Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2166 |
| ensemblid | ENSG00000117480.16 |
| hgncid | 3553 |
| symbol | FAAH |
| name | fatty acid amide hydrolase |
| refseq_nuc | NM_001441.3 |
| refseq_prot | NP_001432.2 |
| ensembl_nuc | ENST00000243167.9 |
| ensembl_prot | ENSP00000243167.8 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 46394317 |
| end | 46413845 |
| strand | + |
| ver | v1.2 |
| region | chr1:46394317-46413845 |
| region5000 | chr1:46389317-46418845 |
| regionname0 | FAAH_chr1_46394317_46413845 |
| regionname5000 | FAAH_chr1_46389317_46418845 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 579 | 258 | 59 | 38 | 111 | 12 | 37 | 88 | FAAH_chr1_46389317_46418845 | FAAH | MVQYE others(574): Show |
chr1 | 46389317 | 46418845 |
| a0002 | 0/1 | 579 | 101 | 24 | 24 | 40 | 4 | 8 | 34 | FAAH_chr1_46389317_46418845 | FAAH | MVQYE others(574): Show |
chr1 | 46389317 | 46418845 |
| a0003 | 0/0 | 116 | 9 | 3 | 0 | 5 | 0 | 1 | 4 | FAAH_chr1_46389317_46418845 | FAAH | MVQYE others(111): Show |
chr1 | 46389317 | 46418845 |
| a0004 | 0/0 | 328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | MVQYE others(323): Show |
chr1 | 46389317 | 46418845 |
| a0005 | 0/0 | 579 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | MVQYE others(574): Show |
chr1 | 46389317 | 46418845 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1737 | 218 | 40 | 34 | 111 | 9 | 24 | FAAH_chr1_46389317_46418845 | FAAH | ATGGT others(1732): Show |
chr1 | 46389317 | 46418845 | ||
| a0001c0003 | 1/0 | 1737 | 38 | 17 | 4 | 0 | 3 | 13 | FAAH_chr1_46389317_46418845 | FAAH | ATGGT others(1732): Show |
chr1 | 46389317 | 46418845 | ||
| a0001c0007 | 0/0 | 1737 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | ATGGT others(1732): Show |
chr1 | 46389317 | 46418845 | ||
| a0002c0002 | 0/0 | 1737 | 95 | 24 | 23 | 40 | 2 | 6 | FAAH_chr1_46389317_46418845 | FAAH | ATGGT others(1732): Show |
chr1 | 46389317 | 46418845 | ||
| a0002c0005 | 0/1 | 1737 | 6 | 0 | 1 | 0 | 2 | 2 | FAAH_chr1_46389317_46418845 | FAAH | ATGGT others(1732): Show |
chr1 | 46389317 | 46418845 | ||
| a0003c0004 | 0/0 | 1729 | 7 | 1 | 0 | 5 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | ATGGT others(1724): Show |
chr1 | 46389317 | 46418845 | ||
| a0003c0006 | 0/0 | 1729 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | ATGGT others(1724): Show |
chr1 | 46389317 | 46418845 | ||
| a0004c0008 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | ATGGT others(1746): Show |
chr1 | 46389317 | 46418845 | ||
| a0005c0009 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | ATGGT others(1732): Show |
chr1 | 46389317 | 46418845 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2042 | 217 | 40 | 33 | 111 | 9 | 24 | FAAH_chr1_46389317_46418845 | FAAH | GTCGC others(2037): Show |
chr1 | 46389317 | 46418845 |
| a0001c0001t0004 | 0/0 | 2042 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | GTCGC others(2037): Show |
chr1 | 46389317 | 46418845 |
| a0001c0003t0001 | 1/0 | 2042 | 37 | 17 | 4 | 0 | 3 | 12 | FAAH_chr1_46389317_46418845 | FAAH | GTCGC others(2037): Show |
chr1 | 46389317 | 46418845 |
| a0001c0003t0003 | 0/0 | 2042 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | GTCGC others(2037): Show |
chr1 | 46389317 | 46418845 |
| a0001c0007t0001 | 0/0 | 2042 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | GTCGC others(2037): Show |
chr1 | 46389317 | 46418845 |
| a0002c0002t0001 | 0/0 | 2042 | 95 | 24 | 23 | 40 | 2 | 6 | FAAH_chr1_46389317_46418845 | FAAH | GTCGC others(2037): Show |
chr1 | 46389317 | 46418845 |
| a0002c0005t0001 | 0/1 | 2042 | 6 | 0 | 1 | 0 | 2 | 2 | FAAH_chr1_46389317_46418845 | FAAH | GTCGC others(2037): Show |
chr1 | 46389317 | 46418845 |
| a0003c0004t0002 | 0/0 | 2021 | 7 | 1 | 0 | 5 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | GTCGC others(2016): Show |
chr1 | 46389317 | 46418845 |
| a0003c0006t0001 | 0/0 | 2034 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | GTCGC others(2029): Show |
chr1 | 46389317 | 46418845 |
| a0004c0008t0001 | 0/0 | 2056 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | GTCGC others(2051): Show |
chr1 | 46389317 | 46418845 |
| a0005c0009t0001 | 0/0 | 2042 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | GTCGC others(2037): Show |
chr1 | 46389317 | 46418845 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 48 | 1 | 8 | 34 | 2 | 3 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0003 | 0/0 | 18 | 0 | 0 | 13 | 0 | 5 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0004 | 0/0 | 18 | 1 | 5 | 5 | 4 | 3 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 6 | 1 | 2 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0008 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0013 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0007 | 0/0 | 10 | 0 | 0 | 0 | 2 | 8 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0025 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0001c0007t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0001 | 0/0 | 43 | 8 | 15 | 15 | 1 | 4 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0015 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0005t0001g0001 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0002c0005t0001g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0003c0004t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0003c0004t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0003c0004t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0003c0004t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0003c0004t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0003c0006t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0003c0006t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0004c0008t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| a0005c0009t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0005 | t0001 | g0001 | EUR | GBR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0007 | EUR | GBR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | GBR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00280 | hp1 | a0002 | c0005 | t0001 | g0001 | EUR | FIN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | FIN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00544 | hp2 | a0003 | c0004 | t0002 | g0022 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0028 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0016 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0061 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00741 | hp1 | a0002 | c0005 | t0001 | g0001 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0050 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0075 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0028 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0016 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0066 | EUR | IBS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01884 | hp2 | a0003 | c0004 | t0002 | g0129 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0139 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0073 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0071 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0141 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0083 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0106 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02602 | hp2 | a0001 | c0003 | t0003 | g0155 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0130 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0076 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0125 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02717 | hp2 | a0001 | c0007 | t0001 | g0021 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0150 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0063 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0062 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0135 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03139 | hp2 | a0003 | c0006 | t0001 | g0127 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0134 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0144 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0077 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0064 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0084 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0023 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03516 | hp1 | a0003 | c0006 | t0001 | g0126 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0052 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03654 | hp1 | a0002 | c0005 | t0001 | g0001 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03834 | hp1 | a0002 | c0005 | t0001 | g0057 | SAS | BEB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03834 | hp2 | a0003 | c0004 | t0002 | g0048 | SAS | BEB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | BEB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0086 | SAS | BEB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | BEB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0067 | AFR | YRI | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18959 | hp1 | a0003 | c0004 | t0002 | g0022 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18969 | hp1 | a0003 | c0004 | t0002 | g0024 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19009 | hp2 | a0003 | c0004 | t0002 | g0074 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | LWK | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19043 | hp1 | a0005 | c0009 | t0001 | g0138 | AFR | LWK | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0051 | AFR | LWK | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19054 | hp2 | a0003 | c0004 | t0002 | g0024 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19240 | hp1 | a0001 | c0007 | t0001 | g0021 | AFR | YRI | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | YRI | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ASW | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0069 | AFR | ASW | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0016 | EUR | TSI | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0007 | EUR | TSI | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | GIH | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | GIH | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0025 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02486 | hp1 | a0004 | c0008 | t0001 | g0001 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0055 | AFR | USA | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | USA | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | USA | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | LWK | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| homoSapiens | chm13v2 | a0002 | c0005 | t0001 | g0078 | REF | REF | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0025 | REF | REF | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:46405089 | C | A | 2 | a0002 a0004 |
101 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(98): Show |
missense_variant | MODERATE | c.385C>A | p.Pro129Thr | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 3/15 | 417/2042 | 385/1740 | 129/579 | chr1 | 46405089 | |||
| chr1:46408494 | C | G | 1 | a0004 | 1 | HG02486.hp1 | stop_gained | HIGH | c.987C>G | p.Tyr329* | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 8/15 | 1019/2042 | 987/1740 | 329/579 | chr1 | 46408494 | |||
| chr1:46408496 | A | ACCCCACC others(7): Show |
1 | a0004 | 1 | HG02486.hp1 | frameshift_variant&stop_gained | HIGH | c.989_990insCCCCACCT others(6): Show |
p.Glu331fs | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 8/15 | 1022/2042 | 990/1740 | 330/579 | chr1 | 46408496 | |||
| chr1:46408574 | C | T | 1 | a0003 | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
missense_variant | MODERATE | c.1067C>T | p.Ala356Val | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 8/15 | 1099/2042 | 1067/1740 | 356/579 | chr1 | 46408574 | |||
| chr1:46409132 | A | G | 1 | a0005 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1109A>G | p.His370Arg | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/15 | 1141/2042 | 1109/1740 | 370/579 | chr1 | 46409132 | |||
| chr1:46412213 | C | G | 1 | a0003 | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
missense_variant | MODERATE | c.1427C>G | p.Ala476Gly | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/15 | 1459/2042 | 1427/1740 | 476/579 | chr1 | 46412213 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:46405702 | C | G | 1 | a0001c0007 | 2 | HG02717.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.693C>G | p.Pro231Pro | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 5/15 | 725/2042 | 693/1740 | 231/579 | chr1 | 46405702 | |||
| chr1:46406041 | G | A | 2 | a0003c0004 a0003c0006 |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
synonymous_variant | LOW | c.789G>A | p.Lys263Lys | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 6/15 | 821/2042 | 789/1740 | 263/579 | chr1 | 46406041 | |||
| chr1:46406074 | G | A | 1 | a0002c0005 | 5 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(2): Show |
synonymous_variant | LOW | c.822G>A | p.Glu274Glu | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 6/15 | 854/2042 | 822/1740 | 274/579 | chr1 | 46406074 | |||
| chr1:46406314 | T | C | 7 | a0001c0001 a0001c0007 a0002c0002 others(4): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(327): Show |
synonymous_variant | LOW | c.897T>C | p.Cys299Cys | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/15 | 929/2042 | 897/1740 | 299/579 | chr1 | 46406314 | |||
| chr1:46410816 | G | C | 1 | a0003c0004 | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.1278G>C | p.Leu426Leu | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/15 | 1310/2042 | 1278/1740 | 426/579 | chr1 | 46410816 | |||
| chr1:46411612 | T | G | 1 | a0003c0004 | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.1317T>G | p.Arg439Arg | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 12/15 | 1349/2042 | 1317/1740 | 439/579 | chr1 | 46411612 | |||
| chr1:46413467 | G | A | 1 | a0003c0004 | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
synonymous_variant | LOW | c.1632G>A | p.Gly544Gly | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 15/15 | 1664/2042 | 1632/1740 | 544/579 | chr1 | 46413467 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:46394338 | C | G | 1 | a0001c0001t0004 | 1 | HG01069.hp2 | 5_prime_UTR_variant | MODIFIER | c.-11C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/15 | 11 | chr1 | 46394338 | ||||||
| chr1:46394339 | T | G | 1 | a0001c0003t0003 | 1 | HG02602.hp2 | 5_prime_UTR_variant | MODIFIER | c.-10T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/15 | 10 | chr1 | 46394339 | ||||||
| chr1:46413589 | A | G | 1 | a0003c0004t0002 | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*14A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 15/15 | 14 | chr1 | 46413589 | ||||||
| chr1:46413769 | C | T | 1 | a0003c0004t0002 | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*194C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 15/15 | 194 | chr1 | 46413769 | ||||||
| chr1:46413771 | TCCTGATC others(6): Show |
T | 1 | a0003c0004t0002 | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*199_*211delTGATCC others(7): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 15/15 | 199 | INFO_REALIGN_3_PRIME | chr1 | 46413771 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:46394552 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.195+9C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46394552 | |||||||
| chr1:46394565 | G | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0020 others(11): Show |
28 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+22G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46394565 | |||||||
| chr1:46394590 | C | A | 1 | a0001c0001t0004g0050 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.195+47C>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46394590 | |||||||
| chr1:46394619 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
5 | HG01243.hp1 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+76G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46394619 | |||||||
| chr1:46394750 | T | C | 2 | a0001c0003t0001g0051 a0001c0003t0001g0052 |
2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.195+207T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46394750 | |||||||
| chr1:46394863 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+320G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46394863 | |||||||
| chr1:46394938 | G | GT | 6 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0156 others(3): Show |
8 | HG00621.hp2 HG02015.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+404dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46394938 | ||||||
| chr1:46394938 | GT | G | 14 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0020 others(11): Show |
28 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+404delT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46394938 | ||||||
| chr1:46394986 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0053 a0001c0001t0001g0153 |
4 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+443C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46394986 | |||||||
| chr1:46395155 | G | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0020 others(11): Show |
28 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+612G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46395155 | |||||||
| chr1:46395215 | G | T | 1 | a0001c0001t0004g0050 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.195+672G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46395215 | |||||||
| chr1:46395472 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.195+929T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46395472 | |||||||
| chr1:46395610 | G | T | 1 | a0001c0001t0004g0050 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.195+1067G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46395610 | |||||||
| chr1:46395634 | A | C | 16 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(13): Show |
33 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.195+1091A>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46395634 | |||||||
| chr1:46395986 | G | C | 1 | a0001c0003t0001g0055 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.195+1443G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46395986 | |||||||
| chr1:46396035 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.195+1492G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396035 | |||||||
| chr1:46396235 | A | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.195+1692A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396235 | |||||||
| chr1:46396270 | T | G | 1 | a0002c0005t0001g0057 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.195+1727T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396270 | |||||||
| chr1:46396327 | A | G | 1 | a0002c0002t0001g0083 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.195+1784A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396327 | |||||||
| chr1:46396345 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.195+1802C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396345 | |||||||
| chr1:46396349 | C | T | 1 | a0001c0001t0004g0050 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.195+1806C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396349 | |||||||
| chr1:46396369 | C | T | 1 | a0001c0003t0001g0150 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.195+1826C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396369 | |||||||
| chr1:46396395 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.195+1852C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396395 | |||||||
| chr1:46396477 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.195+1934C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396477 | |||||||
| chr1:46396608 | TG | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0020 others(11): Show |
28 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+2066delG | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396608 | |||||||
| chr1:46396660 | C | G | 14 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0020 others(11): Show |
28 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+2117C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396660 | |||||||
| chr1:46396683 | A | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.195+2140A>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396683 | |||||||
| chr1:46396746 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0003t0001g0051 others(1): Show |
4 | HG02572.hp2 HG03516.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+2203C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396746 | |||||||
| chr1:46396829 | C | T | 5 | a0002c0002t0001g0005 a0002c0002t0001g0079 a0002c0002t0001g0080 others(2): Show |
15 | HG00673.hp2 HG02040.hp2 NA18950.hp1 others(12): Show |
intron_variant | MODIFIER | c.195+2286C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396829 | |||||||
| chr1:46396883 | C | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0020 others(11): Show |
28 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+2340C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396883 | |||||||
| chr1:46397108 | C | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0020 others(10): Show |
26 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.195+2565C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397108 | |||||||
| chr1:46397221 | C | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0020 others(11): Show |
28 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+2678C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397221 | |||||||
| chr1:46397277 | T | C | 1 | a0001c0007t0001g0021 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.195+2734T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397277 | |||||||
| chr1:46397404 | G | A | 1 | a0002c0002t0001g0058 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.195+2861G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397404 | |||||||
| chr1:46397529 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0149 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.195+2986C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397529 | |||||||
| chr1:46397530 | G | A | 7 | a0001c0001t0001g0037 a0001c0001t0001g0085 a0001c0003t0001g0007 others(4): Show |
19 | HG00140.hp1 HG00733.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.195+2987G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397530 | |||||||
| chr1:46397530 | G | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
5 | HG01243.hp1 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+2987G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397530 | |||||||
| chr1:46397530 | G | T | 5 | a0002c0002t0001g0005 a0002c0002t0001g0079 a0002c0002t0001g0080 others(2): Show |
15 | HG00673.hp2 HG02040.hp2 NA18950.hp1 others(12): Show |
intron_variant | MODIFIER | c.195+2987G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397530 | |||||||
| chr1:46397552 | G | T | 1 | a0001c0001t0001g0145 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.195+3009G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397552 | |||||||
| chr1:46397598 | G | A | 39 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(36): Show |
85 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.195+3055G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397598 | |||||||
| chr1:46397624 | C | T | 1 | a0002c0002t0001g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.195+3081C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397624 | |||||||
| chr1:46397760 | C | T | 1 | a0001c0003t0001g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.195+3217C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397760 | |||||||
| chr1:46397843 | A | G | 17 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(14): Show |
22 | HG00639.hp1 HG00642.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.195+3300A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397843 | |||||||
| chr1:46397874 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.195+3331A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397874 | |||||||
| chr1:46397884 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.195+3341G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397884 | |||||||
| chr1:46397932 | C | CT | 34 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0035 others(31): Show |
58 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.195+3408dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46397932 | ||||||
| chr1:46397932 | C | CTT | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0003t0001g0051 others(3): Show |
6 | HG02895.hp1 HG02897.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+3407_195+3408d others(4): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46397932 | ||||||
| chr1:46397932 | CT | C | 5 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
7 | HG01243.hp1 HG02040.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+3408delT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46397932 | ||||||
| chr1:46397937 | TTTTTTTT others(13): Show |
T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(27): Show |
63 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.195+3395_195+3414d others(22): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397937 | |||||||
| chr1:46398072 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.195+3529T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398072 | |||||||
| chr1:46398156 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.195+3613A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398156 | |||||||
| chr1:46398478 | C | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0020 others(10): Show |
26 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.196-3613C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398478 | |||||||
| chr1:46398539 | C | CTTTTT | 6 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
8 | HG00544.hp2 HG01243.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-3544_196-3540d others(7): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46398539 | ||||||
| chr1:46398539 | C | CTTTTTT | 7 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0044 others(4): Show |
18 | HG00140.hp2 HG00544.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.196-3545_196-3540d others(8): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46398539 | ||||||
| chr1:46398552 | G | A | 1 | a0002c0002t0001g0059 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196-3539G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398552 | |||||||
| chr1:46398560 | G | T | 1 | a0003c0004t0002g0129 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.196-3531G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398560 | |||||||
| chr1:46398582 | G | A | 2 | a0001c0001t0001g0137 a0005c0009t0001g0138 |
2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.196-3509G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398582 | |||||||
| chr1:46398765 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.196-3326C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398765 | |||||||
| chr1:46398819 | G | A | 5 | a0001c0003t0001g0010 a0001c0003t0001g0018 a0001c0003t0001g0055 others(2): Show |
11 | HG01891.hp2 HG02257.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-3272G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398819 | |||||||
| chr1:46398839 | G | A | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.196-3252G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398839 | |||||||
| chr1:46398856 | A | C | 15 | a0001c0001t0001g0107 a0001c0001t0001g0137 a0001c0001t0001g0146 others(12): Show |
21 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.196-3235A>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398856 | |||||||
| chr1:46398878 | C | CTAAACAC others(35): Show |
1 | a0001c0001t0001g0104 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.196-3212_196-3171d others(44): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46398878 | ||||||
| chr1:46398981 | A | AT | 48 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(45): Show |
92 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.196-3104dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46398981 | ||||||
| chr1:46398996 | GC | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
213 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.196-3090delC | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46398996 | ||||||
| chr1:46399055 | A | G | 11 | a0001c0001t0001g0037 a0001c0001t0001g0085 a0001c0001t0001g0124 others(8): Show |
18 | HG01891.hp2 HG01943.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.196-3036A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399055 | |||||||
| chr1:46399108 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.196-2983T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399108 | |||||||
| chr1:46399132 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.196-2959C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399132 | |||||||
| chr1:46399321 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0149 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.196-2770C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399321 | |||||||
| chr1:46399332 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0149 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.196-2759G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399332 | |||||||
| chr1:46399368 | T | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(54): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.196-2723T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399368 | |||||||
| chr1:46399411 | C | T | 1 | a0002c0002t0001g0071 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.196-2680C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399411 | |||||||
| chr1:46399487 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.196-2604T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399487 | |||||||
| chr1:46399522 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.196-2569G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399522 | |||||||
| chr1:46399549 | G | A | 1 | a0002c0002t0001g0060 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.196-2542G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399549 | |||||||
| chr1:46399584 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.196-2507T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399584 | |||||||
| chr1:46399714 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0149 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.196-2377A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399714 | |||||||
| chr1:46399715 | A | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(88): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.196-2376A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399715 | |||||||
| chr1:46399848 | A | T | 1 | a0001c0001t0001g0123 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.196-2243A>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399848 | |||||||
| chr1:46399877 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.196-2214C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399877 | |||||||
| chr1:46399893 | T | C | 1 | a0001c0003t0001g0018 | 3 | HG02896.hp2 HG02897.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.196-2198T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399893 | |||||||
| chr1:46399999 | A | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(49): Show |
133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.196-2092A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399999 | |||||||
| chr1:46400084 | T | A | 1 | a0001c0001t0001g0156 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.196-2007T>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400084 | |||||||
| chr1:46400190 | G | T | 1 | a0001c0001t0001g0149 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196-1901G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400190 | |||||||
| chr1:46400358 | T | C | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-1733T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400358 | |||||||
| chr1:46400412 | G | A | 1 | a0001c0003t0001g0084 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.196-1679G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400412 | |||||||
| chr1:46400413 | CGTGTGAC others(11): Show |
C | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-1676_196-1659d others(20): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46400413 | ||||||
| chr1:46400587 | G | A | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-1504G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400587 | |||||||
| chr1:46400588 | G | T | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-1503G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400588 | |||||||
| chr1:46400662 | A | G | 3 | a0003c0004t0002g0024 a0003c0004t0002g0048 a0003c0004t0002g0074 |
4 | HG03834.hp2 NA18969.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-1429A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400662 | |||||||
| chr1:46400678 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.196-1413G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400678 | |||||||
| chr1:46400905 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.196-1186A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400905 | |||||||
| chr1:46400906 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.196-1185A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400906 | |||||||
| chr1:46400907 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.196-1184A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400907 | |||||||
| chr1:46400962 | G | A | 1 | a0002c0002t0001g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.196-1129G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400962 | |||||||
| chr1:46401052 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.196-1039G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401052 | |||||||
| chr1:46401113 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.196-978G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401113 | |||||||
| chr1:46401159 | TA | T | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-931delA | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401159 | |||||||
| chr1:46401236 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.196-855G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401236 | |||||||
| chr1:46401300 | C | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0043 |
3 | HG02486.hp2 HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.196-791C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401300 | |||||||
| chr1:46401325 | T | C | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-766T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401325 | |||||||
| chr1:46401335 | T | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(40): Show |
89 | HG00408.hp2 HG00423.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.196-756T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401335 | |||||||
| chr1:46401375 | T | C | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-716T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401375 | |||||||
| chr1:46401759 | T | G | 1 | a0001c0001t0001g0131 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.196-332T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401759 | |||||||
| chr1:46401780 | A | T | 1 | a0001c0001t0001g0093 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.196-311A>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401780 | |||||||
| chr1:46401797 | G | A | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-294G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401797 | |||||||
| chr1:46401802 | T | G | 1 | a0002c0002t0001g0064 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.196-289T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401802 | |||||||
| chr1:46401860 | A | C | 1 | a0001c0007t0001g0021 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.196-231A>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401860 | |||||||
| chr1:46401884 | G | GA | 7 | a0001c0001t0001g0034 a0001c0001t0001g0088 a0001c0001t0001g0131 others(4): Show |
8 | HG00642.hp2 HG01515.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-197dupA | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46401884 | ||||||
| chr1:46401884 | GA | G | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-197delA | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46401884 | ||||||
| chr1:46402009 | C | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
9 | HG00639.hp1 HG00642.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-82C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46402009 | |||||||
| chr1:46402196 | GTGGGAAA others(29): Show |
G | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.309+30_309+65delGG others(34): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 46402196 | ||||||
| chr1:46402242 | T | TAAGGCCA others(3): Show |
4 | a0001c0001t0001g0124 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
5 | HG02717.hp2 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+49_309+58dupAA others(8): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 46402242 | ||||||
| chr1:46402351 | G | T | 1 | a0001c0001t0001g0131 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.309+147G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402351 | |||||||
| chr1:46402352 | T | G | 1 | a0001c0001t0001g0131 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.309+148T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402352 | |||||||
| chr1:46402361 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.309+157C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402361 | |||||||
| chr1:46402395 | G | T | 3 | a0003c0004t0002g0024 a0003c0004t0002g0048 a0003c0004t0002g0074 |
4 | HG03834.hp2 NA18969.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+191G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402395 | |||||||
| chr1:46402520 | C | CT | 8 | a0001c0001t0001g0137 a0001c0001t0001g0140 a0003c0004t0002g0022 others(5): Show |
10 | HG00544.hp2 HG03130.hp1 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.309+325dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 46402520 | ||||||
| chr1:46402558 | G | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
10 | HG00423.hp2 HG02056.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.309+354G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402558 | |||||||
| chr1:46402664 | C | A | 1 | a0003c0006t0001g0126 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.309+460C>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402664 | |||||||
| chr1:46402694 | A | AT | 7 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0091 others(4): Show |
8 | HG02897.hp2 HG03669.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.309+506dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 46402694 | ||||||
| chr1:46402694 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.309+490A>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402694 | |||||||
| chr1:46402694 | AT | A | 6 | a0001c0001t0001g0112 a0001c0001t0001g0122 a0001c0001t0001g0157 others(3): Show |
6 | NA18939.hp1 NA18946.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.309+506delT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 46402694 | ||||||
| chr1:46402695 | T | A | 3 | a0001c0001t0001g0111 a0003c0004t0002g0024 a0003c0004t0002g0074 |
4 | NA18969.hp1 NA19009.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+491T>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402695 | |||||||
| chr1:46402696 | T | A | 1 | a0001c0001t0001g0157 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.309+492T>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402696 | |||||||
| chr1:46402735 | C | T | 2 | a0002c0002t0001g0028 a0002c0002t0001g0066 |
3 | HG00733.hp1 HG01192.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.309+531C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402735 | |||||||
| chr1:46403129 | C | T | 2 | a0003c0006t0001g0126 a0003c0006t0001g0127 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.309+925C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46403129 | |||||||
| chr1:46403139 | T | C | 1 | a0001c0003t0001g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.309+935T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46403139 | |||||||
| chr1:46403161 | T | C | 9 | a0001c0001t0001g0137 a0001c0001t0001g0140 a0003c0004t0002g0022 others(6): Show |
11 | HG00544.hp2 HG01884.hp2 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.309+957T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46403161 | |||||||
| chr1:46403255 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.309+1051C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46403255 | |||||||
| chr1:46403455 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.309+1251G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46403455 | |||||||
| chr1:46403730 | C | T | 1 | a0002c0002t0001g0070 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.310-1284C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46403730 | |||||||
| chr1:46403743 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.310-1271A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46403743 | |||||||
| chr1:46404037 | C | A | 1 | a0003c0004t0002g0022 | 2 | HG00544.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.310-977C>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46404037 | |||||||
| chr1:46404253 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0140 a0001c0003t0001g0106 others(1): Show |
4 | HG02280.hp2 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-761G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46404253 | |||||||
| chr1:46404358 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.310-656G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46404358 | |||||||
| chr1:46404383 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.310-631C>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46404383 | |||||||
| chr1:46404520 | A | G | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.310-494A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46404520 | |||||||
| chr1:46404620 | T | C | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.310-394T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46404620 | |||||||
| chr1:46404625 | C | T | 6 | a0001c0001t0001g0124 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
7 | HG02572.hp2 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-389C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46404625 | |||||||
| chr1:46405167 | C | T | 1 | a0001c0003t0001g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.444+19C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 3/14 | chr1 | 46405167 | |||||||
| chr1:46405187 | C | T | 1 | a0003c0004t0002g0022 | 2 | HG00544.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.444+39C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 3/14 | chr1 | 46405187 | |||||||
| chr1:46405367 | C | T | 3 | a0003c0004t0002g0024 a0003c0004t0002g0048 a0003c0004t0002g0074 |
4 | HG03834.hp2 NA18969.hp1 NA19009.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.445-5C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 3/14 | chr1 | 46405367 | |||||||
| chr1:46405887 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.785+93C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 5/14 | chr1 | 46405887 | |||||||
| chr1:46405931 | G | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0157 |
2 | NA19003.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.786-107G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 5/14 | chr1 | 46405931 | |||||||
| chr1:46406203 | G | A | 7 | a0001c0003t0001g0007 a0001c0003t0001g0016 a0001c0003t0001g0084 others(4): Show |
18 | HG00140.hp1 HG00733.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.827-41G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 6/14 | chr1 | 46406203 | |||||||
| chr1:46406393 | A | G | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+25A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406393 | |||||||
| chr1:46406457 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.951+89C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406457 | |||||||
| chr1:46406555 | C | CT | 8 | a0001c0001t0001g0088 a0001c0001t0001g0102 a0001c0001t0001g0116 others(5): Show |
9 | HG03098.hp2 NA18939.hp1 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+200dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 46406555 | ||||||
| chr1:46406555 | CT | C | 9 | a0001c0001t0001g0109 a0001c0001t0001g0122 a0003c0004t0002g0022 others(6): Show |
11 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.951+200delT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 46406555 | ||||||
| chr1:46406583 | C | CT | 8 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0017 others(5): Show |
13 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.951+232dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 46406583 | ||||||
| chr1:46406583 | CT | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(12): Show |
24 | HG00140.hp2 HG00544.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.951+232delT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 46406583 | ||||||
| chr1:46406583 | CTTTTTTT others(4): Show |
C | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+222_951+232del others(11): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 46406583 | ||||||
| chr1:46406584 | T | C | 1 | a0002c0002t0001g0065 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.951+216T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406584 | |||||||
| chr1:46406587 | T | C | 1 | a0002c0002t0001g0067 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.951+219T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406587 | |||||||
| chr1:46406611 | A | C | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+243A>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406611 | |||||||
| chr1:46406654 | C | T | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+286C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406654 | |||||||
| chr1:46406675 | CGGGTTCA others(12): Show |
C | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+328_951+346del others(19): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 46406675 | ||||||
| chr1:46406702 | C | T | 1 | a0002c0002t0001g0060 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.951+334C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406702 | |||||||
| chr1:46406726 | C | T | 4 | a0002c0002t0001g0015 a0002c0002t0001g0063 a0002c0002t0001g0075 others(1): Show |
6 | HG00738.hp1 HG01071.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.951+358C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406726 | |||||||
| chr1:46406750 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0090 |
3 | HG00735.hp2 HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.951+382C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406750 | |||||||
| chr1:46406752 | G | C | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+384G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406752 | |||||||
| chr1:46406758 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.951+390C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406758 | |||||||
| chr1:46406762 | C | T | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+394C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406762 | |||||||
| chr1:46406768 | A | AT | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+408dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 46406768 | ||||||
| chr1:46406784 | TAG | T | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+417_951+418del others(2): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406784 | |||||||
| chr1:46406814 | T | G | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+446T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406814 | |||||||
| chr1:46406827 | G | C | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+459G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406827 | |||||||
| chr1:46406849 | G | A | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+481G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406849 | |||||||
| chr1:46406852 | C | T | 1 | a0001c0003t0001g0062 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.951+484C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406852 | |||||||
| chr1:46406892 | T | C | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+524T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406892 | |||||||
| chr1:46406898 | G | A | 37 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(34): Show |
78 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.951+530G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406898 | |||||||
| chr1:46406900 | C | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0140 |
2 | HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.951+532C>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406900 | |||||||
| chr1:46407026 | A | G | 40 | a0001c0001t0001g0100 a0001c0001t0001g0128 a0001c0001t0001g0133 others(37): Show |
104 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.951+658A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407026 | |||||||
| chr1:46407077 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.951+709G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407077 | |||||||
| chr1:46407079 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.951+711T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407079 | |||||||
| chr1:46407107 | A | G | 7 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+739A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407107 | |||||||
| chr1:46407196 | G | T | 1 | a0001c0001t0001g0115 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.951+828G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407196 | |||||||
| chr1:46407367 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0087 others(6): Show |
26 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.951+999G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407367 | |||||||
| chr1:46407403 | G | A | 1 | a0002c0002t0001g0014 | 3 | HG02717.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.951+1035G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407403 | |||||||
| chr1:46407607 | CTG | C | 7 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0003c0004t0002g0022 others(4): Show |
9 | HG00544.hp2 HG01884.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.952-850_952-849del others(2): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 46407607 | ||||||
| chr1:46407609 | G | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(35): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.952-850G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407609 | |||||||
| chr1:46407621 | G | A | 1 | a0002c0002t0001g0026 | 2 | NA18948.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.952-838G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407621 | |||||||
| chr1:46407875 | G | A | 2 | a0003c0004t0002g0024 a0003c0004t0002g0074 |
3 | NA18969.hp1 NA19009.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.952-584G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407875 | |||||||
| chr1:46407925 | G | A | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.952-534G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407925 | |||||||
| chr1:46407977 | C | T | 7 | a0001c0003t0001g0010 a0001c0003t0001g0018 a0001c0003t0001g0055 others(4): Show |
13 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.952-482C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407977 | |||||||
| chr1:46408201 | C | G | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.952-258C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46408201 | |||||||
| chr1:46408228 | G | T | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.952-231G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46408228 | |||||||
| chr1:46408231 | C | T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(34): Show |
78 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.952-228C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46408231 | |||||||
| chr1:46408388 | C | T | 1 | a0003c0004t0002g0022 | 2 | HG00544.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.952-71C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46408388 | |||||||
| chr1:46408414 | T | C | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.952-45T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46408414 | |||||||
| chr1:46408641 | C | T | 1 | a0003c0004t0002g0129 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1077+57C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 8/14 | chr1 | 46408641 | |||||||
| chr1:46408687 | A | G | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1077+103A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 8/14 | chr1 | 46408687 | |||||||
| chr1:46408711 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
224 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.1077+127A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 8/14 | chr1 | 46408711 | |||||||
| chr1:46409346 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1175+148A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409346 | |||||||
| chr1:46409356 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0085 |
3 | HG02895.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1175+158A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409356 | |||||||
| chr1:46409395 | G | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0019 others(29): Show |
101 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1175+197G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409395 | |||||||
| chr1:46409427 | CT | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(38): Show |
87 | HG00408.hp2 HG00423.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.1175+230delT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409427 | |||||||
| chr1:46409698 | C | T | 3 | a0003c0004t0002g0024 a0003c0004t0002g0048 a0003c0004t0002g0074 |
4 | HG03834.hp2 NA18969.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175+500C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409698 | |||||||
| chr1:46409699 | A | C | 1 | a0003c0004t0002g0129 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1175+501A>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409699 | |||||||
| chr1:46409706 | G | GT | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175+509dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 46409706 | ||||||
| chr1:46409754 | C | A | 1 | a0002c0002t0001g0081 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1175+556C>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409754 | |||||||
| chr1:46409858 | C | T | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176-540C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409858 | |||||||
| chr1:46409875 | C | T | 1 | a0003c0004t0002g0022 | 2 | HG00544.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1176-523C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409875 | |||||||
| chr1:46409922 | T | C | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176-476T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409922 | |||||||
| chr1:46410190 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1176-208T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46410190 | |||||||
| chr1:46410234 | G | A | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176-164G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46410234 | |||||||
| chr1:46410261 | G | A | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176-137G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46410261 | |||||||
| chr1:46410277 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
10 | HG00423.hp2 HG02056.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.1176-121G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46410277 | |||||||
| chr1:46410511 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0085 |
3 | HG02895.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1275+14G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 10/14 | chr1 | 46410511 | |||||||
| chr1:46410570 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1275+73A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 10/14 | chr1 | 46410570 | |||||||
| chr1:46410776 | C | G | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-38C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 10/14 | chr1 | 46410776 | |||||||
| chr1:46410798 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1276-16C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 10/14 | chr1 | 46410798 | |||||||
| chr1:46410857 | A | G | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1316+3A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46410857 | |||||||
| chr1:46410889 | GCC | G | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1316+36_1316+37del others(2): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46410889 | |||||||
| chr1:46410994 | T | C | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1316+140T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46410994 | |||||||
| chr1:46411080 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1316+226G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411080 | |||||||
| chr1:46411155 | A | G | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1316+301A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411155 | |||||||
| chr1:46411212 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1316+358C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411212 | |||||||
| chr1:46411241 | G | T | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1317-371G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411241 | |||||||
| chr1:46411259 | C | T | 2 | a0001c0003t0001g0061 a0001c0003t0001g0062 |
2 | HG00738.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1317-353C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411259 | |||||||
| chr1:46411311 | T | C | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1317-301T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411311 | |||||||
| chr1:46411379 | G | T | 1 | a0002c0002t0001g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1317-233G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411379 | |||||||
| chr1:46411508 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0045 others(4): Show |
16 | HG00140.hp2 HG00544.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1317-104G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411508 | |||||||
| chr1:46411513 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0109 |
4 | NA18946.hp2 NA18972.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317-99C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411513 | |||||||
| chr1:46411566 | C | T | 1 | a0003c0004t0002g0022 | 2 | HG00544.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1317-46C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411566 | |||||||
| chr1:46411591 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1317-21G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411591 | |||||||
| chr1:46411877 | C | T | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1356+226C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 12/14 | chr1 | 46411877 | |||||||
| chr1:46411898 | C | G | 1 | a0002c0002t0001g0068 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1357-245C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 12/14 | chr1 | 46411898 | |||||||
| chr1:46411916 | G | A | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1357-227G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 12/14 | chr1 | 46411916 | |||||||
| chr1:46411933 | T | C | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1357-210T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 12/14 | chr1 | 46411933 | |||||||
| chr1:46412074 | C | A | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1357-69C>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 12/14 | chr1 | 46412074 | |||||||
| chr1:46412138 | C | T | 6 | a0001c0003t0001g0007 a0001c0003t0001g0016 a0001c0003t0001g0084 others(3): Show |
17 | HG00140.hp1 HG00733.hp2 HG01256.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.1357-5C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 12/14 | chr1 | 46412138 | |||||||
| chr1:46412258 | C | G | 1 | a0001c0001t0001g0095 | 1 | NA18979.hp2 | splice_region_variant&intron_variant | LOW | c.1465+7C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412258 | |||||||
| chr1:46412351 | C | T | 1 | a0003c0004t0002g0022 | 2 | HG00544.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1465+100C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412351 | |||||||
| chr1:46412388 | C | G | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1465+137C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412388 | |||||||
| chr1:46412518 | A | C | 1 | a0001c0003t0001g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1465+267A>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412518 | |||||||
| chr1:46412648 | A | C | 6 | a0001c0001t0001g0124 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
7 | HG02572.hp2 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1465+397A>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412648 | |||||||
| chr1:46412667 | T | C | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1466-408T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412667 | |||||||
| chr1:46412708 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1466-367G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412708 | |||||||
| chr1:46412793 | A | T | 1 | a0001c0001t0001g0030 | 2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1466-282A>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412793 | |||||||
| chr1:46412892 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1466-183G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412892 | |||||||
| chr1:46412979 | GAC | G | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1466-92_1466-91del others(2): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 46412979 | ||||||
| chr1:46413000 | T | G | 1 | a0002c0002t0001g0154 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1466-75T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46413000 | |||||||
| chr1:46413040 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1466-35C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46413040 | |||||||
| chr1:46413231 | A | G | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1611+11A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 14/14 | chr1 | 46413231 | |||||||
| chr1:46413355 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1612-92G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 14/14 | chr1 | 46413355 | |||||||
| chr1:46413355 | G | T | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1612-92G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 14/14 | chr1 | 46413355 | |||||||
| chr1:46413412 | T | C | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1612-35T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 14/14 | chr1 | 46413412 | |||||||
| chr1:46413423 | T | C | 5 | a0003c0004t0002g0022 a0003c0004t0002g0024 a0003c0004t0002g0048 others(2): Show |
7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1612-24T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 14/14 | chr1 | 46413423 |