Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6492 |
| ensemblid | ENSG00000112246.10 |
| hgncid | 10882 |
| symbol | SIM1 |
| name | SIM bHLH transcription factor 1 |
| refseq_nuc | NM_005068.3 |
| refseq_prot | NP_005059.2 |
| ensembl_nuc | ENST00000369208.8 |
| ensembl_prot | ENSP00000358210.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 100385009 |
| end | 100464921 |
| strand | - |
| ver | v1.2 |
| region | chr6:100385009-100464921 |
| region5000 | chr6:100380009-100469921 |
| regionname0 | SIM1_chr6_100385009_100464921 |
| regionname5000 | SIM1_chr6_100380009_100469921 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 766 | 237 | 79 | 42 | 78 | 14 | 22 | 57 | SIM1_chr6_100380009_100469921 | SIM1 | MKEKS others(761): Show |
chr6 | 100380009 | 100469921 |
| a0002 | 0/0 | 766 | 79 | 0 | 12 | 55 | 4 | 8 | 43 | SIM1_chr6_100380009_100469921 | SIM1 | MKEKS others(761): Show |
chr6 | 100380009 | 100469921 |
| a0003 | 0/0 | 766 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | MKEKS others(761): Show |
chr6 | 100380009 | 100469921 |
| a0004 | 0/0 | 766 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | MKEKS others(761): Show |
chr6 | 100380009 | 100469921 |
| a0005 | 0/0 | 766 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | MKEKS others(761): Show |
chr6 | 100380009 | 100469921 |
| a0006 | 0/0 | 766 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | MKEKS others(761): Show |
chr6 | 100380009 | 100469921 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2298 | 231 | 78 | 42 | 77 | 13 | 19 | SIM1_chr6_100380009_100469921 | SIM1 | ATGAA others(2293): Show |
chr6 | 100380009 | 100469921 | ||
| a0001c0003 | 0/0 | 2298 | 4 | 0 | 0 | 0 | 1 | 3 | SIM1_chr6_100380009_100469921 | SIM1 | ATGAA others(2293): Show |
chr6 | 100380009 | 100469921 | ||
| a0001c0007 | 0/0 | 2298 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | ATGAA others(2293): Show |
chr6 | 100380009 | 100469921 | ||
| a0001c0009 | 0/0 | 2298 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | ATGAA others(2293): Show |
chr6 | 100380009 | 100469921 | ||
| a0002c0002 | 0/0 | 2298 | 78 | 0 | 12 | 54 | 4 | 8 | SIM1_chr6_100380009_100469921 | SIM1 | ATGAA others(2293): Show |
chr6 | 100380009 | 100469921 | ||
| a0002c0005 | 0/0 | 2298 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | ATGAA others(2293): Show |
chr6 | 100380009 | 100469921 | ||
| a0003c0004 | 0/0 | 2298 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | ATGAA others(2293): Show |
chr6 | 100380009 | 100469921 | ||
| a0004c0008 | 0/0 | 2298 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | ATGAA others(2293): Show |
chr6 | 100380009 | 100469921 | ||
| a0005c0010 | 0/0 | 2298 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | ATGAA others(2293): Show |
chr6 | 100380009 | 100469921 | ||
| a0006c0006 | 0/0 | 2298 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | ATGAA others(2293): Show |
chr6 | 100380009 | 100469921 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8422 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8417): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0002 | 0/0 | 8434 | 42 | 9 | 7 | 16 | 1 | 9 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8429): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0003 | 0/1 | 8432 | 31 | 8 | 7 | 11 | 3 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8427): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0004 | 0/0 | 8419 | 17 | 0 | 5 | 12 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8414): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0005 | 0/0 | 8422 | 18 | 1 | 1 | 13 | 1 | 2 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8417): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0006 | 0/0 | 8430 | 15 | 14 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8425): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0008 | 0/0 | 8419 | 11 | 3 | 5 | 1 | 2 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8414): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0009 | 1/0 | 8428 | 9 | 4 | 3 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8423): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0010 | 0/0 | 8438 | 6 | 3 | 1 | 1 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8433): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0011 | 0/0 | 8436 | 5 | 3 | 0 | 2 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8431): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0012 | 0/0 | 8434 | 4 | 0 | 0 | 4 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8429): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0013 | 0/0 | 8424 | 4 | 0 | 0 | 2 | 2 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8419): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0015 | 0/0 | 8422 | 3 | 3 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8417): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0016 | 0/0 | 8436 | 2 | 0 | 2 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8431): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0018 | 0/0 | 8419 | 2 | 0 | 0 | 2 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8414): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0019 | 0/0 | 8432 | 2 | 0 | 1 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8427): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0020 | 0/0 | 8424 | 2 | 2 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8419): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0021 | 0/0 | 8436 | 2 | 0 | 2 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8431): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0022 | 0/0 | 8432 | 2 | 2 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8427): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0023 | 0/0 | 8436 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8431): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0025 | 0/0 | 8424 | 2 | 2 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8419): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0026 | 0/0 | 8421 | 2 | 0 | 1 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8416): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0027 | 0/0 | 8421 | 2 | 1 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8416): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0028 | 0/0 | 8422 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8417): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0029 | 0/0 | 8440 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8435): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0031 | 0/0 | 8419 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8414): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0032 | 0/0 | 8438 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8433): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0034 | 0/0 | 8434 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8429): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0035 | 0/0 | 8419 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8414): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0036 | 0/0 | 8436 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8431): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0037 | 0/0 | 8436 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8431): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0038 | 0/0 | 8434 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8429): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0039 | 0/0 | 8430 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8425): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0040 | 0/0 | 8428 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8423): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0041 | 0/0 | 8422 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8417): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0042 | 0/0 | 8432 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8427): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0043 | 0/0 | 8430 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8425): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0044 | 0/0 | 8428 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8423): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0045 | 0/0 | 8442 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8437): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0046 | 0/0 | 8438 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8433): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0047 | 0/0 | 8434 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8429): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0048 | 0/0 | 8438 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8433): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0049 | 0/0 | 8428 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8423): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0050 | 0/0 | 8442 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8437): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0051 | 0/0 | 8436 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8431): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0052 | 0/0 | 8434 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8429): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0053 | 0/0 | 8428 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8423): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0054 | 0/0 | 8436 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8431): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0055 | 0/0 | 8430 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8425): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0056 | 0/0 | 8430 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8425): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0057 | 0/0 | 8430 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8425): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0058 | 0/0 | 8430 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8425): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0059 | 0/0 | 8428 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8423): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0060 | 0/0 | 8434 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8429): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0061 | 0/0 | 8417 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8412): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0062 | 0/0 | 8428 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8423): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0063 | 0/0 | 8420 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8415): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0064 | 0/0 | 8418 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8413): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0068 | 0/0 | 8420 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8415): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0069 | 0/0 | 8428 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8423): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0070 | 0/0 | 8416 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8411): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0071 | 0/0 | 8423 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8418): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0072 | 0/0 | 8429 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8424): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0073 | 0/0 | 8417 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8412): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0074 | 0/0 | 8413 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8408): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0075 | 0/0 | 8419 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8414): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0076 | 0/0 | 8434 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8429): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0077 | 0/0 | 8417 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8412): Show |
chr6 | 100380009 | 100469921 |
| a0001c0001t0078 | 0/0 | 8434 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8429): Show |
chr6 | 100380009 | 100469921 |
| a0001c0003t0003 | 0/0 | 8432 | 2 | 0 | 0 | 0 | 1 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8427): Show |
chr6 | 100380009 | 100469921 |
| a0001c0003t0030 | 0/0 | 8432 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8427): Show |
chr6 | 100380009 | 100469921 |
| a0001c0003t0079 | 0/0 | 8432 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8427): Show |
chr6 | 100380009 | 100469921 |
| a0001c0007t0004 | 0/0 | 8419 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8414): Show |
chr6 | 100380009 | 100469921 |
| a0001c0009t0033 | 0/0 | 8418 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8413): Show |
chr6 | 100380009 | 100469921 |
| a0002c0002t0001 | 0/0 | 8422 | 52 | 0 | 6 | 35 | 4 | 7 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8417): Show |
chr6 | 100380009 | 100469921 |
| a0002c0002t0003 | 0/0 | 8432 | 2 | 0 | 0 | 2 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8427): Show |
chr6 | 100380009 | 100469921 |
| a0002c0002t0006 | 0/0 | 8430 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8425): Show |
chr6 | 100380009 | 100469921 |
| a0002c0002t0007 | 0/0 | 8424 | 13 | 0 | 4 | 9 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8419): Show |
chr6 | 100380009 | 100469921 |
| a0002c0002t0014 | 0/0 | 8418 | 4 | 0 | 0 | 4 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8413): Show |
chr6 | 100380009 | 100469921 |
| a0002c0002t0017 | 0/0 | 8422 | 2 | 0 | 2 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8417): Show |
chr6 | 100380009 | 100469921 |
| a0002c0002t0024 | 0/0 | 8420 | 2 | 0 | 0 | 2 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8415): Show |
chr6 | 100380009 | 100469921 |
| a0002c0002t0028 | 0/0 | 8422 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8417): Show |
chr6 | 100380009 | 100469921 |
| a0002c0002t0066 | 0/0 | 8424 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8419): Show |
chr6 | 100380009 | 100469921 |
| a0002c0005t0065 | 0/0 | 8422 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8417): Show |
chr6 | 100380009 | 100469921 |
| a0003c0004t0003 | 0/0 | 8432 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8427): Show |
chr6 | 100380009 | 100469921 |
| a0004c0008t0023 | 0/0 | 8436 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8431): Show |
chr6 | 100380009 | 100469921 |
| a0005c0010t0067 | 0/0 | 8424 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8419): Show |
chr6 | 100380009 | 100469921 |
| a0006c0006t0004 | 0/0 | 8419 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | AAGCT others(8414): Show |
chr6 | 100380009 | 100469921 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0013 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0006g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0006g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0008g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0008g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0008g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0008g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0008g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0008g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0008g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0009g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0009g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0009g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0009g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0009g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0009g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0009g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0009g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0010g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0010g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0010g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0010g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0010g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0011g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0011g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0011g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0011g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0012g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0012g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0012g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0012g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0013g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0013g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0013g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0013g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0015g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0015g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0016g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0018g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0018g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0019g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0019g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0020g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0020g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0021g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0021g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0022g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0022g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0023g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0025g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0025g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0026g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0026g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0027g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0027g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0028g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0029g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0031g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0032g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0034g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0035g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0036g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0037g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0038g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0039g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0040g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0041g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0042g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0043g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0044g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0045g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0046g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0047g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0048g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0049g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0050g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0051g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0052g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0053g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0054g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0055g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0056g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0057g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0058g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0059g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0060g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0061g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0062g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0063g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0064g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0068g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0069g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0070g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0071g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0072g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0073g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0074g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0075g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0076g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0077g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0001t0078g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0003t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0003t0030g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0003t0079g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0007t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0001c0009t0033g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0006g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0007g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0007g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0007g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0007g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0007g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0007g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0007g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0007g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0007g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0007g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0007g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0014g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0014g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0014g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0014g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0017g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0017g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0024g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0024g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0028g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0002t0066g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0002c0005t0065g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0003c0004t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0004c0008t0023g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0005c0010t0067g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| a0006c0006t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0008 | g0225 | EUR | GBR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00099 | hp2 | a0001 | c0001 | t0010 | g0260 | EUR | GBR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00140 | hp1 | a0001 | c0001 | t0037 | g0022 | EUR | GBR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0224 | EUR | GBR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00280 | hp1 | a0001 | c0001 | t0036 | g0302 | EUR | FIN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00280 | hp2 | a0001 | c0001 | t0013 | g0073 | EUR | FIN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0235 | EUR | FIN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00323 | hp2 | a0001 | c0001 | t0013 | g0072 | EUR | FIN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00423 | hp1 | a0001 | c0001 | t0026 | g0216 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00438 | hp1 | a0002 | c0002 | t0014 | g0258 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0243 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00558 | hp2 | a0002 | c0002 | t0024 | g0087 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | CHS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0311 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00733 | hp1 | a0001 | c0001 | t0008 | g0137 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0279 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00738 | hp1 | a0001 | c0001 | t0048 | g0062 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00738 | hp2 | a0002 | c0002 | t0007 | g0245 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0249 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01070 | hp1 | a0001 | c0001 | t0019 | g0019 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01070 | hp2 | a0001 | c0001 | t0008 | g0181 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01074 | hp1 | a0002 | c0002 | t0017 | g0301 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01074 | hp2 | a0001 | c0001 | t0008 | g0047 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01081 | hp1 | a0001 | c0001 | t0021 | g0244 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0275 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0236 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01109 | hp1 | a0001 | c0001 | t0010 | g0005 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0129 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01167 | hp2 | a0001 | c0001 | t0021 | g0063 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01168 | hp1 | a0001 | c0001 | t0009 | g0024 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01168 | hp2 | a0001 | c0001 | t0059 | g0180 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01169 | hp1 | a0001 | c0001 | t0009 | g0025 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0130 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01175 | hp1 | a0001 | c0001 | t0027 | g0053 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0100 | AMR | PUR | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01255 | hp2 | a0001 | c0001 | t0016 | g0001 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01256 | hp1 | a0001 | c0001 | t0038 | g0020 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0070 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0257 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01346 | hp1 | a0001 | c0001 | t0016 | g0001 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0064 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01361 | hp1 | a0002 | c0002 | t0017 | g0303 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0277 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01433 | hp2 | a0001 | c0001 | t0076 | g0136 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01496 | hp2 | a0001 | c0001 | t0026 | g0284 | AMR | CLM | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | IBS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0313 | EUR | IBS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01516 | hp1 | a0001 | c0003 | t0003 | g0102 | EUR | IBS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0312 | EUR | IBS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | IBS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0314 | EUR | IBS | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0293 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01884 | hp2 | a0001 | c0001 | t0060 | g0157 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01891 | hp1 | a0001 | c0001 | t0015 | g0003 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01891 | hp2 | a0001 | c0001 | t0050 | g0156 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01934 | hp1 | a0002 | c0002 | t0007 | g0089 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0278 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01952 | hp2 | a0002 | c0002 | t0007 | g0246 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01993 | hp1 | a0001 | c0001 | t0029 | g0006 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0058 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02027 | hp1 | a0001 | c0001 | t0075 | g0188 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02027 | hp2 | a0001 | c0007 | t0004 | g0287 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02055 | hp1 | a0001 | c0001 | t0074 | g0144 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02056 | hp1 | a0002 | c0002 | t0007 | g0197 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02071 | hp2 | a0003 | c0004 | t0003 | g0032 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0026 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02083 | hp1 | a0001 | c0001 | t0018 | g0309 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02083 | hp2 | a0002 | c0002 | t0014 | g0255 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02129 | hp1 | a0001 | c0001 | t0012 | g0305 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02129 | hp2 | a0001 | c0001 | t0011 | g0060 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02145 | hp1 | a0001 | c0001 | t0069 | g0239 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | CDX | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | CDX | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02165 | hp1 | a0001 | c0001 | t0005 | g0074 | EAS | CDX | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02165 | hp2 | a0001 | c0001 | t0011 | g0274 | EAS | CDX | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0096 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0295 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0261 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02280 | hp1 | a0001 | c0001 | t0022 | g0165 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02280 | hp2 | a0001 | c0001 | t0053 | g0271 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0215 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02300 | hp1 | a0001 | c0001 | t0009 | g0066 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02300 | hp2 | a0002 | c0002 | t0007 | g0099 | AMR | PEL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0159 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02451 | hp2 | a0001 | c0001 | t0025 | g0238 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02523 | hp2 | a0001 | c0001 | t0008 | g0043 | EAS | KHV | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0172 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0141 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02602 | hp1 | a0002 | c0002 | t0006 | g0192 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0281 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02615 | hp1 | a0001 | c0001 | t0039 | g0016 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02615 | hp2 | a0001 | c0001 | t0071 | g0014 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02630 | hp2 | a0001 | c0001 | t0027 | g0098 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02647 | hp2 | a0001 | c0001 | t0051 | g0207 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02683 | hp1 | a0001 | c0001 | t0056 | g0046 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02717 | hp1 | a0001 | c0001 | t0077 | g0252 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02717 | hp2 | a0001 | c0001 | t0068 | g0267 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02723 | hp1 | a0001 | c0001 | t0041 | g0162 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0005 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02738 | hp2 | a0001 | c0003 | t0003 | g0044 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02809 | hp1 | a0001 | c0001 | t0043 | g0229 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02809 | hp2 | a0001 | c0001 | t0040 | g0015 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02886 | hp1 | a0001 | c0001 | t0020 | g0265 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0174 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02922 | hp2 | a0001 | c0001 | t0020 | g0154 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02965 | hp1 | a0001 | c0001 | t0057 | g0028 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0003 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0298 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0213 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03017 | hp1 | a0001 | c0001 | t0049 | g0138 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0189 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0266 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0264 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03098 | hp1 | a0001 | c0001 | t0055 | g0171 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03098 | hp2 | a0001 | c0001 | t0015 | g0219 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03139 | hp1 | a0001 | c0001 | t0058 | g0029 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03139 | hp2 | a0001 | c0001 | t0032 | g0010 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0296 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03225 | hp1 | a0004 | c0008 | t0023 | g0201 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03225 | hp2 | a0001 | c0001 | t0042 | g0054 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0226 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03239 | hp2 | a0001 | c0001 | t0034 | g0011 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0155 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03490 | hp1 | a0001 | c0001 | t0078 | g0299 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03490 | hp2 | a0001 | c0003 | t0030 | g0007 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0268 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03491 | hp2 | a0001 | c0001 | t0035 | g0012 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03492 | hp1 | a0001 | c0003 | t0079 | g0300 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0269 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0297 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03516 | hp2 | a0001 | c0001 | t0025 | g0228 | AFR | ESN | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03540 | hp2 | a0001 | c0001 | t0044 | g0150 | AFR | GWD | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0173 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0170 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0199 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03831 | hp1 | a0001 | c0001 | t0009 | g0049 | SAS | BEB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0272 | SAS | BEB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0035 | SAS | BEB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0033 | SAS | BEB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0220 | SAS | STU | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | STU | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0227 | SAS | BEB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG04184 | hp2 | a0001 | c0001 | t0047 | g0291 | SAS | BEB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0094 | SAS | STU | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0202 | SAS | STU | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18522 | hp1 | a0001 | c0001 | t0022 | g0149 | AFR | YRI | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0212 | AFR | YRI | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | CHB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18747 | hp2 | a0002 | c0002 | t0007 | g0178 | EAS | CHB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18943 | hp1 | a0001 | c0001 | t0045 | g0230 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18943 | hp2 | a0001 | c0001 | t0018 | g0304 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18945 | hp2 | a0001 | c0001 | t0012 | g0308 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18946 | hp1 | a0001 | c0001 | t0010 | g0082 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18947 | hp1 | a0001 | c0001 | t0005 | g0256 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0315 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18948 | hp1 | a0001 | c0001 | t0005 | g0093 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18948 | hp2 | a0002 | c0002 | t0014 | g0254 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18953 | hp1 | a0001 | c0001 | t0064 | g0027 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18957 | hp1 | a0005 | c0010 | t0067 | g0140 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18957 | hp2 | a0002 | c0002 | t0003 | g0051 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18966 | hp1 | a0002 | c0002 | t0007 | g0038 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18966 | hp2 | a0001 | c0001 | t0072 | g0234 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18967 | hp1 | a0002 | c0005 | t0065 | g0116 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18967 | hp2 | a0001 | c0001 | t0052 | g0292 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18973 | hp1 | a0002 | c0002 | t0007 | g0115 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18975 | hp2 | a0001 | c0001 | t0031 | g0008 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18978 | hp1 | a0002 | c0002 | t0028 | g0055 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0289 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18980 | hp1 | a0001 | c0001 | t0013 | g0069 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18982 | hp2 | a0002 | c0002 | t0007 | g0250 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18983 | hp2 | a0002 | c0002 | t0014 | g0121 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18989 | hp1 | a0001 | c0001 | t0046 | g0231 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18992 | hp1 | a0002 | c0002 | t0024 | g0253 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18992 | hp2 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18994 | hp2 | a0001 | c0001 | t0013 | g0059 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18998 | hp1 | a0002 | c0002 | t0066 | g0124 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0104 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19007 | hp1 | a0001 | c0001 | t0012 | g0306 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0262 | AFR | LWK | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19030 | hp2 | a0001 | c0009 | t0033 | g0009 | AFR | LWK | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | LWK | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0163 | AFR | LWK | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19062 | hp1 | a0001 | c0001 | t0073 | g0080 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19062 | hp2 | a0002 | c0002 | t0007 | g0251 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19063 | hp2 | a0001 | c0001 | t0028 | g0232 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19065 | hp2 | a0001 | c0001 | t0054 | g0276 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19066 | hp1 | a0002 | c0002 | t0007 | g0114 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19066 | hp2 | a0006 | c0006 | t0004 | g0090 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19068 | hp1 | a0001 | c0001 | t0012 | g0307 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19078 | hp2 | a0002 | c0002 | t0007 | g0198 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0310 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19082 | hp1 | a0002 | c0002 | t0007 | g0123 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19082 | hp2 | a0001 | c0001 | t0062 | g0071 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19240 | hp1 | a0001 | c0001 | t0061 | g0294 | AFR | YRI | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | YRI | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA20752 | hp1 | a0001 | c0001 | t0019 | g0021 | EUR | TSI | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA20752 | hp2 | a0001 | c0001 | t0008 | g0147 | EUR | TSI | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0132 | EUR | TSI | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0041 | EUR | TSI | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02109 | hp1 | a0001 | c0001 | t0023 | g0097 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02559 | hp1 | a0001 | c0001 | t0070 | g0175 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0205 | AFR | ACB | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | MSL | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0151 | AFR | USA | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | USA | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0263 | AFR | USA | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0206 | AFR | USA | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA21309 | hp1 | a0001 | c0001 | t0063 | g0113 | AFR | LWK | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| NA21309 | hp2 | a0001 | c0001 | t0009 | g0148 | AFR | LWK | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0013 | REF | REF | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0009 | g0131 | REF | REF | SIM1_chr6_100380009_100469921 | SIM1 | chr6 | 100380009 | 100469921 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:100390489 | C | T | 1 | a0004 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.2173G>A | p.Glu725Lys | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2948/8428 | 2173/2301 | 725/766 | chr6 | 100390489 | |||
| chr6:100420836 | C | T | 1 | a0006 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.1121G>A | p.Arg374Gln | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/12 | 1896/8428 | 1121/2301 | 374/766 | chr6 | 100420836 | |||
| chr6:100420845 | G | A | 2 | a0002 a0005 |
80 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
missense_variant | MODERATE | c.1112C>T | p.Ala371Val | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/12 | 1887/8428 | 1112/2301 | 371/766 | chr6 | 100420845 | |||
| chr6:100420903 | G | T | 2 | a0002 a0005 |
80 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
missense_variant | MODERATE | c.1054C>A | p.Pro352Thr | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/12 | 1829/8428 | 1054/2301 | 352/766 | chr6 | 100420903 | |||
| chr6:100449650 | T | C | 1 | a0005 | 1 | NA18957.hp1 | missense_variant | MODERATE | c.398A>G | p.His133Arg | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 5/12 | 1173/8428 | 398/2301 | 133/766 | chr6 | 100449650 | |||
| chr6:100453800 | C | T | 1 | a0003 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.220G>A | p.Asp74Asn | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/12 | 995/8428 | 220/2301 | 74/766 | chr6 | 100453800 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:100390370 | G | A | 1 | a0002c0005 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.2292C>T | p.Asn764Asn | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3067/8428 | 2292/2301 | 764/766 | chr6 | 100390370 | |||
| chr6:100390562 | G | C | 1 | a0001c0009 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.2100C>G | p.Gly700Gly | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2875/8428 | 2100/2301 | 700/766 | chr6 | 100390562 | |||
| chr6:100390703 | G | A | 1 | a0001c0003 | 4 | HG01516.hp1 HG02738.hp2 HG03490.hp2 others(1): Show |
synonymous_variant | LOW | c.1959C>T | p.Thr653Thr | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2734/8428 | 1959/2301 | 653/766 | chr6 | 100390703 | |||
| chr6:100393821 | G | T | 1 | a0001c0007 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.1236C>A | p.Thr412Thr | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/12 | 2011/8428 | 1236/2301 | 412/766 | chr6 | 100393821 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:100385194 | A | G | 1 | a0002c0005t0065 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5167T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 5167 | chr6 | 100385194 | ||||||
| chr6:100385200 | A | G | 1 | a0001c0001t0051 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5161T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 5161 | chr6 | 100385200 | ||||||
| chr6:100385266 | C | T | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0013 others(13): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*5095G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 5095 | chr6 | 100385266 | ||||||
| chr6:100385267 | G | A | 1 | a0001c0001t0052 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5094C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 5094 | chr6 | 100385267 | ||||||
| chr6:100385392 | C | T | 1 | a0001c0001t0059 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4969G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4969 | chr6 | 100385392 | ||||||
| chr6:100385393 | G | A | 1 | a0001c0001t0074 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4968C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4968 | chr6 | 100385393 | ||||||
| chr6:100385411 | G | A | 38 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(35): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*4950C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4950 | chr6 | 100385411 | ||||||
| chr6:100385669 | A | ATG | 8 | a0001c0001t0006 a0001c0001t0039 a0001c0001t0043 others(5): Show |
22 | HG01346.hp2 HG01884.hp1 HG02258.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4690_*4691dupCA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4691 | chr6 | 100385669 | ||||||
| chr6:100385669 | A | ATGTG | 9 | a0001c0001t0003 a0001c0001t0019 a0001c0001t0022 others(6): Show |
42 | HG00544.hp1 HG00558.hp1 HG01070.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*4688_*4691dupCACA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4691 | chr6 | 100385669 | ||||||
| chr6:100385669 | A | ATGTGTG | 9 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0034 others(6): Show |
53 | HG00323.hp1 HG00642.hp1 HG00733.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*4686_*4691dupCACA others(2): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4691 | chr6 | 100385669 | ||||||
| chr6:100385669 | A | ATGTGTGT others(1): Show |
9 | a0001c0001t0011 a0001c0001t0016 a0001c0001t0021 others(6): Show |
15 | HG00140.hp1 HG00280.hp1 HG01081.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4684_*4691dupCACA others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4691 | chr6 | 100385669 | ||||||
| chr6:100385669 | A | ATGTGTGT others(3): Show |
4 | a0001c0001t0010 a0001c0001t0032 a0001c0001t0046 others(1): Show |
9 | HG00099.hp2 HG00738.hp1 HG01109.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4682_*4691dupCACA others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4691 | chr6 | 100385669 | ||||||
| chr6:100385669 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0029 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4680_*4691dupCACA others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4691 | chr6 | 100385669 | ||||||
| chr6:100385669 | A | ATGTGTGT others(7): Show |
2 | a0001c0001t0045 a0001c0001t0050 |
2 | HG01891.hp2 NA18943.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4678_*4691dupCACA others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4691 | chr6 | 100385669 | ||||||
| chr6:100385669 | A | G | 1 | a0001c0001t0049 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4692T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4692 | chr6 | 100385669 | ||||||
| chr6:100385669 | ATGTG | A | 6 | a0001c0001t0013 a0001c0001t0020 a0001c0001t0025 others(3): Show |
23 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4688_*4691delCACA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4688 | chr6 | 100385669 | ||||||
| chr6:100385669 | ATGTGTG | A | 10 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0015 others(7): Show |
81 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*4686_*4691delCACA others(2): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4686 | chr6 | 100385669 | ||||||
| chr6:100385669 | ATGTGTGT others(1): Show |
A | 5 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0063 others(2): Show |
8 | HG00423.hp1 HG00558.hp2 HG01175.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4684_*4691delCACA others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4684 | chr6 | 100385669 | ||||||
| chr6:100385669 | ATGTGTGT others(3): Show |
A | 11 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0018 others(8): Show |
41 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*4682_*4691delCACA others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4682 | chr6 | 100385669 | ||||||
| chr6:100385669 | ATGTGTGT others(5): Show |
A | 4 | a0001c0001t0061 a0001c0001t0070 a0001c0001t0073 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 NA19062.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4680_*4691delCACA others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4680 | chr6 | 100385669 | ||||||
| chr6:100385669 | ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0074 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4676_*4691delCACA others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4676 | chr6 | 100385669 | ||||||
| chr6:100385885 | C | T | 1 | a0001c0001t0074 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4476G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4476 | chr6 | 100385885 | ||||||
| chr6:100385903 | C | T | 11 | a0001c0001t0001 a0001c0001t0028 a0002c0002t0001 others(8): Show |
79 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*4458G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4458 | chr6 | 100385903 | ||||||
| chr6:100386187 | G | C | 5 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0062 others(2): Show |
25 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4174C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4174 | chr6 | 100386187 | ||||||
| chr6:100386226 | T | C | 2 | a0001c0001t0025 a0001c0001t0069 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4135A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 4135 | chr6 | 100386226 | ||||||
| chr6:100386363 | T | C | 1 | a0002c0002t0066 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3998A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3998 | chr6 | 100386363 | ||||||
| chr6:100386374 | A | G | 1 | a0001c0001t0059 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3987T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3987 | chr6 | 100386374 | ||||||
| chr6:100386399 | T | C | 16 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0018 others(13): Show |
45 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*3962A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3962 | chr6 | 100386399 | ||||||
| chr6:100386409 | G | T | 1 | a0001c0001t0034 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3952C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3952 | chr6 | 100386409 | ||||||
| chr6:100386521 | A | G | 1 | a0001c0001t0061 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3840T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3840 | chr6 | 100386521 | ||||||
| chr6:100386555 | A | G | 1 | a0001c0001t0022 | 2 | HG02280.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3806T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3806 | chr6 | 100386555 | ||||||
| chr6:100386556 | T | C | 1 | a0001c0001t0053 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3805A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3805 | chr6 | 100386556 | ||||||
| chr6:100386627 | C | T | 5 | a0001c0001t0016 a0001c0001t0021 a0001c0001t0029 others(2): Show |
7 | HG00738.hp1 HG01081.hp1 HG01167.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3734G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3734 | chr6 | 100386627 | ||||||
| chr6:100386798 | C | T | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0013 others(13): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*3563G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3563 | chr6 | 100386798 | ||||||
| chr6:100386882 | A | G | 1 | a0001c0009t0033 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3479T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3479 | chr6 | 100386882 | ||||||
| chr6:100386904 | C | T | 13 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0018 others(10): Show |
42 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3457G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3457 | chr6 | 100386904 | ||||||
| chr6:100386996 | A | G | 1 | a0001c0001t0047 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3365T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3365 | chr6 | 100386996 | ||||||
| chr6:100387067 | A | T | 2 | a0001c0001t0045 a0001c0001t0046 |
2 | NA18943.hp1 NA18989.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3294T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3294 | chr6 | 100387067 | ||||||
| chr6:100387100 | T | C | 2 | a0001c0001t0025 a0001c0001t0069 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3261A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3261 | chr6 | 100387100 | ||||||
| chr6:100387345 | T | C | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(29): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*3016A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3016 | chr6 | 100387345 | ||||||
| chr6:100387359 | T | C | 2 | a0001c0001t0025 a0001c0001t0069 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3002A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 3002 | chr6 | 100387359 | ||||||
| chr6:100387391 | G | A | 1 | a0005c0010t0067 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2970C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2970 | chr6 | 100387391 | ||||||
| chr6:100387431 | A | T | 10 | a0001c0001t0004 a0001c0001t0018 a0001c0001t0026 others(7): Show |
28 | HG00423.hp1 HG00438.hp2 HG00735.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2930T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2930 | chr6 | 100387431 | ||||||
| chr6:100387453 | A | G | 1 | a0001c0001t0077 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2908T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2908 | chr6 | 100387453 | ||||||
| chr6:100387479 | T | C | 1 | a0001c0001t0054 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2882A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2882 | chr6 | 100387479 | ||||||
| chr6:100387717 | G | A | 1 | a0001c0001t0070 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2644C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2644 | chr6 | 100387717 | ||||||
| chr6:100387782 | T | C | 11 | a0001c0001t0001 a0001c0001t0028 a0002c0002t0001 others(8): Show |
79 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2579A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2579 | chr6 | 100387782 | ||||||
| chr6:100387784 | T | C | 41 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(38): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*2577A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2577 | chr6 | 100387784 | ||||||
| chr6:100387833 | T | C | 1 | a0001c0001t0075 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2528A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2528 | chr6 | 100387833 | ||||||
| chr6:100387945 | C | A | 1 | a0001c0001t0055 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2416G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2416 | chr6 | 100387945 | ||||||
| chr6:100388139 | C | T | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(29): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*2222G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2222 | chr6 | 100388139 | ||||||
| chr6:100388146 | T | C | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0013 others(13): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2215A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2215 | chr6 | 100388146 | ||||||
| chr6:100388274 | C | T | 1 | a0001c0001t0044 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2087G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2087 | chr6 | 100388274 | ||||||
| chr6:100388315 | A | T | 1 | a0001c0001t0071 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2046T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2046 | chr6 | 100388315 | ||||||
| chr6:100388356 | G | GA | 16 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0018 others(13): Show |
45 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2004dupT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 2004 | chr6 | 100388356 | ||||||
| chr6:100388400 | G | A | 1 | a0001c0001t0056 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1961C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 1961 | chr6 | 100388400 | ||||||
| chr6:100388584 | C | T | 1 | a0001c0001t0057 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1777G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 1777 | chr6 | 100388584 | ||||||
| chr6:100388760 | A | T | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0013 others(13): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1601T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 1601 | chr6 | 100388760 | ||||||
| chr6:100388908 | C | A | 16 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0018 others(13): Show |
45 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1453G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 1453 | chr6 | 100388908 | ||||||
| chr6:100389229 | T | G | 2 | a0001c0001t0057 a0001c0001t0058 |
2 | HG02965.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1132A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 1132 | chr6 | 100389229 | ||||||
| chr6:100389362 | A | G | 1 | a0001c0001t0061 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*999T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 999 | chr6 | 100389362 | ||||||
| chr6:100389867 | A | G | 2 | a0001c0001t0042 a0001c0001t0043 |
2 | HG02809.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*494T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 494 | chr6 | 100389867 | ||||||
| chr6:100389891 | G | A | 1 | a0001c0001t0059 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*470C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 470 | chr6 | 100389891 | ||||||
| chr6:100389986 | G | A | 3 | a0001c0001t0023 a0001c0001t0060 a0004c0008t0023 |
3 | HG01884.hp2 HG02109.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*375C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 375 | chr6 | 100389986 | ||||||
| chr6:100390013 | T | A | 38 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(35): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*348A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 348 | chr6 | 100390013 | ||||||
| chr6:100390178 | T | A | 2 | a0001c0001t0028 a0002c0002t0028 |
2 | NA18978.hp1 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*183A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 183 | chr6 | 100390178 | ||||||
| chr6:100390248 | T | A | 1 | a0001c0001t0076 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 113 | chr6 | 100390248 | ||||||
| chr6:100390274 | C | A | 1 | a0001c0001t0077 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*87G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 87 | chr6 | 100390274 | ||||||
| chr6:100390310 | C | T | 2 | a0001c0001t0020 a0001c0001t0041 |
3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*51G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 12/12 | 51 | chr6 | 100390310 | ||||||
| chr6:100463558 | G | T | 2 | a0001c0001t0039 a0001c0001t0040 |
2 | HG02615.hp1 HG02809.hp2 |
5_prime_UTR_variant | MODIFIER | c.-90C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/12 | 90 | chr6 | 100463558 | ||||||
| chr6:100463595 | A | G | 3 | a0001c0001t0019 a0001c0001t0037 a0001c0001t0038 |
4 | HG00140.hp1 HG01070.hp1 HG01256.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-127T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/12 | 127 | chr6 | 100463595 | ||||||
| chr6:100463642 | G | A | 2 | a0001c0001t0078 a0001c0003t0079 |
2 | HG03490.hp1 HG03492.hp1 |
5_prime_UTR_variant | MODIFIER | c.-174C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/12 | 174 | chr6 | 100463642 | ||||||
| chr6:100463724 | C | T | 4 | a0001c0001t0012 a0001c0001t0018 a0001c0001t0036 others(1): Show |
9 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-256G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/12 | 256 | chr6 | 100463724 | ||||||
| chr6:100464648 | C | T | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03239.hp2 HG03491.hp2 |
5_prime_UTR_variant | MODIFIER | c.-502G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/12 | 1180 | chr6 | 100464648 | ||||||
| chr6:100464681 | C | T | 2 | a0001c0001t0032 a0001c0009t0033 |
2 | HG03139.hp2 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-535G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/12 | 1213 | chr6 | 100464681 | ||||||
| chr6:100464749 | C | G | 1 | a0001c0001t0031 | 1 | NA18975.hp2 | 5_prime_UTR_variant | MODIFIER | c.-603G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/12 | 1281 | chr6 | 100464749 | ||||||
| chr6:100464867 | A | G | 3 | a0001c0001t0016 a0001c0001t0029 a0001c0003t0030 |
4 | HG01255.hp2 HG01346.hp1 HG01993.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-721T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/12 | 1399 | chr6 | 100464867 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:100391287 | T | C | 104 | a0001c0001t0001g0067 a0001c0001t0005g0026 a0001c0001t0005g0030 others(101): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1571-196A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391287 | |||||||
| chr6:100391322 | T | C | 1 | a0001c0001t0056g0046 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1571-231A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391322 | |||||||
| chr6:100391418 | T | C | 25 | a0001c0001t0005g0026 a0001c0001t0005g0030 a0001c0001t0005g0041 others(22): Show |
25 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1571-327A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391418 | |||||||
| chr6:100391422 | C | T | 1 | a0001c0001t0005g0074 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1571-331G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391422 | |||||||
| chr6:100391487 | C | A | 4 | a0001c0001t0003g0128 a0001c0001t0003g0210 a0001c0001t0003g0270 others(1): Show |
4 | HG02071.hp2 HG02132.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1571-396G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391487 | |||||||
| chr6:100391497 | T | C | 1 | a0001c0001t0068g0267 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1571-406A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391497 | |||||||
| chr6:100391554 | C | A | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1571-463G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391554 | |||||||
| chr6:100391863 | A | G | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1571-772T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391863 | |||||||
| chr6:100391910 | C | A | 1 | a0001c0009t0033g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1571-819G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391910 | |||||||
| chr6:100391913 | C | G | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1571-822G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391913 | |||||||
| chr6:100391990 | T | C | 3 | a0001c0001t0002g0095 a0001c0001t0003g0160 a0001c0001t0003g0161 |
3 | HG02257.hp1 HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1571-899A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100391990 | |||||||
| chr6:100392082 | G | A | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1571-991C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392082 | |||||||
| chr6:100392128 | C | T | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1571-1037G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392128 | |||||||
| chr6:100392130 | C | T | 1 | a0001c0001t0004g0079 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1571-1039G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392130 | |||||||
| chr6:100392131 | G | A | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1571-1040C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392131 | |||||||
| chr6:100392152 | C | T | 43 | a0001c0001t0004g0056 a0001c0001t0004g0058 a0001c0001t0004g0075 others(40): Show |
43 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1571-1061G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392152 | |||||||
| chr6:100392183 | T | A | 1 | a0002c0002t0007g0197 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1571-1092A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392183 | |||||||
| chr6:100392200 | T | C | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1571-1109A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392200 | |||||||
| chr6:100392215 | A | T | 104 | a0001c0001t0001g0067 a0001c0001t0005g0026 a0001c0001t0005g0030 others(101): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1571-1124T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392215 | |||||||
| chr6:100392244 | A | T | 2 | a0001c0001t0027g0098 a0001c0001t0077g0252 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1571-1153T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392244 | |||||||
| chr6:100392248 | TG | T | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1571-1158delC | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392248 | |||||||
| chr6:100392383 | G | T | 1 | a0001c0001t0002g0040 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1570+1104C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392383 | |||||||
| chr6:100392504 | G | A | 149 | a0001c0001t0001g0067 a0001c0001t0004g0056 a0001c0001t0004g0058 others(146): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1570+983C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392504 | |||||||
| chr6:100392548 | G | T | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1570+939C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392548 | |||||||
| chr6:100392763 | C | T | 1 | a0001c0001t0027g0098 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1570+724G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392763 | |||||||
| chr6:100392880 | C | T | 104 | a0001c0001t0001g0067 a0001c0001t0005g0026 a0001c0001t0005g0030 others(101): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1570+607G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392880 | |||||||
| chr6:100392972 | G | C | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1570+515C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100392972 | |||||||
| chr6:100393091 | T | G | 1 | a0001c0001t0074g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1570+396A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100393091 | |||||||
| chr6:100393353 | G | T | 166 | a0001c0001t0001g0067 a0001c0001t0004g0056 a0001c0001t0004g0058 others(163): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1570+134C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 11/11 | chr6 | 100393353 | |||||||
| chr6:100393996 | G | T | 1 | a0001c0001t0004g0076 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1168-107C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100393996 | |||||||
| chr6:100394092 | A | G | 2 | a0001c0001t0022g0149 a0001c0001t0022g0165 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1168-203T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394092 | |||||||
| chr6:100394130 | A | G | 4 | a0001c0001t0015g0003 a0001c0001t0015g0219 a0001c0001t0068g0267 others(1): Show |
5 | HG01891.hp1 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1168-241T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394130 | |||||||
| chr6:100394220 | TG | T | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-332delC | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394220 | |||||||
| chr6:100394240 | G | C | 1 | a0002c0002t0001g0088 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1168-351C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394240 | |||||||
| chr6:100394455 | G | A | 152 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0004g0056 others(149): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1168-566C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394455 | |||||||
| chr6:100394575 | T | A | 1 | a0002c0002t0001g0037 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1168-686A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394575 | |||||||
| chr6:100394603 | C | G | 26 | a0001c0001t0003g0042 a0001c0001t0005g0026 a0001c0001t0005g0030 others(23): Show |
26 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.1168-714G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394603 | |||||||
| chr6:100394613 | C | G | 152 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0004g0056 others(149): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1168-724G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394613 | |||||||
| chr6:100394889 | T | A | 1 | a0001c0001t0061g0294 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1168-1000A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100394889 | |||||||
| chr6:100395019 | C | T | 152 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0004g0056 others(149): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1168-1130G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395019 | |||||||
| chr6:100395212 | T | A | 1 | a0001c0001t0010g0082 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1168-1323A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395212 | |||||||
| chr6:100395251 | TATTCCAT others(4): Show |
T | 2 | a0001c0001t0015g0003 a0001c0001t0015g0219 |
3 | HG01891.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1168-1373_1168-136 others(15): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395251 | |||||||
| chr6:100395308 | C | T | 1 | a0001c0001t0012g0305 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1168-1419G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395308 | |||||||
| chr6:100395433 | C | T | 6 | a0001c0001t0002g0152 a0001c0001t0002g0204 a0001c0001t0006g0018 others(3): Show |
6 | HG02559.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1168-1544G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395433 | |||||||
| chr6:100395605 | G | C | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-1716C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395605 | |||||||
| chr6:100395716 | A | G | 3 | a0001c0001t0015g0003 a0001c0001t0015g0219 a0001c0001t0068g0267 |
4 | HG01891.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-1827T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395716 | |||||||
| chr6:100395964 | T | C | 3 | a0002c0002t0014g0254 a0002c0002t0014g0255 a0002c0002t0014g0258 |
3 | HG00438.hp1 HG02083.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1168-2075A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395964 | |||||||
| chr6:100395982 | A | T | 1 | a0001c0001t0006g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1168-2093T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100395982 | |||||||
| chr6:100396038 | A | C | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-2149T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396038 | |||||||
| chr6:100396049 | C | T | 1 | a0001c0001t0006g0266 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1168-2160G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396049 | |||||||
| chr6:100396082 | T | C | 1 | a0001c0001t0010g0260 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1168-2193A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396082 | |||||||
| chr6:100396125 | C | T | 1 | a0001c0001t0044g0150 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1168-2236G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396125 | |||||||
| chr6:100396155 | G | A | 1 | a0001c0001t0074g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1168-2266C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396155 | |||||||
| chr6:100396219 | T | C | 156 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0004g0056 others(153): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1168-2330A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396219 | |||||||
| chr6:100396229 | T | C | 27 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(24): Show |
27 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1168-2340A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396229 | |||||||
| chr6:100396392 | T | C | 45 | a0001c0001t0004g0056 a0001c0001t0004g0058 a0001c0001t0004g0075 others(42): Show |
45 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1168-2503A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396392 | |||||||
| chr6:100396545 | G | T | 2 | a0001c0001t0012g0307 a0001c0001t0012g0308 |
2 | NA18945.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1168-2656C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396545 | |||||||
| chr6:100396599 | A | C | 1 | a0002c0002t0007g0114 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1168-2710T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396599 | |||||||
| chr6:100396632 | A | T | 1 | a0002c0002t0001g0125 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1168-2743T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396632 | |||||||
| chr6:100396799 | G | T | 2 | a0001c0001t0015g0003 a0001c0001t0015g0219 |
3 | HG01891.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1168-2910C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396799 | |||||||
| chr6:100396914 | G | A | 3 | a0001c0001t0015g0003 a0001c0001t0015g0219 a0001c0001t0068g0267 |
4 | HG01891.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-3025C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396914 | |||||||
| chr6:100396950 | T | C | 1 | a0001c0009t0033g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1168-3061A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100396950 | |||||||
| chr6:100397230 | G | C | 1 | a0001c0001t0002g0103 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1168-3341C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397230 | |||||||
| chr6:100397478 | A | G | 1 | a0001c0009t0033g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1168-3589T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397478 | |||||||
| chr6:100397553 | C | T | 78 | a0001c0001t0028g0232 a0002c0002t0001g0023 a0002c0002t0001g0031 others(75): Show |
78 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1168-3664G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397553 | |||||||
| chr6:100397719 | G | A | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-3830C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397719 | |||||||
| chr6:100397759 | C | A | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1168-3870G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397759 | |||||||
| chr6:100397768 | A | G | 78 | a0001c0001t0028g0232 a0002c0002t0001g0023 a0002c0002t0001g0031 others(75): Show |
78 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1168-3879T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397768 | |||||||
| chr6:100397912 | A | T | 1 | a0001c0001t0055g0171 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1168-4023T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397912 | |||||||
| chr6:100397963 | A | G | 2 | a0001c0001t0020g0154 a0001c0001t0020g0265 |
2 | HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1168-4074T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397963 | |||||||
| chr6:100397979 | A | G | 2 | a0001c0001t0042g0054 a0001c0001t0043g0229 |
2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1168-4090T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100397979 | |||||||
| chr6:100398025 | A | G | 42 | a0001c0001t0004g0056 a0001c0001t0004g0058 a0001c0001t0004g0075 others(39): Show |
42 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1168-4136T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398025 | |||||||
| chr6:100398280 | G | A | 6 | a0001c0001t0006g0163 a0001c0001t0006g0293 a0001c0001t0006g0295 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168-4391C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398280 | |||||||
| chr6:100398325 | T | C | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1168-4436A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398325 | |||||||
| chr6:100398450 | T | A | 3 | a0001c0001t0020g0154 a0001c0001t0020g0265 a0001c0001t0041g0162 |
3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1168-4561A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398450 | |||||||
| chr6:100398489 | T | C | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-4600A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398489 | |||||||
| chr6:100398712 | G | A | 3 | a0001c0001t0020g0154 a0001c0001t0020g0265 a0001c0001t0041g0162 |
3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1168-4823C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398712 | |||||||
| chr6:100398841 | C | T | 5 | a0001c0001t0002g0135 a0001c0001t0032g0010 a0001c0001t0042g0054 others(2): Show |
5 | HG01433.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1168-4952G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398841 | |||||||
| chr6:100398842 | G | A | 4 | a0001c0001t0020g0154 a0001c0001t0020g0265 a0001c0001t0041g0162 others(1): Show |
4 | HG01168.hp2 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-4953C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398842 | |||||||
| chr6:100398894 | C | T | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-5005G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398894 | |||||||
| chr6:100398933 | T | TTG | 46 | a0001c0001t0002g0040 a0001c0001t0002g0166 a0001c0001t0003g0164 others(43): Show |
46 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.1168-5046_1168-504 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398933 | |||||||
| chr6:100398933 | T | TTGTGTG | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0061g0294 |
3 | HG02451.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1168-5050_1168-504 others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398933 | |||||||
| chr6:100398933 | TTG | T | 9 | a0001c0001t0002g0158 a0001c0001t0002g0167 a0001c0001t0002g0200 others(6): Show |
9 | HG00735.hp1 HG01168.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1168-5046_1168-504 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398933 | |||||||
| chr6:100398951 | GTGTGTGT others(3): Show |
G | 5 | a0001c0001t0028g0232 a0002c0002t0001g0088 a0002c0002t0001g0242 others(2): Show |
5 | HG01261.hp2 HG02071.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1168-5072_1168-506 others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398951 | |||||||
| chr6:100398953 | GTGTGTGT others(1): Show |
G | 70 | a0002c0002t0001g0023 a0002c0002t0001g0031 a0002c0002t0001g0033 others(67): Show |
70 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1168-5072_1168-506 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398953 | |||||||
| chr6:100398955 | GTGTGTA | G | 4 | a0001c0001t0006g0151 a0001c0001t0006g0213 a0002c0002t0001g0037 others(1): Show |
4 | HG02976.hp2 HG06807.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-5072_1168-506 others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398955 | |||||||
| chr6:100398958 | TGTATG | T | 25 | a0001c0001t0003g0042 a0001c0001t0005g0026 a0001c0001t0005g0030 others(22): Show |
25 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1168-5074_1168-507 others(9): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398958 | |||||||
| chr6:100398961 | A | G | 6 | a0001c0001t0015g0003 a0001c0001t0015g0219 a0001c0001t0020g0154 others(3): Show |
7 | HG01891.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1168-5072T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398961 | |||||||
| chr6:100398963 | G | A | 3 | a0001c0001t0020g0154 a0001c0001t0020g0265 a0001c0001t0041g0162 |
3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1168-5074C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398963 | |||||||
| chr6:100398964 | T | A | 28 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(25): Show |
28 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.1168-5075A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398964 | |||||||
| chr6:100398965 | G | A | 2 | a0001c0001t0015g0003 a0001c0001t0015g0219 |
3 | HG01891.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1168-5076C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398965 | |||||||
| chr6:100398966 | T | TG | 2 | a0001c0001t0015g0003 a0001c0001t0015g0219 |
3 | HG01891.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1168-5078_1168-507 others(5): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398966 | |||||||
| chr6:100398966 | TA | T | 3 | a0001c0001t0020g0154 a0001c0001t0020g0265 a0001c0001t0041g0162 |
3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1168-5078delT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398966 | |||||||
| chr6:100398967 | A | T | 2 | a0001c0001t0015g0003 a0001c0001t0015g0219 |
3 | HG01891.hp1 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1168-5078T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100398967 | |||||||
| chr6:100399305 | A | T | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-5416T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100399305 | |||||||
| chr6:100399334 | A | C | 1 | a0001c0009t0033g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1168-5445T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100399334 | |||||||
| chr6:100399366 | T | C | 1 | a0001c0001t0073g0080 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1168-5477A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100399366 | |||||||
| chr6:100399423 | G | C | 2 | a0001c0001t0003g0153 a0001c0001t0009g0170 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1168-5534C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100399423 | |||||||
| chr6:100399744 | C | A | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-5855G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100399744 | |||||||
| chr6:100399752 | A | G | 2 | a0001c0001t0006g0151 a0001c0001t0006g0213 |
2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1168-5863T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100399752 | |||||||
| chr6:100399912 | A | G | 1 | a0001c0001t0008g0047 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1168-6023T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100399912 | |||||||
| chr6:100399997 | G | A | 3 | a0001c0001t0010g0005 a0001c0001t0010g0262 a0001c0001t0011g0261 |
4 | HG01109.hp1 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1168-6108C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100399997 | |||||||
| chr6:100400194 | G | A | 3 | a0001c0001t0020g0154 a0001c0001t0020g0265 a0001c0001t0041g0162 |
3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1168-6305C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100400194 | |||||||
| chr6:100400242 | A | G | 2 | a0001c0001t0003g0002 a0001c0001t0003g0233 |
3 | HG01175.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1168-6353T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100400242 | |||||||
| chr6:100400258 | T | A | 1 | a0001c0001t0001g0067 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1168-6369A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100400258 | |||||||
| chr6:100400308 | G | A | 1 | a0001c0001t0002g0176 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1168-6419C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100400308 | |||||||
| chr6:100400443 | C | A | 126 | a0001c0001t0004g0056 a0001c0001t0004g0058 a0001c0001t0004g0075 others(123): Show |
126 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.1168-6554G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100400443 | |||||||
| chr6:100400980 | GA | G | 81 | a0001c0001t0015g0003 a0001c0001t0015g0219 a0001c0001t0028g0232 others(78): Show |
82 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1168-7092delT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100400980 | |||||||
| chr6:100400995 | A | G | 43 | a0001c0001t0004g0056 a0001c0001t0004g0058 a0001c0001t0004g0075 others(40): Show |
43 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1168-7106T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100400995 | |||||||
| chr6:100401224 | T | C | 130 | a0001c0001t0004g0056 a0001c0001t0004g0058 a0001c0001t0004g0075 others(127): Show |
131 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1168-7335A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401224 | |||||||
| chr6:100401260 | G | C | 1 | a0002c0002t0001g0199 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1168-7371C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401260 | |||||||
| chr6:100401315 | A | C | 4 | a0001c0001t0020g0154 a0001c0001t0020g0265 a0001c0001t0041g0162 others(1): Show |
4 | HG01168.hp2 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-7426T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401315 | |||||||
| chr6:100401450 | T | C | 164 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0004g0056 others(161): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1168-7561A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401450 | |||||||
| chr6:100401462 | T | A | 29 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(26): Show |
29 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1168-7573A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401462 | |||||||
| chr6:100401492 | T | C | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-7603A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401492 | |||||||
| chr6:100401790 | C | T | 1 | a0001c0001t0003g0177 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1168-7901G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401790 | |||||||
| chr6:100401854 | C | T | 164 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0004g0056 others(161): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1168-7965G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401854 | |||||||
| chr6:100401962 | G | A | 5 | a0001c0001t0002g0169 a0001c0001t0002g0179 a0001c0001t0011g0155 others(2): Show |
5 | HG01891.hp2 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1168-8073C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100401962 | |||||||
| chr6:100402092 | T | C | 1 | a0001c0001t0004g0079 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1168-8203A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402092 | |||||||
| chr6:100402165 | A | G | 1 | a0001c0009t0033g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1168-8276T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402165 | |||||||
| chr6:100402259 | T | C | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-8370A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402259 | |||||||
| chr6:100402265 | G | T | 17 | a0002c0002t0001g0023 a0002c0002t0001g0031 a0002c0002t0001g0083 others(14): Show |
17 | HG00621.hp2 HG02293.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.1168-8376C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402265 | |||||||
| chr6:100402295 | T | TA | 28 | a0001c0001t0004g0056 a0001c0001t0004g0058 a0001c0001t0004g0075 others(25): Show |
28 | HG00423.hp1 HG00438.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1168-8407dupT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402295 | |||||||
| chr6:100402420 | T | A | 3 | a0001c0001t0015g0003 a0001c0001t0015g0219 a0001c0001t0068g0267 |
4 | HG01891.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-8531A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402420 | |||||||
| chr6:100402528 | A | G | 29 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(26): Show |
29 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1168-8639T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402528 | |||||||
| chr6:100402565 | C | CTTTTCTC others(6): Show |
15 | a0001c0001t0028g0232 a0002c0002t0001g0033 a0002c0002t0001g0037 others(12): Show |
15 | HG00738.hp2 HG01074.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.1168-8677_1168-867 others(17): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402565 | |||||||
| chr6:100402565 | C | CTTTTCTC others(7): Show |
27 | a0002c0002t0001g0031 a0002c0002t0001g0083 a0002c0002t0001g0084 others(24): Show |
27 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1168-8677_1168-867 others(18): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402565 | |||||||
| chr6:100402565 | C | CTTTTCTC others(8): Show |
20 | a0002c0002t0001g0023 a0002c0002t0001g0039 a0002c0002t0001g0045 others(17): Show |
20 | HG00140.hp2 HG00423.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.1168-8677_1168-867 others(19): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402565 | |||||||
| chr6:100402565 | C | CTTTTCTC others(9): Show |
10 | a0002c0002t0001g0127 a0002c0002t0001g0226 a0002c0002t0001g0236 others(7): Show |
10 | HG00642.hp2 HG01106.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1168-8677_1168-867 others(20): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402565 | |||||||
| chr6:100402565 | C | CTTTTCTC others(10): Show |
1 | a0002c0002t0001g0249 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1168-8677_1168-867 others(21): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402565 | |||||||
| chr6:100402565 | C | CTTTTCTC others(12): Show |
3 | a0002c0002t0001g0100 a0002c0002t0001g0193 a0002c0002t0066g0124 |
3 | HG01192.hp2 HG02135.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1168-8677_1168-867 others(23): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402565 | |||||||
| chr6:100402565 | CTCTTT | C | 27 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(24): Show |
27 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1168-8681_1168-867 others(9): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402565 | |||||||
| chr6:100402567 | C | CT | 22 | a0001c0001t0002g0004 a0001c0001t0002g0135 a0001c0001t0002g0240 others(19): Show |
22 | HG00544.hp1 HG01169.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.1168-8679dupA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402567 | |||||||
| chr6:100402567 | C | CTTT | 32 | a0001c0001t0004g0056 a0001c0001t0004g0058 a0001c0001t0004g0075 others(29): Show |
32 | HG00733.hp1 HG01070.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1168-8681_1168-867 others(7): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402567 | |||||||
| chr6:100402567 | C | CTTTT | 11 | a0001c0001t0004g0076 a0001c0001t0004g0279 a0001c0001t0008g0130 others(8): Show |
11 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1168-8682_1168-867 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402567 | |||||||
| chr6:100402567 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0015g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1168-8688_1168-867 others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402567 | |||||||
| chr6:100402567 | C | T | 78 | a0001c0001t0028g0232 a0002c0002t0001g0023 a0002c0002t0001g0031 others(75): Show |
78 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1168-8678G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402567 | |||||||
| chr6:100402567 | CT | C | 8 | a0001c0001t0002g0158 a0001c0001t0003g0164 a0001c0001t0009g0206 others(5): Show |
8 | HG00735.hp1 HG01167.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1168-8679delA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402567 | |||||||
| chr6:100402569 | T | C | 1 | a0001c0001t0025g0228 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1168-8680A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402569 | |||||||
| chr6:100402570 | T | C | 2 | a0001c0001t0025g0238 a0001c0001t0069g0239 |
2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1168-8681A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402570 | |||||||
| chr6:100402571 | T | C | 1 | a0001c0001t0006g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1168-8682A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402571 | |||||||
| chr6:100402572 | T | C | 1 | a0001c0001t0006g0213 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1168-8683A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402572 | |||||||
| chr6:100402573 | T | C | 1 | a0001c0001t0006g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1168-8684A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402573 | |||||||
| chr6:100402574 | T | C | 1 | a0001c0001t0006g0213 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1168-8685A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402574 | |||||||
| chr6:100402575 | T | C | 27 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(24): Show |
27 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1168-8686A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402575 | |||||||
| chr6:100402577 | T | C | 27 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(24): Show |
27 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1168-8688A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402577 | |||||||
| chr6:100402622 | G | GGCT | 107 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(104): Show |
107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1168-8736_1168-873 others(7): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402622 | |||||||
| chr6:100402673 | G | A | 311 | a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0040 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1168-8784C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402673 | |||||||
| chr6:100402678 | C | T | 311 | a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0040 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1168-8789G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402678 | |||||||
| chr6:100402785 | C | T | 1 | a0002c0002t0001g0037 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1168-8896G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100402785 | |||||||
| chr6:100403100 | T | C | 3 | a0001c0001t0020g0154 a0001c0001t0020g0265 a0001c0001t0041g0162 |
3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1168-9211A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100403100 | |||||||
| chr6:100403317 | G | C | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1168-9428C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100403317 | |||||||
| chr6:100403568 | A | G | 1 | a0001c0001t0002g0273 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1168-9679T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100403568 | |||||||
| chr6:100403754 | A | G | 1 | a0001c0001t0008g0047 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1168-9865T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100403754 | |||||||
| chr6:100403845 | T | G | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-9956A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100403845 | |||||||
| chr6:100403942 | A | G | 44 | a0001c0001t0004g0056 a0001c0001t0004g0058 a0001c0001t0004g0075 others(41): Show |
44 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-10053T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100403942 | |||||||
| chr6:100404027 | C | G | 1 | a0001c0001t0006g0213 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1168-10138G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404027 | |||||||
| chr6:100404098 | C | T | 1 | a0001c0001t0037g0022 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1168-10209G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404098 | |||||||
| chr6:100404140 | C | T | 107 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(104): Show |
107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1168-10251G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404140 | |||||||
| chr6:100404158 | A | G | 29 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(26): Show |
29 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1168-10269T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404158 | |||||||
| chr6:100404229 | C | T | 1 | a0001c0009t0033g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1168-10340G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404229 | |||||||
| chr6:100404303 | A | C | 27 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(24): Show |
27 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1168-10414T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404303 | |||||||
| chr6:100404424 | C | T | 1 | a0001c0001t0027g0098 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1168-10535G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404424 | |||||||
| chr6:100404491 | G | T | 2 | a0001c0001t0006g0151 a0001c0001t0006g0213 |
2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1168-10602C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404491 | |||||||
| chr6:100404692 | T | G | 1 | a0002c0002t0001g0045 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1168-10803A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404692 | |||||||
| chr6:100404793 | C | T | 1 | a0001c0001t0044g0150 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1168-10904G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404793 | |||||||
| chr6:100404877 | T | C | 29 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(26): Show |
29 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1168-10988A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404877 | |||||||
| chr6:100404886 | G | A | 1 | a0001c0001t0008g0263 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1168-10997C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100404886 | |||||||
| chr6:100405076 | A | G | 2 | a0001c0001t0022g0149 a0001c0001t0022g0165 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1168-11187T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405076 | |||||||
| chr6:100405116 | T | C | 44 | a0001c0001t0004g0056 a0001c0001t0004g0058 a0001c0001t0004g0075 others(41): Show |
44 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-11227A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405116 | |||||||
| chr6:100405206 | C | T | 154 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0004g0056 others(151): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1168-11317G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405206 | |||||||
| chr6:100405263 | C | T | 1 | a0001c0009t0033g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1168-11374G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405263 | |||||||
| chr6:100405344 | C | G | 2 | a0001c0001t0022g0149 a0001c0001t0022g0165 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1168-11455G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405344 | |||||||
| chr6:100405526 | A | G | 1 | a0001c0001t0002g0040 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1168-11637T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405526 | |||||||
| chr6:100405551 | C | T | 159 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0004g0056 others(156): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1168-11662G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405551 | |||||||
| chr6:100405729 | C | A | 6 | a0001c0001t0002g0134 a0001c0001t0002g0143 a0001c0001t0002g0235 others(3): Show |
6 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168-11840G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405729 | |||||||
| chr6:100405921 | A | G | 1 | a0001c0001t0009g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1168-12032T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405921 | |||||||
| chr6:100405972 | A | G | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-12083T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405972 | |||||||
| chr6:100405991 | A | G | 1 | a0004c0008t0023g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1168-12102T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100405991 | |||||||
| chr6:100406034 | G | T | 3 | a0001c0001t0002g0282 a0001c0001t0012g0307 a0001c0001t0012g0308 |
3 | NA18945.hp1 NA18945.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1168-12145C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406034 | |||||||
| chr6:100406088 | C | T | 32 | a0001c0001t0002g0240 a0001c0001t0002g0248 a0001c0001t0003g0002 others(29): Show |
33 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1168-12199G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406088 | |||||||
| chr6:100406120 | G | C | 154 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0004g0056 others(151): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1168-12231C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406120 | |||||||
| chr6:100406257 | T | C | 164 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0004g0056 others(161): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1168-12368A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406257 | |||||||
| chr6:100406651 | T | C | 3 | a0001c0001t0020g0154 a0001c0001t0020g0265 a0001c0001t0041g0162 |
3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1168-12762A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406651 | |||||||
| chr6:100406689 | T | C | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1168-12800A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406689 | |||||||
| chr6:100406714 | TTGTATAC others(5): Show |
T | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1168-12837_1168-12 others(18): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406714 | |||||||
| chr6:100406746 | T | C | 47 | a0001c0001t0004g0056 a0001c0001t0004g0058 a0001c0001t0004g0075 others(44): Show |
48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1168-12857A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406746 | |||||||
| chr6:100406908 | G | A | 6 | a0001c0001t0006g0163 a0001c0001t0006g0293 a0001c0001t0006g0295 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168-13019C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406908 | |||||||
| chr6:100406929 | AC | A | 25 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(22): Show |
25 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1168-13041delG | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406929 | |||||||
| chr6:100406931 | A | G | 25 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(22): Show |
25 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1168-13042T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406931 | |||||||
| chr6:100406972 | C | T | 1 | a0001c0001t0005g0289 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1168-13083G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100406972 | |||||||
| chr6:100407059 | T | C | 49 | a0001c0001t0004g0056 a0001c0001t0004g0058 a0001c0001t0004g0075 others(46): Show |
50 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1168-13170A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407059 | |||||||
| chr6:100407119 | T | C | 1 | a0001c0001t0061g0294 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1168-13230A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407119 | |||||||
| chr6:100407338 | C | T | 83 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0028g0232 others(80): Show |
83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1168-13449G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407338 | |||||||
| chr6:100407513 | T | A | 2 | a0001c0001t0002g0117 a0001c0001t0002g0194 |
2 | NA19078.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1167+13277A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407513 | |||||||
| chr6:100407530 | C | A | 1 | a0002c0002t0001g0126 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1167+13260G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407530 | |||||||
| chr6:100407607 | C | T | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1167+13183G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407607 | |||||||
| chr6:100407670 | C | T | 86 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0025g0228 others(83): Show |
86 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1167+13120G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407670 | |||||||
| chr6:100407690 | A | G | 1 | a0001c0001t0002g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1167+13100T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407690 | |||||||
| chr6:100407742 | C | T | 2 | a0001c0001t0003g0002 a0001c0001t0003g0233 |
3 | HG01175.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1167+13048G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407742 | |||||||
| chr6:100407787 | C | A | 1 | a0001c0001t0061g0294 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1167+13003G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407787 | |||||||
| chr6:100407793 | T | A | 1 | a0001c0001t0061g0294 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1167+12997A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100407793 | |||||||
| chr6:100408063 | T | A | 3 | a0002c0002t0001g0259 a0002c0002t0001g0280 a0002c0002t0024g0087 |
3 | HG00558.hp2 NA18970.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1167+12727A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408063 | |||||||
| chr6:100408206 | T | C | 2 | a0001c0001t0006g0151 a0001c0001t0006g0213 |
2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1167+12584A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408206 | |||||||
| chr6:100408566 | T | C | 3 | a0001c0001t0015g0003 a0001c0001t0015g0219 a0001c0001t0068g0267 |
4 | HG01891.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+12224A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408566 | |||||||
| chr6:100408659 | A | G | 2 | a0001c0001t0006g0151 a0001c0001t0006g0213 |
2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1167+12131T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408659 | |||||||
| chr6:100408870 | T | C | 43 | a0001c0001t0004g0056 a0001c0001t0004g0058 a0001c0001t0004g0075 others(40): Show |
43 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1167+11920A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408870 | |||||||
| chr6:100408916 | G | T | 2 | a0001c0001t0006g0151 a0001c0001t0006g0213 |
2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1167+11874C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408916 | |||||||
| chr6:100408929 | G | T | 1 | a0001c0001t0027g0053 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1167+11861C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408929 | |||||||
| chr6:100408933 | T | C | 6 | a0001c0001t0006g0163 a0001c0001t0006g0293 a0001c0001t0006g0295 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1167+11857A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100408933 | |||||||
| chr6:100409120 | A | C | 1 | a0001c0001t0059g0180 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1167+11670T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409120 | |||||||
| chr6:100409136 | G | T | 1 | a0002c0002t0001g0122 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1167+11654C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409136 | |||||||
| chr6:100409198 | C | T | 2 | a0001c0001t0009g0024 a0001c0001t0009g0025 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1167+11592G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409198 | |||||||
| chr6:100409405 | AT | A | 3 | a0001c0001t0003g0042 a0001c0001t0005g0030 a0001c0001t0005g0041 |
3 | HG01109.hp2 HG06807.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1167+11384delA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409405 | |||||||
| chr6:100409428 | A | AT | 46 | a0001c0001t0002g0061 a0001c0001t0004g0056 a0001c0001t0004g0058 others(43): Show |
46 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.1167+11361dupA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409428 | |||||||
| chr6:100409583 | C | A | 6 | a0001c0001t0016g0001 a0001c0001t0021g0063 a0001c0001t0021g0244 others(3): Show |
7 | HG00738.hp1 HG01081.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.1167+11207G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409583 | |||||||
| chr6:100409637 | T | C | 2 | a0001c0001t0070g0175 a0001c0001t0071g0014 |
2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1167+11153A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409637 | |||||||
| chr6:100409643 | C | G | 11 | a0001c0001t0002g0103 a0001c0001t0002g0106 a0001c0001t0002g0111 others(8): Show |
11 | HG00558.hp1 HG02132.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.1167+11147G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409643 | |||||||
| chr6:100409689 | A | T | 86 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0025g0228 others(83): Show |
86 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1167+11101T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409689 | |||||||
| chr6:100409769 | T | C | 6 | a0001c0001t0015g0003 a0001c0001t0015g0219 a0001c0001t0068g0267 others(3): Show |
7 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1167+11021A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409769 | |||||||
| chr6:100409890 | A | G | 2 | a0001c0001t0022g0149 a0001c0001t0022g0165 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1167+10900T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409890 | |||||||
| chr6:100409993 | G | A | 131 | a0001c0001t0004g0056 a0001c0001t0004g0058 a0001c0001t0004g0075 others(128): Show |
131 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1167+10797C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100409993 | |||||||
| chr6:100410351 | A | G | 2 | a0001c0001t0002g0158 a0001c0001t0002g0167 |
2 | HG00735.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1167+10439T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100410351 | |||||||
| chr6:100410400 | G | A | 1 | a0001c0001t0012g0306 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1167+10390C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100410400 | |||||||
| chr6:100410433 | C | T | 1 | a0002c0002t0024g0087 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1167+10357G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100410433 | |||||||
| chr6:100410462 | A | C | 1 | a0001c0001t0061g0294 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1167+10328T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100410462 | |||||||
| chr6:100410651 | T | A | 1 | a0001c0001t0009g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1167+10139A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100410651 | |||||||
| chr6:100411060 | A | T | 25 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(22): Show |
25 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1167+9730T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411060 | |||||||
| chr6:100411164 | G | T | 3 | a0001c0001t0020g0154 a0001c0001t0020g0265 a0001c0001t0041g0162 |
3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1167+9626C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411164 | |||||||
| chr6:100411283 | T | C | 137 | a0001c0001t0004g0056 a0001c0001t0004g0058 a0001c0001t0004g0075 others(134): Show |
138 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.1167+9507A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411283 | |||||||
| chr6:100411313 | A | G | 86 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0025g0228 others(83): Show |
86 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1167+9477T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411313 | |||||||
| chr6:100411452 | T | C | 1 | a0002c0002t0024g0253 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1167+9338A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411452 | |||||||
| chr6:100411472 | G | T | 83 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0028g0232 others(80): Show |
83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1167+9318C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411472 | |||||||
| chr6:100411510 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1167+9280C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411510 | |||||||
| chr6:100411587 | C | T | 1 | a0001c0009t0033g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1167+9203G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411587 | |||||||
| chr6:100411598 | T | G | 1 | a0002c0002t0014g0258 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1167+9192A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411598 | |||||||
| chr6:100411609 | A | G | 2 | a0001c0001t0003g0153 a0001c0001t0009g0170 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1167+9181T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411609 | |||||||
| chr6:100411697 | C | T | 136 | a0001c0001t0004g0056 a0001c0001t0004g0075 a0001c0001t0004g0076 others(133): Show |
137 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1167+9093G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411697 | |||||||
| chr6:100411727 | A | T | 1 | a0002c0002t0007g0251 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1167+9063T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411727 | |||||||
| chr6:100411739 | T | C | 1 | a0001c0001t0026g0216 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1167+9051A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411739 | |||||||
| chr6:100411832 | C | T | 39 | a0001c0001t0004g0056 a0001c0001t0004g0075 a0001c0001t0004g0076 others(36): Show |
39 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1167+8958G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411832 | |||||||
| chr6:100411867 | G | A | 1 | a0001c0001t0060g0157 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1167+8923C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411867 | |||||||
| chr6:100411905 | G | A | 39 | a0001c0001t0004g0056 a0001c0001t0004g0075 a0001c0001t0004g0076 others(36): Show |
39 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1167+8885C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411905 | |||||||
| chr6:100411907 | G | C | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1167+8883C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100411907 | |||||||
| chr6:100412035 | C | T | 1 | a0001c0001t0040g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1167+8755G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412035 | |||||||
| chr6:100412071 | T | C | 166 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0004g0056 others(163): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1167+8719A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412071 | |||||||
| chr6:100412101 | G | A | 3 | a0001c0001t0002g0166 a0001c0001t0003g0164 a0001c0001t0003g0168 |
3 | HG02055.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1167+8689C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412101 | |||||||
| chr6:100412207 | T | C | 2 | a0001c0001t0005g0145 a0001c0001t0005g0146 |
2 | NA18982.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1167+8583A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412207 | |||||||
| chr6:100412226 | T | C | 1 | a0001c0001t0003g0035 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1167+8564A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412226 | |||||||
| chr6:100412461 | C | A | 1 | a0002c0002t0001g0119 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1167+8329G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412461 | |||||||
| chr6:100412462 | A | G | 1 | a0002c0002t0001g0119 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1167+8328T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412462 | |||||||
| chr6:100412534 | CTAAGAAA others(34): Show |
C | 1 | a0002c0002t0001g0280 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1167+8215_1167+825 others(45): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412534 | |||||||
| chr6:100412534 | CTAAGAAA others(38): Show |
C | 1 | a0002c0002t0001g0088 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1167+8211_1167+825 others(49): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412534 | |||||||
| chr6:100412535 | T | A | 81 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0028g0232 others(78): Show |
81 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1167+8255A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412535 | |||||||
| chr6:100412541 | A | G | 2 | a0001c0001t0022g0149 a0001c0001t0022g0165 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1167+8249T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412541 | |||||||
| chr6:100412542 | GAAAGAAA others(6): Show |
G | 10 | a0001c0001t0005g0026 a0001c0001t0005g0070 a0001c0001t0005g0093 others(7): Show |
10 | HG00544.hp2 HG01256.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1167+8235_1167+824 others(17): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412542 | |||||||
| chr6:100412546 | GAAAGAAA others(2): Show |
G | 12 | a0001c0001t0005g0074 a0001c0001t0005g0091 a0001c0001t0005g0092 others(9): Show |
12 | HG00621.hp1 HG00733.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1167+8235_1167+824 others(13): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412546 | |||||||
| chr6:100412548 | AAGAAAGA others(28): Show |
A | 1 | a0001c0001t0005g0220 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1167+8207_1167+824 others(39): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412548 | |||||||
| chr6:100412550 | GAAAGA | G | 7 | a0001c0001t0004g0275 a0001c0001t0004g0277 a0001c0001t0008g0096 others(4): Show |
7 | HG01081.hp2 HG01168.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1167+8235_1167+823 others(9): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412550 | |||||||
| chr6:100412551 | AAAGAAAA others(1): Show |
A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0296 a0001c0001t0006g0297 |
3 | HG03195.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1167+8231_1167+823 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412551 | |||||||
| chr6:100412553 | AGAAAAGA others(63): Show |
A | 1 | a0002c0002t0017g0301 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1167+8167_1167+823 others(74): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412553 | |||||||
| chr6:100412554 | GA | G | 118 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0004g0056 others(115): Show |
118 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1167+8235delT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412554 | |||||||
| chr6:100412555 | A | AAAAG | 17 | a0001c0001t0002g0040 a0001c0001t0002g0191 a0001c0001t0003g0110 others(14): Show |
17 | HG00140.hp1 HG00558.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1167+8231_1167+823 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | |||||||
| chr6:100412555 | A | AAAAGAAA others(1): Show |
5 | a0001c0001t0002g0268 a0001c0001t0003g0128 a0001c0001t0003g0210 others(2): Show |
5 | HG01993.hp1 HG03491.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+8227_1167+823 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | |||||||
| chr6:100412555 | A | AAAAGAAA others(5): Show |
1 | a0001c0001t0002g0202 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1167+8223_1167+823 others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | |||||||
| chr6:100412555 | A | AAAG | 8 | a0001c0001t0004g0076 a0001c0001t0004g0077 a0001c0001t0004g0247 others(5): Show |
8 | HG00438.hp2 HG02723.hp1 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.1167+8234_1167+823 others(7): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | |||||||
| chr6:100412555 | A | AAAGAAAG | 4 | a0001c0001t0004g0079 a0001c0001t0008g0047 a0001c0001t0008g0141 others(1): Show |
4 | HG01074.hp2 HG02572.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8234_1167+823 others(11): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | |||||||
| chr6:100412555 | A | AAAGAAAG others(4): Show |
2 | a0001c0001t0008g0181 a0001c0001t0026g0216 |
2 | HG00423.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1167+8234_1167+823 others(15): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | |||||||
| chr6:100412555 | A | AAAGAAAG others(101): Show |
1 | a0001c0009t0033g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1167+8234_1167+823 others(112): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | |||||||
| chr6:100412555 | AAAAG | A | 56 | a0001c0001t0002g0004 a0001c0001t0002g0052 a0001c0001t0002g0065 others(53): Show |
58 | HG00280.hp1 HG00544.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1167+8231_1167+823 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | |||||||
| chr6:100412555 | AAAAGAAA others(1): Show |
A | 21 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0152 others(18): Show |
21 | HG01109.hp1 HG01433.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.1167+8227_1167+823 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | |||||||
| chr6:100412555 | AAAAGAAA others(5): Show |
A | 13 | a0001c0001t0002g0103 a0001c0001t0002g0106 a0001c0001t0002g0111 others(10): Show |
13 | HG00099.hp2 HG01256.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1167+8223_1167+823 others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | |||||||
| chr6:100412555 | AAAAGAAA others(9): Show |
A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0185 |
2 | NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1167+8219_1167+823 others(20): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | |||||||
| chr6:100412555 | AAAAGAAA others(21): Show |
A | 1 | a0001c0001t0047g0291 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1167+8207_1167+823 others(32): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412555 | |||||||
| chr6:100412559 | G | A | 1 | a0001c0001t0006g0295 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1167+8231C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412559 | |||||||
| chr6:100412563 | G | A | 4 | a0001c0001t0006g0163 a0001c0001t0006g0296 a0001c0001t0006g0297 others(1): Show |
4 | HG02615.hp1 HG03195.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8227C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412563 | |||||||
| chr6:100412569 | AAG | A | 5 | a0001c0001t0013g0059 a0001c0001t0013g0072 a0001c0001t0013g0073 others(2): Show |
5 | HG00280.hp2 HG00323.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.1167+8219_1167+822 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412569 | |||||||
| chr6:100412575 | GAAAGAAA others(55): Show |
G | 3 | a0001c0001t0028g0232 a0002c0002t0001g0312 a0002c0002t0001g0314 |
3 | HG01516.hp2 HG01517.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1167+8153_1167+821 others(66): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412575 | |||||||
| chr6:100412579 | GAAAGAAA others(51): Show |
G | 3 | a0002c0002t0001g0039 a0002c0002t0001g0242 a0002c0002t0001g0313 |
3 | HG01515.hp2 HG02071.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1167+8153_1167+821 others(62): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412579 | |||||||
| chr6:100412581 | AAG | A | 15 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(12): Show |
15 | HG00544.hp2 HG01109.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.1167+8207_1167+820 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412581 | |||||||
| chr6:100412583 | GAAAGAAA others(47): Show |
G | 4 | a0002c0002t0001g0272 a0002c0002t0001g0315 a0002c0002t0006g0192 others(1): Show |
4 | HG02300.hp2 HG02602.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+8153_1167+820 others(58): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412583 | |||||||
| chr6:100412583 | GAAAGAAA others(49): Show |
G | 1 | a0002c0002t0001g0224 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1167+8151_1167+820 others(60): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412583 | |||||||
| chr6:100412583 | GAAAGAAA others(53): Show |
G | 1 | a0002c0002t0024g0253 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1167+8147_1167+820 others(64): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412583 | |||||||
| chr6:100412585 | A | G | 2 | a0002c0002t0007g0038 a0002c0005t0065g0116 |
2 | NA18966.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1167+8205T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412585 | |||||||
| chr6:100412585 | AAGAAAG | A | 5 | a0001c0001t0002g0269 a0001c0003t0003g0044 a0001c0003t0003g0102 others(2): Show |
5 | HG01516.hp1 HG02738.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+8199_1167+820 others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412585 | |||||||
| chr6:100412587 | GAAAGAAA others(43): Show |
G | 2 | a0002c0002t0007g0245 a0002c0002t0007g0246 |
2 | HG00738.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1167+8153_1167+820 others(54): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412587 | |||||||
| chr6:100412587 | GAAAGAAA others(45): Show |
G | 3 | a0002c0002t0001g0193 a0002c0002t0001g0203 a0002c0002t0007g0178 |
3 | HG02135.hp2 NA18747.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1167+8151_1167+820 others(56): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412587 | |||||||
| chr6:100412587 | GAAAGAAA others(49): Show |
G | 1 | a0002c0002t0028g0055 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1167+8147_1167+820 others(60): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412587 | |||||||
| chr6:100412587 | GAAAGAAA others(61): Show |
G | 1 | a0002c0002t0017g0303 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1167+8135_1167+820 others(72): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412587 | |||||||
| chr6:100412589 | A | G | 6 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0002c0002t0001g0227 others(3): Show |
6 | HG00642.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+8201T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412589 | |||||||
| chr6:100412590 | A | G | 1 | a0001c0009t0033g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1167+8200T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412590 | |||||||
| chr6:100412591 | GAAAGAAA others(39): Show |
G | 6 | a0002c0002t0001g0037 a0002c0002t0001g0199 a0002c0002t0001g0237 others(3): Show |
6 | HG00642.hp2 HG02056.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+8153_1167+819 others(50): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412591 | |||||||
| chr6:100412591 | GAAAGAAA others(41): Show |
G | 1 | a0002c0002t0001g0227 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1167+8151_1167+819 others(52): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412591 | |||||||
| chr6:100412591 | GAAAGAAA others(45): Show |
G | 2 | a0002c0002t0001g0214 a0002c0002t0001g0226 |
2 | HG03239.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1167+8147_1167+819 others(56): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412591 | |||||||
| chr6:100412593 | A | G | 9 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0002c0002t0001g0033 others(6): Show |
9 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1167+8197T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412593 | |||||||
| chr6:100412595 | G | GAA | 3 | a0001c0001t0020g0154 a0001c0001t0020g0265 a0001c0001t0041g0162 |
3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1167+8193_1167+819 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412595 | |||||||
| chr6:100412595 | GAAAGAAA others(23): Show |
G | 1 | a0002c0002t0007g0251 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1167+8165_1167+819 others(34): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412595 | |||||||
| chr6:100412595 | GAAAGAAA others(35): Show |
G | 5 | a0002c0002t0001g0094 a0002c0002t0001g0139 a0002c0002t0007g0038 others(2): Show |
5 | HG04204.hp1 NA18966.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.1167+8153_1167+819 others(46): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412595 | |||||||
| chr6:100412595 | GAAAGAAA others(37): Show |
G | 1 | a0002c0002t0007g0089 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1167+8151_1167+819 others(48): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412595 | |||||||
| chr6:100412595 | GAAAGAAA others(41): Show |
G | 4 | a0001c0001t0070g0175 a0002c0002t0001g0045 a0002c0002t0001g0187 others(1): Show |
4 | HG02559.hp1 NA18970.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+8147_1167+819 others(52): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412595 | |||||||
| chr6:100412595 | GAAAGAAA others(42): Show |
G | 1 | a0001c0001t0061g0294 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1167+8146_1167+819 others(53): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412595 | |||||||
| chr6:100412595 | GAAAGAAA others(45): Show |
G | 1 | a0002c0002t0001g0215 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1167+8143_1167+819 others(56): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412595 | |||||||
| chr6:100412595 | GAAAGAAA others(49): Show |
G | 1 | a0002c0002t0001g0281 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1167+8139_1167+819 others(60): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412595 | |||||||
| chr6:100412596 | AAAGAAAG others(17): Show |
A | 4 | a0001c0001t0013g0072 a0001c0001t0013g0073 a0001c0001t0062g0071 others(1): Show |
4 | HG00280.hp2 HG00323.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8170_1167+819 others(28): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412596 | |||||||
| chr6:100412597 | A | G | 8 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0002c0002t0001g0033 others(5): Show |
8 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1167+8193T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412597 | |||||||
| chr6:100412599 | GAAAGAAA others(31): Show |
G | 2 | a0002c0002t0001g0249 a0002c0002t0003g0051 |
2 | HG00741.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1167+8153_1167+819 others(42): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412599 | |||||||
| chr6:100412599 | GAAAGAAA others(33): Show |
G | 4 | a0001c0001t0008g0130 a0002c0002t0001g0033 a0002c0002t0001g0257 others(1): Show |
4 | HG01169.hp2 HG01261.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+8151_1167+819 others(44): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412599 | |||||||
| chr6:100412599 | GAAAGAAA others(36): Show |
G | 1 | a0002c0002t0024g0087 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1167+8148_1167+819 others(47): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412599 | |||||||
| chr6:100412599 | GAAAGAAA others(37): Show |
G | 1 | a0002c0002t0014g0254 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1167+8147_1167+819 others(48): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412599 | |||||||
| chr6:100412599 | GAAAGAAA others(40): Show |
G | 1 | a0002c0002t0014g0258 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1167+8144_1167+819 others(51): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412599 | |||||||
| chr6:100412601 | A | G | 4 | a0001c0001t0008g0129 a0002c0002t0001g0100 a0002c0002t0001g0108 others(1): Show |
4 | HG01167.hp1 HG01192.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8189T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412601 | |||||||
| chr6:100412603 | GAAAGAAA others(16): Show |
G | 1 | a0002c0002t0007g0250 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1167+8164_1167+818 others(27): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412603 | |||||||
| chr6:100412603 | GAAAGAAA others(27): Show |
G | 1 | a0002c0002t0001g0218 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1167+8153_1167+818 others(38): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412603 | |||||||
| chr6:100412603 | GAAAGAAA others(29): Show |
G | 3 | a0002c0002t0001g0086 a0002c0002t0001g0236 a0002c0002t0066g0124 |
3 | HG01106.hp2 NA18998.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1167+8151_1167+818 others(40): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412603 | |||||||
| chr6:100412605 | A | G | 5 | a0001c0001t0008g0129 a0002c0002t0001g0100 a0002c0002t0001g0108 others(2): Show |
5 | HG01167.hp1 HG01192.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+8185T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412605 | |||||||
| chr6:100412607 | GAAAGGAA others(23): Show |
G | 4 | a0002c0002t0001g0084 a0002c0002t0001g0122 a0002c0002t0001g0222 others(1): Show |
4 | NA18950.hp2 NA18957.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8153_1167+818 others(34): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412607 | |||||||
| chr6:100412607 | GAAAGGAA others(25): Show |
G | 1 | a0002c0002t0001g0108 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1167+8151_1167+818 others(36): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412607 | |||||||
| chr6:100412607 | GAAAGGAA others(37): Show |
G | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1167+8139_1167+818 others(48): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412607 | |||||||
| chr6:100412608 | A | G | 20 | a0001c0001t0004g0075 a0001c0001t0004g0081 a0001c0001t0004g0275 others(17): Show |
20 | HG00733.hp1 HG00735.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.1167+8182T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412608 | |||||||
| chr6:100412609 | A | G | 3 | a0002c0002t0001g0100 a0002c0002t0001g0120 a0002c0002t0014g0255 |
3 | HG01192.hp2 HG02083.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1167+8181T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412609 | |||||||
| chr6:100412609 | AAGGAAAG others(7): Show |
A | 1 | a0002c0002t0001g0182 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1167+8167_1167+818 others(18): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412609 | |||||||
| chr6:100412610 | AG | A | 8 | a0001c0001t0013g0059 a0001c0001t0020g0154 a0001c0001t0020g0265 others(5): Show |
8 | HG02074.hp2 HG02886.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1167+8179delC | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412610 | |||||||
| chr6:100412610 | AGGAAAGA others(6): Show |
A | 7 | a0001c0001t0022g0149 a0002c0002t0001g0031 a0002c0002t0001g0085 others(4): Show |
7 | HG00621.hp2 HG02523.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167+8167_1167+817 others(17): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412610 | |||||||
| chr6:100412611 | G | A | 21 | a0001c0001t0004g0075 a0001c0001t0004g0081 a0001c0001t0004g0275 others(18): Show |
22 | HG00733.hp1 HG00735.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.1167+8179C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412611 | |||||||
| chr6:100412611 | GGAAAGAA others(8): Show |
G | 1 | a0002c0002t0001g0057 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1167+8164_1167+817 others(19): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412611 | |||||||
| chr6:100412611 | GGAAAGAA others(12): Show |
G | 3 | a0002c0002t0001g0119 a0002c0002t0001g0127 a0002c0002t0014g0121 |
3 | NA18965.hp1 NA18983.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1167+8160_1167+817 others(23): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412611 | |||||||
| chr6:100412611 | GGAAAGAA others(19): Show |
G | 2 | a0002c0002t0001g0023 a0002c0002t0001g0125 |
2 | NA18989.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1167+8153_1167+817 others(30): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412611 | |||||||
| chr6:100412611 | GGAAAGAA others(20): Show |
G | 1 | a0002c0002t0007g0123 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1167+8152_1167+817 others(31): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412611 | |||||||
| chr6:100412611 | GGAAAGAA others(21): Show |
G | 2 | a0002c0002t0001g0120 a0002c0002t0014g0255 |
2 | HG02083.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1167+8151_1167+817 others(32): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412611 | |||||||
| chr6:100412611 | GGAAAGAA others(22): Show |
G | 1 | a0001c0001t0006g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1167+8150_1167+817 others(33): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412611 | |||||||
| chr6:100412611 | GGAAAGAA others(29): Show |
G | 1 | a0002c0002t0001g0286 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1167+8143_1167+817 others(40): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412611 | |||||||
| chr6:100412614 | A | G | 2 | a0001c0001t0008g0129 a0002c0002t0001g0100 |
2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1167+8176T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412614 | |||||||
| chr6:100412614 | AAG | A | 2 | a0001c0001t0015g0003 a0001c0001t0068g0267 |
3 | HG01891.hp1 HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1167+8174_1167+817 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412614 | |||||||
| chr6:100412615 | A | G | 1 | a0006c0006t0004g0090 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1167+8175T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412615 | |||||||
| chr6:100412616 | GAAAGAAG others(14): Show |
G | 1 | a0001c0001t0003g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1167+8153_1167+817 others(25): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412616 | |||||||
| chr6:100412616 | GAAAGAAG others(16): Show |
G | 1 | a0002c0002t0001g0083 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1167+8151_1167+817 others(27): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412616 | |||||||
| chr6:100412616 | GAAAGAAG others(24): Show |
G | 2 | a0001c0001t0022g0165 a0002c0002t0007g0198 |
2 | HG02280.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1167+8143_1167+817 others(35): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412616 | |||||||
| chr6:100412618 | A | G | 3 | a0001c0001t0006g0213 a0001c0001t0008g0129 a0002c0002t0001g0100 |
3 | HG01167.hp1 HG01192.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1167+8172T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412618 | |||||||
| chr6:100412619 | A | G | 18 | a0001c0001t0004g0075 a0001c0001t0004g0081 a0001c0001t0004g0275 others(15): Show |
18 | HG00733.hp1 HG00735.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1167+8171T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412619 | |||||||
| chr6:100412620 | GAAGGAAA others(10): Show |
G | 2 | a0001c0001t0005g0074 a0001c0001t0063g0113 |
2 | HG02165.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1167+8153_1167+816 others(21): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412620 | |||||||
| chr6:100412622 | A | G | 2 | a0001c0001t0008g0129 a0002c0002t0001g0100 |
2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1167+8168T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412622 | |||||||
| chr6:100412623 | G | A | 49 | a0001c0001t0003g0186 a0001c0001t0004g0075 a0001c0001t0004g0081 others(46): Show |
50 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.1167+8167C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412623 | |||||||
| chr6:100412623 | G | GGAAA | 15 | a0001c0001t0004g0056 a0001c0001t0004g0076 a0001c0001t0004g0077 others(12): Show |
15 | HG00423.hp1 HG00438.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1167+8163_1167+816 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412623 | |||||||
| chr6:100412624 | GAAAGAAA others(6): Show |
G | 2 | a0001c0001t0003g0186 a0001c0001t0005g0196 |
2 | HG00621.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1167+8153_1167+816 others(17): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412624 | |||||||
| chr6:100412626 | A | G | 3 | a0001c0001t0006g0213 a0002c0002t0001g0100 a0002c0002t0001g0182 |
3 | HG01192.hp2 HG02976.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1167+8164T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412626 | |||||||
| chr6:100412628 | GAAAGAAA others(2): Show |
G | 5 | a0001c0001t0005g0026 a0001c0001t0005g0189 a0001c0001t0005g0220 others(2): Show |
5 | HG01168.hp2 HG02074.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+8153_1167+816 others(13): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412628 | |||||||
| chr6:100412630 | A | G | 6 | a0001c0001t0006g0213 a0002c0002t0001g0031 a0002c0002t0001g0057 others(3): Show |
6 | HG02976.hp2 NA18971.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+8160T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412630 | |||||||
| chr6:100412632 | GAAAGA | G | 4 | a0001c0001t0005g0070 a0001c0001t0005g0104 a0001c0001t0005g0289 others(1): Show |
4 | HG01256.hp2 HG02129.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+8153_1167+815 others(9): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412632 | |||||||
| chr6:100412632 | GAAAGAAA others(4): Show |
G | 1 | a0001c0001t0025g0238 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1167+8147_1167+815 others(15): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412632 | |||||||
| chr6:100412632 | GAAAGAAA others(8): Show |
G | 2 | a0001c0001t0025g0228 a0001c0001t0069g0239 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1167+8143_1167+815 others(19): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412632 | |||||||
| chr6:100412634 | A | G | 10 | a0001c0001t0006g0213 a0002c0002t0001g0031 a0002c0002t0001g0057 others(7): Show |
10 | HG02976.hp2 NA18965.hp1 NA18971.hp1 others(7): Show |
intron_variant | MODIFIER | c.1167+8156T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412634 | |||||||
| chr6:100412636 | G | A | 1 | a0006c0006t0004g0090 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1167+8154C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412636 | |||||||
| chr6:100412636 | GA | G | 18 | a0001c0001t0005g0030 a0001c0001t0005g0041 a0001c0001t0005g0091 others(15): Show |
18 | HG00280.hp2 HG00323.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1167+8153delT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412636 | |||||||
| chr6:100412636 | GAAA | G | 6 | a0001c0001t0006g0213 a0002c0002t0001g0031 a0002c0002t0001g0105 others(3): Show |
6 | HG02976.hp2 NA18965.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+8151_1167+815 others(7): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412636 | |||||||
| chr6:100412637 | A | AAAG | 3 | a0001c0001t0020g0154 a0001c0001t0020g0265 a0001c0001t0041g0162 |
3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1167+8152_1167+815 others(7): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412637 | |||||||
| chr6:100412637 | A | G | 2 | a0001c0001t0015g0219 a0006c0006t0004g0090 |
2 | HG03098.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1167+8153T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412637 | |||||||
| chr6:100412637 | AAAAG | A | 3 | a0001c0001t0002g0167 a0001c0001t0009g0206 a0002c0002t0001g0085 |
3 | HG00621.hp2 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1167+8149_1167+815 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412637 | |||||||
| chr6:100412639 | A | G | 24 | a0002c0002t0001g0023 a0002c0002t0001g0037 a0002c0002t0001g0057 others(21): Show |
24 | HG00423.hp2 HG00642.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1167+8151T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412639 | |||||||
| chr6:100412640 | A | G | 8 | a0001c0001t0008g0047 a0001c0001t0008g0141 a0001c0001t0008g0181 others(5): Show |
9 | HG00099.hp1 HG01070.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1167+8150T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412640 | |||||||
| chr6:100412641 | G | A | 5 | a0001c0001t0008g0047 a0001c0001t0008g0141 a0001c0001t0008g0181 others(2): Show |
5 | HG00099.hp1 HG01070.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+8149C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412641 | |||||||
| chr6:100412643 | A | G | 59 | a0001c0001t0006g0213 a0001c0001t0008g0130 a0001c0001t0015g0219 others(56): Show |
59 | HG00140.hp2 HG00423.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1167+8147T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412643 | |||||||
| chr6:100412644 | A | G | 1 | a0001c0001t0006g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1167+8146T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412644 | |||||||
| chr6:100412647 | A | G | 72 | a0001c0001t0005g0243 a0001c0001t0008g0130 a0001c0001t0015g0003 others(69): Show |
73 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1167+8143T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412647 | |||||||
| chr6:100412649 | GAA | G | 6 | a0001c0001t0005g0041 a0001c0001t0005g0091 a0001c0001t0005g0093 others(3): Show |
6 | NA18944.hp1 NA18948.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1167+8139_1167+814 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412649 | |||||||
| chr6:100412649 | GAAAGAAA others(27): Show |
G | 2 | a0001c0001t0008g0129 a0002c0002t0001g0100 |
2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1167+8107_1167+814 others(38): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412649 | |||||||
| chr6:100412651 | A | G | 86 | a0001c0001t0005g0030 a0001c0001t0005g0243 a0001c0001t0006g0151 others(83): Show |
87 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1167+8139T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412651 | |||||||
| chr6:100412655 | A | G | 99 | a0001c0001t0003g0160 a0001c0001t0003g0168 a0001c0001t0005g0030 others(96): Show |
100 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1167+8135T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412655 | |||||||
| chr6:100412655 | AAG | A | 10 | a0001c0001t0002g0040 a0001c0001t0002g0052 a0001c0001t0003g0133 others(7): Show |
10 | HG00733.hp1 HG00733.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1167+8133_1167+813 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412655 | |||||||
| chr6:100412655 | AAGAGAGA others(7): Show |
A | 1 | a0001c0001t0006g0213 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1167+8121_1167+813 others(18): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412655 | |||||||
| chr6:100412657 | G | GAA | 4 | a0001c0001t0008g0047 a0001c0001t0008g0141 a0001c0001t0008g0181 others(1): Show |
4 | HG00099.hp1 HG01070.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+8132_1167+813 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412657 | |||||||
| chr6:100412659 | G | A | 15 | a0001c0001t0003g0186 a0001c0001t0005g0074 a0001c0001t0005g0092 others(12): Show |
15 | HG00280.hp2 HG00323.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1167+8131C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412659 | |||||||
| chr6:100412661 | G | A | 1 | a0001c0001t0005g0243 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1167+8129C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412661 | |||||||
| chr6:100412663 | G | A | 1 | a0001c0001t0020g0265 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1167+8127C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412663 | |||||||
| chr6:100412665 | G | A | 12 | a0001c0001t0005g0030 a0001c0001t0005g0041 a0001c0001t0005g0091 others(9): Show |
12 | HG00544.hp2 HG01169.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1167+8125C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412665 | |||||||
| chr6:100412667 | G | A | 2 | a0001c0001t0013g0059 a0002c0002t0001g0126 |
2 | NA18994.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1167+8123C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412667 | |||||||
| chr6:100412669 | G | A | 12 | a0001c0001t0005g0030 a0001c0001t0005g0041 a0001c0001t0005g0091 others(9): Show |
12 | HG00544.hp2 HG01169.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1167+8121C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412669 | |||||||
| chr6:100412671 | G | A | 27 | a0001c0001t0003g0042 a0001c0001t0003g0160 a0001c0001t0005g0026 others(24): Show |
27 | HG00544.hp2 HG00642.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1167+8119C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412671 | |||||||
| chr6:100412671 | GAGAAAGA others(5): Show |
G | 1 | a0001c0001t0003g0177 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1167+8107_1167+811 others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412671 | |||||||
| chr6:100412673 | G | A | 10 | a0001c0001t0005g0041 a0001c0001t0005g0091 a0001c0001t0005g0093 others(7): Show |
10 | HG01169.hp2 HG02451.hp2 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.1167+8117C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412673 | |||||||
| chr6:100412673 | GAAAGAAA others(37): Show |
G | 1 | a0001c0001t0015g0003 | 2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1167+8073_1167+811 others(48): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412673 | |||||||
| chr6:100412675 | A | G | 40 | a0001c0001t0004g0081 a0001c0001t0020g0265 a0001c0001t0028g0232 others(37): Show |
40 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1167+8115T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412675 | |||||||
| chr6:100412677 | G | A | 1 | a0001c0001t0013g0059 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1167+8113C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412677 | |||||||
| chr6:100412679 | A | G | 17 | a0001c0001t0013g0059 a0001c0001t0028g0232 a0001c0001t0071g0014 others(14): Show |
17 | HG01074.hp1 HG01361.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.1167+8111T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412679 | |||||||
| chr6:100412681 | G | A | 21 | a0001c0001t0003g0042 a0001c0001t0003g0160 a0001c0001t0005g0026 others(18): Show |
21 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1167+8109C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412681 | |||||||
| chr6:100412681 | GAA | G | 12 | a0001c0001t0005g0041 a0001c0001t0005g0091 a0001c0001t0005g0093 others(9): Show |
12 | HG00544.hp2 HG02451.hp2 HG04115.hp1 others(9): Show |
intron_variant | MODIFIER | c.1167+8107_1167+810 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412681 | |||||||
| chr6:100412683 | A | AAAAG | 30 | a0001c0001t0002g0143 a0001c0001t0002g0185 a0001c0001t0002g0208 others(27): Show |
31 | HG00738.hp1 HG01167.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1167+8103_1167+810 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | |||||||
| chr6:100412683 | A | AAAAGAAA others(1): Show |
8 | a0001c0001t0002g0166 a0001c0001t0006g0295 a0001c0001t0021g0244 others(5): Show |
8 | HG01081.hp1 HG01256.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1167+8099_1167+810 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | |||||||
| chr6:100412683 | A | AAAAGAAA others(5): Show |
1 | a0001c0001t0039g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1167+8095_1167+810 others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | |||||||
| chr6:100412683 | A | AAG | 3 | a0001c0001t0005g0030 a0001c0001t0008g0130 a0002c0002t0001g0280 |
3 | HG01169.hp2 HG06807.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1167+8106_1167+810 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | |||||||
| chr6:100412683 | A | G | 37 | a0001c0001t0002g0184 a0001c0001t0003g0042 a0001c0001t0003g0160 others(34): Show |
37 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1167+8107T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | |||||||
| chr6:100412683 | AAAAG | A | 30 | a0001c0001t0001g0067 a0001c0001t0002g0106 a0001c0001t0002g0135 others(27): Show |
32 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1167+8103_1167+810 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | |||||||
| chr6:100412683 | AAAAGAAA others(1): Show |
A | 29 | a0001c0001t0002g0061 a0001c0001t0002g0095 a0001c0001t0002g0118 others(26): Show |
29 | HG00423.hp2 HG00642.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1167+8099_1167+810 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | |||||||
| chr6:100412683 | AAAAGAAA others(5): Show |
A | 11 | a0001c0001t0002g0065 a0001c0001t0002g0152 a0001c0001t0003g0153 others(8): Show |
11 | HG01261.hp1 HG02132.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.1167+8095_1167+810 others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | |||||||
| chr6:100412683 | AAAAGAAA others(9): Show |
A | 6 | a0001c0001t0002g0235 a0001c0001t0003g0034 a0001c0001t0003g0068 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1167+8091_1167+810 others(20): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | |||||||
| chr6:100412683 | AAAAGAAA others(13): Show |
A | 4 | a0001c0001t0003g0128 a0001c0001t0003g0210 a0001c0001t0019g0019 others(1): Show |
4 | HG01070.hp1 HG02071.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+8087_1167+810 others(24): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | |||||||
| chr6:100412683 | AAAAGAAA others(17): Show |
A | 1 | a0004c0008t0023g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1167+8083_1167+810 others(28): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | |||||||
| chr6:100412683 | AAAAGAAA others(37): Show |
A | 2 | a0001c0001t0022g0149 a0001c0001t0022g0165 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1167+8063_1167+810 others(48): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | |||||||
| chr6:100412683 | AAAAGAAA others(41): Show |
A | 2 | a0001c0001t0015g0219 a0001c0001t0068g0267 |
2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1167+8059_1167+810 others(52): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412683 | |||||||
| chr6:100412685 | A | G | 29 | a0001c0001t0002g0111 a0001c0001t0004g0081 a0001c0001t0020g0265 others(26): Show |
29 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.1167+8105T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412685 | |||||||
| chr6:100412687 | G | A | 24 | a0001c0001t0002g0111 a0001c0001t0004g0081 a0001c0001t0020g0265 others(21): Show |
24 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.1167+8103C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412687 | |||||||
| chr6:100412689 | A | G | 1 | a0002c0002t0017g0303 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1167+8101T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412689 | |||||||
| chr6:100412693 | AAG | A | 9 | a0001c0001t0003g0177 a0001c0001t0028g0232 a0001c0001t0071g0014 others(6): Show |
9 | HG00544.hp1 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1167+8095_1167+809 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412693 | |||||||
| chr6:100412695 | G | A | 1 | a0002c0002t0017g0303 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1167+8095C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412695 | |||||||
| chr6:100412696 | AAAGAAAG others(12): Show |
A | 1 | a0001c0001t0002g0202 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1167+8075_1167+809 others(23): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412696 | |||||||
| chr6:100412697 | AAG | A | 4 | a0002c0002t0001g0039 a0002c0002t0001g0203 a0002c0002t0001g0242 others(1): Show |
4 | HG02071.hp1 HG02602.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8091_1167+809 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412697 | |||||||
| chr6:100412738 | AGAAAG | A | 10 | a0001c0001t0004g0076 a0001c0001t0004g0277 a0001c0001t0004g0278 others(7): Show |
10 | HG00438.hp2 HG00733.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.1167+8047_1167+805 others(9): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412738 | |||||||
| chr6:100412742 | A | G | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1167+8048T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412742 | |||||||
| chr6:100412742 | AG | A | 8 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0275 others(5): Show |
8 | HG00423.hp1 HG01081.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1167+8047delC | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412742 | |||||||
| chr6:100412746 | AG | A | 4 | a0001c0001t0004g0078 a0001c0001t0004g0279 a0001c0001t0018g0309 others(1): Show |
4 | HG00735.hp2 HG02083.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8043delC | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412746 | |||||||
| chr6:100412751 | G | A | 5 | a0001c0001t0004g0247 a0001c0001t0008g0181 a0001c0001t0027g0098 others(2): Show |
5 | HG01070.hp2 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+8039C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412751 | |||||||
| chr6:100412751 | GAAAAAAG others(1): Show |
G | 19 | a0001c0001t0004g0076 a0001c0001t0004g0077 a0001c0001t0004g0079 others(16): Show |
19 | HG00423.hp1 HG00438.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.1167+8031_1167+803 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412751 | |||||||
| chr6:100412754 | A | G | 5 | a0001c0001t0004g0247 a0001c0001t0008g0181 a0001c0001t0027g0098 others(2): Show |
5 | HG01070.hp2 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+8036T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412754 | |||||||
| chr6:100412754 | AAAAG | A | 4 | a0001c0001t0004g0078 a0001c0001t0004g0279 a0001c0001t0018g0309 others(1): Show |
4 | HG00735.hp2 HG02083.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8032_1167+803 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412754 | |||||||
| chr6:100412758 | GA | G | 5 | a0001c0001t0004g0247 a0001c0001t0008g0181 a0001c0001t0027g0098 others(2): Show |
5 | HG01070.hp2 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+8031delT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412758 | |||||||
| chr6:100412759 | A | AAAG | 11 | a0001c0001t0004g0056 a0001c0001t0004g0075 a0001c0001t0004g0081 others(8): Show |
11 | HG00099.hp1 HG01074.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.1167+8030_1167+803 others(7): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412759 | |||||||
| chr6:100412759 | A | G | 4 | a0001c0001t0004g0078 a0001c0001t0004g0279 a0001c0001t0018g0309 others(1): Show |
4 | HG00735.hp2 HG02083.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+8031T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412759 | |||||||
| chr6:100412788 | C | T | 1 | a0001c0009t0033g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1167+8002G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412788 | |||||||
| chr6:100412807 | C | T | 8 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0183 others(5): Show |
8 | HG02129.hp1 NA18982.hp1 NA19004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1167+7983G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100412807 | |||||||
| chr6:100413274 | T | C | 3 | a0001c0001t0020g0154 a0001c0001t0020g0265 a0001c0001t0041g0162 |
3 | HG02723.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1167+7516A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413274 | |||||||
| chr6:100413330 | A | T | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1167+7460T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413330 | |||||||
| chr6:100413450 | C | T | 6 | a0001c0001t0016g0001 a0001c0001t0021g0063 a0001c0001t0021g0244 others(3): Show |
7 | HG00738.hp1 HG01081.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.1167+7340G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413450 | |||||||
| chr6:100413550 | G | A | 2 | a0001c0001t0006g0151 a0001c0001t0006g0213 |
2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1167+7240C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413550 | |||||||
| chr6:100413676 | T | C | 1 | a0001c0001t0059g0180 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1167+7114A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413676 | |||||||
| chr6:100413679 | C | T | 1 | a0001c0001t0006g0213 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1167+7111G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413679 | |||||||
| chr6:100413726 | G | A | 311 | a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0040 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1167+7064C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413726 | |||||||
| chr6:100413841 | G | A | 1 | a0002c0002t0007g0089 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1167+6949C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413841 | |||||||
| chr6:100413903 | A | G | 1 | a0001c0001t0003g0283 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1167+6887T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100413903 | |||||||
| chr6:100414072 | G | A | 2 | a0001c0001t0022g0149 a0001c0001t0022g0165 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1167+6718C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414072 | |||||||
| chr6:100414175 | G | A | 31 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(28): Show |
31 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1167+6615C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414175 | |||||||
| chr6:100414246 | T | C | 5 | a0001c0001t0015g0003 a0001c0001t0015g0219 a0001c0001t0022g0149 others(2): Show |
6 | HG01891.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+6544A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414246 | |||||||
| chr6:100414272 | C | T | 2 | a0001c0001t0003g0160 a0001c0001t0003g0161 |
2 | HG02257.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1167+6518G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414272 | |||||||
| chr6:100414368 | T | C | 1 | a0001c0001t0061g0294 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1167+6422A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414368 | |||||||
| chr6:100414401 | C | A | 1 | a0001c0001t0004g0310 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1167+6389G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414401 | |||||||
| chr6:100414415 | C | T | 5 | a0001c0001t0015g0003 a0001c0001t0015g0219 a0001c0001t0022g0149 others(2): Show |
6 | HG01891.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+6375G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414415 | |||||||
| chr6:100414495 | G | T | 5 | a0001c0001t0015g0003 a0001c0001t0015g0219 a0001c0001t0022g0149 others(2): Show |
6 | HG01891.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+6295C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414495 | |||||||
| chr6:100414551 | T | C | 31 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(28): Show |
31 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1167+6239A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414551 | |||||||
| chr6:100414614 | A | G | 1 | a0002c0002t0001g0139 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1167+6176T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414614 | |||||||
| chr6:100414662 | G | T | 1 | a0002c0002t0024g0253 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1167+6128C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414662 | |||||||
| chr6:100414933 | A | G | 7 | a0001c0001t0006g0151 a0001c0001t0006g0213 a0001c0001t0025g0228 others(4): Show |
7 | HG02145.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167+5857T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100414933 | |||||||
| chr6:100415051 | T | C | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1167+5739A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100415051 | |||||||
| chr6:100415121 | G | A | 1 | a0002c0002t0001g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1167+5669C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100415121 | |||||||
| chr6:100415203 | A | G | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1167+5587T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100415203 | |||||||
| chr6:100415312 | T | C | 7 | a0001c0001t0006g0151 a0001c0001t0006g0213 a0001c0001t0025g0228 others(4): Show |
7 | HG02145.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167+5478A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100415312 | |||||||
| chr6:100415388 | C | A | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1167+5402G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100415388 | |||||||
| chr6:100415912 | C | T | 1 | a0001c0001t0078g0299 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1167+4878G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100415912 | |||||||
| chr6:100416242 | C | T | 83 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0028g0232 others(80): Show |
83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1167+4548G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416242 | |||||||
| chr6:100416260 | C | A | 24 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(21): Show |
24 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1167+4530G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416260 | |||||||
| chr6:100416298 | T | C | 1 | a0001c0001t0044g0150 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1167+4492A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416298 | |||||||
| chr6:100416404 | C | G | 4 | a0001c0001t0002g0135 a0001c0001t0032g0010 a0001c0001t0042g0054 others(1): Show |
4 | HG01433.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+4386G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416404 | |||||||
| chr6:100416604 | C | T | 3 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1167+4186G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416604 | |||||||
| chr6:100416948 | T | A | 25 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(22): Show |
25 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1167+3842A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416948 | |||||||
| chr6:100416953 | T | C | 158 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0004g0056 others(155): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1167+3837A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416953 | |||||||
| chr6:100416979 | C | CA | 83 | a0001c0001t0002g0135 a0001c0001t0008g0047 a0001c0001t0008g0129 others(80): Show |
83 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.1167+3810dupT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416979 | |||||||
| chr6:100416979 | C | CAA | 30 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(27): Show |
30 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.1167+3809_1167+381 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416979 | |||||||
| chr6:100416992 | C | A | 5 | a0001c0001t0016g0001 a0001c0001t0021g0063 a0001c0001t0021g0244 others(2): Show |
6 | HG00738.hp1 HG01081.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+3798G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100416992 | |||||||
| chr6:100417062 | T | G | 111 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(108): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.1167+3728A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417062 | |||||||
| chr6:100417084 | A | G | 3 | a0001c0001t0015g0003 a0001c0001t0015g0219 a0001c0001t0068g0267 |
4 | HG01891.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+3706T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417084 | |||||||
| chr6:100417147 | A | G | 2 | a0001c0001t0022g0149 a0001c0001t0022g0165 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1167+3643T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417147 | |||||||
| chr6:100417209 | C | T | 1 | a0001c0001t0010g0082 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1167+3581G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417209 | |||||||
| chr6:100417347 | C | T | 1 | a0001c0001t0078g0299 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1167+3443G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417347 | |||||||
| chr6:100417348 | G | A | 4 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0061g0294 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+3442C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417348 | |||||||
| chr6:100417395 | T | C | 1 | a0001c0001t0004g0058 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1167+3395A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417395 | |||||||
| chr6:100417451 | T | C | 1 | a0001c0001t0059g0180 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1167+3339A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417451 | |||||||
| chr6:100417496 | C | T | 5 | a0001c0001t0002g0169 a0001c0001t0002g0179 a0001c0001t0011g0155 others(2): Show |
5 | HG01891.hp2 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+3294G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417496 | |||||||
| chr6:100417688 | C | T | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1167+3102G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417688 | |||||||
| chr6:100417822 | T | C | 1 | a0001c0001t0019g0021 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1167+2968A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417822 | |||||||
| chr6:100417930 | G | T | 83 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0028g0232 others(80): Show |
83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1167+2860C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100417930 | |||||||
| chr6:100418004 | T | A | 1 | a0001c0001t0018g0304 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1167+2786A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418004 | |||||||
| chr6:100418150 | A | G | 270 | a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0040 others(267): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.1167+2640T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418150 | |||||||
| chr6:100418190 | A | C | 2 | a0001c0001t0002g0184 a0001c0001t0002g0185 |
2 | NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1167+2600T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418190 | |||||||
| chr6:100418198 | A | T | 6 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0059g0180 others(3): Show |
6 | HG01168.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+2592T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418198 | |||||||
| chr6:100418321 | C | T | 1 | a0001c0001t0044g0150 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1167+2469G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418321 | |||||||
| chr6:100418359 | A | AAAAT | 110 | a0001c0001t0002g0065 a0001c0001t0003g0034 a0001c0001t0003g0042 others(107): Show |
110 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1167+2427_1167+243 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418359 | |||||||
| chr6:100418359 | A | AAAATAAA others(1): Show |
7 | a0001c0001t0005g0093 a0001c0001t0005g0112 a0001c0001t0005g0256 others(4): Show |
7 | HG03831.hp2 HG04184.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167+2423_1167+243 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418359 | |||||||
| chr6:100418359 | A | AAAATAAA others(5): Show |
8 | a0001c0001t0004g0079 a0001c0001t0006g0213 a0001c0001t0008g0137 others(5): Show |
8 | HG00733.hp1 HG01168.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1167+2419_1167+243 others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418359 | |||||||
| chr6:100418359 | A | AAAATAAA others(9): Show |
39 | a0001c0001t0004g0056 a0001c0001t0004g0076 a0001c0001t0004g0077 others(36): Show |
40 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1167+2415_1167+243 others(20): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418359 | |||||||
| chr6:100418359 | A | AAAATAAA others(13): Show |
8 | a0001c0001t0002g0095 a0001c0001t0004g0075 a0001c0001t0004g0247 others(5): Show |
8 | HG01175.hp1 HG02083.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1167+2411_1167+243 others(24): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418359 | |||||||
| chr6:100418506 | G | A | 5 | a0001c0001t0015g0003 a0001c0001t0015g0219 a0001c0001t0022g0149 others(2): Show |
6 | HG01891.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+2284C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418506 | |||||||
| chr6:100418740 | A | G | 2 | a0001c0001t0020g0154 a0001c0001t0041g0162 |
2 | HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1167+2050T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418740 | |||||||
| chr6:100418769 | T | A | 4 | a0001c0001t0059g0180 a0001c0001t0061g0294 a0001c0001t0070g0175 others(1): Show |
4 | HG01168.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+2021A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418769 | |||||||
| chr6:100418848 | G | C | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1167+1942C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418848 | |||||||
| chr6:100418888 | C | T | 1 | a0001c0001t0005g0196 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1167+1902G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418888 | |||||||
| chr6:100418957 | G | A | 5 | a0001c0001t0015g0003 a0001c0001t0015g0219 a0001c0001t0022g0149 others(2): Show |
6 | HG01891.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+1833C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100418957 | |||||||
| chr6:100419009 | A | G | 3 | a0001c0001t0059g0180 a0001c0001t0070g0175 a0001c0001t0071g0014 |
3 | HG01168.hp2 HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1167+1781T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419009 | |||||||
| chr6:100419086 | G | A | 128 | a0001c0001t0002g0095 a0001c0001t0004g0056 a0001c0001t0004g0075 others(125): Show |
128 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1167+1704C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419086 | |||||||
| chr6:100419185 | C | A | 1 | a0001c0001t0019g0019 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1167+1605G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419185 | |||||||
| chr6:100419329 | T | C | 1 | a0001c0001t0002g0179 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1167+1461A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419329 | |||||||
| chr6:100419384 | C | T | 2 | a0001c0001t0006g0151 a0001c0001t0006g0213 |
2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1167+1406G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419384 | |||||||
| chr6:100419662 | G | T | 33 | a0002c0002t0001g0023 a0002c0002t0001g0031 a0002c0002t0001g0045 others(30): Show |
33 | HG00621.hp2 HG02056.hp1 HG02293.hp1 others(30): Show |
intron_variant | MODIFIER | c.1167+1128C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419662 | |||||||
| chr6:100419675 | A | G | 1 | a0001c0007t0004g0287 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1167+1115T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419675 | |||||||
| chr6:100419753 | A | T | 2 | a0001c0001t0023g0097 a0001c0001t0060g0157 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1167+1037T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419753 | |||||||
| chr6:100419787 | A | G | 2 | a0001c0001t0022g0149 a0001c0001t0022g0165 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1167+1003T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419787 | |||||||
| chr6:100419923 | A | G | 48 | a0001c0001t0002g0095 a0001c0001t0004g0056 a0001c0001t0004g0075 others(45): Show |
48 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1167+867T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100419923 | |||||||
| chr6:100420039 | G | T | 3 | a0002c0002t0001g0037 a0002c0002t0001g0199 a0002c0002t0006g0192 |
3 | HG02602.hp1 HG03704.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1167+751C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420039 | |||||||
| chr6:100420072 | T | A | 2 | a0001c0001t0006g0151 a0001c0001t0006g0213 |
2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1167+718A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420072 | |||||||
| chr6:100420133 | T | C | 25 | a0001c0001t0003g0042 a0001c0001t0003g0186 a0001c0001t0005g0026 others(22): Show |
25 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1167+657A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420133 | |||||||
| chr6:100420195 | C | T | 6 | a0001c0001t0016g0001 a0001c0001t0021g0063 a0001c0001t0021g0244 others(3): Show |
7 | HG00738.hp1 HG01081.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.1167+595G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420195 | |||||||
| chr6:100420359 | G | A | 2 | a0001c0001t0022g0149 a0001c0001t0022g0165 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1167+431C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420359 | |||||||
| chr6:100420492 | A | T | 1 | a0002c0002t0001g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1167+298T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420492 | |||||||
| chr6:100420499 | G | A | 1 | a0001c0001t0061g0294 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1167+291C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420499 | |||||||
| chr6:100420584 | A | G | 45 | a0001c0001t0002g0095 a0001c0001t0004g0056 a0001c0001t0004g0075 others(42): Show |
45 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1167+206T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420584 | |||||||
| chr6:100420616 | A | T | 163 | a0001c0001t0002g0095 a0001c0001t0003g0042 a0001c0001t0003g0186 others(160): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1167+174T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 10/11 | chr6 | 100420616 | |||||||
| chr6:100421463 | C | G | 2 | a0002c0002t0003g0050 a0002c0002t0003g0051 |
2 | NA18957.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.999-505G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100421463 | |||||||
| chr6:100421680 | T | G | 1 | a0002c0002t0007g0115 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.999-722A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100421680 | |||||||
| chr6:100421722 | T | G | 2 | a0001c0001t0057g0028 a0001c0001t0058g0029 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.999-764A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100421722 | |||||||
| chr6:100421797 | C | T | 8 | a0001c0001t0008g0043 a0001c0001t0008g0047 a0001c0001t0008g0137 others(5): Show |
8 | HG00099.hp1 HG00733.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.999-839G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100421797 | |||||||
| chr6:100421809 | T | C | 1 | a0002c0002t0001g0313 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.999-851A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100421809 | |||||||
| chr6:100421818 | A | G | 1 | a0002c0002t0001g0083 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.999-860T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100421818 | |||||||
| chr6:100421959 | G | A | 2 | a0001c0001t0005g0093 a0001c0001t0005g0112 |
2 | NA18944.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.999-1001C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100421959 | |||||||
| chr6:100421973 | C | A | 45 | a0001c0001t0002g0095 a0001c0001t0004g0056 a0001c0001t0004g0075 others(42): Show |
45 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.999-1015G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100421973 | |||||||
| chr6:100422006 | T | TC | 83 | a0001c0001t0003g0042 a0001c0001t0005g0030 a0001c0001t0005g0041 others(80): Show |
83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.999-1049dupG | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422006 | |||||||
| chr6:100422214 | T | C | 1 | a0001c0001t0013g0073 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.999-1256A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422214 | |||||||
| chr6:100422329 | G | A | 1 | a0001c0001t0073g0080 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.999-1371C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422329 | |||||||
| chr6:100422388 | G | C | 1 | a0001c0001t0005g0243 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.999-1430C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422388 | |||||||
| chr6:100422390 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.999-1432C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422390 | |||||||
| chr6:100422499 | G | A | 1 | a0002c0002t0001g0281 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.999-1541C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422499 | |||||||
| chr6:100422575 | T | C | 1 | a0001c0001t0019g0019 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.999-1617A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422575 | |||||||
| chr6:100422661 | A | C | 45 | a0001c0001t0002g0095 a0001c0001t0004g0056 a0001c0001t0004g0075 others(42): Show |
45 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.999-1703T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422661 | |||||||
| chr6:100422880 | T | C | 2 | a0001c0001t0004g0081 a0006c0006t0004g0090 |
2 | NA19066.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.999-1922A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422880 | |||||||
| chr6:100422910 | T | C | 22 | a0001c0001t0003g0186 a0001c0001t0005g0026 a0001c0001t0005g0070 others(19): Show |
22 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.999-1952A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422910 | |||||||
| chr6:100422922 | A | G | 1 | a0002c0002t0001g0033 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.999-1964T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422922 | |||||||
| chr6:100422954 | C | T | 2 | a0001c0001t0002g0208 a0001c0001t0002g0209 |
2 | HG00642.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.999-1996G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100422954 | |||||||
| chr6:100423048 | C | A | 1 | a0001c0001t0002g0194 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.999-2090G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423048 | |||||||
| chr6:100423077 | T | C | 6 | a0001c0001t0003g0186 a0001c0001t0005g0074 a0001c0001t0005g0092 others(3): Show |
6 | HG00621.hp1 HG02165.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.999-2119A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423077 | |||||||
| chr6:100423126 | C | A | 2 | a0001c0001t0070g0175 a0001c0009t0033g0009 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.999-2168G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423126 | |||||||
| chr6:100423131 | A | G | 1 | a0001c0001t0059g0180 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.999-2173T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423131 | |||||||
| chr6:100423184 | T | A | 4 | a0001c0001t0059g0180 a0001c0001t0070g0175 a0001c0001t0071g0014 others(1): Show |
4 | HG01168.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-2226A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423184 | |||||||
| chr6:100423227 | T | G | 1 | a0001c0001t0003g0068 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.999-2269A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423227 | |||||||
| chr6:100423286 | C | T | 1 | a0001c0001t0004g0277 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.999-2328G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423286 | |||||||
| chr6:100423439 | A | C | 1 | a0001c0001t0005g0092 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.999-2481T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423439 | |||||||
| chr6:100423612 | T | C | 163 | a0001c0001t0002g0095 a0001c0001t0003g0042 a0001c0001t0003g0186 others(160): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.999-2654A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423612 | |||||||
| chr6:100423659 | G | A | 22 | a0001c0001t0003g0186 a0001c0001t0005g0026 a0001c0001t0005g0070 others(19): Show |
22 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.999-2701C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423659 | |||||||
| chr6:100423728 | T | C | 1 | a0002c0002t0006g0192 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.999-2770A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423728 | |||||||
| chr6:100423853 | C | A | 1 | a0001c0001t0002g0111 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.999-2895G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100423853 | |||||||
| chr6:100424066 | C | G | 2 | a0001c0001t0020g0154 a0001c0001t0041g0162 |
2 | HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.999-3108G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424066 | |||||||
| chr6:100424078 | C | T | 1 | a0001c0001t0002g0248 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.999-3120G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424078 | |||||||
| chr6:100424092 | A | T | 3 | a0001c0001t0006g0173 a0001c0001t0057g0028 a0001c0001t0058g0029 |
3 | HG02965.hp1 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.999-3134T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424092 | |||||||
| chr6:100424180 | T | A | 167 | a0001c0001t0002g0095 a0001c0001t0003g0042 a0001c0001t0003g0160 others(164): Show |
168 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.999-3222A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424180 | |||||||
| chr6:100424232 | A | G | 1 | a0002c0002t0007g0245 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.999-3274T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424232 | |||||||
| chr6:100424608 | T | A | 1 | a0002c0002t0007g0089 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.999-3650A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424608 | |||||||
| chr6:100424679 | G | A | 3 | a0001c0001t0015g0003 a0001c0001t0015g0219 a0001c0001t0068g0267 |
4 | HG01891.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-3721C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424679 | |||||||
| chr6:100424770 | T | C | 3 | a0001c0001t0019g0021 a0001c0001t0034g0011 a0001c0001t0056g0046 |
3 | HG02683.hp1 HG03239.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.999-3812A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424770 | |||||||
| chr6:100424827 | T | C | 44 | a0001c0001t0002g0095 a0001c0001t0004g0056 a0001c0001t0004g0075 others(41): Show |
44 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.999-3869A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424827 | |||||||
| chr6:100424911 | C | T | 119 | a0001c0001t0002g0095 a0001c0001t0003g0042 a0001c0001t0004g0056 others(116): Show |
119 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.999-3953G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100424911 | |||||||
| chr6:100425381 | T | C | 83 | a0001c0001t0003g0042 a0001c0001t0005g0030 a0001c0001t0005g0041 others(80): Show |
83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.999-4423A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100425381 | |||||||
| chr6:100425404 | T | C | 2 | a0001c0001t0006g0151 a0001c0001t0006g0213 |
2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.999-4446A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100425404 | |||||||
| chr6:100425425 | A | C | 1 | a0001c0001t0005g0091 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.999-4467T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100425425 | |||||||
| chr6:100425814 | A | G | 4 | a0001c0001t0059g0180 a0001c0001t0070g0175 a0001c0001t0071g0014 others(1): Show |
4 | HG01168.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-4856T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100425814 | |||||||
| chr6:100425914 | T | C | 1 | a0002c0005t0065g0116 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.999-4956A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100425914 | |||||||
| chr6:100426062 | G | A | 26 | a0001c0001t0004g0056 a0001c0001t0004g0075 a0001c0001t0004g0076 others(23): Show |
26 | HG00423.hp1 HG00438.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.999-5104C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426062 | |||||||
| chr6:100426219 | A | G | 1 | a0001c0001t0074g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.999-5261T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426219 | |||||||
| chr6:100426284 | C | T | 6 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0027g0098 others(3): Show |
6 | HG02055.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.999-5326G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426284 | |||||||
| chr6:100426441 | C | T | 5 | a0001c0001t0002g0169 a0001c0001t0002g0179 a0001c0001t0011g0155 others(2): Show |
5 | HG01891.hp2 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.999-5483G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426441 | |||||||
| chr6:100426474 | G | A | 1 | a0001c0001t0037g0022 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.999-5516C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426474 | |||||||
| chr6:100426658 | A | G | 2 | a0001c0001t0003g0153 a0001c0001t0009g0170 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.999-5700T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426658 | |||||||
| chr6:100426709 | TC | T | 4 | a0001c0001t0006g0212 a0001c0001t0010g0005 a0001c0001t0010g0262 others(1): Show |
5 | HG01109.hp1 HG02258.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.999-5752delG | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426709 | |||||||
| chr6:100426713 | G | C | 1 | a0001c0001t0044g0150 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.999-5755C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426713 | |||||||
| chr6:100426727 | A | G | 4 | a0001c0001t0059g0180 a0001c0001t0070g0175 a0001c0001t0071g0014 others(1): Show |
4 | HG01168.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-5769T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426727 | |||||||
| chr6:100426753 | C | T | 3 | a0001c0001t0015g0003 a0001c0001t0015g0219 a0001c0001t0068g0267 |
4 | HG01891.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-5795G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426753 | |||||||
| chr6:100426899 | A | T | 4 | a0001c0001t0003g0195 a0001c0001t0003g0298 a0001c0001t0005g0093 others(1): Show |
4 | HG02896.hp2 HG02970.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-5941T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100426899 | |||||||
| chr6:100427277 | C | T | 2 | a0001c0001t0003g0002 a0001c0001t0003g0233 |
3 | HG01175.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.999-6319G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100427277 | |||||||
| chr6:100427640 | T | C | 88 | a0001c0001t0003g0042 a0001c0001t0004g0288 a0001c0001t0005g0030 others(85): Show |
88 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.999-6682A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100427640 | |||||||
| chr6:100427950 | C | T | 1 | a0001c0001t0064g0027 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.999-6992G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100427950 | |||||||
| chr6:100428050 | T | C | 1 | a0001c0001t0006g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.999-7092A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428050 | |||||||
| chr6:100428213 | G | A | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.999-7255C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428213 | |||||||
| chr6:100428380 | A | G | 3 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0053g0271 |
3 | HG00642.hp1 HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.999-7422T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428380 | |||||||
| chr6:100428436 | A | C | 9 | a0001c0001t0002g0166 a0001c0001t0003g0168 a0001c0001t0003g0195 others(6): Show |
9 | HG02055.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.999-7478T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428436 | |||||||
| chr6:100428577 | G | T | 10 | a0001c0001t0002g0106 a0001c0001t0002g0176 a0001c0001t0002g0240 others(7): Show |
10 | HG02280.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.999-7619C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428577 | |||||||
| chr6:100428628 | T | TAAGAATG others(318): Show |
2 | a0001c0001t0006g0212 a0001c0001t0010g0172 |
2 | HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.999-7671_999-7670i others(327): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | |||||||
| chr6:100428628 | T | TAAGAATG others(328): Show |
4 | a0001c0001t0025g0228 a0001c0001t0025g0238 a0001c0001t0069g0239 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-7671_999-7670i others(337): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | |||||||
| chr6:100428628 | T | TAAGAATG others(329): Show |
2 | a0001c0001t0027g0098 a0001c0001t0074g0144 |
2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.999-7671_999-7670i others(338): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | |||||||
| chr6:100428628 | T | TAAGAATG others(330): Show |
1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.999-7671_999-7670i others(339): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | |||||||
| chr6:100428628 | T | TAAGAATG others(332): Show |
2 | a0001c0001t0006g0174 a0001c0009t0033g0009 |
2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.999-7671_999-7670i others(341): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | |||||||
| chr6:100428628 | T | TAAGAATG others(321): Show |
1 | a0001c0001t0002g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.999-7671_999-7670i others(330): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | |||||||
| chr6:100428628 | T | TAAGAATG others(322): Show |
1 | a0001c0001t0002g0209 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.999-7671_999-7670i others(331): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | |||||||
| chr6:100428628 | T | TAAGAATG others(324): Show |
1 | a0001c0001t0006g0213 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.999-7671_999-7670i others(333): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | |||||||
| chr6:100428628 | T | TAAGAATG others(333): Show |
1 | a0001c0001t0063g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.999-7671_999-7670i others(342): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | |||||||
| chr6:100428628 | T | TAAGAATG others(339): Show |
1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.999-7671_999-7670i others(348): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | |||||||
| chr6:100428628 | T | TAAGAATG others(344): Show |
1 | a0001c0001t0006g0266 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.999-7671_999-7670i others(353): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | |||||||
| chr6:100428628 | T | TAAGAATG others(346): Show |
1 | a0001c0001t0053g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.999-7671_999-7670i others(355): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428628 | |||||||
| chr6:100428667 | G | C | 4 | a0001c0001t0002g0209 a0001c0001t0039g0016 a0001c0001t0043g0229 others(1): Show |
4 | HG00642.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-7709C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428667 | |||||||
| chr6:100428668 | C | G | 1 | a0001c0001t0039g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.999-7710G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428668 | |||||||
| chr6:100428805 | T | C | 1 | a0001c0001t0011g0264 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.999-7847A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428805 | |||||||
| chr6:100428886 | T | C | 1 | a0001c0001t0003g0223 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.999-7928A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100428886 | |||||||
| chr6:100429018 | G | A | 35 | a0001c0001t0002g0111 a0001c0001t0002g0118 a0001c0001t0002g0248 others(32): Show |
35 | HG00558.hp1 HG00741.hp2 HG01516.hp1 others(32): Show |
intron_variant | MODIFIER | c.999-8060C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429018 | |||||||
| chr6:100429068 | A | T | 1 | a0002c0005t0065g0116 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.999-8110T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429068 | |||||||
| chr6:100429076 | T | G | 2 | a0001c0001t0010g0172 a0001c0001t0040g0015 |
2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.999-8118A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429076 | |||||||
| chr6:100429084 | C | T | 6 | a0001c0001t0012g0305 a0001c0001t0012g0306 a0001c0001t0012g0307 others(3): Show |
6 | HG02083.hp1 HG02129.hp1 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.999-8126G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429084 | |||||||
| chr6:100429116 | C | T | 6 | a0001c0001t0012g0305 a0001c0001t0012g0306 a0001c0001t0012g0307 others(3): Show |
6 | HG02083.hp1 HG02129.hp1 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.999-8158G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429116 | |||||||
| chr6:100429174 | A | G | 2 | a0001c0001t0004g0056 a0001c0001t0005g0091 |
2 | HG02056.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.999-8216T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429174 | |||||||
| chr6:100429365 | T | C | 97 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0061 others(94): Show |
97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.999-8407A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429365 | |||||||
| chr6:100429368 | CA | C | 285 | a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0040 others(282): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.999-8411delT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429368 | |||||||
| chr6:100429368 | CAA | C | 7 | a0001c0001t0002g0061 a0001c0001t0002g0248 a0001c0001t0005g0220 others(4): Show |
7 | HG00741.hp2 HG02109.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.999-8412_999-8411d others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429368 | |||||||
| chr6:100429584 | G | A | 1 | a0001c0001t0003g0132 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.999-8626C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429584 | |||||||
| chr6:100429926 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.999-8968A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429926 | |||||||
| chr6:100429952 | T | C | 52 | a0001c0001t0002g0152 a0001c0001t0002g0158 a0001c0001t0002g0166 others(49): Show |
52 | HG00423.hp2 HG00544.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.999-8994A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100429952 | |||||||
| chr6:100430022 | A | G | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.999-9064T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430022 | |||||||
| chr6:100430387 | C | T | 1 | a0001c0001t0008g0047 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.999-9429G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430387 | |||||||
| chr6:100430391 | C | T | 133 | a0001c0001t0002g0004 a0001c0001t0002g0052 a0001c0001t0002g0111 others(130): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.999-9433G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430391 | |||||||
| chr6:100430440 | T | A | 2 | a0001c0001t0039g0016 a0001c0001t0040g0015 |
2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.999-9482A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430440 | |||||||
| chr6:100430466 | C | G | 1 | a0001c0001t0063g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.999-9508G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430466 | |||||||
| chr6:100430582 | G | T | 299 | a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0040 others(296): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.999-9624C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430582 | |||||||
| chr6:100430716 | A | G | 2 | a0001c0001t0057g0028 a0001c0001t0058g0029 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.999-9758T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430716 | |||||||
| chr6:100430762 | T | C | 4 | a0002c0002t0014g0254 a0002c0002t0014g0255 a0002c0002t0014g0258 others(1): Show |
4 | HG00438.hp1 HG02083.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-9804A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430762 | |||||||
| chr6:100430775 | A | G | 1 | a0001c0001t0002g0191 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.999-9817T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430775 | |||||||
| chr6:100430968 | C | G | 3 | a0002c0002t0007g0114 a0002c0002t0007g0115 a0002c0002t0007g0198 |
3 | NA18973.hp1 NA19066.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.999-10010G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430968 | |||||||
| chr6:100430982 | A | G | 132 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0061 others(129): Show |
132 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.999-10024T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100430982 | |||||||
| chr6:100431093 | T | G | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.999-10135A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431093 | |||||||
| chr6:100431140 | C | T | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.999-10182G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431140 | |||||||
| chr6:100431183 | T | C | 2 | a0001c0001t0039g0016 a0001c0001t0040g0015 |
2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.999-10225A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431183 | |||||||
| chr6:100431288 | G | A | 2 | a0001c0001t0032g0010 a0001c0009t0033g0009 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.999-10330C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431288 | |||||||
| chr6:100431382 | C | T | 1 | a0001c0001t0053g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.999-10424G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431382 | |||||||
| chr6:100431505 | T | C | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.999-10547A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431505 | |||||||
| chr6:100431775 | C | T | 167 | a0001c0001t0002g0004 a0001c0001t0002g0052 a0001c0001t0002g0111 others(164): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.999-10817G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431775 | |||||||
| chr6:100431852 | C | T | 10 | a0001c0001t0003g0002 a0001c0001t0012g0305 a0001c0001t0012g0306 others(7): Show |
11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.999-10894G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431852 | |||||||
| chr6:100431977 | C | T | 4 | a0001c0001t0006g0293 a0001c0001t0006g0295 a0001c0001t0006g0296 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-11019G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100431977 | |||||||
| chr6:100432018 | C | T | 1 | a0002c0002t0007g0099 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.999-11060G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432018 | |||||||
| chr6:100432151 | A | G | 5 | a0001c0001t0002g0103 a0001c0001t0002g0106 a0001c0001t0005g0104 others(2): Show |
5 | HG02132.hp1 HG02523.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.999-11193T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432151 | |||||||
| chr6:100432256 | G | C | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.999-11298C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432256 | |||||||
| chr6:100432426 | A | AGTG | 4 | a0001c0001t0018g0304 a0001c0001t0018g0309 a0002c0002t0017g0301 others(1): Show |
4 | HG01074.hp1 HG01361.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-11471_999-1146 others(7): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432426 | |||||||
| chr6:100432429 | GGTT | G | 4 | a0001c0001t0018g0304 a0001c0001t0018g0309 a0002c0002t0017g0301 others(1): Show |
4 | HG01074.hp1 HG01361.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-11474_999-1147 others(7): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432429 | |||||||
| chr6:100432432 | T | G | 6 | a0001c0001t0003g0002 a0001c0001t0012g0305 a0001c0001t0012g0306 others(3): Show |
7 | HG00280.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.999-11474A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432432 | |||||||
| chr6:100432677 | G | T | 1 | a0001c0001t0064g0027 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.999-11719C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432677 | |||||||
| chr6:100432820 | A | G | 142 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0061 others(139): Show |
143 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.999-11862T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432820 | |||||||
| chr6:100432956 | G | A | 2 | a0001c0001t0039g0016 a0001c0001t0040g0015 |
2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.999-11998C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100432956 | |||||||
| chr6:100433018 | T | C | 1 | a0002c0002t0001g0214 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.999-12060A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433018 | |||||||
| chr6:100433083 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.999-12125G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433083 | |||||||
| chr6:100433202 | C | T | 1 | a0001c0001t0010g0172 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.999-12244G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433202 | |||||||
| chr6:100433464 | C | G | 3 | a0001c0001t0003g0002 a0002c0002t0017g0301 a0002c0002t0017g0303 |
4 | HG01074.hp1 HG01361.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-12506G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433464 | |||||||
| chr6:100433670 | G | C | 1 | a0006c0006t0004g0090 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.999-12712C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433670 | |||||||
| chr6:100433736 | C | CCCACCCA others(4): Show |
1 | a0001c0001t0004g0058 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.999-12779_999-1277 others(15): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433736 | |||||||
| chr6:100433736 | C | CCCACCCA others(6): Show |
1 | a0002c0002t0001g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.999-12779_999-1277 others(17): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433736 | |||||||
| chr6:100433740 | C | A | 2 | a0001c0001t0004g0058 a0002c0002t0001g0094 |
2 | HG01993.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.999-12782G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433740 | |||||||
| chr6:100433740 | C | CACACACA others(4): Show |
1 | a0001c0001t0003g0036 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.999-12783_999-1278 others(15): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433740 | |||||||
| chr6:100433740 | C | CCA | 32 | a0001c0001t0002g0273 a0001c0001t0002g0282 a0001c0001t0003g0128 others(29): Show |
32 | HG00423.hp2 HG00735.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.999-12784_999-1278 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433740 | |||||||
| chr6:100433740 | C | CCACACA | 4 | a0001c0001t0002g0204 a0001c0001t0006g0018 a0001c0001t0006g0205 others(1): Show |
4 | HG02559.hp2 HG03540.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-12788_999-1278 others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433740 | |||||||
| chr6:100433740 | C | CCACACAC others(1): Show |
3 | a0001c0001t0009g0148 a0002c0002t0001g0057 a0002c0002t0001g0107 |
3 | HG02523.hp1 NA18990.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.999-12790_999-1278 others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433740 | |||||||
| chr6:100433740 | C | CCACACAC others(3): Show |
86 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(83): Show |
86 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.999-12792_999-1278 others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433740 | |||||||
| chr6:100433740 | C | CCACACAC others(5): Show |
4 | a0001c0001t0005g0091 a0001c0001t0027g0053 a0001c0001t0071g0014 others(1): Show |
4 | HG01175.hp1 HG02615.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-12794_999-1278 others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433740 | |||||||
| chr6:100433740 | C | CCACCCAC others(3): Show |
1 | a0001c0001t0002g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.999-12783_999-1278 others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433740 | |||||||
| chr6:100433742 | A | ACC | 8 | a0001c0001t0012g0305 a0001c0001t0012g0306 a0001c0001t0012g0307 others(5): Show |
8 | HG00280.hp1 HG01074.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.999-12785_999-1278 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433742 | |||||||
| chr6:100433767 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.999-12809A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433767 | |||||||
| chr6:100433986 | C | T | 1 | a0001c0001t0064g0027 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.999-13028G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100433986 | |||||||
| chr6:100434408 | G | T | 1 | a0001c0001t0037g0022 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.998+12860C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100434408 | |||||||
| chr6:100434470 | A | G | 1 | a0001c0001t0076g0136 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.998+12798T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100434470 | |||||||
| chr6:100434520 | C | G | 2 | a0001c0001t0002g0111 a0001c0001t0003g0110 |
2 | HG00558.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.998+12748G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100434520 | |||||||
| chr6:100434529 | G | A | 100 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(97): Show |
100 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.998+12739C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100434529 | |||||||
| chr6:100435126 | T | C | 1 | a0002c0002t0001g0033 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.998+12142A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435126 | |||||||
| chr6:100435273 | T | C | 1 | a0001c0001t0002g0209 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.998+11995A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435273 | |||||||
| chr6:100435458 | C | A | 9 | a0001c0001t0002g0240 a0001c0001t0021g0244 a0002c0002t0001g0257 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.998+11810G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435458 | |||||||
| chr6:100435464 | G | T | 2 | a0001c0001t0032g0010 a0001c0009t0033g0009 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.998+11804C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435464 | |||||||
| chr6:100435492 | C | T | 1 | a0001c0001t0004g0056 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.998+11776G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435492 | |||||||
| chr6:100435562 | C | T | 4 | a0001c0001t0002g0204 a0001c0001t0006g0018 a0001c0001t0006g0205 others(1): Show |
4 | HG02559.hp2 HG03540.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.998+11706G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435562 | |||||||
| chr6:100435609 | A | C | 1 | a0001c0009t0033g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.998+11659T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435609 | |||||||
| chr6:100435663 | A | T | 2 | a0001c0001t0002g0167 a0001c0001t0059g0180 |
2 | HG01168.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.998+11605T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435663 | |||||||
| chr6:100435792 | C | A | 1 | a0001c0001t0008g0225 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.998+11476G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435792 | |||||||
| chr6:100435912 | G | A | 1 | a0001c0001t0005g0092 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.998+11356C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435912 | |||||||
| chr6:100435975 | A | C | 99 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(96): Show |
99 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.998+11293T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435975 | |||||||
| chr6:100435992 | C | T | 1 | a0002c0002t0028g0055 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.998+11276G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435992 | |||||||
| chr6:100435993 | A | C | 1 | a0002c0002t0028g0055 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.998+11275T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435993 | |||||||
| chr6:100435994 | T | A | 1 | a0002c0002t0028g0055 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.998+11274A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435994 | |||||||
| chr6:100435994 | T | TCA | 98 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(95): Show |
98 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.998+11272_998+1127 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435994 | |||||||
| chr6:100435994 | TCACA | T | 24 | a0001c0001t0002g0183 a0001c0001t0002g0184 a0001c0001t0002g0185 others(21): Show |
26 | HG00099.hp2 HG00621.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.998+11270_998+1127 others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100435994 | |||||||
| chr6:100436033 | G | C | 2 | a0001c0001t0032g0010 a0001c0009t0033g0009 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.998+11235C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100436033 | |||||||
| chr6:100436255 | T | C | 4 | a0001c0001t0003g0002 a0001c0001t0036g0302 a0002c0002t0017g0301 others(1): Show |
5 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.998+11013A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100436255 | |||||||
| chr6:100436355 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.998+10913A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100436355 | |||||||
| chr6:100436701 | G | A | 1 | a0001c0001t0034g0011 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.998+10567C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100436701 | |||||||
| chr6:100436742 | A | AT | 7 | a0001c0001t0002g0040 a0001c0001t0003g0101 a0001c0001t0004g0247 others(4): Show |
7 | HG01169.hp1 HG01255.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.998+10525dupA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100436742 | |||||||
| chr6:100436742 | A | ATT | 94 | a0001c0001t0001g0067 a0001c0001t0002g0052 a0001c0001t0002g0061 others(91): Show |
94 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.998+10524_998+1052 others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100436742 | |||||||
| chr6:100436742 | AT | A | 7 | a0001c0001t0006g0266 a0001c0001t0008g0263 a0001c0001t0010g0005 others(4): Show |
8 | HG01109.hp1 HG02258.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.998+10525delA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100436742 | |||||||
| chr6:100436972 | G | A | 10 | a0001c0001t0003g0002 a0001c0001t0012g0305 a0001c0001t0012g0306 others(7): Show |
11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.998+10296C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100436972 | |||||||
| chr6:100437009 | G | T | 114 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(111): Show |
115 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.998+10259C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437009 | |||||||
| chr6:100437013 | G | A | 1 | a0001c0001t0004g0247 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.998+10255C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437013 | |||||||
| chr6:100437077 | A | G | 2 | a0001c0001t0039g0016 a0001c0001t0040g0015 |
2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.998+10191T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437077 | |||||||
| chr6:100437126 | G | A | 1 | a0001c0001t0003g0132 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.998+10142C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437126 | |||||||
| chr6:100437216 | A | G | 1 | a0002c0002t0007g0114 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.998+10052T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437216 | |||||||
| chr6:100437233 | T | C | 1 | a0001c0001t0053g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.998+10035A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437233 | |||||||
| chr6:100437387 | C | T | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.998+9881G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437387 | |||||||
| chr6:100437429 | C | T | 1 | a0001c0001t0061g0294 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.998+9839G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437429 | |||||||
| chr6:100437481 | G | A | 2 | a0001c0001t0034g0011 a0001c0001t0035g0012 |
2 | HG03239.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.998+9787C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437481 | |||||||
| chr6:100437482 | G | A | 1 | a0001c0001t0056g0046 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.998+9786C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437482 | |||||||
| chr6:100437579 | GA | G | 12 | a0001c0001t0003g0002 a0001c0001t0012g0305 a0001c0001t0012g0306 others(9): Show |
13 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.998+9688delT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437579 | |||||||
| chr6:100437587 | AAC | A | 101 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(98): Show |
101 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.998+9679_998+9680d others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437587 | |||||||
| chr6:100437618 | G | T | 1 | a0002c0002t0006g0192 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.998+9650C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437618 | |||||||
| chr6:100437675 | G | A | 1 | a0001c0001t0042g0054 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.998+9593C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437675 | |||||||
| chr6:100437829 | G | A | 1 | a0001c0001t0003g0161 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.998+9439C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437829 | |||||||
| chr6:100437938 | G | A | 1 | a0001c0001t0003g0270 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.998+9330C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100437938 | |||||||
| chr6:100438042 | C | T | 10 | a0001c0001t0003g0002 a0001c0001t0012g0305 a0001c0001t0012g0306 others(7): Show |
11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.998+9226G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438042 | |||||||
| chr6:100438091 | A | G | 26 | a0001c0001t0002g0040 a0001c0001t0002g0052 a0001c0001t0002g0103 others(23): Show |
26 | HG00733.hp2 HG01074.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.998+9177T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438091 | |||||||
| chr6:100438217 | C | A | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.998+9051G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438217 | |||||||
| chr6:100438238 | T | C | 300 | a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0040 others(297): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.998+9030A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438238 | |||||||
| chr6:100438240 | T | A | 300 | a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0040 others(297): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.998+9028A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438240 | |||||||
| chr6:100438422 | C | T | 1 | a0002c0002t0001g0109 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.998+8846G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438422 | |||||||
| chr6:100438530 | A | C | 102 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(99): Show |
102 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.998+8738T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438530 | |||||||
| chr6:100438532 | T | C | 1 | a0001c0001t0005g0093 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.998+8736A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438532 | |||||||
| chr6:100438579 | A | G | 2 | a0001c0001t0032g0010 a0001c0009t0033g0009 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.998+8689T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438579 | |||||||
| chr6:100438749 | G | T | 102 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(99): Show |
102 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.998+8519C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438749 | |||||||
| chr6:100438790 | A | G | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.998+8478T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438790 | |||||||
| chr6:100438879 | A | G | 1 | a0001c0001t0056g0046 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.998+8389T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438879 | |||||||
| chr6:100438987 | G | T | 1 | a0001c0001t0009g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.998+8281C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100438987 | |||||||
| chr6:100439466 | T | C | 1 | a0001c0001t0002g0191 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.998+7802A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100439466 | |||||||
| chr6:100439491 | A | C | 2 | a0001c0001t0026g0216 a0002c0002t0007g0197 |
2 | HG00423.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.998+7777T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100439491 | |||||||
| chr6:100439649 | C | T | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.998+7619G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100439649 | |||||||
| chr6:100439989 | G | A | 11 | a0001c0001t0003g0002 a0001c0001t0012g0305 a0001c0001t0012g0306 others(8): Show |
12 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.998+7279C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100439989 | |||||||
| chr6:100440173 | C | A | 7 | a0001c0001t0002g0183 a0001c0001t0002g0184 a0001c0001t0002g0185 others(4): Show |
7 | NA18944.hp2 NA18950.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.998+7095G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100440173 | |||||||
| chr6:100440182 | A | C | 301 | a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0040 others(298): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.998+7086T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100440182 | |||||||
| chr6:100440532 | G | C | 115 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(112): Show |
116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.998+6736C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100440532 | |||||||
| chr6:100440597 | C | T | 1 | a0002c0002t0001g0045 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.998+6671G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100440597 | |||||||
| chr6:100440749 | C | T | 94 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(91): Show |
94 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.998+6519G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100440749 | |||||||
| chr6:100440775 | A | C | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.998+6493T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100440775 | |||||||
| chr6:100441210 | G | A | 1 | a0002c0002t0001g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.998+6058C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100441210 | |||||||
| chr6:100441624 | C | T | 1 | a0001c0001t0005g0196 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.998+5644G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100441624 | |||||||
| chr6:100441665 | T | G | 13 | a0001c0001t0003g0002 a0001c0001t0012g0305 a0001c0001t0012g0306 others(10): Show |
14 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.998+5603A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100441665 | |||||||
| chr6:100441771 | G | C | 1 | a0001c0001t0003g0132 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.998+5497C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100441771 | |||||||
| chr6:100441790 | G | A | 1 | a0002c0002t0001g0039 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.998+5478C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100441790 | |||||||
| chr6:100441848 | A | G | 2 | a0001c0003t0003g0044 a0001c0003t0003g0102 |
2 | HG01516.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.998+5420T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100441848 | |||||||
| chr6:100441979 | T | A | 99 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(96): Show |
99 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.998+5289A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100441979 | |||||||
| chr6:100442067 | A | G | 1 | a0001c0001t0003g0195 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.998+5201T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100442067 | |||||||
| chr6:100442098 | A | T | 1 | a0001c0001t0003g0195 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.998+5170T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100442098 | |||||||
| chr6:100442702 | C | G | 1 | a0001c0001t0002g0194 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.998+4566G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100442702 | |||||||
| chr6:100442737 | T | A | 2 | a0001c0001t0032g0010 a0001c0009t0033g0009 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.998+4531A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100442737 | |||||||
| chr6:100442775 | A | G | 1 | a0001c0001t0008g0043 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.998+4493T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100442775 | |||||||
| chr6:100442778 | T | A | 128 | a0001c0001t0002g0004 a0001c0001t0002g0111 a0001c0001t0002g0117 others(125): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.998+4490A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100442778 | |||||||
| chr6:100443081 | A | G | 1 | a0002c0002t0001g0214 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.998+4187T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100443081 | |||||||
| chr6:100443115 | A | G | 170 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(167): Show |
171 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.998+4153T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100443115 | |||||||
| chr6:100443255 | T | C | 3 | a0001c0001t0002g0095 a0001c0001t0008g0096 a0001c0001t0023g0097 |
3 | HG02109.hp1 HG02257.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.998+4013A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100443255 | |||||||
| chr6:100443309 | T | C | 22 | a0001c0001t0002g0273 a0001c0001t0002g0282 a0001c0001t0003g0283 others(19): Show |
22 | HG00423.hp2 HG00735.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.998+3959A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100443309 | |||||||
| chr6:100443381 | A | G | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.998+3887T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100443381 | |||||||
| chr6:100443824 | A | G | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.998+3444T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100443824 | |||||||
| chr6:100443891 | A | G | 2 | a0001c0001t0003g0042 a0001c0001t0005g0041 |
2 | HG01109.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.998+3377T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100443891 | |||||||
| chr6:100443968 | A | T | 1 | a0002c0002t0001g0182 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.998+3300T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100443968 | |||||||
| chr6:100444034 | G | A | 1 | a0001c0001t0053g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.998+3234C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100444034 | |||||||
| chr6:100444111 | C | CATTTTCA | 100 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(97): Show |
100 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.998+3156_998+3157i others(9): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100444111 | |||||||
| chr6:100444342 | T | G | 1 | a0002c0002t0001g0315 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.998+2926A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100444342 | |||||||
| chr6:100444419 | T | G | 2 | a0001c0001t0041g0162 a0001c0001t0044g0150 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.998+2849A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100444419 | |||||||
| chr6:100444710 | A | G | 1 | a0001c0001t0006g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.998+2558T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100444710 | |||||||
| chr6:100444829 | C | T | 1 | a0001c0001t0010g0260 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.998+2439G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100444829 | |||||||
| chr6:100444914 | C | T | 1 | a0001c0001t0002g0040 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.998+2354G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100444914 | |||||||
| chr6:100445387 | G | T | 1 | a0002c0002t0001g0242 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.998+1881C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100445387 | |||||||
| chr6:100445644 | G | C | 32 | a0001c0001t0002g0152 a0001c0001t0002g0158 a0001c0001t0002g0166 others(29): Show |
32 | HG00544.hp1 HG00735.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.998+1624C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100445644 | |||||||
| chr6:100445715 | C | G | 1 | a0001c0001t0040g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.998+1553G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100445715 | |||||||
| chr6:100445986 | A | G | 1 | a0001c0009t0033g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.998+1282T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100445986 | |||||||
| chr6:100445986 | A | T | 1 | a0002c0002t0001g0193 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.998+1282T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100445986 | |||||||
| chr6:100446040 | AT | A | 51 | a0001c0001t0002g0152 a0001c0001t0002g0158 a0001c0001t0002g0166 others(48): Show |
51 | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.998+1227delA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100446040 | |||||||
| chr6:100446303 | A | G | 100 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(97): Show |
100 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.998+965T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100446303 | |||||||
| chr6:100446638 | G | T | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.998+630C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100446638 | |||||||
| chr6:100446641 | C | T | 2 | a0001c0001t0006g0212 a0001c0001t0006g0213 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.998+627G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100446641 | |||||||
| chr6:100446711 | G | A | 99 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(96): Show |
99 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.998+557C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100446711 | |||||||
| chr6:100446803 | G | C | 1 | a0001c0001t0027g0098 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.998+465C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100446803 | |||||||
| chr6:100446985 | C | T | 3 | a0001c0001t0021g0244 a0002c0002t0007g0245 a0002c0002t0007g0246 |
3 | HG00738.hp2 HG01081.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.998+283G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 9/11 | chr6 | 100446985 | |||||||
| chr6:100447468 | C | T | 299 | a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0040 others(296): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.851-53G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 8/11 | chr6 | 100447468 | |||||||
| chr6:100447586 | G | T | 109 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(106): Show |
110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.851-171C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 8/11 | chr6 | 100447586 | |||||||
| chr6:100447728 | G | A | 4 | a0001c0001t0002g0166 a0001c0001t0022g0149 a0001c0001t0022g0165 others(1): Show |
4 | HG02280.hp1 HG02647.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-313C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 8/11 | chr6 | 100447728 | |||||||
| chr6:100447749 | C | G | 95 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(92): Show |
95 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.851-334G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 8/11 | chr6 | 100447749 | |||||||
| chr6:100447776 | C | T | 2 | a0001c0001t0002g0235 a0002c0002t0001g0236 |
2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.851-361G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 8/11 | chr6 | 100447776 | |||||||
| chr6:100448042 | G | T | 3 | a0001c0001t0002g0176 a0001c0001t0003g0177 a0002c0002t0007g0178 |
3 | HG00544.hp1 NA18747.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.850+104C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 8/11 | chr6 | 100448042 | |||||||
| chr6:100448305 | C | T | 1 | a0002c0002t0006g0192 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.744-53G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 7/11 | chr6 | 100448305 | |||||||
| chr6:100448320 | C | A | 16 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0003g0128 others(13): Show |
16 | NA18946.hp2 NA18950.hp2 NA18963.hp2 others(13): Show |
intron_variant | MODIFIER | c.744-68G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 7/11 | chr6 | 100448320 | |||||||
| chr6:100448367 | A | G | 96 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(93): Show |
96 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.743+112T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 7/11 | chr6 | 100448367 | |||||||
| chr6:100448367 | A | T | 2 | a0001c0001t0032g0010 a0001c0009t0033g0009 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.743+112T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 7/11 | chr6 | 100448367 | |||||||
| chr6:100448413 | T | G | 97 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(94): Show |
97 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.743+66A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 7/11 | chr6 | 100448413 | |||||||
| chr6:100448693 | T | G | 111 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(108): Show |
112 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.544-15A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 6/11 | chr6 | 100448693 | |||||||
| chr6:100448738 | G | A | 22 | a0001c0001t0002g0152 a0001c0001t0002g0158 a0001c0001t0002g0166 others(19): Show |
22 | HG00544.hp1 HG00735.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.544-60C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 6/11 | chr6 | 100448738 | |||||||
| chr6:100448969 | A | G | 1 | a0002c0002t0006g0192 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.544-291T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 6/11 | chr6 | 100448969 | |||||||
| chr6:100449134 | C | G | 1 | a0001c0001t0018g0304 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.543+229G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 6/11 | chr6 | 100449134 | |||||||
| chr6:100449137 | G | A | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.543+226C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 6/11 | chr6 | 100449137 | |||||||
| chr6:100449303 | C | G | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.543+60G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 6/11 | chr6 | 100449303 | |||||||
| chr6:100449508 | C | T | 1 | a0001c0001t0019g0019 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.458-60G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 5/11 | chr6 | 100449508 | |||||||
| chr6:100449519 | C | T | 1 | a0001c0001t0068g0267 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.458-71G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 5/11 | chr6 | 100449519 | |||||||
| chr6:100449907 | C | T | 2 | a0001c0001t0002g0152 a0001c0001t0003g0153 |
2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.349-208G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 4/11 | chr6 | 100449907 | |||||||
| chr6:100450243 | G | A | 1 | a0001c0001t0008g0141 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.348+24C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 4/11 | chr6 | 100450243 | |||||||
| chr6:100450410 | T | C | 1 | a0001c0001t0003g0241 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.259-54A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450410 | |||||||
| chr6:100450544 | C | G | 1 | a0001c0001t0004g0247 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.259-188G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450544 | |||||||
| chr6:100450665 | G | GTCTCTCT others(1): Show |
8 | a0001c0001t0009g0017 a0001c0001t0016g0001 a0001c0001t0053g0271 others(5): Show |
9 | HG00438.hp1 HG00642.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.259-317_259-310dup others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450665 | |||||||
| chr6:100450665 | G | GTCTCTCT others(3): Show |
1 | a0002c0002t0001g0314 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.259-319_259-310dup others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450665 | |||||||
| chr6:100450665 | G | GTCTCTCT others(5): Show |
2 | a0001c0001t0029g0006 a0002c0002t0001g0224 |
2 | HG00140.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.259-321_259-310dup others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450665 | |||||||
| chr6:100450665 | GTC | G | 6 | a0001c0001t0003g0036 a0001c0001t0071g0014 a0002c0002t0001g0037 others(3): Show |
6 | HG01496.hp1 HG02071.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-311_259-310del others(2): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450665 | |||||||
| chr6:100450665 | GTCTC | G | 10 | a0001c0001t0002g0103 a0001c0001t0002g0106 a0001c0001t0003g0035 others(7): Show |
10 | HG01168.hp1 HG01169.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.259-313_259-310del others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450665 | |||||||
| chr6:100450692 | TCTCTCAC others(3): Show |
T | 13 | a0001c0001t0002g0273 a0001c0001t0003g0283 a0001c0001t0004g0275 others(10): Show |
13 | HG00423.hp2 HG00735.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.259-346_259-337del others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450692 | |||||||
| chr6:100450694 | T | TCACA | 5 | a0001c0001t0003g0002 a0001c0001t0012g0306 a0001c0001t0012g0307 others(2): Show |
6 | HG01361.hp1 HG01515.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-339_259-338ins others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450694 | |||||||
| chr6:100450694 | TCTCA | T | 64 | a0001c0001t0002g0040 a0001c0001t0002g0052 a0001c0001t0002g0061 others(61): Show |
64 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.259-342_259-339del others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450694 | |||||||
| chr6:100450694 | TCTCACA | T | 9 | a0001c0001t0002g0065 a0001c0001t0003g0068 a0001c0001t0003g0101 others(6): Show |
9 | HG01106.hp1 HG01255.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.259-344_259-339del others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450694 | |||||||
| chr6:100450694 | TCTCACAC others(3): Show |
T | 8 | a0001c0001t0002g0282 a0001c0001t0004g0285 a0001c0001t0004g0290 others(5): Show |
8 | HG02165.hp2 HG02602.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-348_259-339del others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450694 | |||||||
| chr6:100450694 | TCTCACAC others(5): Show |
T | 1 | a0001c0001t0006g0163 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.259-350_259-339del others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450694 | |||||||
| chr6:100450696 | T | A | 14 | a0001c0001t0003g0002 a0001c0001t0003g0036 a0001c0001t0012g0305 others(11): Show |
15 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.259-340A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCAC others(1): Show |
6 | a0001c0001t0002g0194 a0001c0001t0002g0217 a0001c0001t0003g0210 others(3): Show |
6 | HG01256.hp1 HG02132.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCAC others(3): Show |
4 | a0001c0001t0002g0248 a0001c0001t0019g0019 a0001c0001t0019g0021 others(1): Show |
4 | HG01070.hp1 HG02109.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCAC others(5): Show |
2 | a0001c0001t0003g0241 a0001c0001t0010g0260 |
2 | HG00099.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.259-341_259-340ins others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCAC others(7): Show |
1 | a0001c0001t0008g0181 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.259-341_259-340ins others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(3): Show |
9 | a0001c0001t0003g0110 a0001c0001t0003g0233 a0001c0001t0006g0151 others(6): Show |
9 | HG00140.hp1 HG00558.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(5): Show |
4 | a0001c0001t0043g0229 a0001c0001t0072g0234 a0001c0001t0075g0188 others(1): Show |
4 | HG02027.hp1 HG02809.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(7): Show |
2 | a0001c0001t0002g0111 a0001c0001t0002g0183 |
2 | NA18953.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.259-341_259-340ins others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(9): Show |
2 | a0001c0001t0003g0195 a0002c0002t0007g0250 |
2 | HG02896.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.259-341_259-340ins others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(3): Show |
6 | a0001c0001t0004g0247 a0001c0001t0004g0310 a0001c0001t0005g0256 others(3): Show |
6 | HG02602.hp1 NA18947.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(5): Show |
15 | a0001c0001t0002g0004 a0001c0001t0002g0190 a0001c0001t0002g0202 others(12): Show |
16 | HG00423.hp1 HG00544.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(7): Show |
5 | a0001c0001t0002g0209 a0001c0001t0002g0235 a0001c0001t0003g0223 others(2): Show |
5 | HG00323.hp1 HG00642.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(9): Show |
3 | a0001c0001t0005g0196 a0002c0002t0001g0187 a0002c0002t0007g0115 |
3 | HG00621.hp1 NA18973.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.259-341_259-340ins others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(5): Show |
11 | a0001c0001t0002g0200 a0001c0001t0005g0189 a0001c0001t0008g0225 others(8): Show |
11 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(7): Show |
5 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0001t0002g0191 others(2): Show |
5 | HG03704.hp1 NA18946.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(9): Show |
18 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0003g0128 others(15): Show |
19 | HG01891.hp1 HG02723.hp2 HG02886.hp1 others(16): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(11): Show |
3 | a0001c0001t0010g0262 a0002c0002t0001g0109 a0002c0002t0001g0193 |
3 | HG02135.hp2 NA18978.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.259-341_259-340ins others(18): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(17): Show |
1 | a0001c0001t0002g0211 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.259-341_259-340ins others(24): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(7): Show |
1 | a0002c0002t0024g0253 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.259-341_259-340ins others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(9): Show |
4 | a0001c0001t0002g0268 a0001c0001t0002g0269 a0002c0002t0001g0125 others(1): Show |
4 | HG03491.hp1 HG03492.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(11): Show |
7 | a0001c0001t0006g0212 a0001c0001t0010g0005 a0001c0001t0011g0261 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-341_259-340ins others(18): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(13): Show |
1 | a0001c0001t0006g0213 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.259-341_259-340ins others(20): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(15): Show |
1 | a0001c0001t0003g0186 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.259-341_259-340ins others(22): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | T | TCTCTCTC others(11): Show |
1 | a0002c0002t0001g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.259-341_259-340ins others(18): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | TCA | T | 5 | a0001c0001t0001g0067 a0001c0001t0032g0010 a0001c0001t0039g0016 others(2): Show |
5 | HG02615.hp1 HG02809.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-342_259-341del others(2): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | TCACA | T | 3 | a0001c0001t0061g0294 a0002c0002t0007g0099 a0002c0002t0024g0087 |
3 | HG00558.hp2 HG02300.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.259-344_259-341del others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450696 | TCACACAC others(1): Show |
T | 30 | a0001c0001t0002g0152 a0001c0001t0002g0158 a0001c0001t0002g0166 others(27): Show |
30 | HG00544.hp1 HG00735.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.259-348_259-341del others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450696 | |||||||
| chr6:100450698 | A | T | 9 | a0001c0001t0002g0204 a0001c0001t0003g0221 a0001c0001t0006g0018 others(6): Show |
10 | HG01255.hp2 HG01346.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.259-342T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450698 | |||||||
| chr6:100450700 | A | T | 2 | a0001c0001t0032g0010 a0001c0009t0033g0009 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.259-344T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450700 | |||||||
| chr6:100450706 | A | T | 29 | a0001c0001t0002g0152 a0001c0001t0002g0158 a0001c0001t0002g0166 others(26): Show |
29 | HG00544.hp1 HG00735.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.259-350T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450706 | |||||||
| chr6:100450803 | A | T | 1 | a0001c0001t0011g0274 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.259-447T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450803 | |||||||
| chr6:100450908 | C | T | 1 | a0001c0001t0003g0034 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.259-552G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450908 | |||||||
| chr6:100450909 | G | A | 4 | a0001c0001t0002g0166 a0001c0001t0022g0149 a0001c0001t0022g0165 others(1): Show |
4 | HG02280.hp1 HG02647.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-553C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450909 | |||||||
| chr6:100450999 | C | G | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.259-643G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100450999 | |||||||
| chr6:100451210 | C | T | 1 | a0001c0001t0009g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-854G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100451210 | |||||||
| chr6:100451225 | C | T | 1 | a0001c0001t0053g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.259-869G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100451225 | |||||||
| chr6:100451315 | G | T | 3 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0217 |
3 | HG03704.hp1 HG03710.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.259-959C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100451315 | |||||||
| chr6:100451584 | A | G | 1 | a0001c0001t0002g0004 | 2 | NA18995.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.259-1228T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100451584 | |||||||
| chr6:100451983 | G | A | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259-1627C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100451983 | |||||||
| chr6:100452000 | C | T | 1 | a0001c0001t0005g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.259-1644G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452000 | |||||||
| chr6:100452083 | G | T | 1 | a0001c0001t0034g0011 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.258+1679C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452083 | |||||||
| chr6:100452209 | CCTT | C | 6 | a0001c0001t0003g0298 a0001c0001t0006g0293 a0001c0001t0006g0295 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+1550_258+1552d others(5): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452209 | |||||||
| chr6:100452289 | A | C | 2 | a0001c0001t0010g0172 a0001c0001t0055g0171 |
2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.258+1473T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452289 | |||||||
| chr6:100452299 | T | C | 10 | a0001c0001t0003g0002 a0001c0001t0012g0305 a0001c0001t0012g0306 others(7): Show |
11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.258+1463A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452299 | |||||||
| chr6:100452360 | G | A | 1 | a0001c0001t0003g0142 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.258+1402C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452360 | |||||||
| chr6:100452380 | G | A | 2 | a0002c0002t0001g0100 a0002c0002t0007g0099 |
2 | HG01192.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.258+1382C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452380 | |||||||
| chr6:100452386 | C | T | 3 | a0001c0001t0002g0169 a0001c0001t0003g0168 a0001c0001t0009g0170 |
3 | HG02055.hp2 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.258+1376G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452386 | |||||||
| chr6:100452418 | C | T | 3 | a0001c0001t0021g0244 a0002c0002t0007g0245 a0002c0002t0007g0246 |
3 | HG00738.hp2 HG01081.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.258+1344G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452418 | |||||||
| chr6:100452630 | C | T | 4 | a0001c0001t0003g0002 a0001c0001t0036g0302 a0002c0002t0017g0301 others(1): Show |
5 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+1132G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452630 | |||||||
| chr6:100452632 | G | A | 312 | a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0040 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.258+1130C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452632 | |||||||
| chr6:100452865 | G | A | 2 | a0001c0001t0006g0212 a0001c0001t0006g0213 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.258+897C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100452865 | |||||||
| chr6:100453286 | G | A | 2 | a0001c0001t0070g0175 a0001c0001t0071g0014 |
2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.258+476C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100453286 | |||||||
| chr6:100453492 | C | T | 2 | a0001c0001t0008g0129 a0001c0001t0008g0130 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.258+270G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100453492 | |||||||
| chr6:100453518 | A | G | 1 | a0002c0002t0001g0033 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.258+244T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100453518 | |||||||
| chr6:100453644 | T | TG | 109 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(106): Show |
110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.258+117dupC | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100453644 | |||||||
| chr6:100453666 | T | G | 1 | a0001c0001t0002g0106 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.258+96A>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 3/11 | chr6 | 100453666 | |||||||
| chr6:100453913 | C | A | 2 | a0001c0001t0070g0175 a0001c0001t0071g0014 |
2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.176-69G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100453913 | |||||||
| chr6:100453961 | G | A | 51 | a0001c0001t0002g0152 a0001c0001t0002g0158 a0001c0001t0002g0166 others(48): Show |
51 | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.176-117C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100453961 | |||||||
| chr6:100453978 | G | T | 2 | a0001c0001t0002g0235 a0002c0002t0001g0236 |
2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.176-134C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100453978 | |||||||
| chr6:100454166 | A | T | 1 | a0001c0001t0009g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.176-322T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454166 | |||||||
| chr6:100454225 | G | A | 2 | a0001c0001t0002g0208 a0001c0001t0002g0209 |
2 | HG00642.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.176-381C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454225 | |||||||
| chr6:100454319 | C | A | 2 | a0001c0001t0039g0016 a0001c0001t0040g0015 |
2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.176-475G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454319 | |||||||
| chr6:100454323 | C | T | 1 | a0002c0002t0001g0031 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.176-479G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454323 | |||||||
| chr6:100454384 | C | T | 1 | a0001c0001t0005g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.176-540G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454384 | |||||||
| chr6:100454518 | C | A | 1 | a0001c0001t0026g0216 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.176-674G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454518 | |||||||
| chr6:100454555 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.176-711G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454555 | |||||||
| chr6:100454595 | G | T | 1 | a0001c0001t0053g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.176-751C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454595 | |||||||
| chr6:100454657 | C | A | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.176-813G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454657 | |||||||
| chr6:100454715 | C | T | 2 | a0001c0001t0070g0175 a0001c0001t0071g0014 |
2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.176-871G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454715 | |||||||
| chr6:100454932 | C | T | 1 | a0001c0001t0009g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.176-1088G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100454932 | |||||||
| chr6:100455105 | T | A | 1 | a0001c0001t0018g0309 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.176-1261A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455105 | |||||||
| chr6:100455110 | A | G | 2 | a0001c0001t0057g0028 a0001c0001t0058g0029 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.176-1266T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455110 | |||||||
| chr6:100455302 | C | T | 10 | a0001c0001t0003g0002 a0001c0001t0012g0305 a0001c0001t0012g0306 others(7): Show |
11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.176-1458G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455302 | |||||||
| chr6:100455370 | T | C | 1 | a0001c0001t0011g0264 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.176-1526A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455370 | |||||||
| chr6:100455405 | G | A | 2 | a0001c0001t0070g0175 a0001c0001t0071g0014 |
2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.176-1561C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455405 | |||||||
| chr6:100455688 | G | C | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.176-1844C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455688 | |||||||
| chr6:100455689 | G | A | 2 | a0001c0001t0032g0010 a0001c0009t0033g0009 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.176-1845C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455689 | |||||||
| chr6:100455934 | C | A | 1 | a0001c0001t0003g0101 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.176-2090G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455934 | |||||||
| chr6:100455947 | C | T | 1 | a0001c0001t0044g0150 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.176-2103G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100455947 | |||||||
| chr6:100456157 | C | T | 1 | a0001c0001t0074g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.176-2313G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100456157 | |||||||
| chr6:100456229 | G | C | 94 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(91): Show |
94 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.176-2385C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100456229 | |||||||
| chr6:100456312 | A | G | 298 | a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0040 others(295): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.176-2468T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100456312 | |||||||
| chr6:100456567 | A | G | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.176-2723T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100456567 | |||||||
| chr6:100456988 | G | T | 1 | a0001c0001t0064g0027 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.176-3144C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100456988 | |||||||
| chr6:100457090 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.176-3246A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457090 | |||||||
| chr6:100457265 | A | G | 2 | a0001c0001t0005g0243 a0001c0001t0072g0234 |
2 | HG00544.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.176-3421T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457265 | |||||||
| chr6:100457350 | C | G | 43 | a0001c0001t0002g0152 a0001c0001t0002g0158 a0001c0001t0002g0166 others(40): Show |
44 | HG00280.hp1 HG00544.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.176-3506G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457350 | |||||||
| chr6:100457419 | G | T | 10 | a0001c0001t0003g0002 a0001c0001t0012g0305 a0001c0001t0012g0306 others(7): Show |
11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.176-3575C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457419 | |||||||
| chr6:100457435 | G | A | 1 | a0001c0001t0009g0017 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.176-3591C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457435 | |||||||
| chr6:100457780 | G | C | 1 | a0001c0001t0074g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.176-3936C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457780 | |||||||
| chr6:100457795 | G | A | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.176-3951C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457795 | |||||||
| chr6:100457822 | G | A | 10 | a0001c0001t0003g0002 a0001c0001t0012g0305 a0001c0001t0012g0306 others(7): Show |
11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.176-3978C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457822 | |||||||
| chr6:100457886 | T | C | 1 | a0001c0001t0039g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.176-4042A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100457886 | |||||||
| chr6:100458005 | TTTCTCTC others(6): Show |
T | 2 | a0001c0001t0003g0002 a0001c0001t0044g0150 |
2 | HG01515.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.176-4174_176-4162d others(15): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458005 | |||||||
| chr6:100458005 | TTTCTCTC others(8): Show |
T | 3 | a0001c0001t0003g0153 a0001c0001t0006g0293 a0005c0010t0067g0140 |
3 | HG01884.hp1 HG03471.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.176-4176_176-4162d others(17): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458005 | |||||||
| chr6:100458005 | TTTCTCTC others(16): Show |
T | 1 | a0001c0001t0006g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.176-4184_176-4162d others(25): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458005 | |||||||
| chr6:100458005 | TTTCTCTC others(18): Show |
T | 1 | a0001c0001t0005g0112 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.176-4186_176-4162d others(27): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458005 | |||||||
| chr6:100458006 | T | C | 1 | a0002c0002t0001g0108 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.176-4162A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | T | TTCTCTCT others(3): Show |
1 | a0001c0001t0053g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.176-4172_176-4163d others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | T | TTCTCTCT others(5): Show |
1 | a0004c0008t0023g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.176-4163_176-4162i others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | T | TTCTCTCT others(13): Show |
1 | a0002c0002t0001g0203 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.176-4163_176-4162i others(22): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTC | T | 7 | a0001c0001t0002g0202 a0001c0001t0010g0005 a0001c0001t0010g0262 others(4): Show |
7 | HG02135.hp2 HG02723.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.176-4164_176-4163d others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTC | T | 8 | a0001c0001t0002g0209 a0001c0001t0008g0263 a0001c0001t0010g0005 others(5): Show |
8 | HG00642.hp1 HG01109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-4166_176-4163d others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTCTC | T | 11 | a0001c0001t0002g0190 a0001c0001t0002g0194 a0001c0001t0002g0208 others(8): Show |
11 | HG00642.hp2 HG02056.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.176-4168_176-4163d others(8): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTCTCT others(1): Show |
T | 21 | a0001c0001t0002g0117 a0001c0001t0002g0217 a0001c0001t0003g0142 others(18): Show |
22 | HG00140.hp2 HG00423.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.176-4170_176-4163d others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTCTCT others(3): Show |
T | 18 | a0001c0001t0002g0004 a0001c0001t0003g0233 a0001c0001t0004g0310 others(15): Show |
19 | HG00280.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.176-4172_176-4163d others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTCTCT others(5): Show |
T | 27 | a0001c0001t0002g0191 a0001c0001t0002g0235 a0001c0001t0002g0240 others(24): Show |
27 | HG00323.hp1 HG01070.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.176-4174_176-4163d others(14): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTCTCT others(7): Show |
T | 38 | a0001c0001t0002g0111 a0001c0001t0002g0135 a0001c0001t0002g0248 others(35): Show |
38 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.176-4176_176-4163d others(16): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTCTCT others(9): Show |
T | 19 | a0001c0001t0002g0118 a0001c0001t0002g0143 a0001c0001t0002g0179 others(16): Show |
19 | HG00558.hp1 HG01192.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.176-4178_176-4163d others(18): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTCTCT others(11): Show |
T | 20 | a0001c0001t0002g0134 a0001c0001t0002g0152 a0001c0001t0002g0158 others(17): Show |
20 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.176-4180_176-4163d others(20): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTCTCT others(13): Show |
T | 9 | a0001c0001t0002g0167 a0001c0001t0002g0169 a0001c0001t0002g0204 others(6): Show |
9 | HG00544.hp1 HG01168.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-4182_176-4163d others(22): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTCTCT others(15): Show |
T | 1 | a0001c0001t0006g0163 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.176-4184_176-4163d others(24): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTCTCT others(17): Show |
T | 2 | a0001c0001t0010g0172 a0001c0001t0039g0016 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.176-4186_176-4163d others(26): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTCTCT others(19): Show |
T | 1 | a0001c0001t0002g0176 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.176-4188_176-4163d others(28): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTCTCT others(21): Show |
T | 4 | a0001c0001t0005g0026 a0001c0001t0040g0015 a0001c0001t0055g0171 others(1): Show |
4 | HG02074.hp1 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.176-4190_176-4163d others(30): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTCTCT others(23): Show |
T | 2 | a0001c0001t0002g0061 a0001c0001t0003g0068 |
2 | HG01106.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.176-4192_176-4163d others(32): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTCTCT others(25): Show |
T | 11 | a0001c0001t0004g0081 a0001c0001t0005g0091 a0001c0001t0005g0093 others(8): Show |
11 | HG00280.hp2 HG00323.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.176-4194_176-4163d others(34): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTCTCT others(27): Show |
T | 49 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0065 others(46): Show |
49 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.176-4196_176-4163d others(36): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458006 | TTCTCTCT others(29): Show |
T | 24 | a0001c0001t0002g0052 a0001c0001t0002g0095 a0001c0001t0002g0103 others(21): Show |
24 | HG00733.hp2 HG01074.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.176-4198_176-4163d others(38): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458006 | |||||||
| chr6:100458007 | T | TCTCTCTC others(3): Show |
1 | a0001c0001t0003g0210 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.176-4164_176-4163i others(12): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458007 | |||||||
| chr6:100458007 | TCTCTCTC others(6): Show |
T | 1 | a0002c0002t0001g0108 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.176-4176_176-4164d others(15): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458007 | |||||||
| chr6:100458009 | T | TCTCTCTC others(1): Show |
3 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0001t0003g0186 |
3 | NA18950.hp1 NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.176-4166_176-4165i others(10): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458009 | |||||||
| chr6:100458011 | TCTCTCTC others(4): Show |
T | 1 | a0001c0007t0004g0287 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.176-4178_176-4168d others(13): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458011 | |||||||
| chr6:100458011 | TCTCTCTC others(6): Show |
T | 1 | a0002c0002t0001g0286 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.176-4180_176-4168d others(15): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458011 | |||||||
| chr6:100458012 | C | T | 1 | a0001c0001t0032g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.176-4168G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458012 | |||||||
| chr6:100458015 | T | TCC | 4 | a0001c0001t0002g0211 a0001c0001t0006g0212 a0001c0001t0006g0213 others(1): Show |
4 | HG02135.hp1 HG02976.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-4172_176-4171i others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458015 | |||||||
| chr6:100458016 | C | T | 1 | a0001c0009t0033g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.176-4172G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458016 | |||||||
| chr6:100458016 | CTCTCTCT | C | 4 | a0001c0001t0026g0216 a0002c0002t0001g0214 a0002c0002t0001g0215 others(1): Show |
4 | HG00423.hp1 HG01516.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.176-4179_176-4173d others(9): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458016 | |||||||
| chr6:100458016 | CTCTCTCT others(4): Show |
C | 1 | a0001c0001t0008g0225 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.176-4183_176-4173d others(13): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458016 | |||||||
| chr6:100458017 | T | C | 2 | a0001c0001t0003g0195 a0001c0001t0008g0181 |
2 | HG01070.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.176-4173A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458017 | |||||||
| chr6:100458018 | C | T | 1 | a0001c0001t0004g0290 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.176-4174G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458018 | |||||||
| chr6:100458019 | T | C | 5 | a0001c0001t0002g0202 a0001c0001t0010g0005 a0001c0001t0010g0262 others(2): Show |
5 | HG02135.hp2 HG02723.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-4175A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458019 | |||||||
| chr6:100458020 | C | T | 1 | a0001c0001t0004g0288 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.176-4176G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458020 | |||||||
| chr6:100458021 | T | C | 5 | a0001c0001t0002g0209 a0001c0001t0008g0263 a0001c0001t0010g0005 others(2): Show |
5 | HG00642.hp1 HG01109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-4177A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458021 | |||||||
| chr6:100458022 | C | T | 1 | a0001c0001t0005g0289 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.176-4178G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458022 | |||||||
| chr6:100458023 | T | C | 8 | a0001c0001t0002g0190 a0001c0001t0002g0194 a0001c0001t0002g0208 others(5): Show |
8 | HG00642.hp2 HG02056.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.176-4179A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458023 | |||||||
| chr6:100458024 | C | T | 3 | a0001c0001t0003g0283 a0001c0001t0004g0285 a0001c0001t0026g0284 |
3 | HG01496.hp2 NA18971.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.176-4180G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458024 | |||||||
| chr6:100458025 | T | C | 14 | a0001c0001t0002g0217 a0001c0001t0003g0221 a0001c0001t0003g0223 others(11): Show |
15 | HG00140.hp2 HG00423.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.176-4181A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458025 | |||||||
| chr6:100458026 | C | T | 9 | a0001c0001t0002g0282 a0001c0001t0004g0275 a0001c0001t0004g0277 others(6): Show |
9 | HG00735.hp2 HG01081.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-4182G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458026 | |||||||
| chr6:100458027 | T | C | 11 | a0001c0001t0002g0004 a0001c0001t0003g0233 a0001c0001t0004g0310 others(8): Show |
12 | HG01175.hp2 HG02809.hp1 HG03239.hp1 others(9): Show |
intron_variant | MODIFIER | c.176-4183A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458027 | |||||||
| chr6:100458028 | C | T | 1 | a0001c0001t0002g0273 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.176-4184G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458028 | |||||||
| chr6:100458029 | T | C | 18 | a0001c0001t0002g0235 a0001c0001t0002g0240 a0001c0001t0002g0268 others(15): Show |
18 | HG00323.hp1 HG01070.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.176-4185A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458029 | |||||||
| chr6:100458030 | C | T | 2 | a0001c0001t0052g0292 a0002c0002t0001g0272 |
2 | HG03831.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.176-4186G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458030 | |||||||
| chr6:100458031 | T | C | 19 | a0001c0001t0002g0248 a0001c0001t0004g0247 a0001c0001t0005g0243 others(16): Show |
19 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.176-4187A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458031 | |||||||
| chr6:100458033 | T | C | 1 | a0002c0002t0001g0259 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.176-4189A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458033 | |||||||
| chr6:100458071 | T | C | 1 | a0001c0001t0010g0260 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.176-4227A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458071 | |||||||
| chr6:100458122 | C | T | 1 | a0001c0001t0075g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.176-4278G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458122 | |||||||
| chr6:100458170 | G | T | 89 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0052 others(86): Show |
89 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.176-4326C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458170 | |||||||
| chr6:100458319 | G | T | 1 | a0001c0001t0005g0026 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.176-4475C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458319 | |||||||
| chr6:100458328 | C | A | 6 | a0001c0001t0003g0298 a0001c0001t0006g0293 a0001c0001t0006g0295 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-4484G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458328 | |||||||
| chr6:100458445 | C | G | 2 | a0001c0001t0009g0024 a0001c0001t0009g0025 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.176-4601G>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458445 | |||||||
| chr6:100458628 | G | A | 21 | a0001c0001t0002g0273 a0001c0001t0002g0282 a0001c0001t0003g0283 others(18): Show |
21 | HG00735.hp2 HG01081.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.175+4666C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458628 | |||||||
| chr6:100458700 | C | A | 7 | a0001c0001t0006g0266 a0001c0001t0008g0263 a0001c0001t0010g0005 others(4): Show |
8 | HG01109.hp1 HG02258.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+4594G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458700 | |||||||
| chr6:100458731 | T | A | 1 | a0001c0001t0010g0172 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175+4563A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458731 | |||||||
| chr6:100458773 | A | T | 6 | a0001c0001t0003g0298 a0001c0001t0006g0293 a0001c0001t0006g0295 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+4521T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458773 | |||||||
| chr6:100458786 | C | A | 33 | a0001c0001t0002g0152 a0001c0001t0002g0158 a0001c0001t0002g0166 others(30): Show |
33 | HG00544.hp1 HG00735.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.175+4508G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458786 | |||||||
| chr6:100458789 | C | A | 1 | a0001c0001t0070g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.175+4505G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100458789 | |||||||
| chr6:100459301 | G | A | 1 | a0001c0003t0003g0102 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.175+3993C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100459301 | |||||||
| chr6:100459333 | G | A | 10 | a0001c0001t0003g0002 a0001c0001t0012g0305 a0001c0001t0012g0306 others(7): Show |
11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+3961C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100459333 | |||||||
| chr6:100459688 | A | G | 3 | a0001c0001t0016g0001 a0001c0001t0029g0006 a0001c0003t0030g0007 |
4 | HG01255.hp2 HG01346.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+3606T>C | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100459688 | |||||||
| chr6:100459911 | C | T | 6 | a0001c0001t0002g0183 a0001c0001t0002g0184 a0001c0001t0002g0185 others(3): Show |
6 | NA18950.hp1 NA18971.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+3383G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100459911 | |||||||
| chr6:100460254 | A | T | 1 | a0001c0001t0003g0270 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.175+3040T>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100460254 | |||||||
| chr6:100460258 | G | A | 2 | a0001c0001t0006g0173 a0001c0001t0006g0174 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.175+3036C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100460258 | |||||||
| chr6:100460304 | T | C | 31 | a0001c0001t0002g0152 a0001c0001t0002g0158 a0001c0001t0002g0166 others(28): Show |
31 | HG00544.hp1 HG00735.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.175+2990A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100460304 | |||||||
| chr6:100460760 | C | T | 1 | a0001c0001t0008g0181 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.175+2534G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100460760 | |||||||
| chr6:100460862 | G | C | 33 | a0001c0001t0002g0152 a0001c0001t0002g0158 a0001c0001t0002g0166 others(30): Show |
33 | HG00544.hp1 HG00735.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.175+2432C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100460862 | |||||||
| chr6:100460921 | C | A | 1 | a0002c0002t0001g0107 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.175+2373G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100460921 | |||||||
| chr6:100460996 | C | T | 32 | a0001c0001t0002g0152 a0001c0001t0002g0158 a0001c0001t0002g0166 others(29): Show |
32 | HG00544.hp1 HG00735.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.175+2298G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100460996 | |||||||
| chr6:100461259 | T | C | 1 | a0001c0001t0068g0267 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.175+2035A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461259 | |||||||
| chr6:100461382 | T | A | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.175+1912A>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461382 | |||||||
| chr6:100461422 | G | T | 1 | a0002c0002t0001g0023 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.175+1872C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461422 | |||||||
| chr6:100461507 | C | A | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.175+1787G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461507 | |||||||
| chr6:100461522 | C | T | 118 | a0001c0001t0002g0004 a0001c0001t0002g0183 a0001c0001t0002g0184 others(115): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.175+1772G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461522 | |||||||
| chr6:100461637 | C | A | 5 | a0001c0001t0002g0103 a0001c0001t0002g0106 a0001c0001t0005g0104 others(2): Show |
5 | HG02132.hp1 HG02523.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+1657G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461637 | |||||||
| chr6:100461777 | C | T | 275 | a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0040 others(272): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.175+1517G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461777 | |||||||
| chr6:100461783 | A | C | 2 | a0001c0001t0032g0010 a0001c0009t0033g0009 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.175+1511T>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461783 | |||||||
| chr6:100461827 | T | TTC | 9 | a0001c0001t0002g0167 a0001c0001t0002g0169 a0001c0001t0003g0168 others(6): Show |
9 | HG01168.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+1465_175+1466d others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461827 | |||||||
| chr6:100461840 | TC | T | 4 | a0001c0001t0002g0167 a0001c0001t0006g0173 a0001c0001t0006g0174 others(1): Show |
4 | HG02572.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+1453delG | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461840 | |||||||
| chr6:100461841 | C | CTT | 6 | a0001c0001t0006g0163 a0001c0001t0009g0017 a0001c0001t0041g0162 others(3): Show |
6 | HG02559.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+1451_175+1452d others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461841 | |||||||
| chr6:100461841 | C | CTTT | 11 | a0001c0001t0002g0166 a0001c0001t0002g0176 a0001c0001t0003g0153 others(8): Show |
11 | HG00544.hp1 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+1450_175+1452d others(5): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461841 | |||||||
| chr6:100461841 | C | CTTTT | 7 | a0001c0001t0002g0152 a0001c0001t0002g0158 a0001c0001t0002g0179 others(4): Show |
7 | HG00735.hp1 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+1449_175+1452d others(6): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461841 | |||||||
| chr6:100461841 | C | T | 1 | a0001c0001t0055g0171 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.175+1453G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461841 | |||||||
| chr6:100461841 | CT | C | 91 | a0001c0001t0002g0040 a0001c0001t0002g0052 a0001c0001t0002g0106 others(88): Show |
92 | HG00438.hp2 HG00558.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.175+1452delA | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461841 | |||||||
| chr6:100461841 | CTT | C | 157 | a0001c0001t0002g0004 a0001c0001t0002g0061 a0001c0001t0002g0065 others(154): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.175+1451_175+1452d others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461841 | |||||||
| chr6:100461841 | CTTT | C | 11 | a0001c0001t0001g0067 a0001c0001t0002g0268 a0001c0001t0004g0247 others(8): Show |
11 | HG00323.hp2 HG01070.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.175+1450_175+1452d others(5): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461841 | |||||||
| chr6:100461846 | T | C | 2 | a0001c0001t0039g0016 a0001c0001t0040g0015 |
2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.175+1448A>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100461846 | |||||||
| chr6:100462293 | C | T | 1 | a0001c0001t0022g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.175+1001G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100462293 | |||||||
| chr6:100462610 | G | A | 9 | a0001c0001t0012g0305 a0001c0001t0012g0306 a0001c0001t0012g0307 others(6): Show |
9 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+684C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100462610 | |||||||
| chr6:100462898 | C | CA | 7 | a0001c0001t0005g0145 a0001c0001t0005g0146 a0001c0001t0008g0147 others(4): Show |
8 | HG01255.hp2 HG01346.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+395dupT | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100462898 | |||||||
| chr6:100462898 | C | CAA | 11 | a0001c0001t0009g0017 a0001c0001t0012g0305 a0001c0001t0012g0306 others(8): Show |
11 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+394_175+395dup others(2): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100462898 | |||||||
| chr6:100462898 | C | CAAA | 26 | a0001c0001t0002g0152 a0001c0001t0002g0158 a0001c0001t0002g0166 others(23): Show |
26 | HG00735.hp1 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.175+393_175+395dup others(3): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100462898 | |||||||
| chr6:100462898 | C | CAAAA | 6 | a0001c0001t0002g0176 a0001c0001t0002g0179 a0001c0001t0003g0177 others(3): Show |
6 | HG00544.hp1 HG01168.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+392_175+395dup others(4): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100462898 | |||||||
| chr6:100462922 | G | A | 187 | a0001c0001t0002g0004 a0001c0001t0002g0152 a0001c0001t0002g0158 others(184): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.175+372C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100462922 | |||||||
| chr6:100463080 | G | A | 1 | a0001c0001t0031g0008 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.175+214C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100463080 | |||||||
| chr6:100463093 | G | C | 6 | a0001c0001t0003g0298 a0001c0001t0006g0293 a0001c0001t0006g0295 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+201C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100463093 | |||||||
| chr6:100463196 | ATATGT | A | 141 | a0001c0001t0002g0004 a0001c0001t0002g0183 a0001c0001t0002g0184 others(138): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.175+93_175+97delAC others(3): Show |
SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 2/11 | chr6 | 100463196 | |||||||
| chr6:100463973 | G | T | 1 | a0001c0001t0006g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-467-38C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100463973 | |||||||
| chr6:100464019 | C | A | 9 | a0001c0001t0012g0305 a0001c0001t0012g0306 a0001c0001t0012g0307 others(6): Show |
9 | HG00280.hp1 HG01074.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.-467-84G>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464019 | |||||||
| chr6:100464196 | C | T | 1 | a0001c0001t0009g0017 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-467-261G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464196 | |||||||
| chr6:100464201 | G | A | 1 | a0001c0001t0004g0310 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-467-266C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464201 | |||||||
| chr6:100464241 | G | A | 4 | a0002c0002t0001g0311 a0002c0002t0001g0312 a0002c0002t0001g0313 others(1): Show |
4 | HG00642.hp2 HG01515.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-467-306C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464241 | |||||||
| chr6:100464260 | G | A | 2 | a0001c0001t0039g0016 a0001c0001t0040g0015 |
2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-467-325C>T | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464260 | |||||||
| chr6:100464261 | C | T | 2 | a0001c0001t0039g0016 a0001c0001t0040g0015 |
2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-467-326G>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464261 | |||||||
| chr6:100464326 | G | T | 1 | a0001c0001t0071g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-468+288C>A | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464326 | |||||||
| chr6:100464497 | G | C | 1 | a0002c0002t0001g0315 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-468+117C>G | SIM1 | ENSG00000112246.10 | transcript | ENST00000369208.8 | protein_coding | 1/11 | chr6 | 100464497 |