Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 29781 |
| ensemblid | ENSG00000025770.19 |
| hgncid | 25071 |
| symbol | NCAPH2 |
| name | non-SMC condensin II complex subunit H2 |
| refseq_nuc | NM_152299.4 |
| refseq_prot | NP_689512.2 |
| ensembl_nuc | ENST00000420993.7 |
| ensembl_prot | ENSP00000410088.2 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 50508224 |
| end | 50524780 |
| strand | + |
| ver | v1.2 |
| region | chr22:50508224-50524780 |
| region5000 | chr22:50503224-50529780 |
| regionname0 | NCAPH2_chr22_50508224_50524780 |
| regionname5000 | NCAPH2_chr22_50503224_50529780 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 605 | 374 | 91 | 75 | 148 | 16 | 42 | 107 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | MEDVE others(600): Show |
chr22 | 50503224 | 50529780 |
| a0002 | 0/0 | 605 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | MEDVE others(600): Show |
chr22 | 50503224 | 50529780 |
| a0003 | 0/0 | 605 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | MEDVE others(600): Show |
chr22 | 50503224 | 50529780 |
| a0004 | 0/0 | 605 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | MEDVE others(600): Show |
chr22 | 50503224 | 50529780 |
| a0005 | 0/0 | 605 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | MEDVE others(600): Show |
chr22 | 50503224 | 50529780 |
| a0006 | 0/0 | 605 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | MEDVE others(600): Show |
chr22 | 50503224 | 50529780 |
| a0007 | 0/0 | 605 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | MEDVE others(600): Show |
chr22 | 50503224 | 50529780 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1815 | 340 | 64 | 73 | 145 | 16 | 41 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0001c0002 | 0/0 | 1815 | 19 | 17 | 2 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0001c0003 | 0/0 | 1815 | 4 | 4 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0001c0006 | 0/0 | 1815 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0001c0007 | 0/0 | 1815 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0001c0009 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0001c0011 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0001c0012 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0001c0013 | 0/1 | 1815 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0001c0015 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0001c0016 | 0/0 | 1815 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0001c0017 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0002c0004 | 0/0 | 1815 | 3 | 2 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0002c0005 | 0/0 | 1815 | 2 | 1 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0003c0018 | 0/0 | 1815 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0004c0019 | 0/0 | 1815 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0005c0008 | 0/0 | 1815 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0006c0014 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 | ||
| a0007c0010 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | ATGGA others(1810): Show |
chr22 | 50503224 | 50529780 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3337 | 212 | 34 | 46 | 100 | 8 | 24 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0001t0002 | 1/0 | 3337 | 103 | 24 | 20 | 44 | 2 | 12 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0001t0003 | 0/0 | 3337 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0001t0004 | 0/0 | 3337 | 8 | 0 | 6 | 0 | 2 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0001t0005 | 0/0 | 3337 | 5 | 1 | 0 | 1 | 1 | 2 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0001t0006 | 0/0 | 3337 | 2 | 0 | 0 | 0 | 0 | 2 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0001t0007 | 0/0 | 3337 | 2 | 0 | 0 | 0 | 2 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0001t0008 | 0/0 | 3337 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0001t0009 | 0/0 | 3337 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0001t0010 | 0/0 | 3337 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0001t0011 | 0/0 | 3337 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0001t0013 | 0/0 | 3372 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3367): Show |
chr22 | 50503224 | 50529780 |
| a0001c0001t0014 | 0/0 | 3337 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0002t0001 | 0/0 | 3337 | 19 | 17 | 2 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0003t0003 | 0/0 | 3337 | 4 | 4 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0006t0002 | 0/0 | 3337 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0007t0003 | 0/0 | 3337 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0009t0001 | 0/0 | 3337 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0011t0001 | 0/0 | 3337 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0012t0001 | 0/0 | 3337 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0013t0001 | 0/1 | 3337 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0015t0005 | 0/0 | 3337 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0016t0001 | 0/0 | 3337 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0001c0017t0012 | 0/0 | 3337 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0002c0004t0003 | 0/0 | 3337 | 3 | 2 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0002c0005t0003 | 0/0 | 3337 | 2 | 1 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0003c0018t0002 | 0/0 | 3337 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0004c0019t0001 | 0/0 | 3337 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0005c0008t0001 | 0/0 | 3337 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0006c0014t0001 | 0/0 | 3337 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| a0007c0010t0001 | 0/0 | 3337 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | GCATT others(3332): Show |
chr22 | 50503224 | 50529780 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 2 | 4 | 4 | 2 | 4 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0002 | 0/0 | 15 | 1 | 3 | 7 | 0 | 4 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0003 | 0/0 | 14 | 1 | 7 | 6 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0004 | 0/0 | 12 | 0 | 1 | 9 | 1 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0008 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0005 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0006 | 0/0 | 9 | 2 | 3 | 1 | 0 | 3 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0036 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0004g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0004g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0007g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0008g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0013g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0001t0014g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0002t0001g0007 | 0/0 | 9 | 7 | 2 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0003t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0003t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0003t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0006t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0006t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0007t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0007t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0009t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0011t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0013t0001g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0015t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0016t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0001c0017t0012g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0002c0004t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0002c0004t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0002c0004t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0002c0005t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0002c0005t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0003c0018t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0004c0019t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0005c0008t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0006c0014t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| a0007c0010t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0163 | EUR | GBR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0164 | EUR | GBR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | GBR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0174 | EUR | GBR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0016 | EUR | FIN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00558 | hp1 | a0001 | c0012 | t0001 | g0001 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00639 | hp1 | a0001 | c0001 | t0013 | g0006 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0176 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01109 | hp1 | a0003 | c0018 | t0002 | g0058 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0171 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01243 | hp1 | a0002 | c0004 | t0003 | g0048 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01256 | hp1 | a0002 | c0005 | t0003 | g0065 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01515 | hp1 | a0001 | c0001 | t0007 | g0014 | EUR | IBS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01517 | hp1 | a0001 | c0001 | t0007 | g0014 | EUR | IBS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01517 | hp2 | a0001 | c0001 | t0014 | g0184 | EUR | IBS | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01934 | hp2 | a0004 | c0019 | t0001 | g0004 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01993 | hp1 | a0005 | c0008 | t0001 | g0008 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02165 | hp1 | a0001 | c0015 | t0005 | g0220 | EAS | CDX | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02257 | hp2 | a0001 | c0007 | t0003 | g0143 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0106 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02622 | hp1 | a0002 | c0005 | t0003 | g0064 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0221 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02717 | hp1 | a0002 | c0004 | t0003 | g0049 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02818 | hp1 | a0001 | c0006 | t0002 | g0066 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | ESN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | ESN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | ESN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0035 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03098 | hp2 | a0001 | c0006 | t0002 | g0227 | AFR | MSL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | ESN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | ESN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | MSL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0012 | AFR | MSL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0045 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03486 | hp2 | a0001 | c0003 | t0003 | g0135 | AFR | MSL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0100 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03492 | hp2 | a0001 | c0001 | t0006 | g0002 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ESN | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0226 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | BEB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | BEB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG04184 | hp1 | a0001 | c0016 | t0001 | g0087 | SAS | BEB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG04184 | hp2 | a0001 | c0001 | t0008 | g0045 | SAS | BEB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | STU | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | STU | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | YRI | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18612 | hp1 | a0006 | c0014 | t0001 | g0092 | EAS | CHB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | CHB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | YRI | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | YRI | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18986 | hp2 | a0007 | c0010 | t0001 | g0090 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19005 | hp2 | a0001 | c0001 | t0005 | g0219 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | LWK | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | LWK | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19087 | hp2 | a0001 | c0011 | t0001 | g0115 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0216 | AFR | YRI | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | YRI | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA20129 | hp1 | a0001 | c0003 | t0003 | g0128 | AFR | ASW | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0225 | EUR | TSI | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | TSI | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | GIH | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02109 | hp2 | a0001 | c0017 | t0012 | g0059 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02486 | hp2 | a0002 | c0004 | t0003 | g0224 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03471 | hp1 | a0001 | c0009 | t0001 | g0011 | AFR | MSL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG03471 | hp2 | a0001 | c0003 | t0003 | g0035 | AFR | MSL | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | USA | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| HG06807 | hp2 | a0001 | c0007 | t0003 | g0142 | AFR | USA | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | LWK | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| homoSapiens | chm13v2 | a0001 | c0013 | t0001 | g0047 | REF | REF | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0036 | REF | REF | NCAPH2_chr22_50503224_50529780 | NCAPH2 | chr22 | 50503224 | 50529780 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:50517614 | G | A | 1 | a0005 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.304G>A | p.Ala102Thr | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 4/20 | 418/3337 | 304/1818 | 102/605 | chr22 | 50517614 | |||
| chr22:50517642 | C | G | 1 | a0004 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.332C>G | p.Pro111Arg | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 4/20 | 446/3337 | 332/1818 | 111/605 | chr22 | 50517642 | |||
| chr22:50519196 | C | G | 1 | a0003 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.737C>G | p.Ser246Cys | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/20 | 851/3337 | 737/1818 | 246/605 | chr22 | 50519196 | |||
| chr22:50521806 | G | A | 1 | a0007 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.1066G>A | p.Ala356Thr | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 12/20 | 1180/3337 | 1066/1818 | 356/605 | chr22 | 50521806 | |||
| chr22:50522362 | G | A | 1 | a0002 | 5 | HG01243.hp1 HG01256.hp1 HG02486.hp2 others(2): Show |
missense_variant | MODERATE | c.1253G>A | p.Arg418Gln | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 15/20 | 1367/3337 | 1253/1818 | 418/605 | chr22 | 50522362 | |||
| chr22:50523074 | C | T | 1 | a0006 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.1585C>T | p.Pro529Ser | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 19/20 | 1699/3337 | 1585/1818 | 529/605 | chr22 | 50523074 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:50518686 | C | T | 3 | a0001c0003 a0001c0007 a0002c0004 |
9 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
synonymous_variant | LOW | c.684C>T | p.Ser228Ser | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 8/20 | 798/3337 | 684/1818 | 228/605 | chr22 | 50518686 | |||
| chr22:50521027 | C | G | 1 | a0001c0017 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.924C>G | p.Ser308Ser | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 10/20 | 1038/3337 | 924/1818 | 308/605 | chr22 | 50521027 | |||
| chr22:50521585 | T | C | 1 | a0001c0009 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.976T>C | p.Leu326Leu | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 11/20 | 1090/3337 | 976/1818 | 326/605 | chr22 | 50521585 | |||
| chr22:50521841 | G | A | 1 | a0001c0011 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.1101G>A | p.Leu367Leu | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 12/20 | 1215/3337 | 1101/1818 | 367/605 | chr22 | 50521841 | |||
| chr22:50522363 | G | A | 1 | a0001c0012 | 1 | HG00558.hp1 | synonymous_variant | LOW | c.1254G>A | p.Arg418Arg | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 15/20 | 1368/3337 | 1254/1818 | 418/605 | chr22 | 50522363 | |||
| chr22:50522363 | G | T | 1 | a0001c0016 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.1254G>T | p.Arg418Arg | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 15/20 | 1368/3337 | 1254/1818 | 418/605 | chr22 | 50522363 | |||
| chr22:50522411 | A | G | 1 | a0001c0015 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.1302A>G | p.Ala434Ala | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 15/20 | 1416/3337 | 1302/1818 | 434/605 | chr22 | 50522411 | |||
| chr22:50522559 | C | T | 2 | a0001c0006 a0003c0018 |
3 | HG01109.hp1 HG02818.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.1365C>T | p.Ala455Ala | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 16/20 | 1479/3337 | 1365/1818 | 455/605 | chr22 | 50522559 | |||
| chr22:50523107 | C | T | 1 | a0001c0002 | 19 | HG01361.hp2 HG01496.hp1 HG01884.hp1 others(16): Show |
synonymous_variant | LOW | c.1618C>T | p.Leu540Leu | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 19/20 | 1732/3337 | 1618/1818 | 540/605 | chr22 | 50523107 | |||
| chr22:50523285 | C | T | 1 | a0001c0007 | 2 | HG02257.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.1728C>T | p.Ala576Ala | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 20/20 | 1842/3337 | 1728/1818 | 576/605 | chr22 | 50523285 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:50523401 | G | C | 1 | a0001c0001t0008 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*26G>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 20/20 | 26 | chr22 | 50523401 | ||||||
| chr22:50523425 | T | C | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(18): Show |
263 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*50T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 20/20 | 50 | chr22 | 50523425 | ||||||
| chr22:50523489 | C | T | 1 | a0001c0001t0010 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 20/20 | 114 | chr22 | 50523489 | ||||||
| chr22:50523635 | C | T | 1 | a0001c0001t0007 | 2 | HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*260C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 20/20 | 260 | chr22 | 50523635 | ||||||
| chr22:50523636 | G | A | 1 | a0001c0001t0011 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*261G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 20/20 | 261 | chr22 | 50523636 | ||||||
| chr22:50523649 | G | T | 1 | a0001c0001t0014 | 1 | HG01517.hp2 | 3_prime_UTR_variant | MODIFIER | c.*274G>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 20/20 | 274 | chr22 | 50523649 | ||||||
| chr22:50523779 | T | G | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(19): Show |
264 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*404T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 20/20 | 404 | chr22 | 50523779 | ||||||
| chr22:50523830 | G | A | 2 | a0001c0001t0004 a0001c0001t0007 |
10 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*455G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 20/20 | 455 | chr22 | 50523830 | ||||||
| chr22:50523956 | T | A | 1 | a0001c0001t0006 | 2 | HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*581T>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 20/20 | 581 | chr22 | 50523956 | ||||||
| chr22:50524085 | G | A | 5 | a0001c0001t0003 a0001c0003t0003 a0001c0007t0003 others(2): Show |
13 | HG01243.hp1 HG01256.hp1 HG02257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*710G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 20/20 | 710 | chr22 | 50524085 | ||||||
| chr22:50524131 | A | G | 1 | a0001c0001t0009 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*756A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 20/20 | 756 | chr22 | 50524131 | ||||||
| chr22:50524285 | G | C | 1 | a0001c0001t0010 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*910G>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 20/20 | 910 | chr22 | 50524285 | ||||||
| chr22:50524353 | C | G | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(18): Show |
263 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*978C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 20/20 | 978 | chr22 | 50524353 | ||||||
| chr22:50524455 | A | AAGGGAAG others(28): Show |
1 | a0001c0001t0013 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1081_*1115dupAGGG others(31): Show |
NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 20/20 | 1116 | INFO_REALIGN_3_PRIME | chr22 | 50524455 | |||||
| chr22:50524519 | G | T | 3 | a0001c0001t0005 a0001c0001t0008 a0001c0015t0005 |
7 | HG02165.hp1 HG02280.hp2 HG03239.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1144G>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 20/20 | 1144 | chr22 | 50524519 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:50508466 | A | C | 1 | a0001c0006t0002g0227 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.108+21A>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50508466 | |||||||
| chr22:50508520 | TGTGGGCG others(33): Show |
T | 1 | a0001c0001t0001g0046 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.108+76_108+115delG others(39): Show |
NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50508520 | |||||||
| chr22:50508527 | G | A | 11 | a0001c0001t0001g0222 a0001c0001t0002g0006 a0001c0001t0005g0045 others(8): Show |
11 | HG01167.hp1 HG02165.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+82G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50508527 | |||||||
| chr22:50508536 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.108+91T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50508536 | |||||||
| chr22:50508767 | T | C | 3 | a0001c0001t0004g0014 a0001c0001t0004g0016 a0001c0001t0007g0014 |
7 | HG00280.hp1 HG00733.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.108+322T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50508767 | |||||||
| chr22:50509002 | C | T | 4 | a0001c0001t0005g0045 a0001c0001t0005g0225 a0001c0001t0005g0226 others(1): Show |
4 | HG03239.hp2 HG03669.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+557C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50509002 | |||||||
| chr22:50509027 | A | G | 1 | a0002c0004t0003g0224 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.108+582A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50509027 | |||||||
| chr22:50509032 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.108+587A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50509032 | |||||||
| chr22:50509104 | AT | A | 5 | a0001c0001t0001g0017 a0001c0001t0003g0024 a0002c0004t0003g0048 others(2): Show |
8 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+667delT | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr22 | 50509104 | ||||||
| chr22:50509112 | T | C | 24 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(21): Show |
36 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.108+667T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50509112 | |||||||
| chr22:50509143 | A | G | 2 | a0001c0001t0001g0222 a0001c0001t0010g0221 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.108+698A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50509143 | |||||||
| chr22:50509171 | G | A | 3 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 |
3 | HG02055.hp2 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.108+726G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50509171 | |||||||
| chr22:50509182 | A | G | 34 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(31): Show |
46 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.108+737A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50509182 | |||||||
| chr22:50509283 | A | T | 1 | a0001c0001t0001g0217 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.108+838A>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50509283 | |||||||
| chr22:50509289 | C | T | 1 | a0001c0001t0011g0216 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.108+844C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50509289 | |||||||
| chr22:50509300 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.108+855A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50509300 | |||||||
| chr22:50509314 | G | C | 1 | a0001c0006t0002g0227 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.108+869G>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50509314 | |||||||
| chr22:50509429 | C | T | 1 | a0001c0006t0002g0066 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.108+984C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50509429 | |||||||
| chr22:50509488 | T | C | 34 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(31): Show |
46 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.108+1043T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50509488 | |||||||
| chr22:50509881 | A | G | 126 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0039 others(123): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.108+1436A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50509881 | |||||||
| chr22:50509927 | T | C | 2 | a0001c0002t0001g0025 a0001c0002t0001g0050 |
3 | HG02257.hp1 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.108+1482T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50509927 | |||||||
| chr22:50509962 | A | G | 37 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(34): Show |
49 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(46): Show |
intron_variant | MODIFIER | c.108+1517A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50509962 | |||||||
| chr22:50510070 | C | T | 6 | a0001c0001t0001g0063 a0001c0001t0002g0060 a0001c0001t0002g0062 others(3): Show |
6 | HG01256.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+1625C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50510070 | |||||||
| chr22:50510075 | C | T | 1 | a0001c0017t0012g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.108+1630C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50510075 | |||||||
| chr22:50510220 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0003g0024 a0002c0004t0003g0048 others(2): Show |
8 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+1775C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50510220 | |||||||
| chr22:50510223 | T | C | 10 | a0001c0001t0001g0056 a0001c0001t0002g0055 a0001c0002t0001g0007 others(7): Show |
19 | HG01361.hp2 HG01496.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.108+1778T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50510223 | |||||||
| chr22:50510262 | G | A | 1 | a0001c0001t0005g0225 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.108+1817G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50510262 | |||||||
| chr22:50510384 | C | T | 6 | a0001c0001t0005g0045 a0001c0001t0005g0219 a0001c0001t0005g0225 others(3): Show |
6 | HG02165.hp1 HG03239.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.108+1939C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50510384 | |||||||
| chr22:50510535 | C | A | 2 | a0001c0001t0002g0013 a0001c0001t0002g0148 |
6 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+2090C>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50510535 | |||||||
| chr22:50510623 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.108+2178C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50510623 | |||||||
| chr22:50510817 | C | T | 34 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(31): Show |
46 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.108+2372C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50510817 | |||||||
| chr22:50510841 | A | G | 24 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(21): Show |
36 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.108+2396A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50510841 | |||||||
| chr22:50510850 | AT | A | 13 | a0001c0001t0001g0026 a0001c0001t0001g0070 a0001c0001t0001g0071 others(10): Show |
14 | HG00558.hp2 HG01168.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.108+2419delT | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr22 | 50510850 | ||||||
| chr22:50510851 | T | A | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.108+2406T>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50510851 | |||||||
| chr22:50510944 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.108+2499T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50510944 | |||||||
| chr22:50510947 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.108+2502C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50510947 | |||||||
| chr22:50510954 | T | A | 10 | a0001c0001t0001g0222 a0001c0001t0005g0045 a0001c0001t0005g0219 others(7): Show |
10 | HG02165.hp1 HG02647.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.108+2509T>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50510954 | |||||||
| chr22:50510967 | T | C | 34 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(31): Show |
46 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.108+2522T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50510967 | |||||||
| chr22:50510988 | A | G | 6 | a0001c0001t0002g0044 a0001c0001t0002g0210 a0001c0001t0002g0211 others(3): Show |
7 | HG01123.hp2 HG01192.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+2543A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50510988 | |||||||
| chr22:50511032 | G | A | 24 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(21): Show |
36 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.108+2587G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511032 | |||||||
| chr22:50511048 | G | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(12): Show |
33 | HG00423.hp2 HG01928.hp2 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.108+2603G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511048 | |||||||
| chr22:50511068 | G | A | 2 | a0001c0001t0001g0027 a0001c0016t0001g0087 |
3 | HG02965.hp2 HG03453.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.108+2623G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511068 | |||||||
| chr22:50511068 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.108+2623G>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511068 | |||||||
| chr22:50511152 | A | G | 1 | a0001c0002t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.108+2707A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511152 | |||||||
| chr22:50511154 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.108+2709T>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511154 | |||||||
| chr22:50511189 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.108+2744G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511189 | |||||||
| chr22:50511285 | C | CT | 21 | a0001c0001t0001g0043 a0001c0001t0001g0078 a0001c0001t0001g0140 others(18): Show |
23 | HG01175.hp2 HG01891.hp2 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.108+2862dupT | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr22 | 50511285 | ||||||
| chr22:50511285 | C | CTTTT | 12 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0002g0055 others(9): Show |
21 | HG01361.hp2 HG01496.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.108+2859_108+2862d others(6): Show |
NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr22 | 50511285 | ||||||
| chr22:50511285 | C | CTTTTTT | 7 | a0001c0001t0001g0017 a0001c0001t0003g0024 a0002c0004t0003g0048 others(4): Show |
10 | HG01243.hp1 HG01256.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.108+2857_108+2862d others(8): Show |
NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr22 | 50511285 | ||||||
| chr22:50511285 | CT | C | 9 | a0001c0001t0001g0071 a0001c0001t0001g0091 a0001c0001t0002g0037 others(6): Show |
10 | HG01192.hp2 HG02897.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+2862delT | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr22 | 50511285 | ||||||
| chr22:50511329 | G | A | 1 | a0002c0004t0003g0224 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.108+2884G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511329 | |||||||
| chr22:50511351 | GCAATCTC others(349): Show |
G | 24 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(21): Show |
36 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.108+2932_108+3287d others(2): Show |
NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr22 | 50511351 | ||||||
| chr22:50511377 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.108+2932C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511377 | |||||||
| chr22:50511382 | T | C | 1 | a0001c0001t0002g0006 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.108+2937T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511382 | |||||||
| chr22:50511394 | A | G | 1 | a0001c0001t0002g0037 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.108+2949A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511394 | |||||||
| chr22:50511527 | A | G | 10 | a0001c0001t0001g0222 a0001c0001t0005g0045 a0001c0001t0005g0219 others(7): Show |
10 | HG02165.hp1 HG02647.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.108+3082A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511527 | |||||||
| chr22:50511647 | A | AT | 40 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0168 others(37): Show |
57 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(54): Show |
intron_variant | MODIFIER | c.108+3215dupT | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr22 | 50511647 | ||||||
| chr22:50511698 | T | G | 2 | a0001c0001t0001g0222 a0001c0001t0010g0221 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.108+3253T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511698 | |||||||
| chr22:50511746 | C | T | 45 | a0001c0001t0001g0022 a0001c0001t0001g0043 a0001c0001t0001g0151 others(42): Show |
67 | HG00408.hp2 HG00597.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.108+3301C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511746 | |||||||
| chr22:50511747 | G | A | 1 | a0006c0014t0001g0092 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.108+3302G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511747 | |||||||
| chr22:50511806 | T | C | 34 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(31): Show |
46 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.108+3361T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511806 | |||||||
| chr22:50511807 | G | A | 2 | a0001c0001t0001g0222 a0001c0001t0010g0221 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.108+3362G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511807 | |||||||
| chr22:50511841 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0146 |
3 | HG02809.hp2 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.108+3396G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50511841 | |||||||
| chr22:50512014 | T | C | 34 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(31): Show |
46 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.108+3569T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512014 | |||||||
| chr22:50512078 | G | A | 2 | a0001c0001t0001g0027 a0001c0016t0001g0087 |
3 | HG02965.hp2 HG03453.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.108+3633G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512078 | |||||||
| chr22:50512229 | T | A | 24 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(21): Show |
36 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.108+3784T>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512229 | |||||||
| chr22:50512278 | A | G | 2 | a0001c0002t0001g0218 a0001c0006t0002g0227 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.108+3833A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512278 | |||||||
| chr22:50512298 | G | A | 34 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(31): Show |
46 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.108+3853G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512298 | |||||||
| chr22:50512371 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0003g0024 a0002c0004t0003g0048 others(2): Show |
8 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+3926C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512371 | |||||||
| chr22:50512386 | C | T | 1 | a0001c0017t0012g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.108+3941C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512386 | |||||||
| chr22:50512438 | C | T | 1 | a0001c0015t0005g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.108+3993C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512438 | |||||||
| chr22:50512474 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.109-3973G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512474 | |||||||
| chr22:50512543 | GTT | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(52): Show |
108 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.109-3892_109-3891d others(4): Show |
NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr22 | 50512543 | ||||||
| chr22:50512549 | T | C | 4 | a0001c0001t0002g0042 a0001c0001t0002g0156 a0001c0001t0002g0203 others(1): Show |
5 | HG01255.hp2 HG02622.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-3898T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512549 | |||||||
| chr22:50512549 | T | G | 34 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(31): Show |
46 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.109-3898T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512549 | |||||||
| chr22:50512555 | T | G | 1 | a0001c0001t0001g0046 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.109-3892T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512555 | |||||||
| chr22:50512557 | G | T | 1 | a0001c0001t0001g0223 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.109-3890G>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512557 | |||||||
| chr22:50512558 | T | G | 1 | a0001c0001t0001g0223 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.109-3889T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512558 | |||||||
| chr22:50512660 | C | T | 1 | a0001c0006t0002g0066 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.109-3787C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512660 | |||||||
| chr22:50512721 | T | C | 3 | a0001c0001t0002g0021 a0001c0001t0002g0158 a0001c0001t0002g0205 |
5 | NA18952.hp2 NA18956.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.109-3726T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512721 | |||||||
| chr22:50512729 | A | G | 5 | a0001c0001t0001g0180 a0001c0001t0002g0021 a0001c0001t0002g0158 others(2): Show |
7 | NA18952.hp2 NA18956.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.109-3718A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512729 | |||||||
| chr22:50512820 | A | G | 1 | a0001c0001t0002g0202 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.109-3627A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512820 | |||||||
| chr22:50512918 | A | G | 10 | a0001c0001t0001g0222 a0001c0001t0005g0045 a0001c0001t0005g0219 others(7): Show |
10 | HG02165.hp1 HG02647.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.109-3529A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512918 | |||||||
| chr22:50512990 | G | A | 1 | a0001c0002t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.109-3457G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50512990 | |||||||
| chr22:50513034 | C | T | 1 | a0001c0006t0002g0066 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.109-3413C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50513034 | |||||||
| chr22:50513062 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.109-3385G>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50513062 | |||||||
| chr22:50513181 | C | A | 1 | a0001c0001t0010g0221 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-3266C>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50513181 | |||||||
| chr22:50513313 | G | C | 34 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(31): Show |
46 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.109-3134G>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50513313 | |||||||
| chr22:50513339 | CTG | C | 17 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0002g0055 others(14): Show |
26 | HG01109.hp1 HG01361.hp2 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.109-3105_109-3104d others(4): Show |
NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr22 | 50513339 | ||||||
| chr22:50513391 | C | T | 1 | a0001c0002t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.109-3056C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50513391 | |||||||
| chr22:50513400 | G | GGGCCGAG others(33): Show |
1 | a0001c0001t0005g0226 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.109-2993_109-2954d others(42): Show |
NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr22 | 50513400 | ||||||
| chr22:50513443 | C | G | 7 | a0001c0001t0001g0017 a0001c0001t0003g0024 a0002c0004t0003g0048 others(4): Show |
10 | HG01243.hp1 HG01256.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.109-3004C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50513443 | |||||||
| chr22:50513448 | G | A | 2 | a0001c0001t0002g0159 a0001c0001t0002g0160 |
2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.109-2999G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50513448 | |||||||
| chr22:50513793 | G | A | 34 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(31): Show |
46 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.109-2654G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50513793 | |||||||
| chr22:50513815 | A | G | 29 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(26): Show |
42 | HG01109.hp1 HG01243.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.109-2632A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50513815 | |||||||
| chr22:50513842 | C | T | 1 | a0001c0006t0002g0227 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.109-2605C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50513842 | |||||||
| chr22:50513859 | G | A | 1 | a0003c0018t0002g0058 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.109-2588G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50513859 | |||||||
| chr22:50513963 | C | A | 10 | a0001c0001t0001g0056 a0001c0001t0002g0055 a0001c0002t0001g0007 others(7): Show |
19 | HG01361.hp2 HG01496.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.109-2484C>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50513963 | |||||||
| chr22:50514038 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.109-2409C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514038 | |||||||
| chr22:50514102 | G | A | 6 | a0001c0001t0002g0013 a0001c0001t0002g0148 a0001c0001t0005g0045 others(3): Show |
10 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.109-2345G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514102 | |||||||
| chr22:50514106 | C | CAAACA | 2 | a0001c0001t0001g0027 a0001c0016t0001g0087 |
3 | HG02965.hp2 HG03453.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.109-2320_109-2316d others(7): Show |
NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr22 | 50514106 | ||||||
| chr22:50514141 | A | C | 1 | a0001c0001t0003g0024 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.109-2306A>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514141 | |||||||
| chr22:50514141 | A | G | 122 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0039 others(119): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.109-2306A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514141 | |||||||
| chr22:50514143 | G | A | 10 | a0001c0001t0001g0222 a0001c0001t0005g0045 a0001c0001t0005g0219 others(7): Show |
10 | HG02165.hp1 HG02647.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.109-2304G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514143 | |||||||
| chr22:50514163 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.109-2284G>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514163 | |||||||
| chr22:50514167 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.109-2280G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514167 | |||||||
| chr22:50514188 | C | T | 3 | a0001c0001t0002g0040 a0001c0001t0002g0152 a0001c0001t0002g0178 |
4 | HG01243.hp2 HG01884.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-2259C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514188 | |||||||
| chr22:50514223 | A | T | 1 | a0001c0001t0002g0201 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.109-2224A>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514223 | |||||||
| chr22:50514301 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0031 others(9): Show |
20 | HG00438.hp2 HG00558.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.109-2146G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514301 | |||||||
| chr22:50514306 | G | A | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG00099.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.109-2141G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514306 | |||||||
| chr22:50514483 | C | T | 3 | a0001c0001t0001g0063 a0001c0001t0002g0060 a0001c0001t0002g0062 |
3 | HG02630.hp2 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.109-1964C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514483 | |||||||
| chr22:50514514 | G | T | 1 | a0001c0001t0002g0086 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.109-1933G>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514514 | |||||||
| chr22:50514560 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG01168.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.109-1887G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514560 | |||||||
| chr22:50514631 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0010g0221 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.109-1816C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514631 | |||||||
| chr22:50514651 | C | T | 2 | a0001c0001t0002g0155 a0001c0001t0002g0200 |
2 | NA18965.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.109-1796C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514651 | |||||||
| chr22:50514674 | C | G | 24 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(21): Show |
36 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.109-1773C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514674 | |||||||
| chr22:50514800 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.109-1647T>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514800 | |||||||
| chr22:50514830 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.109-1617C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514830 | |||||||
| chr22:50514853 | T | C | 1 | a0001c0006t0002g0227 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.109-1594T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50514853 | |||||||
| chr22:50515023 | C | G | 1 | a0001c0001t0002g0160 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.109-1424C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515023 | |||||||
| chr22:50515095 | A | T | 24 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(21): Show |
36 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.109-1352A>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515095 | |||||||
| chr22:50515121 | A | T | 6 | a0001c0001t0005g0045 a0001c0001t0005g0219 a0001c0001t0005g0225 others(3): Show |
6 | HG02165.hp1 HG03239.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-1326A>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515121 | |||||||
| chr22:50515212 | C | T | 1 | a0001c0006t0002g0066 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.109-1235C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515212 | |||||||
| chr22:50515215 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.109-1232G>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515215 | |||||||
| chr22:50515279 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.109-1168G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515279 | |||||||
| chr22:50515431 | C | T | 1 | a0001c0003t0003g0135 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.109-1016C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515431 | |||||||
| chr22:50515436 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.109-1011G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515436 | |||||||
| chr22:50515456 | G | T | 1 | a0001c0001t0001g0177 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.109-991G>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515456 | |||||||
| chr22:50515459 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0002g0040 a0001c0001t0002g0152 |
4 | HG00609.hp1 HG01884.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-988C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515459 | |||||||
| chr22:50515465 | C | T | 1 | a0001c0001t0001g0017 | 3 | HG02559.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.109-982C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515465 | |||||||
| chr22:50515485 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.109-962C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515485 | |||||||
| chr22:50515490 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.109-957A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515490 | |||||||
| chr22:50515497 | T | C | 1 | a0001c0002t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.109-950T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515497 | |||||||
| chr22:50515565 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.109-882T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515565 | |||||||
| chr22:50515586 | C | T | 6 | a0001c0001t0005g0045 a0001c0001t0005g0219 a0001c0001t0005g0225 others(3): Show |
6 | HG02165.hp1 HG03239.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-861C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515586 | |||||||
| chr22:50515597 | C | T | 1 | a0001c0002t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.109-850C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515597 | |||||||
| chr22:50515611 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.109-836T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515611 | |||||||
| chr22:50515617 | C | T | 5 | a0001c0001t0002g0042 a0001c0001t0002g0156 a0001c0001t0002g0203 others(2): Show |
6 | HG01255.hp2 HG02622.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-830C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515617 | |||||||
| chr22:50515647 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.109-800C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515647 | |||||||
| chr22:50515657 | A | G | 1 | a0001c0016t0001g0087 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.109-790A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515657 | |||||||
| chr22:50515675 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.109-772T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515675 | |||||||
| chr22:50515686 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0003g0024 a0002c0004t0003g0048 others(1): Show |
7 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.109-761G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515686 | |||||||
| chr22:50515687 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0003g0024 a0002c0004t0003g0048 others(1): Show |
7 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.109-760C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515687 | |||||||
| chr22:50515688 | A | G | 36 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0063 others(33): Show |
49 | HG01109.hp1 HG01243.hp1 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.109-759A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515688 | |||||||
| chr22:50515695 | C | CT | 57 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0039 others(54): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.109-732dupT | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr22 | 50515695 | ||||||
| chr22:50515695 | C | CTT | 9 | a0001c0001t0001g0120 a0001c0001t0001g0195 a0001c0001t0002g0154 others(6): Show |
9 | HG00597.hp1 NA18994.hp1 NA19000.hp2 others(6): Show |
intron_variant | MODIFIER | c.109-733_109-732dup others(2): Show |
NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr22 | 50515695 | ||||||
| chr22:50515695 | CT | C | 15 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0081 others(12): Show |
19 | HG00609.hp2 HG00733.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.109-732delT | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr22 | 50515695 | ||||||
| chr22:50515767 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0001c0001t0001g0121 others(1): Show |
5 | NA18960.hp1 NA18986.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.109-680G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515767 | |||||||
| chr22:50515803 | A | G | 2 | a0001c0002t0001g0218 a0001c0006t0002g0227 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.109-644A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515803 | |||||||
| chr22:50515925 | A | T | 1 | a0001c0002t0001g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.109-522A>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515925 | |||||||
| chr22:50515935 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.109-512C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515935 | |||||||
| chr22:50515936 | G | A | 1 | a0001c0001t0014g0184 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.109-511G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50515936 | |||||||
| chr22:50516007 | GA | G | 71 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0039 others(68): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.109-439delA | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50516007 | |||||||
| chr22:50516182 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.109-265G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50516182 | |||||||
| chr22:50516206 | G | A | 19 | a0001c0001t0001g0017 a0001c0001t0001g0170 a0001c0001t0002g0172 others(16): Show |
26 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.109-241G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50516206 | |||||||
| chr22:50516256 | G | A | 40 | a0001c0001t0001g0043 a0001c0001t0001g0082 a0001c0001t0001g0151 others(37): Show |
60 | HG00408.hp2 HG00597.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.109-191G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50516256 | |||||||
| chr22:50516325 | T | G | 12 | a0001c0001t0001g0056 a0001c0001t0001g0222 a0001c0001t0002g0055 others(9): Show |
21 | HG01361.hp2 HG01496.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.109-122T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50516325 | |||||||
| chr22:50516395 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0072 a0001c0001t0001g0111 others(1): Show |
6 | HG00323.hp1 HG00735.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-52C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 1/19 | chr22 | 50516395 | |||||||
| chr22:50516603 | C | G | 7 | a0001c0001t0001g0017 a0001c0001t0003g0024 a0002c0004t0003g0048 others(4): Show |
10 | HG01243.hp1 HG01256.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.210+55C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 2/19 | chr22 | 50516603 | |||||||
| chr22:50516638 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0146 |
3 | HG02809.hp2 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.210+90C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 2/19 | chr22 | 50516638 | |||||||
| chr22:50516752 | T | G | 5 | a0002c0004t0003g0048 a0002c0004t0003g0049 a0002c0004t0003g0224 others(2): Show |
5 | HG01243.hp1 HG01256.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+204T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 2/19 | chr22 | 50516752 | |||||||
| chr22:50516787 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.210+239C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 2/19 | chr22 | 50516787 | |||||||
| chr22:50516906 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.210+358C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 2/19 | chr22 | 50516906 | |||||||
| chr22:50516953 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.210+405G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 2/19 | chr22 | 50516953 | |||||||
| chr22:50516970 | C | T | 59 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0132 others(56): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.210+422C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 2/19 | chr22 | 50516970 | |||||||
| chr22:50517043 | A | G | 3 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 |
3 | HG02055.hp2 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.211-384A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 2/19 | chr22 | 50517043 | |||||||
| chr22:50517074 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.211-353C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 2/19 | chr22 | 50517074 | |||||||
| chr22:50517076 | T | C | 1 | a0001c0001t0001g0034 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.211-351T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 2/19 | chr22 | 50517076 | |||||||
| chr22:50517109 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0017 others(142): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.211-318A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 2/19 | chr22 | 50517109 | |||||||
| chr22:50517134 | A | C | 1 | a0001c0001t0001g0083 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.211-293A>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 2/19 | chr22 | 50517134 | |||||||
| chr22:50517167 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.211-260A>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 2/19 | chr22 | 50517167 | |||||||
| chr22:50517186 | C | T | 23 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0026 others(20): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.211-241C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 2/19 | chr22 | 50517186 | |||||||
| chr22:50517351 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.211-76A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 2/19 | chr22 | 50517351 | |||||||
| chr22:50517353 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.211-74C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 2/19 | chr22 | 50517353 | |||||||
| chr22:50517687 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.351+26C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 4/19 | chr22 | 50517687 | |||||||
| chr22:50517713 | C | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0046 a0001c0001t0001g0070 others(7): Show |
17 | HG01928.hp2 HG01993.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.352-28C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 4/19 | chr22 | 50517713 | |||||||
| chr22:50517941 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.421-32G>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 5/19 | chr22 | 50517941 | |||||||
| chr22:50517957 | C | G | 7 | a0001c0001t0001g0140 a0001c0001t0005g0045 a0001c0001t0005g0219 others(4): Show |
7 | HG01175.hp2 HG02165.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-16C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 5/19 | chr22 | 50517957 | |||||||
| chr22:50517957 | C | T | 1 | a0001c0002t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.421-16C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 5/19 | chr22 | 50517957 | |||||||
| chr22:50518072 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.500+20G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 6/19 | chr22 | 50518072 | |||||||
| chr22:50518407 | C | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0138 |
3 | HG01106.hp1 HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.646+129C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 7/19 | chr22 | 50518407 | |||||||
| chr22:50518446 | T | C | 7 | a0001c0001t0002g0060 a0001c0001t0002g0062 a0001c0006t0002g0066 others(4): Show |
7 | HG01109.hp1 HG01256.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.646+168T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 7/19 | chr22 | 50518446 | |||||||
| chr22:50518522 | G | T | 3 | a0001c0001t0002g0042 a0001c0001t0002g0156 a0001c0001t0002g0204 |
4 | HG01255.hp2 HG02622.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.647-127G>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 7/19 | chr22 | 50518522 | |||||||
| chr22:50518754 | G | A | 1 | a0002c0005t0003g0064 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.730+22G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 8/19 | chr22 | 50518754 | |||||||
| chr22:50518897 | C | T | 1 | a0001c0001t0002g0193 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.730+165C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 8/19 | chr22 | 50518897 | |||||||
| chr22:50519033 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.731-157C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 8/19 | chr22 | 50519033 | |||||||
| chr22:50519072 | G | A | 1 | a0001c0001t0004g0174 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.731-118G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 8/19 | chr22 | 50519072 | |||||||
| chr22:50519091 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.731-99G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 8/19 | chr22 | 50519091 | |||||||
| chr22:50519169 | A | G | 9 | a0001c0001t0001g0076 a0001c0001t0001g0140 a0001c0001t0005g0045 others(6): Show |
9 | HG01168.hp2 HG01175.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.731-21A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 8/19 | chr22 | 50519169 | |||||||
| chr22:50519431 | C | G | 1 | a0001c0001t0002g0186 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.861+111C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50519431 | |||||||
| chr22:50519556 | G | A | 4 | a0001c0001t0002g0023 a0001c0001t0002g0139 a0001c0001t0002g0196 others(1): Show |
6 | HG02083.hp1 HG03927.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.861+236G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50519556 | |||||||
| chr22:50519605 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.861+285C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50519605 | |||||||
| chr22:50519627 | C | T | 9 | a0001c0002t0001g0007 a0001c0002t0001g0025 a0001c0002t0001g0050 others(6): Show |
18 | HG01361.hp2 HG01496.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.861+307C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50519627 | |||||||
| chr22:50519763 | G | A | 1 | a0001c0001t0001g0019 | 3 | HG01358.hp1 HG01981.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.861+443G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50519763 | |||||||
| chr22:50519806 | A | G | 1 | a0001c0001t0002g0192 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.861+486A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50519806 | |||||||
| chr22:50519826 | A | G | 3 | a0001c0001t0001g0191 a0001c0001t0001g0194 a0001c0001t0001g0209 |
3 | HG02683.hp1 HG02735.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.861+506A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50519826 | |||||||
| chr22:50519867 | TTG | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0077 others(5): Show |
20 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.861+551_861+552del others(2): Show |
NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr22 | 50519867 | ||||||
| chr22:50519911 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.861+591C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50519911 | |||||||
| chr22:50519913 | C | A | 1 | a0001c0001t0001g0034 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.861+593C>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50519913 | |||||||
| chr22:50519956 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0010g0221 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.861+636C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50519956 | |||||||
| chr22:50519963 | C | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0029 others(29): Show |
52 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.861+643C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50519963 | |||||||
| chr22:50520163 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-802C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520163 | |||||||
| chr22:50520164 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-801C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520164 | |||||||
| chr22:50520165 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-800C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520165 | |||||||
| chr22:50520168 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-797C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520168 | |||||||
| chr22:50520169 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-796C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520169 | |||||||
| chr22:50520170 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-795C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520170 | |||||||
| chr22:50520171 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-794A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520171 | |||||||
| chr22:50520172 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-793C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520172 | |||||||
| chr22:50520173 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-792T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520173 | |||||||
| chr22:50520175 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-790T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520175 | |||||||
| chr22:50520176 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-789T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520176 | |||||||
| chr22:50520177 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-788T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520177 | |||||||
| chr22:50520179 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-786T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520179 | |||||||
| chr22:50520181 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-784T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520181 | |||||||
| chr22:50520182 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-783T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520182 | |||||||
| chr22:50520183 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-782T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520183 | |||||||
| chr22:50520184 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-781T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520184 | |||||||
| chr22:50520185 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-780A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520185 | |||||||
| chr22:50520186 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-779A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520186 | |||||||
| chr22:50520187 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-778A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520187 | |||||||
| chr22:50520189 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-776T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520189 | |||||||
| chr22:50520190 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-775T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520190 | |||||||
| chr22:50520191 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-774T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520191 | |||||||
| chr22:50520192 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-773T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520192 | |||||||
| chr22:50520193 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-772T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520193 | |||||||
| chr22:50520194 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-771C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520194 | |||||||
| chr22:50520195 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-770T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520195 | |||||||
| chr22:50520196 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-769T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520196 | |||||||
| chr22:50520197 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-768A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520197 | |||||||
| chr22:50520201 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-764T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520201 | |||||||
| chr22:50520202 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-763T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520202 | |||||||
| chr22:50520203 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-762T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520203 | |||||||
| chr22:50520204 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-761T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520204 | |||||||
| chr22:50520205 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-760T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520205 | |||||||
| chr22:50520207 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-758T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520207 | |||||||
| chr22:50520208 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-757T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520208 | |||||||
| chr22:50520209 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-756T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520209 | |||||||
| chr22:50520210 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-755T>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520210 | |||||||
| chr22:50520211 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.862-754A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520211 | |||||||
| chr22:50520246 | ATCTTATT others(28): Show |
A | 1 | a0001c0001t0013g0006 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.862-717_862-683del others(35): Show |
NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr22 | 50520246 | ||||||
| chr22:50520280 | C | G | 1 | a0001c0001t0001g0027 | 2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.862-685C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520280 | |||||||
| chr22:50520281 | T | C | 5 | a0001c0001t0001g0043 a0001c0001t0001g0151 a0001c0001t0001g0157 others(2): Show |
6 | NA18944.hp1 NA18951.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.862-684T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520281 | |||||||
| chr22:50520286 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.862-679C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520286 | |||||||
| chr22:50520379 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG00544.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.862-586G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520379 | |||||||
| chr22:50520414 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0129 a0001c0001t0001g0134 others(3): Show |
9 | HG01891.hp2 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.862-551C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520414 | |||||||
| chr22:50520454 | G | C | 1 | a0001c0007t0003g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.862-511G>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520454 | |||||||
| chr22:50520529 | T | C | 11 | a0001c0001t0003g0024 a0001c0003t0003g0035 a0001c0003t0003g0128 others(8): Show |
13 | HG01243.hp1 HG01256.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.862-436T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520529 | |||||||
| chr22:50520534 | G | A | 1 | a0001c0001t0002g0197 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.862-431G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520534 | |||||||
| chr22:50520549 | C | T | 1 | a0001c0015t0005g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.862-416C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520549 | |||||||
| chr22:50520561 | G | GT | 9 | a0001c0001t0001g0034 a0001c0001t0001g0077 a0001c0001t0001g0089 others(6): Show |
10 | HG00741.hp2 HG01175.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.862-388dupT | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr22 | 50520561 | ||||||
| chr22:50520581 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0146 |
2 | HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.862-384C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520581 | |||||||
| chr22:50520623 | A | G | 37 | a0001c0001t0001g0188 a0001c0001t0002g0005 a0001c0001t0002g0013 others(34): Show |
56 | HG00408.hp2 HG00597.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.862-342A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520623 | |||||||
| chr22:50520683 | C | T | 2 | a0001c0001t0002g0156 a0001c0001t0002g0204 |
2 | HG01255.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.862-282C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520683 | |||||||
| chr22:50520688 | A | T | 1 | a0001c0006t0002g0227 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.862-277A>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520688 | |||||||
| chr22:50520707 | C | T | 3 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 |
3 | HG02055.hp2 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.862-258C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520707 | |||||||
| chr22:50520719 | C | T | 11 | a0001c0001t0003g0024 a0001c0001t0005g0219 a0001c0003t0003g0035 others(8): Show |
13 | HG01243.hp1 HG02165.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.862-246C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520719 | |||||||
| chr22:50520796 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.862-169C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 9/19 | chr22 | 50520796 | |||||||
| chr22:50521109 | T | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0217 a0001c0001t0001g0223 |
4 | HG00140.hp1 HG00738.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.933+73T>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 10/19 | chr22 | 50521109 | |||||||
| chr22:50521179 | C | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0029 others(30): Show |
53 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.933+143C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 10/19 | chr22 | 50521179 | |||||||
| chr22:50521182 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.933+146A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 10/19 | chr22 | 50521182 | |||||||
| chr22:50521273 | C | T | 1 | a0002c0004t0003g0224 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.933+237C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 10/19 | chr22 | 50521273 | |||||||
| chr22:50521319 | C | CTGGGAGG others(24): Show |
18 | a0001c0001t0003g0024 a0001c0001t0005g0045 a0001c0001t0005g0106 others(15): Show |
20 | HG01243.hp1 HG01256.hp1 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.934-207_934-177dup others(31): Show |
NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr22 | 50521319 | ||||||
| chr22:50521319 | CTGGGAGG others(58): Show |
C | 12 | a0001c0001t0001g0222 a0001c0001t0010g0221 a0001c0002t0001g0007 others(9): Show |
21 | HG01361.hp2 HG01496.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.934-207_934-143del others(65): Show |
NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr22 | 50521319 | ||||||
| chr22:50521339 | C | CCCCTACT others(24): Show |
123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
221 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.934-177_934-176ins others(31): Show |
NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr22 | 50521339 | ||||||
| chr22:50521416 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.934-127C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 10/19 | chr22 | 50521416 | |||||||
| chr22:50521428 | G | A | 1 | a0001c0001t0002g0189 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.934-115G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 10/19 | chr22 | 50521428 | |||||||
| chr22:50521443 | A | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0164 a0001c0001t0002g0166 |
4 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-100A>C | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 10/19 | chr22 | 50521443 | |||||||
| chr22:50521520 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.934-23G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 10/19 | chr22 | 50521520 | |||||||
| chr22:50521672 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
262 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.1000+63G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 11/19 | chr22 | 50521672 | |||||||
| chr22:50521873 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1108+25G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 12/19 | chr22 | 50521873 | |||||||
| chr22:50522253 | C | T | 61 | a0001c0001t0002g0005 a0001c0001t0002g0013 a0001c0001t0002g0023 others(58): Show |
86 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(83): Show |
splice_donor_variant&intron_variant | HIGH | c.1233+2C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 14/19 | chr22 | 50522253 | |||||||
| chr22:50522422 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18940.hp2 | splice_region_variant&intron_variant | LOW | c.1306+7G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 15/19 | chr22 | 50522422 | |||||||
| chr22:50522423 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18940.hp2 | splice_region_variant&intron_variant | LOW | c.1306+8C>T | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 15/19 | chr22 | 50522423 | |||||||
| chr22:50522740 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.1425+20A>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 17/19 | chr22 | 50522740 | |||||||
| chr22:50522782 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1426-39C>G | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 17/19 | chr22 | 50522782 | |||||||
| chr22:50522936 | G | A | 4 | a0001c0001t0001g0097 a0001c0001t0001g0102 a0001c0001t0001g0107 others(1): Show |
4 | HG00609.hp2 HG00673.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1527+14G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 18/19 | chr22 | 50522936 | |||||||
| chr22:50522989 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1528-28G>A | NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 18/19 | chr22 | 50522989 |