Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23491 |
| ensemblid | ENSG00000172828.13 |
| hgncid | 1865 |
| symbol | CES3 |
| name | carboxylesterase 3 |
| refseq_nuc | NM_024922.6 |
| refseq_prot | NP_079198.2 |
| ensembl_nuc | ENST00000303334.9 |
| ensembl_prot | ENSP00000304782.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 66961266 |
| end | 66975149 |
| strand | + |
| ver | v1.2 |
| region | chr16:66961266-66975149 |
| region5000 | chr16:66956266-66980149 |
| regionname0 | CES3_chr16_66961266_66975149 |
| regionname5000 | CES3_chr16_66956266_66980149 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 571 | 297 | 79 | 51 | 124 | 14 | 27 | 91 | CES3_chr16_66956266_66980149 | CES3 | MERAV others(566): Show |
chr16 | 66956266 | 66980149 |
| a0002 | 0/0 | 571 | 13 | 6 | 1 | 0 | 0 | 6 | 0 | CES3_chr16_66956266_66980149 | CES3 | MERAV others(566): Show |
chr16 | 66956266 | 66980149 |
| a0003 | 0/0 | 571 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | MERAV others(566): Show |
chr16 | 66956266 | 66980149 |
| a0004 | 0/0 | 571 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | MERAV others(566): Show |
chr16 | 66956266 | 66980149 |
| a0005 | 0/0 | 429 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | MERAV others(424): Show |
chr16 | 66956266 | 66980149 |
| a0006 | 0/0 | 571 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CES3_chr16_66956266_66980149 | CES3 | MERAV others(566): Show |
chr16 | 66956266 | 66980149 |
| a0007 | 0/0 | 571 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | MERAV others(566): Show |
chr16 | 66956266 | 66980149 |
| a0008 | 0/0 | 571 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | MERAV others(566): Show |
chr16 | 66956266 | 66980149 |
| a0009 | 0/0 | 571 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | MERAV others(566): Show |
chr16 | 66956266 | 66980149 |
| a0010 | 0/0 | 571 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | MERAV others(566): Show |
chr16 | 66956266 | 66980149 |
| a0011 | 0/0 | 571 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CES3_chr16_66956266_66980149 | CES3 | MERAV others(566): Show |
chr16 | 66956266 | 66980149 |
| a0012 | 0/0 | 571 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | MERAV others(566): Show |
chr16 | 66956266 | 66980149 |
| a0013 | 0/0 | 571 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | MERAV others(566): Show |
chr16 | 66956266 | 66980149 |
| a0014 | 0/0 | 571 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | MERAV others(566): Show |
chr16 | 66956266 | 66980149 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1713 | 263 | 69 | 40 | 112 | 14 | 26 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0001c0002 | 0/0 | 1713 | 20 | 0 | 7 | 12 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0001c0004 | 0/0 | 1713 | 8 | 8 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0001c0006 | 0/0 | 1713 | 4 | 0 | 4 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0001c0010 | 0/0 | 1713 | 2 | 2 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0002c0003 | 0/0 | 1713 | 11 | 4 | 1 | 0 | 0 | 6 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0002c0012 | 0/0 | 1713 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0002c0013 | 0/0 | 1713 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0003c0005 | 0/0 | 1713 | 6 | 5 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0004c0008 | 0/0 | 1713 | 2 | 0 | 2 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0005c0009 | 0/0 | 1713 | 2 | 2 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0006c0007 | 0/0 | 1713 | 2 | 0 | 0 | 2 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0007c0019 | 0/0 | 1713 | 1 | 0 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0008c0018 | 0/0 | 1713 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0009c0011 | 0/0 | 1713 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0010c0014 | 0/0 | 1713 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0011c0020 | 0/0 | 1713 | 1 | 0 | 0 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0012c0015 | 0/0 | 1713 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0013c0017 | 0/0 | 1713 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 | ||
| a0014c0016 | 0/0 | 1713 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATGGA others(1708): Show |
chr16 | 66956266 | 66980149 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3858 | 208 | 56 | 31 | 81 | 14 | 24 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0001t0002 | 0/0 | 3858 | 31 | 1 | 4 | 25 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0001t0003 | 0/0 | 3858 | 11 | 10 | 0 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0001t0006 | 0/0 | 3858 | 2 | 0 | 0 | 2 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0001t0007 | 0/0 | 3858 | 2 | 0 | 2 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0001t0008 | 0/0 | 3858 | 2 | 1 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0001t0009 | 0/0 | 3858 | 2 | 0 | 0 | 2 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0001t0010 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0001t0015 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0001t0016 | 0/0 | 3858 | 1 | 0 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0001t0018 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0001t0019 | 0/0 | 3858 | 1 | 0 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0002t0002 | 0/0 | 3858 | 16 | 0 | 6 | 9 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0002t0005 | 0/0 | 3858 | 3 | 0 | 0 | 3 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0002t0012 | 0/0 | 3858 | 1 | 0 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0004t0001 | 0/0 | 3858 | 8 | 8 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0006t0001 | 0/0 | 3858 | 4 | 0 | 4 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0001c0010t0001 | 0/0 | 3858 | 2 | 2 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0002c0003t0004 | 0/0 | 3858 | 10 | 4 | 1 | 0 | 0 | 5 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0002c0003t0017 | 0/0 | 3858 | 1 | 0 | 0 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0002c0012t0001 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0002c0013t0001 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0003c0005t0001 | 0/0 | 3858 | 6 | 5 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0004c0008t0001 | 0/0 | 3858 | 2 | 0 | 2 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0005c0009t0011 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0005c0009t0014 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0006c0007t0001 | 0/0 | 3858 | 2 | 0 | 0 | 2 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0007c0019t0001 | 0/0 | 3858 | 1 | 0 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0008c0018t0013 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0009c0011t0001 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0010c0014t0001 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0011c0020t0001 | 0/0 | 3858 | 1 | 0 | 0 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0012c0015t0002 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0013c0017t0001 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| a0014c0016t0001 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | ATTCC others(3853): Show |
chr16 | 66956266 | 66980149 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 105 | 16 | 16 | 53 | 6 | 13 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0003 | 0/0 | 17 | 9 | 0 | 6 | 1 | 1 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0004 | 0/1 | 15 | 1 | 6 | 0 | 4 | 3 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0005 | 0/0 | 14 | 14 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0008 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0002g0002 | 0/0 | 27 | 1 | 4 | 21 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0003g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0003g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0006g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0007g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0008g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0009g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0010g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0015g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0016g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0018g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0001t0019g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0002t0002g0002 | 0/0 | 11 | 0 | 5 | 6 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0002t0005g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0002t0012g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0004t0001g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0006t0001g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0001c0010t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0002c0003t0004g0007 | 0/0 | 8 | 4 | 0 | 0 | 0 | 4 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0002c0003t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0002c0003t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0002c0003t0017g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0002c0012t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0002c0013t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0003c0005t0001g0003 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0004c0008t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0005c0009t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0005c0009t0014g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0006c0007t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0007c0019t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0008c0018t0013g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0009c0011t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0010c0014t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0011c0020t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0012c0015t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0013c0017t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| a0014c0016t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00597 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | CHS | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | CHS | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0053 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00738 | hp1 | a0001 | c0001 | t0019 | g0021 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00738 | hp2 | a0003 | c0005 | t0001 | g0003 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00741 | hp1 | a0007 | c0019 | t0001 | g0034 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0003 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0003 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01109 | hp1 | a0002 | c0003 | t0004 | g0066 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01256 | hp1 | a0001 | c0006 | t0001 | g0001 | AMR | CLM | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01256 | hp2 | a0001 | c0001 | t0016 | g0001 | AMR | CLM | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01258 | hp2 | a0001 | c0006 | t0001 | g0001 | AMR | CLM | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01433 | hp1 | a0004 | c0008 | t0001 | g0001 | AMR | CLM | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01433 | hp2 | a0001 | c0001 | t0008 | g0022 | AMR | CLM | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01496 | hp2 | a0001 | c0006 | t0001 | g0001 | AMR | CLM | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01884 | hp1 | a0001 | c0004 | t0001 | g0006 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01884 | hp2 | a0008 | c0018 | t0013 | g0060 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01891 | hp1 | a0005 | c0009 | t0014 | g0069 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01934 | hp1 | a0004 | c0008 | t0001 | g0001 | AMR | PEL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01952 | hp1 | a0001 | c0006 | t0001 | g0001 | AMR | PEL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01981 | hp1 | a0001 | c0002 | t0012 | g0002 | AMR | PEL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02055 | hp2 | a0001 | c0010 | t0001 | g0008 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02056 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02145 | hp1 | a0002 | c0003 | t0004 | g0007 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02155 | hp1 | a0009 | c0011 | t0001 | g0047 | EAS | CDX | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02523 | hp1 | a0001 | c0001 | t0018 | g0064 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02523 | hp2 | a0001 | c0001 | t0009 | g0040 | EAS | KHV | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02572 | hp1 | a0003 | c0005 | t0001 | g0003 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02602 | hp1 | a0002 | c0003 | t0004 | g0007 | SAS | PJL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02622 | hp1 | a0001 | c0004 | t0001 | g0006 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02630 | hp2 | a0002 | c0003 | t0004 | g0007 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02818 | hp1 | a0002 | c0013 | t0001 | g0025 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02895 | hp1 | a0003 | c0005 | t0001 | g0003 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02895 | hp2 | a0002 | c0003 | t0004 | g0007 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0062 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02897 | hp2 | a0003 | c0005 | t0001 | g0003 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ESN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02970 | hp1 | a0002 | c0012 | t0001 | g0031 | AFR | ESN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | MSL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03130 | hp1 | a0003 | c0005 | t0001 | g0003 | AFR | ESN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03195 | hp2 | a0010 | c0014 | t0001 | g0006 | AFR | ESN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03225 | hp1 | a0001 | c0001 | t0015 | g0002 | AFR | MSL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03486 | hp1 | a0001 | c0010 | t0001 | g0008 | AFR | MSL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0006 | AFR | MSL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03491 | hp2 | a0002 | c0003 | t0004 | g0007 | SAS | PJL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03516 | hp1 | a0001 | c0004 | t0001 | g0006 | AFR | ESN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0006 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03540 | hp2 | a0005 | c0009 | t0011 | g0068 | AFR | GWD | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03654 | hp1 | a0002 | c0003 | t0004 | g0007 | SAS | PJL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0054 | SAS | STU | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03688 | hp2 | a0002 | c0003 | t0004 | g0065 | SAS | STU | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03704 | hp2 | a0011 | c0020 | t0001 | g0019 | SAS | PJL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03927 | hp2 | a0002 | c0003 | t0017 | g0007 | SAS | BEB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG04115 | hp1 | a0002 | c0003 | t0004 | g0007 | SAS | STU | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18942 | hp2 | a0012 | c0015 | t0002 | g0057 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18947 | hp1 | a0013 | c0017 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18971 | hp2 | a0006 | c0007 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18992 | hp1 | a0001 | c0002 | t0005 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19012 | hp1 | a0001 | c0002 | t0005 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | LWK | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19054 | hp1 | a0014 | c0016 | t0001 | g0011 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19057 | hp1 | a0001 | c0001 | t0010 | g0013 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19077 | hp1 | a0001 | c0002 | t0005 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19080 | hp2 | a0006 | c0007 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0006 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02559 | hp1 | a0003 | c0005 | t0001 | g0003 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG06807 | hp1 | a0002 | c0003 | t0004 | g0007 | AFR | USA | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0006 | AFR | USA | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | USA | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0004 | REF | REF | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | CES3_chr16_66956266_66980149 | CES3 | chr16 | 66956266 | 66980149 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:66963233 | G | A | 1 | a0006 | 2 | NA18971.hp2 NA19080.hp2 |
missense_variant | MODERATE | c.137G>A | p.Arg46Gln | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 2/13 | 179/3858 | 137/1716 | 46/571 | chr16 | 66963233 | |||
| chr16:66963514 | T | C | 1 | a0009 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.311T>C | p.Met104Thr | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 3/13 | 353/3858 | 311/1716 | 104/571 | chr16 | 66963514 | |||
| chr16:66963588 | G | A | 1 | a0002 | 13 | HG01109.hp1 HG02145.hp1 HG02602.hp1 others(10): Show |
missense_variant | MODERATE | c.385G>A | p.Val129Ile | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 3/13 | 427/3858 | 385/1716 | 129/571 | chr16 | 66963588 | |||
| chr16:66963807 | G | A | 1 | a0010 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.432G>A | p.Met144Ile | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 4/13 | 474/3858 | 432/1716 | 144/571 | chr16 | 66963807 | |||
| chr16:66963853 | T | C | 1 | a0004 | 2 | HG01433.hp1 HG01934.hp1 |
missense_variant | MODERATE | c.478T>C | p.Tyr160His | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 4/13 | 520/3858 | 478/1716 | 160/571 | chr16 | 66963853 | |||
| chr16:66964367 | G | A | 1 | a0003 | 6 | HG00738.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
missense_variant | MODERATE | c.571G>A | p.Glu191Lys | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 5/13 | 613/3858 | 571/1716 | 191/571 | chr16 | 66964367 | |||
| chr16:66964434 | T | A | 1 | a0012 | 1 | NA18942.hp2 | missense_variant | MODERATE | c.638T>A | p.Ile213Asn | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 5/13 | 680/3858 | 638/1716 | 213/571 | chr16 | 66964434 | |||
| chr16:66966250 | G | A | 1 | a0014 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.826G>A | p.Ala276Thr | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 7/13 | 868/3858 | 826/1716 | 276/571 | chr16 | 66966250 | |||
| chr16:66966861 | C | T | 1 | a0011 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.1058C>T | p.Pro353Leu | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/13 | 1100/3858 | 1058/1716 | 353/571 | chr16 | 66966861 | |||
| chr16:66969715 | C | T | 1 | a0007 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1099C>T | p.Arg367Trp | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/13 | 1141/3858 | 1099/1716 | 367/571 | chr16 | 66969715 | |||
| chr16:66971175 | G | A | 1 | a0005 | 2 | HG01891.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.1147G>A | p.Val383Met | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 10/13 | 1189/3858 | 1147/1716 | 383/571 | chr16 | 66971175 | |||
| chr16:66971316 | C | T | 1 | a0005 | 2 | HG01891.hp1 HG03540.hp2 |
stop_gained | HIGH | c.1288C>T | p.Arg430* | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 10/13 | 1330/3858 | 1288/1716 | 430/571 | chr16 | 66971316 | |||
| chr16:66972461 | T | G | 1 | a0013 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.1397T>G | p.Phe466Cys | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 11/13 | 1439/3858 | 1397/1716 | 466/571 | chr16 | 66972461 | |||
| chr16:66972694 | A | G | 1 | a0008 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1468A>G | p.Lys490Glu | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 12/13 | 1510/3858 | 1468/1716 | 490/571 | chr16 | 66972694 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:66963810 | A | G | 1 | a0002c0003 | 11 | HG01109.hp1 HG02145.hp1 HG02602.hp1 others(8): Show |
synonymous_variant | LOW | c.435A>G | p.Val145Val | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 4/13 | 477/3858 | 435/1716 | 145/571 | chr16 | 66963810 | |||
| chr16:66964649 | G | A | 1 | a0002c0012 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.741G>A | p.Leu247Leu | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 6/13 | 783/3858 | 741/1716 | 247/571 | chr16 | 66964649 | |||
| chr16:66966279 | C | A | 1 | a0005c0009 | 2 | HG01891.hp1 HG03540.hp2 |
synonymous_variant | LOW | c.855C>A | p.Ser285Ser | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 7/13 | 897/3858 | 855/1716 | 285/571 | chr16 | 66966279 | |||
| chr16:66969744 | C | T | 2 | a0001c0004 a0010c0014 |
9 | HG01884.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
synonymous_variant | LOW | c.1128C>T | p.Pro376Pro | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/13 | 1170/3858 | 1128/1716 | 376/571 | chr16 | 66969744 | |||
| chr16:66971252 | G | A | 1 | a0001c0006 | 4 | HG01256.hp1 HG01258.hp2 HG01496.hp2 others(1): Show |
synonymous_variant | LOW | c.1224G>A | p.Ala408Ala | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 10/13 | 1266/3858 | 1224/1716 | 408/571 | chr16 | 66971252 | |||
| chr16:66972890 | A | G | 1 | a0001c0010 | 2 | HG02055.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.1557A>G | p.Gln519Gln | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 1599/3858 | 1557/1716 | 519/571 | chr16 | 66972890 | |||
| chr16:66972935 | G | A | 1 | a0001c0002 | 20 | HG00733.hp2 HG01081.hp2 HG01123.hp2 others(17): Show |
synonymous_variant | LOW | c.1602G>A | p.Arg534Arg | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 1644/3858 | 1602/1716 | 534/571 | chr16 | 66972935 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:66973244 | G | C | 1 | a0001c0001t0010 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*195G>C | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 195 | chr16 | 66973244 | ||||||
| chr16:66973687 | G | C | 1 | a0001c0001t0010 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*638G>C | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 638 | chr16 | 66973687 | ||||||
| chr16:66973691 | G | A | 1 | a0001c0001t0006 | 2 | HG00597.hp1 HG00621.hp2 |
3_prime_UTR_variant | MODIFIER | c.*642G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 642 | chr16 | 66973691 | ||||||
| chr16:66973945 | G | A | 1 | a0005c0009t0011 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*896G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 896 | chr16 | 66973945 | ||||||
| chr16:66974011 | C | T | 2 | a0001c0001t0003 a0001c0001t0019 |
12 | HG00738.hp1 HG02280.hp1 HG02451.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*962C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 962 | chr16 | 66974011 | ||||||
| chr16:66974204 | C | T | 1 | a0001c0002t0005 | 3 | NA18992.hp1 NA19012.hp1 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1155C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 1155 | chr16 | 66974204 | ||||||
| chr16:66974243 | C | T | 2 | a0001c0001t0003 a0001c0001t0019 |
12 | HG00738.hp1 HG02280.hp1 HG02451.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1194C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 1194 | chr16 | 66974243 | ||||||
| chr16:66974289 | C | A | 1 | a0001c0001t0007 | 2 | HG01070.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1240C>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 1240 | chr16 | 66974289 | ||||||
| chr16:66974289 | C | T | 1 | a0001c0001t0018 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1240C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 1240 | chr16 | 66974289 | ||||||
| chr16:66974316 | G | A | 1 | a0001c0002t0012 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1267G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 1267 | chr16 | 66974316 | ||||||
| chr16:66974321 | C | A | 1 | a0008c0018t0013 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1272C>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 1272 | chr16 | 66974321 | ||||||
| chr16:66974325 | C | G | 1 | a0002c0003t0017 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1276C>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 1276 | chr16 | 66974325 | ||||||
| chr16:66974443 | T | C | 2 | a0005c0009t0011 a0005c0009t0014 |
2 | HG01891.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1394T>C | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 1394 | chr16 | 66974443 | ||||||
| chr16:66974511 | C | T | 1 | a0001c0001t0019 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1462C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 1462 | chr16 | 66974511 | ||||||
| chr16:66974516 | C | A | 1 | a0001c0001t0008 | 2 | HG01433.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1467C>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 1467 | chr16 | 66974516 | ||||||
| chr16:66974516 | C | G | 1 | a0005c0009t0014 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1467C>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 1467 | chr16 | 66974516 | ||||||
| chr16:66974554 | C | T | 2 | a0002c0003t0004 a0002c0003t0017 |
11 | HG01109.hp1 HG02145.hp1 HG02602.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1505C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 1505 | chr16 | 66974554 | ||||||
| chr16:66974893 | T | C | 7 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0015 others(4): Show |
55 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1844T>C | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 1844 | chr16 | 66974893 | ||||||
| chr16:66975068 | A | G | 1 | a0001c0001t0009 | 2 | HG02056.hp2 HG02523.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2019A>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 2019 | chr16 | 66975068 | ||||||
| chr16:66975073 | C | T | 1 | a0001c0001t0016 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2024C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 2024 | chr16 | 66975073 | ||||||
| chr16:66975100 | C | T | 6 | a0001c0001t0002 a0001c0001t0006 a0001c0002t0002 others(3): Show |
54 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2051C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 13/13 | 2051 | chr16 | 66975100 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:66961430 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG00741.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.82+41G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 1/12 | chr16 | 66961430 | |||||||
| chr16:66961452 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.82+63G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 1/12 | chr16 | 66961452 | |||||||
| chr16:66961595 | C | T | 2 | a0005c0009t0011g0068 a0005c0009t0014g0069 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.82+206C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 1/12 | chr16 | 66961595 | |||||||
| chr16:66961650 | G | A | 1 | a0002c0013t0001g0025 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.82+261G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 1/12 | chr16 | 66961650 | |||||||
| chr16:66962180 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.82+791C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 1/12 | chr16 | 66962180 | |||||||
| chr16:66962253 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0026 others(2): Show |
20 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.82+864G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 1/12 | chr16 | 66962253 | |||||||
| chr16:66962289 | T | A | 1 | a0005c0009t0011g0068 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.83-890T>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 1/12 | chr16 | 66962289 | |||||||
| chr16:66962395 | A | T | 4 | a0002c0003t0004g0007 a0002c0003t0004g0065 a0002c0003t0004g0066 others(1): Show |
11 | HG01109.hp1 HG02145.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.83-784A>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 1/12 | chr16 | 66962395 | |||||||
| chr16:66962458 | G | A | 1 | a0001c0002t0002g0029 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.83-721G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 1/12 | chr16 | 66962458 | |||||||
| chr16:66962571 | C | A | 1 | a0001c0001t0003g0016 | 2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.83-608C>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 1/12 | chr16 | 66962571 | |||||||
| chr16:66962969 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.83-210G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 1/12 | chr16 | 66962969 | |||||||
| chr16:66963052 | G | A | 1 | a0002c0012t0001g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.83-127G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 1/12 | chr16 | 66963052 | |||||||
| chr16:66963718 | C | T | 1 | a0001c0001t0018g0064 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.427-84C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 3/12 | chr16 | 66963718 | |||||||
| chr16:66963973 | G | A | 1 | a0005c0009t0011g0068 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.560+38G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 4/12 | chr16 | 66963973 | |||||||
| chr16:66964257 | C | A | 1 | a0001c0001t0001g0032 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.561-100C>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 4/12 | chr16 | 66964257 | |||||||
| chr16:66965037 | C | A | 1 | a0001c0001t0001g0033 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.819+310C>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 6/12 | chr16 | 66965037 | |||||||
| chr16:66965239 | G | T | 1 | a0001c0002t0002g0063 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.819+512G>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 6/12 | chr16 | 66965239 | |||||||
| chr16:66965240 | G | A | 1 | a0007c0019t0001g0034 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.819+513G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 6/12 | chr16 | 66965240 | |||||||
| chr16:66965339 | G | A | 1 | a0001c0001t0001g0017 | 2 | NA18960.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.819+612G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 6/12 | chr16 | 66965339 | |||||||
| chr16:66965467 | A | G | 50 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
154 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(151): Show |
intron_variant | MODIFIER | c.819+740A>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 6/12 | chr16 | 66965467 | |||||||
| chr16:66965630 | GGAGA | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0010g0013 |
4 | NA18942.hp1 NA18979.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-611_820-608del others(4): Show |
CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 66965630 | ||||||
| chr16:66965643 | C | G | 1 | a0001c0001t0003g0010 | 5 | HG02280.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.820-601C>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 6/12 | chr16 | 66965643 | |||||||
| chr16:66965716 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.820-528G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 6/12 | chr16 | 66965716 | |||||||
| chr16:66966364 | G | A | 5 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0016 others(2): Show |
12 | HG00738.hp1 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.921+19G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 7/12 | chr16 | 66966364 | |||||||
| chr16:66966450 | A | G | 1 | a0001c0004t0001g0062 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.921+105A>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 7/12 | chr16 | 66966450 | |||||||
| chr16:66966451 | C | T | 1 | a0001c0004t0001g0062 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.921+106C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 7/12 | chr16 | 66966451 | |||||||
| chr16:66967060 | C | CT | 4 | a0002c0003t0004g0007 a0002c0003t0004g0065 a0002c0003t0004g0066 others(1): Show |
11 | HG01109.hp1 HG02145.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.1062+205dupT | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 66967060 | ||||||
| chr16:66967075 | TTTTG | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(13): Show |
44 | HG00738.hp1 HG01255.hp1 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.1062+230_1062+233d others(6): Show |
CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 66967075 | ||||||
| chr16:66967114 | G | C | 2 | a0005c0009t0011g0068 a0005c0009t0014g0069 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1062+249G>C | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66967114 | |||||||
| chr16:66967256 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0051 a0001c0001t0007g0003 others(1): Show |
26 | HG00609.hp2 HG00738.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1062+391G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66967256 | |||||||
| chr16:66967406 | C | G | 2 | a0002c0012t0001g0031 a0002c0013t0001g0025 |
2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1062+541C>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66967406 | |||||||
| chr16:66967490 | A | G | 2 | a0002c0012t0001g0031 a0002c0013t0001g0025 |
2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1062+625A>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66967490 | |||||||
| chr16:66967649 | C | A | 1 | a0001c0001t0001g0036 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1062+784C>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66967649 | |||||||
| chr16:66967685 | C | CT | 6 | a0001c0001t0001g0050 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
6 | HG01109.hp1 HG01361.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1062+835dupT | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 66967685 | ||||||
| chr16:66967793 | G | C | 1 | a0001c0001t0001g0004 | 14 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1062+928G>C | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66967793 | |||||||
| chr16:66967890 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1062+1025C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66967890 | |||||||
| chr16:66968206 | G | C | 4 | a0002c0012t0001g0031 a0002c0013t0001g0025 a0005c0009t0011g0068 others(1): Show |
4 | HG01891.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062+1341G>C | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66968206 | |||||||
| chr16:66968268 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1062+1403G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66968268 | |||||||
| chr16:66968309 | C | T | 1 | a0002c0013t0001g0025 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1063-1370C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66968309 | |||||||
| chr16:66968576 | C | T | 1 | a0002c0003t0004g0065 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1063-1103C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66968576 | |||||||
| chr16:66968635 | C | T | 2 | a0001c0001t0003g0021 a0001c0001t0019g0021 |
2 | HG00738.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1063-1044C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66968635 | |||||||
| chr16:66968766 | T | G | 2 | a0005c0009t0011g0068 a0005c0009t0014g0069 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1063-913T>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66968766 | |||||||
| chr16:66968775 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1063-904G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66968775 | |||||||
| chr16:66968963 | G | A | 1 | a0001c0001t0008g0022 | 2 | HG01433.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1063-716G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66968963 | |||||||
| chr16:66968971 | C | A | 1 | a0001c0001t0001g0037 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1063-708C>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66968971 | |||||||
| chr16:66969051 | T | G | 8 | a0002c0003t0004g0007 a0002c0003t0004g0065 a0002c0003t0004g0066 others(5): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1063-628T>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66969051 | |||||||
| chr16:66969065 | G | A | 1 | a0008c0018t0013g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1063-614G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66969065 | |||||||
| chr16:66969136 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1063-543C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66969136 | |||||||
| chr16:66969141 | C | A | 1 | a0001c0001t0001g0038 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1063-538C>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66969141 | |||||||
| chr16:66969260 | G | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0026 others(2): Show |
20 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1063-419G>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66969260 | |||||||
| chr16:66969480 | C | T | 1 | a0009c0011t0001g0047 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1063-199C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66969480 | |||||||
| chr16:66969518 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG01361.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1063-161G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66969518 | |||||||
| chr16:66969596 | C | T | 4 | a0002c0012t0001g0031 a0002c0013t0001g0025 a0005c0009t0011g0068 others(1): Show |
4 | HG01891.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063-83C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66969596 | |||||||
| chr16:66969615 | A | G | 1 | a0012c0015t0002g0057 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1063-64A>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 8/12 | chr16 | 66969615 | |||||||
| chr16:66969932 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0037 |
9 | NA18952.hp2 NA18954.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143+173A>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | chr16 | 66969932 | |||||||
| chr16:66969952 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1143+193C>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | chr16 | 66969952 | |||||||
| chr16:66969981 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1143+222C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | chr16 | 66969981 | |||||||
| chr16:66970026 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1143+267C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | chr16 | 66970026 | |||||||
| chr16:66970054 | T | A | 8 | a0002c0003t0004g0007 a0002c0003t0004g0065 a0002c0003t0004g0066 others(5): Show |
15 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1143+295T>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | chr16 | 66970054 | |||||||
| chr16:66970072 | T | G | 1 | a0001c0001t0001g0018 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1143+313T>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | chr16 | 66970072 | |||||||
| chr16:66970089 | T | A | 1 | a0007c0019t0001g0034 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1143+330T>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | chr16 | 66970089 | |||||||
| chr16:66970109 | GT | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(36): Show |
136 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+367delT | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr16 | 66970109 | ||||||
| chr16:66970109 | GTT | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0061 others(3): Show |
7 | HG01891.hp1 HG03209.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+366_1143+367d others(4): Show |
CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr16 | 66970109 | ||||||
| chr16:66970234 | G | A | 1 | a0001c0002t0002g0053 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1143+475G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | chr16 | 66970234 | |||||||
| chr16:66970354 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0010g0013 |
4 | NA18942.hp1 NA18979.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143+595C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | chr16 | 66970354 | |||||||
| chr16:66970418 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1143+659T>C | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | chr16 | 66970418 | |||||||
| chr16:66970434 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1143+675C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | chr16 | 66970434 | |||||||
| chr16:66970690 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0043 |
2 | HG02135.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1144-482C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | chr16 | 66970690 | |||||||
| chr16:66970811 | G | C | 1 | a0001c0001t0009g0040 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1144-361G>C | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | chr16 | 66970811 | |||||||
| chr16:66970822 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1144-350C>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | chr16 | 66970822 | |||||||
| chr16:66970866 | G | A | 2 | a0001c0001t0001g0019 a0011c0020t0001g0019 |
2 | HG03704.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1144-306G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 9/12 | chr16 | 66970866 | |||||||
| chr16:66971551 | G | A | 4 | a0002c0003t0004g0007 a0002c0003t0004g0065 a0002c0003t0004g0066 others(1): Show |
11 | HG01109.hp1 HG02145.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.1291+232G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 10/12 | chr16 | 66971551 | |||||||
| chr16:66971704 | G | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
153 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.1291+385G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 10/12 | chr16 | 66971704 | |||||||
| chr16:66971705 | A | G | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
153 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.1291+386A>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 10/12 | chr16 | 66971705 | |||||||
| chr16:66971706 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
153 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.1291+387C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 10/12 | chr16 | 66971706 | |||||||
| chr16:66971707 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
153 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.1291+388C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 10/12 | chr16 | 66971707 | |||||||
| chr16:66971708 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
153 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.1291+389C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 10/12 | chr16 | 66971708 | |||||||
| chr16:66971709 | A | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
153 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.1291+390A>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 10/12 | chr16 | 66971709 | |||||||
| chr16:66971710 | G | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
153 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.1291+391G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 10/12 | chr16 | 66971710 | |||||||
| chr16:66971736 | C | T | 1 | a0001c0002t0002g0055 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1291+417C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 10/12 | chr16 | 66971736 | |||||||
| chr16:66971739 | C | T | 1 | a0005c0009t0011g0068 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1291+420C>T | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 10/12 | chr16 | 66971739 | |||||||
| chr16:66971823 | T | C | 1 | a0002c0012t0001g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1291+504T>C | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 10/12 | chr16 | 66971823 | |||||||
| chr16:66971905 | G | A | 1 | a0001c0001t0001g0020 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1292-451G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 10/12 | chr16 | 66971905 | |||||||
| chr16:66971954 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1292-402A>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 10/12 | chr16 | 66971954 | |||||||
| chr16:66972582 | G | A | 1 | a0001c0002t0002g0054 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1441+77G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 11/12 | chr16 | 66972582 | |||||||
| chr16:66972609 | T | G | 1 | a0001c0001t0001g0012 | 3 | HG02109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1442-59T>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 11/12 | chr16 | 66972609 | |||||||
| chr16:66972636 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1442-32C>G | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 11/12 | chr16 | 66972636 | |||||||
| chr16:66972639 | G | A | 4 | a0002c0003t0004g0007 a0002c0003t0004g0065 a0002c0003t0004g0066 others(1): Show |
11 | HG01109.hp1 HG02145.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.1442-29G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 11/12 | chr16 | 66972639 | |||||||
| chr16:66972667 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG03209.hp2 HG03453.hp2 |
splice_acceptor_variant&intron_variant | HIGH | c.1442-1G>A | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 11/12 | chr16 | 66972667 | |||||||
| chr16:66972808 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1521-46G>C | CES3 | ENSG00000172828.13 | transcript | ENST00000303334.9 | protein_coding | 12/12 | chr16 | 66972808 |