Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3070 |
| ensemblid | ENSG00000119969.16 |
| hgncid | 4861 |
| symbol | HELLS |
| name | helicase, lymphoid specific |
| refseq_nuc | NM_018063.5 |
| refseq_prot | NP_060533.2 |
| ensembl_nuc | ENST00000348459.10 |
| ensembl_prot | ENSP00000239027.7 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 94545788 |
| end | 94602099 |
| strand | + |
| ver | v1.2 |
| region | chr10:94545788-94602099 |
| region5000 | chr10:94540788-94607099 |
| regionname0 | HELLS_chr10_94545788_94602099 |
| regionname5000 | HELLS_chr10_94540788_94607099 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 838 | 349 | 86 | 54 | 147 | 16 | 44 | 109 | HELLS_chr10_94540788_94607099 | HELLS | MPAER others(833): Show |
chr10 | 94540788 | 94607099 |
| a0002 | 0/0 | 838 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | HELLS_chr10_94540788_94607099 | HELLS | MPAER others(833): Show |
chr10 | 94540788 | 94607099 |
| a0003 | 0/0 | 838 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | MPAER others(833): Show |
chr10 | 94540788 | 94607099 |
| a0004 | 0/0 | 822 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | MVEQL others(817): Show |
chr10 | 94540788 | 94607099 |
| a0005 | 0/0 | 838 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | MPAER others(833): Show |
chr10 | 94540788 | 94607099 |
| a0006 | 0/0 | 838 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | MPAER others(833): Show |
chr10 | 94540788 | 94607099 |
| a0007 | 0/0 | 838 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | MPAER others(833): Show |
chr10 | 94540788 | 94607099 |
| a0008 | 0/0 | 838 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | MPAER others(833): Show |
chr10 | 94540788 | 94607099 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2514 | 172 | 28 | 17 | 100 | 7 | 20 | HELLS_chr10_94540788_94607099 | HELLS | ATGCC others(2509): Show |
chr10 | 94540788 | 94607099 | ||
| a0001c0002 | 1/1 | 2514 | 162 | 46 | 36 | 46 | 9 | 23 | HELLS_chr10_94540788_94607099 | HELLS | ATGCC others(2509): Show |
chr10 | 94540788 | 94607099 | ||
| a0001c0003 | 0/0 | 2514 | 10 | 10 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | ATGCC others(2509): Show |
chr10 | 94540788 | 94607099 | ||
| a0001c0007 | 0/0 | 2514 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | ATGCC others(2509): Show |
chr10 | 94540788 | 94607099 | ||
| a0001c0009 | 0/0 | 2514 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | ATGCC others(2509): Show |
chr10 | 94540788 | 94607099 | ||
| a0001c0011 | 0/0 | 2514 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | ATGCC others(2509): Show |
chr10 | 94540788 | 94607099 | ||
| a0001c0012 | 0/0 | 2514 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | ATGCC others(2509): Show |
chr10 | 94540788 | 94607099 | ||
| a0001c0014 | 0/0 | 2514 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | ATGCC others(2509): Show |
chr10 | 94540788 | 94607099 | ||
| a0002c0004 | 0/0 | 2514 | 3 | 0 | 0 | 3 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | ATGCC others(2509): Show |
chr10 | 94540788 | 94607099 | ||
| a0003c0006 | 0/0 | 2514 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | ATGCC others(2509): Show |
chr10 | 94540788 | 94607099 | ||
| a0004c0005 | 0/0 | 2514 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | ACGCC others(2509): Show |
chr10 | 94540788 | 94607099 | ||
| a0005c0013 | 0/0 | 2514 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | ATGCC others(2509): Show |
chr10 | 94540788 | 94607099 | ||
| a0006c0010 | 0/0 | 2514 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | ATGCC others(2509): Show |
chr10 | 94540788 | 94607099 | ||
| a0007c0015 | 0/0 | 2514 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | ATGCC others(2509): Show |
chr10 | 94540788 | 94607099 | ||
| a0008c0008 | 0/0 | 2514 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | ATGCC others(2509): Show |
chr10 | 94540788 | 94607099 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3128 | 92 | 17 | 12 | 50 | 5 | 8 | HELLS_chr10_94540788_94607099 | HELLS | GAAGG others(3123): Show |
chr10 | 94540788 | 94607099 |
| a0001c0001t0002 | 0/0 | 3128 | 80 | 11 | 5 | 50 | 2 | 12 | HELLS_chr10_94540788_94607099 | HELLS | GAAGG others(3123): Show |
chr10 | 94540788 | 94607099 |
| a0001c0002t0001 | 1/1 | 3128 | 162 | 46 | 36 | 46 | 9 | 23 | HELLS_chr10_94540788_94607099 | HELLS | GAAGG others(3123): Show |
chr10 | 94540788 | 94607099 |
| a0001c0003t0001 | 0/0 | 3128 | 10 | 10 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | GAAGG others(3123): Show |
chr10 | 94540788 | 94607099 |
| a0001c0007t0001 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | GAAGG others(3123): Show |
chr10 | 94540788 | 94607099 |
| a0001c0009t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | GAAGG others(3123): Show |
chr10 | 94540788 | 94607099 |
| a0001c0011t0001 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | GAAGG others(3123): Show |
chr10 | 94540788 | 94607099 |
| a0001c0012t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | GAAGG others(3123): Show |
chr10 | 94540788 | 94607099 |
| a0001c0014t0002 | 0/0 | 3128 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | GAAGG others(3123): Show |
chr10 | 94540788 | 94607099 |
| a0002c0004t0001 | 0/0 | 3128 | 3 | 0 | 0 | 3 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | GAAGG others(3123): Show |
chr10 | 94540788 | 94607099 |
| a0003c0006t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | GAAGG others(3123): Show |
chr10 | 94540788 | 94607099 |
| a0004c0005t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | GAAGG others(3123): Show |
chr10 | 94540788 | 94607099 |
| a0005c0013t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | GAAGG others(3123): Show |
chr10 | 94540788 | 94607099 |
| a0006c0010t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | GAAGG others(3123): Show |
chr10 | 94540788 | 94607099 |
| a0007c0015t0001 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | GAAGG others(3123): Show |
chr10 | 94540788 | 94607099 |
| a0008c0008t0001 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | GAAGG others(3123): Show |
chr10 | 94540788 | 94607099 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0300 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0315 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0003t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0007t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0009t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0011t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0012t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0001c0014t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0002c0004t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0002c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0003c0006t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0004c0005t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0005c0013t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0006c0010t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0007c0015t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| a0008c0008t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0148 | EUR | GBR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0018 | EUR | GBR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0090 | EUR | FIN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | FIN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | FIN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0269 | EUR | FIN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | CHS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | CHS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | CHS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | CHS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0251 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0250 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0326 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0248 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0254 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0322 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0320 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0226 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0304 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0253 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0232 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0278 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0310 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0235 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0288 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0228 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0294 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0325 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0219 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0295 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0276 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0270 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0316 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0255 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0229 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0245 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | IBS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0297 | EUR | IBS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0279 | EUR | IBS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0024 | EUR | IBS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0323 | EUR | IBS | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0225 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0291 | AMR | PEL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0274 | AMR | PEL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0271 | AMR | PEL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0285 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0060 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | CDX | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CDX | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02257 | hp1 | a0001 | c0012 | t0001 | g0027 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0268 | AMR | PEL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02293 | hp2 | a0001 | c0014 | t0002 | g0113 | AMR | PEL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0312 | AMR | PEL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02451 | hp2 | a0004 | c0005 | t0001 | g0321 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0230 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0242 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0327 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0265 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0258 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0062 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0234 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02738 | hp1 | a0001 | c0007 | t0001 | g0244 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0311 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0026 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0314 | AFR | ESN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02965 | hp2 | a0001 | c0009 | t0001 | g0215 | AFR | ESN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | ESN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | ESN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0222 | AFR | ESN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | ESN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0224 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0328 | AFR | ESN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0239 | AFR | ESN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0063 | AFR | ESN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0299 | AFR | ESN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0059 | AFR | ESN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0214 | AFR | MSL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03225 | hp2 | a0005 | c0013 | t0001 | g0073 | AFR | MSL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0220 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0302 | AFR | MSL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | MSL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | MSL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0237 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0044 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0303 | AFR | ESN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0238 | AFR | ESN | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03540 | hp1 | a0006 | c0010 | t0001 | g0191 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0241 | AFR | GWD | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0223 | AFR | MSL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0272 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0309 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0217 | SAS | STU | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | STU | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0227 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0221 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0034 | SAS | BEB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | BEB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0317 | SAS | BEB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | BEB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0287 | SAS | BEB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0293 | SAS | STU | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | STU | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | STU | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | STU | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0236 | AFR | YRI | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | CHB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0065 | AFR | YRI | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | YRI | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18948 | hp2 | a0002 | c0004 | t0001 | g0021 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18989 | hp1 | a0002 | c0004 | t0001 | g0021 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18995 | hp1 | a0007 | c0015 | t0001 | g0165 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19003 | hp2 | a0002 | c0004 | t0001 | g0262 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19010 | hp1 | a0001 | c0011 | t0001 | g0201 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | LWK | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | LWK | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19088 | hp2 | a0008 | c0008 | t0001 | g0261 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | YRI | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | YRI | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | ASW | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0301 | AFR | ASW | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0249 | EUR | TSI | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0252 | EUR | TSI | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0260 | EUR | TSI | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | TSI | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0024 | SAS | GIH | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0275 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0246 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02109 | hp2 | a0003 | c0006 | t0001 | g0064 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0298 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0058 | AFR | ACB | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | MSL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0061 | AFR | USA | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | USA | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0319 | AFR | USA | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0292 | AFR | USA | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | LWK | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0315 | REF | REF | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0300 | REF | REF | HELLS_chr10_94540788_94607099 | HELLS | chr10 | 94540788 | 94607099 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:94545923 | T | C | 1 | a0004 | 1 | HG02451.hp2 | start_lost | HIGH | c.2T>C | p.Met1? | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 1/22 | 136/3128 | 2/2517 | 1/838 | chr10 | 94545923 | |||
| chr10:94546415 | G | C | 1 | a0003 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.70G>C | p.Ala24Pro | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/22 | 204/3128 | 70/2517 | 24/838 | chr10 | 94546415 | |||
| chr10:94562698 | A | T | 1 | a0007 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.341A>T | p.Asn114Ile | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 5/22 | 475/3128 | 341/2517 | 114/838 | chr10 | 94562698 | |||
| chr10:94576672 | T | C | 1 | a0006 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.899T>C | p.Met300Thr | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/22 | 1033/3128 | 899/2517 | 300/838 | chr10 | 94576672 | |||
| chr10:94590458 | A | G | 1 | a0002 | 3 | NA18948.hp2 NA18989.hp1 NA19003.hp2 |
missense_variant | MODERATE | c.1534A>G | p.Thr512Ala | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 14/22 | 1668/3128 | 1534/2517 | 512/838 | chr10 | 94590458 | |||
| chr10:94593532 | A | G | 1 | a0008 | 1 | NA19088.hp2 | missense_variant | MODERATE | c.2005A>G | p.Ile669Val | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 18/22 | 2139/3128 | 2005/2517 | 669/838 | chr10 | 94593532 | |||
| chr10:94601551 | A | G | 1 | a0005 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.2446A>G | p.Ile816Val | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 22/22 | 2580/3128 | 2446/2517 | 816/838 | chr10 | 94601551 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:94554203 | A | C | 10 | a0001c0001 a0001c0003 a0001c0011 others(7): Show |
190 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
synonymous_variant | LOW | c.231A>C | p.Ile77Ile | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/22 | 365/3128 | 231/2517 | 77/838 | chr10 | 94554203 | |||
| chr10:94554242 | A | G | 2 | a0001c0003 a0003c0006 |
11 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
synonymous_variant | LOW | c.270A>G | p.Gln90Gln | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/22 | 404/3128 | 270/2517 | 90/838 | chr10 | 94554242 | |||
| chr10:94592508 | A | G | 1 | a0001c0014 | 1 | HG02293.hp2 | synonymous_variant | LOW | c.1965A>G | p.Glu655Glu | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 17/22 | 2099/3128 | 1965/2517 | 655/838 | chr10 | 94592508 | |||
| chr10:94592514 | C | T | 1 | a0001c0009 | 1 | HG02965.hp2 | splice_region_variant&synonymous_variant | LOW | c.1971C>T | p.Asn657Asn | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 17/22 | 2105/3128 | 1971/2517 | 657/838 | chr10 | 94592514 | |||
| chr10:94593516 | G | A | 1 | a0001c0011 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.1989G>A | p.Thr663Thr | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 18/22 | 2123/3128 | 1989/2517 | 663/838 | chr10 | 94593516 | |||
| chr10:94594724 | T | C | 1 | a0001c0012 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.2118T>C | p.Asp706Asp | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/22 | 2252/3128 | 2118/2517 | 706/838 | chr10 | 94594724 | |||
| chr10:94594790 | C | T | 1 | a0001c0007 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.2184C>T | p.Ile728Ile | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/22 | 2318/3128 | 2184/2517 | 728/838 | chr10 | 94594790 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:94602019 | C | T | 2 | a0001c0001t0002 a0001c0014t0002 |
81 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*397C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 22/22 | 397 | chr10 | 94602019 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:94545972 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(197): Show |
218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.31+20T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 1/21 | chr10 | 94545972 | |||||||
| chr10:94546073 | G | A | 53 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(50): Show |
59 | HG01884.hp1 HG01891.hp2 HG01978.hp2 others(56): Show |
intron_variant | MODIFIER | c.31+121G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 1/21 | chr10 | 94546073 | |||||||
| chr10:94546152 | A | G | 3 | a0001c0002t0001g0025 a0001c0002t0001g0327 a0001c0002t0001g0328 |
4 | HG02451.hp1 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+200A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 1/21 | chr10 | 94546152 | |||||||
| chr10:94546247 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.32-130T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 1/21 | chr10 | 94546247 | |||||||
| chr10:94546352 | A | G | 1 | a0005c0013t0001g0073 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.32-25A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 1/21 | chr10 | 94546352 | |||||||
| chr10:94546357 | A | G | 1 | a0001c0002t0001g0326 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.32-20A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 1/21 | chr10 | 94546357 | |||||||
| chr10:94546592 | G | A | 1 | a0001c0003t0001g0026 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.153+94G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94546592 | |||||||
| chr10:94546657 | T | C | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.153+159T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94546657 | |||||||
| chr10:94546752 | T | C | 48 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0002t0001g0003 others(45): Show |
54 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.153+254T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94546752 | |||||||
| chr10:94546848 | C | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(176): Show |
195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.153+350C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94546848 | |||||||
| chr10:94546925 | G | T | 10 | a0001c0001t0002g0086 a0001c0001t0002g0100 a0001c0001t0002g0107 others(7): Show |
10 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.153+427G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94546925 | |||||||
| chr10:94547077 | A | G | 8 | a0001c0001t0001g0017 a0001c0001t0001g0204 a0001c0001t0001g0205 others(5): Show |
9 | HG01361.hp2 HG01981.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+579A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94547077 | |||||||
| chr10:94547095 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.153+597T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94547095 | |||||||
| chr10:94547105 | A | G | 1 | a0001c0002t0001g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.153+607A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94547105 | |||||||
| chr10:94547181 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.153+683T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94547181 | |||||||
| chr10:94547286 | A | G | 2 | a0001c0001t0002g0203 a0001c0002t0001g0320 |
2 | HG01099.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.153+788A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94547286 | |||||||
| chr10:94547419 | T | G | 6 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(3): Show |
6 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+921T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94547419 | |||||||
| chr10:94547679 | A | G | 1 | a0001c0002t0001g0319 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.153+1181A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94547679 | |||||||
| chr10:94547981 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(249): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.153+1483C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94547981 | |||||||
| chr10:94548095 | T | C | 1 | a0004c0005t0001g0321 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.153+1597T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94548095 | |||||||
| chr10:94548212 | T | C | 1 | a0001c0002t0001g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.153+1714T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94548212 | |||||||
| chr10:94548379 | A | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+1881A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94548379 | |||||||
| chr10:94548404 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.153+1906A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94548404 | |||||||
| chr10:94548453 | A | G | 1 | a0001c0002t0001g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.153+1955A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94548453 | |||||||
| chr10:94549014 | G | A | 1 | a0001c0001t0002g0075 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.153+2516G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94549014 | |||||||
| chr10:94549069 | G | A | 28 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 others(25): Show |
32 | HG01884.hp1 HG01891.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.153+2571G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94549069 | |||||||
| chr10:94549197 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.153+2699A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94549197 | |||||||
| chr10:94549208 | A | G | 1 | a0001c0002t0001g0318 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.153+2710A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94549208 | |||||||
| chr10:94549500 | G | C | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | NA18990.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.153+3002G>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94549500 | |||||||
| chr10:94549666 | G | T | 1 | a0001c0002t0001g0249 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.153+3168G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94549666 | |||||||
| chr10:94549672 | A | G | 2 | a0001c0002t0001g0247 a0001c0002t0001g0248 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.153+3174A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94549672 | |||||||
| chr10:94550012 | C | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0005c0013t0001g0073 |
3 | HG02717.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.153+3514C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94550012 | |||||||
| chr10:94550030 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+3532C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94550030 | |||||||
| chr10:94550072 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.153+3574C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94550072 | |||||||
| chr10:94550150 | C | T | 1 | a0001c0001t0002g0202 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.153+3652C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94550150 | |||||||
| chr10:94550310 | C | T | 1 | a0001c0002t0001g0246 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.153+3812C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94550310 | |||||||
| chr10:94550311 | C | G | 1 | a0001c0002t0001g0246 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.153+3813C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94550311 | |||||||
| chr10:94550435 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 |
4 | HG01884.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-3691C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94550435 | |||||||
| chr10:94550532 | G | T | 2 | a0001c0002t0001g0316 a0001c0002t0001g0317 |
2 | HG01361.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.154-3594G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94550532 | |||||||
| chr10:94550617 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(63): Show |
74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.154-3509C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94550617 | |||||||
| chr10:94550632 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | NA18944.hp1 NA18959.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.154-3494G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94550632 | |||||||
| chr10:94550908 | G | T | 10 | a0001c0003t0001g0007 a0001c0003t0001g0026 a0001c0003t0001g0058 others(7): Show |
11 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.154-3218G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94550908 | |||||||
| chr10:94551344 | G | C | 1 | a0001c0001t0002g0081 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.154-2782G>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94551344 | |||||||
| chr10:94551356 | G | A | 1 | a0005c0013t0001g0073 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.154-2770G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94551356 | |||||||
| chr10:94551527 | A | G | 1 | a0001c0001t0002g0149 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.154-2599A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94551527 | |||||||
| chr10:94551567 | A | C | 25 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0030 others(22): Show |
28 | HG01891.hp2 HG02071.hp1 HG02280.hp1 others(25): Show |
intron_variant | MODIFIER | c.154-2559A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94551567 | |||||||
| chr10:94551659 | A | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-2467A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94551659 | |||||||
| chr10:94551770 | C | T | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.154-2356C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94551770 | |||||||
| chr10:94551796 | G | T | 1 | a0001c0002t0001g0245 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.154-2330G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94551796 | |||||||
| chr10:94551833 | G | A | 1 | a0001c0002t0001g0256 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.154-2293G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94551833 | |||||||
| chr10:94551841 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.154-2285G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94551841 | |||||||
| chr10:94551900 | C | T | 1 | a0001c0002t0001g0314 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.154-2226C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94551900 | |||||||
| chr10:94551975 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.154-2151G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94551975 | |||||||
| chr10:94551982 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.154-2144G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94551982 | |||||||
| chr10:94552009 | G | A | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.154-2117G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94552009 | |||||||
| chr10:94552099 | AACC | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.154-2022_154-2020d others(5): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 94552099 | ||||||
| chr10:94552246 | T | TTGTCTAG others(2): Show |
169 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(166): Show |
183 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.154-1877_154-1876i others(11): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 94552246 | ||||||
| chr10:94552504 | G | A | 1 | a0001c0001t0002g0081 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.154-1622G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94552504 | |||||||
| chr10:94552735 | G | C | 1 | a0001c0001t0002g0083 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.154-1391G>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94552735 | |||||||
| chr10:94552746 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.154-1380C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94552746 | |||||||
| chr10:94552808 | CA | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(163): Show |
180 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.154-1306delA | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 94552808 | ||||||
| chr10:94552809 | A | C | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG01361.hp2 HG01981.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.154-1317A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94552809 | |||||||
| chr10:94552810 | A | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.154-1316A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94552810 | |||||||
| chr10:94552931 | A | G | 1 | a0001c0007t0001g0244 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.154-1195A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94552931 | |||||||
| chr10:94553058 | A | G | 1 | a0001c0001t0002g0149 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.154-1068A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94553058 | |||||||
| chr10:94553175 | T | A | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.154-951T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94553175 | |||||||
| chr10:94553252 | C | CT | 8 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0002t0001g0050 others(5): Show |
8 | HG00140.hp1 HG01891.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-861dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 94553252 | ||||||
| chr10:94553329 | A | G | 1 | a0001c0002t0001g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.154-797A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94553329 | |||||||
| chr10:94553340 | C | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.154-786C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94553340 | |||||||
| chr10:94553349 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.154-777A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94553349 | |||||||
| chr10:94553432 | A | C | 1 | a0001c0001t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.154-694A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94553432 | |||||||
| chr10:94553441 | G | T | 2 | a0001c0001t0002g0145 a0001c0001t0002g0146 |
2 | NA18939.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.154-685G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94553441 | |||||||
| chr10:94553538 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.154-588C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94553538 | |||||||
| chr10:94553552 | A | AT | 35 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(32): Show |
38 | HG01175.hp2 HG01433.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.154-555dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 94553552 | ||||||
| chr10:94553552 | AT | A | 70 | a0001c0001t0001g0098 a0001c0001t0001g0103 a0001c0001t0001g0105 others(67): Show |
73 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.154-555delT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 94553552 | ||||||
| chr10:94553577 | G | A | 29 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 others(26): Show |
33 | HG01884.hp1 HG01891.hp2 HG02071.hp1 others(30): Show |
intron_variant | MODIFIER | c.154-549G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94553577 | |||||||
| chr10:94553688 | A | G | 4 | a0001c0002t0001g0305 a0001c0002t0001g0306 a0001c0002t0001g0307 others(1): Show |
4 | HG02056.hp1 NA18969.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-438A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94553688 | |||||||
| chr10:94553721 | T | C | 1 | a0001c0002t0001g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.154-405T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94553721 | |||||||
| chr10:94553763 | G | T | 1 | a0001c0002t0001g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.154-363G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94553763 | |||||||
| chr10:94553843 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0057 |
3 | HG01884.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.154-283C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94553843 | |||||||
| chr10:94553973 | A | AT | 10 | a0001c0003t0001g0007 a0001c0003t0001g0026 a0001c0003t0001g0058 others(7): Show |
11 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.154-143dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr10 | 94553973 | ||||||
| chr10:94553987 | A | G | 2 | a0001c0002t0001g0241 a0001c0002t0001g0242 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.154-139A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 2/21 | chr10 | 94553987 | |||||||
| chr10:94554347 | G | A | 66 | a0001c0002t0001g0004 a0001c0002t0001g0022 a0001c0002t0001g0023 others(63): Show |
71 | HG00323.hp2 HG00408.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.276+99G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94554347 | |||||||
| chr10:94554396 | C | G | 1 | a0001c0001t0001g0071 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.276+148C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94554396 | |||||||
| chr10:94554636 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.276+388G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94554636 | |||||||
| chr10:94554644 | G | GT | 31 | a0001c0001t0002g0080 a0001c0001t0002g0082 a0001c0001t0002g0132 others(28): Show |
34 | HG00140.hp1 HG01258.hp1 HG02129.hp1 others(31): Show |
intron_variant | MODIFIER | c.276+407dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr10 | 94554644 | ||||||
| chr10:94554652 | T | TG | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.276+404_276+405ins others(1): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94554652 | |||||||
| chr10:94554653 | T | G | 12 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0003t0001g0007 others(9): Show |
13 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.276+405T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94554653 | |||||||
| chr10:94554654 | T | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.276+406T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94554654 | |||||||
| chr10:94554655 | TG | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(45): Show |
55 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.276+408delG | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94554655 | |||||||
| chr10:94554656 | G | T | 178 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(175): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.276+408G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94554656 | |||||||
| chr10:94554842 | T | G | 1 | a0001c0001t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.276+594T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94554842 | |||||||
| chr10:94555034 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.276+786T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94555034 | |||||||
| chr10:94555469 | G | A | 1 | a0001c0002t0001g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.276+1221G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94555469 | |||||||
| chr10:94555603 | C | T | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.276+1355C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94555603 | |||||||
| chr10:94555745 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.276+1497C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94555745 | |||||||
| chr10:94555767 | T | G | 10 | a0001c0003t0001g0007 a0001c0003t0001g0026 a0001c0003t0001g0058 others(7): Show |
11 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.276+1519T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94555767 | |||||||
| chr10:94556020 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.276+1772G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94556020 | |||||||
| chr10:94556066 | C | T | 1 | a0001c0001t0002g0131 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.276+1818C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94556066 | |||||||
| chr10:94556131 | C | T | 71 | a0001c0002t0001g0004 a0001c0002t0001g0022 a0001c0002t0001g0023 others(68): Show |
76 | HG00323.hp2 HG00408.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.276+1883C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94556131 | |||||||
| chr10:94556134 | A | G | 1 | a0001c0002t0001g0297 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.276+1886A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94556134 | |||||||
| chr10:94556228 | G | A | 1 | a0001c0001t0002g0138 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.277-1911G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94556228 | |||||||
| chr10:94556711 | A | G | 1 | a0001c0002t0001g0246 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.277-1428A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94556711 | |||||||
| chr10:94556714 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0057 |
3 | HG01884.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.277-1425T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94556714 | |||||||
| chr10:94556751 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.277-1388C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94556751 | |||||||
| chr10:94556834 | ATGT | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.277-1300_277-1298d others(5): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr10 | 94556834 | ||||||
| chr10:94557051 | G | A | 10 | a0001c0003t0001g0007 a0001c0003t0001g0026 a0001c0003t0001g0058 others(7): Show |
11 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.277-1088G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94557051 | |||||||
| chr10:94557218 | A | C | 1 | a0001c0002t0001g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.277-921A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94557218 | |||||||
| chr10:94557264 | A | G | 1 | a0001c0001t0002g0130 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.277-875A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94557264 | |||||||
| chr10:94557312 | A | G | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | NA18990.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.277-827A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94557312 | |||||||
| chr10:94557450 | A | C | 1 | a0001c0001t0001g0166 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.277-689A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94557450 | |||||||
| chr10:94557519 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 |
4 | HG01884.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-620C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94557519 | |||||||
| chr10:94557821 | T | C | 2 | a0001c0002t0001g0020 a0001c0002t0001g0237 |
3 | HG03239.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.277-318T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | chr10 | 94557821 | |||||||
| chr10:94558081 | G | GT | 7 | a0001c0001t0001g0128 a0001c0001t0002g0129 a0001c0002t0001g0024 others(4): Show |
8 | HG01099.hp1 HG01256.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.277-48dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr10 | 94558081 | ||||||
| chr10:94558495 | T | G | 11 | a0001c0002t0001g0042 a0001c0003t0001g0007 a0001c0003t0001g0026 others(8): Show |
12 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.333+300T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94558495 | |||||||
| chr10:94558569 | G | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(170): Show |
188 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.333+374G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94558569 | |||||||
| chr10:94558602 | A | G | 70 | a0001c0002t0001g0004 a0001c0002t0001g0022 a0001c0002t0001g0023 others(67): Show |
75 | HG00323.hp2 HG00408.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.333+407A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94558602 | |||||||
| chr10:94558602 | A | T | 1 | a0001c0002t0001g0296 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.333+407A>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94558602 | |||||||
| chr10:94558613 | C | A | 77 | a0001c0001t0001g0098 a0001c0001t0001g0103 a0001c0001t0001g0105 others(74): Show |
81 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.333+418C>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94558613 | |||||||
| chr10:94558625 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.333+430G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94558625 | |||||||
| chr10:94558750 | C | T | 1 | a0001c0002t0001g0023 | 2 | NA18953.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.333+555C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94558750 | |||||||
| chr10:94559002 | T | G | 1 | a0001c0002t0001g0246 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.333+807T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94559002 | |||||||
| chr10:94559038 | T | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(64): Show |
75 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.333+843T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94559038 | |||||||
| chr10:94559135 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.333+940A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94559135 | |||||||
| chr10:94559270 | A | T | 1 | a0001c0001t0001g0195 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.333+1075A>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94559270 | |||||||
| chr10:94559432 | ATTTATTT others(3): Show |
A | 1 | a0001c0001t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.333+1256_333+1265d others(12): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr10 | 94559432 | ||||||
| chr10:94559526 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 |
4 | HG01884.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+1331A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94559526 | |||||||
| chr10:94559629 | A | G | 2 | a0001c0002t0001g0294 a0001c0002t0001g0295 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.333+1434A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94559629 | |||||||
| chr10:94559788 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.333+1593T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94559788 | |||||||
| chr10:94560101 | C | T | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.333+1906C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94560101 | |||||||
| chr10:94560110 | G | T | 3 | a0001c0002t0001g0025 a0001c0002t0001g0327 a0001c0002t0001g0328 |
4 | HG02451.hp1 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+1915G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94560110 | |||||||
| chr10:94560533 | A | G | 1 | a0001c0001t0002g0011 | 2 | NA18943.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.334-2158A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94560533 | |||||||
| chr10:94560656 | C | T | 1 | a0001c0002t0001g0325 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.334-2035C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94560656 | |||||||
| chr10:94560696 | C | CTAAA | 22 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0029 others(19): Show |
24 | HG01978.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.334-1976_334-1973d others(6): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr10 | 94560696 | ||||||
| chr10:94561055 | C | CA | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0167 others(4): Show |
7 | HG02015.hp1 HG02056.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-1625dupA | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr10 | 94561055 | ||||||
| chr10:94561074 | A | C | 1 | a0001c0002t0001g0031 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.334-1617A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94561074 | |||||||
| chr10:94561075 | C | A | 1 | a0001c0002t0001g0031 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.334-1616C>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94561075 | |||||||
| chr10:94561075 | CA | C | 39 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0019 others(36): Show |
44 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.334-1606delA | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr10 | 94561075 | ||||||
| chr10:94561191 | C | T | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0194 others(2): Show |
5 | HG01109.hp2 HG02717.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.334-1500C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94561191 | |||||||
| chr10:94561531 | T | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.334-1160T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94561531 | |||||||
| chr10:94561560 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.334-1131G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94561560 | |||||||
| chr10:94561658 | G | A | 28 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 others(25): Show |
32 | HG01884.hp1 HG01891.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.334-1033G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94561658 | |||||||
| chr10:94561777 | T | G | 1 | a0004c0005t0001g0321 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.334-914T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94561777 | |||||||
| chr10:94561859 | AATGTATG others(6): Show |
A | 28 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 others(25): Show |
32 | HG01884.hp1 HG01891.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.334-829_334-817del others(13): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr10 | 94561859 | ||||||
| chr10:94561883 | A | AGTATTCC others(23): Show |
1 | a0001c0001t0001g0068 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.334-808_334-807ins others(30): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94561883 | |||||||
| chr10:94561884 | A | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.334-807A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94561884 | |||||||
| chr10:94562013 | C | T | 1 | a0001c0002t0001g0320 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.334-678C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94562013 | |||||||
| chr10:94562022 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.334-669C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94562022 | |||||||
| chr10:94562027 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.334-664C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94562027 | |||||||
| chr10:94562037 | T | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.334-654T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94562037 | |||||||
| chr10:94562166 | G | T | 46 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0019 others(43): Show |
52 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.334-525G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94562166 | |||||||
| chr10:94562175 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.334-516G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94562175 | |||||||
| chr10:94562345 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.334-346A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94562345 | |||||||
| chr10:94562365 | T | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.334-326T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94562365 | |||||||
| chr10:94562432 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(64): Show |
75 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.334-259A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94562432 | |||||||
| chr10:94562647 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(194): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.334-44G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 4/21 | chr10 | 94562647 | |||||||
| chr10:94562785 | T | C | 1 | a0001c0002t0001g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.371-27T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 5/21 | chr10 | 94562785 | |||||||
| chr10:94563001 | A | G | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.435+125A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94563001 | |||||||
| chr10:94563343 | G | T | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.435+467G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94563343 | |||||||
| chr10:94563808 | C | CT | 15 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(12): Show |
17 | HG00639.hp1 HG01978.hp2 HG03490.hp2 others(14): Show |
intron_variant | MODIFIER | c.435+948dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 94563808 | ||||||
| chr10:94563808 | C | CTT | 134 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(131): Show |
145 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.435+947_435+948dup others(2): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 94563808 | ||||||
| chr10:94563808 | C | CTTT | 6 | a0001c0001t0001g0151 a0001c0001t0001g0168 a0001c0001t0001g0193 others(3): Show |
6 | HG01361.hp2 HG02071.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.435+946_435+948dup others(3): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 94563808 | ||||||
| chr10:94564035 | C | T | 1 | a0001c0002t0001g0213 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.435+1159C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94564035 | |||||||
| chr10:94564353 | C | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435+1477C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94564353 | |||||||
| chr10:94564370 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435+1494G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94564370 | |||||||
| chr10:94564394 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.435+1518A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94564394 | |||||||
| chr10:94564654 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.435+1778C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94564654 | |||||||
| chr10:94564674 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 |
4 | HG01884.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+1798C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94564674 | |||||||
| chr10:94564682 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435+1806G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94564682 | |||||||
| chr10:94564686 | A | G | 1 | a0001c0001t0002g0192 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.435+1810A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94564686 | |||||||
| chr10:94564718 | G | A | 3 | a0001c0002t0001g0301 a0001c0002t0001g0302 a0001c0002t0001g0304 |
3 | HG01109.hp2 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.435+1842G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94564718 | |||||||
| chr10:94564777 | T | A | 2 | a0001c0003t0001g0059 a0001c0003t0001g0060 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.435+1901T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94564777 | |||||||
| chr10:94565088 | G | A | 1 | a0001c0002t0001g0034 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.435+2212G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94565088 | |||||||
| chr10:94565189 | T | C | 43 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0019 others(40): Show |
48 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.435+2313T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94565189 | |||||||
| chr10:94565278 | T | A | 1 | a0001c0001t0002g0089 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.435+2402T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94565278 | |||||||
| chr10:94565440 | G | A | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.435+2564G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94565440 | |||||||
| chr10:94565563 | C | G | 2 | a0001c0001t0001g0190 a0006c0010t0001g0191 |
2 | HG01261.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.435+2687C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94565563 | |||||||
| chr10:94565690 | C | T | 71 | a0001c0002t0001g0004 a0001c0002t0001g0022 a0001c0002t0001g0023 others(68): Show |
76 | HG00323.hp2 HG00408.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.435+2814C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94565690 | |||||||
| chr10:94565712 | A | C | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.435+2836A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94565712 | |||||||
| chr10:94565766 | T | A | 1 | a0001c0001t0002g0090 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.435+2890T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94565766 | |||||||
| chr10:94565780 | C | T | 2 | a0001c0001t0002g0125 a0001c0001t0002g0126 |
2 | HG01071.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.435+2904C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94565780 | |||||||
| chr10:94565817 | C | T | 1 | a0001c0002t0001g0254 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.435+2941C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94565817 | |||||||
| chr10:94565900 | A | AT | 67 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(64): Show |
75 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.435+3037dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 94565900 | ||||||
| chr10:94565900 | AT | A | 13 | a0001c0001t0002g0125 a0001c0002t0001g0247 a0001c0002t0001g0259 others(10): Show |
14 | HG01069.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.435+3037delT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 94565900 | ||||||
| chr10:94565920 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(224): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.435+3044G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94565920 | |||||||
| chr10:94565920 | G | C | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.435+3044G>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94565920 | |||||||
| chr10:94565970 | GCAGCCTC others(7): Show |
G | 1 | a0001c0002t0001g0035 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.435+3098_435+3111d others(16): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 94565970 | ||||||
| chr10:94566113 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435+3237G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94566113 | |||||||
| chr10:94566177 | C | T | 2 | a0001c0002t0001g0291 a0001c0002t0001g0292 |
2 | HG01928.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.435+3301C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94566177 | |||||||
| chr10:94566407 | A | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435+3531A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94566407 | |||||||
| chr10:94566454 | C | A | 1 | a0001c0001t0002g0091 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.435+3578C>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94566454 | |||||||
| chr10:94566628 | A | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0005c0013t0001g0073 |
3 | HG02717.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435+3752A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94566628 | |||||||
| chr10:94566690 | C | T | 1 | a0001c0001t0002g0124 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.435+3814C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94566690 | |||||||
| chr10:94566710 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.435+3834T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94566710 | |||||||
| chr10:94566801 | C | G | 1 | a0001c0001t0002g0129 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.435+3925C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94566801 | |||||||
| chr10:94566812 | G | A | 3 | a0001c0001t0002g0011 a0001c0001t0002g0081 a0001c0001t0002g0092 |
4 | NA18943.hp2 NA18977.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+3936G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94566812 | |||||||
| chr10:94566820 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.435+3944G>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94566820 | |||||||
| chr10:94566823 | T | A | 1 | a0001c0001t0001g0197 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.435+3947T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94566823 | |||||||
| chr10:94566886 | C | G | 28 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 others(25): Show |
32 | HG01884.hp1 HG01891.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.435+4010C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94566886 | |||||||
| chr10:94566953 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(197): Show |
218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.435+4077T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94566953 | |||||||
| chr10:94567071 | T | C | 1 | a0001c0002t0001g0256 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.435+4195T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567071 | |||||||
| chr10:94567076 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.435+4200G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567076 | |||||||
| chr10:94567180 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.436-4208C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567180 | |||||||
| chr10:94567384 | C | T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0136 |
3 | HG02698.hp2 HG03834.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.436-4004C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567384 | |||||||
| chr10:94567423 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.436-3965C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567423 | |||||||
| chr10:94567513 | G | A | 2 | a0001c0001t0002g0125 a0001c0001t0002g0126 |
2 | HG01071.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.436-3875G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567513 | |||||||
| chr10:94567686 | A | G | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.436-3702A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567686 | |||||||
| chr10:94567719 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.436-3669A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567719 | |||||||
| chr10:94567739 | C | G | 40 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0019 others(37): Show |
45 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.436-3649C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567739 | |||||||
| chr10:94567776 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.436-3612T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567776 | |||||||
| chr10:94567810 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(194): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.436-3578A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567810 | |||||||
| chr10:94567874 | A | G | 1 | a0001c0001t0002g0123 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.436-3514A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567874 | |||||||
| chr10:94567879 | A | G | 1 | a0001c0002t0001g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.436-3509A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567879 | |||||||
| chr10:94567905 | G | GT | 27 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(24): Show |
30 | HG00609.hp2 HG01099.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.436-3461dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 94567905 | ||||||
| chr10:94567905 | G | GTT | 26 | a0001c0001t0001g0071 a0001c0002t0001g0002 a0001c0002t0001g0005 others(23): Show |
30 | HG01891.hp2 HG02071.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.436-3462_436-3461d others(4): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 94567905 | ||||||
| chr10:94567905 | G | GTTT | 11 | a0001c0001t0001g0056 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
11 | HG02145.hp1 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.436-3463_436-3461d others(5): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 94567905 | ||||||
| chr10:94567905 | GT | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.436-3461delT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 94567905 | ||||||
| chr10:94567905 | GTTTTTTT others(5): Show |
G | 1 | a0001c0002t0001g0260 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.436-3472_436-3461d others(14): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 94567905 | ||||||
| chr10:94567912 | T | G | 4 | a0001c0001t0001g0189 a0001c0001t0001g0194 a0001c0001t0001g0197 others(1): Show |
4 | HG01433.hp1 HG03041.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-3476T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567912 | |||||||
| chr10:94567913 | T | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(141): Show |
156 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.436-3475T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567913 | |||||||
| chr10:94567927 | T | G | 1 | a0001c0001t0002g0130 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.436-3461T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567927 | |||||||
| chr10:94567929 | G | T | 46 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0019 others(43): Show |
52 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.436-3459G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94567929 | |||||||
| chr10:94568038 | T | G | 3 | a0001c0001t0002g0093 a0001c0001t0002g0094 a0001c0001t0002g0095 |
3 | NA18950.hp2 NA18952.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.436-3350T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94568038 | |||||||
| chr10:94568069 | C | G | 1 | a0001c0002t0001g0320 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.436-3319C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94568069 | |||||||
| chr10:94568208 | C | CT | 69 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(66): Show |
77 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.436-3164dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 94568208 | ||||||
| chr10:94568208 | CT | C | 6 | a0001c0001t0002g0086 a0001c0001t0002g0096 a0001c0001t0002g0097 others(3): Show |
6 | HG02451.hp2 HG02895.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.436-3164delT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 94568208 | ||||||
| chr10:94568278 | G | A | 1 | a0001c0002t0001g0314 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.436-3110G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94568278 | |||||||
| chr10:94568414 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.436-2974G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94568414 | |||||||
| chr10:94568544 | T | C | 2 | a0001c0002t0001g0241 a0001c0002t0001g0242 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.436-2844T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94568544 | |||||||
| chr10:94568812 | A | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.436-2576A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94568812 | |||||||
| chr10:94568840 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.436-2548T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94568840 | |||||||
| chr10:94568845 | C | CT | 143 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(140): Show |
155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.436-2530dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 94568845 | ||||||
| chr10:94568862 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.436-2526A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94568862 | |||||||
| chr10:94568897 | A | G | 4 | a0001c0003t0001g0058 a0001c0003t0001g0059 a0001c0003t0001g0060 others(1): Show |
4 | HG02145.hp1 HG02486.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.436-2491A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94568897 | |||||||
| chr10:94569092 | G | A | 10 | a0001c0003t0001g0007 a0001c0003t0001g0026 a0001c0003t0001g0058 others(7): Show |
11 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.436-2296G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94569092 | |||||||
| chr10:94569140 | A | G | 1 | a0001c0002t0001g0236 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.436-2248A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94569140 | |||||||
| chr10:94569397 | T | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.436-1991T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94569397 | |||||||
| chr10:94569535 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.436-1853C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94569535 | |||||||
| chr10:94569611 | C | T | 1 | a0001c0002t0001g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.436-1777C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94569611 | |||||||
| chr10:94569650 | A | G | 2 | a0001c0001t0002g0121 a0001c0001t0002g0138 |
2 | HG00423.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.436-1738A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94569650 | |||||||
| chr10:94569793 | G | A | 76 | a0001c0001t0001g0098 a0001c0001t0001g0103 a0001c0001t0001g0105 others(73): Show |
79 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.436-1595G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94569793 | |||||||
| chr10:94570023 | G | GT | 4 | a0001c0001t0001g0168 a0001c0001t0001g0188 a0001c0001t0002g0120 others(1): Show |
4 | HG01175.hp1 HG01243.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-1358dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 94570023 | ||||||
| chr10:94570031 | A | AT | 28 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(25): Show |
31 | HG01891.hp2 HG02071.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.436-1346dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr10 | 94570031 | ||||||
| chr10:94570037 | T | A | 3 | a0001c0002t0001g0214 a0001c0002t0001g0238 a0001c0009t0001g0215 |
3 | HG02965.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.436-1351T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94570037 | |||||||
| chr10:94570049 | A | T | 4 | a0001c0003t0001g0058 a0001c0003t0001g0059 a0001c0003t0001g0060 others(1): Show |
4 | HG02145.hp1 HG02486.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.436-1339A>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94570049 | |||||||
| chr10:94570052 | T | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.436-1336T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94570052 | |||||||
| chr10:94570989 | A | G | 1 | a0001c0001t0002g0012 | 2 | HG00639.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.436-399A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94570989 | |||||||
| chr10:94571241 | T | C | 1 | a0001c0001t0002g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.436-147T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94571241 | |||||||
| chr10:94571277 | A | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.436-111A>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94571277 | |||||||
| chr10:94571326 | GAATAAAT others(8): Show |
G | 1 | a0001c0001t0002g0119 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.436-61_436-47delAA others(13): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94571326 | |||||||
| chr10:94571328 | A | G | 2 | a0001c0002t0001g0241 a0001c0002t0001g0242 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.436-60A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 6/21 | chr10 | 94571328 | |||||||
| chr10:94571467 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.477+38A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 7/21 | chr10 | 94571467 | |||||||
| chr10:94571839 | G | A | 4 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0124 others(1): Show |
4 | NA18944.hp2 NA18949.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.477+410G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 7/21 | chr10 | 94571839 | |||||||
| chr10:94572270 | A | ACAGT | 149 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(146): Show |
161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.477+846_477+849dup others(4): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr10 | 94572270 | ||||||
| chr10:94572276 | A | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.477+847A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 7/21 | chr10 | 94572276 | |||||||
| chr10:94572332 | T | C | 1 | a0001c0002t0001g0035 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.477+903T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 7/21 | chr10 | 94572332 | |||||||
| chr10:94572515 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(173): Show |
191 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.477+1086C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 7/21 | chr10 | 94572515 | |||||||
| chr10:94572786 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 |
4 | HG01884.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-1174G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 7/21 | chr10 | 94572786 | |||||||
| chr10:94572998 | C | T | 2 | a0001c0002t0001g0234 a0001c0002t0001g0235 |
2 | HG01192.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.478-962C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 7/21 | chr10 | 94572998 | |||||||
| chr10:94573149 | AGTGT | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.478-808_478-805del others(4): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr10 | 94573149 | ||||||
| chr10:94573194 | A | G | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.478-766A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 7/21 | chr10 | 94573194 | |||||||
| chr10:94573367 | G | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0029 others(18): Show |
23 | HG01978.hp2 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.478-593G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 7/21 | chr10 | 94573367 | |||||||
| chr10:94573453 | A | ATATTT | 73 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(70): Show |
81 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.478-480_478-476dup others(5): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr10 | 94573453 | ||||||
| chr10:94573453 | ATATTTTA others(3): Show |
A | 1 | a0001c0002t0001g0051 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.478-485_478-476del others(10): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr10 | 94573453 | ||||||
| chr10:94573800 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.478-160G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 7/21 | chr10 | 94573800 | |||||||
| chr10:94574218 | C | T | 1 | a0001c0002t0001g0317 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.705+31C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 8/21 | chr10 | 94574218 | |||||||
| chr10:94574279 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.705+92A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 8/21 | chr10 | 94574279 | |||||||
| chr10:94574821 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(169): Show |
187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.888+85T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94574821 | |||||||
| chr10:94575064 | T | C | 2 | a0001c0001t0002g0011 a0001c0001t0002g0092 |
3 | NA18943.hp2 NA19080.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.888+328T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575064 | |||||||
| chr10:94575098 | A | AT | 48 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0029 others(45): Show |
51 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.888+385dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575098 | ||||||
| chr10:94575098 | A | ATT | 6 | a0001c0001t0001g0067 a0001c0003t0001g0007 a0001c0003t0001g0061 others(3): Show |
7 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.888+384_888+385dup others(2): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575098 | ||||||
| chr10:94575098 | AT | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0155 others(10): Show |
14 | HG01069.hp2 HG01168.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.888+385delT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575098 | ||||||
| chr10:94575139 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.888+403A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575139 | |||||||
| chr10:94575188 | C | T | 1 | a0001c0002t0001g0037 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.888+452C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575188 | |||||||
| chr10:94575394 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(249): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.888+658T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575394 | |||||||
| chr10:94575438 | T | C | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.888+702T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575438 | |||||||
| chr10:94575455 | G | A | 1 | a0001c0002t0001g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.888+719G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575455 | |||||||
| chr10:94575533 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.888+797C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575533 | |||||||
| chr10:94575572 | A | C | 1 | a0001c0001t0002g0012 | 2 | HG00639.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.888+836A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575572 | |||||||
| chr10:94575722 | A | G | 1 | a0001c0002t0001g0289 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.889-940A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575722 | |||||||
| chr10:94575754 | TG | T | 22 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0055 others(19): Show |
23 | HG01978.hp2 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.889-898delG | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575754 | ||||||
| chr10:94575754 | TGG | T | 140 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0002t0001g0002 others(137): Show |
155 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.889-899_889-898del others(2): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575754 | ||||||
| chr10:94575762 | GGGTTGTG others(3): Show |
G | 2 | a0001c0002t0001g0041 a0001c0002t0001g0047 |
2 | NA19089.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.889-898_889-889del others(10): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575762 | ||||||
| chr10:94575762 | GGGTTGTG others(5): Show |
G | 1 | a0001c0002t0001g0046 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.889-898_889-887del others(12): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575762 | ||||||
| chr10:94575762 | GGGTTGTG others(7): Show |
G | 1 | a0001c0001t0001g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.889-898_889-885del others(14): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575762 | ||||||
| chr10:94575764 | G | T | 1 | a0001c0001t0001g0008 | 2 | HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.889-898G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575764 | |||||||
| chr10:94575764 | GTTGTGTT others(3): Show |
G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG00408.hp1 NA18956.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.889-897_889-888del others(10): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575764 | |||||||
| chr10:94575765 | T | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(121): Show |
136 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.889-897T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575765 | |||||||
| chr10:94575766 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.889-896T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575766 | |||||||
| chr10:94575766 | TGTGTTTG | T | 55 | a0001c0001t0001g0103 a0001c0001t0001g0128 a0001c0001t0001g0161 others(52): Show |
59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.889-895_889-889del others(7): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575766 | |||||||
| chr10:94575766 | TGTGTTTG others(2): Show |
T | 19 | a0001c0001t0001g0074 a0001c0001t0001g0098 a0001c0001t0001g0150 others(16): Show |
19 | HG00438.hp1 HG01257.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.889-895_889-887del others(9): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575766 | |||||||
| chr10:94575766 | TGTGTTTG others(4): Show |
T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(45): Show |
56 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.889-895_889-885del others(11): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575766 | |||||||
| chr10:94575766 | TGTGTTTG others(6): Show |
T | 1 | a0004c0005t0001g0321 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.889-895_889-883del others(13): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575766 | |||||||
| chr10:94575767 | GTGTT | G | 11 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0032 others(8): Show |
14 | HG01891.hp2 HG02071.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.889-891_889-888del others(4): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575767 | ||||||
| chr10:94575769 | G | C | 1 | a0001c0001t0001g0008 | 2 | HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.889-893G>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575769 | |||||||
| chr10:94575769 | GT | G | 5 | a0001c0002t0001g0287 a0001c0002t0001g0290 a0001c0002t0001g0292 others(2): Show |
5 | HG03942.hp2 NA18949.hp2 NA19084.hp1 others(2): Show |
intron_variant | MODIFIER | c.889-890delT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575769 | ||||||
| chr10:94575769 | GTT | G | 4 | a0001c0002t0001g0035 a0001c0002t0001g0040 a0001c0002t0001g0042 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.889-891_889-890del others(2): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575769 | ||||||
| chr10:94575770 | T | G | 7 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(4): Show |
7 | HG02135.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.889-892T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575770 | |||||||
| chr10:94575771 | T | G | 2 | a0001c0001t0001g0008 a0001c0002t0001g0034 |
3 | HG03490.hp2 HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.889-891T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575771 | |||||||
| chr10:94575771 | T | TTG | 11 | a0001c0001t0001g0055 a0001c0002t0001g0294 a0001c0002t0001g0295 others(8): Show |
12 | HG00408.hp2 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.889-849_889-848dup others(2): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575771 | ||||||
| chr10:94575771 | TTG | T | 58 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0070 others(55): Show |
63 | HG00323.hp2 HG00609.hp2 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.889-849_889-848del others(2): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575771 | ||||||
| chr10:94575771 | TTGTG | T | 28 | a0001c0001t0002g0203 a0001c0002t0001g0003 a0001c0002t0001g0019 others(25): Show |
32 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.889-851_889-848del others(4): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575771 | ||||||
| chr10:94575771 | TTGTGTGT others(1): Show |
T | 9 | a0001c0001t0002g0086 a0001c0001t0002g0108 a0001c0001t0002g0109 others(6): Show |
9 | HG01243.hp2 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.889-855_889-848del others(8): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575771 | ||||||
| chr10:94575771 | TTGTGTGT others(3): Show |
T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0002g0107 |
3 | HG02717.hp2 HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.889-857_889-848del others(10): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575771 | ||||||
| chr10:94575771 | TTGTGTGT others(5): Show |
T | 1 | a0001c0002t0001g0314 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.889-859_889-848del others(12): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr10 | 94575771 | ||||||
| chr10:94575773 | G | T | 2 | a0001c0002t0001g0041 a0001c0002t0001g0047 |
2 | NA19089.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.889-889G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575773 | |||||||
| chr10:94575774 | T | G | 2 | a0001c0001t0001g0164 a0006c0010t0001g0191 |
2 | HG02056.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.889-888T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575774 | |||||||
| chr10:94575775 | G | T | 3 | a0001c0001t0001g0164 a0001c0002t0001g0046 a0006c0010t0001g0191 |
3 | HG02056.hp2 HG03540.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.889-887G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575775 | |||||||
| chr10:94575776 | T | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG00408.hp1 NA18956.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.889-886T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575776 | |||||||
| chr10:94575777 | G | T | 14 | a0001c0001t0001g0056 a0001c0001t0001g0076 a0001c0001t0001g0077 others(11): Show |
14 | HG00408.hp1 HG02055.hp1 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.889-885G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575777 | |||||||
| chr10:94575779 | G | T | 55 | a0001c0001t0001g0103 a0001c0001t0001g0128 a0001c0001t0001g0161 others(52): Show |
59 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.889-883G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575779 | |||||||
| chr10:94575781 | G | T | 18 | a0001c0001t0001g0074 a0001c0001t0001g0098 a0001c0001t0001g0150 others(15): Show |
18 | HG01257.hp1 HG01261.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.889-881G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575781 | |||||||
| chr10:94575783 | G | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(49): Show |
60 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.889-879G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575783 | |||||||
| chr10:94575785 | G | T | 1 | a0004c0005t0001g0321 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.889-877G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94575785 | |||||||
| chr10:94576025 | G | A | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.889-637G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94576025 | |||||||
| chr10:94576026 | A | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.889-636A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94576026 | |||||||
| chr10:94576027 | C | T | 2 | a0001c0002t0001g0241 a0001c0002t0001g0242 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.889-635C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94576027 | |||||||
| chr10:94576126 | T | G | 28 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 others(25): Show |
32 | HG01884.hp1 HG01891.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.889-536T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94576126 | |||||||
| chr10:94576134 | G | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.889-528G>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94576134 | |||||||
| chr10:94576157 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0029 others(18): Show |
23 | HG01978.hp2 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.889-505A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94576157 | |||||||
| chr10:94576158 | G | T | 1 | a0001c0001t0002g0081 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.889-504G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94576158 | |||||||
| chr10:94576173 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.889-489G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94576173 | |||||||
| chr10:94576174 | C | T | 1 | a0001c0001t0002g0106 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.889-488C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94576174 | |||||||
| chr10:94576219 | G | A | 28 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 others(25): Show |
32 | HG01884.hp1 HG01891.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.889-443G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94576219 | |||||||
| chr10:94576294 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.889-368G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94576294 | |||||||
| chr10:94576394 | G | A | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.889-268G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94576394 | |||||||
| chr10:94576426 | A | G | 4 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0124 others(1): Show |
4 | NA18944.hp2 NA18949.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.889-236A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94576426 | |||||||
| chr10:94576463 | T | A | 28 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 others(25): Show |
32 | HG01884.hp1 HG01891.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.889-199T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94576463 | |||||||
| chr10:94576482 | A | G | 1 | a0005c0013t0001g0073 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.889-180A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94576482 | |||||||
| chr10:94576526 | T | C | 2 | a0001c0001t0002g0083 a0001c0001t0002g0087 |
2 | HG02155.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.889-136T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 9/21 | chr10 | 94576526 | |||||||
| chr10:94576815 | A | T | 2 | a0001c0002t0001g0241 a0001c0002t0001g0242 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1032+10A>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94576815 | |||||||
| chr10:94576938 | A | G | 1 | a0001c0002t0001g0303 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1032+133A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94576938 | |||||||
| chr10:94577022 | C | T | 1 | a0004c0005t0001g0321 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1032+217C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94577022 | |||||||
| chr10:94577075 | A | G | 25 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0030 others(22): Show |
28 | HG01891.hp2 HG02071.hp1 HG02280.hp1 others(25): Show |
intron_variant | MODIFIER | c.1032+270A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94577075 | |||||||
| chr10:94577112 | G | A | 2 | a0001c0001t0002g0096 a0001c0001t0002g0133 |
2 | NA19076.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1032+307G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94577112 | |||||||
| chr10:94577171 | G | C | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | NA18944.hp1 NA18959.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1032+366G>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94577171 | |||||||
| chr10:94577271 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1032+466T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94577271 | |||||||
| chr10:94577467 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 |
4 | HG01884.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1032+662C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94577467 | |||||||
| chr10:94577612 | G | T | 1 | a0001c0002t0001g0266 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1032+807G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94577612 | |||||||
| chr10:94577659 | G | A | 28 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 others(25): Show |
32 | HG01884.hp1 HG01891.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1032+854G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94577659 | |||||||
| chr10:94577700 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1032+895C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94577700 | |||||||
| chr10:94577717 | G | C | 1 | a0001c0002t0001g0034 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1032+912G>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94577717 | |||||||
| chr10:94578027 | C | T | 4 | a0001c0003t0001g0058 a0001c0003t0001g0059 a0001c0003t0001g0060 others(1): Show |
4 | HG02145.hp1 HG02486.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032+1222C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94578027 | |||||||
| chr10:94578070 | C | CA | 31 | a0001c0001t0001g0053 a0001c0001t0001g0189 a0001c0001t0001g0190 others(28): Show |
33 | HG00408.hp2 HG00735.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.1032+1292dupA | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94578070 | ||||||
| chr10:94578070 | CA | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(80): Show |
90 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1032+1292delA | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94578070 | ||||||
| chr10:94578070 | CAA | C | 71 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0076 others(68): Show |
76 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1032+1291_1032+129 others(6): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94578070 | ||||||
| chr10:94578070 | CAAAAAAA others(2): Show |
C | 27 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 others(24): Show |
31 | HG01884.hp1 HG01891.hp2 HG02071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1032+1284_1032+129 others(13): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94578070 | ||||||
| chr10:94578070 | CAAAAAAA others(6): Show |
C | 1 | a0001c0002t0001g0224 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1032+1280_1032+129 others(17): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94578070 | ||||||
| chr10:94578080 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1032+1275A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94578080 | |||||||
| chr10:94578098 | T | A | 1 | a0001c0001t0001g0178 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1032+1293T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94578098 | |||||||
| chr10:94578101 | A | C | 1 | a0001c0002t0001g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1032+1296A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94578101 | |||||||
| chr10:94578257 | T | TAGTC | 21 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0029 others(18): Show |
23 | HG01978.hp2 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1032+1453_1032+145 others(8): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94578257 | ||||||
| chr10:94578538 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1032+1733A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94578538 | |||||||
| chr10:94578681 | A | G | 1 | a0003c0006t0001g0064 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1032+1876A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94578681 | |||||||
| chr10:94578805 | A | G | 1 | a0001c0001t0002g0104 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1032+2000A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94578805 | |||||||
| chr10:94579181 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1033-2145C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94579181 | |||||||
| chr10:94579201 | C | CT | 151 | a0001c0001t0001g0071 a0001c0001t0001g0076 a0001c0001t0001g0077 others(148): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1033-2108dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94579201 | ||||||
| chr10:94579201 | CTTT | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0117 a0001c0001t0001g0150 others(8): Show |
11 | HG00438.hp2 HG00597.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.1033-2110_1033-210 others(7): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94579201 | ||||||
| chr10:94579201 | CTTTT | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(54): Show |
64 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.1033-2111_1033-210 others(8): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94579201 | ||||||
| chr10:94579264 | G | A | 2 | a0001c0001t0002g0145 a0001c0001t0002g0146 |
2 | NA18939.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1033-2062G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94579264 | |||||||
| chr10:94579464 | G | GAACTACT others(15): Show |
1 | a0001c0001t0002g0192 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1033-1859_1033-183 others(26): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94579464 | ||||||
| chr10:94579598 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1033-1728G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94579598 | |||||||
| chr10:94579605 | G | C | 1 | a0001c0001t0002g0081 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1033-1721G>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94579605 | |||||||
| chr10:94579707 | G | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0057 |
3 | HG01884.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1033-1619G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94579707 | |||||||
| chr10:94580034 | C | G | 1 | a0001c0002t0001g0233 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1033-1292C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580034 | |||||||
| chr10:94580117 | G | GTA | 5 | a0001c0001t0001g0117 a0001c0001t0001g0186 a0001c0001t0001g0197 others(2): Show |
5 | HG02083.hp1 HG03927.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.1033-1164_1033-116 others(6): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580117 | ||||||
| chr10:94580117 | G | GTATATAT others(3): Show |
1 | a0001c0002t0001g0289 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1033-1172_1033-116 others(14): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580117 | ||||||
| chr10:94580117 | GTA | G | 6 | a0001c0001t0001g0053 a0001c0002t0001g0004 a0001c0002t0001g0260 others(3): Show |
8 | HG01361.hp1 HG02129.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1033-1164_1033-116 others(6): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580117 | ||||||
| chr10:94580117 | GTATA | G | 17 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0190 others(14): Show |
17 | HG00423.hp2 HG01069.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1033-1166_1033-116 others(8): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580117 | ||||||
| chr10:94580117 | GTATATA | G | 17 | a0001c0001t0001g0167 a0001c0001t0001g0172 a0001c0001t0001g0177 others(14): Show |
17 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(14): Show |
intron_variant | MODIFIER | c.1033-1168_1033-116 others(10): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580117 | ||||||
| chr10:94580117 | GTATATAT others(1): Show |
G | 15 | a0001c0001t0001g0076 a0001c0001t0001g0159 a0001c0001t0001g0188 others(12): Show |
16 | HG00323.hp2 HG01175.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.1033-1170_1033-116 others(12): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580117 | ||||||
| chr10:94580117 | GTATATAT others(3): Show |
G | 17 | a0001c0001t0001g0156 a0001c0002t0001g0022 a0001c0002t0001g0250 others(14): Show |
18 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1033-1172_1033-116 others(14): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580117 | ||||||
| chr10:94580117 | GTATATAT others(5): Show |
G | 7 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0002t0001g0267 others(4): Show |
7 | HG02293.hp1 HG02300.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1033-1174_1033-116 others(16): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580117 | ||||||
| chr10:94580117 | GTATATAT others(7): Show |
G | 5 | a0001c0001t0001g0105 a0001c0001t0001g0151 a0001c0001t0001g0193 others(2): Show |
5 | HG03225.hp2 NA18973.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.1033-1176_1033-116 others(18): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580117 | ||||||
| chr10:94580117 | GTATATAT others(9): Show |
G | 1 | a0001c0001t0002g0095 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1033-1178_1033-116 others(20): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580117 | ||||||
| chr10:94580117 | GTATATAT others(11): Show |
G | 7 | a0001c0001t0002g0081 a0001c0001t0002g0093 a0001c0001t0002g0094 others(4): Show |
7 | NA18947.hp2 NA18950.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.1033-1180_1033-116 others(22): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580117 | ||||||
| chr10:94580117 | GTATATAT others(13): Show |
G | 68 | a0001c0001t0001g0098 a0001c0001t0001g0103 a0001c0001t0001g0128 others(65): Show |
71 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1033-1182_1033-116 others(24): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580117 | ||||||
| chr10:94580117 | GTATATAT others(15): Show |
G | 2 | a0001c0001t0002g0082 a0001c0014t0002g0113 |
2 | HG02129.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1033-1184_1033-116 others(26): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580117 | ||||||
| chr10:94580117 | GTATATAT others(17): Show |
G | 1 | a0004c0005t0001g0321 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1033-1186_1033-116 others(28): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580117 | ||||||
| chr10:94580117 | GTATATAT others(21): Show |
G | 4 | a0001c0001t0001g0074 a0001c0002t0001g0301 a0001c0002t0001g0302 others(1): Show |
4 | HG01109.hp2 HG02040.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1033-1190_1033-116 others(32): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580117 | ||||||
| chr10:94580117 | GTATATAT others(23): Show |
G | 1 | a0001c0001t0001g0152 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1033-1192_1033-116 others(34): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580117 | ||||||
| chr10:94580121 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0029 others(18): Show |
23 | HG01978.hp2 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1033-1205A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580121 | |||||||
| chr10:94580130 | TATATATA others(27): Show |
T | 5 | a0001c0002t0001g0024 a0001c0002t0001g0322 a0001c0002t0001g0323 others(2): Show |
6 | HG01099.hp1 HG01256.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1033-1194_1033-116 others(38): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580130 | ||||||
| chr10:94580140 | TATATATA others(19): Show |
T | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1033-1184_1033-115 others(30): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580140 | ||||||
| chr10:94580140 | TATATATA others(21): Show |
T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.1033-1184_1033-115 others(32): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580140 | ||||||
| chr10:94580142 | TATATATA others(15): Show |
T | 3 | a0001c0002t0001g0035 a0001c0002t0001g0043 a0001c0002t0001g0044 |
3 | HG03490.hp1 HG03492.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1033-1182_1033-116 others(26): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580142 | ||||||
| chr10:94580142 | TATATATA others(19): Show |
T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1033-1182_1033-115 others(30): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580142 | ||||||
| chr10:94580144 | TATATATA others(13): Show |
T | 1 | a0001c0001t0002g0012 | 2 | HG00639.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1033-1180_1033-116 others(24): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580144 | ||||||
| chr10:94580144 | TATATATA others(17): Show |
T | 6 | a0001c0003t0001g0007 a0001c0003t0001g0026 a0001c0003t0001g0061 others(3): Show |
7 | HG02109.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1033-1180_1033-115 others(28): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580144 | ||||||
| chr10:94580146 | TATATATA others(13): Show |
T | 4 | a0001c0003t0001g0058 a0001c0003t0001g0059 a0001c0003t0001g0060 others(1): Show |
4 | HG02145.hp1 HG02486.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1033-1178_1033-115 others(24): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580146 | ||||||
| chr10:94580149 | ATATATAT | A | 16 | a0001c0002t0001g0018 a0001c0002t0001g0214 a0001c0002t0001g0217 others(13): Show |
17 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1033-1176_1033-117 others(11): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580149 | |||||||
| chr10:94580151 | ATATAT | A | 13 | a0001c0002t0001g0019 a0001c0002t0001g0211 a0001c0002t0001g0212 others(10): Show |
13 | HG01109.hp1 HG01192.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1033-1174_1033-117 others(9): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580151 | |||||||
| chr10:94580152 | TATATATA others(5): Show |
T | 6 | a0001c0002t0001g0002 a0001c0002t0001g0033 a0001c0002t0001g0045 others(3): Show |
8 | HG02280.hp1 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1033-1172_1033-116 others(16): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580152 | ||||||
| chr10:94580152 | TATATATA others(9): Show |
T | 1 | a0001c0001t0001g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1033-1172_1033-115 others(20): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580152 | ||||||
| chr10:94580152 | TATATATA others(11): Show |
T | 2 | a0001c0002t0001g0042 a0001c0002t0001g0049 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1033-1172_1033-115 others(22): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580152 | ||||||
| chr10:94580153 | ATAT | A | 11 | a0001c0002t0001g0003 a0001c0002t0001g0019 a0001c0002t0001g0020 others(8): Show |
13 | HG01081.hp2 HG01884.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.1033-1172_1033-117 others(7): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580153 | |||||||
| chr10:94580154 | TATATATA others(3): Show |
T | 2 | a0001c0002t0001g0046 a0001c0002t0001g0051 |
2 | HG01891.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1033-1170_1033-116 others(14): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580154 | ||||||
| chr10:94580154 | TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0057 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1033-1170_1033-115 others(18): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580154 | ||||||
| chr10:94580156 | TATATATA others(1): Show |
T | 2 | a0001c0002t0001g0005 a0001c0002t0001g0032 |
3 | HG02071.hp1 NA19054.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1033-1168_1033-116 others(12): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580156 | ||||||
| chr10:94580158 | TATATACA others(3): Show |
T | 1 | a0001c0001t0001g0006 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1033-1166_1033-115 others(14): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580158 | ||||||
| chr10:94580160 | T | C | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0076 others(3): Show |
6 | HG02258.hp1 HG02717.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1033-1166T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580160 | |||||||
| chr10:94580160 | TATAC | T | 6 | a0001c0002t0001g0025 a0001c0002t0001g0030 a0001c0002t0001g0031 others(3): Show |
7 | HG02451.hp1 HG02647.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.1033-1164_1033-116 others(8): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580160 | ||||||
| chr10:94580162 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0053 others(21): Show |
27 | HG00408.hp1 HG00408.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.1033-1164T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580162 | |||||||
| chr10:94580162 | T | TATAC | 3 | a0001c0002t0001g0279 a0001c0002t0001g0294 a0001c0002t0001g0295 |
3 | HG01256.hp1 HG01258.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1033-1163_1033-116 others(8): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580162 | ||||||
| chr10:94580162 | TACACACA others(3): Show |
T | 1 | a0001c0002t0001g0236 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1033-1150_1033-114 others(14): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580162 | ||||||
| chr10:94580164 | C | T | 48 | a0001c0001t0001g0015 a0001c0001t0001g0163 a0001c0001t0001g0164 others(45): Show |
53 | HG00140.hp2 HG00639.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.1033-1162C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580164 | |||||||
| chr10:94580170 | C | T | 1 | a0001c0002t0001g0302 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1033-1156C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580170 | |||||||
| chr10:94580183 | AC | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0002t0001g0034 others(3): Show |
6 | HG02258.hp2 HG02922.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1033-1142delC | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580183 | |||||||
| chr10:94580183 | ACATT | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0179 a0001c0001t0001g0185 others(4): Show |
10 | HG01361.hp2 HG02083.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.1033-1142_1033-113 others(8): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580183 | |||||||
| chr10:94580185 | A | AT | 12 | a0001c0002t0001g0024 a0001c0002t0001g0265 a0001c0002t0001g0266 others(9): Show |
13 | HG00408.hp2 HG01099.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1033-1122dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580185 | ||||||
| chr10:94580185 | A | T | 8 | a0001c0001t0001g0076 a0001c0002t0001g0004 a0001c0002t0001g0034 others(5): Show |
9 | HG02129.hp2 HG02258.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.1033-1141A>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580185 | |||||||
| chr10:94580185 | AT | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(11): Show |
16 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.1033-1122delT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580185 | ||||||
| chr10:94580185 | ATT | A | 118 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0016 others(115): Show |
124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.1033-1123_1033-112 others(6): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr10 | 94580185 | ||||||
| chr10:94580186 | T | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0164 |
3 | HG02056.hp2 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1033-1140T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580186 | |||||||
| chr10:94580186 | T | C | 26 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0098 others(23): Show |
26 | HG01175.hp1 HG01257.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.1033-1140T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580186 | |||||||
| chr10:94580187 | T | A | 26 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0098 others(23): Show |
26 | HG01175.hp1 HG01257.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.1033-1139T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580187 | |||||||
| chr10:94580193 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0057 |
3 | HG01884.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1033-1133T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580193 | |||||||
| chr10:94580349 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 |
4 | HG01884.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1033-977T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580349 | |||||||
| chr10:94580440 | C | G | 2 | a0001c0001t0001g0199 a0004c0005t0001g0321 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1033-886C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580440 | |||||||
| chr10:94580486 | A | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.1033-840A>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580486 | |||||||
| chr10:94580575 | T | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0029 others(7): Show |
11 | HG01978.hp2 HG02258.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.1033-751T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580575 | |||||||
| chr10:94580579 | T | C | 2 | a0001c0001t0002g0075 a0001c0001t0002g0082 |
2 | HG02129.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1033-747T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580579 | |||||||
| chr10:94580860 | A | G | 3 | a0001c0001t0002g0088 a0001c0001t0002g0115 a0001c0001t0002g0144 |
3 | NA18978.hp1 NA18983.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1033-466A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94580860 | |||||||
| chr10:94581127 | A | G | 2 | a0001c0001t0001g0168 a0007c0015t0001g0165 |
2 | NA18985.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1033-199A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94581127 | |||||||
| chr10:94581184 | T | C | 10 | a0001c0003t0001g0007 a0001c0003t0001g0026 a0001c0003t0001g0058 others(7): Show |
11 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1033-142T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94581184 | |||||||
| chr10:94581282 | T | C | 1 | a0001c0002t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1033-44T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 10/21 | chr10 | 94581282 | |||||||
| chr10:94581553 | C | A | 1 | a0001c0002t0001g0260 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1229+31C>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 11/21 | chr10 | 94581553 | |||||||
| chr10:94581571 | T | TA | 10 | a0001c0003t0001g0007 a0001c0003t0001g0026 a0001c0003t0001g0058 others(7): Show |
11 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1229+50dupA | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr10 | 94581571 | ||||||
| chr10:94581579 | A | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1229+57A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 11/21 | chr10 | 94581579 | |||||||
| chr10:94581782 | T | C | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1229+260T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 11/21 | chr10 | 94581782 | |||||||
| chr10:94581804 | A | T | 1 | a0001c0001t0002g0138 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1229+282A>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 11/21 | chr10 | 94581804 | |||||||
| chr10:94581855 | T | C | 4 | a0001c0003t0001g0058 a0001c0003t0001g0059 a0001c0003t0001g0060 others(1): Show |
4 | HG02145.hp1 HG02486.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1229+333T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 11/21 | chr10 | 94581855 | |||||||
| chr10:94582173 | T | C | 2 | a0001c0002t0001g0020 a0001c0002t0001g0237 |
3 | HG03239.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1229+651T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 11/21 | chr10 | 94582173 | |||||||
| chr10:94582231 | T | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1229+709T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 11/21 | chr10 | 94582231 | |||||||
| chr10:94582251 | C | G | 2 | a0001c0001t0001g0199 a0004c0005t0001g0321 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1230-712C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 11/21 | chr10 | 94582251 | |||||||
| chr10:94582263 | T | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1230-700T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 11/21 | chr10 | 94582263 | |||||||
| chr10:94582384 | G | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0196 |
2 | HG02300.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1230-579G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 11/21 | chr10 | 94582384 | |||||||
| chr10:94582415 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1230-548A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 11/21 | chr10 | 94582415 | |||||||
| chr10:94582584 | G | A | 1 | a0001c0002t0001g0218 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1230-379G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 11/21 | chr10 | 94582584 | |||||||
| chr10:94582674 | T | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1230-289T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 11/21 | chr10 | 94582674 | |||||||
| chr10:94583118 | C | T | 1 | a0001c0002t0001g0325 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1326+59C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94583118 | |||||||
| chr10:94583132 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1326+73T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94583132 | |||||||
| chr10:94583305 | G | A | 1 | a0001c0011t0001g0201 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1326+246G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94583305 | |||||||
| chr10:94583410 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1326+351G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94583410 | |||||||
| chr10:94583471 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1326+412G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94583471 | |||||||
| chr10:94583703 | TTGTGTAA others(5): Show |
T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1326+650_1326+661d others(14): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr10 | 94583703 | ||||||
| chr10:94583724 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1326+665A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94583724 | |||||||
| chr10:94583942 | C | G | 1 | a0001c0002t0001g0303 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1326+883C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94583942 | |||||||
| chr10:94584267 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1326+1208A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94584267 | |||||||
| chr10:94584328 | T | G | 1 | a0004c0005t0001g0321 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1326+1269T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94584328 | |||||||
| chr10:94584574 | T | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1326+1515T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94584574 | |||||||
| chr10:94584701 | T | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1326+1642T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94584701 | |||||||
| chr10:94584845 | A | G | 2 | a0001c0002t0001g0241 a0001c0002t0001g0242 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1326+1786A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94584845 | |||||||
| chr10:94585090 | C | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(169): Show |
187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.1326+2031C>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94585090 | |||||||
| chr10:94585362 | G | GT | 12 | a0001c0002t0001g0002 a0001c0002t0001g0033 a0001c0002t0001g0042 others(9): Show |
14 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1326+2315dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr10 | 94585362 | ||||||
| chr10:94585362 | GT | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(173): Show |
192 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1326+2315delT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr10 | 94585362 | ||||||
| chr10:94585371 | T | G | 2 | a0001c0001t0002g0203 a0001c0002t0001g0032 |
2 | HG02071.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1326+2312T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94585371 | |||||||
| chr10:94585385 | GT | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
8 | HG01884.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1326+2337delT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr10 | 94585385 | ||||||
| chr10:94585385 | GTT | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(165): Show |
182 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.1326+2336_1326+233 others(6): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr10 | 94585385 | ||||||
| chr10:94585396 | T | G | 1 | a0004c0005t0001g0321 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1326+2337T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94585396 | |||||||
| chr10:94585406 | GT | G | 27 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(24): Show |
30 | HG01884.hp1 HG01978.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1326+2359delT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr10 | 94585406 | ||||||
| chr10:94585437 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1326+2378G>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94585437 | |||||||
| chr10:94585572 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1326+2513C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94585572 | |||||||
| chr10:94585689 | A | AT | 11 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(8): Show |
12 | HG01978.hp2 HG02071.hp1 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.1327-2523dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr10 | 94585689 | ||||||
| chr10:94585742 | A | AGTAGT | 25 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0030 others(22): Show |
28 | HG01891.hp2 HG02071.hp1 HG02280.hp1 others(25): Show |
intron_variant | MODIFIER | c.1327-2485_1327-248 others(9): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr10 | 94585742 | ||||||
| chr10:94585896 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1327-2333A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94585896 | |||||||
| chr10:94586110 | T | A | 5 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG02258.hp1 HG02602.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-2119T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94586110 | |||||||
| chr10:94586131 | A | AT | 46 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0019 others(43): Show |
52 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.1327-2091dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr10 | 94586131 | ||||||
| chr10:94586189 | C | T | 1 | a0005c0013t0001g0073 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1327-2040C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94586189 | |||||||
| chr10:94586190 | G | A | 1 | a0001c0002t0001g0213 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1327-2039G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94586190 | |||||||
| chr10:94586195 | A | T | 1 | a0001c0001t0002g0083 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1327-2034A>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94586195 | |||||||
| chr10:94586207 | A | G | 201 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(198): Show |
219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1327-2022A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94586207 | |||||||
| chr10:94586273 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1327-1956A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94586273 | |||||||
| chr10:94586411 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0005c0013t0001g0073 |
3 | HG02717.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1327-1818G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94586411 | |||||||
| chr10:94586417 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0160 others(1): Show |
6 | HG00639.hp2 HG01123.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1327-1812G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94586417 | |||||||
| chr10:94586548 | A | G | 28 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 others(25): Show |
32 | HG01884.hp1 HG01891.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1327-1681A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94586548 | |||||||
| chr10:94586622 | A | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.1327-1607A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94586622 | |||||||
| chr10:94586688 | T | G | 27 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0002t0001g0002 others(24): Show |
30 | HG01891.hp2 HG02071.hp1 HG02280.hp1 others(27): Show |
intron_variant | MODIFIER | c.1327-1541T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94586688 | |||||||
| chr10:94586691 | G | T | 24 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
27 | HG01978.hp2 HG02109.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.1327-1538G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94586691 | |||||||
| chr10:94586694 | G | T | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1327-1535G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94586694 | |||||||
| chr10:94586991 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1327-1238G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94586991 | |||||||
| chr10:94587029 | C | T | 4 | a0001c0001t0002g0099 a0001c0001t0002g0116 a0001c0001t0002g0149 others(1): Show |
4 | HG02027.hp1 HG02132.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327-1200C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94587029 | |||||||
| chr10:94587072 | T | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.1327-1157T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94587072 | |||||||
| chr10:94587078 | C | T | 1 | a0001c0002t0001g0314 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1327-1151C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94587078 | |||||||
| chr10:94587096 | T | C | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | NA18990.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1327-1133T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94587096 | |||||||
| chr10:94587192 | C | T | 17 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(14): Show |
17 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1327-1037C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94587192 | |||||||
| chr10:94587235 | ATTAAAAA others(11): Show |
A | 1 | a0001c0001t0001g0186 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1327-985_1327-968d others(20): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr10 | 94587235 | ||||||
| chr10:94587341 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1327-888A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94587341 | |||||||
| chr10:94587354 | C | A | 1 | a0001c0001t0002g0142 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1327-875C>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94587354 | |||||||
| chr10:94587427 | T | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 |
4 | HG01884.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327-802T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94587427 | |||||||
| chr10:94587427 | T | TTGTG | 4 | a0001c0003t0001g0058 a0001c0003t0001g0059 a0001c0003t0001g0060 others(1): Show |
4 | HG02145.hp1 HG02486.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1327-787_1327-784d others(6): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr10 | 94587427 | ||||||
| chr10:94587667 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1327-562T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94587667 | |||||||
| chr10:94587834 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1327-395G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94587834 | |||||||
| chr10:94588045 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.1327-184G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94588045 | |||||||
| chr10:94588165 | C | T | 1 | a0001c0002t0001g0230 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1327-64C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 12/21 | chr10 | 94588165 | |||||||
| chr10:94588396 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0207 |
3 | HG02071.hp2 NA18942.hp1 NA18984.hp1 |
splice_region_variant&intron_variant | LOW | c.1488+6G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94588396 | |||||||
| chr10:94588478 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0160 |
5 | HG00639.hp2 HG01123.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1488+88C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94588478 | |||||||
| chr10:94588497 | G | A | 69 | a0001c0002t0001g0004 a0001c0002t0001g0022 a0001c0002t0001g0023 others(66): Show |
74 | HG00323.hp2 HG00408.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.1488+107G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94588497 | |||||||
| chr10:94588577 | C | T | 325 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(322): Show |
355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.1488+187C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94588577 | |||||||
| chr10:94588651 | G | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG01978.hp2 HG03710.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1488+261G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94588651 | |||||||
| chr10:94588873 | A | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(193): Show |
214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1488+483A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94588873 | |||||||
| chr10:94588937 | G | A | 2 | a0001c0001t0002g0140 a0001c0001t0002g0148 |
2 | HG00140.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.1488+547G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94588937 | |||||||
| chr10:94589016 | G | T | 1 | a0001c0002t0001g0281 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1488+626G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589016 | |||||||
| chr10:94589128 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(194): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1488+738G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589128 | |||||||
| chr10:94589161 | T | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.1488+771T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589161 | |||||||
| chr10:94589161 | TA | T | 28 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 others(25): Show |
32 | HG01884.hp1 HG01891.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1488+781delA | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr10 | 94589161 | ||||||
| chr10:94589354 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1488+964T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589354 | |||||||
| chr10:94589365 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1488+975A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589365 | |||||||
| chr10:94589409 | G | A | 10 | a0001c0001t0002g0086 a0001c0001t0002g0100 a0001c0001t0002g0107 others(7): Show |
10 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1489-1004G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589409 | |||||||
| chr10:94589414 | G | T | 4 | a0001c0002t0001g0022 a0001c0002t0001g0280 a0001c0002t0001g0283 others(1): Show |
5 | NA18973.hp1 NA18991.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489-999G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589414 | |||||||
| chr10:94589459 | C | T | 5 | a0001c0002t0001g0024 a0001c0002t0001g0322 a0001c0002t0001g0323 others(2): Show |
6 | HG01099.hp1 HG01256.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1489-954C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589459 | |||||||
| chr10:94589460 | A | G | 5 | a0001c0002t0001g0024 a0001c0002t0001g0322 a0001c0002t0001g0323 others(2): Show |
6 | HG01099.hp1 HG01256.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1489-953A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589460 | |||||||
| chr10:94589491 | A | T | 1 | a0005c0013t0001g0073 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1489-922A>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589491 | |||||||
| chr10:94589535 | TATC | T | 10 | a0001c0003t0001g0007 a0001c0003t0001g0026 a0001c0003t0001g0058 others(7): Show |
11 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1489-875_1489-873d others(5): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr10 | 94589535 | ||||||
| chr10:94589596 | C | G | 10 | a0001c0003t0001g0007 a0001c0003t0001g0026 a0001c0003t0001g0058 others(7): Show |
11 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1489-817C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589596 | |||||||
| chr10:94589680 | C | CT | 46 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(43): Show |
52 | HG00735.hp2 HG01192.hp1 HG01496.hp1 others(49): Show |
intron_variant | MODIFIER | c.1489-709dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr10 | 94589680 | ||||||
| chr10:94589680 | CT | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(63): Show |
74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1489-709delT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr10 | 94589680 | ||||||
| chr10:94589680 | CTTTT | C | 70 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(67): Show |
74 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1489-712_1489-709d others(6): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr10 | 94589680 | ||||||
| chr10:94589717 | C | T | 1 | a0001c0002t0001g0233 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1489-696C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589717 | |||||||
| chr10:94589760 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1489-653T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589760 | |||||||
| chr10:94589773 | G | C | 1 | a0001c0002t0001g0289 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1489-640G>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589773 | |||||||
| chr10:94589844 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1489-569G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589844 | |||||||
| chr10:94589908 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1489-505C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589908 | |||||||
| chr10:94589933 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1489-480C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589933 | |||||||
| chr10:94589945 | C | T | 1 | a0001c0002t0001g0238 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1489-468C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94589945 | |||||||
| chr10:94590189 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 |
4 | HG01884.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1489-224A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94590189 | |||||||
| chr10:94590266 | A | G | 2 | a0001c0002t0001g0045 a0001c0002t0001g0048 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1489-147A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 13/21 | chr10 | 94590266 | |||||||
| chr10:94590852 | G | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0029 others(18): Show |
23 | HG01978.hp2 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1767+76G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 15/21 | chr10 | 94590852 | |||||||
| chr10:94591003 | T | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1767+227T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 15/21 | chr10 | 94591003 | |||||||
| chr10:94591015 | A | G | 4 | a0001c0002t0001g0025 a0001c0002t0001g0072 a0001c0002t0001g0327 others(1): Show |
5 | HG02451.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1767+239A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 15/21 | chr10 | 94591015 | |||||||
| chr10:94591125 | C | T | 3 | a0001c0001t0001g0167 a0001c0001t0001g0184 a0001c0001t0001g0195 |
3 | HG02027.hp2 NA19004.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1767+349C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 15/21 | chr10 | 94591125 | |||||||
| chr10:94591490 | C | T | 77 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(74): Show |
81 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.1767+714C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 15/21 | chr10 | 94591490 | |||||||
| chr10:94591643 | G | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1768-586G>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 15/21 | chr10 | 94591643 | |||||||
| chr10:94591646 | G | A | 1 | a0001c0002t0001g0287 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1768-583G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 15/21 | chr10 | 94591646 | |||||||
| chr10:94591755 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0160 others(1): Show |
6 | HG00639.hp2 HG01123.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1768-474A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 15/21 | chr10 | 94591755 | |||||||
| chr10:94592532 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1971+18A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 17/21 | chr10 | 94592532 | |||||||
| chr10:94592638 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0005c0013t0001g0073 |
3 | HG02717.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1971+124G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 17/21 | chr10 | 94592638 | |||||||
| chr10:94592725 | TTAA | T | 10 | a0001c0003t0001g0007 a0001c0003t0001g0026 a0001c0003t0001g0058 others(7): Show |
11 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1971+217_1971+219d others(5): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr10 | 94592725 | ||||||
| chr10:94592936 | T | G | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1971+422T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 17/21 | chr10 | 94592936 | |||||||
| chr10:94593081 | G | A | 1 | a0001c0002t0001g0243 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1972-418G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 17/21 | chr10 | 94593081 | |||||||
| chr10:94593106 | T | C | 4 | a0001c0001t0002g0010 a0001c0001t0002g0114 a0001c0001t0002g0136 others(1): Show |
5 | HG02698.hp2 HG03017.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1972-393T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 17/21 | chr10 | 94593106 | |||||||
| chr10:94593175 | C | G | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1972-324C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 17/21 | chr10 | 94593175 | |||||||
| chr10:94593210 | T | C | 28 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 others(25): Show |
32 | HG01884.hp1 HG01891.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1972-289T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 17/21 | chr10 | 94593210 | |||||||
| chr10:94593276 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1972-223G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 17/21 | chr10 | 94593276 | |||||||
| chr10:94593422 | T | G | 1 | a0001c0001t0001g0077 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1972-77T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 17/21 | chr10 | 94593422 | |||||||
| chr10:94593444 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
212 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.1972-55G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 17/21 | chr10 | 94593444 | |||||||
| chr10:94593665 | AT | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(244): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.2088+65delT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr10 | 94593665 | ||||||
| chr10:94593731 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 |
4 | HG01884.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+116C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 18/21 | chr10 | 94593731 | |||||||
| chr10:94593740 | G | A | 28 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 others(25): Show |
32 | HG01884.hp1 HG01891.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.2088+125G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 18/21 | chr10 | 94593740 | |||||||
| chr10:94593903 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0057 |
3 | HG01884.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2088+288C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 18/21 | chr10 | 94593903 | |||||||
| chr10:94593960 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2088+345C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 18/21 | chr10 | 94593960 | |||||||
| chr10:94593971 | A | AT | 11 | a0001c0001t0001g0029 a0001c0001t0001g0157 a0001c0001t0002g0080 others(8): Show |
11 | HG01109.hp2 HG01358.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.2088+377dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr10 | 94593971 | ||||||
| chr10:94593971 | AT | A | 17 | a0001c0001t0001g0128 a0001c0001t0001g0166 a0001c0001t0001g0183 others(14): Show |
18 | HG01192.hp1 HG01257.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.2088+377delT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr10 | 94593971 | ||||||
| chr10:94594003 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.2088+388T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 18/21 | chr10 | 94594003 | |||||||
| chr10:94594058 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 |
4 | HG01884.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+443C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 18/21 | chr10 | 94594058 | |||||||
| chr10:94594061 | G | A | 1 | a0005c0013t0001g0073 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2088+446G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 18/21 | chr10 | 94594061 | |||||||
| chr10:94594383 | A | G | 78 | a0001c0001t0001g0128 a0001c0001t0002g0009 a0001c0001t0002g0010 others(75): Show |
82 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.2089-312A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 18/21 | chr10 | 94594383 | |||||||
| chr10:94594413 | A | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(5): Show |
9 | HG01978.hp2 HG03490.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.2089-282A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 18/21 | chr10 | 94594413 | |||||||
| chr10:94594527 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.2089-168G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 18/21 | chr10 | 94594527 | |||||||
| chr10:94594619 | G | A | 1 | a0001c0001t0001g0006 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2089-76G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 18/21 | chr10 | 94594619 | |||||||
| chr10:94595015 | G | C | 1 | a0001c0001t0002g0120 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2248+161G>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94595015 | |||||||
| chr10:94595054 | C | G | 1 | a0001c0001t0002g0090 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2248+200C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94595054 | |||||||
| chr10:94595091 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.2248+237G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94595091 | |||||||
| chr10:94595103 | C | CT | 25 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0030 others(22): Show |
28 | HG01891.hp2 HG02071.hp1 HG02280.hp1 others(25): Show |
intron_variant | MODIFIER | c.2248+250dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr10 | 94595103 | ||||||
| chr10:94595176 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2248+322C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94595176 | |||||||
| chr10:94595227 | C | CA | 74 | a0001c0001t0001g0128 a0001c0001t0002g0009 a0001c0001t0002g0010 others(71): Show |
77 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.2248+384dupA | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr10 | 94595227 | ||||||
| chr10:94595307 | C | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0005c0013t0001g0073 |
3 | HG02717.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2248+453C>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94595307 | |||||||
| chr10:94595309 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.2248+455C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94595309 | |||||||
| chr10:94595358 | A | G | 1 | a0001c0001t0002g0126 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2248+504A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94595358 | |||||||
| chr10:94595629 | T | C | 3 | a0001c0003t0001g0059 a0001c0003t0001g0060 a0001c0003t0001g0065 |
3 | HG02145.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2248+775T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94595629 | |||||||
| chr10:94595647 | G | A | 1 | a0001c0002t0001g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2248+793G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94595647 | |||||||
| chr10:94595771 | T | A | 1 | a0001c0002t0001g0212 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2248+917T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94595771 | |||||||
| chr10:94596055 | A | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.2249-805A>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94596055 | |||||||
| chr10:94596213 | T | C | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2249-647T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94596213 | |||||||
| chr10:94596424 | C | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(169): Show |
187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.2249-436C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94596424 | |||||||
| chr10:94596448 | A | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0184 |
2 | NA19004.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2249-412A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94596448 | |||||||
| chr10:94596449 | T | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0029 others(19): Show |
24 | HG01081.hp2 HG01978.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.2249-411T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94596449 | |||||||
| chr10:94596588 | CTGT | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2249-271_2249-269d others(5): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94596588 | |||||||
| chr10:94596751 | A | G | 1 | a0001c0012t0001g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2249-109A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94596751 | |||||||
| chr10:94596814 | A | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.2249-46A>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 19/21 | chr10 | 94596814 | |||||||
| chr10:94597265 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.2422+154A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94597265 | |||||||
| chr10:94597579 | CTGGAGTG others(4): Show |
C | 1 | a0001c0002t0001g0034 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2422+469_2422+479d others(13): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94597579 | |||||||
| chr10:94597588 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2422+477G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94597588 | |||||||
| chr10:94597764 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(249): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.2422+653T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94597764 | |||||||
| chr10:94598004 | C | CT | 6 | a0001c0001t0002g0088 a0001c0002t0001g0274 a0001c0002t0001g0275 others(3): Show |
6 | HG01123.hp1 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2422+907dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr10 | 94598004 | ||||||
| chr10:94598004 | CT | C | 13 | a0001c0001t0001g0188 a0001c0002t0001g0003 a0001c0002t0001g0019 others(10): Show |
16 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.2422+907delT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr10 | 94598004 | ||||||
| chr10:94598018 | T | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2422+907T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94598018 | |||||||
| chr10:94598039 | C | CTTA | 6 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0001c0002t0001g0252 others(3): Show |
6 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+930_2422+932d others(5): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr10 | 94598039 | ||||||
| chr10:94598328 | T | C | 1 | a0001c0001t0002g0121 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2422+1217T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94598328 | |||||||
| chr10:94598379 | A | C | 1 | a0001c0001t0001g0029 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2422+1268A>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94598379 | |||||||
| chr10:94598420 | A | G | 5 | a0001c0002t0001g0024 a0001c0002t0001g0322 a0001c0002t0001g0323 others(2): Show |
6 | HG01099.hp1 HG01256.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2422+1309A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94598420 | |||||||
| chr10:94598606 | G | GT | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0002t0001g0034 others(3): Show |
6 | HG01433.hp2 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2422+1514dupT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr10 | 94598606 | ||||||
| chr10:94598606 | GT | G | 6 | a0001c0002t0001g0219 a0001c0002t0001g0232 a0001c0002t0001g0237 others(3): Show |
6 | HG01169.hp1 HG01257.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.2422+1514delT | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr10 | 94598606 | ||||||
| chr10:94598606 | GTT | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(166): Show |
184 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.2422+1513_2422+151 others(6): Show |
HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr10 | 94598606 | ||||||
| chr10:94598613 | T | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.2422+1502T>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94598613 | |||||||
| chr10:94598625 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2422+1514T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94598625 | |||||||
| chr10:94598626 | A | T | 2 | a0001c0002t0001g0241 a0001c0002t0001g0242 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2422+1515A>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94598626 | |||||||
| chr10:94598680 | C | A | 1 | a0001c0001t0002g0111 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2422+1569C>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94598680 | |||||||
| chr10:94598709 | T | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2422+1598T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94598709 | |||||||
| chr10:94598768 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(249): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.2422+1657A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94598768 | |||||||
| chr10:94598855 | T | C | 6 | a0001c0003t0001g0007 a0001c0003t0001g0026 a0001c0003t0001g0061 others(3): Show |
7 | HG02109.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2422+1744T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94598855 | |||||||
| chr10:94598863 | A | G | 1 | a0001c0002t0001g0303 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2422+1752A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94598863 | |||||||
| chr10:94599116 | A | G | 1 | a0001c0002t0001g0266 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2422+2005A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94599116 | |||||||
| chr10:94599116 | A | T | 1 | a0001c0001t0002g0130 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2422+2005A>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94599116 | |||||||
| chr10:94599132 | G | C | 1 | a0001c0001t0002g0127 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2422+2021G>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94599132 | |||||||
| chr10:94599384 | C | T | 1 | a0001c0002t0001g0238 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2423-2144C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94599384 | |||||||
| chr10:94599605 | C | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.2423-1923C>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94599605 | |||||||
| chr10:94599734 | T | A | 1 | a0001c0001t0002g0131 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2423-1794T>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94599734 | |||||||
| chr10:94599903 | T | C | 1 | a0001c0002t0001g0229 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2423-1625T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94599903 | |||||||
| chr10:94600033 | A | G | 1 | a0001c0002t0001g0213 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2423-1495A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94600033 | |||||||
| chr10:94600041 | A | G | 78 | a0001c0001t0001g0128 a0001c0001t0002g0009 a0001c0001t0002g0010 others(75): Show |
82 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.2423-1487A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94600041 | |||||||
| chr10:94600108 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 |
4 | HG01884.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2423-1420C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94600108 | |||||||
| chr10:94600151 | C | A | 1 | a0001c0002t0001g0303 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2423-1377C>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94600151 | |||||||
| chr10:94600219 | A | G | 10 | a0001c0003t0001g0007 a0001c0003t0001g0026 a0001c0003t0001g0058 others(7): Show |
11 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2423-1309A>G | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94600219 | |||||||
| chr10:94600262 | G | T | 1 | a0001c0002t0001g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2423-1266G>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94600262 | |||||||
| chr10:94600292 | T | TA | 158 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(155): Show |
171 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.2423-1219dupA | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr10 | 94600292 | ||||||
| chr10:94600375 | A | T | 1 | a0001c0002t0001g0220 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2423-1153A>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94600375 | |||||||
| chr10:94600416 | G | A | 1 | a0001c0002t0001g0236 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2423-1112G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94600416 | |||||||
| chr10:94600692 | C | T | 1 | a0001c0002t0001g0269 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2423-836C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94600692 | |||||||
| chr10:94600921 | T | C | 2 | a0001c0002t0001g0045 a0001c0002t0001g0048 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2423-607T>C | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94600921 | |||||||
| chr10:94601003 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(194): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.2423-525G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94601003 | |||||||
| chr10:94601167 | C | T | 2 | a0001c0001t0001g0156 a0001c0002t0001g0236 |
2 | NA18522.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2423-361C>T | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94601167 | |||||||
| chr10:94601300 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2423-228G>A | HELLS | ENSG00000119969.16 | transcript | ENST00000348459.10 | protein_coding | 21/21 | chr10 | 94601300 |