Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2327 |
| ensemblid | ENSG00000094963.14 |
| hgncid | 3770 |
| symbol | FMO2 |
| name | flavin containing dimethylaniline monoxygenase 2 |
| refseq_nuc | NM_001460.5 |
| refseq_prot | NP_001451.2 |
| ensembl_nuc | ENST00000209929.10 |
| ensembl_prot | ENSP00000209929.8 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 171185300 |
| end | 171212686 |
| strand | + |
| ver | v1.2 |
| region | chr1:171185300-171212686 |
| region5000 | chr1:171180300-171217686 |
| regionname0 | FMO2_chr1_171185300_171212686 |
| regionname5000 | FMO2_chr1_171180300_171217686 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 471 | 108 | 12 | 18 | 61 | 5 | 11 | 50 | FMO2_chr1_171180300_171217686 | FMO2 | MAKKV others(466): Show |
chr1 | 171180300 | 171217686 |
| a0002 | 0/0 | 471 | 73 | 4 | 10 | 45 | 2 | 12 | 38 | FMO2_chr1_171180300_171217686 | FMO2 | MAKKV others(466): Show |
chr1 | 171180300 | 171217686 |
| a0003 | 0/0 | 471 | 49 | 1 | 7 | 28 | 1 | 12 | 21 | FMO2_chr1_171180300_171217686 | FMO2 | MAKKV others(466): Show |
chr1 | 171180300 | 171217686 |
| a0004 | 0/0 | 471 | 44 | 12 | 9 | 22 | 1 | 0 | 18 | FMO2_chr1_171180300_171217686 | FMO2 | MAKKV others(466): Show |
chr1 | 171180300 | 171217686 |
| a0005 | 0/0 | 471 | 36 | 17 | 7 | 7 | 2 | 3 | 3 | FMO2_chr1_171180300_171217686 | FMO2 | MAKKV others(466): Show |
chr1 | 171180300 | 171217686 |
| a0006 | 0/0 | 113 | 24 | 18 | 3 | 1 | 2 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | MAKKV others(108): Show |
chr1 | 171180300 | 171217686 |
| a0007 | 1/0 | 535 | 11 | 10 | 0 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | MAKKV others(530): Show |
chr1 | 171180300 | 171217686 |
| a0008 | 0/0 | 535 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | MAKKV others(530): Show |
chr1 | 171180300 | 171217686 |
| a0009 | 0/0 | 471 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | MAKKV others(466): Show |
chr1 | 171180300 | 171217686 |
| a0010 | 0/0 | 471 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | MAKKV others(466): Show |
chr1 | 171180300 | 171217686 |
| a0011 | 0/0 | 471 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | MAKKV others(466): Show |
chr1 | 171180300 | 171217686 |
| a0012 | 0/0 | 471 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | MAKKV others(466): Show |
chr1 | 171180300 | 171217686 |
| a0013 | 0/0 | 535 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | MAKKV others(530): Show |
chr1 | 171180300 | 171217686 |
| a0014 | 0/0 | 471 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | MAKKV others(466): Show |
chr1 | 171180300 | 171217686 |
| a0015 | 0/0 | 471 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | MAKKV others(466): Show |
chr1 | 171180300 | 171217686 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1605 | 105 | 12 | 15 | 61 | 5 | 11 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 | ||
| a0001c0015 | 0/0 | 1605 | 3 | 0 | 3 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 | ||
| a0002c0002 | 0/0 | 1606 | 72 | 4 | 10 | 44 | 2 | 12 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1601): Show |
chr1 | 171180300 | 171217686 | ||
| a0002c0019 | 0/0 | 1606 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1601): Show |
chr1 | 171180300 | 171217686 | ||
| a0003c0003 | 0/0 | 1605 | 46 | 1 | 7 | 25 | 1 | 12 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 | ||
| a0003c0016 | 0/0 | 1605 | 3 | 0 | 0 | 3 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 | ||
| a0004c0005 | 0/0 | 1605 | 28 | 0 | 6 | 22 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 | ||
| a0004c0008 | 0/0 | 1605 | 8 | 4 | 3 | 0 | 1 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 | ||
| a0004c0009 | 0/0 | 1606 | 8 | 8 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1601): Show |
chr1 | 171180300 | 171217686 | ||
| a0005c0004 | 0/0 | 1605 | 36 | 17 | 7 | 7 | 2 | 3 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 | ||
| a0006c0006 | 0/0 | 1607 | 24 | 18 | 3 | 1 | 2 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1602): Show |
chr1 | 171180300 | 171217686 | ||
| a0007c0007 | 0/0 | 1605 | 10 | 10 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 | ||
| a0007c0018 | 1/0 | 1605 | 1 | 0 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 | ||
| a0008c0010 | 0/0 | 1605 | 4 | 4 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 | ||
| a0009c0011 | 0/0 | 1605 | 4 | 4 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 | ||
| a0010c0013 | 0/0 | 1605 | 3 | 0 | 2 | 0 | 1 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 | ||
| a0011c0014 | 0/0 | 1605 | 3 | 3 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 | ||
| a0012c0012 | 0/0 | 1605 | 3 | 3 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 | ||
| a0013c0017 | 0/0 | 1605 | 2 | 2 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 | ||
| a0014c0020 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 | ||
| a0015c0021 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ATGGC others(1600): Show |
chr1 | 171180300 | 171217686 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5215 | 77 | 10 | 15 | 38 | 5 | 9 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0001c0001t0002 | 0/0 | 5215 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0001c0001t0007 | 0/0 | 5215 | 13 | 0 | 0 | 13 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0001c0001t0010 | 0/0 | 5215 | 5 | 0 | 0 | 5 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0001c0001t0013 | 0/0 | 5051 | 4 | 0 | 0 | 4 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5046): Show |
chr1 | 171180300 | 171217686 |
| a0001c0001t0018 | 0/0 | 5215 | 1 | 0 | 0 | 0 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0001c0001t0019 | 0/0 | 5195 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5190): Show |
chr1 | 171180300 | 171217686 |
| a0001c0001t0020 | 0/0 | 5215 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0001c0001t0021 | 0/0 | 5215 | 1 | 0 | 0 | 0 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0001c0001t0023 | 0/1 | 5133 | 1 | 0 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5128): Show |
chr1 | 171180300 | 171217686 |
| a0001c0015t0003 | 0/0 | 5215 | 3 | 0 | 3 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0002c0002t0004 | 0/0 | 5216 | 49 | 3 | 0 | 32 | 2 | 12 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5211): Show |
chr1 | 171180300 | 171217686 |
| a0002c0002t0005 | 0/0 | 5215 | 22 | 0 | 10 | 12 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0002c0002t0025 | 0/0 | 5216 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5211): Show |
chr1 | 171180300 | 171217686 |
| a0002c0019t0004 | 0/0 | 5216 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5211): Show |
chr1 | 171180300 | 171217686 |
| a0003c0003t0001 | 0/0 | 5215 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0003c0003t0002 | 0/0 | 5215 | 41 | 1 | 7 | 20 | 1 | 12 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0003c0003t0014 | 0/0 | 5215 | 4 | 0 | 0 | 4 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0003c0016t0002 | 0/0 | 5215 | 3 | 0 | 0 | 3 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0004c0005t0003 | 0/0 | 5215 | 28 | 0 | 6 | 22 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0004c0008t0002 | 0/0 | 5215 | 7 | 4 | 3 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0004c0008t0022 | 0/0 | 5215 | 1 | 0 | 0 | 0 | 1 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0004c0009t0004 | 0/0 | 5216 | 8 | 8 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5211): Show |
chr1 | 171180300 | 171217686 |
| a0005c0004t0003 | 0/0 | 5215 | 27 | 8 | 7 | 7 | 2 | 3 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0005c0004t0008 | 0/0 | 5215 | 9 | 9 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0006c0006t0006 | 0/0 | 5217 | 17 | 12 | 2 | 1 | 2 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5212): Show |
chr1 | 171180300 | 171217686 |
| a0006c0006t0011 | 0/0 | 5217 | 4 | 3 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5212): Show |
chr1 | 171180300 | 171217686 |
| a0006c0006t0016 | 0/0 | 5217 | 3 | 3 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5212): Show |
chr1 | 171180300 | 171217686 |
| a0007c0007t0009 | 0/0 | 5443 | 6 | 6 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5438): Show |
chr1 | 171180300 | 171217686 |
| a0007c0007t0012 | 0/0 | 5216 | 4 | 4 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5211): Show |
chr1 | 171180300 | 171217686 |
| a0007c0018t0001 | 1/0 | 5215 | 1 | 0 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0008c0010t0015 | 0/0 | 5219 | 3 | 3 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5214): Show |
chr1 | 171180300 | 171217686 |
| a0008c0010t0024 | 0/0 | 5219 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5214): Show |
chr1 | 171180300 | 171217686 |
| a0009c0011t0002 | 0/0 | 5215 | 4 | 4 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0010c0013t0001 | 0/0 | 5215 | 3 | 0 | 2 | 0 | 1 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0011c0014t0006 | 0/0 | 5215 | 3 | 3 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0012c0012t0002 | 0/0 | 5215 | 3 | 3 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0013c0017t0017 | 0/0 | 5215 | 2 | 2 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0014c0020t0001 | 0/0 | 5215 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| a0015c0021t0002 | 0/0 | 5215 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | ACACA others(5210): Show |
chr1 | 171180300 | 171217686 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 25 | 4 | 7 | 9 | 3 | 2 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0005 | 0/0 | 13 | 0 | 1 | 9 | 0 | 3 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0012 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0007g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0007g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0007g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0007g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0007g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0010g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0010g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0013g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0013g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0013g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0018g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0019g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0020g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0021g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0001t0023g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0015t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0015t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0001c0015t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0003 | 0/0 | 12 | 0 | 0 | 5 | 2 | 5 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0008 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0039 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0005g0003 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0005g0008 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0005g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0005g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0005g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0002t0025g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0002c0019t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0002g0002 | 0/0 | 20 | 1 | 1 | 11 | 0 | 7 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0002g0020 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0002g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0002g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0003t0014g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0016t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0003c0016t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0005t0003g0004 | 0/0 | 17 | 0 | 4 | 13 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0005t0003g0027 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0005t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0005t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0005t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0005t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0005t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0005t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0005t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0008t0002g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0008t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0008t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0008t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0008t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0008t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0008t0022g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0009t0004g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0009t0004g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0009t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0004c0009t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0003g0011 | 0/0 | 6 | 3 | 1 | 0 | 1 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0003g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0003g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0003g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0008g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0008g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0005c0004t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0006c0006t0006g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0006c0006t0006g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0006c0006t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0006c0006t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0006c0006t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0006c0006t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0006c0006t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0006c0006t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0006c0006t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0006c0006t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0006c0006t0006g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0006c0006t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0006c0006t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0006c0006t0011g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0006c0006t0011g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0006c0006t0016g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0007c0007t0009g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0007c0007t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0007c0007t0009g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0007c0007t0009g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0007c0007t0012g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0007c0007t0012g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0007c0007t0012g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0007c0007t0012g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0007c0018t0001g0033 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0008c0010t0015g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0008c0010t0015g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0008c0010t0015g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0008c0010t0024g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0009c0011t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0009c0011t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0010c0013t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0011c0014t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0011c0014t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0011c0014t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0012c0012t0002g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0013c0017t0017g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0013c0017t0017g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0014c0020t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| a0015c0021t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00140 | hp2 | a0002 | c0002 | t0004 | g0003 | EUR | GBR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00280 | hp2 | a0005 | c0004 | t0003 | g0011 | EUR | FIN | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | FIN | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00323 | hp2 | a0005 | c0004 | t0003 | g0144 | EUR | FIN | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00423 | hp1 | a0001 | c0001 | t0007 | g0006 | EAS | CHS | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00423 | hp2 | a0004 | c0005 | t0003 | g0004 | EAS | CHS | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00438 | hp1 | a0003 | c0003 | t0002 | g0045 | EAS | CHS | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00438 | hp2 | a0004 | c0005 | t0003 | g0004 | EAS | CHS | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00544 | hp2 | a0002 | c0002 | t0004 | g0135 | EAS | CHS | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00597 | hp1 | a0014 | c0020 | t0001 | g0164 | EAS | CHS | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00597 | hp2 | a0004 | c0005 | t0003 | g0038 | EAS | CHS | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00639 | hp2 | a0004 | c0008 | t0002 | g0145 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00642 | hp1 | a0005 | c0004 | t0003 | g0138 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00673 | hp1 | a0005 | c0004 | t0003 | g0018 | EAS | CHS | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00673 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | CHS | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG00741 | hp2 | a0002 | c0002 | t0005 | g0008 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01069 | hp1 | a0005 | c0004 | t0003 | g0042 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01069 | hp2 | a0001 | c0015 | t0003 | g0061 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01071 | hp2 | a0001 | c0015 | t0003 | g0068 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01074 | hp1 | a0005 | c0004 | t0003 | g0141 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01074 | hp2 | a0005 | c0004 | t0003 | g0142 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01081 | hp2 | a0004 | c0008 | t0002 | g0036 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01099 | hp1 | a0005 | c0004 | t0003 | g0042 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01109 | hp1 | a0010 | c0013 | t0001 | g0021 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01109 | hp2 | a0004 | c0008 | t0002 | g0126 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01168 | hp1 | a0003 | c0003 | t0002 | g0020 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01169 | hp2 | a0003 | c0003 | t0002 | g0020 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01192 | hp1 | a0006 | c0006 | t0006 | g0107 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01192 | hp2 | a0002 | c0002 | t0005 | g0110 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01243 | hp1 | a0006 | c0006 | t0011 | g0007 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01243 | hp2 | a0004 | c0005 | t0003 | g0004 | AMR | PUR | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01256 | hp1 | a0003 | c0003 | t0002 | g0044 | AMR | CLM | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01256 | hp2 | a0002 | c0002 | t0005 | g0008 | AMR | CLM | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01261 | hp2 | a0004 | c0005 | t0003 | g0027 | AMR | CLM | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01358 | hp1 | a0001 | c0015 | t0003 | g0049 | AMR | CLM | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01358 | hp2 | a0004 | c0005 | t0003 | g0004 | AMR | CLM | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01361 | hp1 | a0005 | c0004 | t0003 | g0143 | AMR | CLM | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01496 | hp1 | a0003 | c0003 | t0002 | g0155 | AMR | CLM | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01496 | hp2 | a0002 | c0002 | t0005 | g0121 | AMR | CLM | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01515 | hp1 | a0002 | c0002 | t0004 | g0003 | EUR | IBS | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01515 | hp2 | a0006 | c0006 | t0006 | g0037 | EUR | IBS | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01517 | hp1 | a0010 | c0013 | t0001 | g0021 | EUR | IBS | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01517 | hp2 | a0006 | c0006 | t0006 | g0037 | EUR | IBS | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01884 | hp1 | a0006 | c0006 | t0016 | g0025 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01884 | hp2 | a0008 | c0010 | t0024 | g0086 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01891 | hp1 | a0011 | c0014 | t0006 | g0082 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01891 | hp2 | a0006 | c0006 | t0016 | g0025 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01934 | hp1 | a0002 | c0002 | t0005 | g0009 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01934 | hp2 | a0003 | c0003 | t0002 | g0165 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01952 | hp1 | a0002 | c0002 | t0005 | g0122 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01978 | hp1 | a0003 | c0003 | t0002 | g0002 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01978 | hp2 | a0002 | c0002 | t0005 | g0003 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01981 | hp1 | a0004 | c0005 | t0003 | g0004 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01993 | hp1 | a0010 | c0013 | t0001 | g0021 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01993 | hp2 | a0004 | c0005 | t0003 | g0004 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02004 | hp2 | a0002 | c0002 | t0005 | g0134 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02015 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02015 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02027 | hp1 | a0001 | c0001 | t0007 | g0006 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02027 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02040 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02056 | hp1 | a0005 | c0004 | t0003 | g0139 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02080 | hp1 | a0003 | c0003 | t0014 | g0002 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02080 | hp2 | a0002 | c0002 | t0004 | g0008 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02083 | hp1 | a0002 | c0002 | t0004 | g0010 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02129 | hp1 | a0004 | c0005 | t0003 | g0120 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02129 | hp2 | a0005 | c0004 | t0003 | g0146 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02132 | hp1 | a0003 | c0003 | t0014 | g0002 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02132 | hp2 | a0002 | c0002 | t0004 | g0010 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02135 | hp1 | a0006 | c0006 | t0006 | g0098 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02135 | hp2 | a0015 | c0021 | t0002 | g0002 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02148 | hp1 | a0004 | c0005 | t0003 | g0027 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02148 | hp2 | a0003 | c0003 | t0002 | g0045 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02155 | hp1 | a0003 | c0003 | t0014 | g0002 | EAS | CDX | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02155 | hp2 | a0002 | c0002 | t0005 | g0003 | EAS | CDX | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02257 | hp1 | a0001 | c0001 | t0020 | g0076 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02258 | hp1 | a0011 | c0014 | t0006 | g0078 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02258 | hp2 | a0007 | c0007 | t0009 | g0090 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02273 | hp1 | a0002 | c0002 | t0005 | g0003 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02273 | hp2 | a0005 | c0004 | t0003 | g0011 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02280 | hp1 | a0006 | c0006 | t0011 | g0007 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02280 | hp2 | a0004 | c0009 | t0004 | g0016 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02293 | hp1 | a0002 | c0002 | t0005 | g0003 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02451 | hp1 | a0005 | c0004 | t0008 | g0017 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02523 | hp1 | a0001 | c0001 | t0010 | g0013 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02572 | hp1 | a0005 | c0004 | t0003 | g0043 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02572 | hp2 | a0006 | c0006 | t0016 | g0025 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02615 | hp1 | a0005 | c0004 | t0008 | g0029 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02615 | hp2 | a0006 | c0006 | t0006 | g0007 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02622 | hp1 | a0005 | c0004 | t0003 | g0011 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02622 | hp2 | a0006 | c0006 | t0006 | g0108 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02630 | hp2 | a0006 | c0006 | t0006 | g0106 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02647 | hp1 | a0005 | c0004 | t0003 | g0043 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02647 | hp2 | a0004 | c0009 | t0004 | g0094 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02698 | hp1 | a0003 | c0003 | t0002 | g0002 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02698 | hp2 | a0002 | c0002 | t0004 | g0039 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02717 | hp1 | a0009 | c0011 | t0002 | g0023 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02717 | hp2 | a0005 | c0004 | t0008 | g0017 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02723 | hp1 | a0004 | c0009 | t0004 | g0016 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02735 | hp1 | a0002 | c0002 | t0004 | g0003 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02735 | hp2 | a0003 | c0003 | t0002 | g0002 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02738 | hp1 | a0001 | c0001 | t0021 | g0032 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02738 | hp2 | a0002 | c0002 | t0004 | g0114 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02809 | hp1 | a0006 | c0006 | t0006 | g0109 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02809 | hp2 | a0008 | c0010 | t0015 | g0085 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02818 | hp2 | a0006 | c0006 | t0011 | g0105 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02886 | hp1 | a0004 | c0008 | t0002 | g0097 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02895 | hp1 | a0005 | c0004 | t0003 | g0148 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02896 | hp1 | a0007 | c0007 | t0012 | g0088 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02896 | hp2 | a0009 | c0011 | t0002 | g0023 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02897 | hp2 | a0007 | c0007 | t0012 | g0087 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02922 | hp1 | a0013 | c0017 | t0017 | g0150 | AFR | ESN | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02922 | hp2 | a0012 | c0012 | t0002 | g0024 | AFR | ESN | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02965 | hp1 | a0004 | c0008 | t0002 | g0095 | AFR | ESN | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02965 | hp2 | a0006 | c0006 | t0006 | g0104 | AFR | ESN | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02970 | hp1 | a0007 | c0007 | t0009 | g0022 | AFR | ESN | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02970 | hp2 | a0005 | c0004 | t0003 | g0011 | AFR | ESN | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02976 | hp1 | a0005 | c0004 | t0008 | g0140 | AFR | ESN | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02976 | hp2 | a0004 | c0009 | t0004 | g0096 | AFR | ESN | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03017 | hp1 | a0002 | c0002 | t0004 | g0003 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03041 | hp1 | a0013 | c0017 | t0017 | g0151 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03041 | hp2 | a0004 | c0009 | t0004 | g0035 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03098 | hp1 | a0007 | c0007 | t0009 | g0089 | AFR | MSL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03098 | hp2 | a0004 | c0008 | t0002 | g0093 | AFR | MSL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03130 | hp1 | a0011 | c0014 | t0006 | g0083 | AFR | ESN | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03130 | hp2 | a0003 | c0003 | t0002 | g0002 | AFR | ESN | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03139 | hp1 | a0006 | c0006 | t0006 | g0007 | AFR | ESN | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03139 | hp2 | a0002 | c0002 | t0004 | g0028 | AFR | ESN | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03209 | hp1 | a0005 | c0004 | t0003 | g0136 | AFR | MSL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03209 | hp2 | a0005 | c0004 | t0003 | g0137 | AFR | MSL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03225 | hp1 | a0007 | c0007 | t0012 | g0084 | AFR | MSL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03225 | hp2 | a0006 | c0006 | t0006 | g0100 | AFR | MSL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03239 | hp2 | a0003 | c0003 | t0002 | g0002 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03453 | hp1 | a0012 | c0012 | t0002 | g0024 | AFR | MSL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03453 | hp2 | a0005 | c0004 | t0008 | g0147 | AFR | MSL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03486 | hp1 | a0006 | c0006 | t0006 | g0102 | AFR | MSL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03486 | hp2 | a0002 | c0002 | t0004 | g0028 | AFR | MSL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03490 | hp1 | a0005 | c0004 | t0003 | g0011 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03490 | hp2 | a0002 | c0002 | t0004 | g0003 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03491 | hp1 | a0005 | c0004 | t0003 | g0149 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03491 | hp2 | a0003 | c0003 | t0002 | g0020 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03492 | hp1 | a0003 | c0003 | t0002 | g0020 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03492 | hp2 | a0002 | c0002 | t0004 | g0003 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03540 | hp1 | a0005 | c0004 | t0008 | g0017 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03540 | hp2 | a0004 | c0009 | t0004 | g0035 | AFR | GWD | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03579 | hp1 | a0012 | c0012 | t0002 | g0024 | AFR | MSL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03579 | hp2 | a0006 | c0006 | t0006 | g0007 | AFR | MSL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03669 | hp2 | a0003 | c0003 | t0002 | g0159 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03704 | hp1 | a0002 | c0002 | t0004 | g0009 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03704 | hp2 | a0003 | c0003 | t0002 | g0002 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03710 | hp2 | a0002 | c0002 | t0004 | g0133 | SAS | PJL | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03831 | hp1 | a0001 | c0001 | t0018 | g0066 | SAS | BEB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03831 | hp2 | a0003 | c0003 | t0002 | g0002 | SAS | BEB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03942 | hp1 | a0003 | c0003 | t0002 | g0162 | SAS | BEB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG04115 | hp2 | a0003 | c0003 | t0002 | g0166 | SAS | STU | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG04184 | hp1 | a0003 | c0003 | t0002 | g0002 | SAS | BEB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG04199 | hp1 | a0005 | c0004 | t0003 | g0041 | SAS | STU | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG04199 | hp2 | a0002 | c0002 | t0004 | g0003 | SAS | STU | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG04204 | hp1 | a0002 | c0002 | t0004 | g0008 | SAS | STU | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | STU | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG04228 | hp1 | a0002 | c0002 | t0004 | g0008 | SAS | STU | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG04228 | hp2 | a0003 | c0003 | t0002 | g0002 | SAS | STU | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18522 | hp1 | a0005 | c0004 | t0008 | g0017 | AFR | YRI | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18522 | hp2 | a0004 | c0009 | t0004 | g0016 | AFR | YRI | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18612 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | CHB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18612 | hp2 | a0001 | c0001 | t0007 | g0006 | EAS | CHB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18747 | hp1 | a0005 | c0004 | t0003 | g0018 | EAS | CHB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18747 | hp2 | a0002 | c0002 | t0005 | g0003 | EAS | CHB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18906 | hp1 | a0008 | c0010 | t0015 | g0080 | AFR | YRI | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18906 | hp2 | a0004 | c0008 | t0002 | g0036 | AFR | YRI | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18941 | hp1 | a0002 | c0002 | t0004 | g0010 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18942 | hp2 | a0003 | c0003 | t0002 | g0156 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18943 | hp1 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18943 | hp2 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18945 | hp2 | a0002 | c0002 | t0005 | g0003 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18946 | hp1 | a0002 | c0002 | t0004 | g0123 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18947 | hp1 | a0001 | c0001 | t0007 | g0059 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18947 | hp2 | a0002 | c0002 | t0004 | g0118 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18949 | hp2 | a0003 | c0003 | t0002 | g0163 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18950 | hp1 | a0003 | c0003 | t0001 | g0157 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18950 | hp2 | a0002 | c0002 | t0004 | g0128 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18951 | hp1 | a0005 | c0004 | t0003 | g0041 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18954 | hp2 | a0004 | c0005 | t0003 | g0027 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18956 | hp2 | a0002 | c0002 | t0005 | g0008 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18959 | hp1 | a0001 | c0001 | t0019 | g0074 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18959 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18960 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18961 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18961 | hp2 | a0002 | c0002 | t0005 | g0003 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18963 | hp2 | a0002 | c0002 | t0004 | g0026 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18965 | hp1 | a0002 | c0002 | t0005 | g0003 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18967 | hp2 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18968 | hp2 | a0002 | c0002 | t0004 | g0152 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18970 | hp1 | a0003 | c0016 | t0002 | g0019 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18970 | hp2 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18971 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18972 | hp1 | a0002 | c0002 | t0004 | g0010 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18973 | hp1 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18973 | hp2 | a0003 | c0003 | t0002 | g0019 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18978 | hp1 | a0003 | c0003 | t0002 | g0153 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18978 | hp2 | a0001 | c0001 | t0013 | g0055 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18979 | hp1 | a0002 | c0002 | t0005 | g0008 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18980 | hp1 | a0002 | c0002 | t0004 | g0030 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18981 | hp2 | a0002 | c0002 | t0004 | g0115 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18982 | hp1 | a0002 | c0002 | t0004 | g0132 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18983 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18985 | hp1 | a0002 | c0002 | t0005 | g0003 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18986 | hp1 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18986 | hp2 | a0002 | c0002 | t0004 | g0030 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18989 | hp1 | a0004 | c0005 | t0003 | g0112 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18989 | hp2 | a0001 | c0001 | t0013 | g0012 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18990 | hp1 | a0002 | c0002 | t0004 | g0030 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18991 | hp1 | a0002 | c0002 | t0004 | g0129 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18991 | hp2 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18994 | hp1 | a0002 | c0002 | t0004 | g0010 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18995 | hp1 | a0003 | c0003 | t0002 | g0160 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18995 | hp2 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18998 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18998 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18999 | hp1 | a0001 | c0001 | t0013 | g0048 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA18999 | hp2 | a0002 | c0002 | t0005 | g0111 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19000 | hp1 | a0002 | c0002 | t0005 | g0009 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19000 | hp2 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19001 | hp1 | a0002 | c0019 | t0004 | g0003 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19002 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19002 | hp2 | a0003 | c0003 | t0014 | g0002 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19003 | hp2 | a0004 | c0005 | t0003 | g0113 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19004 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19004 | hp2 | a0002 | c0002 | t0004 | g0040 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19005 | hp2 | a0002 | c0002 | t0004 | g0009 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19009 | hp1 | a0004 | c0005 | t0003 | g0116 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19009 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19011 | hp1 | a0002 | c0002 | t0004 | g0026 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19011 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19012 | hp1 | a0001 | c0001 | t0013 | g0012 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19012 | hp2 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19030 | hp1 | a0002 | c0002 | t0025 | g0028 | AFR | LWK | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19030 | hp2 | a0007 | c0007 | t0009 | g0022 | AFR | LWK | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19043 | hp1 | a0008 | c0010 | t0015 | g0081 | AFR | LWK | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19043 | hp2 | a0009 | c0011 | t0002 | g0092 | AFR | LWK | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19054 | hp1 | a0002 | c0002 | t0004 | g0010 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19056 | hp1 | a0005 | c0004 | t0003 | g0018 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19057 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19057 | hp2 | a0005 | c0004 | t0003 | g0018 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19060 | hp1 | a0002 | c0002 | t0004 | g0009 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19060 | hp2 | a0003 | c0003 | t0002 | g0154 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19062 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19062 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19064 | hp1 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19064 | hp2 | a0003 | c0016 | t0002 | g0019 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19065 | hp1 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19066 | hp1 | a0004 | c0005 | t0003 | g0038 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19066 | hp2 | a0002 | c0002 | t0004 | g0130 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19068 | hp1 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19068 | hp2 | a0002 | c0002 | t0004 | g0131 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19072 | hp2 | a0004 | c0005 | t0003 | g0117 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19074 | hp1 | a0002 | c0002 | t0005 | g0125 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19075 | hp1 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19075 | hp2 | a0002 | c0002 | t0005 | g0009 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19077 | hp2 | a0004 | c0005 | t0003 | g0127 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19079 | hp1 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19079 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19085 | hp1 | a0003 | c0016 | t0002 | g0161 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19085 | hp2 | a0003 | c0003 | t0002 | g0158 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19087 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19087 | hp2 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19088 | hp1 | a0002 | c0002 | t0004 | g0040 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19088 | hp2 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19089 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19089 | hp2 | a0003 | c0003 | t0002 | g0019 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19090 | hp2 | a0002 | c0002 | t0004 | g0026 | EAS | JPT | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19240 | hp1 | a0005 | c0004 | t0008 | g0029 | AFR | YRI | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA19240 | hp2 | a0007 | c0007 | t0009 | g0022 | AFR | YRI | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ASW | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA20129 | hp2 | a0006 | c0006 | t0006 | g0007 | AFR | ASW | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA20752 | hp2 | a0004 | c0008 | t0022 | g0046 | EUR | TSI | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA20805 | hp2 | a0003 | c0003 | t0002 | g0044 | EUR | TSI | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA20905 | hp2 | a0002 | c0002 | t0004 | g0119 | SAS | GIH | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01123 | hp1 | a0006 | c0006 | t0006 | g0101 | AMR | CLM | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02109 | hp1 | a0006 | c0006 | t0006 | g0103 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02109 | hp2 | a0009 | c0011 | t0002 | g0023 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02486 | hp1 | a0006 | c0006 | t0011 | g0007 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02486 | hp2 | a0007 | c0007 | t0009 | g0091 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02559 | hp1 | a0007 | c0007 | t0012 | g0079 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG02559 | hp2 | a0005 | c0004 | t0008 | g0029 | AFR | ACB | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG06807 | hp1 | a0004 | c0009 | t0004 | g0016 | AFR | USA | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA20300 | hp1 | a0006 | c0006 | t0006 | g0099 | AFR | USA | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | USA | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA21309 | hp1 | a0005 | c0004 | t0003 | g0011 | AFR | LWK | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| NA21309 | hp2 | a0002 | c0002 | t0004 | g0039 | AFR | LWK | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0023 | g0058 | REF | REF | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| homoSapiens | grch38p0 | a0007 | c0018 | t0001 | g0033 | REF | REF | FMO2_chr1_171180300_171217686 | FMO2 | chr1 | 171180300 | 171217686 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:171185820 | A | G | 4 | a0003 a0009 a0014 others(1): Show |
55 | HG00438.hp1 HG00597.hp1 HG01168.hp1 others(52): Show |
missense_variant | MODERATE | c.107A>G | p.Asp36Gly | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/9 | 173/5215 | 107/1608 | 36/535 | chr1 | 171185820 | |||
| chr1:171193377 | G | A | 1 | a0012 | 3 | HG02922.hp2 HG03453.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.175G>A | p.Val59Ile | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/9 | 241/5215 | 175/1608 | 59/535 | chr1 | 171193377 | |||
| chr1:171193408 | T | A | 1 | a0009 | 4 | HG02109.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
missense_variant | MODERATE | c.206T>A | p.Phe69Tyr | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/9 | 272/5215 | 206/1608 | 69/535 | chr1 | 171193408 | |||
| chr1:171193412 | T | TGAC | 1 | a0006 | 24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
conservative_inframe_insertion | MODERATE | c.211_213dupGAC | p.Asp71dup | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/9 | 280/5215 | 214/1608 | 72/535 | INFO_REALIGN_3_PRIME | chr1 | 171193412 | ||
| chr1:171193444 | T | C | 1 | a0006 | 24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
missense_variant | MODERATE | c.242T>C | p.Phe81Ser | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/9 | 308/5215 | 242/1608 | 81/535 | chr1 | 171193444 | |||
| chr1:171196663 | TG | T | 1 | a0006 | 24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
frameshift_variant | HIGH | c.337delG | p.Val113fs | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/9 | 403/5215 | 337/1608 | 113/535 | chr1 | 171196663 | |||
| chr1:171199358 | T | C | 1 | a0010 | 3 | HG01109.hp1 HG01517.hp1 HG01993.hp1 |
missense_variant | MODERATE | c.497T>C | p.Phe166Ser | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/9 | 563/5215 | 497/1608 | 166/535 | chr1 | 171199358 | |||
| chr1:171199406 | T | C | 1 | a0005 | 36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
missense_variant | MODERATE | c.545T>C | p.Phe182Ser | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/9 | 611/5215 | 545/1608 | 182/535 | chr1 | 171199406 | |||
| chr1:171199445 | C | T | 7 | a0002 a0003 a0004 others(4): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
missense_variant | MODERATE | c.584C>T | p.Ser195Leu | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/9 | 650/5215 | 584/1608 | 195/535 | chr1 | 171199445 | |||
| chr1:171203950 | G | A | 1 | a0008 | 4 | HG01884.hp2 HG02809.hp2 NA18906.hp1 others(1): Show |
missense_variant | MODERATE | c.713G>A | p.Arg238Gln | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 6/9 | 779/5215 | 713/1608 | 238/535 | chr1 | 171203950 | |||
| chr1:171205392 | A | G | 1 | a0002 | 73 | HG00140.hp2 HG00544.hp2 HG00741.hp2 others(70): Show |
missense_variant | MODERATE | c.941A>G | p.Glu314Gly | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 7/9 | 1007/5215 | 941/1608 | 314/535 | chr1 | 171205392 | |||
| chr1:171205550 | G | A | 1 | a0015 | 1 | HG02135.hp2 | missense_variant | MODERATE | c.1099G>A | p.Ala367Thr | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 7/9 | 1165/5215 | 1099/1608 | 367/535 | chr1 | 171205550 | |||
| chr1:171205623 | G | C | 1 | a0013 | 2 | HG02922.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.1172G>C | p.Arg391Thr | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 7/9 | 1238/5215 | 1172/1608 | 391/535 | chr1 | 171205623 | |||
| chr1:171207773 | T | G | 2 | a0006 a0011 |
27 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(24): Show |
missense_variant | MODERATE | c.1239T>G | p.Asn413Lys | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/9 | 1305/5215 | 1239/1608 | 413/535 | chr1 | 171207773 | |||
| chr1:171208951 | C | T | 12 | a0001 a0002 a0003 others(9): Show |
348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
stop_gained | HIGH | c.1414C>T | p.Gln472* | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1480/5215 | 1414/1608 | 472/535 | chr1 | 171208951 | |||
| chr1:171209006 | C | T | 1 | a0002 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.1469C>T | p.Thr490Ile | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1535/5215 | 1469/1608 | 490/535 | chr1 | 171209006 | |||
| chr1:171209118 | C | CT | 2 | a0002 a0004 |
81 | HG00140.hp2 HG00544.hp2 HG00741.hp2 others(78): Show |
frameshift_variant | HIGH | c.1588dupT | p.Cys530fs | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1655/5215 | 1589/1608 | 530/535 | INFO_REALIGN_3_PRIME | chr1 | 171209118 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:171199446 | A | G | 12 | a0002c0002 a0002c0019 a0003c0003 others(9): Show |
234 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(231): Show |
synonymous_variant | LOW | c.585A>G | p.Ser195Ser | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/9 | 651/5215 | 585/1608 | 195/535 | chr1 | 171199446 | |||
| chr1:171205552 | G | A | 3 | a0007c0007 a0008c0010 a0013c0017 |
16 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(13): Show |
synonymous_variant | LOW | c.1101G>A | p.Ala367Ala | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 7/9 | 1167/5215 | 1101/1608 | 367/535 | chr1 | 171205552 | |||
| chr1:171207740 | G | A | 3 | a0007c0007 a0008c0010 a0013c0017 |
16 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(13): Show |
synonymous_variant | LOW | c.1206G>A | p.Glu402Glu | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/9 | 1272/5215 | 1206/1608 | 402/535 | chr1 | 171207740 | |||
| chr1:171209013 | A | G | 3 | a0001c0015 a0004c0005 a0005c0004 |
67 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(64): Show |
synonymous_variant | LOW | c.1476A>G | p.Lys492Lys | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1542/5215 | 1476/1608 | 492/535 | chr1 | 171209013 | |||
| chr1:171209092 | C | T | 1 | a0003c0016 | 3 | NA18970.hp1 NA19064.hp2 NA19085.hp1 |
synonymous_variant | LOW | c.1555C>T | p.Leu519Leu | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1621/5215 | 1555/1608 | 519/535 | chr1 | 171209092 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:171209281 | A | G | 1 | a0003c0003t0014 | 4 | HG02080.hp1 HG02132.hp1 HG02155.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*136A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 136 | chr1 | 171209281 | ||||||
| chr1:171209351 | C | T | 5 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0025 others(2): Show |
81 | HG00140.hp2 HG00544.hp2 HG00741.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*206C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 206 | chr1 | 171209351 | ||||||
| chr1:171209377 | C | T | 1 | a0008c0010t0024 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*232C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 232 | chr1 | 171209377 | ||||||
| chr1:171209402 | G | A | 1 | a0001c0001t0018 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*257G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 257 | chr1 | 171209402 | ||||||
| chr1:171209486 | TG | T | 1 | a0002c0002t0005 | 22 | HG00741.hp2 HG01192.hp2 HG01256.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*343delG | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 343 | INFO_REALIGN_3_PRIME | chr1 | 171209486 | |||||
| chr1:171209706 | ATATTAAG others(13): Show |
A | 1 | a0001c0001t0019 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*562_*581delTATTAA others(14): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 562 | chr1 | 171209706 | ||||||
| chr1:171209844 | T | C | 1 | a0006c0006t0011 | 4 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*699T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 699 | chr1 | 171209844 | ||||||
| chr1:171209886 | T | C | 5 | a0007c0007t0009 a0007c0007t0012 a0008c0010t0015 others(2): Show |
16 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*741T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 741 | chr1 | 171209886 | ||||||
| chr1:171210099 | A | G | 2 | a0008c0010t0015 a0008c0010t0024 |
4 | HG01884.hp2 HG02809.hp2 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*954A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 954 | chr1 | 171210099 | ||||||
| chr1:171210148 | C | T | 12 | a0001c0001t0002 a0001c0015t0003 a0003c0003t0002 others(9): Show |
131 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1003C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1003 | chr1 | 171210148 | ||||||
| chr1:171210212 | A | T | 5 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0025 others(2): Show |
81 | HG00140.hp2 HG00544.hp2 HG00741.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1067A>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1067 | chr1 | 171210212 | ||||||
| chr1:171210332 | T | C | 1 | a0001c0001t0020 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1187T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1187 | chr1 | 171210332 | ||||||
| chr1:171210338 | C | T | 17 | a0001c0001t0002 a0001c0015t0003 a0003c0003t0002 others(14): Show |
147 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*1193C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1193 | chr1 | 171210338 | ||||||
| chr1:171210506 | G | A | 1 | a0001c0001t0010 | 5 | HG00673.hp2 HG02015.hp1 HG02523.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1361G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1361 | chr1 | 171210506 | ||||||
| chr1:171210527 | C | T | 1 | a0001c0001t0007 | 13 | HG00423.hp1 HG02027.hp1 NA18612.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1382C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1382 | chr1 | 171210527 | ||||||
| chr1:171210531 | C | G | 8 | a0001c0001t0002 a0003c0003t0002 a0003c0003t0014 others(5): Show |
64 | HG00438.hp1 HG00639.hp2 HG01081.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1386C>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1386 | chr1 | 171210531 | ||||||
| chr1:171210640 | A | G | 9 | a0006c0006t0006 a0006c0006t0011 a0006c0006t0016 others(6): Show |
43 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1495A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1495 | chr1 | 171210640 | ||||||
| chr1:171210672 | CTTA | C | 2 | a0007c0007t0009 a0007c0007t0012 |
10 | HG02258.hp2 HG02486.hp2 HG02559.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1530_*1532delATT | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1530 | INFO_REALIGN_3_PRIME | chr1 | 171210672 | |||||
| chr1:171210717 | TGTACTTC others(157): Show |
T | 1 | a0001c0001t0013 | 4 | NA18978.hp2 NA18989.hp2 NA18999.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1655_*1818del | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1655 | INFO_REALIGN_3_PRIME | chr1 | 171210717 | |||||
| chr1:171210882 | G | T | 21 | a0001c0001t0002 a0001c0015t0003 a0003c0003t0002 others(18): Show |
174 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*1737G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1737 | chr1 | 171210882 | ||||||
| chr1:171210932 | A | G | 9 | a0006c0006t0006 a0006c0006t0011 a0006c0006t0016 others(6): Show |
43 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1787A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1787 | chr1 | 171210932 | ||||||
| chr1:171211062 | T | C | 9 | a0006c0006t0006 a0006c0006t0011 a0006c0006t0016 others(6): Show |
43 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1917T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1917 | chr1 | 171211062 | ||||||
| chr1:171211101 | T | TGTAA | 4 | a0007c0007t0009 a0007c0007t0012 a0008c0010t0015 others(1): Show |
14 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1959_*1962dupAAGT | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 1963 | INFO_REALIGN_3_PRIME | chr1 | 171211101 | |||||
| chr1:171211346 | C | T | 1 | a0004c0008t0022 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2201C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 2201 | chr1 | 171211346 | ||||||
| chr1:171211541 | G | GAAATATT others(215): Show |
1 | a0007c0007t0009 | 6 | HG02258.hp2 HG02486.hp2 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2399_*2400insTATT others(218): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 2400 | INFO_REALIGN_3_PRIME | chr1 | 171211541 | |||||
| chr1:171211550 | A | AGATAT | 1 | a0007c0007t0009 | 6 | HG02258.hp2 HG02486.hp2 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2405_*2406insGATA others(1): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 2406 | chr1 | 171211550 | ||||||
| chr1:171211933 | C | A | 1 | a0005c0004t0008 | 9 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2788C>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 2788 | chr1 | 171211933 | ||||||
| chr1:171212070 | T | G | 1 | a0002c0002t0025 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2925T>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 2925 | chr1 | 171212070 | ||||||
| chr1:171212306 | G | A | 1 | a0001c0001t0021 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3161G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 3161 | chr1 | 171212306 | ||||||
| chr1:171212615 | G | A | 3 | a0006c0006t0006 a0006c0006t0011 a0011c0014t0006 |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3470G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 9/9 | 3470 | chr1 | 171212615 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:171185467 | A | G | 1 | a0003c0003t0002g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-7+108A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 1/8 | chr1 | 171185467 | |||||||
| chr1:171185504 | AG | A | 22 | a0003c0003t0001g0157 a0003c0003t0002g0002 a0003c0003t0002g0019 others(19): Show |
51 | HG00438.hp1 HG00597.hp1 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.-7+147delG | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 171185504 | ||||||
| chr1:171185515 | A | G | 1 | a0004c0009t0004g0035 | 2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-7+156A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 1/8 | chr1 | 171185515 | |||||||
| chr1:171185679 | G | T | 2 | a0003c0003t0002g0045 a0003c0003t0002g0165 |
3 | HG00438.hp1 HG01934.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.-6-29G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 1/8 | chr1 | 171185679 | |||||||
| chr1:171185893 | G | A | 1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.132+48G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171185893 | |||||||
| chr1:171185964 | C | T | 134 | a0001c0001t0001g0124 a0001c0001t0002g0077 a0001c0001t0020g0076 others(131): Show |
257 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.132+119C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171185964 | |||||||
| chr1:171186043 | C | T | 2 | a0002c0002t0004g0030 a0002c0002t0004g0152 |
4 | NA18968.hp2 NA18980.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+198C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171186043 | |||||||
| chr1:171186122 | C | T | 2 | a0013c0017t0017g0150 a0013c0017t0017g0151 |
2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.132+277C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171186122 | |||||||
| chr1:171186493 | A | G | 117 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(114): Show |
238 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.132+648A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171186493 | |||||||
| chr1:171186709 | A | G | 4 | a0007c0007t0009g0022 a0007c0007t0009g0089 a0007c0007t0009g0090 others(1): Show |
6 | HG02258.hp2 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+864A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171186709 | |||||||
| chr1:171186716 | C | T | 21 | a0004c0008t0002g0145 a0005c0004t0003g0011 a0005c0004t0003g0018 others(18): Show |
37 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.132+871C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171186716 | |||||||
| chr1:171186788 | A | G | 44 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(41): Show |
103 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.132+943A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171186788 | |||||||
| chr1:171186895 | T | C | 24 | a0003c0003t0001g0157 a0003c0003t0002g0002 a0003c0003t0002g0019 others(21): Show |
55 | HG00438.hp1 HG00597.hp1 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.132+1050T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171186895 | |||||||
| chr1:171186961 | A | G | 24 | a0003c0003t0001g0157 a0003c0003t0002g0002 a0003c0003t0002g0019 others(21): Show |
55 | HG00438.hp1 HG00597.hp1 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.132+1116A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171186961 | |||||||
| chr1:171187292 | A | G | 133 | a0001c0001t0001g0124 a0001c0001t0002g0077 a0002c0002t0004g0003 others(130): Show |
256 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.132+1447A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171187292 | |||||||
| chr1:171187344 | A | G | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.132+1499A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171187344 | |||||||
| chr1:171187376 | G | A | 1 | a0002c0002t0005g0110 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.132+1531G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171187376 | |||||||
| chr1:171187402 | G | C | 1 | a0001c0001t0002g0077 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.132+1557G>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171187402 | |||||||
| chr1:171187405 | T | C | 51 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(48): Show |
115 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.132+1560T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171187405 | |||||||
| chr1:171187451 | T | A | 2 | a0001c0001t0001g0047 a0002c0002t0005g0111 |
2 | NA18999.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.132+1606T>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171187451 | |||||||
| chr1:171187625 | A | C | 1 | a0002c0002t0004g0135 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.132+1780A>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171187625 | |||||||
| chr1:171187627 | C | CA | 19 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0050 others(16): Show |
32 | HG00423.hp1 HG00642.hp1 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.132+1809dupA | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171187627 | ||||||
| chr1:171187627 | CA | C | 18 | a0001c0001t0001g0034 a0001c0001t0001g0073 a0001c0001t0019g0074 others(15): Show |
21 | HG01168.hp2 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.132+1809delA | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171187627 | ||||||
| chr1:171187627 | CAA | C | 11 | a0001c0001t0001g0075 a0002c0002t0004g0009 a0002c0002t0004g0030 others(8): Show |
17 | HG01934.hp1 HG02486.hp2 HG02738.hp2 others(14): Show |
intron_variant | MODIFIER | c.132+1808_132+1809d others(4): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171187627 | ||||||
| chr1:171187627 | CAAA | C | 41 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(38): Show |
99 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.132+1807_132+1809d others(5): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171187627 | ||||||
| chr1:171187627 | CAAAA | C | 22 | a0002c0002t0004g0132 a0002c0002t0004g0133 a0002c0002t0005g0134 others(19): Show |
32 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.132+1806_132+1809d others(6): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171187627 | ||||||
| chr1:171187627 | CAAAAA | C | 21 | a0003c0003t0001g0157 a0003c0003t0002g0002 a0003c0003t0002g0019 others(18): Show |
50 | HG00438.hp1 HG00597.hp1 HG01168.hp1 others(47): Show |
intron_variant | MODIFIER | c.132+1805_132+1809d others(7): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171187627 | ||||||
| chr1:171187627 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0047 a0004c0009t0004g0096 |
2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.132+1800_132+1809d others(12): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171187627 | ||||||
| chr1:171187643 | A | T | 1 | a0012c0012t0002g0024 | 3 | HG02922.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.132+1798A>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171187643 | |||||||
| chr1:171187687 | T | C | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.132+1842T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171187687 | |||||||
| chr1:171187688 | G | A | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.132+1843G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171187688 | |||||||
| chr1:171187810 | A | C | 4 | a0005c0004t0008g0017 a0005c0004t0008g0029 a0005c0004t0008g0140 others(1): Show |
9 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.132+1965A>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171187810 | |||||||
| chr1:171187858 | G | A | 113 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(110): Show |
232 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.132+2013G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171187858 | |||||||
| chr1:171187864 | C | A | 1 | a0007c0007t0012g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.132+2019C>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171187864 | |||||||
| chr1:171187906 | T | C | 1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.132+2061T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171187906 | |||||||
| chr1:171187913 | C | G | 1 | a0003c0003t0002g0020 | 4 | HG01168.hp1 HG01169.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+2068C>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171187913 | |||||||
| chr1:171187944 | G | T | 1 | a0006c0006t0006g0098 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.132+2099G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171187944 | |||||||
| chr1:171188029 | AATTTTTT others(3): Show |
A | 15 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(12): Show |
23 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.132+2185_132+2194d others(12): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171188029 | |||||||
| chr1:171188029 | AATTTTTT others(4): Show |
A | 1 | a0006c0006t0006g0099 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.132+2185_132+2195d others(13): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171188029 | |||||||
| chr1:171188030 | A | AT | 67 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(64): Show |
115 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.132+2209dupT | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171188030 | ||||||
| chr1:171188030 | A | ATT | 19 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0010 others(16): Show |
31 | HG00140.hp2 HG00423.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.132+2208_132+2209d others(4): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171188030 | ||||||
| chr1:171188030 | AT | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0004c0008t0002g0097 others(2): Show |
7 | HG02523.hp2 HG02886.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.132+2209delT | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171188030 | ||||||
| chr1:171188030 | ATTT | A | 5 | a0001c0001t0001g0001 a0005c0004t0003g0011 a0005c0004t0008g0017 others(2): Show |
8 | HG02257.hp2 HG02273.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.132+2207_132+2209d others(5): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171188030 | ||||||
| chr1:171188030 | ATTTT | A | 19 | a0001c0001t0001g0001 a0004c0008t0002g0145 a0005c0004t0003g0011 others(16): Show |
31 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.132+2206_132+2209d others(6): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171188030 | ||||||
| chr1:171188030 | ATTTTTTT | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0032 others(6): Show |
14 | HG00673.hp2 HG02015.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.132+2203_132+2209d others(9): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171188030 | ||||||
| chr1:171188030 | ATTTTTTT others(6): Show |
A | 1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.132+2197_132+2209d others(15): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171188030 | ||||||
| chr1:171188050 | T | C | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.132+2205T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171188050 | |||||||
| chr1:171188301 | C | G | 1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.132+2456C>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171188301 | |||||||
| chr1:171188330 | A | C | 91 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(88): Show |
194 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.132+2485A>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171188330 | |||||||
| chr1:171188478 | T | C | 3 | a0002c0002t0004g0010 a0002c0002t0004g0115 a0002c0002t0004g0132 |
8 | HG02083.hp1 HG02132.hp2 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.132+2633T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171188478 | |||||||
| chr1:171188569 | C | G | 91 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(88): Show |
194 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.132+2724C>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171188569 | |||||||
| chr1:171188620 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.132+2775T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171188620 | |||||||
| chr1:171188722 | C | A | 1 | a0001c0001t0001g0031 | 2 | NA18945.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.132+2877C>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171188722 | |||||||
| chr1:171188736 | G | A | 113 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(110): Show |
232 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.132+2891G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171188736 | |||||||
| chr1:171188748 | A | G | 3 | a0002c0002t0004g0129 a0002c0002t0004g0130 a0002c0002t0004g0131 |
3 | NA18991.hp1 NA19066.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.132+2903A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171188748 | |||||||
| chr1:171188869 | T | A | 23 | a0003c0003t0001g0157 a0003c0003t0002g0002 a0003c0003t0002g0019 others(20): Show |
54 | HG00438.hp1 HG01168.hp1 HG01169.hp2 others(51): Show |
intron_variant | MODIFIER | c.132+3024T>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171188869 | |||||||
| chr1:171189082 | G | A | 51 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(48): Show |
115 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.132+3237G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171189082 | |||||||
| chr1:171189088 | G | C | 116 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(113): Show |
237 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.132+3243G>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171189088 | |||||||
| chr1:171189115 | T | C | 2 | a0004c0005t0003g0112 a0004c0005t0003g0116 |
2 | NA18989.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.132+3270T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171189115 | |||||||
| chr1:171189145 | C | T | 90 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(87): Show |
193 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.132+3300C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171189145 | |||||||
| chr1:171189212 | AT | A | 90 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(87): Show |
193 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.132+3375delT | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171189212 | ||||||
| chr1:171189217 | T | C | 90 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(87): Show |
193 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.132+3372T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171189217 | |||||||
| chr1:171189360 | T | C | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.132+3515T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171189360 | |||||||
| chr1:171189373 | T | TA | 90 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(87): Show |
193 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.132+3531dupA | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171189373 | ||||||
| chr1:171189601 | A | T | 1 | a0008c0010t0024g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.133-3734A>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171189601 | |||||||
| chr1:171189654 | C | CT | 14 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(11): Show |
22 | HG01192.hp1 HG01243.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.133-3677dupT | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171189654 | ||||||
| chr1:171189654 | C | CTTTTTT | 5 | a0002c0002t0004g0129 a0002c0002t0004g0130 a0002c0002t0004g0133 others(2): Show |
9 | HG02280.hp2 HG02723.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.133-3677_133-3676i others(8): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171189654 | ||||||
| chr1:171189654 | C | CTTTTTTT | 36 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0009 others(33): Show |
88 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.133-3677_133-3676i others(9): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171189654 | ||||||
| chr1:171189654 | C | CTTTTTTT others(1): Show |
10 | a0002c0002t0004g0008 a0002c0002t0004g0028 a0002c0002t0004g0114 others(7): Show |
18 | HG00741.hp2 HG01109.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.133-3677_133-3676i others(10): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171189654 | ||||||
| chr1:171189657 | TTC | T | 23 | a0003c0003t0001g0157 a0003c0003t0002g0002 a0003c0003t0002g0019 others(20): Show |
51 | HG00438.hp1 HG01168.hp1 HG01169.hp2 others(48): Show |
intron_variant | MODIFIER | c.133-3676_133-3675d others(4): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171189657 | ||||||
| chr1:171189659 | C | CT | 6 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG01069.hp1 HG02895.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-3659dupT | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171189659 | ||||||
| chr1:171189659 | C | CTT | 19 | a0004c0008t0002g0145 a0005c0004t0003g0011 a0005c0004t0003g0018 others(16): Show |
33 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.133-3660_133-3659d others(4): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171189659 | ||||||
| chr1:171189659 | C | T | 66 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(63): Show |
138 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.133-3676C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171189659 | |||||||
| chr1:171189659 | CT | C | 15 | a0001c0001t0002g0077 a0004c0008t0022g0046 a0007c0007t0012g0079 others(12): Show |
15 | HG01884.hp2 HG01891.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.133-3659delT | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171189659 | ||||||
| chr1:171189659 | CTT | C | 6 | a0004c0008t0002g0097 a0007c0007t0009g0022 a0007c0007t0009g0089 others(3): Show |
10 | HG02258.hp2 HG02486.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.133-3660_133-3659d others(4): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171189659 | ||||||
| chr1:171189691 | C | T | 74 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(71): Show |
169 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.133-3644C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171189691 | |||||||
| chr1:171189796 | C | T | 3 | a0005c0004t0003g0018 a0005c0004t0003g0139 a0005c0004t0003g0146 |
6 | HG00673.hp1 HG02056.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-3539C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171189796 | |||||||
| chr1:171189847 | T | C | 90 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(87): Show |
193 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.133-3488T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171189847 | |||||||
| chr1:171190024 | T | A | 1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.133-3311T>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171190024 | |||||||
| chr1:171190151 | A | G | 90 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(87): Show |
193 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.133-3184A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171190151 | |||||||
| chr1:171190229 | A | G | 1 | a0002c0002t0005g0125 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.133-3106A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171190229 | |||||||
| chr1:171190233 | A | T | 90 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(87): Show |
193 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.133-3102A>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171190233 | |||||||
| chr1:171190729 | AT | A | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.133-2602delT | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171190729 | ||||||
| chr1:171190804 | C | T | 2 | a0002c0002t0004g0040 a0002c0002t0004g0128 |
3 | NA18950.hp2 NA19004.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.133-2531C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171190804 | |||||||
| chr1:171190872 | G | A | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.133-2463G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171190872 | |||||||
| chr1:171190927 | C | T | 2 | a0008c0010t0015g0085 a0008c0010t0024g0086 |
2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.133-2408C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171190927 | |||||||
| chr1:171190935 | C | T | 3 | a0004c0008t0002g0036 a0004c0008t0002g0093 a0004c0008t0002g0095 |
4 | HG01081.hp2 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-2400C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171190935 | |||||||
| chr1:171190976 | C | A | 20 | a0005c0004t0003g0011 a0005c0004t0003g0018 a0005c0004t0003g0041 others(17): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.133-2359C>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171190976 | |||||||
| chr1:171190982 | C | T | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.133-2353C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171190982 | |||||||
| chr1:171191001 | T | C | 112 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(109): Show |
231 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.133-2334T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171191001 | |||||||
| chr1:171191027 | C | A | 91 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(88): Show |
194 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.133-2308C>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171191027 | |||||||
| chr1:171191094 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.133-2241G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171191094 | |||||||
| chr1:171191126 | C | A | 52 | a0001c0001t0001g0124 a0002c0002t0004g0003 a0002c0002t0004g0008 others(49): Show |
116 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.133-2209C>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171191126 | |||||||
| chr1:171191145 | CA | C | 89 | a0001c0001t0001g0052 a0001c0001t0001g0124 a0002c0002t0004g0003 others(86): Show |
192 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.133-2178delA | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171191145 | ||||||
| chr1:171191330 | T | C | 20 | a0005c0004t0003g0011 a0005c0004t0003g0018 a0005c0004t0003g0041 others(17): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.133-2005T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171191330 | |||||||
| chr1:171191344 | A | T | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.133-1991A>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171191344 | |||||||
| chr1:171191559 | T | C | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.133-1776T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171191559 | |||||||
| chr1:171191749 | C | T | 1 | a0004c0009t0004g0035 | 2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.133-1586C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171191749 | |||||||
| chr1:171191786 | T | G | 111 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(108): Show |
230 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.133-1549T>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171191786 | |||||||
| chr1:171191816 | G | C | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.133-1519G>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171191816 | |||||||
| chr1:171191825 | AC | A | 2 | a0009c0011t0002g0023 a0009c0011t0002g0092 |
4 | HG02109.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-1508delC | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171191825 | ||||||
| chr1:171191860 | C | CA | 12 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0056 others(9): Show |
18 | HG01069.hp1 HG01099.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.133-1455dupA | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171191860 | ||||||
| chr1:171191860 | C | CAA | 8 | a0001c0001t0013g0055 a0008c0010t0015g0080 a0008c0010t0015g0081 others(5): Show |
8 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.133-1456_133-1455d others(4): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171191860 | ||||||
| chr1:171191860 | CA | C | 48 | a0001c0001t0001g0072 a0002c0002t0004g0003 a0002c0002t0004g0008 others(45): Show |
111 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.133-1455delA | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171191860 | ||||||
| chr1:171191860 | CAA | C | 22 | a0003c0003t0001g0157 a0003c0003t0002g0002 a0003c0003t0002g0019 others(19): Show |
51 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.133-1456_133-1455d others(4): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171191860 | ||||||
| chr1:171191880 | AT | A | 1 | a0012c0012t0002g0024 | 3 | HG02922.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.133-1454delT | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171191880 | |||||||
| chr1:171191933 | A | G | 111 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(108): Show |
230 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.133-1402A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171191933 | |||||||
| chr1:171191945 | G | GGAA | 180 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
362 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.133-1388_133-1387i others(5): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171191945 | ||||||
| chr1:171191976 | C | T | 91 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(88): Show |
194 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.133-1359C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171191976 | |||||||
| chr1:171192016 | C | G | 2 | a0006c0006t0006g0099 a0006c0006t0006g0102 |
2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.133-1319C>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171192016 | |||||||
| chr1:171192026 | C | A | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.133-1309C>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171192026 | |||||||
| chr1:171192153 | A | G | 91 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(88): Show |
194 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.133-1182A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171192153 | |||||||
| chr1:171192221 | C | G | 91 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(88): Show |
194 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.133-1114C>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171192221 | |||||||
| chr1:171192222 | T | C | 2 | a0004c0008t0002g0097 a0012c0012t0002g0024 |
4 | HG02886.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-1113T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171192222 | |||||||
| chr1:171192291 | G | A | 91 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(88): Show |
194 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.133-1044G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171192291 | |||||||
| chr1:171192355 | A | G | 1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.133-980A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171192355 | |||||||
| chr1:171192359 | T | C | 91 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(88): Show |
194 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.133-976T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171192359 | |||||||
| chr1:171192361 | C | T | 2 | a0007c0007t0012g0079 a0007c0007t0012g0084 |
2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.133-974C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171192361 | |||||||
| chr1:171192475 | C | T | 1 | a0006c0006t0006g0108 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.133-860C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171192475 | |||||||
| chr1:171192565 | T | C | 3 | a0007c0007t0009g0022 a0007c0007t0009g0089 a0007c0007t0009g0090 |
5 | HG02258.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-770T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171192565 | |||||||
| chr1:171192618 | T | G | 2 | a0004c0009t0004g0016 a0004c0009t0004g0035 |
6 | HG02280.hp2 HG02723.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-717T>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171192618 | |||||||
| chr1:171192765 | C | CA | 13 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0057 others(10): Show |
15 | HG01358.hp1 HG02486.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.133-548dupA | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171192765 | ||||||
| chr1:171192765 | CAAAA | C | 16 | a0003c0003t0002g0154 a0006c0006t0006g0007 a0006c0006t0006g0037 others(13): Show |
24 | HG01123.hp1 HG01243.hp1 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.133-551_133-548del others(4): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171192765 | ||||||
| chr1:171192765 | CAAAAA | C | 24 | a0003c0003t0001g0157 a0003c0003t0002g0002 a0003c0003t0002g0019 others(21): Show |
53 | HG00438.hp1 HG00639.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.133-552_133-548del others(5): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171192765 | ||||||
| chr1:171192765 | CAAAAAA | C | 52 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(49): Show |
120 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.133-553_133-548del others(6): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171192765 | ||||||
| chr1:171192765 | CAAAAAAA others(1): Show |
C | 20 | a0005c0004t0003g0011 a0005c0004t0003g0018 a0005c0004t0003g0041 others(17): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.133-555_133-548del others(8): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 171192765 | ||||||
| chr1:171192827 | A | G | 1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.133-508A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171192827 | |||||||
| chr1:171192921 | T | C | 49 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(46): Show |
113 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.133-414T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171192921 | |||||||
| chr1:171193066 | A | G | 3 | a0011c0014t0006g0078 a0011c0014t0006g0082 a0011c0014t0006g0083 |
3 | HG01891.hp1 HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.133-269A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171193066 | |||||||
| chr1:171193136 | C | T | 77 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(74): Show |
174 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.133-199C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171193136 | |||||||
| chr1:171193164 | G | A | 3 | a0004c0008t0002g0036 a0004c0008t0002g0093 a0004c0008t0002g0095 |
4 | HG01081.hp2 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-171G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171193164 | |||||||
| chr1:171193299 | C | T | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.133-36C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 2/8 | chr1 | 171193299 | |||||||
| chr1:171193547 | G | T | 1 | a0002c0002t0004g0123 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.321+24G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171193547 | |||||||
| chr1:171193596 | T | A | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.321+73T>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171193596 | |||||||
| chr1:171193655 | C | T | 1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.321+132C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171193655 | |||||||
| chr1:171193740 | G | A | 113 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(110): Show |
234 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.321+217G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171193740 | |||||||
| chr1:171193776 | C | CT | 25 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0070 others(22): Show |
41 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.321+268dupT | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 171193776 | ||||||
| chr1:171193791 | T | C | 4 | a0004c0008t0002g0036 a0004c0008t0002g0093 a0004c0008t0002g0095 others(1): Show |
5 | HG01081.hp2 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.321+268T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171193791 | |||||||
| chr1:171193791 | T | TC | 87 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(84): Show |
191 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.321+269dupC | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 171193791 | ||||||
| chr1:171193821 | T | C | 93 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(90): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.321+298T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171193821 | |||||||
| chr1:171193899 | C | T | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.321+376C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171193899 | |||||||
| chr1:171193969 | G | A | 1 | a0002c0002t0004g0152 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.321+446G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171193969 | |||||||
| chr1:171194031 | C | T | 2 | a0004c0008t0002g0097 a0012c0012t0002g0024 |
4 | HG02886.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.321+508C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171194031 | |||||||
| chr1:171194041 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.321+518A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171194041 | |||||||
| chr1:171194197 | A | G | 3 | a0004c0008t0002g0036 a0004c0008t0002g0093 a0004c0008t0002g0095 |
4 | HG01081.hp2 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+674A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171194197 | |||||||
| chr1:171194443 | T | G | 93 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(90): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.321+920T>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171194443 | |||||||
| chr1:171194484 | A | G | 93 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(90): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.321+961A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171194484 | |||||||
| chr1:171194601 | T | A | 1 | a0005c0004t0003g0149 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.321+1078T>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171194601 | |||||||
| chr1:171194673 | T | C | 113 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(110): Show |
234 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.321+1150T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171194673 | |||||||
| chr1:171194806 | A | AT | 93 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(90): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.321+1288dupT | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 171194806 | ||||||
| chr1:171194900 | A | G | 2 | a0009c0011t0002g0023 a0009c0011t0002g0092 |
4 | HG02109.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+1377A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171194900 | |||||||
| chr1:171194972 | A | G | 27 | a0003c0003t0001g0157 a0003c0003t0002g0002 a0003c0003t0002g0019 others(24): Show |
60 | HG00438.hp1 HG00639.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.321+1449A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171194972 | |||||||
| chr1:171194999 | G | A | 27 | a0003c0003t0001g0157 a0003c0003t0002g0002 a0003c0003t0002g0019 others(24): Show |
60 | HG00438.hp1 HG00639.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.321+1476G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171194999 | |||||||
| chr1:171195043 | G | T | 3 | a0008c0010t0015g0080 a0008c0010t0015g0085 a0008c0010t0024g0086 |
3 | HG01884.hp2 HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.321+1520G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171195043 | |||||||
| chr1:171195056 | A | C | 93 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(90): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.321+1533A>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171195056 | |||||||
| chr1:171195076 | T | C | 2 | a0004c0008t0002g0097 a0012c0012t0002g0024 |
4 | HG02886.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.321+1553T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171195076 | |||||||
| chr1:171195167 | G | A | 93 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(90): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.322-1482G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171195167 | |||||||
| chr1:171195341 | A | T | 93 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(90): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.322-1308A>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171195341 | |||||||
| chr1:171195405 | C | T | 113 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(110): Show |
234 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.322-1244C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171195405 | |||||||
| chr1:171195723 | G | A | 1 | a0001c0001t0007g0059 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.322-926G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171195723 | |||||||
| chr1:171195796 | TA | T | 93 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(90): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.322-846delA | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 171195796 | ||||||
| chr1:171195915 | C | CTG | 3 | a0007c0007t0009g0022 a0007c0007t0009g0089 a0007c0007t0009g0090 |
5 | HG02258.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-733_322-732dup others(2): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 171195915 | ||||||
| chr1:171195940 | A | C | 1 | a0001c0001t0001g0051 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.322-709A>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171195940 | |||||||
| chr1:171196023 | C | A | 1 | a0006c0006t0006g0100 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.322-626C>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171196023 | |||||||
| chr1:171196025 | T | A | 1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.322-624T>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171196025 | |||||||
| chr1:171196522 | A | G | 20 | a0005c0004t0003g0011 a0005c0004t0003g0018 a0005c0004t0003g0041 others(17): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.322-127A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 3/8 | chr1 | 171196522 | |||||||
| chr1:171197142 | C | G | 2 | a0004c0009t0004g0094 a0004c0009t0004g0096 |
2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.484+331C>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171197142 | |||||||
| chr1:171197173 | C | A | 1 | a0003c0003t0002g0155 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.484+362C>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171197173 | |||||||
| chr1:171197256 | T | C | 2 | a0007c0007t0012g0079 a0007c0007t0012g0084 |
2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.484+445T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171197256 | |||||||
| chr1:171197393 | A | G | 93 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(90): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.484+582A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171197393 | |||||||
| chr1:171197535 | G | C | 93 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(90): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.484+724G>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171197535 | |||||||
| chr1:171197786 | A | G | 23 | a0003c0003t0001g0157 a0003c0003t0002g0002 a0003c0003t0002g0019 others(20): Show |
52 | HG00438.hp1 HG00639.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.484+975A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171197786 | |||||||
| chr1:171198018 | C | T | 113 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(110): Show |
234 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.484+1207C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171198018 | |||||||
| chr1:171198136 | G | A | 20 | a0005c0004t0003g0011 a0005c0004t0003g0018 a0005c0004t0003g0041 others(17): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.485-1210G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171198136 | |||||||
| chr1:171198214 | C | G | 30 | a0003c0003t0001g0157 a0003c0003t0002g0002 a0003c0003t0002g0019 others(27): Show |
64 | HG00438.hp1 HG00639.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.485-1132C>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171198214 | |||||||
| chr1:171198249 | T | TACA | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.485-1096_485-1094d others(5): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 171198249 | ||||||
| chr1:171198267 | A | T | 93 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(90): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.485-1079A>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171198267 | |||||||
| chr1:171198336 | TCTAA | T | 31 | a0001c0001t0001g0065 a0003c0003t0001g0157 a0003c0003t0002g0002 others(28): Show |
65 | HG00438.hp1 HG00639.hp2 HG01081.hp2 others(62): Show |
intron_variant | MODIFIER | c.485-1006_485-1003d others(6): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 171198336 | ||||||
| chr1:171198394 | G | C | 1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.485-952G>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171198394 | |||||||
| chr1:171198410 | A | AT | 19 | a0001c0001t0001g0064 a0006c0006t0006g0007 a0006c0006t0006g0037 others(16): Show |
29 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.485-921dupT | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 171198410 | ||||||
| chr1:171198410 | AT | A | 52 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(49): Show |
120 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.485-921delT | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 171198410 | ||||||
| chr1:171198427 | A | G | 3 | a0003c0003t0002g0019 a0003c0016t0002g0019 a0003c0016t0002g0161 |
5 | NA18970.hp1 NA18973.hp2 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.485-919A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171198427 | |||||||
| chr1:171198564 | G | A | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.485-782G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171198564 | |||||||
| chr1:171198653 | C | T | 2 | a0013c0017t0017g0150 a0013c0017t0017g0151 |
2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.485-693C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171198653 | |||||||
| chr1:171198657 | C | T | 20 | a0005c0004t0003g0011 a0005c0004t0003g0018 a0005c0004t0003g0041 others(17): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.485-689C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171198657 | |||||||
| chr1:171198789 | G | T | 1 | a0002c0002t0005g0121 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.485-557G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171198789 | |||||||
| chr1:171198880 | T | C | 1 | a0002c0002t0004g0039 | 2 | HG02698.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.485-466T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171198880 | |||||||
| chr1:171198895 | T | C | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.485-451T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171198895 | |||||||
| chr1:171198935 | C | T | 7 | a0008c0010t0015g0080 a0008c0010t0015g0081 a0008c0010t0015g0085 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.485-411C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171198935 | |||||||
| chr1:171198944 | C | T | 95 | a0001c0001t0001g0050 a0001c0001t0001g0063 a0002c0002t0004g0003 others(92): Show |
200 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.485-402C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171198944 | |||||||
| chr1:171198971 | G | A | 2 | a0004c0008t0002g0097 a0012c0012t0002g0024 |
4 | HG02886.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-375G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171198971 | |||||||
| chr1:171199027 | C | T | 28 | a0003c0003t0001g0157 a0003c0003t0002g0002 a0003c0003t0002g0019 others(25): Show |
60 | HG00438.hp1 HG00639.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.485-319C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171199027 | |||||||
| chr1:171199163 | G | C | 113 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(110): Show |
234 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.485-183G>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | chr1 | 171199163 | |||||||
| chr1:171199240 | CA | C | 20 | a0005c0004t0003g0011 a0005c0004t0003g0018 a0005c0004t0003g0041 others(17): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.485-103delA | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 171199240 | ||||||
| chr1:171199554 | C | T | 30 | a0003c0003t0001g0157 a0003c0003t0002g0002 a0003c0003t0002g0019 others(27): Show |
64 | HG00438.hp1 HG00639.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.627+66C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171199554 | |||||||
| chr1:171199573 | T | TC | 2 | a0002c0002t0004g0028 a0002c0002t0025g0028 |
3 | HG03139.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.627+87dupC | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 171199573 | ||||||
| chr1:171199665 | A | C | 113 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(110): Show |
234 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.627+177A>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171199665 | |||||||
| chr1:171199858 | G | A | 1 | a0001c0001t0020g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.627+370G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171199858 | |||||||
| chr1:171199936 | C | A | 20 | a0005c0004t0003g0011 a0005c0004t0003g0018 a0005c0004t0003g0041 others(17): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.627+448C>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171199936 | |||||||
| chr1:171199984 | T | C | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.627+496T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171199984 | |||||||
| chr1:171200053 | G | T | 93 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(90): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.627+565G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171200053 | |||||||
| chr1:171200157 | A | G | 1 | a0006c0006t0006g0037 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.627+669A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171200157 | |||||||
| chr1:171200162 | T | C | 1 | a0005c0004t0003g0137 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.627+674T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171200162 | |||||||
| chr1:171200205 | G | C | 30 | a0003c0003t0001g0157 a0003c0003t0002g0002 a0003c0003t0002g0019 others(27): Show |
64 | HG00438.hp1 HG00639.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.627+717G>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171200205 | |||||||
| chr1:171200206 | G | A | 23 | a0003c0003t0001g0157 a0003c0003t0002g0002 a0003c0003t0002g0019 others(20): Show |
52 | HG00438.hp1 HG00639.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.627+718G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171200206 | |||||||
| chr1:171200261 | C | A | 1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.627+773C>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171200261 | |||||||
| chr1:171200283 | A | G | 3 | a0001c0001t0002g0077 a0007c0007t0012g0079 a0007c0007t0012g0084 |
3 | HG02559.hp1 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.627+795A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171200283 | |||||||
| chr1:171200297 | C | T | 20 | a0005c0004t0003g0011 a0005c0004t0003g0018 a0005c0004t0003g0041 others(17): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.627+809C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171200297 | |||||||
| chr1:171200312 | T | C | 113 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(110): Show |
234 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.627+824T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171200312 | |||||||
| chr1:171200363 | C | T | 113 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(110): Show |
234 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.627+875C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171200363 | |||||||
| chr1:171200408 | C | T | 93 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(90): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.627+920C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171200408 | |||||||
| chr1:171200564 | T | C | 4 | a0007c0007t0009g0022 a0007c0007t0009g0089 a0007c0007t0009g0090 others(1): Show |
6 | HG02258.hp2 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.627+1076T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171200564 | |||||||
| chr1:171200584 | C | T | 2 | a0013c0017t0017g0150 a0013c0017t0017g0151 |
2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.627+1096C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171200584 | |||||||
| chr1:171200858 | G | C | 20 | a0005c0004t0003g0011 a0005c0004t0003g0018 a0005c0004t0003g0041 others(17): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.627+1370G>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171200858 | |||||||
| chr1:171200870 | A | C | 46 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(43): Show |
109 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.627+1382A>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171200870 | |||||||
| chr1:171200885 | T | A | 20 | a0005c0004t0003g0011 a0005c0004t0003g0018 a0005c0004t0003g0041 others(17): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.627+1397T>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171200885 | |||||||
| chr1:171201041 | G | C | 1 | a0002c0002t0004g0118 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.627+1553G>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201041 | |||||||
| chr1:171201070 | T | C | 93 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(90): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.627+1582T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201070 | |||||||
| chr1:171201105 | A | T | 113 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(110): Show |
234 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.627+1617A>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201105 | |||||||
| chr1:171201412 | A | G | 93 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(90): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.627+1924A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201412 | |||||||
| chr1:171201435 | C | G | 93 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(90): Show |
198 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.627+1947C>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201435 | |||||||
| chr1:171201497 | G | A | 1 | a0002c0002t0004g0119 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.627+2009G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201497 | |||||||
| chr1:171201553 | A | C | 15 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(12): Show |
21 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.627+2065A>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201553 | |||||||
| chr1:171201594 | A | T | 20 | a0005c0004t0003g0011 a0005c0004t0003g0018 a0005c0004t0003g0041 others(17): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.627+2106A>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201594 | |||||||
| chr1:171201595 | T | C | 1 | a0001c0001t0002g0077 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.627+2107T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201595 | |||||||
| chr1:171201678 | C | T | 1 | a0002c0002t0004g0026 | 3 | NA18963.hp2 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.628-2187C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201678 | |||||||
| chr1:171201713 | T | C | 20 | a0005c0004t0003g0011 a0005c0004t0003g0018 a0005c0004t0003g0041 others(17): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.628-2152T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201713 | |||||||
| chr1:171201769 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.628-2096G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201769 | |||||||
| chr1:171201824 | G | A | 14 | a0001c0001t0002g0077 a0004c0008t0002g0097 a0007c0007t0009g0091 others(11): Show |
14 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.628-2041G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201824 | |||||||
| chr1:171201832 | A | C | 20 | a0005c0004t0003g0011 a0005c0004t0003g0018 a0005c0004t0003g0041 others(17): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.628-2033A>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201832 | |||||||
| chr1:171201833 | G | T | 20 | a0005c0004t0003g0011 a0005c0004t0003g0018 a0005c0004t0003g0041 others(17): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.628-2032G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201833 | |||||||
| chr1:171201863 | G | A | 16 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(13): Show |
24 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.628-2002G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201863 | |||||||
| chr1:171201916 | C | T | 20 | a0005c0004t0003g0011 a0005c0004t0003g0018 a0005c0004t0003g0041 others(17): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.628-1949C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171201916 | |||||||
| chr1:171202031 | A | G | 1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.628-1834A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171202031 | |||||||
| chr1:171202354 | G | T | 2 | a0003c0003t0002g0160 a0003c0003t0002g0163 |
2 | NA18949.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.628-1511G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171202354 | |||||||
| chr1:171202632 | A | G | 1 | a0001c0015t0003g0049 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.628-1233A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171202632 | |||||||
| chr1:171202843 | A | T | 1 | a0006c0006t0016g0025 | 3 | HG01884.hp1 HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.628-1022A>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171202843 | |||||||
| chr1:171202957 | T | C | 1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.628-908T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171202957 | |||||||
| chr1:171203008 | G | T | 45 | a0001c0001t0002g0077 a0003c0003t0002g0002 a0003c0003t0002g0019 others(42): Show |
81 | HG00438.hp1 HG00639.hp2 HG01081.hp2 others(78): Show |
intron_variant | MODIFIER | c.628-857G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171203008 | |||||||
| chr1:171203273 | T | C | 33 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(30): Show |
73 | HG00140.hp2 HG00544.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.628-592T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171203273 | |||||||
| chr1:171203321 | T | TCA | 8 | a0007c0007t0012g0079 a0007c0007t0012g0084 a0008c0010t0015g0080 others(5): Show |
8 | HG01884.hp2 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-543_628-542ins others(2): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 171203321 | ||||||
| chr1:171203321 | TCTCACAC others(7): Show |
T | 4 | a0007c0007t0009g0022 a0007c0007t0009g0089 a0007c0007t0009g0090 others(1): Show |
6 | HG02258.hp2 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-542_628-529del others(14): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 171203321 | ||||||
| chr1:171203323 | T | A | 8 | a0007c0007t0012g0079 a0007c0007t0012g0084 a0008c0010t0015g0080 others(5): Show |
8 | HG01884.hp2 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-542T>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171203323 | |||||||
| chr1:171203323 | T | TCA | 37 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(34): Show |
71 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.628-507_628-506dup others(2): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 171203323 | ||||||
| chr1:171203323 | T | TCACA | 27 | a0001c0001t0001g0057 a0001c0001t0001g0070 a0001c0001t0019g0074 others(24): Show |
52 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.628-509_628-506dup others(4): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 171203323 | ||||||
| chr1:171203323 | T | TCACACAC others(1): Show |
6 | a0003c0003t0002g0020 a0003c0003t0002g0159 a0003c0003t0002g0162 others(3): Show |
12 | HG01081.hp2 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.628-513_628-506dup others(8): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 171203323 | ||||||
| chr1:171203323 | T | TCACACAC others(5): Show |
1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.628-517_628-506dup others(12): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 171203323 | ||||||
| chr1:171203323 | TCA | T | 4 | a0003c0003t0002g0044 a0003c0003t0002g0155 a0010c0013t0001g0021 others(1): Show |
7 | HG01109.hp1 HG01256.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-507_628-506del others(2): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 171203323 | ||||||
| chr1:171203323 | TCACA | T | 1 | a0009c0011t0002g0023 | 3 | HG02109.hp2 HG02717.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.628-509_628-506del others(4): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 171203323 | ||||||
| chr1:171203323 | TCACACA | T | 2 | a0004c0009t0004g0016 a0004c0009t0004g0035 |
6 | HG02280.hp2 HG02723.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-511_628-506del others(6): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 171203323 | ||||||
| chr1:171203323 | TCACACAC others(1): Show |
T | 35 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(32): Show |
75 | HG00140.hp2 HG00544.hp2 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.628-513_628-506del others(8): Show |
FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 171203323 | ||||||
| chr1:171203369 | C | A | 1 | a0005c0004t0008g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.628-496C>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171203369 | |||||||
| chr1:171203399 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.628-466C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171203399 | |||||||
| chr1:171203469 | G | A | 2 | a0005c0004t0003g0138 a0005c0004t0003g0141 |
2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.628-396G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171203469 | |||||||
| chr1:171203641 | C | T | 14 | a0007c0007t0009g0022 a0007c0007t0009g0089 a0007c0007t0009g0090 others(11): Show |
16 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.628-224C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 5/8 | chr1 | 171203641 | |||||||
| chr1:171204103 | T | C | 14 | a0007c0007t0009g0022 a0007c0007t0009g0089 a0007c0007t0009g0090 others(11): Show |
16 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.827+39T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 6/8 | chr1 | 171204103 | |||||||
| chr1:171204272 | T | C | 33 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(30): Show |
73 | HG00140.hp2 HG00544.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.827+208T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 6/8 | chr1 | 171204272 | |||||||
| chr1:171204300 | G | C | 1 | a0005c0004t0003g0148 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.827+236G>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 6/8 | chr1 | 171204300 | |||||||
| chr1:171204603 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.827+539G>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 6/8 | chr1 | 171204603 | |||||||
| chr1:171204729 | T | C | 1 | a0003c0003t0002g0155 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.828-550T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 6/8 | chr1 | 171204729 | |||||||
| chr1:171204743 | A | G | 1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.828-536A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 6/8 | chr1 | 171204743 | |||||||
| chr1:171205013 | G | T | 37 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(34): Show |
81 | HG00140.hp2 HG00544.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.828-266G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 6/8 | chr1 | 171205013 | |||||||
| chr1:171205060 | C | T | 1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.828-219C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 6/8 | chr1 | 171205060 | |||||||
| chr1:171205173 | T | A | 37 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(34): Show |
81 | HG00140.hp2 HG00544.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.828-106T>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 6/8 | chr1 | 171205173 | |||||||
| chr1:171205196 | G | T | 2 | a0004c0008t0002g0097 a0012c0012t0002g0024 |
4 | HG02886.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.828-83G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 6/8 | chr1 | 171205196 | |||||||
| chr1:171205682 | G | A | 14 | a0007c0007t0009g0022 a0007c0007t0009g0089 a0007c0007t0009g0090 others(11): Show |
16 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1183+48G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 7/8 | chr1 | 171205682 | |||||||
| chr1:171205724 | T | C | 6 | a0001c0001t0002g0077 a0004c0008t0002g0036 a0004c0008t0002g0093 others(3): Show |
9 | HG01081.hp2 HG02109.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183+90T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 7/8 | chr1 | 171205724 | |||||||
| chr1:171206262 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1183+628G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 7/8 | chr1 | 171206262 | |||||||
| chr1:171206406 | T | C | 1 | a0004c0005t0003g0127 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1183+772T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 7/8 | chr1 | 171206406 | |||||||
| chr1:171206447 | G | A | 37 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(34): Show |
81 | HG00140.hp2 HG00544.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.1183+813G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 7/8 | chr1 | 171206447 | |||||||
| chr1:171206511 | G | T | 32 | a0001c0015t0003g0049 a0001c0015t0003g0061 a0001c0015t0003g0068 others(29): Show |
67 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1183+877G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 7/8 | chr1 | 171206511 | |||||||
| chr1:171206819 | C | G | 1 | a0001c0001t0001g0067 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1184-899C>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 7/8 | chr1 | 171206819 | |||||||
| chr1:171206917 | A | G | 134 | a0001c0001t0002g0077 a0001c0001t0020g0076 a0001c0015t0003g0049 others(131): Show |
257 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1184-801A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 7/8 | chr1 | 171206917 | |||||||
| chr1:171206959 | T | A | 14 | a0007c0007t0009g0022 a0007c0007t0009g0089 a0007c0007t0009g0090 others(11): Show |
16 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1184-759T>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 7/8 | chr1 | 171206959 | |||||||
| chr1:171206991 | C | T | 1 | a0002c0002t0004g0115 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1184-727C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 7/8 | chr1 | 171206991 | |||||||
| chr1:171207096 | T | C | 30 | a0001c0001t0002g0077 a0003c0003t0002g0002 a0003c0003t0002g0019 others(27): Show |
64 | HG00438.hp1 HG00639.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.1184-622T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 7/8 | chr1 | 171207096 | |||||||
| chr1:171207251 | C | T | 2 | a0013c0017t0017g0150 a0013c0017t0017g0151 |
2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1184-467C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 7/8 | chr1 | 171207251 | |||||||
| chr1:171207929 | G | A | 2 | a0013c0017t0017g0150 a0013c0017t0017g0151 |
2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1256+139G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/8 | chr1 | 171207929 | |||||||
| chr1:171207980 | T | C | 22 | a0003c0003t0002g0002 a0003c0003t0002g0019 a0003c0003t0002g0020 others(19): Show |
51 | HG00438.hp1 HG00639.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.1256+190T>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/8 | chr1 | 171207980 | |||||||
| chr1:171208045 | T | G | 1 | a0005c0004t0003g0043 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1256+255T>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/8 | chr1 | 171208045 | |||||||
| chr1:171208066 | G | T | 133 | a0001c0001t0002g0077 a0001c0015t0003g0049 a0001c0015t0003g0061 others(130): Show |
256 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.1256+276G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/8 | chr1 | 171208066 | |||||||
| chr1:171208134 | A | G | 114 | a0001c0001t0002g0077 a0001c0015t0003g0049 a0001c0015t0003g0061 others(111): Show |
229 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.1256+344A>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/8 | chr1 | 171208134 | |||||||
| chr1:171208172 | G | A | 4 | a0001c0001t0002g0077 a0004c0008t0002g0036 a0004c0008t0002g0093 others(1): Show |
5 | HG01081.hp2 HG02723.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1256+382G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/8 | chr1 | 171208172 | |||||||
| chr1:171208197 | G | C | 2 | a0007c0007t0012g0087 a0007c0007t0012g0088 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1256+407G>C | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/8 | chr1 | 171208197 | |||||||
| chr1:171208277 | G | A | 19 | a0006c0006t0006g0007 a0006c0006t0006g0037 a0006c0006t0006g0098 others(16): Show |
27 | HG01123.hp1 HG01192.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1256+487G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/8 | chr1 | 171208277 | |||||||
| chr1:171208342 | C | T | 37 | a0002c0002t0004g0003 a0002c0002t0004g0008 a0002c0002t0004g0009 others(34): Show |
81 | HG00140.hp2 HG00544.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.1257-452C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/8 | chr1 | 171208342 | |||||||
| chr1:171208386 | G | T | 30 | a0001c0001t0002g0077 a0003c0003t0002g0002 a0003c0003t0002g0019 others(27): Show |
64 | HG00438.hp1 HG00639.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.1257-408G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/8 | chr1 | 171208386 | |||||||
| chr1:171208475 | C | G | 2 | a0009c0011t0002g0023 a0009c0011t0002g0092 |
4 | HG02109.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1257-319C>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/8 | chr1 | 171208475 | |||||||
| chr1:171208529 | C | T | 14 | a0007c0007t0009g0022 a0007c0007t0009g0089 a0007c0007t0009g0090 others(11): Show |
16 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1257-265C>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/8 | chr1 | 171208529 | |||||||
| chr1:171208552 | G | T | 2 | a0007c0007t0012g0079 a0007c0007t0012g0084 |
2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1257-242G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/8 | chr1 | 171208552 | |||||||
| chr1:171208564 | G | A | 1 | a0004c0008t0022g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1257-230G>A | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/8 | chr1 | 171208564 | |||||||
| chr1:171208719 | G | T | 2 | a0013c0017t0017g0150 a0013c0017t0017g0151 |
2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1257-75G>T | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/8 | chr1 | 171208719 | |||||||
| chr1:171208739 | T | G | 1 | a0004c0008t0002g0097 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1257-55T>G | FMO2 | ENSG00000094963.14 | transcript | ENST00000209929.10 | protein_coding | 8/8 | chr1 | 171208739 |