGATCATTAC | 75725 |
rs213171308 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036879 | ATATTTTATCCATTA[C/T]TTGTCTATCAGGAGT | 75725 |
rs213183395 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11963018 | ATCAACCATACTGCA[C/T]GGTGTCTTGAAGTGT | 75725 |
rs213184718 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11952635 | GGCCTTTAGTCTCTT[A/G]TGTTTATTTGTGATT | 75725 |
rs213189230 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12096812 | TACTATTGAGGATGC[C/T]AAACCTCTGAAGCTG | 75725 |
rs213196495 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12030496 | GGACAACATTATCTT[A/G]CTCCTAATTTTAGTG | 75725 |
rs213198579 | in-del | -/CT | | | intron-variant | Phf14 | Mm_Celera | 6:12075758 | GTAGCAACAAGTGTC[-/CT]CTCTGAGCATAGCAC | 75725 |
rs213208885 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12046477 | ATATGGCATTTGTCA[A/G]TTTCATTTTATTCAC | 75725 |
rs213239736 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12076817 | AGTTTACAAGGTGAA[-/C]ATATTCAGATTTTAA | 75725 |
rs213244157 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12023890 | TATAGCCCTGGATGT[C/G]CTGGAACTCACTCTA | 75725 |
rs213244168 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12072392 | GGATCAAAATATATT[C/G]CCGACTCTTGCAGAA | 75725 |
rs213258354 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11915531 | AACAAACAAATAGAC[A/C]AAGACTTCTATGCCA | 75725 |
rs213284049 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11990690 | ATTTAAGAAAAATTT[A/C]ATTGTAGTGATTTTA | 75725 |
rs213284510 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12059322 | TTTGATAAGGTTGGA[A/T]ACCATCACAGTCCTT | 75725 |
rs213311568 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008004 | AGGAATAAAAAAATG[A/G]TAAAACACATATTTG | 75725 |
rs213317416 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11995744 | TTGGGTACCAATCTG[C/G]TCTGGTATATCAAGT | 75725 |
rs213344826 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11938197 | TGCCATCTATAACTT[A/T]CTTATCTAATTTCTA | 75725 |
rs213367603 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11928347 | ACAAGGAAAGGGAAA[A/G]GAGGTAAATGACTTC | 75725 |
rs213380058 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12053658 | GTAATAATTCAAAAC[A/C]CCAAGAATATTTAAA | 75725 |
rs213407696 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12043036 | CAGACGAGTTTCAGG[C/T]ACGGAAATGTCTAAT | 75725 |
rs213413034 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11911882 | TGTAGACCATACATA[C/T]AAAATGTTCTTAACA | 75725 |
rs213420410 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054099 | ATCAGTTTGTTATAC[A/T]ACAAATGTCCTTAAG | 75725 |
rs213421983 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12046141 | CCAAATAATGGTATT[C/T]TTTATAACATTTCCG | 75725 |
rs213426877 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11998307 | AAGTGAGGTCTCAGC[A/G/T]ATGAGACGTGCTAGA | 75725 |
rs213434819 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11985980 | GTAGGCAAGTGTTGT[A/G]TGGATGTGCTATACA | 75725 |
rs213444974 | in-del | -/CATCTGTACTAA | | | intron-variant | Phf14 | Mm_Celera | 6:12056173 | CGTTTATGCCCCAGT[-/CATCTGTACTAA]CTAGACTGAAAACTC | 75725 |
rs213446871 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11921033 | GATCTTGAGACATTA[A/G]GGTACTTGTACTTAA | 75725 |
rs213478862 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12096971 | ATAGCTTACCAACAC[A/G]GGGCATGCTTGCCTT | 75725 |
rs213482041 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11989860 | ATGCAGTTGTAGCTT[C/T]ATAATAGAAGTAGTT | 75725 |
rs213495186 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11990942 | GCCTGTAGTGTAAAC[A/G]TTAGTGCATGAACAC | 75725 |
rs213504737 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12046646 | TAACTATCTCACACT[C/T]CCATGTGCCTGCATG | 75725 |
rs213512122 | in-del | -/GACATT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083357 | ATTCCCCTACACTAG[-/GACATT]GACATCGAACCGCCT | 75725 |
rs213522014 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11915109 | AGAAAGGAATATGGC[A/G]GTATGAAGAGTATTA | 75725 |
rs213533011 | in-del | -/GTTTCTCT | | | intron-variant | Phf14 | Mm_Celera | 6:11917395 | CTAGAAACATTTTGG[-/GTTTCTCT]GTTATTAATGGTACC | 75725 |
rs213573844 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11915582 | TAAGAAGCCACTATA[A/G]TGTGTCTAAGATCAT | 75725 |
rs213582507 | in-del | -/AAAGA | | | intron-variant | Phf14 | Mm_Celera | 6:12020211 | AGCAACTTAAACAGG[-/AAAGA]TTTTATTTCACTCAC | 75725 |
rs213584998 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12078795 | AGCACCTACATGGGG[A/G]TTGAGAACCATCTAT | 75725 |
rs213587404 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Ndufa4, Phf14 | Mm_Celera | 6:11907761 | GGTCCGCTGGCAGTG[C/T]GCTCGGCGGGCGCGG | 75725 |
rs213597781 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12080960 | TTTTGCTGGTAAGAA[A/G]TGTAGGATTTAATGT | 75725 |
rs213603646 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12087724 | TGGAACTATACTGAA[A/T]GTAATAACAATATCA | 75725 |
rs213624945 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12071458 | AGCCTCATGTGGCGG[A/G]GATTATATAGGAGTG | 75725 |
rs213635203 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12073546 | GTTACCATCACTCTC[A/C]GGATGTGACATTCGA | 75725 |
rs213640621 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11976934 | CAGACACAGAAGTAT[A/G]ACTGAAGCATAGGCC | 75725 |
rs213648464 | snp | G/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908592 | TCCTTTGGCTATGAA[G/T]AATGGAGTAGATAAA | 75725 |
rs213653431 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12023365 | TCCACTCCCTTCCCT[A/C]CCCGCCAATCCCCCC | 75725 |
rs213676914 | in-del | -/ATCCTGATA | | | intron-variant | Phf14 | Mm_Celera | 6:12078077 | ACTTTATAAGCGAGC[-/ATCCTGATA]AGGAAGTCAGCCAAC | 75725 |
rs213683604 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11987752 | TTGTGATTTTATTGT[A/T]TTTCTATGTTTCAGT | 75725 |
rs213684778 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12032431 | TATATAAATAGCAGT[A/G]AGTAGAAACATGTTT | 75725 |
rs213688691 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052794 | TTTTAACTGAAAATA[C/T]TCTTGAGTAACAGGA | 75725 |
rs213696529 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:11914644 | AATAGTTTTATGGTT[-/G]GGGGTCACCACAGCA | 75725 |
rs213696973 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906272 | GGATTGAAGCAGTGT[C/T]TCTTTCAATTGTATT | 75725 |
rs213702679 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11919234 | AGCACGACATACTAC[A/G]TATAGTCCTCTTTAT | 75725 |
rs213743209 | snp | G/T | | | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | Phf14 | Mm_Celera | 6:11988760 | GCAAAATCTGAATGG[G/T]AAACTTCGAAGTGAA | 75725 |
rs213747215 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11945066 | GTGTAAGAAGCTTGG[C/T]TCCCAGTGTTGTAGT | 75725 |
rs213759822 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12078930 | TAAAAAATATCAAAG[-/A]TATGTGGCCATTTTG | 75725 |
rs213764700 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11920285 | AGTTTTACAGAGACA[A/G]GTTAAGCAGAACAAT | 75725 |
rs213766251 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11955996 | ATTTCAAATGTGATC[C/T]CCTGTCCTAGTTTCC | 75725 |
rs213782160 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11914260 | CTGCTCCCTGGTTTC[A/G]TATGGGCGTTAGAGA | 75725 |
rs213824820 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079173 | CATTTAGACAGGAGG[A/G]ATATAATATACAGAA | 75725 |
rs213826971 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12050331 | TTCTGTACAGAAAGA[A/C]TCTCTGATGGAATGT | 75725 |
rs213832565 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12095097 | TTCAGCTCCGTGTGA[A/G]AAGCCACATGAATGG | 75725 |
rs213862693 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12060012 | AAGATTGGCATGGTT[A/C]TTTTGTTTGTTTTGT | 75725 |
rs213870952 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12096238 | CTCATTTACATCGTA[C/T]TGTGGTTTGAATAAG | 75725 |
rs213873578 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12044345 | AGGCATAAGAGAAAA[G/T]TTTAAGTTAGATATG | 75725 |
rs213897978 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12079671 | AGAAAATGAAGATTT[A/C]ATTTTTAATAGGTTG | 75725 |
rs213899212 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11928912 | TTAAATAATAGTCAA[C/T]GGCAGGTGAGTCTTC | 75725 |
rs213902239 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11995466 | TCTCCTCCCCTCCAG[A/C]TCTCCTCCAAGTTCT | 75725 |
rs213907547 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12072425 | AGAAGCTTGTTTAGT[C/T]GATGGAGTCCTATCT | 75725 |
rs213915186 | in-del | -/GTGT | | | intron-variant | Phf14 | Mm_Celera | 6:11916132 | CACAATATTAAACAA[-/GTGT]GTGTGCGCGCACACA | 75725 |
rs213918068 | snp | G/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009015 | TAATATTTATTTTTT[G/T]TATATGAGTACACTG | 75725 |
rs213922877 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12033620 | ACTTTTTCTAGGTCC[-/T]TTTTTTATCTGCAAT | 75725 |
rs213928412 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11945977 | TTGTTGATGTGTCAT[A/G]TAGAGACTTCTGTTG | 75725 |
rs213936050 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12072748 | TAGTTCTTAAACTAT[A/C]AGAACTAAAAAAATA | 75725 |
rs213947828 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031517 | TTCAGTTTCCATGAG[C/T]TTGAAGGCTTTCTGT | 75725 |
rs213948991 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12024091 | TTGTAGACCAGGCTG[A/G]CCTCGAACTCAGAAA | 75725 |
rs213956622 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12042982 | TAAAATCTTTCCCAG[A/G]GCATGAGCAGAGGGA | 75725 |
rs213997769 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12024451 | TCCTCCTACAGGGCC[A/G]CCCTTTTCAGCTTCT | 75725 |
rs213998453 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036946 | ATATATCATTTTGGC[C/T]GGGCAGTAGTGTCAC | 75725 |
rs214020538 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11946477 | GCTATTTTGCTGCCA[A/G]TTTGGCATTTGGAAG | 75725 |
rs214020798 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11937247 | AAATCAAGCACAGGA[C/T]CCAATGAATACAAAG | 75725 |
rs214028584 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921553 | TAGTAAAACACATTC[C/T]GTACATCTAAAGGTA | 75725 |
rs214045673 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950425 | CTAATCCTTCCAAAA[C/T]ATTTAGACTGTGGAT | 75725 |
rs214053599 | snp | A/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906357 | AACTTCCTTACATGG[A/T]TTAAATTATATGAAC | 75725 |
rs214065701 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11963290 | AGTTTCTAGAGATTA[C/T]ATGCAGCATAAGAGT | 75725 |
rs214106980 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11951046 | TGTAATTTGCCCTCC[A/G]TGGGTGTGCACTGTA | 75725 |
rs214121463 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029879 | CTTAATAACTAATAT[C/T]CACATATAAGTGAAC | 75725 |
rs214135856 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11953899 | GTGGGATTGCCCCCC[A/C]TCCCCCATTTGATGC | 75725 |
rs214142374 | in-del | -/AC | | | intron-variant | Phf14 | Mm_Celera | 6:12054930 | TTATCAAATACACAG[-/AC]ACACACACACACATA | 75725 |
rs214142733 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12088580 | TCTGCTCCTTTAATA[C/T]CGTTAGAAAACTAAT | 75725 |
rs214164939 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12038654 | TGACTATTAATCTAT[A/T]CAGCTCTAAATATGT | 75725 |
rs214191244 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12081856 | GACCTAGCTTTCTTA[A/C]ACAACCTGGCCACAG | 75725 |
rs214192327 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12023260 | TTTATTACTCCCCAT[A/G]TTAGTTTTTTCTAAT | 75725 |
rs214200201 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032895 | TGAGCTCTGGGTAGT[C/T]TTGGTCGATATTGTT | 75725 |
rs214211129 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11943829 | TGTTTTTTGTCATTT[A/T]CTGTTTCTGTTTAAT | 75725 |
rs214259658 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12043754 | CAGCAGTCGGTTCTC[C/T]AGATGCTCATGTTTC | 75725 |
rs214274507 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11944736 | GGCATAGTATATTGC[A/T]TGTTCTGTGCTTATA | 75725 |
rs214279106 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12065514 | CACAGTCAAGATTTT[A/G]TTGACCATTTAAGTG | 75725 |
rs214281792 | in-del | -/A | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011291 | TTTTAAATGTCTGAC[-/A]TTCCTAATGTTTTTT | 75725 |
rs214283260 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12085421 | GGGGACTTGTGTTCC[G/T]GTATGCAATAACTGC | 75725 |
rs214283267 | in-del | -/GTG | | | intron-variant | Phf14 | Mm_Celera | 6:12000566 | ACAGTGCTTTTTGTT[-/GTG]GTTGTTCTCAGATTG | 75725 |
rs214311466 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11962312 | AAAATGATCACCTTT[C/T]TTCAACATAGTAAAA | 75725 |
rs214339198 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11935654 | ACCTATATTTAAGTA[A/G]TGCCCACATAGACTG | 75725 |
rs214341062 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11960770 | TGCAAGCAAACAGAT[A/G]TGTAATAAATGAATA | 75725 |
rs214357393 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12052333 | TTGTTTTGTAGCAGC[A/G]GTTGAGATTTAGAAT | 75725 |
rs214360984 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11905751 | AACATAAACAAGCAA[A/G]CAAACAACAACAACA | 75725 |
rs214414832 | in-del | -/TTTT | | | intron-variant | Phf14 | Mm_Celera | 6:12031138 | CATTGATTCTTTGTA[-/TTTT]TTTTTTAATTGCTTT | 75725 |
rs214416880 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11996435 | ACATTTGAAAGTACA[A/C]ATATCAGCGCATAAA | 75725 |
rs214426869 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11931236 | TCACAACTTCGTGAT[-/A]TTTGTAAAGTTTACC | 75725 |
rs214438238 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11986329 | CTTCCTTTCTTTTTC[-/T]TTTTTTTTTTAGGAT | 75725 |
rs214473811 | snp | A/G | | | missense, nc-transcript-variant | Phf14 | Mm_Celera | 6:11941452 | TGATTCTTGAGAAGA[A/G]TCAAAATTGGAGTTC | 75725 |
rs214502159 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12086575 | ACAGGATTCTCCACA[-/G]GAGCTAAAGATGGGG | 75725 |
rs214519126 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:12071138 | ATTAAAAAAAAAAAA[A/C]AAAAAAAAACACCAA | 75725 |
rs214536471 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924689 | ATGTTCTGAATAAAG[C/T]TAGCTATTGCATGAG | 75725 |
rs214542072 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12056802 | CACGAGTGTTTGAGT[A/C]TTTACTTTGTCTTTG | 75725 |
rs214546859 | snp | A/C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12050363 | GATTTGCTAAGTCTA[A/C/T]TTGTTTATTTATTGA | 75725 |
rs214559890 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12001978 | GTGGTCTCCATTCAC[A/C]AATAAAATGAGACAG | 75725 |
rs214564450 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12063655 | ACTATTTCCTTCTTA[A/G]GAAAGTATCTGTAAA | 75725 |
rs214565587 | in-del | -/TTTTTTTC | | | intron-variant | Phf14 | Mm_Celera | 6:12088646 | TTATATTCTTTTTCA[-/TTTTTTTC]TTTTTTTCTATTAGA | 75725 |
rs214580653 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12002822 | AGGGTAAAATGGATC[C/T]TTTTAATTAATGTTC | 75725 |
rs214619751 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11993867 | TGGGCCACCCTCTGA[C/T]TTTTCCACATCCCAC | 75725 |
rs214628687 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12050879 | TCTAAAGACAGTCTG[A/C]GCTACATAGCAAGAC | 75725 |
rs214637250 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11936132 | TTCTCTATTTTGCCT[A/G]TAGGTGTTGAGAAAC | 75725 |
rs214640409 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11994377 | TCCTACTCTGAGCCT[A/G]TTGCTGGACCTCTTT | 75725 |
rs214647661 | in-del | -/TTTG | | | intron-variant | Phf14 | Mm_Celera | 6:11945186 | AATGTCTAGGAAGAA[-/TTTG]TTTGTTTGTTTGCCT | 75725 |
rs214700776 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927342 | CCTTGAGTGCTTGCT[G/T]ATTCCAGTTAGTGAT | 75725 |
rs214702545 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12069402 | TGTTGCTTTCAAACA[-/T]TTTGAGAACTCCATA | 75725 |
rs214705939 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11917977 | TGTTAGTGAAAGGCA[A/G]CAAAGTGCCGGCCAC | 75725 |
rs214718930 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12004868 | TTGATGAATATTTTT[G/T]AATGTAAGCTTAGGA | 75725 |
rs214719194 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11910829 | CCAACAGCATGTCAA[A/T]GTCTGTATACAGTCC | 75725 |
rs214724200 | snp | A/C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083808 | CAGTCTCAGCTCCAC[A/C/T]CTTTGTCTCCATATT | 75725 |
rs214764091 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12084252 | AATATGAGGTTTATG[A/G]TGCTGCTTGTCATGT | 75725 |
rs214764125 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12076757 | AAAGGGAATTCTATG[C/T]CTTTTTATGATCTTA | 75725 |
rs214779231 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11911555 | GAGTACCTGAGATTT[C/T]ATCCCTAGAACTCAA | 75725 |
rs214788681 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12070499 | TTCTCTTCAAACTGT[A/G]GTTTGTTTTTTATTT | 75725 |
rs214797688 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12029259 | TAGTACATGTGTTGA[A/C]TTTTTGAGAAACCTA | 75725 |
rs214804084 | in-del | -/TACT | | | intron-variant | Phf14 | Mm_Celera | 6:12002717 | TGAAGTGCTTTTAAA[-/TACT]TACTAATCTAATGAA | 75725 |
rs214860274 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12071420 | TTAGTACTTTGAATA[A/G]TCCATTGTTTCAACT | 75725 |
rs214870380 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11931307 | TGAGCTTTAGGGTTG[-/T]TTTTATTGGCTGATA | 75725 |
rs214888314 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12014705 | ATCTAATAACTAGGA[A/G]AGAGTGTGGGAAGAA | 75725 |
rs214889948 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12061968 | AGTCTGGTCAATTCC[C/G]TATTGAAATAAAGAC | 75725 |
rs214897174 | snp | G/T | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099389 | ACAGGCTTGCCTACA[G/T]CCTGATCTTAGGAAG | 75725 |
rs214898236 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12063708 | ACGTATAGTTCATTG[A/T]TTTCTTTGTTAAGTT | 75725 |
rs214913135 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12023278 | AGTTTTTTCTAATTT[A/G]TTTTGCCTTGAGGAA | 75725 |
rs214920933 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11932807 | ATAGACAGTTTTACA[A/G]GGCTAACATTGTTTT | 75725 |
rs214930741 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11936157 | AGAAACCTGTAGGTC[C/T]ACTCTAGAGTAGAGA | 75725 |
rs214938282 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12013715 | TAGTCAATGAGTATA[A/T]TTACATTGTACTTAT | 75725 |
rs214959567 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12003599 | AATATGAAAGTAGTA[C/G]CACACAAATACTCAA | 75725 |
rs214972412 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12015457 | CCACAAAGAATCACT[C/T]CTCTGACTTCCCCAG | 75725 |
rs214984120 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12016312 | TTGTCAGATGGCTCA[A/G]TAGCTGACTTAGCAC | 75725 |
rs214984165 | in-del | -/ACAAAC | | | intron-variant | Phf14 | Mm_Celera | 6:11936519 | TTAGATATTCTAAAA[-/ACAAAC]ACAAAAACAAAACTA | 75725 |
rs214984551 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11934911 | TCTTAAACTGGTAGA[G/T]TTTCTTTATGCTTTA | 75725 |
rs214989124 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12064443 | ATTGCAGGGCTACAG[C/G]TTGTGAACTGCCATG | 75725 |
rs214999853 | snp | A/G | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11926139 | GTGGGGAGGGACAGT[A/G]GCCCACCCCCGGGGT | 75725 |
rs215027364 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11976072 | CAGTGCAGACTAGTC[C/T]CTGAGGGACCCGGGA | 75725 |
rs215041704 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11937100 | TCTTTTATGCTTAAT[G/T]ATAGATGTCATTTGA | 75725 |
rs215043097 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11927363 | AGTTAGTGATGTGAA[A/G]AGGTGGTGAACTTGT | 75725 |
rs215051948 | in-del | -/TA | | | intron-variant | Phf14 | Mm_Celera | 6:11993596 | TATATTATAGGGATT[-/TA]TATATATTTGTAAAG | 75725 |
rs215056502 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12072087 | GATTAATGGCCTTAC[-/T]TTTGGGGAAAATAGC | 75725 |
rs215057436 | snp | G/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925384 | AGGAACTCAAGCAGG[G/T]CAGGAACTTGGAGGC | 75725 |
rs215102428 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11927748 | CTCTGACATGTTACC[A/G]TCCCATCAGGCAGTC | 75725 |
rs215103778 | in-del | -/CAAGCTGTTGAA | | | intron-variant | Phf14 | Mm_Celera | 6:12002080 | GACTCTACCACGGAG[-/CAAGCTGTTGAA]CAAGATATACCAAAA | 75725 |
rs215113012 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12095195 | AAAAAAAAAAAAAAA[C/T]GGCTACTCAGCAAGG | 75725 |
rs215114408 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916139 | ttaaacaagtgtgtg[C/T]gcgcgcacacacaca | 75725 |
rs215147630 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12044661 | CACATTAAAAATTGG[C/G]TTTGTTTGATCTCAC | 75725 |
rs215156669 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12042471 | AAGATCTGTTTAAAA[A/T]TTCAGAAGAATTCTG | 75725 |
rs215160007 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12093675 | TGCTTTACTCTCTGC[A/T]ACTTCACAACCTGAA | 75725 |
rs215163212 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12094334 | TTAACAGAAGGAGTA[A/G]TTAGTGTGAGTCATG | 75725 |
rs215177106 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12042662 | GAATGCGAACAAAGA[C/T]GGGATTTACAAGTGG | 75725 |
rs215179199 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12061529 | ACTCTTTACTGTCTT[A/C]AGGGAAAAGAGAATA | 75725 |
rs215197912 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12095923 | ACCGGAAGTTGAGAG[A/T]TCATATCTCAAACTG | 75725 |
rs215231735 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11985856 | CTACAAGTTTTTATG[G/T]AAGTATACATACATA | 75725 |
rs215233874 | in-del | -/AA | | | intron-variant | Phf14 | Mm_Celera | 6:12028720 | AAGTGCAGACTGAAT[-/AA]TTTTTTTTTCAAAAA | 75725 |