Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 950 |
| ensemblid | ENSG00000138760.11 |
| hgncid | 1665 |
| symbol | SCARB2 |
| name | scavenger receptor class B member 2 |
| refseq_nuc | NM_005506.4 |
| refseq_prot | NP_005497.1 |
| ensembl_nuc | ENST00000264896.8 |
| ensembl_prot | ENSP00000264896.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 76158737 |
| end | 76213824 |
| strand | - |
| ver | v1.2 |
| region | chr4:76158737-76213824 |
| region5000 | chr4:76153737-76218824 |
| regionname0 | SCARB2_chr4_76158737_76213824 |
| regionname5000 | SCARB2_chr4_76153737_76218824 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 478 | 363 | 83 | 62 | 163 | 15 | 38 | 127 | SCARB2_chr4_76153737_76218824 | SCARB2 | MGRCC others(473): Show |
chr4 | 76153737 | 76218824 |
| a0002 | 0/0 | 478 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | MGRCC others(473): Show |
chr4 | 76153737 | 76218824 |
| a0003 | 0/0 | 478 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | MGRCC others(473): Show |
chr4 | 76153737 | 76218824 |
| a0004 | 0/0 | 478 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SCARB2_chr4_76153737_76218824 | SCARB2 | MGRCC others(473): Show |
chr4 | 76153737 | 76218824 |
| a0005 | 0/0 | 478 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SCARB2_chr4_76153737_76218824 | SCARB2 | MGRCC others(473): Show |
chr4 | 76153737 | 76218824 |
| a0006 | 0/0 | 478 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | MGRCC others(473): Show |
chr4 | 76153737 | 76218824 |
| a0007 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | MGRCC others(473): Show |
chr4 | 76153737 | 76218824 |
| a0008 | 0/0 | 225 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | MGRCC others(220): Show |
chr4 | 76153737 | 76218824 |
| a0009 | 0/0 | 478 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | MGRCC others(473): Show |
chr4 | 76153737 | 76218824 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1434 | 346 | 66 | 62 | 163 | 15 | 38 | SCARB2_chr4_76153737_76218824 | SCARB2 | ATGGG others(1429): Show |
chr4 | 76153737 | 76218824 | ||
| a0001c0002 | 0/0 | 1434 | 16 | 16 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ATGGG others(1429): Show |
chr4 | 76153737 | 76218824 | ||
| a0001c0008 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ATGGG others(1429): Show |
chr4 | 76153737 | 76218824 | ||
| a0002c0003 | 0/0 | 1434 | 7 | 7 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ATGGG others(1429): Show |
chr4 | 76153737 | 76218824 | ||
| a0003c0006 | 0/0 | 1434 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ATGGG others(1429): Show |
chr4 | 76153737 | 76218824 | ||
| a0003c0009 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ATGGG others(1429): Show |
chr4 | 76153737 | 76218824 | ||
| a0004c0004 | 0/0 | 1434 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ATGGG others(1429): Show |
chr4 | 76153737 | 76218824 | ||
| a0005c0005 | 0/0 | 1434 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ATGGG others(1429): Show |
chr4 | 76153737 | 76218824 | ||
| a0006c0007 | 0/0 | 1434 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ATGGG others(1429): Show |
chr4 | 76153737 | 76218824 | ||
| a0007c0010 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ATGGG others(1429): Show |
chr4 | 76153737 | 76218824 | ||
| a0008c0011 | 0/0 | 1052 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ATGGG others(1047): Show |
chr4 | 76153737 | 76218824 | ||
| a0009c0012 | 0/0 | 1434 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ATGGG others(1429): Show |
chr4 | 76153737 | 76218824 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4694 | 93 | 7 | 23 | 52 | 4 | 7 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0002 | 0/0 | 4694 | 82 | 18 | 10 | 43 | 2 | 9 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0003 | 0/0 | 4694 | 62 | 3 | 8 | 39 | 1 | 11 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0004 | 0/0 | 4694 | 26 | 8 | 4 | 11 | 1 | 2 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0005 | 0/1 | 4694 | 22 | 1 | 12 | 0 | 4 | 4 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0006 | 0/0 | 4694 | 9 | 7 | 1 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0007 | 0/0 | 4694 | 10 | 1 | 2 | 0 | 2 | 5 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0008 | 0/0 | 4694 | 12 | 12 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0009 | 0/0 | 4694 | 11 | 2 | 0 | 9 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0010 | 0/0 | 4694 | 5 | 0 | 0 | 5 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0011 | 0/0 | 4694 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0012 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0015 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0016 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0017 | 0/0 | 4694 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0018 | 0/0 | 4694 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0020 | 1/0 | 4694 | 1 | 0 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0021 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0025 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0026 | 0/0 | 4694 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0027 | 0/0 | 4694 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0029 | 0/0 | 4694 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0001t0030 | 0/0 | 4694 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0002t0006 | 0/0 | 4694 | 10 | 10 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0002t0008 | 0/0 | 4694 | 3 | 3 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0002t0009 | 0/0 | 4694 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0002t0023 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0001c0008t0012 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0002c0003t0004 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0002c0003t0006 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0002c0003t0014 | 0/0 | 4694 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0002c0003t0019 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0002c0003t0022 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0002c0003t0024 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0003c0006t0013 | 0/0 | 4694 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0003c0009t0028 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0004c0004t0004 | 0/0 | 4694 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0005c0005t0007 | 0/0 | 4694 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0006c0007t0007 | 0/0 | 4694 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0007c0010t0002 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| a0008c0011t0002 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4307): Show |
chr4 | 76153737 | 76218824 |
| a0009c0012t0001 | 0/0 | 4694 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | ACTCT others(4689): Show |
chr4 | 76153737 | 76218824 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0003 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0001 | 0/0 | 12 | 0 | 4 | 5 | 1 | 2 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0008 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0045 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0005g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0007g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0007g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0007g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0008g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0008g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0008g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0008g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0009g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0009g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0009g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0009g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0009g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0009g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0009g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0010g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0010g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0010g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0011g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0011g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0012g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0015g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0016g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0017g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0018g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0020g0193 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0021g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0025g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0026g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0027g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0029g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0001t0030g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0002t0006g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0002t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0002t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0002t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0002t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0002t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0002t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0002t0008g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0002t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0002t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0002t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0002t0023g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0001c0008t0012g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0002c0003t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0002c0003t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0002c0003t0014g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0002c0003t0014g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0002c0003t0019g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0002c0003t0022g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0002c0003t0024g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0003c0006t0013g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0003c0006t0013g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0003c0009t0028g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0004c0004t0004g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0005c0005t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0005c0005t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0005c0005t0007g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0006c0007t0007g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0007c0010t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0008c0011t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| a0009c0012t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0234 | EUR | GBR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | FIN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0044 | EUR | FIN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00323 | hp1 | a0001 | c0001 | t0017 | g0072 | EUR | FIN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0218 | EUR | FIN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00438 | hp2 | a0006 | c0007 | t0007 | g0035 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0279 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00621 | hp2 | a0006 | c0007 | t0007 | g0035 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0222 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00673 | hp2 | a0001 | c0001 | t0009 | g0195 | EAS | CHS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0039 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0238 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0040 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0040 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0043 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0215 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0180 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0113 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01175 | hp1 | a0001 | c0001 | t0029 | g0206 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0122 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0225 | AMR | PUR | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01257 | hp2 | a0001 | c0001 | t0030 | g0289 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0043 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0244 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0237 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0219 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0039 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0242 | EUR | IBS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0224 | EUR | IBS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01516 | hp2 | a0001 | c0001 | t0007 | g0036 | EUR | IBS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01517 | hp1 | a0001 | c0001 | t0007 | g0036 | EUR | IBS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01884 | hp2 | a0001 | c0002 | t0006 | g0166 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01891 | hp1 | a0003 | c0009 | t0028 | g0226 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0015 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0250 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0221 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0177 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02083 | hp1 | a0001 | c0001 | t0009 | g0006 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02129 | hp2 | a0001 | c0001 | t0027 | g0280 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02145 | hp1 | a0001 | c0002 | t0006 | g0005 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0247 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02280 | hp2 | a0002 | c0003 | t0004 | g0227 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02451 | hp1 | a0001 | c0002 | t0006 | g0005 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0063 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02572 | hp1 | a0001 | c0001 | t0016 | g0029 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0176 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02615 | hp2 | a0003 | c0006 | t0013 | g0169 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02630 | hp2 | a0001 | c0002 | t0006 | g0171 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0187 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0173 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0199 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0283 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0153 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02809 | hp2 | a0002 | c0003 | t0014 | g0228 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02818 | hp1 | a0002 | c0003 | t0019 | g0096 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02886 | hp1 | a0001 | c0002 | t0006 | g0170 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02896 | hp1 | a0001 | c0002 | t0008 | g0037 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02897 | hp2 | a0001 | c0002 | t0008 | g0037 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0015 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0185 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02970 | hp1 | a0001 | c0001 | t0011 | g0108 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0174 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02976 | hp2 | a0001 | c0001 | t0011 | g0109 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0216 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03041 | hp1 | a0002 | c0003 | t0014 | g0274 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03041 | hp2 | a0001 | c0002 | t0006 | g0165 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03098 | hp1 | a0001 | c0002 | t0006 | g0172 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03098 | hp2 | a0001 | c0001 | t0025 | g0230 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03130 | hp1 | a0002 | c0003 | t0006 | g0175 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0182 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03139 | hp2 | a0001 | c0002 | t0023 | g0167 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0192 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03209 | hp1 | a0001 | c0001 | t0015 | g0097 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0209 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0188 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0233 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03453 | hp2 | a0001 | c0008 | t0012 | g0183 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0189 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0178 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0081 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03516 | hp1 | a0001 | c0001 | t0021 | g0186 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0181 | AFR | ESN | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0184 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03540 | hp2 | a0002 | c0003 | t0024 | g0202 | AFR | GWD | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0114 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0285 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0214 | SAS | PJL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03831 | hp1 | a0001 | c0001 | t0007 | g0062 | SAS | BEB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0243 | SAS | BEB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0085 | SAS | BEB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0262 | SAS | STU | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0045 | SAS | STU | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | BEB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0069 | SAS | STU | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG04199 | hp2 | a0001 | c0001 | t0007 | g0091 | SAS | STU | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG04204 | hp1 | a0001 | c0001 | t0007 | g0061 | SAS | STU | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0217 | SAS | STU | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0022 | SAS | STU | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0191 | AFR | YRI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | YRI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | CHB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | CHB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0232 | AFR | YRI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18906 | hp2 | a0001 | c0002 | t0009 | g0163 | AFR | YRI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18939 | hp1 | a0004 | c0004 | t0004 | g0019 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18941 | hp1 | a0004 | c0004 | t0004 | g0019 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18948 | hp1 | a0001 | c0001 | t0009 | g0006 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18949 | hp1 | a0005 | c0005 | t0007 | g0150 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18949 | hp2 | a0001 | c0001 | t0018 | g0134 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18950 | hp2 | a0005 | c0005 | t0007 | g0151 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18962 | hp2 | a0001 | c0001 | t0009 | g0197 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18965 | hp1 | a0001 | c0001 | t0026 | g0252 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18966 | hp1 | a0001 | c0001 | t0009 | g0006 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18970 | hp1 | a0001 | c0001 | t0010 | g0014 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18974 | hp2 | a0001 | c0001 | t0009 | g0006 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18978 | hp1 | a0008 | c0011 | t0002 | g0264 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18979 | hp2 | a0005 | c0005 | t0007 | g0149 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18994 | hp2 | a0001 | c0001 | t0009 | g0196 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18995 | hp2 | a0001 | c0001 | t0009 | g0198 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA18999 | hp2 | a0001 | c0001 | t0010 | g0014 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19004 | hp2 | a0004 | c0004 | t0004 | g0019 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19010 | hp1 | a0001 | c0001 | t0010 | g0129 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0038 | AFR | LWK | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19043 | hp2 | a0001 | c0002 | t0006 | g0162 | AFR | LWK | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19064 | hp1 | a0001 | c0001 | t0009 | g0194 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19066 | hp2 | a0001 | c0001 | t0006 | g0201 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19078 | hp1 | a0001 | c0001 | t0010 | g0123 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19087 | hp2 | a0001 | c0001 | t0010 | g0014 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0015 | AFR | YRI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA19240 | hp2 | a0001 | c0002 | t0006 | g0005 | AFR | YRI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA20129 | hp1 | a0001 | c0001 | t0009 | g0038 | AFR | ASW | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA20129 | hp2 | a0001 | c0002 | t0006 | g0005 | AFR | ASW | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | TSI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0041 | EUR | TSI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0236 | EUR | TSI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA20805 | hp2 | a0009 | c0012 | t0001 | g0095 | EUR | TSI | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0044 | AMR | CLM | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG02559 | hp2 | a0001 | c0002 | t0009 | g0164 | AFR | ACB | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03471 | hp1 | a0007 | c0010 | t0002 | g0204 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG03471 | hp2 | a0001 | c0002 | t0008 | g0161 | AFR | MSL | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | USA | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0179 | AFR | USA | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | USA | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA20300 | hp2 | a0003 | c0006 | t0013 | g0168 | AFR | USA | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA21309 | hp1 | a0002 | c0003 | t0022 | g0200 | AFR | LWK | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0190 | AFR | LWK | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0220 | REF | REF | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0020 | g0193 | REF | REF | SCARB2_chr4_76153737_76218824 | SCARB2 | chr4 | 76153737 | 76218824 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76158737 | T | C | 1 | a0001 | 1 | HG02572.hp1 | splice_region_variant | LOW | c.*2976A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | chr4 | 76158737 | |||||||
| chr4:76163238 | C | T | 1 | a0004 | 3 | NA18939.hp1 NA18941.hp1 NA19004.hp2 |
missense_variant | MODERATE | c.1385G>A | p.Gly462Glu | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/12 | 1666/4694 | 1385/1437 | 462/478 | chr4 | 76163238 | |||
| chr4:76163311 | T | G | 1 | a0007 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1312A>C | p.Ile438Leu | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/12 | 1593/4694 | 1312/1437 | 438/478 | chr4 | 76163311 | |||
| chr4:76166279 | T | C | 1 | a0006 | 2 | HG00438.hp2 HG00621.hp2 |
missense_variant | MODERATE | c.1210A>G | p.Met404Val | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/12 | 1491/4694 | 1210/1437 | 404/478 | chr4 | 76166279 | |||
| chr4:76168404 | C | T | 1 | a0002 | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
missense_variant&splice_region_variant | MODERATE | c.1186G>A | p.Val396Ile | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/12 | 1467/4694 | 1186/1437 | 396/478 | chr4 | 76168404 | |||
| chr4:76172721 | TTGCCCAG others(4076): Show |
T | 1 | a0008 | 1 | NA18978.hp1 | exon_loss_variant | HIGH | c.613-276_994+1422de others(1): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/12 | chr4 | 76172721 | |||||||
| chr4:76179654 | T | C | 1 | a0009 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.475A>G | p.Met159Val | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/12 | 756/4694 | 475/1437 | 159/478 | chr4 | 76179654 | |||
| chr4:76179699 | T | A | 1 | a0005 | 3 | NA18949.hp1 NA18950.hp2 NA18979.hp2 |
missense_variant | MODERATE | c.430A>T | p.Ile144Leu | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/12 | 711/4694 | 430/1437 | 144/478 | chr4 | 76179699 | |||
| chr4:76181015 | C | T | 1 | a0003 | 3 | HG01891.hp1 HG02615.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.362G>A | p.Arg121Gln | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/12 | 643/4694 | 362/1437 | 121/478 | chr4 | 76181015 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76195736 | C | G | 1 | a0001c0008 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.246G>C | p.Arg82Arg | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/12 | 527/4694 | 246/1437 | 82/478 | chr4 | 76195736 | |||
| chr4:76213496 | C | G | 2 | a0001c0002 a0003c0006 |
18 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(15): Show |
synonymous_variant | LOW | c.48G>C | p.Leu16Leu | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/12 | 329/4694 | 48/1437 | 16/478 | chr4 | 76213496 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76158925 | T | G | 1 | a0001c0001t0021 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2788A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 2788 | chr4 | 76158925 | ||||||
| chr4:76158944 | G | A | 1 | a0001c0001t0011 | 2 | HG02970.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2769C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 2769 | chr4 | 76158944 | ||||||
| chr4:76159229 | T | C | 1 | a0001c0001t0029 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2484A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 2484 | chr4 | 76159229 | ||||||
| chr4:76159242 | G | A | 1 | a0001c0001t0027 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2471C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 2471 | chr4 | 76159242 | ||||||
| chr4:76159325 | G | A | 2 | a0003c0006t0013 a0003c0009t0028 |
3 | HG01891.hp1 HG02615.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2388C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 2388 | chr4 | 76159325 | ||||||
| chr4:76159504 | G | A | 4 | a0002c0003t0014 a0002c0003t0019 a0002c0003t0022 others(1): Show |
5 | HG02809.hp2 HG02818.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2209C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 2209 | chr4 | 76159504 | ||||||
| chr4:76159646 | C | T | 16 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(13): Show |
124 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*2067G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 2067 | chr4 | 76159646 | ||||||
| chr4:76159678 | T | C | 21 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(18): Show |
144 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*2035A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 2035 | chr4 | 76159678 | ||||||
| chr4:76159754 | A | G | 1 | a0001c0001t0015 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1959T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1959 | chr4 | 76159754 | ||||||
| chr4:76159854 | A | G | 1 | a0001c0001t0018 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1859T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1859 | chr4 | 76159854 | ||||||
| chr4:76159933 | T | A | 18 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(15): Show |
126 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*1780A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1780 | chr4 | 76159933 | ||||||
| chr4:76160575 | T | C | 1 | a0001c0001t0026 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1138A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1138 | chr4 | 76160575 | ||||||
| chr4:76160612 | G | A | 3 | a0001c0001t0009 a0001c0001t0010 a0001c0002t0009 |
18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1101C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1101 | chr4 | 76160612 | ||||||
| chr4:76160624 | T | A | 1 | a0001c0001t0017 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1089A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1089 | chr4 | 76160624 | ||||||
| chr4:76160661 | G | C | 16 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(13): Show |
124 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1052C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1052 | chr4 | 76160661 | ||||||
| chr4:76160683 | G | A | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(32): Show |
344 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(341): Show |
3_prime_UTR_variant | MODIFIER | c.*1030C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1030 | chr4 | 76160683 | ||||||
| chr4:76160684 | C | A | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(32): Show |
344 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(341): Show |
3_prime_UTR_variant | MODIFIER | c.*1029G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 1029 | chr4 | 76160684 | ||||||
| chr4:76160932 | A | G | 1 | a0001c0001t0025 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*781T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 781 | chr4 | 76160932 | ||||||
| chr4:76161120 | T | C | 2 | a0001c0001t0029 a0001c0002t0023 |
2 | HG01175.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*593A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 593 | chr4 | 76161120 | ||||||
| chr4:76161250 | G | A | 3 | a0001c0001t0009 a0001c0001t0010 a0001c0002t0009 |
18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*463C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 463 | chr4 | 76161250 | ||||||
| chr4:76161596 | C | T | 3 | a0001c0001t0009 a0001c0001t0010 a0001c0002t0009 |
18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*117G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 117 | chr4 | 76161596 | ||||||
| chr4:76161646 | G | C | 3 | a0001c0001t0009 a0001c0001t0010 a0001c0002t0009 |
18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*67C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 12/12 | 67 | chr4 | 76161646 | ||||||
| chr4:76213554 | G | A | 1 | a0001c0001t0030 | 1 | HG01257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-11C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/12 | 11 | chr4 | 76213554 | ||||||
| chr4:76213633 | C | T | 13 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(10): Show |
183 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
5_prime_UTR_variant | MODIFIER | c.-90G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/12 | 90 | chr4 | 76213633 | ||||||
| chr4:76213675 | G | C | 1 | a0002c0003t0024 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-132C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/12 | 132 | chr4 | 76213675 | ||||||
| chr4:76213717 | G | A | 14 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(11): Show |
143 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
5_prime_UTR_variant | MODIFIER | c.-174C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/12 | 174 | chr4 | 76213717 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76161794 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1399-43C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76161794 | |||||||
| chr4:76161917 | TCAG | T | 160 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(157): Show |
222 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.1399-169_1399-167d others(5): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76161917 | |||||||
| chr4:76161929 | A | T | 58 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(55): Show |
80 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1399-178T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76161929 | |||||||
| chr4:76161956 | C | T | 1 | a0001c0001t0005g0233 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1399-205G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76161956 | |||||||
| chr4:76161957 | T | C | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1399-206A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76161957 | |||||||
| chr4:76161971 | C | A | 12 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(9): Show |
18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.1399-220G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76161971 | |||||||
| chr4:76162031 | G | A | 2 | a0001c0001t0005g0039 a0001c0001t0007g0036 |
4 | HG00738.hp1 HG01361.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399-280C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162031 | |||||||
| chr4:76162161 | C | T | 1 | a0001c0001t0005g0043 | 2 | HG01081.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1399-410G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162161 | |||||||
| chr4:76162197 | G | A | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1399-446C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162197 | |||||||
| chr4:76162226 | G | A | 33 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0099 others(30): Show |
37 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1399-475C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162226 | |||||||
| chr4:76162416 | T | TA | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1399-666dupT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162416 | |||||||
| chr4:76162481 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1399-730G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162481 | |||||||
| chr4:76162601 | T | C | 90 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(87): Show |
124 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1398+624A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162601 | |||||||
| chr4:76162648 | C | T | 2 | a0001c0001t0003g0056 a0001c0001t0004g0018 |
4 | HG00558.hp1 HG02071.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398+577G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162648 | |||||||
| chr4:76162846 | G | A | 1 | a0001c0001t0015g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1398+379C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 11/11 | chr4 | 76162846 | |||||||
| chr4:76163436 | T | C | 55 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(52): Show |
77 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1240-53A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76163436 | |||||||
| chr4:76163498 | C | A | 1 | a0001c0001t0003g0087 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1240-115G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76163498 | |||||||
| chr4:76163714 | C | T | 8 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0004g0042 others(5): Show |
9 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1240-331G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76163714 | |||||||
| chr4:76163720 | G | A | 8 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0004g0042 others(5): Show |
9 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1240-337C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76163720 | |||||||
| chr4:76163819 | G | A | 1 | a0001c0001t0002g0267 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1240-436C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76163819 | |||||||
| chr4:76164013 | A | G | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1240-630T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164013 | |||||||
| chr4:76164221 | C | T | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1240-838G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164221 | |||||||
| chr4:76164250 | A | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(255): Show |
345 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.1240-867T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164250 | |||||||
| chr4:76164284 | G | C | 1 | a0001c0001t0005g0222 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1240-901C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164284 | |||||||
| chr4:76164480 | C | G | 90 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(87): Show |
124 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1240-1097G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164480 | |||||||
| chr4:76164498 | G | A | 75 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(72): Show |
108 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1240-1115C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164498 | |||||||
| chr4:76164504 | G | A | 33 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0099 others(30): Show |
37 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1240-1121C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164504 | |||||||
| chr4:76164550 | G | C | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1240-1167C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164550 | |||||||
| chr4:76164576 | C | A | 162 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(159): Show |
224 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.1240-1193G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164576 | |||||||
| chr4:76164637 | GA | G | 91 | a0001c0001t0002g0235 a0001c0001t0003g0001 a0001c0001t0003g0007 others(88): Show |
125 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.1240-1255delT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164637 | |||||||
| chr4:76164691 | C | A | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1240-1308G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164691 | |||||||
| chr4:76164722 | G | C | 1 | a0001c0001t0008g0191 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1240-1339C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164722 | |||||||
| chr4:76164767 | G | C | 92 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(89): Show |
126 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.1240-1384C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164767 | |||||||
| chr4:76164791 | C | CA | 94 | a0001c0001t0001g0090 a0001c0001t0002g0231 a0001c0001t0002g0245 others(91): Show |
128 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.1240-1409dupT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164791 | |||||||
| chr4:76164857 | A | G | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1239+1393T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76164857 | |||||||
| chr4:76165253 | G | A | 1 | a0001c0001t0002g0284 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1239+997C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165253 | |||||||
| chr4:76165274 | T | C | 1 | a0001c0001t0015g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1239+976A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165274 | |||||||
| chr4:76165281 | A | C | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1239+969T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165281 | |||||||
| chr4:76165298 | T | C | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1239+952A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165298 | |||||||
| chr4:76165322 | T | A | 1 | a0001c0001t0001g0058 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1239+928A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165322 | |||||||
| chr4:76165433 | T | G | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1239+817A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165433 | |||||||
| chr4:76165495 | T | C | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1239+755A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165495 | |||||||
| chr4:76165688 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1239+562C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165688 | |||||||
| chr4:76165763 | G | GT | 70 | a0001c0001t0001g0030 a0001c0001t0001g0143 a0001c0001t0001g0146 others(67): Show |
100 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.1239+486dupA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165763 | |||||||
| chr4:76165763 | G | GTT | 7 | a0001c0001t0003g0077 a0001c0001t0003g0081 a0001c0001t0003g0082 others(4): Show |
7 | HG00673.hp1 HG01934.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+485_1239+486d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165763 | |||||||
| chr4:76165858 | A | C | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1239+392T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165858 | |||||||
| chr4:76165859 | T | C | 3 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0003c0006t0013g0168 |
3 | HG02055.hp2 HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1239+391A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76165859 | |||||||
| chr4:76166025 | A | G | 1 | a0001c0001t0006g0187 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1239+225T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76166025 | |||||||
| chr4:76166113 | A | G | 1 | a0001c0001t0003g0026 | 2 | NA18986.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1239+137T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76166113 | |||||||
| chr4:76166236 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1239+14C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 10/11 | chr4 | 76166236 | |||||||
| chr4:76166551 | G | T | 106 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(103): Show |
139 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.1188-250C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76166551 | |||||||
| chr4:76166560 | G | C | 1 | a0001c0001t0008g0015 | 3 | HG01891.hp2 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1188-259C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76166560 | |||||||
| chr4:76166653 | GAGCCAAC others(5): Show |
G | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1188-364_1188-353d others(14): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76166653 | |||||||
| chr4:76166834 | T | C | 2 | a0001c0001t0002g0231 a0001c0001t0025g0230 |
2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1188-533A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76166834 | |||||||
| chr4:76166844 | C | G | 37 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0004g0042 others(34): Show |
42 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.1188-543G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76166844 | |||||||
| chr4:76166913 | C | T | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1188-612G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76166913 | |||||||
| chr4:76167014 | A | G | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1188-713T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167014 | |||||||
| chr4:76167089 | T | C | 1 | a0001c0001t0002g0249 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1188-788A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167089 | |||||||
| chr4:76167252 | C | T | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1188-951G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167252 | |||||||
| chr4:76167409 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1187+994A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167409 | |||||||
| chr4:76167498 | C | T | 38 | a0001c0001t0001g0124 a0001c0001t0003g0107 a0001c0001t0003g0110 others(35): Show |
43 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.1187+905G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167498 | |||||||
| chr4:76167610 | C | T | 9 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187+793G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167610 | |||||||
| chr4:76167672 | T | TC | 24 | a0001c0001t0001g0034 a0001c0001t0001g0094 a0001c0001t0001g0099 others(21): Show |
27 | HG00438.hp2 HG00621.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1187+730dupG | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167672 | |||||||
| chr4:76167672 | TC | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(137): Show |
212 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1187+730delG | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167672 | |||||||
| chr4:76167681 | C | G | 21 | a0001c0001t0004g0054 a0001c0001t0004g0209 a0001c0001t0004g0225 others(18): Show |
25 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1187+722G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167681 | |||||||
| chr4:76167682 | C | G | 7 | a0001c0001t0002g0251 a0001c0001t0003g0107 a0001c0001t0003g0110 others(4): Show |
8 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1187+721G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167682 | |||||||
| chr4:76167682 | CG | C | 22 | a0001c0001t0004g0054 a0001c0001t0004g0209 a0001c0001t0004g0225 others(19): Show |
26 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1187+720delC | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167682 | |||||||
| chr4:76167682 | CGCT | C | 7 | a0001c0002t0006g0165 a0002c0003t0004g0227 a0002c0003t0006g0175 others(4): Show |
7 | HG02280.hp2 HG02818.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1187+718_1187+720d others(5): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167682 | |||||||
| chr4:76167683 | G | C | 9 | a0001c0001t0002g0251 a0001c0001t0003g0107 a0001c0001t0003g0110 others(6): Show |
10 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1187+720C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167683 | |||||||
| chr4:76167684 | C | T | 28 | a0001c0001t0002g0251 a0001c0001t0003g0107 a0001c0001t0003g0110 others(25): Show |
33 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.1187+719G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167684 | |||||||
| chr4:76167685 | T | C | 1 | a0002c0003t0014g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1187+718A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167685 | |||||||
| chr4:76167705 | C | T | 9 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187+698G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167705 | |||||||
| chr4:76167706 | A | T | 2 | a0001c0001t0005g0219 a0001c0001t0007g0063 |
2 | HG01358.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1187+697T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167706 | |||||||
| chr4:76167767 | C | T | 9 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187+636G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167767 | |||||||
| chr4:76167768 | G | A | 12 | a0001c0001t0002g0282 a0001c0001t0004g0209 a0001c0001t0004g0229 others(9): Show |
15 | HG00408.hp2 HG01109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1187+635C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167768 | |||||||
| chr4:76167792 | T | C | 9 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187+611A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167792 | |||||||
| chr4:76167930 | T | C | 4 | a0001c0001t0003g0110 a0001c0001t0004g0042 a0001c0002t0006g0165 others(1): Show |
5 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1187+473A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167930 | |||||||
| chr4:76167971 | A | G | 3 | a0001c0001t0003g0079 a0001c0001t0003g0080 a0001c0001t0004g0275 |
3 | HG00423.hp2 HG02040.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1187+432T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76167971 | |||||||
| chr4:76168158 | G | C | 84 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(81): Show |
118 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.1187+245C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76168158 | |||||||
| chr4:76168322 | G | C | 9 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187+81C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76168322 | |||||||
| chr4:76168346 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1187+57G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76168346 | |||||||
| chr4:76168351 | C | T | 3 | a0001c0001t0003g0022 a0001c0001t0003g0076 a0001c0001t0003g0081 |
4 | HG03490.hp1 HG03491.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1187+52G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 9/11 | chr4 | 76168351 | |||||||
| chr4:76168775 | C | G | 82 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(79): Show |
116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.1114-299G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76168775 | |||||||
| chr4:76168927 | G | A | 9 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-451C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76168927 | |||||||
| chr4:76168934 | G | A | 9 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-458C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76168934 | |||||||
| chr4:76169012 | C | T | 9 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-536G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169012 | |||||||
| chr4:76169212 | T | C | 91 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(88): Show |
125 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.1113+655A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169212 | |||||||
| chr4:76169287 | G | A | 9 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113+580C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169287 | |||||||
| chr4:76169296 | T | C | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1113+571A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169296 | |||||||
| chr4:76169317 | T | TAC | 6 | a0001c0001t0001g0067 a0001c0001t0001g0093 a0001c0001t0002g0259 others(3): Show |
6 | HG01257.hp2 HG03831.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+548_1113+549d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169317 | |||||||
| chr4:76169317 | T | TACAC | 57 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(54): Show |
78 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1113+546_1113+549d others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169317 | |||||||
| chr4:76169325 | C | G | 1 | a0001c0001t0004g0243 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1113+542G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169325 | |||||||
| chr4:76169335 | C | T | 68 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(65): Show |
96 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1113+532G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169335 | |||||||
| chr4:76169341 | C | CACACACA | 8 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(5): Show |
8 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+525_1113+526i others(9): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169341 | |||||||
| chr4:76169341 | C | CACACACA others(11): Show |
1 | a0001c0001t0006g0187 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1113+525_1113+526i others(20): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169341 | |||||||
| chr4:76169341 | C | CACACACA others(9): Show |
24 | a0001c0001t0003g0007 a0001c0001t0003g0056 a0001c0001t0003g0057 others(21): Show |
32 | HG00558.hp1 HG00673.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1113+525_1113+526i others(18): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169341 | |||||||
| chr4:76169341 | C | CACACACA others(7): Show |
44 | a0001c0001t0003g0001 a0001c0001t0003g0008 a0001c0001t0003g0011 others(41): Show |
66 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1113+525_1113+526i others(16): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169341 | |||||||
| chr4:76169341 | C | CACACACA others(5): Show |
5 | a0001c0001t0003g0009 a0001c0001t0003g0025 a0001c0001t0003g0027 others(2): Show |
9 | HG01099.hp2 HG01243.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1113+525_1113+526i others(14): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169341 | |||||||
| chr4:76169341 | C | CACACACA others(3): Show |
7 | a0001c0001t0003g0156 a0001c0001t0004g0276 a0001c0001t0004g0278 others(4): Show |
7 | HG00558.hp2 HG02129.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+525_1113+526i others(12): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169341 | |||||||
| chr4:76169342 | G | A | 9 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113+525C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169342 | |||||||
| chr4:76169476 | T | G | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1113+391A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169476 | |||||||
| chr4:76169692 | T | C | 1 | a0001c0001t0002g0213 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1113+175A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169692 | |||||||
| chr4:76169853 | A | T | 82 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(79): Show |
116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.1113+14T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 8/11 | chr4 | 76169853 | |||||||
| chr4:76170033 | AAGCTG | A | 91 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(88): Show |
125 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.995-53_995-49delCA others(3): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170033 | |||||||
| chr4:76170096 | A | G | 1 | a0001c0001t0002g0271 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.995-111T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170096 | |||||||
| chr4:76170437 | G | A | 91 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(88): Show |
125 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.995-452C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170437 | |||||||
| chr4:76170440 | G | A | 56 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(53): Show |
78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.995-455C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170440 | |||||||
| chr4:76170463 | C | G | 1 | a0001c0001t0001g0031 | 2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.995-478G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170463 | |||||||
| chr4:76170508 | C | T | 82 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(79): Show |
116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.995-523G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170508 | |||||||
| chr4:76170528 | A | T | 1 | a0001c0008t0012g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.995-543T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170528 | |||||||
| chr4:76170529 | T | A | 2 | a0001c0001t0029g0206 a0001c0002t0023g0167 |
2 | HG01175.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.995-544A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170529 | |||||||
| chr4:76170533 | T | G | 6 | a0001c0001t0001g0029 a0001c0001t0001g0106 a0001c0001t0002g0203 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.995-548A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170533 | |||||||
| chr4:76170540 | T | TTTTTG | 3 | a0001c0001t0021g0186 a0001c0001t0029g0206 a0001c0002t0023g0167 |
3 | HG01175.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.995-560_995-556dup others(5): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170540 | |||||||
| chr4:76170671 | C | T | 19 | a0001c0001t0004g0054 a0001c0001t0004g0209 a0001c0001t0004g0229 others(16): Show |
23 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.995-686G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170671 | |||||||
| chr4:76170714 | T | C | 82 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(79): Show |
116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.995-729A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170714 | |||||||
| chr4:76170845 | G | A | 9 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.995-860C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170845 | |||||||
| chr4:76170945 | A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0259 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.995-961_995-960ins others(13): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170945 | |||||||
| chr4:76170945 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.995-961_995-960ins others(17): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170945 | |||||||
| chr4:76170945 | AAT | A | 62 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0099 others(59): Show |
72 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.995-962_995-961del others(2): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170945 | |||||||
| chr4:76170945 | AATAT | A | 2 | a0001c0001t0001g0105 a0001c0001t0002g0049 |
3 | HG03195.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.995-964_995-961del others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170945 | |||||||
| chr4:76170945 | AATATAT | A | 60 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0030 others(57): Show |
81 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.995-966_995-961del others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170945 | |||||||
| chr4:76170945 | AATATATA others(1): Show |
A | 101 | a0001c0001t0001g0029 a0001c0001t0001g0106 a0001c0001t0002g0203 others(98): Show |
141 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.995-968_995-961del others(8): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170945 | |||||||
| chr4:76170971 | T | A | 6 | a0001c0001t0001g0139 a0001c0001t0002g0259 a0001c0001t0006g0185 others(3): Show |
6 | HG01175.hp1 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.995-986A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170971 | |||||||
| chr4:76170971 | T | TATATATA others(3): Show |
30 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0020 others(27): Show |
43 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.995-987_995-986ins others(10): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170971 | |||||||
| chr4:76170971 | T | TATATATA others(5): Show |
10 | a0001c0001t0001g0013 a0001c0001t0001g0066 a0001c0001t0001g0117 others(7): Show |
12 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.995-987_995-986ins others(12): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170971 | |||||||
| chr4:76170971 | T | TATATATA others(7): Show |
2 | a0001c0001t0001g0065 a0001c0001t0001g0144 |
2 | NA19064.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.995-987_995-986ins others(14): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170971 | |||||||
| chr4:76170971 | T | TATATATA others(9): Show |
13 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
19 | HG01168.hp2 HG01169.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.995-987_995-986ins others(16): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170971 | |||||||
| chr4:76170971 | T | TATATATA others(11): Show |
2 | a0001c0001t0001g0112 a0001c0001t0001g0132 |
2 | HG00597.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.995-987_995-986ins others(18): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170971 | |||||||
| chr4:76170971 | T | TATATATA others(17): Show |
1 | a0001c0001t0001g0152 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.995-987_995-986ins others(24): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76170971 | |||||||
| chr4:76171268 | C | G | 7 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0014g0228 others(4): Show |
7 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.995-1283G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171268 | |||||||
| chr4:76171323 | C | A | 82 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(79): Show |
116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.995-1338G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171323 | |||||||
| chr4:76171345 | C | T | 3 | a0003c0006t0013g0168 a0003c0006t0013g0169 a0003c0009t0028g0226 |
3 | HG01891.hp1 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.995-1360G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171345 | |||||||
| chr4:76171519 | A | T | 2 | a0001c0001t0003g0008 a0004c0004t0004g0019 |
6 | HG04184.hp1 NA18939.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.995-1534T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171519 | |||||||
| chr4:76171549 | G | A | 1 | a0001c0001t0007g0122 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.995-1564C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171549 | |||||||
| chr4:76171549 | GT | G | 9 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.995-1565delA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171549 | |||||||
| chr4:76171703 | CA | C | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.995-1719delT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171703 | |||||||
| chr4:76171706 | C | A | 82 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(79): Show |
116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.995-1721G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171706 | |||||||
| chr4:76171755 | TG | T | 82 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(79): Show |
116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.995-1771delC | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171755 | |||||||
| chr4:76171863 | T | C | 1 | a0001c0001t0008g0174 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.995-1878A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171863 | |||||||
| chr4:76171967 | AGT | A | 82 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(79): Show |
116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.995-1984_995-1983d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171967 | |||||||
| chr4:76171975 | T | G | 9 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.995-1990A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171975 | |||||||
| chr4:76171985 | C | T | 9 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.995-2000G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76171985 | |||||||
| chr4:76172004 | C | CTATA | 9 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.995-2023_995-2020d others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172004 | |||||||
| chr4:76172200 | G | A | 1 | a0001c0001t0002g0282 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.994+1944C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172200 | |||||||
| chr4:76172200 | GTA | G | 12 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(9): Show |
18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.994+1942_994+1943d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172200 | |||||||
| chr4:76172202 | A | G | 1 | a0001c0001t0002g0047 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.994+1942T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172202 | |||||||
| chr4:76172204 | ATATATAT others(1): Show |
A | 9 | a0001c0001t0012g0177 a0001c0008t0012g0183 a0002c0003t0004g0227 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.994+1932_994+1939d others(10): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172204 | |||||||
| chr4:76172209 | T | C | 82 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(79): Show |
116 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.994+1935A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172209 | |||||||
| chr4:76172679 | CT | C | 77 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(74): Show |
105 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.994+1464delA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172679 | |||||||
| chr4:76172679 | CTT | C | 83 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(80): Show |
117 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.994+1463_994+1464d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172679 | |||||||
| chr4:76172752 | C | T | 1 | a0001c0001t0001g0012 | 2 | NA18964.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.994+1392G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172752 | |||||||
| chr4:76172779 | A | G | 2 | a0001c0001t0029g0206 a0001c0002t0023g0167 |
2 | HG01175.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.994+1365T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172779 | |||||||
| chr4:76172799 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.994+1345C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172799 | |||||||
| chr4:76172905 | A | G | 56 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(53): Show |
78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.994+1239T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76172905 | |||||||
| chr4:76173053 | CA | C | 2 | a0001c0001t0003g0025 a0001c0001t0004g0214 |
3 | HG01099.hp2 HG02109.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.994+1090delT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173053 | |||||||
| chr4:76173220 | C | G | 1 | a0001c0001t0005g0040 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.994+924G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173220 | |||||||
| chr4:76173328 | CT | C | 21 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(18): Show |
27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.994+815delA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173328 | |||||||
| chr4:76173328 | CTT | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(132): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.994+814_994+815del others(2): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173328 | |||||||
| chr4:76173328 | CTTT | C | 74 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(71): Show |
106 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.994+813_994+815del others(3): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173328 | |||||||
| chr4:76173329 | T | G | 1 | a0001c0001t0008g0188 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.994+815A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173329 | |||||||
| chr4:76173388 | C | T | 76 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(73): Show |
104 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.994+756G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173388 | |||||||
| chr4:76173425 | G | A | 1 | a0001c0001t0003g0074 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.994+719C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173425 | |||||||
| chr4:76173580 | C | T | 1 | a0001c0001t0008g0015 | 3 | HG01891.hp2 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.994+564G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173580 | |||||||
| chr4:76173627 | C | T | 21 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(18): Show |
27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.994+517G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173627 | |||||||
| chr4:76173678 | T | G | 138 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(135): Show |
194 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.994+466A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173678 | |||||||
| chr4:76173686 | C | T | 1 | a0001c0001t0002g0050 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.994+458G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173686 | |||||||
| chr4:76173820 | T | G | 1 | a0001c0001t0003g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.994+324A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173820 | |||||||
| chr4:76173864 | T | C | 2 | a0001c0001t0005g0215 a0001c0001t0005g0218 |
2 | HG00323.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.994+280A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173864 | |||||||
| chr4:76173882 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.994+262A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173882 | |||||||
| chr4:76173895 | A | G | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.994+249T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173895 | |||||||
| chr4:76173950 | T | C | 1 | a0001c0001t0004g0243 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.994+194A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173950 | |||||||
| chr4:76173990 | A | G | 56 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(53): Show |
78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.994+154T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76173990 | |||||||
| chr4:76174062 | C | T | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.994+82G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76174062 | |||||||
| chr4:76174096 | C | G | 5 | a0002c0003t0014g0228 a0002c0003t0014g0274 a0002c0003t0019g0096 others(2): Show |
5 | HG02809.hp2 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.994+48G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76174096 | |||||||
| chr4:76174118 | A | G | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.994+26T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 7/11 | chr4 | 76174118 | |||||||
| chr4:76174421 | C | T | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.825-108G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174421 | |||||||
| chr4:76174436 | G | A | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.825-123C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174436 | |||||||
| chr4:76174504 | G | A | 2 | a0001c0001t0006g0178 a0001c0001t0006g0190 |
2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.825-191C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174504 | |||||||
| chr4:76174629 | T | A | 1 | a0001c0001t0002g0285 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.825-316A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174629 | |||||||
| chr4:76174637 | T | C | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.825-324A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174637 | |||||||
| chr4:76174787 | C | T | 13 | a0001c0001t0003g0001 a0001c0001t0003g0023 a0001c0001t0003g0060 others(10): Show |
14 | HG00597.hp1 HG03834.hp1 NA18942.hp1 others(11): Show |
intron_variant | MODIFIER | c.825-474G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174787 | |||||||
| chr4:76174803 | C | A | 7 | a0001c0001t0004g0209 a0001c0001t0004g0229 a0001c0001t0004g0232 others(4): Show |
9 | HG01109.hp2 HG02451.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.825-490G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174803 | |||||||
| chr4:76174870 | A | T | 56 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(53): Show |
78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.825-557T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174870 | |||||||
| chr4:76174965 | G | A | 33 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0099 others(30): Show |
37 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.825-652C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76174965 | |||||||
| chr4:76175004 | C | T | 1 | a0001c0001t0001g0002 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.825-691G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175004 | |||||||
| chr4:76175067 | A | G | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.824+724T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175067 | |||||||
| chr4:76175073 | G | GT | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.824+717dupA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175073 | |||||||
| chr4:76175366 | A | G | 92 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(89): Show |
126 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.824+425T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175366 | |||||||
| chr4:76175453 | G | T | 145 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(142): Show |
201 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.824+338C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175453 | |||||||
| chr4:76175533 | G | A | 6 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0004g0042 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.824+258C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175533 | |||||||
| chr4:76175576 | C | A | 1 | a0001c0001t0021g0186 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.824+215G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175576 | |||||||
| chr4:76175578 | A | G | 1 | a0001c0001t0012g0177 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.824+213T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175578 | |||||||
| chr4:76175624 | T | C | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.824+167A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175624 | |||||||
| chr4:76175690 | C | T | 56 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(53): Show |
78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.824+101G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 6/11 | chr4 | 76175690 | |||||||
| chr4:76175984 | T | C | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.705-74A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76175984 | |||||||
| chr4:76176036 | C | T | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.705-126G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176036 | |||||||
| chr4:76176093 | C | A | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.705-183G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176093 | |||||||
| chr4:76176132 | G | A | 1 | a0005c0005t0007g0149 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.705-222C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176132 | |||||||
| chr4:76176134 | G | A | 1 | a0005c0005t0007g0149 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.705-224C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176134 | |||||||
| chr4:76176136 | T | C | 1 | a0005c0005t0007g0149 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.705-226A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176136 | |||||||
| chr4:76176137 | T | A | 1 | a0005c0005t0007g0149 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.705-227A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176137 | |||||||
| chr4:76176138 | T | C | 1 | a0005c0005t0007g0149 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.705-228A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176138 | |||||||
| chr4:76176139 | G | A | 1 | a0005c0005t0007g0149 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.705-229C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176139 | |||||||
| chr4:76176183 | C | T | 56 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(53): Show |
78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.704+254G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176183 | |||||||
| chr4:76176220 | A | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(58): Show |
82 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.704+217T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176220 | |||||||
| chr4:76176421 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.704+16T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 5/11 | chr4 | 76176421 | |||||||
| chr4:76176605 | T | C | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.613-77A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76176605 | |||||||
| chr4:76176798 | G | A | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.613-270C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76176798 | |||||||
| chr4:76176987 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.613-459A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76176987 | |||||||
| chr4:76177021 | CT | C | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.613-494delA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76177021 | |||||||
| chr4:76177278 | T | A | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.613-750A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76177278 | |||||||
| chr4:76177445 | A | G | 1 | a0001c0001t0002g0263 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.613-917T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76177445 | |||||||
| chr4:76177676 | C | T | 1 | a0001c0001t0002g0262 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.613-1148G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76177676 | |||||||
| chr4:76177713 | G | A | 75 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(72): Show |
108 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.613-1185C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76177713 | |||||||
| chr4:76177785 | T | C | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.613-1257A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76177785 | |||||||
| chr4:76177832 | C | T | 1 | a0001c0001t0006g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.613-1304G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76177832 | |||||||
| chr4:76178019 | G | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.613-1491C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178019 | |||||||
| chr4:76178077 | C | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.612+1440G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178077 | |||||||
| chr4:76178175 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.612+1342A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178175 | |||||||
| chr4:76178231 | A | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(58): Show |
82 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.612+1286T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178231 | |||||||
| chr4:76178493 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.612+1024A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178493 | |||||||
| chr4:76178508 | A | C | 160 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(157): Show |
222 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.612+1009T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178508 | |||||||
| chr4:76178520 | C | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.612+997G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178520 | |||||||
| chr4:76178591 | C | A | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.612+926G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178591 | |||||||
| chr4:76178602 | A | G | 2 | a0001c0002t0009g0163 a0001c0002t0009g0164 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.612+915T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178602 | |||||||
| chr4:76178638 | A | G | 1 | a0001c0001t0006g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.612+879T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178638 | |||||||
| chr4:76178666 | A | C | 2 | a0001c0001t0005g0039 a0001c0001t0007g0036 |
4 | HG00738.hp1 HG01361.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.612+851T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178666 | |||||||
| chr4:76178746 | A | G | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.612+771T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178746 | |||||||
| chr4:76178966 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.612+551A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76178966 | |||||||
| chr4:76179028 | G | GGTTTTT | 4 | a0001c0001t0001g0010 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
6 | HG01106.hp1 HG01123.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.612+483_612+488dup others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179028 | |||||||
| chr4:76179028 | GGTTTTT | G | 13 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(10): Show |
19 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.612+483_612+488del others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179028 | |||||||
| chr4:76179047 | GTTTTTGT others(1): Show |
G | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.612+462_612+469del others(8): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179047 | |||||||
| chr4:76179047 | GTTTTTGT others(4): Show |
G | 1 | a0001c0001t0004g0237 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.612+459_612+469del others(11): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179047 | |||||||
| chr4:76179053 | GTTTTT | G | 90 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(87): Show |
124 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.612+459_612+463del others(5): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179053 | |||||||
| chr4:76179054 | T | G | 1 | a0001c0001t0001g0002 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.612+463A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179054 | |||||||
| chr4:76179059 | T | G | 4 | a0001c0001t0001g0111 a0001c0001t0002g0016 a0001c0001t0002g0041 others(1): Show |
7 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.612+458A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179059 | |||||||
| chr4:76179119 | T | C | 56 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(53): Show |
78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.612+398A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179119 | |||||||
| chr4:76179290 | A | G | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.612+227T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179290 | |||||||
| chr4:76179440 | CAA | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0139 a0001c0001t0001g0152 others(1): Show |
6 | NA18964.hp2 NA18971.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.612+75_612+76delTT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 4/11 | chr4 | 76179440 | |||||||
| chr4:76179748 | A | G | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.424-43T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76179748 | |||||||
| chr4:76179915 | T | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(58): Show |
82 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.424-210A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76179915 | |||||||
| chr4:76180062 | G | A | 86 | a0001c0001t0001g0030 a0001c0001t0003g0001 a0001c0001t0003g0007 others(83): Show |
121 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.424-357C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180062 | |||||||
| chr4:76180084 | T | C | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.424-379A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180084 | |||||||
| chr4:76180225 | A | C | 71 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(68): Show |
99 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.424-520T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180225 | |||||||
| chr4:76180484 | C | G | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.423+470G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180484 | |||||||
| chr4:76180512 | T | G | 1 | a0001c0001t0015g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.423+442A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180512 | |||||||
| chr4:76180595 | T | C | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.423+359A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180595 | |||||||
| chr4:76180705 | C | T | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.423+249G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180705 | |||||||
| chr4:76180773 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.423+181T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180773 | |||||||
| chr4:76180819 | G | A | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.423+135C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180819 | |||||||
| chr4:76180853 | C | G | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.423+101G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 3/11 | chr4 | 76180853 | |||||||
| chr4:76181270 | G | A | 12 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(9): Show |
18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-169C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76181270 | |||||||
| chr4:76181321 | C | A | 1 | a0001c0001t0006g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.276-220G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76181321 | |||||||
| chr4:76181373 | G | A | 1 | a0001c0001t0004g0225 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.276-272C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76181373 | |||||||
| chr4:76181386 | G | A | 1 | a0001c0001t0003g0024 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.276-285C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76181386 | |||||||
| chr4:76182001 | T | C | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.276-900A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182001 | |||||||
| chr4:76182043 | C | CAAAATTT others(6): Show |
80 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(77): Show |
113 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.276-955_276-943dup others(13): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182043 | |||||||
| chr4:76182311 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.276-1210A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182311 | |||||||
| chr4:76182376 | T | C | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-1275A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182376 | |||||||
| chr4:76182469 | T | C | 1 | a0001c0001t0015g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.276-1368A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182469 | |||||||
| chr4:76182510 | G | A | 1 | a0001c0001t0006g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.276-1409C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182510 | |||||||
| chr4:76182536 | G | C | 1 | a0002c0003t0024g0202 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.276-1435C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182536 | |||||||
| chr4:76182655 | G | A | 56 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(53): Show |
85 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.276-1554C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182655 | |||||||
| chr4:76182705 | T | C | 1 | a0001c0001t0002g0272 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.276-1604A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182705 | |||||||
| chr4:76182776 | G | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-1675C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182776 | |||||||
| chr4:76182935 | C | CAT | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-1836_276-1835d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182935 | |||||||
| chr4:76182999 | T | C | 160 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(157): Show |
222 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.276-1898A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76182999 | |||||||
| chr4:76183124 | T | C | 54 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(51): Show |
76 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.276-2023A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76183124 | |||||||
| chr4:76183356 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.276-2255C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76183356 | |||||||
| chr4:76183376 | T | C | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-2275A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76183376 | |||||||
| chr4:76183571 | T | TA | 4 | a0001c0001t0001g0073 a0001c0001t0001g0101 a0001c0001t0002g0246 others(1): Show |
4 | HG01361.hp1 HG01496.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-2471dupT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76183571 | |||||||
| chr4:76183731 | G | C | 2 | a0001c0001t0003g0056 a0001c0001t0004g0018 |
4 | HG00558.hp1 HG02071.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-2630C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76183731 | |||||||
| chr4:76183776 | T | A | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.276-2675A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76183776 | |||||||
| chr4:76183790 | C | T | 1 | a0001c0001t0015g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.276-2689G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76183790 | |||||||
| chr4:76184021 | G | A | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-2920C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184021 | |||||||
| chr4:76184163 | C | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3062G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184163 | |||||||
| chr4:76184251 | A | C | 12 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(9): Show |
18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-3150T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184251 | |||||||
| chr4:76184269 | C | T | 56 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(53): Show |
78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.276-3168G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184269 | |||||||
| chr4:76184463 | C | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3362G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184463 | |||||||
| chr4:76184472 | C | T | 1 | a0002c0003t0024g0202 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.276-3371G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184472 | |||||||
| chr4:76184491 | C | T | 1 | a0001c0001t0009g0194 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.276-3390G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184491 | |||||||
| chr4:76184547 | T | G | 160 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(157): Show |
222 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.276-3446A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184547 | |||||||
| chr4:76184605 | A | C | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.276-3504T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184605 | |||||||
| chr4:76184613 | A | T | 1 | a0001c0001t0015g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.276-3512T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184613 | |||||||
| chr4:76184642 | C | T | 1 | a0001c0001t0015g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.276-3541G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184642 | |||||||
| chr4:76184758 | A | G | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3657T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184758 | |||||||
| chr4:76184785 | CA | C | 106 | a0001c0001t0001g0094 a0001c0001t0001g0140 a0001c0001t0003g0001 others(103): Show |
146 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.276-3685delT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184785 | |||||||
| chr4:76184785 | CAA | C | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3686_276-3685d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184785 | |||||||
| chr4:76184797 | A | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3696T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184797 | |||||||
| chr4:76184798 | A | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3697T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184798 | |||||||
| chr4:76184799 | A | T | 147 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(144): Show |
204 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.276-3698T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184799 | |||||||
| chr4:76184893 | A | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3792T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184893 | |||||||
| chr4:76184962 | T | A | 6 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0001t0002g0257 others(3): Show |
8 | NA18943.hp1 NA18962.hp1 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.276-3861A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184962 | |||||||
| chr4:76184984 | G | C | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3883C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76184984 | |||||||
| chr4:76185068 | T | C | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-3967A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185068 | |||||||
| chr4:76185209 | G | A | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(86): Show |
123 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.276-4108C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185209 | |||||||
| chr4:76185332 | G | C | 160 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(157): Show |
222 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.276-4231C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185332 | |||||||
| chr4:76185426 | C | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-4325G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185426 | |||||||
| chr4:76185607 | T | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0139 a0001c0001t0001g0152 others(1): Show |
6 | NA18964.hp2 NA18971.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.276-4506A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185607 | |||||||
| chr4:76185659 | G | A | 54 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(51): Show |
76 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.276-4558C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185659 | |||||||
| chr4:76185717 | T | A | 160 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(157): Show |
222 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.276-4616A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185717 | |||||||
| chr4:76185721 | G | A | 2 | a0001c0001t0005g0219 a0001c0001t0007g0063 |
2 | HG01358.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.276-4620C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185721 | |||||||
| chr4:76185915 | G | A | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-4814C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76185915 | |||||||
| chr4:76186139 | C | T | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.276-5038G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76186139 | |||||||
| chr4:76186250 | G | A | 2 | a0001c0002t0009g0163 a0001c0002t0009g0164 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.276-5149C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76186250 | |||||||
| chr4:76186409 | G | A | 103 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(100): Show |
143 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.276-5308C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76186409 | |||||||
| chr4:76186415 | G | A | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.276-5314C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76186415 | |||||||
| chr4:76186521 | G | A | 6 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0004g0042 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.276-5420C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76186521 | |||||||
| chr4:76187005 | T | TA | 7 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0004g0042 others(4): Show |
8 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.276-5905dupT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187005 | |||||||
| chr4:76187107 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.276-6006A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187107 | |||||||
| chr4:76187153 | C | T | 160 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(157): Show |
222 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.276-6052G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187153 | |||||||
| chr4:76187436 | G | A | 12 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(9): Show |
18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-6335C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187436 | |||||||
| chr4:76187515 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.276-6414T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187515 | |||||||
| chr4:76187530 | C | G | 2 | a0001c0001t0002g0210 a0001c0001t0002g0211 |
2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.276-6429G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187530 | |||||||
| chr4:76187560 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0104 |
3 | HG01070.hp1 HG01943.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.276-6459A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187560 | |||||||
| chr4:76187614 | T | C | 3 | a0001c0001t0003g0156 a0001c0001t0004g0276 a0001c0001t0004g0277 |
3 | HG02027.hp2 NA18747.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.276-6513A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187614 | |||||||
| chr4:76187620 | A | T | 1 | a0001c0001t0015g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.276-6519T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187620 | |||||||
| chr4:76187641 | T | A | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-6540A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187641 | |||||||
| chr4:76187690 | T | C | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.276-6589A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187690 | |||||||
| chr4:76187799 | A | C | 1 | a0001c0001t0002g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.276-6698T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187799 | |||||||
| chr4:76187850 | C | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-6749G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76187850 | |||||||
| chr4:76188080 | C | T | 1 | a0001c0001t0005g0244 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.276-6979G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188080 | |||||||
| chr4:76188128 | T | G | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.276-7027A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188128 | |||||||
| chr4:76188286 | T | G | 1 | a0001c0001t0003g0007 | 3 | NA19002.hp2 NA19003.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.276-7185A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188286 | |||||||
| chr4:76188365 | AGACT | A | 56 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(53): Show |
78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.276-7268_276-7265d others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188365 | |||||||
| chr4:76188427 | T | G | 56 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(53): Show |
78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.275+7280A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188427 | |||||||
| chr4:76188473 | A | C | 1 | a0001c0001t0005g0043 | 2 | HG01081.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.275+7234T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188473 | |||||||
| chr4:76188490 | GTTAGGCC others(1): Show |
G | 56 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(53): Show |
78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.275+7209_275+7216d others(10): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188490 | |||||||
| chr4:76188548 | C | T | 56 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(53): Show |
78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.275+7159G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188548 | |||||||
| chr4:76188556 | T | C | 56 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(53): Show |
78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.275+7151A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188556 | |||||||
| chr4:76188557 | G | A | 55 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(52): Show |
77 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.275+7150C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188557 | |||||||
| chr4:76188704 | T | C | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+7003A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188704 | |||||||
| chr4:76188726 | A | C | 76 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(73): Show |
109 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.275+6981T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188726 | |||||||
| chr4:76188852 | A | G | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+6855T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188852 | |||||||
| chr4:76188870 | T | G | 2 | a0001c0001t0003g0009 a0001c0001t0003g0027 |
5 | NA18946.hp1 NA18981.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.275+6837A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188870 | |||||||
| chr4:76188881 | A | C | 3 | a0005c0005t0007g0149 a0005c0005t0007g0150 a0005c0005t0007g0151 |
3 | NA18949.hp1 NA18950.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.275+6826T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76188881 | |||||||
| chr4:76189010 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+6697G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189010 | |||||||
| chr4:76189114 | T | C | 56 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(53): Show |
78 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.275+6593A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189114 | |||||||
| chr4:76189136 | T | C | 7 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0004g0042 others(4): Show |
8 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.275+6571A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189136 | |||||||
| chr4:76189157 | C | T | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+6550G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189157 | |||||||
| chr4:76189158 | C | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0205 a0001c0001t0002g0208 |
8 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.275+6549G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189158 | |||||||
| chr4:76189158 | C | G | 183 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(180): Show |
243 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.275+6549G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189158 | |||||||
| chr4:76189212 | C | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(90): Show |
118 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.275+6495G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189212 | |||||||
| chr4:76189238 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.275+6469C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189238 | |||||||
| chr4:76189262 | T | C | 2 | a0001c0001t0010g0014 a0001c0001t0010g0129 |
4 | NA18970.hp1 NA18999.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+6445A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189262 | |||||||
| chr4:76189427 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0102 |
2 | NA18944.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.275+6280G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189427 | |||||||
| chr4:76189470 | T | C | 1 | a0001c0001t0005g0234 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.275+6237A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189470 | |||||||
| chr4:76189474 | C | CTGTTGT | 225 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0020 others(222): Show |
306 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.275+6227_275+6232d others(8): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189474 | |||||||
| chr4:76189474 | C | CTGTTGTT others(2): Show |
15 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0138 others(12): Show |
18 | HG00280.hp1 HG01515.hp1 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.275+6224_275+6232d others(11): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189474 | |||||||
| chr4:76189474 | C | CTGTTGTT others(5): Show |
1 | a0001c0002t0006g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.275+6221_275+6232d others(14): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189474 | |||||||
| chr4:76189474 | C | CTGTTGTT others(8): Show |
4 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0006g0192 others(1): Show |
4 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+6218_275+6232d others(17): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189474 | |||||||
| chr4:76189474 | C | CTGTTGTT others(11): Show |
1 | a0001c0001t0004g0042 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.275+6215_275+6232d others(20): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189474 | |||||||
| chr4:76189474 | CTGTTGT | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0115 a0001c0001t0001g0117 others(1): Show |
6 | HG01106.hp1 HG01123.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.275+6227_275+6232d others(8): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189474 | |||||||
| chr4:76189575 | G | A | 3 | a0001c0001t0003g0077 a0001c0001t0003g0078 a0001c0001t0004g0256 |
3 | NA18974.hp1 NA19062.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.275+6132C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189575 | |||||||
| chr4:76189658 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.275+6049C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189658 | |||||||
| chr4:76189684 | T | C | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+6023A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189684 | |||||||
| chr4:76189806 | T | C | 10 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(7): Show |
10 | HG01891.hp1 HG02280.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.275+5901A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189806 | |||||||
| chr4:76189814 | C | G | 1 | a0001c0001t0007g0036 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.275+5893G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189814 | |||||||
| chr4:76189863 | C | T | 1 | a0001c0001t0018g0134 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.275+5844G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189863 | |||||||
| chr4:76189864 | G | A | 42 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0099 others(39): Show |
46 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.275+5843C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189864 | |||||||
| chr4:76189876 | C | A | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+5831G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189876 | |||||||
| chr4:76189879 | C | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(102): Show |
136 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.275+5828G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189879 | |||||||
| chr4:76189880 | C | T | 7 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0004g0042 others(4): Show |
8 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.275+5827G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189880 | |||||||
| chr4:76189947 | G | A | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.275+5760C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76189947 | |||||||
| chr4:76190008 | ACTTT | A | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+5695_275+5698d others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190008 | |||||||
| chr4:76190009 | CT | C | 26 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0033 others(23): Show |
33 | HG00673.hp2 HG01515.hp1 HG01517.hp1 others(30): Show |
intron_variant | MODIFIER | c.275+5697delA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190009 | |||||||
| chr4:76190011 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0002g0207 |
2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.275+5696A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190011 | |||||||
| chr4:76190136 | G | T | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+5571C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190136 | |||||||
| chr4:76190166 | G | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+5541C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190166 | |||||||
| chr4:76190199 | G | A | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.275+5508C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190199 | |||||||
| chr4:76190238 | A | G | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+5469T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190238 | |||||||
| chr4:76190257 | A | G | 255 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(252): Show |
342 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.275+5450T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190257 | |||||||
| chr4:76190328 | A | T | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+5379T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190328 | |||||||
| chr4:76190365 | T | G | 1 | a0001c0001t0004g0238 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.275+5342A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190365 | |||||||
| chr4:76190523 | C | T | 10 | a0001c0001t0001g0111 a0001c0001t0002g0016 a0001c0001t0002g0041 others(7): Show |
13 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.275+5184G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190523 | |||||||
| chr4:76190602 | G | A | 55 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(52): Show |
77 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.275+5105C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190602 | |||||||
| chr4:76190610 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+5097G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190610 | |||||||
| chr4:76190645 | C | T | 1 | a0001c0001t0005g0219 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.275+5062G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190645 | |||||||
| chr4:76190721 | T | C | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+4986A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190721 | |||||||
| chr4:76190738 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.275+4969G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190738 | |||||||
| chr4:76190739 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0120 a0001c0001t0002g0048 |
4 | NA18983.hp1 NA19012.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+4968C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190739 | |||||||
| chr4:76190785 | AAAAC | A | 15 | a0001c0001t0003g0024 a0001c0001t0009g0006 a0001c0001t0009g0038 others(12): Show |
22 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.275+4918_275+4921d others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190785 | |||||||
| chr4:76190956 | G | A | 1 | a0001c0001t0003g0075 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.275+4751C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190956 | |||||||
| chr4:76190982 | C | A | 19 | a0001c0001t0004g0054 a0001c0001t0004g0209 a0001c0001t0004g0229 others(16): Show |
23 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.275+4725G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76190982 | |||||||
| chr4:76191039 | C | T | 1 | a0004c0004t0004g0019 | 3 | NA18939.hp1 NA18941.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.275+4668G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191039 | |||||||
| chr4:76191078 | TAAC | T | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+4626_275+4628d others(5): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191078 | |||||||
| chr4:76191291 | A | G | 2 | a0001c0001t0002g0259 a0001c0001t0002g0260 |
2 | NA18947.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.275+4416T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191291 | |||||||
| chr4:76191295 | A | T | 1 | a0001c0002t0006g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.275+4412T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191295 | |||||||
| chr4:76191318 | A | G | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+4389T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191318 | |||||||
| chr4:76191404 | C | CACCA | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+4302_275+4303i others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191404 | |||||||
| chr4:76191487 | T | C | 76 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(73): Show |
109 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.275+4220A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191487 | |||||||
| chr4:76191533 | T | C | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+4174A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191533 | |||||||
| chr4:76191552 | C | T | 1 | a0002c0003t0024g0202 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.275+4155G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191552 | |||||||
| chr4:76191574 | A | G | 1 | a0001c0001t0015g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.275+4133T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191574 | |||||||
| chr4:76191690 | G | T | 1 | a0001c0001t0006g0201 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.275+4017C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191690 | |||||||
| chr4:76191698 | C | T | 224 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(221): Show |
307 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.275+4009G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191698 | |||||||
| chr4:76191731 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(57): Show |
81 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.275+3976G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191731 | |||||||
| chr4:76191737 | CCCCT | C | 12 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(9): Show |
18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.275+3966_275+3969d others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191737 | |||||||
| chr4:76191759 | C | T | 220 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(217): Show |
303 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(300): Show |
intron_variant | MODIFIER | c.275+3948G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191759 | |||||||
| chr4:76191766 | T | G | 1 | a0001c0001t0015g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.275+3941A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191766 | |||||||
| chr4:76191779 | C | CT | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+3927dupA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191779 | |||||||
| chr4:76191848 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0002g0207 |
2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.275+3859C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191848 | |||||||
| chr4:76191855 | C | T | 1 | a0001c0001t0004g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.275+3852G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76191855 | |||||||
| chr4:76192197 | G | C | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+3510C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192197 | |||||||
| chr4:76192218 | G | T | 1 | a0001c0001t0008g0191 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.275+3489C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192218 | |||||||
| chr4:76192250 | A | T | 76 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(73): Show |
109 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.275+3457T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192250 | |||||||
| chr4:76192406 | T | C | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+3301A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192406 | |||||||
| chr4:76192491 | G | A | 1 | a0001c0001t0003g0088 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.275+3216C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192491 | |||||||
| chr4:76192526 | T | C | 1 | a0001c0001t0006g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.275+3181A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192526 | |||||||
| chr4:76192628 | G | A | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+3079C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192628 | |||||||
| chr4:76192637 | G | GA | 21 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(18): Show |
27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+3069dupT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192637 | |||||||
| chr4:76192649 | C | T | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+3058G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192649 | |||||||
| chr4:76192651 | C | T | 1 | a0001c0001t0005g0218 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.275+3056G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192651 | |||||||
| chr4:76192654 | T | C | 21 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(18): Show |
27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+3053A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192654 | |||||||
| chr4:76192681 | CA | C | 8 | a0001c0001t0004g0238 a0002c0003t0004g0227 a0002c0003t0006g0175 others(5): Show |
8 | HG01069.hp1 HG02280.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.275+3025delT | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192681 | |||||||
| chr4:76192681 | CAA | C | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+3024_275+3025d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192681 | |||||||
| chr4:76192765 | A | T | 21 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(18): Show |
27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+2942T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76192765 | |||||||
| chr4:76193034 | C | G | 2 | a0001c0001t0001g0152 a0001c0001t0002g0245 |
2 | NA19058.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.275+2673G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193034 | |||||||
| chr4:76193037 | A | G | 21 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(18): Show |
27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+2670T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193037 | |||||||
| chr4:76193100 | C | G | 1 | a0001c0001t0001g0136 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.275+2607G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193100 | |||||||
| chr4:76193107 | A | C | 1 | a0001c0001t0002g0273 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.275+2600T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193107 | |||||||
| chr4:76193120 | A | C | 21 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(18): Show |
27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+2587T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193120 | |||||||
| chr4:76193365 | C | T | 9 | a0001c0001t0005g0216 a0001c0001t0005g0217 a0002c0003t0004g0227 others(6): Show |
9 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.275+2342G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193365 | |||||||
| chr4:76193412 | G | T | 1 | a0001c0001t0015g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.275+2295C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193412 | |||||||
| chr4:76193595 | T | A | 33 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0099 others(30): Show |
37 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.275+2112A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193595 | |||||||
| chr4:76193731 | T | C | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+1976A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193731 | |||||||
| chr4:76193783 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(57): Show |
81 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.275+1924G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193783 | |||||||
| chr4:76193862 | A | G | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+1845T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193862 | |||||||
| chr4:76193919 | G | A | 1 | a0001c0001t0021g0186 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.275+1788C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193919 | |||||||
| chr4:76193998 | G | A | 76 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(73): Show |
109 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.275+1709C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76193998 | |||||||
| chr4:76194034 | G | A | 1 | a0001c0001t0008g0188 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.275+1673C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194034 | |||||||
| chr4:76194037 | G | C | 1 | a0001c0001t0008g0191 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.275+1670C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194037 | |||||||
| chr4:76194050 | G | C | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+1657C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194050 | |||||||
| chr4:76194113 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+1594G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194113 | |||||||
| chr4:76194296 | C | T | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+1411G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194296 | |||||||
| chr4:76194346 | C | T | 3 | a0001c0001t0003g0079 a0001c0001t0003g0080 a0001c0001t0004g0275 |
3 | HG00423.hp2 HG02040.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.275+1361G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194346 | |||||||
| chr4:76194367 | C | CATA | 21 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(18): Show |
27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+1339_275+1340i others(5): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194367 | |||||||
| chr4:76194400 | T | C | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+1307A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194400 | |||||||
| chr4:76194410 | G | T | 1 | a0001c0001t0006g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.275+1297C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194410 | |||||||
| chr4:76194474 | A | AGGC | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+1230_275+1232d others(5): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194474 | |||||||
| chr4:76194494 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+1213G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194494 | |||||||
| chr4:76194521 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+1186G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194521 | |||||||
| chr4:76194696 | C | A | 1 | a0001c0001t0006g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.275+1011G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194696 | |||||||
| chr4:76194696 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+1011G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194696 | |||||||
| chr4:76194749 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.275+958A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194749 | |||||||
| chr4:76194793 | C | G | 21 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(18): Show |
27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+914G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194793 | |||||||
| chr4:76194815 | T | C | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+892A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194815 | |||||||
| chr4:76194831 | C | A | 1 | a0001c0001t0006g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.275+876G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194831 | |||||||
| chr4:76194841 | C | G | 1 | a0001c0001t0002g0282 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.275+866G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194841 | |||||||
| chr4:76194842 | G | A | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+865C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194842 | |||||||
| chr4:76194918 | C | G | 1 | a0001c0001t0012g0177 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.275+789G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194918 | |||||||
| chr4:76194942 | G | C | 21 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(18): Show |
27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+765C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194942 | |||||||
| chr4:76194964 | G | C | 76 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(73): Show |
109 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.275+743C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194964 | |||||||
| chr4:76194965 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0137 |
3 | HG00642.hp2 HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.275+742G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194965 | |||||||
| chr4:76194990 | T | C | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+717A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76194990 | |||||||
| chr4:76195064 | G | C | 2 | a0001c0001t0002g0259 a0001c0001t0002g0260 |
2 | NA18947.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.275+643C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195064 | |||||||
| chr4:76195091 | A | G | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.275+616T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195091 | |||||||
| chr4:76195186 | T | C | 1 | a0003c0009t0028g0226 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.275+521A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195186 | |||||||
| chr4:76195194 | G | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+513C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195194 | |||||||
| chr4:76195196 | C | A | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+511G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195196 | |||||||
| chr4:76195249 | C | T | 21 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(18): Show |
27 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.275+458G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195249 | |||||||
| chr4:76195374 | T | A | 1 | a0001c0001t0004g0225 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.275+333A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195374 | |||||||
| chr4:76195448 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.275+259T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195448 | |||||||
| chr4:76195506 | G | A | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+201C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195506 | |||||||
| chr4:76195575 | G | A | 6 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0004g0042 others(3): Show |
7 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+132C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 2/11 | chr4 | 76195575 | |||||||
| chr4:76195871 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01358.hp2 | splice_region_variant&intron_variant | LOW | c.118-7T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76195871 | |||||||
| chr4:76195891 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-27G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76195891 | |||||||
| chr4:76195943 | G | A | 75 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(72): Show |
108 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.118-79C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76195943 | |||||||
| chr4:76195958 | C | T | 1 | a0001c0001t0012g0177 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.118-94G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76195958 | |||||||
| chr4:76196060 | G | A | 1 | a0004c0004t0004g0019 | 3 | NA18939.hp1 NA18941.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.118-196C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196060 | |||||||
| chr4:76196072 | G | A | 75 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(72): Show |
108 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.118-208C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196072 | |||||||
| chr4:76196156 | G | A | 33 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0099 others(30): Show |
37 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.118-292C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196156 | |||||||
| chr4:76196308 | G | A | 1 | a0002c0003t0019g0096 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.118-444C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196308 | |||||||
| chr4:76196318 | A | T | 1 | a0001c0001t0003g0024 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.118-454T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196318 | |||||||
| chr4:76196384 | T | C | 3 | a0001c0001t0003g0107 a0001c0001t0006g0192 a0001c0002t0006g0162 |
3 | HG03195.hp1 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.118-520A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196384 | |||||||
| chr4:76196421 | A | C | 131 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(128): Show |
186 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.118-557T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196421 | |||||||
| chr4:76196596 | G | A | 73 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(70): Show |
106 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.118-732C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196596 | |||||||
| chr4:76196774 | G | A | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-910C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196774 | |||||||
| chr4:76196913 | G | A | 1 | a0001c0001t0002g0255 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.118-1049C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196913 | |||||||
| chr4:76196980 | G | A | 2 | a0001c0001t0006g0192 a0001c0002t0006g0162 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.118-1116C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196980 | |||||||
| chr4:76196981 | GT | G | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1118delA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76196981 | |||||||
| chr4:76197083 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.118-1219G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197083 | |||||||
| chr4:76197096 | C | T | 4 | a0001c0001t0006g0185 a0001c0001t0021g0186 a0001c0001t0029g0206 others(1): Show |
4 | HG01175.hp1 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-1232G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197096 | |||||||
| chr4:76197102 | T | G | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1238A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197102 | |||||||
| chr4:76197132 | T | A | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1268A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197132 | |||||||
| chr4:76197214 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1350G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197214 | |||||||
| chr4:76197302 | T | G | 1 | a0001c0001t0002g0246 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118-1438A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197302 | |||||||
| chr4:76197340 | G | T | 9 | a0001c0001t0009g0006 a0001c0001t0009g0194 a0001c0001t0009g0195 others(6): Show |
14 | HG00673.hp2 HG02083.hp1 NA18948.hp1 others(11): Show |
intron_variant | MODIFIER | c.118-1476C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197340 | |||||||
| chr4:76197344 | C | A | 1 | a0001c0001t0008g0188 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.118-1480G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197344 | |||||||
| chr4:76197344 | C | T | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.118-1480G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197344 | |||||||
| chr4:76197469 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0002g0245 |
2 | NA19058.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.118-1605C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197469 | |||||||
| chr4:76197516 | T | TCAAACTG others(6): Show |
7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1653_118-1652i others(15): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197516 | |||||||
| chr4:76197518 | G | C | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1654C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197518 | |||||||
| chr4:76197578 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1714G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197578 | |||||||
| chr4:76197586 | T | C | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1722A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197586 | |||||||
| chr4:76197630 | C | G | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1766G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197630 | |||||||
| chr4:76197766 | T | A | 1 | a0001c0001t0004g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.118-1902A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197766 | |||||||
| chr4:76197895 | C | CT | 8 | a0001c0001t0008g0188 a0002c0003t0004g0227 a0002c0003t0006g0175 others(5): Show |
8 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-2032dupA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197895 | |||||||
| chr4:76197985 | G | A | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.118-2121C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76197985 | |||||||
| chr4:76198054 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.118-2190C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198054 | |||||||
| chr4:76198065 | C | A | 75 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0008 others(72): Show |
108 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.118-2201G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198065 | |||||||
| chr4:76198143 | T | C | 2 | a0001c0001t0003g0074 a0001c0001t0003g0075 |
2 | NA18979.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.118-2279A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198143 | |||||||
| chr4:76198293 | T | C | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.118-2429A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198293 | |||||||
| chr4:76198308 | C | T | 1 | a0001c0001t0008g0188 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.118-2444G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198308 | |||||||
| chr4:76198328 | G | A | 1 | a0001c0002t0008g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.118-2464C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198328 | |||||||
| chr4:76198348 | G | A | 1 | a0001c0001t0006g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.118-2484C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198348 | |||||||
| chr4:76198365 | A | G | 2 | a0001c0001t0007g0091 a0001c0001t0007g0114 |
2 | HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.118-2501T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198365 | |||||||
| chr4:76198394 | G | A | 57 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(54): Show |
79 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.118-2530C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198394 | |||||||
| chr4:76198471 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0002g0255 |
2 | NA19057.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.118-2607A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198471 | |||||||
| chr4:76198488 | A | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-2624T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198488 | |||||||
| chr4:76198581 | C | A | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-2717G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198581 | |||||||
| chr4:76198608 | CCT | C | 13 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(10): Show |
19 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.118-2746_118-2745d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198608 | |||||||
| chr4:76198631 | A | G | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-2767T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198631 | |||||||
| chr4:76198789 | T | C | 7 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0004g0042 others(4): Show |
8 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-2925A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198789 | |||||||
| chr4:76198821 | C | A | 7 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0004g0042 others(4): Show |
8 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-2957G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198821 | |||||||
| chr4:76198837 | AGTGAGT | A | 3 | a0001c0002t0009g0163 a0001c0002t0009g0164 a0001c0008t0012g0183 |
3 | HG02559.hp2 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.118-2979_118-2974d others(8): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198837 | |||||||
| chr4:76198837 | AGTGAGTG others(1): Show |
A | 9 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(6): Show |
15 | HG00673.hp2 HG02083.hp1 NA18948.hp1 others(12): Show |
intron_variant | MODIFIER | c.118-2981_118-2974d others(10): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198837 | |||||||
| chr4:76198837 | AGTGAGTG others(5): Show |
A | 1 | a0001c0001t0009g0197 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.118-2985_118-2974d others(14): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198837 | |||||||
| chr4:76198839 | TGA | T | 6 | a0002c0003t0004g0227 a0002c0003t0014g0228 a0002c0003t0014g0274 others(3): Show |
6 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-2977_118-2976d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198839 | |||||||
| chr4:76198841 | A | AGT | 25 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0059 others(22): Show |
28 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.118-2979_118-2978d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | |||||||
| chr4:76198841 | A | AGTGAGT | 3 | a0001c0001t0003g0110 a0001c0002t0006g0165 a0001c0002t0006g0166 |
3 | HG01884.hp2 HG02145.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.118-2978_118-2977i others(8): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | |||||||
| chr4:76198841 | A | AGTGAGTG others(3): Show |
2 | a0001c0001t0006g0192 a0001c0002t0006g0162 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.118-2978_118-2977i others(12): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | |||||||
| chr4:76198841 | A | AGTGT | 19 | a0001c0001t0001g0002 a0001c0001t0001g0128 a0001c0001t0001g0136 others(16): Show |
26 | HG00609.hp1 HG01192.hp2 HG02572.hp2 others(23): Show |
intron_variant | MODIFIER | c.118-2981_118-2978d others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | |||||||
| chr4:76198841 | A | AGTGTGT | 36 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(33): Show |
49 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.118-2983_118-2978d others(8): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | |||||||
| chr4:76198841 | A | AGTGTGTG others(1): Show |
12 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0089 others(9): Show |
13 | HG00423.hp1 HG01070.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.118-2985_118-2978d others(10): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | |||||||
| chr4:76198841 | A | AGTGTGTG others(3): Show |
3 | a0001c0001t0003g0156 a0001c0001t0029g0206 a0001c0002t0023g0167 |
3 | HG01175.hp1 HG03139.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.118-2987_118-2978d others(12): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | |||||||
| chr4:76198841 | A | T | 1 | a0002c0003t0006g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.118-2977T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | |||||||
| chr4:76198841 | AGT | A | 57 | a0001c0001t0001g0133 a0001c0001t0001g0146 a0001c0001t0002g0046 others(54): Show |
81 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.118-2979_118-2978d others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | |||||||
| chr4:76198841 | AGTGT | A | 4 | a0001c0001t0006g0178 a0001c0001t0006g0190 a0005c0005t0007g0150 others(1): Show |
4 | HG03486.hp2 NA18949.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-2981_118-2978d others(6): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | |||||||
| chr4:76198841 | AGTGTGT | A | 3 | a0001c0001t0003g0022 a0001c0001t0003g0076 a0001c0001t0003g0081 |
4 | HG03490.hp1 HG03491.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-2983_118-2978d others(8): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | |||||||
| chr4:76198841 | AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0003g0060 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.118-2989_118-2978d others(14): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198841 | |||||||
| chr4:76198843 | T | TGA | 2 | a0001c0001t0003g0008 a0004c0004t0004g0019 |
6 | HG04184.hp1 NA18939.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-2980_118-2979i others(4): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198843 | |||||||
| chr4:76198873 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.118-3009A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198873 | |||||||
| chr4:76198882 | G | A | 1 | a0001c0001t0002g0254 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.118-3018C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198882 | |||||||
| chr4:76198883 | A | G | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3019T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76198883 | |||||||
| chr4:76199036 | C | T | 4 | a0001c0001t0006g0185 a0001c0001t0021g0186 a0001c0001t0029g0206 others(1): Show |
4 | HG01175.hp1 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-3172G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199036 | |||||||
| chr4:76199216 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3352G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199216 | |||||||
| chr4:76199252 | C | T | 1 | a0001c0001t0002g0246 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118-3388G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199252 | |||||||
| chr4:76199330 | T | A | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3466A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199330 | |||||||
| chr4:76199392 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3528G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199392 | |||||||
| chr4:76199393 | A | G | 13 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(10): Show |
19 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.118-3529T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199393 | |||||||
| chr4:76199393 | A | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3529T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199393 | |||||||
| chr4:76199556 | C | T | 1 | a0001c0002t0006g0170 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.118-3692G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199556 | |||||||
| chr4:76199568 | A | AT | 12 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(9): Show |
18 | HG00673.hp2 HG02083.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.118-3705dupA | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199568 | |||||||
| chr4:76199611 | T | G | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3747A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199611 | |||||||
| chr4:76199720 | G | A | 20 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(17): Show |
26 | HG00673.hp2 HG02083.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.118-3856C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199720 | |||||||
| chr4:76199745 | G | A | 7 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0004g0042 others(4): Show |
8 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-3881C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199745 | |||||||
| chr4:76199762 | C | G | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3898G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199762 | |||||||
| chr4:76199863 | G | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-3999C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76199863 | |||||||
| chr4:76200050 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0002g0270 |
2 | HG01081.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.118-4186C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200050 | |||||||
| chr4:76200056 | T | C | 1 | a0001c0001t0008g0188 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.118-4192A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200056 | |||||||
| chr4:76200193 | A | G | 247 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(244): Show |
333 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.118-4329T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200193 | |||||||
| chr4:76200343 | G | A | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-4479C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200343 | |||||||
| chr4:76200349 | A | G | 4 | a0001c0001t0003g0110 a0001c0001t0004g0042 a0001c0002t0006g0165 others(1): Show |
5 | HG01884.hp2 HG02145.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-4485T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200349 | |||||||
| chr4:76200411 | T | C | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-4547A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200411 | |||||||
| chr4:76200735 | A | G | 1 | a0001c0001t0002g0257 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.118-4871T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200735 | |||||||
| chr4:76200925 | T | C | 2 | a0001c0001t0012g0177 a0001c0008t0012g0183 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.118-5061A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200925 | |||||||
| chr4:76200954 | G | C | 20 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(17): Show |
26 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(23): Show |
intron_variant | MODIFIER | c.118-5090C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200954 | |||||||
| chr4:76200961 | A | G | 2 | a0002c0003t0004g0227 a0002c0003t0006g0175 |
2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.118-5097T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76200961 | |||||||
| chr4:76201028 | C | A | 4 | a0001c0001t0001g0071 a0001c0001t0002g0052 a0001c0001t0002g0271 others(1): Show |
5 | HG02129.hp1 NA18947.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-5164G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201028 | |||||||
| chr4:76201057 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-5193G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201057 | |||||||
| chr4:76201348 | T | C | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-5484A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201348 | |||||||
| chr4:76201354 | G | C | 14 | a0001c0001t0009g0006 a0001c0001t0009g0038 a0001c0001t0009g0194 others(11): Show |
20 | HG00673.hp2 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.118-5490C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201354 | |||||||
| chr4:76201356 | G | A | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-5492C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201356 | |||||||
| chr4:76201487 | C | G | 6 | a0001c0001t0003g0023 a0001c0001t0003g0060 a0001c0001t0003g0077 others(3): Show |
7 | NA18974.hp1 NA18977.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-5623G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201487 | |||||||
| chr4:76201539 | T | C | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-5675A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201539 | |||||||
| chr4:76201785 | T | C | 3 | a0001c0001t0003g0107 a0001c0001t0006g0192 a0001c0002t0006g0162 |
3 | HG03195.hp1 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.118-5921A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201785 | |||||||
| chr4:76201864 | A | G | 3 | a0001c0001t0001g0130 a0001c0001t0005g0216 a0001c0001t0005g0217 |
3 | HG02735.hp2 HG03017.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.118-6000T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201864 | |||||||
| chr4:76201979 | A | G | 3 | a0001c0001t0008g0181 a0001c0001t0008g0182 a0001c0002t0008g0161 |
3 | HG03130.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.118-6115T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76201979 | |||||||
| chr4:76202081 | A | G | 2 | a0001c0001t0003g0022 a0001c0001t0003g0076 |
3 | HG03491.hp2 HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.118-6217T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76202081 | |||||||
| chr4:76202161 | G | C | 1 | a0001c0008t0012g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-6297C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76202161 | |||||||
| chr4:76202355 | G | A | 1 | a0001c0008t0012g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-6491C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76202355 | |||||||
| chr4:76202365 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.118-6501C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76202365 | |||||||
| chr4:76202551 | G | A | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-6687C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76202551 | |||||||
| chr4:76202688 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-6824G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76202688 | |||||||
| chr4:76202785 | G | C | 8 | a0001c0008t0012g0183 a0002c0003t0004g0227 a0002c0003t0006g0175 others(5): Show |
8 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-6921C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76202785 | |||||||
| chr4:76202891 | C | T | 1 | a0001c0001t0004g0214 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.118-7027G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76202891 | |||||||
| chr4:76203001 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.118-7137G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203001 | |||||||
| chr4:76203043 | A | G | 286 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(283): Show |
379 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.118-7179T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203043 | |||||||
| chr4:76203125 | C | T | 1 | a0001c0008t0012g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-7261G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203125 | |||||||
| chr4:76203212 | T | A | 1 | a0001c0008t0012g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-7348A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203212 | |||||||
| chr4:76203270 | T | C | 1 | a0001c0008t0012g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-7406A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203270 | |||||||
| chr4:76203297 | G | T | 1 | a0001c0008t0012g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-7433C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203297 | |||||||
| chr4:76203409 | T | C | 1 | a0001c0008t0012g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-7545A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203409 | |||||||
| chr4:76203413 | C | A | 1 | a0001c0008t0012g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-7549G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203413 | |||||||
| chr4:76203462 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-7598G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203462 | |||||||
| chr4:76203464 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-7600G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203464 | |||||||
| chr4:76203592 | A | G | 66 | a0001c0001t0001g0020 a0001c0001t0001g0064 a0001c0001t0001g0065 others(63): Show |
97 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.118-7728T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203592 | |||||||
| chr4:76203614 | A | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-7750T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203614 | |||||||
| chr4:76203772 | C | T | 3 | a0001c0001t0004g0042 a0001c0002t0006g0165 a0001c0002t0006g0166 |
4 | HG01884.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-7908G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203772 | |||||||
| chr4:76203788 | A | G | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-7924T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76203788 | |||||||
| chr4:76204159 | T | C | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-8295A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204159 | |||||||
| chr4:76204180 | G | A | 1 | a0001c0001t0002g0016 | 3 | HG01069.hp2 HG01071.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.118-8316C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204180 | |||||||
| chr4:76204181 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-8317G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204181 | |||||||
| chr4:76204192 | G | A | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-8328C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204192 | |||||||
| chr4:76204359 | C | G | 8 | a0001c0008t0012g0183 a0002c0003t0004g0227 a0002c0003t0006g0175 others(5): Show |
8 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-8495G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204359 | |||||||
| chr4:76204523 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.118-8659C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204523 | |||||||
| chr4:76204598 | G | A | 2 | a0001c0001t0006g0178 a0001c0001t0006g0190 |
2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.118-8734C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204598 | |||||||
| chr4:76204725 | C | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(203): Show |
284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.117+8702G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204725 | |||||||
| chr4:76204890 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0002g0285 |
2 | HG02080.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.117+8537G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204890 | |||||||
| chr4:76204905 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0002g0255 |
2 | NA19057.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.117+8522T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76204905 | |||||||
| chr4:76205068 | G | A | 1 | a0001c0008t0012g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.117+8359C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205068 | |||||||
| chr4:76205071 | A | G | 5 | a0001c0001t0002g0017 a0001c0001t0002g0251 a0001c0001t0002g0253 others(2): Show |
7 | NA18941.hp2 NA18965.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+8356T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205071 | |||||||
| chr4:76205138 | C | A | 1 | a0001c0002t0006g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.117+8289G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205138 | |||||||
| chr4:76205172 | T | C | 1 | a0003c0006t0013g0168 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.117+8255A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205172 | |||||||
| chr4:76205187 | G | C | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+8240C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205187 | |||||||
| chr4:76205349 | A | AAAAAT | 46 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0099 others(43): Show |
56 | HG00140.hp1 HG00673.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.117+8073_117+8077d others(7): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205349 | |||||||
| chr4:76205423 | A | T | 1 | a0001c0001t0001g0055 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.117+8004T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205423 | |||||||
| chr4:76205784 | C | T | 1 | a0001c0001t0003g0057 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.117+7643G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205784 | |||||||
| chr4:76205865 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.117+7562A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205865 | |||||||
| chr4:76205875 | C | G | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+7552G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205875 | |||||||
| chr4:76205951 | G | A | 45 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0099 others(42): Show |
55 | HG00140.hp1 HG00673.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.117+7476C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76205951 | |||||||
| chr4:76206159 | G | A | 1 | a0001c0008t0012g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.117+7268C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206159 | |||||||
| chr4:76206230 | G | T | 1 | a0001c0001t0005g0244 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.117+7197C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206230 | |||||||
| chr4:76206391 | A | G | 4 | a0001c0001t0004g0054 a0003c0006t0013g0168 a0003c0006t0013g0169 others(1): Show |
5 | HG01891.hp1 HG02615.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+7036T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206391 | |||||||
| chr4:76206440 | A | G | 1 | a0001c0001t0005g0215 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.117+6987T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206440 | |||||||
| chr4:76206618 | T | A | 46 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0099 others(43): Show |
56 | HG00140.hp1 HG00673.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.117+6809A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206618 | |||||||
| chr4:76206663 | G | A | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+6764C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206663 | |||||||
| chr4:76206740 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+6687G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206740 | |||||||
| chr4:76206741 | G | A | 1 | a0001c0001t0006g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.117+6686C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206741 | |||||||
| chr4:76206822 | G | C | 1 | a0001c0001t0009g0198 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.117+6605C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206822 | |||||||
| chr4:76206873 | A | G | 256 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(253): Show |
339 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(336): Show |
intron_variant | MODIFIER | c.117+6554T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206873 | |||||||
| chr4:76206967 | T | C | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+6460A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206967 | |||||||
| chr4:76206995 | T | A | 3 | a0001c0001t0003g0110 a0001c0001t0029g0206 a0001c0002t0023g0167 |
3 | HG01175.hp1 HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.117+6432A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76206995 | |||||||
| chr4:76207005 | A | G | 1 | a0001c0001t0004g0214 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.117+6422T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207005 | |||||||
| chr4:76207068 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+6359G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207068 | |||||||
| chr4:76207100 | G | C | 76 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0099 others(73): Show |
90 | HG00140.hp1 HG00673.hp2 HG00738.hp2 others(87): Show |
intron_variant | MODIFIER | c.117+6327C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207100 | |||||||
| chr4:76207287 | A | G | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+6140T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207287 | |||||||
| chr4:76207481 | C | T | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+5946G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207481 | |||||||
| chr4:76207495 | T | C | 1 | a0001c0001t0002g0273 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.117+5932A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207495 | |||||||
| chr4:76207571 | G | A | 34 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0099 others(31): Show |
38 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.117+5856C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207571 | |||||||
| chr4:76207734 | C | T | 2 | a0001c0001t0003g0074 a0001c0001t0003g0075 |
2 | NA18979.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.117+5693G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207734 | |||||||
| chr4:76207758 | T | C | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+5669A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207758 | |||||||
| chr4:76207941 | G | A | 7 | a0002c0003t0004g0227 a0002c0003t0006g0175 a0002c0003t0014g0228 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+5486C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207941 | |||||||
| chr4:76207964 | T | G | 19 | a0001c0001t0004g0054 a0001c0001t0004g0209 a0001c0001t0004g0229 others(16): Show |
23 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+5463A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76207964 | |||||||
| chr4:76208119 | T | G | 4 | a0001c0001t0003g0110 a0001c0001t0029g0206 a0001c0002t0023g0167 others(1): Show |
4 | HG01175.hp1 HG02145.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+5308A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208119 | |||||||
| chr4:76208237 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0002g0207 |
2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.117+5190A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208237 | |||||||
| chr4:76208392 | C | T | 1 | a0001c0008t0012g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.117+5035G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208392 | |||||||
| chr4:76208404 | C | T | 7 | a0001c0001t0003g0110 a0001c0001t0004g0042 a0001c0001t0029g0206 others(4): Show |
8 | HG01175.hp1 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+5023G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208404 | |||||||
| chr4:76208415 | C | G | 35 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0098 others(32): Show |
39 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.117+5012G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208415 | |||||||
| chr4:76208531 | C | T | 2 | a0001c0002t0006g0165 a0001c0002t0006g0166 |
2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.117+4896G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208531 | |||||||
| chr4:76208626 | T | C | 15 | a0001c0001t0004g0054 a0001c0001t0004g0209 a0001c0001t0004g0229 others(12): Show |
19 | HG01891.hp1 HG02145.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.117+4801A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208626 | |||||||
| chr4:76208659 | T | C | 18 | a0001c0001t0002g0004 a0001c0001t0002g0208 a0001c0001t0004g0054 others(15): Show |
27 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.117+4768A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208659 | |||||||
| chr4:76208687 | G | A | 77 | a0001c0001t0001g0073 a0001c0001t0001g0089 a0001c0001t0001g0090 others(74): Show |
111 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.117+4740C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208687 | |||||||
| chr4:76208702 | T | C | 1 | a0002c0003t0019g0096 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.117+4725A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208702 | |||||||
| chr4:76208755 | C | A | 245 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(242): Show |
328 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(325): Show |
intron_variant | MODIFIER | c.117+4672G>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208755 | |||||||
| chr4:76208756 | T | C | 1 | a0001c0001t0006g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.117+4671A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208756 | |||||||
| chr4:76208809 | G | A | 16 | a0001c0001t0002g0223 a0001c0001t0003g0110 a0001c0001t0004g0054 others(13): Show |
21 | HG01175.hp1 HG02145.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.117+4618C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208809 | |||||||
| chr4:76208823 | T | C | 3 | a0001c0001t0006g0190 a0001c0001t0021g0186 a0003c0009t0028g0226 |
3 | HG01891.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.117+4604A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76208823 | |||||||
| chr4:76209052 | T | C | 8 | a0001c0001t0002g0004 a0001c0001t0002g0208 a0001c0001t0004g0209 others(5): Show |
13 | HG01884.hp1 HG02622.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+4375A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209052 | |||||||
| chr4:76209101 | C | T | 2 | a0001c0001t0004g0225 a0003c0009t0028g0226 |
2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.117+4326G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209101 | |||||||
| chr4:76209132 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(56): Show |
83 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.117+4295C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209132 | |||||||
| chr4:76209167 | A | G | 75 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0059 others(72): Show |
97 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.117+4260T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209167 | |||||||
| chr4:76209188 | G | C | 1 | a0001c0001t0001g0157 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.117+4239C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209188 | |||||||
| chr4:76209437 | T | C | 5 | a0001c0001t0001g0098 a0001c0001t0006g0192 a0001c0001t0008g0181 others(2): Show |
5 | HG03130.hp2 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+3990A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209437 | |||||||
| chr4:76209493 | C | T | 1 | a0001c0001t0007g0113 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.117+3934G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209493 | |||||||
| chr4:76209505 | A | C | 1 | a0001c0001t0002g0245 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.117+3922T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209505 | |||||||
| chr4:76209553 | G | C | 1 | a0001c0001t0004g0243 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.117+3874C>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209553 | |||||||
| chr4:76209554 | A | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
8 | HG01106.hp1 HG01123.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+3873T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209554 | |||||||
| chr4:76209649 | G | A | 10 | a0001c0001t0002g0231 a0001c0001t0004g0042 a0001c0001t0004g0225 others(7): Show |
11 | HG01169.hp1 HG01243.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.117+3778C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209649 | |||||||
| chr4:76209781 | T | C | 15 | a0001c0001t0002g0235 a0001c0001t0002g0240 a0001c0001t0002g0241 others(12): Show |
18 | HG00140.hp2 HG00280.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.117+3646A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209781 | |||||||
| chr4:76209916 | T | C | 95 | a0001c0001t0001g0098 a0001c0001t0001g0160 a0001c0001t0002g0003 others(92): Show |
126 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.117+3511A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209916 | |||||||
| chr4:76209932 | C | T | 1 | a0001c0001t0015g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117+3495G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76209932 | |||||||
| chr4:76210095 | A | C | 1 | a0001c0001t0006g0187 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.117+3332T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76210095 | |||||||
| chr4:76210100 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.117+3327A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76210100 | |||||||
| chr4:76210141 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(56): Show |
82 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.117+3286C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76210141 | |||||||
| chr4:76210251 | G | T | 3 | a0001c0001t0001g0055 a0001c0001t0003g0007 a0001c0001t0003g0056 |
5 | NA18747.hp2 NA18994.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+3176C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76210251 | |||||||
| chr4:76210357 | C | T | 1 | a0002c0003t0024g0202 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.117+3070G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76210357 | |||||||
| chr4:76210917 | T | C | 1 | a0001c0001t0005g0244 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.117+2510A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76210917 | |||||||
| chr4:76210919 | G | A | 22 | a0001c0001t0002g0203 a0001c0001t0002g0205 a0001c0001t0006g0185 others(19): Show |
28 | HG01175.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.117+2508C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76210919 | |||||||
| chr4:76210989 | A | G | 1 | a0001c0001t0002g0207 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.117+2438T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76210989 | |||||||
| chr4:76211207 | T | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(232): Show |
315 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.117+2220A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211207 | |||||||
| chr4:76211270 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.117+2157C>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211270 | |||||||
| chr4:76211271 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.117+2156T>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211271 | |||||||
| chr4:76211300 | A | G | 1 | a0002c0003t0019g0096 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.117+2127T>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211300 | |||||||
| chr4:76211361 | T | TAAGTA | 241 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(238): Show |
321 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.117+2065_117+2066i others(7): Show |
SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211361 | |||||||
| chr4:76211369 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.117+2058C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211369 | |||||||
| chr4:76211398 | T | A | 14 | a0001c0002t0006g0005 a0001c0002t0006g0162 a0001c0002t0006g0165 others(11): Show |
18 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.117+2029A>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211398 | |||||||
| chr4:76211404 | T | G | 72 | a0001c0001t0001g0160 a0001c0001t0002g0003 a0001c0001t0002g0017 others(69): Show |
97 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.117+2023A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211404 | |||||||
| chr4:76211469 | A | C | 1 | a0001c0001t0015g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117+1958T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211469 | |||||||
| chr4:76211481 | C | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(159): Show |
217 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.117+1946G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211481 | |||||||
| chr4:76211786 | C | T | 1 | a0002c0003t0019g0096 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.117+1641G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211786 | |||||||
| chr4:76211895 | T | C | 58 | a0001c0001t0001g0160 a0001c0001t0002g0003 a0001c0001t0002g0017 others(55): Show |
79 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.117+1532A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211895 | |||||||
| chr4:76211926 | A | C | 183 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(180): Show |
242 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.117+1501T>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76211926 | |||||||
| chr4:76212022 | G | A | 14 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(11): Show |
18 | HG00673.hp2 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.117+1405C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212022 | |||||||
| chr4:76212300 | C | T | 3 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 |
3 | HG01109.hp2 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.117+1127G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212300 | |||||||
| chr4:76212426 | G | A | 1 | a0001c0001t0012g0177 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+1001C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212426 | |||||||
| chr4:76212448 | T | C | 1 | a0001c0001t0012g0177 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+979A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212448 | |||||||
| chr4:76212491 | G | A | 1 | a0001c0001t0006g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.117+936C>T | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212491 | |||||||
| chr4:76212492 | C | G | 1 | a0001c0001t0006g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.117+935G>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212492 | |||||||
| chr4:76212576 | C | T | 1 | a0009c0012t0001g0095 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.117+851G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212576 | |||||||
| chr4:76212630 | T | C | 2 | a0001c0001t0002g0287 a0001c0001t0004g0288 |
2 | NA18980.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.117+797A>G | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212630 | |||||||
| chr4:76212762 | T | G | 1 | a0001c0001t0008g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.117+665A>C | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76212762 | |||||||
| chr4:76213058 | TC | T | 108 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0016 others(105): Show |
143 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.117+368delG | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76213058 | |||||||
| chr4:76213130 | TG | T | 52 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0055 others(49): Show |
77 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.117+296delC | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76213130 | |||||||
| chr4:76213257 | C | T | 1 | a0001c0001t0012g0177 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+170G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76213257 | |||||||
| chr4:76213312 | C | T | 4 | a0001c0001t0008g0173 a0001c0001t0008g0174 a0001c0001t0008g0176 others(1): Show |
4 | HG02572.hp2 HG02723.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+115G>A | SCARB2 | ENSG00000138760.11 | transcript | ENST00000264896.8 | protein_coding | 1/11 | chr4 | 76213312 |