Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1071 |
| ensemblid | ENSG00000087237.12 |
| hgncid | 1869 |
| symbol | CETP |
| name | cholesteryl ester transfer protein |
| refseq_nuc | NM_000078.3 |
| refseq_prot | NP_000069.2 |
| ensembl_nuc | ENST00000200676.8 |
| ensembl_prot | ENSP00000200676.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 56961950 |
| end | 56983845 |
| strand | + |
| ver | v1.2 |
| region | chr16:56961950-56983845 |
| region5000 | chr16:56956950-56988845 |
| regionname0 | CETP_chr16_56961950_56983845 |
| regionname5000 | CETP_chr16_56956950_56988845 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 493 | 211 | 29 | 42 | 97 | 13 | 29 | 65 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| a0002 | 1/0 | 493 | 209 | 56 | 26 | 108 | 3 | 15 | 91 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| a0003 | 0/0 | 493 | 12 | 0 | 11 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| a0004 | 0/0 | 493 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| a0005 | 0/0 | 493 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| a0006 | 0/0 | 493 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| a0007 | 0/0 | 493 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| a0008 | 0/0 | 493 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| a0009 | 0/0 | 493 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| a0010 | 0/0 | 493 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| a0011 | 0/0 | 493 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| a0012 | 0/0 | 493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| a0013 | 0/0 | 493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| a0014 | 0/0 | 493 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| a0015 | 0/0 | 493 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| a0016 | 0/0 | 493 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| a0017 | 0/0 | 493 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | MLAAT others(488): Show |
chr16 | 56956950 | 56988845 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1479 | 207 | 29 | 42 | 93 | 13 | 29 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0001c0010 | 0/0 | 1479 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0001c0016 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0002c0002 | 1/0 | 1479 | 168 | 29 | 25 | 101 | 2 | 10 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0002c0003 | 0/0 | 1479 | 17 | 12 | 1 | 0 | 1 | 3 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0002c0005 | 0/0 | 1479 | 9 | 0 | 0 | 7 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0002c0006 | 0/0 | 1479 | 6 | 6 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0002c0009 | 0/0 | 1479 | 5 | 5 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0002c0014 | 0/0 | 1479 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0002c0019 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0002c0025 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0003c0004 | 0/0 | 1479 | 12 | 0 | 11 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0004c0007 | 0/0 | 1479 | 6 | 6 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0005c0008 | 0/0 | 1479 | 5 | 0 | 0 | 5 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0006c0013 | 0/0 | 1479 | 3 | 2 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0007c0011 | 0/0 | 1479 | 3 | 0 | 1 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0008c0012 | 0/0 | 1479 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0009c0017 | 0/0 | 1479 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0009c0018 | 0/0 | 1479 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0010c0023 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0011c0027 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0012c0021 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0013c0026 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0014c0022 | 0/0 | 1479 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0015c0024 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0016c0020 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 | ||
| a0017c0015 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | ATGCT others(1474): Show |
chr16 | 56956950 | 56988845 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1691 | 207 | 29 | 42 | 93 | 13 | 29 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0001c0010t0001 | 0/0 | 1691 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0001c0016t0001 | 0/0 | 1691 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0002c0002t0001 | 1/0 | 1691 | 130 | 25 | 19 | 77 | 1 | 7 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0002c0002t0002 | 0/0 | 1691 | 37 | 3 | 6 | 24 | 1 | 3 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0002c0002t0003 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0002c0003t0002 | 0/0 | 1691 | 17 | 12 | 1 | 0 | 1 | 3 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0002c0005t0001 | 0/0 | 1691 | 9 | 0 | 0 | 7 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0002c0006t0001 | 0/0 | 1691 | 6 | 6 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0002c0009t0001 | 0/0 | 1691 | 5 | 5 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0002c0014t0001 | 0/0 | 1691 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0002c0019t0001 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0002c0025t0001 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0003c0004t0001 | 0/0 | 1691 | 12 | 0 | 11 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0004c0007t0001 | 0/0 | 1691 | 6 | 6 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0005c0008t0001 | 0/0 | 1691 | 5 | 0 | 0 | 5 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0006c0013t0001 | 0/0 | 1691 | 3 | 2 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0007c0011t0001 | 0/0 | 1691 | 3 | 0 | 1 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0008c0012t0001 | 0/0 | 1691 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0009c0017t0002 | 0/0 | 1691 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0009c0018t0002 | 0/0 | 1691 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0010c0023t0001 | 0/0 | 1691 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0011c0027t0001 | 0/0 | 1691 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0012c0021t0001 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0013c0026t0001 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0014c0022t0002 | 0/0 | 1691 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0015c0024t0001 | 0/0 | 1691 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0016c0020t0001 | 0/0 | 1691 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| a0017c0015t0001 | 0/0 | 1691 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | GGGCC others(1686): Show |
chr16 | 56956950 | 56988845 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 15 | 2 | 2 | 8 | 1 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0002 | 0/0 | 15 | 4 | 3 | 4 | 3 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0005 | 0/0 | 7 | 1 | 0 | 5 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0033 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0060 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0062 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0063 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0065 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0267 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0010t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0010t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0010t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0001c0016t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0003 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0006 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0009 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0014 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0066 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0007 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0002t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0003t0002g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0003t0002g0022 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0003t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0003t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0003t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0003t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0003t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0003t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0003t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0005t0001g0018 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0005t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0005t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0005t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0005t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0005t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0006t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0006t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0006t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0006t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0009t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0009t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0009t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0009t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0009t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0014t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0014t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0019t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0002c0025t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0003c0004t0001g0010 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0003c0004t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0003c0004t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0003c0004t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0003c0004t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0003c0004t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0003c0004t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0003c0004t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0004c0007t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0004c0007t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0004c0007t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0004c0007t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0005c0008t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0005c0008t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0005c0008t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0005c0008t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0006c0013t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0006c0013t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0006c0013t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0007c0011t0001g0059 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0007c0011t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0008c0012t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0008c0012t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0008c0012t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0009c0017t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0009c0018t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0010c0023t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0011c0027t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0012c0021t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0013c0026t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0014c0022t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0015c0024t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0016c0020t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| a0017c0015t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0286 | EUR | GBR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00099 | hp2 | a0002 | c0003 | t0002 | g0022 | EUR | GBR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | FIN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0009 | EUR | FIN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00438 | hp1 | a0002 | c0005 | t0001 | g0208 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00438 | hp2 | a0001 | c0010 | t0001 | g0210 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00733 | hp1 | a0003 | c0004 | t0001 | g0226 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0140 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00741 | hp1 | a0002 | c0003 | t0002 | g0295 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0107 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0294 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0253 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01167 | hp1 | a0003 | c0004 | t0001 | g0046 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0150 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01169 | hp1 | a0003 | c0004 | t0001 | g0163 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0153 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0274 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01255 | hp2 | a0003 | c0004 | t0001 | g0010 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0158 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0148 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0262 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01433 | hp1 | a0010 | c0023 | t0001 | g0004 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0276 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0193 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01891 | hp1 | a0002 | c0006 | t0001 | g0194 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01928 | hp2 | a0003 | c0004 | t0001 | g0010 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01952 | hp1 | a0003 | c0004 | t0001 | g0010 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01975 | hp1 | a0003 | c0004 | t0001 | g0010 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01978 | hp2 | a0007 | c0011 | t0001 | g0221 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0108 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02055 | hp1 | a0008 | c0012 | t0001 | g0195 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02056 | hp2 | a0011 | c0027 | t0001 | g0131 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0202 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02148 | hp2 | a0003 | c0004 | t0001 | g0218 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CDX | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CDX | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CDX | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | CDX | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02258 | hp2 | a0012 | c0021 | t0001 | g0095 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02273 | hp1 | a0003 | c0004 | t0001 | g0109 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02280 | hp1 | a0002 | c0003 | t0002 | g0013 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0241 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02300 | hp1 | a0003 | c0004 | t0001 | g0215 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02451 | hp1 | a0002 | c0003 | t0002 | g0082 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02451 | hp2 | a0002 | c0009 | t0001 | g0178 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0201 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0233 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0188 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02622 | hp2 | a0002 | c0009 | t0001 | g0162 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02630 | hp1 | a0008 | c0012 | t0001 | g0198 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02647 | hp1 | a0004 | c0007 | t0001 | g0027 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0166 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02717 | hp2 | a0002 | c0014 | t0001 | g0098 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02723 | hp1 | a0002 | c0025 | t0001 | g0085 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02735 | hp2 | a0003 | c0004 | t0001 | g0010 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0044 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02818 | hp1 | a0002 | c0009 | t0001 | g0177 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02886 | hp1 | a0002 | c0006 | t0001 | g0055 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02895 | hp1 | a0002 | c0003 | t0002 | g0045 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02896 | hp1 | a0002 | c0003 | t0002 | g0013 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02897 | hp2 | a0002 | c0003 | t0002 | g0045 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02965 | hp1 | a0006 | c0013 | t0001 | g0167 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0235 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02970 | hp1 | a0002 | c0006 | t0001 | g0055 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0176 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0191 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03017 | hp1 | a0014 | c0022 | t0002 | g0120 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0165 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0234 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0068 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03130 | hp1 | a0002 | c0003 | t0002 | g0013 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03130 | hp2 | a0002 | c0009 | t0001 | g0090 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03139 | hp1 | a0008 | c0012 | t0001 | g0197 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03195 | hp1 | a0002 | c0019 | t0001 | g0240 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0280 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0181 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0067 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03453 | hp1 | a0002 | c0006 | t0001 | g0054 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0214 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03486 | hp2 | a0002 | c0003 | t0002 | g0022 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03490 | hp1 | a0002 | c0003 | t0002 | g0036 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03491 | hp1 | a0007 | c0011 | t0001 | g0059 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03492 | hp2 | a0007 | c0011 | t0001 | g0059 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03516 | hp1 | a0002 | c0003 | t0002 | g0013 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03516 | hp2 | a0002 | c0014 | t0001 | g0099 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03540 | hp1 | a0004 | c0007 | t0001 | g0027 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03540 | hp2 | a0002 | c0003 | t0002 | g0084 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03579 | hp2 | a0006 | c0013 | t0001 | g0172 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03654 | hp1 | a0002 | c0003 | t0002 | g0072 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0266 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03704 | hp2 | a0002 | c0005 | t0001 | g0018 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03710 | hp2 | a0009 | c0017 | t0002 | g0232 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03831 | hp1 | a0002 | c0003 | t0002 | g0036 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0159 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03927 | hp1 | a0009 | c0018 | t0002 | g0229 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0130 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG04184 | hp2 | a0002 | c0005 | t0001 | g0073 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0083 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0009 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0128 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0279 | AFR | YRI | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0174 | AFR | YRI | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18612 | hp2 | a0001 | c0010 | t0001 | g0213 | EAS | CHB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | YRI | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18940 | hp1 | a0005 | c0008 | t0001 | g0245 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18941 | hp1 | a0002 | c0005 | t0001 | g0212 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18942 | hp1 | a0002 | c0005 | t0001 | g0211 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18952 | hp2 | a0005 | c0008 | t0001 | g0040 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18963 | hp1 | a0015 | c0024 | t0001 | g0186 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18971 | hp2 | a0002 | c0005 | t0001 | g0018 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18977 | hp2 | a0001 | c0010 | t0001 | g0209 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18978 | hp2 | a0005 | c0008 | t0001 | g0004 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18990 | hp2 | a0016 | c0020 | t0001 | g0287 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18991 | hp1 | a0005 | c0008 | t0001 | g0251 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19030 | hp1 | a0004 | c0007 | t0001 | g0171 | AFR | LWK | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19043 | hp2 | a0002 | c0006 | t0001 | g0179 | AFR | LWK | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19056 | hp1 | a0002 | c0005 | t0001 | g0018 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19060 | hp2 | a0001 | c0016 | t0001 | g0281 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19066 | hp2 | a0002 | c0005 | t0001 | g0018 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19075 | hp1 | a0002 | c0005 | t0001 | g0207 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19077 | hp1 | a0017 | c0015 | t0001 | g0017 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19080 | hp1 | a0005 | c0008 | t0001 | g0040 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0301 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19240 | hp1 | a0004 | c0007 | t0001 | g0169 | AFR | YRI | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | ASW | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA20129 | hp2 | a0002 | c0002 | t0003 | g0088 | AFR | ASW | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0139 | EUR | TSI | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | GIH | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0119 | SAS | GIH | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01123 | hp1 | a0003 | c0004 | t0001 | g0110 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG01123 | hp2 | a0006 | c0013 | t0001 | g0168 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02109 | hp1 | a0002 | c0009 | t0001 | g0091 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02109 | hp2 | a0002 | c0003 | t0002 | g0297 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02486 | hp2 | a0002 | c0003 | t0002 | g0022 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG02559 | hp2 | a0013 | c0026 | t0001 | g0199 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG03471 | hp2 | a0002 | c0006 | t0001 | g0054 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG06807 | hp1 | a0002 | c0003 | t0002 | g0296 | AFR | USA | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| HG06807 | hp2 | a0004 | c0007 | t0001 | g0027 | AFR | USA | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA20300 | hp1 | a0004 | c0007 | t0001 | g0170 | AFR | USA | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0093 | AFR | USA | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0267 | REF | REF | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0283 | REF | REF | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:56962023 | C | G | 2 | a0004 a0006 |
9 | HG01123.hp2 HG02647.hp1 HG02965.hp1 others(6): Show |
missense_variant | MODERATE | c.44C>G | p.Ala15Gly | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/16 | 74/1691 | 44/1482 | 15/493 | chr16 | 56962023 | |||
| chr16:56962047 | C | T | 1 | a0011 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.68C>T | p.Ser23Leu | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/16 | 98/1691 | 68/1482 | 23/493 | chr16 | 56962047 | |||
| chr16:56969934 | C | T | 2 | a0008 a0013 |
4 | HG02055.hp1 HG02559.hp2 HG02630.hp1 others(1): Show |
missense_variant | MODERATE | c.460C>T | p.Arg154Trp | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/16 | 490/1691 | 460/1482 | 154/493 | chr16 | 56969934 | |||
| chr16:56971324 | T | G | 1 | a0017 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.601T>G | p.Cys201Gly | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/16 | 631/1691 | 601/1482 | 201/493 | chr16 | 56971324 | |||
| chr16:56971996 | C | A | 1 | a0009 | 2 | HG03710.hp2 HG03927.hp1 |
missense_variant | MODERATE | c.663C>A | p.Ser221Arg | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/16 | 693/1691 | 663/1482 | 221/493 | chr16 | 56971996 | |||
| chr16:56973364 | C | A | 1 | a0016 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.784C>A | p.Leu262Ile | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/16 | 814/1691 | 784/1482 | 262/493 | chr16 | 56973364 | |||
| chr16:56981164 | G | A | 1 | a0012 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1153G>A | p.Val385Met | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/16 | 1183/1691 | 1153/1482 | 385/493 | chr16 | 56981164 | |||
| chr16:56981179 | G | C | 2 | a0003 a0007 |
15 | HG00733.hp1 HG01123.hp1 HG01167.hp1 others(12): Show |
missense_variant | MODERATE | c.1168G>C | p.Ala390Pro | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/16 | 1198/1691 | 1168/1482 | 390/493 | chr16 | 56981179 | |||
| chr16:56981201 | T | A | 1 | a0014 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1190T>A | p.Leu397His | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/16 | 1220/1691 | 1190/1482 | 397/493 | chr16 | 56981201 | |||
| chr16:56982180 | G | A | 9 | a0001 a0003 a0005 others(6): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
missense_variant | MODERATE | c.1264G>A | p.Val422Ile | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/16 | 1294/1691 | 1264/1482 | 422/493 | chr16 | 56982180 | |||
| chr16:56983331 | G | A | 1 | a0010 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.1327G>A | p.Glu443Lys | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 15/16 | 1357/1691 | 1327/1482 | 443/493 | chr16 | 56983331 | |||
| chr16:56983370 | A | C | 1 | a0015 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.1366A>C | p.Ser456Arg | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 15/16 | 1396/1691 | 1366/1482 | 456/493 | chr16 | 56983370 | |||
| chr16:56983380 | A | G | 1 | a0005 | 5 | NA18940.hp1 NA18952.hp2 NA18978.hp2 others(2): Show |
missense_variant | MODERATE | c.1376A>G | p.Asp459Gly | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 15/16 | 1406/1691 | 1376/1482 | 459/493 | chr16 | 56983380 | |||
| chr16:56983407 | G | A | 1 | a0003 | 12 | HG00733.hp1 HG01123.hp1 HG01167.hp1 others(9): Show |
missense_variant | MODERATE | c.1403G>A | p.Arg468Gln | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 15/16 | 1433/1691 | 1403/1482 | 468/493 | chr16 | 56983407 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:56962045 | C | A | 1 | a0002c0006 | 6 | HG01891.hp1 HG02886.hp1 HG02970.hp1 others(3): Show |
synonymous_variant | LOW | c.66C>A | p.Thr22Thr | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/16 | 96/1691 | 66/1482 | 22/493 | chr16 | 56962045 | |||
| chr16:56971039 | G | A | 2 | a0001c0010 a0002c0005 |
12 | HG00438.hp1 HG00438.hp2 HG03704.hp2 others(9): Show |
synonymous_variant | LOW | c.534G>A | p.Gly178Gly | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 6/16 | 564/1691 | 534/1482 | 178/493 | chr16 | 56971039 | |||
| chr16:56971359 | C | T | 1 | a0002c0014 | 2 | HG02717.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.636C>T | p.Ala212Ala | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/16 | 666/1691 | 636/1482 | 212/493 | chr16 | 56971359 | |||
| chr16:56971362 | T | C | 1 | a0001c0016 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.639T>C | p.Asp213Asp | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/16 | 669/1691 | 639/1482 | 213/493 | chr16 | 56971362 | |||
| chr16:56973336 | T | C | 1 | a0002c0019 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.756T>C | p.His252His | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/16 | 786/1691 | 756/1482 | 252/493 | chr16 | 56973336 | |||
| chr16:56973441 | C | T | 2 | a0002c0003 a0009c0018 |
18 | HG00099.hp2 HG00741.hp1 HG02109.hp2 others(15): Show |
synonymous_variant | LOW | c.861C>T | p.Phe287Phe | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/16 | 891/1691 | 861/1482 | 287/493 | chr16 | 56973441 | |||
| chr16:56981172 | C | G | 1 | a0002c0009 | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
synonymous_variant | LOW | c.1161C>G | p.Thr387Thr | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/16 | 1191/1691 | 1161/1482 | 387/493 | chr16 | 56981172 | |||
| chr16:56981172 | C | T | 2 | a0002c0025 a0013c0026 |
2 | HG02559.hp2 HG02723.hp1 |
synonymous_variant | LOW | c.1161C>T | p.Thr387Thr | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/16 | 1191/1691 | 1161/1482 | 387/493 | chr16 | 56981172 | |||
| chr16:56982215 | G | A | 1 | a0002c0009 | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
synonymous_variant | LOW | c.1299G>A | p.Val433Val | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/16 | 1329/1691 | 1299/1482 | 433/493 | chr16 | 56982215 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:56983711 | C | G | 1 | a0002c0002t0003 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*45C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 16/16 | 45 | chr16 | 56983711 | ||||||
| chr16:56983750 | G | A | 5 | a0002c0002t0002 a0002c0003t0002 a0009c0017t0002 others(2): Show |
57 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*84G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 16/16 | 84 | chr16 | 56983750 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:56962130 | G | A | 1 | a0002c0002t0001g0067 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.118+33G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962130 | |||||||
| chr16:56962148 | C | A | 1 | a0002c0002t0001g0068 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.118+51C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962148 | |||||||
| chr16:56962155 | G | A | 4 | a0001c0001t0001g0020 a0002c0002t0001g0069 a0002c0002t0001g0070 others(1): Show |
6 | HG00544.hp1 HG02155.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+58G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962155 | |||||||
| chr16:56962192 | C | A | 22 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0037 others(19): Show |
36 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.118+95C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962192 | |||||||
| chr16:56962246 | T | C | 172 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0015 others(169): Show |
253 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.118+149T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962246 | |||||||
| chr16:56962299 | G | A | 114 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0025 others(111): Show |
170 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.118+202G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962299 | |||||||
| chr16:56962367 | C | T | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | HG01081.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.118+270C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962367 | |||||||
| chr16:56962376 | G | A | 114 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0025 others(111): Show |
170 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.118+279G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962376 | |||||||
| chr16:56962391 | T | A | 1 | a0001c0001t0001g0200 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.118+294T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962391 | |||||||
| chr16:56962677 | G | A | 1 | a0002c0002t0001g0201 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.119-333G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962677 | |||||||
| chr16:56962733 | GCC | G | 107 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0025 others(104): Show |
161 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.119-274_119-273del others(2): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 56962733 | ||||||
| chr16:56962737 | C | A | 107 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0025 others(104): Show |
161 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.119-273C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962737 | |||||||
| chr16:56962751 | G | A | 3 | a0002c0002t0001g0202 a0002c0003t0002g0072 a0006c0013t0001g0167 |
3 | HG02145.hp1 HG02965.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.119-259G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962751 | |||||||
| chr16:56962795 | G | T | 2 | a0001c0001t0001g0050 a0002c0002t0001g0166 |
3 | HG02647.hp2 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.119-215G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962795 | |||||||
| chr16:56962860 | C | A | 1 | a0002c0002t0001g0086 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.119-150C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962860 | |||||||
| chr16:56963160 | A | G | 8 | a0001c0001t0001g0196 a0002c0006t0001g0054 a0002c0006t0001g0055 others(5): Show |
10 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+36A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963160 | |||||||
| chr16:56963168 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.233+44G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963168 | |||||||
| chr16:56963277 | C | A | 1 | a0002c0002t0003g0088 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.233+153C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963277 | |||||||
| chr16:56963321 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0038 others(54): Show |
92 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.233+197G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963321 | |||||||
| chr16:56963406 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0173 a0002c0002t0001g0175 others(2): Show |
7 | HG02615.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+282G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963406 | |||||||
| chr16:56963437 | C | CA | 78 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0028 others(75): Show |
119 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.233+315dupA | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56963437 | ||||||
| chr16:56963456 | T | A | 1 | a0002c0002t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.233+332T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963456 | |||||||
| chr16:56963457 | A | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(205): Show |
313 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.233+333A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963457 | |||||||
| chr16:56963458 | A | T | 1 | a0001c0001t0001g0049 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.233+334A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963458 | |||||||
| chr16:56963639 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(194): Show |
299 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.233+515C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963639 | |||||||
| chr16:56963744 | G | C | 34 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0037 others(31): Show |
52 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.233+620G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963744 | |||||||
| chr16:56963990 | T | TTTTA | 8 | a0001c0001t0001g0087 a0001c0001t0001g0164 a0001c0001t0001g0293 others(5): Show |
8 | HG01169.hp1 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+917_233+920dup others(4): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56963990 | ||||||
| chr16:56963990 | TTTTA | T | 113 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(110): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.233+917_233+920del others(4): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56963990 | ||||||
| chr16:56963990 | TTTTATTT others(1): Show |
T | 52 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0025 others(49): Show |
83 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.233+913_233+920del others(8): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56963990 | ||||||
| chr16:56963990 | TTTTATTT others(5): Show |
T | 10 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0242 others(7): Show |
10 | HG01884.hp1 HG02165.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+909_233+920del others(12): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56963990 | ||||||
| chr16:56963990 | TTTTATTT others(13): Show |
T | 11 | a0001c0010t0001g0209 a0001c0010t0001g0210 a0001c0010t0001g0213 others(8): Show |
14 | HG00438.hp1 HG00438.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+901_233+920del others(20): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56963990 | ||||||
| chr16:56963990 | TTTTATTT others(17): Show |
T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0028 others(38): Show |
74 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.233+897_233+920del others(24): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56963990 | ||||||
| chr16:56963994 | A | T | 4 | a0002c0003t0002g0022 a0002c0003t0002g0045 a0002c0003t0002g0082 others(1): Show |
5 | HG02451.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+870A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963994 | |||||||
| chr16:56964002 | ATTTATTT others(18): Show |
A | 1 | a0002c0002t0001g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.233+881_233+905del others(25): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56964002 | ||||||
| chr16:56964034 | ATTTATTT others(2): Show |
A | 6 | a0001c0001t0001g0096 a0001c0001t0001g0102 a0002c0002t0001g0024 others(3): Show |
9 | HG00621.hp2 NA18942.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.233+912_233+920del others(9): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56964034 | ||||||
| chr16:56964108 | C | G | 1 | a0002c0002t0001g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.233+984C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56964108 | |||||||
| chr16:56964425 | T | A | 1 | a0001c0001t0001g0243 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.233+1301T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56964425 | |||||||
| chr16:56964656 | ACCCGCGC others(4): Show |
A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
8 | NA18944.hp2 NA18953.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.233+1533_233+1543d others(13): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56964656 | |||||||
| chr16:56964660 | G | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0019 others(73): Show |
125 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.233+1536G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56964660 | |||||||
| chr16:56964797 | C | T | 2 | a0008c0012t0001g0198 a0013c0026t0001g0199 |
2 | HG02559.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.233+1673C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56964797 | |||||||
| chr16:56964849 | T | G | 23 | a0001c0001t0001g0025 a0002c0002t0001g0003 a0002c0002t0001g0014 others(20): Show |
39 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.233+1725T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56964849 | |||||||
| chr16:56964982 | G | A | 1 | a0002c0002t0002g0258 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.233+1858G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56964982 | |||||||
| chr16:56965006 | A | G | 79 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0043 others(76): Show |
114 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(111): Show |
intron_variant | MODIFIER | c.233+1882A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965006 | |||||||
| chr16:56965015 | G | A | 2 | a0002c0009t0001g0177 a0002c0009t0001g0178 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.233+1891G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965015 | |||||||
| chr16:56965040 | A | T | 2 | a0002c0014t0001g0098 a0002c0014t0001g0099 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.233+1916A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965040 | |||||||
| chr16:56965133 | G | C | 1 | a0001c0001t0001g0074 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.233+2009G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965133 | |||||||
| chr16:56965146 | C | T | 1 | a0002c0002t0001g0201 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.233+2022C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965146 | |||||||
| chr16:56965188 | T | A | 4 | a0008c0012t0001g0195 a0008c0012t0001g0197 a0008c0012t0001g0198 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+2064T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965188 | |||||||
| chr16:56965267 | C | T | 1 | a0002c0006t0001g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.233+2143C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965267 | |||||||
| chr16:56965272 | AT | A | 20 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0037 others(17): Show |
33 | HG00099.hp2 HG00423.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.233+2149delT | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965272 | |||||||
| chr16:56965346 | A | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0025 others(94): Show |
151 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.233+2222A>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965346 | |||||||
| chr16:56965416 | C | T | 78 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0043 others(75): Show |
113 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.233+2292C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965416 | |||||||
| chr16:56965440 | TC | T | 43 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0037 others(40): Show |
65 | HG00099.hp2 HG00423.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.233+2317delC | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965440 | |||||||
| chr16:56965470 | G | A | 2 | a0002c0014t0001g0098 a0002c0014t0001g0099 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.233+2346G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965470 | |||||||
| chr16:56965651 | C | A | 3 | a0002c0002t0001g0176 a0002c0002t0001g0193 a0002c0025t0001g0085 |
3 | HG01884.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.233+2527C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965651 | |||||||
| chr16:56965866 | C | T | 7 | a0002c0002t0001g0023 a0002c0002t0001g0029 a0002c0002t0001g0092 others(4): Show |
11 | HG02257.hp1 HG02622.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.233+2742C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965866 | |||||||
| chr16:56965866 | CG | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0028 others(54): Show |
95 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+2744delG | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56965866 | ||||||
| chr16:56965925 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.233+2801C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965925 | |||||||
| chr16:56966036 | C | T | 1 | a0001c0010t0001g0213 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.233+2912C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966036 | |||||||
| chr16:56966037 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(224): Show |
340 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.233+2913A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966037 | |||||||
| chr16:56966048 | G | C | 2 | a0002c0002t0001g0175 a0002c0002t0002g0174 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.233+2924G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966048 | |||||||
| chr16:56966072 | T | TA | 7 | a0002c0002t0001g0104 a0002c0002t0002g0279 a0002c0002t0002g0280 others(4): Show |
9 | HG01123.hp2 HG02647.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.233+2956dupA | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56966072 | ||||||
| chr16:56966090 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.233+2966G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966090 | |||||||
| chr16:56966232 | G | A | 2 | a0002c0002t0002g0119 a0014c0022t0002g0120 |
2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.233+3108G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966232 | |||||||
| chr16:56966233 | C | T | 19 | a0001c0001t0001g0025 a0002c0002t0001g0003 a0002c0002t0001g0014 others(16): Show |
35 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.233+3109C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966233 | |||||||
| chr16:56966234 | T | C | 1 | a0002c0003t0002g0072 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.233+3110T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966234 | |||||||
| chr16:56966279 | A | G | 2 | a0002c0009t0001g0177 a0002c0009t0001g0178 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.234-3107A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966279 | |||||||
| chr16:56966297 | C | A | 8 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0111 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.234-3089C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966297 | |||||||
| chr16:56966300 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.234-3086G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966300 | |||||||
| chr16:56966309 | C | T | 3 | a0002c0002t0001g0176 a0002c0002t0001g0193 a0002c0025t0001g0085 |
3 | HG01884.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.234-3077C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966309 | |||||||
| chr16:56966330 | A | G | 14 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0187 others(11): Show |
19 | HG03942.hp1 HG04115.hp2 NA18612.hp1 others(16): Show |
intron_variant | MODIFIER | c.234-3056A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966330 | |||||||
| chr16:56966364 | T | A | 5 | a0002c0002t0001g0034 a0002c0002t0001g0035 a0002c0002t0001g0039 others(2): Show |
8 | HG00558.hp1 HG02071.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.234-3022T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966364 | |||||||
| chr16:56966372 | G | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(163): Show |
255 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.234-3014G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966372 | |||||||
| chr16:56966463 | G | T | 1 | a0002c0002t0002g0280 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.234-2923G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966463 | |||||||
| chr16:56966484 | C | T | 1 | a0002c0002t0001g0145 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.234-2902C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966484 | |||||||
| chr16:56966485 | G | A | 2 | a0002c0009t0001g0177 a0002c0009t0001g0178 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.234-2901G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966485 | |||||||
| chr16:56966524 | T | C | 1 | a0012c0021t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.234-2862T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966524 | |||||||
| chr16:56966593 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.234-2793T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966593 | |||||||
| chr16:56966598 | T | G | 1 | a0002c0002t0001g0104 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.234-2788T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966598 | |||||||
| chr16:56966599 | G | T | 1 | a0002c0002t0001g0104 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.234-2787G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966599 | |||||||
| chr16:56966761 | G | A | 1 | a0002c0005t0001g0207 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.234-2625G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966761 | |||||||
| chr16:56966764 | TA | T | 18 | a0001c0001t0001g0025 a0002c0002t0001g0003 a0002c0002t0001g0014 others(15): Show |
34 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.234-2620delA | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56966764 | ||||||
| chr16:56966768 | CT | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0025 others(96): Show |
154 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.234-2602delT | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56966768 | ||||||
| chr16:56966770 | T | C | 1 | a0002c0002t0001g0105 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.234-2616T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966770 | |||||||
| chr16:56966784 | T | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0025 others(81): Show |
138 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.234-2602T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966784 | |||||||
| chr16:56966973 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0028 others(53): Show |
93 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.234-2413G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966973 | |||||||
| chr16:56967026 | G | A | 16 | a0001c0001t0001g0058 a0001c0001t0001g0216 a0001c0001t0001g0217 others(13): Show |
22 | HG00642.hp2 HG00733.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.234-2360G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967026 | |||||||
| chr16:56967119 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.234-2267G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967119 | |||||||
| chr16:56967173 | C | G | 6 | a0002c0002t0002g0279 a0002c0002t0002g0280 a0004c0007t0001g0027 others(3): Show |
8 | HG01123.hp2 HG02647.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.234-2213C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967173 | |||||||
| chr16:56967191 | T | C | 2 | a0002c0009t0001g0177 a0002c0009t0001g0178 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.234-2195T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967191 | |||||||
| chr16:56967202 | C | A | 1 | a0001c0001t0001g0227 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.234-2184C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967202 | |||||||
| chr16:56967304 | C | T | 81 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0043 others(78): Show |
117 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.234-2082C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967304 | |||||||
| chr16:56967338 | T | C | 9 | a0002c0002t0001g0067 a0002c0002t0001g0175 a0002c0002t0001g0176 others(6): Show |
9 | HG01884.hp1 HG02717.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.234-2048T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967338 | |||||||
| chr16:56967342 | T | TCACA | 55 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0028 others(52): Show |
93 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.234-2041_234-2038d others(6): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56967342 | ||||||
| chr16:56967349 | A | C | 2 | a0002c0005t0001g0208 a0003c0004t0001g0215 |
2 | HG00438.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.234-2037A>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967349 | |||||||
| chr16:56967362 | AC | A | 48 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0043 others(45): Show |
74 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.234-2023delC | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967362 | |||||||
| chr16:56967363 | C | A | 32 | a0001c0001t0001g0049 a0001c0001t0001g0121 a0001c0001t0001g0136 others(29): Show |
42 | HG00673.hp1 HG00738.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.234-2023C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967363 | |||||||
| chr16:56967425 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.234-1961G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967425 | |||||||
| chr16:56967475 | T | G | 20 | a0001c0001t0001g0025 a0002c0002t0001g0003 a0002c0002t0001g0014 others(17): Show |
36 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.234-1911T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967475 | |||||||
| chr16:56967526 | G | A | 81 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0043 others(78): Show |
117 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.234-1860G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967526 | |||||||
| chr16:56967604 | G | A | 20 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0037 others(17): Show |
33 | HG00099.hp2 HG00423.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.234-1782G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967604 | |||||||
| chr16:56967654 | C | CA | 19 | a0001c0001t0001g0079 a0001c0001t0001g0115 a0001c0001t0001g0216 others(16): Show |
20 | HG00438.hp1 HG01109.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.234-1715dupA | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56967654 | ||||||
| chr16:56967654 | CA | C | 9 | a0002c0002t0001g0067 a0002c0002t0001g0175 a0002c0002t0001g0214 others(6): Show |
9 | HG02451.hp2 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.234-1715delA | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56967654 | ||||||
| chr16:56967661 | A | G | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0111 |
3 | HG02630.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.234-1725A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967661 | |||||||
| chr16:56967668 | AAAAC | A | 8 | a0002c0002t0001g0112 a0002c0002t0001g0114 a0002c0002t0001g0155 others(5): Show |
8 | HG00642.hp1 HG02055.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.234-1715_234-1712d others(6): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56967668 | ||||||
| chr16:56967669 | AAAC | A | 76 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0043 others(73): Show |
111 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.234-1714_234-1712d others(5): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56967669 | ||||||
| chr16:56967672 | C | A | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.234-1714C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967672 | |||||||
| chr16:56967680 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0077 |
5 | NA18947.hp1 NA18973.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-1706T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967680 | |||||||
| chr16:56967792 | C | T | 2 | a0002c0006t0001g0179 a0004c0007t0001g0170 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.234-1594C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967792 | |||||||
| chr16:56967795 | A | G | 1 | a0012c0021t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.234-1591A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967795 | |||||||
| chr16:56967882 | G | A | 7 | a0002c0002t0001g0026 a0002c0002t0001g0042 a0002c0002t0001g0117 others(4): Show |
10 | HG01346.hp1 HG01981.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.234-1504G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967882 | |||||||
| chr16:56967900 | AGTGAACT | A | 4 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0177 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-1481_234-1475d others(9): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56967900 | ||||||
| chr16:56967977 | TA | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.234-1396delA | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56967977 | ||||||
| chr16:56968053 | T | A | 8 | a0001c0001t0001g0033 a0001c0001t0001g0097 a0001c0001t0001g0261 others(5): Show |
10 | HG00423.hp2 HG02015.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1333T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968053 | |||||||
| chr16:56968073 | A | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.234-1313A>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968073 | |||||||
| chr16:56968180 | C | A | 1 | a0006c0013t0001g0168 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.234-1206C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968180 | |||||||
| chr16:56968189 | A | G | 1 | a0001c0001t0001g0278 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.234-1197A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968189 | |||||||
| chr16:56968206 | G | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0144 |
3 | HG01981.hp2 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.234-1180G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968206 | |||||||
| chr16:56968209 | A | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0144 |
3 | HG01981.hp2 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.234-1177A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968209 | |||||||
| chr16:56968240 | T | C | 36 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0052 others(33): Show |
53 | HG00099.hp2 HG00741.hp1 HG01515.hp2 others(50): Show |
intron_variant | MODIFIER | c.234-1146T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968240 | |||||||
| chr16:56968330 | C | T | 40 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0052 others(37): Show |
58 | HG00099.hp2 HG00741.hp1 HG01515.hp2 others(55): Show |
intron_variant | MODIFIER | c.234-1056C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968330 | |||||||
| chr16:56968336 | C | G | 4 | a0002c0002t0001g0241 a0002c0006t0001g0055 a0002c0006t0001g0179 others(1): Show |
5 | HG02280.hp2 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-1050C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968336 | |||||||
| chr16:56968346 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0077 a0001c0001t0001g0080 others(1): Show |
7 | HG00423.hp1 NA18947.hp1 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.234-1040C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968346 | |||||||
| chr16:56968359 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.234-1027T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968359 | |||||||
| chr16:56968376 | G | A | 1 | a0002c0003t0002g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.234-1010G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968376 | |||||||
| chr16:56968387 | A | G | 3 | a0002c0002t0001g0176 a0002c0002t0001g0193 a0002c0025t0001g0085 |
3 | HG01884.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.234-999A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968387 | |||||||
| chr16:56968463 | A | G | 4 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0177 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-923A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968463 | |||||||
| chr16:56968478 | C | T | 1 | a0002c0003t0002g0084 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.234-908C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968478 | |||||||
| chr16:56968492 | C | A | 84 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.234-894C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968492 | |||||||
| chr16:56968729 | C | CT | 34 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0079 others(31): Show |
51 | HG00099.hp2 HG00733.hp2 HG02109.hp2 others(48): Show |
intron_variant | MODIFIER | c.234-642dupT | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56968729 | ||||||
| chr16:56968729 | CT | C | 24 | a0001c0001t0001g0025 a0002c0002t0001g0003 a0002c0002t0001g0014 others(21): Show |
40 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.234-642delT | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56968729 | ||||||
| chr16:56968751 | C | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
258 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.234-635C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968751 | |||||||
| chr16:56968798 | A | G | 4 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0111 others(1): Show |
4 | HG02145.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-588A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968798 | |||||||
| chr16:56968820 | T | G | 246 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(243): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.234-566T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968820 | |||||||
| chr16:56969113 | G | T | 20 | a0001c0001t0001g0025 a0002c0002t0001g0003 a0002c0002t0001g0014 others(17): Show |
36 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.234-273G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56969113 | |||||||
| chr16:56969131 | C | T | 6 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0177 others(3): Show |
6 | HG02109.hp1 HG02451.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.234-255C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56969131 | |||||||
| chr16:56969234 | T | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0028 others(19): Show |
49 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.234-152T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56969234 | |||||||
| chr16:56969278 | G | A | 1 | a0002c0002t0001g0107 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.234-108G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56969278 | |||||||
| chr16:56969322 | A | T | 1 | a0002c0009t0001g0162 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.234-64A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56969322 | |||||||
| chr16:56969338 | C | A | 9 | a0001c0010t0001g0209 a0001c0010t0001g0210 a0001c0010t0001g0213 others(6): Show |
12 | HG00438.hp1 HG00438.hp2 HG03704.hp2 others(9): Show |
intron_variant | MODIFIER | c.234-48C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56969338 | |||||||
| chr16:56969549 | T | C | 2 | a0002c0002t0001g0175 a0002c0002t0002g0174 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.368+29T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 3/15 | chr16 | 56969549 | |||||||
| chr16:56969811 | G | T | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(283): Show |
436 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(433): Show |
intron_variant | MODIFIER | c.440-103G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 4/15 | chr16 | 56969811 | |||||||
| chr16:56969877 | G | A | 1 | a0002c0002t0002g0119 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.440-37G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 4/15 | chr16 | 56969877 | |||||||
| chr16:56970065 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(287): Show |
440 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(437): Show |
intron_variant | MODIFIER | c.527+64T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970065 | |||||||
| chr16:56970068 | T | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(296): Show |
452 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(449): Show |
intron_variant | MODIFIER | c.527+67T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970068 | |||||||
| chr16:56970402 | G | A | 1 | a0002c0014t0001g0098 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.527+401G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970402 | |||||||
| chr16:56970547 | G | A | 6 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0177 others(3): Show |
6 | HG02109.hp1 HG02451.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.528-486G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970547 | |||||||
| chr16:56970551 | C | T | 1 | a0002c0002t0002g0165 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.528-482C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970551 | |||||||
| chr16:56970576 | C | T | 1 | a0002c0002t0001g0094 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.528-457C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970576 | |||||||
| chr16:56970750 | C | T | 6 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0177 others(3): Show |
6 | HG02109.hp1 HG02451.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.528-283C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970750 | |||||||
| chr16:56970756 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.528-277C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970756 | |||||||
| chr16:56970757 | A | G | 1 | a0003c0004t0001g0226 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.528-276A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970757 | |||||||
| chr16:56970835 | A | G | 6 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0177 others(3): Show |
6 | HG02109.hp1 HG02451.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.528-198A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970835 | |||||||
| chr16:56970859 | A | G | 2 | a0002c0002t0002g0160 a0002c0002t0002g0161 |
2 | NA19001.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.528-174A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970859 | |||||||
| chr16:56970898 | G | A | 1 | a0004c0007t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.528-135G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970898 | |||||||
| chr16:56970956 | G | C | 1 | a0001c0001t0001g0247 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.528-77G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970956 | |||||||
| chr16:56970977 | G | A | 94 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0043 others(91): Show |
133 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.528-56G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970977 | |||||||
| chr16:56970999 | G | A | 1 | a0002c0002t0001g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.528-34G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970999 | |||||||
| chr16:56971389 | C | T | 85 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0043 others(82): Show |
121 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(118): Show |
splice_region_variant&intron_variant | LOW | c.658+8C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971389 | |||||||
| chr16:56971468 | A | G | 1 | a0002c0002t0003g0088 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.658+87A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971468 | |||||||
| chr16:56971513 | T | C | 8 | a0002c0002t0001g0023 a0002c0002t0001g0029 a0002c0002t0001g0092 others(5): Show |
12 | HG02257.hp1 HG02622.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.658+132T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971513 | |||||||
| chr16:56971567 | C | A | 85 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0043 others(82): Show |
121 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(118): Show |
intron_variant | MODIFIER | c.658+186C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971567 | |||||||
| chr16:56971638 | C | T | 26 | a0001c0001t0001g0049 a0001c0001t0001g0121 a0001c0001t0001g0136 others(23): Show |
35 | HG00673.hp1 HG00738.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.658+257C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971638 | |||||||
| chr16:56971690 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.659-302T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971690 | |||||||
| chr16:56971708 | T | C | 39 | a0001c0001t0001g0025 a0001c0001t0001g0100 a0001c0001t0001g0101 others(36): Show |
58 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.659-284T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971708 | |||||||
| chr16:56971852 | C | G | 10 | a0002c0002t0001g0067 a0002c0002t0001g0175 a0002c0002t0002g0174 others(7): Show |
10 | HG02055.hp1 HG02559.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.659-140C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971852 | |||||||
| chr16:56971970 | C | T | 10 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0111 others(7): Show |
10 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.659-22C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971970 | |||||||
| chr16:56972160 | G | A | 2 | a0002c0003t0002g0295 a0002c0003t0002g0296 |
2 | HG00741.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.750+77G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972160 | |||||||
| chr16:56972387 | GC | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(203): Show |
312 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.750+313delC | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 56972387 | ||||||
| chr16:56972393 | C | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.750+310C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972393 | |||||||
| chr16:56972394 | C | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0237 |
2 | HG01109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.750+311C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972394 | |||||||
| chr16:56972402 | G | A | 1 | a0002c0002t0002g0160 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.750+319G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972402 | |||||||
| chr16:56972440 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.750+357A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972440 | |||||||
| chr16:56972466 | A | G | 42 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0028 others(39): Show |
75 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.750+383A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972466 | |||||||
| chr16:56972493 | C | G | 1 | a0004c0007t0001g0170 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.750+410C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972493 | |||||||
| chr16:56972533 | C | T | 1 | a0002c0003t0002g0297 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.750+450C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972533 | |||||||
| chr16:56972535 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.750+452C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972535 | |||||||
| chr16:56972678 | C | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0028 others(74): Show |
119 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.750+595C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972678 | |||||||
| chr16:56972684 | G | C | 2 | a0002c0002t0002g0156 a0002c0002t0002g0258 |
2 | HG02015.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.750+601G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972684 | |||||||
| chr16:56972806 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.751-525C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972806 | |||||||
| chr16:56972917 | T | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.751-414T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972917 | |||||||
| chr16:56972970 | C | T | 1 | a0002c0002t0001g0068 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.751-361C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972970 | |||||||
| chr16:56973023 | G | A | 1 | a0002c0002t0001g0246 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.751-308G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56973023 | |||||||
| chr16:56973027 | T | A | 2 | a0002c0002t0001g0176 a0002c0002t0001g0193 |
2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.751-304T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56973027 | |||||||
| chr16:56973038 | G | A | 2 | a0002c0002t0001g0176 a0002c0002t0001g0193 |
2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.751-293G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56973038 | |||||||
| chr16:56973128 | C | T | 2 | a0001c0001t0001g0056 a0002c0002t0001g0254 |
3 | HG01070.hp1 HG01071.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.751-203C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56973128 | |||||||
| chr16:56973280 | T | C | 14 | a0001c0001t0001g0058 a0001c0001t0001g0118 a0001c0001t0001g0286 others(11): Show |
22 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.751-51T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56973280 | |||||||
| chr16:56973534 | T | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0028 others(88): Show |
146 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.930+24T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973534 | |||||||
| chr16:56973539 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(203): Show |
304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.930+29G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973539 | |||||||
| chr16:56973600 | G | A | 22 | a0001c0010t0001g0209 a0002c0002t0001g0003 a0002c0002t0001g0014 others(19): Show |
37 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.930+90G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973600 | |||||||
| chr16:56973698 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(131): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.930+188G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973698 | |||||||
| chr16:56973716 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.930+206C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973716 | |||||||
| chr16:56973740 | A | G | 2 | a0002c0003t0002g0295 a0002c0003t0002g0296 |
2 | HG00741.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.930+230A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973740 | |||||||
| chr16:56973774 | C | T | 1 | a0002c0002t0001g0201 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.930+264C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973774 | |||||||
| chr16:56973806 | C | T | 1 | a0004c0007t0001g0169 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.930+296C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973806 | |||||||
| chr16:56973822 | A | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(129): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.930+312A>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973822 | |||||||
| chr16:56973906 | C | T | 1 | a0002c0002t0001g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.930+396C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973906 | |||||||
| chr16:56973921 | C | T | 1 | a0007c0011t0001g0221 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.930+411C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973921 | |||||||
| chr16:56973928 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.930+418C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973928 | |||||||
| chr16:56973980 | T | C | 1 | a0002c0002t0001g0246 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.930+470T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973980 | |||||||
| chr16:56974017 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.930+507G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974017 | |||||||
| chr16:56974075 | G | C | 1 | a0005c0008t0001g0040 | 2 | NA18952.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.930+565G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974075 | |||||||
| chr16:56974136 | G | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
195 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.930+626G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974136 | |||||||
| chr16:56974212 | G | A | 1 | a0001c0001t0001g0060 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.930+702G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974212 | |||||||
| chr16:56974249 | G | A | 9 | a0002c0002t0001g0023 a0002c0002t0001g0029 a0002c0002t0001g0092 others(6): Show |
13 | HG02257.hp1 HG02622.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.930+739G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974249 | |||||||
| chr16:56974275 | A | G | 1 | a0003c0004t0001g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.930+765A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974275 | |||||||
| chr16:56974288 | TAA | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0133 |
3 | HG01074.hp2 HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.930+779_930+780del others(2): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974288 | |||||||
| chr16:56974315 | G | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(182): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.931-786G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974315 | |||||||
| chr16:56974316 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.931-785G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974316 | |||||||
| chr16:56974375 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(195): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.931-726A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974375 | |||||||
| chr16:56974465 | C | A | 1 | a0001c0001t0001g0136 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.931-636C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974465 | |||||||
| chr16:56974493 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.931-608T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974493 | |||||||
| chr16:56974586 | T | G | 20 | a0002c0002t0001g0003 a0002c0002t0001g0014 a0002c0002t0001g0034 others(17): Show |
35 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.931-515T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974586 | |||||||
| chr16:56974596 | A | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(228): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.931-505A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974596 | |||||||
| chr16:56974857 | G | A | 1 | a0016c0020t0001g0287 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.931-244G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974857 | |||||||
| chr16:56974993 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0256 a0001c0001t0001g0261 others(1): Show |
4 | NA18960.hp1 NA18993.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-108G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974993 | |||||||
| chr16:56975189 | G | A | 1 | a0002c0002t0001g0142 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.981+38G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975189 | |||||||
| chr16:56975253 | A | G | 2 | a0002c0002t0002g0279 a0002c0002t0002g0280 |
2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.981+102A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975253 | |||||||
| chr16:56975283 | T | G | 33 | a0002c0002t0001g0003 a0002c0002t0001g0014 a0002c0002t0001g0023 others(30): Show |
52 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.981+132T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975283 | |||||||
| chr16:56975288 | C | T | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+137C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975288 | |||||||
| chr16:56975289 | G | A | 2 | a0002c0002t0001g0047 a0002c0002t0001g0155 |
3 | NA18957.hp2 NA18975.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.981+138G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975289 | |||||||
| chr16:56975329 | T | G | 1 | a0001c0001t0001g0244 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.981+178T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975329 | |||||||
| chr16:56975464 | T | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(158): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.981+313T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975464 | |||||||
| chr16:56975476 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.981+325G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975476 | |||||||
| chr16:56975599 | C | T | 9 | a0002c0002t0001g0023 a0002c0002t0001g0092 a0002c0002t0001g0093 others(6): Show |
11 | HG02572.hp1 HG02717.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.981+448C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975599 | |||||||
| chr16:56975632 | T | C | 20 | a0002c0002t0001g0003 a0002c0002t0001g0014 a0002c0002t0001g0034 others(17): Show |
35 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.981+481T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975632 | |||||||
| chr16:56975696 | A | G | 13 | a0002c0002t0001g0023 a0002c0002t0001g0029 a0002c0002t0001g0092 others(10): Show |
17 | HG02257.hp1 HG02572.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.981+545A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975696 | |||||||
| chr16:56975739 | TC | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.981+594delC | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 56975739 | ||||||
| chr16:56975857 | T | A | 29 | a0002c0002t0001g0006 a0002c0002t0001g0009 a0002c0002t0001g0024 others(26): Show |
42 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.981+706T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975857 | |||||||
| chr16:56975887 | C | A | 15 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0002c0002t0001g0023 others(12): Show |
19 | HG02257.hp1 HG02572.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.981+736C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975887 | |||||||
| chr16:56975916 | C | A | 1 | a0002c0002t0003g0088 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.981+765C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975916 | |||||||
| chr16:56975939 | G | A | 1 | a0014c0022t0002g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.981+788G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975939 | |||||||
| chr16:56975966 | G | A | 4 | a0002c0002t0001g0132 a0002c0005t0001g0018 a0002c0005t0001g0207 others(1): Show |
7 | HG03704.hp2 NA18942.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.981+815G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975966 | |||||||
| chr16:56975970 | C | G | 13 | a0002c0002t0001g0023 a0002c0002t0001g0029 a0002c0002t0001g0092 others(10): Show |
17 | HG02257.hp1 HG02572.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.981+819C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975970 | |||||||
| chr16:56976005 | C | T | 2 | a0002c0002t0001g0107 a0002c0002t0001g0108 |
2 | HG01099.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.981+854C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976005 | |||||||
| chr16:56976020 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(178): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.981+869C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976020 | |||||||
| chr16:56976029 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(183): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.981+878T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976029 | |||||||
| chr16:56976073 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(70): Show |
118 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.981+922T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976073 | |||||||
| chr16:56976075 | T | G | 20 | a0002c0002t0001g0003 a0002c0002t0001g0014 a0002c0002t0001g0034 others(17): Show |
35 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.981+924T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976075 | |||||||
| chr16:56976119 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.981+968A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976119 | |||||||
| chr16:56976197 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.981+1046C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976197 | |||||||
| chr16:56976203 | G | A | 13 | a0002c0002t0001g0023 a0002c0002t0001g0029 a0002c0002t0001g0092 others(10): Show |
17 | HG02257.hp1 HG02572.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.981+1052G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976203 | |||||||
| chr16:56976205 | G | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0277 a0001c0001t0001g0291 |
4 | HG03139.hp2 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.981+1054G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976205 | |||||||
| chr16:56976320 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0144 |
7 | HG00140.hp1 HG01361.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.981+1169C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976320 | |||||||
| chr16:56976420 | A | G | 13 | a0002c0002t0001g0023 a0002c0002t0001g0029 a0002c0002t0001g0092 others(10): Show |
17 | HG02257.hp1 HG02572.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.981+1269A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976420 | |||||||
| chr16:56976470 | T | G | 9 | a0001c0001t0001g0056 a0001c0001t0001g0079 a0001c0001t0001g0203 others(6): Show |
10 | HG00280.hp2 HG00735.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.981+1319T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976470 | |||||||
| chr16:56976475 | CT | C | 8 | a0001c0001t0001g0065 a0001c0001t0001g0151 a0001c0001t0001g0189 others(5): Show |
9 | HG01069.hp1 HG02148.hp2 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.981+1338delT | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 56976475 | ||||||
| chr16:56976574 | C | T | 7 | a0003c0004t0001g0010 a0003c0004t0001g0109 a0003c0004t0001g0110 others(4): Show |
11 | HG00733.hp1 HG01123.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.981+1423C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976574 | |||||||
| chr16:56976769 | G | A | 1 | a0002c0002t0001g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.982-1322G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976769 | |||||||
| chr16:56976915 | T | A | 2 | a0001c0001t0001g0250 a0002c0002t0001g0202 |
2 | HG02145.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.982-1176T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976915 | |||||||
| chr16:56976916 | A | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(68): Show |
116 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.982-1175A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976916 | |||||||
| chr16:56976929 | A | T | 1 | a0001c0001t0001g0244 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.982-1162A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976929 | |||||||
| chr16:56976940 | C | T | 1 | a0002c0002t0002g0141 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.982-1151C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976940 | |||||||
| chr16:56976992 | T | A | 1 | a0002c0019t0001g0240 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.982-1099T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976992 | |||||||
| chr16:56977036 | T | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(223): Show |
348 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.982-1055T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977036 | |||||||
| chr16:56977043 | G | C | 14 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0002c0002t0001g0017 others(11): Show |
19 | HG00438.hp1 HG03942.hp1 HG04115.hp2 others(16): Show |
intron_variant | MODIFIER | c.982-1048G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977043 | |||||||
| chr16:56977082 | T | G | 21 | a0002c0002t0002g0007 a0002c0002t0002g0016 a0002c0002t0002g0030 others(18): Show |
32 | HG01081.hp2 HG01175.hp2 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.982-1009T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977082 | |||||||
| chr16:56977201 | G | A | 1 | a0001c0016t0001g0281 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.982-890G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977201 | |||||||
| chr16:56977208 | G | A | 1 | a0002c0002t0001g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.982-883G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977208 | |||||||
| chr16:56977211 | G | A | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.982-880G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977211 | |||||||
| chr16:56977273 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
172 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.982-818G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977273 | |||||||
| chr16:56977331 | C | T | 21 | a0002c0002t0002g0007 a0002c0002t0002g0016 a0002c0002t0002g0030 others(18): Show |
32 | HG01081.hp2 HG01175.hp2 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.982-760C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977331 | |||||||
| chr16:56977342 | A | G | 1 | a0002c0002t0001g0154 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.982-749A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977342 | |||||||
| chr16:56977540 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.982-551G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977540 | |||||||
| chr16:56977632 | G | A | 1 | a0002c0002t0001g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.982-459G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977632 | |||||||
| chr16:56977665 | CT | C | 1 | a0001c0001t0001g0028 | 3 | HG02615.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.982-425delT | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977665 | |||||||
| chr16:56977794 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.982-297C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977794 | |||||||
| chr16:56977847 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.982-244G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977847 | |||||||
| chr16:56977884 | T | A | 2 | a0005c0008t0001g0245 a0005c0008t0001g0251 |
2 | NA18940.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.982-207T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977884 | |||||||
| chr16:56977905 | A | G | 1 | a0002c0002t0001g0154 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.982-186A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977905 | |||||||
| chr16:56977914 | C | T | 20 | a0002c0002t0001g0003 a0002c0002t0001g0014 a0002c0002t0001g0034 others(17): Show |
35 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.982-177C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977914 | |||||||
| chr16:56977944 | C | G | 1 | a0001c0001t0001g0037 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.982-147C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977944 | |||||||
| chr16:56977972 | C | T | 2 | a0002c0002t0001g0176 a0002c0002t0001g0193 |
2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.982-119C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977972 | |||||||
| chr16:56978024 | C | T | 40 | a0002c0002t0001g0003 a0002c0002t0001g0014 a0002c0002t0001g0023 others(37): Show |
58 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.982-67C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56978024 | |||||||
| chr16:56978262 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG01496.hp1 | splice_region_variant&intron_variant | LOW | c.1146+7C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978262 | |||||||
| chr16:56978442 | C | T | 2 | a0002c0002t0001g0068 a0002c0002t0001g0241 |
2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1146+187C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978442 | |||||||
| chr16:56978467 | T | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(65): Show |
109 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1146+212T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978467 | |||||||
| chr16:56978548 | A | G | 1 | a0002c0003t0002g0296 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1146+293A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978548 | |||||||
| chr16:56978650 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1146+395T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978650 | |||||||
| chr16:56978650 | TA | T | 21 | a0002c0002t0001g0003 a0002c0002t0001g0014 a0002c0002t0001g0034 others(18): Show |
36 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1146+406delA | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 56978650 | ||||||
| chr16:56978651 | A | T | 70 | a0002c0002t0001g0006 a0002c0002t0001g0009 a0002c0002t0001g0024 others(67): Show |
101 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.1146+396A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978651 | |||||||
| chr16:56978787 | A | G | 90 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1146+532A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978787 | |||||||
| chr16:56978880 | C | T | 1 | a0011c0027t0001g0131 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1146+625C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978880 | |||||||
| chr16:56978975 | G | A | 21 | a0002c0002t0002g0007 a0002c0002t0002g0016 a0002c0002t0002g0030 others(18): Show |
32 | HG01081.hp2 HG01175.hp2 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.1146+720G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978975 | |||||||
| chr16:56979019 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1146+764G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979019 | |||||||
| chr16:56979024 | G | A | 1 | a0001c0001t0001g0019 | 4 | HG02055.hp2 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146+769G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979024 | |||||||
| chr16:56979104 | G | A | 20 | a0002c0002t0001g0003 a0002c0002t0001g0014 a0002c0002t0001g0034 others(17): Show |
35 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1146+849G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979104 | |||||||
| chr16:56979484 | G | C | 1 | a0002c0002t0002g0139 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1146+1229G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979484 | |||||||
| chr16:56979517 | A | AT | 28 | a0001c0001t0001g0077 a0002c0002t0001g0003 a0002c0002t0001g0014 others(25): Show |
43 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.1146+1273dupT | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 56979517 | ||||||
| chr16:56979517 | A | ATT | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(195): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1146+1272_1146+127 others(6): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 56979517 | ||||||
| chr16:56979572 | G | A | 1 | a0002c0002t0001g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1146+1317G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979572 | |||||||
| chr16:56979614 | G | A | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146+1359G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979614 | |||||||
| chr16:56979619 | G | A | 2 | a0002c0002t0001g0070 a0002c0002t0001g0290 |
2 | NA18961.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1146+1364G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979619 | |||||||
| chr16:56979659 | C | T | 8 | a0002c0002t0001g0068 a0002c0002t0001g0176 a0002c0002t0001g0193 others(5): Show |
8 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1146+1404C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979659 | |||||||
| chr16:56979660 | G | A | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146+1405G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979660 | |||||||
| chr16:56979661 | C | T | 2 | a0002c0002t0001g0014 a0002c0002t0001g0260 |
5 | HG02129.hp2 HG03239.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1146+1406C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979661 | |||||||
| chr16:56979671 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1146+1416C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979671 | |||||||
| chr16:56979672 | G | A | 1 | a0002c0002t0001g0134 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1146+1417G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979672 | |||||||
| chr16:56979753 | T | C | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-1405T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979753 | |||||||
| chr16:56979787 | A | G | 11 | a0002c0002t0001g0023 a0002c0002t0001g0029 a0002c0002t0001g0092 others(8): Show |
15 | HG02257.hp1 HG02622.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1147-1371A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979787 | |||||||
| chr16:56979822 | A | G | 2 | a0001c0001t0001g0187 a0001c0001t0001g0189 |
2 | HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1147-1336A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979822 | |||||||
| chr16:56979831 | TA | T | 21 | a0002c0002t0002g0007 a0002c0002t0002g0016 a0002c0002t0002g0030 others(18): Show |
32 | HG01081.hp2 HG01175.hp2 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.1147-1324delA | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 56979831 | ||||||
| chr16:56979842 | G | A | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-1316G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979842 | |||||||
| chr16:56979934 | G | T | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-1224G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979934 | |||||||
| chr16:56980123 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1147-1035G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980123 | |||||||
| chr16:56980125 | C | T | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-1033C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980125 | |||||||
| chr16:56980137 | C | T | 1 | a0007c0011t0001g0059 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1147-1021C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980137 | |||||||
| chr16:56980144 | C | T | 1 | a0002c0002t0001g0183 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1147-1014C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980144 | |||||||
| chr16:56980296 | G | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0243 a0001c0001t0001g0265 others(1): Show |
6 | HG00609.hp2 HG00621.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.1147-862G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980296 | |||||||
| chr16:56980337 | T | C | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-821T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980337 | |||||||
| chr16:56980407 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1147-751A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980407 | |||||||
| chr16:56980427 | C | T | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-731C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980427 | |||||||
| chr16:56980483 | T | C | 3 | a0002c0002t0002g0016 a0002c0002t0002g0141 a0002c0002t0002g0157 |
6 | HG02056.hp1 HG02165.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1147-675T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980483 | |||||||
| chr16:56980510 | C | T | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-648C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980510 | |||||||
| chr16:56980625 | A | T | 1 | a0002c0002t0001g0103 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1147-533A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980625 | |||||||
| chr16:56980646 | G | A | 1 | a0002c0002t0001g0067 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1147-512G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980646 | |||||||
| chr16:56980694 | T | C | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-464T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980694 | |||||||
| chr16:56980698 | T | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(233): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1147-460T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980698 | |||||||
| chr16:56980778 | C | T | 1 | a0002c0002t0001g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1147-380C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980778 | |||||||
| chr16:56980852 | G | A | 1 | a0002c0002t0001g0128 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1147-306G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980852 | |||||||
| chr16:56980897 | G | A | 2 | a0002c0006t0001g0054 a0002c0006t0001g0194 |
3 | HG01891.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1147-261G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980897 | |||||||
| chr16:56980908 | T | C | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-250T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980908 | |||||||
| chr16:56980932 | A | G | 1 | a0013c0026t0001g0199 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1147-226A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980932 | |||||||
| chr16:56980963 | A | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1147-195A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980963 | |||||||
| chr16:56981333 | T | C | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1214+108T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981333 | |||||||
| chr16:56981377 | A | C | 3 | a0002c0002t0001g0083 a0002c0002t0002g0279 a0002c0002t0002g0280 |
3 | HG03209.hp1 HG04204.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1214+152A>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981377 | |||||||
| chr16:56981390 | G | C | 2 | a0002c0014t0001g0098 a0002c0014t0001g0099 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1214+165G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981390 | |||||||
| chr16:56981423 | GCTGCCAG others(5): Show |
G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(225): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1214+199_1214+210d others(14): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981423 | |||||||
| chr16:56981464 | G | A | 1 | a0002c0014t0001g0099 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1215-183G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981464 | |||||||
| chr16:56981468 | A | G | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1215-179A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981468 | |||||||
| chr16:56981507 | G | A | 3 | a0002c0002t0001g0083 a0002c0002t0002g0279 a0002c0002t0002g0280 |
3 | HG03209.hp1 HG04204.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1215-140G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981507 | |||||||
| chr16:56981535 | C | G | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1215-112C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981535 | |||||||
| chr16:56981551 | G | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(291): Show |
447 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(444): Show |
intron_variant | MODIFIER | c.1215-96G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981551 | |||||||
| chr16:56981632 | G | T | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1215-15G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981632 | |||||||
| chr16:56981633 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(57): Show |
101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1215-14C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981633 | |||||||
| chr16:56981796 | A | T | 1 | a0002c0002t0001g0130 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1248+116A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 13/15 | chr16 | 56981796 | |||||||
| chr16:56981813 | T | C | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1248+133T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 13/15 | chr16 | 56981813 | |||||||
| chr16:56981869 | A | G | 1 | a0014c0022t0002g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1248+189A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 13/15 | chr16 | 56981869 | |||||||
| chr16:56982238 | G | A | 1 | a0001c0001t0001g0051 | 2 | NA18948.hp2 NA19081.hp2 |
splice_donor_variant&intron_variant | HIGH | c.1321+1G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982238 | |||||||
| chr16:56982366 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1321+129C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982366 | |||||||
| chr16:56982390 | T | C | 25 | a0002c0002t0001g0003 a0002c0002t0001g0014 a0002c0002t0001g0034 others(22): Show |
40 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.1321+153T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982390 | |||||||
| chr16:56982397 | C | A | 2 | a0002c0014t0001g0098 a0002c0014t0001g0099 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1321+160C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982397 | |||||||
| chr16:56982479 | C | A | 1 | a0002c0002t0001g0269 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1321+242C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982479 | |||||||
| chr16:56982503 | T | TTTGGTGT others(17): Show |
1 | a0001c0001t0001g0152 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1321+266_1321+267i others(26): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982503 | |||||||
| chr16:56982533 | C | G | 25 | a0002c0002t0001g0003 a0002c0002t0001g0014 a0002c0002t0001g0034 others(22): Show |
40 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.1321+296C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982533 | |||||||
| chr16:56982573 | C | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0102 a0001c0001t0001g0257 others(2): Show |
9 | NA18944.hp2 NA18953.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.1321+336C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982573 | |||||||
| chr16:56982607 | T | C | 25 | a0002c0002t0001g0003 a0002c0002t0001g0014 a0002c0002t0001g0034 others(22): Show |
40 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.1321+370T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982607 | |||||||
| chr16:56982610 | T | C | 1 | a0002c0005t0001g0211 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1321+373T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982610 | |||||||
| chr16:56982615 | T | G | 5 | a0002c0009t0001g0090 a0002c0009t0001g0091 a0002c0009t0001g0162 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1321+378T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982615 | |||||||
| chr16:56982672 | G | T | 2 | a0001c0010t0001g0209 a0001c0010t0001g0213 |
2 | NA18612.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1321+435G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982672 | |||||||
| chr16:56982693 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1321+456T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982693 | |||||||
| chr16:56982736 | G | A | 26 | a0002c0002t0001g0003 a0002c0002t0001g0014 a0002c0002t0001g0034 others(23): Show |
41 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.1321+499G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982736 | |||||||
| chr16:56982888 | G | A | 1 | a0002c0002t0001g0129 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1322-438G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982888 | |||||||
| chr16:56982911 | A | T | 1 | a0001c0001t0001g0080 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1322-415A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982911 | |||||||
| chr16:56983038 | C | T | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(296): Show |
452 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(449): Show |
intron_variant | MODIFIER | c.1322-288C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56983038 | |||||||
| chr16:56983090 | T | G | 16 | a0002c0002t0002g0139 a0002c0002t0002g0140 a0002c0002t0002g0158 others(13): Show |
23 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1322-236T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56983090 | |||||||
| chr16:56983178 | G | T | 1 | a0001c0001t0001g0256 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1322-148G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56983178 | |||||||
| chr16:56983254 | C | T | 2 | a0002c0002t0001g0068 a0002c0002t0001g0241 |
2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1322-72C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56983254 | |||||||
| chr16:56983487 | G | A | 1 | a0002c0002t0002g0030 | 3 | NA18992.hp2 NA19005.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1407+76G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 15/15 | chr16 | 56983487 | |||||||
| chr16:56983562 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(167): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.1408-30G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 15/15 | chr16 | 56983562 |