Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23397 |
| ensemblid | ENSG00000121152.10 |
| hgncid | 1112 |
| symbol | NCAPH |
| name | non-SMC condensin I complex subunit H |
| refseq_nuc | NM_015341.5 |
| refseq_prot | NP_056156.2 |
| ensembl_nuc | ENST00000240423.9 |
| ensembl_prot | ENSP00000240423.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 96335766 |
| end | 96377091 |
| strand | + |
| ver | v1.2 |
| region | chr2:96335766-96377091 |
| region5000 | chr2:96330766-96382091 |
| regionname0 | NCAPH_chr2_96335766_96377091 |
| regionname5000 | NCAPH_chr2_96330766_96382091 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 741 | 204 | 61 | 35 | 91 | 7 | 8 | 64 | NCAPH_chr2_96330766_96382091 | NCAPH | MGPPG others(736): Show |
chr2 | 96330766 | 96382091 |
| a0002 | 0/0 | 741 | 142 | 24 | 25 | 66 | 3 | 24 | 58 | NCAPH_chr2_96330766_96382091 | NCAPH | MGPPG others(736): Show |
chr2 | 96330766 | 96382091 |
| a0003 | 0/0 | 741 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | MGPPG others(736): Show |
chr2 | 96330766 | 96382091 |
| a0004 | 0/0 | 741 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NCAPH_chr2_96330766_96382091 | NCAPH | MGPPG others(736): Show |
chr2 | 96330766 | 96382091 |
| a0005 | 0/0 | 741 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | MGPPG others(736): Show |
chr2 | 96330766 | 96382091 |
| a0006 | 0/0 | 741 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | MGPPG others(736): Show |
chr2 | 96330766 | 96382091 |
| a0007 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | MGPPG others(736): Show |
chr2 | 96330766 | 96382091 |
| a0008 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | MGPPG others(736): Show |
chr2 | 96330766 | 96382091 |
| a0009 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | MGPPG others(736): Show |
chr2 | 96330766 | 96382091 |
| a0010 | 0/0 | 741 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | MGPPG others(736): Show |
chr2 | 96330766 | 96382091 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2223 | 203 | 61 | 35 | 90 | 7 | 8 | NCAPH_chr2_96330766_96382091 | NCAPH | ATGGG others(2218): Show |
chr2 | 96330766 | 96382091 | ||
| a0001c0008 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | ATGGG others(2218): Show |
chr2 | 96330766 | 96382091 | ||
| a0002c0002 | 0/0 | 2223 | 101 | 2 | 20 | 54 | 3 | 22 | NCAPH_chr2_96330766_96382091 | NCAPH | ATGGG others(2218): Show |
chr2 | 96330766 | 96382091 | ||
| a0002c0003 | 0/0 | 2223 | 39 | 22 | 5 | 10 | 0 | 2 | NCAPH_chr2_96330766_96382091 | NCAPH | ATGGG others(2218): Show |
chr2 | 96330766 | 96382091 | ||
| a0002c0006 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | ATGGG others(2218): Show |
chr2 | 96330766 | 96382091 | ||
| a0002c0009 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | ATGGG others(2218): Show |
chr2 | 96330766 | 96382091 | ||
| a0003c0005 | 0/0 | 2223 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | ATGGG others(2218): Show |
chr2 | 96330766 | 96382091 | ||
| a0004c0004 | 0/0 | 2223 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | ATGGG others(2218): Show |
chr2 | 96330766 | 96382091 | ||
| a0005c0010 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | ATGGG others(2218): Show |
chr2 | 96330766 | 96382091 | ||
| a0006c0011 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | ATGGG others(2218): Show |
chr2 | 96330766 | 96382091 | ||
| a0007c0013 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | ATGGG others(2218): Show |
chr2 | 96330766 | 96382091 | ||
| a0008c0014 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | ATGGG others(2218): Show |
chr2 | 96330766 | 96382091 | ||
| a0009c0012 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | ATGGG others(2218): Show |
chr2 | 96330766 | 96382091 | ||
| a0010c0007 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | ATGGG others(2218): Show |
chr2 | 96330766 | 96382091 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6030 | 154 | 47 | 18 | 77 | 4 | 8 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0001c0001t0002 | 0/0 | 6030 | 15 | 0 | 8 | 7 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0001c0001t0003 | 0/0 | 6031 | 9 | 6 | 3 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6026): Show |
chr2 | 96330766 | 96382091 |
| a0001c0001t0005 | 1/1 | 6030 | 7 | 0 | 2 | 0 | 3 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0001c0001t0006 | 0/0 | 6030 | 6 | 0 | 4 | 2 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0001c0001t0007 | 0/0 | 6030 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0001c0001t0008 | 0/0 | 6031 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GCTAC others(6026): Show |
chr2 | 96330766 | 96382091 |
| a0001c0001t0009 | 0/0 | 6031 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6026): Show |
chr2 | 96330766 | 96382091 |
| a0001c0001t0012 | 0/0 | 6030 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0001c0001t0013 | 0/0 | 6030 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0001c0001t0014 | 0/0 | 6030 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0001c0001t0016 | 0/0 | 6030 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0001c0001t0018 | 0/0 | 6030 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0001c0008t0001 | 0/0 | 6030 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0002c0002t0001 | 0/0 | 6030 | 96 | 2 | 20 | 50 | 3 | 21 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0002c0002t0002 | 0/0 | 6030 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0002c0002t0010 | 0/0 | 6030 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0002c0002t0015 | 0/0 | 6030 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0002c0002t0017 | 0/0 | 6030 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0002c0003t0001 | 0/0 | 6030 | 29 | 20 | 5 | 2 | 0 | 2 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0002c0003t0004 | 0/0 | 6030 | 8 | 0 | 0 | 8 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0002c0003t0011 | 0/0 | 6030 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0002c0006t0001 | 0/0 | 6030 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0002c0009t0001 | 0/0 | 6030 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0003c0005t0001 | 0/0 | 6030 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0004c0004t0001 | 0/0 | 6030 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0005c0010t0003 | 0/0 | 6031 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6026): Show |
chr2 | 96330766 | 96382091 |
| a0006c0011t0001 | 0/0 | 6030 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0007c0013t0001 | 0/0 | 6030 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0008c0014t0001 | 0/0 | 6030 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0009c0012t0001 | 0/0 | 6030 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| a0010c0007t0001 | 0/0 | 6030 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | GTTAC others(6025): Show |
chr2 | 96330766 | 96382091 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 11 | 1 | 3 | 7 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0003g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0005g0015 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0005g0244 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0006g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0007g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0008g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0009g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0012g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0013g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0014g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0016g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0001t0018g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0001c0008t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0001 | 0/0 | 15 | 0 | 3 | 11 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0004 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0008 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0010g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0010g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0015g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0002t0017g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0011g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0003t0011g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0006t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0002c0009t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0003c0005t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0003c0005t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0004c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0004c0004t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0005c0010t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0006c0011t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0007c0013t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0008c0014t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0009c0012t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| a0010c0007t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0085 | EUR | GBR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0068 | EUR | GBR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | GBR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | CHS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | CHS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00673 | hp1 | a0002 | c0003 | t0004 | g0057 | EAS | CHS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00673 | hp2 | a0001 | c0001 | t0014 | g0043 | EAS | CHS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0103 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0173 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01081 | hp2 | a0002 | c0003 | t0001 | g0126 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01099 | hp1 | a0002 | c0003 | t0001 | g0020 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0142 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0071 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0104 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01243 | hp1 | a0005 | c0010 | t0003 | g0221 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | CLM | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0119 | AMR | CLM | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01358 | hp2 | a0006 | c0011 | t0001 | g0208 | AMR | CLM | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0124 | AMR | CLM | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0109 | EUR | IBS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0211 | EUR | IBS | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01884 | hp2 | a0002 | c0003 | t0001 | g0005 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0266 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0049 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01928 | hp1 | a0001 | c0001 | t0006 | g0230 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0006 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0098 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0076 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0061 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01993 | hp1 | a0002 | c0003 | t0001 | g0125 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0029 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | KHV | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | KHV | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02055 | hp1 | a0002 | c0003 | t0001 | g0267 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0105 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | KHV | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | KHV | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02083 | hp2 | a0007 | c0013 | t0001 | g0004 | EAS | KHV | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02132 | hp2 | a0002 | c0006 | t0001 | g0038 | EAS | KHV | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02145 | hp2 | a0002 | c0003 | t0011 | g0034 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02148 | hp2 | a0002 | c0003 | t0001 | g0080 | AMR | PEL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CDX | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | CDX | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0235 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0183 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02572 | hp1 | a0002 | c0003 | t0001 | g0136 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0064 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02622 | hp1 | a0002 | c0003 | t0011 | g0035 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0115 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0096 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0070 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0062 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0123 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0262 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02896 | hp2 | a0002 | c0003 | t0001 | g0033 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0261 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0242 | AFR | ESN | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0236 | AFR | ESN | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0040 | AFR | ESN | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02970 | hp2 | a0001 | c0001 | t0016 | g0028 | AFR | ESN | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0113 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03017 | hp2 | a0002 | c0003 | t0001 | g0020 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03130 | hp2 | a0002 | c0003 | t0001 | g0005 | AFR | ESN | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0005 | AFR | ESN | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03195 | hp1 | a0002 | c0003 | t0001 | g0233 | AFR | ESN | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03453 | hp2 | a0003 | c0005 | t0001 | g0174 | AFR | MSL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0239 | AFR | MSL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0089 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0030 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0005 | AFR | ESN | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03540 | hp1 | a0001 | c0001 | t0012 | g0028 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0234 | AFR | MSL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0127 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0069 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0021 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0131 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0088 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0102 | SAS | PJL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03834 | hp1 | a0002 | c0003 | t0001 | g0117 | SAS | BEB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0022 | SAS | BEB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0063 | SAS | STU | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0110 | SAS | STU | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0090 | SAS | BEB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0082 | SAS | STU | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG04199 | hp2 | a0002 | c0002 | t0017 | g0121 | SAS | STU | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0022 | SAS | STU | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | YRI | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0263 | AFR | YRI | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18747 | hp2 | a0001 | c0008 | t0001 | g0128 | EAS | CHB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | YRI | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | YRI | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18939 | hp2 | a0002 | c0003 | t0004 | g0053 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18940 | hp1 | a0002 | c0003 | t0001 | g0036 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18946 | hp2 | a0002 | c0003 | t0004 | g0058 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18949 | hp2 | a0001 | c0001 | t0007 | g0259 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18960 | hp2 | a0002 | c0003 | t0004 | g0059 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18966 | hp2 | a0002 | c0002 | t0015 | g0012 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18967 | hp1 | a0002 | c0003 | t0004 | g0056 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18968 | hp1 | a0002 | c0002 | t0010 | g0092 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18973 | hp1 | a0008 | c0014 | t0001 | g0129 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18973 | hp2 | a0002 | c0003 | t0001 | g0037 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18974 | hp2 | a0002 | c0002 | t0010 | g0067 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18997 | hp1 | a0009 | c0012 | t0001 | g0078 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | LWK | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | LWK | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19043 | hp2 | a0010 | c0007 | t0001 | g0241 | AFR | LWK | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19055 | hp1 | a0002 | c0003 | t0004 | g0055 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19060 | hp1 | a0004 | c0004 | t0001 | g0215 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19070 | hp1 | a0001 | c0001 | t0007 | g0139 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19070 | hp2 | a0002 | c0009 | t0001 | g0039 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19074 | hp2 | a0002 | c0003 | t0004 | g0054 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19075 | hp1 | a0004 | c0004 | t0001 | g0203 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19077 | hp1 | a0002 | c0003 | t0004 | g0060 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19079 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19081 | hp2 | a0001 | c0001 | t0006 | g0229 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19088 | hp1 | a0001 | c0001 | t0007 | g0260 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0243 | AFR | YRI | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA19240 | hp2 | a0001 | c0001 | t0018 | g0161 | AFR | YRI | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ASW | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA20129 | hp2 | a0002 | c0003 | t0001 | g0005 | AFR | ASW | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0015 | EUR | TSI | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | TSI | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0190 | EUR | TSI | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0005 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02559 | hp1 | a0001 | c0001 | t0013 | g0157 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG06807 | hp1 | a0002 | c0003 | t0001 | g0118 | AFR | USA | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| HG06807 | hp2 | a0003 | c0005 | t0001 | g0226 | AFR | USA | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | USA | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | USA | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | LWK | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0015 | REF | REF | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0244 | REF | REF | NCAPH_chr2_96330766_96382091 | NCAPH | chr2 | 96330766 | 96382091 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:96341719 | G | T | 1 | a0008 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.97G>T | p.Val33Leu | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 2/18 | 161/6030 | 97/2226 | 33/741 | chr2 | 96341719 | |||
| chr2:96341726 | C | T | 1 | a0007 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.104C>T | p.Pro35Leu | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 2/18 | 168/6030 | 104/2226 | 35/741 | chr2 | 96341726 | |||
| chr2:96342072 | A | G | 1 | a0003 | 2 | HG03453.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.295A>G | p.Ile99Val | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 3/18 | 359/6030 | 295/2226 | 99/741 | chr2 | 96342072 | |||
| chr2:96344170 | A | G | 1 | a0009 | 1 | NA18997.hp1 | missense_variant | MODERATE | c.661A>G | p.Arg221Gly | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/18 | 725/6030 | 661/2226 | 221/741 | chr2 | 96344170 | |||
| chr2:96351940 | C | T | 1 | a0006 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.830C>T | p.Pro277Leu | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 7/18 | 894/6030 | 830/2226 | 277/741 | chr2 | 96351940 | |||
| chr2:96353363 | A | G | 1 | a0004 | 2 | NA19060.hp1 NA19075.hp1 |
missense_variant | MODERATE | c.968A>G | p.Gln323Arg | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 8/18 | 1032/6030 | 968/2226 | 323/741 | chr2 | 96353363 | |||
| chr2:96354309 | G | A | 1 | a0010 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1129G>A | p.Asp377Asn | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/18 | 1193/6030 | 1129/2226 | 377/741 | chr2 | 96354309 | |||
| chr2:96359085 | A | G | 1 | a0005 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.1249A>G | p.Met417Val | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 10/18 | 1313/6030 | 1249/2226 | 417/741 | chr2 | 96359085 | |||
| chr2:96364509 | T | C | 4 | a0002 a0007 a0008 others(1): Show |
145 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(142): Show |
missense_variant | MODERATE | c.1616T>C | p.Val539Ala | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 13/18 | 1680/6030 | 1616/2226 | 539/741 | chr2 | 96364509 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:96354275 | C | A | 1 | a0002c0006 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.1095C>A | p.Pro365Pro | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/18 | 1159/6030 | 1095/2226 | 365/741 | chr2 | 96354275 | |||
| chr2:96354311 | T | C | 4 | a0001c0008 a0002c0002 a0007c0013 others(1): Show |
104 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(101): Show |
synonymous_variant | LOW | c.1131T>C | p.Asp377Asp | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/18 | 1195/6030 | 1131/2226 | 377/741 | chr2 | 96354311 | |||
| chr2:96359102 | T | C | 1 | a0002c0009 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.1266T>C | p.Ser422Ser | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 10/18 | 1330/6030 | 1266/2226 | 422/741 | chr2 | 96359102 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:96335767 | T | C | 1 | a0001c0001t0008 | 2 | NA18906.hp2 NA19043.hp1 |
5_prime_UTR_variant | MODIFIER | c.-63T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/18 | 63 | chr2 | 96335767 | ||||||
| chr2:96335772 | G | C | 1 | a0001c0001t0012 | 1 | HG03540.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58G>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/18 | 58 | chr2 | 96335772 | ||||||
| chr2:96335813 | G | A | 1 | a0001c0001t0013 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/18 | 17 | chr2 | 96335813 | ||||||
| chr2:96335829 | G | A | 1 | a0001c0001t0007 | 3 | NA18949.hp2 NA19070.hp1 NA19088.hp1 |
5_prime_UTR_variant | MODIFIER | c.-1G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/18 | 1 | chr2 | 96335829 | ||||||
| chr2:96373420 | G | A | 2 | a0001c0001t0002 a0002c0002t0002 |
16 | HG00544.hp2 HG00639.hp2 HG00741.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*69G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 18/18 | 69 | chr2 | 96373420 | ||||||
| chr2:96373470 | C | T | 1 | a0002c0003t0011 | 2 | HG02145.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*119C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 18/18 | 119 | chr2 | 96373470 | ||||||
| chr2:96373928 | C | A | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(28): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*577C>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 18/18 | 577 | chr2 | 96373928 | ||||||
| chr2:96374101 | T | C | 1 | a0001c0001t0006 | 6 | HG01109.hp1 HG01928.hp1 HG01934.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*750T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 18/18 | 750 | chr2 | 96374101 | ||||||
| chr2:96374257 | G | A | 1 | a0001c0001t0009 | 2 | HG01891.hp2 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*906G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 18/18 | 906 | chr2 | 96374257 | ||||||
| chr2:96374359 | A | G | 1 | a0001c0001t0018 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1008A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 18/18 | 1008 | chr2 | 96374359 | ||||||
| chr2:96374939 | G | T | 1 | a0002c0003t0004 | 8 | HG00673.hp1 NA18939.hp2 NA18946.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1588G>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 18/18 | 1588 | chr2 | 96374939 | ||||||
| chr2:96375030 | A | C | 1 | a0002c0003t0004 | 8 | HG00673.hp1 NA18939.hp2 NA18946.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1679A>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 18/18 | 1679 | chr2 | 96375030 | ||||||
| chr2:96375038 | T | G | 1 | a0001c0001t0014 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1687T>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 18/18 | 1687 | chr2 | 96375038 | ||||||
| chr2:96375166 | C | T | 1 | a0002c0003t0004 | 8 | HG00673.hp1 NA18939.hp2 NA18946.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1815C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 18/18 | 1815 | chr2 | 96375166 | ||||||
| chr2:96375213 | C | CA | 4 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0009 others(1): Show |
14 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1873dupA | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 18/18 | 1874 | INFO_REALIGN_3_PRIME | chr2 | 96375213 | |||||
| chr2:96375543 | G | C | 1 | a0002c0003t0004 | 8 | HG00673.hp1 NA18939.hp2 NA18946.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2192G>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 18/18 | 2192 | chr2 | 96375543 | ||||||
| chr2:96375554 | G | A | 1 | a0002c0002t0015 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2203G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 18/18 | 2203 | chr2 | 96375554 | ||||||
| chr2:96376655 | G | A | 1 | a0001c0001t0016 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3304G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 18/18 | 3304 | chr2 | 96376655 | ||||||
| chr2:96376747 | C | T | 1 | a0002c0002t0010 | 2 | NA18968.hp1 NA18974.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3396C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 18/18 | 3396 | chr2 | 96376747 | ||||||
| chr2:96377081 | A | T | 1 | a0002c0002t0017 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3730A>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 18/18 | 3730 | chr2 | 96377081 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:96335954 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.19+106C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96335954 | |||||||
| chr2:96336018 | C | G | 2 | a0002c0003t0001g0266 a0002c0003t0001g0267 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.19+170C>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96336018 | |||||||
| chr2:96336123 | TG | T | 9 | a0002c0003t0001g0020 a0002c0003t0001g0033 a0002c0003t0001g0036 others(6): Show |
10 | HG01099.hp1 HG02132.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.19+279delG | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 96336123 | ||||||
| chr2:96336169 | C | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0042 others(7): Show |
18 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.19+321C>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96336169 | |||||||
| chr2:96336278 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.19+430A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96336278 | |||||||
| chr2:96336297 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.19+449T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96336297 | |||||||
| chr2:96336337 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0009g0049 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.19+489T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96336337 | |||||||
| chr2:96336541 | T | A | 1 | a0001c0001t0001g0051 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.19+693T>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96336541 | |||||||
| chr2:96336709 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.19+861T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96336709 | |||||||
| chr2:96337391 | C | G | 1 | a0001c0001t0001g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.19+1543C>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96337391 | |||||||
| chr2:96337545 | G | A | 8 | a0002c0003t0004g0053 a0002c0003t0004g0054 a0002c0003t0004g0055 others(5): Show |
8 | HG00673.hp1 NA18939.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+1697G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96337545 | |||||||
| chr2:96337931 | C | CT | 4 | a0001c0001t0003g0019 a0001c0001t0003g0261 a0001c0001t0003g0262 others(1): Show |
6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+2094dupT | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 96337931 | ||||||
| chr2:96337947 | G | T | 2 | a0001c0001t0007g0259 a0001c0001t0007g0260 |
2 | NA18949.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.19+2099G>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96337947 | |||||||
| chr2:96338061 | G | A | 1 | a0002c0003t0004g0053 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.19+2213G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96338061 | |||||||
| chr2:96338128 | T | C | 2 | a0002c0002t0001g0061 a0002c0002t0001g0062 |
2 | HG01981.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.19+2280T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96338128 | |||||||
| chr2:96338241 | G | GA | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(158): Show |
211 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.19+2415dupA | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 96338241 | ||||||
| chr2:96338241 | G | GAA | 84 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0073 others(81): Show |
108 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.19+2414_19+2415dup others(2): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 96338241 | ||||||
| chr2:96338241 | G | GAAA | 6 | a0002c0002t0001g0008 a0002c0002t0001g0063 a0002c0002t0001g0064 others(3): Show |
9 | HG01981.hp2 HG02155.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2413_19+2415dup others(3): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 96338241 | ||||||
| chr2:96338241 | GAAAAAA | G | 10 | a0001c0001t0001g0018 a0001c0001t0001g0250 a0001c0001t0001g0251 others(7): Show |
12 | HG02040.hp2 HG02056.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.19+2410_19+2415del others(6): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 96338241 | ||||||
| chr2:96338384 | C | G | 1 | a0002c0002t0001g0131 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.19+2536C>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96338384 | |||||||
| chr2:96338455 | G | T | 4 | a0001c0008t0001g0128 a0002c0002t0001g0130 a0002c0002t0001g0249 others(1): Show |
4 | NA18747.hp2 NA18970.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+2607G>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96338455 | |||||||
| chr2:96338493 | G | T | 1 | a0002c0002t0001g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.19+2645G>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96338493 | |||||||
| chr2:96338589 | T | A | 1 | a0001c0001t0001g0132 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.19+2741T>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96338589 | |||||||
| chr2:96338620 | G | A | 2 | a0002c0002t0001g0068 a0002c0002t0001g0069 |
2 | HG00099.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.19+2772G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96338620 | |||||||
| chr2:96338755 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0268 |
2 | HG00423.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.20-2887T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96338755 | |||||||
| chr2:96338758 | A | T | 1 | a0002c0003t0001g0040 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.20-2884A>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96338758 | |||||||
| chr2:96338959 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.20-2683C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96338959 | |||||||
| chr2:96339102 | C | T | 75 | a0001c0008t0001g0128 a0002c0002t0001g0001 a0002c0002t0001g0004 others(72): Show |
104 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.20-2540C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96339102 | |||||||
| chr2:96339253 | T | C | 1 | a0002c0003t0001g0080 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.20-2389T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96339253 | |||||||
| chr2:96339445 | A | G | 9 | a0002c0003t0001g0020 a0002c0003t0001g0033 a0002c0003t0001g0036 others(6): Show |
10 | HG01099.hp1 HG02132.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-2197A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96339445 | |||||||
| chr2:96339481 | A | T | 1 | a0001c0001t0001g0237 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.20-2161A>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96339481 | |||||||
| chr2:96339537 | G | A | 78 | a0001c0008t0001g0128 a0002c0002t0001g0001 a0002c0002t0001g0004 others(75): Show |
107 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.20-2105G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96339537 | |||||||
| chr2:96339589 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.20-2053T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96339589 | |||||||
| chr2:96339590 | C | CA | 6 | a0001c0001t0001g0072 a0001c0001t0001g0133 a0001c0001t0007g0259 others(3): Show |
6 | NA18939.hp1 NA18949.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-2033dupA | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 96339590 | ||||||
| chr2:96339590 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.20-2052C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96339590 | |||||||
| chr2:96339591 | A | C | 1 | a0001c0001t0001g0132 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.20-2051A>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96339591 | |||||||
| chr2:96339747 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.20-1895G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96339747 | |||||||
| chr2:96339830 | G | C | 3 | a0002c0002t0001g0082 a0002c0002t0001g0083 a0002c0002t0001g0084 |
3 | HG01106.hp2 HG01934.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.20-1812G>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96339830 | |||||||
| chr2:96339908 | CCTT | C | 5 | a0002c0003t0001g0005 a0002c0003t0001g0233 a0002c0003t0001g0234 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.20-1730_20-1728del others(3): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 96339908 | ||||||
| chr2:96339975 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.20-1667T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96339975 | |||||||
| chr2:96339993 | G | T | 1 | a0002c0003t0001g0080 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.20-1649G>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96339993 | |||||||
| chr2:96340131 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0009g0049 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.20-1511C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96340131 | |||||||
| chr2:96340295 | G | A | 1 | a0002c0002t0001g0085 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.20-1347G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96340295 | |||||||
| chr2:96340383 | C | CT | 14 | a0001c0001t0001g0042 a0001c0001t0001g0079 a0001c0001t0001g0224 others(11): Show |
14 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.20-1235dupT | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 96340383 | ||||||
| chr2:96340383 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.20-1259C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96340383 | |||||||
| chr2:96340383 | CT | C | 87 | a0001c0001t0001g0073 a0001c0001t0001g0135 a0001c0001t0001g0137 others(84): Show |
120 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.20-1235delT | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 96340383 | ||||||
| chr2:96340483 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.20-1159C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96340483 | |||||||
| chr2:96340571 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.20-1071A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96340571 | |||||||
| chr2:96340783 | C | CT | 16 | a0001c0001t0001g0141 a0001c0001t0001g0219 a0001c0001t0001g0220 others(13): Show |
21 | HG00544.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.20-841dupT | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 96340783 | ||||||
| chr2:96340783 | CT | C | 12 | a0001c0001t0001g0135 a0001c0001t0001g0143 a0001c0001t0001g0145 others(9): Show |
15 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.20-841delT | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 96340783 | ||||||
| chr2:96340870 | T | G | 1 | a0001c0001t0001g0149 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.20-772T>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96340870 | |||||||
| chr2:96340947 | T | C | 79 | a0001c0008t0001g0128 a0002c0002t0001g0001 a0002c0002t0001g0004 others(76): Show |
108 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.20-695T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96340947 | |||||||
| chr2:96341097 | T | A | 1 | a0001c0001t0001g0132 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.20-545T>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96341097 | |||||||
| chr2:96341164 | A | C | 5 | a0002c0003t0001g0005 a0002c0003t0001g0233 a0002c0003t0001g0234 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.20-478A>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96341164 | |||||||
| chr2:96341240 | C | A | 1 | a0001c0001t0001g0132 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.20-402C>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96341240 | |||||||
| chr2:96341269 | C | T | 9 | a0002c0003t0001g0020 a0002c0003t0001g0033 a0002c0003t0001g0036 others(6): Show |
10 | HG01099.hp1 HG02132.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-373C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96341269 | |||||||
| chr2:96341430 | C | A | 1 | a0002c0003t0004g0054 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.20-212C>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96341430 | |||||||
| chr2:96341615 | G | A | 2 | a0001c0001t0003g0261 a0001c0001t0003g0262 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.20-27G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 1/17 | chr2 | 96341615 | |||||||
| chr2:96341949 | G | T | 2 | a0002c0003t0001g0242 a0002c0003t0001g0243 |
2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.272+55G>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 2/17 | chr2 | 96341949 | |||||||
| chr2:96342198 | A | G | 1 | a0002c0003t0001g0243 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.363+58A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 3/17 | chr2 | 96342198 | |||||||
| chr2:96342320 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.363+180C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 3/17 | chr2 | 96342320 | |||||||
| chr2:96343057 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.457-109C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 4/17 | chr2 | 96343057 | |||||||
| chr2:96343358 | G | C | 2 | a0002c0002t0001g0068 a0002c0002t0001g0069 |
2 | HG00099.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.595+54G>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 5/17 | chr2 | 96343358 | |||||||
| chr2:96343451 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0250 a0001c0001t0001g0251 others(7): Show |
12 | HG02040.hp2 HG02056.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.595+147C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 5/17 | chr2 | 96343451 | |||||||
| chr2:96343452 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.595+148G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 5/17 | chr2 | 96343452 | |||||||
| chr2:96343479 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG00621.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.595+175A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 5/17 | chr2 | 96343479 | |||||||
| chr2:96343933 | C | A | 1 | a0001c0001t0001g0150 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.596-172C>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 5/17 | chr2 | 96343933 | |||||||
| chr2:96344247 | C | T | 2 | a0002c0002t0001g0068 a0002c0002t0001g0069 |
2 | HG00099.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.720+18C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96344247 | |||||||
| chr2:96344394 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.720+165A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96344394 | |||||||
| chr2:96344467 | T | A | 1 | a0001c0001t0001g0151 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.720+238T>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96344467 | |||||||
| chr2:96344687 | T | C | 1 | a0002c0003t0001g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.720+458T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96344687 | |||||||
| chr2:96344924 | A | G | 8 | a0002c0003t0004g0053 a0002c0003t0004g0054 a0002c0003t0004g0055 others(5): Show |
8 | HG00673.hp1 NA18939.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.720+695A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96344924 | |||||||
| chr2:96345177 | C | A | 5 | a0002c0003t0001g0005 a0002c0003t0001g0233 a0002c0003t0001g0234 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.720+948C>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96345177 | |||||||
| chr2:96345259 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.720+1030G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96345259 | |||||||
| chr2:96345265 | C | G | 1 | a0002c0003t0001g0243 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.720+1036C>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96345265 | |||||||
| chr2:96345369 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.720+1140G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96345369 | |||||||
| chr2:96345424 | A | T | 1 | a0005c0010t0003g0221 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.720+1195A>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96345424 | |||||||
| chr2:96345581 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.720+1352T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96345581 | |||||||
| chr2:96345624 | C | T | 106 | a0001c0008t0001g0128 a0002c0002t0001g0001 a0002c0002t0001g0004 others(103): Show |
141 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.720+1395C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96345624 | |||||||
| chr2:96345820 | A | G | 1 | a0002c0003t0001g0040 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.720+1591A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96345820 | |||||||
| chr2:96345848 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.720+1619G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96345848 | |||||||
| chr2:96345933 | A | G | 4 | a0001c0008t0001g0128 a0002c0002t0001g0130 a0002c0002t0001g0249 others(1): Show |
4 | NA18747.hp2 NA18970.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+1704A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96345933 | |||||||
| chr2:96346180 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.720+1951G>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96346180 | |||||||
| chr2:96346354 | G | A | 17 | a0001c0001t0001g0013 a0001c0001t0001g0137 a0001c0001t0001g0141 others(14): Show |
19 | HG01261.hp1 HG02258.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.720+2125G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96346354 | |||||||
| chr2:96346417 | C | T | 107 | a0001c0001t0001g0264 a0001c0008t0001g0128 a0002c0002t0001g0001 others(104): Show |
142 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.720+2188C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96346417 | |||||||
| chr2:96346570 | G | A | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG00140.hp2 HG00741.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+2341G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96346570 | |||||||
| chr2:96347278 | G | GT | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(86): Show |
117 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.720+3065dupT | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr2 | 96347278 | ||||||
| chr2:96347278 | G | GTT | 9 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0151 others(6): Show |
10 | HG00558.hp2 HG00733.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.720+3064_720+3065d others(4): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr2 | 96347278 | ||||||
| chr2:96347416 | GTAATATC | G | 70 | a0001c0008t0001g0128 a0002c0002t0001g0001 a0002c0002t0001g0004 others(67): Show |
99 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.720+3191_720+3197d others(9): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr2 | 96347416 | ||||||
| chr2:96347422 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.720+3193T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96347422 | |||||||
| chr2:96347489 | A | G | 1 | a0001c0001t0003g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.720+3260A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96347489 | |||||||
| chr2:96347723 | A | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0132 a0001c0001t0001g0212 |
5 | NA18972.hp2 NA18995.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+3494A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96347723 | |||||||
| chr2:96347749 | G | A | 2 | a0002c0003t0004g0058 a0002c0003t0004g0059 |
2 | NA18946.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.720+3520G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96347749 | |||||||
| chr2:96347863 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.720+3634A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96347863 | |||||||
| chr2:96347958 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0222 |
4 | NA18971.hp1 NA19009.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+3729G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96347958 | |||||||
| chr2:96347967 | G | T | 1 | a0001c0001t0001g0189 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.720+3738G>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96347967 | |||||||
| chr2:96347996 | A | G | 4 | a0001c0008t0001g0128 a0002c0002t0001g0130 a0002c0002t0001g0249 others(1): Show |
4 | NA18747.hp2 NA18970.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+3767A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96347996 | |||||||
| chr2:96348049 | C | T | 1 | a0005c0010t0003g0221 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.721-3782C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96348049 | |||||||
| chr2:96348192 | T | C | 1 | a0001c0001t0005g0190 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.721-3639T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96348192 | |||||||
| chr2:96348226 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.721-3605G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96348226 | |||||||
| chr2:96348250 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.721-3581C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96348250 | |||||||
| chr2:96348251 | G | A | 1 | a0002c0003t0001g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.721-3580G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96348251 | |||||||
| chr2:96348345 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.721-3486A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96348345 | |||||||
| chr2:96348350 | C | T | 1 | a0002c0003t0001g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.721-3481C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96348350 | |||||||
| chr2:96348351 | G | T | 3 | a0002c0003t0001g0242 a0002c0003t0001g0243 a0010c0007t0001g0241 |
3 | HG02922.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.721-3480G>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96348351 | |||||||
| chr2:96348482 | G | A | 4 | a0001c0001t0001g0151 a0001c0001t0001g0191 a0001c0001t0001g0192 others(1): Show |
4 | NA18950.hp2 NA18974.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-3349G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96348482 | |||||||
| chr2:96348664 | A | T | 8 | a0002c0003t0004g0053 a0002c0003t0004g0054 a0002c0003t0004g0055 others(5): Show |
8 | HG00673.hp1 NA18939.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.721-3167A>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96348664 | |||||||
| chr2:96348700 | G | C | 1 | a0002c0002t0001g0064 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.721-3131G>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96348700 | |||||||
| chr2:96348709 | G | A | 104 | a0001c0008t0001g0128 a0002c0002t0001g0001 a0002c0002t0001g0004 others(101): Show |
139 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.721-3122G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96348709 | |||||||
| chr2:96348974 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.721-2857C>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96348974 | |||||||
| chr2:96349168 | C | T | 1 | a0002c0009t0001g0039 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.721-2663C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96349168 | |||||||
| chr2:96349332 | T | G | 1 | a0002c0002t0001g0088 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.721-2499T>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96349332 | |||||||
| chr2:96349335 | T | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(71): Show |
103 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.721-2496T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96349335 | |||||||
| chr2:96349486 | A | G | 2 | a0001c0001t0001g0151 a0001c0001t0001g0192 |
2 | NA18974.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.721-2345A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96349486 | |||||||
| chr2:96349633 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.721-2198C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96349633 | |||||||
| chr2:96349670 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.721-2161C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96349670 | |||||||
| chr2:96349707 | G | T | 1 | a0002c0003t0001g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.721-2124G>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96349707 | |||||||
| chr2:96349765 | C | T | 2 | a0002c0002t0001g0061 a0002c0002t0001g0062 |
2 | HG01981.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.721-2066C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96349765 | |||||||
| chr2:96349919 | A | G | 1 | a0002c0002t0001g0114 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.721-1912A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96349919 | |||||||
| chr2:96349929 | A | G | 1 | a0002c0002t0002g0087 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.721-1902A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96349929 | |||||||
| chr2:96350127 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.721-1704C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96350127 | |||||||
| chr2:96350201 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.721-1630A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96350201 | |||||||
| chr2:96350208 | C | T | 1 | a0001c0001t0003g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.721-1623C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96350208 | |||||||
| chr2:96350432 | A | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0143 a0001c0001t0001g0185 others(1): Show |
4 | HG02647.hp2 HG02723.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-1399A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96350432 | |||||||
| chr2:96350497 | G | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(173): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.721-1334G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96350497 | |||||||
| chr2:96350596 | G | A | 78 | a0001c0001t0001g0072 a0001c0001t0001g0193 a0001c0001t0001g0194 others(75): Show |
107 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.721-1235G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96350596 | |||||||
| chr2:96350723 | T | C | 4 | a0001c0001t0003g0019 a0001c0001t0003g0261 a0001c0001t0003g0262 others(1): Show |
6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.721-1108T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96350723 | |||||||
| chr2:96350817 | G | T | 8 | a0002c0003t0004g0053 a0002c0003t0004g0054 a0002c0003t0004g0055 others(5): Show |
8 | HG00673.hp1 NA18939.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.721-1014G>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96350817 | |||||||
| chr2:96350858 | C | T | 5 | a0002c0003t0001g0020 a0002c0003t0001g0033 a0002c0003t0001g0037 others(2): Show |
6 | HG01099.hp1 HG02132.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.721-973C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96350858 | |||||||
| chr2:96351416 | C | T | 2 | a0002c0003t0001g0266 a0002c0003t0001g0267 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.721-415C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96351416 | |||||||
| chr2:96351557 | A | G | 1 | a0002c0003t0004g0057 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.721-274A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96351557 | |||||||
| chr2:96351577 | A | G | 1 | a0001c0001t0006g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.721-254A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96351577 | |||||||
| chr2:96351647 | G | A | 1 | a0002c0002t0001g0089 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.721-184G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96351647 | |||||||
| chr2:96351667 | C | CA | 10 | a0001c0001t0001g0077 a0001c0001t0001g0154 a0001c0001t0001g0220 others(7): Show |
11 | HG02027.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.721-146dupA | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr2 | 96351667 | ||||||
| chr2:96351667 | CA | C | 13 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0217 others(10): Show |
13 | HG00642.hp1 HG00673.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.721-146delA | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr2 | 96351667 | ||||||
| chr2:96351686 | C | A | 3 | a0001c0001t0001g0237 a0002c0003t0011g0034 a0002c0003t0011g0035 |
3 | HG02145.hp2 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.721-145C>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96351686 | |||||||
| chr2:96351797 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.721-34G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 6/17 | chr2 | 96351797 | |||||||
| chr2:96352207 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.910+187C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 7/17 | chr2 | 96352207 | |||||||
| chr2:96352548 | C | T | 1 | a0002c0002t0001g0110 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.910+528C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 7/17 | chr2 | 96352548 | |||||||
| chr2:96352584 | G | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0155 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.910+564G>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 7/17 | chr2 | 96352584 | |||||||
| chr2:96352689 | T | G | 2 | a0002c0002t0001g0012 a0002c0002t0015g0012 |
3 | NA18966.hp2 NA18990.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.911-617T>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 7/17 | chr2 | 96352689 | |||||||
| chr2:96352692 | C | T | 1 | a0002c0003t0001g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.911-614C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 7/17 | chr2 | 96352692 | |||||||
| chr2:96353097 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.911-209G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 7/17 | chr2 | 96353097 | |||||||
| chr2:96353188 | G | A | 1 | a0002c0003t0011g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.911-118G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 7/17 | chr2 | 96353188 | |||||||
| chr2:96353243 | G | A | 2 | a0002c0002t0010g0067 a0002c0002t0010g0092 |
2 | NA18968.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.911-63G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 7/17 | chr2 | 96353243 | |||||||
| chr2:96353276 | C | T | 1 | a0002c0003t0001g0243 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.911-30C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 7/17 | chr2 | 96353276 | |||||||
| chr2:96353465 | A | G | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0018g0161 |
3 | HG01261.hp1 HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1002+68A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 8/17 | chr2 | 96353465 | |||||||
| chr2:96353622 | C | G | 1 | a0001c0001t0001g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1002+225C>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 8/17 | chr2 | 96353622 | |||||||
| chr2:96353734 | C | T | 1 | a0002c0003t0004g0054 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1002+337C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 8/17 | chr2 | 96353734 | |||||||
| chr2:96354432 | A | C | 73 | a0001c0008t0001g0128 a0002c0002t0001g0001 a0002c0002t0001g0004 others(70): Show |
104 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1208+44A>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96354432 | |||||||
| chr2:96354490 | T | C | 1 | a0002c0003t0001g0233 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1208+102T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96354490 | |||||||
| chr2:96354491 | T | C | 2 | a0002c0002t0001g0093 a0002c0002t0001g0094 |
2 | HG02027.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1208+103T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96354491 | |||||||
| chr2:96354501 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1208+113A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96354501 | |||||||
| chr2:96354689 | G | C | 5 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0198 others(2): Show |
5 | HG00544.hp2 NA18948.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208+301G>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96354689 | |||||||
| chr2:96354968 | C | G | 1 | a0002c0002t0001g0084 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1208+580C>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96354968 | |||||||
| chr2:96355580 | T | A | 8 | a0002c0003t0004g0053 a0002c0003t0004g0054 a0002c0003t0004g0055 others(5): Show |
8 | HG00673.hp1 NA18939.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1208+1192T>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96355580 | |||||||
| chr2:96355615 | A | G | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(1): Show |
4 | HG03130.hp1 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208+1227A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96355615 | |||||||
| chr2:96355645 | G | GT | 14 | a0001c0001t0001g0031 a0001c0001t0001g0046 a0001c0001t0001g0258 others(11): Show |
15 | HG01081.hp2 HG01515.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1208+1271dupT | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 96355645 | ||||||
| chr2:96355645 | G | T | 1 | a0001c0001t0001g0184 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1208+1257G>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96355645 | |||||||
| chr2:96355791 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1208+1403G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96355791 | |||||||
| chr2:96355905 | A | ATTAC | 8 | a0002c0003t0004g0053 a0002c0003t0004g0054 a0002c0003t0004g0055 others(5): Show |
8 | HG00673.hp1 NA18939.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1208+1518_1208+152 others(8): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 96355905 | ||||||
| chr2:96355925 | C | T | 8 | a0002c0003t0004g0053 a0002c0003t0004g0054 a0002c0003t0004g0055 others(5): Show |
8 | HG00673.hp1 NA18939.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1208+1537C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96355925 | |||||||
| chr2:96355926 | G | T | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(67): Show |
97 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1208+1538G>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96355926 | |||||||
| chr2:96356038 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1208+1650G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96356038 | |||||||
| chr2:96356320 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1208+1932G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96356320 | |||||||
| chr2:96356429 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1208+2041A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96356429 | |||||||
| chr2:96356588 | A | G | 2 | a0001c0001t0012g0028 a0001c0001t0016g0028 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1208+2200A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96356588 | |||||||
| chr2:96356757 | C | T | 107 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0008 others(104): Show |
144 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1209-2288C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96356757 | |||||||
| chr2:96356796 | C | G | 18 | a0001c0001t0001g0013 a0001c0001t0001g0137 a0001c0001t0001g0141 others(15): Show |
20 | HG01261.hp1 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1209-2249C>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96356796 | |||||||
| chr2:96356837 | A | T | 1 | a0001c0001t0001g0258 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1209-2208A>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96356837 | |||||||
| chr2:96356839 | C | T | 1 | a0002c0003t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1209-2206C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96356839 | |||||||
| chr2:96356917 | C | A | 1 | a0001c0001t0001g0150 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1209-2128C>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96356917 | |||||||
| chr2:96357092 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1209-1953C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96357092 | |||||||
| chr2:96357555 | A | G | 1 | a0001c0001t0002g0199 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1209-1490A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96357555 | |||||||
| chr2:96357636 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1209-1409T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96357636 | |||||||
| chr2:96357708 | G | C | 1 | a0001c0001t0001g0265 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1209-1337G>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96357708 | |||||||
| chr2:96357847 | G | A | 1 | a0002c0002t0001g0095 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1209-1198G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96357847 | |||||||
| chr2:96357902 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1209-1143G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96357902 | |||||||
| chr2:96358195 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0219 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1209-850A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96358195 | |||||||
| chr2:96358342 | G | A | 1 | a0002c0009t0001g0039 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1209-703G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96358342 | |||||||
| chr2:96358486 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1209-559T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96358486 | |||||||
| chr2:96358561 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0219 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1209-484T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96358561 | |||||||
| chr2:96358618 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1209-427G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96358618 | |||||||
| chr2:96358661 | C | G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(77): Show |
96 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.1209-384C>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96358661 | |||||||
| chr2:96358682 | G | A | 11 | a0001c0001t0001g0170 a0001c0001t0001g0201 a0001c0001t0002g0196 others(8): Show |
12 | HG01099.hp1 HG01346.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1209-363G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96358682 | |||||||
| chr2:96358690 | G | A | 2 | a0002c0002t0001g0082 a0002c0002t0001g0090 |
2 | HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1209-355G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96358690 | |||||||
| chr2:96358703 | T | C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0175 a0001c0001t0001g0250 others(4): Show |
9 | HG02074.hp1 HG02602.hp2 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.1209-342T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96358703 | |||||||
| chr2:96358710 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1209-335C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96358710 | |||||||
| chr2:96358719 | T | A | 1 | a0001c0001t0002g0196 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1209-326T>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96358719 | |||||||
| chr2:96358745 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0219 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1209-300A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96358745 | |||||||
| chr2:96358760 | G | A | 1 | a0002c0002t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1209-285G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 9/17 | chr2 | 96358760 | |||||||
| chr2:96359250 | C | T | 7 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0177 others(4): Show |
8 | HG02280.hp1 HG02486.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1357+57C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 10/17 | chr2 | 96359250 | |||||||
| chr2:96359268 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1357+75A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 10/17 | chr2 | 96359268 | |||||||
| chr2:96359476 | G | A | 1 | a0002c0002t0001g0096 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1357+283G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 10/17 | chr2 | 96359476 | |||||||
| chr2:96359536 | T | C | 3 | a0002c0003t0001g0036 a0002c0003t0001g0037 a0002c0009t0001g0039 |
3 | NA18940.hp1 NA18973.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1357+343T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 10/17 | chr2 | 96359536 | |||||||
| chr2:96359715 | C | T | 2 | a0002c0003t0001g0266 a0002c0003t0001g0267 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1358-428C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 10/17 | chr2 | 96359715 | |||||||
| chr2:96359821 | G | A | 8 | a0002c0003t0004g0053 a0002c0003t0004g0054 a0002c0003t0004g0055 others(5): Show |
8 | HG00673.hp1 NA18939.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358-322G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 10/17 | chr2 | 96359821 | |||||||
| chr2:96360311 | A | T | 2 | a0002c0002t0001g0107 a0002c0002t0001g0108 |
2 | NA19054.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1464+62A>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 11/17 | chr2 | 96360311 | |||||||
| chr2:96360319 | G | A | 1 | a0002c0003t0001g0124 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1464+70G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 11/17 | chr2 | 96360319 | |||||||
| chr2:96360441 | T | G | 3 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0001g0097 |
3 | HG02027.hp2 HG02080.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1465-147T>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 11/17 | chr2 | 96360441 | |||||||
| chr2:96360573 | T | A | 1 | a0001c0001t0001g0138 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1465-15T>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 11/17 | chr2 | 96360573 | |||||||
| chr2:96360740 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0188 |
3 | HG01884.hp1 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1587+30C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96360740 | |||||||
| chr2:96360838 | C | T | 99 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0008 others(96): Show |
136 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.1587+128C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96360838 | |||||||
| chr2:96360880 | G | A | 1 | a0005c0010t0003g0221 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1587+170G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96360880 | |||||||
| chr2:96361040 | C | CT | 41 | a0001c0001t0001g0031 a0001c0001t0001g0163 a0001c0001t0001g0166 others(38): Show |
42 | HG00609.hp2 HG00621.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1587+356dupT | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361040 | ||||||
| chr2:96361040 | C | CTT | 60 | a0001c0001t0001g0189 a0001c0001t0009g0183 a0002c0002t0001g0001 others(57): Show |
91 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1587+355_1587+356d others(4): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361040 | ||||||
| chr2:96361040 | C | CTTT | 19 | a0001c0001t0003g0019 a0001c0001t0003g0261 a0001c0001t0003g0262 others(16): Show |
26 | HG01175.hp2 HG01261.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1587+354_1587+356d others(5): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361040 | ||||||
| chr2:96361040 | CT | C | 10 | a0001c0001t0001g0140 a0001c0001t0001g0151 a0001c0001t0001g0168 others(7): Show |
13 | HG00639.hp2 HG01109.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1587+356delT | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361040 | ||||||
| chr2:96361105 | A | G | 1 | a0002c0002t0001g0238 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1587+395A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361105 | |||||||
| chr2:96361180 | C | A | 1 | a0002c0002t0001g0131 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1587+470C>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361180 | |||||||
| chr2:96361237 | A | G | 1 | a0002c0002t0001g0099 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1587+527A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361237 | |||||||
| chr2:96361459 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0227 |
2 | NA18990.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1587+749G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361459 | |||||||
| chr2:96361601 | C | T | 3 | a0002c0003t0001g0242 a0002c0003t0001g0243 a0010c0007t0001g0241 |
3 | HG02922.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1587+891C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361601 | |||||||
| chr2:96361749 | G | GAT | 5 | a0001c0001t0001g0135 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | HG01891.hp2 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1587+1057_1587+105 others(6): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361749 | ||||||
| chr2:96361749 | GAT | G | 3 | a0002c0003t0001g0037 a0002c0003t0001g0235 a0004c0004t0001g0203 |
3 | HG02257.hp1 NA18973.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1587+1057_1587+105 others(6): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361749 | ||||||
| chr2:96361749 | GATATATA others(53): Show |
G | 1 | a0001c0001t0001g0180 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1587+1059_1587+111 others(64): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361749 | ||||||
| chr2:96361763 | T | TATAC | 5 | a0002c0002t0001g0104 a0002c0002t0001g0110 a0002c0003t0001g0115 others(2): Show |
5 | HG01192.hp2 HG02647.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1587+1056_1587+105 others(8): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361763 | ||||||
| chr2:96361763 | TATATACA others(15): Show |
T | 1 | a0002c0002t0001g0065 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1587+1059_1587+108 others(26): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361763 | ||||||
| chr2:96361765 | T | TAC | 66 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0008 others(63): Show |
95 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1587+1056_1587+105 others(6): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361765 | ||||||
| chr2:96361767 | T | C | 19 | a0001c0001t0001g0186 a0002c0002t0001g0061 a0002c0002t0001g0082 others(16): Show |
24 | HG00673.hp1 HG01106.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1587+1057T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361767 | |||||||
| chr2:96361769 | C | T | 83 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0008 others(80): Show |
117 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1587+1059C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361769 | |||||||
| chr2:96361769 | CAT | C | 4 | a0001c0001t0003g0019 a0001c0001t0003g0261 a0001c0001t0003g0262 others(1): Show |
6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.1587+1071_1587+107 others(6): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361769 | ||||||
| chr2:96361778 | A | ATATATAC others(19): Show |
1 | a0002c0003t0004g0058 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1587+1072_1587+107 others(30): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361778 | ||||||
| chr2:96361783 | C | T | 102 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0008 others(99): Show |
137 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1587+1073C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361783 | |||||||
| chr2:96361787 | T | C | 2 | a0002c0003t0001g0266 a0002c0003t0001g0267 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1587+1077T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361787 | |||||||
| chr2:96361804 | G | GTATATAC others(17): Show |
7 | a0002c0003t0004g0053 a0002c0003t0004g0054 a0002c0003t0004g0055 others(4): Show |
7 | HG00673.hp1 NA18939.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.1587+1095_1587+109 others(28): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361804 | ||||||
| chr2:96361806 | G | GTA | 10 | a0001c0001t0001g0134 a0001c0001t0001g0153 a0001c0001t0001g0156 others(7): Show |
10 | HG02257.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1587+1118_1587+111 others(6): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361806 | ||||||
| chr2:96361806 | G | GTATA | 4 | a0001c0001t0003g0019 a0001c0001t0003g0261 a0001c0001t0003g0262 others(1): Show |
6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.1587+1116_1587+111 others(8): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361806 | ||||||
| chr2:96361806 | GTA | G | 16 | a0001c0001t0001g0026 a0001c0001t0001g0188 a0002c0002t0001g0023 others(13): Show |
19 | HG00733.hp2 HG01071.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.1587+1118_1587+111 others(6): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361806 | ||||||
| chr2:96361808 | A | G | 13 | a0002c0002t0001g0001 a0002c0003t0001g0080 a0002c0003t0001g0117 others(10): Show |
13 | HG00673.hp1 HG01081.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1587+1098A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361808 | |||||||
| chr2:96361812 | A | G | 1 | a0002c0002t0001g0104 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1587+1102A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361812 | |||||||
| chr2:96361818 | A | ATATG | 8 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0145 others(5): Show |
10 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1587+1111_1587+111 others(8): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361818 | ||||||
| chr2:96361818 | A | ATG | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(60): Show |
90 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1587+1109_1587+111 others(6): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361818 | ||||||
| chr2:96361820 | A | G | 2 | a0001c0001t0001g0207 a0001c0001t0002g0148 |
2 | NA18950.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1587+1110A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361820 | |||||||
| chr2:96361826 | A | T | 2 | a0001c0001t0001g0228 a0001c0001t0001g0255 |
2 | HG02523.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.1587+1116A>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361826 | |||||||
| chr2:96361826 | ATAT | A | 5 | a0002c0002t0001g0001 a0002c0003t0001g0005 a0002c0003t0001g0233 others(2): Show |
9 | HG01884.hp2 HG02109.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1587+1118_1587+112 others(7): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361826 | ||||||
| chr2:96361828 | A | AT | 7 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0258 others(4): Show |
8 | HG01106.hp1 HG01515.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1587+1133dupT | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361828 | ||||||
| chr2:96361828 | A | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0162 others(6): Show |
11 | HG01261.hp1 HG02523.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1587+1118A>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361828 | |||||||
| chr2:96361828 | AT | A | 11 | a0001c0001t0001g0018 a0001c0001t0001g0150 a0001c0001t0001g0216 others(8): Show |
13 | HG00642.hp1 HG01167.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.1587+1133delT | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361828 | ||||||
| chr2:96361828 | ATT | A | 59 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0008 others(56): Show |
85 | HG00099.hp2 HG00544.hp1 HG01081.hp2 others(82): Show |
intron_variant | MODIFIER | c.1587+1132_1587+113 others(6): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 96361828 | ||||||
| chr2:96361829 | T | TA | 7 | a0001c0001t0001g0075 a0001c0001t0001g0163 a0001c0001t0001g0170 others(4): Show |
7 | HG01346.hp1 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1587+1119_1587+112 others(5): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361829 | |||||||
| chr2:96361830 | T | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
128 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1587+1120T>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361830 | |||||||
| chr2:96361831 | T | A | 8 | a0001c0001t0001g0152 a0001c0001t0001g0207 a0001c0001t0001g0217 others(5): Show |
8 | HG00642.hp1 HG01167.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1587+1121T>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361831 | |||||||
| chr2:96361832 | T | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0017 others(78): Show |
105 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1587+1122T>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361832 | |||||||
| chr2:96361833 | T | A | 4 | a0001c0001t0001g0207 a0001c0001t0009g0049 a0002c0002t0001g0101 others(1): Show |
4 | HG01167.hp1 HG01891.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1587+1123T>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361833 | |||||||
| chr2:96361834 | T | A | 5 | a0002c0002t0001g0063 a0002c0002t0001g0082 a0002c0002t0001g0084 others(2): Show |
5 | HG01934.hp2 HG02027.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.1587+1124T>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361834 | |||||||
| chr2:96361848 | G | T | 2 | a0001c0001t0009g0049 a0001c0001t0009g0183 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1587+1138G>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361848 | |||||||
| chr2:96361965 | A | G | 18 | a0001c0001t0001g0013 a0001c0001t0001g0137 a0001c0001t0001g0141 others(15): Show |
20 | HG01261.hp1 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1587+1255A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361965 | |||||||
| chr2:96361993 | C | T | 1 | a0002c0003t0001g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1587+1283C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96361993 | |||||||
| chr2:96362184 | C | T | 2 | a0002c0002t0001g0024 a0002c0002t0001g0106 |
3 | HG01071.hp1 HG01175.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1587+1474C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96362184 | |||||||
| chr2:96362378 | C | G | 1 | a0001c0001t0006g0076 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1587+1668C>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96362378 | |||||||
| chr2:96362587 | AGT | A | 105 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0008 others(102): Show |
140 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1587+1878_1587+187 others(6): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96362587 | |||||||
| chr2:96362590 | A | C | 105 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0008 others(102): Show |
140 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1587+1880A>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96362590 | |||||||
| chr2:96362633 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0138 a0001c0001t0001g0175 others(2): Show |
9 | HG00609.hp1 HG02559.hp2 HG04204.hp2 others(6): Show |
intron_variant | MODIFIER | c.1588-1848A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96362633 | |||||||
| chr2:96363024 | T | C | 108 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0008 others(105): Show |
145 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1588-1457T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96363024 | |||||||
| chr2:96363183 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG03942.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1588-1298A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96363183 | |||||||
| chr2:96363419 | G | C | 8 | a0002c0003t0004g0053 a0002c0003t0004g0054 a0002c0003t0004g0055 others(5): Show |
8 | HG00673.hp1 NA18939.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1588-1062G>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96363419 | |||||||
| chr2:96363430 | G | A | 70 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0008 others(67): Show |
101 | HG00099.hp2 HG00544.hp1 HG00733.hp2 others(98): Show |
intron_variant | MODIFIER | c.1588-1051G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96363430 | |||||||
| chr2:96363714 | A | G | 8 | a0002c0003t0004g0053 a0002c0003t0004g0054 a0002c0003t0004g0055 others(5): Show |
8 | HG00673.hp1 NA18939.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1588-767A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96363714 | |||||||
| chr2:96364092 | G | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(183): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1588-389G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96364092 | |||||||
| chr2:96364221 | A | G | 1 | a0001c0001t0002g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1588-260A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96364221 | |||||||
| chr2:96364258 | C | T | 1 | a0010c0007t0001g0241 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1588-223C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96364258 | |||||||
| chr2:96364365 | A | T | 1 | a0002c0003t0001g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1588-116A>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | chr2 | 96364365 | |||||||
| chr2:96364625 | T | G | 5 | a0002c0003t0001g0005 a0002c0003t0001g0233 a0002c0003t0001g0234 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1698+34T>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 13/17 | chr2 | 96364625 | |||||||
| chr2:96364656 | A | G | 1 | a0002c0009t0001g0039 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1698+65A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 13/17 | chr2 | 96364656 | |||||||
| chr2:96365050 | T | C | 2 | a0002c0003t0001g0266 a0002c0003t0001g0267 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1698+459T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 13/17 | chr2 | 96365050 | |||||||
| chr2:96365108 | G | A | 1 | a0002c0002t0001g0114 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1698+517G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 13/17 | chr2 | 96365108 | |||||||
| chr2:96365235 | G | GA | 8 | a0002c0003t0004g0053 a0002c0003t0004g0054 a0002c0003t0004g0055 others(5): Show |
8 | HG00673.hp1 NA18939.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1699-634dupA | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 96365235 | ||||||
| chr2:96365493 | A | G | 42 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(39): Show |
52 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1699-383A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 13/17 | chr2 | 96365493 | |||||||
| chr2:96365503 | T | A | 2 | a0002c0002t0001g0024 a0002c0002t0001g0106 |
3 | HG01071.hp1 HG01175.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1699-373T>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 13/17 | chr2 | 96365503 | |||||||
| chr2:96366359 | A | G | 5 | a0002c0003t0001g0080 a0002c0003t0001g0117 a0002c0003t0001g0124 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1881+301A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 14/17 | chr2 | 96366359 | |||||||
| chr2:96366421 | G | A | 1 | a0002c0002t0001g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1881+363G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 14/17 | chr2 | 96366421 | |||||||
| chr2:96366854 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1882-403G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 14/17 | chr2 | 96366854 | |||||||
| chr2:96366876 | C | CA | 10 | a0001c0001t0001g0077 a0001c0001t0001g0225 a0001c0001t0001g0228 others(7): Show |
10 | HG00733.hp2 HG00741.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1882-357dupA | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 96366876 | ||||||
| chr2:96366876 | CA | C | 13 | a0001c0001t0001g0046 a0001c0001t0001g0168 a0001c0001t0001g0178 others(10): Show |
13 | HG01069.hp2 HG01081.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.1882-357delA | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 96366876 | ||||||
| chr2:96366913 | G | A | 2 | a0002c0003t0001g0115 a0002c0003t0001g0118 |
2 | HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1882-344G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 14/17 | chr2 | 96366913 | |||||||
| chr2:96366937 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1882-320A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 14/17 | chr2 | 96366937 | |||||||
| chr2:96366958 | A | G | 2 | a0003c0005t0001g0174 a0003c0005t0001g0226 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1882-299A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 14/17 | chr2 | 96366958 | |||||||
| chr2:96367009 | T | C | 3 | a0002c0003t0001g0267 a0003c0005t0001g0174 a0003c0005t0001g0226 |
3 | HG02055.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1882-248T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 14/17 | chr2 | 96367009 | |||||||
| chr2:96367010 | C | T | 1 | a0002c0002t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1882-247C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 14/17 | chr2 | 96367010 | |||||||
| chr2:96367057 | T | C | 2 | a0002c0003t0001g0115 a0002c0003t0001g0118 |
2 | HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1882-200T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 14/17 | chr2 | 96367057 | |||||||
| chr2:96367109 | C | T | 1 | a0002c0002t0001g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1882-148C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 14/17 | chr2 | 96367109 | |||||||
| chr2:96367584 | G | T | 1 | a0002c0002t0001g0094 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1998+211G>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 15/17 | chr2 | 96367584 | |||||||
| chr2:96367691 | T | G | 1 | a0001c0001t0001g0193 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1998+318T>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 15/17 | chr2 | 96367691 | |||||||
| chr2:96367719 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1998+346A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 15/17 | chr2 | 96367719 | |||||||
| chr2:96367760 | A | G | 1 | a0002c0003t0001g0267 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1998+387A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 15/17 | chr2 | 96367760 | |||||||
| chr2:96368124 | G | A | 42 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(39): Show |
52 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1998+751G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 15/17 | chr2 | 96368124 | |||||||
| chr2:96368202 | G | A | 77 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0008 others(74): Show |
106 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.1999-770G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 15/17 | chr2 | 96368202 | |||||||
| chr2:96368262 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1999-710A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 15/17 | chr2 | 96368262 | |||||||
| chr2:96368525 | C | T | 21 | a0002c0003t0001g0005 a0002c0003t0001g0020 a0002c0003t0001g0033 others(18): Show |
27 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1999-447C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 15/17 | chr2 | 96368525 | |||||||
| chr2:96368635 | G | A | 2 | a0002c0002t0001g0093 a0002c0002t0001g0094 |
2 | HG02027.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1999-337G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 15/17 | chr2 | 96368635 | |||||||
| chr2:96368651 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1999-321G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 15/17 | chr2 | 96368651 | |||||||
| chr2:96368698 | T | C | 2 | a0002c0002t0001g0061 a0002c0002t0001g0062 |
2 | HG01981.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1999-274T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 15/17 | chr2 | 96368698 | |||||||
| chr2:96369174 | T | C | 2 | a0002c0003t0001g0242 a0002c0003t0001g0243 |
2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2090+111T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 16/17 | chr2 | 96369174 | |||||||
| chr2:96369175 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2090+112G>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 16/17 | chr2 | 96369175 | |||||||
| chr2:96369387 | G | A | 1 | a0002c0002t0002g0087 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2091-38G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 16/17 | chr2 | 96369387 | |||||||
| chr2:96369421 | C | G | 7 | a0001c0001t0002g0009 a0001c0001t0002g0074 a0001c0001t0002g0144 others(4): Show |
10 | HG00639.hp2 HG00741.hp2 HG01109.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.2091-4C>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 16/17 | chr2 | 96369421 | |||||||
| chr2:96369575 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2166+75T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96369575 | |||||||
| chr2:96369999 | G | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0051 others(8): Show |
15 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.2166+499G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96369999 | |||||||
| chr2:96370234 | A | G | 1 | a0002c0002t0001g0022 | 2 | HG03834.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2166+734A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96370234 | |||||||
| chr2:96370251 | G | A | 1 | a0002c0003t0001g0126 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2166+751G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96370251 | |||||||
| chr2:96370329 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2166+829G>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96370329 | |||||||
| chr2:96370333 | T | G | 1 | a0002c0003t0004g0055 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2166+833T>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96370333 | |||||||
| chr2:96370362 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2166+862C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96370362 | |||||||
| chr2:96370447 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2166+947C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96370447 | |||||||
| chr2:96370458 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2166+958G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96370458 | |||||||
| chr2:96370701 | G | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(185): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.2166+1201G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96370701 | |||||||
| chr2:96370741 | A | G | 4 | a0002c0003t0001g0266 a0002c0003t0001g0267 a0003c0005t0001g0174 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2166+1241A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96370741 | |||||||
| chr2:96370932 | C | T | 11 | a0002c0003t0001g0037 a0002c0003t0001g0115 a0002c0003t0001g0118 others(8): Show |
11 | HG00673.hp1 HG02647.hp1 HG06807.hp1 others(8): Show |
intron_variant | MODIFIER | c.2166+1432C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96370932 | |||||||
| chr2:96371143 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0018g0161 |
2 | HG01261.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2166+1643C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96371143 | |||||||
| chr2:96371166 | G | GC | 3 | a0002c0003t0001g0242 a0002c0003t0001g0243 a0010c0007t0001g0241 |
3 | HG02922.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2166+1668dupC | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 96371166 | ||||||
| chr2:96371168 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2166+1668C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96371168 | |||||||
| chr2:96371811 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2167-1481G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96371811 | |||||||
| chr2:96371826 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2167-1466T>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96371826 | |||||||
| chr2:96371914 | A | G | 1 | a0002c0003t0001g0239 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2167-1378A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96371914 | |||||||
| chr2:96371973 | A | G | 1 | a0001c0001t0001g0041 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2167-1319A>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96371973 | |||||||
| chr2:96372027 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0172 |
2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2167-1265C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96372027 | |||||||
| chr2:96372195 | C | T | 1 | a0002c0003t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2167-1097C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96372195 | |||||||
| chr2:96372343 | C | G | 1 | a0002c0003t0001g0243 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2167-949C>G | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96372343 | |||||||
| chr2:96372345 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2167-947G>A | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96372345 | |||||||
| chr2:96372391 | G | C | 8 | a0002c0003t0004g0053 a0002c0003t0004g0054 a0002c0003t0004g0055 others(5): Show |
8 | HG00673.hp1 NA18939.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.2167-901G>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96372391 | |||||||
| chr2:96372657 | A | C | 1 | a0002c0003t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2167-635A>C | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96372657 | |||||||
| chr2:96372802 | A | T | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2167-490A>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96372802 | |||||||
| chr2:96372931 | C | T | 1 | a0002c0003t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2167-361C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96372931 | |||||||
| chr2:96372984 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2167-308C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96372984 | |||||||
| chr2:96373019 | C | T | 1 | a0002c0002t0001g0102 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2167-273C>T | NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 17/17 | chr2 | 96373019 |