Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8634 |
| ensemblid | ENSG00000137996.13 |
| hgncid | 17981 |
| symbol | RTCA |
| name | RNA 3'-terminal phosphate cyclase |
| refseq_nuc | NM_003729.4 |
| refseq_prot | NP_003720.1 |
| ensembl_nuc | ENST00000370128.9 |
| ensembl_prot | ENSP00000359146.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 100266216 |
| end | 100292769 |
| strand | + |
| ver | v1.2 |
| region | chr1:100266216-100292769 |
| region5000 | chr1:100261216-100297769 |
| regionname0 | RTCA_chr1_100266216_100292769 |
| regionname5000 | RTCA_chr1_100261216_100297769 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 366 | 291 | 85 | 51 | 111 | 12 | 30 | 74 | RTCA_chr1_100261216_100297769 | RTCA | MAGPR others(361): Show |
chr1 | 100261216 | 100297769 |
| a0002 | 0/0 | 366 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | MAGPR others(361): Show |
chr1 | 100261216 | 100297769 |
| a0003 | 0/0 | 366 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | MAGPR others(361): Show |
chr1 | 100261216 | 100297769 |
| a0004 | 0/0 | 366 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | MAGPR others(361): Show |
chr1 | 100261216 | 100297769 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1098 | 287 | 84 | 50 | 111 | 10 | 30 | RTCA_chr1_100261216_100297769 | RTCA | ATGGC others(1093): Show |
chr1 | 100261216 | 100297769 | ||
| a0001c0003 | 0/0 | 1098 | 2 | 0 | 1 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | ATGGC others(1093): Show |
chr1 | 100261216 | 100297769 | ||
| a0001c0005 | 0/0 | 1098 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | ATGGC others(1093): Show |
chr1 | 100261216 | 100297769 | ||
| a0001c0007 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | ATGGC others(1093): Show |
chr1 | 100261216 | 100297769 | ||
| a0002c0002 | 0/0 | 1098 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | ATGGC others(1093): Show |
chr1 | 100261216 | 100297769 | ||
| a0003c0006 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | ATGGC others(1093): Show |
chr1 | 100261216 | 100297769 | ||
| a0004c0004 | 0/0 | 1098 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | ATGGC others(1093): Show |
chr1 | 100261216 | 100297769 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2527 | 187 | 41 | 36 | 82 | 5 | 22 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0002 | 0/0 | 2527 | 35 | 17 | 6 | 8 | 2 | 2 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0003 | 1/0 | 2526 | 18 | 13 | 0 | 3 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2521): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0004 | 0/0 | 2526 | 14 | 2 | 0 | 9 | 0 | 3 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2521): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0005 | 0/0 | 2528 | 7 | 1 | 1 | 5 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2523): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0006 | 0/0 | 2527 | 6 | 0 | 4 | 0 | 2 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0007 | 0/0 | 2527 | 3 | 0 | 2 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0008 | 0/0 | 2527 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0009 | 0/0 | 2516 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2511): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0010 | 0/0 | 2544 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2539): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0011 | 0/0 | 2527 | 2 | 0 | 0 | 0 | 0 | 2 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0012 | 0/0 | 2527 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0013 | 0/0 | 2527 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0014 | 0/0 | 2527 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0015 | 0/0 | 2527 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0016 | 0/0 | 2527 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0017 | 0/0 | 2527 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| a0001c0001t0018 | 0/0 | 2544 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2539): Show |
chr1 | 100261216 | 100297769 |
| a0001c0003t0001 | 0/0 | 2527 | 2 | 0 | 1 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| a0001c0005t0001 | 0/0 | 2527 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| a0001c0007t0001 | 0/0 | 2527 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| a0002c0002t0001 | 0/0 | 2527 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| a0003c0006t0005 | 0/0 | 2528 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2523): Show |
chr1 | 100261216 | 100297769 |
| a0004c0004t0001 | 0/0 | 2527 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | AGTGT others(2522): Show |
chr1 | 100261216 | 100297769 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 1 | 6 | 5 | 0 | 2 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0002 | 0/0 | 13 | 0 | 3 | 7 | 0 | 3 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0003 | 0/0 | 9 | 4 | 1 | 4 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0005 | 0/0 | 6 | 1 | 3 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0012 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0008 | 0/0 | 6 | 3 | 2 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0009 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0005g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0006g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0006g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0008g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0008g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0010g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0011g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0012g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0013g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0014g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0015g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0016g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0017g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0018g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0005t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0007t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0002c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0003c0006t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0004c0004t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0005 | t0001 | g0001 | EUR | GBR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | GBR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | FIN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | FIN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0058 | EUR | FIN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0178 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0034 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01074 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0034 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01261 | hp2 | a0001 | c0001 | t0015 | g0006 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0016 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0016 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01515 | hp2 | a0001 | c0001 | t0007 | g0108 | EUR | IBS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0041 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02015 | hp1 | a0003 | c0006 | t0005 | g0005 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CDX | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | CDX | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02280 | hp1 | a0001 | c0001 | t0013 | g0057 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02293 | hp1 | a0004 | c0004 | t0001 | g0002 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02572 | hp2 | a0001 | c0001 | t0018 | g0164 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0162 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0136 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0107 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0029 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0159 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0041 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0163 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03490 | hp1 | a0001 | c0001 | t0011 | g0009 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03492 | hp2 | a0001 | c0001 | t0011 | g0009 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | BEB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0140 | SAS | BEB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0039 | SAS | STU | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | STU | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0142 | SAS | STU | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18522 | hp1 | a0001 | c0007 | t0001 | g0055 | AFR | YRI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | CHB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | CHB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18747 | hp1 | a0001 | c0001 | t0014 | g0003 | EAS | CHB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | YRI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18939 | hp2 | a0001 | c0001 | t0017 | g0091 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18995 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0056 | AFR | LWK | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | LWK | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19067 | hp2 | a0001 | c0001 | t0016 | g0011 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19072 | hp1 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | YRI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ASW | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ASW | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0016 | EUR | TSI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0177 | EUR | TSI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0165 | EUR | TSI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | GIH | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01123 | hp1 | a0001 | c0001 | t0007 | g0065 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0095 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | USA | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | USA | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | USA | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0089 | REF | REF | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0133 | REF | REF | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:100266412 | A | G | 1 | a0002 | 3 | HG02258.hp1 HG02559.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.37A>G | p.Met13Val | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 1/11 | 197/2526 | 37/1101 | 13/366 | chr1 | 100266412 | |||
| chr1:100266569 | G | A | 1 | a0004 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.91G>A | p.Gly31Ser | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/11 | 251/2526 | 91/1101 | 31/366 | chr1 | 100266569 | |||
| chr1:100287174 | G | A | 1 | a0003 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.970G>A | p.Ala324Thr | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/11 | 1130/2526 | 970/1101 | 324/366 | chr1 | 100287174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:100270665 | C | T | 1 | a0001c0003 | 2 | HG00738.hp2 NA20752.hp2 |
synonymous_variant | LOW | c.399C>T | p.Ile133Ile | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/11 | 559/2526 | 399/1101 | 133/366 | chr1 | 100270665 | |||
| chr1:100274929 | T | C | 1 | a0001c0005 | 1 | HG00140.hp1 | synonymous_variant | LOW | c.579T>C | p.Tyr193Tyr | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 6/11 | 739/2526 | 579/1101 | 193/366 | chr1 | 100274929 | |||
| chr1:100287176 | G | A | 1 | a0001c0007 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.972G>A | p.Ala324Ala | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/11 | 1132/2526 | 972/1101 | 324/366 | chr1 | 100287176 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:100266248 | C | T | 1 | a0001c0001t0018 | 1 | HG02572.hp2 | 5_prime_UTR_variant | MODIFIER | c.-128C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 1/11 | 128 | chr1 | 100266248 | ||||||
| chr1:100266259 | C | A | 1 | a0001c0001t0012 | 1 | NA18995.hp1 | 5_prime_UTR_variant | MODIFIER | c.-117C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 1/11 | 117 | chr1 | 100266259 | ||||||
| chr1:100266263 | C | CA | 17 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(14): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
5_prime_UTR_variant | MODIFIER | c.-113_-112insA | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 1/11 | 112 | chr1 | 100266263 | ||||||
| chr1:100266264 | G | A | 17 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(14): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
5_prime_UTR_variant | MODIFIER | c.-112G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 1/11 | 112 | chr1 | 100266264 | ||||||
| chr1:100291620 | T | G | 1 | a0001c0001t0007 | 3 | HG01074.hp1 HG01123.hp1 HG01515.hp2 |
3_prime_UTR_variant | MODIFIER | c.*116T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 116 | chr1 | 100291620 | ||||||
| chr1:100291863 | T | C | 1 | a0001c0001t0013 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*359T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 359 | chr1 | 100291863 | ||||||
| chr1:100291912 | A | T | 1 | a0001c0001t0017 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*408A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 408 | chr1 | 100291912 | ||||||
| chr1:100291929 | C | CT | 4 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0011 others(1): Show |
45 | HG00140.hp2 HG00597.hp1 HG00642.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*443dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 444 | INFO_REALIGN_3_PRIME | chr1 | 100291929 | |||||
| chr1:100291929 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0009 | 3 | HG02622.hp1 HG02723.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*434_*443delTTTTTT others(4): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 434 | INFO_REALIGN_3_PRIME | chr1 | 100291929 | |||||
| chr1:100291959 | G | C | 1 | a0001c0001t0014 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*455G>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 455 | chr1 | 100291959 | ||||||
| chr1:100292068 | C | T | 1 | a0001c0001t0004 | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*564C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 564 | chr1 | 100292068 | ||||||
| chr1:100292197 | C | T | 1 | a0001c0001t0016 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*693C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 693 | chr1 | 100292197 | ||||||
| chr1:100292198 | G | A | 2 | a0001c0001t0008 a0001c0001t0011 |
5 | HG02630.hp2 HG02647.hp1 HG03490.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*694G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 694 | chr1 | 100292198 | ||||||
| chr1:100292207 | T | C | 18 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(15): Show |
234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*703T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 703 | chr1 | 100292207 | ||||||
| chr1:100292213 | C | T | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*709C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 709 | chr1 | 100292213 | ||||||
| chr1:100292268 | C | T | 1 | a0001c0001t0006 | 6 | HG00323.hp2 HG01070.hp2 HG01099.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*764C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 764 | chr1 | 100292268 | ||||||
| chr1:100292427 | C | T | 1 | a0001c0001t0004 | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*923C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 923 | chr1 | 100292427 | ||||||
| chr1:100292543 | C | T | 1 | a0001c0001t0004 | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1039C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 1039 | chr1 | 100292543 | ||||||
| chr1:100292599 | T | C | 18 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(15): Show |
234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*1095T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 1095 | chr1 | 100292599 | ||||||
| chr1:100292641 | T | TATGTTTT others(11): Show |
2 | a0001c0001t0010 a0001c0001t0018 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1139_*1156dupTGTT others(14): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 1157 | INFO_REALIGN_3_PRIME | chr1 | 100292641 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:100266670 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.146+46G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100266670 | |||||||
| chr1:100266766 | T | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.146+142T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100266766 | |||||||
| chr1:100266848 | A | G | 2 | a0001c0003t0001g0177 a0001c0003t0001g0178 |
2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.146+224A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100266848 | |||||||
| chr1:100266877 | G | A | 1 | a0001c0001t0003g0045 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.146+253G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100266877 | |||||||
| chr1:100266894 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.146+270T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100266894 | |||||||
| chr1:100266947 | A | G | 5 | a0001c0001t0003g0013 a0001c0001t0003g0173 a0001c0001t0003g0174 others(2): Show |
8 | HG02257.hp2 HG02486.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.146+323A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100266947 | |||||||
| chr1:100266964 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.146+340T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100266964 | |||||||
| chr1:100266970 | C | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.146+346C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100266970 | |||||||
| chr1:100267045 | A | C | 11 | a0001c0001t0002g0009 a0001c0001t0002g0165 a0001c0001t0002g0166 others(8): Show |
14 | HG00597.hp1 HG01257.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.146+421A>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100267045 | |||||||
| chr1:100267125 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.146+501A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100267125 | |||||||
| chr1:100267141 | G | T | 7 | a0001c0001t0003g0013 a0001c0001t0003g0173 a0001c0001t0003g0174 others(4): Show |
11 | HG01891.hp1 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.146+517G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100267141 | |||||||
| chr1:100267299 | T | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
5 | HG00323.hp2 HG01928.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.146+675T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100267299 | |||||||
| chr1:100267460 | CAG | C | 12 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(9): Show |
14 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.147-689_147-688del others(2): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 100267460 | ||||||
| chr1:100267651 | G | GT | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.147-487dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 100267651 | ||||||
| chr1:100267651 | G | GTT | 8 | a0001c0001t0001g0037 a0001c0001t0001g0132 a0001c0001t0002g0160 others(5): Show |
9 | HG02055.hp1 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.147-488_147-487dup others(2): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 100267651 | ||||||
| chr1:100267709 | A | G | 5 | a0001c0001t0003g0013 a0001c0001t0003g0173 a0001c0001t0003g0174 others(2): Show |
8 | HG02257.hp2 HG02486.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.147-443A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100267709 | |||||||
| chr1:100267725 | G | T | 2 | a0001c0001t0004g0156 a0001c0001t0004g0157 |
2 | NA18969.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.147-427G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100267725 | |||||||
| chr1:100267779 | A | G | 6 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(3): Show |
6 | HG00438.hp1 HG00609.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.147-373A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100267779 | |||||||
| chr1:100267996 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.147-156T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100267996 | |||||||
| chr1:100268328 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.290+33C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100268328 | |||||||
| chr1:100268403 | G | GT | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
129 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.290+120dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 100268403 | ||||||
| chr1:100268571 | T | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
5 | HG02055.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+276T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100268571 | |||||||
| chr1:100268615 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0007t0001g0055 |
3 | HG03486.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.290+320G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100268615 | |||||||
| chr1:100268810 | G | C | 1 | a0001c0001t0003g0173 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.290+515G>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100268810 | |||||||
| chr1:100268913 | G | T | 1 | a0001c0001t0001g0088 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.290+618G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100268913 | |||||||
| chr1:100268927 | G | A | 17 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0043 others(14): Show |
22 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.290+632G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100268927 | |||||||
| chr1:100269005 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.290+710A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269005 | |||||||
| chr1:100269048 | T | C | 1 | a0001c0001t0008g0029 | 2 | HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.290+753T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269048 | |||||||
| chr1:100269049 | A | ATG | 15 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(12): Show |
17 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.290+755_290+756ins others(2): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 100269049 | ||||||
| chr1:100269052 | A | T | 1 | a0001c0001t0001g0086 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.290+757A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269052 | |||||||
| chr1:100269191 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.290+896C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269191 | |||||||
| chr1:100269222 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.290+927G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269222 | |||||||
| chr1:100269328 | C | T | 12 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0019 others(9): Show |
21 | HG00140.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.290+1033C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269328 | |||||||
| chr1:100269337 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
9 | HG00639.hp1 HG01255.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.290+1042C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269337 | |||||||
| chr1:100269362 | TC | T | 2 | a0001c0001t0005g0036 a0001c0001t0005g0122 |
3 | NA18612.hp2 NA18956.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.290+1068delC | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269362 | |||||||
| chr1:100269363 | C | CT | 16 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0147 others(13): Show |
20 | HG00597.hp1 HG01257.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.290+1086dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 100269363 | ||||||
| chr1:100269363 | CT | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.290+1086delT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 100269363 | ||||||
| chr1:100269364 | T | G | 2 | a0001c0001t0005g0036 a0001c0001t0005g0122 |
3 | NA18612.hp2 NA18956.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.290+1069T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269364 | |||||||
| chr1:100269400 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.290+1105G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269400 | |||||||
| chr1:100269739 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.291-818C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269739 | |||||||
| chr1:100269843 | T | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.291-714T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269843 | |||||||
| chr1:100269875 | C | G | 3 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0003g0153 |
3 | HG02809.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.291-682C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269875 | |||||||
| chr1:100269983 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.291-574A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269983 | |||||||
| chr1:100270035 | C | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.291-522C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100270035 | |||||||
| chr1:100270180 | G | T | 15 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(12): Show |
17 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.291-377G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100270180 | |||||||
| chr1:100270200 | TGAA | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.291-352_291-350del others(3): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 100270200 | ||||||
| chr1:100270208 | G | A | 4 | a0001c0001t0003g0045 a0001c0001t0003g0136 a0001c0001t0003g0137 others(1): Show |
4 | HG02622.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.291-349G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100270208 | |||||||
| chr1:100270320 | T | G | 1 | a0001c0001t0002g0147 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.291-237T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100270320 | |||||||
| chr1:100270347 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.291-210A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100270347 | |||||||
| chr1:100270352 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.291-205G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100270352 | |||||||
| chr1:100270696 | G | C | 1 | a0001c0001t0002g0018 | 3 | HG02257.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.414+16G>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100270696 | |||||||
| chr1:100270815 | C | CT | 13 | a0001c0001t0001g0131 a0001c0001t0004g0039 a0001c0001t0004g0040 others(10): Show |
15 | HG00609.hp1 HG02109.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.414+146dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 100270815 | ||||||
| chr1:100270821 | T | A | 1 | a0001c0001t0002g0165 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.414+141T>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100270821 | |||||||
| chr1:100270932 | C | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.414+252C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100270932 | |||||||
| chr1:100270961 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.414+281T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100270961 | |||||||
| chr1:100271041 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG00408.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.414+361C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271041 | |||||||
| chr1:100271131 | T | C | 2 | a0001c0003t0001g0177 a0001c0003t0001g0178 |
2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.414+451T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271131 | |||||||
| chr1:100271215 | A | G | 1 | a0001c0001t0002g0165 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.414+535A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271215 | |||||||
| chr1:100271275 | C | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0031 |
5 | HG02451.hp1 HG02486.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+595C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271275 | |||||||
| chr1:100271287 | AT | A | 4 | a0001c0001t0003g0045 a0001c0001t0003g0136 a0001c0001t0003g0137 others(1): Show |
4 | HG02622.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+608delT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271287 | |||||||
| chr1:100271561 | A | T | 1 | a0001c0001t0002g0170 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.414+881A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271561 | |||||||
| chr1:100271576 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02129.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.414+896A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271576 | |||||||
| chr1:100271614 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.414+934A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271614 | |||||||
| chr1:100271632 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.414+952G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271632 | |||||||
| chr1:100271637 | C | T | 2 | a0001c0001t0002g0160 a0001c0001t0002g0161 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.414+957C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271637 | |||||||
| chr1:100271672 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.414+992C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271672 | |||||||
| chr1:100271856 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.414+1176C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271856 | |||||||
| chr1:100272226 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.415-1168C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100272226 | |||||||
| chr1:100272565 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.415-829G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100272565 | |||||||
| chr1:100272572 | T | C | 1 | a0001c0003t0001g0177 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.415-822T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100272572 | |||||||
| chr1:100272642 | T | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.415-752T>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100272642 | |||||||
| chr1:100272676 | A | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0007t0001g0055 |
3 | HG03486.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.415-718A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100272676 | |||||||
| chr1:100272894 | G | A | 1 | a0001c0001t0017g0091 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.415-500G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100272894 | |||||||
| chr1:100273083 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.415-311A>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100273083 | |||||||
| chr1:100273117 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.415-277C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100273117 | |||||||
| chr1:100273167 | G | A | 5 | a0001c0001t0003g0013 a0001c0001t0003g0173 a0001c0001t0003g0174 others(2): Show |
8 | HG02257.hp2 HG02486.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-227G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100273167 | |||||||
| chr1:100273228 | T | C | 1 | a0001c0001t0009g0162 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.415-166T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100273228 | |||||||
| chr1:100273317 | G | A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
10 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.415-77G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100273317 | |||||||
| chr1:100273639 | C | T | 5 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(2): Show |
5 | HG00597.hp1 HG02071.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+187C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100273639 | |||||||
| chr1:100273973 | C | T | 12 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0139 others(9): Show |
14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.473+521C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100273973 | |||||||
| chr1:100273990 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.473+538C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100273990 | |||||||
| chr1:100274090 | C | G | 11 | a0001c0001t0002g0009 a0001c0001t0002g0165 a0001c0001t0002g0166 others(8): Show |
14 | HG00597.hp1 HG01257.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.473+638C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274090 | |||||||
| chr1:100274169 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.474-655A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274169 | |||||||
| chr1:100274251 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.474-573T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274251 | |||||||
| chr1:100274277 | C | A | 1 | a0001c0001t0001g0092 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.474-547C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274277 | |||||||
| chr1:100274278 | G | A | 2 | a0001c0001t0010g0041 a0001c0001t0018g0164 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.474-546G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274278 | |||||||
| chr1:100274508 | A | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.474-316A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274508 | |||||||
| chr1:100274524 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.474-300T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274524 | |||||||
| chr1:100274649 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.474-175C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274649 | |||||||
| chr1:100274741 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.474-83T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274741 | |||||||
| chr1:100274976 | T | C | 1 | a0001c0001t0007g0065 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.615+11T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 6/10 | chr1 | 100274976 | |||||||
| chr1:100275050 | GAACTT | G | 12 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0019 others(9): Show |
21 | HG00140.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.615+89_615+93delTT others(3): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 100275050 | ||||||
| chr1:100275104 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG00280.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.615+139C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 6/10 | chr1 | 100275104 | |||||||
| chr1:100275138 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.615+173G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 6/10 | chr1 | 100275138 | |||||||
| chr1:100275228 | C | G | 2 | a0001c0001t0010g0041 a0001c0001t0018g0164 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.615+263C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 6/10 | chr1 | 100275228 | |||||||
| chr1:100275310 | A | G | 2 | a0001c0001t0004g0145 a0001c0001t0004g0146 |
2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.616-289A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 6/10 | chr1 | 100275310 | |||||||
| chr1:100275391 | AATATATG others(1): Show |
A | 12 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0139 others(9): Show |
14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.616-205_616-198del others(8): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 100275391 | ||||||
| chr1:100275867 | G | A | 2 | a0001c0001t0002g0160 a0001c0001t0002g0161 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.740+144G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100275867 | |||||||
| chr1:100275980 | C | T | 1 | a0001c0001t0003g0173 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.740+257C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100275980 | |||||||
| chr1:100276037 | G | A | 2 | a0001c0001t0009g0162 a0001c0001t0009g0163 |
2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.740+314G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276037 | |||||||
| chr1:100276231 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG02572.hp1 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.740+508T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276231 | |||||||
| chr1:100276352 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.740+629G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276352 | |||||||
| chr1:100276417 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.740+694A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276417 | |||||||
| chr1:100276432 | A | G | 1 | a0001c0001t0001g0026 | 2 | HG00280.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.740+709A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276432 | |||||||
| chr1:100276478 | A | G | 11 | a0001c0001t0002g0009 a0001c0001t0002g0165 a0001c0001t0002g0166 others(8): Show |
14 | HG00597.hp1 HG01257.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.740+755A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276478 | |||||||
| chr1:100276609 | G | A | 5 | a0001c0001t0003g0013 a0001c0001t0003g0173 a0001c0001t0003g0174 others(2): Show |
8 | HG02257.hp2 HG02486.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.741-649G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276609 | |||||||
| chr1:100276648 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG04184.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.741-610G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276648 | |||||||
| chr1:100276843 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.741-415C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276843 | |||||||
| chr1:100276866 | C | G | 5 | a0001c0001t0001g0027 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
6 | HG00408.hp1 HG00597.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.741-392C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276866 | |||||||
| chr1:100276937 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.741-321A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276937 | |||||||
| chr1:100277114 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.741-144A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100277114 | |||||||
| chr1:100277436 | T | C | 1 | a0001c0003t0001g0178 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.799+120T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100277436 | |||||||
| chr1:100277522 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.799+206A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100277522 | |||||||
| chr1:100277659 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0052 |
3 | HG02055.hp2 HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.799+343A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100277659 | |||||||
| chr1:100277802 | T | G | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0005g0095 |
3 | HG02559.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.799+486T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100277802 | |||||||
| chr1:100277802 | T | TG | 22 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0052 others(19): Show |
31 | HG00738.hp2 HG01257.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.799+495dupG | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100277802 | ||||||
| chr1:100277828 | CT | C | 2 | a0001c0001t0003g0013 a0001c0001t0003g0174 |
5 | HG02486.hp1 HG03579.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.799+513delT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100277828 | |||||||
| chr1:100278044 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.799+728C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100278044 | |||||||
| chr1:100278549 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.799+1233T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100278549 | |||||||
| chr1:100278864 | C | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.799+1548C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100278864 | |||||||
| chr1:100278898 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.799+1582C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100278898 | |||||||
| chr1:100278899 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.799+1583G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100278899 | |||||||
| chr1:100279094 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.799+1778A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279094 | |||||||
| chr1:100279242 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.799+1926G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279242 | |||||||
| chr1:100279326 | T | C | 7 | a0001c0001t0003g0013 a0001c0001t0003g0173 a0001c0001t0003g0174 others(4): Show |
11 | HG01891.hp1 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.799+2010T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279326 | |||||||
| chr1:100279591 | A | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0134 a0001c0001t0002g0135 |
4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.799+2275A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279591 | |||||||
| chr1:100279614 | A | AT | 23 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(20): Show |
43 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.799+2311dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100279614 | ||||||
| chr1:100279614 | A | T | 1 | a0001c0001t0002g0135 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.799+2298A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279614 | |||||||
| chr1:100279675 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.799+2359A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279675 | |||||||
| chr1:100279729 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.799+2413A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279729 | |||||||
| chr1:100279752 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.799+2436T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279752 | |||||||
| chr1:100279873 | C | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0037 others(7): Show |
22 | HG00438.hp2 HG00735.hp1 HG02717.hp2 others(19): Show |
intron_variant | MODIFIER | c.799+2557C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279873 | |||||||
| chr1:100279933 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.799+2617T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279933 | |||||||
| chr1:100280083 | A | G | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0084 |
3 | HG02280.hp2 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.799+2767A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280083 | |||||||
| chr1:100280095 | A | G | 5 | a0001c0001t0003g0013 a0001c0001t0003g0173 a0001c0001t0003g0174 others(2): Show |
8 | HG02257.hp2 HG02486.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.799+2779A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280095 | |||||||
| chr1:100280218 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.799+2902C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280218 | |||||||
| chr1:100280236 | G | T | 1 | a0001c0001t0003g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.799+2920G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280236 | |||||||
| chr1:100280400 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.799+3084G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280400 | |||||||
| chr1:100280500 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.799+3184A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280500 | |||||||
| chr1:100280510 | T | A | 15 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(12): Show |
17 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.799+3194T>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280510 | |||||||
| chr1:100280603 | T | G | 25 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(22): Show |
45 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.799+3287T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280603 | |||||||
| chr1:100280736 | G | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.799+3420G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280736 | |||||||
| chr1:100280823 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.799+3507G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280823 | |||||||
| chr1:100281167 | G | C | 1 | a0001c0001t0002g0138 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.799+3851G>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100281167 | |||||||
| chr1:100281322 | TAGAG | T | 12 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(9): Show |
14 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.800-3903_800-3900d others(6): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100281322 | ||||||
| chr1:100281516 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.800-3712G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100281516 | |||||||
| chr1:100281635 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.800-3593A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100281635 | |||||||
| chr1:100281871 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.800-3357C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100281871 | |||||||
| chr1:100282362 | T | G | 2 | a0001c0001t0002g0018 a0001c0001t0002g0148 |
4 | HG01109.hp1 HG02257.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.800-2866T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100282362 | |||||||
| chr1:100282569 | A | T | 32 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(29): Show |
45 | HG00140.hp2 HG00597.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.800-2659A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100282569 | |||||||
| chr1:100282578 | G | T | 1 | a0001c0001t0002g0169 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.800-2650G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100282578 | |||||||
| chr1:100282658 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.800-2570A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100282658 | |||||||
| chr1:100282727 | C | CA | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.800-2497dupA | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100282727 | ||||||
| chr1:100282956 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0134 a0001c0001t0002g0135 |
4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-2272G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100282956 | |||||||
| chr1:100283077 | G | A | 11 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0139 others(8): Show |
13 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(10): Show |
intron_variant | MODIFIER | c.800-2151G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283077 | |||||||
| chr1:100283160 | C | CT | 26 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0002g0008 others(23): Show |
39 | HG00140.hp2 HG00597.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.800-2045dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283160 | ||||||
| chr1:100283160 | CT | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(107): Show |
191 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.800-2045delT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283160 | ||||||
| chr1:100283160 | CTT | C | 21 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0046 others(18): Show |
25 | HG00323.hp2 HG00609.hp1 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.800-2046_800-2045d others(4): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283160 | ||||||
| chr1:100283203 | A | G | 1 | a0001c0001t0008g0107 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.800-2025A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283203 | |||||||
| chr1:100283234 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.800-1994G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283234 | |||||||
| chr1:100283237 | C | T | 2 | a0001c0001t0002g0160 a0001c0001t0002g0161 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.800-1991C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283237 | |||||||
| chr1:100283239 | C | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.800-1989C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283239 | |||||||
| chr1:100283352 | G | A | 11 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0139 others(8): Show |
13 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(10): Show |
intron_variant | MODIFIER | c.800-1876G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283352 | |||||||
| chr1:100283437 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.800-1791T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283437 | |||||||
| chr1:100283572 | G | C | 1 | a0001c0001t0001g0114 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.800-1656G>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283572 | |||||||
| chr1:100283633 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.800-1595A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283633 | |||||||
| chr1:100283827 | C | A | 12 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0139 others(9): Show |
14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.800-1401C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283827 | |||||||
| chr1:100283931 | AAAAGAAA others(12): Show |
A | 10 | a0001c0001t0004g0039 a0001c0001t0004g0139 a0001c0001t0004g0140 others(7): Show |
11 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(8): Show |
intron_variant | MODIFIER | c.800-1293_800-1275d others(21): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283931 | ||||||
| chr1:100283932 | AAAGAAAA others(11): Show |
A | 2 | a0001c0001t0004g0040 a0001c0001t0004g0144 |
2 | NA18969.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.800-1293_800-1276d others(20): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283932 | ||||||
| chr1:100283933 | AAGAAAAA others(10): Show |
A | 1 | a0001c0001t0004g0040 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.800-1293_800-1277d others(19): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283933 | ||||||
| chr1:100283935 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.800-1293G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283935 | |||||||
| chr1:100283935 | G | GA | 5 | a0001c0001t0003g0013 a0001c0001t0003g0173 a0001c0001t0003g0174 others(2): Show |
8 | HG02257.hp2 HG02486.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.800-1279dupA | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283935 | ||||||
| chr1:100283935 | G | GAA | 28 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(25): Show |
40 | HG00140.hp2 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.800-1280_800-1279d others(4): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283935 | ||||||
| chr1:100283935 | G | GAAA | 7 | a0001c0001t0002g0019 a0001c0001t0002g0135 a0001c0001t0002g0160 others(4): Show |
7 | HG00642.hp2 HG02055.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.800-1281_800-1279d others(5): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283935 | ||||||
| chr1:100283943 | AAAAAAAG others(7): Show |
A | 1 | a0001c0001t0001g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.800-1282_800-1269d others(16): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283943 | ||||||
| chr1:100283944 | AAAAAAGA others(6): Show |
A | 14 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(11): Show |
15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.800-1281_800-1269d others(15): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283944 | ||||||
| chr1:100283945 | AAAAAGAA others(5): Show |
A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0052 a0001c0003t0001g0178 others(1): Show |
4 | HG00323.hp1 HG00738.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-1280_800-1269d others(14): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283945 | ||||||
| chr1:100283946 | AAAAGAAA others(4): Show |
A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
159 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.800-1279_800-1269d others(13): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283946 | ||||||
| chr1:100283947 | AAAGAAAA others(3): Show |
A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(33): Show |
38 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.800-1262_800-1253d others(12): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283947 | ||||||
| chr1:100283949 | AGAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0035 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.800-1278_800-1268d others(13): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283949 | |||||||
| chr1:100283957 | C | A | 12 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0139 others(9): Show |
14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.800-1271C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283957 | |||||||
| chr1:100283999 | C | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0052 |
3 | HG02055.hp2 HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.800-1229C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283999 | |||||||
| chr1:100284350 | C | CT | 13 | a0001c0001t0001g0075 a0001c0001t0004g0039 a0001c0001t0004g0040 others(10): Show |
15 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(12): Show |
intron_variant | MODIFIER | c.800-871dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100284350 | ||||||
| chr1:100284397 | A | AT | 29 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0035 others(26): Show |
50 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.800-815dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100284397 | ||||||
| chr1:100284467 | C | A | 1 | a0001c0001t0001g0097 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.800-761C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100284467 | |||||||
| chr1:100284699 | C | A | 12 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0139 others(9): Show |
14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.800-529C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100284699 | |||||||
| chr1:100284747 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.800-481T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100284747 | |||||||
| chr1:100284814 | C | G | 2 | a0001c0001t0006g0016 a0001c0001t0006g0034 |
5 | HG01070.hp2 HG01099.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-414C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100284814 | |||||||
| chr1:100284890 | G | A | 1 | a0001c0001t0003g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.800-338G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100284890 | |||||||
| chr1:100284998 | A | G | 15 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(12): Show |
17 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.800-230A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100284998 | |||||||
| chr1:100285177 | AGTTTT | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.800-25_800-21delGT others(3): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100285177 | ||||||
| chr1:100285177 | AGTTTTGT others(3): Show |
A | 1 | a0001c0001t0001g0050 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.800-30_800-21delGT others(8): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100285177 | ||||||
| chr1:100285387 | A | T | 12 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0139 others(9): Show |
14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.894+65A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285387 | |||||||
| chr1:100285428 | C | T | 7 | a0001c0001t0003g0013 a0001c0001t0003g0173 a0001c0001t0003g0174 others(4): Show |
11 | HG01891.hp1 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.894+106C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285428 | |||||||
| chr1:100285499 | G | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.894+177G>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285499 | |||||||
| chr1:100285505 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.894+183A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285505 | |||||||
| chr1:100285516 | C | G | 1 | a0001c0001t0004g0142 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.894+194C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285516 | |||||||
| chr1:100285517 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.894+195G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285517 | |||||||
| chr1:100285556 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.894+234C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285556 | |||||||
| chr1:100285705 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.894+383G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285705 | |||||||
| chr1:100285720 | A | G | 1 | a0001c0001t0004g0141 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.894+398A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285720 | |||||||
| chr1:100285723 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.894+401G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285723 | |||||||
| chr1:100286002 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0006g0016 a0001c0001t0006g0034 |
7 | HG00323.hp1 HG01070.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.894+680C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286002 | |||||||
| chr1:100286249 | G | A | 15 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(12): Show |
17 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.895-850G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286249 | |||||||
| chr1:100286315 | G | A | 12 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0139 others(9): Show |
14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.895-784G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286315 | |||||||
| chr1:100286315 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.895-784G>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286315 | |||||||
| chr1:100286322 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.895-777C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286322 | |||||||
| chr1:100286346 | C | T | 2 | a0001c0003t0001g0177 a0001c0003t0001g0178 |
2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.895-753C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286346 | |||||||
| chr1:100286352 | G | T | 12 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0139 others(9): Show |
14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.895-747G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286352 | |||||||
| chr1:100286386 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.895-713G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286386 | |||||||
| chr1:100286450 | G | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0084 |
3 | HG02280.hp2 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.895-649G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286450 | |||||||
| chr1:100286454 | C | CA | 66 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(63): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.895-623dupA | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 100286454 | ||||||
| chr1:100286454 | C | CAA | 15 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0052 others(12): Show |
18 | HG00642.hp2 HG01109.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.895-624_895-623dup others(2): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 100286454 | ||||||
| chr1:100286484 | C | CA | 4 | a0001c0001t0003g0013 a0001c0001t0003g0173 a0001c0001t0003g0174 others(1): Show |
7 | HG02257.hp2 HG02486.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.895-607dupA | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 100286484 | ||||||
| chr1:100286876 | A | G | 12 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0139 others(9): Show |
14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.895-223A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286876 | |||||||
| chr1:100287018 | T | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0007t0001g0055 |
3 | HG03486.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.895-81T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100287018 | |||||||
| chr1:100287385 | G | A | 11 | a0001c0001t0002g0009 a0001c0001t0002g0165 a0001c0001t0002g0166 others(8): Show |
14 | HG00597.hp1 HG01257.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.999+182G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100287385 | |||||||
| chr1:100287435 | A | T | 1 | a0001c0001t0003g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.999+232A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100287435 | |||||||
| chr1:100287436 | T | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.999+233T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100287436 | |||||||
| chr1:100287586 | A | T | 15 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(12): Show |
17 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.999+383A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100287586 | |||||||
| chr1:100287642 | CATTTT | C | 12 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0139 others(9): Show |
14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.999+445_999+449del others(5): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 100287642 | ||||||
| chr1:100287794 | CT | C | 50 | a0001c0001t0001g0061 a0001c0001t0002g0008 a0001c0001t0002g0009 others(47): Show |
69 | HG00140.hp2 HG00597.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.999+608delT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 100287794 | ||||||
| chr1:100287794 | CTT | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.999+607_999+608del others(2): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 100287794 | ||||||
| chr1:100287825 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.999+622A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100287825 | |||||||
| chr1:100287859 | T | C | 1 | a0001c0001t0004g0143 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.999+656T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100287859 | |||||||
| chr1:100288049 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.999+846C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288049 | |||||||
| chr1:100288079 | C | T | 7 | a0001c0001t0003g0013 a0001c0001t0003g0173 a0001c0001t0003g0174 others(4): Show |
11 | HG01891.hp1 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.999+876C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288079 | |||||||
| chr1:100288171 | A | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0002c0002t0001g0021 others(1): Show |
5 | HG01891.hp2 HG02258.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.999+968A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288171 | |||||||
| chr1:100288245 | C | T | 2 | a0001c0001t0009g0162 a0001c0001t0009g0163 |
2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.999+1042C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288245 | |||||||
| chr1:100288285 | C | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.999+1082C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288285 | |||||||
| chr1:100288347 | A | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.999+1144A>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288347 | |||||||
| chr1:100288514 | C | T | 12 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0139 others(9): Show |
14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.999+1311C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288514 | |||||||
| chr1:100288534 | G | A | 6 | a0001c0001t0002g0009 a0001c0001t0002g0165 a0001c0001t0002g0166 others(3): Show |
9 | HG01257.hp1 HG01261.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.999+1331G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288534 | |||||||
| chr1:100288538 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.999+1335T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288538 | |||||||
| chr1:100288546 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG00438.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.999+1343C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288546 | |||||||
| chr1:100288634 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.999+1431T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288634 | |||||||
| chr1:100288640 | C | G | 12 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0139 others(9): Show |
14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.999+1437C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288640 | |||||||
| chr1:100288688 | G | A | 2 | a0001c0003t0001g0177 a0001c0003t0001g0178 |
2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.999+1485G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288688 | |||||||
| chr1:100288690 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.999+1487C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288690 | |||||||
| chr1:100288815 | TTTTTC | T | 3 | a0001c0001t0002g0038 a0001c0001t0002g0134 a0001c0001t0002g0135 |
4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.999+1622_999+1626d others(7): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 100288815 | ||||||
| chr1:100288825 | C | A | 3 | a0001c0001t0002g0169 a0001c0001t0002g0171 a0001c0001t0002g0172 |
3 | HG02071.hp1 HG02074.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.999+1622C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288825 | |||||||
| chr1:100288878 | A | G | 32 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0018 others(29): Show |
45 | HG00140.hp2 HG00597.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.999+1675A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288878 | |||||||
| chr1:100288926 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.999+1723A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288926 | |||||||
| chr1:100289027 | T | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.999+1824T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100289027 | |||||||
| chr1:100289104 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.999+1901A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100289104 | |||||||
| chr1:100289304 | T | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0046 a0001c0001t0001g0074 others(3): Show |
7 | HG00558.hp1 HG01255.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1000-2099T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100289304 | |||||||
| chr1:100289306 | G | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.1000-2097G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100289306 | |||||||
| chr1:100289308 | T | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.1000-2095T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100289308 | |||||||
| chr1:100289376 | C | T | 4 | a0001c0001t0003g0013 a0001c0001t0003g0173 a0001c0001t0003g0174 others(1): Show |
7 | HG02257.hp2 HG02486.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1000-2027C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100289376 | |||||||
| chr1:100289475 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1000-1928T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100289475 | |||||||
| chr1:100289946 | T | C | 15 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(12): Show |
17 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1000-1457T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100289946 | |||||||
| chr1:100290387 | C | T | 2 | a0001c0001t0004g0145 a0001c0001t0004g0146 |
2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1000-1016C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100290387 | |||||||
| chr1:100290523 | C | T | 7 | a0001c0001t0003g0013 a0001c0001t0003g0173 a0001c0001t0003g0174 others(4): Show |
11 | HG01891.hp1 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1000-880C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100290523 | |||||||
| chr1:100290670 | G | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0101 a0001c0001t0001g0109 |
3 | HG01167.hp1 HG01169.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1000-733G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100290670 | |||||||
| chr1:100290696 | G | A | 3 | a0001c0001t0009g0159 a0001c0001t0009g0162 a0001c0001t0009g0163 |
3 | HG02622.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1000-707G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100290696 | |||||||
| chr1:100290715 | G | T | 2 | a0001c0003t0001g0177 a0001c0003t0001g0178 |
2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1000-688G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100290715 | |||||||
| chr1:100290765 | C | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
5 | HG02055.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000-638C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100290765 | |||||||
| chr1:100291245 | ATTAAGTT | A | 12 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0139 others(9): Show |
14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.1000-156_1000-150d others(9): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 100291245 | ||||||
| chr1:100291249 | A | C | 2 | a0002c0002t0001g0021 a0002c0002t0001g0056 |
3 | HG02258.hp1 HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1000-154A>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100291249 | |||||||
| chr1:100291306 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1000-97G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100291306 | |||||||
| chr1:100291309 | C | A | 1 | a0001c0001t0002g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1000-94C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100291309 | |||||||
| chr1:100291328 | CT | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0076 a0001c0001t0005g0024 |
3 | HG00642.hp1 HG01255.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1000-74delT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100291328 | |||||||
| chr1:100291332 | A | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0134 a0001c0001t0002g0135 |
4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-71A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100291332 | |||||||
| chr1:100291371 | G | C | 1 | a0001c0001t0001g0037 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1000-32G>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100291371 |