Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23119 |
| ensemblid | ENSG00000169635.10 |
| hgncid | 18595 |
| symbol | HIC2 |
| name | HIC ZBTB transcriptional repressor 2 |
| refseq_nuc | NM_015094.3 |
| refseq_prot | NP_055909.2 |
| ensembl_nuc | ENST00000407464.7 |
| ensembl_prot | ENSP00000385319.2 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 21417371 |
| end | 21451463 |
| strand | + |
| ver | v1.2 |
| region | chr22:21417371-21451463 |
| region5000 | chr22:21412371-21456463 |
| regionname0 | HIC2_chr22_21417371_21451463 |
| regionname5000 | HIC2_chr22_21412371_21456463 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 615 | 278 | 74 | 53 | 106 | 8 | 36 | 76 | HIC2_chr22_21412371_21456463 | HIC2 | MVSGP others(610): Show |
chr22 | 21412371 | 21456463 |
| a0002 | 0/1 | 615 | 5 | 2 | 1 | 1 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | MVSGP others(610): Show |
chr22 | 21412371 | 21456463 |
| a0003 | 0/0 | 615 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | MVSGP others(610): Show |
chr22 | 21412371 | 21456463 |
| a0004 | 0/0 | 615 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | MVSGP others(610): Show |
chr22 | 21412371 | 21456463 |
| a0005 | 0/0 | 615 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | MVSGP others(610): Show |
chr22 | 21412371 | 21456463 |
| a0006 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | MVSGP others(610): Show |
chr22 | 21412371 | 21456463 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1845 | 249 | 73 | 52 | 88 | 8 | 28 | HIC2_chr22_21412371_21456463 | HIC2 | ATGGT others(1840): Show |
chr22 | 21412371 | 21456463 | ||
| a0001c0002 | 1/0 | 1845 | 14 | 0 | 0 | 5 | 0 | 8 | HIC2_chr22_21412371_21456463 | HIC2 | ATGGT others(1840): Show |
chr22 | 21412371 | 21456463 | ||
| a0001c0003 | 0/0 | 1845 | 7 | 1 | 0 | 6 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ATGGT others(1840): Show |
chr22 | 21412371 | 21456463 | ||
| a0001c0005 | 0/0 | 1845 | 4 | 0 | 1 | 3 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ATGGT others(1840): Show |
chr22 | 21412371 | 21456463 | ||
| a0001c0007 | 0/0 | 1845 | 2 | 0 | 0 | 2 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ATGGT others(1840): Show |
chr22 | 21412371 | 21456463 | ||
| a0001c0008 | 0/0 | 1845 | 2 | 0 | 0 | 2 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ATGGT others(1840): Show |
chr22 | 21412371 | 21456463 | ||
| a0002c0004 | 0/1 | 1845 | 5 | 2 | 1 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ATGGT others(1840): Show |
chr22 | 21412371 | 21456463 | ||
| a0003c0006 | 0/0 | 1845 | 2 | 0 | 0 | 0 | 0 | 2 | HIC2_chr22_21412371_21456463 | HIC2 | ATGGT others(1840): Show |
chr22 | 21412371 | 21456463 | ||
| a0004c0009 | 0/0 | 1845 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ATGGT others(1840): Show |
chr22 | 21412371 | 21456463 | ||
| a0005c0011 | 0/0 | 1845 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ATGGT others(1840): Show |
chr22 | 21412371 | 21456463 | ||
| a0006c0010 | 0/0 | 1845 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ATGGT others(1840): Show |
chr22 | 21412371 | 21456463 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6830 | 63 | 14 | 15 | 16 | 3 | 15 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0002 | 0/0 | 6832 | 55 | 0 | 16 | 28 | 3 | 8 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0003 | 0/0 | 6830 | 25 | 23 | 2 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0004 | 0/0 | 6830 | 20 | 0 | 0 | 20 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0006 | 0/0 | 6831 | 8 | 6 | 2 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6826): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0007 | 0/0 | 6830 | 8 | 4 | 3 | 0 | 1 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0008 | 0/0 | 6833 | 5 | 1 | 1 | 3 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6828): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0009 | 0/0 | 6832 | 4 | 4 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0010 | 0/0 | 6830 | 5 | 5 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0011 | 0/0 | 6830 | 3 | 0 | 0 | 3 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0013 | 0/0 | 6831 | 3 | 0 | 0 | 3 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6826): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0014 | 0/0 | 6826 | 3 | 3 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6821): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0015 | 0/0 | 6830 | 3 | 1 | 1 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0016 | 0/0 | 6832 | 3 | 0 | 0 | 3 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0017 | 0/0 | 6830 | 3 | 0 | 3 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0018 | 0/0 | 6830 | 2 | 0 | 2 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0019 | 0/0 | 6830 | 2 | 2 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0021 | 0/0 | 6832 | 2 | 0 | 2 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0022 | 0/0 | 6832 | 2 | 2 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0023 | 0/0 | 6832 | 2 | 1 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0024 | 0/0 | 6832 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0029 | 0/0 | 6833 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6828): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0030 | 0/0 | 6827 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6822): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0031 | 0/0 | 6831 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6826): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0032 | 0/0 | 6830 | 1 | 0 | 0 | 0 | 1 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0033 | 0/0 | 6830 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0034 | 0/0 | 6830 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0035 | 0/0 | 6830 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0036 | 0/0 | 6831 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6826): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0037 | 0/0 | 6831 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6826): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0038 | 0/0 | 6830 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0039 | 0/0 | 6830 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0040 | 0/0 | 6828 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6823): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0041 | 0/0 | 6830 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0043 | 0/0 | 6830 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0044 | 0/0 | 6830 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0045 | 0/0 | 6830 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0046 | 0/0 | 6830 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0047 | 0/0 | 6830 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0050 | 0/0 | 6832 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0051 | 0/0 | 6832 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0052 | 0/0 | 6832 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0053 | 0/0 | 6832 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0054 | 0/0 | 6832 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0055 | 0/0 | 6832 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0056 | 0/0 | 6832 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0057 | 0/0 | 6832 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0001t0059 | 0/0 | 6830 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0002t0005 | 1/0 | 6831 | 13 | 0 | 0 | 5 | 0 | 7 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6826): Show |
chr22 | 21412371 | 21456463 |
| a0001c0002t0026 | 0/0 | 6831 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6826): Show |
chr22 | 21412371 | 21456463 |
| a0001c0003t0002 | 0/0 | 6832 | 4 | 1 | 0 | 3 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0003t0008 | 0/0 | 6833 | 2 | 0 | 0 | 2 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6828): Show |
chr22 | 21412371 | 21456463 |
| a0001c0003t0058 | 0/0 | 6832 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0005t0012 | 0/0 | 6830 | 3 | 0 | 1 | 2 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0001c0005t0028 | 0/0 | 6831 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6826): Show |
chr22 | 21412371 | 21456463 |
| a0001c0007t0005 | 0/0 | 6831 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6826): Show |
chr22 | 21412371 | 21456463 |
| a0001c0007t0027 | 0/0 | 6832 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0001c0008t0004 | 0/0 | 6830 | 2 | 0 | 0 | 2 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0002c0004t0020 | 0/1 | 6830 | 2 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0002c0004t0025 | 0/0 | 6830 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0002c0004t0048 | 0/0 | 6830 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0002c0004t0049 | 0/0 | 6830 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| a0003c0006t0002 | 0/0 | 6832 | 2 | 0 | 0 | 0 | 0 | 2 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0004c0009t0009 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0005c0011t0042 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6827): Show |
chr22 | 21412371 | 21456463 |
| a0006c0010t0001 | 0/0 | 6830 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | ACAAG others(6825): Show |
chr22 | 21412371 | 21456463 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 1 | 3 | 3 | 2 | 5 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0002 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0013 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0004g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0004g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0006g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0007g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0007g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0008g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0008g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0008g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0008g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0009g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0010g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0010g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0010g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0011g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0011g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0013g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0014g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0014g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0014g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0015g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0015g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0015g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0016g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0016g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0016g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0017g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0017g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0018g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0018g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0019g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0019g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0021g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0022g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0023g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0023g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0024g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0029g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0030g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0031g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0032g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0033g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0034g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0035g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0036g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0037g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0038g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0039g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0040g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0041g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0043g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0044g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0045g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0046g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0047g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0050g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0051g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0052g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0053g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0054g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0055g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0056g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0057g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0001t0059g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0002t0005g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0002t0005g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0002t0005g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0002t0005g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0002t0005g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0002t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0002t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0002t0005g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0002t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0002t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0002t0026g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0003t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0003t0008g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0003t0008g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0003t0058g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0005t0012g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0005t0012g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0005t0012g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0005t0028g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0007t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0007t0027g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0008t0004g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0001c0008t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0002c0004t0020g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0002c0004t0020g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0002c0004t0025g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0002c0004t0048g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0002c0004t0049g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0003c0006t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0003c0006t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0004c0009t0009g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0005c0011t0042g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| a0006c0010t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00099 | hp2 | a0001 | c0001 | t0032 | g0135 | EUR | GBR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | GBR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0037 | EUR | GBR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0070 | EUR | FIN | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00438 | hp2 | a0001 | c0001 | t0059 | g0181 | EAS | CHS | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0120 | EAS | CHS | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00621 | hp1 | a0001 | c0007 | t0027 | g0213 | EAS | CHS | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00621 | hp2 | a0001 | c0001 | t0011 | g0140 | EAS | CHS | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0030 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00673 | hp2 | a0001 | c0001 | t0036 | g0101 | EAS | CHS | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00733 | hp2 | a0001 | c0001 | t0018 | g0125 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00738 | hp2 | a0001 | c0001 | t0007 | g0187 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00741 | hp1 | a0001 | c0001 | t0021 | g0009 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG00741 | hp2 | a0001 | c0001 | t0023 | g0163 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01071 | hp1 | a0002 | c0004 | t0049 | g0179 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01099 | hp1 | a0001 | c0001 | t0015 | g0148 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01099 | hp2 | a0001 | c0001 | t0008 | g0203 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01168 | hp1 | a0001 | c0001 | t0018 | g0124 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0020 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0145 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0020 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01261 | hp2 | a0001 | c0001 | t0041 | g0086 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0189 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01496 | hp1 | a0001 | c0001 | t0017 | g0021 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01496 | hp2 | a0001 | c0001 | t0007 | g0126 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01884 | hp1 | a0001 | c0001 | t0023 | g0188 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01975 | hp1 | a0001 | c0001 | t0017 | g0049 | AMR | PEL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01981 | hp1 | a0001 | c0001 | t0021 | g0009 | AMR | PEL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01993 | hp2 | a0001 | c0001 | t0055 | g0003 | AMR | PEL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PEL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02004 | hp2 | a0001 | c0001 | t0057 | g0076 | AMR | PEL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02027 | hp1 | a0001 | c0002 | t0005 | g0156 | EAS | KHV | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02027 | hp2 | a0001 | c0001 | t0056 | g0069 | EAS | KHV | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | KHV | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | KHV | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0201 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0191 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02056 | hp1 | a0001 | c0001 | t0038 | g0001 | EAS | KHV | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02056 | hp2 | a0001 | c0007 | t0005 | g0212 | EAS | KHV | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | KHV | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02083 | hp1 | a0001 | c0008 | t0004 | g0001 | EAS | KHV | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02129 | hp1 | a0001 | c0002 | t0005 | g0155 | EAS | KHV | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | KHV | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02132 | hp2 | a0001 | c0003 | t0058 | g0064 | EAS | KHV | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02135 | hp2 | a0001 | c0003 | t0008 | g0211 | EAS | KHV | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0194 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | CDX | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0185 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0122 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02273 | hp1 | a0001 | c0001 | t0017 | g0021 | AMR | PEL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02273 | hp2 | a0001 | c0005 | t0012 | g0160 | AMR | PEL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02451 | hp1 | a0001 | c0001 | t0022 | g0019 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02451 | hp2 | a0001 | c0001 | t0014 | g0077 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02572 | hp1 | a0001 | c0001 | t0030 | g0078 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02572 | hp2 | a0001 | c0001 | t0047 | g0084 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0173 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0006 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02738 | hp2 | a0001 | c0001 | t0035 | g0214 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0184 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02809 | hp2 | a0004 | c0009 | t0009 | g0176 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0195 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0180 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02886 | hp2 | a0005 | c0011 | t0042 | g0190 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0167 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02895 | hp2 | a0001 | c0001 | t0046 | g0175 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02896 | hp1 | a0001 | c0001 | t0015 | g0147 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0006 | AFR | ESN | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02976 | hp2 | a0001 | c0001 | t0019 | g0222 | AFR | ESN | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0219 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | MSL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | ESN | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | ESN | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | ESN | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0193 | AFR | ESN | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03225 | hp1 | a0002 | c0004 | t0020 | g0094 | AFR | MSL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0006 | AFR | MSL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | MSL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03486 | hp2 | a0001 | c0001 | t0033 | g0081 | AFR | MSL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03491 | hp1 | a0001 | c0002 | t0005 | g0017 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03492 | hp1 | a0001 | c0002 | t0005 | g0017 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | ESN | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03516 | hp2 | a0001 | c0001 | t0019 | g0223 | AFR | ESN | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03540 | hp1 | a0001 | c0001 | t0044 | g0198 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03540 | hp2 | a0002 | c0004 | t0048 | g0183 | AFR | GWD | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03579 | hp1 | a0001 | c0001 | t0043 | g0031 | AFR | MSL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03579 | hp2 | a0001 | c0001 | t0014 | g0207 | AFR | MSL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03669 | hp2 | a0001 | c0001 | t0040 | g0093 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03704 | hp1 | a0001 | c0002 | t0005 | g0005 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03704 | hp2 | a0001 | c0002 | t0005 | g0154 | SAS | PJL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03831 | hp1 | a0003 | c0006 | t0002 | g0036 | SAS | BEB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03834 | hp1 | a0001 | c0001 | t0024 | g0131 | SAS | BEB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03834 | hp2 | a0003 | c0006 | t0002 | g0043 | SAS | BEB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03927 | hp1 | a0001 | c0002 | t0005 | g0153 | SAS | BEB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03927 | hp2 | a0001 | c0001 | t0037 | g0085 | SAS | BEB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03942 | hp1 | a0001 | c0002 | t0005 | g0159 | SAS | BEB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG04115 | hp1 | a0001 | c0002 | t0026 | g0005 | SAS | STU | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG04184 | hp1 | a0001 | c0001 | t0015 | g0209 | SAS | BEB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | STU | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | STU | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | STU | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18747 | hp1 | a0001 | c0001 | t0011 | g0118 | EAS | CHB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18747 | hp2 | a0001 | c0003 | t0002 | g0058 | EAS | CHB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18941 | hp1 | a0001 | c0002 | t0005 | g0018 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18941 | hp2 | a0001 | c0003 | t0008 | g0044 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18942 | hp2 | a0001 | c0001 | t0008 | g0055 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18943 | hp2 | a0001 | c0001 | t0051 | g0003 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18946 | hp1 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18946 | hp2 | a0001 | c0001 | t0016 | g0072 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18948 | hp1 | a0001 | c0001 | t0034 | g0134 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18948 | hp2 | a0001 | c0001 | t0052 | g0004 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18952 | hp2 | a0001 | c0008 | t0004 | g0012 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18975 | hp1 | a0001 | c0005 | t0028 | g0002 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18978 | hp1 | a0001 | c0001 | t0029 | g0104 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18978 | hp2 | a0001 | c0001 | t0008 | g0074 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18980 | hp1 | a0002 | c0004 | t0025 | g0178 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18982 | hp2 | a0001 | c0005 | t0012 | g0098 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18984 | hp1 | a0001 | c0001 | t0054 | g0052 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18990 | hp1 | a0001 | c0002 | t0005 | g0158 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19003 | hp1 | a0001 | c0003 | t0002 | g0038 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19004 | hp1 | a0001 | c0001 | t0008 | g0028 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19011 | hp1 | a0001 | c0003 | t0002 | g0047 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19012 | hp1 | a0001 | c0005 | t0012 | g0133 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19012 | hp2 | a0006 | c0010 | t0001 | g0141 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0171 | AFR | LWK | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19057 | hp1 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19057 | hp2 | a0001 | c0001 | t0016 | g0149 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19062 | hp2 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19066 | hp1 | a0001 | c0001 | t0039 | g0001 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19070 | hp1 | a0001 | c0001 | t0053 | g0079 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19070 | hp2 | a0001 | c0001 | t0045 | g0032 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19076 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19079 | hp1 | a0001 | c0001 | t0016 | g0071 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19086 | hp1 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19086 | hp2 | a0001 | c0002 | t0005 | g0018 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0162 | AFR | YRI | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA19240 | hp2 | a0001 | c0001 | t0031 | g0216 | AFR | YRI | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0197 | AFR | ASW | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA20129 | hp2 | a0001 | c0001 | t0014 | g0152 | AFR | ASW | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA20752 | hp1 | a0001 | c0001 | t0007 | g0182 | EUR | TSI | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0204 | EUR | TSI | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA20905 | hp1 | a0001 | c0002 | t0005 | g0005 | SAS | GIH | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG01123 | hp2 | a0001 | c0001 | t0050 | g0003 | AMR | CLM | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG02559 | hp2 | a0001 | c0001 | t0022 | g0019 | AFR | ACB | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | MSL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | MSL | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | USA | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0196 | AFR | USA | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | USA | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0034 | AFR | USA | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | LWK | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| homoSapiens | chm13v2 | a0002 | c0004 | t0020 | g0150 | REF | REF | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0005 | g0157 | REF | REF | HIC2_chr22_21412371_21456463 | HIC2 | chr22 | 21412371 | 21456463 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:21445469 | C | T | 1 | a0005 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.574C>T | p.Pro192Ser | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 837/6831 | 574/1848 | 192/615 | chr22 | 21445469 | |||
| chr22:21445754 | C | T | 1 | a0006 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.859C>T | p.Pro287Ser | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1122/6831 | 859/1848 | 287/615 | chr22 | 21445754 | |||
| chr22:21445938 | C | G | 1 | a0004 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1043C>G | p.Ser348Cys | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1306/6831 | 1043/1848 | 348/615 | chr22 | 21445938 | |||
| chr22:21445980 | C | T | 1 | a0002 | 4 | HG01071.hp1 HG03225.hp1 HG03540.hp2 others(1): Show |
missense_variant | MODERATE | c.1085C>T | p.Pro362Leu | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1348/6831 | 1085/1848 | 362/615 | chr22 | 21445980 | |||
| chr22:21445988 | G | A | 1 | a0003 | 2 | HG03831.hp1 HG03834.hp2 |
missense_variant | MODERATE | c.1093G>A | p.Glu365Lys | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1356/6831 | 1093/1848 | 365/615 | chr22 | 21445988 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:21445036 | C | T | 1 | a0001c0005 | 4 | HG02273.hp2 NA18975.hp1 NA18982.hp2 others(1): Show |
synonymous_variant | LOW | c.141C>T | p.Asp47Asp | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 404/6831 | 141/1848 | 47/615 | chr22 | 21445036 | |||
| chr22:21445753 | T | C | 9 | a0001c0001 a0001c0003 a0001c0005 others(6): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
synonymous_variant | LOW | c.858T>C | p.Ala286Ala | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1121/6831 | 858/1848 | 286/615 | chr22 | 21445753 | |||
| chr22:21445753 | T | G | 1 | a0006c0010 | 1 | NA19012.hp2 | synonymous_variant | LOW | c.858T>G | p.Ala286Ala | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1121/6831 | 858/1848 | 286/615 | chr22 | 21445753 | |||
| chr22:21445840 | C | T | 1 | a0001c0003 | 7 | HG02132.hp2 HG02135.hp2 NA18747.hp2 others(4): Show |
synonymous_variant | LOW | c.945C>T | p.His315His | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1208/6831 | 945/1848 | 315/615 | chr22 | 21445840 | |||
| chr22:21445891 | C | T | 1 | a0001c0008 | 2 | HG02083.hp1 NA18952.hp2 |
synonymous_variant | LOW | c.996C>T | p.His332His | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1259/6831 | 996/1848 | 332/615 | chr22 | 21445891 | |||
| chr22:21446131 | C | T | 1 | a0005c0011 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.1236C>T | p.Ser412Ser | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1499/6831 | 1236/1848 | 412/615 | chr22 | 21446131 | |||
| chr22:21446155 | T | C | 9 | a0001c0001 a0001c0003 a0001c0005 others(6): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
synonymous_variant | LOW | c.1260T>C | p.His420His | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1523/6831 | 1260/1848 | 420/615 | chr22 | 21446155 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:21417417 | G | C | 1 | a0001c0001t0024 | 1 | HG03834.hp1 | 5_prime_UTR_variant | MODIFIER | c.-217G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/3 | 25415 | chr22 | 21417417 | ||||||
| chr22:21417483 | G | A | 1 | a0002c0004t0025 | 1 | NA18980.hp1 | 5_prime_UTR_variant | MODIFIER | c.-151G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/3 | 25349 | chr22 | 21417483 | ||||||
| chr22:21442795 | C | G | 1 | a0001c0001t0059 | 1 | HG00438.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/3 | 37 | chr22 | 21442795 | ||||||
| chr22:21442803 | A | AG | 6 | a0001c0001t0008 a0001c0001t0029 a0001c0001t0030 others(3): Show |
11 | HG01099.hp2 HG02055.hp1 HG02135.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-28dupG | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/3 | 27 | INFO_REALIGN_3_PRIME | chr22 | 21442803 | |||||
| chr22:21442805 | C | G | 56 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(53): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
5_prime_UTR_variant | MODIFIER | c.-27C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/3 | 27 | chr22 | 21442805 | ||||||
| chr22:21442813 | G | C | 60 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(57): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
5_prime_UTR_variant | MODIFIER | c.-19G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/3 | 19 | chr22 | 21442813 | ||||||
| chr22:21447056 | C | G | 2 | a0001c0001t0010 a0001c0001t0031 |
6 | HG02257.hp2 HG02622.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*313C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 313 | chr22 | 21447056 | ||||||
| chr22:21447147 | T | G | 1 | a0001c0001t0032 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404T>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 404 | chr22 | 21447147 | ||||||
| chr22:21447200 | C | A | 20 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(17): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*457C>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 457 | chr22 | 21447200 | ||||||
| chr22:21447264 | ACAGT | A | 2 | a0001c0001t0014 a0001c0001t0030 |
4 | HG02451.hp2 HG02572.hp1 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*525_*528delTCAG | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 525 | INFO_REALIGN_3_PRIME | chr22 | 21447264 | |||||
| chr22:21447284 | G | A | 1 | a0001c0001t0033 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*541G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 541 | chr22 | 21447284 | ||||||
| chr22:21447299 | T | A | 62 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(59): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*556T>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 556 | chr22 | 21447299 | ||||||
| chr22:21447359 | C | A | 1 | a0001c0001t0041 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*616C>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 616 | chr22 | 21447359 | ||||||
| chr22:21447478 | G | A | 1 | a0001c0001t0018 | 2 | HG00733.hp2 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*735G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 735 | chr22 | 21447478 | ||||||
| chr22:21447512 | C | T | 2 | a0001c0001t0014 a0001c0001t0030 |
4 | HG02451.hp2 HG02572.hp1 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*769C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 769 | chr22 | 21447512 | ||||||
| chr22:21447646 | T | G | 1 | a0001c0001t0034 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*903T>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 903 | chr22 | 21447646 | ||||||
| chr22:21447681 | T | C | 1 | a0005c0011t0042 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*938T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 938 | chr22 | 21447681 | ||||||
| chr22:21447781 | C | CGT | 24 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(21): Show |
97 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1051_*1052dupGT | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1053 | INFO_REALIGN_3_PRIME | chr22 | 21447781 | |||||
| chr22:21447814 | CTA | C | 2 | a0001c0001t0017 a0001c0001t0040 |
4 | HG01496.hp1 HG01975.hp1 HG02273.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1073_*1074delAT | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1073 | INFO_REALIGN_3_PRIME | chr22 | 21447814 | |||||
| chr22:21448094 | G | T | 5 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0029 others(2): Show |
27 | HG00558.hp1 HG00673.hp1 HG02040.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1351G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1351 | chr22 | 21448094 | ||||||
| chr22:21448308 | C | A | 1 | a0001c0001t0043 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1565C>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1565 | chr22 | 21448308 | ||||||
| chr22:21448412 | T | G | 1 | a0001c0001t0050 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1669T>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1669 | chr22 | 21448412 | ||||||
| chr22:21448511 | C | T | 1 | a0002c0004t0049 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1768C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1768 | chr22 | 21448511 | ||||||
| chr22:21448543 | T | TC | 1 | a0001c0001t0006 | 8 | HG01257.hp1 HG01258.hp2 HG02055.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1800_*1801insC | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1801 | chr22 | 21448543 | ||||||
| chr22:21448593 | C | T | 2 | a0001c0001t0014 a0001c0001t0030 |
4 | HG02451.hp2 HG02572.hp1 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1850C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1850 | chr22 | 21448593 | ||||||
| chr22:21448617 | A | G | 1 | a0001c0007t0027 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1874A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1874 | chr22 | 21448617 | ||||||
| chr22:21448672 | T | G | 22 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(19): Show |
99 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1929T>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 1929 | chr22 | 21448672 | ||||||
| chr22:21448757 | C | T | 1 | a0001c0001t0001 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2014C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 2014 | chr22 | 21448757 | ||||||
| chr22:21448761 | C | T | 1 | a0001c0001t0057 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2018C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 2018 | chr22 | 21448761 | ||||||
| chr22:21448840 | T | A | 1 | a0001c0001t0035 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2097T>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 2097 | chr22 | 21448840 | ||||||
| chr22:21448883 | C | T | 1 | a0001c0001t0016 | 3 | NA18946.hp2 NA19057.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2140C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 2140 | chr22 | 21448883 | ||||||
| chr22:21448887 | A | AC | 4 | a0001c0001t0013 a0001c0001t0036 a0001c0001t0037 others(1): Show |
6 | HG00621.hp1 HG00673.hp2 HG03927.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2148dupC | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 2149 | INFO_REALIGN_3_PRIME | chr22 | 21448887 | |||||
| chr22:21448943 | T | C | 2 | a0001c0001t0014 a0001c0001t0030 |
4 | HG02451.hp2 HG02572.hp1 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2200T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 2200 | chr22 | 21448943 | ||||||
| chr22:21448949 | C | T | 1 | a0001c0001t0045 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2206C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 2206 | chr22 | 21448949 | ||||||
| chr22:21449073 | C | T | 1 | a0001c0001t0039 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2330C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 2330 | chr22 | 21449073 | ||||||
| chr22:21449074 | G | A | 1 | a0001c0001t0019 | 2 | HG02976.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2331G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 2331 | chr22 | 21449074 | ||||||
| chr22:21449463 | A | G | 1 | a0001c0001t0050 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2720A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 2720 | chr22 | 21449463 | ||||||
| chr22:21449662 | G | A | 1 | a0001c0001t0044 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2919G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 2919 | chr22 | 21449662 | ||||||
| chr22:21449719 | C | T | 1 | a0002c0004t0048 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2976C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 2976 | chr22 | 21449719 | ||||||
| chr22:21449766 | T | C | 1 | a0001c0001t0051 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3023T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 3023 | chr22 | 21449766 | ||||||
| chr22:21449846 | C | T | 1 | a0001c0001t0021 | 2 | HG00741.hp1 HG01981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3103C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 3103 | chr22 | 21449846 | ||||||
| chr22:21449981 | T | C | 2 | a0001c0001t0022 a0001c0001t0046 |
3 | HG02451.hp1 HG02559.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3238T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 3238 | chr22 | 21449981 | ||||||
| chr22:21450043 | G | A | 1 | a0001c0001t0023 | 2 | HG00741.hp2 HG01884.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3300G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 3300 | chr22 | 21450043 | ||||||
| chr22:21450136 | C | T | 2 | a0001c0001t0014 a0001c0001t0030 |
4 | HG02451.hp2 HG02572.hp1 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3393C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 3393 | chr22 | 21450136 | ||||||
| chr22:21450210 | A | C | 1 | a0001c0001t0056 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3467A>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 3467 | chr22 | 21450210 | ||||||
| chr22:21450228 | CA | C | 62 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(59): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*3495delA | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 3495 | INFO_REALIGN_3_PRIME | chr22 | 21450228 | |||||
| chr22:21450600 | A | G | 1 | a0001c0001t0055 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3857A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 3857 | chr22 | 21450600 | ||||||
| chr22:21450614 | C | T | 4 | a0002c0004t0020 a0002c0004t0025 a0002c0004t0048 others(1): Show |
4 | HG01071.hp1 HG03225.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3871C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 3871 | chr22 | 21450614 | ||||||
| chr22:21450652 | G | T | 1 | a0001c0001t0018 | 2 | HG00733.hp2 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3909G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 3909 | chr22 | 21450652 | ||||||
| chr22:21450674 | C | G | 1 | a0001c0001t0054 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3931C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 3931 | chr22 | 21450674 | ||||||
| chr22:21450783 | C | T | 1 | a0001c0002t0026 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4040C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 4040 | chr22 | 21450783 | ||||||
| chr22:21450796 | G | A | 1 | a0001c0001t0047 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4053G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 4053 | chr22 | 21450796 | ||||||
| chr22:21450880 | A | G | 1 | a0001c0001t0056 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4137A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 4137 | chr22 | 21450880 | ||||||
| chr22:21450888 | C | T | 1 | a0001c0001t0053 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4145C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 4145 | chr22 | 21450888 | ||||||
| chr22:21450902 | T | C | 2 | a0001c0001t0011 a0001c0001t0036 |
4 | HG00621.hp2 HG00673.hp2 NA18747.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4159T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 4159 | chr22 | 21450902 | ||||||
| chr22:21450963 | T | G | 3 | a0001c0001t0038 a0001c0005t0012 a0001c0005t0028 |
5 | HG02056.hp1 HG02273.hp2 NA18975.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4220T>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 4220 | chr22 | 21450963 | ||||||
| chr22:21451118 | G | A | 1 | a0001c0001t0038 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4375G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 4375 | chr22 | 21451118 | ||||||
| chr22:21451220 | G | T | 1 | a0001c0001t0015 | 3 | HG01099.hp1 HG02896.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4477G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 4477 | chr22 | 21451220 | ||||||
| chr22:21451368 | A | C | 1 | a0001c0001t0052 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4625A>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 3/3 | 4625 | chr22 | 21451368 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:21417582 | C | CG | 8 | a0001c0001t0002g0210 a0001c0001t0002g0215 a0001c0001t0003g0208 others(5): Show |
8 | HG00621.hp1 HG02056.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.-74+28dupG | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21417582 | ||||||
| chr22:21417588 | G | T | 8 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 others(5): Show |
8 | HG02109.hp2 HG02145.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.-74+28G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21417588 | |||||||
| chr22:21417609 | C | CGGGGCCG others(6): Show |
1 | a0001c0001t0014g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-74+53_-74+65dupGC others(11): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21417609 | ||||||
| chr22:21417684 | G | C | 1 | a0001c0001t0002g0023 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-74+124G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21417684 | |||||||
| chr22:21417712 | G | T | 6 | a0001c0001t0002g0022 a0001c0001t0002g0204 a0001c0001t0002g0205 others(3): Show |
8 | HG01099.hp2 HG01496.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.-74+152G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21417712 | |||||||
| chr22:21417742 | G | T | 5 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0202 others(2): Show |
5 | HG01109.hp1 HG01168.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.-74+182G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21417742 | |||||||
| chr22:21417957 | C | G | 2 | a0001c0001t0019g0222 a0001c0001t0019g0223 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-74+397C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21417957 | |||||||
| chr22:21417985 | T | G | 86 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(83): Show |
98 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.-74+425T>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21417985 | |||||||
| chr22:21417986 | T | C | 86 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(83): Show |
98 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.-74+426T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21417986 | |||||||
| chr22:21418108 | G | T | 1 | a0001c0001t0053g0079 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-74+548G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21418108 | |||||||
| chr22:21418136 | C | G | 1 | a0001c0001t0044g0198 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-74+576C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21418136 | |||||||
| chr22:21418347 | G | C | 1 | a0001c0001t0003g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-74+787G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21418347 | |||||||
| chr22:21418350 | GGGGT | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(88): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.-74+794_-74+797del others(4): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21418350 | ||||||
| chr22:21418351 | GGGT | G | 79 | a0001c0001t0001g0161 a0001c0001t0001g0166 a0001c0001t0001g0169 others(76): Show |
87 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.-74+794_-74+796del others(3): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21418351 | ||||||
| chr22:21418352 | GGT | G | 36 | a0001c0001t0001g0168 a0001c0001t0002g0004 a0001c0001t0002g0008 others(33): Show |
38 | HG00438.hp2 HG00741.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.-74+794_-74+795del others(2): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21418352 | ||||||
| chr22:21418353 | GT | G | 14 | a0001c0001t0002g0205 a0001c0001t0003g0080 a0001c0001t0003g0218 others(11): Show |
16 | HG01257.hp1 HG01258.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-74+794delT | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21418353 | |||||||
| chr22:21418354 | T | G | 9 | a0001c0001t0003g0217 a0001c0001t0003g0220 a0001c0001t0003g0221 others(6): Show |
9 | HG00621.hp1 HG02055.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.-74+794T>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21418354 | |||||||
| chr22:21418717 | A | G | 8 | a0001c0001t0003g0192 a0001c0001t0006g0020 a0001c0001t0006g0191 others(5): Show |
9 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-74+1157A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21418717 | |||||||
| chr22:21418729 | T | C | 2 | a0001c0001t0003g0151 a0001c0001t0033g0081 |
2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-74+1169T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21418729 | |||||||
| chr22:21419176 | G | C | 3 | a0001c0001t0019g0222 a0001c0001t0019g0223 a0001c0001t0031g0216 |
3 | HG02976.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-74+1616G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21419176 | |||||||
| chr22:21419291 | G | A | 1 | a0001c0002t0005g0017 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-74+1731G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21419291 | |||||||
| chr22:21419433 | C | G | 2 | a0001c0001t0014g0077 a0001c0001t0030g0078 |
2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-74+1873C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21419433 | |||||||
| chr22:21419437 | G | A | 1 | a0001c0001t0008g0028 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-74+1877G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21419437 | |||||||
| chr22:21419438 | G | C | 1 | a0001c0001t0014g0152 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-74+1878G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21419438 | |||||||
| chr22:21419559 | A | C | 4 | a0001c0001t0001g0016 a0001c0001t0003g0189 a0001c0001t0023g0188 others(1): Show |
5 | HG01346.hp1 HG01884.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+1999A>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21419559 | |||||||
| chr22:21419676 | G | T | 2 | a0001c0001t0019g0222 a0001c0001t0019g0223 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-74+2116G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21419676 | |||||||
| chr22:21419679 | G | T | 2 | a0001c0001t0019g0222 a0001c0001t0019g0223 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-74+2119G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21419679 | |||||||
| chr22:21419687 | G | T | 2 | a0001c0001t0019g0222 a0001c0001t0019g0223 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-74+2127G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21419687 | |||||||
| chr22:21419688 | G | C | 2 | a0001c0001t0019g0222 a0001c0001t0019g0223 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-74+2128G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21419688 | |||||||
| chr22:21419690 | A | T | 2 | a0001c0001t0019g0222 a0001c0001t0019g0223 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-74+2130A>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21419690 | |||||||
| chr22:21419691 | C | T | 2 | a0001c0001t0019g0222 a0001c0001t0019g0223 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-74+2131C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21419691 | |||||||
| chr22:21419696 | C | A | 2 | a0001c0001t0019g0222 a0001c0001t0019g0223 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-74+2136C>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21419696 | |||||||
| chr22:21419754 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(220): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-74+2194A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21419754 | |||||||
| chr22:21419968 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0007g0187 |
2 | HG00738.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.-74+2408C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21419968 | |||||||
| chr22:21420032 | A | G | 1 | a0001c0001t0057g0076 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-74+2472A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21420032 | |||||||
| chr22:21420068 | C | T | 1 | a0001c0002t0005g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-74+2508C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21420068 | |||||||
| chr22:21420381 | G | T | 77 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(74): Show |
90 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-74+2821G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21420381 | |||||||
| chr22:21420446 | C | T | 2 | a0001c0001t0015g0147 a0001c0001t0015g0148 |
2 | HG01099.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-74+2886C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21420446 | |||||||
| chr22:21420513 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-74+2953G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21420513 | |||||||
| chr22:21420532 | C | T | 74 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(71): Show |
85 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-74+2972C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21420532 | |||||||
| chr22:21420594 | C | G | 77 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(74): Show |
90 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-74+3034C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21420594 | |||||||
| chr22:21420729 | C | T | 2 | a0001c0001t0002g0075 a0001c0001t0008g0074 |
2 | HG02040.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.-74+3169C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21420729 | |||||||
| chr22:21420767 | T | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(222): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.-74+3207T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21420767 | |||||||
| chr22:21420816 | A | C | 8 | a0001c0001t0003g0192 a0001c0001t0006g0020 a0001c0001t0006g0191 others(5): Show |
9 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-74+3256A>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21420816 | |||||||
| chr22:21420907 | C | T | 1 | a0002c0004t0048g0183 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-74+3347C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21420907 | |||||||
| chr22:21421074 | A | AG | 70 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(67): Show |
80 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-74+3514_-74+3515i others(3): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21421074 | |||||||
| chr22:21421076 | G | GGGGCTGA others(59): Show |
1 | a0001c0001t0002g0073 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-74+3517_-74+3582d others(68): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21421076 | ||||||
| chr22:21421376 | C | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(140): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.-74+3816C>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21421376 | |||||||
| chr22:21421377 | G | A | 86 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(83): Show |
101 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.-74+3817G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21421377 | |||||||
| chr22:21421470 | T | TC | 3 | a0001c0001t0010g0006 a0001c0001t0010g0184 a0001c0001t0010g0185 |
5 | HG02257.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+3912dupC | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21421470 | ||||||
| chr22:21421635 | A | C | 24 | a0001c0001t0001g0186 a0001c0001t0002g0022 a0001c0001t0002g0202 others(21): Show |
28 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.-74+4075A>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21421635 | |||||||
| chr22:21421653 | A | T | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0007g0180 others(3): Show |
8 | HG01109.hp2 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-74+4093A>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21421653 | |||||||
| chr22:21421657 | GC | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(96): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.-74+4099delC | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21421657 | ||||||
| chr22:21421658 | C | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0090 others(4): Show |
8 | HG00621.hp1 HG02056.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.-74+4098C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21421658 | |||||||
| chr22:21421678 | G | GT | 3 | a0001c0001t0002g0206 a0001c0001t0008g0201 a0001c0003t0008g0211 |
3 | HG02055.hp1 HG02135.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-74+4124dupT | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21421678 | ||||||
| chr22:21421842 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-74+4282G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21421842 | |||||||
| chr22:21422373 | T | C | 1 | a0001c0001t0003g0219 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-74+4813T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21422373 | |||||||
| chr22:21422475 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-74+4915A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21422475 | |||||||
| chr22:21422500 | G | A | 4 | a0001c0001t0007g0030 a0001c0001t0007g0182 a0001c0001t0015g0209 others(1): Show |
4 | HG00639.hp2 HG04184.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.-74+4940G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21422500 | |||||||
| chr22:21422570 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(145): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-74+5010G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21422570 | |||||||
| chr22:21422610 | G | A | 45 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0022 others(42): Show |
51 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.-74+5050G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21422610 | |||||||
| chr22:21422620 | A | G | 4 | a0001c0001t0014g0077 a0001c0001t0014g0152 a0001c0001t0014g0207 others(1): Show |
4 | HG02451.hp2 HG02572.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-74+5060A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21422620 | |||||||
| chr22:21422642 | A | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0177 others(2): Show |
6 | HG02083.hp2 NA18942.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-74+5082A>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21422642 | |||||||
| chr22:21422646 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(148): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-74+5086C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21422646 | |||||||
| chr22:21422726 | G | A | 2 | a0001c0001t0003g0095 a0002c0004t0020g0094 |
2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-74+5166G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21422726 | |||||||
| chr22:21422857 | G | T | 1 | a0001c0001t0002g0073 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-74+5297G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21422857 | |||||||
| chr22:21422867 | A | C | 1 | a0001c0001t0002g0042 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-74+5307A>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21422867 | |||||||
| chr22:21422873 | GTCT | G | 8 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 others(5): Show |
10 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-74+5320_-74+5322d others(5): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21422873 | ||||||
| chr22:21422939 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(148): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-74+5379A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21422939 | |||||||
| chr22:21422977 | C | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(148): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-74+5417C>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21422977 | |||||||
| chr22:21423106 | GCTATAAG others(6): Show |
G | 1 | a0001c0001t0003g0096 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-74+5548_-74+5560d others(15): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21423106 | ||||||
| chr22:21423156 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-74+5596G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21423156 | |||||||
| chr22:21423207 | C | G | 1 | a0001c0001t0002g0073 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-74+5647C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21423207 | |||||||
| chr22:21423217 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(150): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-74+5657G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21423217 | |||||||
| chr22:21423232 | G | A | 3 | a0001c0001t0010g0006 a0001c0001t0010g0184 a0001c0001t0010g0185 |
5 | HG02257.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+5672G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21423232 | |||||||
| chr22:21423289 | A | G | 1 | a0001c0001t0014g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-74+5729A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21423289 | |||||||
| chr22:21423385 | C | T | 1 | a0001c0001t0011g0140 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-74+5825C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21423385 | |||||||
| chr22:21423407 | T | A | 1 | a0001c0001t0002g0073 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-74+5847T>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21423407 | |||||||
| chr22:21423630 | C | T | 30 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0022 others(27): Show |
36 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-74+6070C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21423630 | |||||||
| chr22:21423667 | T | C | 2 | a0001c0005t0012g0098 a0001c0005t0012g0160 |
2 | HG02273.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.-74+6107T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21423667 | |||||||
| chr22:21423925 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-74+6365C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21423925 | |||||||
| chr22:21424112 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-74+6552T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21424112 | |||||||
| chr22:21424147 | C | T | 5 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 others(2): Show |
5 | HG02109.hp2 HG02145.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+6587C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21424147 | |||||||
| chr22:21424156 | G | T | 1 | a0001c0001t0002g0042 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-74+6596G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21424156 | |||||||
| chr22:21424287 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-74+6727G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21424287 | |||||||
| chr22:21424328 | C | G | 1 | a0001c0001t0053g0079 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-74+6768C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21424328 | |||||||
| chr22:21424476 | G | A | 1 | a0002c0004t0048g0183 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-74+6916G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21424476 | |||||||
| chr22:21424519 | A | C | 2 | a0001c0001t0001g0186 a0001c0001t0007g0187 |
2 | HG00738.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.-74+6959A>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21424519 | |||||||
| chr22:21424557 | A | G | 45 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0022 others(42): Show |
53 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-74+6997A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21424557 | |||||||
| chr22:21424579 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(194): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.-74+7019A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21424579 | |||||||
| chr22:21424630 | G | A | 42 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0024 others(39): Show |
48 | HG00544.hp1 HG00558.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-74+7070G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21424630 | |||||||
| chr22:21424658 | A | G | 3 | a0001c0001t0010g0006 a0001c0001t0010g0184 a0001c0001t0010g0185 |
5 | HG02257.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+7098A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21424658 | |||||||
| chr22:21424780 | C | T | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0061 others(1): Show |
4 | HG01433.hp1 HG02004.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.-74+7220C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21424780 | |||||||
| chr22:21424803 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0040g0093 a0004c0009t0009g0176 |
3 | HG02809.hp2 HG02976.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-74+7243C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21424803 | |||||||
| chr22:21424852 | C | T | 8 | a0001c0001t0003g0192 a0001c0001t0006g0020 a0001c0001t0006g0191 others(5): Show |
9 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-74+7292C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21424852 | |||||||
| chr22:21424942 | G | A | 1 | a0001c0001t0036g0101 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-74+7382G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21424942 | |||||||
| chr22:21424992 | C | G | 1 | a0001c0003t0002g0058 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-74+7432C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21424992 | |||||||
| chr22:21425009 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-74+7449A>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21425009 | |||||||
| chr22:21425165 | T | TAAAAAAA | 10 | a0001c0001t0002g0022 a0001c0001t0002g0057 a0001c0001t0002g0073 others(7): Show |
12 | HG01099.hp2 HG01168.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.-74+7613_-74+7619d others(9): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21425165 | ||||||
| chr22:21425165 | T | TAAAAAAA others(1): Show |
51 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(48): Show |
61 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-74+7612_-74+7619d others(10): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21425165 | ||||||
| chr22:21425165 | T | TAAAAAAA others(2): Show |
17 | a0001c0001t0002g0027 a0001c0001t0002g0042 a0001c0001t0002g0045 others(14): Show |
17 | HG00323.hp2 HG01192.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.-74+7611_-74+7619d others(11): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21425165 | ||||||
| chr22:21425165 | T | TAAAAAAA others(3): Show |
3 | a0001c0001t0008g0074 a0001c0001t0031g0216 a0001c0003t0008g0044 |
3 | NA18941.hp2 NA18978.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-74+7610_-74+7619d others(12): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21425165 | ||||||
| chr22:21425165 | T | TAAAAAAA others(4): Show |
4 | a0001c0001t0007g0030 a0001c0001t0007g0182 a0001c0001t0015g0209 others(1): Show |
4 | HG00639.hp2 HG04184.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.-74+7609_-74+7619d others(13): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21425165 | ||||||
| chr22:21425165 | T | TAAAAAAA others(5): Show |
9 | a0001c0001t0003g0219 a0001c0001t0003g0220 a0001c0001t0003g0221 others(6): Show |
11 | HG01071.hp1 HG02622.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.-74+7608_-74+7619d others(14): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21425165 | ||||||
| chr22:21425165 | T | TAAAAAAA others(6): Show |
13 | a0001c0001t0001g0144 a0001c0001t0003g0080 a0001c0001t0003g0189 others(10): Show |
14 | HG01257.hp1 HG01258.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.-74+7607_-74+7619d others(15): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21425165 | ||||||
| chr22:21425165 | T | TAAAAAAA others(7): Show |
68 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.-74+7606_-74+7619d others(16): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21425165 | ||||||
| chr22:21425165 | T | TAAAAAAA others(8): Show |
40 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0001t0001g0105 others(37): Show |
48 | HG00438.hp2 HG00621.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.-74+7619_-74+7620i others(17): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21425165 | ||||||
| chr22:21425165 | T | TAAAAAAA others(9): Show |
6 | a0001c0001t0001g0013 a0001c0001t0001g0102 a0001c0001t0003g0083 others(3): Show |
7 | HG02572.hp2 HG02895.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-74+7619_-74+7620i others(18): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21425165 | ||||||
| chr22:21425165 | T | TAAAAAAA others(10): Show |
1 | a0001c0001t0003g0082 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-74+7619_-74+7620i others(19): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21425165 | ||||||
| chr22:21425312 | A | T | 1 | a0001c0001t0002g0073 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-74+7752A>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21425312 | |||||||
| chr22:21425320 | C | T | 5 | a0001c0001t0009g0162 a0001c0001t0022g0019 a0001c0001t0023g0163 others(2): Show |
6 | HG00741.hp2 HG01884.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-74+7760C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21425320 | |||||||
| chr22:21425375 | G | A | 6 | a0001c0001t0003g0164 a0001c0001t0003g0165 a0001c0001t0003g0208 others(3): Show |
6 | HG02976.hp2 HG03130.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-74+7815G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21425375 | |||||||
| chr22:21425455 | A | G | 50 | a0001c0001t0001g0139 a0001c0001t0002g0008 a0001c0001t0002g0010 others(47): Show |
56 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.-74+7895A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21425455 | |||||||
| chr22:21425491 | C | T | 1 | a0001c0001t0002g0073 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-74+7931C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21425491 | |||||||
| chr22:21425519 | C | T | 1 | a0001c0001t0003g0189 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-74+7959C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21425519 | |||||||
| chr22:21425542 | C | CT | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(112): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.-74+7999dupT | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21425542 | ||||||
| chr22:21425542 | C | CTT | 7 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0166 others(4): Show |
7 | HG01891.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-74+7998_-74+7999d others(4): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21425542 | ||||||
| chr22:21425543 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-74+7983T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21425543 | |||||||
| chr22:21425557 | T | TC | 8 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 others(5): Show |
10 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-74+7997_-74+7998i others(3): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21425557 | |||||||
| chr22:21425573 | GCCCTGTC others(164): Show |
G | 2 | a0001c0001t0002g0041 a0001c0001t0002g0070 |
2 | HG00323.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-74+8044_-74+8214d others(2): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21425573 | ||||||
| chr22:21425681 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-74+8121C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21425681 | |||||||
| chr22:21425714 | CT | C | 44 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0022 others(41): Show |
52 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-74+8170delT | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21425714 | ||||||
| chr22:21426186 | T | C | 12 | a0001c0001t0003g0164 a0001c0001t0003g0165 a0001c0001t0003g0192 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-74+8626T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21426186 | |||||||
| chr22:21426204 | C | T | 2 | a0001c0001t0003g0217 a0001c0001t0003g0218 |
2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-74+8644C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21426204 | |||||||
| chr22:21426209 | G | A | 1 | a0001c0001t0006g0195 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-74+8649G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21426209 | |||||||
| chr22:21426234 | G | A | 3 | a0002c0004t0025g0178 a0002c0004t0048g0183 a0002c0004t0049g0179 |
3 | HG01071.hp1 HG03540.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.-74+8674G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21426234 | |||||||
| chr22:21426262 | T | C | 1 | a0001c0002t0005g0155 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-74+8702T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21426262 | |||||||
| chr22:21426272 | A | G | 2 | a0001c0001t0003g0151 a0001c0001t0043g0031 |
2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-74+8712A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21426272 | |||||||
| chr22:21426297 | G | C | 6 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0062 others(3): Show |
7 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.-74+8737G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21426297 | |||||||
| chr22:21426321 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0168 |
2 | HG03017.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-74+8761G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21426321 | |||||||
| chr22:21426337 | A | AT | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(199): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.-74+8796dupT | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21426337 | ||||||
| chr22:21426337 | A | ATT | 11 | a0001c0001t0001g0113 a0001c0001t0001g0168 a0001c0001t0002g0056 others(8): Show |
11 | HG02055.hp2 HG02080.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-74+8795_-74+8796d others(4): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21426337 | ||||||
| chr22:21426476 | TG | T | 5 | a0001c0001t0002g0041 a0001c0001t0002g0070 a0001c0001t0002g0073 others(2): Show |
5 | HG00323.hp2 NA18941.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.-74+8917delG | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21426476 | |||||||
| chr22:21426477 | G | GT | 9 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0128 others(6): Show |
9 | HG02056.hp1 HG03669.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.-74+8930dupT | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21426477 | ||||||
| chr22:21426477 | G | T | 40 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0010 others(37): Show |
46 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.-74+8917G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21426477 | |||||||
| chr22:21426591 | C | T | 1 | a0001c0001t0002g0073 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-74+9031C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21426591 | |||||||
| chr22:21426629 | C | T | 1 | a0001c0001t0033g0081 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-74+9069C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21426629 | |||||||
| chr22:21426641 | G | A | 2 | a0001c0005t0012g0098 a0001c0005t0012g0160 |
2 | HG02273.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.-74+9081G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21426641 | |||||||
| chr22:21426730 | T | C | 1 | a0001c0001t0007g0030 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-74+9170T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21426730 | |||||||
| chr22:21427080 | A | G | 1 | a0001c0001t0002g0027 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-74+9520A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21427080 | |||||||
| chr22:21427300 | C | CT | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(175): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.-74+9754dupT | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21427300 | ||||||
| chr22:21427300 | C | CTT | 14 | a0001c0001t0002g0003 a0001c0001t0002g0025 a0001c0001t0002g0048 others(11): Show |
15 | HG00558.hp2 HG00639.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.-74+9753_-74+9754d others(4): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21427300 | ||||||
| chr22:21427334 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-74+9774G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21427334 | |||||||
| chr22:21427357 | G | A | 1 | a0001c0001t0002g0042 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-74+9797G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21427357 | |||||||
| chr22:21427395 | G | A | 2 | a0001c0001t0007g0007 a0001c0001t0007g0029 |
3 | HG01891.hp1 HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-74+9835G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21427395 | |||||||
| chr22:21427421 | C | T | 1 | a0001c0001t0014g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-74+9861C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21427421 | |||||||
| chr22:21427474 | A | C | 1 | a0001c0001t0011g0140 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-74+9914A>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21427474 | |||||||
| chr22:21427476 | A | G | 3 | a0001c0001t0003g0189 a0001c0001t0022g0019 a0001c0001t0046g0175 |
4 | HG01346.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-74+9916A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21427476 | |||||||
| chr22:21427781 | T | A | 1 | a0001c0002t0005g0156 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-74+10221T>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21427781 | |||||||
| chr22:21427793 | T | A | 1 | a0001c0001t0003g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-74+10233T>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21427793 | |||||||
| chr22:21427798 | G | GT | 83 | a0001c0001t0001g0177 a0001c0001t0002g0003 a0001c0001t0002g0004 others(80): Show |
94 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-74+10250dupT | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21427798 | ||||||
| chr22:21427822 | T | C | 1 | a0001c0001t0015g0209 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-74+10262T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21427822 | |||||||
| chr22:21428141 | G | T | 8 | a0001c0001t0003g0192 a0001c0001t0006g0020 a0001c0001t0006g0191 others(5): Show |
9 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-74+10581G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21428141 | |||||||
| chr22:21428325 | ACCTACCT others(47): Show |
A | 1 | a0001c0001t0001g0137 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-74+10769_-74+1082 others(58): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21428325 | ||||||
| chr22:21428392 | A | T | 3 | a0001c0001t0002g0026 a0001c0001t0002g0061 a0001c0001t0002g0065 |
3 | HG01358.hp1 HG02004.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-74+10832A>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21428392 | |||||||
| chr22:21428403 | C | T | 1 | a0002c0004t0048g0183 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-74+10843C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21428403 | |||||||
| chr22:21428492 | A | C | 1 | a0001c0001t0003g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-74+10932A>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21428492 | |||||||
| chr22:21428507 | C | T | 1 | a0001c0001t0006g0194 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-74+10947C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21428507 | |||||||
| chr22:21428544 | G | A | 1 | a0001c0001t0014g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-74+10984G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21428544 | |||||||
| chr22:21428546 | G | A | 2 | a0001c0001t0016g0071 a0001c0001t0016g0072 |
2 | NA18946.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-74+10986G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21428546 | |||||||
| chr22:21428551 | C | T | 75 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(72): Show |
87 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.-74+10991C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21428551 | |||||||
| chr22:21428683 | A | AG | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(127): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.-74+11124dupG | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21428683 | ||||||
| chr22:21428684 | G | GAAA | 70 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(67): Show |
82 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.-74+11139_-74+1114 others(7): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21428684 | ||||||
| chr22:21428684 | G | GGA | 18 | a0001c0001t0001g0102 a0001c0001t0001g0112 a0001c0001t0001g0144 others(15): Show |
20 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.-74+11124_-74+1112 others(6): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21428684 | |||||||
| chr22:21428685 | A | G | 4 | a0001c0001t0001g0136 a0001c0001t0015g0147 a0001c0001t0015g0148 others(1): Show |
4 | HG01099.hp1 HG01258.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-74+11125A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21428685 | |||||||
| chr22:21428926 | G | T | 72 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(69): Show |
83 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.-74+11366G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21428926 | |||||||
| chr22:21429119 | T | C | 8 | a0001c0001t0003g0192 a0001c0001t0006g0020 a0001c0001t0006g0191 others(5): Show |
9 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-74+11559T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21429119 | |||||||
| chr22:21429297 | C | T | 73 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(70): Show |
84 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.-74+11737C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21429297 | |||||||
| chr22:21429336 | G | A | 5 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 others(2): Show |
5 | HG02109.hp2 HG02145.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+11776G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21429336 | |||||||
| chr22:21429356 | C | T | 1 | a0001c0001t0032g0135 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-74+11796C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21429356 | |||||||
| chr22:21429500 | G | A | 1 | a0001c0001t0007g0030 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-74+11940G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21429500 | |||||||
| chr22:21429611 | G | T | 1 | a0001c0001t0002g0025 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-74+12051G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21429611 | |||||||
| chr22:21429629 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(104): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-74+12069A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21429629 | |||||||
| chr22:21429712 | A | G | 3 | a0001c0001t0003g0145 a0001c0001t0003g0146 a0001c0001t0059g0181 |
3 | HG00438.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-74+12152A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21429712 | |||||||
| chr22:21429818 | G | A | 1 | a0001c0001t0043g0031 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-74+12258G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21429818 | |||||||
| chr22:21429908 | T | C | 5 | a0001c0001t0003g0164 a0001c0001t0003g0165 a0001c0001t0003g0208 others(2): Show |
5 | HG02976.hp2 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+12348T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21429908 | |||||||
| chr22:21430305 | CCTCTTTC others(6): Show |
C | 6 | a0001c0001t0002g0022 a0001c0001t0002g0204 a0001c0001t0002g0205 others(3): Show |
8 | HG01099.hp2 HG01496.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73-12442_-73-1243 others(17): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21430305 | ||||||
| chr22:21430336 | T | C | 1 | a0001c0001t0059g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-73-12423T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21430336 | |||||||
| chr22:21430342 | C | T | 2 | a0001c0001t0019g0222 a0001c0001t0019g0223 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-73-12417C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21430342 | |||||||
| chr22:21430344 | C | G | 1 | a0001c0001t0059g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-73-12415C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21430344 | |||||||
| chr22:21430348 | G | C | 2 | a0001c0001t0003g0164 a0001c0001t0003g0192 |
2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-73-12411G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21430348 | |||||||
| chr22:21430348 | G | T | 1 | a0001c0001t0059g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-73-12411G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21430348 | |||||||
| chr22:21430352 | T | G | 1 | a0001c0001t0059g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-73-12407T>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21430352 | |||||||
| chr22:21430377 | T | A | 1 | a0001c0001t0059g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-73-12382T>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21430377 | |||||||
| chr22:21430399 | G | T | 1 | a0001c0001t0059g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-73-12360G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21430399 | |||||||
| chr22:21430452 | A | G | 2 | a0001c0001t0003g0220 a0001c0001t0003g0221 |
2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-73-12307A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21430452 | |||||||
| chr22:21430574 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-73-12185T>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21430574 | |||||||
| chr22:21430602 | A | G | 1 | a0001c0001t0059g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-73-12157A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21430602 | |||||||
| chr22:21430722 | T | C | 1 | a0001c0001t0059g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-73-12037T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21430722 | |||||||
| chr22:21430864 | C | CA | 17 | a0001c0001t0001g0105 a0001c0001t0001g0119 a0001c0001t0001g0139 others(14): Show |
17 | HG00558.hp1 HG00738.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.-73-11876dupA | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21430864 | ||||||
| chr22:21430864 | CA | C | 95 | a0001c0001t0001g0014 a0001c0001t0002g0003 a0001c0001t0002g0004 others(92): Show |
111 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.-73-11876delA | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21430864 | ||||||
| chr22:21430898 | A | G | 1 | a0001c0001t0011g0118 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-73-11861A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21430898 | |||||||
| chr22:21430899 | T | C | 1 | a0001c0001t0059g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-73-11860T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21430899 | |||||||
| chr22:21430955 | T | C | 1 | a0001c0001t0059g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-73-11804T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21430955 | |||||||
| chr22:21430996 | C | T | 1 | a0001c0001t0007g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-73-11763C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21430996 | |||||||
| chr22:21431051 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-73-11708A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21431051 | |||||||
| chr22:21431075 | C | T | 1 | a0005c0011t0042g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-73-11684C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21431075 | |||||||
| chr22:21431242 | T | C | 1 | a0001c0001t0059g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-73-11517T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21431242 | |||||||
| chr22:21431371 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-73-11388C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21431371 | |||||||
| chr22:21431666 | T | C | 5 | a0001c0001t0003g0106 a0001c0001t0003g0114 a0001c0001t0003g0121 others(2): Show |
5 | HG02258.hp2 HG02486.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-73-11093T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21431666 | |||||||
| chr22:21431832 | ATTGG | A | 3 | a0001c0001t0002g0022 a0001c0001t0002g0046 a0001c0001t0002g0205 |
4 | HG02698.hp1 HG03490.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73-10922_-73-1091 others(8): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21431832 | ||||||
| chr22:21431915 | G | A | 1 | a0001c0001t0045g0032 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-73-10844G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21431915 | |||||||
| chr22:21431927 | C | T | 1 | a0001c0005t0012g0133 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-73-10832C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21431927 | |||||||
| chr22:21432011 | C | CT | 92 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(89): Show |
104 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-73-10732dupT | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21432011 | ||||||
| chr22:21432200 | T | C | 1 | a0001c0001t0008g0028 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-73-10559T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21432200 | |||||||
| chr22:21432306 | C | T | 2 | a0001c0001t0003g0146 a0001c0001t0059g0181 |
2 | HG00438.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-73-10453C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21432306 | |||||||
| chr22:21432335 | C | T | 10 | a0001c0001t0003g0164 a0001c0001t0003g0165 a0001c0001t0003g0208 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.-73-10424C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21432335 | |||||||
| chr22:21432448 | G | A | 1 | a0001c0001t0057g0076 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-73-10311G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21432448 | |||||||
| chr22:21432675 | TCA | T | 10 | a0001c0001t0003g0164 a0001c0001t0003g0165 a0001c0001t0003g0208 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.-73-10083_-73-1008 others(6): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21432675 | |||||||
| chr22:21432676 | C | CA | 13 | a0001c0001t0001g0166 a0001c0001t0002g0050 a0001c0001t0003g0080 others(10): Show |
13 | HG01071.hp1 HG01346.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-73-10063dupA | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21432676 | ||||||
| chr22:21432676 | CA | C | 9 | a0001c0001t0004g0111 a0001c0001t0007g0029 a0001c0001t0008g0203 others(6): Show |
9 | HG01099.hp1 HG01099.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.-73-10063delA | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21432676 | ||||||
| chr22:21432677 | A | G | 2 | a0001c0001t0019g0223 a0001c0002t0005g0156 |
2 | HG02027.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-73-10082A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21432677 | |||||||
| chr22:21432678 | A | G | 10 | a0001c0001t0003g0164 a0001c0001t0003g0165 a0001c0001t0003g0208 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.-73-10081A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21432678 | |||||||
| chr22:21432758 | G | C | 1 | a0001c0001t0002g0066 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-73-10001G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21432758 | |||||||
| chr22:21432911 | T | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(221): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.-73-9848T>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21432911 | |||||||
| chr22:21433136 | G | A | 1 | a0001c0001t0059g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-73-9623G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21433136 | |||||||
| chr22:21433217 | G | C | 1 | a0001c0001t0002g0060 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-73-9542G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21433217 | |||||||
| chr22:21433220 | A | G | 14 | a0001c0001t0003g0164 a0001c0001t0003g0165 a0001c0001t0003g0208 others(11): Show |
16 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-73-9539A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21433220 | |||||||
| chr22:21433237 | G | A | 1 | a0001c0001t0018g0124 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-73-9522G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21433237 | |||||||
| chr22:21433535 | A | G | 1 | a0001c0001t0004g0132 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-73-9224A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21433535 | |||||||
| chr22:21433536 | C | CAGCTAGC others(5): Show |
219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-73-9218_-73-9207d others(14): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21433536 | ||||||
| chr22:21433536 | C | CAGCTAGC others(9): Show |
2 | a0001c0001t0002g0054 a0001c0001t0037g0085 |
2 | HG03927.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-73-9222_-73-9207d others(18): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21433536 | ||||||
| chr22:21433536 | C | CAGCTAGC others(17): Show |
1 | a0001c0001t0023g0163 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-73-9207_-73-9206i others(26): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21433536 | ||||||
| chr22:21433539 | C | CTAGCTAG others(5): Show |
1 | a0001c0001t0003g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-73-9209_-73-9208i others(14): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21433539 | ||||||
| chr22:21433557 | G | T | 1 | a0001c0001t0059g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-73-9202G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21433557 | |||||||
| chr22:21433845 | C | T | 1 | a0001c0001t0014g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-73-8914C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21433845 | |||||||
| chr22:21433895 | A | G | 1 | a0001c0001t0024g0131 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-73-8864A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21433895 | |||||||
| chr22:21434063 | C | T | 1 | a0001c0001t0004g0120 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-73-8696C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21434063 | |||||||
| chr22:21434490 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(222): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.-73-8269A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21434490 | |||||||
| chr22:21434863 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-73-7896G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21434863 | |||||||
| chr22:21435321 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-73-7438C>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21435321 | |||||||
| chr22:21435475 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-73-7284A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21435475 | |||||||
| chr22:21435511 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-73-7248G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21435511 | |||||||
| chr22:21435555 | G | A | 11 | a0001c0001t0003g0164 a0001c0001t0003g0165 a0001c0001t0003g0192 others(8): Show |
11 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-73-7204G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21435555 | |||||||
| chr22:21435596 | G | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(211): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.-73-7163G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21435596 | |||||||
| chr22:21435687 | C | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG01109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-73-7072C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21435687 | |||||||
| chr22:21435912 | A | T | 6 | a0001c0001t0003g0164 a0001c0001t0003g0165 a0001c0001t0003g0192 others(3): Show |
6 | HG01884.hp2 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73-6847A>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21435912 | |||||||
| chr22:21435931 | T | G | 86 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(83): Show |
98 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.-73-6828T>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21435931 | |||||||
| chr22:21435991 | C | T | 7 | a0001c0001t0006g0020 a0001c0001t0006g0191 a0001c0001t0006g0193 others(4): Show |
8 | HG01257.hp1 HG01258.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-73-6768C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21435991 | |||||||
| chr22:21436014 | C | G | 1 | a0005c0011t0042g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-73-6745C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21436014 | |||||||
| chr22:21436175 | G | A | 4 | a0001c0001t0007g0030 a0001c0001t0007g0182 a0001c0001t0015g0147 others(1): Show |
4 | HG00639.hp2 HG02896.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73-6584G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21436175 | |||||||
| chr22:21436217 | G | T | 1 | a0001c0001t0004g0110 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-73-6542G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21436217 | |||||||
| chr22:21436528 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-73-6231C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21436528 | |||||||
| chr22:21436668 | C | T | 1 | a0001c0001t0004g0091 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-73-6091C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21436668 | |||||||
| chr22:21436684 | G | T | 1 | a0001c0001t0002g0039 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-73-6075G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21436684 | |||||||
| chr22:21437269 | A | C | 1 | a0001c0001t0006g0020 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-73-5490A>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21437269 | |||||||
| chr22:21437323 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-73-5436G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21437323 | |||||||
| chr22:21437833 | G | T | 4 | a0001c0001t0010g0006 a0001c0001t0010g0184 a0001c0001t0010g0185 others(1): Show |
6 | HG02257.hp2 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73-4926G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21437833 | |||||||
| chr22:21437959 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-73-4800A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21437959 | |||||||
| chr22:21438050 | A | G | 1 | a0005c0011t0042g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-73-4709A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21438050 | |||||||
| chr22:21438077 | G | A | 1 | a0001c0001t0032g0135 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-73-4682G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21438077 | |||||||
| chr22:21438180 | T | G | 73 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(70): Show |
84 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.-73-4579T>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21438180 | |||||||
| chr22:21438402 | C | T | 126 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(123): Show |
141 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.-73-4357C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21438402 | |||||||
| chr22:21438435 | C | T | 2 | a0001c0001t0003g0164 a0001c0001t0003g0192 |
2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-73-4324C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21438435 | |||||||
| chr22:21438566 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-73-4193G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21438566 | |||||||
| chr22:21438651 | G | A | 4 | a0002c0004t0020g0094 a0002c0004t0025g0178 a0002c0004t0048g0183 others(1): Show |
4 | HG01071.hp1 HG03225.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73-4108G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21438651 | |||||||
| chr22:21438866 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(220): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-73-3893T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21438866 | |||||||
| chr22:21438872 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(177): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-73-3887A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21438872 | |||||||
| chr22:21439316 | A | G | 1 | a0001c0001t0007g0187 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-73-3443A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21439316 | |||||||
| chr22:21439330 | C | T | 1 | a0001c0001t0007g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-73-3429C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21439330 | |||||||
| chr22:21439516 | A | T | 9 | a0001c0001t0001g0016 a0001c0001t0001g0097 a0001c0001t0001g0107 others(6): Show |
10 | HG01256.hp1 HG01258.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.-73-3243A>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21439516 | |||||||
| chr22:21439791 | G | A | 1 | a0001c0001t0002g0059 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-73-2968G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21439791 | |||||||
| chr22:21439958 | C | CA | 8 | a0001c0001t0003g0151 a0001c0001t0006g0020 a0001c0001t0006g0193 others(5): Show |
9 | HG00733.hp2 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-73-2787dupA | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21439958 | ||||||
| chr22:21439958 | CA | C | 12 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 others(9): Show |
14 | HG01071.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-73-2787delA | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr22 | 21439958 | ||||||
| chr22:21440197 | G | C | 6 | a0001c0001t0003g0164 a0001c0001t0003g0165 a0001c0001t0003g0192 others(3): Show |
6 | HG01884.hp2 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73-2562G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21440197 | |||||||
| chr22:21440249 | A | G | 3 | a0001c0001t0014g0077 a0001c0001t0014g0152 a0001c0001t0030g0078 |
3 | HG02451.hp2 HG02572.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-73-2510A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21440249 | |||||||
| chr22:21440293 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-73-2466C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21440293 | |||||||
| chr22:21440340 | C | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(220): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-73-2419C>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21440340 | |||||||
| chr22:21440549 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-73-2210C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21440549 | |||||||
| chr22:21440811 | C | G | 3 | a0001c0001t0001g0112 a0001c0001t0001g0172 a0001c0001t0032g0135 |
3 | HG00099.hp2 HG03669.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-73-1948C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21440811 | |||||||
| chr22:21440864 | G | A | 1 | a0001c0001t0044g0198 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-73-1895G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21440864 | |||||||
| chr22:21440873 | C | G | 3 | a0001c0001t0001g0109 a0001c0001t0001g0161 a0001c0001t0033g0081 |
3 | HG03195.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-73-1886C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21440873 | |||||||
| chr22:21441254 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-73-1505A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21441254 | |||||||
| chr22:21441369 | T | A | 19 | a0001c0001t0002g0045 a0001c0001t0002g0048 a0001c0001t0002g0070 others(16): Show |
19 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.-73-1390T>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21441369 | |||||||
| chr22:21441393 | C | T | 1 | a0001c0001t0002g0024 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-73-1366C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21441393 | |||||||
| chr22:21441966 | T | C | 2 | a0001c0001t0002g0035 a0001c0001t0002g0037 |
2 | HG00140.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.-73-793T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21441966 | |||||||
| chr22:21442095 | C | G | 2 | a0001c0001t0002g0050 a0001c0001t0002g0053 |
2 | NA18940.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-73-664C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21442095 | |||||||
| chr22:21442176 | G | A | 68 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0008 others(65): Show |
78 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-73-583G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21442176 | |||||||
| chr22:21442180 | T | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0186 |
2 | HG00738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-73-579T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21442180 | |||||||
| chr22:21442524 | C | G | 2 | a0001c0001t0059g0181 a0001c0003t0058g0064 |
2 | HG00438.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.-73-235C>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21442524 | |||||||
| chr22:21442549 | C | T | 2 | a0001c0001t0059g0181 a0001c0003t0058g0064 |
2 | HG00438.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.-73-210C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21442549 | |||||||
| chr22:21442631 | C | T | 1 | a0001c0001t0059g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-73-128C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21442631 | |||||||
| chr22:21442643 | G | T | 1 | a0002c0004t0049g0179 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-73-116G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 1/2 | chr22 | 21442643 | |||||||
| chr22:21442872 | A | AG | 7 | a0001c0001t0001g0090 a0001c0001t0001g0128 a0001c0001t0007g0126 others(4): Show |
7 | HG00741.hp2 HG01496.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+21dupG | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr22 | 21442872 | ||||||
| chr22:21442941 | A | G | 2 | a0001c0001t0019g0222 a0001c0001t0019g0223 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.26+84A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21442941 | |||||||
| chr22:21443289 | T | C | 1 | a0001c0001t0054g0052 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.26+432T>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21443289 | |||||||
| chr22:21443523 | C | T | 4 | a0001c0001t0014g0077 a0001c0001t0014g0152 a0001c0001t0014g0207 others(1): Show |
4 | HG02451.hp2 HG02572.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+666C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21443523 | |||||||
| chr22:21443698 | G | GGACACTG others(25): Show |
1 | a0001c0001t0034g0134 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.26+850_26+851insGG others(30): Show |
HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr22 | 21443698 | ||||||
| chr22:21443815 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.26+958G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21443815 | |||||||
| chr22:21443910 | C | T | 6 | a0001c0001t0003g0080 a0001c0001t0003g0151 a0002c0004t0020g0094 others(3): Show |
6 | HG01071.hp1 HG03098.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-1012C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21443910 | |||||||
| chr22:21443928 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.27-994A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21443928 | |||||||
| chr22:21443957 | C | A | 2 | a0002c0004t0025g0178 a0002c0004t0049g0179 |
2 | HG01071.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.27-965C>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21443957 | |||||||
| chr22:21443988 | G | C | 1 | a0001c0001t0003g0121 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.27-934G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21443988 | |||||||
| chr22:21444025 | G | T | 1 | a0001c0001t0044g0198 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.27-897G>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21444025 | |||||||
| chr22:21444043 | G | GCT | 4 | a0001c0001t0014g0077 a0001c0001t0014g0152 a0001c0001t0014g0207 others(1): Show |
4 | HG02451.hp2 HG02572.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-877_27-876dupTC | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr22 | 21444043 | ||||||
| chr22:21444062 | G | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(90): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.27-860G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21444062 | |||||||
| chr22:21444118 | G | C | 1 | a0001c0001t0047g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.27-804G>C | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21444118 | |||||||
| chr22:21444258 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.27-664C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21444258 | |||||||
| chr22:21444300 | G | A | 1 | a0001c0001t0032g0135 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.27-622G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21444300 | |||||||
| chr22:21444428 | G | A | 4 | a0001c0001t0014g0077 a0001c0001t0014g0152 a0001c0001t0014g0207 others(1): Show |
4 | HG02451.hp2 HG02572.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-494G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21444428 | |||||||
| chr22:21444430 | C | T | 2 | a0001c0001t0018g0124 a0001c0001t0018g0125 |
2 | HG00733.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.27-492C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21444430 | |||||||
| chr22:21444432 | C | T | 21 | a0001c0001t0003g0080 a0001c0001t0003g0151 a0001c0001t0003g0164 others(18): Show |
23 | HG01071.hp1 HG01884.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.27-490C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21444432 | |||||||
| chr22:21444570 | A | AGG | 5 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0003g0088 others(2): Show |
5 | HG01261.hp2 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.27-350_27-349dupGG | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr22 | 21444570 | ||||||
| chr22:21444618 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(91): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.27-304A>G | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21444618 | |||||||
| chr22:21444782 | C | T | 3 | a0001c0001t0014g0077 a0001c0001t0014g0152 a0001c0001t0030g0078 |
3 | HG02451.hp2 HG02572.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.27-140C>T | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21444782 | |||||||
| chr22:21444783 | G | A | 1 | a0001c0001t0022g0019 | 2 | HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.27-139G>A | HIC2 | ENSG00000169635.10 | transcript | ENST00000407464.7 | protein_coding | 2/2 | chr22 | 21444783 |