Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10585 |
| ensemblid | ENSG00000130714.19 |
| hgncid | 9202 |
| symbol | POMT1 |
| name | protein O-mannosyltransferase 1 |
| refseq_nuc | NM_001077365.2 |
| refseq_prot | NP_001070833.1 |
| ensembl_nuc | ENST00000402686.8 |
| ensembl_prot | ENSP00000385797.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 131502918 |
| end | 131523799 |
| strand | + |
| ver | v1.2 |
| region | chr9:131502918-131523799 |
| region5000 | chr9:131497918-131528799 |
| regionname0 | POMT1_chr9_131502918_131523799 |
| regionname5000 | POMT1_chr9_131497918_131528799 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 725 | 284 | 76 | 63 | 99 | 14 | 30 | 68 | POMT1_chr9_131497918_131528799 | POMT1 | MWGFL others(720): Show |
chr9 | 131497918 | 131528799 |
| a0002 | 0/0 | 725 | 32 | 2 | 4 | 21 | 3 | 2 | 16 | POMT1_chr9_131497918_131528799 | POMT1 | MWGFL others(720): Show |
chr9 | 131497918 | 131528799 |
| a0003 | 0/0 | 725 | 9 | 7 | 1 | 0 | 0 | 1 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | MWGFL others(720): Show |
chr9 | 131497918 | 131528799 |
| a0004 | 0/0 | 725 | 3 | 0 | 0 | 0 | 1 | 2 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | MWGFL others(720): Show |
chr9 | 131497918 | 131528799 |
| a0005 | 0/0 | 725 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | MWGFL others(720): Show |
chr9 | 131497918 | 131528799 |
| a0006 | 0/0 | 725 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | MWGFL others(720): Show |
chr9 | 131497918 | 131528799 |
| a0007 | 0/0 | 725 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | MWGFL others(720): Show |
chr9 | 131497918 | 131528799 |
| a0008 | 0/0 | 725 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | MCGFL others(720): Show |
chr9 | 131497918 | 131528799 |
| a0009 | 0/0 | 725 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | MWGFL others(720): Show |
chr9 | 131497918 | 131528799 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2175 | 241 | 50 | 55 | 91 | 14 | 30 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0001c0003 | 1/0 | 2175 | 16 | 13 | 1 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0001c0004 | 0/0 | 2175 | 11 | 0 | 5 | 6 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0001c0006 | 0/0 | 2175 | 5 | 5 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0001c0007 | 0/0 | 2175 | 4 | 4 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0001c0009 | 0/0 | 2175 | 2 | 2 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0001c0010 | 0/0 | 2175 | 2 | 2 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0001c0013 | 0/0 | 2175 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0001c0014 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0001c0015 | 0/0 | 2175 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0002c0002 | 0/0 | 2175 | 32 | 2 | 4 | 21 | 3 | 2 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0003c0005 | 0/0 | 2175 | 8 | 7 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0003c0018 | 0/0 | 2175 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0004c0008 | 0/0 | 2175 | 3 | 0 | 0 | 0 | 1 | 2 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0005c0012 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0005c0017 | 0/0 | 2175 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0006c0016 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0007c0019 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0008c0020 | 0/0 | 2175 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 | ||
| a0009c0011 | 0/0 | 2175 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | ATGTG others(2170): Show |
chr9 | 131497918 | 131528799 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3057 | 204 | 35 | 43 | 89 | 8 | 28 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0001t0003 | 0/0 | 3057 | 15 | 13 | 2 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0001t0004 | 0/0 | 3057 | 17 | 0 | 9 | 0 | 6 | 2 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0001t0008 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0001t0009 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0001t0010 | 0/0 | 3057 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0001t0011 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0001t0015 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0003t0002 | 0/0 | 3057 | 4 | 4 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0003t0005 | 1/0 | 3057 | 6 | 4 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0003t0006 | 0/0 | 3057 | 5 | 5 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0003t0012 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0004t0001 | 0/0 | 3057 | 11 | 0 | 5 | 6 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0006t0007 | 0/0 | 3057 | 5 | 5 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0007t0002 | 0/0 | 3057 | 4 | 4 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0009t0004 | 0/0 | 3057 | 2 | 2 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0010t0013 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0010t0014 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0013t0001 | 0/0 | 3057 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0014t0001 | 0/0 | 3057 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0001c0015t0003 | 0/0 | 3057 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0002c0002t0002 | 0/0 | 3057 | 32 | 2 | 4 | 21 | 3 | 2 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0003c0005t0003 | 0/0 | 3057 | 8 | 7 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0003c0018t0003 | 0/0 | 3057 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0004c0008t0001 | 0/0 | 3057 | 3 | 0 | 0 | 0 | 1 | 2 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0005c0012t0001 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0005c0017t0001 | 0/0 | 3057 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0006c0016t0003 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0007c0019t0002 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0008c0020t0001 | 0/0 | 3057 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| a0009c0011t0001 | 0/0 | 3057 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | GTCTG others(3052): Show |
chr9 | 131497918 | 131528799 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 17 | 9 | 1 | 6 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0002 | 0/0 | 11 | 0 | 2 | 7 | 0 | 2 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0003 | 0/0 | 11 | 0 | 1 | 8 | 0 | 2 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0004 | 0/0 | 8 | 1 | 1 | 3 | 1 | 2 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0005 | 0/0 | 4 | 1 | 0 | 2 | 1 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0006 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0041 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0003g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0003g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0004g0009 | 0/0 | 5 | 0 | 1 | 0 | 3 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0004g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0004g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0004g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0009g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0010g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0011g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0001t0015g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0003t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0003t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0003t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0003t0005g0014 | 1/0 | 4 | 2 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0003t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0003t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0003t0006g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0003t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0003t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0003t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0003t0012g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0004t0001g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0004t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0004t0001g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0004t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0004t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0006t0007g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0007t0002g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0007t0002g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0009t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0009t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0010t0013g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0010t0014g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0013t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0014t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0001c0015t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0008 | 0/0 | 6 | 1 | 1 | 1 | 3 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0049 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0003c0005t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0003c0005t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0003c0005t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0003c0005t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0003c0005t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0003c0005t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0003c0018t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0004c0008t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0004c0008t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0005c0012t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0005c0017t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0006c0016t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0007c0019t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0008c0020t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| a0009c0011t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0096 | EUR | GBR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00140 | hp1 | a0004 | c0008 | t0001 | g0003 | EUR | GBR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | GBR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0009 | EUR | FIN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0009 | EUR | FIN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | FIN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | CHS | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00642 | hp2 | a0001 | c0001 | t0010 | g0189 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00741 | hp1 | a0001 | c0013 | t0001 | g0002 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01081 | hp2 | a0001 | c0003 | t0005 | g0014 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01099 | hp2 | a0001 | c0004 | t0001 | g0005 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01106 | hp1 | a0001 | c0015 | t0003 | g0054 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0185 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0074 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0018 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0038 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0187 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0038 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01358 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0008 | EUR | IBS | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0086 | EUR | IBS | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0009 | EUR | IBS | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0008 | EUR | IBS | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01891 | hp1 | a0001 | c0003 | t0006 | g0181 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01891 | hp2 | a0001 | c0010 | t0014 | g0055 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01928 | hp1 | a0001 | c0004 | t0001 | g0005 | AMR | PEL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01928 | hp2 | a0001 | c0004 | t0001 | g0142 | AMR | PEL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01943 | hp1 | a0003 | c0005 | t0003 | g0063 | AMR | PEL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01952 | hp2 | a0001 | c0004 | t0001 | g0140 | AMR | PEL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0097 | AMR | PEL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0186 | AMR | PEL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02027 | hp2 | a0001 | c0001 | t0009 | g0093 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02055 | hp2 | a0001 | c0007 | t0002 | g0052 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02135 | hp2 | a0001 | c0014 | t0001 | g0042 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CDX | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02258 | hp1 | a0003 | c0005 | t0003 | g0075 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02258 | hp2 | a0003 | c0005 | t0003 | g0170 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02451 | hp2 | a0001 | c0003 | t0006 | g0050 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02572 | hp2 | a0003 | c0005 | t0003 | g0091 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02647 | hp1 | a0001 | c0006 | t0007 | g0011 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02698 | hp2 | a0004 | c0008 | t0001 | g0002 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02723 | hp2 | a0001 | c0007 | t0002 | g0051 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0049 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02818 | hp2 | a0006 | c0016 | t0003 | g0164 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02886 | hp2 | a0007 | c0019 | t0002 | g0180 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02896 | hp1 | a0001 | c0003 | t0002 | g0168 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02896 | hp2 | a0001 | c0003 | t0002 | g0047 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02897 | hp1 | a0001 | c0003 | t0002 | g0047 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | ESN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02965 | hp1 | a0001 | c0009 | t0004 | g0073 | AFR | ESN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02965 | hp2 | a0001 | c0003 | t0005 | g0166 | AFR | ESN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | ESN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02970 | hp2 | a0003 | c0005 | t0003 | g0025 | AFR | ESN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02976 | hp1 | a0001 | c0003 | t0005 | g0014 | AFR | ESN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0032 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03195 | hp2 | a0001 | c0003 | t0005 | g0014 | AFR | ESN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03209 | hp1 | a0001 | c0006 | t0007 | g0011 | AFR | MSL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03209 | hp2 | a0003 | c0005 | t0003 | g0024 | AFR | MSL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0009 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03453 | hp1 | a0003 | c0005 | t0003 | g0024 | AFR | MSL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03453 | hp2 | a0001 | c0009 | t0004 | g0072 | AFR | MSL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03486 | hp1 | a0001 | c0006 | t0007 | g0011 | AFR | MSL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03486 | hp2 | a0001 | c0003 | t0005 | g0167 | AFR | MSL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03490 | hp1 | a0008 | c0020 | t0001 | g0154 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03516 | hp2 | a0003 | c0005 | t0003 | g0025 | AFR | ESN | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03540 | hp2 | a0001 | c0007 | t0002 | g0051 | AFR | GWD | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | MSL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03654 | hp2 | a0009 | c0011 | t0001 | g0094 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0100 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03688 | hp1 | a0005 | c0017 | t0001 | g0110 | SAS | STU | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03710 | hp2 | a0003 | c0018 | t0003 | g0064 | SAS | PJL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | STU | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0183 | SAS | STU | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0175 | AFR | YRI | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | CHB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18906 | hp1 | a0001 | c0003 | t0002 | g0174 | AFR | YRI | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0080 | AFR | YRI | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18941 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18944 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18952 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18969 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18970 | hp1 | a0001 | c0001 | t0015 | g0046 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18987 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18997 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19030 | hp1 | a0001 | c0003 | t0006 | g0172 | AFR | LWK | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19030 | hp2 | a0001 | c0010 | t0013 | g0056 | AFR | LWK | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19043 | hp1 | a0001 | c0003 | t0006 | g0179 | AFR | LWK | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | LWK | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19068 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19078 | hp2 | a0001 | c0003 | t0012 | g0182 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA20129 | hp1 | a0005 | c0012 | t0001 | g0123 | AFR | ASW | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA20129 | hp2 | a0001 | c0007 | t0002 | g0052 | AFR | ASW | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0018 | EUR | TSI | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0008 | EUR | TSI | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA20905 | hp2 | a0004 | c0008 | t0001 | g0003 | SAS | GIH | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG06807 | hp1 | a0001 | c0003 | t0006 | g0050 | AFR | USA | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| HG06807 | hp2 | a0001 | c0006 | t0007 | g0011 | AFR | USA | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | USA | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | USA | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA21309 | hp1 | a0001 | c0006 | t0007 | g0011 | AFR | LWK | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0156 | REF | REF | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0005 | g0014 | REF | REF | POMT1_chr9_131497918_131528799 | POMT1 | chr9 | 131497918 | 131528799 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131504224 | G | T | 1 | a0008 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.6G>T | p.Trp2Cys | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/20 | 192/3057 | 6/2178 | 2/725 | chr9 | 131504224 | |||
| chr9:131511394 | G | A | 1 | a0002 | 32 | HG00558.hp2 HG01192.hp1 HG01257.hp2 others(29): Show |
missense_variant | MODERATE | c.913G>A | p.Val305Ile | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 10/20 | 1099/3057 | 913/2178 | 305/725 | chr9 | 131511394 | |||
| chr9:131515483 | C | A | 1 | a0004 | 3 | HG00140.hp1 HG02698.hp2 NA20905.hp2 |
missense_variant | MODERATE | c.1233C>A | p.Asp411Glu | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/20 | 1419/3057 | 1233/2178 | 411/725 | chr9 | 131515483 | |||
| chr9:131518475 | G | A | 1 | a0009 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.1303G>A | p.Val435Ile | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 14/20 | 1489/3057 | 1303/2178 | 435/725 | chr9 | 131518475 | |||
| chr9:131518945 | C | G | 1 | a0007 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.1474C>G | p.Arg492Gly | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 15/20 | 1660/3057 | 1474/2178 | 492/725 | chr9 | 131518945 | |||
| chr9:131519401 | G | A | 1 | a0005 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.1499G>A | p.Arg500Lys | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 16/20 | 1685/3057 | 1499/2178 | 500/725 | chr9 | 131519401 | |||
| chr9:131519402 | G | T | 1 | a0005 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1500G>T | p.Arg500Ser | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 16/20 | 1686/3057 | 1500/2178 | 500/725 | chr9 | 131519402 | |||
| chr9:131522077 | C | T | 2 | a0003 a0006 |
10 | HG01943.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
missense_variant | MODERATE | c.1856C>T | p.Ala619Val | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/20 | 2042/3057 | 1856/2178 | 619/725 | chr9 | 131522077 | |||
| chr9:131523096 | G | A | 1 | a0006 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.2168G>A | p.Arg723Gln | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 2354/3057 | 2168/2178 | 723/725 | chr9 | 131523096 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131504296 | G | A | 1 | a0001c0009 | 2 | HG02965.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.78G>A | p.Gly26Gly | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/20 | 264/3057 | 78/2178 | 26/725 | chr9 | 131504296 | |||
| chr9:131511357 | T | C | 15 | a0001c0001 a0001c0004 a0001c0009 others(12): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
synonymous_variant | LOW | c.876T>C | p.Thr292Thr | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 10/20 | 1062/3057 | 876/2178 | 292/725 | chr9 | 131511357 | |||
| chr9:131511372 | G | A | 1 | a0001c0004 | 11 | HG01099.hp2 HG01358.hp1 HG01928.hp1 others(8): Show |
synonymous_variant | LOW | c.891G>A | p.Leu297Leu | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 10/20 | 1077/3057 | 891/2178 | 297/725 | chr9 | 131511372 | |||
| chr9:131512101 | T | C | 15 | a0001c0001 a0001c0004 a0001c0009 others(12): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
synonymous_variant | LOW | c.1047T>C | p.Asp349Asp | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/20 | 1233/3057 | 1047/2178 | 349/725 | chr9 | 131512101 | |||
| chr9:131513281 | C | T | 1 | a0001c0007 | 4 | HG02055.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
synonymous_variant | LOW | c.1125C>T | p.His375His | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/20 | 1311/3057 | 1125/2178 | 375/725 | chr9 | 131513281 | |||
| chr9:131513305 | C | T | 1 | a0003c0018 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.1149C>T | p.His383His | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/20 | 1335/3057 | 1149/2178 | 383/725 | chr9 | 131513305 | |||
| chr9:131518447 | A | G | 1 | a0001c0006 | 5 | HG02647.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.1275A>G | p.Glu425Glu | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 14/20 | 1461/3057 | 1275/2178 | 425/725 | chr9 | 131518447 | |||
| chr9:131518950 | C | T | 1 | a0001c0007 | 4 | HG02055.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
synonymous_variant | LOW | c.1479C>T | p.Tyr493Tyr | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 15/20 | 1665/3057 | 1479/2178 | 493/725 | chr9 | 131518950 | |||
| chr9:131520187 | G | A | 1 | a0001c0013 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.1692G>A | p.Arg564Arg | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/20 | 1878/3057 | 1692/2178 | 564/725 | chr9 | 131520187 | |||
| chr9:131520193 | C | T | 1 | a0001c0010 | 2 | HG01891.hp2 NA19030.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1698C>T | p.Ser566Ser | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/20 | 1884/3057 | 1698/2178 | 566/725 | chr9 | 131520193 | |||
| chr9:131522207 | C | T | 1 | a0001c0015 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.1986C>T | p.Ile662Ile | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/20 | 2172/3057 | 1986/2178 | 662/725 | chr9 | 131522207 | |||
| chr9:131523010 | G | A | 1 | a0001c0014 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.2082G>A | p.Leu694Leu | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 2268/3057 | 2082/2178 | 694/725 | chr9 | 131523010 | |||
| chr9:131523043 | G | A | 1 | a0007c0019 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.2115G>A | p.Ser705Ser | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 2301/3057 | 2115/2178 | 705/725 | chr9 | 131523043 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131502987 | C | T | 1 | a0001c0001t0015 | 1 | NA18970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-117C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 1/20 | 1232 | chr9 | 131502987 | ||||||
| chr9:131504199 | T | C | 1 | a0001c0001t0008 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-20T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/20 | 20 | chr9 | 131504199 | ||||||
| chr9:131504213 | T | G | 1 | a0001c0003t0006 | 5 | HG01891.hp1 HG02451.hp2 HG06807.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-6T>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/20 | 6 | chr9 | 131504213 | ||||||
| chr9:131523131 | C | T | 2 | a0001c0010t0013 a0001c0010t0014 |
2 | HG01891.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*25C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 25 | chr9 | 131523131 | ||||||
| chr9:131523138 | G | C | 1 | a0001c0010t0013 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*32G>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 32 | chr9 | 131523138 | ||||||
| chr9:131523144 | G | A | 1 | a0001c0001t0009 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*38G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 38 | chr9 | 131523144 | ||||||
| chr9:131523147 | T | C | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(20): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*41T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 41 | chr9 | 131523147 | ||||||
| chr9:131523312 | A | G | 1 | a0001c0003t0006 | 5 | HG01891.hp1 HG02451.hp2 HG06807.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*206A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 206 | chr9 | 131523312 | ||||||
| chr9:131523332 | T | C | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(20): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*226T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 226 | chr9 | 131523332 | ||||||
| chr9:131523384 | T | C | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(21): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*278T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 278 | chr9 | 131523384 | ||||||
| chr9:131523391 | A | G | 30 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(27): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
3_prime_UTR_variant | MODIFIER | c.*285A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 285 | chr9 | 131523391 | ||||||
| chr9:131523444 | T | G | 1 | a0001c0001t0010 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*338T>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 338 | chr9 | 131523444 | ||||||
| chr9:131523454 | C | T | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(19): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*348C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 348 | chr9 | 131523454 | ||||||
| chr9:131523527 | G | A | 2 | a0001c0001t0004 a0001c0009t0004 |
19 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*421G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 421 | chr9 | 131523527 | ||||||
| chr9:131523542 | G | A | 1 | a0001c0001t0011 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*436G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 436 | chr9 | 131523542 | ||||||
| chr9:131523559 | T | C | 15 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(12): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*453T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 453 | chr9 | 131523559 | ||||||
| chr9:131523635 | G | A | 1 | a0001c0006t0007 | 5 | HG02647.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*529G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 20/20 | 529 | chr9 | 131523635 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131503109 | C | G | 1 | a0001c0001t0001g0053 | 2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-31+36C>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 1/19 | chr9 | 131503109 | |||||||
| chr9:131503152 | T | C | 1 | a0001c0001t0001g0015 | 3 | HG01070.hp1 HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-31+79T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 1/19 | chr9 | 131503152 | |||||||
| chr9:131503247 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-31+174C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 1/19 | chr9 | 131503247 | |||||||
| chr9:131503465 | T | C | 1 | a0001c0015t0003g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-31+392T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 1/19 | chr9 | 131503465 | |||||||
| chr9:131503485 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-31+412G>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 1/19 | chr9 | 131503485 | |||||||
| chr9:131503656 | A | G | 27 | a0001c0001t0001g0171 a0001c0001t0010g0189 a0001c0003t0002g0047 others(24): Show |
40 | HG00558.hp2 HG00642.hp2 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.-30-533A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 1/19 | chr9 | 131503656 | |||||||
| chr9:131503657 | A | C | 1 | a0001c0001t0010g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-30-532A>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 1/19 | chr9 | 131503657 | |||||||
| chr9:131503983 | G | A | 1 | a0001c0001t0001g0022 | 2 | NA18948.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.-30-206G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 1/19 | chr9 | 131503983 | |||||||
| chr9:131504157 | T | C | 2 | a0001c0010t0013g0056 a0001c0010t0014g0055 |
2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-30-32T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 1/19 | chr9 | 131504157 | |||||||
| chr9:131504160 | T | G | 1 | a0001c0001t0001g0057 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-30-29T>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 1/19 | chr9 | 131504160 | |||||||
| chr9:131504588 | T | C | 3 | a0001c0001t0003g0023 a0001c0001t0003g0058 a0001c0001t0003g0059 |
4 | HG01361.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+248T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504588 | |||||||
| chr9:131504661 | C | T | 1 | a0003c0005t0003g0170 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122+321C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504661 | |||||||
| chr9:131504746 | A | AAT | 16 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(13): Show |
34 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.122+407_122+408dup others(2): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504746 | ||||||
| chr9:131504747 | A | ATATG | 25 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0019 others(22): Show |
45 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.122+408_122+409ins others(4): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504747 | ||||||
| chr9:131504747 | A | ATATGTG | 23 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0034 others(20): Show |
45 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.122+408_122+409ins others(6): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504747 | ||||||
| chr9:131504747 | A | ATATGTGT others(1): Show |
35 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(32): Show |
63 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.122+408_122+409ins others(8): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504747 | ||||||
| chr9:131504747 | A | ATATGTGT others(3): Show |
18 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0135 others(15): Show |
25 | HG01099.hp1 HG01099.hp2 HG01928.hp1 others(22): Show |
intron_variant | MODIFIER | c.122+408_122+409ins others(10): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504747 | ||||||
| chr9:131504747 | A | ATATGTGT others(5): Show |
3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG02735.hp1 NA18972.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.122+408_122+409ins others(12): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504747 | ||||||
| chr9:131504747 | A | ATATGTGT others(7): Show |
5 | a0001c0001t0001g0045 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
6 | HG01109.hp1 HG03490.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+408_122+409ins others(14): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504747 | ||||||
| chr9:131504747 | A | ATATGTGT others(9): Show |
3 | a0001c0001t0001g0046 a0001c0001t0001g0155 a0001c0001t0015g0046 |
3 | NA18970.hp1 NA19003.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.122+408_122+409ins others(16): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504747 | ||||||
| chr9:131504747 | ATGTGTG | A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0010t0013g0056 |
3 | HG00408.hp2 NA18970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.122+409_122+414del others(6): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504747 | ||||||
| chr9:131504747 | ATGTGTGT others(5): Show |
A | 1 | a0001c0001t0001g0163 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.122+415_122+426del others(12): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504747 | ||||||
| chr9:131504749 | G | A | 32 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0060 others(29): Show |
44 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.122+409G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504749 | |||||||
| chr9:131504751 | GTGTA | G | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG02056.hp1 HG02155.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+415_122+418del others(4): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504751 | ||||||
| chr9:131504753 | GTA | G | 5 | a0001c0001t0004g0074 a0003c0005t0003g0024 a0003c0005t0003g0075 others(2): Show |
6 | HG01243.hp1 HG02258.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+415_122+416del others(2): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504753 | ||||||
| chr9:131504755 | A | ATG | 2 | a0001c0003t0005g0167 a0001c0006t0007g0011 |
6 | HG02647.hp1 HG03209.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+451_122+452dup others(2): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504755 | ||||||
| chr9:131504755 | A | ATGTGTGT others(5): Show |
1 | a0001c0003t0006g0181 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.122+441_122+452dup others(12): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504755 | ||||||
| chr9:131504755 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.122+415A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504755 | |||||||
| chr9:131504755 | ATG | A | 3 | a0001c0001t0003g0165 a0001c0003t0002g0047 a0001c0003t0002g0174 |
4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+451_122+452del others(2): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504755 | ||||||
| chr9:131504755 | ATGTG | A | 4 | a0001c0003t0002g0168 a0001c0003t0012g0182 a0001c0015t0003g0054 others(1): Show |
4 | HG01106.hp1 HG02896.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+449_122+452del others(4): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504755 | ||||||
| chr9:131504755 | ATGTGTG | A | 16 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0021 others(13): Show |
31 | HG00558.hp2 HG01192.hp1 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.122+447_122+452del others(6): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504755 | ||||||
| chr9:131504755 | ATGTGTGT others(15): Show |
A | 2 | a0001c0007t0002g0051 a0001c0007t0002g0052 |
4 | HG02055.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+431_122+452del others(22): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131504755 | ||||||
| chr9:131504761 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.122+421G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504761 | |||||||
| chr9:131504779 | G | A | 2 | a0001c0007t0002g0051 a0001c0007t0002g0052 |
4 | HG02055.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+439G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504779 | |||||||
| chr9:131504792 | T | TGTGTG | 3 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0066 |
3 | HG00673.hp1 HG01496.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.122+452_122+453ins others(5): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504792 | |||||||
| chr9:131504792 | T | TGTGTGTG | 6 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0069 others(3): Show |
10 | HG00673.hp2 HG00738.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.122+452_122+453ins others(7): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504792 | |||||||
| chr9:131504792 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0060 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.122+452_122+453ins others(11): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504792 | |||||||
| chr9:131504793 | T | G | 8 | a0001c0001t0001g0087 a0001c0001t0003g0030 a0001c0001t0003g0033 others(5): Show |
10 | HG01167.hp1 HG02451.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.122+453T>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504793 | |||||||
| chr9:131504794 | T | G | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0003g0062 |
3 | HG00673.hp1 HG02145.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.122+454T>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504794 | |||||||
| chr9:131504795 | T | G | 1 | a0001c0001t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.122+455T>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504795 | |||||||
| chr9:131504796 | T | G | 1 | a0002c0002t0002g0173 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.122+456T>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504796 | |||||||
| chr9:131504801 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.122+461C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504801 | |||||||
| chr9:131504817 | C | T | 11 | a0001c0001t0001g0147 a0002c0002t0002g0007 a0002c0002t0002g0008 others(8): Show |
22 | HG01192.hp1 HG01257.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.122+477C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504817 | |||||||
| chr9:131504837 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.122+497G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504837 | |||||||
| chr9:131504964 | G | C | 1 | a0001c0001t0010g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.122+624G>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131504964 | |||||||
| chr9:131505056 | G | A | 1 | a0001c0001t0011g0080 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.122+716G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131505056 | |||||||
| chr9:131505086 | TTTTG | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.122+750_122+753del others(4): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131505086 | ||||||
| chr9:131505162 | C | A | 1 | a0002c0002t0002g0008 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.122+822C>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131505162 | |||||||
| chr9:131505201 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.122+861C>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131505201 | |||||||
| chr9:131505297 | A | AT | 30 | a0001c0001t0001g0103 a0001c0001t0001g0114 a0001c0001t0003g0058 others(27): Show |
53 | HG00558.hp2 HG01192.hp1 HG01257.hp2 others(50): Show |
intron_variant | MODIFIER | c.123-801dupT | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131505297 | ||||||
| chr9:131505297 | A | ATT | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.123-802_123-801dup others(2): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131505297 | ||||||
| chr9:131505297 | A | ATTT | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(16): Show |
36 | HG00323.hp2 HG01070.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.123-803_123-801dup others(3): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131505297 | ||||||
| chr9:131505297 | A | T | 1 | a0001c0001t0003g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.123-817A>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131505297 | |||||||
| chr9:131505347 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.123-767A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131505347 | |||||||
| chr9:131505361 | A | C | 1 | a0002c0002t0002g0173 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.123-753A>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131505361 | |||||||
| chr9:131505388 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.123-726G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131505388 | |||||||
| chr9:131505419 | C | T | 2 | a0002c0002t0002g0007 a0002c0002t0002g0169 |
8 | HG02056.hp2 NA18612.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.123-695C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131505419 | |||||||
| chr9:131505482 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.123-632T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131505482 | |||||||
| chr9:131505594 | A | C | 1 | a0002c0002t0002g0173 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.123-520A>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131505594 | |||||||
| chr9:131505610 | C | T | 1 | a0001c0003t0005g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123-504C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131505610 | |||||||
| chr9:131505723 | A | C | 1 | a0002c0002t0002g0173 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.123-391A>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131505723 | |||||||
| chr9:131505752 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.123-362G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131505752 | |||||||
| chr9:131505861 | G | C | 1 | a0001c0003t0005g0166 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.123-253G>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | chr9 | 131505861 | |||||||
| chr9:131506100 | G | GT | 11 | a0001c0001t0004g0009 a0001c0001t0004g0018 a0001c0001t0004g0027 others(8): Show |
19 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(16): Show |
splice_region_variant&intron_variant | LOW | c.123-5dupT | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131506100 | ||||||
| chr9:131506100 | G | GTT | 8 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(5): Show |
10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.123-6_123-5dupTT | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 131506100 | ||||||
| chr9:131506484 | G | A | 3 | a0001c0001t0003g0023 a0001c0001t0003g0058 a0001c0001t0003g0059 |
4 | HG01361.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+31G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131506484 | |||||||
| chr9:131506487 | C | T | 1 | a0001c0015t0003g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.280+34C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131506487 | |||||||
| chr9:131506554 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.280+101A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131506554 | |||||||
| chr9:131506713 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.280+260C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131506713 | |||||||
| chr9:131506724 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.280+271G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131506724 | |||||||
| chr9:131506796 | C | T | 2 | a0001c0007t0002g0051 a0001c0007t0002g0052 |
4 | HG02055.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+343C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131506796 | |||||||
| chr9:131506797 | G | A | 17 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(14): Show |
26 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.280+344G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131506797 | |||||||
| chr9:131506819 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.280+366G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131506819 | |||||||
| chr9:131506884 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.280+431T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131506884 | |||||||
| chr9:131506896 | G | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.280+443G>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131506896 | |||||||
| chr9:131506959 | C | A | 1 | a0001c0001t0001g0116 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.281-409C>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131506959 | |||||||
| chr9:131506960 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0105 |
9 | HG00735.hp2 HG01123.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.281-408G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131506960 | |||||||
| chr9:131506998 | C | T | 8 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(5): Show |
10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.281-370C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131506998 | |||||||
| chr9:131507024 | G | A | 2 | a0001c0001t0003g0165 a0001c0001t0010g0189 |
2 | HG00642.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.281-344G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131507024 | |||||||
| chr9:131507118 | G | A | 1 | a0001c0001t0004g0100 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.281-250G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131507118 | |||||||
| chr9:131507169 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.281-199G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131507169 | |||||||
| chr9:131507208 | C | T | 3 | a0001c0001t0003g0023 a0001c0001t0003g0058 a0001c0001t0003g0059 |
4 | HG01361.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-160C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131507208 | |||||||
| chr9:131507283 | C | T | 1 | a0001c0003t0002g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.281-85C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131507283 | |||||||
| chr9:131507286 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.281-82C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 4/19 | chr9 | 131507286 | |||||||
| chr9:131507555 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0112 |
2 | HG01074.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.427+41G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 5/19 | chr9 | 131507555 | |||||||
| chr9:131507772 | C | T | 9 | a0001c0001t0004g0009 a0001c0001t0004g0018 a0001c0001t0004g0038 others(6): Show |
16 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.427+258C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 5/19 | chr9 | 131507772 | |||||||
| chr9:131507894 | G | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0135 |
3 | HG02132.hp1 NA18971.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.427+380G>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 5/19 | chr9 | 131507894 | |||||||
| chr9:131507896 | C | T | 1 | a0001c0001t0003g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.427+382C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 5/19 | chr9 | 131507896 | |||||||
| chr9:131507907 | C | T | 1 | a0001c0015t0003g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.427+393C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 5/19 | chr9 | 131507907 | |||||||
| chr9:131507950 | A | C | 1 | a0002c0002t0002g0188 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.427+436A>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 5/19 | chr9 | 131507950 | |||||||
| chr9:131507993 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.427+479A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 5/19 | chr9 | 131507993 | |||||||
| chr9:131508191 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.427+677T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 5/19 | chr9 | 131508191 | |||||||
| chr9:131508231 | C | T | 1 | a0001c0015t0003g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.428-680C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 5/19 | chr9 | 131508231 | |||||||
| chr9:131508519 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.428-392G>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 5/19 | chr9 | 131508519 | |||||||
| chr9:131508571 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.428-340C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 5/19 | chr9 | 131508571 | |||||||
| chr9:131508679 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.428-232A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 5/19 | chr9 | 131508679 | |||||||
| chr9:131508773 | T | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0031 others(8): Show |
18 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.428-138T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 5/19 | chr9 | 131508773 | |||||||
| chr9:131508890 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.428-21T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 5/19 | chr9 | 131508890 | |||||||
| chr9:131509113 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.539+91C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 6/19 | chr9 | 131509113 | |||||||
| chr9:131509125 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.539+103C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 6/19 | chr9 | 131509125 | |||||||
| chr9:131509126 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.539+104A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 6/19 | chr9 | 131509126 | |||||||
| chr9:131509216 | T | C | 1 | a0002c0002t0002g0169 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.539+194T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 6/19 | chr9 | 131509216 | |||||||
| chr9:131509219 | C | G | 1 | a0003c0005t0003g0063 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.539+197C>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 6/19 | chr9 | 131509219 | |||||||
| chr9:131509276 | G | A | 5 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0132 others(2): Show |
5 | NA18948.hp1 NA18949.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.539+254G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 6/19 | chr9 | 131509276 | |||||||
| chr9:131509279 | T | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | NA18963.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.539+257T>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 6/19 | chr9 | 131509279 | |||||||
| chr9:131509522 | T | C | 2 | a0001c0010t0013g0056 a0001c0010t0014g0055 |
2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.540-221T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 6/19 | chr9 | 131509522 | |||||||
| chr9:131510048 | C | T | 17 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(14): Show |
26 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.699+52C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 8/19 | chr9 | 131510048 | |||||||
| chr9:131510049 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.699+53A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 8/19 | chr9 | 131510049 | |||||||
| chr9:131510165 | GT | G | 19 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(16): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.700-92delT | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 131510165 | ||||||
| chr9:131510212 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.700-48A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 8/19 | chr9 | 131510212 | |||||||
| chr9:131510230 | G | T | 1 | a0001c0001t0004g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.700-30G>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 8/19 | chr9 | 131510230 | |||||||
| chr9:131510590 | G | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.855+175G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 9/19 | chr9 | 131510590 | |||||||
| chr9:131510640 | A | G | 9 | a0001c0001t0004g0009 a0001c0001t0004g0018 a0001c0001t0004g0038 others(6): Show |
16 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.855+225A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 9/19 | chr9 | 131510640 | |||||||
| chr9:131510795 | C | T | 1 | a0001c0015t0003g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.855+380C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 9/19 | chr9 | 131510795 | |||||||
| chr9:131510855 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.855+440C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 9/19 | chr9 | 131510855 | |||||||
| chr9:131510969 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.856-368C>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 9/19 | chr9 | 131510969 | |||||||
| chr9:131511038 | T | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.856-299T>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 9/19 | chr9 | 131511038 | |||||||
| chr9:131511229 | C | T | 1 | a0005c0017t0001g0110 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.856-108C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 9/19 | chr9 | 131511229 | |||||||
| chr9:131511272 | G | A | 15 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0020 others(12): Show |
24 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.856-65G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 9/19 | chr9 | 131511272 | |||||||
| chr9:131511288 | T | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.856-49T>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 9/19 | chr9 | 131511288 | |||||||
| chr9:131511516 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.986+49G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 10/19 | chr9 | 131511516 | |||||||
| chr9:131511651 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.986+184G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 10/19 | chr9 | 131511651 | |||||||
| chr9:131511655 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.986+188C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 10/19 | chr9 | 131511655 | |||||||
| chr9:131511658 | G | A | 2 | a0001c0003t0002g0047 a0001c0003t0002g0174 |
3 | HG02896.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.986+191G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 10/19 | chr9 | 131511658 | |||||||
| chr9:131511713 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.986+246G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 10/19 | chr9 | 131511713 | |||||||
| chr9:131511746 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.986+279T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 10/19 | chr9 | 131511746 | |||||||
| chr9:131511767 | C | T | 3 | a0001c0001t0003g0023 a0001c0001t0003g0058 a0001c0001t0003g0059 |
4 | HG01361.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-274C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 10/19 | chr9 | 131511767 | |||||||
| chr9:131511868 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.987-173C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 10/19 | chr9 | 131511868 | |||||||
| chr9:131511921 | G | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0015g0046 |
3 | NA18970.hp1 NA18971.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.987-120G>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 10/19 | chr9 | 131511921 | |||||||
| chr9:131511928 | C | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.987-113C>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 10/19 | chr9 | 131511928 | |||||||
| chr9:131511939 | G | A | 19 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(16): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.987-102G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 10/19 | chr9 | 131511939 | |||||||
| chr9:131512152 | G | A | 25 | a0001c0001t0003g0023 a0001c0001t0003g0030 a0001c0001t0003g0033 others(22): Show |
35 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.1082+16G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131512152 | |||||||
| chr9:131512251 | C | T | 2 | a0001c0010t0013g0056 a0001c0010t0014g0055 |
2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1082+115C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131512251 | |||||||
| chr9:131512606 | T | A | 1 | a0002c0002t0002g0175 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1082+470T>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131512606 | |||||||
| chr9:131512632 | G | T | 25 | a0001c0001t0003g0023 a0001c0001t0003g0030 a0001c0001t0003g0033 others(22): Show |
35 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.1082+496G>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131512632 | |||||||
| chr9:131512642 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1082+506C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131512642 | |||||||
| chr9:131512659 | T | C | 2 | a0002c0002t0002g0048 a0002c0002t0002g0176 |
3 | NA18951.hp1 NA18997.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1082+523T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131512659 | |||||||
| chr9:131512681 | G | A | 1 | a0001c0001t0003g0088 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1082+545G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131512681 | |||||||
| chr9:131512698 | G | T | 1 | a0001c0001t0001g0129 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1083-541G>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131512698 | |||||||
| chr9:131512714 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1083-525T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131512714 | |||||||
| chr9:131512891 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1083-348T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131512891 | |||||||
| chr9:131512904 | G | A | 2 | a0001c0001t0003g0165 a0001c0001t0010g0189 |
2 | HG00642.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1083-335G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131512904 | |||||||
| chr9:131512910 | C | A | 1 | a0001c0001t0003g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1083-329C>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131512910 | |||||||
| chr9:131512953 | T | TC | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1083-284dupC | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr9 | 131512953 | ||||||
| chr9:131512977 | T | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0066 others(5): Show |
14 | HG00735.hp2 HG01123.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1083-262T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131512977 | |||||||
| chr9:131512978 | C | T | 1 | a0002c0002t0002g0176 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1083-261C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131512978 | |||||||
| chr9:131512986 | T | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0066 others(6): Show |
15 | HG00735.hp2 HG01123.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1083-253T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131512986 | |||||||
| chr9:131513015 | G | A | 17 | a0002c0002t0002g0007 a0002c0002t0002g0008 a0002c0002t0002g0021 others(14): Show |
32 | HG00558.hp2 HG01192.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.1083-224G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131513015 | |||||||
| chr9:131513028 | G | A | 2 | a0001c0001t0001g0057 a0002c0002t0002g0183 |
2 | HG04228.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1083-211G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131513028 | |||||||
| chr9:131513045 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1083-194G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131513045 | |||||||
| chr9:131513059 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1083-180G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131513059 | |||||||
| chr9:131513175 | C | T | 17 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(14): Show |
26 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.1083-64C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 11/19 | chr9 | 131513175 | |||||||
| chr9:131513402 | G | A | 1 | a0001c0015t0003g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1175+71G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131513402 | |||||||
| chr9:131513421 | G | A | 1 | a0005c0012t0001g0123 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1175+90G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131513421 | |||||||
| chr9:131513428 | CCT | C | 8 | a0001c0001t0003g0023 a0001c0001t0003g0058 a0001c0001t0003g0059 others(5): Show |
9 | HG00642.hp2 HG01106.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1175+98_1175+99del others(2): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131513428 | |||||||
| chr9:131513505 | C | T | 2 | a0001c0009t0004g0072 a0001c0009t0004g0073 |
2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1175+174C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131513505 | |||||||
| chr9:131513573 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1175+242C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131513573 | |||||||
| chr9:131513579 | A | G | 2 | a0001c0010t0013g0056 a0001c0010t0014g0055 |
2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1175+248A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131513579 | |||||||
| chr9:131513683 | C | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1175+352C>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131513683 | |||||||
| chr9:131513831 | C | A | 1 | a0001c0003t0002g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1175+500C>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131513831 | |||||||
| chr9:131513859 | TC | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0128 |
3 | HG01358.hp2 HG01496.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1175+530delC | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr9 | 131513859 | ||||||
| chr9:131513914 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1175+583C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131513914 | |||||||
| chr9:131514011 | C | T | 1 | a0001c0001t0003g0033 | 2 | HG01167.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1175+680C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131514011 | |||||||
| chr9:131514094 | T | C | 1 | a0001c0009t0004g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1175+763T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131514094 | |||||||
| chr9:131514124 | C | A | 1 | a0003c0018t0003g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1175+793C>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131514124 | |||||||
| chr9:131514138 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1175+807C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131514138 | |||||||
| chr9:131514225 | C | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0015g0046 |
3 | NA18970.hp1 NA18971.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1175+894C>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131514225 | |||||||
| chr9:131514483 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1176-943C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131514483 | |||||||
| chr9:131514533 | C | T | 1 | a0001c0001t0004g0096 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1176-893C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131514533 | |||||||
| chr9:131514659 | G | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0066 others(6): Show |
15 | HG00735.hp2 HG01123.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1176-767G>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131514659 | |||||||
| chr9:131514691 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1176-735C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131514691 | |||||||
| chr9:131514694 | A | G | 1 | a0001c0009t0004g0073 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1176-732A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131514694 | |||||||
| chr9:131514785 | G | A | 1 | a0001c0001t0003g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1176-641G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131514785 | |||||||
| chr9:131514810 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1176-616G>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131514810 | |||||||
| chr9:131514893 | T | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0066 others(5): Show |
14 | HG00735.hp2 HG01123.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1176-533T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131514893 | |||||||
| chr9:131514907 | G | T | 2 | a0001c0007t0002g0051 a0001c0007t0002g0052 |
4 | HG02055.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1176-519G>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131514907 | |||||||
| chr9:131515115 | A | G | 2 | a0001c0007t0002g0051 a0001c0007t0002g0052 |
4 | HG02055.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1176-311A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131515115 | |||||||
| chr9:131515131 | C | T | 1 | a0001c0003t0006g0050 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1176-295C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131515131 | |||||||
| chr9:131515161 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1176-265G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131515161 | |||||||
| chr9:131515285 | G | A | 1 | a0001c0015t0003g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1176-141G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131515285 | |||||||
| chr9:131515333 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1176-93C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131515333 | |||||||
| chr9:131515410 | G | C | 1 | a0003c0005t0003g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1176-16G>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 12/19 | chr9 | 131515410 | |||||||
| chr9:131515606 | C | T | 21 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0003t0002g0047 others(18): Show |
39 | HG00558.hp2 HG01192.hp1 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.1272+84C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515606 | |||||||
| chr9:131515704 | AACACTTC others(118): Show |
A | 5 | a0001c0001t0004g0009 a0001c0001t0004g0074 a0001c0001t0004g0086 others(2): Show |
9 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.1272+209_1272+333d others(2): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515704 | ||||||
| chr9:131515705 | A | G | 8 | a0001c0001t0001g0057 a0001c0001t0001g0109 a0001c0001t0001g0114 others(5): Show |
11 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.1272+183A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515705 | |||||||
| chr9:131515715 | A | C | 3 | a0001c0001t0003g0023 a0001c0001t0003g0058 a0001c0001t0003g0059 |
4 | HG01361.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1272+193A>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515715 | |||||||
| chr9:131515718 | C | G | 3 | a0001c0001t0001g0057 a0001c0001t0001g0114 a0001c0001t0001g0131 |
3 | NA18747.hp2 NA18960.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1272+196C>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515718 | |||||||
| chr9:131515718 | C | T | 4 | a0001c0001t0003g0033 a0001c0001t0003g0101 a0001c0001t0003g0113 others(1): Show |
5 | HG01167.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1272+196C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515718 | |||||||
| chr9:131515728 | CCTGTAAC others(135): Show |
C | 6 | a0001c0001t0004g0018 a0001c0001t0004g0027 a0001c0001t0004g0038 others(3): Show |
10 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272+209_1272+350d others(2): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515728 | ||||||
| chr9:131515731 | G | C | 5 | a0001c0001t0001g0057 a0001c0001t0001g0109 a0001c0001t0001g0114 others(2): Show |
5 | HG00099.hp1 HG00738.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.1272+209G>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515731 | |||||||
| chr9:131515733 | AACAGGAC others(48): Show |
A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0114 a0001c0001t0001g0131 |
3 | NA18747.hp2 NA18960.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1272+249_1272+303d others(57): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515733 | ||||||
| chr9:131515752 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1272+230C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515752 | |||||||
| chr9:131515764 | T | TCACATGG others(78): Show |
1 | a0001c0001t0001g0109 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1272+243_1272+244i others(87): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515764 | ||||||
| chr9:131515767 | A | AACACAGG others(27): Show |
119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1272+248_1272+249i others(36): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515767 | ||||||
| chr9:131515767 | A | AACACAGG others(201): Show |
1 | a0001c0001t0001g0044 | 2 | NA18612.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1272+248_1272+249i others(210): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515767 | ||||||
| chr9:131515767 | A | C | 1 | a0001c0001t0001g0109 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1272+245A>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515767 | |||||||
| chr9:131515771 | T | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0028 a0001c0001t0001g0044 others(1): Show |
8 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272+249T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515771 | |||||||
| chr9:131515771 | T | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1272+249T>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515771 | |||||||
| chr9:131515771 | T | TGGAGAAC others(137): Show |
1 | a0001c0001t0003g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1272+253_1272+254i others(146): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515771 | ||||||
| chr9:131515772 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0028 |
5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1272+250G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515772 | |||||||
| chr9:131515774 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0028 |
5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1272+252A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515774 | |||||||
| chr9:131515775 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0028 a0001c0001t0001g0044 |
7 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.1272+253G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515775 | |||||||
| chr9:131515782 | CTG | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0028 |
5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1272+262_1272+263d others(4): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515782 | ||||||
| chr9:131515784 | G | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1272+262G>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515784 | |||||||
| chr9:131515784 | G | GTAACACA others(29): Show |
2 | a0001c0001t0001g0077 a0001c0001t0001g0157 |
2 | HG02155.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1272+299_1272+334d others(38): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515784 | ||||||
| chr9:131515784 | G | GTAACACA others(137): Show |
12 | a0001c0001t0010g0189 a0001c0010t0013g0056 a0001c0010t0014g0055 others(9): Show |
14 | HG00642.hp2 HG01106.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1272+334_1272+335i others(146): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515784 | ||||||
| chr9:131515786 | A | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0028 |
5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1272+264A>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515786 | |||||||
| chr9:131515786 | AAC | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1272+268_1272+269d others(4): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515786 | ||||||
| chr9:131515791 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0028 |
5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1272+269A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515791 | |||||||
| chr9:131515793 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0028 |
5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1272+271G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515793 | |||||||
| chr9:131515794 | A | ACACTTCC others(46): Show |
1 | a0007c0019t0002g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1272+285_1272+337d others(55): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515794 | ||||||
| chr9:131515794 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0028 |
5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1272+272A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515794 | |||||||
| chr9:131515807 | C | CGGAGCAC others(10): Show |
1 | a0001c0001t0003g0059 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1272+298_1272+299i others(19): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515807 | ||||||
| chr9:131515807 | C | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0028 |
5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1272+285C>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515807 | |||||||
| chr9:131515820 | CTA | C | 10 | a0001c0001t0003g0023 a0001c0001t0003g0030 a0001c0001t0003g0033 others(7): Show |
13 | HG01167.hp1 HG01361.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1272+299_1272+300d others(4): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515820 | |||||||
| chr9:131515822 | AAC | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0028 |
5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1272+304_1272+305d others(4): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515822 | ||||||
| chr9:131515826 | C | G | 10 | a0001c0001t0003g0023 a0001c0001t0003g0030 a0001c0001t0003g0033 others(7): Show |
13 | HG01167.hp1 HG01361.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1272+304C>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515826 | |||||||
| chr9:131515827 | A | G | 10 | a0001c0001t0003g0023 a0001c0001t0003g0030 a0001c0001t0003g0033 others(7): Show |
13 | HG01167.hp1 HG01361.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1272+305A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515827 | |||||||
| chr9:131515829 | G | A | 10 | a0001c0001t0003g0023 a0001c0001t0003g0030 a0001c0001t0003g0033 others(7): Show |
13 | HG01167.hp1 HG01361.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1272+307G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515829 | |||||||
| chr9:131515830 | A | G | 15 | a0001c0001t0003g0023 a0001c0001t0003g0030 a0001c0001t0003g0033 others(12): Show |
22 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.1272+308A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515830 | |||||||
| chr9:131515839 | C | CTA | 10 | a0001c0001t0003g0023 a0001c0001t0003g0030 a0001c0001t0003g0033 others(7): Show |
13 | HG01167.hp1 HG01361.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1272+317_1272+318i others(4): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515839 | |||||||
| chr9:131515844 | G | A | 10 | a0001c0001t0003g0023 a0001c0001t0003g0030 a0001c0001t0003g0033 others(7): Show |
13 | HG01167.hp1 HG01361.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1272+322G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515844 | |||||||
| chr9:131515846 | A | G | 10 | a0001c0001t0003g0023 a0001c0001t0003g0030 a0001c0001t0003g0033 others(7): Show |
13 | HG01167.hp1 HG01361.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1272+324A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515846 | |||||||
| chr9:131515847 | G | A | 10 | a0001c0001t0003g0023 a0001c0001t0003g0030 a0001c0001t0003g0033 others(7): Show |
13 | HG01167.hp1 HG01361.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1272+325G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515847 | |||||||
| chr9:131515847 | G | GCACTTCC others(12): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0028 a0001c0001t0003g0059 |
6 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.1272+334_1272+335i others(21): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515847 | ||||||
| chr9:131515853 | CCTCACAG others(10): Show |
C | 5 | a0001c0001t0004g0009 a0001c0001t0004g0074 a0001c0001t0004g0086 others(2): Show |
9 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.1272+335_1272+351d others(19): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515853 | ||||||
| chr9:131515860 | G | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.1272+338G>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515860 | |||||||
| chr9:131515870 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
307 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1272+348T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515870 | |||||||
| chr9:131515875 | AAC | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0138 others(5): Show |
8 | HG00099.hp1 HG02155.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272+357_1272+358d others(4): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515875 | ||||||
| chr9:131515896 | T | C | 19 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0138 others(16): Show |
22 | HG00099.hp1 HG01167.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1272+374T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515896 | |||||||
| chr9:131515900 | G | GCACTTCC others(12): Show |
2 | a0001c0001t0003g0023 a0001c0001t0003g0058 |
3 | HG01361.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1272+387_1272+388i others(21): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515900 | ||||||
| chr9:131515909 | C | CTA | 8 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0138 others(5): Show |
8 | HG00099.hp1 HG02155.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272+387_1272+388i others(4): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515909 | |||||||
| chr9:131515913 | T | C | 19 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0138 others(16): Show |
22 | HG00099.hp1 HG01167.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1272+391T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515913 | |||||||
| chr9:131515914 | G | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0138 others(5): Show |
8 | HG00099.hp1 HG02155.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272+392G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515914 | |||||||
| chr9:131515916 | A | G | 8 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0138 others(5): Show |
8 | HG00099.hp1 HG02155.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272+394A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515916 | |||||||
| chr9:131515917 | G | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0138 others(5): Show |
8 | HG00099.hp1 HG02155.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272+395G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515917 | |||||||
| chr9:131515926 | C | CTA | 8 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(5): Show |
10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272+404_1272+405i others(4): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515926 | |||||||
| chr9:131515930 | G | C | 16 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0138 others(13): Show |
18 | HG00099.hp1 HG01167.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1272+408G>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515930 | |||||||
| chr9:131515931 | G | A | 8 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(5): Show |
10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272+409G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515931 | |||||||
| chr9:131515933 | A | G | 8 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(5): Show |
10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272+411A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515933 | |||||||
| chr9:131515934 | G | A | 8 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(5): Show |
10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272+412G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515934 | |||||||
| chr9:131515947 | C | T | 8 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(5): Show |
10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272+425C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515947 | |||||||
| chr9:131515951 | A | G | 16 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0138 others(13): Show |
18 | HG00099.hp1 HG01167.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1272+429A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515951 | |||||||
| chr9:131515951 | ACACTTCC others(37): Show |
A | 1 | a0001c0001t0001g0118 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1272+458_1272+501d others(46): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515951 | ||||||
| chr9:131515951 | ACACTTCC others(90): Show |
A | 6 | a0001c0001t0004g0018 a0001c0001t0004g0027 a0001c0001t0004g0038 others(3): Show |
10 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272+458_1272+554d others(99): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515951 | ||||||
| chr9:131515960 | CTA | C | 8 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(5): Show |
10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272+439_1272+440d others(4): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515960 | |||||||
| chr9:131515966 | C | T | 8 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(5): Show |
10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272+444C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515966 | |||||||
| chr9:131515967 | A | G | 8 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(5): Show |
10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272+445A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515967 | |||||||
| chr9:131515969 | G | A | 8 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(5): Show |
10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272+447G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515969 | |||||||
| chr9:131515970 | A | G | 8 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(5): Show |
10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272+448A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515970 | |||||||
| chr9:131515976 | CCT | C | 9 | a0001c0001t0001g0044 a0001c0001t0001g0077 a0001c0001t0001g0109 others(6): Show |
10 | HG00099.hp1 HG02155.hp1 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272+458_1272+459d others(4): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515976 | ||||||
| chr9:131515976 | CCTCTCAC others(1): Show |
C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1272+458_1272+465d others(10): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515976 | ||||||
| chr9:131515980 | T | A | 8 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(5): Show |
10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272+458T>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515980 | |||||||
| chr9:131515982 | A | AGGGAG | 8 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(5): Show |
10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272+460_1272+461i others(7): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515982 | |||||||
| chr9:131515984 | A | ACTTC | 8 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(5): Show |
10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272+464_1272+465i others(6): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515984 | ||||||
| chr9:131515984 | A | ATGGAGCA others(38): Show |
8 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0138 others(5): Show |
8 | HG00099.hp1 HG02155.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272+462_1272+463i others(47): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515984 | |||||||
| chr9:131515984 | A | ATGGAGCA others(316): Show |
1 | a0001c0001t0001g0044 | 2 | NA18612.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1272+462_1272+463i others(325): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515984 | |||||||
| chr9:131515995 | G | A | 16 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0138 others(13): Show |
18 | HG00099.hp1 HG01167.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1272+473G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131515995 | |||||||
| chr9:131515995 | GCACTTCC others(12): Show |
G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1272+483_1272+501d others(21): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131515995 | ||||||
| chr9:131516023 | C | CTCACACT others(39): Show |
1 | a0001c0001t0010g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1272+501_1272+502i others(48): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516023 | |||||||
| chr9:131516028 | G | A | 1 | a0001c0001t0003g0059 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1272+506G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516028 | |||||||
| chr9:131516040 | C | CACACGGA others(12): Show |
43 | a0001c0001t0003g0023 a0001c0001t0003g0058 a0001c0001t0003g0059 others(40): Show |
69 | HG00558.hp2 HG01106.hp1 HG01192.hp1 others(66): Show |
intron_variant | MODIFIER | c.1272+523_1272+541d others(21): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131516040 | ||||||
| chr9:131516040 | C | CTA | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1272+518_1272+519i others(4): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516040 | |||||||
| chr9:131516041 | A | T | 1 | a0001c0001t0001g0066 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1272+519A>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516041 | |||||||
| chr9:131516042 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1272+520C>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516042 | |||||||
| chr9:131516045 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1272+523G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516045 | |||||||
| chr9:131516045 | G | GGAGCACT others(12): Show |
16 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0138 others(13): Show |
18 | HG00099.hp1 HG01167.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1272+525_1272+543d others(21): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131516045 | ||||||
| chr9:131516045 | G | GGAGCACT others(152): Show |
1 | a0001c0001t0001g0044 | 2 | NA18612.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1272+557_1272+558i others(161): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131516045 | ||||||
| chr9:131516066 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1272+544G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516066 | |||||||
| chr9:131516067 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1272+545A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516067 | |||||||
| chr9:131516081 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1272+559G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516081 | |||||||
| chr9:131516083 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1272+561A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516083 | |||||||
| chr9:131516084 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1272+562G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516084 | |||||||
| chr9:131516097 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1272+575T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516097 | |||||||
| chr9:131516124 | C | T | 1 | a0001c0015t0003g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1272+602C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516124 | |||||||
| chr9:131516156 | A | ACTTC | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1272+636_1272+637i others(6): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131516156 | ||||||
| chr9:131516192 | G | C | 3 | a0001c0001t0003g0023 a0001c0001t0003g0058 a0001c0001t0003g0059 |
4 | HG01361.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1272+670G>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516192 | |||||||
| chr9:131516228 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1272+706G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516228 | |||||||
| chr9:131516228 | GCACTTCC others(10): Show |
G | 14 | a0001c0001t0003g0023 a0001c0001t0003g0058 a0001c0001t0003g0059 others(11): Show |
17 | HG00642.hp2 HG01106.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.1272+744_1272+760d others(19): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131516228 | ||||||
| chr9:131516249 | T | TTCCTCAC others(10): Show |
2 | a0001c0010t0013g0056 a0001c0010t0014g0055 |
2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1272+743_1272+744i others(19): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131516249 | ||||||
| chr9:131516262 | A | ACACCTCC others(27): Show |
1 | a0001c0001t0001g0153 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1272+743_1272+744i others(36): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131516262 | ||||||
| chr9:131516262 | A | ACACTTCC others(44): Show |
1 | a0001c0001t0001g0129 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1272+770_1272+771i others(53): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131516262 | ||||||
| chr9:131516266 | T | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0003g0134 |
3 | HG02293.hp2 HG02818.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1272+744T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516266 | |||||||
| chr9:131516296 | A | ACACTTCC others(44): Show |
123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1272+801_1272+851d others(53): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131516296 | ||||||
| chr9:131516296 | A | ACACTTCC others(112): Show |
1 | a0001c0001t0001g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1272+811_1272+812i others(121): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131516296 | ||||||
| chr9:131516296 | A | ACACTTCC others(44): Show |
1 | a0001c0001t0001g0118 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1272+807_1272+808i others(53): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131516296 | ||||||
| chr9:131516296 | A | ACACTTCC others(44): Show |
1 | a0001c0004t0001g0142 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1272+786_1272+787i others(53): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131516296 | ||||||
| chr9:131516296 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0153 |
2 | NA18954.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1272+774A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516296 | |||||||
| chr9:131516300 | T | TTCCTCAC others(27): Show |
1 | a0001c0001t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1272+794_1272+795i others(36): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131516300 | ||||||
| chr9:131516300 | T | TTCCTCAC others(27): Show |
2 | a0001c0001t0001g0143 a0001c0001t0001g0160 |
2 | NA18966.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1272+808_1272+841d others(36): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131516300 | ||||||
| chr9:131516309 | C | T | 2 | a0001c0001t0003g0023 a0001c0001t0003g0058 |
3 | HG01361.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1272+787C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516309 | |||||||
| chr9:131516326 | C | CGGAACAC others(44): Show |
1 | a0001c0001t0001g0098 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1272+851_1272+852i others(53): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131516326 | ||||||
| chr9:131516364 | GCACTTCC others(10): Show |
G | 1 | a0001c0001t0010g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1272+852_1272+868d others(19): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131516364 | ||||||
| chr9:131516481 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1272+959G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516481 | |||||||
| chr9:131516531 | A | G | 6 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0069 others(3): Show |
7 | HG00673.hp2 HG02083.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.1272+1009A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516531 | |||||||
| chr9:131516583 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1272+1061C>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131516583 | |||||||
| chr9:131517008 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1273-1437A>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517008 | |||||||
| chr9:131517009 | T | C | 19 | a0001c0001t0003g0030 a0001c0001t0003g0033 a0001c0001t0003g0062 others(16): Show |
29 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1273-1436T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517009 | |||||||
| chr9:131517128 | C | T | 1 | a0001c0003t0005g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1273-1317C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517128 | |||||||
| chr9:131517166 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1273-1279C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517166 | |||||||
| chr9:131517167 | G | A | 2 | a0002c0002t0002g0048 a0002c0002t0002g0176 |
3 | NA18951.hp1 NA18997.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1273-1278G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517167 | |||||||
| chr9:131517235 | C | CT | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1273-1197dupT | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr9 | 131517235 | ||||||
| chr9:131517266 | T | C | 1 | a0001c0006t0007g0011 | 5 | HG02647.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1273-1179T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517266 | |||||||
| chr9:131517292 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1273-1153G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517292 | |||||||
| chr9:131517307 | T | C | 27 | a0001c0001t0010g0189 a0001c0003t0002g0047 a0001c0003t0002g0168 others(24): Show |
44 | HG00558.hp2 HG00642.hp2 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.1273-1138T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517307 | |||||||
| chr9:131517321 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1273-1124C>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517321 | |||||||
| chr9:131517383 | G | A | 1 | a0002c0002t0002g0175 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1273-1062G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517383 | |||||||
| chr9:131517458 | T | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1273-987T>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517458 | |||||||
| chr9:131517461 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1273-984G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517461 | |||||||
| chr9:131517477 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1273-968T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517477 | |||||||
| chr9:131517517 | G | A | 3 | a0001c0001t0003g0023 a0001c0001t0003g0058 a0001c0001t0003g0059 |
4 | HG01361.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273-928G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517517 | |||||||
| chr9:131517543 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1273-902C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517543 | |||||||
| chr9:131517589 | T | C | 2 | a0001c0007t0002g0051 a0001c0007t0002g0052 |
4 | HG02055.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273-856T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517589 | |||||||
| chr9:131517832 | G | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0084 a0001c0001t0001g0109 others(2): Show |
6 | HG00099.hp1 HG01346.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1273-613G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517832 | |||||||
| chr9:131517899 | G | A | 1 | a0001c0015t0003g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1273-546G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517899 | |||||||
| chr9:131517909 | T | C | 2 | a0002c0002t0002g0021 a0002c0002t0002g0177 |
4 | HG00558.hp2 NA18949.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273-536T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517909 | |||||||
| chr9:131517913 | G | A | 1 | a0001c0001t0010g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1273-532G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517913 | |||||||
| chr9:131517946 | T | G | 2 | a0001c0010t0013g0056 a0001c0010t0014g0055 |
2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1273-499T>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131517946 | |||||||
| chr9:131518244 | C | T | 2 | a0001c0010t0013g0056 a0001c0010t0014g0055 |
2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1273-201C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131518244 | |||||||
| chr9:131518375 | C | T | 9 | a0001c0001t0003g0165 a0003c0005t0003g0024 a0003c0005t0003g0025 others(6): Show |
11 | HG01943.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1273-70C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 13/19 | chr9 | 131518375 | |||||||
| chr9:131518614 | C | T | 3 | a0001c0001t0003g0023 a0001c0001t0003g0058 a0001c0001t0003g0059 |
4 | HG01361.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1365+77C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 14/19 | chr9 | 131518614 | |||||||
| chr9:131518661 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1365+124C>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 14/19 | chr9 | 131518661 | |||||||
| chr9:131518776 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1366-61A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 14/19 | chr9 | 131518776 | |||||||
| chr9:131519009 | C | T | 1 | a0001c0015t0003g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1486+52C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 15/19 | chr9 | 131519009 | |||||||
| chr9:131519093 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | NA18963.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1486+136C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 15/19 | chr9 | 131519093 | |||||||
| chr9:131519223 | G | A | 22 | a0001c0001t0003g0059 a0001c0003t0002g0047 a0001c0003t0002g0174 others(19): Show |
38 | HG00558.hp2 HG01192.hp1 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.1487-166G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 15/19 | chr9 | 131519223 | |||||||
| chr9:131519225 | G | A | 22 | a0001c0001t0003g0059 a0001c0003t0002g0047 a0001c0003t0002g0174 others(19): Show |
38 | HG00558.hp2 HG01192.hp1 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.1487-164G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 15/19 | chr9 | 131519225 | |||||||
| chr9:131519259 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1487-130A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 15/19 | chr9 | 131519259 | |||||||
| chr9:131520060 | A | C | 1 | a0001c0001t0001g0076 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1585-20A>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 16/19 | chr9 | 131520060 | |||||||
| chr9:131520066 | C | T | 2 | a0001c0010t0013g0056 a0001c0010t0014g0055 |
2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1585-14C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 16/19 | chr9 | 131520066 | |||||||
| chr9:131520204 | G | C | 1 | a0001c0001t0003g0059 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1698+11G>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | chr9 | 131520204 | |||||||
| chr9:131520241 | C | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1698+48C>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | chr9 | 131520241 | |||||||
| chr9:131520263 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1698+70A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | chr9 | 131520263 | |||||||
| chr9:131520300 | C | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1698+107C>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | chr9 | 131520300 | |||||||
| chr9:131520352 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1698+159A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | chr9 | 131520352 | |||||||
| chr9:131520426 | C | T | 11 | a0001c0001t0004g0009 a0001c0001t0004g0018 a0001c0001t0004g0027 others(8): Show |
19 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.1698+233C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | chr9 | 131520426 | |||||||
| chr9:131520510 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0126 |
2 | HG01071.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1698+317C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | chr9 | 131520510 | |||||||
| chr9:131520571 | G | A | 1 | a0001c0001t0001g0015 | 3 | HG01070.hp1 HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1698+378G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | chr9 | 131520571 | |||||||
| chr9:131520575 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1698+382G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | chr9 | 131520575 | |||||||
| chr9:131520615 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1698+422C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | chr9 | 131520615 | |||||||
| chr9:131520693 | C | G | 2 | a0001c0003t0002g0047 a0001c0003t0002g0174 |
3 | HG02896.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1698+500C>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | chr9 | 131520693 | |||||||
| chr9:131520717 | G | C | 1 | a0002c0002t0002g0177 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1698+524G>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | chr9 | 131520717 | |||||||
| chr9:131520747 | G | A | 1 | a0001c0007t0002g0051 | 2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1698+554G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | chr9 | 131520747 | |||||||
| chr9:131520755 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1698+562C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | chr9 | 131520755 | |||||||
| chr9:131520827 | C | CTG | 15 | a0001c0001t0003g0023 a0001c0001t0003g0058 a0001c0001t0003g0059 others(12): Show |
18 | HG01106.hp1 HG01361.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1699-505_1699-504d others(4): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr9 | 131520827 | ||||||
| chr9:131520993 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1699-353C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | chr9 | 131520993 | |||||||
| chr9:131521007 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1699-339A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 17/19 | chr9 | 131521007 | |||||||
| chr9:131521490 | AT | A | 3 | a0001c0001t0003g0030 a0001c0001t0003g0079 a0001c0001t0003g0088 |
4 | HG02922.hp1 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825+19delT | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 18/19 | chr9 | 131521490 | |||||||
| chr9:131521497 | T | G | 2 | a0001c0010t0013g0056 a0001c0010t0014g0055 |
2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1825+25T>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 18/19 | chr9 | 131521497 | |||||||
| chr9:131521530 | G | A | 3 | a0003c0005t0003g0024 a0003c0005t0003g0075 a0003c0005t0003g0170 |
4 | HG02258.hp1 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825+58G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 18/19 | chr9 | 131521530 | |||||||
| chr9:131521581 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0141 |
2 | HG02155.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1825+109C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 18/19 | chr9 | 131521581 | |||||||
| chr9:131521645 | G | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0158 a0001c0001t0001g0162 others(1): Show |
4 | HG00408.hp2 HG00423.hp2 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825+173G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 18/19 | chr9 | 131521645 | |||||||
| chr9:131521670 | C | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1825+198C>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 18/19 | chr9 | 131521670 | |||||||
| chr9:131521709 | T | C | 4 | a0001c0003t0006g0050 a0001c0003t0006g0172 a0001c0003t0006g0179 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+237T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 18/19 | chr9 | 131521709 | |||||||
| chr9:131521769 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0163 |
2 | NA18964.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1826-278C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 18/19 | chr9 | 131521769 | |||||||
| chr9:131521778 | C | A | 1 | a0001c0001t0003g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1826-269C>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 18/19 | chr9 | 131521778 | |||||||
| chr9:131521779 | G | A | 25 | a0001c0003t0002g0047 a0001c0003t0002g0174 a0001c0003t0006g0050 others(22): Show |
42 | HG00558.hp2 HG01192.hp1 HG01257.hp2 others(39): Show |
intron_variant | MODIFIER | c.1826-268G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 18/19 | chr9 | 131521779 | |||||||
| chr9:131521799 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1826-248T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 18/19 | chr9 | 131521799 | |||||||
| chr9:131522007 | G | A | 2 | a0002c0002t0002g0173 a0002c0002t0002g0185 |
2 | HG01192.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1826-40G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 18/19 | chr9 | 131522007 | |||||||
| chr9:131522040 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG00738.hp1 | splice_region_variant&intron_variant | LOW | c.1826-7C>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 18/19 | chr9 | 131522040 | |||||||
| chr9:131522041 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG00738.hp1 | splice_region_variant&intron_variant | LOW | c.1826-6C>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 18/19 | chr9 | 131522041 | |||||||
| chr9:131522237 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.2003+13C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522237 | |||||||
| chr9:131522345 | C | T | 1 | a0009c0011t0001g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2003+121C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522345 | |||||||
| chr9:131522356 | G | A | 1 | a0001c0001t0004g0027 | 2 | HG00639.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.2003+132G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522356 | |||||||
| chr9:131522369 | G | A | 1 | a0001c0003t0002g0174 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2003+145G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522369 | |||||||
| chr9:131522376 | A | G | 1 | a0001c0015t0003g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2003+152A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522376 | |||||||
| chr9:131522575 | G | A | 1 | a0001c0004t0001g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2003+351G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522575 | |||||||
| chr9:131522724 | G | C | 1 | a0002c0002t0002g0178 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2004-208G>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522724 | |||||||
| chr9:131522727 | G | C | 1 | a0002c0002t0002g0178 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2004-205G>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522727 | |||||||
| chr9:131522730 | G | T | 1 | a0002c0002t0002g0178 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2004-202G>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522730 | |||||||
| chr9:131522735 | A | G | 1 | a0002c0002t0002g0178 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2004-197A>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522735 | |||||||
| chr9:131522740 | T | C | 1 | a0002c0002t0002g0178 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2004-192T>C | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522740 | |||||||
| chr9:131522743 | T | G | 1 | a0002c0002t0002g0178 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2004-189T>G | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522743 | |||||||
| chr9:131522744 | C | T | 1 | a0002c0002t0002g0178 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2004-188C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522744 | |||||||
| chr9:131522747 | G | GCAATATT others(282): Show |
1 | a0002c0002t0002g0178 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2004-185_2004-184i others(291): Show |
POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522747 | |||||||
| chr9:131522749 | G | T | 1 | a0002c0002t0002g0178 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2004-183G>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522749 | |||||||
| chr9:131522805 | C | T | 1 | a0002c0002t0002g0187 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2004-127C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522805 | |||||||
| chr9:131522834 | CG | C | 9 | a0001c0001t0003g0165 a0003c0005t0003g0024 a0003c0005t0003g0025 others(6): Show |
11 | HG01943.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2004-92delG | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 131522834 | ||||||
| chr9:131522846 | G | A | 1 | a0002c0002t0002g0186 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2004-86G>A | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522846 | |||||||
| chr9:131522862 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.2004-70C>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522862 | |||||||
| chr9:131522868 | G | T | 1 | a0001c0003t0002g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2004-64G>T | POMT1 | ENSG00000130714.19 | transcript | ENST00000402686.8 | protein_coding | 19/19 | chr9 | 131522868 |