Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64399 |
| ensemblid | ENSG00000164161.10 |
| hgncid | 14866 |
| symbol | HHIP |
| name | hedgehog interacting protein |
| refseq_nuc | NM_022475.3 |
| refseq_prot | NP_071920.1 |
| ensembl_nuc | ENST00000296575.8 |
| ensembl_prot | ENSP00000296575.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 144646156 |
| end | 144745271 |
| strand | + |
| ver | v1.2 |
| region | chr4:144646156-144745271 |
| region5000 | chr4:144641156-144750271 |
| regionname0 | HHIP_chr4_144646156_144745271 |
| regionname5000 | HHIP_chr4_144641156_144750271 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 700 | 305 | 74 | 45 | 148 | 10 | 26 | 120 | HHIP_chr4_144641156_144750271 | HHIP | MLKML others(695): Show |
chr4 | 144641156 | 144750271 |
| a0002 | 0/0 | 700 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | MLKML others(695): Show |
chr4 | 144641156 | 144750271 |
| a0003 | 0/0 | 700 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HHIP_chr4_144641156_144750271 | HHIP | MLKML others(695): Show |
chr4 | 144641156 | 144750271 |
| a0004 | 0/0 | 700 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | MLKML others(695): Show |
chr4 | 144641156 | 144750271 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2100 | 300 | 73 | 43 | 148 | 8 | 26 | HHIP_chr4_144641156_144750271 | HHIP | ATGCT others(2095): Show |
chr4 | 144641156 | 144750271 | ||
| a0001c0003 | 0/0 | 2100 | 4 | 0 | 2 | 0 | 2 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGCT others(2095): Show |
chr4 | 144641156 | 144750271 | ||
| a0001c0006 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGCT others(2095): Show |
chr4 | 144641156 | 144750271 | ||
| a0002c0002 | 0/0 | 2100 | 8 | 7 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGCT others(2095): Show |
chr4 | 144641156 | 144750271 | ||
| a0003c0004 | 0/0 | 2100 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGCT others(2095): Show |
chr4 | 144641156 | 144750271 | ||
| a0004c0005 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGCT others(2095): Show |
chr4 | 144641156 | 144750271 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9930 | 72 | 12 | 8 | 48 | 0 | 4 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0002 | 0/0 | 9934 | 68 | 4 | 9 | 49 | 2 | 4 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9929): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0003 | 0/0 | 9930 | 44 | 1 | 14 | 19 | 4 | 6 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0004 | 0/0 | 9930 | 14 | 6 | 3 | 4 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0005 | 0/0 | 9930 | 15 | 14 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0006 | 0/0 | 9929 | 7 | 6 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9924): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0007 | 0/0 | 9930 | 7 | 0 | 0 | 7 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0009 | 0/0 | 9934 | 5 | 0 | 1 | 2 | 2 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9929): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0010 | 0/0 | 9930 | 5 | 4 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0011 | 0/0 | 9930 | 5 | 0 | 0 | 4 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0012 | 0/0 | 9929 | 3 | 0 | 0 | 2 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9924): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0013 | 0/0 | 9934 | 3 | 3 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9929): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0014 | 0/0 | 9934 | 3 | 3 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9929): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0015 | 0/0 | 9930 | 3 | 3 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0016 | 0/0 | 9930 | 3 | 0 | 1 | 0 | 0 | 2 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0017 | 0/0 | 9933 | 3 | 1 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9928): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0018 | 0/0 | 9935 | 3 | 3 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9930): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0019 | 0/0 | 9876 | 2 | 1 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9871): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0020 | 0/0 | 9930 | 2 | 0 | 1 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0021 | 0/0 | 9934 | 2 | 1 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9929): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0022 | 0/0 | 9930 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0023 | 0/0 | 9930 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0024 | 0/0 | 9930 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0025 | 0/0 | 9930 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0026 | 0/1 | 9877 | 1 | 0 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9872): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0027 | 0/0 | 9930 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0028 | 0/0 | 9930 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0029 | 0/0 | 9930 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0030 | 0/0 | 9934 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9929): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0031 | 0/0 | 9929 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9924): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0032 | 0/0 | 9930 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0033 | 0/0 | 9929 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9924): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0034 | 0/0 | 9930 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0035 | 0/0 | 9930 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0036 | 0/0 | 9889 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9884): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0037 | 0/0 | 9930 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0038 | 0/0 | 9934 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9929): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0039 | 0/0 | 9934 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9929): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0040 | 0/0 | 9934 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9929): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0041 | 0/0 | 9930 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0042 | 0/0 | 9934 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9929): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0043 | 1/0 | 9937 | 1 | 0 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9932): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0044 | 0/0 | 9937 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9932): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0045 | 0/0 | 9908 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9903): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0046 | 0/0 | 9930 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0047 | 0/0 | 9934 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9929): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0048 | 0/0 | 9930 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0049 | 0/0 | 9935 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9930): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0050 | 0/0 | 9930 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0051 | 0/0 | 9930 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0001t0054 | 0/0 | 9930 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0001c0003t0002 | 0/0 | 9934 | 4 | 0 | 2 | 0 | 2 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9929): Show |
chr4 | 144641156 | 144750271 |
| a0001c0006t0004 | 0/0 | 9930 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0002c0002t0008 | 0/0 | 9930 | 6 | 6 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0002c0002t0052 | 0/0 | 9934 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9929): Show |
chr4 | 144641156 | 144750271 |
| a0002c0002t0053 | 0/0 | 9930 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0003c0004t0004 | 0/0 | 9930 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| a0004c0005t0005 | 0/0 | 9930 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | ATGAG others(9925): Show |
chr4 | 144641156 | 144750271 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0007g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0007g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0009g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0009g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0009g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0009g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0009g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0010g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0010g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0010g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0010g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0011g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0011g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0011g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0011g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0011g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0012g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0012g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0012g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0013g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0013g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0014g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0014g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0014g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0015g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0015g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0015g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0016g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0016g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0016g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0017g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0017g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0017g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0018g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0018g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0018g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0019g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0019g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0020g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0020g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0021g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0021g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0022g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0023g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0024g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0025g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0026g0184 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0027g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0028g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0029g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0030g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0031g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0032g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0033g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0034g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0035g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0036g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0037g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0038g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0039g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0040g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0041g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0042g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0043g0287 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0044g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0045g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0046g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0047g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0048g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0049g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0050g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0051g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0001t0054g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0003t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0003t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0001c0006t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0002c0002t0008g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0002c0002t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0002c0002t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0002c0002t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0002c0002t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0002c0002t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0002c0002t0052g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0002c0002t0053g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0003c0004t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0003c0004t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| a0004c0005t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0002 | g0113 | EUR | GBR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00099 | hp2 | a0001 | c0001 | t0009 | g0183 | EUR | GBR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0102 | EUR | FIN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0153 | EUR | FIN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0096 | EUR | FIN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0191 | EUR | FIN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00408 | hp2 | a0001 | c0001 | t0009 | g0158 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00423 | hp2 | a0001 | c0001 | t0047 | g0249 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0154 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00621 | hp1 | a0001 | c0001 | t0011 | g0045 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0224 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00642 | hp2 | a0001 | c0001 | t0016 | g0089 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0275 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01074 | hp2 | a0001 | c0001 | t0020 | g0087 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01081 | hp2 | a0001 | c0001 | t0051 | g0110 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0292 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01106 | hp2 | a0001 | c0001 | t0009 | g0225 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01109 | hp1 | a0001 | c0003 | t0002 | g0101 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01192 | hp1 | a0002 | c0002 | t0053 | g0138 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0228 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01243 | hp2 | a0001 | c0001 | t0019 | g0161 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0223 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0150 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0293 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0080 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01515 | hp1 | a0001 | c0001 | t0009 | g0175 | EUR | IBS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0168 | EUR | IBS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0169 | EUR | IBS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0099 | EUR | IBS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01884 | hp1 | a0001 | c0001 | t0010 | g0297 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01891 | hp2 | a0001 | c0001 | t0032 | g0142 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01943 | hp2 | a0001 | c0001 | t0034 | g0060 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0205 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02015 | hp1 | a0001 | c0001 | t0033 | g0001 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02055 | hp2 | a0002 | c0002 | t0008 | g0136 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02056 | hp1 | a0001 | c0001 | t0025 | g0159 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0222 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0193 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02145 | hp1 | a0001 | c0001 | t0014 | g0122 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02145 | hp2 | a0001 | c0001 | t0018 | g0147 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CDX | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CDX | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02257 | hp1 | a0001 | c0001 | t0029 | g0199 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02258 | hp1 | a0002 | c0002 | t0052 | g0139 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0281 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0131 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0272 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02572 | hp2 | a0001 | c0001 | t0045 | g0082 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02615 | hp1 | a0001 | c0001 | t0010 | g0146 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0276 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0219 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02622 | hp2 | a0001 | c0001 | t0031 | g0079 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0214 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02630 | hp2 | a0002 | c0002 | t0008 | g0134 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02698 | hp1 | a0001 | c0001 | t0040 | g0017 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0208 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0073 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02723 | hp1 | a0001 | c0001 | t0019 | g0162 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02735 | hp1 | a0001 | c0001 | t0021 | g0090 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0197 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02809 | hp1 | a0001 | c0001 | t0014 | g0130 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02896 | hp2 | a0001 | c0001 | t0013 | g0014 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02897 | hp1 | a0001 | c0001 | t0013 | g0014 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0277 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02965 | hp2 | a0002 | c0002 | t0008 | g0135 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02970 | hp1 | a0001 | c0001 | t0023 | g0218 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02970 | hp2 | a0002 | c0002 | t0008 | g0137 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0078 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03041 | hp1 | a0002 | c0002 | t0008 | g0140 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03041 | hp2 | a0004 | c0005 | t0005 | g0118 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03130 | hp1 | a0002 | c0002 | t0008 | g0133 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0076 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03209 | hp1 | a0001 | c0001 | t0018 | g0149 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03209 | hp2 | a0001 | c0001 | t0017 | g0115 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03225 | hp1 | a0001 | c0001 | t0015 | g0119 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0278 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03239 | hp2 | a0001 | c0001 | t0012 | g0189 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03486 | hp1 | a0001 | c0001 | t0015 | g0072 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03516 | hp1 | a0001 | c0001 | t0050 | g0132 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03516 | hp2 | a0001 | c0001 | t0015 | g0144 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0216 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0273 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0141 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0188 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03654 | hp2 | a0001 | c0001 | t0016 | g0083 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03669 | hp1 | a0001 | c0001 | t0020 | g0088 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0176 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03704 | hp1 | a0001 | c0001 | t0011 | g0295 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0178 | SAS | BEB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03831 | hp2 | a0001 | c0001 | t0016 | g0085 | SAS | BEB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03927 | hp1 | a0001 | c0001 | t0037 | g0022 | SAS | BEB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0186 | SAS | BEB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | BEB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0187 | SAS | STU | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | STU | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0291 | SAS | STU | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG04204 | hp2 | a0001 | c0001 | t0036 | g0040 | SAS | STU | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG04228 | hp1 | a0001 | c0001 | t0028 | g0217 | SAS | STU | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG04228 | hp2 | a0001 | c0001 | t0027 | g0165 | SAS | STU | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0074 | AFR | YRI | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | CHB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0220 | AFR | YRI | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18940 | hp2 | a0001 | c0001 | t0035 | g0027 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18941 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18942 | hp1 | a0001 | c0001 | t0030 | g0230 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18942 | hp2 | a0001 | c0001 | t0022 | g0157 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18947 | hp2 | a0001 | c0001 | t0012 | g0211 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18948 | hp2 | a0003 | c0004 | t0004 | g0207 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18951 | hp1 | a0001 | c0001 | t0017 | g0250 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18953 | hp2 | a0001 | c0001 | t0017 | g0240 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18960 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18965 | hp2 | a0001 | c0001 | t0011 | g0049 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18967 | hp1 | a0001 | c0001 | t0007 | g0029 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18971 | hp2 | a0001 | c0001 | t0007 | g0066 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18973 | hp1 | a0001 | c0001 | t0042 | g0006 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18983 | hp1 | a0001 | c0001 | t0024 | g0212 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18984 | hp1 | a0001 | c0001 | t0011 | g0259 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18986 | hp2 | a0001 | c0001 | t0011 | g0234 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18988 | hp2 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18991 | hp2 | a0001 | c0001 | t0039 | g0093 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18993 | hp1 | a0001 | c0001 | t0054 | g0180 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19002 | hp2 | a0003 | c0004 | t0004 | g0206 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19010 | hp1 | a0001 | c0001 | t0012 | g0210 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0215 | AFR | LWK | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | LWK | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | LWK | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19043 | hp2 | a0001 | c0001 | t0018 | g0148 | AFR | LWK | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19068 | hp2 | a0001 | c0001 | t0009 | g0172 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19074 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19075 | hp1 | a0001 | c0001 | t0041 | g0057 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19084 | hp1 | a0001 | c0001 | t0007 | g0046 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0077 | AFR | YRI | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0274 | AFR | YRI | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA20129 | hp1 | a0001 | c0001 | t0010 | g0145 | AFR | ASW | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0296 | AFR | ASW | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02109 | hp1 | a0001 | c0001 | t0046 | g0270 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0114 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02486 | hp2 | a0001 | c0001 | t0038 | g0269 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02559 | hp1 | a0001 | c0001 | t0014 | g0128 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG02559 | hp2 | a0001 | c0001 | t0021 | g0226 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03471 | hp1 | a0001 | c0001 | t0049 | g0075 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG03471 | hp2 | a0001 | c0001 | t0013 | g0285 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG06807 | hp1 | a0001 | c0001 | t0048 | g0129 | AFR | USA | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| HG06807 | hp2 | a0001 | c0001 | t0044 | g0286 | AFR | USA | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA21309 | hp1 | a0001 | c0006 | t0004 | g0213 | AFR | LWK | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0026 | g0184 | REF | REF | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0043 | g0287 | REF | REF | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:144659714 | G | A | 1 | a0002 | 8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
missense_variant | MODERATE | c.707G>A | p.Gly236Glu | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/13 | 1227/9937 | 707/2103 | 236/700 | chr4 | 144659714 | |||
| chr4:144708220 | G | A | 1 | a0004 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.1210G>A | p.Val404Met | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/13 | 1730/9937 | 1210/2103 | 404/700 | chr4 | 144708220 | |||
| chr4:144737949 | A | G | 1 | a0003 | 2 | NA18948.hp2 NA19002.hp2 |
missense_variant | MODERATE | c.2095A>G | p.Ile699Val | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2615/9937 | 2095/2103 | 699/700 | chr4 | 144737949 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:144715396 | C | T | 1 | a0001c0006 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.1644C>T | p.Ser548Ser | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/13 | 2164/9937 | 1644/2103 | 548/700 | chr4 | 144715396 | |||
| chr4:144737912 | T | C | 1 | a0001c0003 | 4 | HG00099.hp1 HG00280.hp1 HG01106.hp1 others(1): Show |
synonymous_variant | LOW | c.2058T>C | p.Ile686Ile | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2578/9937 | 2058/2103 | 686/700 | chr4 | 144737912 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:144646226 | G | T | 1 | a0001c0001t0054 | 1 | NA18993.hp1 | 5_prime_UTR_variant | MODIFIER | c.-450G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/13 | 450 | chr4 | 144646226 | ||||||
| chr4:144646243 | C | T | 3 | a0002c0002t0008 a0002c0002t0052 a0002c0002t0053 |
8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-433C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/13 | 433 | chr4 | 144646243 | ||||||
| chr4:144646319 | T | A | 15 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0009 others(12): Show |
79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
5_prime_UTR_variant | MODIFIER | c.-357T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/13 | 357 | chr4 | 144646319 | ||||||
| chr4:144646536 | T | G | 1 | a0001c0001t0030 | 1 | NA18942.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-140T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/13 | chr4 | 144646536 | |||||||
| chr4:144738046 | C | T | 2 | a0001c0001t0029 a0001c0001t0051 |
2 | HG01081.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*89C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 89 | chr4 | 144738046 | ||||||
| chr4:144738143 | A | G | 1 | a0001c0001t0050 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 186 | chr4 | 144738143 | ||||||
| chr4:144738268 | T | C | 1 | a0001c0001t0019 | 2 | HG01243.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*311T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 311 | chr4 | 144738268 | ||||||
| chr4:144738373 | T | A | 1 | a0001c0001t0019 | 2 | HG01243.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*416T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 416 | chr4 | 144738373 | ||||||
| chr4:144738438 | A | G | 1 | a0001c0001t0049 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*481A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 481 | chr4 | 144738438 | ||||||
| chr4:144738495 | A | G | 3 | a0001c0001t0048 a0002c0002t0008 a0002c0002t0053 |
8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*538A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 538 | chr4 | 144738495 | ||||||
| chr4:144738537 | A | T | 1 | a0001c0001t0028 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*580A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 580 | chr4 | 144738537 | ||||||
| chr4:144738561 | T | C | 1 | a0001c0001t0022 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*604T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 604 | chr4 | 144738561 | ||||||
| chr4:144738574 | T | C | 1 | a0001c0001t0019 | 2 | HG01243.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*617T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 617 | chr4 | 144738574 | ||||||
| chr4:144739230 | T | C | 2 | a0001c0001t0006 a0001c0001t0031 |
8 | HG01496.hp2 HG02622.hp2 HG02976.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1273T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 1273 | chr4 | 144739230 | ||||||
| chr4:144739399 | A | G | 1 | a0001c0001t0027 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1442A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 1442 | chr4 | 144739399 | ||||||
| chr4:144739582 | A | T | 2 | a0001c0001t0006 a0001c0001t0031 |
8 | HG01496.hp2 HG02622.hp2 HG02976.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1625A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 1625 | chr4 | 144739582 | ||||||
| chr4:144739931 | A | C | 1 | a0001c0001t0019 | 2 | HG01243.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1974A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 1974 | chr4 | 144739931 | ||||||
| chr4:144739985 | T | C | 1 | a0001c0001t0013 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2028T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2028 | chr4 | 144739985 | ||||||
| chr4:144740224 | A | C | 1 | a0001c0001t0047 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2267A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2267 | chr4 | 144740224 | ||||||
| chr4:144740328 | A | T | 1 | a0001c0001t0046 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2371A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2371 | chr4 | 144740328 | ||||||
| chr4:144740499 | G | C | 21 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(18): Show |
128 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*2542G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2542 | chr4 | 144740499 | ||||||
| chr4:144740758 | G | A | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(48): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*2801G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2801 | chr4 | 144740758 | ||||||
| chr4:144740763 | G | T | 2 | a0001c0001t0016 a0001c0001t0020 |
5 | HG00642.hp2 HG01074.hp2 HG03654.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2806G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2806 | chr4 | 144740763 | ||||||
| chr4:144740816 | G | A | 2 | a0001c0001t0020 a0001c0001t0049 |
3 | HG01074.hp2 HG03471.hp1 HG03669.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2859G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2859 | chr4 | 144740816 | ||||||
| chr4:144740923 | T | C | 1 | a0001c0001t0032 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2966T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2966 | chr4 | 144740923 | ||||||
| chr4:144740946 | G | C | 1 | a0001c0001t0038 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2989G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2989 | chr4 | 144740946 | ||||||
| chr4:144740980 | C | G | 1 | a0001c0001t0015 | 3 | HG03225.hp1 HG03486.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3023C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3023 | chr4 | 144740980 | ||||||
| chr4:144740980 | CT | C | 2 | a0001c0001t0006 a0001c0001t0031 |
8 | HG01496.hp2 HG02622.hp2 HG02976.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3025delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3025 | INFO_REALIGN_3_PRIME | chr4 | 144740980 | |||||
| chr4:144741020 | C | T | 1 | a0002c0002t0053 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3063C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3063 | chr4 | 144741020 | ||||||
| chr4:144741142 | TA | T | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(48): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*3186delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3186 | chr4 | 144741142 | ||||||
| chr4:144741145 | A | T | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(48): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*3188A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3188 | chr4 | 144741145 | ||||||
| chr4:144741363 | GT | G | 11 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(8): Show |
15 | HG01081.hp2 HG01256.hp1 HG01515.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3422delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3422 | INFO_REALIGN_3_PRIME | chr4 | 144741363 | |||||
| chr4:144741379 | T | C | 1 | a0001c0001t0049 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3422T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3422 | chr4 | 144741379 | ||||||
| chr4:144741385 | CT | C | 4 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0033 others(1): Show |
8 | HG02015.hp1 HG03209.hp2 HG03239.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3443delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3443 | INFO_REALIGN_3_PRIME | chr4 | 144741385 | |||||
| chr4:144741465 | C | T | 1 | a0001c0001t0042 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3508C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3508 | chr4 | 144741465 | ||||||
| chr4:144741541 | G | A | 1 | a0001c0001t0010 | 5 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3584G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3584 | chr4 | 144741541 | ||||||
| chr4:144741670 | C | A | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(48): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*3713C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3713 | chr4 | 144741670 | ||||||
| chr4:144741678 | A | G | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(48): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*3721A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3721 | chr4 | 144741678 | ||||||
| chr4:144741690 | C | T | 11 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0012 others(8): Show |
60 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*3733C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3733 | chr4 | 144741690 | ||||||
| chr4:144742006 | G | A | 2 | a0001c0001t0016 a0001c0001t0020 |
5 | HG00642.hp2 HG01074.hp2 HG03654.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4049G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4049 | chr4 | 144742006 | ||||||
| chr4:144742014 | G | A | 1 | a0001c0001t0034 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4057G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4057 | chr4 | 144742014 | ||||||
| chr4:144742035 | GTA | G | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(48): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*4088_*4089delAT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4088 | INFO_REALIGN_3_PRIME | chr4 | 144742035 | |||||
| chr4:144742060 | TAC | T | 2 | a0001c0001t0018 a0001c0001t0045 |
4 | HG02145.hp2 HG02572.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4119_*4120delCA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4119 | INFO_REALIGN_3_PRIME | chr4 | 144742060 | |||||
| chr4:144742062 | C | T | 14 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0009 others(11): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*4105C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4105 | chr4 | 144742062 | ||||||
| chr4:144742064 | C | T | 1 | a0001c0001t0047 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4107C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4107 | chr4 | 144742064 | ||||||
| chr4:144742074 | CACAT | C | 37 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(34): Show |
211 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*4135_*4138delCATA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4135 | INFO_REALIGN_3_PRIME | chr4 | 144742074 | |||||
| chr4:144742076 | CAT | C | 13 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0013 others(10): Show |
94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*4121_*4122delTA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4121 | INFO_REALIGN_3_PRIME | chr4 | 144742076 | |||||
| chr4:144742078 | T | C | 2 | a0001c0001t0047 a0001c0001t0049 |
2 | HG00423.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4121T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4121 | chr4 | 144742078 | ||||||
| chr4:144742261 | A | G | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(52): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*4304A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4304 | chr4 | 144742261 | ||||||
| chr4:144742569 | A | T | 1 | a0001c0001t0041 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4612A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4612 | chr4 | 144742569 | ||||||
| chr4:144742646 | G | A | 11 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0012 others(8): Show |
60 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*4689G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4689 | chr4 | 144742646 | ||||||
| chr4:144742663 | T | A | 1 | a0001c0001t0035 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4706T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4706 | chr4 | 144742663 | ||||||
| chr4:144742832 | GTTATATA others(20): Show |
G | 1 | a0001c0001t0045 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4892_*4918delATAT others(23): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4892 | INFO_REALIGN_3_PRIME | chr4 | 144742832 | |||||
| chr4:144742849 | A | T | 2 | a0001c0001t0018 a0001c0001t0036 |
4 | HG02145.hp2 HG03209.hp1 HG04204.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4892A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4892 | chr4 | 144742849 | ||||||
| chr4:144742862 | ATATATAT others(34): Show |
A | 1 | a0001c0001t0036 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4918_*4958delTTTA others(37): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4918 | INFO_REALIGN_3_PRIME | chr4 | 144742862 | |||||
| chr4:144742872 | C | A | 1 | a0001c0001t0001 | 3 | NA18962.hp1 NA18994.hp2 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4915C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4915 | chr4 | 144742872 | ||||||
| chr4:144742874 | TTTTATAT others(45): Show |
T | 1 | a0001c0001t0018 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4945_*4996delTTTA others(48): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4945 | INFO_REALIGN_3_PRIME | chr4 | 144742874 | |||||
| chr4:144742889 | ATATATAT others(7): Show |
A | 48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(45): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*4945_*4958delTTTA others(10): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4945 | INFO_REALIGN_3_PRIME | chr4 | 144742889 | |||||
| chr4:144742899 | CTT | C | 2 | a0001c0001t0019 a0001c0001t0049 |
3 | HG01243.hp2 HG02723.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4946_*4947delTT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4946 | INFO_REALIGN_3_PRIME | chr4 | 144742899 | |||||
| chr4:144742899 | CTTTTTAT others(8): Show |
C | 1 | a0001c0001t0035 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4944_*4958delTTTT others(11): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4944 | INFO_REALIGN_3_PRIME | chr4 | 144742899 | |||||
| chr4:144742900 | TTTTTATA others(9): Show |
T | 1 | a0001c0001t0001 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4945_*4960delTTTA others(12): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4945 | INFO_REALIGN_3_PRIME | chr4 | 144742900 | |||||
| chr4:144742901 | T | TATATATA others(4): Show |
1 | a0001c0001t0002 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4944_*4945insATAT others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4945 | chr4 | 144742901 | ||||||
| chr4:144742901 | TTTTATAT others(5): Show |
T | 1 | a0001c0001t0010 | 5 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4947_*4958delTATA others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4947 | INFO_REALIGN_3_PRIME | chr4 | 144742901 | |||||
| chr4:144742901 | TTTTATAT others(90): Show |
T | 1 | a0001c0001t0002 | 2 | HG02056.hp2 NA18944.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4945_*5041delTTTA others(93): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4945 | chr4 | 144742901 | ||||||
| chr4:144742914 | T | A | 1 | a0001c0001t0010 | 5 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4957T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4957 | chr4 | 144742914 | ||||||
| chr4:144742927 | TTTATATA others(54): Show |
T | 1 | a0001c0001t0019 | 2 | HG01243.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4972_*5032delTATA others(57): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4972 | INFO_REALIGN_3_PRIME | chr4 | 144742927 | |||||
| chr4:144742955 | TACATATA others(36): Show |
T | 1 | a0001c0001t0021 | 2 | HG02559.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5000_*5042delCATA others(39): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5000 | INFO_REALIGN_3_PRIME | chr4 | 144742955 | |||||
| chr4:144742964 | GATATATG others(31): Show |
G | 1 | a0001c0001t0049 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5014_*5051delGTAT others(34): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5014 | INFO_REALIGN_3_PRIME | chr4 | 144742964 | |||||
| chr4:144742971 | G | A | 50 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(47): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*5014G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5014 | chr4 | 144742971 | ||||||
| chr4:144742972 | TATATATA others(33): Show |
T | 50 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(47): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*5016_*5055delATAT others(36): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5016 | chr4 | 144742972 | ||||||
| chr4:144742993 | T | C | 1 | a0001c0001t0019 | 2 | HG01243.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5036T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5036 | chr4 | 144742993 | ||||||
| chr4:144743000 | T | G | 1 | a0001c0001t0019 | 2 | HG01243.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5043T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5043 | chr4 | 144743000 | ||||||
| chr4:144743009 | A | C | 1 | a0001c0001t0002 | 2 | HG02056.hp2 NA18944.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5052A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5052 | chr4 | 144743009 | ||||||
| chr4:144743024 | T | G | 1 | a0001c0001t0021 | 2 | HG02559.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5067T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5067 | chr4 | 144743024 | ||||||
| chr4:144743120 | A | T | 1 | a0001c0001t0044 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5163A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5163 | chr4 | 144743120 | ||||||
| chr4:144743220 | T | C | 1 | a0001c0001t0045 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5263T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5263 | chr4 | 144743220 | ||||||
| chr4:144743360 | A | G | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(48): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*5403A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5403 | chr4 | 144743360 | ||||||
| chr4:144743703 | C | A | 1 | a0001c0001t0039 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5746C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5746 | chr4 | 144743703 | ||||||
| chr4:144743738 | A | T | 1 | a0001c0001t0037 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5781A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5781 | chr4 | 144743738 | ||||||
| chr4:144743790 | C | T | 1 | a0001c0001t0025 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5833C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5833 | chr4 | 144743790 | ||||||
| chr4:144743929 | T | C | 1 | a0001c0001t0040 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5972T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5972 | chr4 | 144743929 | ||||||
| chr4:144744082 | G | T | 1 | a0001c0001t0040 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6125G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 6125 | chr4 | 144744082 | ||||||
| chr4:144744112 | T | C | 1 | a0001c0001t0024 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6155T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 6155 | chr4 | 144744112 | ||||||
| chr4:144744143 | A | G | 1 | a0001c0001t0006 | 7 | HG01496.hp2 HG02976.hp2 HG03130.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6186A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 6186 | chr4 | 144744143 | ||||||
| chr4:144744449 | C | A | 1 | a0001c0001t0049 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6492C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 6492 | chr4 | 144744449 | ||||||
| chr4:144744516 | A | G | 1 | a0001c0001t0007 | 7 | NA18941.hp2 NA18960.hp1 NA18967.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6559A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 6559 | chr4 | 144744516 | ||||||
| chr4:144744776 | AG | A | 52 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(49): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*6826delG | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 6826 | INFO_REALIGN_3_PRIME | chr4 | 144744776 | |||||
| chr4:144744800 | G | A | 1 | a0001c0001t0018 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6843G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 6843 | chr4 | 144744800 | ||||||
| chr4:144745218 | G | A | 1 | a0001c0001t0027 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7261G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 7261 | chr4 | 144745218 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:144647200 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.279+246T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144647200 | |||||||
| chr4:144647299 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(60): Show |
67 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+345G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144647299 | |||||||
| chr4:144647368 | G | A | 2 | a0001c0001t0002g0070 a0001c0001t0002g0071 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.279+414G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144647368 | |||||||
| chr4:144647373 | C | T | 1 | a0001c0001t0021g0226 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.279+419C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144647373 | |||||||
| chr4:144647394 | C | A | 1 | a0001c0001t0015g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.279+440C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144647394 | |||||||
| chr4:144647530 | A | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(60): Show |
67 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+576A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144647530 | |||||||
| chr4:144647636 | C | A | 1 | a0001c0001t0001g0015 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.279+682C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144647636 | |||||||
| chr4:144647692 | T | TTAAC | 77 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(74): Show |
79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.279+741_279+742ins others(4): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 144647692 | ||||||
| chr4:144647704 | A | C | 1 | a0001c0001t0009g0225 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.279+750A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144647704 | |||||||
| chr4:144647988 | T | TA | 10 | a0001c0001t0005g0073 a0001c0001t0006g0074 a0001c0001t0006g0076 others(7): Show |
10 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.279+1046dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 144647988 | ||||||
| chr4:144647988 | TA | T | 80 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(77): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.279+1046delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 144647988 | ||||||
| chr4:144648202 | T | C | 1 | a0001c0001t0003g0150 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.279+1248T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144648202 | |||||||
| chr4:144648450 | T | C | 10 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(7): Show |
10 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.279+1496T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144648450 | |||||||
| chr4:144648529 | C | A | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.279+1575C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144648529 | |||||||
| chr4:144648540 | C | T | 77 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(74): Show |
79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.279+1586C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144648540 | |||||||
| chr4:144648680 | C | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(60): Show |
67 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+1726C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144648680 | |||||||
| chr4:144649235 | G | GA | 36 | a0001c0001t0002g0006 a0001c0001t0002g0070 a0001c0001t0002g0071 others(33): Show |
36 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.279+2292dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 144649235 | ||||||
| chr4:144649353 | T | C | 1 | a0001c0001t0002g0227 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.279+2399T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144649353 | |||||||
| chr4:144650135 | G | A | 1 | a0001c0001t0010g0228 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.280-2470G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144650135 | |||||||
| chr4:144650542 | A | C | 79 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(76): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.280-2063A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144650542 | |||||||
| chr4:144650894 | T | C | 79 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(76): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.280-1711T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144650894 | |||||||
| chr4:144651073 | A | T | 1 | a0001c0001t0015g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.280-1532A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651073 | |||||||
| chr4:144651183 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280-1422A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651183 | |||||||
| chr4:144651225 | T | C | 1 | a0001c0001t0016g0083 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.280-1380T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651225 | |||||||
| chr4:144651331 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.280-1274C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651331 | |||||||
| chr4:144651387 | C | T | 1 | a0001c0001t0032g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.280-1218C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651387 | |||||||
| chr4:144651449 | A | T | 79 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(76): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.280-1156A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651449 | |||||||
| chr4:144651530 | A | G | 1 | a0001c0001t0021g0226 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.280-1075A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651530 | |||||||
| chr4:144651761 | A | AT | 79 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(76): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.280-843dupT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 144651761 | ||||||
| chr4:144651785 | A | G | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.280-820A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651785 | |||||||
| chr4:144651901 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.280-704C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651901 | |||||||
| chr4:144651979 | T | C | 1 | a0001c0001t0005g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.280-626T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651979 | |||||||
| chr4:144652134 | T | G | 1 | a0001c0001t0002g0084 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.280-471T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144652134 | |||||||
| chr4:144652476 | T | C | 1 | a0001c0001t0017g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.280-129T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144652476 | |||||||
| chr4:144652802 | GA | G | 44 | a0001c0001t0002g0006 a0001c0001t0002g0070 a0001c0001t0002g0071 others(41): Show |
44 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.472+14delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 144652802 | ||||||
| chr4:144653044 | A | G | 11 | a0001c0001t0002g0288 a0001c0001t0002g0289 a0001c0001t0002g0290 others(8): Show |
11 | HG00735.hp2 HG01106.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.472+247A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144653044 | |||||||
| chr4:144653087 | G | T | 35 | a0001c0001t0002g0006 a0001c0001t0002g0070 a0001c0001t0002g0071 others(32): Show |
35 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.472+290G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144653087 | |||||||
| chr4:144653110 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.472+313T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144653110 | |||||||
| chr4:144653304 | C | A | 1 | a0001c0001t0040g0017 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.472+507C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144653304 | |||||||
| chr4:144653442 | A | G | 1 | a0001c0001t0006g0141 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.472+645A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144653442 | |||||||
| chr4:144653692 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.472+895A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144653692 | |||||||
| chr4:144653698 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.472+901A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144653698 | |||||||
| chr4:144653722 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 |
3 | HG00597.hp1 NA18952.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.472+925T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144653722 | |||||||
| chr4:144654027 | C | G | 2 | a0001c0001t0004g0223 a0001c0001t0004g0224 |
2 | HG00642.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.472+1230C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654027 | |||||||
| chr4:144654028 | T | C | 1 | a0001c0001t0032g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.472+1231T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654028 | |||||||
| chr4:144654097 | T | C | 1 | a0001c0001t0001g0021 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.472+1300T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654097 | |||||||
| chr4:144654256 | G | A | 1 | a0001c0001t0016g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.472+1459G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654256 | |||||||
| chr4:144654435 | C | A | 1 | a0001c0001t0003g0150 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.472+1638C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654435 | |||||||
| chr4:144654536 | T | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.472+1739T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654536 | |||||||
| chr4:144654716 | A | G | 1 | a0001c0001t0003g0150 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.472+1919A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654716 | |||||||
| chr4:144654759 | T | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(60): Show |
67 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.472+1962T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654759 | |||||||
| chr4:144654868 | T | C | 3 | a0001c0001t0002g0229 a0001c0001t0002g0231 a0001c0001t0030g0230 |
3 | NA18942.hp1 NA18962.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.472+2071T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654868 | |||||||
| chr4:144655188 | G | T | 1 | a0001c0001t0017g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.472+2391G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144655188 | |||||||
| chr4:144655403 | A | G | 1 | a0001c0001t0004g0222 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.472+2606A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144655403 | |||||||
| chr4:144655406 | G | A | 77 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(74): Show |
79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.472+2609G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144655406 | |||||||
| chr4:144655504 | T | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.472+2707T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144655504 | |||||||
| chr4:144655753 | C | CTCTT | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
193 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.472+2957_472+2958i others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 144655753 | ||||||
| chr4:144656039 | A | G | 1 | a0001c0001t0015g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.473-2751A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656039 | |||||||
| chr4:144656056 | C | T | 1 | a0001c0003t0002g0113 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.473-2734C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656056 | |||||||
| chr4:144656143 | G | C | 1 | a0001c0001t0002g0232 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.473-2647G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656143 | |||||||
| chr4:144656165 | G | C | 8 | a0002c0002t0008g0133 a0002c0002t0008g0134 a0002c0002t0008g0135 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.473-2625G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656165 | |||||||
| chr4:144656218 | A | G | 16 | a0001c0001t0002g0086 a0001c0001t0006g0074 a0001c0001t0006g0076 others(13): Show |
16 | HG00642.hp2 HG01074.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.473-2572A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656218 | |||||||
| chr4:144656241 | G | A | 1 | a0001c0001t0015g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.473-2549G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656241 | |||||||
| chr4:144656314 | A | C | 2 | a0001c0001t0013g0014 a0001c0001t0013g0285 |
3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.473-2476A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656314 | |||||||
| chr4:144656379 | C | A | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.473-2411C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656379 | |||||||
| chr4:144656446 | G | A | 6 | a0001c0001t0004g0219 a0001c0001t0004g0220 a0001c0001t0004g0221 others(3): Show |
6 | HG01243.hp2 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.473-2344G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656446 | |||||||
| chr4:144656484 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
203 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.473-2306T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656484 | |||||||
| chr4:144656766 | A | G | 1 | a0001c0001t0017g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.473-2024A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656766 | |||||||
| chr4:144656977 | C | A | 1 | a0001c0001t0002g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.473-1813C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656977 | |||||||
| chr4:144657001 | C | G | 1 | a0001c0001t0007g0066 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.473-1789C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144657001 | |||||||
| chr4:144657002 | G | T | 1 | a0001c0001t0028g0217 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.473-1788G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144657002 | |||||||
| chr4:144657389 | T | C | 1 | a0002c0002t0008g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.473-1401T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144657389 | |||||||
| chr4:144657515 | T | C | 78 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(75): Show |
80 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.473-1275T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144657515 | |||||||
| chr4:144657647 | C | T | 77 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(74): Show |
79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.473-1143C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144657647 | |||||||
| chr4:144657661 | A | G | 2 | a0001c0001t0002g0013 a0001c0001t0002g0284 |
3 | NA18947.hp1 NA18955.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.473-1129A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144657661 | |||||||
| chr4:144658261 | A | G | 2 | a0001c0001t0016g0085 a0001c0001t0021g0090 |
2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.473-529A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144658261 | |||||||
| chr4:144658351 | G | GTATT | 28 | a0001c0001t0002g0092 a0001c0001t0002g0288 a0001c0001t0002g0289 others(25): Show |
29 | HG00735.hp2 HG01192.hp1 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.473-409_473-406dup others(4): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 144658351 | ||||||
| chr4:144658351 | G | GTATTTAT others(1): Show |
5 | a0001c0001t0002g0233 a0001c0001t0002g0235 a0001c0001t0003g0163 others(2): Show |
5 | HG03516.hp2 NA18952.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.473-413_473-406dup others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 144658351 | ||||||
| chr4:144658351 | GTATT | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
99 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.473-409_473-406del others(4): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 144658351 | ||||||
| chr4:144658438 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
193 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.473-352T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144658438 | |||||||
| chr4:144658439 | G | C | 1 | a0001c0001t0015g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.473-351G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144658439 | |||||||
| chr4:144658462 | C | T | 1 | a0001c0001t0009g0225 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.473-328C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144658462 | |||||||
| chr4:144658514 | G | A | 4 | a0001c0001t0005g0114 a0001c0001t0010g0145 a0001c0001t0010g0146 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-276G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144658514 | |||||||
| chr4:144658755 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
203 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.473-35G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144658755 | |||||||
| chr4:144659020 | T | C | 11 | a0001c0001t0002g0023 a0001c0001t0003g0164 a0001c0001t0003g0174 others(8): Show |
11 | HG01074.hp1 HG01515.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.629+74T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 3/12 | chr4 | 144659020 | |||||||
| chr4:144659138 | C | A | 68 | a0001c0001t0002g0023 a0001c0001t0003g0007 a0001c0001t0003g0008 others(65): Show |
70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.629+192C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 3/12 | chr4 | 144659138 | |||||||
| chr4:144659216 | T | C | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.629+270T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 3/12 | chr4 | 144659216 | |||||||
| chr4:144659319 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.630-318G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 3/12 | chr4 | 144659319 | |||||||
| chr4:144659433 | A | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
203 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.630-204A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 3/12 | chr4 | 144659433 | |||||||
| chr4:144659487 | G | C | 4 | a0001c0001t0005g0114 a0001c0001t0010g0145 a0001c0001t0010g0146 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.630-150G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 3/12 | chr4 | 144659487 | |||||||
| chr4:144659535 | A | T | 1 | a0001c0001t0001g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.630-102A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 3/12 | chr4 | 144659535 | |||||||
| chr4:144659907 | A | G | 7 | a0001c0001t0003g0007 a0001c0001t0003g0163 a0001c0001t0003g0170 others(4): Show |
8 | HG02165.hp1 NA18957.hp2 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.831+69A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144659907 | |||||||
| chr4:144660033 | A | G | 7 | a0002c0002t0008g0134 a0002c0002t0008g0135 a0002c0002t0008g0136 others(4): Show |
7 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+195A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660033 | |||||||
| chr4:144660306 | C | A | 2 | a0001c0001t0009g0183 a0001c0001t0009g0225 |
2 | HG00099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.831+468C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660306 | |||||||
| chr4:144660403 | C | T | 3 | a0001c0001t0010g0228 a0001c0001t0010g0296 a0001c0001t0010g0297 |
3 | HG01243.hp1 HG01884.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.831+565C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660403 | |||||||
| chr4:144660444 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
203 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.831+606T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660444 | |||||||
| chr4:144660485 | C | T | 5 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
5 | HG01081.hp1 HG01358.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+647C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660485 | |||||||
| chr4:144660589 | A | C | 2 | a0001c0001t0016g0085 a0001c0001t0021g0090 |
2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.831+751A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660589 | |||||||
| chr4:144660679 | G | A | 1 | a0001c0001t0032g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.831+841G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660679 | |||||||
| chr4:144660748 | C | T | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+910C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660748 | |||||||
| chr4:144660761 | A | G | 7 | a0001c0001t0002g0086 a0001c0001t0016g0083 a0001c0001t0016g0085 others(4): Show |
7 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+923A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660761 | |||||||
| chr4:144660799 | T | C | 1 | a0001c0001t0032g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.831+961T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660799 | |||||||
| chr4:144660842 | A | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(80): Show |
89 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.831+1004A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660842 | |||||||
| chr4:144661384 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
203 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.831+1546A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144661384 | |||||||
| chr4:144661499 | C | T | 1 | a0001c0001t0021g0226 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.831+1661C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144661499 | |||||||
| chr4:144661583 | C | T | 5 | a0001c0001t0003g0164 a0001c0001t0003g0179 a0001c0001t0003g0181 others(2): Show |
5 | NA18944.hp2 NA18969.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1745C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144661583 | |||||||
| chr4:144661668 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
203 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.831+1830T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144661668 | |||||||
| chr4:144661837 | C | T | 1 | a0001c0001t0002g0283 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.831+1999C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144661837 | |||||||
| chr4:144661920 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.831+2082C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144661920 | |||||||
| chr4:144662114 | A | G | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+2276A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144662114 | |||||||
| chr4:144662689 | GTGTGTGT others(3): Show |
G | 8 | a0002c0002t0008g0133 a0002c0002t0008g0134 a0002c0002t0008g0135 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.831+2860_831+2869d others(12): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144662689 | ||||||
| chr4:144662710 | C | A | 9 | a0001c0001t0006g0074 a0001c0001t0006g0076 a0001c0001t0006g0077 others(6): Show |
9 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.831+2872C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144662710 | |||||||
| chr4:144662946 | T | G | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+3108T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144662946 | |||||||
| chr4:144663023 | T | G | 16 | a0001c0001t0002g0086 a0001c0001t0006g0074 a0001c0001t0006g0076 others(13): Show |
16 | HG00642.hp2 HG01074.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.831+3185T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144663023 | |||||||
| chr4:144663055 | T | G | 79 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(76): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.831+3217T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144663055 | |||||||
| chr4:144663512 | C | A | 1 | a0001c0001t0015g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.831+3674C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144663512 | |||||||
| chr4:144663557 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.831+3719C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144663557 | |||||||
| chr4:144663893 | G | T | 7 | a0001c0001t0002g0086 a0001c0001t0016g0083 a0001c0001t0016g0085 others(4): Show |
7 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+4055G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144663893 | |||||||
| chr4:144663960 | C | A | 1 | a0001c0006t0004g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.831+4122C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144663960 | |||||||
| chr4:144664179 | G | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.831+4341G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664179 | |||||||
| chr4:144664202 | A | T | 79 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(76): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.831+4364A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664202 | |||||||
| chr4:144664210 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.831+4372G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664210 | |||||||
| chr4:144664221 | G | A | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+4383G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664221 | |||||||
| chr4:144664300 | G | A | 2 | a0001c0001t0005g0114 a0004c0005t0005g0118 |
2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.831+4462G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664300 | |||||||
| chr4:144664369 | G | A | 79 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(76): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.831+4531G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664369 | |||||||
| chr4:144664531 | G | A | 1 | a0001c0001t0003g0185 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.831+4693G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664531 | |||||||
| chr4:144664645 | T | C | 10 | a0001c0001t0003g0007 a0001c0001t0003g0163 a0001c0001t0003g0166 others(7): Show |
11 | HG02165.hp1 HG04228.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+4807T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664645 | |||||||
| chr4:144664781 | A | G | 1 | a0001c0001t0015g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.831+4943A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664781 | |||||||
| chr4:144664791 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.831+4953C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664791 | |||||||
| chr4:144664883 | G | A | 2 | a0001c0001t0005g0073 a0001c0001t0017g0115 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.831+5045G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664883 | |||||||
| chr4:144664891 | T | C | 79 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(76): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.831+5053T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664891 | |||||||
| chr4:144665007 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | NA18950.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.831+5169G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665007 | |||||||
| chr4:144665307 | A | G | 100 | a0001c0001t0002g0086 a0001c0001t0003g0007 a0001c0001t0003g0008 others(97): Show |
102 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.831+5469A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665307 | |||||||
| chr4:144665400 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.831+5562A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665400 | |||||||
| chr4:144665701 | A | G | 7 | a0001c0001t0002g0086 a0001c0001t0016g0083 a0001c0001t0016g0085 others(4): Show |
7 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+5863A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665701 | |||||||
| chr4:144665748 | G | A | 79 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(76): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.831+5910G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665748 | |||||||
| chr4:144665761 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.831+5923C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665761 | |||||||
| chr4:144665788 | T | C | 3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 |
3 | HG01346.hp1 HG01496.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.831+5950T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665788 | |||||||
| chr4:144665830 | C | A | 1 | a0001c0001t0003g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.831+5992C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665830 | |||||||
| chr4:144665866 | C | T | 1 | a0001c0001t0050g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.831+6028C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665866 | |||||||
| chr4:144665963 | G | C | 1 | a0001c0001t0005g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.831+6125G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665963 | |||||||
| chr4:144666217 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.831+6379C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144666217 | |||||||
| chr4:144666248 | CGT | C | 11 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0004g0219 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.831+6456_831+6457d others(4): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144666248 | ||||||
| chr4:144666248 | CGTGT | C | 15 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0054 others(12): Show |
15 | HG02109.hp2 HG02451.hp1 HG03041.hp2 others(12): Show |
intron_variant | MODIFIER | c.831+6454_831+6457d others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144666248 | ||||||
| chr4:144666248 | CGTGTGT | C | 106 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0025 others(103): Show |
111 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.831+6452_831+6457d others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144666248 | ||||||
| chr4:144666248 | CGTGTGTG others(1): Show |
C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(66): Show |
72 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.831+6450_831+6457d others(10): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144666248 | ||||||
| chr4:144666248 | CGTGTGTG others(3): Show |
C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0120 a0001c0001t0001g0236 others(78): Show |
87 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.831+6448_831+6457d others(12): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144666248 | ||||||
| chr4:144666248 | CGTGTGTG others(5): Show |
C | 12 | a0001c0001t0001g0059 a0001c0001t0001g0143 a0001c0001t0006g0074 others(9): Show |
12 | HG01081.hp1 HG01496.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+6446_831+6457d others(14): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144666248 | ||||||
| chr4:144666248 | CGTGTGTG others(7): Show |
C | 3 | a0001c0001t0002g0233 a0001c0001t0002g0235 a0001c0001t0011g0234 |
3 | NA18952.hp2 NA18986.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.831+6444_831+6457d others(16): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144666248 | ||||||
| chr4:144666248 | CGTGTGTG others(9): Show |
C | 2 | a0001c0001t0010g0145 a0001c0001t0010g0146 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.831+6442_831+6457d others(18): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144666248 | ||||||
| chr4:144666294 | T | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0052 a0001c0001t0035g0027 |
3 | NA18940.hp2 NA19006.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.831+6456T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144666294 | |||||||
| chr4:144666549 | C | T | 2 | a0001c0001t0019g0161 a0001c0001t0019g0162 |
2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.831+6711C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144666549 | |||||||
| chr4:144666793 | A | C | 1 | a0001c0001t0015g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.831+6955A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144666793 | |||||||
| chr4:144666964 | A | T | 81 | a0001c0001t0002g0023 a0001c0001t0003g0007 a0001c0001t0003g0008 others(78): Show |
83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.831+7126A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144666964 | |||||||
| chr4:144667072 | G | T | 7 | a0001c0001t0002g0086 a0001c0001t0016g0083 a0001c0001t0016g0085 others(4): Show |
7 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+7234G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144667072 | |||||||
| chr4:144667484 | T | G | 1 | a0001c0001t0003g0152 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.831+7646T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144667484 | |||||||
| chr4:144667753 | T | A | 16 | a0001c0001t0002g0086 a0001c0001t0006g0074 a0001c0001t0006g0076 others(13): Show |
16 | HG00642.hp2 HG01074.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.831+7915T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144667753 | |||||||
| chr4:144667819 | A | G | 16 | a0001c0001t0002g0086 a0001c0001t0006g0074 a0001c0001t0006g0076 others(13): Show |
16 | HG00642.hp2 HG01074.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.831+7981A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144667819 | |||||||
| chr4:144667999 | A | AATT | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+8180_831+8182d others(5): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144667999 | ||||||
| chr4:144668080 | G | A | 5 | a0001c0001t0003g0151 a0001c0001t0003g0153 a0001c0001t0003g0155 others(2): Show |
5 | HG00280.hp2 HG00609.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+8242G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144668080 | |||||||
| chr4:144668195 | T | G | 6 | a0001c0001t0004g0219 a0001c0001t0004g0220 a0001c0001t0004g0221 others(3): Show |
6 | HG01243.hp2 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+8357T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144668195 | |||||||
| chr4:144668454 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.831+8616G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144668454 | |||||||
| chr4:144668692 | C | A | 74 | a0001c0001t0002g0023 a0001c0001t0003g0007 a0001c0001t0003g0008 others(71): Show |
76 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.831+8854C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144668692 | |||||||
| chr4:144668796 | C | T | 2 | a0001c0001t0002g0288 a0001c0001t0002g0291 |
2 | HG00735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.831+8958C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144668796 | |||||||
| chr4:144668853 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
202 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.831+9015C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144668853 | |||||||
| chr4:144668864 | T | C | 1 | a0001c0001t0004g0214 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.831+9026T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144668864 | |||||||
| chr4:144668904 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0034g0060 |
2 | HG01943.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.831+9066G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144668904 | |||||||
| chr4:144669022 | T | C | 2 | a0001c0001t0016g0085 a0001c0001t0021g0090 |
2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.831+9184T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669022 | |||||||
| chr4:144669279 | A | C | 3 | a0001c0001t0004g0214 a0001c0001t0004g0215 a0001c0001t0004g0216 |
3 | HG02630.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.831+9441A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669279 | |||||||
| chr4:144669293 | A | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(78): Show |
87 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.831+9455A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669293 | |||||||
| chr4:144669411 | G | A | 5 | a0001c0001t0001g0239 a0001c0001t0002g0009 a0001c0001t0002g0241 others(2): Show |
6 | NA18950.hp1 NA18953.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+9573G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669411 | |||||||
| chr4:144669414 | G | T | 3 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0009g0172 |
3 | NA18961.hp2 NA19068.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.831+9576G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669414 | |||||||
| chr4:144669576 | A | G | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+9738A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669576 | |||||||
| chr4:144669639 | A | C | 2 | a0001c0001t0005g0073 a0001c0001t0017g0115 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.831+9801A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669639 | |||||||
| chr4:144669710 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.831+9872C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669710 | |||||||
| chr4:144669781 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
192 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.831+9943A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669781 | |||||||
| chr4:144669805 | AG | A | 80 | a0001c0001t0002g0023 a0001c0001t0003g0007 a0001c0001t0003g0008 others(77): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.831+9968delG | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669805 | |||||||
| chr4:144669807 | T | A | 80 | a0001c0001t0002g0023 a0001c0001t0003g0007 a0001c0001t0003g0008 others(77): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.831+9969T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669807 | |||||||
| chr4:144669909 | A | G | 80 | a0001c0001t0002g0023 a0001c0001t0003g0007 a0001c0001t0003g0008 others(77): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.831+10071A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669909 | |||||||
| chr4:144669978 | T | TA | 172 | a0001c0001t0001g0028 a0001c0001t0001g0236 a0001c0001t0001g0237 others(169): Show |
178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.831+10156dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144669978 | ||||||
| chr4:144669989 | A | G | 1 | a0001c0001t0002g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.831+10151A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669989 | |||||||
| chr4:144670059 | G | A | 80 | a0001c0001t0002g0023 a0001c0001t0003g0007 a0001c0001t0003g0008 others(77): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.831+10221G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670059 | |||||||
| chr4:144670106 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(78): Show |
87 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.831+10268A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670106 | |||||||
| chr4:144670142 | C | CA | 81 | a0001c0001t0002g0023 a0001c0001t0003g0007 a0001c0001t0003g0008 others(78): Show |
83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.831+10315dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144670142 | ||||||
| chr4:144670157 | GAATTGGT others(10): Show |
G | 8 | a0002c0002t0008g0133 a0002c0002t0008g0134 a0002c0002t0008g0135 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.831+10337_831+1035 others(21): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144670157 | ||||||
| chr4:144670169 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.831+10331C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670169 | |||||||
| chr4:144670274 | C | A | 83 | a0001c0001t0002g0023 a0001c0001t0003g0007 a0001c0001t0003g0008 others(80): Show |
85 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.831+10436C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670274 | |||||||
| chr4:144670289 | C | T | 3 | a0001c0001t0003g0209 a0001c0001t0012g0210 a0001c0001t0012g0211 |
3 | NA18947.hp2 NA19010.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.831+10451C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670289 | |||||||
| chr4:144670455 | C | CA | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
108 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.831+10633dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144670455 | ||||||
| chr4:144670455 | C | CAA | 83 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0023 others(80): Show |
85 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.831+10632_831+1063 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144670455 | ||||||
| chr4:144670543 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.831+10705C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670543 | |||||||
| chr4:144670635 | G | C | 1 | a0001c0001t0006g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.831+10797G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670635 | |||||||
| chr4:144670707 | G | GA | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
81 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.831+10883dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144670707 | ||||||
| chr4:144670718 | A | C | 5 | a0001c0001t0002g0266 a0001c0001t0006g0074 a0001c0001t0006g0078 others(2): Show |
5 | HG01496.hp2 HG02622.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+10880A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670718 | |||||||
| chr4:144670722 | C | A | 1 | a0001c0001t0002g0084 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.831+10884C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670722 | |||||||
| chr4:144670764 | GA | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(36): Show |
42 | HG00099.hp1 HG00597.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.831+10950delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144670764 | ||||||
| chr4:144670764 | GAA | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(61): Show |
68 | HG00423.hp1 HG00621.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.831+10949_831+1095 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144670764 | ||||||
| chr4:144670764 | GAAA | G | 84 | a0001c0001t0001g0021 a0001c0001t0002g0023 a0001c0001t0003g0007 others(81): Show |
86 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.831+10948_831+1095 others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144670764 | ||||||
| chr4:144670768 | A | G | 1 | a0001c0001t0010g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.831+10930A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670768 | |||||||
| chr4:144670769 | A | G | 1 | a0001c0001t0010g0145 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.831+10931A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670769 | |||||||
| chr4:144670785 | A | G | 7 | a0001c0001t0001g0282 a0001c0001t0002g0232 a0001c0001t0002g0264 others(4): Show |
7 | HG02145.hp2 HG03209.hp1 NA19043.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+10947A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670785 | |||||||
| chr4:144671207 | T | C | 4 | a0001c0001t0002g0023 a0001c0001t0004g0176 a0001c0001t0004g0177 others(1): Show |
4 | HG01515.hp1 HG01934.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+11369T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144671207 | |||||||
| chr4:144671226 | A | G | 1 | a0004c0005t0005g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.831+11388A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144671226 | |||||||
| chr4:144671318 | GT | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
193 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.831+11494delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144671318 | ||||||
| chr4:144671534 | G | A | 6 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(3): Show |
6 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+11696G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144671534 | |||||||
| chr4:144671703 | T | G | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+11865T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144671703 | |||||||
| chr4:144671780 | C | T | 1 | a0001c0006t0004g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.831+11942C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144671780 | |||||||
| chr4:144671809 | C | G | 8 | a0002c0002t0008g0133 a0002c0002t0008g0134 a0002c0002t0008g0135 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.831+11971C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144671809 | |||||||
| chr4:144671876 | T | C | 81 | a0001c0001t0002g0023 a0001c0001t0003g0007 a0001c0001t0003g0008 others(78): Show |
83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.831+12038T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144671876 | |||||||
| chr4:144671930 | G | T | 6 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(3): Show |
6 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+12092G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144671930 | |||||||
| chr4:144672119 | T | C | 2 | a0001c0001t0004g0193 a0001c0001t0004g0222 |
2 | HG02071.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.831+12281T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672119 | |||||||
| chr4:144672522 | G | C | 80 | a0001c0001t0002g0023 a0001c0001t0003g0007 a0001c0001t0003g0008 others(77): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.831+12684G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672522 | |||||||
| chr4:144672549 | G | C | 6 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(3): Show |
6 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+12711G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672549 | |||||||
| chr4:144672688 | AT | A | 6 | a0001c0001t0004g0219 a0001c0001t0004g0220 a0001c0001t0004g0221 others(3): Show |
6 | HG01243.hp2 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+12857delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144672688 | ||||||
| chr4:144672697 | A | T | 1 | a0001c0001t0001g0034 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.831+12859A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672697 | |||||||
| chr4:144672728 | G | A | 1 | a0001c0001t0005g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.831+12890G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672728 | |||||||
| chr4:144672747 | G | C | 1 | a0001c0001t0001g0034 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.831+12909G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672747 | |||||||
| chr4:144672748 | C | G | 1 | a0001c0001t0001g0034 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.831+12910C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672748 | |||||||
| chr4:144672750 | G | A | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+12912G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672750 | |||||||
| chr4:144672801 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
81 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.831+12963A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672801 | |||||||
| chr4:144672836 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0002g0243 |
2 | NA18944.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.831+12998G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672836 | |||||||
| chr4:144672851 | G | T | 1 | a0001c0001t0001g0048 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.831+13013G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672851 | |||||||
| chr4:144673082 | T | C | 1 | a0001c0001t0002g0294 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.831+13244T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144673082 | |||||||
| chr4:144673335 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.831+13497A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144673335 | |||||||
| chr4:144673448 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.831+13610C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144673448 | |||||||
| chr4:144673661 | T | G | 1 | a0001c0001t0001g0034 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.831+13823T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144673661 | |||||||
| chr4:144674028 | T | C | 1 | a0001c0001t0002g0084 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.831+14190T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144674028 | |||||||
| chr4:144674130 | T | C | 1 | a0001c0001t0005g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.831+14292T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144674130 | |||||||
| chr4:144674292 | T | G | 1 | a0001c0001t0003g0191 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.831+14454T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144674292 | |||||||
| chr4:144674312 | G | A | 1 | a0001c0001t0003g0151 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.831+14474G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144674312 | |||||||
| chr4:144674608 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(77): Show |
86 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.831+14770C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144674608 | |||||||
| chr4:144674873 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0120 a0001c0001t0015g0072 |
5 | HG02257.hp2 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+15035G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144674873 | |||||||
| chr4:144675041 | C | T | 7 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(4): Show |
7 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+15203C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144675041 | |||||||
| chr4:144675253 | C | T | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+15415C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144675253 | |||||||
| chr4:144675351 | A | G | 13 | a0001c0001t0005g0073 a0001c0001t0006g0074 a0001c0001t0006g0076 others(10): Show |
13 | HG01496.hp2 HG02145.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.831+15513A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144675351 | |||||||
| chr4:144675541 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.831+15703G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144675541 | |||||||
| chr4:144675681 | T | C | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+15843T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144675681 | |||||||
| chr4:144675733 | A | C | 4 | a0001c0001t0003g0191 a0001c0001t0003g0208 a0001c0001t0004g0223 others(1): Show |
4 | HG00323.hp2 HG00642.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+15895A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144675733 | |||||||
| chr4:144675910 | A | G | 1 | a0001c0001t0002g0261 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.831+16072A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144675910 | |||||||
| chr4:144675923 | G | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
85 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.831+16085G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144675923 | |||||||
| chr4:144676221 | T | C | 1 | a0001c0001t0005g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.831+16383T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144676221 | |||||||
| chr4:144676395 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.831+16557A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144676395 | |||||||
| chr4:144676607 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
201 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.831+16769A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144676607 | |||||||
| chr4:144676679 | C | T | 2 | a0001c0001t0003g0166 a0001c0001t0003g0167 |
2 | NA18939.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.831+16841C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144676679 | |||||||
| chr4:144676945 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.831+17107T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144676945 | |||||||
| chr4:144677163 | C | T | 91 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(88): Show |
97 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.831+17325C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144677163 | |||||||
| chr4:144677316 | C | G | 1 | a0001c0001t0032g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.831+17478C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144677316 | |||||||
| chr4:144677333 | C | T | 10 | a0001c0001t0005g0073 a0001c0001t0006g0074 a0001c0001t0006g0076 others(7): Show |
10 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.831+17495C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144677333 | |||||||
| chr4:144677382 | TGTA | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0048 |
3 | NA18962.hp1 NA18994.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.831+17546_831+1754 others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144677382 | ||||||
| chr4:144677397 | C | G | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+17559C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144677397 | |||||||
| chr4:144677774 | C | T | 6 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(3): Show |
6 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+17936C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144677774 | |||||||
| chr4:144677972 | C | T | 2 | a0003c0004t0004g0206 a0003c0004t0004g0207 |
2 | NA18948.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.831+18134C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144677972 | |||||||
| chr4:144677977 | G | A | 1 | a0001c0001t0003g0170 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.831+18139G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144677977 | |||||||
| chr4:144678382 | G | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
201 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.831+18544G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144678382 | |||||||
| chr4:144678429 | A | T | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+18591A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144678429 | |||||||
| chr4:144678539 | C | G | 2 | a0001c0001t0002g0260 a0001c0001t0011g0259 |
2 | HG00673.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.831+18701C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144678539 | |||||||
| chr4:144678756 | G | A | 78 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(75): Show |
80 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.831+18918G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144678756 | |||||||
| chr4:144678928 | G | A | 4 | a0001c0001t0003g0191 a0001c0001t0003g0208 a0001c0001t0004g0223 others(1): Show |
4 | HG00323.hp2 HG00642.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+19090G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144678928 | |||||||
| chr4:144678928 | G | C | 4 | a0001c0001t0016g0085 a0001c0001t0020g0087 a0001c0001t0020g0088 others(1): Show |
4 | HG01074.hp2 HG02735.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+19090G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144678928 | |||||||
| chr4:144678976 | A | G | 7 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(4): Show |
7 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+19138A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144678976 | |||||||
| chr4:144679140 | G | GT | 9 | a0001c0001t0006g0074 a0001c0001t0006g0076 a0001c0001t0006g0077 others(6): Show |
9 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.831+19312dupT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144679140 | ||||||
| chr4:144679223 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
85 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.831+19385G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144679223 | |||||||
| chr4:144679618 | A | G | 5 | a0001c0001t0004g0214 a0001c0001t0004g0215 a0001c0001t0004g0216 others(2): Show |
5 | HG02615.hp1 HG02630.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+19780A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144679618 | |||||||
| chr4:144679623 | T | C | 5 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
5 | HG01081.hp1 HG01358.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+19785T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144679623 | |||||||
| chr4:144679658 | G | A | 1 | a0001c0001t0003g0194 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.831+19820G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144679658 | |||||||
| chr4:144680013 | G | T | 1 | a0001c0001t0003g0156 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.831+20175G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680013 | |||||||
| chr4:144680040 | T | A | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+20202T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680040 | |||||||
| chr4:144680247 | AC | A | 11 | a0001c0001t0005g0012 a0001c0001t0005g0271 a0001c0001t0005g0272 others(8): Show |
12 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.831+20410delC | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680247 | |||||||
| chr4:144680279 | T | C | 1 | a0001c0001t0002g0291 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.831+20441T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680279 | |||||||
| chr4:144680289 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.831+20451A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680289 | |||||||
| chr4:144680468 | A | T | 1 | a0001c0001t0001g0033 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.831+20630A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680468 | |||||||
| chr4:144680656 | G | T | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+20818G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680656 | |||||||
| chr4:144680711 | A | G | 69 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(66): Show |
71 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.831+20873A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680711 | |||||||
| chr4:144680820 | G | A | 1 | a0001c0001t0006g0081 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.831+20982G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680820 | |||||||
| chr4:144680972 | C | A | 14 | a0001c0001t0006g0074 a0001c0001t0006g0076 a0001c0001t0006g0077 others(11): Show |
14 | HG00642.hp2 HG01074.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.831+21134C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680972 | |||||||
| chr4:144681110 | T | C | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+21272T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681110 | |||||||
| chr4:144681237 | T | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.831+21399T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681237 | |||||||
| chr4:144681345 | T | C | 10 | a0001c0001t0002g0086 a0001c0001t0002g0092 a0001c0001t0002g0288 others(7): Show |
10 | HG00735.hp2 HG01106.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.831+21507T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681345 | |||||||
| chr4:144681421 | CT | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
112 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.831+21605delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144681421 | ||||||
| chr4:144681421 | CTT | C | 79 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(76): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.831+21604_831+2160 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144681421 | ||||||
| chr4:144681517 | C | T | 1 | a0002c0002t0052g0139 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.831+21679C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681517 | |||||||
| chr4:144681545 | C | T | 4 | a0001c0001t0005g0131 a0001c0001t0015g0119 a0001c0001t0015g0144 others(1): Show |
4 | HG02451.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+21707C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681545 | |||||||
| chr4:144681616 | G | T | 14 | a0001c0001t0006g0074 a0001c0001t0006g0076 a0001c0001t0006g0077 others(11): Show |
14 | HG00642.hp2 HG01074.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.831+21778G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681616 | |||||||
| chr4:144681624 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.831+21786C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681624 | |||||||
| chr4:144681669 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0056 |
2 | NA18979.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.831+21831C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681669 | |||||||
| chr4:144681675 | G | A | 66 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(63): Show |
68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.831+21837G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681675 | |||||||
| chr4:144681711 | C | T | 1 | a0001c0001t0051g0110 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.831+21873C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681711 | |||||||
| chr4:144681946 | T | C | 1 | a0001c0001t0014g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.831+22108T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681946 | |||||||
| chr4:144682216 | C | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.831+22378C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144682216 | |||||||
| chr4:144682303 | C | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG00673.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.831+22465C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144682303 | |||||||
| chr4:144682549 | AAG | A | 8 | a0002c0002t0008g0133 a0002c0002t0008g0134 a0002c0002t0008g0135 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.831+22723_831+2272 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144682549 | ||||||
| chr4:144682577 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0120 a0001c0001t0015g0072 |
5 | HG02257.hp2 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+22739C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144682577 | |||||||
| chr4:144682751 | C | A | 1 | a0001c0001t0015g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.831+22913C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144682751 | |||||||
| chr4:144683239 | A | T | 1 | a0001c0001t0002g0084 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.832-23292A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683239 | |||||||
| chr4:144683442 | C | T | 1 | a0001c0001t0002g0242 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.832-23089C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683442 | |||||||
| chr4:144683639 | C | T | 1 | a0001c0001t0002g0262 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.832-22892C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683639 | |||||||
| chr4:144683683 | T | C | 1 | a0001c0001t0002g0268 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.832-22848T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683683 | |||||||
| chr4:144683701 | G | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
201 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.832-22830G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683701 | |||||||
| chr4:144683839 | A | G | 2 | a0001c0001t0003g0192 a0001c0001t0003g0205 |
2 | HG01978.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.832-22692A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683839 | |||||||
| chr4:144683873 | A | G | 9 | a0001c0001t0002g0092 a0001c0001t0002g0288 a0001c0001t0002g0289 others(6): Show |
9 | HG00735.hp2 HG01106.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.832-22658A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683873 | |||||||
| chr4:144683881 | T | C | 67 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(64): Show |
69 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.832-22650T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683881 | |||||||
| chr4:144683923 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
201 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.832-22608T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683923 | |||||||
| chr4:144683937 | T | C | 1 | a0001c0001t0003g0196 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.832-22594T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683937 | |||||||
| chr4:144684061 | T | TA | 67 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(64): Show |
69 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.832-22460dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684061 | ||||||
| chr4:144684121 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
201 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.832-22410T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684121 | |||||||
| chr4:144684227 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.832-22304A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684227 | |||||||
| chr4:144684232 | A | ATT | 14 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0112 others(11): Show |
14 | HG00741.hp1 HG02071.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.832-22256_832-2225 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | A | ATTT | 11 | a0001c0001t0002g0006 a0001c0001t0002g0111 a0001c0001t0002g0227 others(8): Show |
11 | HG00597.hp2 HG00621.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.832-22257_832-2225 others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | NA18946.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.832-22266_832-2225 others(16): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | AT | A | 27 | a0001c0001t0001g0244 a0001c0001t0002g0010 a0001c0001t0002g0011 others(24): Show |
31 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.832-22255delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATT | A | 22 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0246 others(19): Show |
22 | HG01106.hp1 HG01168.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.832-22256_832-2225 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTT | A | 8 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0245 others(5): Show |
8 | HG01943.hp1 HG02056.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.832-22257_832-2225 others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTTTT | A | 6 | a0001c0001t0006g0074 a0001c0001t0006g0077 a0001c0001t0006g0080 others(3): Show |
6 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-22259_832-2225 others(9): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTTTTT | A | 6 | a0001c0001t0005g0131 a0001c0001t0006g0076 a0001c0001t0006g0078 others(3): Show |
6 | HG02145.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-22260_832-2225 others(10): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.832-22265_832-2225 others(15): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0051 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.832-22266_832-2225 others(16): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTTTTTT others(6): Show |
A | 26 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0033 others(23): Show |
26 | HG00621.hp1 HG01261.hp2 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.832-22267_832-2225 others(17): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTTTTTT others(7): Show |
A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
44 | HG00597.hp1 HG00673.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.832-22268_832-2225 others(18): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTTTTTT others(8): Show |
A | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(34): Show |
40 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.832-22269_832-2225 others(19): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTTTTTT others(9): Show |
A | 37 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(34): Show |
39 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.832-22270_832-2225 others(20): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTTTTTT others(10): Show |
A | 10 | a0001c0001t0003g0164 a0001c0001t0003g0187 a0001c0001t0005g0114 others(7): Show |
10 | HG00642.hp2 HG01192.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.832-22271_832-2225 others(21): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTTTTTT others(11): Show |
A | 12 | a0001c0001t0004g0220 a0001c0001t0004g0221 a0001c0001t0016g0083 others(9): Show |
12 | HG01074.hp2 HG01243.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-22272_832-2225 others(22): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTTTTTT others(12): Show |
A | 2 | a0001c0001t0032g0142 a0002c0002t0008g0134 |
2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.832-22273_832-2225 others(23): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTTTTTT others(13): Show |
A | 3 | a0001c0001t0001g0117 a0001c0001t0002g0235 a0001c0006t0004g0213 |
3 | HG01884.hp2 NA18989.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.832-22274_832-2225 others(24): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTTTTTT others(14): Show |
A | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.832-22275_832-2225 others(25): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTTTTTT others(15): Show |
A | 2 | a0001c0001t0002g0233 a0001c0001t0005g0073 |
2 | HG02717.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.832-22276_832-2225 others(26): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTTTTTT others(18): Show |
A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0048 a0001c0001t0001g0052 others(1): Show |
4 | NA18940.hp2 NA18962.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-22279_832-2225 others(29): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684232 | ATTTTTTT others(22): Show |
A | 1 | a0001c0003t0002g0113 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.832-22283_832-2225 others(33): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | ||||||
| chr4:144684303 | G | T | 1 | a0001c0001t0002g0242 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.832-22228G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684303 | |||||||
| chr4:144684320 | G | A | 11 | a0001c0001t0005g0114 a0001c0001t0019g0161 a0001c0001t0019g0162 others(8): Show |
11 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.832-22211G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684320 | |||||||
| chr4:144684419 | C | T | 1 | a0001c0001t0007g0046 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.832-22112C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684419 | |||||||
| chr4:144684568 | C | T | 6 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(3): Show |
6 | HG00642.hp2 HG01074.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-21963C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684568 | |||||||
| chr4:144684647 | C | G | 1 | a0001c0001t0017g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.832-21884C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684647 | |||||||
| chr4:144684869 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
201 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.832-21662C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684869 | |||||||
| chr4:144684895 | A | C | 1 | a0001c0003t0002g0292 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.832-21636A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684895 | |||||||
| chr4:144685157 | A | C | 6 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(3): Show |
6 | HG00642.hp2 HG01074.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-21374A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144685157 | |||||||
| chr4:144685209 | G | A | 2 | a0001c0001t0006g0076 a0001c0001t0006g0081 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.832-21322G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144685209 | |||||||
| chr4:144685300 | T | A | 1 | a0001c0001t0002g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.832-21231T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144685300 | |||||||
| chr4:144685432 | G | A | 2 | a0001c0001t0019g0161 a0001c0001t0019g0162 |
2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.832-21099G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144685432 | |||||||
| chr4:144685768 | C | A | 2 | a0001c0001t0001g0282 a0001c0001t0002g0264 |
2 | NA19062.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.832-20763C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144685768 | |||||||
| chr4:144686351 | C | T | 3 | a0001c0001t0002g0229 a0001c0001t0002g0231 a0001c0001t0030g0230 |
3 | NA18942.hp1 NA18962.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.832-20180C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144686351 | |||||||
| chr4:144686542 | A | G | 1 | a0001c0006t0004g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.832-19989A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144686542 | |||||||
| chr4:144686694 | C | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
199 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.832-19837C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144686694 | |||||||
| chr4:144686730 | C | G | 1 | a0001c0001t0003g0171 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.832-19801C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144686730 | |||||||
| chr4:144686750 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
183 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.832-19781G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144686750 | |||||||
| chr4:144687713 | T | A | 3 | a0001c0001t0005g0131 a0001c0001t0015g0119 a0001c0001t0015g0144 |
3 | HG02451.hp1 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.832-18818T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144687713 | |||||||
| chr4:144687751 | C | CT | 23 | a0001c0001t0001g0239 a0001c0001t0002g0011 a0001c0001t0002g0084 others(20): Show |
24 | HG00597.hp2 HG00673.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.832-18752dupT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144687751 | ||||||
| chr4:144687751 | CT | C | 23 | a0001c0001t0001g0037 a0001c0001t0001g0068 a0001c0001t0001g0121 others(20): Show |
23 | HG00642.hp1 HG00642.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.832-18752delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144687751 | ||||||
| chr4:144687751 | CTT | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(140): Show |
151 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.832-18753_832-1875 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144687751 | ||||||
| chr4:144687751 | CTTT | C | 17 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0039 others(14): Show |
17 | HG01192.hp1 HG01884.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.832-18754_832-1875 others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144687751 | ||||||
| chr4:144687848 | C | T | 1 | a0001c0001t0003g0167 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.832-18683C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144687848 | |||||||
| chr4:144687921 | C | T | 2 | a0001c0001t0005g0073 a0004c0005t0005g0118 |
2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.832-18610C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144687921 | |||||||
| chr4:144688107 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0120 a0001c0001t0015g0072 |
5 | HG02257.hp2 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-18424A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144688107 | |||||||
| chr4:144688367 | G | A | 2 | a0001c0001t0005g0073 a0004c0005t0005g0118 |
2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.832-18164G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144688367 | |||||||
| chr4:144688775 | AGAACGGA others(22): Show |
A | 14 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(11): Show |
14 | HG01261.hp2 HG02055.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.832-17755_832-1772 others(33): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144688775 | |||||||
| chr4:144688871 | G | T | 2 | a0001c0001t0005g0073 a0004c0005t0005g0118 |
2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.832-17660G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144688871 | |||||||
| chr4:144688894 | T | C | 3 | a0001c0001t0004g0214 a0001c0001t0004g0215 a0001c0001t0004g0216 |
3 | HG02630.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.832-17637T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144688894 | |||||||
| chr4:144688907 | A | C | 6 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(3): Show |
6 | HG00642.hp2 HG01074.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-17624A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144688907 | |||||||
| chr4:144688985 | A | G | 1 | a0001c0001t0003g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.832-17546A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144688985 | |||||||
| chr4:144689060 | T | C | 8 | a0002c0002t0008g0133 a0002c0002t0008g0134 a0002c0002t0008g0135 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.832-17471T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144689060 | |||||||
| chr4:144689255 | T | C | 1 | a0001c0001t0002g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.832-17276T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144689255 | |||||||
| chr4:144689407 | G | T | 1 | a0001c0001t0003g0194 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.832-17124G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144689407 | |||||||
| chr4:144689427 | G | C | 1 | a0001c0001t0013g0285 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.832-17104G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144689427 | |||||||
| chr4:144689590 | A | C | 1 | a0001c0001t0005g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.832-16941A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144689590 | |||||||
| chr4:144689695 | T | C | 12 | a0001c0001t0005g0073 a0001c0001t0006g0074 a0001c0001t0006g0076 others(9): Show |
12 | HG01496.hp2 HG01891.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-16836T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144689695 | |||||||
| chr4:144689874 | T | C | 8 | a0002c0002t0008g0133 a0002c0002t0008g0134 a0002c0002t0008g0135 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.832-16657T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144689874 | |||||||
| chr4:144689982 | T | C | 2 | a0001c0001t0003g0152 a0001c0001t0009g0158 |
2 | HG00408.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.832-16549T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144689982 | |||||||
| chr4:144690144 | A | C | 2 | a0001c0001t0012g0210 a0001c0001t0012g0211 |
2 | NA18947.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.832-16387A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144690144 | |||||||
| chr4:144690315 | G | T | 8 | a0001c0001t0006g0074 a0001c0001t0006g0076 a0001c0001t0006g0077 others(5): Show |
8 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.832-16216G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144690315 | |||||||
| chr4:144690394 | T | C | 1 | a0001c0001t0002g0258 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.832-16137T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144690394 | |||||||
| chr4:144690616 | A | G | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832-15915A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144690616 | |||||||
| chr4:144690784 | CTA | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
166 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.832-15745_832-1574 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144690784 | ||||||
| chr4:144690925 | A | G | 3 | a0001c0001t0005g0073 a0001c0001t0005g0131 a0004c0005t0005g0118 |
3 | HG02451.hp1 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.832-15606A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144690925 | |||||||
| chr4:144690967 | A | C | 13 | a0001c0001t0005g0073 a0001c0001t0005g0131 a0001c0001t0006g0074 others(10): Show |
13 | HG01496.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-15564A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144690967 | |||||||
| chr4:144690968 | G | T | 13 | a0001c0001t0005g0073 a0001c0001t0005g0131 a0001c0001t0006g0074 others(10): Show |
13 | HG01496.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-15563G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144690968 | |||||||
| chr4:144691007 | G | A | 3 | a0001c0001t0005g0114 a0001c0001t0019g0161 a0001c0001t0019g0162 |
3 | HG01243.hp2 HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.832-15524G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691007 | |||||||
| chr4:144691057 | T | A | 2 | a0001c0001t0015g0119 a0001c0001t0015g0144 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.832-15474T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691057 | |||||||
| chr4:144691160 | C | T | 16 | a0001c0001t0005g0073 a0001c0001t0005g0131 a0001c0001t0006g0074 others(13): Show |
16 | HG01496.hp2 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.832-15371C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691160 | |||||||
| chr4:144691178 | A | C | 13 | a0001c0001t0005g0073 a0001c0001t0005g0131 a0001c0001t0006g0074 others(10): Show |
13 | HG01496.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-15353A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691178 | |||||||
| chr4:144691192 | A | T | 2 | a0001c0001t0003g0185 a0001c0001t0003g0204 |
2 | HG01168.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.832-15339A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691192 | |||||||
| chr4:144691399 | C | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.832-15132C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691399 | |||||||
| chr4:144691400 | A | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.832-15131A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691400 | |||||||
| chr4:144691465 | T | C | 1 | a0001c0001t0045g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.832-15066T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691465 | |||||||
| chr4:144691593 | G | C | 1 | a0001c0001t0002g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.832-14938G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691593 | |||||||
| chr4:144691633 | A | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0120 a0001c0001t0015g0072 |
5 | HG02257.hp2 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-14898A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691633 | |||||||
| chr4:144691790 | C | T | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832-14741C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691790 | |||||||
| chr4:144691838 | G | T | 1 | a0001c0001t0004g0223 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.832-14693G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691838 | |||||||
| chr4:144691896 | GA | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(68): Show |
75 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.832-14625delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144691896 | ||||||
| chr4:144691906 | AT | A | 4 | a0001c0001t0001g0054 a0001c0001t0005g0114 a0001c0001t0019g0161 others(1): Show |
4 | HG01243.hp2 HG02109.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-14621delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144691906 | ||||||
| chr4:144692028 | A | G | 3 | a0001c0001t0005g0114 a0001c0001t0019g0161 a0001c0001t0019g0162 |
3 | HG01243.hp2 HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.832-14503A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692028 | |||||||
| chr4:144692098 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.832-14433C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692098 | |||||||
| chr4:144692270 | T | C | 6 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(3): Show |
6 | HG00642.hp2 HG01074.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-14261T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692270 | |||||||
| chr4:144692309 | C | T | 1 | a0002c0002t0008g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.832-14222C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692309 | |||||||
| chr4:144692399 | A | G | 65 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(62): Show |
67 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.832-14132A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692399 | |||||||
| chr4:144692568 | C | T | 2 | a0001c0001t0009g0183 a0001c0001t0009g0225 |
2 | HG00099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.832-13963C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692568 | |||||||
| chr4:144692607 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.832-13924G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692607 | |||||||
| chr4:144692655 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.832-13876G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692655 | |||||||
| chr4:144692750 | G | C | 5 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(2): Show |
5 | HG00642.hp2 HG01074.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.832-13781G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692750 | |||||||
| chr4:144692805 | C | A | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832-13726C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692805 | |||||||
| chr4:144692891 | A | AGAG | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
200 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.832-13636_832-1363 others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144692891 | ||||||
| chr4:144692949 | C | A | 1 | a0001c0001t0004g0222 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.832-13582C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692949 | |||||||
| chr4:144693183 | T | C | 2 | a0001c0001t0015g0119 a0001c0001t0015g0144 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.832-13348T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144693183 | |||||||
| chr4:144693240 | T | A | 1 | a0001c0001t0002g0013 | 2 | NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.832-13291T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144693240 | |||||||
| chr4:144693472 | C | T | 1 | a0001c0001t0016g0089 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.832-13059C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144693472 | |||||||
| chr4:144693549 | A | C | 1 | a0001c0001t0005g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.832-12982A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144693549 | |||||||
| chr4:144693738 | G | A | 1 | a0001c0001t0002g0261 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.832-12793G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144693738 | |||||||
| chr4:144693832 | G | A | 57 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(54): Show |
59 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.832-12699G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144693832 | |||||||
| chr4:144693863 | G | A | 1 | a0001c0001t0005g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.832-12668G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144693863 | |||||||
| chr4:144693884 | A | G | 1 | a0001c0001t0012g0210 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.832-12647A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144693884 | |||||||
| chr4:144694221 | A | G | 7 | a0002c0002t0008g0133 a0002c0002t0008g0134 a0002c0002t0008g0135 others(4): Show |
7 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-12310A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144694221 | |||||||
| chr4:144694246 | T | G | 1 | a0001c0001t0001g0032 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.832-12285T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144694246 | |||||||
| chr4:144694273 | T | C | 4 | a0001c0001t0002g0009 a0001c0001t0002g0241 a0001c0001t0002g0267 others(1): Show |
5 | NA18950.hp1 NA18953.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.832-12258T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144694273 | |||||||
| chr4:144694334 | G | GT | 10 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0003g0205 others(7): Show |
10 | HG01192.hp1 HG01978.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.832-12187dupT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144694334 | ||||||
| chr4:144694434 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(71): Show |
78 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.832-12097T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144694434 | |||||||
| chr4:144694518 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0120 |
4 | HG02257.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-12013A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144694518 | |||||||
| chr4:144694953 | G | A | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832-11578G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144694953 | |||||||
| chr4:144695126 | ACAAG | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0120 a0001c0001t0015g0072 |
5 | HG02257.hp2 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-11404_832-1140 others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144695126 | |||||||
| chr4:144695301 | C | T | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832-11230C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144695301 | |||||||
| chr4:144695590 | T | G | 1 | a0001c0001t0001g0125 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.832-10941T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144695590 | |||||||
| chr4:144695625 | C | T | 3 | a0001c0001t0010g0228 a0001c0001t0010g0296 a0001c0001t0010g0297 |
3 | HG01243.hp1 HG01884.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.832-10906C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144695625 | |||||||
| chr4:144695803 | C | T | 6 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(3): Show |
6 | HG00642.hp2 HG01074.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-10728C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144695803 | |||||||
| chr4:144696029 | TACTTGAG others(27): Show |
T | 3 | a0001c0001t0005g0114 a0001c0001t0019g0161 a0001c0001t0019g0162 |
3 | HG01243.hp2 HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.832-10500_832-1046 others(38): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144696029 | ||||||
| chr4:144696258 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.832-10273T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144696258 | |||||||
| chr4:144696266 | T | G | 1 | a0001c0001t0041g0057 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.832-10265T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144696266 | |||||||
| chr4:144696275 | C | CT | 25 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(22): Show |
25 | HG01192.hp1 HG01261.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.832-10246dupT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144696275 | ||||||
| chr4:144696549 | G | A | 1 | a0001c0001t0002g0293 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.832-9982G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144696549 | |||||||
| chr4:144696596 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
200 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.832-9935G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144696596 | |||||||
| chr4:144696607 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.832-9924A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144696607 | |||||||
| chr4:144696794 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
195 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.832-9737C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144696794 | |||||||
| chr4:144697414 | T | A | 2 | a0001c0001t0003g0168 a0001c0001t0003g0169 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.832-9117T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144697414 | |||||||
| chr4:144697456 | C | T | 2 | a0001c0001t0002g0279 a0002c0002t0052g0139 |
2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.832-9075C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144697456 | |||||||
| chr4:144697567 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
171 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.832-8964T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144697567 | |||||||
| chr4:144697795 | G | A | 1 | a0001c0001t0045g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.832-8736G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144697795 | |||||||
| chr4:144697991 | G | T | 2 | a0001c0001t0019g0161 a0001c0001t0019g0162 |
2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.832-8540G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144697991 | |||||||
| chr4:144698044 | G | T | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.832-8487G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698044 | |||||||
| chr4:144698094 | C | T | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832-8437C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698094 | |||||||
| chr4:144698181 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.832-8350C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698181 | |||||||
| chr4:144698261 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.832-8270T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698261 | |||||||
| chr4:144698288 | T | A | 1 | a0001c0006t0004g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.832-8243T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698288 | |||||||
| chr4:144698501 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.832-8030G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698501 | |||||||
| chr4:144698589 | A | G | 1 | a0002c0002t0052g0139 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.832-7942A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698589 | |||||||
| chr4:144698812 | T | C | 13 | a0001c0001t0005g0073 a0001c0001t0005g0131 a0001c0001t0006g0074 others(10): Show |
13 | HG01496.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-7719T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698812 | |||||||
| chr4:144698888 | A | C | 1 | a0001c0001t0011g0045 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.832-7643A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698888 | |||||||
| chr4:144699141 | T | C | 1 | a0001c0001t0011g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.832-7390T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144699141 | |||||||
| chr4:144699156 | C | A | 2 | a0001c0001t0002g0232 a0001c0001t0002g0265 |
2 | NA19078.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.832-7375C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144699156 | |||||||
| chr4:144699260 | T | C | 1 | a0001c0001t0002g0258 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.832-7271T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144699260 | |||||||
| chr4:144699304 | T | C | 1 | a0001c0001t0017g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.832-7227T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144699304 | |||||||
| chr4:144699402 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
171 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.832-7129G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144699402 | |||||||
| chr4:144699447 | A | T | 1 | a0001c0001t0005g0131 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.832-7084A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144699447 | |||||||
| chr4:144699484 | G | A | 5 | a0001c0001t0004g0193 a0001c0001t0004g0195 a0001c0001t0004g0222 others(2): Show |
5 | HG02071.hp2 HG02074.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.832-7047G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144699484 | |||||||
| chr4:144699494 | C | A | 3 | a0001c0001t0005g0114 a0001c0001t0019g0161 a0001c0001t0019g0162 |
3 | HG01243.hp2 HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.832-7037C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144699494 | |||||||
| chr4:144700153 | A | G | 10 | a0001c0001t0005g0114 a0001c0001t0019g0161 a0001c0001t0019g0162 others(7): Show |
10 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.832-6378A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144700153 | |||||||
| chr4:144700176 | G | A | 4 | a0001c0001t0051g0110 a0001c0003t0002g0101 a0001c0003t0002g0102 others(1): Show |
4 | HG00099.hp1 HG00280.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-6355G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144700176 | |||||||
| chr4:144700367 | G | A | 1 | a0001c0003t0002g0292 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.832-6164G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144700367 | |||||||
| chr4:144700585 | G | A | 13 | a0001c0001t0005g0073 a0001c0001t0005g0131 a0001c0001t0006g0074 others(10): Show |
13 | HG01496.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-5946G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144700585 | |||||||
| chr4:144700770 | A | C | 1 | a0001c0001t0001g0015 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.832-5761A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144700770 | |||||||
| chr4:144700852 | T | C | 3 | a0001c0001t0004g0214 a0001c0001t0004g0215 a0001c0001t0004g0216 |
3 | HG02630.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.832-5679T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144700852 | |||||||
| chr4:144700881 | G | C | 1 | a0001c0001t0032g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.832-5650G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144700881 | |||||||
| chr4:144701004 | CTT | C | 3 | a0001c0001t0005g0073 a0001c0001t0005g0131 a0004c0005t0005g0118 |
3 | HG02451.hp1 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.832-5523_832-5522d others(4): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144701004 | ||||||
| chr4:144701048 | G | A | 1 | a0001c0001t0009g0183 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.832-5483G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701048 | |||||||
| chr4:144701077 | T | C | 8 | a0001c0001t0006g0074 a0001c0001t0006g0076 a0001c0001t0006g0077 others(5): Show |
8 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.832-5454T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701077 | |||||||
| chr4:144701278 | G | T | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832-5253G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701278 | |||||||
| chr4:144701291 | T | A | 1 | a0001c0001t0001g0237 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.832-5240T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701291 | |||||||
| chr4:144701323 | C | CT | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(169): Show |
178 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.832-5195dupT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144701323 | ||||||
| chr4:144701323 | C | CTT | 17 | a0001c0001t0001g0003 a0001c0001t0001g0120 a0001c0001t0005g0131 others(14): Show |
19 | HG01496.hp2 HG01891.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.832-5196_832-5195d others(4): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144701323 | ||||||
| chr4:144701499 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
171 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.832-5032T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701499 | |||||||
| chr4:144701646 | A | G | 8 | a0001c0001t0006g0074 a0001c0001t0006g0076 a0001c0001t0006g0077 others(5): Show |
8 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.832-4885A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701646 | |||||||
| chr4:144701649 | T | C | 1 | a0001c0001t0015g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.832-4882T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701649 | |||||||
| chr4:144701686 | G | C | 2 | a0001c0001t0010g0145 a0001c0001t0010g0146 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.832-4845G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701686 | |||||||
| chr4:144701713 | C | T | 3 | a0001c0001t0005g0073 a0001c0001t0005g0131 a0004c0005t0005g0118 |
3 | HG02451.hp1 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.832-4818C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701713 | |||||||
| chr4:144701741 | T | G | 1 | a0004c0005t0005g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.832-4790T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701741 | |||||||
| chr4:144701798 | C | G | 1 | a0001c0001t0002g0294 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.832-4733C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701798 | |||||||
| chr4:144701800 | C | T | 1 | a0001c0001t0004g0195 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.832-4731C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701800 | |||||||
| chr4:144701871 | G | A | 13 | a0001c0001t0005g0073 a0001c0001t0005g0131 a0001c0001t0006g0074 others(10): Show |
13 | HG01496.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-4660G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701871 | |||||||
| chr4:144701955 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
198 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.832-4576G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701955 | |||||||
| chr4:144702009 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.832-4522T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144702009 | |||||||
| chr4:144702681 | T | G | 1 | a0001c0001t0007g0046 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.832-3850T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144702681 | |||||||
| chr4:144702703 | A | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0120 a0001c0001t0015g0072 |
5 | HG02257.hp2 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-3828A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144702703 | |||||||
| chr4:144702837 | A | C | 1 | a0001c0001t0032g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.832-3694A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144702837 | |||||||
| chr4:144702976 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.832-3555G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144702976 | |||||||
| chr4:144703045 | T | C | 1 | a0001c0001t0002g0227 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.832-3486T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703045 | |||||||
| chr4:144703082 | CAAGTGCC others(3): Show |
C | 1 | a0001c0001t0010g0145 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.832-3446_832-3437d others(12): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144703082 | ||||||
| chr4:144703163 | G | A | 6 | a0002c0002t0008g0134 a0002c0002t0008g0135 a0002c0002t0008g0136 others(3): Show |
6 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-3368G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703163 | |||||||
| chr4:144703214 | C | CA | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
163 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.832-3305dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144703214 | ||||||
| chr4:144703279 | C | T | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.832-3252C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703279 | |||||||
| chr4:144703295 | C | T | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832-3236C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703295 | |||||||
| chr4:144703332 | T | G | 13 | a0001c0001t0005g0012 a0001c0001t0005g0271 a0001c0001t0005g0272 others(10): Show |
14 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.832-3199T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703332 | |||||||
| chr4:144703554 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.832-2977T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703554 | |||||||
| chr4:144703729 | C | T | 7 | a0001c0001t0006g0074 a0001c0001t0006g0076 a0001c0001t0006g0077 others(4): Show |
7 | HG01496.hp2 HG02622.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-2802C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703729 | |||||||
| chr4:144703748 | C | A | 2 | a0001c0001t0019g0161 a0001c0001t0019g0162 |
2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.832-2783C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703748 | |||||||
| chr4:144703761 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.832-2770C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703761 | |||||||
| chr4:144704217 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.832-2314C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144704217 | |||||||
| chr4:144704561 | A | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0006t0004g0213 |
3 | HG01884.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.832-1970A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144704561 | |||||||
| chr4:144704578 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.832-1953C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144704578 | |||||||
| chr4:144704799 | A | G | 3 | a0001c0001t0015g0072 a0001c0001t0015g0119 a0001c0001t0015g0144 |
3 | HG03225.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.832-1732A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144704799 | |||||||
| chr4:144704944 | C | G | 65 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(62): Show |
67 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.832-1587C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144704944 | |||||||
| chr4:144705182 | C | T | 1 | a0001c0003t0002g0292 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.832-1349C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144705182 | |||||||
| chr4:144705223 | C | T | 2 | a0001c0001t0020g0087 a0001c0001t0020g0088 |
2 | HG01074.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.832-1308C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144705223 | |||||||
| chr4:144705262 | C | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
168 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.832-1269C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144705262 | |||||||
| chr4:144705506 | A | C | 1 | a0001c0001t0004g0216 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.832-1025A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144705506 | |||||||
| chr4:144705860 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
183 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.832-671G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144705860 | |||||||
| chr4:144705881 | G | A | 5 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(2): Show |
5 | HG00642.hp2 HG01074.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.832-650G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144705881 | |||||||
| chr4:144706245 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.832-286C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144706245 | |||||||
| chr4:144706253 | G | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.832-278G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144706253 | |||||||
| chr4:144706306 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.832-225A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144706306 | |||||||
| chr4:144706431 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.832-100T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144706431 | |||||||
| chr4:144706506 | C | A | 1 | a0001c0001t0040g0017 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.832-25C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144706506 | |||||||
| chr4:144706716 | C | G | 1 | a0001c0001t0016g0089 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.983+34C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 5/12 | chr4 | 144706716 | |||||||
| chr4:144707464 | G | A | 1 | a0001c0001t0032g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1157+204G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | chr4 | 144707464 | |||||||
| chr4:144707576 | C | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0006t0004g0213 |
3 | HG01884.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1157+316C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | chr4 | 144707576 | |||||||
| chr4:144707646 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0053 a0001c0001t0001g0056 |
2 | NA18979.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1157+389_1157+398d others(12): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 144707646 | ||||||
| chr4:144707646 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0005g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1157+388_1157+398d others(13): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 144707646 | ||||||
| chr4:144707646 | C | CAAAAAAA others(5): Show |
15 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0002g0099 others(12): Show |
15 | HG01168.hp1 HG01243.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.1157+387_1157+398d others(14): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 144707646 | ||||||
| chr4:144707646 | C | CAAAAAAA others(6): Show |
106 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(103): Show |
112 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1157+398_1157+399i others(15): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 144707646 | ||||||
| chr4:144707646 | C | CAAAAAAA others(7): Show |
145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
153 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.1157+398_1157+399i others(16): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 144707646 | ||||||
| chr4:144707646 | C | CAAAAAAA others(8): Show |
25 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0039 others(22): Show |
25 | HG00621.hp1 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1157+398_1157+399i others(17): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 144707646 | ||||||
| chr4:144707646 | C | CAAAAAAA others(9): Show |
4 | a0001c0001t0015g0144 a0002c0002t0008g0134 a0002c0002t0008g0137 others(1): Show |
4 | HG01192.hp1 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1157+398_1157+399i others(18): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 144707646 | ||||||
| chr4:144707649 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0009g0172 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1157+398_1157+399i others(15): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 144707649 | ||||||
| chr4:144707709 | G | T | 1 | a0001c0001t0034g0060 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1157+449G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | chr4 | 144707709 | |||||||
| chr4:144707786 | T | G | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1158-382T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | chr4 | 144707786 | |||||||
| chr4:144707861 | C | A | 2 | a0001c0001t0001g0282 a0001c0001t0002g0264 |
2 | NA19062.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1158-307C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | chr4 | 144707861 | |||||||
| chr4:144707888 | C | T | 2 | a0001c0001t0019g0161 a0001c0001t0019g0162 |
2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1158-280C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | chr4 | 144707888 | |||||||
| chr4:144707907 | C | T | 3 | a0001c0001t0015g0072 a0001c0001t0015g0119 a0001c0001t0015g0144 |
3 | HG03225.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1158-261C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | chr4 | 144707907 | |||||||
| chr4:144708102 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1158-66A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | chr4 | 144708102 | |||||||
| chr4:144708478 | A | T | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.1301+167A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144708478 | |||||||
| chr4:144708636 | TAG | T | 3 | a0001c0001t0004g0214 a0001c0001t0004g0215 a0001c0001t0004g0216 |
3 | HG02630.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1301+331_1301+332d others(4): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 144708636 | ||||||
| chr4:144708650 | T | TTTTGA | 8 | a0001c0001t0048g0129 a0002c0002t0008g0133 a0002c0002t0008g0134 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1301+344_1301+348d others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 144708650 | ||||||
| chr4:144708744 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1301+433C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144708744 | |||||||
| chr4:144708797 | T | C | 3 | a0001c0001t0015g0072 a0001c0001t0015g0119 a0001c0001t0015g0144 |
3 | HG03225.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1301+486T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144708797 | |||||||
| chr4:144708838 | G | T | 5 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(2): Show |
5 | HG00642.hp2 HG01074.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1301+527G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144708838 | |||||||
| chr4:144708990 | G | T | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1301+679G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144708990 | |||||||
| chr4:144709141 | A | T | 3 | a0001c0001t0005g0114 a0001c0001t0019g0161 a0001c0001t0019g0162 |
3 | HG01243.hp2 HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1301+830A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144709141 | |||||||
| chr4:144709243 | T | A | 3 | a0001c0001t0015g0072 a0001c0001t0015g0119 a0001c0001t0015g0144 |
3 | HG03225.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1301+932T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144709243 | |||||||
| chr4:144709931 | C | T | 1 | a0001c0001t0037g0022 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1301+1620C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144709931 | |||||||
| chr4:144710131 | C | T | 1 | a0002c0002t0008g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1302-1819C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144710131 | |||||||
| chr4:144710319 | A | G | 1 | a0001c0001t0007g0046 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1302-1631A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144710319 | |||||||
| chr4:144710416 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1302-1534G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144710416 | |||||||
| chr4:144710447 | T | C | 5 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(2): Show |
5 | HG00642.hp2 HG01074.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302-1503T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144710447 | |||||||
| chr4:144710496 | T | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1302-1454T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144710496 | |||||||
| chr4:144710637 | T | C | 3 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG01081.hp1 HG01358.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1302-1313T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144710637 | |||||||
| chr4:144710715 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1302-1235G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144710715 | |||||||
| chr4:144710845 | T | C | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1302-1105T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144710845 | |||||||
| chr4:144711028 | T | C | 2 | a0001c0001t0002g0013 a0001c0001t0002g0284 |
3 | NA18947.hp1 NA18955.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1302-922T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144711028 | |||||||
| chr4:144711046 | T | TCCTA | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1302-901_1302-900i others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 144711046 | ||||||
| chr4:144711138 | C | T | 1 | a0001c0001t0003g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1302-812C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144711138 | |||||||
| chr4:144711373 | G | T | 1 | a0001c0001t0002g0258 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1302-577G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144711373 | |||||||
| chr4:144711540 | C | G | 2 | a0001c0001t0002g0070 a0001c0001t0002g0071 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1302-410C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144711540 | |||||||
| chr4:144711926 | T | C | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0006t0004g0213 |
3 | HG01884.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1302-24T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144711926 | |||||||
| chr4:144712280 | G | C | 3 | a0001c0001t0005g0114 a0001c0001t0019g0161 a0001c0001t0019g0162 |
3 | HG01243.hp2 HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1423+209G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144712280 | |||||||
| chr4:144712334 | C | A | 1 | a0001c0001t0003g0155 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1423+263C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144712334 | |||||||
| chr4:144712348 | T | C | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1423+277T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144712348 | |||||||
| chr4:144712378 | A | G | 1 | a0001c0001t0021g0226 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1423+307A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144712378 | |||||||
| chr4:144712559 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1423+488C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144712559 | |||||||
| chr4:144712885 | G | GGTGT | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1423+834_1423+837d others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 144712885 | ||||||
| chr4:144712885 | G | GGTGTGT | 5 | a0001c0001t0001g0048 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
5 | HG01884.hp2 HG03831.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1423+832_1423+837d others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 144712885 | ||||||
| chr4:144712953 | G | GA | 18 | a0001c0001t0002g0106 a0001c0001t0002g0261 a0001c0001t0005g0114 others(15): Show |
18 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1423+897dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 144712953 | ||||||
| chr4:144712962 | A | G | 1 | a0001c0001t0003g0188 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1423+891A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144712962 | |||||||
| chr4:144713007 | T | C | 1 | a0001c0001t0005g0131 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1423+936T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144713007 | |||||||
| chr4:144713250 | A | C | 2 | a0001c0001t0020g0087 a0001c0001t0020g0088 |
2 | HG01074.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1424-975A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144713250 | |||||||
| chr4:144713336 | G | T | 1 | a0001c0001t0037g0022 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1424-889G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144713336 | |||||||
| chr4:144713890 | GT | G | 6 | a0001c0001t0002g0267 a0001c0001t0002g0294 a0001c0001t0011g0045 others(3): Show |
6 | HG00621.hp1 HG03225.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1424-325delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 144713890 | ||||||
| chr4:144714035 | A | G | 1 | a0001c0001t0002g0112 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1424-190A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144714035 | |||||||
| chr4:144714195 | C | A | 8 | a0001c0001t0048g0129 a0002c0002t0008g0133 a0002c0002t0008g0134 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1424-30C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144714195 | |||||||
| chr4:144714358 | C | G | 1 | a0004c0005t0005g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1547+10C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 9/12 | chr4 | 144714358 | |||||||
| chr4:144714487 | T | C | 1 | a0001c0001t0002g0092 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1547+139T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 9/12 | chr4 | 144714487 | |||||||
| chr4:144714861 | C | T | 1 | a0001c0001t0031g0079 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1548-439C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 9/12 | chr4 | 144714861 | |||||||
| chr4:144715155 | G | A | 2 | a0001c0001t0013g0014 a0001c0001t0013g0285 |
3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1548-145G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 9/12 | chr4 | 144715155 | |||||||
| chr4:144715580 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1678+150T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144715580 | |||||||
| chr4:144715620 | G | A | 5 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(2): Show |
5 | HG00642.hp2 HG01074.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1678+190G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144715620 | |||||||
| chr4:144715767 | A | T | 1 | a0001c0001t0001g0248 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1678+337A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144715767 | |||||||
| chr4:144715790 | A | G | 1 | a0001c0001t0048g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1678+360A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144715790 | |||||||
| chr4:144715923 | A | T | 60 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(57): Show |
62 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1678+493A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144715923 | |||||||
| chr4:144716217 | C | T | 1 | a0001c0001t0003g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1678+787C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716217 | |||||||
| chr4:144716263 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1678+833T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716263 | |||||||
| chr4:144716297 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1678+867T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716297 | |||||||
| chr4:144716496 | C | T | 4 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 others(1): Show |
4 | HG02145.hp2 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1678+1066C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716496 | |||||||
| chr4:144716540 | CAA | C | 4 | a0001c0001t0003g0150 a0001c0001t0003g0190 a0001c0001t0003g0200 others(1): Show |
4 | HG00741.hp2 HG01192.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678+1111_1678+111 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716540 | |||||||
| chr4:144716657 | G | A | 8 | a0001c0001t0048g0129 a0002c0002t0008g0133 a0002c0002t0008g0134 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+1227G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716657 | |||||||
| chr4:144716684 | C | A | 1 | a0001c0001t0021g0226 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1678+1254C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716684 | |||||||
| chr4:144716721 | C | G | 2 | a0001c0001t0019g0161 a0001c0001t0019g0162 |
2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1678+1291C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716721 | |||||||
| chr4:144716831 | A | G | 4 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0247 others(1): Show |
6 | HG00609.hp2 NA18939.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+1401A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716831 | |||||||
| chr4:144716854 | G | GA | 11 | a0001c0001t0002g0084 a0001c0001t0002g0098 a0001c0001t0002g0104 others(8): Show |
11 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.1678+1458dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | ||||||
| chr4:144716854 | GA | G | 60 | a0001c0001t0001g0244 a0001c0001t0002g0009 a0001c0001t0002g0010 others(57): Show |
65 | HG00099.hp1 HG00609.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.1678+1458delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | ||||||
| chr4:144716854 | GAA | G | 41 | a0001c0001t0001g0026 a0001c0001t0001g0037 a0001c0001t0001g0043 others(38): Show |
41 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.1678+1457_1678+145 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | ||||||
| chr4:144716854 | GAAA | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
110 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1678+1456_1678+145 others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | ||||||
| chr4:144716854 | GAAAA | G | 14 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0048 others(11): Show |
14 | HG01168.hp2 HG01243.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.1678+1455_1678+145 others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | ||||||
| chr4:144716854 | GAAAAAAA others(3): Show |
G | 3 | a0001c0001t0003g0192 a0001c0001t0003g0205 a0001c0001t0015g0119 |
3 | HG01978.hp2 HG02004.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1678+1449_1678+145 others(14): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | ||||||
| chr4:144716854 | GAAAAAAA others(4): Show |
G | 9 | a0001c0001t0002g0268 a0001c0001t0048g0129 a0001c0001t0049g0075 others(6): Show |
9 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1678+1448_1678+145 others(15): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | ||||||
| chr4:144716854 | GAAAAAAA others(5): Show |
G | 1 | a0002c0002t0008g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1678+1447_1678+145 others(16): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | ||||||
| chr4:144716854 | GAAAAAAA others(8): Show |
G | 9 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(6): Show |
9 | HG01346.hp1 HG01496.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1678+1444_1678+145 others(19): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | ||||||
| chr4:144716854 | GAAAAAAA others(9): Show |
G | 10 | a0001c0001t0001g0058 a0001c0001t0003g0164 a0001c0001t0006g0074 others(7): Show |
10 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1678+1443_1678+145 others(20): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | ||||||
| chr4:144716854 | GAAAAAAA others(10): Show |
G | 1 | a0001c0001t0024g0212 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1678+1442_1678+145 others(21): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | ||||||
| chr4:144716854 | GAAAAAAA others(11): Show |
G | 1 | a0001c0001t0001g0067 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1678+1441_1678+145 others(22): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | ||||||
| chr4:144716854 | GAAAAAAA others(14): Show |
G | 1 | a0001c0001t0001g0032 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1678+1438_1678+145 others(25): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | ||||||
| chr4:144716919 | A | T | 1 | a0001c0001t0002g0289 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1678+1489A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716919 | |||||||
| chr4:144716920 | T | C | 8 | a0001c0001t0048g0129 a0002c0002t0008g0133 a0002c0002t0008g0134 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+1490T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716920 | |||||||
| chr4:144717003 | G | A | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1678+1573G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144717003 | |||||||
| chr4:144717026 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
164 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1678+1596C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144717026 | |||||||
| chr4:144717043 | A | C | 2 | a0001c0001t0001g0244 a0001c0001t0002g0243 |
2 | NA18944.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1678+1613A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144717043 | |||||||
| chr4:144717111 | C | A | 1 | a0001c0001t0031g0079 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1678+1681C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144717111 | |||||||
| chr4:144717115 | G | C | 2 | a0001c0001t0019g0161 a0001c0001t0019g0162 |
2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1678+1685G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144717115 | |||||||
| chr4:144717576 | T | C | 1 | a0001c0001t0020g0087 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1679-1299T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144717576 | |||||||
| chr4:144717881 | G | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1679-994G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144717881 | |||||||
| chr4:144718166 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
164 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1679-709G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144718166 | |||||||
| chr4:144718302 | A | G | 1 | a0001c0001t0001g0031 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1679-573A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144718302 | |||||||
| chr4:144718557 | G | A | 14 | a0001c0001t0005g0012 a0001c0001t0005g0073 a0001c0001t0005g0271 others(11): Show |
15 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1679-318G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144718557 | |||||||
| chr4:144718578 | A | G | 1 | a0001c0001t0003g0196 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1679-297A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144718578 | |||||||
| chr4:144718748 | T | C | 4 | a0001c0001t0003g0164 a0001c0001t0003g0181 a0001c0001t0003g0182 others(1): Show |
4 | NA18944.hp2 NA18969.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1679-127T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144718748 | |||||||
| chr4:144719002 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(76): Show |
83 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.1760+46C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144719002 | |||||||
| chr4:144719115 | G | T | 1 | a0001c0001t0005g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1760+159G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144719115 | |||||||
| chr4:144719193 | C | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1760+237C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144719193 | |||||||
| chr4:144719466 | C | T | 4 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0020g0087 others(1): Show |
4 | HG01074.hp2 HG03654.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1760+510C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144719466 | |||||||
| chr4:144719550 | G | C | 1 | a0001c0001t0005g0281 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1760+594G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144719550 | |||||||
| chr4:144719833 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1760+877A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144719833 | |||||||
| chr4:144720064 | T | C | 1 | a0001c0001t0015g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1760+1108T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720064 | |||||||
| chr4:144720089 | T | A | 3 | a0001c0001t0015g0072 a0001c0001t0015g0119 a0001c0001t0015g0144 |
3 | HG03225.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1760+1133T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720089 | |||||||
| chr4:144720137 | A | G | 5 | a0001c0001t0004g0193 a0001c0001t0004g0195 a0001c0001t0004g0222 others(2): Show |
5 | HG02071.hp2 HG02074.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1760+1181A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720137 | |||||||
| chr4:144720336 | A | G | 1 | a0001c0001t0005g0131 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1760+1380A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720336 | |||||||
| chr4:144720597 | G | T | 1 | a0001c0001t0002g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1760+1641G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720597 | |||||||
| chr4:144720676 | G | T | 1 | a0001c0001t0039g0093 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1760+1720G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720676 | |||||||
| chr4:144720679 | C | T | 1 | a0001c0001t0003g0188 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1760+1723C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720679 | |||||||
| chr4:144720909 | G | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0006t0004g0213 |
3 | HG01884.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1760+1953G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720909 | |||||||
| chr4:144720985 | A | T | 1 | a0001c0001t0005g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1760+2029A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720985 | |||||||
| chr4:144721522 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1760+2566T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144721522 | |||||||
| chr4:144721561 | T | A | 3 | a0001c0001t0004g0214 a0001c0001t0004g0215 a0001c0001t0004g0216 |
3 | HG02630.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1760+2605T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144721561 | |||||||
| chr4:144721563 | GA | G | 6 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0005g0114 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1760+2611delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144721563 | ||||||
| chr4:144721594 | GA | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(167): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.1760+2656delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144721594 | ||||||
| chr4:144721771 | C | T | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1760+2815C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144721771 | |||||||
| chr4:144721811 | G | A | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+2855G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144721811 | |||||||
| chr4:144721820 | T | C | 1 | a0001c0001t0013g0285 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1760+2864T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144721820 | |||||||
| chr4:144721927 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1760+2971G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144721927 | |||||||
| chr4:144722111 | C | T | 1 | a0001c0001t0016g0089 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1760+3155C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144722111 | |||||||
| chr4:144722174 | G | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1760+3218G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144722174 | |||||||
| chr4:144722334 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
205 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.1760+3378T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144722334 | |||||||
| chr4:144722395 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1760+3439G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144722395 | |||||||
| chr4:144722431 | T | C | 1 | a0001c0001t0002g0235 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1760+3475T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144722431 | |||||||
| chr4:144722548 | G | T | 1 | a0001c0001t0002g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1760+3592G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144722548 | |||||||
| chr4:144722619 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1760+3663G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144722619 | |||||||
| chr4:144722728 | C | T | 1 | a0001c0006t0004g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1760+3772C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144722728 | |||||||
| chr4:144723010 | G | A | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+4054G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144723010 | |||||||
| chr4:144723214 | C | T | 1 | a0001c0001t0032g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1760+4258C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144723214 | |||||||
| chr4:144723651 | C | T | 1 | a0001c0003t0002g0102 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1760+4695C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144723651 | |||||||
| chr4:144723907 | A | C | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1760+4951A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144723907 | |||||||
| chr4:144723971 | C | T | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1760+5015C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144723971 | |||||||
| chr4:144724074 | G | A | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5118G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724074 | |||||||
| chr4:144724086 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1760+5130T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724086 | |||||||
| chr4:144724121 | T | C | 1 | a0001c0001t0005g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1760+5165T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724121 | |||||||
| chr4:144724338 | A | T | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5382A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724338 | |||||||
| chr4:144724358 | G | A | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1760+5402G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724358 | |||||||
| chr4:144724372 | T | G | 1 | a0001c0001t0003g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1760+5416T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724372 | |||||||
| chr4:144724385 | G | A | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5429G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724385 | |||||||
| chr4:144724401 | A | C | 2 | a0001c0001t0001g0282 a0001c0001t0002g0264 |
2 | NA19062.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1760+5445A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724401 | |||||||
| chr4:144724444 | A | T | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5488A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724444 | |||||||
| chr4:144724475 | T | C | 14 | a0001c0001t0005g0012 a0001c0001t0005g0073 a0001c0001t0005g0271 others(11): Show |
15 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1760+5519T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724475 | |||||||
| chr4:144724598 | G | A | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5642G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724598 | |||||||
| chr4:144724611 | A | G | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5655A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724611 | |||||||
| chr4:144724648 | T | TTG | 3 | a0001c0001t0002g0086 a0001c0001t0005g0274 a0001c0001t0046g0270 |
3 | HG02109.hp1 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1760+5712_1760+571 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144724648 | ||||||
| chr4:144724648 | TTG | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
119 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.1760+5712_1760+571 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144724648 | ||||||
| chr4:144724652 | G | GTGTGTGT others(67): Show |
1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5705_1760+570 others(78): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144724652 | ||||||
| chr4:144724668 | G | A | 3 | a0001c0001t0003g0008 a0001c0001t0012g0189 a0001c0001t0016g0085 |
4 | HG01261.hp1 HG01346.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1760+5712G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724668 | |||||||
| chr4:144724687 | T | C | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5731T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724687 | |||||||
| chr4:144724695 | TAA | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1760+5740_1760+574 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724695 | |||||||
| chr4:144724696 | A | G | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5740A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724696 | |||||||
| chr4:144724697 | A | T | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5741A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724697 | |||||||
| chr4:144724698 | G | A | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5742G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724698 | |||||||
| chr4:144724738 | C | T | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5782C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724738 | |||||||
| chr4:144724768 | G | T | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5812G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724768 | |||||||
| chr4:144724773 | C | A | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1760+5817C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724773 | |||||||
| chr4:144724808 | T | C | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5852T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724808 | |||||||
| chr4:144724851 | T | C | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1760+5895T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724851 | |||||||
| chr4:144724859 | T | C | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5903T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724859 | |||||||
| chr4:144725031 | G | T | 1 | a0001c0001t0002g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1760+6075G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725031 | |||||||
| chr4:144725059 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1760+6103C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725059 | |||||||
| chr4:144725257 | C | T | 1 | a0001c0003t0002g0292 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1760+6301C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725257 | |||||||
| chr4:144725402 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1760+6446G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725402 | |||||||
| chr4:144725470 | T | C | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+6514T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725470 | |||||||
| chr4:144725492 | G | T | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+6536G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725492 | |||||||
| chr4:144725626 | C | A | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+6670C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725626 | |||||||
| chr4:144725663 | C | CGT | 9 | a0001c0001t0006g0074 a0001c0001t0006g0076 a0001c0001t0006g0077 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1760+6726_1760+672 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144725663 | ||||||
| chr4:144725663 | C | T | 63 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0003g0007 others(60): Show |
65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.1760+6707C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725663 | |||||||
| chr4:144725663 | CGT | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(108): Show |
117 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.1760+6726_1760+672 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144725663 | ||||||
| chr4:144725782 | C | T | 1 | a0001c0001t0032g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1760+6826C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725782 | |||||||
| chr4:144725859 | G | T | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+6903G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725859 | |||||||
| chr4:144725891 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1760+6935G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725891 | |||||||
| chr4:144725916 | C | T | 3 | a0001c0001t0002g0229 a0001c0001t0002g0231 a0001c0001t0030g0230 |
3 | NA18942.hp1 NA18962.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1760+6960C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725916 | |||||||
| chr4:144725922 | C | T | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+6966C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725922 | |||||||
| chr4:144725969 | G | C | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+7013G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725969 | |||||||
| chr4:144726019 | T | C | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+7063T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726019 | |||||||
| chr4:144726086 | T | C | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1760+7130T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726086 | |||||||
| chr4:144726092 | T | C | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+7136T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726092 | |||||||
| chr4:144726224 | A | C | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+7268A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726224 | |||||||
| chr4:144726286 | T | C | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+7330T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726286 | |||||||
| chr4:144726296 | T | A | 1 | a0001c0001t0001g0053 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1760+7340T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726296 | |||||||
| chr4:144726791 | G | T | 2 | a0001c0001t0032g0142 a0001c0001t0049g0075 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1760+7835G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726791 | |||||||
| chr4:144726867 | A | G | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1761-7874A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726867 | |||||||
| chr4:144726880 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1761-7861T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726880 | |||||||
| chr4:144727020 | C | T | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1761-7721C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727020 | |||||||
| chr4:144727269 | CACTTCTT others(9): Show |
C | 2 | a0001c0001t0013g0014 a0001c0001t0013g0285 |
3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1761-7470_1761-745 others(20): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144727269 | ||||||
| chr4:144727288 | A | G | 2 | a0001c0001t0013g0014 a0001c0001t0013g0285 |
3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1761-7453A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727288 | |||||||
| chr4:144727289 | A | G | 2 | a0001c0001t0013g0014 a0001c0001t0013g0285 |
3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1761-7452A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727289 | |||||||
| chr4:144727290 | T | G | 2 | a0001c0001t0013g0014 a0001c0001t0013g0285 |
3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1761-7451T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727290 | |||||||
| chr4:144727291 | C | G | 2 | a0001c0001t0013g0014 a0001c0001t0013g0285 |
3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1761-7450C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727291 | |||||||
| chr4:144727339 | T | C | 2 | a0001c0001t0013g0014 a0001c0001t0013g0285 |
3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1761-7402T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727339 | |||||||
| chr4:144727429 | C | T | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1761-7312C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727429 | |||||||
| chr4:144727485 | G | A | 2 | a0003c0004t0004g0206 a0003c0004t0004g0207 |
2 | NA18948.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1761-7256G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727485 | |||||||
| chr4:144727631 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1761-7110C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727631 | |||||||
| chr4:144727789 | A | G | 8 | a0001c0001t0048g0129 a0002c0002t0008g0133 a0002c0002t0008g0134 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1761-6952A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727789 | |||||||
| chr4:144727818 | T | C | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1761-6923T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727818 | |||||||
| chr4:144727889 | G | T | 5 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(2): Show |
5 | HG00642.hp2 HG01074.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761-6852G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727889 | |||||||
| chr4:144728090 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1761-6651C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728090 | |||||||
| chr4:144728208 | G | T | 1 | a0001c0001t0017g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1761-6533G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728208 | |||||||
| chr4:144728218 | A | G | 6 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0005g0114 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1761-6523A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728218 | |||||||
| chr4:144728324 | G | A | 6 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0005g0114 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1761-6417G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728324 | |||||||
| chr4:144728347 | A | T | 2 | a0001c0001t0003g0152 a0001c0001t0009g0158 |
2 | HG00408.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1761-6394A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728347 | |||||||
| chr4:144728469 | G | T | 2 | a0001c0001t0003g0185 a0001c0001t0003g0204 |
2 | HG01168.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1761-6272G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728469 | |||||||
| chr4:144728508 | T | C | 1 | a0001c0001t0015g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1761-6233T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728508 | |||||||
| chr4:144728828 | G | A | 2 | a0001c0001t0032g0142 a0001c0001t0049g0075 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1761-5913G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728828 | |||||||
| chr4:144728833 | A | G | 1 | a0001c0001t0003g0194 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1761-5908A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728833 | |||||||
| chr4:144728869 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
173 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1761-5872G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728869 | |||||||
| chr4:144728943 | C | T | 1 | a0001c0001t0002g0260 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1761-5798C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728943 | |||||||
| chr4:144728983 | GAAGA | G | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1761-5751_1761-574 others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144728983 | ||||||
| chr4:144729165 | G | T | 1 | a0001c0006t0004g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1761-5576G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144729165 | |||||||
| chr4:144729239 | T | A | 1 | a0001c0001t0001g0048 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1761-5502T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144729239 | |||||||
| chr4:144729469 | A | G | 1 | a0001c0001t0002g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1761-5272A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144729469 | |||||||
| chr4:144729601 | T | C | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1761-5140T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144729601 | |||||||
| chr4:144729815 | C | CA | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1761-4926_1761-492 others(5): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144729815 | |||||||
| chr4:144729852 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
222 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1761-4889C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144729852 | |||||||
| chr4:144729995 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
184 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1761-4746A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144729995 | |||||||
| chr4:144730107 | T | A | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1761-4634T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144730107 | |||||||
| chr4:144730242 | AT | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
189 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1761-4492delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144730242 | ||||||
| chr4:144730511 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
189 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1761-4230A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144730511 | |||||||
| chr4:144730541 | G | A | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1761-4200G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144730541 | |||||||
| chr4:144730585 | C | T | 1 | a0001c0001t0032g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1761-4156C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144730585 | |||||||
| chr4:144730826 | T | C | 1 | a0001c0001t0011g0045 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1761-3915T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144730826 | |||||||
| chr4:144730828 | A | G | 1 | a0001c0001t0028g0217 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1761-3913A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144730828 | |||||||
| chr4:144730989 | C | T | 1 | a0001c0001t0002g0252 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1761-3752C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144730989 | |||||||
| chr4:144731280 | C | T | 1 | a0001c0001t0032g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1761-3461C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144731280 | |||||||
| chr4:144731323 | C | T | 1 | a0001c0001t0049g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1761-3418C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144731323 | |||||||
| chr4:144731330 | T | C | 6 | a0002c0002t0008g0134 a0002c0002t0008g0135 a0002c0002t0008g0136 others(3): Show |
6 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1761-3411T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144731330 | |||||||
| chr4:144731443 | G | A | 1 | a0001c0001t0002g0266 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1761-3298G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144731443 | |||||||
| chr4:144731578 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1761-3163C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144731578 | |||||||
| chr4:144732011 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1761-2730G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144732011 | |||||||
| chr4:144732026 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0034g0060 |
2 | HG01943.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1761-2715G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144732026 | |||||||
| chr4:144732242 | A | C | 7 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0005g0114 others(4): Show |
7 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1761-2499A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144732242 | |||||||
| chr4:144732480 | A | C | 8 | a0001c0001t0048g0129 a0002c0002t0008g0133 a0002c0002t0008g0134 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1761-2261A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144732480 | |||||||
| chr4:144732527 | T | C | 1 | a0001c0001t0039g0093 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1761-2214T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144732527 | |||||||
| chr4:144732542 | T | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
170 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.1761-2199T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144732542 | |||||||
| chr4:144732688 | C | G | 8 | a0001c0001t0048g0129 a0002c0002t0008g0133 a0002c0002t0008g0134 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1761-2053C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144732688 | |||||||
| chr4:144732799 | T | G | 1 | a0001c0001t0006g0141 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1761-1942T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144732799 | |||||||
| chr4:144733085 | G | A | 1 | a0001c0006t0004g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1761-1656G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733085 | |||||||
| chr4:144733108 | T | G | 3 | a0001c0001t0004g0193 a0001c0001t0004g0195 a0001c0001t0004g0222 |
3 | HG02071.hp2 HG02074.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.1761-1633T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733108 | |||||||
| chr4:144733345 | G | T | 60 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(57): Show |
62 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1761-1396G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733345 | |||||||
| chr4:144733546 | A | G | 16 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0005g0114 others(13): Show |
16 | HG00642.hp2 HG01074.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1761-1195A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733546 | |||||||
| chr4:144733744 | C | T | 2 | a0001c0001t0051g0110 a0001c0003t0002g0113 |
2 | HG00099.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1761-997C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733744 | |||||||
| chr4:144733761 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1761-980T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733761 | |||||||
| chr4:144733917 | A | T | 8 | a0001c0001t0006g0074 a0001c0001t0006g0076 a0001c0001t0006g0077 others(5): Show |
8 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1761-824A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733917 | |||||||
| chr4:144733920 | G | A | 1 | a0001c0001t0025g0159 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1761-821G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733920 | |||||||
| chr4:144733956 | A | G | 14 | a0001c0001t0016g0083 a0001c0001t0016g0085 a0001c0001t0016g0089 others(11): Show |
14 | HG00642.hp2 HG01074.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1761-785A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733956 | |||||||
| chr4:144734237 | A | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
179 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.1761-504A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144734237 | |||||||
| chr4:144734339 | T | G | 2 | a0001c0001t0002g0099 a0001c0001t0002g0103 |
2 | HG01433.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1761-402T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144734339 | |||||||
| chr4:144734380 | T | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1761-361T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144734380 | |||||||
| chr4:144734490 | G | A | 1 | a0001c0001t0021g0226 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1761-251G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144734490 | |||||||
| chr4:144734617 | T | TA | 84 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(81): Show |
86 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.1761-111dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144734617 | ||||||
| chr4:144734617 | TA | T | 6 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0058 others(3): Show |
6 | HG02165.hp2 HG02622.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1761-111delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144734617 | ||||||
| chr4:144734902 | G | C | 8 | a0001c0001t0048g0129 a0002c0002t0008g0133 a0002c0002t0008g0134 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1909+13G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144734902 | |||||||
| chr4:144735059 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1909+170T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735059 | |||||||
| chr4:144735149 | A | C | 1 | a0001c0001t0016g0083 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1909+260A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735149 | |||||||
| chr4:144735268 | A | T | 1 | a0001c0001t0001g0053 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1909+379A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735268 | |||||||
| chr4:144735426 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1909+537G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735426 | |||||||
| chr4:144735462 | A | C | 1 | a0001c0001t0001g0063 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1909+573A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735462 | |||||||
| chr4:144735466 | A | G | 2 | a0001c0001t0019g0161 a0001c0001t0019g0162 |
2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1909+577A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735466 | |||||||
| chr4:144735660 | G | A | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1909+771G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735660 | |||||||
| chr4:144735682 | CT | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
173 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1909+795delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 144735682 | ||||||
| chr4:144735742 | C | T | 1 | a0001c0001t0002g0262 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1909+853C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735742 | |||||||
| chr4:144735765 | A | T | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+876A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735765 | |||||||
| chr4:144736014 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
190 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1909+1125T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736014 | |||||||
| chr4:144736025 | G | A | 2 | a0001c0001t0010g0145 a0001c0001t0010g0146 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1909+1136G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736025 | |||||||
| chr4:144736032 | A | G | 9 | a0001c0001t0048g0129 a0001c0001t0049g0075 a0002c0002t0008g0133 others(6): Show |
9 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1909+1143A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736032 | |||||||
| chr4:144736059 | T | C | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1909+1170T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736059 | |||||||
| chr4:144736136 | C | CTTT | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
171 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.1909+1262_1909+126 others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 144736136 | ||||||
| chr4:144736136 | C | CTTTT | 16 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0021 others(13): Show |
17 | HG00642.hp2 HG01074.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1909+1261_1909+126 others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 144736136 | ||||||
| chr4:144736259 | C | T | 2 | a0001c0001t0002g0070 a0001c0001t0002g0071 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1909+1370C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736259 | |||||||
| chr4:144736342 | G | A | 8 | a0001c0001t0048g0129 a0002c0002t0008g0133 a0002c0002t0008g0134 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1910-1422G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736342 | |||||||
| chr4:144736590 | CTATA | C | 3 | a0001c0001t0018g0147 a0001c0001t0018g0148 a0001c0001t0018g0149 |
3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1910-1169_1910-116 others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 144736590 | ||||||
| chr4:144736866 | C | T | 1 | a0001c0001t0003g0198 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1910-898C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736866 | |||||||
| chr4:144736875 | TC | T | 8 | a0001c0001t0048g0129 a0002c0002t0008g0133 a0002c0002t0008g0134 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1910-886delC | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 144736875 | ||||||
| chr4:144736880 | T | G | 8 | a0001c0001t0048g0129 a0002c0002t0008g0133 a0002c0002t0008g0134 others(5): Show |
8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1910-884T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736880 | |||||||
| chr4:144736914 | G | A | 7 | a0001c0001t0006g0074 a0001c0001t0006g0076 a0001c0001t0006g0077 others(4): Show |
7 | HG01496.hp2 HG02622.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1910-850G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736914 | |||||||
| chr4:144737134 | C | T | 58 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0150 others(55): Show |
60 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1910-630C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144737134 | |||||||
| chr4:144737184 | C | T | 2 | a0001c0001t0019g0161 a0001c0001t0019g0162 |
2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1910-580C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144737184 | |||||||
| chr4:144737277 | T | C | 132 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0236 others(129): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1910-487T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144737277 | |||||||
| chr4:144737671 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1910-93C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144737671 | |||||||
| chr4:144737733 | G | A | 3 | a0001c0001t0004g0214 a0001c0001t0004g0215 a0001c0001t0004g0216 |
3 | HG02630.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1910-31G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144737733 |