Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6996 |
| ensemblid | ENSG00000139372.15 |
| hgncid | 11700 |
| symbol | TDG |
| name | thymine DNA glycosylase |
| refseq_nuc | NM_003211.6 |
| refseq_prot | NP_003202.3 |
| ensembl_nuc | ENST00000392872.8 |
| ensembl_prot | ENSP00000376611.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 103965872 |
| end | 103988874 |
| strand | + |
| ver | v1.2 |
| region | chr12:103965872-103988874 |
| region5000 | chr12:103960872-103993874 |
| regionname0 | TDG_chr12_103965872_103988874 |
| regionname5000 | TDG_chr12_103960872_103993874 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 410 | 294 | 81 | 55 | 96 | 13 | 47 | 71 | TDG_chr12_103960872_103993874 | TDG | MEAEN others(405): Show |
chr12 | 103960872 | 103993874 |
| a0002 | 0/0 | 410 | 85 | 1 | 11 | 68 | 2 | 3 | 53 | TDG_chr12_103960872_103993874 | TDG | MEAEN others(405): Show |
chr12 | 103960872 | 103993874 |
| a0003 | 0/0 | 410 | 63 | 14 | 6 | 41 | 2 | 0 | 33 | TDG_chr12_103960872_103993874 | TDG | MEAEN others(405): Show |
chr12 | 103960872 | 103993874 |
| a0004 | 0/0 | 410 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | MEAEN others(405): Show |
chr12 | 103960872 | 103993874 |
| a0005 | 0/0 | 410 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | MEAEN others(405): Show |
chr12 | 103960872 | 103993874 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1230 | 289 | 77 | 55 | 95 | 13 | 47 | TDG_chr12_103960872_103993874 | TDG | ATGGA others(1225): Show |
chr12 | 103960872 | 103993874 | ||
| a0001c0005 | 0/0 | 1230 | 4 | 4 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | ATGGA others(1225): Show |
chr12 | 103960872 | 103993874 | ||
| a0001c0007 | 0/0 | 1230 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | ATGGA others(1225): Show |
chr12 | 103960872 | 103993874 | ||
| a0002c0002 | 0/0 | 1230 | 78 | 1 | 11 | 61 | 2 | 3 | TDG_chr12_103960872_103993874 | TDG | ATGGA others(1225): Show |
chr12 | 103960872 | 103993874 | ||
| a0002c0004 | 0/0 | 1230 | 7 | 0 | 0 | 7 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | ATGGA others(1225): Show |
chr12 | 103960872 | 103993874 | ||
| a0003c0003 | 0/0 | 1230 | 60 | 11 | 6 | 41 | 2 | 0 | TDG_chr12_103960872_103993874 | TDG | ATGGA others(1225): Show |
chr12 | 103960872 | 103993874 | ||
| a0003c0006 | 0/0 | 1230 | 3 | 3 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | ATGGA others(1225): Show |
chr12 | 103960872 | 103993874 | ||
| a0004c0009 | 0/0 | 1230 | 1 | 0 | 0 | 0 | 1 | 0 | TDG_chr12_103960872_103993874 | TDG | ATGGA others(1225): Show |
chr12 | 103960872 | 103993874 | ||
| a0005c0008 | 0/0 | 1230 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | ATGGA others(1225): Show |
chr12 | 103960872 | 103993874 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3185 | 210 | 32 | 44 | 92 | 9 | 32 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0001c0001t0002 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0001c0001t0003 | 1/0 | 3183 | 28 | 16 | 7 | 0 | 2 | 2 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3178): Show |
chr12 | 103960872 | 103993874 |
| a0001c0001t0004 | 0/0 | 3185 | 17 | 9 | 2 | 1 | 0 | 5 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0001c0001t0005 | 0/0 | 3178 | 16 | 16 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3173): Show |
chr12 | 103960872 | 103993874 |
| a0001c0001t0007 | 0/0 | 3185 | 8 | 1 | 0 | 0 | 0 | 7 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0001c0001t0008 | 0/0 | 3185 | 3 | 2 | 0 | 0 | 1 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0001c0001t0010 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0001c0001t0011 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0001c0001t0012 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 1 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0001c0001t0015 | 0/0 | 3185 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0001c0001t0016 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0001c0001t0017 | 0/0 | 3183 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3178): Show |
chr12 | 103960872 | 103993874 |
| a0001c0005t0003 | 0/0 | 3183 | 4 | 4 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3178): Show |
chr12 | 103960872 | 103993874 |
| a0001c0007t0001 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0002c0002t0002 | 0/0 | 3185 | 77 | 1 | 10 | 61 | 2 | 3 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0002c0002t0014 | 0/0 | 3185 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0002c0004t0002 | 0/0 | 3185 | 6 | 0 | 0 | 6 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0002c0004t0009 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0003c0003t0001 | 0/0 | 3185 | 47 | 7 | 0 | 40 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0003c0003t0006 | 0/0 | 3185 | 12 | 4 | 6 | 0 | 2 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0003c0003t0013 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0003c0006t0001 | 0/0 | 3185 | 3 | 3 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0004c0009t0001 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 1 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| a0005c0008t0002 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | AGAAG others(3180): Show |
chr12 | 103960872 | 103993874 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 13 | 2 | 0 | 10 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0004 | 0/0 | 13 | 0 | 0 | 10 | 0 | 3 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0008 | 0/0 | 7 | 1 | 5 | 0 | 1 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0022 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0034 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0035 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0036 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0063 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0064 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0065 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0066 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0069 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0072 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0073 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0074 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0003g0005 | 0/0 | 7 | 5 | 1 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0003g0014 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0003g0021 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0003g0033 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0003g0070 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0003g0071 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0004g0067 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0004g0068 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0005g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0005g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0005g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0005g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0007g0012 | 0/0 | 5 | 0 | 0 | 0 | 0 | 5 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0007g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0008g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0008g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0010g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0011g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0012g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0015g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0016g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0001t0017g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0005t0003g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0005t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0001c0007t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0002 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0006 | 0/0 | 7 | 0 | 3 | 0 | 2 | 2 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0058 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0060 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0061 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0002t0014g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0004t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0004t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0004t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0004t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0002c0004t0009g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0001 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0062 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0006g0023 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0006g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0006g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0006g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0006g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0003t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0003c0006t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0004c0009t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| a0005c0008t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0012 | g0031 | EUR | GBR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00099 | hp2 | a0004 | c0009 | t0001 | g0013 | EUR | GBR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00140 | hp1 | a0003 | c0003 | t0006 | g0038 | EUR | GBR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | GBR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00280 | hp2 | a0003 | c0003 | t0006 | g0039 | EUR | FIN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | FIN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00323 | hp2 | a0001 | c0001 | t0008 | g0142 | EUR | FIN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00408 | hp2 | a0003 | c0003 | t0001 | g0121 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00423 | hp1 | a0003 | c0003 | t0001 | g0127 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00597 | hp1 | a0001 | c0007 | t0001 | g0010 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00597 | hp2 | a0003 | c0003 | t0001 | g0126 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0166 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00621 | hp2 | a0003 | c0003 | t0001 | g0046 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00642 | hp2 | a0003 | c0003 | t0006 | g0023 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | CHS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0189 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01074 | hp2 | a0001 | c0001 | t0015 | g0008 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01081 | hp1 | a0003 | c0003 | t0006 | g0039 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0184 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01109 | hp2 | a0003 | c0003 | t0006 | g0040 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01192 | hp2 | a0003 | c0003 | t0006 | g0076 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01255 | hp1 | a0001 | c0001 | t0017 | g0014 | AMR | CLM | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | CLM | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01256 | hp2 | a0003 | c0003 | t0006 | g0038 | AMR | CLM | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01257 | hp2 | a0003 | c0003 | t0006 | g0023 | AMR | CLM | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0186 | AMR | CLM | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01496 | hp1 | a0002 | c0002 | t0014 | g0018 | AMR | CLM | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0209 | AMR | CLM | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0006 | EUR | IBS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | IBS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0006 | EUR | IBS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | IBS | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01884 | hp2 | a0003 | c0003 | t0001 | g0139 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0078 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0160 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0061 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0212 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02040 | hp2 | a0003 | c0003 | t0001 | g0124 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0167 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02056 | hp2 | a0003 | c0003 | t0001 | g0049 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0176 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0185 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | CDX | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02165 | hp1 | a0003 | c0003 | t0001 | g0122 | EAS | CDX | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CDX | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0215 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0134 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02280 | hp1 | a0003 | c0003 | t0001 | g0194 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02451 | hp2 | a0001 | c0005 | t0003 | g0229 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0132 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0223 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02615 | hp2 | a0001 | c0005 | t0003 | g0005 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0115 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0208 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0211 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02723 | hp1 | a0003 | c0006 | t0001 | g0026 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0068 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02735 | hp2 | a0001 | c0001 | t0007 | g0012 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0052 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0052 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02922 | hp1 | a0003 | c0006 | t0001 | g0026 | AFR | ESN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0068 | AFR | ESN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | ESN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ESN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02970 | hp1 | a0001 | c0005 | t0003 | g0005 | AFR | ESN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0210 | AFR | ESN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02976 | hp2 | a0003 | c0003 | t0006 | g0040 | AFR | ESN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0012 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03041 | hp1 | a0003 | c0003 | t0006 | g0075 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0130 | AFR | MSL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03130 | hp2 | a0003 | c0006 | t0001 | g0026 | AFR | ESN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03139 | hp2 | a0001 | c0001 | t0016 | g0243 | AFR | ESN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | ESN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0051 | AFR | ESN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | MSL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0216 | AFR | MSL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | MSL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0143 | AFR | MSL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | MSL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03453 | hp2 | a0003 | c0003 | t0006 | g0023 | AFR | MSL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03516 | hp1 | a0003 | c0003 | t0001 | g0050 | AFR | ESN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | ESN | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0213 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03540 | hp2 | a0003 | c0003 | t0001 | g0050 | AFR | GWD | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | MSL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0207 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03669 | hp2 | a0001 | c0001 | t0007 | g0012 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0228 | SAS | BEB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03834 | hp2 | a0001 | c0001 | t0007 | g0012 | SAS | BEB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0012 | SAS | BEB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0067 | SAS | STU | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0060 | SAS | BEB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG04199 | hp1 | a0001 | c0001 | t0007 | g0128 | SAS | STU | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG04199 | hp2 | a0001 | c0001 | t0011 | g0041 | SAS | STU | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG04204 | hp2 | a0001 | c0001 | t0007 | g0133 | SAS | STU | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | STU | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0131 | AFR | YRI | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | YRI | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18747 | hp1 | a0003 | c0003 | t0001 | g0116 | EAS | CHB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | CHB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0129 | AFR | YRI | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | YRI | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18945 | hp2 | a0003 | c0003 | t0001 | g0125 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18946 | hp2 | a0002 | c0004 | t0002 | g0006 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18947 | hp1 | a0003 | c0003 | t0001 | g0016 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18948 | hp2 | a0003 | c0003 | t0001 | g0118 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18950 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18951 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18954 | hp2 | a0003 | c0003 | t0001 | g0016 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18959 | hp2 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18960 | hp1 | a0002 | c0004 | t0002 | g0222 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18962 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18963 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18967 | hp1 | a0003 | c0003 | t0001 | g0016 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18973 | hp2 | a0003 | c0003 | t0001 | g0046 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18975 | hp1 | a0001 | c0001 | t0010 | g0083 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18980 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18981 | hp1 | a0002 | c0004 | t0009 | g0187 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0172 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18984 | hp2 | a0003 | c0003 | t0013 | g0001 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18986 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18987 | hp2 | a0003 | c0003 | t0001 | g0120 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18988 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18989 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18993 | hp2 | a0002 | c0004 | t0002 | g0190 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18994 | hp2 | a0003 | c0003 | t0001 | g0049 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18998 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18999 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19002 | hp2 | a0002 | c0004 | t0002 | g0188 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19003 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19006 | hp2 | a0003 | c0003 | t0001 | g0117 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19007 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19010 | hp2 | a0002 | c0004 | t0002 | g0006 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | LWK | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0214 | AFR | LWK | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0062 | AFR | LWK | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0227 | AFR | LWK | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19055 | hp1 | a0005 | c0008 | t0002 | g0164 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19062 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19063 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19065 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19067 | hp1 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19070 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19072 | hp1 | a0003 | c0003 | t0001 | g0217 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19080 | hp1 | a0003 | c0003 | t0001 | g0016 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19086 | hp2 | a0003 | c0003 | t0001 | g0119 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19087 | hp1 | a0002 | c0004 | t0002 | g0191 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19090 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19240 | hp1 | a0003 | c0003 | t0006 | g0077 | AFR | YRI | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA19240 | hp2 | a0001 | c0005 | t0003 | g0005 | AFR | YRI | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0062 | AFR | ASW | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ASW | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | TSI | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0070 | EUR | TSI | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0064 | EUR | TSI | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | GIH | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | GIH | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0051 | AFR | ACB | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | USA | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA18955 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | USA | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | USA | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| NA21309 | hp2 | a0001 | c0001 | t0008 | g0145 | AFR | LWK | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0198 | REF | REF | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0033 | REF | REF | TDG_chr12_103960872_103993874 | TDG | chr12 | 103960872 | 103993874 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:103979860 | A | G | 1 | a0004 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.196A>G | p.Arg66Gly | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 3/10 | 362/3183 | 196/1233 | 66/410 | chr12 | 103979860 | |||
| chr12:103982915 | G | A | 1 | a0003 | 63 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(60): Show |
missense_variant | MODERATE | c.595G>A | p.Gly199Ser | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 5/10 | 761/3183 | 595/1233 | 199/410 | chr12 | 103982915 | |||
| chr12:103983158 | C | G | 1 | a0005 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.637C>G | p.Arg213Gly | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 6/10 | 803/3183 | 637/1233 | 213/410 | chr12 | 103983158 | |||
| chr12:103983159 | G | C | 1 | a0005 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.638G>C | p.Arg213Pro | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 6/10 | 804/3183 | 638/1233 | 213/410 | chr12 | 103983159 | |||
| chr12:103983218 | T | A | 1 | a0005 | 1 | NA19055.hp1 | missense_variant&splice_region_variant | MODERATE | c.697T>A | p.Cys233Ser | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 6/10 | 863/3183 | 697/1233 | 233/410 | chr12 | 103983218 | |||
| chr12:103986956 | G | A | 2 | a0002 a0005 |
86 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
missense_variant | MODERATE | c.1099G>A | p.Val367Met | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 1265/3183 | 1099/1233 | 367/410 | chr12 | 103986956 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:103980907 | G | A | 1 | a0003c0006 | 3 | HG02723.hp1 HG02922.hp1 HG03130.hp2 |
synonymous_variant | LOW | c.423G>A | p.Pro141Pro | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/10 | 589/3183 | 423/1233 | 141/410 | chr12 | 103980907 | |||
| chr12:103984823 | C | T | 1 | a0001c0005 | 4 | HG02451.hp2 HG02615.hp2 HG02970.hp1 others(1): Show |
synonymous_variant | LOW | c.867C>T | p.Tyr289Tyr | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/10 | 1033/3183 | 867/1233 | 289/410 | chr12 | 103984823 | |||
| chr12:103984886 | G | A | 1 | a0002c0004 | 7 | NA18946.hp2 NA18960.hp1 NA18981.hp1 others(4): Show |
synonymous_variant | LOW | c.930G>A | p.Glu310Glu | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/10 | 1096/3183 | 930/1233 | 310/410 | chr12 | 103984886 | |||
| chr12:103986988 | C | T | 1 | a0001c0007 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.1131C>T | p.Gly377Gly | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 1297/3183 | 1131/1233 | 377/410 | chr12 | 103986988 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:103965996 | G | T | 1 | a0001c0001t0017 | 1 | HG01255.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-42G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/10 | chr12 | 103965996 | |||||||
| chr12:103987118 | T | C | 1 | a0002c0004t0009 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 28 | chr12 | 103987118 | ||||||
| chr12:103987340 | T | C | 1 | a0003c0003t0006 | 12 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*250T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 250 | chr12 | 103987340 | ||||||
| chr12:103987427 | C | CTG | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(19): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
3_prime_UTR_variant | MODIFIER | c.*338_*339dupTG | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 340 | INFO_REALIGN_3_PRIME | chr12 | 103987427 | |||||
| chr12:103987441 | A | G | 1 | a0001c0001t0016 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*351A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 351 | chr12 | 103987441 | ||||||
| chr12:103987443 | A | C | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*353A>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 353 | chr12 | 103987443 | ||||||
| chr12:103987510 | GTTGATTT | G | 1 | a0001c0001t0005 | 16 | HG02055.hp1 HG02258.hp1 HG02559.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*424_*430delATTTTT others(1): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 424 | INFO_REALIGN_3_PRIME | chr12 | 103987510 | |||||
| chr12:103987527 | A | G | 1 | a0002c0002t0014 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*437A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 437 | chr12 | 103987527 | ||||||
| chr12:103987604 | T | G | 1 | a0001c0001t0010 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*514T>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 514 | chr12 | 103987604 | ||||||
| chr12:103987632 | G | C | 1 | a0001c0001t0010 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*542G>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 542 | chr12 | 103987632 | ||||||
| chr12:103987907 | A | C | 1 | a0001c0001t0008 | 3 | HG00323.hp2 HG03225.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*817A>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 817 | chr12 | 103987907 | ||||||
| chr12:103988305 | T | G | 6 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0014 others(3): Show |
87 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1215T>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 1215 | chr12 | 103988305 | ||||||
| chr12:103988377 | T | C | 1 | a0001c0001t0011 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1287T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 1287 | chr12 | 103988377 | ||||||
| chr12:103988486 | G | A | 1 | a0001c0001t0007 | 8 | HG02258.hp2 HG02735.hp2 HG03017.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1396G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 1396 | chr12 | 103988486 | ||||||
| chr12:103988498 | G | A | 1 | a0001c0001t0004 | 17 | HG01496.hp2 HG01891.hp2 HG02004.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1408G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 1408 | chr12 | 103988498 | ||||||
| chr12:103988599 | G | T | 1 | a0003c0003t0013 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1509G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 1509 | chr12 | 103988599 | ||||||
| chr12:103988669 | G | A | 1 | a0001c0001t0012 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1579G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 10/10 | 1579 | chr12 | 103988669 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:103966083 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0242 a0001c0001t0016g0243 |
4 | HG02559.hp1 HG03139.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.23+23C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103966083 | |||||||
| chr12:103966112 | G | C | 1 | a0001c0001t0001g0037 | 2 | HG02738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.23+52G>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103966112 | |||||||
| chr12:103966153 | T | A | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.23+93T>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103966153 | |||||||
| chr12:103966154 | C | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0034 others(19): Show |
40 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.23+94C>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103966154 | |||||||
| chr12:103966204 | C | A | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.23+144C>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103966204 | |||||||
| chr12:103966214 | T | G | 7 | a0003c0003t0006g0023 a0003c0003t0006g0038 a0003c0003t0006g0039 others(4): Show |
12 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.23+154T>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103966214 | |||||||
| chr12:103966308 | T | A | 1 | a0001c0001t0004g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.23+248T>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103966308 | |||||||
| chr12:103966507 | G | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(43): Show |
80 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.23+447G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103966507 | |||||||
| chr12:103966665 | CAA | C | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.23+606_23+607delAA | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103966665 | |||||||
| chr12:103966825 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.23+765T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103966825 | |||||||
| chr12:103966849 | A | T | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.23+789A>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103966849 | |||||||
| chr12:103966888 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.23+828T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103966888 | |||||||
| chr12:103966935 | G | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(43): Show |
80 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.23+875G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103966935 | |||||||
| chr12:103967273 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0112 |
3 | HG01891.hp1 HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.23+1213A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103967273 | |||||||
| chr12:103967398 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0034 others(19): Show |
40 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.23+1338C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103967398 | |||||||
| chr12:103967456 | C | CT | 21 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0034 others(18): Show |
39 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.23+1415dupT | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103967456 | ||||||
| chr12:103967456 | CT | C | 169 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(166): Show |
309 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(306): Show |
intron_variant | MODIFIER | c.23+1415delT | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103967456 | ||||||
| chr12:103967519 | G | A | 34 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(31): Show |
47 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.23+1459G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103967519 | |||||||
| chr12:103967569 | G | T | 14 | a0001c0001t0004g0067 a0001c0001t0004g0068 a0001c0001t0004g0078 others(11): Show |
16 | HG01496.hp2 HG01891.hp2 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.23+1509G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103967569 | |||||||
| chr12:103967828 | T | G | 58 | a0001c0001t0001g0047 a0001c0001t0001g0054 a0001c0001t0001g0069 others(55): Show |
103 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.23+1768T>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103967828 | |||||||
| chr12:103967831 | GT | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(196): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.23+1786delT | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103967831 | ||||||
| chr12:103967834 | T | G | 15 | a0001c0001t0001g0032 a0001c0001t0001g0054 a0001c0001t0001g0069 others(12): Show |
20 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.23+1774T>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103967834 | |||||||
| chr12:103967835 | T | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(196): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.23+1775T>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103967835 | |||||||
| chr12:103967836 | T | G | 1 | a0003c0003t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.23+1776T>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103967836 | |||||||
| chr12:103967837 | T | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG01167.hp1 HG02257.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.23+1777T>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103967837 | |||||||
| chr12:103967838 | T | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(76): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.23+1778T>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103967838 | |||||||
| chr12:103967841 | T | G | 4 | a0001c0001t0001g0041 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
4 | HG02896.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.23+1781T>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103967841 | |||||||
| chr12:103967880 | G | A | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.23+1820G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103967880 | |||||||
| chr12:103967891 | C | G | 50 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0018 others(47): Show |
85 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.23+1831C>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103967891 | |||||||
| chr12:103967901 | T | TCACTGCA others(33): Show |
22 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0034 others(19): Show |
40 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.23+1843_23+1882dup others(40): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103967901 | ||||||
| chr12:103967934 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.23+1874T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103967934 | |||||||
| chr12:103968043 | G | A | 1 | a0001c0001t0004g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.23+1983G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103968043 | |||||||
| chr12:103968141 | G | T | 2 | a0001c0001t0004g0078 a0001c0001t0004g0216 |
2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.23+2081G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103968141 | |||||||
| chr12:103968329 | T | C | 1 | a0001c0001t0008g0142 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.23+2269T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103968329 | |||||||
| chr12:103968354 | C | A | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.23+2294C>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103968354 | |||||||
| chr12:103968414 | T | C | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.23+2354T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103968414 | |||||||
| chr12:103968542 | A | G | 1 | a0001c0001t0004g0215 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.23+2482A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103968542 | |||||||
| chr12:103968698 | A | T | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.23+2638A>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103968698 | |||||||
| chr12:103968716 | G | A | 7 | a0003c0003t0006g0023 a0003c0003t0006g0038 a0003c0003t0006g0039 others(4): Show |
12 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.23+2656G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103968716 | |||||||
| chr12:103968746 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.23+2686C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103968746 | |||||||
| chr12:103968958 | G | A | 23 | a0001c0001t0001g0047 a0001c0001t0001g0123 a0003c0003t0001g0001 others(20): Show |
48 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.23+2898G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103968958 | |||||||
| chr12:103968958 | G | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0241 |
2 | HG01069.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.23+2898G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103968958 | |||||||
| chr12:103969051 | A | T | 12 | a0001c0001t0001g0032 a0001c0001t0001g0054 a0001c0001t0001g0137 others(9): Show |
16 | HG01167.hp1 HG02055.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.23+2991A>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103969051 | |||||||
| chr12:103969079 | G | A | 1 | a0001c0001t0007g0128 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.23+3019G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103969079 | |||||||
| chr12:103969122 | A | G | 3 | a0001c0001t0001g0054 a0001c0001t0001g0137 a0001c0001t0001g0138 |
4 | HG02055.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.23+3062A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103969122 | |||||||
| chr12:103969154 | A | T | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.23+3094A>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103969154 | |||||||
| chr12:103969389 | G | A | 1 | a0003c0003t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.23+3329G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103969389 | |||||||
| chr12:103969403 | A | G | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.23+3343A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103969403 | |||||||
| chr12:103969549 | G | C | 1 | a0003c0003t0001g0050 | 2 | HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.23+3489G>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103969549 | |||||||
| chr12:103969637 | G | A | 8 | a0001c0001t0001g0032 a0001c0001t0001g0140 a0001c0001t0001g0141 others(5): Show |
11 | HG01167.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.23+3577G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103969637 | |||||||
| chr12:103969832 | C | T | 47 | a0001c0001t0001g0047 a0001c0001t0001g0069 a0001c0001t0001g0112 others(44): Show |
91 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.23+3772C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103969832 | |||||||
| chr12:103969915 | A | T | 1 | a0003c0003t0001g0217 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.23+3855A>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103969915 | |||||||
| chr12:103969981 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.23+3921A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103969981 | |||||||
| chr12:103970064 | A | G | 1 | a0003c0003t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.23+4004A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103970064 | |||||||
| chr12:103970713 | C | T | 8 | a0001c0001t0001g0032 a0001c0001t0001g0140 a0001c0001t0001g0141 others(5): Show |
11 | HG01167.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.23+4653C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103970713 | |||||||
| chr12:103970748 | TA | T | 235 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(232): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.23+4698delA | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103970748 | ||||||
| chr12:103970936 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.23+4876A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103970936 | |||||||
| chr12:103971344 | G | A | 72 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0034 others(69): Show |
125 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.23+5284G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103971344 | |||||||
| chr12:103971427 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.23+5367G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103971427 | |||||||
| chr12:103971542 | C | T | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.24-5376C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103971542 | |||||||
| chr12:103971600 | G | A | 1 | a0001c0001t0003g0224 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.24-5318G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103971600 | |||||||
| chr12:103971609 | C | G | 1 | a0001c0001t0001g0028 | 3 | HG00544.hp2 NA18968.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.24-5309C>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103971609 | |||||||
| chr12:103971672 | G | A | 50 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0018 others(47): Show |
85 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.24-5246G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103971672 | |||||||
| chr12:103971712 | G | T | 1 | a0003c0003t0001g0127 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.24-5206G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103971712 | |||||||
| chr12:103971733 | G | A | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(213): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.24-5185G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103971733 | |||||||
| chr12:103971753 | G | A | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(213): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.24-5165G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103971753 | |||||||
| chr12:103971884 | C | T | 34 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(31): Show |
47 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.24-5034C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103971884 | |||||||
| chr12:103971912 | C | T | 4 | a0001c0001t0007g0012 a0001c0001t0007g0128 a0001c0001t0007g0133 others(1): Show |
8 | HG02258.hp2 HG02735.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.24-5006C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103971912 | |||||||
| chr12:103972050 | C | A | 1 | a0001c0001t0001g0084 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.24-4868C>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103972050 | |||||||
| chr12:103972157 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0034 others(19): Show |
40 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.24-4761C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103972157 | |||||||
| chr12:103972186 | TTG | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0085 a0001c0001t0001g0086 |
4 | HG00438.hp2 HG02015.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.24-4731_24-4730del others(2): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103972186 | |||||||
| chr12:103972276 | G | A | 23 | a0001c0001t0001g0047 a0001c0001t0001g0123 a0003c0003t0001g0001 others(20): Show |
48 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.24-4642G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103972276 | |||||||
| chr12:103972338 | C | T | 46 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0019 others(43): Show |
78 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.24-4580C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103972338 | |||||||
| chr12:103972521 | T | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0137 a0001c0001t0001g0138 |
4 | HG02055.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.24-4397T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103972521 | |||||||
| chr12:103972562 | C | T | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.24-4356C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103972562 | |||||||
| chr12:103972626 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.24-4292A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103972626 | |||||||
| chr12:103972699 | T | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(247): Show |
439 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(436): Show |
intron_variant | MODIFIER | c.24-4219T>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103972699 | |||||||
| chr12:103972702 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0034 others(19): Show |
40 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.24-4216A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103972702 | |||||||
| chr12:103972752 | T | C | 1 | a0001c0001t0007g0128 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.24-4166T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103972752 | |||||||
| chr12:103972767 | T | G | 47 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(44): Show |
81 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.24-4151T>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103972767 | |||||||
| chr12:103972895 | A | T | 23 | a0001c0001t0001g0047 a0001c0001t0001g0123 a0003c0003t0001g0001 others(20): Show |
48 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.24-4023A>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103972895 | |||||||
| chr12:103973037 | G | A | 38 | a0002c0002t0002g0002 a0002c0002t0002g0018 a0002c0002t0002g0019 others(35): Show |
65 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.24-3881G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103973037 | |||||||
| chr12:103973086 | A | ATTTTTT | 15 | a0001c0001t0004g0207 a0001c0001t0005g0011 a0001c0001t0005g0051 others(12): Show |
27 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.24-3822_24-3817dup others(6): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103973086 | ||||||
| chr12:103973086 | A | ATTTTTTT | 69 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(66): Show |
112 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.24-3823_24-3817dup others(7): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103973086 | ||||||
| chr12:103973086 | A | ATTTTTTT others(1): Show |
134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(131): Show |
247 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.24-3824_24-3817dup others(8): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103973086 | ||||||
| chr12:103973086 | A | ATTTTTTT others(2): Show |
19 | a0001c0001t0001g0015 a0001c0001t0001g0054 a0001c0001t0001g0073 others(16): Show |
24 | HG01175.hp1 HG01934.hp2 HG01978.hp2 others(21): Show |
intron_variant | MODIFIER | c.24-3825_24-3817dup others(9): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103973086 | ||||||
| chr12:103973107 | G | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0137 a0001c0001t0001g0138 |
4 | HG02055.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.24-3811G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103973107 | |||||||
| chr12:103973294 | G | A | 2 | a0002c0002t0002g0163 a0005c0008t0002g0164 |
2 | HG00609.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.24-3624G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103973294 | |||||||
| chr12:103973569 | G | T | 1 | a0001c0001t0001g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.24-3349G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103973569 | |||||||
| chr12:103973715 | G | A | 1 | a0003c0003t0001g0050 | 2 | HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.24-3203G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103973715 | |||||||
| chr12:103973786 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.24-3132T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103973786 | |||||||
| chr12:103973821 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.24-3097C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103973821 | |||||||
| chr12:103973948 | G | T | 2 | a0002c0002t0002g0177 a0002c0002t0002g0178 |
2 | HG02080.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.24-2970G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103973948 | |||||||
| chr12:103974034 | A | T | 1 | a0001c0005t0003g0229 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.24-2884A>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103974034 | |||||||
| chr12:103974184 | C | CT | 6 | a0001c0001t0001g0066 a0001c0001t0001g0195 a0001c0001t0001g0204 others(3): Show |
8 | HG01256.hp1 HG01516.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.24-2724dupT | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103974184 | ||||||
| chr12:103974271 | T | TTTG | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(234): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.24-2629_24-2627dup others(3): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103974271 | ||||||
| chr12:103974350 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.24-2568C>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103974350 | |||||||
| chr12:103974381 | A | G | 1 | a0003c0003t0001g0125 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.24-2537A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103974381 | |||||||
| chr12:103974417 | T | C | 51 | a0001c0001t0002g0147 a0002c0002t0002g0002 a0002c0002t0002g0006 others(48): Show |
86 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.24-2501T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103974417 | |||||||
| chr12:103974448 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(43): Show |
80 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.24-2470T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103974448 | |||||||
| chr12:103974659 | A | G | 51 | a0001c0001t0002g0147 a0002c0002t0002g0002 a0002c0002t0002g0006 others(48): Show |
86 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.24-2259A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103974659 | |||||||
| chr12:103974671 | A | C | 108 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0034 others(105): Show |
193 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.24-2247A>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103974671 | |||||||
| chr12:103974706 | C | T | 2 | a0003c0003t0001g0062 a0003c0003t0001g0194 |
3 | HG02280.hp1 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.24-2212C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103974706 | |||||||
| chr12:103974753 | G | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG01168.hp1 HG01516.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.24-2165G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103974753 | |||||||
| chr12:103974823 | A | G | 1 | a0001c0001t0010g0083 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.24-2095A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103974823 | |||||||
| chr12:103974838 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(43): Show |
80 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.24-2080T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103974838 | |||||||
| chr12:103974879 | G | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(43): Show |
80 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.24-2039G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103974879 | |||||||
| chr12:103974879 | G | T | 1 | a0001c0001t0007g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.24-2039G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103974879 | |||||||
| chr12:103974974 | C | CA | 8 | a0001c0001t0001g0092 a0001c0001t0001g0102 a0001c0001t0001g0111 others(5): Show |
8 | HG00673.hp1 HG03098.hp2 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.24-1925dupA | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103974974 | ||||||
| chr12:103974974 | CA | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0035 others(19): Show |
39 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.24-1925delA | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103974974 | ||||||
| chr12:103974988 | AAAAAAG | A | 33 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(30): Show |
44 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.24-1913_24-1908del others(6): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103974988 | ||||||
| chr12:103974989 | A | G | 1 | a0003c0003t0001g0127 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.24-1929A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103974989 | |||||||
| chr12:103974989 | AAAAAG | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0201 a0003c0003t0001g0001 others(2): Show |
6 | HG01261.hp1 HG01358.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.24-1924_24-1920del others(5): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103974989 | ||||||
| chr12:103974990 | AAAAG | A | 30 | a0001c0001t0001g0047 a0001c0001t0001g0069 a0001c0001t0001g0112 others(27): Show |
55 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.24-1924_24-1921del others(4): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103974990 | ||||||
| chr12:103974991 | AAAG | A | 6 | a0001c0001t0001g0047 a0003c0003t0001g0016 a0003c0003t0001g0049 others(3): Show |
8 | HG02723.hp1 HG02922.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.24-1924_24-1922del others(3): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103974991 | ||||||
| chr12:103975032 | G | C | 35 | a0001c0001t0001g0047 a0001c0001t0001g0069 a0001c0001t0001g0112 others(32): Show |
67 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.24-1886G>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103975032 | |||||||
| chr12:103975153 | T | C | 1 | a0003c0003t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.24-1765T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103975153 | |||||||
| chr12:103975153 | T | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0034 others(19): Show |
40 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.24-1765T>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103975153 | |||||||
| chr12:103975167 | C | A | 1 | a0001c0001t0003g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.24-1751C>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103975167 | |||||||
| chr12:103975225 | G | A | 8 | a0001c0001t0005g0011 a0001c0001t0005g0051 a0001c0001t0005g0052 others(5): Show |
16 | HG02055.hp1 HG02258.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.24-1693G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103975225 | |||||||
| chr12:103975268 | A | G | 34 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(31): Show |
47 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.24-1650A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103975268 | |||||||
| chr12:103975348 | T | C | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(234): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.24-1570T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103975348 | |||||||
| chr12:103975501 | T | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0137 a0001c0001t0001g0138 |
4 | HG02055.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.24-1417T>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103975501 | |||||||
| chr12:103975509 | T | C | 51 | a0001c0001t0002g0147 a0002c0002t0002g0002 a0002c0002t0002g0006 others(48): Show |
86 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.24-1409T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103975509 | |||||||
| chr12:103975705 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.24-1213A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103975705 | |||||||
| chr12:103975822 | C | T | 1 | a0001c0001t0001g0045 | 2 | HG02083.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.24-1096C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103975822 | |||||||
| chr12:103976059 | CA | C | 33 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(30): Show |
46 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.24-848delA | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103976059 | ||||||
| chr12:103976270 | G | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(43): Show |
80 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.24-648G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103976270 | |||||||
| chr12:103976275 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0034 others(20): Show |
41 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.24-643C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103976275 | |||||||
| chr12:103976282 | G | A | 1 | a0003c0003t0001g0117 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.24-636G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103976282 | |||||||
| chr12:103976406 | C | CCACACAC others(5): Show |
1 | a0003c0003t0001g0050 | 2 | HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.24-511_24-510insAC others(10): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103976406 | ||||||
| chr12:103976408 | C | A | 2 | a0002c0002t0002g0166 a0003c0003t0001g0050 |
3 | HG00609.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.24-510C>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103976408 | |||||||
| chr12:103976408 | C | CCA | 54 | a0001c0001t0001g0036 a0001c0001t0001g0054 a0001c0001t0001g0100 others(51): Show |
93 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.24-483_24-482dupCA | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103976408 | ||||||
| chr12:103976408 | C | CCACA | 4 | a0002c0002t0002g0165 a0002c0002t0002g0175 a0002c0002t0002g0176 others(1): Show |
4 | HG02135.hp1 NA18973.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.24-485_24-482dupCA others(2): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103976408 | ||||||
| chr12:103976408 | C | CCACACA | 8 | a0001c0001t0001g0069 a0001c0001t0001g0112 a0003c0003t0006g0023 others(5): Show |
14 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.24-487_24-482dupCA others(4): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103976408 | ||||||
| chr12:103976408 | C | CCACACAC others(3): Show |
3 | a0003c0003t0001g0116 a0003c0003t0001g0117 a0003c0003t0001g0118 |
3 | NA18747.hp1 NA18948.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.24-491_24-482dupCA others(8): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103976408 | ||||||
| chr12:103976408 | C | CCACACAC others(5): Show |
3 | a0003c0003t0001g0115 a0003c0003t0001g0119 a0003c0006t0001g0026 |
5 | HG02630.hp2 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.24-493_24-482dupCA others(10): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103976408 | ||||||
| chr12:103976408 | C | CCACACAC others(7): Show |
16 | a0001c0001t0001g0047 a0001c0001t0001g0123 a0003c0003t0001g0001 others(13): Show |
38 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.24-495_24-482dupCA others(12): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103976408 | ||||||
| chr12:103976408 | C | CCACACAC others(9): Show |
2 | a0003c0003t0001g0048 a0003c0003t0001g0139 |
3 | HG01884.hp2 NA18959.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.24-497_24-482dupCA others(14): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103976408 | ||||||
| chr12:103976408 | CCA | C | 10 | a0001c0001t0001g0082 a0001c0001t0004g0144 a0001c0001t0005g0011 others(7): Show |
17 | HG00323.hp2 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.24-483_24-482delCA | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 103976408 | ||||||
| chr12:103976549 | A | G | 8 | a0001c0001t0005g0011 a0001c0001t0005g0051 a0001c0001t0005g0052 others(5): Show |
16 | HG02055.hp1 HG02258.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.24-369A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103976549 | |||||||
| chr12:103976615 | C | T | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(234): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.24-303C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103976615 | |||||||
| chr12:103976664 | G | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0027 others(19): Show |
47 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.24-254G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103976664 | |||||||
| chr12:103976694 | T | C | 51 | a0001c0001t0002g0147 a0002c0002t0002g0002 a0002c0002t0002g0006 others(48): Show |
86 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.24-224T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103976694 | |||||||
| chr12:103976701 | A | G | 51 | a0001c0001t0002g0147 a0002c0002t0002g0002 a0002c0002t0002g0006 others(48): Show |
86 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.24-217A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103976701 | |||||||
| chr12:103976724 | A | T | 1 | a0001c0001t0001g0099 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.24-194A>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 1/9 | chr12 | 103976724 | |||||||
| chr12:103977072 | A | G | 50 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0018 others(47): Show |
85 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.166+12A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103977072 | |||||||
| chr12:103977347 | T | C | 50 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0018 others(47): Show |
85 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.166+287T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103977347 | |||||||
| chr12:103977351 | G | T | 50 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0018 others(47): Show |
85 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.166+291G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103977351 | |||||||
| chr12:103977385 | T | C | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(234): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.166+325T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103977385 | |||||||
| chr12:103977400 | A | G | 1 | a0003c0003t0001g0124 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.166+340A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103977400 | |||||||
| chr12:103977418 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.166+358C>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103977418 | |||||||
| chr12:103977447 | C | T | 50 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0018 others(47): Show |
85 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.166+387C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103977447 | |||||||
| chr12:103977492 | T | C | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(234): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.166+432T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103977492 | |||||||
| chr12:103977587 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.166+527A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103977587 | |||||||
| chr12:103977589 | G | A | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(234): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.166+529G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103977589 | |||||||
| chr12:103977651 | T | C | 1 | a0001c0001t0001g0072 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.166+591T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103977651 | |||||||
| chr12:103977846 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0034 others(20): Show |
41 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.166+786C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103977846 | |||||||
| chr12:103977881 | T | C | 1 | a0001c0001t0001g0035 | 3 | HG00735.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.166+821T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103977881 | |||||||
| chr12:103977911 | G | A | 1 | a0002c0002t0002g0184 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.166+851G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103977911 | |||||||
| chr12:103978059 | TCAAAAA | T | 57 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0022 others(54): Show |
104 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.166+1029_166+1034d others(8): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 103978059 | ||||||
| chr12:103978059 | TCAAAAAC others(5): Show |
T | 44 | a0001c0001t0001g0047 a0001c0001t0001g0069 a0001c0001t0001g0112 others(41): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.166+1023_166+1034d others(14): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 103978059 | ||||||
| chr12:103978179 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.166+1119A>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103978179 | |||||||
| chr12:103978213 | A | G | 1 | a0002c0002t0002g0060 | 2 | HG02071.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.166+1153A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103978213 | |||||||
| chr12:103978278 | G | T | 1 | a0001c0001t0005g0051 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.166+1218G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103978278 | |||||||
| chr12:103978878 | A | G | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(126): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.167-953A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103978878 | |||||||
| chr12:103978917 | A | G | 2 | a0001c0001t0001g0155 a0001c0005t0003g0229 |
2 | HG02074.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.167-914A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103978917 | |||||||
| chr12:103978992 | G | A | 8 | a0001c0001t0005g0011 a0001c0001t0005g0051 a0001c0001t0005g0052 others(5): Show |
16 | HG02055.hp1 HG02258.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.167-839G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103978992 | |||||||
| chr12:103979095 | T | TTTC | 8 | a0001c0001t0005g0011 a0001c0001t0005g0051 a0001c0001t0005g0052 others(5): Show |
16 | HG02055.hp1 HG02258.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.167-733_167-731dup others(3): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 103979095 | ||||||
| chr12:103979109 | C | CTTTTTTT | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(154): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.167-716_167-710dup others(7): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 103979109 | ||||||
| chr12:103979109 | C | CTTTTTTT others(1): Show |
66 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0034 others(63): Show |
109 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.167-717_167-710dup others(8): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 103979109 | ||||||
| chr12:103979109 | C | CTTTTTTT others(2): Show |
7 | a0001c0001t0001g0239 a0002c0002t0002g0020 a0002c0002t0002g0162 others(4): Show |
10 | HG02148.hp2 NA18940.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.167-718_167-710dup others(9): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 103979109 | ||||||
| chr12:103979109 | C | CTTTTTTT others(3): Show |
1 | a0002c0002t0002g0173 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.167-719_167-710dup others(10): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 103979109 | ||||||
| chr12:103979339 | G | T | 37 | a0001c0001t0001g0032 a0001c0001t0001g0047 a0001c0001t0001g0069 others(34): Show |
71 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.167-492G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103979339 | |||||||
| chr12:103979590 | T | C | 84 | a0001c0001t0001g0047 a0001c0001t0001g0069 a0001c0001t0001g0112 others(81): Show |
151 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.167-241T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103979590 | |||||||
| chr12:103979592 | T | C | 19 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(16): Show |
30 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.167-239T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103979592 | |||||||
| chr12:103979651 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0098 |
3 | HG02080.hp1 HG03654.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.167-180A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103979651 | |||||||
| chr12:103979661 | T | C | 5 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(2): Show |
5 | HG00423.hp2 NA18939.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.167-170T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103979661 | |||||||
| chr12:103979684 | T | C | 56 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(53): Show |
91 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.167-147T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103979684 | |||||||
| chr12:103979755 | G | A | 1 | a0002c0002t0002g0179 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.167-76G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103979755 | |||||||
| chr12:103979822 | G | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(79): Show |
153 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.167-9G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103979822 | |||||||
| chr12:103979824 | A | G | 1 | a0002c0002t0002g0171 | 1 | NA18960.hp2 | splice_region_variant&intron_variant | LOW | c.167-7A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 2/9 | chr12 | 103979824 | |||||||
| chr12:103980177 | A | C | 58 | a0001c0001t0001g0032 a0001c0001t0001g0047 a0001c0001t0001g0054 others(55): Show |
96 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.408+105A>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 3/9 | chr12 | 103980177 | |||||||
| chr12:103980259 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.408+187G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 3/9 | chr12 | 103980259 | |||||||
| chr12:103980380 | A | G | 1 | a0003c0003t0001g0125 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.408+308A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 3/9 | chr12 | 103980380 | |||||||
| chr12:103980498 | A | G | 51 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0018 others(48): Show |
86 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.409-395A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 3/9 | chr12 | 103980498 | |||||||
| chr12:103980527 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.409-366C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 3/9 | chr12 | 103980527 | |||||||
| chr12:103980637 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.409-256C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 3/9 | chr12 | 103980637 | |||||||
| chr12:103980664 | A | G | 44 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0022 others(41): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.409-229A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 3/9 | chr12 | 103980664 | |||||||
| chr12:103980761 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.409-132A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 3/9 | chr12 | 103980761 | |||||||
| chr12:103980854 | G | T | 2 | a0003c0003t0001g0062 a0003c0003t0001g0194 |
3 | HG02280.hp1 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.409-39G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 3/9 | chr12 | 103980854 | |||||||
| chr12:103980884 | G | A | 1 | a0001c0001t0003g0224 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.409-9G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 3/9 | chr12 | 103980884 | |||||||
| chr12:103981053 | GAA | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0112 |
3 | HG01891.hp1 HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.478+93_478+94delAA | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 103981053 | ||||||
| chr12:103981106 | C | G | 9 | a0001c0001t0001g0113 a0001c0001t0005g0011 a0001c0001t0005g0051 others(6): Show |
17 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.478+144C>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103981106 | |||||||
| chr12:103981157 | AT | A | 5 | a0001c0001t0001g0094 a0001c0001t0007g0012 a0001c0001t0007g0128 others(2): Show |
9 | HG02155.hp1 HG02258.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.478+196delT | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103981157 | |||||||
| chr12:103981226 | C | CT | 24 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0054 others(21): Show |
33 | HG01175.hp1 HG01243.hp1 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.478+290dupT | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 103981226 | ||||||
| chr12:103981226 | CT | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(99): Show |
169 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.478+290delT | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 103981226 | ||||||
| chr12:103981226 | CTT | C | 37 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0036 others(34): Show |
67 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.478+289_478+290del others(2): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 103981226 | ||||||
| chr12:103981230 | T | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0107 a0001c0001t0001g0111 |
5 | HG01123.hp2 HG01975.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.478+268T>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103981230 | |||||||
| chr12:103981304 | C | T | 1 | a0001c0001t0004g0212 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.478+342C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103981304 | |||||||
| chr12:103981514 | C | T | 1 | a0003c0003t0006g0040 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.478+552C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103981514 | |||||||
| chr12:103981593 | C | T | 2 | a0002c0002t0002g0135 a0002c0002t0002g0136 |
2 | NA19062.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.478+631C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103981593 | |||||||
| chr12:103981594 | G | A | 32 | a0003c0003t0001g0001 a0003c0003t0001g0016 a0003c0003t0001g0017 others(29): Show |
63 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.478+632G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103981594 | |||||||
| chr12:103981669 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0112 |
3 | HG01891.hp1 HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.478+707A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103981669 | |||||||
| chr12:103981691 | A | C | 34 | a0001c0001t0001g0069 a0001c0001t0001g0112 a0003c0003t0001g0001 others(31): Show |
66 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.478+729A>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103981691 | |||||||
| chr12:103982016 | AAAAACAA others(5): Show |
A | 34 | a0001c0001t0001g0069 a0001c0001t0001g0112 a0003c0003t0001g0001 others(31): Show |
66 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.479-771_479-760del others(12): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 103982016 | ||||||
| chr12:103982060 | T | C | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0199 others(1): Show |
6 | HG00323.hp1 HG00738.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.479-739T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103982060 | |||||||
| chr12:103982262 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0123 |
3 | NA18964.hp1 NA19082.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.479-537G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103982262 | |||||||
| chr12:103982291 | T | C | 34 | a0001c0001t0001g0069 a0001c0001t0001g0112 a0003c0003t0001g0001 others(31): Show |
66 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.479-508T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103982291 | |||||||
| chr12:103982337 | G | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG01167.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.479-462G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103982337 | |||||||
| chr12:103982350 | A | T | 1 | a0001c0001t0001g0236 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.479-449A>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103982350 | |||||||
| chr12:103982436 | G | A | 4 | a0001c0001t0007g0012 a0001c0001t0007g0128 a0001c0001t0007g0133 others(1): Show |
8 | HG02258.hp2 HG02735.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.479-363G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103982436 | |||||||
| chr12:103982474 | A | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.479-325A>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103982474 | |||||||
| chr12:103982490 | A | G | 235 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(232): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.479-309A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103982490 | |||||||
| chr12:103982680 | G | T | 1 | a0002c0002t0002g0160 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.479-119G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103982680 | |||||||
| chr12:103982720 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0112 |
3 | HG01891.hp1 HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.479-79G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103982720 | |||||||
| chr12:103982723 | C | G | 1 | a0001c0001t0016g0243 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.479-76C>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 4/9 | chr12 | 103982723 | |||||||
| chr12:103983254 | A | G | 21 | a0003c0003t0001g0001 a0003c0003t0001g0016 a0003c0003t0001g0017 others(18): Show |
45 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.697+36A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 6/9 | chr12 | 103983254 | |||||||
| chr12:103983652 | T | C | 1 | a0003c0003t0006g0077 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.792+263T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 7/9 | chr12 | 103983652 | |||||||
| chr12:103983829 | G | A | 34 | a0001c0001t0001g0069 a0001c0001t0001g0112 a0003c0003t0001g0001 others(31): Show |
66 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.792+440G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 7/9 | chr12 | 103983829 | |||||||
| chr12:103984021 | G | A | 1 | a0003c0003t0001g0016 | 4 | NA18947.hp1 NA18954.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+632G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 7/9 | chr12 | 103984021 | |||||||
| chr12:103984101 | A | G | 1 | a0001c0001t0001g0064 | 2 | HG00323.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.793-648A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 7/9 | chr12 | 103984101 | |||||||
| chr12:103984161 | A | G | 1 | a0002c0002t0002g0170 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.793-588A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 7/9 | chr12 | 103984161 | |||||||
| chr12:103984285 | G | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0109 |
2 | NA18987.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.793-464G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 7/9 | chr12 | 103984285 | |||||||
| chr12:103984330 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.793-419A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 7/9 | chr12 | 103984330 | |||||||
| chr12:103984355 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | NA18982.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.793-394A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 7/9 | chr12 | 103984355 | |||||||
| chr12:103984468 | G | A | 51 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0018 others(48): Show |
86 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.793-281G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 7/9 | chr12 | 103984468 | |||||||
| chr12:103984472 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.793-277T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 7/9 | chr12 | 103984472 | |||||||
| chr12:103984473 | A | G | 1 | a0001c0001t0005g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.793-276A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 7/9 | chr12 | 103984473 | |||||||
| chr12:103984704 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.793-45A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 7/9 | chr12 | 103984704 | |||||||
| chr12:103984984 | C | CAT | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(67): Show |
130 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.964+72_964+73dupTA | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103984984 | ||||||
| chr12:103985028 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.964+108T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985028 | |||||||
| chr12:103985048 | C | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
157 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.964+128C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985048 | |||||||
| chr12:103985061 | ATG | A | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(198): Show |
361 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(358): Show |
intron_variant | MODIFIER | c.964+145_964+146del others(2): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985061 | ||||||
| chr12:103985065 | G | A | 36 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(33): Show |
49 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.964+145G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985065 | |||||||
| chr12:103985072 | T | C | 36 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(33): Show |
49 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.964+152T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985072 | |||||||
| chr12:103985074 | C | T | 36 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(33): Show |
49 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.964+154C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985074 | |||||||
| chr12:103985080 | T | C | 36 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(33): Show |
49 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.964+160T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985080 | |||||||
| chr12:103985141 | ATG | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(122): Show |
224 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.964+229_964+230del others(2): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985141 | ||||||
| chr12:103985141 | ATGTG | A | 12 | a0002c0002t0002g0006 a0002c0002t0002g0061 a0002c0002t0002g0184 others(9): Show |
20 | HG00733.hp1 HG01070.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.964+227_964+230del others(4): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985141 | ||||||
| chr12:103985143 | G | T | 1 | a0001c0001t0001g0034 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.964+223G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985143 | |||||||
| chr12:103985162 | C | CACAT | 25 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0024 others(22): Show |
46 | HG00438.hp2 HG01123.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.964+246_964+249dup others(4): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985162 | ||||||
| chr12:103985166 | T | C | 1 | a0003c0003t0001g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.964+246T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985166 | |||||||
| chr12:103985166 | T | TAC | 11 | a0001c0001t0001g0032 a0001c0001t0001g0193 a0001c0001t0003g0005 others(8): Show |
23 | HG00408.hp2 HG01943.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.964+288_964+289dup others(2): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985166 | ||||||
| chr12:103985166 | T | TACAC | 4 | a0001c0001t0001g0192 a0001c0001t0003g0021 a0001c0001t0003g0071 others(1): Show |
11 | HG01255.hp2 HG02886.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.964+286_964+289dup others(4): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985166 | ||||||
| chr12:103985166 | T | TACACACA others(7): Show |
1 | a0001c0001t0003g0225 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.964+276_964+289dup others(14): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985166 | ||||||
| chr12:103985166 | T | TACATAC | 31 | a0001c0001t0001g0031 a0001c0001t0001g0043 a0001c0001t0001g0056 others(28): Show |
47 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.964+249_964+250ins others(6): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985166 | ||||||
| chr12:103985166 | T | TACATACA others(1): Show |
48 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0047 others(45): Show |
76 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.964+249_964+250ins others(8): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985166 | ||||||
| chr12:103985166 | T | TACATACA others(3): Show |
15 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0064 others(12): Show |
27 | HG00323.hp1 HG00609.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.964+249_964+250ins others(10): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985166 | ||||||
| chr12:103985166 | T | TACATACA others(5): Show |
11 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0057 others(8): Show |
27 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.964+249_964+250ins others(12): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985166 | ||||||
| chr12:103985166 | T | TACATACA others(7): Show |
4 | a0001c0001t0001g0027 a0001c0001t0001g0201 a0002c0002t0002g0059 others(1): Show |
7 | HG00642.hp1 HG01261.hp1 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.964+249_964+250ins others(14): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985166 | ||||||
| chr12:103985166 | TAC | T | 8 | a0001c0001t0001g0084 a0001c0001t0001g0095 a0001c0001t0001g0141 others(5): Show |
9 | HG00140.hp1 HG01256.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.964+288_964+289del others(2): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985166 | ||||||
| chr12:103985166 | TACAC | T | 11 | a0001c0001t0001g0202 a0001c0001t0003g0070 a0001c0001t0005g0131 others(8): Show |
16 | HG00597.hp2 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.964+286_964+289del others(4): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985166 | ||||||
| chr12:103985166 | TACACAC | T | 5 | a0001c0001t0001g0069 a0001c0001t0001g0112 a0001c0001t0001g0196 others(2): Show |
7 | HG00280.hp2 HG01081.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+284_964+289del others(6): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985166 | ||||||
| chr12:103985166 | TACACACA others(1): Show |
T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0137 a0001c0001t0001g0138 |
4 | HG02055.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+282_964+289del others(8): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985166 | ||||||
| chr12:103985166 | TACACACA others(3): Show |
T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0034 others(19): Show |
40 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.964+280_964+289del others(10): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985166 | ||||||
| chr12:103985166 | TACACACA others(9): Show |
T | 1 | a0003c0003t0001g0046 | 2 | HG00621.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.964+274_964+289del others(16): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985166 | ||||||
| chr12:103985166 | TACACACA others(11): Show |
T | 1 | a0001c0001t0007g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.964+272_964+289del others(18): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985166 | ||||||
| chr12:103985166 | TACACACA others(13): Show |
T | 3 | a0001c0001t0007g0012 a0001c0001t0007g0128 a0001c0001t0007g0133 |
7 | HG02735.hp2 HG03017.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.964+270_964+289del others(20): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985166 | ||||||
| chr12:103985168 | C | CAT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0088 a0001c0001t0001g0094 others(4): Show |
15 | HG02155.hp1 HG02258.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.964+249_964+250ins others(2): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 103985168 | ||||||
| chr12:103985170 | C | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0044 others(14): Show |
29 | HG00558.hp1 HG00597.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.964+250C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985170 | |||||||
| chr12:103985172 | C | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0095 a0001c0001t0005g0129 |
3 | HG04228.hp1 NA18906.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.964+252C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985172 | |||||||
| chr12:103985174 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0005g0131 |
2 | HG00735.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.964+254C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985174 | |||||||
| chr12:103985176 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.964+256C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985176 | |||||||
| chr12:103985178 | C | T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0137 a0001c0001t0001g0138 |
4 | HG02055.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+258C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985178 | |||||||
| chr12:103985180 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0034 others(19): Show |
40 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.964+260C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985180 | |||||||
| chr12:103985188 | C | T | 1 | a0001c0001t0007g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.964+268C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985188 | |||||||
| chr12:103985190 | C | T | 3 | a0001c0001t0007g0012 a0001c0001t0007g0128 a0001c0001t0007g0133 |
7 | HG02735.hp2 HG03017.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.964+270C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985190 | |||||||
| chr12:103985208 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0034 others(19): Show |
40 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.964+288C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985208 | |||||||
| chr12:103985210 | T | C | 2 | a0003c0003t0001g0062 a0003c0003t0001g0194 |
3 | HG02280.hp1 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.964+290T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985210 | |||||||
| chr12:103985353 | T | C | 36 | a0001c0001t0001g0032 a0001c0001t0001g0069 a0001c0001t0001g0112 others(33): Show |
70 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.965-250T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985353 | |||||||
| chr12:103985356 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.965-247T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985356 | |||||||
| chr12:103985545 | G | C | 23 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0027 others(20): Show |
48 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.965-58G>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 8/9 | chr12 | 103985545 | |||||||
| chr12:103985950 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1090+222C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103985950 | |||||||
| chr12:103986007 | C | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0158 |
3 | HG01099.hp1 HG01943.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1090+279C>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986007 | |||||||
| chr12:103986073 | C | T | 51 | a0001c0001t0002g0147 a0002c0002t0002g0002 a0002c0002t0002g0006 others(48): Show |
86 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1090+345C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986073 | |||||||
| chr12:103986112 | A | G | 1 | a0003c0003t0001g0119 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1090+384A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986112 | |||||||
| chr12:103986123 | G | A | 2 | a0001c0001t0007g0133 a0002c0002t0002g0166 |
2 | HG00609.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1090+395G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986123 | |||||||
| chr12:103986216 | C | T | 2 | a0001c0001t0001g0205 a0002c0002t0002g0185 |
2 | HG02148.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1090+488C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986216 | |||||||
| chr12:103986268 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG01167.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1090+540A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986268 | |||||||
| chr12:103986300 | A | G | 23 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0027 others(20): Show |
48 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.1090+572A>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986300 | |||||||
| chr12:103986317 | T | G | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1090+589T>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986317 | |||||||
| chr12:103986332 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0151 a0001c0001t0001g0153 |
4 | HG02135.hp2 NA18612.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1090+604C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986332 | |||||||
| chr12:103986448 | G | A | 1 | a0001c0001t0008g0143 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1091-500G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986448 | |||||||
| chr12:103986524 | C | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0112 |
3 | HG01891.hp1 HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1091-424C>G | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986524 | |||||||
| chr12:103986551 | A | AGCTGG | 235 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(232): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1091-395_1091-394i others(7): Show |
TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 103986551 | ||||||
| chr12:103986639 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0109 |
2 | NA18987.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1091-309G>A | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986639 | |||||||
| chr12:103986675 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1091-273T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986675 | |||||||
| chr12:103986707 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG01167.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1091-241C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986707 | |||||||
| chr12:103986747 | C | T | 1 | a0001c0001t0008g0143 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1091-201C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986747 | |||||||
| chr12:103986792 | G | T | 1 | a0001c0001t0003g0224 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1091-156G>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986792 | |||||||
| chr12:103986816 | T | C | 29 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0034 others(26): Show |
48 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1091-132T>C | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986816 | |||||||
| chr12:103986877 | C | T | 1 | a0001c0001t0001g0074 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1091-71C>T | TDG | ENSG00000139372.15 | transcript | ENST00000392872.8 | protein_coding | 9/9 | chr12 | 103986877 |