SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6181992 | snp | A/T | 0.304688 | 0.243945 | intron-variant | Hecw2 | Mm_Celera | 1:53868717 | ATGACGATTTCCTTA[A/T]GANTCCGAGGAGAAA | 329152 |
rs6182012 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53868720 | ACGATTTCCTTANGA[C/T]TCCGAGGAGAAAGGA | 329152 |
rs6182708 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54066337 | ggcaggtgaattcag[C/T]tcaccaaccaaaggc | 329152 |
rs6182819 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54066395 | acaggactggagggt[A/G]gagacaggcagatcc | 329152 |
rs6183140 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Hecw2 | GRCm38.p3 | 1:53868949 | AAACGGTACAGATGC[C/T]CATGATAGGCTTTGT | 329152 |
rs6184001 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54066601 | tttttttgttgtttt[A/G]gtttttttttttttt | 329152 |
rs6187190 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Hecw2 | Mm_Celera | 1:54060553 | TTAAACCCATGTCTA[A/C]GTTTTCCAAACCCAT | 329152 |
rs6187747 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54060636 | CATTAGCATCTAAAC[A/T]GATTCCAATTTCATT | 329152 |
rs6188229 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Hecw2 | Mm_Celera | 1:54060734 | TATAACTGTCATTGT[A/G]GAGGCCTTTACTGTC | 329152 |
rs6188762 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Hecw2 | Mm_Celera | 1:54060855 | TAATAACCATGAAGA[C/G]TCTACCAAACCCTAA | 329152 |
rs6189197 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54060910 | TGGGTGACTAAGCTT[A/T]GACATTCAGTCATCT | 329152 |
rs6195969 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:53869036 | CTTAATAAGTGGCAC[G/T]GTGCTATGGGACTTT | 329152 |
rs6197054 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53869202 | ggcagtggtggccac[A/G]cctttaatcccagca | 329152 |
rs6203033 | snp | C/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53994627 | tgacaggaacttaag[C/G]agggcaggaacntgg | 329152 |
rs6203055 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53994639 | aagnagggcaggaac[A/G]tggaggcaagagttg | 329152 |
rs6203092 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:53994663 | agagttgatgcaggg[A/G]ccatggagggtgctg | 329152 |
rs6203600 | snp | C/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53994723 | taaaacccaggacca[C/G]cacgcagggattata | 329152 |
rs6204154 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:53994818 | atcttatggaggcat[A/T]ttctgaattgagatt | 329152 |
rs6205282 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:53995007 | TAAAATATAGCTCAA[C/T]TNGGCTAAAACAANA | 329152 |
rs6205283 | snp | A/C | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:53995009 | AAATATAGCTCAANT[A/C]GGCTAAAACAANAGC | 329152 |
rs6205310 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:53995021 | ANTNGGCTAAAACAA[C/T]AGCAATGGCCAGATC | 329152 |
rs6205364 | snp | G/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53995059 | TTTTGTTTTCTTAAC[G/T]AGTTACTTCAGATTA | 329152 |
rs6248481 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54115186 | cacatctgagtttag[A/G]tgtcaccctagaaag | 329152 |
rs6263382 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Hecw2 | Mm_Celera | 1:54115715 | GTATCAACTTAAGGA[A/C]TGCTACTATCACCAG | 329152 |
rs6286542 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54149880 | tctggggattacaag[C/T]tcacagtccaaacag | 329152 |
rs6286999 | snp | C/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54149951 | cctttctccttaact[C/G]tntgcattccngtgt | 329152 |
rs6287001 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54149953 | tttctccttaactnt[A/T]tgcattccngtgttt | 329152 |
rs6287017 | snp | G/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54149962 | aactntntgcattcc[G/T]gtgtttcttcctacn | 329152 |
rs6287051 | snp | A/C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54149977 | ngtgtttcttcctac[A/C/T]atcctcnctctgagc | 329152 |
rs6287055 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54149984 | cttcctacnatcctc[C/T]ctctgagcattttct | 329152 |
rs6287504 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54150000 | ctctgagcattttct[C/T]tgaatggatttccct | 329152 |
rs6287557 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54150032 | ttcaataactatcca[A/T]gttatcctggagnaa | 329152 |
rs6287579 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54150045 | cangttatcctggag[A/G]aaggcacagcattca | 329152 |
rs6287628 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54150072 | ttcattttaacttga[A/T]tacttctaggaagac | 329152 |
rs6287666 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54150088 | tacttctaggaagac[C/T]gtgcctccaaataaa | 329152 |
rs6295895 | snp | A/C | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54123743 | TCCTGTAATAAATTT[A/C]CTTAAGTAAAAATGA | 329152 |
rs6307292 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Hecw2 | Mm_Celera | 1:53933559 | GCTATAATTCCAGCA[C/G]AGGGCTCTCCAAGGT | 329152 |
rs6323965 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53934418 | CTCTCGGGAAGGAAT[A/G]GACTGGTCCACAAGA | 329152 |
rs6324449 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Hecw2 | Mm_Celera | 1:53934486 | GGCTGGCTAATGACA[C/G]AGTCAGCAGTGGAAT | 329152 |
rs6324992 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Hecw2 | Mm_Celera | 1:53934573 | CACTGCATGAGATCT[C/T]GATTGGTGGCTGCCC | 329152 |
rs6325545 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53934669 | GGCTCCCAGTAGTTC[C/T]ATTNTGGATGCNTCA | 329152 |
rs6325562 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53934673 | CCCAGTAGTTCNATT[A/T]TGGATGCNTCACTAT | 329152 |
rs6325579 | snp | G/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53934681 | TTCNATTNTGGATGC[G/T]TCACTATTAAATGCA | 329152 |
rs6336416 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Hecw2 | Mm_Celera | 1:53856327 | GGGTACTCTAGACAC[G/T]AAATAGGATACCTCC | 329152 |
rs6336988 | snp | C/G | 0.484429 | 0.0868505 | intron-variant | Hecw2 | GRCm38.p3 | 1:53856431 | TTATAAGAAGCCCTC[C/G]ATGAGTCATCTATAT | 329152 |
rs6337597 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53856526 | TCTGGAGGCTTGTCT[A/G]GGGAGATATAAACCT | 329152 |
rs6338179 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53856635 | Gcagtggctctcaac[A/G]ttgagcacatatcag | 329152 |
rs6338206 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53856655 | gcacatatcagaatc[C/T]cataggaactttaaa | 329152 |
rs6338652 | snp | G/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53856675 | ggaactttaaaaaat[G/T]ccaaagcccagtcca | 329152 |
rs6338779 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53856758 | gttttctacagctgt[C/T]caggtgagtccaaaa | 329152 |
rs6371761 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54095234 | AGTAGTTAAAGGTAA[C/T]CCAAGAAAGTCTAGC | 329152 |
rs6372274 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54095352 | GTTTCCTAACCTTTA[C/T]GTTGGCTTGTGGGGC | 329152 |
rs6386920 | snp | A/C/T | 0.494922 | 0.202172 | intron-variant | Hecw2 | GRCm38.p3 | 1:54095723 | TAAAGGCTAGGACAC[A/C/T]GCATCCGAGAGAACG | 329152 |
rs6389572 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54168221 | GACTACAAGGCTGGC[A/G]GCTGTAGTCNCCCTA | 329152 |
rs6389589 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Hecw2 | Mm_Celera | 1:54168231 | CTGGCNGCTGTAGTC[A/G]CCCTAACCCTGTCTT | 329152 |
rs6389621 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Hecw2 | Mm_Celera | 1:54168262 | ACCAAGTTTCAAGAT[C/T]ACCTCAACCTAACCC | 329152 |
rs6406541 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Hecw2 | Mm_Celera | 1:54024190 | AAGCAGTTAACCACT[A/G]AAACAAAACTCTTCT | 329152 |
rs6406690 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:54024268 | ATTCATCTAGAGGAG[C/T]TTAGGGAGNGAGGGA | 329152 |
rs6407117 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:54024277 | GAGGAGNTTAGGGAG[A/G]GAGGGATATCTACAA | 329152 |
rs6408803 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54024606 | aagtactcatatggt[A/G]actcacaaccatcag | 329152 |
rs29552601 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:53920125 | AAGGGAGCAAAAACC[A/T]TTCAGTGGAAAAAGG | 329152 |
rs30458955 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54075696 | TATTCTTGGCTATTC[A/T]TGGCTGTCAACTACA | 329152 |
rs30464765 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54184262 | CAAATGTGGTGGAAA[A/G]GCTGTGGATGTGTGG | 329152 |
rs30476938 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54133594 | TGCTCCTTCATTCCT[A/G]CCACATGGACTAAGG | 329152 |
rs30496792 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54120540 | AGCTCACAACCACCT[A/G]GACCTCCAACCCCAG | 329152 |
rs30506354 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54111300 | AACTGCCTACTCTAC[C/T]TTTACTTACAAAATA | 329152 |
rs30507791 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54105059 | ATAAACACACCACTG[A/T]GTGTTGACAACTCAC | 329152 |
rs30508615 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54187940 | TTCCAGCTGAGTTTC[C/T]AAGTGTCTCTTCAAT | 329152 |
rs30517470 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54161814 | TTTGATTATCTTATG[A/G]ATCAGCATCACCTGA | 329152 |
rs30518194 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54178762 | TTAAATGTCTACAGG[A/C]CCCAAGAAGTTCTGC | 329152 |
rs30521120 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54175742 | AATAGGACAAGTGAG[A/G]TAATATCTAATGTCT | 329152 |
rs30525025 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54183485 | TTAACATTCTGTACC[A/G]ATTTAATATCTGATT | 329152 |
rs30573767 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Hecw2 | Mm_Celera | 1:54162763 | ACGAACTTCAGAAAT[A/G]AAATGGCAGCTTGTG | 329152 |
rs30596250 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54101273 | TAAGGTATGTCAGAC[C/T]GTAATTCTTACAAAC | 329152 |
rs30598652 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54087059 | ATTGGATACTAGATC[C/T]ACACCAGGCCAGCAG | 329152 |
rs30602485 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54182163 | ACTCCTAGAATGAAG[G/T]TTTTACTCCTACTTT | 329152 |
rs30612203 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54075697 | ATTCTTGGCTATTCT[A/T]GGCTGTCAACTACAT | 329152 |
rs30689709 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54084551 | TTTCCATTAAAGACT[C/T]GTTGTCTAATTAAAT | 329152 |
rs30702290 | snp | G/T | 0.42 | 0.183303 | intron-variant | Hecw2 | Mm_Celera | 1:54091250 | TGCAAGCACTCTTCC[G/T]AGCATGAGTCAGGCC | 329152 |
rs30731025 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Hecw2 | GRCm38.p3 | 1:54196327 | ATAGCAACCCTCTAT[C/T]TGTTTTTATACTCTT | 329152 |
rs30764783 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Hecw2 | Mm_Celera | 1:54160662 | CTGAGGGTGATGCTG[G/T]GCTAACAGGAGGAGT | 329152 |
rs30801997 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Hecw2 | Mm_Celera | 1:54107428 | CTTCAGGAATTCTCA[A/G]TTAAGTGAGGAAGAC | 329152 |
rs30858737 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Hecw2 | Mm_Celera | 1:54127590 | TTTTTCCCTTCTGGT[C/T]CTGGCATGACTCTTA | 329152 |
rs30864847 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54101986 | AGGGCTCTCTGAGCT[A/G]CCAGTCTAGTCTAAT | 329152 |
rs30893340 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54186112 | TCTTTTATCACCACA[A/G]TCTGCAAGTTATGCA | 329152 |
rs30895908 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54110222 | ACCTCTACAGATGAG[C/T]TATGGCATGTTTGGA | 329152 |
rs30915980 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54165841 | TCACAGCAATAGTAA[C/T]CCTAACTAAGACAGT | 329152 |
rs30916566 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:54155688 | TGTCTTACAGAGATT[A/G]CAATTCAGTGTATGA | 329152 |
rs30989983 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54167376 | TTCGAGACAGGGTTT[C/T]TCTGTATAGCCCTGG | 329152 |
rs31010809 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54183921 | TTTTTCAATTGTCTA[G/T]CAAAAGACAGTTGGA | 329152 |
rs31029571 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Hecw2 | Mm_Celera | 1:54159344 | TCCCATTTGAAAGCC[A/G]GTCTTTTAACTCTCT | 329152 |
rs31040575 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54177437 | ACATGGACTATTTTT[A/T]AAAATTGAGACTGGG | 329152 |
rs31055451 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54127734 | GGATCGTAATGTAAA[C/T]ATCTGATATGCAGGA | 329152 |
rs31086025 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54117480 | AAGGAGGGCACAAGG[A/G]AGGATGCTTGAATCT | 329152 |
rs31087875 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Hecw2 | Mm_Celera | 1:54118895 | GCCCCCAGCCTTCTG[C/G]TCTTGTATCTCTGCC | 329152 |
rs31158149 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54180533 | TGAACAATGACTGTG[C/T]TGACAAGCATGACCA | 329152 |
rs31186167 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54187146 | CCCCATCCCTTCCAC[A/G]GTGCATCGTAAGTTC | 329152 |
rs31234094 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:53869244 | GAGGCAGGCAGATTT[C/T]TGAGTTTGAGGCCAG | 329152 |
rs31249365 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54107153 | TGGGCAATGGTAGTA[A/G]TTTATGCTGTTTGAG | 329152 |
rs31302932 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54173992 | GGAGAAAGCAAAGAG[C/T]TCACAAAGCACTATG | 329152 |
rs31330466 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Hecw2 | Mm_Celera | 1:54153162 | ACGCCTCCTGACACT[A/G]TGGATTACATGCAGT | 329152 |
rs31334572 | snp | A/C | 0.612245 | 0.0999792 | intron-variant | Hecw2 | Mm_Celera | 1:53920053 | AAAGTAGACCAATGG[A/C]ATAGAATTGTAGACC | 329152 |
rs31351043 | snp | A/C | 0.455 | 0.143091 | intron-variant | Hecw2 | Mm_Celera | 1:54146474 | TCGTCTATTTCCTTA[A/C]GCCACTTTTAGGTGA | 329152 |
rs31388308 | snp | A/C/T | 0.415225 | 0.187619 | intron-variant | Hecw2 | GRCm38.p3 | 1:54107410 | GTCACTGTTGGTACC[A/C/T]GTCTTCAGGAATTCT | 329152 |
rs31392798 | snp | A/G/T | 0.417778 | 0.252357 | intron-variant | Hecw2 | Mm_Celera | 1:54129632 | TTAGTAACACTGACT[A/G/T]GTCAAGGTGCAGTCT | 329152 |
rs31395105 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Hecw2 | Mm_Celera | 1:54153032 | CGGGCTCTGGCCTCA[A/G]TATTGCTTCTTCCTC | 329152 |
rs31401868 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54120219 | CACCCCGAGAGAGGC[A/G]ACCTGAGGGATTCTC | 329152 |
rs31401904 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54094566 | GCCAGTAAGGAACAT[C/T]CCTCCATGGCCTCTG | 329152 |
rs31426694 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54157196 | GGGTTTTTTTGTTTG[G/T]TTGGTTGGTTGGTTG | 329152 |
rs31434153 | snp | C/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54091914 | GAAGTCACATATAAA[C/G]AAGAGTTTGATGCCT | 329152 |
rs31451952 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Hecw2 | Mm_Celera | 1:54105478 | GACCCTGAGATTACC[C/T]ACCATTGCTCTGCAT | 329152 |
rs31452855 | snp | A/C | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54135285 | AAGAAGAAGAAGAAG[A/C]AGCAGCAGCAGCAGC | 329152 |
rs31473217 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Hecw2 | Mm_Celera | 1:54105394 | GATACCTTGCTAGTA[C/T]CTATATTCAAGGCAC | 329152 |
rs31474765 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Hecw2 | Mm_Celera | 1:54104473 | AGCAGGAAGCAGAGA[A/C]GTTTTAATGGACTAA | 329152 |
rs31519824 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54094602 | GCTCCTGCTTCCTGA[C/T]CTGCTTGAGTTCCAG | 329152 |
rs31545822 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54141053 | CAGAAAACAAGAAAC[A/T]AAACAATACATTTTA | 329152 |
rs31548564 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54091362 | GTAAGAACAATTAAA[A/T]CTGATTCTCTTGGGT | 329152 |
rs31549651 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54109470 | TTCAGCAATAGCTGG[C/T]TTTGCCTCCGCCTAG | 329152 |
rs31572949 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Hecw2 | Mm_Celera | 1:54128052 | TAGTCATATGTTATG[C/T]GTAACTAACAATCTG | 329152 |
rs31591624 | snp | A/C | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54157739 | CTTTGAATAATAATT[A/C]TTCCCAACAGGGGAA | 329152 |
rs31592902 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54111305 | CCTACTCTACTTTTA[C/T]TTACAAAATAAGTTC | 329152 |
rs31605116 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54090751 | AACTACCGCATATGC[A/G]CACATATATGGTAAA | 329152 |
rs31613514 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54084352 | GGCCTGCCCCACCCC[G/T]CCCCACCCGACCCTG | 329152 |
rs31639250 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54183448 | TCCTGTCGTTTTTTT[A/T]AAATACAAAAATGTT | 329152 |
rs31643984 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54174037 | AAGAGAGGGAAAGAG[A/G]AGGGAAGGGAGGGGA | 329152 |
rs31655468 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54188243 | GAACCCAGTTTTTTT[A/T]AAAAAAAATGCTTTC | 329152 |
rs31660908 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:54091003 | TTGTTTAAATATAAT[A/G]GTATGTAAAGATCAT | 329152 |
rs31671978 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54193105 | CCGAGGTGCCAAGTA[C/T]ATGCAAGGGCCAATA | 329152 |
rs31713013 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54182957 | GTGTTTGCACACATG[C/T]GCATTTGTCTGCTGT | 329152 |
rs31731153 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54185440 | TAGAGACATTTTGGG[A/G]GCTCCAGGCCAGAGA | 329152 |
rs31747477 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Hecw2 | GRCm38.p3 | 1:53828108 | CAATTTAAGATTAAG[A/G]AACAGGACTGCAAAT | 329152 |
rs31767536 | snp | C/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54181383 | ACACACACACACACA[C/G]AGAGAGAGAGAGAGA | 329152 |
rs31779234 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54187930 | TCCTTAAACTTTCCA[A/G]CTGAGTTTCTAAGTG | 329152 |
rs31782093 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54131989 | TACTTATCCTAACAC[C/T]AATAAGAAAAGAAAC | 329152 |
rs31783208 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54180422 | CTGGGGATACAGTAG[A/T]CAGTGAAGCATCAAC | 329152 |
rs31789561 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54091897 | ATCAAAATTAATAAA[C/T]GGAAGTCACATATAA | 329152 |
rs31798076 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54086310 | ATGACCTAGAAAGAT[A/G]GATTGTGACCCAGCT | 329152 |
rs31809882 | snp | A/C | 0.465374 | 0.126941 | intron-variant | Hecw2 | Mm_Celera | 1:54139813 | GCCACATACATAAAA[A/C]AGAAAAGATCAGAAA | 329152 |
rs31815236 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54187920 | GGAATTTCAGTCCTT[A/T]AACTTTCCAGCTGAG | 329152 |
rs31819442 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54178569 | TCTCTGCTCAAAGAG[A/G]ACATGATTATATACA | 329152 |
rs31840990 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54181725 | AAGAGAGAAAGAGAA[A/G]GAAAAGTATGATCCA | 329152 |
rs31842343 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Hecw2 | Mm_Celera | 1:54148848 | ACTCAGATGTAATTG[A/G]TTTGCAAGATTTTGG | 329152 |
rs31860195 | snp | A/T | 0.455 | 0.143091 | intron-variant | Hecw2 | Mm_Celera | 1:54123434 | TCATATTATGAGTAA[A/T]GCATTCCTGATTAGG | 329152 |
rs31874836 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54091591 | CTTGGTTTTGCACAC[C/T]TGGTCCCCAGGTGCT | 329152 |
rs31886270 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54136809 | AAATTAATTAATAGG[A/G]GTTTTGTTCAATTTT | 329152 |
rs31907816 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54177577 | CGACCTCTTCTGGTG[A/T]GTCTGAAGTCAGCTA | 329152 |
rs31912292 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Hecw2 | Mm_Celera | 1:54137473 | AGCCCCAAGAGATTC[C/T]GACCGGGGCAGACTC | 329152 |
rs31914015 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54127635 | AACCTTCCTAATGCT[A/G]CCTCCCTTGTATGCA | 329152 |
rs31939991 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54103514 | GTGTGACCCCTTGTC[A/G]AGTTCCCTCCCTACT | 329152 |
rs31949040 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Hecw2 | Mm_Celera | 1:54110953 | GGACTTGCCTACACG[A/G]CACAGGAAGAATGTG | 329152 |
rs31959237 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Hecw2 | Mm_Celera | 1:54133185 | GCAAATGATGGAGAA[C/T]GTGGGTAACTGCTCT | 329152 |
rs31971644 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Hecw2 | Mm_Celera | 1:54118601 | TTTCCACCCTGGGCC[G/T]CAGCTAAAATATGAG | 329152 |
rs31976178 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54116995 | CTATCCTCTTCAGGA[C/T]CCTCAATCCTTCCTC | 329152 |
rs31980723 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Hecw2 | GRCm38.p3 | 1:53845264 | GTTCCCAGAATGATA[A/C]TCAGTAGAGGCTCTA | 329152 |
rs31993878 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Hecw2 | Mm_Celera | 1:54105413 | TATTCAAGGCACTCG[C/T]TCCACTGGGGATTTA | 329152 |
rs32003126 | snp | A/C | 0.265928 | 0.249492 | intron-variant | Hecw2 | Mm_Celera | 1:54128189 | CAAATGATTATTAAA[A/C]GATTGTATGAACTAT | 329152 |
rs32004478 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54088487 | TACCGGAGGATCCAG[A/C/T]AATACCTCTTCTGGG | 329152 |
rs32014398 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Hecw2 | Mm_Celera | 1:54108529 | AAAGAAAAAACATAT[A/G]ACCATCACATGACTC | 329152 |
rs32022954 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54177457 | TTGAGACTGGGCTGG[C/T]GATATGGCTCAGCAG | 329152 |
rs32027204 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54191866 | TAAAGCAAAAGGAAC[A/T]TGAATTCAAGGATAG | 329152 |
rs32028946 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54084555 | CATTAAAGACTTGTT[A/G]TCTAATTAAATGTTC | 329152 |
rs32035239 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54127268 | CAACCTCAGGCACCA[C/T]ATGGGAGCTCACGCT | 329152 |
rs32043581 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Hecw2 | Mm_Celera | 1:54127430 | TTGAAATTTTGTAAA[C/T]TGATGCATTTCAGAG | 329152 |
rs32046735 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54182318 | TACCCTGCTGCAGGG[C/T]TCCCGCCTAACATGG | 329152 |
rs32057812 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Hecw2 | Mm_Celera | 1:54137267 | AGGAGCCTAGCACAC[A/G]GGCTTGAGAATTCCA | 329152 |
rs32079703 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54093417 | TGATGACAGGTTCTG[G/T]CAGGACATGTTCTGC | 329152 |
rs32081313 | snp | C/G | 0.375 | 0.216506 | intron-variant | Hecw2 | GRCm38.p3 | 1:54181385 | ACACACACACACAGA[C/G]AGAGAGAGAGAGAGA | 329152 |
rs32089921 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54183779 | AGTCACTGCTGTCCA[C/G]CCCTCTTGTGAGGCA | 329152 |
rs32104221 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Hecw2 | Mm_Celera | 1:54133284 | TTGTTTTTCTGCGAC[A/G]GCTCCCACATCTACT | 329152 |
rs32145937 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:53819983 | ACCAAAACCAAAAAA[A/G]AAAAGAAAAGAAAAG | 329152 |
rs32158924 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54117438 | ATACCCACACTATAA[A/T]CCACAGATCCTAAGA | 329152 |
rs32177835 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Hecw2 | Mm_Celera | 1:54090443 | TAAGTTGGCAGTACT[A/C]TGGAGAGATGGTTGA | 329152 |
rs32179999 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54088259 | CTTCTTGGCCCTGGC[A/G]TTCCCCTGTACTGAG | 329152 |
rs32180540 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54183591 | ATACTGGGCATTATA[C/T]AGTCTGGCCAGACTT | 329152 |
rs32184851 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Hecw2 | Mm_Celera | 1:54132138 | GCTGGGAGTGTGATC[A/G]TACAACTATAATAGT | 329152 |
rs32226367 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Hecw2 | Mm_Celera | 1:54153089 | CAATGACTGCTGTTG[C/T]CAGCCATAAGAAAAT | 329152 |
rs32237350 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54183131 | TTCCAAAAGATAAAT[G/T]TTTGAGGAATGGGTA | 329152 |
rs32267392 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54171714 | TAAAAAAATTCTAAG[A/G]AATGCTCTGAAAAGT | 329152 |
rs32271617 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54128125 | TGCAGACACAATTTT[C/T]CTAAGAACTGCTGCC | 329152 |
rs32275619 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Hecw2 | Mm_Celera | 1:54127936 | GAGTTTTACCAGCAG[A/G]GTAGAGCACTTGGTT | 329152 |
rs32306384 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54084725 | CCAGTCAATATTTTA[C/T]CTTCTGAGCCTGGCA | 329152 |
rs32313689 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54182120 | GCTACACTTCAAAGG[C/T]AAATAAGAAGAAATT | 329152 |
rs32315659 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54186680 | AAGGGTCTCAGGAGT[A/G]GGCTAGTAACATGAC | 329152 |
rs32322251 | snp | A/C | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54165789 | TGAATAAAATAAACC[A/C]TTTCCTTCTCAAGTT | 329152 |
rs32359359 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54182321 | CCTGCTGCAGGGTTC[C/G]CGCCTAACATGGAGA | 329152 |
rs32365005 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54160127 | GGACAACTTAAATAC[A/G]CCAGCAATCTCCTTT | 329152 |
rs32392361 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54091908 | TAAACGGAAGTCACA[C/T]ATAAAGAAGAGTTTG | 329152 |
rs32409511 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Hecw2 | Mm_Celera | 1:54136519 | ATAAACTAGGTCCTG[A/G]GAGCCACAGGGTCCT | 329152 |
rs32421254 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Hecw2 | Mm_Celera | 1:54131689 | GTTCTCTTCAGTCCT[C/T]AGAGCCCATCAAATC | 329152 |
rs32422064 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Hecw2 | Mm_Celera | 1:54161230 | TGTAAACATAGAGAT[A/G]GTGCCACAATGTAGA | 329152 |
rs32426956 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:53920106 | TGGTCACTTGATCTT[C/T]GACAAGGGAGCTAAA | 329152 |
rs32428353 | snp | C/G/T | 0.375 | 0.216506 | intron-variant | Hecw2 | GRCm38.p3 | 1:54192100 | CCTCTCTAACCTCTC[C/G/T]TTCACATCCTGATAC | 329152 |
rs32434080 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54091078 | ATACACATTCGGGTA[C/T]GTGTTAGCACAACGG | 329152 |
rs32435638 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Hecw2 | Mm_Celera | 1:54155182 | GACCAAAAAATTCTT[C/G]TTTTAGGCAACAGAT | 329152 |
rs32440645 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54165619 | GTTGGTGCCATCAGT[A/G]GGCTGATGGTCCTGG | 329152 |
rs32446135 | snp | A/C | 0.465374 | 0.126941 | intron-variant | Hecw2 | Mm_Celera | 1:54139577 | TTGCAAGGCTAAGCA[A/C]TTAACTATCAGAGTC | 329152 |
rs32455114 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Hecw2 | Mm_Celera | 1:54133603 | ATTCCTGCCACATGG[A/G]CTAAGGTGCTCACAC | 329152 |
rs32467834 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54110165 | AATCCCAAGGACACA[C/T]GTGGAGGAAGGGACA | 329152 |
rs32473888 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54183981 | TTCAGATACTTCCTA[C/T]GACAGAATCACTGAG | 329152 |
rs32478938 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54161529 | GGGGTTCTGAGAGAA[A/G]AGGTTTCTGGGAGTG | 329152 |
rs32492034 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54181794 | GACAATTTTTACAGT[G/T]TATTAATTATATCTT | 329152 |
rs32532610 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Hecw2 | Mm_Celera | 1:54087188 | ATGCATATGTCTTCA[C/T]TTCCCATACACCTAA | 329152 |
rs32535397 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54177495 | CACTGACTGTTCTTC[C/T]AAAAAGTCCTGAGTT | 329152 |
rs32548885 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54183291 | TAATGCAGATTCTAA[C/T]TCAATAGGTCTGGTA | 329152 |
rs32554981 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54094559 | GAAGCAAGCCAGTAA[A/G]GAACATTCCTCCATG | 329152 |
rs32576323 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54192520 | TATCCTCAACTACAG[C/T]AACAACTTGCTTGGA | 329152 |
rs32578936 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54191556 | ATGGGGCTTTAGAAC[A/C]ATGGCAGACACTTTG | 329152 |
rs32584979 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54120223 | CCGAGAGAGGCAACC[C/T]GAGGGATTCTCTTTT | 329152 |
rs32590861 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Hecw2 | Mm_Celera | 1:54132171 | AGGCTTAGCTTGCAT[A/G]AGAACATGGATTTAA | 329152 |
rs32594155 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Hecw2 | Mm_Celera | 1:54171637 | TAGAAATTTTTGCAA[A/G]TGAAATTAAATTACT | 329152 |
rs32594903 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54091724 | TGGGTCTGCAGCCTC[C/T]TGATTGTTTTGGTGA | 329152 |
rs32604588 | snp | A/C | 0.455 | 0.143091 | intron-variant | Hecw2 | Mm_Celera | 1:54128115 | CCAACTTGTTTGCAG[A/C]CACAATTTTTCTAAG | 329152 |
rs32605573 | snp | C/G | 0.375 | 0.216506 | intron-variant | Hecw2 | GRCm38.p3 | 1:54181518 | CAAGAAAGAAAATGA[C/G]CAAATTTTCTTCAAC | 329152 |
rs32612864 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54091649 | TCAGGAGGTGGGGCC[A/G]TGCAAGAGGAAGCAG | 329152 |
rs32615662 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Hecw2 | Mm_Celera | 1:54111344 | TAATCAAGGCACAGA[A/C]TTTTTGCATGATACA | 329152 |
rs32646075 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Hecw2 | Mm_Celera | 1:54101342 | GAACAGTAAAAGTCC[C/T]GAACCACACACAATA | 329152 |
rs32676984 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54086994 | TAGATAGATAGATAG[A/G]TAGATAGATAGATAG | 329152 |
rs32677095 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Hecw2 | Mm_Celera | 1:54120779 | TCCTTTAGTATTTCA[C/T]ATTAGTTAGCAAGAT | 329152 |
rs32677719 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54144985 | AAACTTAGTGGGTGA[C/T]AGATAGATAGATAGA | 329152 |
rs32682276 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54111260 | AAAGACAGAGAAATT[A/T]AAAAAAAAAATGACT | 329152 |
rs32700268 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54104477 | GGAAGCAGAGAAGTT[C/T]TAATGGACTAATTCA | 329152 |
rs32711221 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Hecw2 | Mm_Celera | 1:54119182 | CAATGAGACTGTGGG[G/T]TTTTTTTTTCCTTTA | 329152 |
rs32712289 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54158813 | GGAAGAGCTCTTATA[C/T]ACACACACACACACA | 329152 |
rs32713119 | snp | A/C | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54183216 | CCATGATATGTACAA[A/C]TGAGTGTTATACATG | 329152 |
rs32715039 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54118887 | GCCAGAATGCCCCCA[A/G]CCTTCTGGTCTTGTA | 329152 |
rs32715381 | snp | A/C | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54177564 | TGATGAGATCTGACG[A/C]CCTCTTCTGGTGAGT | 329152 |
rs32738089 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54161638 | CAGCTTTCCAACTTT[C/T]TCTCTGGTCTGCTCT | 329152 |
rs32739754 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54089822 | GTCCCAGTTTCATGA[C/T]GGTAACTGCACTCTT | 329152 |
rs32742851 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54183215 | CCCATGATATGTACA[A/G]CTGAGTGTTATACAT | 329152 |
rs32753115 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54091893 | GCACATCAAAATTAA[C/T]AAACGGAAGTCACAT | 329152 |
rs32758422 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54084517 | GAATAAGAAGTTACA[A/T]CAGAAATGTATACAT | 329152 |
rs32760777 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54107447 | AGTGAGGAAGACAGG[C/T]CACACCCCCAATGAT | 329152 |
rs32766047 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54108671 | CTTCCTTCTTCTCTT[C/T]CTTCCTTCTTTCCTT | 329152 |
rs32797393 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54175779 | AACCAGAGAAGGGTG[A/G]TTAGTCATGTCTACT | 329152 |
rs32805462 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54190662 | TCCCAGACTAAATAT[A/G]AAGGAGAAAGCCAGA | 329152 |
rs33825675 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw2 | GRCm38.p3 | 1:53972705 | GATGACGATGATGAA[A/G]TACCTCAGTCCTAAT | 329152 |
rs33825678 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53972770 | TCCTGCTGCTACAGA[A/T]TTTCTACCGTAAAGA | 329152 |
rs33825681 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | GRCm38.p3 | 1:53972797 | AAGATTGAAGTAAAC[A/G]ATCTTTTCCTAGCAA | 329152 |
rs33826594 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53974600 | ACAGTAATGAAAAAG[A/G]TGCTCACTCCTTAGA | 329152 |
rs33826597 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hecw2 | Mm_Celera | 1:53975166 | ACACACACACACACA[C/T]GCTCGAGAAGCATAA | 329152 |
rs33826600 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53975167 | CACACACACACACAC[A/G]CTCGAGAAGCATAAA | 329152 |
rs33826603 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw2 | GRCm38.p3 | 1:53975286 | ATGAACAAAGTAATG[A/G]CACATGACTGTACAC | 329152 |
rs33827266 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53985864 | AGGTGTAAGAGGAGG[A/C]TCATGGGTGTATGTG | 329152 |
rs33827269 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:53985902 | ACACAATGGATAATG[C/T]CACAATAATAACTAC | 329152 |
rs33827272 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53985943 | TTGCCAGGACCTTTA[A/G]CGAGGAAGACTGAAA | 329152 |
rs33827496 | snp | A/C/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53975416 | TTAATTTGGGGAAAC[A/C/G]TGTTAGTAGGTCAAA | 329152 |
rs33827499 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53975480 | AAGAAAGTAACAATC[A/G]TAGACAGGATGGAGA | 329152 |
rs33827502 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Hecw2 | GRCm38.p3 | 1:53976036 | TCAAACCACCATCAT[A/G]TAATTTCATTCTTTA | 329152 |
rs33828225 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:53986268 | CAATATAAAGGATTG[C/T]AAAATAATATCAAGT | 329152 |
rs33828228 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53986292 | ATCAAGTGAGCAGCA[A/C]GGAGCCCGGGGCAGC | 329152 |
rs33828231 | snp | C/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53986334 | TGTGTTAGTGTCCCT[C/G]GTGTGGCCAGTAGGA | 329152 |
rs33828515 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:53976376 | TAGTGTATAAAATTC[G/T]AATGGTACCTGGCTT | 329152 |
rs33828518 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:53976420 | TGAGGATATGAATAG[A/G]CGGTGCAAGCCTGGA | 329152 |
rs33828521 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:53976442 | AAGCCTGGAAACCAC[C/G]GGAGTGAAACACGTA | 329152 |
rs33829124 | snp | C/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53986359 | GTAGGAAAGACTAAA[C/G]CACTGACACAGAATC | 329152 |
rs33829127 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Hecw2 | GRCm38.p3 | 1:53986501 | CTCATGCGAACAGAT[C/T]CTGCTCAAATTTTCA | 329152 |
rs33829130 | snp | G/T | 0.426035 | 0.177515 | intron-variant | Hecw2 | GRCm38.p3 | 1:53986551 | TTTGGAAGAGAAAAC[G/T]TGCCTATTTTCAACT | 329152 |
rs33829133 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53986602 | TTCCTTCAGTTTATT[A/G]CACACACTCGTTTCA | 329152 |
rs33829324 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:53976531 | GCAAAGCACATTCCT[C/T]CATGTTTTCACATTT | 329152 |
rs33829327 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:53977170 | ATGCTTAATGCACCT[A/T]AGTCTAGTTCTATTA | 329152 |
rs33829330 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:53977195 | CTATTAGAACCACAC[A/G]GAGGTGCCCTCTTCT | 329152 |
rs33829333 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Hecw2 | GRCm38.p3 | 1:53977226 | CTCTACACAAGGAAC[C/G]CAGAACAAATTTTTC | 329152 |
rs33829593 | snp | C/T | 0.128419 | 0.218444 | intron-variant | Hecw2 | Mm_Celera | 1:53970382 | TTGCTATTTCCTGTA[C/T]AGAACGTCATCCATA | 329152 |
rs33829806 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53986660 | AGCAAATAAAGCTGA[A/T]ATCGTAGGACATCTT | 329152 |
rs33829809 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw2 | GRCm38.p3 | 1:53986686 | ATCTTTGTGAGAGTC[A/G]ATGGCATCCATCCAA | 329152 |
rs33829812 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53986858 | GTTTCTATATAAACA[G/T]CTCAATAAAATGTTT | 329152 |
rs33829896 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53977255 | TCAGCAGCACGTGTA[C/T]AAGACGAATGACAAT | 329152 |
rs33829899 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:53977649 | CCTTTTGTTTTTAAT[C/T]TTAATATCATTGTTA | 329152 |
rs33829902 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53977685 | TGGTCTCTGGGACAC[A/G]TCTCCACAGCTCGTC | 329152 |
rs33830214 | snp | A/G | 0.244898 | 0.249948 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Hecw2 | Mm_Celera | 1:53978765 | GTCTGATAGAGTCTG[A/G]ACAGAGAAGCTGCTC | 329152 |
rs33830217 | snp | C/T | 0.336735 | 0.234472 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Hecw2 | Mm_Celera | 1:53978847 | AGCTAGTGAATGGAC[C/T]GGGAGCAGCCACATC | 329152 |
rs33830220 | snp | C/T | 0.32 | 0.24 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Hecw2 | Mm_Celera | 1:53978892 | TCTGTAGACTTATCA[C/T]CTCAAATTATTAAAA | 329152 |
rs33830223 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53980943 | GAGGAAAGGCAGAAA[A/G]TTTCAAAAATAAAAA | 329152 |
rs33830224 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54001885 | TATGACTCCTGGGGT[A/G]CCCTGTCCCCAAATC | 329152 |
rs33830227 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hecw2 | Mm_Celera | 1:54001959 | CAACTCTGAGGACAA[A/G]TGAATGTCCACAGCG | 329152 |
rs33830230 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54002240 | ACTTTGAAATGTCAA[C/T]TGCATGTGCATTTCA | 329152 |
rs33830233 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54002326 | GAAACACGCAGATGT[A/G]CCCTATTTCCTGTGC | 329152 |
rs33830266 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:53970471 | AGCCAAGTCCTAACC[A/G]CTGCCAGCCAGAACA | 329152 |
rs33830269 | snp | A/T | 0.328181 | 0.237461 | intron-variant | Hecw2 | Mm_Celera | 1:53970502 | TACACAATTCCAGAC[A/T]TTCAGGGTGGAGGCA | 329152 |
rs33830272 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:53970534 | GAAGTGCCAAGCAAC[C/T]TCCTGTACAAAATGT | 329152 |
rs33830295 | snp | A/G | 0.42 | 0.183303 | intron-variant | Hecw2 | Mm_Celera | 1:53995189 | CAATGCTAGGACAGG[A/G]AAAAACTGTCTGTTC | 329152 |
rs33830298 | snp | C/G | 0.396694 | 0.202437 | intron-variant | Hecw2 | Mm_Celera | 1:53995213 | TCTGTTCAACTCTGA[C/G]ATATATTTGAATTTG | 329152 |
rs33830301 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Hecw2 | GRCm38.p3 | 1:53995352 | GACAAAAAACAAAAC[A/T]TTAAAACTTGTCAAA | 329152 |
rs33830325 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54004457 | TCTTCTAAAACTCGG[C/G]TACAGTAAGAGAGTC | 329152 |
rs33830328 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54004923 | TGTCTTAATCCCAGT[C/T]TTAACTGAGTATCTA | 329152 |
rs33830331 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54004986 | GTGGAAGCTACTGTA[C/T]GTACATGATCAAATC | 329152 |
rs33830386 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Hecw2 | GRCm38.p3 | 1:54022874 | CCTGTATTTTTGAGT[A/G]CTGTGTTCACATTCA | 329152 |
rs33830389 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Hecw2 | Mm_Celera | 1:54023171 | ACATCACCAGTTATA[A/T]GTCCCATTAAATCCC | 329152 |
rs33830392 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:54023220 | TTCTATAGAGACCAT[C/T]TCTCTGTTCCATAAA | 329152 |
rs33830395 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54009856 | TATCTATATCCTGAG[A/G]CACAGCTGCCATCCA | 329152 |
rs33830398 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Hecw2 | Mm_Celera | 1:54009878 | TGCCATCCATTAAGC[A/C]GCGCTTCAGGCATAA | 329152 |
rs33830401 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54009973 | TCCGAGGTCACCGGT[A/C]CACAAAATTGCTTGT | 329152 |
rs33830475 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54069514 | CTGGGTTCAGTAGTA[C/T]CTACTAAAATCCCTG | 329152 |
rs33830478 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54069684 | AGAGGATAAAGAAAA[A/C]GAGGTACAAAACACT | 329152 |
rs33830481 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54069756 | AGCACTTACAGCTAT[A/G]TATCTGCTGGCTCTC | 329152 |
rs33830488 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw2 | GRCm38.p3 | 1:54060762 | GTCTTTACCTCTGAA[C/T]TCCCATGGAGGGCCA | 329152 |
rs33830492 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54061032 | ATAACTCTCTAATTA[A/T]CCTCACTGGCAATGC | 329152 |
rs33830514 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54015079 | CCTGAAGGCTCAGAG[A/G]AGAATTTGCATAATG | 329152 |
rs33830516 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | GRCm38.p3 | 1:54015086 | GCTCAGAGGAGAATT[A/T]GCATAATGTCATACT | 329152 |
rs33830519 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54015118 | TTGGCCACAGCAACT[C/G]ATTCAGGAAAGGGCT | 329152 |
rs33830522 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54015403 | ACATCCAACTGAACA[C/T]TTACATCCTTCAGAG | 329152 |
rs33830524 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54046805 | GAATTAGCTTGAGAG[C/T]ACCATCAGCTCTGTT | 329152 |
rs33830527 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hecw2 | GRCm38.p3 | 1:54047692 | GAAGATGCTTGTATT[G/T]TCCAAGAGAGCTCTC | 329152 |
rs33830530 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hecw2 | GRCm38.p3 | 1:54048232 | ACCTCACTCTGCCTC[A/G]ATACATCCATTATAT | 329152 |
rs33830533 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Hecw2 | Mm_Celera | 1:54049211 | GACTTGGAAACAGTT[G/T]GCAATGAGGGAATAA | 329152 |
rs33830675 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53986875 | TCAATAAAATGTTTG[A/G]AAAAAAAAAGCAAGT | 329152 |
rs33830678 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53986876 | CAATAAAATGTTTGG[A/G]AAAAAAAAGCAAGTT | 329152 |
rs33830681 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53986954 | GTTGCAGGAAGGTAA[C/T]AGCTGTCACATGAAA | 329152 |
rs33830735 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:54041244 | AGGCGAGCATCTTTA[A/C]CCCAGAGACTCGGTG | 329152 |
rs33830738 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw2 | GRCm38.p3 | 1:54041295 | CTCTCTTCTGAGCCC[A/G]CTGCTTGTCACCCTG | 329152 |
rs33830741 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54041666 | CTCTTATTCTGTGCA[A/C]TCAGACTCTTGCAAT | 329152 |
rs33830765 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:53977728 | CCTTTGAAGAGAAAC[A/G]TGCTTTAGCACCTCA | 329152 |
rs33830767 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:53977746 | CTTTAGCACCTCATG[C/T]CCTGAAAGAAAAGCT | 329152 |
rs33830770 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53977815 | CTTTCTCCAGGGGCA[G/T]ATAATCTAACCTGCT | 329152 |
rs33830773 | snp | C/T | 0.336735 | 0.234472 | intron-variant, utr-variant-5-prime | Hecw2 | Mm_Celera | 1:53978060 | GGCAAACACAGCACA[C/T]AGCTCACTAGTCACC | 329152 |
rs33830864 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54090360 | CATCCCCAAAGCATT[A/G]ACATGGTGAAGGCCT | 329152 |
rs33830869 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hecw2 | Mm_Celera | 1:54090712 | TTTAAGCAGTTCTCT[C/T]CGATTATCTTGTCAC | 329152 |
rs33830872 | snp | A/C | 0.18 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54090803 | AAGATGACTCACTTT[A/C]GATCACAGGATTTTT | 329152 |
rs33831156 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54002363 | TATCAGAGATACAGA[A/G]CACATTCTTGTTGGC | 329152 |
rs33831159 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54002387 | TGTTGGCTACTATTT[C/T]CCCCAAAGGTTGGAA | 329152 |
rs33831161 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54002423 | AGATATTCCAAGTAA[C/T]ATCAAGTGATTTAAT | 329152 |
rs33831205 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53970702 | GGGAAGCAGGCGAGC[A/C]ATGGTTTACATAAGA | 329152 |
rs33831208 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:53970745 | CAAGGATGCCACATA[A/G]ATGTGTTGAGCTGTG | 329152 |
rs33831211 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53971553 | TTGTGCTTGCTCATG[C/T]TACTCTGTTTTTACT | 329152 |
rs33831224 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hecw2 | Mm_Celera | 1:53995616 | TAGTAACGTATTTCA[C/T]TGAAGAGCAGCAGTG | 329152 |
rs33831227 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:53995818 | CCATGTATTGCTTAA[A/T]GTTCTTTATAACTCC | 329152 |
rs33831230 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | GRCm38.p3 | 1:53995853 | AACTCAGAAAATAAT[C/T]TGGCAGGTTGGAGAT | 329152 |
rs33831232 | snp | A/C/G | 0.297521 | 0.245442 | intron-variant | Hecw2 | GRCm38.p3 | 1:53996144 | GCTTTCAGAGGTAAA[A/C/G]CAATAGTACTGTCAG | 329152 |
rs33831276 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54096026 | TCTCATAGATAGCAA[A/G]ACCTTAACTTGGATA | 329152 |
rs33831279 | snp | A/T | 0.396694 | 0.202437 | intron-variant | Hecw2 | Mm_Celera | 1:54096126 | TTACCATATATCTTA[A/T]AGCCTTATCATACAG | 329152 |
rs33831282 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54096308 | CAGTACCAAAGACAT[C/T]CATCAAAACTGCACC | 329152 |
rs33831285 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54105552 | CAGCACACAGTGAGT[A/T]CGCTCTTCTACCAGC | 329152 |
rs33831288 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54105553 | AGCACACAGTGAGTT[A/C]GCTCTTCTACCAGCA | 329152 |
rs33831291 | snp | C/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54105627 | ATGACACCAGACACA[C/G]TGCAGATGATCAATA | 329152 |
rs33831295 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53981244 | TTTTAAATAGAAAAG[A/T]GCTCTGTGAAGCTAT | 329152 |
rs33831298 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53981309 | TACTTGCTGAATGCA[A/G]TCTAAGACTATAAAA | 329152 |
rs33831301 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53981455 | TTCTGTGTTGTTCCT[G/T]TGACCCTAACACCCA | 329152 |
rs33831303 | snp | C/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53981576 | GGGACAAATCATCAC[C/G]CTTTTCCTGCGTGGG | 329152 |
rs33831355 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hecw2 | Mm_Celera | 1:54023352 | GACACGTGTGCTATT[A/G]TTATGAAACCCAGGT | 329152 |
rs33831358 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Hecw2 | GRCm38.p3 | 1:54023375 | ACCCAGGTTCTCAGA[A/G]CATCCACTTGACAGT | 329152 |
rs33831361 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54023545 | GAATAAATAAATAAA[A/T]CCTAACCAATAGCAA | 329152 |
rs33831384 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54005046 | GTGGTTAAATAAATG[A/T]TGGAACAATCATGCC | 329152 |
rs33831386 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54005061 | ATGGAACAATCATGC[C/T]GAGCGCTTTAAAGAT | 329152 |
rs33831389 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54005448 | TTTCTCTTTAACAGC[C/T]TTACTTCTAATCACA | 329152 |
rs33831392 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54005530 | TTTCACAGAGATCTT[A/G]TACGTCCTGGGTATT | 329152 |
rs33831406 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Hecw2 | GRCm38.p3 | 1:54049269 | CTTTTGGGCGAATCT[A/G]AAGTTAAGAGATAGA | 329152 |
rs33831409 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hecw2 | GRCm38.p3 | 1:54051094 | TGTATCTCAGGACCA[A/G]TGCTGTTTTGTGTAA | 329152 |
rs33831412 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hecw2 | GRCm38.p3 | 1:54051125 | ACATCCTCCCTCATC[C/T]CAGACTCCTTCAGTT | 329152 |
rs33831414 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54010521 | GTCTGTCATAGGGAG[C/T]AGAATTGACAAACAG | 329152 |
rs33831417 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54011973 | TATTTATGTCAATCT[A/G]TTATATCTAACCAAA | 329152 |
rs33831420 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54012155 | TTAAAATCCTTATGG[A/G]AGAAGCAAATCTTTA | 329152 |
rs33831423 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54012168 | GGAAGAAGCAAATCT[C/T]TATTGAACTTGCATT | 329152 |
rs33831515 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Hecw2 | GRCm38.p3 | 1:54015808 | AACTGTATTGAGAGA[G/T]AAAACTTCCAGCATC | 329152 |
rs33831518 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw2 | GRCm38.p3 | 1:54015876 | AGCAGTGGGTTGAAA[A/G]GAAGGAAATCCGCAG | 329152 |
rs33831521 | snp | C/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54016048 | GGGAGGGTCCTTCCA[C/G]AGTTACAGACAAGTG | 329152 |
rs33831574 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Hecw2 | GRCm38.p3 | 1:53986955 | TTGCAGGAAGGTAAC[A/G]GCTGTCACATGAAAA | 329152 |
rs33831577 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53987059 | TGGCTTTTCACATTG[A/G]CCTCTAAGACTCTGC | 329152 |
rs33831580 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:53987265 | AAAAAGGATGAGAAA[C/T]TCACAGTGTGCACAT | 329152 |
rs33831583 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:53987267 | AAAGGATGAGAAACT[C/T]ACAGTGTGCACATTA | 329152 |
rs33831614 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54069789 | CCCCCTTCACTAAAG[C/T]AAATTTCTTATTCAA | 329152 |
rs33831617 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54069929 | CTGCCAAGAGGCTAA[A/G]GTTGACTATACGTCT | 329152 |
rs33831620 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54074484 | TCCACCATGAAAATT[A/C]AAAGATCCAGTTCCA | 329152 |
rs33831623 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54074593 | TATGAGAGATAACAA[A/G]ACACCAGATCAGAAG | 329152 |
rs33831624 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54041741 | GTTAGCATGAGATTC[C/T]ACTTAAAAACAAACT | 329152 |
rs33831627 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54041750 | AGATTCTACTTAAAA[A/G]CAAACTAGTTGGGCT | 329152 |
rs33831630 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54041970 | AAACTAGTTACTCTC[C/T]AGTGTCCTATTTGTA | 329152 |
rs33831632 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54042049 | AGAAAAGGCTCCCCG[A/G]CTTTTCCCATTTCTC | 329152 |
rs33831684 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54061069 | CTGTAAGGACCCAGG[A/G]TTAGTACCTTGACAA | 329152 |
rs33831686 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54061385 | TTGAATTGCTTTTTA[A/G]AATCTCAAGTTATAA | 329152 |
rs33831689 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54061494 | ATCTAGAACAATCTA[C/T]GAAGCAGTCGTTGGC | 329152 |
rs33831692 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54061525 | CTTAATTAGGAACTA[A/C]AGTTCAAACAGTTAA | 329152 |
rs33831795 | snp | C/T | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Hecw2 | Mm_Celera | 1:53978078 | CTCACTAGTCACCAC[C/T]GGTAACCAATGGAGA | 329152 |
rs33831798 | snp | C/G | 0.46281 | 0.131194 | intron-variant, utr-variant-5-prime | Hecw2 | GRCm38.p3 | 1:53978127 | TCTCAGAGAGAGGCA[C/G]AGAGAGGCACAAACC | 329152 |
rs33831801 | snp | A/G | 0.336735 | 0.234472 | intron-variant, utr-variant-5-prime | Hecw2 | Mm_Celera | 1:53978164 | TGGACAAGGAAGTCA[A/G]GTAGGAGTCCAGACT | 329152 |
rs33831925 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Hecw2 | Mm_Celera | 1:54090809 | ACTCACTTTCGATCA[C/T]AGGATTTTTGTGGAA | 329152 |
rs33831928 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54090848 | AATCAGTGTAAAGAA[C/T]TTTTAACGTTATTTT | 329152 |
rs33831930 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54090878 | TTTAAAGTATACGAC[A/G]TTTTCAAACAATGTG | 329152 |
rs33831932 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54091130 | TATGGAAATGGCATC[A/G]GGACCCTTGCACTTC | 329152 |
rs33832045 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54096319 | ACATCCATCAAAACT[A/G]CACCAGCTTTAACGG | 329152 |
rs33832048 | snp | C/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54096362 | TTTTAGGATATTTTA[C/G]ACTTAAATTAGCTGC | 329152 |
rs33832051 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Hecw2 | Mm_Celera | 1:54097100 | CACAAGGCCAGACTA[C/T]GGTATATAGTGAAAC | 329152 |
rs33832053 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54097180 | ATCTTGGAGTCACAC[C/T]CAAATGCTAACCTGC | 329152 |
rs33832114 | snp | A/C/T | 0.132653 | 0.220748 | intron-variant | Hecw2 | GRCm38.p3 | 1:54002508 | TTAAGTTAAAGACTT[A/C/T]GAATAATTTAGACCT | 329152 |
rs33832117 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54002611 | GGTAGAAACCTCCAA[A/G]AAGCCCTATTTTAAG | 329152 |
rs33832120 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54002816 | TCAAGTTTAAGCAGG[C/T]AGTCAATGACAAAGG | 329152 |
rs33832123 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hecw2 | Mm_Celera | 1:54002819 | AGTTTAAGCAGGTAG[C/T]CAATGACAAAGGCGG | 329152 |
rs33832174 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Hecw2 | Mm_Celera | 1:53971581 | ACTGAATATCTTAGT[A/T]TTCTCTCTTGATTAT | 329152 |
rs33832177 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:53971647 | TTGAAATATACAGAC[A/G]AGAAACAGCATTCTC | 329152 |
rs33832180 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53971880 | GTCGTTCTAAACTCT[A/C]AATCTTTAAAGCAAT | 329152 |
rs33832183 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:53971927 | TCTCAACTCAGGCAC[G/T]TTTAGCTGATACTCA | 329152 |
rs33832184 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw2 | Mm_Celera | 1:54106011 | CCAGAAAACTAAACA[C/T]GCTCAGCCTGCACAT | 329152 |
rs33832187 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54106092 | AAACCCACACAACAC[A/G]AAAGGGCAGGTGAGC | 329152 |
rs33832190 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54106131 | ACTCTTGTAGTAAAA[G/T]AACCTGGTCTTGCAT | 329152 |
rs33832193 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54106216 | TCTTTCAGTTGCCGC[A/T]AGGATTTCATGAGAC | 329152 |
rs33832245 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Hecw2 | GRCm38.p3 | 1:53996214 | TGCCTTTTCCTTAAG[C/T]ACTAGGGGCAGGGCT | 329152 |
rs33832248 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hecw2 | GRCm38.p3 | 1:53996300 | CAACCTTTAAAAGCA[C/T]CCAGAAAACCAGAGC | 329152 |
rs33832251 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | GRCm38.p3 | 1:53996319 | GAAAACCAGAGCTTA[C/T]AGAATCTGAAGCATG | 329152 |
rs33832275 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Hecw2 | Mm_Celera | 1:54054174 | AGCCTCCAACCCACA[C/T]CTACAGATCATCATA | 329152 |
rs33832278 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hecw2 | Mm_Celera | 1:54054462 | GTATCATCCAGGCTT[A/G]GAGGTTTCTGTAGGA | 329152 |
rs33832281 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hecw2 | GRCm38.p3 | 1:54054878 | AGATTAGGATCTGAG[A/G]CCAACTACAGAGGAG | 329152 |
rs33832306 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54012424 | CAGTTTTACAGGATA[A/T]TACCCCTTCTAAAGG | 329152 |
rs33832309 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54012884 | ATGGTGTATTAGGCA[A/G]TATGTTTCCAGTTTT | 329152 |
rs33832312 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | GRCm38.p3 | 1:54013531 | TTGATGAGGGAGAGA[C/G]ACAGATCAACTCATT | 329152 |
rs33832316 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53982253 | TCCAGGCCTGATCGT[C/T]ATACATAGGTATGGC | 329152 |
rs33832319 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:53982267 | TCATACATAGGTATG[A/G]CACCTCAGCTGACTC | 329152 |
rs33832322 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:53982978 | AGAGAAATAAATAAC[A/G]GCATTAAAATGGGGG | 329152 |
rs33832396 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Hecw2 | Mm_Celera | 1:54024230 | TTTGAATGCAGTTGT[C/T]TAACCCACCTGTGCC | 329152 |
rs33832399 | snp | A/T | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:54024357 | CTTTCACATACAACA[A/T]GAACCTTGGAGTGCC | 329152 |
rs33832402 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw2 | GRCm38.p3 | 1:54024436 | AGATTGGTATCTCAG[A/G]GTTCATCACAGAAAT | 329152 |
rs33832486 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:53987533 | AAAAATCAAAGAATA[C/G]GACAGGCAGGCATCG | 329152 |
rs33832489 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53987640 | ATGGTCATCTCCAAT[G/T]TACAGGAAATGTGGA | 329152 |
rs33832492 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53987713 | CGGCATCTCAGAGGA[C/T]AAGTCAGAGAGCTTT | 329152 |
rs33832504 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54111196 | CTGCCCTAATTGGCT[A/G]GGCTAAGTCATATCC | 329152 |
rs33832511 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54111354 | ACAGAATTTTTGCAT[A/G]ATACAAAGTACTTTG | 329152 |
rs33832524 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Hecw2 | Mm_Celera | 1:54016395 | CATATATATCAGCCT[G/T]TTCTATGCCCAGAGC | 329152 |
rs33832527 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Hecw2 | Mm_Celera | 1:54017832 | AAAATCCAGAACTTC[A/C]TTATCAGCCTCCAAC | 329152 |
rs33832530 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hecw2 | GRCm38.p3 | 1:54018063 | CATGTGCTCTCCTGT[A/G]ACCTTGCTCAAATCA | 329152 |
rs33832533 | snp | A/C | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54018957 | TATAAAGGATAACCA[A/C]CAGGATTAAACTAGA | 329152 |
rs33832534 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Hecw2 | Mm_Celera | 1:54005925 | CTCTGTAACTTCAGA[C/T]CTTGAAGACACCATC | 329152 |
rs33832537 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54006162 | GGAAACTTCACTCAC[A/G]GTGGGGAAGATAAGA | 329152 |
rs33832539 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54006251 | GGTAACAAGGGCCTC[A/G]GGTCCTTTGAAGGCA | 329152 |
rs33832542 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54006384 | ACTTCCTCATCATAC[C/T]GTAGCTGGCTTTTCC | 329152 |
rs33832616 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54074673 | CTTTCTTGCTTCTGA[C/T]CAAACTGCTGTTCTT | 329152 |
rs33832619 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54075101 | ACCTCGGCCAGGCTT[C/T]ATCTGTCCTAACAGC | 329152 |
rs33832622 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54075155 | TTCTTTGCACATTTC[C/T]AGTCAAATCACATCC | 329152 |
rs33832635 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54061834 | CTGCCCAGCAGTCCC[A/G]GACAACCTGTTGCTC | 329152 |
rs33832638 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Hecw2 | Mm_Celera | 1:54061993 | CCTTAGATCAATTAT[C/G]TAGCCAATACTTACT | 329152 |
rs33832641 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | GRCm38.p3 | 1:54062091 | ATCTTTGTTCAAACC[G/T]AATCCCATAACCTCT | 329152 |
rs33832643 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54062582 | CTATTGGTGGTTATG[A/G]ATCACATCAACTGAA | 329152 |
rs33832654 | snp | A/G | 0.32 | 0.24 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Hecw2 | Mm_Celera | 1:53978260 | CAGCTCGATCCCGGC[A/G]CAGGAAGCAGCAAGA | 329152 |
rs33832657 | snp | C/T | 0.32 | 0.24 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Hecw2 | Mm_Celera | 1:53978302 | CATTCTGCTTAAAAG[C/T]ATGCACCTGGCCTAG | 329152 |
rs33832660 | snp | C/T | 0.32 | 0.24 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Hecw2 | Mm_Celera | 1:53978314 | AAGCATGCACCTGGC[C/T]TAGACCCTTGGCAGC | 329152 |
rs33832663 | snp | A/G | 0.32 | 0.24 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Hecw2 | Mm_Celera | 1:53978371 | GGCCACAGCAGGCCC[A/G]GAGTCCTCAGGTGTT | 329152 |
rs33832684 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54042892 | GCCATCACGGTGCTC[A/G]TGTTTCCATGAATAC | 329152 |
rs33832687 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54043048 | AATGTGAAGTAACTT[A/G]GATTTCTAGGCAAGA | 329152 |
rs33832689 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54043126 | TTCTCTAGGTCAATG[A/G]CATTAAGTTCGTGTC | 329152 |
rs33832692 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54043156 | CCTTGTTCACTGAAT[C/T]GAGTTCATACTTCTG | 329152 |
rs33832976 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54002906 | AGTAGGACAGACATG[C/T]GAGGCCTCCTACTCA | 329152 |
rs33832979 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54002946 | GGTAGCAAACAGTAG[A/C]AGATTTTTGAACAAA | 329152 |
rs33832982 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:54002967 | TTTGAACAAAGGGCA[C/T]GATGGCTGCCTACCA | 329152 |
rs33832985 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54097274 | ATGGGCTGACCAGGT[A/G]AGTTGCCTGTGACCT | 329152 |
rs33832987 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Hecw2 | Mm_Celera | 1:54097402 | CCCAGTCGGAAGTCC[C/T]GCTCGTGTGCTCTAT | 329152 |
rs33832990 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54101079 | GTCTGTCCCATCAAC[A/G]ATGCTCATTGTCACA | 329152 |
rs33832993 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Hecw2 | Mm_Celera | 1:54101172 | TCACCATTTCAGTCC[G/T]CCAAGGTGTGAGAAA | 329152 |
rs33832996 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hecw2 | Mm_Celera | 1:54091877 | AATAAAAGTGACTAA[C/T]GCACATCAAAATTAA | 329152 |
rs33832999 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hecw2 | Mm_Celera | 1:54091898 | TCAAAATTAATAAAC[A/G]GAAGTCACATATAAA | 329152 |
rs33833001 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54092167 | CTAGGCTACTTTTGA[A/G]CATTAAAAGCCCTAC | 329152 |
rs33833003 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54092207 | CACAGCAGTTCAAGA[C/T]TTCCTACGACATGGA | 329152 |
rs33833034 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Hecw2 | GRCm38.p3 | 1:53996383 | TGATGTGCAGGCTTC[G/T]GTGGAGTAGCTACTT | 329152 |
rs33833037 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hecw2 | Mm_Celera | 1:53996457 | CTCCCCATCAGGCAC[A/G]GCCACTGGACACCAA | 329152 |
rs33833040 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | GRCm38.p3 | 1:53996539 | CTTGTTGCAGGCAGA[C/T]GGGTGTGCCAGCAAA | 329152 |
rs33833043 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Hecw2 | Mm_Celera | 1:53996711 | CACTGATTGGCCCAG[A/G]GAACCTTTTCTAAGA | 329152 |
rs33833074 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Hecw2 | GRCm38.p3 | 1:54055050 | CAAACCATATCAAAA[C/G]GTGACGACCTAAATG | 329152 |
rs33833077 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hecw2 | GRCm38.p3 | 1:54055094 | GTGGTGAGACAGGGA[A/G]AAGAAGTACCTTTGT | 329152 |
rs33833080 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Hecw2 | Mm_Celera | 1:54056905 | TACAATAGCTCTCAA[A/C]AAACATGTACTCTCA | 329152 |
rs33833083 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Hecw2 | Mm_Celera | 1:54057226 | AACTGTAAATCATTA[C/T]ACCAGAGACAATTTT | 329152 |
rs33833146 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53971958 | GCTTTGCAGCCAACA[C/T]ATAAAGACACAAGGA | 329152 |
rs33833149 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:53972020 | TGAAACATCTTCAAC[A/G]TGGTTTTGCTGTTAT | 329152 |
rs33833152 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw2 | GRCm38.p3 | 1:53972034 | CATGGTTTTGCTGTT[A/G]TTGTCGTCCTGGTCA | 329152 |
rs33833175 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | GRCm38.p3 | 1:54024512 | GGGGGAGGTTAAGAA[A/G]CTCTGTCTTGGGGGC | 329152 |
rs33833178 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54036069 | CTTCTCATATCTCAA[A/T]GGCCAGAAGAGATGT | 329152 |
rs33833181 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54037373 | GTTAGCATATCCCTT[A/G]AGGGTTAGAGATAAC | 329152 |
rs33833196 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54106280 | AACAAGCAAGGAATT[G/T]AGCAGAAATTTGGAG | 329152 |
rs33833199 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54106315 | AGAATATCGATGTGA[C/T]CACAGCATAGACTTT | 329152 |
rs33833202 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54106340 | GACTTTACAGAGTTA[A/T]TGCCATAAAGTGGAA | 329152 |
rs33833216 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | GRCm38.p3 | 1:54019490 | ACACAAATCAGTACA[A/T]GATCTTAGTCTTTGG | 329152 |
rs33833219 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54019517 | TTGGAACAAACTACA[C/T]GACCAGATGCACTTT | 329152 |
rs33833222 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hecw2 | Mm_Celera | 1:54019581 | CACTGACTATTGGCC[A/G]AAGAGTCAAACTCTC | 329152 |
rs33833225 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53987728 | TAAGTCAGAGAGCTT[C/T]TGTGTCACCAAGACA | 329152 |
rs33833228 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:53987844 | TTTTGGAAGTCAACT[C/G]TTATGAGGATTTTGG | 329152 |
rs33833231 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Hecw2 | Mm_Celera | 1:53988534 | AACAACTAACATCTA[A/C]ACAAAACAAAAATTC | 329152 |
rs33833265 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53983082 | GATACAGAAGGGACA[A/T]GGTCTAAACAGAAGG | 329152 |
rs33833268 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:53983181 | GAGCTGCTACCCAAA[A/C]GACCCAATCCATGGA | 329152 |
rs33833271 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53983343 | ATGGCAAAGGATCAG[C/T]GTGACCAGAGCACAG | 329152 |
rs33833275 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | GRCm38.p3 | 1:54013571 | CCGTAAGACCAGTTG[A/G]TTTACCATCGAACCG | 329152 |
rs33833278 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54013602 | TGAGGTCAGGACTTA[A/G]CCATGGACTGCATCA | 329152 |
rs33833281 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54013624 | ACTGCATCAAGTGCA[A/G]CATTTACATAGGTAC | 329152 |
rs33833305 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54006436 | CGAAGTCAAGCCGCA[C/T]CATGTCTTTCAGGCC | 329152 |
rs33833307 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54006470 | CACTCACATTAGCTC[A/G]ACATTTTAGTATTTT | 329152 |
rs33833310 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54006505 | TGCAAGCACTTGATG[C/T]CTAAAGTTGGATAAC | 329152 |
rs33833312 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54006586 | GAATCCACATAATAA[A/C]GGGATGGTTTAGAAC | 329152 |
rs33833346 | snp | A/C | 0.32 | 0.24 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Hecw2 | Mm_Celera | 1:53978491 | GGTGACCTATACAGA[A/C]CAGTCCTGTCCAGCT | 329152 |
rs33833349 | snp | C/G | 0.32 | 0.24 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Hecw2 | GRCm38.p3 | 1:53978547 | CACACATCAAGTCTT[C/G]TTACTGCCCAGGCAT | 329152 |
rs33833425 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54062705 | CAGAACAGGGTCACA[A/G]GAACTATGTGAAAAG | 329152 |
rs33833428 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | GRCm38.p3 | 1:54062725 | TATGTGAAAAGAGGT[A/G]TGATGTACTTTACAA | 329152 |
rs33833431 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54062767 | AATATTGCTCAACTC[A/G]TTGTTTTCCAGCTCT | 329152 |
rs33833485 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54076289 | GTTACAGTTCAGCAC[C/T]GGCTTTTCTTCCACT | 329152 |
rs33833488 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54076567 | TTCCAATTGGTCCAT[A/G]CATACTTAGTCTCAC | 329152 |
rs33833491 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54077051 | CACTGTATTAAGAAG[C/T]CACAGGGTTATTCAG | 329152 |
rs33833495 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54043554 | TGTGTGTTTTAGCAT[A/G]ACCTATATTTAAACA | 329152 |
rs33833498 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54044297 | CTATAAATTTACTCT[A/G]TAATCTCTGACTGTT | 329152 |
rs33833501 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54044421 | ACCAATGTCTAATTC[G/T]TGTCATTCTAAGGAA | 329152 |
rs33833514 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hecw2 | Mm_Celera | 1:54111472 | GACCACGAGTGCTCC[A/G]GAGACATTGTCTTTA | 329152 |
rs33833517 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54111519 | TCAAATACTGTAGCA[C/T]GTCAGAAAGAAGTTG | 329152 |
rs33833520 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54111627 | TCATGTGCTTCATAT[C/T]AGGAGAGTACAGGGT | 329152 |
rs33833523 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54111978 | TTTACTGCACTTGAG[A/G]CTTCCCTGGTTAGAA | 329152 |
rs33833675 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54002970 | GAACAAAGGGCACGA[A/T]GGCTGCCTACCACTG | 329152 |
rs33833678 | snp | A/G/T | 0.35503 | 0.226867 | intron-variant | Hecw2 | GRCm38.p3 | 1:54003021 | CAGCCAGGAGAAACT[A/G/T]TACTGGGTGTTGCCA | 329152 |
rs33833681 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54003032 | AACTTTACTGGGTGT[A/T]GCCAAACTCAACTTT | 329152 |
rs33833686 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hecw2 | Mm_Celera | 1:54057632 | CTAAAGATATTGATG[A/G]ATGGTGTCAAATGAC | 329152 |
rs33833689 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hecw2 | GRCm38.p3 | 1:54058261 | GTGAGCCAGACCCTA[C/T]GCTGTGCGTTTACAT | 329152 |
rs33833692 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54058379 | AGTCTTCCAAAAACA[C/T]ATTGCAAATGGCACA | 329152 |
rs33833726 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Hecw2 | Mm_Celera | 1:54101351 | AAGTCCTGAACCACA[C/T]ACAATAAACAGTGAT | 329152 |
rs33833728 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hecw2 | Mm_Celera | 1:54101521 | ACACGTTGTTAAAAA[A/G]TAGAAAGTATACATC | 329152 |
rs33833731 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Hecw2 | Mm_Celera | 1:54101716 | AAATTTTTTCCTAAA[C/T]TGATTATGACTTTTA | 329152 |
rs33833735 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Hecw2 | Mm_Celera | 1:53996880 | ACAACATGGCAAAGG[C/T]AACTCTTTTTTAATT | 329152 |
rs33833738 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Hecw2 | GRCm38.p3 | 1:53997574 | GTCAGAAATAGTTCT[C/T]TCTGCCTTAAAGGTT | 329152 |
rs33833741 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Hecw2 | Mm_Celera | 1:53997713 | ATTACACTGCTCATA[A/C]TAAACTCTGTAGCCA | 329152 |
rs33833774 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hecw2 | GRCm38.p3 | 1:53988741 | AGCATGTGAGAACCC[A/G]GAAGGCACCATGGGC | 329152 |
rs33833777 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Hecw2 | Mm_Celera | 1:53990076 | AATCCTTGAGTGGTG[A/G]TAGTTCATCAGGGAT | 329152 |
rs33833780 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Hecw2 | Mm_Celera | 1:53990205 | CTACAATGAAGCTGG[A/G]GATGAAATAAGTAAG | 329152 |
rs33833782 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | GRCm38.p3 | 1:53994315 | AACCCTTTACAATAA[A/G]CAGTTGCTAAGAAGA | 329152 |
rs33833795 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | GRCm38.p3 | 1:54019680 | AAATGGACAATCTTG[A/G]TGCCAAAGAATTTGA | 329152 |
rs33833798 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54020055 | TAAAGTTCCTATTCA[A/G]TGCTCTTTTGTCCTA | 329152 |
rs33833801 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54020532 | TAGGTTTCCAAGAAA[C/T]AGATTTTATTGTCAT | 329152 |
rs33833854 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54037412 | TCTACTATTTCCTGC[C/T]AGAGATCTATGAGAA | 329152 |
rs33833857 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54038510 | TTAGACAGGAAAATG[C/T]AACAGTTTGAGGGGA | 329152 |
rs33833860 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54038686 | ATTTTAAACCACCAT[A/T]TTTTATTTGCAATGT | 329152 |
rs33833863 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54039071 | TTTCAAAAGAAAATT[C/G]TTAGTCCCCAAAGAA | 329152 |
rs33833886 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54092255 | TGATGGCAAAACAGA[A/G]GCAAGTCCCATCCTG | 329152 |
rs33833889 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54092375 | ACTCCCCAGGAGCCT[A/G]CACGCCCAGTACAAA | 329152 |
rs33833892 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54092506 | TTTACTTGGGACTGG[A/G]TCATGATGCATCCAT | 329152 |
rs33833935 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Hecw2 | Mm_Celera | 1:53972465 | CACCAGGCCTAGCAA[A/C]ACTCAAGCTCTTTGA | 329152 |
rs33833938 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:53972530 | TGTATGCCAACCAGG[A/G]AACCTGCATGCGATT | 329152 |
rs33833941 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hecw2 | GRCm38.p3 | 1:53972585 | AGTAACACTATGAAA[A/G]TATAGTAAGTCATTT | 329152 |
rs33833984 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54013782 | GGAAACCAGAATCCT[G/T]GGCCAATAGAAGACA | 329152 |
rs33833987 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54013883 | CATCTTAACTCACTA[C/T]GAAAGCAGTTCACTA | 329152 |
rs33833990 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54013910 | ACTAGAAAGACCCTT[C/G]TGGCTTAGGACATAG | 329152 |
rs33833993 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54014212 | GCTCACCTCCTCACG[A/C]CTCCCTTTTCTCAAC | 329152 |
rs33833994 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:53983539 | TCCCAGCTCCACCAG[A/T]TCACTCCCTGAAACC | 329152 |
rs33833997 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:53984079 | AAATCTCCCAGAGGA[A/G]ACACATTTCTACATG | 329152 |
rs33834000 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:53984104 | TACATGAATCAGAAA[A/G]TTGTTCTTAATGTAC | 329152 |
rs33834003 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:53984135 | ATAAAAGTCAGATCC[C/T]GGATTTAAAAAAAAA | 329152 |
rs33834005 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54006823 | TGTCATATGGGCTAC[A/G]TTTAACAAAGAGATT | 329152 |
rs33834008 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw2 | GRCm38.p3 | 1:54006881 | AATCTGTTATCATTT[C/T]GTAACACCCAACAAT | 329152 |
rs33834011 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Hecw2 | GRCm38.p3 | 1:54006900 | ACACCCAACAATCCC[G/T]GACTTCCCAGATTCA | 329152 |
rs33834025 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54106343 | TTTACAGAGTTATTG[C/G]CATAAAGTGGAAAAT | 329152 |
rs33834028 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw2 | Mm_Celera | 1:54106519 | GAATGGCCTGCTTCG[C/T]ACCCAGTGCTAGACA | 329152 |
rs33834031 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw2 | Mm_Celera | 1:54106642 | AATGTATGTATAGAA[C/T]GCATGAAAGCATTTG | 329152 |
rs33834034 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54044543 | AGTTGTGGTTTTCCA[A/G]TTTGTGTACACTCAT | 329152 |
rs33834037 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54044692 | GAGGTGTGATTAAAT[C/T]GTAAGCTCTGATTCT | 329152 |
rs33834040 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54044750 | ACTTAATCTCTAGCT[A/T]AAACAGCGAAATTTT | 329152 |
rs33834118 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54116067 | TGTAATTGGAAAATC[C/T]ATGTTACTTGCCAAA | 329152 |
rs33834121 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54116087 | TACTTGCCAAATTAA[A/G]TTAATTACCTAACTA | 329152 |
rs33834134 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54062885 | GTTACCTGGCCACTA[A/G]CTGCAAGCCTCGTTC | 329152 |
rs33834137 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54062897 | CTAGCTGCAAGCCTC[A/G]TTCTGAGACATACAC | 329152 |
rs33834140 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54063975 | TACTACTTACCTACA[C/T]CCTCTGCCCTATACA | 329152 |
rs33834143 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54065707 | TGTTTTATAAAGCCA[A/G]AAAAGAAATCTGTTT | 329152 |
rs33834164 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Hecw2 | Mm_Celera | 1:54003053 | ACTCAACTTTCAACA[C/G]GAGAAAAGAAATTCT | 329152 |
rs33834167 | snp | C/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54003067 | AGGAGAAAAGAAATT[C/G]TGGATTTAAATAAGC | 329152 |
rs33834170 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54003126 | GCACAGCAATCATAT[A/G]ACAAATAACAGAGCT | 329152 |
rs33834173 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54003200 | TGGCAAATGGTGGTG[G/T]CATGGAGAGTCTGTC | 329152 |
rs33834185 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Hecw2 | GRCm38.p3 | 1:54058798 | CTGTTCCTGTTTACT[C/G]CTCTCATGGGGCATG | 329152 |
rs33834187 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54059047 | TAGTTGGAGGAGCCA[A/G]GAGATTCTCCAGTAA | 329152 |
rs33834190 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54059073 | AGTAATAGGTTTACT[A/G]ATCCATAGAGATTGA | 329152 |
rs33834193 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Hecw2 | Mm_Celera | 1:54059292 | TGCTTGATATATCTG[C/G]CTCCACCCTGATGCT | 329152 |
rs33834224 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Hecw2 | Mm_Celera | 1:53997770 | ACATCATTAGATATT[G/T]CAAGACCTTAAGTCT | 329152 |
rs33834227 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hecw2 | GRCm38.p3 | 1:53999347 | ACTCTGTACTTAGCA[G/T]TCTAGGTGTTTCTAT | 329152 |
rs33834230 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Hecw2 | GRCm38.p3 | 1:53999459 | TGTGCTGTGAGATGT[A/C]CAAGGGTCCTGCCAG | 329152 |
rs33834233 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Hecw2 | GRCm38.p3 | 1:53999550 | ATGCTTAGTTCTTAG[C/T]TGTATATAGCTAACT | 329152 |
rs33834245 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54121443 | AGGCCCAGTATAACT[G/T]TGAGGGATTTGGACA | 329152 |
rs33834248 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54121508 | GGAGAGAGTGAGTCA[C/T]GATGACCCACATTAG | 329152 |
rs33834251 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54121684 | GAGAAGAGCACATGT[A/G]GTATGAGCCACACCA | 329152 |
rs33834296 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54112013 | CAGCAACCATAACAA[C/T]TTCTAAGTCTCAGTT | 329152 |
rs33834299 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54112039 | CAGTTTCTATACAGT[C/T]CCTCAAACGAACCAA | 329152 |
rs33834302 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54112058 | CAAACGAACCAAGAG[A/C]TCCCTAAGTCACACC | 329152 |
rs33834314 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw2 | Mm_Celera | 1:54020800 | TTAAAAGGCTAAATA[A/G]TTGTTTCTAGGTCAT | 329152 |
rs33834317 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54020804 | AAGGCTAAATAGTTG[G/T]TTCTAGGTCATTCAG | 329152 |
rs33834320 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54020921 | GTGTACTGTGTGTCA[C/T]GTTTTTCATATTTGA | 329152 |
rs33834323 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw2 | Mm_Celera | 1:54021230 | CACCATTGCTTAGTA[C/T]GAGGCCATGGTAGAA | 329152 |
rs33834334 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54101859 | ACTTAAAAATTCAAT[A/G]TTTAAAAAGCATTCA | 329152 |
rs33834337 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54101903 | AAAGAAAGCTCTCCT[C/T]TTGCAAAGCCAAGCA | 329152 |
rs33834340 | snp | A/C | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54102463 | ATTGTCTGCTCTTCC[A/C]GTAATCTCAACCCTT | 329152 |
rs33834343 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54102585 | CCAAAGGCAGCATGA[A/G]GCTGTAATTAGAGGG | 329152 |
rs33834356 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw2 | GRCm38.p3 | 1:54039343 | AGGACTCCTTGTTTA[C/T]TCCTTACACAGCAAC | 329152 |
rs33834359 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54039379 | CAAGACGCTTGACTC[A/G]TAACTTACAGTGAAA | 329152 |
rs33834362 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Hecw2 | Mm_Celera | 1:54039927 | CCTCTTTCCAAGTCA[C/T]GACGGTGTCTCAAGA | 329152 |
rs33834364 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hecw2 | Mm_Celera | 1:54077515 | TTTTTCTTACATTTT[C/T]TGTATGCCACATACT | 329152 |
rs33834367 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54077667 | ATTACTGCCTTCCAA[A/T]TCTATGCTTGCTTCT | 329152 |
rs33834370 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Hecw2 | Mm_Celera | 1:54077890 | GGCTTGTACTGTGTG[A/T]CCCAGGATTCAACAA | 329152 |
rs33834373 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54077891 | GCTTGTACTGTGTGT[C/T]CCAGGATTCAACAAC | 329152 |
rs33834384 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Hecw2 | GRCm38.p3 | 1:53994361 | CCAAAGTCCTTCTTA[G/T]ATGCTGTTCTGTACC | 329152 |
rs33834387 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | GRCm38.p3 | 1:53994438 | TAAGGGTTACATCAG[C/T]ATAAAACCATCCCTC | 329152 |
rs33834390 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53995075 | AGTTACTTCAGATTA[A/G]TCCAATGGAAACTAA | 329152 |
rs33834475 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54131414 | CTTCTGGACTATTTC[A/C]TGAAAGGAAGGAAAT | 329152 |
rs33834478 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54131434 | AGGAAGGAAATTTAT[A/G]TCTTGTGTGTGCTGC | 329152 |
rs33834481 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54131458 | GTGCTGCTATAATCT[A/G]GAGGACTTTTCTTAC | 329152 |
rs33834494 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Hecw2 | Mm_Celera | 1:54127004 | CTCAGCTCAGGACGC[C/T]GGAGGGTAGTAAACT | 329152 |
rs33834497 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54127012 | AGGACGCTGGAGGGT[A/G]GTAAACTAGCATCAT | 329152 |
rs33834500 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54127028 | GTAAACTAGCATCAT[A/T]GCCTGCCACTCCTCC | 329152 |
rs33834503 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54127195 | AAAAAAAAATCTCCC[A/G]GGCTGATGTTTTAGA | 329152 |
rs33834514 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54136923 | TTAGAATCTGAAAGG[G/T]TACTGTGTCTGTGTG | 329152 |
rs33834517 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Hecw2 | Mm_Celera | 1:54136941 | CTGTGTCTGTGTGTC[C/T]TTCTGAATGTGTCCA | 329152 |
rs33834522 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54137420 | ATGAGATCTCAGGGC[C/T]TGTGTGCACGTTTGG | 329152 |
rs33834536 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54129911 | GACCACCAATAAACC[C/G]CACAAACCAAGTCCC | 329152 |
rs33834539 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54129986 | ACTATTCTGTCTGTG[C/T]ATTTAAATCTCTCTA | 329152 |
rs33834542 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54130067 | CATAAAAGTTCAAGA[C/T]TCTTGGAAAAGAAAA | 329152 |
rs33834634 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54007095 | ACCGGATCACAGGAT[C/T]TTCTAATGCCACCTC | 329152 |
rs33834636 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54007250 | TAGAAACTTTTTTGA[C/T]TTTAGGTACAGGTCT | 329152 |
rs33834639 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54007305 | CCCTTTAGCCGGTCC[C/T]TACTCTGGAAGACAA | 329152 |
rs33834642 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54007430 | AAAAGGACACCATTT[A/T]AAATAGCACTGTCTC | 329152 |
rs33834646 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54045241 | AAAACAGCACATATT[C/T]CTTTCTACAAAAGTG | 329152 |
rs33834649 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54045655 | GCTTTACAGGGAAAC[A/G]GTCAGGTCTTAGACA | 329152 |
rs33834652 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54045684 | CACTTAGGAAGGTCT[G/T]GGGCTTCTGTTCATT | 329152 |
rs33834695 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54092638 | TTGGCTTTTGTGGTT[C/T]CTCATGATATTAACG | 329152 |
rs33834698 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54092675 | TGTTTGGGGATGAGA[A/G]AAACAATGCCAGACT | 329152 |
rs33834701 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Hecw2 | Mm_Celera | 1:54092920 | GGCAATTTGGTGACC[C/T]GACAGAGAGTAAGTA | 329152 |
rs33834766 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54161000 | TGCATCTCCTGAAAC[C/T]GTGGAAGGAACAGCA | 329152 |
rs33834769 | snp | A/G/T | 0.32 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:54161093 | CAAGCAGGATGCCTC[A/G/T]AGTCCATTACTCAGA | 329152 |
rs33834772 | snp | C/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54161215 | CAAATCTATCTCTTA[C/T]GTAAACATAGAGATG | 329152 |
rs33834856 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54142940 | CATTTTGCTAAACAA[C/T]TTTTATTATCTCTTT | 329152 |
rs33834859 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54143026 | GACAAATTATAAGAC[A/G]GGAAGAGAAGGATCT | 329152 |
rs33834862 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54143058 | ATAACCTATAGAAAA[C/T]AGGACCTCGAAGTTC | 329152 |
rs33834874 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Hecw2 | GRCm38.p3 | 1:54174424 | TGAGGCCACTCCAAT[A/G]GTGCCTGCTGCTTCC | 329152 |
rs33834877 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hecw2 | GRCm38.p3 | 1:54174437 | ATGGTGCCTGCTGCT[C/T]CCATGTAATTATTAG | 329152 |
rs33834879 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Hecw2 | Mm_Celera | 1:54174487 | GTTGGAGAAGTTGTT[A/G]CAGACACACAGCCAG | 329152 |
rs33834881 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Hecw2 | Mm_Celera | 1:54174535 | GTGAACGTCTTTGGA[A/G]CACAGCTTTTTCTCT | 329152 |
rs33834886 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54014242 | CCTCAGTGCTGGTCC[C/T]GATGGAAATGCCAAC | 329152 |
rs33834889 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54014259 | ATGGAAATGCCAACA[C/T]CATTCTTAGGGAAGA | 329152 |
rs33834892 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw2 | GRCm38.p3 | 1:54014429 | GCTCCAAGATGACCA[C/T]TCCCCAGCTTTCTGT | 329152 |
rs33834926 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:53984142 | TCAGATCCCGGATTT[A/T]AAAAAAAAAAAATAG | 329152 |
rs33834928 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:53984163 | AAAAAAATAGGGCTT[C/T]AAATCTAACCCCAAG | 329152 |
rs33834930 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Hecw2 | Mm_Celera | 1:53984185 | AACCCCAAGTTGATA[A/T]ACATATATGAAATAC | 329152 |
rs33834933 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53984248 | AACCAACTTCAATAA[A/T]AAGGGATGGCCATTA | 329152 |
rs33834945 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54170625 | CTGGCCCTTTTCTCA[G/T]GTTCTCCTCATAAAC | 329152 |
rs33834948 | snp | A/C/G | 0.391111 | 0.206368 | intron-variant | Hecw2 | GRCm38.p3 | 1:54170976 | CAGTTTCATGAAACT[A/C/G]GTGAAAATCCATCAG | 329152 |
rs33834951 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54171246 | CAAAATCCAAACTAA[A/G]GTTGTCTCTTTATGA | 329152 |
rs33834974 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54106761 | TGGGTACTAAGTAAC[C/T]GCTATATAGTATGCA | 329152 |
rs33834977 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54106852 | ATTCTTCTCAGGCAC[C/T]TTTATAACTATCACA | 329152 |
rs33834980 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Hecw2 | Mm_Celera | 1:54107273 | AACTCTTTTCTCCAC[A/T]CCACATCTAGCCTAT | 329152 |
rs33834983 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54107290 | CACATCTAGCCTATG[C/T]TTTAGCAGTGAGCTG | 329152 |
rs33834986 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hecw2 | Mm_Celera | 1:54067671 | GTAGGCAGACAGACA[A/G]AGGAGGGCTTGGAGG | 329152 |
rs33834989 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54067991 | AGATAGTCAGACAAC[A/C]ACTGCAGAGCTCACG | 329152 |
rs33834992 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54068021 | GGTACACTAAACAGT[A/G]AAACTCTGACCCACT | 329152 |
rs33834994 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Hecw2 | Mm_Celera | 1:54116118 | ATGCAATTTTATAAG[A/T]ACTTATCTGAATACC | 329152 |
rs33834997 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54116172 | CCAGCATCAGCTGCT[A/G]GCACATGGATGAGTT | 329152 |
rs33835000 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54116191 | CATGGATGAGTTATT[C/T]GAGAAACATTTTACA | 329152 |
rs33835002 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54116278 | AATATTTCAAAGAAC[A/G]ATTTAGCATGACAAA | 329152 |
rs33835038 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54153191 | GTCACTTAAAAGATG[G/T]TTTCGAATCAAAGTT | 329152 |
rs33835041 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54153414 | GGGCATCACAAATGG[C/T]AATGCATGTTTATAC | 329152 |
rs33835045 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54147532 | CCAGCTACTGTATGA[A/G]CAAATAAAGGCTGTG | 329152 |
rs33835048 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54147538 | ACTGTATGAGCAAAT[A/G]AAGGCTGTGCCATAT | 329152 |
rs33835051 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54147583 | CTTTTAAGCACAAAT[C/T]TTGTCTAGGTTAGAT | 329152 |
rs33835106 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | GRCm38.p3 | 1:54003393 | TTGTTATGTCCATCA[A/G]CAAGGAAATGGGACA | 329152 |
rs33835109 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54003673 | ATTCTCCTTCTACTC[C/T]ATAGTCTAACTAAAG | 329152 |
rs33835112 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54003760 | TTACTTAAAAACCAC[A/G]AAAACTTACTAAATA | 329152 |
rs33835146 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54021244 | ATGAGGCCATGGTAG[A/C]AAGTAGTGAGTTGCA | 329152 |
rs33835149 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54021383 | ATAGTATAGCTGATA[A/G]GACAACTTTCCAAAA | 329152 |
rs33835152 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | GRCm38.p3 | 1:54021392 | CTGATAAGACAACTT[C/T]CCAAAACAATCAGGA | 329152 |
rs33835156 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | GRCm38.p3 | 1:54059351 | TGGTGTACTATCCTT[G/T]TGCTTTTACACAGAA | 329152 |
rs33835159 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54059388 | GATGAAGGACCTCCA[A/G]ACAGTCTAGCCAAAT | 329152 |
rs33835162 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54059436 | TTCTCAGTGATGGAC[A/G]AGTGGGTGACTTTTT | 329152 |
rs33835176 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | GRCm38.p3 | 1:54102693 | CAGAACTGAAAGGGG[A/C/T]AGCTGTTCCCACCCT | 329152 |
rs33835179 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54102900 | TCCACACTAAAATGA[C/T]AGTCTCGGTAGGTAA | 329152 |
rs33835182 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54103926 | TTTTATTCTTCTTGG[C/T]ATCTTTAATCTTGCA | 329152 |
rs33835184 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54123395 | GGGGACGATACAACA[A/G]TGAAAATACACACAC | 329152 |
rs33835189 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54123528 | ACTGGCTGAGTTGTA[C/T]TTCAATAATTCTACT | 329152 |
rs33835192 | snp | A/C | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54123575 | AATGACAGGATGTCA[A/C]TAATAGATCTTCAAC | 329152 |
rs33835196 | snp | A/G | 0.18 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:53999579 | CTCACAGACTAATAA[A/G]TGAAGATTGTGTCTG | 329152 |
rs33835199 | snp | C/G | 0.426035 | 0.177515 | intron-variant | Hecw2 | GRCm38.p3 | 1:53999754 | TCTCAGAAATACTGC[C/G]GGCAACCATGACAGG | 329152 |
rs33835202 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Hecw2 | GRCm38.p3 | 1:53999791 | GGGCACAAGTCAACA[A/C]AGAAACAAGTTTGTA | 329152 |
rs33835275 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Hecw2 | Mm_Celera | 1:54112103 | CATATCAATGAAAGC[A/G]CCCTTCAGTAGTAAT | 329152 |
rs33835278 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Hecw2 | Mm_Celera | 1:54112161 | ATGACTTGATTTTTT[A/T]AAATGTTTTTAAAAC | 329152 |
rs33835281 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54112581 | ACTCAGACACTGGGA[A/G]CGCCCTAGTACAACT | 329152 |
rs33835296 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54078320 | TCCAGGTGGCTGAAT[A/G]ACTTTACCTCTTCAG | 329152 |
rs33835299 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54079130 | AGACTTCAGAGACCA[C/T]GACTTGTTACAGTGA | 329152 |
rs33835302 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54079171 | GCTAAATGGAATACC[C/T]CCTTACACCTTTTCC | 329152 |
rs33835315 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Hecw2 | Mm_Celera | 1:54039950 | TCTCAAGAACAACAA[G/T]AAAGGGAAGAGAAAA | 329152 |
rs33835318 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hecw2 | Mm_Celera | 1:54039958 | ACAACAATAAAGGGA[A/G]GAGAAAATCCAGCGG | 329152 |
rs33835321 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54040089 | AATCTGCTTTGTCTA[C/T]TTGTGTATGAAAACC | 329152 |
rs33835344 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54131474 | GAGGACTTTTCTTAC[A/C]AACAGCTAGCTTAGG | 329152 |
rs33835347 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54131512 | AAATGTACTCATATA[C/T]TAAATGTGTTTTAGG | 329152 |
rs33835352 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54131860 | AATCCTTCCGTACTC[C/T]GCTCTAGTGGTTGCA | 329152 |
rs33835395 | snp | C/G | 0.18 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54130157 | TTTGGACGACTTACT[C/G]CATCCTTCAGAGGAG | 329152 |
rs33835398 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54130261 | TCTAGTTAACTTTGC[A/T]ACCGTCATGAAATAC | 329152 |
rs33835401 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54130333 | TGAAGTTCAGGCCTG[A/T]CTACCAGCAGATGGT | 329152 |
rs33835406 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54127236 | AATCTGGCTAAATCA[C/T]GTGGAGACTTTCTTT | 329152 |
rs33835413 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54127911 | TTACCACGACTGCAG[C/T]GATGGACGGGAGTTT | 329152 |
rs33835467 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:54138410 | CCTTGTGGCTTCTTC[A/G]GACTGACCTGCTTAC | 329152 |
rs33835470 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw2 | Mm_Celera | 1:54138422 | TTCGGACTGACCTGC[C/T]TACCTACCTTTGCTG | 329152 |
rs33835473 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54138841 | ACACTATATAGTGGT[C/T]ACATTGAGTCAACAC | 329152 |
rs33835515 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54045701 | GGCTTCTGTTCATTC[C/T]GGTGCCAAACCAGTG | 329152 |
rs33835517 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54045720 | GCCAAACCAGTGGGA[C/T]TCAAATTTCACACAA | 329152 |
rs33835519 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54045747 | ACAATCTGGGTTTTA[C/T]TCATGGAGGTTAACC | 329152 |
rs33835521 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54045784 | GAGTAATCCTTCGTT[A/G]CTCTACTGAGGTGTC | 329152 |
rs33835594 | snp | A/T | 0.396694 | 0.202437 | intron-variant | Hecw2 | Mm_Celera | 1:54093025 | ACCTGGAAAACCACC[A/T]TTTCCCATTTCTAGG | 329152 |
rs33835597 | snp | G/T | 0.46875 | 0.121031 | intron-variant | Hecw2 | Mm_Celera | 1:54093082 | ATTAATATTCAGAAT[G/T]CGAAAGAATTTCTCT | 329152 |
rs33835600 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54093362 | AGGAAATGCAACAAA[C/T]TAGCAGCACAGAATA | 329152 |
rs33835603 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54093738 | ACTTTGGGGGAAGGC[A/G]AAACCATAGCAAAGA | 329152 |
rs33835615 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54007468 | TTATCATCTCCAGCC[C/T]CTAAAAGTATAAGAG | 329152 |
rs33835618 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hecw2 | Mm_Celera | 1:54007477 | CCAGCCCCTAAAAGT[A/G]TAAGAGTTAGGTGGA | 329152 |
rs33835621 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54007610 | ATGCAATATAGAAGC[A/C]GAGTCTTTATGGACA | 329152 |
rs33835627 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54161302 | CACAAGGATAGGGTC[A/G]GCGGTGTTAACGATG | 329152 |
rs33835630 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54161326 | AACGATGCTGGTGCT[A/G]CTACAGCGACCACCC | 329152 |
rs33835633 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54161340 | TGCTACAGCGACCAC[C/T]CTTTTCTAGCAAAAC | 329152 |
rs33835695 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54014443 | ACTCCCCAGCTTTCT[G/T]TTCTTGGCTGCCTTT | 329152 |
rs33835698 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54014615 | CCTCTCCCCGGCAAC[A/T]CCATTCTGTATCCCA | 329152 |
rs33835701 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw2 | GRCm38.p3 | 1:54014641 | TCCCAATTTACTCAG[C/T]CTTGGCTGCCTCAGC | 329152 |
rs33835725 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54143077 | ACCTCGAAGTTCAAC[A/G]TGTTGATGCTGAGAG | 329152 |
rs33835728 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hecw2 | Mm_Celera | 1:54143138 | TTCCTGTTACTAAGA[A/G]GTGATATTCAGTGAT | 329152 |
rs33835731 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54143168 | TTATCATTTTTCATC[A/T]GTGTTTTATTCATAT | 329152 |
rs33835774 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Hecw2 | Mm_Celera | 1:54171252 | CCAAACTAAGGTTGT[C/T]TCTTTATGAAAAATA | 329152 |
rs33835777 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw2 | Mm_Celera | 1:54171460 | ATAAGGAATTTAAAG[C/T]TTATATCCATCAGCC | 329152 |
rs33835782 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hecw2 | Mm_Celera | 1:54171976 | AGCAATCCCAATTAA[A/G]CTCACTGGATTACAA | 329152 |
rs33835795 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54068113 | ACTCACTAAAACATA[A/G]TTGTGTAAGCACAAG | 329152 |
rs33835798 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54068212 | GATATTTTGGTCCTC[A/G]ATTCATTAAATTGTA | 329152 |
rs33835801 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54068399 | TCTACAAAGACTGCA[G/T]AAGGCATTTACTCTC | 329152 |
rs33835809 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54107642 | TTTTGAGGTAACTTT[C/T]ATCTCCTGGCTTCTT | 329152 |
rs33835811 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54107672 | TTTTATTGAACTTTG[A/G]TTTATATCATCACAA | 329152 |
rs33835855 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54116433 | TAGAAAGCATAAGGC[A/G]TATCAACAGTAACAA | 329152 |
rs33835858 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54116486 | AAACACAATACCTTC[C/T]GATTTTAAATCTAGA | 329152 |
rs33835861 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54117984 | CCAAGTGAGTATATT[G/T]TATTCCAAACAACCA | 329152 |
rs33835884 | snp | A/C/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54147606 | GGTTAGATTCATCAA[A/C/G]GATCTCCCCTATTGA | 329152 |
rs33835887 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54147653 | GTCCTGGTTCCACAG[A/G]GAGGAGCAAATTGCC | 329152 |
rs33835890 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54147888 | AGAATAATATTGAAG[A/G]TTTTACAAATGTGGT | 329152 |
rs33835893 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54148026 | CTGTCTCAACAAACT[A/G]AGAGGCAAGGAGGCA | 329152 |
rs33835894 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Hecw2 | Mm_Celera | 1:54174614 | TAACATTACAAGGTA[C/T]GGTACGTGGGGAAGT | 329152 |
rs33835897 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54174740 | TCCATGAGGCCCTCG[A/G]TTCAACTCCCAGCAA | 329152 |
rs33835900 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Hecw2 | Mm_Celera | 1:54174815 | AAGAACTTAGCAGAG[A/T]GGTCACAGAAAGTCA | 329152 |
rs33835903 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54175084 | TGAGAAATTACCTCA[C/T]AAAAATCTCAGTTCA | 329152 |
rs33835925 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Hecw2 | Mm_Celera | 1:54021455 | TGACCTCATTTCCAT[G/T]AACAGGAAGAATATG | 329152 |
rs33835928 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Hecw2 | Mm_Celera | 1:54021525 | CAACAAGCTGTAGGA[C/T]GGCACTATGCCAGGC | 329152 |
rs33835931 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54021531 | GCTGTAGGATGGCAC[C/T]ATGCCAGGCTCTAGT | 329152 |
rs33835944 | snp | C/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54153808 | ACCACTCCTGACTCA[C/G]TGCATACATTTTAAC | 329152 |
rs33835947 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Hecw2 | Mm_Celera | 1:54153856 | AAGTAACTTGAATCA[A/T]CGATGTCCAATATAC | 329152 |
rs33835950 | snp | C/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54153942 | AGTTTCCAATTGGTA[C/G]AGCAGGTACATCACT | 329152 |
rs33835953 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Hecw2 | Mm_Celera | 1:54154271 | AGCCAAGAAGATAGT[A/T]ATCTCCAAGTTTTTT | 329152 |
rs33835956 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53985319 | TGCTTTAGATGATTT[C/T]CAGTGATTGAGAGAG | 329152 |
rs33835959 | snp | C/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53985332 | TTTCAGTGATTGAGA[C/G]AGCAGTTAGGTCAGG | 329152 |
rs33835962 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53985365 | TACATCCAAGAGCTG[C/T]CCTGCTGAAAGCATG | 329152 |
rs33835995 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hecw2 | Mm_Celera | 1:53999813 | AAGTTTGTAAATAAA[C/T]GCAGAAAACAAGAAT | 329152 |
rs33835998 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hecw2 | GRCm38.p3 | 1:53999984 | TTAGACAGAGGGAAA[A/G]TCACATATCCCGACC | 329152 |
rs33836001 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | GRCm38.p3 | 1:54000103 | ACCACAAGCTTTCAG[A/G]CCACCCCGCATGCAT | 329152 |
rs33836005 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54104030 | AGACTTATTTTACTG[A/G]CAAAACAACAAAGGC | 329152 |
rs33836012 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54104569 | TCTGTCAAAGGCTTA[C/T]CTGACAATAATGGAA | 329152 |
rs33836025 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54003858 | GACATCTCTTTGAGC[A/C]ACTAACTTGCATTCT | 329152 |
rs33836028 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54003902 | ATACAAAGTTTAACT[A/T]CCATTTTTATATTCA | 329152 |
rs33836031 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Hecw2 | Mm_Celera | 1:54004022 | AACTTGTAATTCTTA[C/T]CATTAGAGAAACATA | 329152 |
rs33836095 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54059520 | CATGGGGCATGCAGT[A/G]TCCCAGTGATATCTC | 329152 |
rs33836098 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54059546 | ATCTCCCTTAATAGT[C/T]ACTTGTGATCTTACT | 329152 |
rs33836101 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54059571 | CTTACTATGAGTCCC[G/T]TGGGGAAAGAGAGGG | 329152 |
rs33836115 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54123912 | GCTCACCAGACACTA[C/T]GGAGAGGACCAACTG | 329152 |
rs33836118 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54123970 | CCATAATAATTCAAA[A/G]CACTGCTCAAGAATA | 329152 |
rs33836121 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54124090 | ATGTTTGCATTAATC[A/G]AGTATTCCTAACTAA | 329152 |
rs33836134 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54112633 | CCACTGCAGCCAGTG[A/G]CACTGCAAGGACCCT | 329152 |
rs33836137 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw2 | Mm_Celera | 1:54112730 | GTCAGGCACTGTGCT[A/G]AGGAGTGAAGGATCC | 329152 |
rs33836140 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54112749 | AGTGAAGGATCCTGG[A/C]AGATGGAGCACCTGT | 329152 |
rs33836143 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Hecw2 | Mm_Celera | 1:54112969 | TATTCCTATTCTTAT[G/T]TATTGAACCTAGAAG | 329152 |
rs33836159 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54132143 | GAGTGTGATCGTACA[A/G]CTATAATAGTGTAGG | 329152 |
rs33836175 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Hecw2 | Mm_Celera | 1:54080014 | CTCCTCTTTTAGCTT[G/T]TCGCCTACCCCTTTA | 329152 |
rs33836178 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54080494 | AGGCTCTGCTACACG[C/T]TAGGCATCATGCCAG | 329152 |
rs33836181 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Hecw2 | Mm_Celera | 1:54082562 | ATAACCACAACTATA[G/T]ACATCTATATTTATT | 329152 |
rs33836204 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54040184 | TGAGCCACATGCAAG[A/T]CTTCACCCAGACTCA | 329152 |
rs33836207 | snp | G/T | 0.35503 | 0.226867 | synonymous-codon | Hecw2 | Mm_Celera | 1:54040202 | TCACCCAGACTCACC[G/T]ATGTGATAGAGTCCT | 329152 |
rs33836210 | snp | A/T | 0.124444 | 0.216185 | synonymous-codon | Hecw2 | Mm_Celera | 1:54040427 | GTTCTCTGGGCTCAG[A/T]GTGTACCGCATCTGT | 329152 |
rs33836213 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54040561 | CATAAAACATCAGTG[C/T]TAAAAGGTGAGGAGT | 329152 |
rs33836224 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54130367 | TTAAAATAGTTAATT[C/T]CTGTTTCCTTCATTC | 329152 |
rs33836227 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54130386 | TTTCCTTCATTCTGT[A/G]TAGTAGACAAGCGTC | 329152 |
rs33836230 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54130394 | ATTCTGTGTAGTAGA[C/T]AAGCGTCCCTACACA | 329152 |
rs33836233 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Hecw2 | Mm_Celera | 1:54130420 | ACACAGTCCAAGCTG[C/T]CATAGTCGGTCTCAG | 329152 |
rs33836376 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54138893 | CTTGCATAAGCTCCT[C/T]CAGGTTCCTTGAGGC | 329152 |
rs33836379 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54138991 | TCTCTCTCTTTTAAT[A/G]AGGGCAAATCTAGTG | 329152 |
rs33836382 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54139171 | ATAGGAAAATACAAC[A/G]GCTTTTATAAATAGC | 329152 |
rs33836516 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54093752 | CGAAACCATAGCAAA[A/G]ATCACCATGAAACAA | 329152 |
rs33836519 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54094886 | AAGTGAAACAACAAG[A/G]AAGTCAAAAGATCGG | 329152 |
rs33836522 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hecw2 | Mm_Celera | 1:54094929 | AGAGAAACATTCCAA[A/G]CACAGGAGACAGACC | 329152 |
rs33836536 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54162631 | TCTCCCCTAACAGCC[A/C]TTCAATGACTTCTCA | 329152 |
rs33836539 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54162672 | CATTAACCAGAGAAC[A/G]GCATGTATGCAGGCC | 329152 |
rs33836542 | snp | C/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54162722 | GGATGGCAATGGTCA[C/G]CAGGAAATGAAATTC | 329152 |
rs33836564 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54007621 | AAGCAGAGTCTTTAT[A/G]GACACCAAATTGTGA | 329152 |
rs33836567 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54007934 | TCAGAAATGTGTGAA[A/G]AAATCAGAATCCAGA | 329152 |
rs33836570 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54009165 | GCAAAAATGCTAAGC[A/G]GGAGAAGACAATCGC | 329152 |
rs33836573 | snp | C/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54009193 | CGCAGAGTGTTAGAA[C/G]CTATTGCTAACTGCT | 329152 |
rs33836574 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54045816 | TAAAGTTTCCTGTTT[C/T]AAACAGCTACATTAC | 329152 |
rs33836577 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54045897 | AACAATGTCTAGCCC[A/G]TCCTATGTGTTCAAT | 329152 |
rs33836580 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54045923 | TCAATTAAGATTAGC[A/T]ACTAATTATCTTGTT | 329152 |
rs33836583 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54046106 | GAACAGCCTAGTAGC[A/G]CAGAAGAACTCACCT | 329152 |
rs33836654 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw2 | GRCm38.p3 | 1:54014712 | CATGGGAGTTCTACC[A/G]AGGACAGAAAATAGT | 329152 |
rs33836657 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | GRCm38.p3 | 1:54014741 | GTGTCTTCCTGCATC[A/G]TGGATAATGTTATCT | 329152 |
rs33836660 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hecw2 | GRCm38.p3 | 1:54014764 | TGTTATCTGTGAAGG[G/T]TAAGCAACCGGCCAG | 329152 |
rs33836663 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54014767 | TATCTGTGAAGGGTA[A/G]GCAACCGGCCAGCGT | 329152 |
rs33836704 | snp | G/T | 0.42 | 0.183303 | intron-variant | Hecw2 | Mm_Celera | 1:54143422 | ATTTTAACATCTATG[G/T]AAATATGCAAATGTT | 329152 |
rs33836707 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54143459 | CCCACCCAGTATAAA[C/T]GATAGATACCGTATT | 329152 |
rs33836710 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hecw2 | Mm_Celera | 1:54143487 | ATTGCCGCAGATACA[A/G]AGGTTACTCCACGAA | 329152 |
rs33836713 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54143549 | CCTTTGTGTGTTTCC[C/T]TTTTGATCTAAGCTC | 329152 |
rs33836724 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54068625 | AGTGAGGTTAGAACC[A/T]ACCTAGAATTCCTGG | 329152 |
rs33836727 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54068657 | GCTGAGCAGCTCACA[A/G]AGCGCACAGGCCCTA | 329152 |
rs33836729 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54068911 | TGCTGACCTCTCTGG[C/T]CAGCTCACAGTAGGT | 329152 |
rs33836732 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54069016 | TGGTCAGTATCATCA[A/G]AGGCAGCTTGAATAT | 329152 |
rs33836734 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54118050 | AAAACTCACAATTAG[A/G]AAAGAAGGCCCTGAG | 329152 |
rs33836737 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54118119 | AGGGAAAGTCAACTC[A/G]CTGTTTCTTGGCCCA | 329152 |
rs33836740 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54118151 | CATCAGATGGTTTAA[A/G]ACAGTCCACTGAAGA | 329152 |
rs33836743 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54118216 | ATGCCTTTTTGGTAA[C/T]AATAAGCCCTGGAAG | 329152 |
rs33836745 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54172293 | TGCCAATTTTCTGTG[G/T]AGAGGTGTTACCAGA | 329152 |
rs33836748 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Hecw2 | Mm_Celera | 1:54172345 | CAGGTGCAACCTTCC[C/G]TCGGGCTGGAACACA | 329152 |
rs33836751 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54172361 | TCGGGCTGGAACACA[A/T]GTGGAAGTCAGGCAG | 329152 |
rs33836796 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54154338 | GACGGCAAAATCTAC[A/G]TAACTCAGTGATTCC | 329152 |
rs33836799 | snp | A/C/G | 0.42 | 0.183303 | intron-variant | Hecw2 | GRCm38.p3 | 1:54154353 | ATAACTCAGTGATTC[A/C/G]TGGTCACTGTTTCAT | 329152 |
rs33836802 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54154412 | AGAGTTGACAAATGA[C/T]TCAAAGATCTATCAT | 329152 |
rs33836815 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hecw2 | Mm_Celera | 1:54148116 | CCTTTTAAAATATAT[C/T]CTGAAACTCTGATAC | 329152 |
rs33836817 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54148452 | GACTCAGCCAGAAAC[A/C]GAAGCAAAGGCCATA | 329152 |
rs33836820 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54148518 | TAGTGACTGGTCAGG[G/T]AACACAAAGGCTACA | 329152 |
rs33836823 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54148561 | AATTTCATTTTCAGC[C/T]CTTTATTTCTAATAG | 329152 |
rs33836846 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54175107 | TCAGTTCAATTTCTC[A/G]GATTATCATGATCTT | 329152 |
rs33836849 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Hecw2 | Mm_Celera | 1:54175288 | AAGGGGGCATATCTC[A/G]AATCTTAGGGCAACA | 329152 |
rs33836865 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Hecw2 | Mm_Celera | 1:53985448 | TAGAATTTAACATGG[C/T]ATACTATGAGTCAGA | 329152 |
rs33836867 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53985536 | CATGTGGGTTACGAT[C/T]GCCTGCGACTCTTGT | 329152 |
rs33836870 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53985558 | GACTCTTGTTTAAGA[C/T]TCAGATTTCAAGAAA | 329152 |
rs33836873 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53985609 | TTTGGTAAAGGGCAT[C/T]ATGAATCTGTGTTTC | 329152 |
rs33836874 | snp | G/T | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54022091 | GCCTACCATCAACTA[G/T]AGTACTTTTTGGAGA | 329152 |
rs33836877 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Hecw2 | Mm_Celera | 1:54022169 | ACACCAGGTCAACCA[A/G]CTCAGTAAAACAGTG | 329152 |
rs33836880 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Hecw2 | Mm_Celera | 1:54022246 | ATAAACAGAAGGCAC[A/G]TTAACAAACTCCTAA | 329152 |
rs33836883 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw2 | Mm_Celera | 1:54022318 | ACGCTGAAGAACATG[C/T]ATGCTCTACTCAAGG | 329152 |
rs33836914 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54004078 | AAGGGCTTTGCTAAA[A/T]CTACATGTTTCTAAG | 329152 |
rs33836917 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw2 | Mm_Celera | 1:54004172 | CAGGAATTACATTTG[C/T]TTAGAAATATTAGCA | 329152 |
rs33836920 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54004221 | GGACACTCCTGTGAG[C/T]CCAGCTTGTGAGAAG | 329152 |
rs33836923 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54004316 | GGAGACACTGGCACG[A/G]ATGTCCAAAGACACA | 329152 |
rs33836944 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54000308 | GTCTGTGGACAAGGA[A/G]GTGCTAGGAAGATGA | 329152 |
rs33836947 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hecw2 | GRCm38.p3 | 1:54000877 | CAAATCACAATGATA[A/G]CGTAGCTAGCACATG | 329152 |
rs33836950 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hecw2 | Mm_Celera | 1:54000913 | ACACAGTGCTTGGCA[C/T]CAAGCTATCTCCCCA | 329152 |
rs33836953 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Hecw2 | GRCm38.p3 | 1:54001193 | TACTGGGAAAGGCTA[A/G]TGATTAAATGATGGG | 329152 |
rs33836986 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54040703 | AATAACGTCTAGGAC[A/G]GAGATCACAAGATGG | 329152 |
rs33836989 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54040722 | ATCACAAGATGGCCA[A/G]GCTGTCATACACCTC | 329152 |
rs33836992 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54040884 | TAAATTTTCAACCAG[C/T]AAGATACATGCTAAA | 329152 |
rs33836994 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54059988 | TAAAAACTGCAACTG[C/T]AAAGAGAAAATTTAA | 329152 |
rs33836996 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54060248 | TCTTCCTCACCCAGC[A/G]GTACTTTGAGTGGGA | 329152 |
rs33836999 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54060352 | ACTGGGGCTTCTCTT[A/G]GAGCCAGGAAAGAAA | 329152 |
rs33837002 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | GRCm38.p3 | 1:54060508 | TCTCTCCCTGCTTCC[C/T]ATGAAGCCGTGCCCT | 329152 |
rs33837014 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54124292 | AGGGCTGTACTGCCT[A/G]CAGAGTGCTAGCCTA | 329152 |
rs33837017 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54124483 | GCTTGTCTTCAAAAT[A/C]ATATGCTCCATCCCA | 329152 |
rs33837019 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54124542 | TCCCTTGGTGCCTTG[C/G]TCCACTTTCCCTCAA | 329152 |
rs33837022 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54124564 | TTCCCTCAAGTCACT[A/C]AGATCCACCCTCACT | 329152 |
rs33837075 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54104757 | CTTCCCCAAGATAGG[C/T]ATGGATTGAGGGAGC | 329152 |
rs33837077 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54105154 | GCCTCACCTTGAGTA[C/G]CCCAGTCCAATCTCT | 329152 |
rs33837079 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54105262 | CAGACAAAATCCAAC[A/G]AACCCTTACACACAT | 329152 |
rs33837082 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54105285 | ACACACATGCCATGC[A/C]AGGACATCTTTGACA | 329152 |
rs33837114 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Hecw2 | Mm_Celera | 1:54082832 | TATTCTCCATAAATT[C/T]CAATCTGAGTTTGCA | 329152 |
rs33837117 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Hecw2 | Mm_Celera | 1:54083472 | CCCAACACCTCATTC[A/T]CTATTTTAATCACAT | 329152 |
rs33837120 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hecw2 | Mm_Celera | 1:54085530 | TGAATTTATTTTTTT[A/G]AAGGAGAGGAGGTGA | 329152 |
rs33837123 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hecw2 | Mm_Celera | 1:54085550 | AGAGGAGGTGAACCA[C/T]AACAAATTCAAAAGC | 329152 |
rs33837136 | snp | C/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54130446 | CTCAGGGAAGTTCCA[C/G]CAGAGCCGCCTGGTC | 329152 |
rs33837139 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54130453 | AAGTTCCACCAGAGC[C/T]GCCTGGTCACCAGCC | 329152 |
rs33837142 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Hecw2 | Mm_Celera | 1:54130513 | TTATTAAAATCAGAG[C/T]CAACTTTCTATATGC | 329152 |
rs33837146 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54113373 | AGAGGTCAGAAAGGA[A/G]GTGTTTCTACCTCAA | 329152 |
rs33837149 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54113589 | GAAAGAGAAAAGTCA[A/G]TATTCTGTTAACAGG | 329152 |
rs33837152 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hecw2 | Mm_Celera | 1:54114166 | ATTAAAAAAAAAAAA[A/G]ACTCGAGTGCAGTTC | 329152 |
rs33837154 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Hecw2 | Mm_Celera | 1:54107865 | CCAGCCCAGCTCAAT[A/C]CTGGGTGCAGCAGAT | 329152 |
rs33837157 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Hecw2 | Mm_Celera | 1:54108264 | GGCACACCTTGGCAT[A/G]GGCCTGCCAGGTACA | 329152 |
rs33837162 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54109409 | GGAATTTGCTTAATT[C/T]CATTGTTCTTGATTG | 329152 |
rs33837224 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54132200 | AATCCCTTGCATTAC[A/C]CCTCAAACACATGGA | 329152 |
rs33837227 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54132810 | TTTCTTTCCTTCTTG[A/G]TTTCCGTCTCCCTCC | 329152 |
rs33837230 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54132912 | TCAGCACACCACACG[C/T]ACCCTCATCCGTGAT | 329152 |
rs33837235 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54139224 | TCCCAGCTGTGAAAG[G/T]TGGTGGTCTGAAAAG | 329152 |
rs33837238 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54139308 | ATCAGAAGTCCAGAA[A/G]CACATTACAGTCTTA | 329152 |
rs33837241 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54139343 | AAAGCTAAGGATGGA[C/T]TAGTAAAGTAGGCAT | 329152 |
rs33837417 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54166336 | GGAAGTATTCAAAGA[A/G]TGAAGGAGTTATATA | 329152 |
rs33837420 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54166500 | AATCCTCTGAAAGCC[A/C]TAGTATGGTGGTGTA | 329152 |
rs33837423 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Hecw2 | Mm_Celera | 1:54166566 | GAAAGATCAGAGAGA[G/T]CAGGACACTCACGCT | 329152 |
rs33837466 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54009265 | GTTACCCAGAATGGA[A/G]CTACTTGTGACTTGA | 329152 |
rs33837469 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hecw2 | Mm_Celera | 1:54009324 | TTTTGTTTTAAAGAA[C/T]TAATCAGTTCCTCGT | 329152 |
rs33837472 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54009420 | AGAACAAAGGGAAGG[C/T]TTATAACTCTCACCC | 329152 |
rs33837485 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54094945 | CACAGGAGACAGACC[C/T]TCAGAATGAGCTGAA | 329152 |
rs33837488 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54095353 | TTTCCTAACCTTTAC[A/G]TTGGCTTGTGGGGCT | 329152 |
rs33837491 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54095509 | AGCCCATGGCTTCTG[C/T]CAGCATGACACAACT | 329152 |
rs33837496 | snp | C/G | 0.495868 | 0.0452663 | intron-variant | Hecw2 | Mm_Celera | 1:54046138 | CCAAGAAACCCCAAT[C/G]TGGGGCTCAGGCCCC | 329152 |
rs33837499 | snp | C/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54046178 | CTGTTCTTCAGTGCA[C/G]AAGCCAGGAATAAAG | 329152 |
rs33837502 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw2 | Mm_Celera | 1:54046345 | AAAAGTCAAAACCTG[A/G]ACACATTACTTATGA | 329152 |
rs33837514 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54128226 | TGATTTTTTTATGGC[C/T]TGGTTGAAACTGGAT | 329152 |
rs33837517 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54128502 | CACACACACACACAC[A/G]TATGATCAGGATTCC | 329152 |
rs33837520 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54128533 | TTACACCTTTGTTTA[C/T]GGAGACTGTAAATAG | 329152 |
rs33837523 | snp | A/C/T | 0.32 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:54128597 | GTCTACATTTCCCAA[A/C/T]ACATGTCTTTAATAG | 329152 |
rs33837594 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Hecw2 | Mm_Celera | 1:54172602 | ACCTCAGCTCACCCA[A/G]TTATAGGATCGGGTA | 329152 |
rs33837597 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Hecw2 | Mm_Celera | 1:54172705 | AACAGCAAAGACTGC[G/T]AACTAGAAAGGCTCA | 329152 |
rs33837600 | snp | C/T | 0.42 | 0.183303 | intron-variant | Hecw2 | Mm_Celera | 1:54172737 | AAGACAAACTCTTGT[C/T]TGTCACAGTGAAATA | 329152 |
rs33837603 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Hecw2 | Mm_Celera | 1:54172767 | AGCCAGCAATATCTG[C/T]CATCTGTTACCTAGA | 329152 |
rs33837616 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | GRCm38.p3 | 1:54014801 | GACAGAAAGCAACAG[C/T]AGGCTAAACAGTGCA | 329152 |
rs33837619 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54014871 | AGGGGAAAAAAAAAA[A/C]CACTGGTACATTTAG | 329152 |
rs33837622 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Hecw2 | GRCm38.p3 | 1:54014890 | TGGTACATTTAGCCT[G/T]GAAGACTAGTTTAAC | 329152 |
rs33837626 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54118336 | ATGGGGTAAATAACT[A/G]GGCCGGTTTATGCAG | 329152 |
rs33837629 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54118467 | TTGACCTACTTTTAC[C/T]AACTGCCTTTCTACC | 329152 |
rs33837632 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54118541 | GGGGGCTGCTCGTGC[A/G]TGTCCATGCATGTCT | 329152 |
rs33837665 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54154448 | TTAAGAAATATTTAT[C/T]TGCTAATTACAGAAT | 329152 |
rs33837668 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54154563 | GCTAATTCTGTTTTA[C/T]TTTCAATCAAATTTA | 329152 |
rs33837673 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54155240 | TAGAGCTTCCAAGTT[A/G]CACATAGCACTCTGT | 329152 |
rs33837686 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54143567 | TTGATCTAAGCTCTT[A/C]ATCAGAAGGACAAAT | 329152 |
rs33837689 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54143624 | ACACTGTGACACAAT[G/T]TTGTCACCCACAAAT | 329152 |
rs33837692 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54143744 | ATTAAGCCAACCAAA[C/T]AGCCCTGCACTCCAC | 329152 |
rs33837745 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54069219 | TCTATTCCTAATCTT[C/T]GGGAGCATTTCATAA | 329152 |
rs33837748 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Hecw2 | Mm_Celera | 1:54069261 | AGGAAAAAAAGTGTC[A/G]AAAAGAACCAGAAGA | 329152 |
rs33837751 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54069299 | ACTCTTAACAGATTC[A/C]GCAACCTTTCATTTG | 329152 |
rs33837796 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | GRCm38.p3 | 1:54004358 | TCCACTGAGTACTTT[A/G]GTCATTCACTCGGAG | 329152 |
rs33837799 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54004387 | AGCAGTGAAAGAGAC[A/G]TTCTAAGAGTCCAGT | 329152 |
rs33837802 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54004438 | TGGTACACATGATAC[A/G]TCTTCTTCTAAAACT | 329152 |
rs33837806 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54022663 | GAGTACAGTGTCTTT[G/T]TATGTGTGCCTTTTA | 329152 |
rs33837809 | snp | A/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54022792 | TTCTGAGAACCATCT[A/G]CAAGGAAATCTTGTC | 329152 |
rs33837812 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Hecw2 | Mm_Celera | 1:54022820 | GTCTAGAAATCTTCA[C/G/T]GGTGTGTGTGAGATT | 329152 |
rs33837816 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw2 | GRCm38.p3 | 1:54001231 | AAACGTATTTAATAA[C/T]TGGGTAAAATGCTAT | 329152 |
rs33837819 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Hecw2 | Mm_Celera | 1:54001722 | CTGGGACTGGCCGGC[C/T]GCAACAATGGAGAAA | 329152 |
rs33837825 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54130525 | GAGTCAACTTTCTAT[A/G]TGCCAAACACAGGTC | 329152 |
rs33837828 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54130552 | GGTCCCTTCTTTCAA[G/T]AGTCTTATGTTTACT | 329152 |
rs33837831 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54130697 | AAACAGGAAGATGGT[A/G]GCTATCATACATACA | 329152 |
rs33837836 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:53985625 | ATGAATCTGTGTTTC[A/G]ATAACAAATCCAAGC | 329152 |
rs33837839 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:53985642 | TAACAAATCCAAGCA[A/G]TTCTAATACAAGCAA | 329152 |
rs33837842 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:53985679 | AGCCATAGTTTGAAA[A/G]ATTGATTGGCATTCT | 329152 |
rs33837855 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54040907 | ATGCTAAATGCAGAC[A/G]ATGAACGCTACTGAT | 329152 |
rs33837858 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Hecw2 | GRCm38.p3 | 1:54041001 | AGCTTGCGCAAATGT[G/T]GCCCCTGCACTTAAA | 329152 |
rs33837861 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54041089 | TTTCTCTGTAAAGTC[C/T]GATTTGCCATATGAT | 329152 |
rs33837876 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54148590 | AGACAGTGACAGTTG[G/T]CAGCTATCAAACATG | 329152 |
rs33837881 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54149087 | TAATTACAGCCATTG[A/C]TAGTTTGAAGTATAA | 329152 |
rs33837957 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54060607 | GCATTTCAATTGCTT[C/T]CCACTTCAGAGCCCA | 329152 |
rs33837975 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54124609 | GCATCACATCTGCCT[A/G]CATAAACACAGGATG | 329152 |
rs33837978 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54124636 | GATGTACCATGTTTG[C/T]ACAGCACTTGAGAAC | 329152 |
rs33837981 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54124856 | AACAGGATGAGAAGC[A/G]GTAACAGAGCCAATC | 329152 |
rs33837996 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Hecw2 | Mm_Celera | 1:54085561 | ACCATAACAAATTCA[A/T]AAGCAGCCTCCATTT | 329152 |
rs33837998 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Hecw2 | Mm_Celera | 1:54085868 | AGTGCTTAGCTATGT[C/T]AAAAATCTTACTAAT | 329152 |
rs33838002 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54087665 | TCAGTGCATGGATGA[A/G]GCCTTACACAGCCAG | 329152 |
rs33838075 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54114508 | ATGTTTGTTTCTGAA[A/C]TTGCTTGCTATATTT | 329152 |
rs33838078 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hecw2 | Mm_Celera | 1:54114531 | CTATATTTTACATTC[A/G]CCTCATTTACTCTTC | 329152 |
rs33838081 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54114532 | TATATTTTACATTCA[C/G]CTCATTTACTCTTCA | 329152 |
rs33838084 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54139523 | GGTTGGTTGAGAAAC[C/T]CTGAACGTGCCCAAA | 329152 |
rs33838089 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54139680 | GCATCTCCCTTTATC[A/G]CCCACTTTTCTATAA | 329152 |
rs33838092 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54139713 | AAGAACAGAAATCAC[C/T]ATGGAGAAGCACAGT | 329152 |
rs33838137 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54133395 | AACTGAATGAGATCA[A/G]ACGGTTTAAAATTGG | 329152 |
rs33838140 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54133545 | GGGTGTCCAGACCTC[C/T]AGGCCTTTATCTTGC | 329152 |
rs33838207 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54110537 | TAGCACAGAAATAAT[A/G]CCAGCAAAAGGCAGC | 329152 |
rs33838210 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54110563 | GCAGCTGTTTCTCTC[A/G]CTAAGAGAATAAGTG | 329152 |
rs33838213 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54110625 | GAACATTTCCCAGGT[A/G]CTTTGTTTTTTCAAA | 329152 |
rs33838306 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54166579 | GATCAGGACACTCAC[A/G]CTCCCTCAAGCTCAC | 329152 |
rs33838309 | snp | C/G | 0.396694 | 0.202437 | intron-variant | Hecw2 | Mm_Celera | 1:54166635 | AAGACAAATTGGCTT[C/G]TGGAAAGCCAGGGTC | 329152 |
rs33838312 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54166785 | AAGTAAACAAACCTT[A/G]AATATTCTACAACTG | 329152 |
rs33838315 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54009725 | TGCTTAGCTTTTGAG[A/G]CGCATCAAAGAAAGT | 329152 |
rs33838355 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54046787 | GAGACCCGGGAATAC[A/T]GTGAATTAGCTTGAG | 329152 |
rs33838426 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54128628 | ACTCGATTCTATAAA[C/T]GCAGAGATCCTGCCA | 329152 |
rs33838429 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54128745 | GATTTTTCAAAGTCA[G/T]TGCTGAAGGCTTGTT | 329152 |
rs33838432 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54128878 | AGGCTTTTCTATTGT[A/G]CAAGTCCCAGGCATT | 329152 |
rs33838454 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54095563 | CAGCAGCCCTGAGTA[A/T]CCTCTGTATACCCAC | 329152 |
rs33838459 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Hecw2 | Mm_Celera | 1:54095802 | TCTAAGTAGAGAAAC[A/G]TAAGCACCTTCGCCC | 329152 |
rs33838462 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54095825 | CTTCGCCCCTCTCAC[C/T]GATGGCAGGAAAGTA | 329152 |
rs33838526 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54172775 | ATATCTGCCATCTGT[C/T]ACCTAGAAGGTAAAC | 329152 |
rs33838529 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hecw2 | Mm_Celera | 1:54172847 | GTTCAGGAAGAAATC[C/T]CTGTCACTCTTGAGT | 329152 |
rs33838532 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Hecw2 | Mm_Celera | 1:54172969 | GTAGGATGCATTAAT[A/G]TGTTGGTAGGATGAT | 329152 |
rs33838584 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54069339 | CAGGCTGAGACACAT[A/G]GTCTTATCTCAACAC | 329152 |
rs33838595 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54143786 | TTTCCAGGTAAGGGG[C/T]GTACAGAGAAAAGAT | 329152 |
rs33838598 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54143920 | CCTAGACCCTATCAT[A/G]GAACCCTGAAAGACA | 329152 |
rs33838601 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hecw2 | Mm_Celera | 1:54145135 | TAGTACTTAAGTATT[C/T]TGTGAATAAACAGAC | 329152 |
rs33838609 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54118915 | GTATCTCTGCCTGCT[A/G]CTCTGGCCCTGAAGC | 329152 |
rs33838612 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54119005 | AAGAGAACTCCATTA[A/T]TTCCTACAGGATTTT | 329152 |
rs33838626 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54155277 | TCAAAGAACATCAAA[C/T]CTACAAGGTCACTCA | 329152 |
rs33838629 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Hecw2 | Mm_Celera | 1:54156098 | AGCCTCTCAAGTTAA[A/G]TACTTTTCTAAAAAG | 329152 |
rs33838632 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54156272 | ACCACAATCTTGACA[C/T]AATCATATTTCACCT | 329152 |
rs33838655 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Hecw2 | GRCm38.p3 | 1:54014908 | AGACTAGTTTAACTA[C/T]GATAACATGGGGAAG | 329152 |
rs33838658 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Hecw2 | GRCm38.p3 | 1:54014957 | TATGTATTCAGTCAT[A/G]AAATGGGTCAAAAAG | 329152 |
rs33838661 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54015058 | GTCTCATCAACCCCA[C/G]AAGAACCTGAAGGCT | 329152 |
rs33838744 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hecw2 | Mm_Celera | 1:54130719 | ATACATACATACAAA[A/G]GATGGTTGGTAAATA | 329152 |
rs33838747 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54130824 | AATCCGTTTGAATTG[A/G]ATGGATTCAGGCTTC | 329152 |
rs33838750 | snp | G/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54130857 | TGCCCAGGCCTGTCA[G/T]GCTTCTGTAACCCAG | 329152 |
rs33838753 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hecw2 | Mm_Celera | 1:54130882 | ACCCAGAACTGCCAT[A/G]CCCAACCCTGACTAT | 329152 |
rs33838834 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54125042 | TCAAAACAGACGATC[A/G]GGGTCTGGATCCTTT | 329152 |
rs33838836 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54125131 | GCTATAAAATGTTTT[A/C]TCTCCTTGCTCCTGG | 329152 |
rs33838839 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54125515 | TGAGCTAAACACATT[C/T]ATTTTACACTTTTCT | 329152 |
rs33838842 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hecw2 | Mm_Celera | 1:54125815 | TTTTCACAAACACTG[C/T]GTAGCTTAACAAACA | 329152 |
rs33838854 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:53985762 | GTCAGTAGCTGGCAC[A/T]GAGGTCCCTACAGTT | 329152 |
rs33838856 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | GRCm38.p3 | 1:53985799 | TTTGCTACAAAAATG[C/T]TGCCAAGAATAACTT | 329152 |
rs33838915 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54166941 | CTTATATGAAATGCC[A/C]TGTGGTACACAGCAC | 329152 |
rs33838918 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54166973 | TCATACAATAAATAG[A/T]CACAATAAAAATTAA | 329152 |
rs33838921 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Hecw2 | Mm_Celera | 1:54167001 | TAATCAGTTTAAAAG[C/T]AAAATACAAATATTT | 329152 |
rs33838924 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Hecw2 | Mm_Celera | 1:54114612 | TTCGACTACACGTGT[A/G]TATGGATGCCAGATC | 329152 |
rs33838927 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54114867 | CCTGAACTCACAAAG[A/G]GTATGCAAGTTCCTG | 329152 |
rs33838930 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54114881 | GGGTATGCAAGTTCC[C/T]GAGAAGCATAAAGCC | 329152 |
rs33838933 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hecw2 | Mm_Celera | 1:54114943 | GAGTCTGGAAAACTA[C/T]AGTTACGGTAGCCCC | 329152 |
rs33838954 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54149104 | AGTTTGAAGTATAAA[C/T]TCAGGGATCCATTAC | 329152 |
rs33838957 | snp | C/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54149185 | TTAATAGCACAGACA[C/T]TAGAAATCCAGGGTT | 329152 |
rs33838960 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54149290 | ACGCCCTTTACCACC[A/G]GCTGGACTTTATCAT | 329152 |
rs33838963 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54149619 | GATAAGAGCTAGATG[A/G]CCTGAGAATAAACCA | 329152 |
rs33838987 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54139950 | CCAAACAGCCCGCTT[A/G]GCCAAAGTACTACAT | 329152 |
rs33838990 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54140034 | GCTGAGTTGTGTGCC[C/T]ATAAAACTATCTATG | 329152 |
rs33838993 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54140602 | AATGTGATAAAGGCA[A/G]GTATCTAACAATATA | 329152 |
rs33839085 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54134077 | GTAAAAATCAAATCC[C/T]ATTTCAATTCCCATA | 329152 |
rs33839088 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hecw2 | Mm_Celera | 1:54134188 | CTTCCTTCTGTACCA[A/G]TTTATCCAGGAAAAT | 329152 |
rs33839091 | snp | C/G | 0.486111 | 0.0821678 | intron-variant | Hecw2 | Mm_Celera | 1:54134551 | AAGAAATAAATAAAT[C/G]TGGGTTTCTTTCAGA | 329152 |
rs33839186 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hecw2 | Mm_Celera | 1:54110846 | ATTATACAATTTAGC[A/G]TCTTAAGACTATCAA | 329152 |
rs33839191 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Hecw2 | Mm_Celera | 1:54111075 | CAGCAATGCTGACTT[G/T]CTAAGGCTCGAGGTT | 329152 |
rs33839195 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hecw2 | Mm_Celera | 1:54129147 | GTGAAATACCTCCTA[A/C]ACTGTCAAGTGATAC | 329152 |
rs33839198 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54129256 | ATGCCTCTCTTGCAT[A/C]ATGTCCTCAGAGGCT | 329152 |
rs33839201 | snp | G/T | 0.473373 | 0.11227 | intron-variant | Hecw2 | Mm_Celera | 1:54129453 | CCATCCCTAGTAATG[G/T]CAAAAGTGATTAGAA | 329152 |
rs33839245 | snp | A/C/T | 0.489796 | 0.070696 | intron-variant | Hecw2 | GRCm38.p3 | 1:54172998 | ATGTTTCTCCCTAAA[A/C/T]GAGAAATAAACAAAC | 329152 |
rs33839248 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Hecw2 | Mm_Celera | 1:54173232 | TTTGGTGTTGAAAAC[A/G]TCATCATTATAGGAG | 329152 |
rs33839251 | snp | C/G | 0.5 | 0 | intron-variant | Hecw2 | Mm_Celera | 1:54173247 | GTCATCATTATAGGA[C/G]GGCACTATTTTGGGG | 329152 |
rs33839264 | snp | A/T | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54087926 | CTTAAGCATTATGAA[A/T]GTTCTATCTCCTTTA | 329152 |
rs33839267 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54090308 | AAAAAGCAAGCGCTG[A/C]TCCTGATACCTCTTG | 329152 |
rs33839375 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Hecw2 | Mm_Celera | 1:54095900 | AAAGTCCCTCTGCTT[A/G]TTTCTTATATTTTTG | 329152 |
rs33839404 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hecw2 | Mm_Celera | 1:54145358 | ACACTCTAGAAATCT[A/G]CAGCCCACATAGTAC | 329152 |
rs33839407 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hecw2 | Mm_Celera | 1:54145368 | AATCTGCAGCCCACA[C/T]AGTACAAATGCAAAA | 329152 |
rs33839410 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54145453 | GTATTTGTACAACAC[A/G]CTGTATCACGGGAAA | 329152 |
rs33839413 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54145606 | TTCCCTTCTTGTAAA[A/C]TGGGATGCCATACAC | 329152 |
rs33839415 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Hecw2 | Mm_Celera | 1:54156995 | CAAGCATACTGCACA[A/T]TATTAAATAAATGTA | 329152 |
rs33839418 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hecw2 | Mm_Celera | 1:54157162 | ACCAGAGCTCCAAAG[A/G]TTCTTTGGTTGGTTG | 329152 |
rs33839421 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54157503 | AAAGGCTGTGGATGA[A/G]CAGTAATAGAAAGAT | 329152 |
rs33839486 | snp | A/C | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54130920 | GAAAGAAACTTCCAT[A/C]CACTCTGAGCTGTTG | 329152 |
rs33839489 | snp | A/G | 0.32 | 0.24 | intron-variant | Hecw2 | Mm_Celera | 1:54130935 | ACACTCTGAGCTGTT[A/G]TCATCTGTACTCTCT | 329152 |