Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8909 |
| ensemblid | ENSG00000111405.9 |
| hgncid | 14369 |
| symbol | ENDOU |
| name | endonuclease, poly(U) specific |
| refseq_nuc | NM_001172439.2 |
| refseq_prot | NP_001165910.1 |
| ensembl_nuc | ENST00000422538.8 |
| ensembl_prot | ENSP00000397679.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 47709734 |
| end | 47725490 |
| strand | - |
| ver | v1.2 |
| region | chr12:47709734-47725490 |
| region5000 | chr12:47704734-47730490 |
| regionname0 | ENDOU_chr12_47709734_47725490 |
| regionname5000 | ENDOU_chr12_47704734_47730490 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 410 | 396 | 84 | 63 | 188 | 16 | 43 | 152 | ENDOU_chr12_47704734_47730490 | ENDOU | MRACI others(405): Show |
chr12 | 47704734 | 47730490 |
| a0002 | 0/0 | 410 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | MRACI others(405): Show |
chr12 | 47704734 | 47730490 |
| a0003 | 0/0 | 62 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | ENDOU_chr12_47704734_47730490 | ENDOU | MRACI others(57): Show |
chr12 | 47704734 | 47730490 |
| a0004 | 0/0 | 410 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | MRACI others(405): Show |
chr12 | 47704734 | 47730490 |
| a0005 | 0/0 | 410 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | MRACI others(405): Show |
chr12 | 47704734 | 47730490 |
| a0006 | 0/0 | 410 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | MRACI others(405): Show |
chr12 | 47704734 | 47730490 |
| a0007 | 0/0 | 410 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | MRACI others(405): Show |
chr12 | 47704734 | 47730490 |
| a0008 | 0/0 | 410 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ENDOU_chr12_47704734_47730490 | ENDOU | MRACI others(405): Show |
chr12 | 47704734 | 47730490 |
| a0009 | 0/0 | 410 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | MRACI others(405): Show |
chr12 | 47704734 | 47730490 |
| a0010 | 0/0 | 410 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | MRACI others(405): Show |
chr12 | 47704734 | 47730490 |
| a0011 | 0/0 | 410 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | MRACI others(405): Show |
chr12 | 47704734 | 47730490 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1230 | 380 | 71 | 61 | 187 | 16 | 43 | ENDOU_chr12_47704734_47730490 | ENDOU | ATGAG others(1225): Show |
chr12 | 47704734 | 47730490 | ||
| a0001c0002 | 0/0 | 1230 | 9 | 7 | 1 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | ATGAG others(1225): Show |
chr12 | 47704734 | 47730490 | ||
| a0001c0005 | 0/0 | 1230 | 4 | 4 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | ATGAG others(1225): Show |
chr12 | 47704734 | 47730490 | ||
| a0001c0008 | 0/0 | 1230 | 2 | 1 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | ATGAG others(1225): Show |
chr12 | 47704734 | 47730490 | ||
| a0001c0014 | 0/0 | 1230 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | ATGAG others(1225): Show |
chr12 | 47704734 | 47730490 | ||
| a0002c0003 | 0/0 | 1230 | 7 | 7 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | ATGAG others(1225): Show |
chr12 | 47704734 | 47730490 | ||
| a0003c0004 | 0/0 | 1230 | 5 | 0 | 0 | 5 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | ATGAG others(1225): Show |
chr12 | 47704734 | 47730490 | ||
| a0004c0006 | 0/0 | 1230 | 3 | 3 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | ATGAG others(1225): Show |
chr12 | 47704734 | 47730490 | ||
| a0005c0007 | 0/0 | 1230 | 2 | 1 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | ATGAG others(1225): Show |
chr12 | 47704734 | 47730490 | ||
| a0006c0009 | 0/0 | 1230 | 2 | 0 | 1 | 0 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | ATGAG others(1225): Show |
chr12 | 47704734 | 47730490 | ||
| a0007c0011 | 0/0 | 1230 | 2 | 0 | 0 | 2 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | ATGAG others(1225): Show |
chr12 | 47704734 | 47730490 | ||
| a0008c0010 | 0/0 | 1230 | 2 | 0 | 0 | 2 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | ATGAG others(1225): Show |
chr12 | 47704734 | 47730490 | ||
| a0009c0012 | 0/0 | 1230 | 1 | 0 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | ATGAG others(1225): Show |
chr12 | 47704734 | 47730490 | ||
| a0010c0013 | 0/0 | 1230 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | ATGAG others(1225): Show |
chr12 | 47704734 | 47730490 | ||
| a0011c0015 | 0/0 | 1230 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | ATGAG others(1225): Show |
chr12 | 47704734 | 47730490 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2379 | 201 | 25 | 41 | 105 | 8 | 21 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2374): Show |
chr12 | 47704734 | 47730490 |
| a0001c0001t0002 | 1/0 | 2378 | 162 | 37 | 17 | 81 | 7 | 19 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2373): Show |
chr12 | 47704734 | 47730490 |
| a0001c0001t0003 | 0/0 | 2379 | 8 | 1 | 3 | 0 | 1 | 3 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2374): Show |
chr12 | 47704734 | 47730490 |
| a0001c0001t0004 | 0/0 | 2379 | 7 | 7 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2374): Show |
chr12 | 47704734 | 47730490 |
| a0001c0001t0005 | 0/0 | 2379 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2374): Show |
chr12 | 47704734 | 47730490 |
| a0001c0001t0006 | 0/0 | 2379 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2374): Show |
chr12 | 47704734 | 47730490 |
| a0001c0002t0001 | 0/0 | 2379 | 9 | 7 | 1 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2374): Show |
chr12 | 47704734 | 47730490 |
| a0001c0005t0001 | 0/0 | 2379 | 4 | 4 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2374): Show |
chr12 | 47704734 | 47730490 |
| a0001c0008t0001 | 0/0 | 2379 | 2 | 1 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2374): Show |
chr12 | 47704734 | 47730490 |
| a0001c0014t0001 | 0/0 | 2379 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2374): Show |
chr12 | 47704734 | 47730490 |
| a0002c0003t0004 | 0/0 | 2379 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2374): Show |
chr12 | 47704734 | 47730490 |
| a0002c0003t0005 | 0/0 | 2379 | 6 | 6 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2374): Show |
chr12 | 47704734 | 47730490 |
| a0003c0004t0001 | 0/0 | 2379 | 5 | 0 | 0 | 5 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2374): Show |
chr12 | 47704734 | 47730490 |
| a0004c0006t0002 | 0/0 | 2378 | 3 | 3 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2373): Show |
chr12 | 47704734 | 47730490 |
| a0005c0007t0002 | 0/0 | 2378 | 2 | 1 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2373): Show |
chr12 | 47704734 | 47730490 |
| a0006c0009t0002 | 0/0 | 2378 | 2 | 0 | 1 | 0 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2373): Show |
chr12 | 47704734 | 47730490 |
| a0007c0011t0002 | 0/0 | 2378 | 2 | 0 | 0 | 2 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2373): Show |
chr12 | 47704734 | 47730490 |
| a0008c0010t0001 | 0/0 | 2379 | 2 | 0 | 0 | 2 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2374): Show |
chr12 | 47704734 | 47730490 |
| a0009c0012t0002 | 0/0 | 2378 | 1 | 0 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2373): Show |
chr12 | 47704734 | 47730490 |
| a0010c0013t0002 | 0/0 | 2378 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2373): Show |
chr12 | 47704734 | 47730490 |
| a0011c0015t0002 | 0/0 | 2378 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | GTCTG others(2373): Show |
chr12 | 47704734 | 47730490 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 62 | 3 | 15 | 37 | 3 | 3 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0002 | 0/0 | 34 | 7 | 9 | 16 | 0 | 2 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0006 | 0/0 | 15 | 1 | 2 | 9 | 1 | 2 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0007 | 0/0 | 15 | 0 | 5 | 9 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0008 | 0/0 | 11 | 0 | 5 | 6 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0027 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0003 | 0/0 | 25 | 1 | 1 | 18 | 3 | 2 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0004 | 0/0 | 23 | 6 | 7 | 5 | 2 | 3 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0005 | 0/0 | 22 | 1 | 1 | 15 | 0 | 5 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0009 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0011 | 0/0 | 8 | 4 | 1 | 1 | 0 | 2 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0012 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0015 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0003g0010 | 0/0 | 8 | 1 | 3 | 0 | 1 | 3 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0004g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0004g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0002t0001g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0002t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0005t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0005t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0005t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0008t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0008t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0001c0014t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0002c0003t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0002c0003t0005g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0002c0003t0005g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0003c0004t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0003c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0003c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0004c0006t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0004c0006t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0005c0007t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0005c0007t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0006c0009t0002g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0007c0011t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0007c0011t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0008c0010t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0009c0012t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0010c0013t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| a0011c0015t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0010 | EUR | FIN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | FIN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01109 | hp1 | a0005 | c0007 | t0002 | g0119 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01255 | hp2 | a0001 | c0008 | t0001 | g0106 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01884 | hp1 | a0004 | c0006 | t0002 | g0047 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02015 | hp1 | a0007 | c0011 | t0002 | g0132 | EAS | KHV | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02040 | hp2 | a0001 | c0001 | t0006 | g0059 | EAS | KHV | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02055 | hp1 | a0002 | c0003 | t0005 | g0020 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02165 | hp1 | a0007 | c0011 | t0002 | g0133 | EAS | CDX | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02257 | hp1 | a0002 | c0003 | t0005 | g0020 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02258 | hp2 | a0010 | c0013 | t0002 | g0125 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02622 | hp2 | a0001 | c0008 | t0001 | g0105 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0082 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02717 | hp2 | a0001 | c0014 | t0001 | g0108 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02723 | hp1 | a0001 | c0005 | t0001 | g0092 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02735 | hp2 | a0006 | c0009 | t0002 | g0049 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02886 | hp1 | a0004 | c0006 | t0002 | g0122 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02886 | hp2 | a0002 | c0003 | t0005 | g0020 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | ESN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02922 | hp2 | a0001 | c0005 | t0001 | g0037 | AFR | ESN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | ESN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | ESN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | ESN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02976 | hp1 | a0001 | c0005 | t0001 | g0037 | AFR | ESN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | ESN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03139 | hp1 | a0002 | c0003 | t0005 | g0021 | AFR | ESN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03209 | hp1 | a0002 | c0003 | t0005 | g0021 | AFR | MSL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | MSL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | MSL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | MSL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | MSL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | STU | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | BEB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | BEB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | STU | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | STU | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | STU | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | STU | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | STU | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | STU | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18522 | hp1 | a0002 | c0003 | t0004 | g0061 | AFR | YRI | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | CHB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18906 | hp1 | a0002 | c0003 | t0005 | g0021 | AFR | YRI | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | YRI | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18959 | hp1 | a0011 | c0015 | t0002 | g0081 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18965 | hp2 | a0003 | c0004 | t0001 | g0069 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18966 | hp2 | a0003 | c0004 | t0001 | g0026 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18971 | hp1 | a0003 | c0004 | t0001 | g0026 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18979 | hp2 | a0003 | c0004 | t0001 | g0070 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19030 | hp2 | a0001 | c0005 | t0001 | g0093 | AFR | LWK | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | LWK | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19062 | hp2 | a0008 | c0010 | t0001 | g0031 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19083 | hp2 | a0003 | c0004 | t0001 | g0026 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19087 | hp2 | a0008 | c0010 | t0001 | g0031 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | YRI | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA19240 | hp2 | a0004 | c0006 | t0002 | g0047 | AFR | YRI | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ASW | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | ASW | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0044 | EUR | TSI | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0094 | EUR | TSI | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | GIH | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01123 | hp1 | a0006 | c0009 | t0002 | g0049 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG01123 | hp2 | a0009 | c0012 | t0002 | g0072 | AMR | CLM | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02109 | hp1 | a0005 | c0007 | t0002 | g0118 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | USA | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | USA | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | USA | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | LWK | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | LWK | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0088 | REF | REF | ENDOU_chr12_47704734_47730490 | ENDOU | chr12 | 47704734 | 47730490 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:47711700 | T | C | 1 | a0005 | 2 | HG01109.hp1 HG02109.hp1 |
missense_variant | MODERATE | c.1048A>G | p.Ile350Val | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 9/10 | 1125/2378 | 1048/1233 | 350/410 | chr12 | 47711700 | |||
| chr12:47716419 | C | T | 1 | a0004 | 3 | HG01884.hp1 HG02886.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.632G>A | p.Arg211Gln | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/10 | 709/2378 | 632/1233 | 211/410 | chr12 | 47716419 | |||
| chr12:47716449 | G | A | 1 | a0002 | 7 | HG02055.hp1 HG02257.hp1 HG02886.hp2 others(4): Show |
missense_variant | MODERATE | c.602C>T | p.Ala201Val | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/10 | 679/2378 | 602/1233 | 201/410 | chr12 | 47716449 | |||
| chr12:47716486 | C | T | 1 | a0010 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.565G>A | p.Val189Ile | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/10 | 642/2378 | 565/1233 | 189/410 | chr12 | 47716486 | |||
| chr12:47716890 | G | A | 1 | a0011 | 1 | NA18959.hp1 | missense_variant&splice_region_variant | MODERATE | c.551C>T | p.Pro184Leu | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 5/10 | 628/2378 | 551/1233 | 184/410 | chr12 | 47716890 | |||
| chr12:47717622 | C | T | 1 | a0009 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.278G>A | p.Arg93His | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 4/10 | 355/2378 | 278/1233 | 93/410 | chr12 | 47717622 | |||
| chr12:47718186 | T | A | 1 | a0003 | 5 | NA18965.hp2 NA18966.hp2 NA18971.hp1 others(2): Show |
stop_gained | HIGH | c.187A>T | p.Lys63* | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 3/10 | 264/2378 | 187/1233 | 63/410 | chr12 | 47718186 | |||
| chr12:47720828 | C | A | 1 | a0006 | 2 | HG01123.hp1 HG02735.hp2 |
missense_variant | MODERATE | c.103G>T | p.Asp35Tyr | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/10 | 180/2378 | 103/1233 | 35/410 | chr12 | 47720828 | |||
| chr12:47720831 | G | A | 1 | a0008 | 2 | NA19062.hp2 NA19087.hp2 |
missense_variant | MODERATE | c.100C>T | p.Arg34Trp | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/10 | 177/2378 | 100/1233 | 34/410 | chr12 | 47720831 | |||
| chr12:47725362 | C | A | 1 | a0007 | 2 | HG02015.hp1 HG02165.hp1 |
missense_variant | MODERATE | c.52G>T | p.Ala18Ser | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/10 | 129/2378 | 52/1233 | 18/410 | chr12 | 47725362 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:47712525 | G | A | 1 | a0001c0014 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.963C>T | p.Tyr321Tyr | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 8/10 | 1040/2378 | 963/1233 | 321/410 | chr12 | 47712525 | |||
| chr12:47712537 | G | A | 1 | a0001c0005 | 4 | HG02723.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
synonymous_variant | LOW | c.951C>T | p.Tyr317Tyr | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 8/10 | 1028/2378 | 951/1233 | 317/410 | chr12 | 47712537 | |||
| chr12:47716367 | G | A | 1 | a0001c0002 | 9 | HG01167.hp2 HG02922.hp1 HG02965.hp1 others(6): Show |
synonymous_variant | LOW | c.684C>T | p.Asp228Asp | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/10 | 761/2378 | 684/1233 | 228/410 | chr12 | 47716367 | |||
| chr12:47716898 | G | A | 1 | a0001c0008 | 2 | HG01255.hp2 HG02622.hp2 |
synonymous_variant | LOW | c.543C>T | p.Cys181Cys | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 5/10 | 620/2378 | 543/1233 | 181/410 | chr12 | 47716898 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:47710007 | C | CA | 13 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(10): Show |
247 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*794dupT | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 10/10 | 794 | chr12 | 47710007 | ||||||
| chr12:47710338 | A | C | 2 | a0001c0001t0004 a0002c0003t0004 |
8 | HG02257.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*464T>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 10/10 | 464 | chr12 | 47710338 | ||||||
| chr12:47710342 | T | A | 2 | a0001c0001t0005 a0002c0003t0005 |
7 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*460A>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 10/10 | 460 | chr12 | 47710342 | ||||||
| chr12:47710429 | G | T | 1 | a0001c0001t0003 | 8 | HG00280.hp1 HG00741.hp1 HG01243.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*373C>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 10/10 | 373 | chr12 | 47710429 | ||||||
| chr12:47710448 | C | T | 1 | a0001c0001t0006 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*354G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 10/10 | 354 | chr12 | 47710448 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:47710963 | G | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(99): Show |
333 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(330): Show |
intron_variant | MODIFIER | c.1116-44C>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 9/9 | chr12 | 47710963 | |||||||
| chr12:47711393 | C | T | 6 | a0001c0001t0001g0103 a0001c0001t0001g0121 a0001c0001t0001g0129 others(3): Show |
12 | HG01167.hp2 HG02723.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1115+240G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 9/9 | chr12 | 47711393 | |||||||
| chr12:47711422 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1115+211C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 9/9 | chr12 | 47711422 | |||||||
| chr12:47711423 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1115+210T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 9/9 | chr12 | 47711423 | |||||||
| chr12:47711469 | C | G | 1 | a0001c0001t0002g0116 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1115+164G>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 9/9 | chr12 | 47711469 | |||||||
| chr12:47711898 | C | T | 1 | a0001c0001t0001g0040 | 2 | HG03239.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.973-123G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 8/9 | chr12 | 47711898 | |||||||
| chr12:47711909 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.973-134C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 8/9 | chr12 | 47711909 | |||||||
| chr12:47711935 | T | C | 1 | a0001c0001t0002g0111 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.973-160A>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 8/9 | chr12 | 47711935 | |||||||
| chr12:47711989 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.973-214G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 8/9 | chr12 | 47711989 | |||||||
| chr12:47712196 | G | A | 1 | a0002c0003t0005g0020 | 3 | HG02055.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.972+320C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 8/9 | chr12 | 47712196 | |||||||
| chr12:47712459 | CAG | C | 5 | a0001c0001t0001g0050 a0001c0001t0002g0022 a0001c0001t0002g0042 others(2): Show |
8 | HG02280.hp2 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.972+55_972+56delCT | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 8/9 | chr12 | 47712459 | |||||||
| chr12:47712505 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.972+11G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 8/9 | chr12 | 47712505 | |||||||
| chr12:47712686 | T | G | 1 | a0001c0001t0001g0041 | 2 | HG00558.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.866-64A>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 7/9 | chr12 | 47712686 | |||||||
| chr12:47712705 | G | T | 30 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0074 others(27): Show |
80 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.866-83C>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 7/9 | chr12 | 47712705 | |||||||
| chr12:47712938 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.866-316A>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 7/9 | chr12 | 47712938 | |||||||
| chr12:47712976 | C | G | 1 | a0001c0001t0002g0126 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.865+299G>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 7/9 | chr12 | 47712976 | |||||||
| chr12:47713029 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.865+246G>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 7/9 | chr12 | 47713029 | |||||||
| chr12:47713060 | T | C | 1 | a0001c0001t0001g0014 | 4 | NA18940.hp2 NA18981.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.865+215A>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 7/9 | chr12 | 47713060 | |||||||
| chr12:47713112 | AC | A | 4 | a0001c0001t0001g0121 a0001c0001t0001g0129 a0001c0002t0001g0017 others(1): Show |
10 | HG01167.hp2 HG02723.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.865+162delG | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 7/9 | chr12 | 47713112 | |||||||
| chr12:47713115 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.865+160G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 7/9 | chr12 | 47713115 | |||||||
| chr12:47713119 | C | T | 4 | a0001c0001t0001g0121 a0001c0001t0001g0129 a0001c0002t0001g0017 others(1): Show |
10 | HG01167.hp2 HG02723.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.865+156G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 7/9 | chr12 | 47713119 | |||||||
| chr12:47713193 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.865+82T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 7/9 | chr12 | 47713193 | |||||||
| chr12:47713496 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.752-108C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47713496 | |||||||
| chr12:47713550 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0003g0010 |
12 | HG00280.hp1 HG00741.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.752-162G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47713550 | |||||||
| chr12:47713564 | A | G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0001g0121 others(4): Show |
22 | HG00280.hp1 HG00741.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.752-176T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47713564 | |||||||
| chr12:47713610 | C | T | 1 | a0001c0001t0002g0032 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.752-222G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47713610 | |||||||
| chr12:47713698 | A | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(30): Show |
133 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.752-310T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47713698 | |||||||
| chr12:47713740 | C | CG | 33 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0035 others(30): Show |
98 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.752-353dupC | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47713740 | |||||||
| chr12:47713740 | C | CGG | 28 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0040 others(25): Show |
65 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.752-354_752-353dup others(2): Show |
ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47713740 | |||||||
| chr12:47713740 | CGG | C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(22): Show |
110 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.752-354_752-353del others(2): Show |
ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47713740 | |||||||
| chr12:47713750 | G | T | 25 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(22): Show |
110 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.752-362C>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47713750 | |||||||
| chr12:47713752 | G | T | 1 | a0001c0001t0002g0117 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.752-364C>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47713752 | |||||||
| chr12:47713860 | A | G | 18 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(15): Show |
98 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.752-472T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47713860 | |||||||
| chr12:47714734 | G | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0001g0121 others(4): Show |
22 | HG00280.hp1 HG00741.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.752-1346C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47714734 | |||||||
| chr12:47714740 | G | A | 4 | a0001c0001t0001g0121 a0001c0001t0001g0129 a0001c0002t0001g0017 others(1): Show |
10 | HG01167.hp2 HG02723.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.752-1352C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47714740 | |||||||
| chr12:47714939 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(99): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.751+1361T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47714939 | |||||||
| chr12:47715241 | A | G | 30 | a0001c0001t0001g0048 a0001c0001t0002g0004 a0001c0001t0002g0009 others(27): Show |
87 | HG00140.hp1 HG00639.hp1 HG00673.hp1 others(84): Show |
intron_variant | MODIFIER | c.751+1059T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47715241 | |||||||
| chr12:47715459 | T | C | 1 | a0001c0001t0002g0077 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.751+841A>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47715459 | |||||||
| chr12:47715530 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.751+770G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47715530 | |||||||
| chr12:47715623 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0003g0010 |
12 | HG00280.hp1 HG00741.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.751+677C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47715623 | |||||||
| chr12:47715787 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.751+513G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47715787 | |||||||
| chr12:47715789 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.751+511C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47715789 | |||||||
| chr12:47715822 | C | A | 2 | a0001c0001t0001g0051 a0001c0014t0001g0108 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.751+478G>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47715822 | |||||||
| chr12:47715841 | G | C | 4 | a0001c0001t0001g0121 a0001c0001t0001g0129 a0001c0002t0001g0017 others(1): Show |
10 | HG01167.hp2 HG02723.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.751+459C>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47715841 | |||||||
| chr12:47715881 | T | G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0001g0121 others(4): Show |
22 | HG00280.hp1 HG00741.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.751+419A>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47715881 | |||||||
| chr12:47715885 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0003g0010 |
12 | HG00280.hp1 HG00741.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.751+415C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47715885 | |||||||
| chr12:47715911 | C | T | 1 | a0001c0001t0002g0032 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.751+389G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47715911 | |||||||
| chr12:47715917 | G | C | 2 | a0001c0001t0002g0032 a0001c0001t0005g0082 |
3 | HG01167.hp1 HG01169.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.751+383C>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47715917 | |||||||
| chr12:47715948 | G | A | 1 | a0001c0001t0001g0029 | 2 | NA18954.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.751+352C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47715948 | |||||||
| chr12:47716040 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
13 | HG00280.hp1 HG00741.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.751+260C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47716040 | |||||||
| chr12:47716083 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.751+217G>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47716083 | |||||||
| chr12:47716188 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.751+112G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47716188 | |||||||
| chr12:47716253 | C | T | 3 | a0001c0005t0001g0037 a0001c0005t0001g0092 a0001c0005t0001g0093 |
4 | HG02723.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.751+47G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47716253 | |||||||
| chr12:47716272 | G | A | 1 | a0001c0001t0002g0022 | 3 | HG02895.hp1 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.751+28C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 6/9 | chr12 | 47716272 | |||||||
| chr12:47716542 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): Show |
415 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(412): Show |
intron_variant | MODIFIER | c.552-43T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 5/9 | chr12 | 47716542 | |||||||
| chr12:47716598 | T | C | 3 | a0001c0001t0002g0016 a0005c0007t0002g0118 a0005c0007t0002g0119 |
6 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.552-99A>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 5/9 | chr12 | 47716598 | |||||||
| chr12:47716639 | GTC | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
13 | HG00280.hp1 HG00741.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.552-142_552-141del others(2): Show |
ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 5/9 | chr12 | 47716639 | |||||||
| chr12:47716768 | A | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(117): Show |
384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.551+122T>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 5/9 | chr12 | 47716768 | |||||||
| chr12:47716797 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.551+93C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 5/9 | chr12 | 47716797 | |||||||
| chr12:47716825 | A | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(58): Show |
211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.551+65T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 5/9 | chr12 | 47716825 | |||||||
| chr12:47716827 | A | G | 1 | a0001c0001t0002g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.551+63T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 5/9 | chr12 | 47716827 | |||||||
| chr12:47716830 | G | A | 39 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(36): Show |
105 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.551+60C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 5/9 | chr12 | 47716830 | |||||||
| chr12:47716846 | G | T | 1 | a0001c0001t0002g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.551+44C>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 5/9 | chr12 | 47716846 | |||||||
| chr12:47716860 | G | C | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | NA18941.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.551+30C>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 5/9 | chr12 | 47716860 | |||||||
| chr12:47716887 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18957.hp2 | splice_region_variant&intron_variant | LOW | c.551+3G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 5/9 | chr12 | 47716887 | |||||||
| chr12:47717273 | T | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
13 | HG00280.hp1 HG00741.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.383-215A>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 4/9 | chr12 | 47717273 | |||||||
| chr12:47717408 | T | A | 1 | a0001c0001t0001g0107 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.382+110A>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 4/9 | chr12 | 47717408 | |||||||
| chr12:47717725 | G | A | 2 | a0001c0001t0002g0114 a0001c0001t0002g0123 |
2 | HG02280.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.245-70C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 3/9 | chr12 | 47717725 | |||||||
| chr12:47717751 | T | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(15): Show |
70 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.245-96A>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 3/9 | chr12 | 47717751 | |||||||
| chr12:47717981 | C | G | 4 | a0001c0001t0001g0121 a0001c0001t0001g0129 a0001c0002t0001g0017 others(1): Show |
10 | HG01167.hp2 HG02723.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.244+148G>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 3/9 | chr12 | 47717981 | |||||||
| chr12:47718321 | G | C | 4 | a0001c0001t0001g0121 a0001c0001t0001g0129 a0001c0002t0001g0017 others(1): Show |
10 | HG01167.hp2 HG02723.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.179-127C>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47718321 | |||||||
| chr12:47718339 | G | T | 1 | a0001c0001t0002g0036 | 2 | HG02055.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.179-145C>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47718339 | |||||||
| chr12:47718466 | C | T | 1 | a0001c0001t0002g0046 | 2 | NA18945.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.179-272G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47718466 | |||||||
| chr12:47718467 | G | A | 1 | a0001c0001t0005g0082 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.179-273C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47718467 | |||||||
| chr12:47718594 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(108): Show |
357 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.179-400G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47718594 | |||||||
| chr12:47718653 | T | C | 1 | a0001c0001t0002g0124 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.179-459A>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47718653 | |||||||
| chr12:47718812 | G | C | 11 | a0001c0001t0001g0048 a0001c0001t0002g0012 a0001c0001t0002g0016 others(8): Show |
23 | HG00738.hp2 HG01109.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.179-618C>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47718812 | |||||||
| chr12:47718891 | C | T | 5 | a0001c0001t0001g0100 a0001c0001t0001g0121 a0001c0001t0001g0129 others(2): Show |
11 | HG01167.hp2 HG02723.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.179-697G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47718891 | |||||||
| chr12:47718987 | T | A | 1 | a0001c0001t0002g0083 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.179-793A>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47718987 | |||||||
| chr12:47719075 | A | G | 1 | a0001c0001t0002g0120 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.179-881T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47719075 | |||||||
| chr12:47719482 | T | G | 1 | a0002c0003t0005g0021 | 3 | HG03139.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.178+1271A>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47719482 | |||||||
| chr12:47719507 | G | A | 2 | a0001c0001t0001g0051 a0001c0014t0001g0108 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.178+1246C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47719507 | |||||||
| chr12:47719528 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.178+1225C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47719528 | |||||||
| chr12:47719575 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.178+1178G>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47719575 | |||||||
| chr12:47719577 | C | T | 1 | a0001c0001t0004g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.178+1176G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47719577 | |||||||
| chr12:47719744 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
13 | HG00280.hp1 HG00741.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.178+1009C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47719744 | |||||||
| chr12:47719813 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.178+940G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47719813 | |||||||
| chr12:47719942 | T | C | 1 | a0001c0001t0002g0085 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.178+811A>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47719942 | |||||||
| chr12:47719984 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.178+769G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47719984 | |||||||
| chr12:47719989 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(115): Show |
382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.178+764G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47719989 | |||||||
| chr12:47720100 | C | A | 1 | a0001c0001t0002g0091 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.178+653G>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47720100 | |||||||
| chr12:47720233 | A | G | 6 | a0001c0001t0002g0012 a0001c0001t0002g0016 a0001c0001t0002g0028 others(3): Show |
17 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.178+520T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47720233 | |||||||
| chr12:47720254 | G | A | 2 | a0001c0001t0002g0042 a0001c0001t0002g0111 |
3 | HG02451.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.178+499C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47720254 | |||||||
| chr12:47720417 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.178+336T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47720417 | |||||||
| chr12:47720521 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.178+232A>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47720521 | |||||||
| chr12:47720628 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.178+125G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47720628 | |||||||
| chr12:47720677 | C | T | 1 | a0001c0001t0002g0032 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.178+76G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47720677 | |||||||
| chr12:47720702 | A | C | 1 | a0001c0001t0002g0032 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.178+51T>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 2/9 | chr12 | 47720702 | |||||||
| chr12:47720978 | C | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(15): Show |
70 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.56-103G>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47720978 | |||||||
| chr12:47721303 | T | G | 35 | a0001c0001t0001g0048 a0001c0001t0001g0121 a0001c0001t0001g0129 others(32): Show |
98 | HG00140.hp1 HG00639.hp1 HG00673.hp1 others(95): Show |
intron_variant | MODIFIER | c.56-428A>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47721303 | |||||||
| chr12:47721530 | C | T | 6 | a0001c0001t0002g0009 a0001c0001t0002g0043 a0001c0001t0002g0045 others(3): Show |
18 | HG00673.hp1 HG02135.hp1 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.56-655G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47721530 | |||||||
| chr12:47721656 | A | G | 1 | a0001c0001t0002g0115 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.56-781T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47721656 | |||||||
| chr12:47722135 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0051 a0001c0001t0001g0053 others(2): Show |
14 | HG00280.hp1 HG00741.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.56-1260C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47722135 | |||||||
| chr12:47722200 | G | C | 1 | a0001c0001t0001g0050 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.56-1325C>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47722200 | |||||||
| chr12:47722214 | G | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(20): Show |
107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.56-1339C>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47722214 | |||||||
| chr12:47722416 | T | A | 1 | a0001c0001t0002g0036 | 2 | HG02055.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.56-1541A>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47722416 | |||||||
| chr12:47722472 | A | G | 35 | a0001c0001t0001g0048 a0001c0001t0001g0121 a0001c0001t0001g0129 others(32): Show |
98 | HG00140.hp1 HG00639.hp1 HG00673.hp1 others(95): Show |
intron_variant | MODIFIER | c.56-1597T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47722472 | |||||||
| chr12:47722552 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG00280.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.56-1677C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47722552 | |||||||
| chr12:47722599 | G | A | 3 | a0001c0005t0001g0037 a0001c0005t0001g0092 a0001c0005t0001g0093 |
4 | HG02723.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-1724C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47722599 | |||||||
| chr12:47722716 | T | G | 1 | a0001c0001t0002g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.56-1841A>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47722716 | |||||||
| chr12:47722790 | G | A | 35 | a0001c0001t0001g0048 a0001c0001t0001g0121 a0001c0001t0001g0129 others(32): Show |
98 | HG00140.hp1 HG00639.hp1 HG00673.hp1 others(95): Show |
intron_variant | MODIFIER | c.56-1915C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47722790 | |||||||
| chr12:47722843 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.56-1968C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47722843 | |||||||
| chr12:47722850 | G | C | 35 | a0001c0001t0001g0048 a0001c0001t0001g0121 a0001c0001t0001g0129 others(32): Show |
98 | HG00140.hp1 HG00639.hp1 HG00673.hp1 others(95): Show |
intron_variant | MODIFIER | c.56-1975C>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47722850 | |||||||
| chr12:47723134 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0095 a0001c0001t0002g0096 |
4 | HG00438.hp2 NA18943.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+2225C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47723134 | |||||||
| chr12:47723195 | A | G | 1 | a0001c0001t0002g0071 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.55+2164T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47723195 | |||||||
| chr12:47723307 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.55+2052T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47723307 | |||||||
| chr12:47723354 | G | A | 1 | a0001c0001t0002g0011 | 3 | HG01884.hp2 HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.55+2005C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47723354 | |||||||
| chr12:47723404 | C | T | 1 | a0001c0001t0001g0039 | 2 | HG02040.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.55+1955G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47723404 | |||||||
| chr12:47723417 | A | G | 1 | a0007c0011t0002g0132 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.55+1942T>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47723417 | |||||||
| chr12:47723512 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.55+1847G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47723512 | |||||||
| chr12:47723568 | C | G | 1 | a0001c0001t0001g0055 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.55+1791G>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47723568 | |||||||
| chr12:47723568 | C | T | 1 | a0003c0004t0001g0070 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.55+1791G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47723568 | |||||||
| chr12:47723582 | A | T | 39 | a0001c0001t0001g0019 a0001c0001t0001g0048 a0001c0001t0001g0053 others(36): Show |
111 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.55+1777T>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47723582 | |||||||
| chr12:47723651 | G | A | 1 | a0008c0010t0001g0031 | 2 | NA19062.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.55+1708C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47723651 | |||||||
| chr12:47723752 | G | T | 35 | a0001c0001t0001g0048 a0001c0001t0001g0121 a0001c0001t0001g0129 others(32): Show |
98 | HG00140.hp1 HG00639.hp1 HG00673.hp1 others(95): Show |
intron_variant | MODIFIER | c.55+1607C>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47723752 | |||||||
| chr12:47723924 | T | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(17): Show |
72 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.55+1435A>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47723924 | |||||||
| chr12:47724058 | C | G | 1 | a0003c0004t0001g0069 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.55+1301G>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47724058 | |||||||
| chr12:47724110 | G | C | 1 | a0001c0001t0002g0130 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.55+1249C>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47724110 | |||||||
| chr12:47724115 | C | T | 1 | a0001c0001t0002g0032 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.55+1244G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47724115 | |||||||
| chr12:47724159 | A | C | 3 | a0001c0001t0002g0044 a0001c0001t0002g0113 a0001c0001t0002g0114 |
4 | HG01261.hp2 HG02698.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+1200T>G | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47724159 | |||||||
| chr12:47724172 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(21): Show |
108 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.55+1187G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47724172 | |||||||
| chr12:47724374 | C | T | 40 | a0001c0001t0001g0019 a0001c0001t0001g0048 a0001c0001t0001g0050 others(37): Show |
112 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.55+985G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47724374 | |||||||
| chr12:47724404 | C | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
13 | HG00280.hp1 HG00741.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.55+955G>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47724404 | |||||||
| chr12:47724434 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.55+925C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47724434 | |||||||
| chr12:47724493 | CA | C | 2 | a0001c0001t0002g0043 a0001c0001t0002g0112 |
3 | NA18966.hp1 NA19064.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.55+865delT | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47724493 | |||||||
| chr12:47724644 | C | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
13 | HG00280.hp1 HG00741.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.55+715G>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47724644 | |||||||
| chr12:47724793 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.55+566G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47724793 | |||||||
| chr12:47724862 | G | A | 2 | a0001c0001t0002g0042 a0001c0001t0002g0111 |
3 | HG02451.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.55+497C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47724862 | |||||||
| chr12:47725181 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.55+178G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47725181 | |||||||
| chr12:47725190 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.55+169G>A | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47725190 | |||||||
| chr12:47725233 | C | G | 35 | a0001c0001t0001g0048 a0001c0001t0001g0121 a0001c0001t0001g0129 others(32): Show |
98 | HG00140.hp1 HG00639.hp1 HG00673.hp1 others(95): Show |
intron_variant | MODIFIER | c.55+126G>C | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47725233 | |||||||
| chr12:47725266 | G | A | 35 | a0001c0001t0001g0048 a0001c0001t0001g0121 a0001c0001t0001g0129 others(32): Show |
98 | HG00140.hp1 HG00639.hp1 HG00673.hp1 others(95): Show |
intron_variant | MODIFIER | c.55+93C>T | ENDOU | ENSG00000111405.9 | transcript | ENST00000422538.8 | protein_coding | 1/9 | chr12 | 47725266 |