Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 81493 |
| ensemblid | ENSG00000162520.15 |
| hgncid | 28897 |
| symbol | SYNC |
| name | syncoilin, intermediate filament protein |
| refseq_nuc | NM_030786.3 |
| refseq_prot | NP_110413.3 |
| ensembl_nuc | ENST00000409190.8 |
| ensembl_prot | ENSP00000386439.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 32679906 |
| end | 32702770 |
| strand | - |
| ver | v1.2 |
| region | chr1:32679906-32702770 |
| region5000 | chr1:32674906-32707770 |
| regionname0 | SYNC_chr1_32679906_32702770 |
| regionname5000 | SYNC_chr1_32674906_32707770 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 482 | 242 | 74 | 39 | 82 | 12 | 34 | 58 | SYNC_chr1_32674906_32707770 | SYNC | MASPE others(477): Show |
chr1 | 32674906 | 32707770 |
| a0002 | 0/0 | 482 | 39 | 0 | 14 | 23 | 0 | 2 | 18 | SYNC_chr1_32674906_32707770 | SYNC | MASPE others(477): Show |
chr1 | 32674906 | 32707770 |
| a0003 | 1/0 | 482 | 22 | 13 | 3 | 5 | 0 | 0 | 4 | SYNC_chr1_32674906_32707770 | SYNC | MASPE others(477): Show |
chr1 | 32674906 | 32707770 |
| a0004 | 0/0 | 482 | 8 | 5 | 3 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | MASPE others(477): Show |
chr1 | 32674906 | 32707770 |
| a0005 | 0/0 | 482 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | MASPE others(477): Show |
chr1 | 32674906 | 32707770 |
| a0006 | 0/0 | 482 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | MASPE others(477): Show |
chr1 | 32674906 | 32707770 |
| a0007 | 0/0 | 482 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | MASPE others(477): Show |
chr1 | 32674906 | 32707770 |
| a0008 | 0/0 | 482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | MASPE others(477): Show |
chr1 | 32674906 | 32707770 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1446 | 241 | 74 | 39 | 82 | 12 | 33 | SYNC_chr1_32674906_32707770 | SYNC | ATGGC others(1441): Show |
chr1 | 32674906 | 32707770 | ||
| a0001c0006 | 0/0 | 1446 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | ATGGC others(1441): Show |
chr1 | 32674906 | 32707770 | ||
| a0002c0002 | 0/0 | 1446 | 39 | 0 | 14 | 23 | 0 | 2 | SYNC_chr1_32674906_32707770 | SYNC | ATGGC others(1441): Show |
chr1 | 32674906 | 32707770 | ||
| a0003c0003 | 1/0 | 1446 | 22 | 13 | 3 | 5 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | ATGGC others(1441): Show |
chr1 | 32674906 | 32707770 | ||
| a0004c0004 | 0/0 | 1446 | 8 | 5 | 3 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | ATGGC others(1441): Show |
chr1 | 32674906 | 32707770 | ||
| a0005c0005 | 0/0 | 1446 | 4 | 3 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | ATGGC others(1441): Show |
chr1 | 32674906 | 32707770 | ||
| a0006c0008 | 0/0 | 1446 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | ATGGC others(1441): Show |
chr1 | 32674906 | 32707770 | ||
| a0007c0009 | 0/0 | 1446 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | ATGGC others(1441): Show |
chr1 | 32674906 | 32707770 | ||
| a0008c0007 | 0/0 | 1446 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | ATGGC others(1441): Show |
chr1 | 32674906 | 32707770 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3503 | 137 | 15 | 30 | 63 | 8 | 20 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| a0001c0001t0002 | 0/0 | 3503 | 70 | 32 | 7 | 17 | 4 | 10 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| a0001c0001t0004 | 0/0 | 3496 | 26 | 25 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3491): Show |
chr1 | 32674906 | 32707770 |
| a0001c0001t0009 | 0/0 | 3496 | 2 | 2 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3491): Show |
chr1 | 32674906 | 32707770 |
| a0001c0001t0011 | 0/0 | 3503 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| a0001c0001t0012 | 0/0 | 3503 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| a0001c0001t0013 | 0/0 | 3503 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| a0001c0001t0015 | 0/0 | 3503 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| a0001c0001t0016 | 0/0 | 3503 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| a0001c0001t0017 | 0/0 | 3503 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| a0001c0006t0001 | 0/0 | 3503 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| a0002c0002t0003 | 0/0 | 3504 | 39 | 0 | 14 | 23 | 0 | 2 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3499): Show |
chr1 | 32674906 | 32707770 |
| a0003c0003t0005 | 1/0 | 3503 | 9 | 6 | 2 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| a0003c0003t0006 | 0/0 | 3502 | 5 | 0 | 0 | 5 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3497): Show |
chr1 | 32674906 | 32707770 |
| a0003c0003t0008 | 0/0 | 3502 | 4 | 4 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3497): Show |
chr1 | 32674906 | 32707770 |
| a0003c0003t0010 | 0/0 | 3503 | 2 | 2 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| a0003c0003t0014 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| a0003c0003t0018 | 0/0 | 3503 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| a0004c0004t0005 | 0/0 | 3503 | 8 | 5 | 3 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| a0005c0005t0007 | 0/0 | 3502 | 4 | 3 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3497): Show |
chr1 | 32674906 | 32707770 |
| a0006c0008t0001 | 0/0 | 3503 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| a0007c0009t0002 | 0/0 | 3503 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| a0008c0007t0002 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | GGGAT others(3498): Show |
chr1 | 32674906 | 32707770 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 1 | 2 | 0 | 3 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0006 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0007 | 0/0 | 4 | 1 | 0 | 2 | 1 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0011 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0012 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0004g0002 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0004g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0004g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0004g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0009g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0009g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0011g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0012g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0013g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0015g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0016g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0001t0017g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0001c0006t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0001 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0002c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0003c0003t0005g0004 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0003c0003t0005g0015 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0003c0003t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0003c0003t0006g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0003c0003t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0003c0003t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0003c0003t0006g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0003c0003t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0003c0003t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0003c0003t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0003c0003t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0003c0003t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0003c0003t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0003c0003t0014g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0003c0003t0018g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0004c0004t0005g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0004c0004t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0004c0004t0005g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0004c0004t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0004c0004t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0005c0005t0007g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0005c0005t0007g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0005c0005t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0006c0008t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0007c0009t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| a0008c0007t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | GBR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0178 | EUR | GBR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0164 | EUR | FIN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00423 | hp2 | a0002 | c0002 | t0003 | g0221 | EAS | CHS | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00544 | hp1 | a0002 | c0002 | t0003 | g0210 | EAS | CHS | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | CHS | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00621 | hp2 | a0002 | c0002 | t0003 | g0224 | EAS | CHS | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0036 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00639 | hp2 | a0004 | c0004 | t0005 | g0017 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00642 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00733 | hp2 | a0003 | c0003 | t0018 | g0247 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00735 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG00738 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01069 | hp1 | a0003 | c0003 | t0005 | g0004 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01070 | hp2 | a0004 | c0004 | t0005 | g0017 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01071 | hp2 | a0003 | c0003 | t0005 | g0015 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01109 | hp2 | a0005 | c0005 | t0007 | g0020 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01168 | hp1 | a0002 | c0002 | t0003 | g0001 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01243 | hp1 | a0004 | c0004 | t0005 | g0019 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | CLM | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01261 | hp1 | a0002 | c0002 | t0003 | g0209 | AMR | CLM | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01358 | hp1 | a0002 | c0002 | t0003 | g0216 | AMR | CLM | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01358 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | CLM | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01496 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | CLM | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | IBS | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0136 | EUR | IBS | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01891 | hp1 | a0003 | c0003 | t0005 | g0004 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01928 | hp1 | a0001 | c0001 | t0015 | g0064 | AMR | PEL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01928 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | PEL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01943 | hp2 | a0002 | c0002 | t0003 | g0205 | AMR | PEL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01975 | hp1 | a0002 | c0002 | t0003 | g0208 | AMR | PEL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01981 | hp2 | a0002 | c0002 | t0003 | g0035 | AMR | PEL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02015 | hp2 | a0002 | c0002 | t0003 | g0207 | EAS | KHV | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0240 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02083 | hp1 | a0003 | c0003 | t0006 | g0244 | EAS | KHV | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02132 | hp2 | a0002 | c0002 | t0003 | g0206 | EAS | KHV | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02145 | hp1 | a0003 | c0003 | t0005 | g0004 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CDX | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02280 | hp2 | a0004 | c0004 | t0005 | g0019 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02293 | hp2 | a0002 | c0002 | t0003 | g0035 | AMR | PEL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0230 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02451 | hp2 | a0003 | c0003 | t0008 | g0051 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02572 | hp1 | a0003 | c0003 | t0005 | g0004 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02717 | hp1 | a0003 | c0003 | t0014 | g0041 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02723 | hp1 | a0004 | c0004 | t0005 | g0045 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02809 | hp2 | a0005 | c0005 | t0007 | g0020 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0236 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02922 | hp2 | a0003 | c0003 | t0010 | g0049 | AFR | ESN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0231 | AFR | ESN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | ESN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | ESN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03017 | hp2 | a0001 | c0001 | t0013 | g0146 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03041 | hp1 | a0003 | c0003 | t0005 | g0228 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03041 | hp2 | a0004 | c0004 | t0005 | g0044 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0232 | AFR | MSL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03098 | hp2 | a0003 | c0003 | t0005 | g0015 | AFR | MSL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ESN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0239 | AFR | ESN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03139 | hp2 | a0003 | c0003 | t0010 | g0048 | AFR | ESN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03195 | hp2 | a0004 | c0004 | t0005 | g0018 | AFR | ESN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0229 | AFR | MSL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03453 | hp1 | a0005 | c0005 | t0007 | g0047 | AFR | MSL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03453 | hp2 | a0003 | c0003 | t0008 | g0050 | AFR | MSL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | MSL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ESN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0241 | AFR | ESN | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03579 | hp2 | a0003 | c0003 | t0005 | g0004 | AFR | MSL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03654 | hp2 | a0001 | c0001 | t0016 | g0166 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03669 | hp2 | a0002 | c0002 | t0003 | g0218 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03710 | hp2 | a0001 | c0001 | t0017 | g0070 | SAS | PJL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | BEB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | BEB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | BEB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG04115 | hp1 | a0002 | c0002 | t0003 | g0217 | SAS | STU | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | STU | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | STU | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | STU | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | YRI | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18522 | hp2 | a0005 | c0005 | t0007 | g0197 | AFR | YRI | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | CHB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | YRI | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | YRI | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18944 | hp1 | a0001 | c0001 | t0011 | g0095 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18946 | hp1 | a0002 | c0002 | t0003 | g0226 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18950 | hp1 | a0002 | c0002 | t0003 | g0214 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18951 | hp2 | a0006 | c0008 | t0001 | g0179 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18952 | hp2 | a0003 | c0003 | t0006 | g0040 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18964 | hp2 | a0002 | c0002 | t0003 | g0034 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18969 | hp2 | a0002 | c0002 | t0003 | g0220 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18973 | hp2 | a0002 | c0002 | t0003 | g0034 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18977 | hp2 | a0002 | c0002 | t0003 | g0016 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18979 | hp2 | a0002 | c0002 | t0003 | g0215 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18982 | hp2 | a0002 | c0002 | t0003 | g0014 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18987 | hp2 | a0002 | c0002 | t0003 | g0219 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18989 | hp2 | a0002 | c0002 | t0003 | g0227 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18993 | hp1 | a0003 | c0003 | t0006 | g0246 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18993 | hp2 | a0002 | c0002 | t0003 | g0225 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18994 | hp1 | a0002 | c0002 | t0003 | g0223 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18994 | hp2 | a0001 | c0001 | t0012 | g0083 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA18998 | hp2 | a0003 | c0003 | t0006 | g0040 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | LWK | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | LWK | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19065 | hp1 | a0002 | c0002 | t0003 | g0014 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19068 | hp1 | a0007 | c0009 | t0002 | g0054 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19074 | hp1 | a0002 | c0002 | t0003 | g0213 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19079 | hp2 | a0002 | c0002 | t0003 | g0014 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19082 | hp1 | a0002 | c0002 | t0003 | g0016 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19083 | hp1 | a0003 | c0003 | t0006 | g0243 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19084 | hp2 | a0002 | c0002 | t0003 | g0212 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19085 | hp1 | a0002 | c0002 | t0003 | g0222 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | YRI | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | YRI | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0237 | AFR | ASW | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA20129 | hp2 | a0003 | c0003 | t0008 | g0046 | AFR | ASW | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | TSI | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA20905 | hp1 | a0001 | c0006 | t0001 | g0074 | SAS | GIH | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | GIH | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG01123 | hp2 | a0002 | c0002 | t0003 | g0211 | AMR | CLM | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02109 | hp1 | a0004 | c0004 | t0005 | g0018 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03471 | hp1 | a0003 | c0003 | t0008 | g0052 | AFR | MSL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | MSL | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0234 | AFR | USA | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | USA | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA20300 | hp1 | a0008 | c0007 | t0002 | g0133 | AFR | USA | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | USA | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | LWK | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0137 | REF | REF | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0005 | g0015 | REF | REF | SYNC_chr1_32674906_32707770 | SYNC | chr1 | 32674906 | 32707770 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:32694909 | C | T | 1 | a0005 | 4 | HG01109.hp2 HG02809.hp2 HG03453.hp1 others(1): Show |
missense_variant | MODERATE | c.1189G>A | p.Ala397Thr | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/5 | 1299/3503 | 1189/1449 | 397/482 | chr1 | 32694909 | |||
| chr1:32695043 | T | G | 1 | a0002 | 39 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
missense_variant | MODERATE | c.1055A>C | p.Glu352Ala | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/5 | 1165/3503 | 1055/1449 | 352/482 | chr1 | 32695043 | |||
| chr1:32695140 | C | T | 1 | a0008 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.958G>A | p.Glu320Lys | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/5 | 1068/3503 | 958/1449 | 320/482 | chr1 | 32695140 | |||
| chr1:32695266 | T | C | 1 | a0006 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.832A>G | p.Thr278Ala | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/5 | 942/3503 | 832/1449 | 278/482 | chr1 | 32695266 | |||
| chr1:32695277 | C | T | 4 | a0001 a0006 a0007 others(1): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
missense_variant | MODERATE | c.821G>A | p.Arg274Gln | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/5 | 931/3503 | 821/1449 | 274/482 | chr1 | 32695277 | |||
| chr1:32695307 | T | C | 1 | a0004 | 8 | HG00639.hp2 HG01070.hp2 HG01243.hp1 others(5): Show |
missense_variant | MODERATE | c.791A>G | p.Gln264Arg | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/5 | 901/3503 | 791/1449 | 264/482 | chr1 | 32695307 | |||
| chr1:32695611 | T | C | 4 | a0001 a0006 a0007 others(1): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
missense_variant | MODERATE | c.487A>G | p.Met163Val | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/5 | 597/3503 | 487/1449 | 163/482 | chr1 | 32695611 | |||
| chr1:32695719 | G | C | 1 | a0007 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.379C>G | p.Pro127Ala | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/5 | 489/3503 | 379/1449 | 127/482 | chr1 | 32695719 | |||
| chr1:32695853 | G | C | 1 | a0007 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.245C>G | p.Ala82Gly | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/5 | 355/3503 | 245/1449 | 82/482 | chr1 | 32695853 | |||
| chr1:32695856 | T | C | 1 | a0007 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.242A>G | p.Glu81Gly | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/5 | 352/3503 | 242/1449 | 81/482 | chr1 | 32695856 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:32695663 | C | T | 1 | a0002c0002 | 39 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
synonymous_variant | LOW | c.435G>A | p.Arg145Arg | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/5 | 545/3503 | 435/1449 | 145/482 | chr1 | 32695663 | |||
| chr1:32695717 | T | G | 1 | a0007c0009 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.381A>C | p.Pro127Pro | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/5 | 491/3503 | 381/1449 | 127/482 | chr1 | 32695717 | |||
| chr1:32695801 | C | T | 1 | a0001c0006 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.297G>A | p.Glu99Glu | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/5 | 407/3503 | 297/1449 | 99/482 | chr1 | 32695801 | |||
| chr1:32695855 | C | T | 1 | a0007c0009 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.243G>A | p.Glu81Glu | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/5 | 353/3503 | 243/1449 | 81/482 | chr1 | 32695855 | |||
| chr1:32696011 | T | G | 1 | a0002c0002 | 39 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
synonymous_variant | LOW | c.87A>C | p.Pro29Pro | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/5 | 197/3503 | 87/1449 | 29/482 | chr1 | 32696011 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:32679951 | A | G | 1 | a0001c0001t0016 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1899T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 1899 | chr1 | 32679951 | ||||||
| chr1:32680009 | G | A | 1 | a0001c0001t0009 | 2 | HG02818.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1841C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 1841 | chr1 | 32680009 | ||||||
| chr1:32680141 | A | G | 8 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(5): Show |
143 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*1709T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 1709 | chr1 | 32680141 | ||||||
| chr1:32680162 | TCTTGACA others(1): Show |
T | 2 | a0001c0001t0004 a0001c0001t0009 |
28 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1680_*1687delGTGT others(4): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 1680 | chr1 | 32680162 | ||||||
| chr1:32680267 | C | T | 1 | a0001c0001t0015 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1583G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 1583 | chr1 | 32680267 | ||||||
| chr1:32680347 | T | TG | 3 | a0001c0001t0004 a0001c0001t0009 a0002c0002t0003 |
67 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1502_*1503insC | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 1502 | chr1 | 32680347 | ||||||
| chr1:32680349 | T | G | 1 | a0003c0003t0014 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1501A>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 1501 | chr1 | 32680349 | ||||||
| chr1:32680349 | TG | T | 2 | a0003c0003t0006 a0003c0003t0008 |
9 | HG02083.hp1 HG02451.hp2 HG03453.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1500delC | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 1500 | chr1 | 32680349 | ||||||
| chr1:32680350 | G | T | 4 | a0003c0003t0010 a0003c0003t0014 a0004c0004t0005 others(1): Show |
14 | HG00639.hp2 HG01070.hp2 HG01109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1500C>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 1500 | chr1 | 32680350 | ||||||
| chr1:32680357 | G | GT | 10 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(7): Show |
50 | HG00558.hp1 HG00733.hp1 HG00733.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1492dupA | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 1492 | chr1 | 32680357 | ||||||
| chr1:32680747 | TG | T | 1 | a0005c0005t0007 | 4 | HG01109.hp2 HG02809.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1102delC | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 1102 | chr1 | 32680747 | ||||||
| chr1:32680851 | A | G | 1 | a0001c0001t0013 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*999T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 999 | chr1 | 32680851 | ||||||
| chr1:32680900 | A | G | 18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0011 others(15): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*950T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 950 | chr1 | 32680900 | ||||||
| chr1:32681137 | G | T | 1 | a0003c0003t0006 | 5 | HG02083.hp1 NA18952.hp2 NA18993.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*713C>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 713 | chr1 | 32681137 | ||||||
| chr1:32681143 | G | A | 2 | a0001c0001t0004 a0001c0001t0009 |
28 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*707C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 707 | chr1 | 32681143 | ||||||
| chr1:32681362 | G | A | 1 | a0001c0001t0017 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*488C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 488 | chr1 | 32681362 | ||||||
| chr1:32681497 | T | C | 1 | a0003c0003t0010 | 2 | HG02922.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*353A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 353 | chr1 | 32681497 | ||||||
| chr1:32681542 | C | T | 21 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(18): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
3_prime_UTR_variant | MODIFIER | c.*308G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 308 | chr1 | 32681542 | ||||||
| chr1:32681578 | A | T | 3 | a0001c0001t0004 a0001c0001t0009 a0002c0002t0003 |
67 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*272T>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 272 | chr1 | 32681578 | ||||||
| chr1:32681741 | A | G | 1 | a0001c0001t0012 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*109T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 109 | chr1 | 32681741 | ||||||
| chr1:32681752 | C | T | 1 | a0001c0001t0011 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*98G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 98 | chr1 | 32681752 | ||||||
| chr1:32681756 | T | G | 1 | a0003c0003t0018 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*94A>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 5/5 | 94 | chr1 | 32681756 | ||||||
| chr1:32702693 | T | A | 1 | a0003c0003t0018 | 1 | HG00733.hp2 | 5_prime_UTR_variant | MODIFIER | c.-33A>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/5 | 33 | chr1 | 32702693 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:32682129 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0184 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1439-269G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32682129 | |||||||
| chr1:32682441 | A | T | 2 | a0003c0003t0010g0048 a0003c0003t0010g0049 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1439-581T>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32682441 | |||||||
| chr1:32682443 | A | AAAAAT | 46 | a0001c0001t0004g0002 a0001c0001t0004g0036 a0001c0001t0004g0037 others(43): Show |
67 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1439-588_1439-584d others(7): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32682443 | |||||||
| chr1:32682444 | A | AAAATG | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1439-585_1439-584i others(7): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32682444 | |||||||
| chr1:32682761 | A | ACT | 238 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(235): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1439-903_1439-902d others(4): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32682761 | |||||||
| chr1:32682768 | CA | C | 28 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0016 others(25): Show |
39 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1439-909delT | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32682768 | |||||||
| chr1:32682800 | A | G | 2 | a0001c0001t0009g0234 a0001c0001t0009g0236 |
2 | HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1439-940T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32682800 | |||||||
| chr1:32682854 | G | A | 28 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0016 others(25): Show |
39 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1439-994C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32682854 | |||||||
| chr1:32682861 | C | G | 2 | a0003c0003t0010g0048 a0003c0003t0010g0049 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1439-1001G>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32682861 | |||||||
| chr1:32682962 | G | A | 2 | a0003c0003t0010g0048 a0003c0003t0010g0049 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1438+1048C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32682962 | |||||||
| chr1:32683040 | C | T | 238 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(235): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1438+970G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32683040 | |||||||
| chr1:32683152 | C | G | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0099 |
3 | NA18964.hp1 NA19010.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1438+858G>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32683152 | |||||||
| chr1:32683196 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1438+814G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32683196 | |||||||
| chr1:32683264 | CA | C | 33 | a0001c0001t0001g0068 a0001c0001t0001g0086 a0001c0001t0001g0107 others(30): Show |
38 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1438+745delT | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32683264 | |||||||
| chr1:32683264 | CAA | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1438+744_1438+745d others(4): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32683264 | |||||||
| chr1:32683334 | G | A | 29 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0012 others(26): Show |
37 | HG00544.hp2 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1438+676C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32683334 | |||||||
| chr1:32683445 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1438+565C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32683445 | |||||||
| chr1:32683568 | C | T | 28 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0016 others(25): Show |
39 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1438+442G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32683568 | |||||||
| chr1:32683654 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1438+356C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32683654 | |||||||
| chr1:32683740 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1438+270G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32683740 | |||||||
| chr1:32683957 | T | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0094 |
2 | HG00609.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1438+53A>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 4/4 | chr1 | 32683957 | |||||||
| chr1:32684097 | AAG | A | 46 | a0001c0001t0004g0002 a0001c0001t0004g0036 a0001c0001t0004g0037 others(43): Show |
67 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1359-10_1359-9delC others(1): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 3/4 | chr1 | 32684097 | |||||||
| chr1:32684656 | G | C | 1 | a0001c0001t0001g0169 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1234-274C>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32684656 | |||||||
| chr1:32684708 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1234-326T>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32684708 | |||||||
| chr1:32684946 | A | C | 1 | a0003c0003t0014g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1234-564T>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32684946 | |||||||
| chr1:32684982 | T | G | 1 | a0003c0003t0014g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1234-600A>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32684982 | |||||||
| chr1:32684995 | G | A | 1 | a0003c0003t0014g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1234-613C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32684995 | |||||||
| chr1:32684996 | C | T | 238 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(235): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1234-614G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32684996 | |||||||
| chr1:32684997 | T | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1234-615A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32684997 | |||||||
| chr1:32685015 | T | TTTC | 46 | a0001c0001t0004g0002 a0001c0001t0004g0036 a0001c0001t0004g0037 others(43): Show |
67 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1234-636_1234-634d others(5): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32685015 | |||||||
| chr1:32685042 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1234-660C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32685042 | |||||||
| chr1:32685117 | T | C | 238 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(235): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1234-735A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32685117 | |||||||
| chr1:32685264 | G | A | 238 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(235): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1234-882C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32685264 | |||||||
| chr1:32685350 | T | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1234-968A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32685350 | |||||||
| chr1:32685741 | C | T | 18 | a0001c0001t0004g0002 a0001c0001t0004g0036 a0001c0001t0004g0037 others(15): Show |
28 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1234-1359G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32685741 | |||||||
| chr1:32685751 | T | C | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0112 |
3 | NA18971.hp1 NA19004.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1234-1369A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32685751 | |||||||
| chr1:32685936 | C | T | 1 | a0001c0001t0004g0039 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1234-1554G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32685936 | |||||||
| chr1:32686057 | A | C | 1 | a0001c0001t0001g0154 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1234-1675T>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32686057 | |||||||
| chr1:32686062 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1234-1680A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32686062 | |||||||
| chr1:32686571 | G | A | 8 | a0001c0001t0002g0031 a0001c0001t0002g0132 a0001c0001t0002g0136 others(5): Show |
9 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1234-2189C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32686571 | |||||||
| chr1:32686741 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(75): Show |
95 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1234-2359C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32686741 | |||||||
| chr1:32686784 | CAG | C | 4 | a0003c0003t0006g0040 a0003c0003t0006g0243 a0003c0003t0006g0244 others(1): Show |
5 | HG02083.hp1 NA18952.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-2404_1234-240 others(6): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32686784 | |||||||
| chr1:32686790 | TTAAG | T | 46 | a0001c0001t0004g0002 a0001c0001t0004g0036 a0001c0001t0004g0037 others(43): Show |
67 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1234-2412_1234-240 others(8): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32686790 | |||||||
| chr1:32686862 | A | G | 1 | a0004c0004t0005g0018 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1234-2480T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32686862 | |||||||
| chr1:32686908 | C | G | 2 | a0003c0003t0008g0051 a0003c0003t0008g0052 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1234-2526G>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32686908 | |||||||
| chr1:32686989 | T | C | 1 | a0001c0001t0004g0239 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1234-2607A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32686989 | |||||||
| chr1:32687131 | G | A | 4 | a0003c0003t0006g0040 a0003c0003t0006g0243 a0003c0003t0006g0244 others(1): Show |
5 | HG02083.hp1 NA18952.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-2749C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687131 | |||||||
| chr1:32687158 | G | A | 28 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0016 others(25): Show |
39 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1234-2776C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687158 | |||||||
| chr1:32687361 | C | CA | 182 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1234-2980dupT | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687361 | |||||||
| chr1:32687361 | C | CAA | 41 | a0001c0001t0001g0080 a0001c0001t0001g0093 a0001c0001t0001g0108 others(38): Show |
53 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.1234-2981_1234-298 others(6): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687361 | |||||||
| chr1:32687361 | CA | C | 7 | a0003c0003t0006g0040 a0003c0003t0006g0243 a0003c0003t0006g0244 others(4): Show |
8 | HG02083.hp1 HG02451.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.1234-2980delT | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687361 | |||||||
| chr1:32687382 | A | G | 1 | a0005c0005t0007g0020 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1234-3000T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687382 | |||||||
| chr1:32687447 | T | C | 238 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(235): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1234-3065A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687447 | |||||||
| chr1:32687625 | T | C | 28 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0016 others(25): Show |
39 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1234-3243A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687625 | |||||||
| chr1:32687657 | C | T | 7 | a0001c0001t0002g0013 a0001c0001t0002g0198 a0001c0001t0002g0199 others(4): Show |
9 | HG02055.hp1 HG02257.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1234-3275G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687657 | |||||||
| chr1:32687664 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1234-3282G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687664 | |||||||
| chr1:32687670 | C | CA | 182 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1234-3289dupT | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687670 | |||||||
| chr1:32687670 | C | CAA | 10 | a0001c0001t0001g0182 a0001c0001t0002g0204 a0003c0003t0006g0040 others(7): Show |
11 | HG00733.hp2 HG02055.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1234-3290_1234-328 others(6): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687670 | |||||||
| chr1:32687696 | G | C | 1 | a0003c0003t0018g0247 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1234-3314C>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687696 | |||||||
| chr1:32687772 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1234-3390A>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687772 | |||||||
| chr1:32687828 | C | G | 1 | a0008c0007t0002g0133 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1234-3446G>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687828 | |||||||
| chr1:32687833 | A | AATAATTA others(5): Show |
1 | a0003c0003t0008g0050 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1234-3452_1234-345 others(16): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687833 | |||||||
| chr1:32687833 | A | AATT | 5 | a0004c0004t0005g0017 a0004c0004t0005g0018 a0004c0004t0005g0019 others(2): Show |
8 | HG00639.hp2 HG01070.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1234-3454_1234-345 others(7): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687833 | |||||||
| chr1:32687833 | A | AATTATTA others(2): Show |
4 | a0003c0003t0006g0040 a0003c0003t0006g0243 a0003c0003t0006g0244 others(1): Show |
5 | HG02083.hp1 NA18952.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-3460_1234-345 others(13): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687833 | |||||||
| chr1:32687833 | A | AATTATTA others(5): Show |
6 | a0001c0001t0004g0237 a0001c0001t0004g0239 a0001c0001t0009g0236 others(3): Show |
6 | HG02451.hp2 HG02818.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1234-3463_1234-345 others(16): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687833 | |||||||
| chr1:32687833 | A | AATTATTA others(8): Show |
4 | a0001c0001t0004g0036 a0001c0001t0004g0229 a0001c0001t0004g0231 others(1): Show |
5 | HG00639.hp1 HG02717.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-3466_1234-345 others(19): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687833 | |||||||
| chr1:32687833 | A | AATTATTA others(11): Show |
14 | a0001c0001t0004g0002 a0001c0001t0004g0037 a0001c0001t0004g0230 others(11): Show |
22 | HG00423.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1234-3469_1234-345 others(22): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687833 | |||||||
| chr1:32687833 | A | AATTATTA others(14): Show |
17 | a0001c0001t0001g0195 a0001c0001t0004g0038 a0001c0001t0004g0241 others(14): Show |
20 | HG00544.hp1 HG01123.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.1234-3472_1234-345 others(25): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687833 | |||||||
| chr1:32687833 | A | AATTATTA others(17): Show |
5 | a0002c0002t0003g0016 a0002c0002t0003g0207 a0002c0002t0003g0224 others(2): Show |
7 | HG00621.hp2 HG01109.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.1234-3475_1234-345 others(28): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687833 | |||||||
| chr1:32687833 | A | AATTATTA others(20): Show |
2 | a0001c0001t0001g0134 a0002c0002t0003g0213 |
2 | NA19068.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1234-3478_1234-345 others(31): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687833 | |||||||
| chr1:32687839 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1234-3457A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687839 | |||||||
| chr1:32687843 | A | ATTATTAT others(15): Show |
5 | a0002c0002t0003g0001 a0002c0002t0003g0035 a0002c0002t0003g0205 others(2): Show |
12 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1234-3462_1234-346 others(26): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687843 | |||||||
| chr1:32687843 | A | ATTATTAT others(18): Show |
1 | a0002c0002t0003g0208 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1234-3462_1234-346 others(29): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687843 | |||||||
| chr1:32687854 | T | TATTATTA others(14): Show |
1 | a0001c0001t0004g0039 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1234-3473_1234-347 others(25): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687854 | |||||||
| chr1:32687855 | A | ATTATTAT others(4): Show |
3 | a0001c0001t0001g0087 a0001c0001t0002g0160 a0001c0001t0016g0166 |
3 | HG03654.hp2 HG03831.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1234-3474_1234-347 others(15): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687855 | |||||||
| chr1:32687855 | A | ATTATTAT others(7): Show |
4 | a0001c0001t0001g0022 a0001c0001t0001g0147 a0001c0001t0002g0159 others(1): Show |
5 | HG02155.hp2 HG03710.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234-3474_1234-347 others(18): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687855 | |||||||
| chr1:32687855 | A | ATTATTAT others(10): Show |
27 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0056 others(24): Show |
35 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.1234-3474_1234-347 others(21): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687855 | |||||||
| chr1:32687855 | A | ATTATTAT others(13): Show |
63 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0025 others(60): Show |
77 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1234-3474_1234-347 others(24): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687855 | |||||||
| chr1:32687855 | A | ATTATTAT others(16): Show |
48 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(45): Show |
60 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.1234-3474_1234-347 others(27): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687855 | |||||||
| chr1:32687855 | A | ATTATTAT others(19): Show |
16 | a0001c0001t0001g0027 a0001c0001t0001g0042 a0001c0001t0001g0043 others(13): Show |
19 | HG00099.hp1 HG00609.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1234-3474_1234-347 others(30): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687855 | |||||||
| chr1:32687855 | A | ATTATTAT others(22): Show |
7 | a0001c0001t0001g0065 a0001c0001t0001g0113 a0001c0001t0001g0114 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1234-3474_1234-347 others(33): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687855 | |||||||
| chr1:32687855 | A | ATTATTAT others(25): Show |
1 | a0001c0001t0001g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1234-3474_1234-347 others(36): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687855 | |||||||
| chr1:32687855 | A | ATTATTAT others(18): Show |
1 | a0001c0001t0002g0024 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1234-3474_1234-347 others(29): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687855 | |||||||
| chr1:32687858 | A | ATTATTAT others(7): Show |
3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0112 |
3 | NA18971.hp1 NA19004.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1234-3477_1234-347 others(18): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687858 | |||||||
| chr1:32687861 | A | ATTATTAT others(8): Show |
1 | a0003c0003t0014g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1234-3480_1234-347 others(19): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687861 | |||||||
| chr1:32687861 | A | ATTATTAT others(5): Show |
1 | a0003c0003t0018g0247 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1234-3480_1234-347 others(16): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687861 | |||||||
| chr1:32687863 | T | TATTATTA others(9): Show |
1 | a0002c0002t0003g0216 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1234-3482_1234-348 others(20): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687863 | |||||||
| chr1:32687864 | T | A | 3 | a0003c0003t0008g0050 a0003c0003t0008g0051 a0003c0003t0008g0052 |
3 | HG02451.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1234-3482A>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687864 | |||||||
| chr1:32687895 | G | C | 1 | a0001c0001t0001g0077 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1234-3513C>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687895 | |||||||
| chr1:32687936 | A | G | 46 | a0001c0001t0004g0002 a0001c0001t0004g0036 a0001c0001t0004g0037 others(43): Show |
67 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1234-3554T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32687936 | |||||||
| chr1:32688084 | C | A | 1 | a0001c0001t0001g0161 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1234-3702G>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32688084 | |||||||
| chr1:32688232 | C | A | 12 | a0001c0001t0004g0002 a0001c0001t0004g0036 a0001c0001t0004g0037 others(9): Show |
21 | HG00639.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1234-3850G>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32688232 | |||||||
| chr1:32688261 | C | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0169 a0001c0001t0001g0193 |
3 | HG00558.hp2 NA18942.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1234-3879G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32688261 | |||||||
| chr1:32688365 | C | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0098 a0001c0001t0001g0189 |
3 | NA18950.hp2 NA18952.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1234-3983G>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32688365 | |||||||
| chr1:32688371 | A | G | 1 | a0001c0001t0004g0037 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1234-3989T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32688371 | |||||||
| chr1:32688412 | G | A | 1 | a0003c0003t0008g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1234-4030C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32688412 | |||||||
| chr1:32688599 | C | T | 1 | a0003c0003t0014g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1234-4217G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32688599 | |||||||
| chr1:32688723 | C | T | 1 | a0003c0003t0014g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1234-4341G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32688723 | |||||||
| chr1:32688732 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1234-4350T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32688732 | |||||||
| chr1:32688766 | C | T | 181 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1234-4384G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32688766 | |||||||
| chr1:32688949 | T | A | 1 | a0003c0003t0014g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1234-4567A>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32688949 | |||||||
| chr1:32689007 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0143 |
2 | HG00280.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1234-4625G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689007 | |||||||
| chr1:32689019 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1234-4637T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689019 | |||||||
| chr1:32689164 | C | A | 3 | a0005c0005t0007g0020 a0005c0005t0007g0047 a0005c0005t0007g0197 |
4 | HG01109.hp2 HG02809.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234-4782G>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689164 | |||||||
| chr1:32689188 | G | A | 1 | a0001c0001t0004g0241 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1234-4806C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689188 | |||||||
| chr1:32689221 | G | C | 243 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1234-4839C>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689221 | |||||||
| chr1:32689235 | C | CT | 4 | a0003c0003t0005g0004 a0003c0003t0006g0243 a0003c0003t0008g0051 others(1): Show |
8 | HG01069.hp1 HG01891.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1234-4854dupA | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689235 | |||||||
| chr1:32689235 | C | CTTTTTTT | 10 | a0001c0001t0002g0059 a0001c0001t0002g0061 a0001c0001t0002g0106 others(7): Show |
10 | HG00733.hp2 HG01257.hp1 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1234-4860_1234-485 others(11): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689235 | |||||||
| chr1:32689235 | C | CTTTTTTT others(1): Show |
42 | a0001c0001t0001g0030 a0001c0001t0001g0043 a0001c0001t0001g0123 others(39): Show |
54 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.1234-4861_1234-485 others(12): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689235 | |||||||
| chr1:32689235 | C | CTTTTTTT others(2): Show |
55 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0027 others(52): Show |
65 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1234-4862_1234-485 others(13): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689235 | |||||||
| chr1:32689235 | C | CTTTTTTT others(3): Show |
40 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(37): Show |
52 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1234-4863_1234-485 others(14): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689235 | |||||||
| chr1:32689235 | C | CTTTTTTT others(4): Show |
17 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0025 others(14): Show |
20 | HG00621.hp1 HG00735.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1234-4864_1234-485 others(15): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689235 | |||||||
| chr1:32689235 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0067 a0001c0001t0001g0120 a0001c0001t0001g0144 |
3 | HG01496.hp1 HG01934.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1234-4865_1234-485 others(16): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689235 | |||||||
| chr1:32689235 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0090 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1234-4866_1234-485 others(17): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689235 | |||||||
| chr1:32689235 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0170 a0002c0002t0003g0212 a0002c0002t0003g0217 others(1): Show |
4 | HG00423.hp2 HG04115.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234-4863_1234-485 others(14): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689235 | |||||||
| chr1:32689235 | CTTTTTTT others(4): Show |
C | 28 | a0001c0001t0004g0229 a0001c0001t0004g0232 a0001c0001t0004g0233 others(25): Show |
39 | HG00544.hp1 HG00621.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1234-4864_1234-485 others(15): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689235 | |||||||
| chr1:32689235 | CTTTTTTT others(5): Show |
C | 16 | a0001c0001t0001g0116 a0001c0001t0004g0002 a0001c0001t0004g0036 others(13): Show |
26 | HG00639.hp1 HG01192.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1234-4865_1234-485 others(16): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689235 | |||||||
| chr1:32689481 | C | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1234-5099G>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689481 | |||||||
| chr1:32689487 | G | A | 1 | a0004c0004t0005g0017 | 2 | HG00639.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.1234-5105C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689487 | |||||||
| chr1:32689492 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG01106.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1234-5110C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689492 | |||||||
| chr1:32689499 | A | G | 2 | a0001c0001t0004g0036 a0001c0001t0004g0231 |
3 | HG00639.hp1 HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1234-5117T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689499 | |||||||
| chr1:32689502 | C | A | 4 | a0001c0001t0004g0039 a0001c0001t0004g0230 a0001c0001t0004g0240 others(1): Show |
5 | HG01884.hp2 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-5120G>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689502 | |||||||
| chr1:32689680 | T | C | 3 | a0004c0004t0005g0017 a0004c0004t0005g0044 a0004c0004t0005g0045 |
4 | HG00639.hp2 HG01070.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+5185A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689680 | |||||||
| chr1:32689758 | T | C | 18 | a0001c0001t0004g0002 a0001c0001t0004g0036 a0001c0001t0004g0037 others(15): Show |
28 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1233+5107A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689758 | |||||||
| chr1:32689810 | G | A | 1 | a0002c0002t0003g0016 | 2 | NA18977.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1233+5055C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689810 | |||||||
| chr1:32689939 | C | CA | 7 | a0001c0001t0004g0241 a0003c0003t0006g0040 a0003c0003t0006g0243 others(4): Show |
8 | HG02083.hp1 HG03453.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1233+4925dupT | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689939 | |||||||
| chr1:32689939 | CA | C | 193 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(190): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1233+4925delT | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689939 | |||||||
| chr1:32689942 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1233+4923T>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32689942 | |||||||
| chr1:32690021 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1233+4844C>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32690021 | |||||||
| chr1:32690418 | G | C | 1 | a0003c0003t0008g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1233+4447C>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32690418 | |||||||
| chr1:32690429 | G | A | 1 | a0001c0001t0004g0238 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1233+4436C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32690429 | |||||||
| chr1:32690569 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1233+4296C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32690569 | |||||||
| chr1:32690584 | C | T | 1 | a0003c0003t0008g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1233+4281G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32690584 | |||||||
| chr1:32690649 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1233+4216T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32690649 | |||||||
| chr1:32690666 | TAGAG | T | 27 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0016 others(24): Show |
38 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1233+4195_1233+419 others(8): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32690666 | |||||||
| chr1:32690670 | G | T | 1 | a0002c0002t0003g0215 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1233+4195C>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32690670 | |||||||
| chr1:32690905 | G | A | 28 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0016 others(25): Show |
39 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1233+3960C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32690905 | |||||||
| chr1:32690934 | A | G | 18 | a0001c0001t0004g0002 a0001c0001t0004g0036 a0001c0001t0004g0037 others(15): Show |
28 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1233+3931T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32690934 | |||||||
| chr1:32690941 | G | A | 4 | a0002c0002t0003g0016 a0002c0002t0003g0212 a0002c0002t0003g0213 others(1): Show |
5 | NA18950.hp1 NA18977.hp2 NA19074.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+3924C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32690941 | |||||||
| chr1:32691084 | G | A | 3 | a0005c0005t0007g0020 a0005c0005t0007g0047 a0005c0005t0007g0197 |
4 | HG01109.hp2 HG02809.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+3781C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32691084 | |||||||
| chr1:32691160 | GTGAGCCC others(170): Show |
G | 28 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0016 others(25): Show |
39 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1233+3528_1233+370 others(4): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32691160 | |||||||
| chr1:32691240 | A | C | 210 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1233+3625T>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32691240 | |||||||
| chr1:32691255 | C | T | 1 | a0003c0003t0008g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1233+3610G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32691255 | |||||||
| chr1:32691392 | T | TA | 237 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(234): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1233+3472dupT | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32691392 | |||||||
| chr1:32691502 | G | A | 8 | a0003c0003t0006g0040 a0003c0003t0006g0243 a0003c0003t0006g0244 others(5): Show |
9 | HG00733.hp2 HG02083.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1233+3363C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32691502 | |||||||
| chr1:32691568 | AG | A | 6 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0127 others(3): Show |
6 | HG01192.hp2 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1233+3296delC | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32691568 | |||||||
| chr1:32691568 | AGT | A | 186 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1233+3295_1233+329 others(6): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32691568 | |||||||
| chr1:32691570 | T | A | 6 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0127 others(3): Show |
6 | HG01192.hp2 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1233+3295A>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32691570 | |||||||
| chr1:32691585 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1233+3280C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32691585 | |||||||
| chr1:32691697 | TTAGA | T | 2 | a0004c0004t0005g0018 a0004c0004t0005g0019 |
4 | HG01243.hp1 HG02109.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+3164_1233+316 others(8): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32691697 | |||||||
| chr1:32691830 | T | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1233+3035A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32691830 | |||||||
| chr1:32692003 | C | T | 46 | a0001c0001t0004g0002 a0001c0001t0004g0036 a0001c0001t0004g0037 others(43): Show |
67 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1233+2862G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32692003 | |||||||
| chr1:32692028 | G | C | 238 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(235): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1233+2837C>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32692028 | |||||||
| chr1:32692094 | C | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1233+2771G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32692094 | |||||||
| chr1:32692125 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0119 a0001c0001t0001g0126 |
3 | HG00280.hp2 HG01081.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1233+2740C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32692125 | |||||||
| chr1:32692223 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1233+2642C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32692223 | |||||||
| chr1:32692241 | C | A | 232 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(229): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1233+2624G>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32692241 | |||||||
| chr1:32692244 | C | A | 31 | a0001c0001t0001g0081 a0001c0001t0002g0174 a0001c0001t0004g0002 others(28): Show |
42 | HG00423.hp2 HG00639.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1233+2621G>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32692244 | |||||||
| chr1:32692247 | C | A | 1 | a0003c0003t0018g0247 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1233+2618G>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32692247 | |||||||
| chr1:32692263 | C | T | 46 | a0001c0001t0004g0002 a0001c0001t0004g0036 a0001c0001t0004g0037 others(43): Show |
67 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1233+2602G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32692263 | |||||||
| chr1:32692485 | A | G | 2 | a0003c0003t0010g0048 a0003c0003t0010g0049 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1233+2380T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32692485 | |||||||
| chr1:32692544 | C | T | 2 | a0001c0001t0002g0141 a0001c0001t0002g0142 |
2 | NA18945.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1233+2321G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32692544 | |||||||
| chr1:32692743 | G | T | 28 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0016 others(25): Show |
39 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1233+2122C>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32692743 | |||||||
| chr1:32692769 | C | G | 28 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0016 others(25): Show |
39 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1233+2096G>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32692769 | |||||||
| chr1:32692921 | T | C | 1 | a0001c0001t0015g0064 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1233+1944A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32692921 | |||||||
| chr1:32692940 | T | C | 28 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0016 others(25): Show |
39 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1233+1925A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32692940 | |||||||
| chr1:32693066 | G | GT | 45 | a0001c0001t0001g0010 a0001c0001t0001g0075 a0001c0001t0001g0079 others(42): Show |
58 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1233+1798dupA | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32693066 | |||||||
| chr1:32693074 | T | C | 2 | a0003c0003t0010g0048 a0003c0003t0010g0049 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1233+1791A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32693074 | |||||||
| chr1:32693077 | G | T | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1233+1788C>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32693077 | |||||||
| chr1:32693080 | T | G | 1 | a0001c0001t0002g0132 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1233+1785A>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32693080 | |||||||
| chr1:32693080 | T | TG | 3 | a0001c0001t0001g0135 a0001c0001t0001g0182 a0001c0001t0002g0136 |
3 | HG01516.hp1 HG01516.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1233+1784dupC | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32693080 | |||||||
| chr1:32693080 | T | TTG | 4 | a0001c0001t0001g0065 a0001c0001t0001g0112 a0002c0002t0003g0206 others(1): Show |
4 | HG01261.hp2 HG02132.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+1784_1233+178 others(6): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32693080 | |||||||
| chr1:32693081 | G | GT | 2 | a0004c0004t0005g0018 a0004c0004t0005g0019 |
4 | HG01243.hp1 HG02109.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+1783dupA | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32693081 | |||||||
| chr1:32693082 | T | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(227): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1233+1783A>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32693082 | |||||||
| chr1:32693085 | G | T | 243 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1233+1780C>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32693085 | |||||||
| chr1:32693230 | G | A | 1 | a0002c0002t0003g0216 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1233+1635C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32693230 | |||||||
| chr1:32693273 | G | C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG01106.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1233+1592C>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32693273 | |||||||
| chr1:32693284 | T | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1233+1581A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32693284 | |||||||
| chr1:32693364 | C | T | 18 | a0001c0001t0004g0002 a0001c0001t0004g0036 a0001c0001t0004g0037 others(15): Show |
28 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1233+1501G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32693364 | |||||||
| chr1:32693427 | C | G | 1 | a0001c0001t0004g0240 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1233+1438G>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32693427 | |||||||
| chr1:32693897 | A | G | 1 | a0001c0001t0004g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1233+968T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32693897 | |||||||
| chr1:32693904 | G | A | 28 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0016 others(25): Show |
39 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1233+961C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32693904 | |||||||
| chr1:32694011 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1233+854G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32694011 | |||||||
| chr1:32694061 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1233+804T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32694061 | |||||||
| chr1:32694078 | A | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0112 |
3 | NA18971.hp1 NA19004.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1233+787T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32694078 | |||||||
| chr1:32694125 | G | T | 7 | a0003c0003t0008g0046 a0003c0003t0010g0048 a0003c0003t0010g0049 others(4): Show |
8 | HG01109.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1233+740C>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32694125 | |||||||
| chr1:32694143 | G | A | 3 | a0003c0003t0008g0050 a0003c0003t0008g0051 a0003c0003t0008g0052 |
3 | HG02451.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1233+722C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32694143 | |||||||
| chr1:32694192 | G | A | 2 | a0004c0004t0005g0018 a0004c0004t0005g0019 |
4 | HG01243.hp1 HG02109.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+673C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32694192 | |||||||
| chr1:32694289 | G | T | 1 | a0008c0007t0002g0133 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1233+576C>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32694289 | |||||||
| chr1:32694299 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1233+566G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32694299 | |||||||
| chr1:32694375 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1233+490G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32694375 | |||||||
| chr1:32694381 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1233+484G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32694381 | |||||||
| chr1:32694549 | A | G | 238 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(235): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1233+316T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32694549 | |||||||
| chr1:32694611 | A | C | 4 | a0001c0001t0004g0039 a0001c0001t0004g0230 a0001c0001t0004g0240 others(1): Show |
5 | HG01884.hp2 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+254T>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32694611 | |||||||
| chr1:32694653 | C | CA | 12 | a0001c0001t0001g0072 a0001c0001t0001g0112 a0001c0001t0001g0115 others(9): Show |
13 | HG00099.hp2 HG01109.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.1233+211dupT | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32694653 | |||||||
| chr1:32694653 | C | CAA | 8 | a0003c0003t0006g0040 a0003c0003t0006g0243 a0003c0003t0006g0244 others(5): Show |
9 | HG00733.hp2 HG02083.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1233+210_1233+211d others(4): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32694653 | |||||||
| chr1:32694665 | A | C | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0118 |
3 | NA18945.hp1 NA18973.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1233+200T>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32694665 | |||||||
| chr1:32694667 | C | A | 1 | a0007c0009t0002g0054 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1233+198G>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 2/4 | chr1 | 32694667 | |||||||
| chr1:32696198 | C | A | 1 | a0001c0001t0001g0131 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.54-154G>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32696198 | |||||||
| chr1:32696205 | C | T | 195 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.54-161G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32696205 | |||||||
| chr1:32696208 | C | T | 1 | a0005c0005t0007g0197 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.54-164G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32696208 | |||||||
| chr1:32696454 | G | A | 1 | a0001c0001t0015g0064 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.54-410C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32696454 | |||||||
| chr1:32696503 | A | G | 8 | a0003c0003t0006g0040 a0003c0003t0006g0243 a0003c0003t0006g0244 others(5): Show |
9 | HG00733.hp2 HG02083.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.54-459T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32696503 | |||||||
| chr1:32696511 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.54-467C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32696511 | |||||||
| chr1:32696748 | C | A | 1 | a0007c0009t0002g0054 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.54-704G>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32696748 | |||||||
| chr1:32696768 | T | C | 238 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(235): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.54-724A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32696768 | |||||||
| chr1:32696895 | G | C | 4 | a0001c0001t0001g0065 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-851C>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32696895 | |||||||
| chr1:32696975 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.54-931A>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32696975 | |||||||
| chr1:32697160 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.54-1116C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32697160 | |||||||
| chr1:32697171 | G | A | 1 | a0005c0005t0007g0197 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.54-1127C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32697171 | |||||||
| chr1:32697368 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.54-1324C>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32697368 | |||||||
| chr1:32697371 | G | A | 1 | a0001c0001t0004g0229 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.54-1327C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32697371 | |||||||
| chr1:32697426 | G | A | 1 | a0003c0003t0008g0050 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.54-1382C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32697426 | |||||||
| chr1:32697438 | CA | C | 18 | a0001c0001t0002g0132 a0002c0002t0003g0205 a0003c0003t0006g0040 others(15): Show |
20 | HG00733.hp2 HG01109.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.54-1395delT | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32697438 | |||||||
| chr1:32697460 | G | A | 238 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(235): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.54-1416C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32697460 | |||||||
| chr1:32697472 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.54-1428C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32697472 | |||||||
| chr1:32697568 | C | G | 1 | a0001c0001t0001g0072 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.54-1524G>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32697568 | |||||||
| chr1:32697700 | C | A | 28 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0016 others(25): Show |
39 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.54-1656G>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32697700 | |||||||
| chr1:32697751 | A | T | 15 | a0003c0003t0006g0040 a0003c0003t0006g0243 a0003c0003t0006g0244 others(12): Show |
17 | HG00733.hp2 HG01109.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.54-1707T>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32697751 | |||||||
| chr1:32698201 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.54-2157G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698201 | |||||||
| chr1:32698214 | CA | C | 19 | a0002c0002t0003g0035 a0002c0002t0003g0217 a0002c0002t0003g0218 others(16): Show |
22 | HG00621.hp2 HG00733.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.54-2171delT | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698214 | |||||||
| chr1:32698214 | CAA | C | 23 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0016 others(20): Show |
33 | HG00423.hp2 HG00544.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.54-2172_54-2171del others(2): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698214 | |||||||
| chr1:32698214 | CAAAA | C | 18 | a0001c0001t0001g0023 a0001c0001t0001g0066 a0001c0001t0001g0118 others(15): Show |
19 | HG00099.hp1 HG00280.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.54-2174_54-2171del others(4): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698214 | |||||||
| chr1:32698214 | CAAAAA | C | 175 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.54-2175_54-2171del others(5): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698214 | |||||||
| chr1:32698241 | G | A | 2 | a0001c0001t0004g0229 a0001c0001t0004g0239 |
2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.54-2197C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698241 | |||||||
| chr1:32698257 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.54-2213C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698257 | |||||||
| chr1:32698293 | C | T | 1 | a0001c0001t0017g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.54-2249G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698293 | |||||||
| chr1:32698388 | G | A | 2 | a0005c0005t0007g0020 a0005c0005t0007g0047 |
3 | HG01109.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.54-2344C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698388 | |||||||
| chr1:32698691 | A | G | 1 | a0001c0001t0002g0199 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.54-2647T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698691 | |||||||
| chr1:32698706 | G | A | 4 | a0003c0003t0006g0040 a0003c0003t0006g0243 a0003c0003t0006g0244 others(1): Show |
5 | HG02083.hp1 NA18952.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-2662C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698706 | |||||||
| chr1:32698783 | C | CT | 8 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(5): Show |
9 | HG01934.hp1 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.54-2740dupA | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698783 | |||||||
| chr1:32698783 | CT | C | 14 | a0003c0003t0006g0040 a0003c0003t0006g0243 a0003c0003t0006g0244 others(11): Show |
16 | HG01109.hp2 HG02083.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.54-2740delA | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698783 | |||||||
| chr1:32698843 | T | C | 1 | a0003c0003t0008g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.54-2799A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698843 | |||||||
| chr1:32698933 | G | A | 2 | a0003c0003t0010g0048 a0003c0003t0010g0049 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.54-2889C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698933 | |||||||
| chr1:32698942 | G | A | 3 | a0005c0005t0007g0020 a0005c0005t0007g0047 a0005c0005t0007g0197 |
4 | HG01109.hp2 HG02809.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-2898C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698942 | |||||||
| chr1:32698947 | T | C | 7 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0062 others(4): Show |
9 | HG01934.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.54-2903A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32698947 | |||||||
| chr1:32699153 | C | CTT | 114 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0025 others(111): Show |
148 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.54-3111_54-3110dup others(2): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32699153 | |||||||
| chr1:32699153 | C | CTTT | 75 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(72): Show |
90 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.54-3112_54-3110dup others(3): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32699153 | |||||||
| chr1:32699153 | CT | C | 17 | a0002c0002t0003g0225 a0002c0002t0003g0226 a0002c0002t0003g0227 others(14): Show |
19 | HG00733.hp2 HG01109.hp2 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.54-3110delA | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32699153 | |||||||
| chr1:32699446 | C | T | 2 | a0003c0003t0010g0048 a0003c0003t0010g0049 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.53+3162G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32699446 | |||||||
| chr1:32699500 | C | T | 15 | a0003c0003t0006g0040 a0003c0003t0006g0243 a0003c0003t0006g0244 others(12): Show |
17 | HG00733.hp2 HG01109.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.53+3108G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32699500 | |||||||
| chr1:32699618 | C | T | 1 | a0003c0003t0008g0050 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.53+2990G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32699618 | |||||||
| chr1:32699636 | AAC | A | 15 | a0003c0003t0006g0040 a0003c0003t0006g0243 a0003c0003t0006g0244 others(12): Show |
17 | HG00733.hp2 HG01109.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.53+2970_53+2971del others(2): Show |
SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32699636 | |||||||
| chr1:32699687 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.53+2921G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32699687 | |||||||
| chr1:32699728 | CT | C | 232 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(229): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.53+2879delA | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32699728 | |||||||
| chr1:32699878 | G | A | 3 | a0005c0005t0007g0020 a0005c0005t0007g0047 a0005c0005t0007g0197 |
4 | HG01109.hp2 HG02809.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.53+2730C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32699878 | |||||||
| chr1:32699954 | G | A | 4 | a0003c0003t0006g0040 a0003c0003t0006g0243 a0003c0003t0006g0244 others(1): Show |
5 | HG02083.hp1 NA18952.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+2654C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32699954 | |||||||
| chr1:32699984 | G | A | 4 | a0001c0001t0004g0039 a0001c0001t0004g0230 a0001c0001t0004g0240 others(1): Show |
5 | HG01884.hp2 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+2624C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32699984 | |||||||
| chr1:32700051 | C | T | 1 | a0001c0001t0015g0064 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.53+2557G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32700051 | |||||||
| chr1:32700242 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.53+2366G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32700242 | |||||||
| chr1:32700318 | G | A | 10 | a0002c0002t0003g0014 a0002c0002t0003g0219 a0002c0002t0003g0220 others(7): Show |
12 | HG00423.hp2 HG00621.hp2 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.53+2290C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32700318 | |||||||
| chr1:32700477 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.53+2131G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32700477 | |||||||
| chr1:32700499 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.53+2109G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32700499 | |||||||
| chr1:32700506 | G | A | 2 | a0003c0003t0010g0048 a0003c0003t0010g0049 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.53+2102C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32700506 | |||||||
| chr1:32700557 | T | C | 3 | a0003c0003t0008g0050 a0003c0003t0008g0051 a0003c0003t0008g0052 |
3 | HG02451.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.53+2051A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32700557 | |||||||
| chr1:32700567 | T | C | 243 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.53+2041A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32700567 | |||||||
| chr1:32700855 | G | A | 195 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.53+1753C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32700855 | |||||||
| chr1:32700919 | C | CT | 10 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0060 others(7): Show |
11 | HG02040.hp1 HG02083.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.53+1688dupA | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32700919 | |||||||
| chr1:32700933 | G | T | 28 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0016 others(25): Show |
39 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.53+1675C>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32700933 | |||||||
| chr1:32701166 | C | T | 1 | a0001c0001t0002g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.53+1442G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32701166 | |||||||
| chr1:32701174 | C | T | 3 | a0001c0001t0002g0053 a0001c0001t0002g0055 a0007c0009t0002g0054 |
3 | HG01978.hp2 NA18987.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.53+1434G>A | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32701174 | |||||||
| chr1:32701286 | G | A | 194 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.53+1322C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32701286 | |||||||
| chr1:32701392 | T | G | 1 | a0001c0001t0001g0195 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.53+1216A>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32701392 | |||||||
| chr1:32701488 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.53+1120A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32701488 | |||||||
| chr1:32701516 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.53+1092T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32701516 | |||||||
| chr1:32701650 | T | C | 17 | a0001c0001t0004g0002 a0001c0001t0004g0036 a0001c0001t0004g0037 others(14): Show |
27 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.53+958A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32701650 | |||||||
| chr1:32701749 | G | A | 8 | a0001c0001t0002g0013 a0001c0001t0002g0198 a0001c0001t0002g0199 others(5): Show |
10 | HG02055.hp1 HG02257.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.53+859C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32701749 | |||||||
| chr1:32701853 | G | A | 2 | a0003c0003t0006g0040 a0003c0003t0006g0246 |
3 | NA18952.hp2 NA18993.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.53+755C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32701853 | |||||||
| chr1:32701903 | G | A | 27 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0034 others(24): Show |
37 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.53+705C>T | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32701903 | |||||||
| chr1:32701967 | A | G | 243 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.53+641T>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32701967 | |||||||
| chr1:32702098 | C | G | 1 | a0003c0003t0018g0247 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.53+510G>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32702098 | |||||||
| chr1:32702448 | A | C | 1 | a0003c0003t0014g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.53+160T>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32702448 | |||||||
| chr1:32702459 | T | C | 1 | a0001c0001t0004g0241 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.53+149A>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32702459 | |||||||
| chr1:32702497 | G | C | 18 | a0001c0001t0004g0002 a0001c0001t0004g0036 a0001c0001t0004g0037 others(15): Show |
28 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.53+111C>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32702497 | |||||||
| chr1:32702567 | T | G | 1 | a0001c0001t0002g0242 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.53+41A>C | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32702567 | |||||||
| chr1:32702584 | G | C | 5 | a0001c0001t0001g0245 a0003c0003t0006g0040 a0003c0003t0006g0243 others(2): Show |
6 | HG00408.hp2 HG02083.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+24C>G | SYNC | ENSG00000162520.15 | transcript | ENST00000409190.8 | protein_coding | 1/4 | chr1 | 32702584 |