Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27128 |
| ensemblid | ENSG00000100055.21 |
| hgncid | 9505 |
| symbol | CYTH4 |
| name | cytohesin 4 |
| refseq_nuc | NM_013385.5 |
| refseq_prot | NP_037517.1 |
| ensembl_nuc | ENST00000248901.11 |
| ensembl_prot | ENSP00000248901.6 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 37282508 |
| end | 37315341 |
| strand | + |
| ver | v1.2 |
| region | chr22:37282508-37315341 |
| region5000 | chr22:37277508-37320341 |
| regionname0 | CYTH4_chr22_37282508_37315341 |
| regionname5000 | CYTH4_chr22_37277508_37320341 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 394 | 393 | 90 | 69 | 181 | 14 | 37 | 136 | CYTH4_chr22_37277508_37320341 | CYTH4 | MDLCH others(389): Show |
chr22 | 37277508 | 37320341 |
| a0002 | 0/0 | 394 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | MDLCH others(389): Show |
chr22 | 37277508 | 37320341 |
| a0003 | 0/0 | 394 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | MDLCH others(389): Show |
chr22 | 37277508 | 37320341 |
| a0004 | 0/0 | 394 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | MDLCH others(389): Show |
chr22 | 37277508 | 37320341 |
| a0005 | 0/0 | 394 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | MDLCH others(389): Show |
chr22 | 37277508 | 37320341 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1182 | 256 | 63 | 44 | 110 | 10 | 28 | CYTH4_chr22_37277508_37320341 | CYTH4 | ATGGA others(1177): Show |
chr22 | 37277508 | 37320341 | ||
| a0001c0002 | 1/0 | 1182 | 125 | 20 | 22 | 70 | 4 | 8 | CYTH4_chr22_37277508_37320341 | CYTH4 | ATGGA others(1177): Show |
chr22 | 37277508 | 37320341 | ||
| a0001c0004 | 0/0 | 1182 | 6 | 3 | 3 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | ATGGA others(1177): Show |
chr22 | 37277508 | 37320341 | ||
| a0001c0005 | 0/0 | 1182 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | ATGGA others(1177): Show |
chr22 | 37277508 | 37320341 | ||
| a0001c0006 | 0/0 | 1182 | 2 | 0 | 0 | 1 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | ATGGA others(1177): Show |
chr22 | 37277508 | 37320341 | ||
| a0001c0009 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | ATGGA others(1177): Show |
chr22 | 37277508 | 37320341 | ||
| a0001c0012 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | ATGGA others(1177): Show |
chr22 | 37277508 | 37320341 | ||
| a0002c0003 | 0/0 | 1182 | 7 | 7 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | ATGGA others(1177): Show |
chr22 | 37277508 | 37320341 | ||
| a0003c0010 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | ATGGA others(1177): Show |
chr22 | 37277508 | 37320341 | ||
| a0003c0011 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | ATGGA others(1177): Show |
chr22 | 37277508 | 37320341 | ||
| a0004c0007 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | ATGGA others(1177): Show |
chr22 | 37277508 | 37320341 | ||
| a0005c0008 | 0/0 | 1182 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | ATGGA others(1177): Show |
chr22 | 37277508 | 37320341 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3077 | 62 | 24 | 2 | 25 | 2 | 9 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0002 | 0/0 | 3077 | 26 | 0 | 9 | 15 | 0 | 2 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAACA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0003 | 0/0 | 3077 | 56 | 1 | 11 | 40 | 1 | 3 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAACA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0004 | 0/1 | 3077 | 53 | 8 | 10 | 20 | 4 | 10 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0005 | 0/0 | 3077 | 13 | 1 | 5 | 3 | 2 | 2 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0006 | 0/0 | 3077 | 4 | 0 | 2 | 0 | 1 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0007 | 0/0 | 3077 | 5 | 5 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0008 | 0/0 | 3071 | 8 | 7 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3066): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0009 | 0/0 | 3077 | 5 | 5 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0010 | 0/0 | 3077 | 4 | 4 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0011 | 0/0 | 3077 | 3 | 2 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0012 | 0/0 | 3077 | 3 | 0 | 0 | 3 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0015 | 0/0 | 3077 | 2 | 0 | 2 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAACA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0016 | 0/0 | 3077 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAACA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0018 | 0/0 | 3077 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAACA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0020 | 0/0 | 3071 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3066): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0022 | 0/0 | 3077 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAACA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0024 | 0/0 | 3077 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAACA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0028 | 0/0 | 3077 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0030 | 0/0 | 3077 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0033 | 0/0 | 3077 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0034 | 0/0 | 3077 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0039 | 0/0 | 3077 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0001t0040 | 0/0 | 3093 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3088): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0002 | 1/0 | 3077 | 36 | 0 | 9 | 24 | 2 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAACA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0004 | 0/0 | 3077 | 2 | 1 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0005 | 0/0 | 3077 | 32 | 2 | 8 | 16 | 2 | 4 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0006 | 0/0 | 3077 | 30 | 3 | 2 | 22 | 0 | 3 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0007 | 0/0 | 3077 | 5 | 5 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0008 | 0/0 | 3071 | 4 | 3 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3066): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0009 | 0/0 | 3077 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0014 | 0/0 | 3075 | 3 | 3 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3070): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0017 | 0/0 | 3077 | 2 | 0 | 0 | 2 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAACA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0018 | 0/0 | 3077 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAACA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0020 | 0/0 | 3071 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3066): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0021 | 0/0 | 3077 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAACA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0025 | 0/0 | 3077 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAACA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0026 | 0/0 | 3077 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0027 | 0/0 | 3077 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0029 | 0/0 | 3077 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0036 | 0/0 | 3077 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0037 | 0/0 | 3077 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0002t0038 | 0/0 | 3077 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0004t0013 | 0/0 | 3077 | 3 | 1 | 2 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0004t0019 | 0/0 | 3077 | 2 | 1 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0004t0032 | 0/0 | 3077 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0005t0006 | 0/0 | 3077 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0005t0035 | 0/0 | 3077 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0006t0003 | 0/0 | 3077 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAACA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0006t0004 | 0/0 | 3077 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0009t0001 | 0/0 | 3077 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0001c0012t0023 | 0/0 | 3077 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAACA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0002c0003t0007 | 0/0 | 3077 | 7 | 7 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0003c0010t0007 | 0/0 | 3077 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0003c0011t0009 | 0/0 | 3077 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0004c0007t0001 | 0/0 | 3077 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3072): Show |
chr22 | 37277508 | 37320341 |
| a0005c0008t0031 | 0/0 | 3075 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | GAGCA others(3070): Show |
chr22 | 37277508 | 37320341 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0006 | 0/0 | 5 | 2 | 0 | 0 | 1 | 2 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0002 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0316 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0005g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0005g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0005g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0006g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0008g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0008g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0008g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0008g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0009g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0009g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0009g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0010g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0010g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0010g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0011g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0011g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0012g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0012g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0012g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0015g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0015g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0016g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0016g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0018g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0020g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0022g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0024g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0028g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0030g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0033g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0034g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0039g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0001t0040g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0001 | 1/0 | 8 | 0 | 0 | 7 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0004 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0006g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0007g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0008g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0008g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0009g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0014g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0014g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0014g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0017g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0018g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0020g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0021g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0025g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0026g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0027g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0029g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0036g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0037g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0002t0038g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0004t0013g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0004t0013g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0004t0013g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0004t0019g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0004t0019g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0004t0032g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0005t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0005t0035g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0006t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0006t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0009t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0001c0012t0023g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0002c0003t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0002c0003t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0002c0003t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0002c0003t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0002c0003t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0002c0003t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0002c0003t0007g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0003c0010t0007g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0003c0011t0009g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0004c0007t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| a0005c0008t0031g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0319 | EUR | GBR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0043 | EUR | GBR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0033 | EUR | GBR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0286 | EUR | FIN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0144 | EUR | FIN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0215 | EUR | FIN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00323 | hp2 | a0001 | c0002 | t0005 | g0241 | EUR | FIN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | CHS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | CHS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | CHS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00423 | hp2 | a0001 | c0002 | t0006 | g0130 | EAS | CHS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | CHS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | CHS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | CHS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0254 | EAS | CHS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | CHS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | CHS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | CHS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | CHS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00639 | hp1 | a0001 | c0001 | t0008 | g0108 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0223 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00735 | hp1 | a0001 | c0004 | t0019 | g0299 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00735 | hp2 | a0001 | c0001 | t0030 | g0318 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0030 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0184 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01069 | hp1 | a0001 | c0004 | t0013 | g0150 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0270 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0227 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0039 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01071 | hp2 | a0001 | c0004 | t0013 | g0151 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01074 | hp1 | a0001 | c0002 | t0005 | g0324 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01081 | hp1 | a0001 | c0002 | t0037 | g0156 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01099 | hp1 | a0001 | c0002 | t0005 | g0292 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0053 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01106 | hp2 | a0001 | c0002 | t0005 | g0014 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01109 | hp2 | a0001 | c0001 | t0011 | g0244 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0038 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0315 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01168 | hp1 | a0001 | c0002 | t0005 | g0283 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01168 | hp2 | a0001 | c0001 | t0015 | g0172 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01169 | hp1 | a0001 | c0001 | t0015 | g0173 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0038 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0175 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0039 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01243 | hp1 | a0003 | c0010 | t0007 | g0098 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0314 | AMR | PUR | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0027 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0040 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01257 | hp1 | a0001 | c0002 | t0005 | g0037 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01258 | hp1 | a0001 | c0002 | t0005 | g0037 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0027 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01261 | hp1 | a0001 | c0002 | t0005 | g0293 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0327 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01346 | hp2 | a0001 | c0002 | t0006 | g0004 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0082 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0040 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0228 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0317 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01433 | hp2 | a0001 | c0002 | t0036 | g0005 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01496 | hp1 | a0001 | c0002 | t0008 | g0160 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01496 | hp2 | a0001 | c0002 | t0005 | g0289 | AMR | CLM | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0265 | EUR | IBS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01515 | hp2 | a0001 | c0002 | t0005 | g0320 | EUR | IBS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0028 | EUR | IBS | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01884 | hp1 | a0001 | c0002 | t0007 | g0059 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0035 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0119 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0030 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02015 | hp2 | a0001 | c0002 | t0029 | g0279 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02027 | hp2 | a0001 | c0006 | t0004 | g0256 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02040 | hp1 | a0004 | c0007 | t0001 | g0149 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02040 | hp2 | a0001 | c0001 | t0039 | g0060 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02055 | hp1 | a0001 | c0002 | t0014 | g0061 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0312 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02056 | hp2 | a0001 | c0002 | t0005 | g0303 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02080 | hp1 | a0001 | c0002 | t0006 | g0072 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0269 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02132 | hp2 | a0001 | c0002 | t0005 | g0287 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0046 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02148 | hp1 | a0001 | c0002 | t0006 | g0047 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | CDX | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CDX | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | CDX | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | CDX | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02257 | hp2 | a0001 | c0004 | t0032 | g0103 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0102 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0036 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02280 | hp1 | a0002 | c0003 | t0007 | g0302 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0273 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0272 | EAS | KHV | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0093 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02602 | hp2 | a0001 | c0002 | t0005 | g0310 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02615 | hp1 | a0001 | c0004 | t0019 | g0083 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02622 | hp1 | a0001 | c0001 | t0034 | g0068 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02630 | hp2 | a0001 | c0002 | t0007 | g0101 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0062 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0081 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02683 | hp1 | a0005 | c0008 | t0031 | g0296 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0325 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0322 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02698 | hp2 | a0001 | c0002 | t0005 | g0285 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0290 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02717 | hp2 | a0001 | c0002 | t0038 | g0075 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02723 | hp1 | a0001 | c0002 | t0005 | g0328 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0262 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0208 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0260 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02809 | hp1 | a0002 | c0003 | t0007 | g0048 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0157 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02818 | hp2 | a0001 | c0001 | t0016 | g0058 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02886 | hp1 | a0001 | c0002 | t0008 | g0057 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0311 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02895 | hp1 | a0001 | c0001 | t0028 | g0077 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0297 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02896 | hp1 | a0001 | c0004 | t0013 | g0067 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0313 | AFR | ESN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | ESN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02965 | hp2 | a0001 | c0005 | t0006 | g0158 | AFR | ESN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0109 | AFR | ESN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0064 | AFR | ESN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02976 | hp1 | a0001 | c0002 | t0008 | g0097 | AFR | ESN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0252 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03017 | hp2 | a0001 | c0002 | t0006 | g0135 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03041 | hp2 | a0001 | c0001 | t0020 | g0277 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03098 | hp1 | a0002 | c0003 | t0007 | g0055 | AFR | MSL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03130 | hp1 | a0001 | c0002 | t0009 | g0304 | AFR | ESN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0105 | AFR | ESN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0036 | AFR | ESN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03139 | hp2 | a0001 | c0002 | t0006 | g0070 | AFR | ESN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03195 | hp1 | a0001 | c0001 | t0016 | g0099 | AFR | ESN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0065 | AFR | ESN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | MSL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03209 | hp2 | a0001 | c0005 | t0035 | g0115 | AFR | MSL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03225 | hp1 | a0003 | c0011 | t0009 | g0281 | AFR | MSL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0242 | AFR | MSL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0266 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03239 | hp2 | a0001 | c0002 | t0005 | g0321 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03486 | hp1 | a0001 | c0009 | t0001 | g0152 | AFR | MSL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03486 | hp2 | a0001 | c0001 | t0011 | g0034 | AFR | MSL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0189 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0145 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03516 | hp2 | a0002 | c0003 | t0007 | g0044 | AFR | ESN | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03540 | hp1 | a0002 | c0003 | t0007 | g0071 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03579 | hp1 | a0001 | c0001 | t0033 | g0104 | AFR | MSL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03579 | hp2 | a0001 | c0001 | t0010 | g0019 | AFR | MSL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03688 | hp2 | a0001 | c0002 | t0006 | g0164 | SAS | STU | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03704 | hp1 | a0001 | c0001 | t0022 | g0190 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0261 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0264 | SAS | BEB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0258 | SAS | BEB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03834 | hp1 | a0001 | c0002 | t0026 | g0015 | SAS | BEB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03927 | hp1 | a0001 | c0002 | t0005 | g0284 | SAS | BEB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0255 | SAS | BEB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG04115 | hp2 | a0001 | c0002 | t0006 | g0129 | SAS | STU | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0013 | SAS | BEB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG04199 | hp1 | a0001 | c0006 | t0003 | g0092 | SAS | STU | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0253 | SAS | STU | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0089 | SAS | STU | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0323 | SAS | STU | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18522 | hp1 | a0001 | c0002 | t0004 | g0305 | AFR | YRI | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0113 | AFR | YRI | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | CHB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0280 | EAS | CHB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | CHB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18906 | hp1 | a0001 | c0002 | t0006 | g0069 | AFR | YRI | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0243 | AFR | YRI | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18939 | hp2 | a0001 | c0002 | t0005 | g0015 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18940 | hp1 | a0001 | c0002 | t0006 | g0288 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18941 | hp2 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18945 | hp1 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18948 | hp1 | a0001 | c0002 | t0006 | g0138 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18951 | hp2 | a0001 | c0002 | t0005 | g0032 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18953 | hp1 | a0001 | c0002 | t0006 | g0137 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18954 | hp2 | a0001 | c0002 | t0005 | g0291 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18956 | hp1 | a0001 | c0002 | t0006 | g0134 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18965 | hp1 | a0001 | c0001 | t0012 | g0309 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18965 | hp2 | a0001 | c0002 | t0005 | g0251 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18967 | hp1 | a0001 | c0002 | t0006 | g0136 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18967 | hp2 | a0001 | c0002 | t0025 | g0185 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18969 | hp1 | a0001 | c0002 | t0005 | g0294 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18970 | hp2 | a0001 | c0002 | t0017 | g0011 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18971 | hp2 | a0001 | c0002 | t0006 | g0004 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18973 | hp1 | a0001 | c0002 | t0006 | g0004 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18974 | hp1 | a0001 | c0002 | t0018 | g0029 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18974 | hp2 | a0001 | c0001 | t0018 | g0177 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18975 | hp1 | a0001 | c0002 | t0006 | g0073 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18977 | hp2 | a0001 | c0002 | t0005 | g0012 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18981 | hp2 | a0001 | c0002 | t0005 | g0282 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18982 | hp2 | a0001 | c0002 | t0021 | g0231 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18988 | hp1 | a0001 | c0002 | t0006 | g0012 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18991 | hp1 | a0001 | c0002 | t0006 | g0005 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19000 | hp1 | a0001 | c0002 | t0006 | g0005 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19003 | hp1 | a0001 | c0002 | t0005 | g0295 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19005 | hp1 | a0001 | c0002 | t0006 | g0074 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19007 | hp2 | a0001 | c0002 | t0006 | g0004 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19009 | hp1 | a0001 | c0002 | t0005 | g0014 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19010 | hp2 | a0001 | c0002 | t0017 | g0011 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19011 | hp2 | a0001 | c0002 | t0005 | g0032 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19030 | hp1 | a0001 | c0002 | t0007 | g0154 | AFR | LWK | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19043 | hp1 | a0001 | c0002 | t0007 | g0161 | AFR | LWK | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0298 | AFR | LWK | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19057 | hp1 | a0001 | c0002 | t0005 | g0014 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19057 | hp2 | a0001 | c0001 | t0012 | g0308 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19060 | hp2 | a0001 | c0002 | t0027 | g0301 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19070 | hp1 | a0001 | c0001 | t0024 | g0197 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19070 | hp2 | a0001 | c0002 | t0006 | g0012 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19076 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19076 | hp2 | a0001 | c0001 | t0040 | g0147 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19080 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19080 | hp2 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19081 | hp1 | a0001 | c0002 | t0006 | g0005 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19084 | hp2 | a0001 | c0002 | t0005 | g0029 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19085 | hp2 | a0001 | c0002 | t0006 | g0005 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19086 | hp2 | a0001 | c0002 | t0006 | g0004 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19087 | hp1 | a0001 | c0002 | t0005 | g0249 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19091 | hp1 | a0001 | c0002 | t0004 | g0300 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19240 | hp1 | a0001 | c0002 | t0008 | g0159 | AFR | YRI | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA20129 | hp1 | a0001 | c0002 | t0014 | g0114 | AFR | ASW | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA20129 | hp2 | a0001 | c0012 | t0023 | g0084 | AFR | ASW | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0275 | EUR | TSI | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0076 | EUR | TSI | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0063 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02486 | hp2 | a0001 | c0002 | t0006 | g0066 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02559 | hp1 | a0001 | c0002 | t0007 | g0140 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03471 | hp1 | a0001 | c0002 | t0020 | g0015 | AFR | MSL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG06807 | hp1 | a0002 | c0003 | t0007 | g0050 | AFR | USA | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| HG06807 | hp2 | a0001 | c0001 | t0011 | g0034 | AFR | USA | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18955 | hp1 | a0001 | c0002 | t0005 | g0263 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA18955 | hp2 | a0001 | c0001 | t0012 | g0307 | EAS | JPT | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA20300 | hp1 | a0001 | c0001 | t0009 | g0306 | AFR | USA | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA20300 | hp2 | a0001 | c0002 | t0005 | g0326 | AFR | USA | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA21309 | hp1 | a0001 | c0002 | t0014 | g0051 | AFR | LWK | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| NA21309 | hp2 | a0002 | c0003 | t0007 | g0056 | AFR | LWK | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0316 | REF | REF | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0001 | REF | REF | CYTH4_chr22_37277508_37320341 | CYTH4 | chr22 | 37277508 | 37320341 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37292626 | G | A | 1 | a0004 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.25G>A | p.Ala9Thr | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/13 | 87/3077 | 25/1185 | 9/394 | chr22 | 37292626 | |||
| chr22:37296051 | A | G | 1 | a0002 | 7 | HG02280.hp1 HG02809.hp1 HG03098.hp1 others(4): Show |
missense_variant | MODERATE | c.220A>G | p.Met74Val | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/13 | 282/3077 | 220/1185 | 74/394 | chr22 | 37296051 | |||
| chr22:37297648 | A | C | 1 | a0003 | 2 | HG01243.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.319A>C | p.Asn107His | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/13 | 381/3077 | 319/1185 | 107/394 | chr22 | 37297648 | |||
| chr22:37299245 | G | A | 1 | a0005 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.373G>A | p.Val125Ile | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/13 | 435/3077 | 373/1185 | 125/394 | chr22 | 37299245 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37294716 | G | A | 1 | a0001c0005 | 2 | HG02965.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.159G>A | p.Ala53Ala | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/13 | 221/3077 | 159/1185 | 53/394 | chr22 | 37294716 | |||
| chr22:37296059 | C | T | 1 | a0001c0012 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.228C>T | p.Pro76Pro | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/13 | 290/3077 | 228/1185 | 76/394 | chr22 | 37296059 | |||
| chr22:37297591 | C | T | 2 | a0003c0010 a0003c0011 |
2 | HG01243.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.262C>T | p.Leu88Leu | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/13 | 324/3077 | 262/1185 | 88/394 | chr22 | 37297591 | |||
| chr22:37297605 | C | T | 1 | a0001c0009 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.276C>T | p.Asp92Asp | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/13 | 338/3077 | 276/1185 | 92/394 | chr22 | 37297605 | |||
| chr22:37300937 | C | T | 1 | a0001c0006 | 2 | HG02027.hp2 HG04199.hp1 |
synonymous_variant | LOW | c.465C>T | p.Gly155Gly | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/13 | 527/3077 | 465/1185 | 155/394 | chr22 | 37300937 | |||
| chr22:37303336 | T | C | 10 | a0001c0001 a0001c0004 a0001c0005 others(7): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): Show |
synonymous_variant | LOW | c.630T>C | p.Phe210Phe | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/13 | 692/3077 | 630/1185 | 210/394 | chr22 | 37303336 | |||
| chr22:37311031 | C | T | 1 | a0001c0004 | 6 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
synonymous_variant | LOW | c.852C>T | p.Thr284Thr | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 10/13 | 914/3077 | 852/1185 | 284/394 | chr22 | 37311031 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37282510 | A | G | 43 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(40): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
5_prime_UTR_variant | MODIFIER | c.-60A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/13 | 60 | chr22 | 37282510 | ||||||
| chr22:37282524 | G | A | 19 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(16): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
5_prime_UTR_variant | MODIFIER | c.-46G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/13 | 46 | chr22 | 37282524 | ||||||
| chr22:37282531 | G | C | 2 | a0001c0001t0033 a0001c0004t0032 |
2 | HG02257.hp2 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-39G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/13 | 39 | chr22 | 37282531 | ||||||
| chr22:37313579 | C | T | 6 | a0001c0001t0008 a0001c0001t0020 a0001c0002t0008 others(3): Show |
18 | HG00639.hp1 HG01496.hp1 HG02055.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*68C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 68 | chr22 | 37313579 | ||||||
| chr22:37313938 | G | T | 5 | a0001c0001t0008 a0001c0001t0020 a0001c0002t0008 others(2): Show |
17 | HG00639.hp1 HG01496.hp1 HG02055.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*427G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 427 | chr22 | 37313938 | ||||||
| chr22:37313972 | C | T | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(14): Show |
187 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*461C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 461 | chr22 | 37313972 | ||||||
| chr22:37313984 | C | A | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*473C>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 473 | chr22 | 37313984 | ||||||
| chr22:37313988 | T | C | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*477T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 477 | chr22 | 37313988 | ||||||
| chr22:37313989 | T | C | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*478T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 478 | chr22 | 37313989 | ||||||
| chr22:37313990 | G | A | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*479G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 479 | chr22 | 37313990 | ||||||
| chr22:37313991 | G | A | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*480G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 480 | chr22 | 37313991 | ||||||
| chr22:37313994 | T | G | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*483T>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 483 | chr22 | 37313994 | ||||||
| chr22:37313995 | T | A | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*484T>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 484 | chr22 | 37313995 | ||||||
| chr22:37314001 | T | G | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*490T>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 490 | chr22 | 37314001 | ||||||
| chr22:37314002 | C | G | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*491C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 491 | chr22 | 37314002 | ||||||
| chr22:37314004 | C | T | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*493C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 493 | chr22 | 37314004 | ||||||
| chr22:37314005 | T | G | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494T>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 494 | chr22 | 37314005 | ||||||
| chr22:37314014 | G | T | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*503G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 503 | chr22 | 37314014 | ||||||
| chr22:37314016 | G | T | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*505G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 505 | chr22 | 37314016 | ||||||
| chr22:37314018 | T | C | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*507T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 507 | chr22 | 37314018 | ||||||
| chr22:37314028 | C | A | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*517C>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 517 | chr22 | 37314028 | ||||||
| chr22:37314034 | T | G | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*523T>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 523 | chr22 | 37314034 | ||||||
| chr22:37314039 | C | G | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*528C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 528 | chr22 | 37314039 | ||||||
| chr22:37314042 | A | C | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*531A>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 531 | chr22 | 37314042 | ||||||
| chr22:37314043 | C | T | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*532C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 532 | chr22 | 37314043 | ||||||
| chr22:37314044 | G | T | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*533G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 533 | chr22 | 37314044 | ||||||
| chr22:37314046 | A | C | 1 | a0001c0001t0024 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*535A>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 535 | chr22 | 37314046 | ||||||
| chr22:37314055 | C | T | 1 | a0001c0001t0005 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*544C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 544 | chr22 | 37314055 | ||||||
| chr22:37314090 | C | T | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(14): Show |
187 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*579C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 579 | chr22 | 37314090 | ||||||
| chr22:37314136 | G | A | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(13): Show |
186 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*625G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 625 | chr22 | 37314136 | ||||||
| chr22:37314150 | C | T | 1 | a0001c0002t0038 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*639C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 639 | chr22 | 37314150 | ||||||
| chr22:37314197 | A | ACGTATTG others(9): Show |
1 | a0001c0001t0040 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*687_*702dupCGTATT others(10): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 703 | INFO_REALIGN_3_PRIME | chr22 | 37314197 | |||||
| chr22:37314218 | C | G | 1 | a0001c0002t0029 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*707C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 707 | chr22 | 37314218 | ||||||
| chr22:37314251 | G | A | 4 | a0001c0001t0039 a0001c0004t0013 a0001c0004t0019 others(1): Show |
7 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*740G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 740 | chr22 | 37314251 | ||||||
| chr22:37314254 | G | A | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(14): Show |
187 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*743G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 743 | chr22 | 37314254 | ||||||
| chr22:37314260 | G | A | 1 | a0001c0001t0030 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*749G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 749 | chr22 | 37314260 | ||||||
| chr22:37314340 | G | A | 1 | a0001c0002t0026 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*829G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 829 | chr22 | 37314340 | ||||||
| chr22:37314371 | A | T | 1 | a0001c0002t0017 | 2 | NA18970.hp2 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*860A>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 860 | chr22 | 37314371 | ||||||
| chr22:37314395 | T | A | 2 | a0001c0002t0021 a0001c0002t0027 |
2 | NA18982.hp2 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*884T>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 884 | chr22 | 37314395 | ||||||
| chr22:37314473 | T | C | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(14): Show |
187 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*962T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 962 | chr22 | 37314473 | ||||||
| chr22:37314506 | A | C | 1 | a0001c0002t0037 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*995A>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 995 | chr22 | 37314506 | ||||||
| chr22:37314528 | G | T | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(14): Show |
187 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*1017G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1017 | chr22 | 37314528 | ||||||
| chr22:37314566 | G | A | 1 | a0005c0008t0031 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1055G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1055 | chr22 | 37314566 | ||||||
| chr22:37314590 | C | A | 2 | a0001c0001t0018 a0001c0002t0018 |
2 | NA18974.hp1 NA18974.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1079C>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1079 | chr22 | 37314590 | ||||||
| chr22:37314629 | A | C | 2 | a0001c0001t0018 a0001c0002t0018 |
2 | NA18974.hp1 NA18974.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1118A>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1118 | chr22 | 37314629 | ||||||
| chr22:37314658 | T | C | 2 | a0001c0001t0011 a0001c0001t0034 |
4 | HG01109.hp2 HG02622.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1147T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1147 | chr22 | 37314658 | ||||||
| chr22:37314673 | C | T | 1 | a0001c0002t0036 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1162C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1162 | chr22 | 37314673 | ||||||
| chr22:37314694 | G | A | 4 | a0001c0004t0013 a0001c0004t0019 a0001c0004t0032 others(1): Show |
7 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1183G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1183 | chr22 | 37314694 | ||||||
| chr22:37314798 | C | T | 40 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(37): Show |
249 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*1287C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1287 | chr22 | 37314798 | ||||||
| chr22:37314799 | C | T | 2 | a0001c0001t0010 a0001c0001t0028 |
5 | HG02647.hp1 HG02895.hp1 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1288C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1288 | chr22 | 37314799 | ||||||
| chr22:37314802 | C | A | 1 | a0001c0001t0015 | 2 | HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1291C>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1291 | chr22 | 37314802 | ||||||
| chr22:37314910 | C | T | 4 | a0001c0001t0008 a0001c0001t0020 a0001c0002t0008 others(1): Show |
14 | HG00639.hp1 HG01496.hp1 HG02145.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1399C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1399 | chr22 | 37314910 | ||||||
| chr22:37314947 | G | A | 1 | a0001c0001t0012 | 3 | NA18955.hp2 NA18965.hp1 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1436G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1436 | chr22 | 37314947 | ||||||
| chr22:37315024 | G | A | 1 | a0001c0002t0021 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1513G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1513 | chr22 | 37315024 | ||||||
| chr22:37315037 | C | G | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(14): Show |
187 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*1526C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1526 | chr22 | 37315037 | ||||||
| chr22:37315141 | G | A | 1 | a0001c0012t0023 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1630G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1630 | chr22 | 37315141 | ||||||
| chr22:37315235 | T | C | 1 | a0001c0001t0022 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1724T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1724 | chr22 | 37315235 | ||||||
| chr22:37315252 | CAT | C | 6 | a0001c0001t0008 a0001c0001t0020 a0001c0002t0008 others(3): Show |
18 | HG00639.hp1 HG01496.hp1 HG02055.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1742_*1743delAT | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1742 | chr22 | 37315252 | ||||||
| chr22:37315316 | AAGAG | A | 4 | a0001c0001t0008 a0001c0001t0020 a0001c0002t0008 others(1): Show |
14 | HG00639.hp1 HG01496.hp1 HG02145.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1809_*1812delGAGA | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1809 | INFO_REALIGN_3_PRIME | chr22 | 37315316 | |||||
| chr22:37315330 | C | A | 1 | a0001c0001t0040 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1819C>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1819 | chr22 | 37315330 | ||||||
| chr22:37315333 | C | T | 2 | a0001c0001t0010 a0001c0001t0028 |
5 | HG02647.hp1 HG02895.hp1 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1822C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 13/13 | 1822 | chr22 | 37315333 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37282620 | C | A | 5 | a0001c0001t0002g0017 a0001c0001t0003g0018 a0001c0001t0003g0041 others(2): Show |
7 | HG00140.hp1 HG01928.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.19+32C>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37282620 | |||||||
| chr22:37282773 | C | T | 107 | a0001c0001t0001g0016 a0001c0001t0001g0245 a0001c0001t0004g0016 others(104): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.19+185C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37282773 | |||||||
| chr22:37282796 | C | T | 106 | a0001c0001t0001g0016 a0001c0001t0001g0245 a0001c0001t0004g0016 others(103): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.19+208C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37282796 | |||||||
| chr22:37282958 | G | A | 1 | a0002c0003t0007g0044 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.19+370G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37282958 | |||||||
| chr22:37283186 | T | TAG | 106 | a0001c0001t0001g0045 a0001c0001t0001g0245 a0001c0001t0004g0031 others(103): Show |
121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.19+601_19+602dupAG | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr22 | 37283186 | ||||||
| chr22:37283198 | A | G | 1 | a0001c0001t0004g0240 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.19+610A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283198 | |||||||
| chr22:37283349 | T | A | 231 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(228): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.19+761T>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283349 | |||||||
| chr22:37283446 | C | G | 114 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(111): Show |
146 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.19+858C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283446 | |||||||
| chr22:37283446 | C | T | 6 | a0001c0001t0002g0238 a0001c0001t0003g0236 a0001c0001t0003g0237 others(3): Show |
7 | NA18950.hp2 NA18951.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.19+858C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283446 | |||||||
| chr22:37283545 | A | C | 231 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(228): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.19+957A>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283545 | |||||||
| chr22:37283630 | C | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.19+1042C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283630 | |||||||
| chr22:37283665 | G | T | 118 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0054 others(115): Show |
131 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.19+1077G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283665 | |||||||
| chr22:37283666 | A | T | 118 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0054 others(115): Show |
131 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.19+1078A>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283666 | |||||||
| chr22:37283722 | A | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(217): Show |
265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.19+1134A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283722 | |||||||
| chr22:37283813 | T | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(215): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.19+1225T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283813 | |||||||
| chr22:37283831 | C | T | 1 | a0001c0002t0005g0326 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.19+1243C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283831 | |||||||
| chr22:37283883 | G | C | 6 | a0001c0001t0002g0025 a0001c0001t0002g0167 a0001c0001t0003g0168 others(3): Show |
7 | NA18942.hp2 NA18950.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+1295G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283883 | |||||||
| chr22:37283884 | G | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(218): Show |
266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.19+1296G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283884 | |||||||
| chr22:37283905 | T | C | 4 | a0001c0001t0002g0174 a0001c0001t0015g0172 a0001c0001t0015g0173 others(1): Show |
4 | HG01081.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+1317T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283905 | |||||||
| chr22:37283907 | C | T | 185 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0022 others(182): Show |
217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.19+1319C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283907 | |||||||
| chr22:37283911 | C | T | 10 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0006g0053 others(7): Show |
10 | HG01106.hp1 HG01516.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+1323C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283911 | |||||||
| chr22:37283972 | C | T | 1 | a0001c0002t0005g0310 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.19+1384C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37283972 | |||||||
| chr22:37284034 | C | T | 3 | a0001c0001t0012g0307 a0001c0001t0012g0308 a0001c0001t0012g0309 |
3 | NA18955.hp2 NA18965.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.19+1446C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284034 | |||||||
| chr22:37284086 | G | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
142 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.19+1498G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284086 | |||||||
| chr22:37284173 | G | A | 10 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0006g0053 others(7): Show |
10 | HG01106.hp1 HG01516.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+1585G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284173 | |||||||
| chr22:37284206 | C | T | 10 | a0001c0001t0007g0065 a0001c0001t0008g0063 a0001c0001t0010g0019 others(7): Show |
11 | HG02486.hp1 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.19+1618C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284206 | |||||||
| chr22:37284380 | G | A | 2 | a0001c0001t0001g0049 a0002c0003t0007g0048 |
2 | HG01891.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.19+1792G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284380 | |||||||
| chr22:37284431 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.19+1843T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284431 | |||||||
| chr22:37284441 | G | A | 1 | a0001c0002t0038g0075 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.19+1853G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284441 | |||||||
| chr22:37284471 | G | A | 34 | a0001c0001t0001g0049 a0001c0001t0001g0079 a0001c0001t0001g0080 others(31): Show |
38 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.19+1883G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284471 | |||||||
| chr22:37284589 | G | A | 1 | a0001c0002t0007g0101 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.19+2001G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284589 | |||||||
| chr22:37284648 | C | T | 1 | a0001c0001t0004g0240 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.19+2060C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284648 | |||||||
| chr22:37284667 | C | T | 2 | a0001c0001t0016g0099 a0003c0010t0007g0098 |
2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.19+2079C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284667 | |||||||
| chr22:37284753 | C | T | 3 | a0001c0001t0002g0174 a0001c0001t0003g0233 a0001c0002t0002g0175 |
3 | HG01081.hp2 HG01192.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.19+2165C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284753 | |||||||
| chr22:37284759 | G | A | 36 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0110 others(33): Show |
37 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.19+2171G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284759 | |||||||
| chr22:37284797 | G | A | 2 | a0001c0001t0001g0049 a0002c0003t0007g0048 |
2 | HG01891.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.19+2209G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284797 | |||||||
| chr22:37284817 | T | C | 10 | a0001c0001t0003g0176 a0001c0001t0004g0031 a0001c0001t0004g0246 others(7): Show |
12 | HG02027.hp1 HG02155.hp1 NA18951.hp2 others(9): Show |
intron_variant | MODIFIER | c.19+2229T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284817 | |||||||
| chr22:37284936 | G | A | 1 | a0001c0001t0008g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.19+2348G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284936 | |||||||
| chr22:37284947 | TG | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(112): Show |
138 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.19+2366delG | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr22 | 37284947 | ||||||
| chr22:37284950 | G | C | 4 | a0001c0001t0001g0049 a0001c0001t0033g0104 a0001c0004t0032g0103 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+2362G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284950 | |||||||
| chr22:37284957 | G | A | 110 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(107): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.19+2369G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284957 | |||||||
| chr22:37284958 | C | T | 110 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(107): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.19+2370C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37284958 | |||||||
| chr22:37285225 | G | C | 1 | a0001c0002t0005g0321 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.19+2637G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285225 | |||||||
| chr22:37285233 | C | T | 1 | a0001c0002t0005g0251 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.19+2645C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285233 | |||||||
| chr22:37285350 | T | TGTG | 30 | a0001c0001t0001g0016 a0001c0001t0001g0049 a0001c0001t0001g0052 others(27): Show |
32 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.19+2783_19+2785dup others(3): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr22 | 37285350 | ||||||
| chr22:37285350 | TGTGGTG | T | 1 | a0001c0002t0006g0010 | 3 | NA18941.hp2 NA18945.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.19+2780_19+2785del others(6): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr22 | 37285350 | ||||||
| chr22:37285374 | A | G | 10 | a0001c0001t0001g0016 a0001c0001t0001g0049 a0001c0001t0001g0162 others(7): Show |
11 | HG01243.hp2 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.19+2786A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285374 | |||||||
| chr22:37285397 | T | G | 10 | a0001c0001t0001g0016 a0001c0001t0001g0049 a0001c0001t0001g0142 others(7): Show |
11 | HG01243.hp2 HG01496.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.19+2809T>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285397 | |||||||
| chr22:37285433 | T | C | 4 | a0001c0001t0002g0200 a0001c0001t0003g0176 a0001c0001t0004g0246 others(1): Show |
4 | HG03017.hp1 NA18957.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+2845T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285433 | |||||||
| chr22:37285517 | C | T | 1 | a0001c0002t0005g0303 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.19+2929C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285517 | |||||||
| chr22:37285568 | G | A | 1 | a0001c0001t0011g0034 | 2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.19+2980G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285568 | |||||||
| chr22:37285572 | C | G | 1 | a0001c0001t0004g0250 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.19+2984C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285572 | |||||||
| chr22:37285648 | T | C | 7 | a0001c0001t0009g0262 a0001c0001t0009g0306 a0001c0001t0011g0034 others(4): Show |
8 | HG01109.hp2 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+3060T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285648 | |||||||
| chr22:37285667 | G | C | 1 | a0001c0001t0004g0253 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.19+3079G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285667 | |||||||
| chr22:37285672 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.19+3084C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285672 | |||||||
| chr22:37285683 | C | G | 8 | a0001c0002t0004g0305 a0001c0002t0006g0066 a0001c0002t0006g0069 others(5): Show |
8 | HG02486.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+3095C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285683 | |||||||
| chr22:37285703 | A | G | 1 | a0001c0002t0008g0159 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.19+3115A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285703 | |||||||
| chr22:37285706 | G | A | 2 | a0001c0002t0005g0263 a0001c0002t0008g0057 |
2 | HG02886.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.19+3118G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285706 | |||||||
| chr22:37285709 | T | TCAAA | 11 | a0001c0002t0007g0059 a0001c0002t0008g0160 a0001c0005t0006g0158 others(8): Show |
11 | HG01496.hp1 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.19+3142_19+3145dup others(4): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr22 | 37285709 | ||||||
| chr22:37285848 | C | T | 2 | a0001c0001t0001g0054 a0001c0012t0023g0084 |
2 | HG01516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.19+3260C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285848 | |||||||
| chr22:37285870 | AC | A | 3 | a0001c0002t0002g0232 a0001c0002t0014g0061 a0001c0002t0014g0114 |
3 | HG02055.hp1 NA18961.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.19+3285delC | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr22 | 37285870 | ||||||
| chr22:37285881 | G | A | 1 | a0001c0001t0004g0247 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.19+3293G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285881 | |||||||
| chr22:37285882 | G | T | 1 | a0001c0001t0001g0165 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.19+3294G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285882 | |||||||
| chr22:37285884 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.19+3296T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285884 | |||||||
| chr22:37285921 | G | T | 4 | a0001c0001t0004g0259 a0001c0002t0004g0300 a0001c0002t0021g0231 others(1): Show |
4 | HG00609.hp2 NA18982.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+3333G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285921 | |||||||
| chr22:37285945 | G | A | 133 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0023 others(130): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.19+3357G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285945 | |||||||
| chr22:37285949 | G | A | 1 | a0001c0001t0002g0201 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.19+3361G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37285949 | |||||||
| chr22:37286012 | T | C | 1 | a0001c0012t0023g0084 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.19+3424T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286012 | |||||||
| chr22:37286098 | G | A | 1 | a0001c0001t0008g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.19+3510G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286098 | |||||||
| chr22:37286109 | GT | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.19+3522delT | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286109 | |||||||
| chr22:37286115 | G | T | 2 | a0001c0001t0011g0034 a0001c0001t0011g0244 |
3 | HG01109.hp2 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.19+3527G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286115 | |||||||
| chr22:37286188 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0003g0236 |
2 | HG00597.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.19+3600G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286188 | |||||||
| chr22:37286191 | C | A | 1 | a0001c0001t0001g0165 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.19+3603C>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286191 | |||||||
| chr22:37286290 | C | A | 1 | a0001c0001t0001g0165 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.19+3702C>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286290 | |||||||
| chr22:37286321 | T | C | 1 | a0001c0001t0004g0264 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.19+3733T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286321 | |||||||
| chr22:37286324 | C | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(198): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.19+3736C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286324 | |||||||
| chr22:37286330 | A | G | 5 | a0001c0001t0004g0298 a0001c0001t0005g0297 a0001c0001t0016g0099 others(2): Show |
5 | HG00735.hp1 HG02683.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+3742A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286330 | |||||||
| chr22:37286354 | G | A | 2 | a0001c0001t0008g0102 a0001c0001t0008g0105 |
2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.19+3766G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286354 | |||||||
| chr22:37286402 | T | C | 1 | a0001c0001t0010g0062 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.19+3814T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286402 | |||||||
| chr22:37286430 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.19+3842G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286430 | |||||||
| chr22:37286455 | G | C | 5 | a0001c0001t0004g0275 a0001c0004t0013g0067 a0001c0004t0013g0150 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+3867G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286455 | |||||||
| chr22:37286533 | C | T | 3 | a0001c0002t0014g0051 a0001c0002t0014g0061 a0001c0002t0014g0114 |
3 | HG02055.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.19+3945C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286533 | |||||||
| chr22:37286633 | G | A | 3 | a0001c0001t0009g0262 a0001c0001t0009g0306 a0001c0001t0016g0058 |
3 | HG02723.hp2 HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.19+4045G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286633 | |||||||
| chr22:37286658 | G | A | 4 | a0001c0001t0004g0298 a0001c0001t0005g0297 a0001c0004t0019g0299 others(1): Show |
4 | HG00735.hp1 HG02683.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+4070G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286658 | |||||||
| chr22:37286680 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.19+4092G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286680 | |||||||
| chr22:37286703 | G | C | 2 | a0003c0010t0007g0098 a0003c0011t0009g0281 |
2 | HG01243.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.19+4115G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286703 | |||||||
| chr22:37286772 | T | C | 1 | a0001c0012t0023g0084 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.19+4184T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286772 | |||||||
| chr22:37286784 | A | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(198): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.19+4196A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286784 | |||||||
| chr22:37286790 | G | A | 3 | a0001c0002t0014g0051 a0001c0002t0014g0061 a0001c0002t0014g0114 |
3 | HG02055.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.19+4202G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286790 | |||||||
| chr22:37286869 | T | C | 4 | a0001c0001t0004g0298 a0001c0001t0005g0297 a0001c0004t0019g0299 others(1): Show |
4 | HG00735.hp1 HG02683.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+4281T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286869 | |||||||
| chr22:37286914 | T | C | 200 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(197): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.19+4326T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286914 | |||||||
| chr22:37286923 | C | T | 200 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(197): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.19+4335C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286923 | |||||||
| chr22:37286929 | C | T | 2 | a0001c0001t0011g0034 a0001c0001t0011g0244 |
3 | HG01109.hp2 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.19+4341C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286929 | |||||||
| chr22:37286969 | A | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(184): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.19+4381A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37286969 | |||||||
| chr22:37287177 | A | G | 200 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(197): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.19+4589A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37287177 | |||||||
| chr22:37287239 | G | C | 200 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(197): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.19+4651G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37287239 | |||||||
| chr22:37287248 | A | G | 1 | a0001c0001t0004g0275 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.19+4660A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37287248 | |||||||
| chr22:37287255 | A | G | 198 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(195): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.19+4667A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37287255 | |||||||
| chr22:37287335 | T | C | 200 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(197): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.19+4747T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37287335 | |||||||
| chr22:37287352 | C | A | 88 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0022 others(85): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.19+4764C>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37287352 | |||||||
| chr22:37287415 | C | T | 5 | a0001c0001t0001g0054 a0001c0002t0004g0300 a0001c0002t0021g0231 others(2): Show |
5 | HG01516.hp1 NA18982.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+4827C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37287415 | |||||||
| chr22:37287430 | C | A | 2 | a0001c0001t0015g0172 a0001c0001t0015g0173 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.19+4842C>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37287430 | |||||||
| chr22:37287557 | C | T | 1 | a0001c0001t0004g0269 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.19+4969C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37287557 | |||||||
| chr22:37287601 | G | T | 1 | a0002c0003t0007g0071 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.19+5013G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37287601 | |||||||
| chr22:37287642 | C | T | 167 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(164): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.20-4979C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37287642 | |||||||
| chr22:37287784 | G | A | 3 | a0001c0001t0001g0131 a0001c0001t0002g0178 a0001c0005t0035g0115 |
3 | HG02083.hp2 HG03209.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.20-4837G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37287784 | |||||||
| chr22:37287898 | T | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.20-4723T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37287898 | |||||||
| chr22:37287949 | G | A | 1 | a0001c0002t0005g0310 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.20-4672G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37287949 | |||||||
| chr22:37287977 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.20-4644C>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37287977 | |||||||
| chr22:37288031 | G | C | 202 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(199): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.20-4590G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37288031 | |||||||
| chr22:37288044 | C | T | 1 | a0002c0003t0007g0056 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.20-4577C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37288044 | |||||||
| chr22:37288148 | C | T | 201 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(198): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.20-4473C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37288148 | |||||||
| chr22:37288410 | CA | C | 4 | a0001c0001t0001g0052 a0001c0001t0001g0080 a0001c0001t0001g0106 others(1): Show |
4 | HG01891.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-4204delA | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr22 | 37288410 | ||||||
| chr22:37288510 | T | G | 4 | a0002c0003t0007g0044 a0002c0003t0007g0050 a0002c0003t0007g0055 others(1): Show |
4 | HG03098.hp1 HG03516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-4111T>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37288510 | |||||||
| chr22:37288583 | C | CA | 190 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.20-4025dupA | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr22 | 37288583 | ||||||
| chr22:37288584 | A | G | 1 | a0001c0002t0014g0061 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.20-4037A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37288584 | |||||||
| chr22:37288730 | G | T | 1 | a0001c0004t0019g0083 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.20-3891G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37288730 | |||||||
| chr22:37288844 | C | T | 1 | a0001c0001t0004g0040 | 2 | HG01256.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.20-3777C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37288844 | |||||||
| chr22:37288914 | G | T | 2 | a0001c0002t0005g0294 a0001c0002t0005g0295 |
2 | NA18969.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.20-3707G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37288914 | |||||||
| chr22:37289104 | T | C | 1 | a0001c0001t0004g0278 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.20-3517T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37289104 | |||||||
| chr22:37289280 | C | T | 1 | a0001c0002t0005g0293 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.20-3341C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37289280 | |||||||
| chr22:37289344 | G | A | 3 | a0002c0003t0007g0048 a0002c0003t0007g0071 a0002c0003t0007g0302 |
3 | HG02280.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.20-3277G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37289344 | |||||||
| chr22:37289359 | T | C | 233 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(230): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.20-3262T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37289359 | |||||||
| chr22:37289445 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0049 a0001c0001t0004g0016 |
4 | HG01891.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-3176G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37289445 | |||||||
| chr22:37289597 | G | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.20-3024G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37289597 | |||||||
| chr22:37289663 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.20-2958G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37289663 | |||||||
| chr22:37289698 | G | A | 200 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(197): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.20-2923G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37289698 | |||||||
| chr22:37289757 | C | T | 1 | a0001c0002t0005g0320 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.20-2864C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37289757 | |||||||
| chr22:37289855 | G | A | 199 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(196): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.20-2766G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37289855 | |||||||
| chr22:37289872 | G | A | 3 | a0001c0002t0014g0051 a0001c0002t0014g0061 a0001c0002t0014g0114 |
3 | HG02055.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.20-2749G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37289872 | |||||||
| chr22:37289875 | C | T | 2 | a0003c0010t0007g0098 a0003c0011t0009g0281 |
2 | HG01243.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.20-2746C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37289875 | |||||||
| chr22:37289882 | G | A | 1 | a0001c0002t0005g0282 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.20-2739G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37289882 | |||||||
| chr22:37290072 | C | G | 200 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(197): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.20-2549C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37290072 | |||||||
| chr22:37290081 | G | A | 11 | a0001c0001t0001g0052 a0001c0001t0001g0080 a0001c0001t0001g0106 others(8): Show |
11 | HG01891.hp2 HG02280.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.20-2540G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37290081 | |||||||
| chr22:37290224 | C | T | 13 | a0001c0001t0001g0052 a0001c0001t0001g0080 a0001c0001t0001g0106 others(10): Show |
14 | HG01109.hp2 HG01891.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.20-2397C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37290224 | |||||||
| chr22:37290351 | T | C | 1 | a0001c0012t0023g0084 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.20-2270T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37290351 | |||||||
| chr22:37290669 | T | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(215): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.20-1952T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37290669 | |||||||
| chr22:37290741 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.20-1880C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37290741 | |||||||
| chr22:37290861 | G | A | 5 | a0001c0001t0002g0202 a0001c0001t0004g0082 a0001c0001t0004g0265 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-1760G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37290861 | |||||||
| chr22:37290946 | G | T | 4 | a0001c0001t0004g0298 a0001c0001t0005g0297 a0001c0004t0019g0299 others(1): Show |
4 | HG00735.hp1 HG02683.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-1675G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37290946 | |||||||
| chr22:37290995 | T | C | 1 | a0001c0002t0002g0009 | 4 | NA18940.hp2 NA18942.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-1626T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37290995 | |||||||
| chr22:37291222 | TGGATAGG others(3): Show |
T | 11 | a0001c0001t0001g0052 a0001c0001t0001g0080 a0001c0001t0001g0106 others(8): Show |
11 | HG01891.hp2 HG02280.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.20-1397_20-1388del others(10): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr22 | 37291222 | ||||||
| chr22:37291265 | G | A | 1 | a0001c0002t0005g0283 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.20-1356G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37291265 | |||||||
| chr22:37291267 | T | G | 1 | a0001c0001t0022g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.20-1354T>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37291267 | |||||||
| chr22:37291294 | C | T | 1 | a0001c0002t0002g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.20-1327C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37291294 | |||||||
| chr22:37291381 | C | T | 2 | a0003c0010t0007g0098 a0003c0011t0009g0281 |
2 | HG01243.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.20-1240C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37291381 | |||||||
| chr22:37291435 | A | G | 2 | a0001c0001t0011g0034 a0001c0001t0011g0244 |
3 | HG01109.hp2 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.20-1186A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37291435 | |||||||
| chr22:37291449 | C | T | 4 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(1): Show |
4 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-1172C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37291449 | |||||||
| chr22:37291467 | C | T | 4 | a0001c0002t0002g0027 a0001c0002t0005g0292 a0001c0002t0005g0320 others(1): Show |
5 | HG01099.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-1154C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37291467 | |||||||
| chr22:37291549 | A | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0094 others(15): Show |
23 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.20-1072A>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37291549 | |||||||
| chr22:37291662 | A | G | 1 | a0001c0001t0008g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.20-959A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37291662 | |||||||
| chr22:37291835 | G | A | 5 | a0001c0001t0002g0025 a0001c0001t0002g0100 a0001c0001t0002g0178 others(2): Show |
6 | HG00558.hp1 NA18950.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-786G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37291835 | |||||||
| chr22:37291882 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0094 others(15): Show |
23 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.20-739A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37291882 | |||||||
| chr22:37292063 | C | T | 41 | a0001c0001t0001g0023 a0001c0001t0001g0045 a0001c0001t0001g0127 others(38): Show |
45 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.20-558C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37292063 | |||||||
| chr22:37292094 | G | C | 8 | a0001c0001t0004g0298 a0001c0001t0005g0297 a0001c0001t0007g0065 others(5): Show |
8 | HG00735.hp1 HG02683.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.20-527G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37292094 | |||||||
| chr22:37292275 | G | A | 3 | a0001c0001t0009g0262 a0001c0001t0009g0306 a0001c0001t0016g0058 |
3 | HG02723.hp2 HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.20-346G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37292275 | |||||||
| chr22:37292444 | G | A | 1 | a0001c0002t0005g0294 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.20-177G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37292444 | |||||||
| chr22:37292515 | A | C | 3 | a0001c0001t0009g0262 a0001c0001t0009g0306 a0001c0001t0016g0058 |
3 | HG02723.hp2 HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.20-106A>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37292515 | |||||||
| chr22:37292589 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.20-32A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 1/12 | chr22 | 37292589 | |||||||
| chr22:37292830 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.102+127C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37292830 | |||||||
| chr22:37293065 | A | G | 1 | a0001c0001t0009g0036 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.102+362A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37293065 | |||||||
| chr22:37293092 | A | G | 8 | a0001c0001t0002g0238 a0001c0002t0002g0009 a0001c0002t0002g0011 others(5): Show |
13 | HG00423.hp2 HG00741.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.102+389A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37293092 | |||||||
| chr22:37293334 | G | A | 1 | a0001c0001t0009g0036 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.102+631G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37293334 | |||||||
| chr22:37293364 | T | C | 1 | a0001c0002t0005g0326 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.102+661T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37293364 | |||||||
| chr22:37293387 | A | G | 10 | a0001c0001t0001g0079 a0001c0001t0004g0290 a0001c0001t0004g0312 others(7): Show |
10 | HG02055.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.102+684A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37293387 | |||||||
| chr22:37293393 | AC | A | 89 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0022 others(86): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.102+693delC | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr22 | 37293393 | ||||||
| chr22:37293716 | G | A | 1 | a0001c0001t0003g0211 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.103-944G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37293716 | |||||||
| chr22:37293895 | C | T | 11 | a0001c0001t0001g0052 a0001c0001t0001g0080 a0001c0001t0001g0106 others(8): Show |
11 | HG01891.hp2 HG02280.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-765C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37293895 | |||||||
| chr22:37293927 | G | A | 1 | a0001c0001t0005g0038 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.103-733G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37293927 | |||||||
| chr22:37293931 | T | C | 1 | a0001c0002t0005g0284 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.103-729T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37293931 | |||||||
| chr22:37294018 | G | T | 2 | a0001c0002t0002g0088 a0001c0002t0002g0194 |
2 | HG00621.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.103-642G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37294018 | |||||||
| chr22:37294035 | A | G | 11 | a0001c0001t0001g0052 a0001c0001t0001g0080 a0001c0001t0001g0106 others(8): Show |
11 | HG01891.hp2 HG02280.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-625A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37294035 | |||||||
| chr22:37294056 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.103-604G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37294056 | |||||||
| chr22:37294139 | C | T | 7 | a0002c0003t0007g0044 a0002c0003t0007g0048 a0002c0003t0007g0050 others(4): Show |
7 | HG02280.hp1 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-521C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37294139 | |||||||
| chr22:37294149 | AGGCAGGG others(80): Show |
A | 1 | a0001c0001t0003g0199 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.103-461_103-375del others(87): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr22 | 37294149 | ||||||
| chr22:37294212 | G | A | 1 | a0001c0001t0007g0065 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.103-448G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37294212 | |||||||
| chr22:37294221 | AGGCAGGG others(8): Show |
A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0117 |
2 | HG00544.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.103-425_103-411del others(15): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr22 | 37294221 | ||||||
| chr22:37294310 | G | T | 2 | a0001c0001t0007g0065 a0001c0001t0007g0093 |
2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.103-350G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37294310 | |||||||
| chr22:37294459 | C | A | 5 | a0001c0001t0001g0127 a0001c0001t0003g0183 a0001c0001t0003g0215 others(2): Show |
5 | HG00323.hp1 HG02040.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-201C>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37294459 | |||||||
| chr22:37294597 | C | CA | 3 | a0001c0002t0006g0066 a0001c0002t0006g0069 a0001c0002t0006g0070 |
3 | HG02486.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.103-60dupA | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr22 | 37294597 | ||||||
| chr22:37294606 | G | A | 1 | a0001c0001t0003g0188 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.103-54G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 2/12 | chr22 | 37294606 | |||||||
| chr22:37294900 | G | C | 5 | a0001c0001t0007g0065 a0001c0001t0007g0093 a0001c0001t0009g0262 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.167+176G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37294900 | |||||||
| chr22:37294912 | G | T | 1 | a0001c0001t0008g0157 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.167+188G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37294912 | |||||||
| chr22:37294945 | C | T | 5 | a0001c0002t0014g0051 a0001c0002t0014g0061 a0001c0002t0014g0114 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.167+221C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37294945 | |||||||
| chr22:37295034 | G | A | 3 | a0001c0001t0004g0298 a0001c0001t0005g0297 a0005c0008t0031g0296 |
3 | HG02683.hp1 HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.167+310G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295034 | |||||||
| chr22:37295041 | A | T | 18 | a0001c0001t0001g0123 a0001c0001t0001g0143 a0001c0001t0001g0146 others(15): Show |
20 | HG00597.hp2 HG00609.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.167+317A>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295041 | |||||||
| chr22:37295099 | G | A | 1 | a0001c0002t0005g0285 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.167+375G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295099 | |||||||
| chr22:37295274 | T | G | 176 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(173): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.167+550T>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295274 | |||||||
| chr22:37295287 | A | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0094 others(21): Show |
30 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.167+563A>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295287 | |||||||
| chr22:37295339 | C | T | 2 | a0001c0001t0004g0252 a0001c0001t0004g0258 |
2 | HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.167+615C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295339 | |||||||
| chr22:37295373 | C | T | 1 | a0004c0007t0001g0149 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.168-626C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295373 | |||||||
| chr22:37295374 | ACATGCAC others(11): Show |
A | 2 | a0001c0001t0008g0102 a0001c0001t0008g0105 |
2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.168-608_168-591del others(18): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 37295374 | ||||||
| chr22:37295391 | CGCATGCA others(11): Show |
C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0094 others(12): Show |
20 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.168-557_168-540del others(18): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 37295391 | ||||||
| chr22:37295396 | GCA | G | 7 | a0002c0003t0007g0044 a0002c0003t0007g0048 a0002c0003t0007g0050 others(4): Show |
7 | HG02280.hp1 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-592_168-591del others(2): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 37295396 | ||||||
| chr22:37295409 | A | T | 2 | a0001c0001t0008g0102 a0001c0001t0008g0105 |
2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.168-590A>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295409 | |||||||
| chr22:37295459 | C | T | 1 | a0001c0001t0003g0196 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.168-540C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295459 | |||||||
| chr22:37295468 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.168-531G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295468 | |||||||
| chr22:37295539 | C | G | 1 | a0001c0001t0008g0157 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.168-460C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295539 | |||||||
| chr22:37295553 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0080 a0001c0001t0001g0106 others(1): Show |
4 | HG01891.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-446C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295553 | |||||||
| chr22:37295577 | A | G | 232 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.168-422A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295577 | |||||||
| chr22:37295656 | G | A | 7 | a0002c0003t0007g0044 a0002c0003t0007g0048 a0002c0003t0007g0050 others(4): Show |
7 | HG02280.hp1 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-343G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295656 | |||||||
| chr22:37295746 | C | G | 8 | a0001c0002t0004g0305 a0001c0002t0007g0059 a0001c0002t0007g0101 others(5): Show |
8 | HG01496.hp1 HG01884.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-253C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295746 | |||||||
| chr22:37295782 | G | A | 1 | a0001c0001t0003g0085 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.168-217G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295782 | |||||||
| chr22:37295784 | G | A | 1 | a0001c0006t0004g0256 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.168-215G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295784 | |||||||
| chr22:37295866 | A | G | 166 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(163): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.168-133A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295866 | |||||||
| chr22:37295867 | T | A | 1 | a0001c0002t0014g0114 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.168-132T>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295867 | |||||||
| chr22:37295983 | G | A | 3 | a0001c0001t0009g0262 a0001c0001t0009g0306 a0001c0001t0016g0058 |
3 | HG02723.hp2 HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.168-16G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 3/12 | chr22 | 37295983 | |||||||
| chr22:37296371 | G | A | 1 | a0001c0001t0004g0247 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.234+306G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/12 | chr22 | 37296371 | |||||||
| chr22:37296669 | G | A | 9 | a0001c0001t0001g0107 a0001c0001t0008g0046 a0001c0001t0008g0063 others(6): Show |
9 | HG00639.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.234+604G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/12 | chr22 | 37296669 | |||||||
| chr22:37296684 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0007g0078 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.234+619G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/12 | chr22 | 37296684 | |||||||
| chr22:37296758 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.234+693C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/12 | chr22 | 37296758 | |||||||
| chr22:37296778 | C | T | 2 | a0001c0001t0011g0034 a0001c0001t0011g0244 |
3 | HG01109.hp2 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.234+713C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/12 | chr22 | 37296778 | |||||||
| chr22:37296796 | C | T | 2 | a0001c0004t0013g0150 a0001c0004t0013g0151 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.234+731C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/12 | chr22 | 37296796 | |||||||
| chr22:37296799 | C | T | 7 | a0002c0003t0007g0044 a0002c0003t0007g0048 a0002c0003t0007g0050 others(4): Show |
7 | HG02280.hp1 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+734C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/12 | chr22 | 37296799 | |||||||
| chr22:37296809 | C | G | 4 | a0001c0001t0004g0298 a0001c0001t0005g0297 a0001c0004t0019g0299 others(1): Show |
4 | HG00735.hp1 HG02683.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+744C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/12 | chr22 | 37296809 | |||||||
| chr22:37296897 | C | T | 169 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(166): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.235-667C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/12 | chr22 | 37296897 | |||||||
| chr22:37296933 | C | G | 5 | a0001c0001t0004g0275 a0001c0004t0013g0067 a0001c0004t0013g0150 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-631C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/12 | chr22 | 37296933 | |||||||
| chr22:37296970 | G | A | 164 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(161): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.235-594G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/12 | chr22 | 37296970 | |||||||
| chr22:37296996 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.235-568G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/12 | chr22 | 37296996 | |||||||
| chr22:37297058 | A | C | 2 | a0001c0001t0011g0034 a0001c0001t0011g0244 |
3 | HG01109.hp2 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.235-506A>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/12 | chr22 | 37297058 | |||||||
| chr22:37297080 | C | G | 2 | a0001c0001t0011g0034 a0001c0001t0011g0244 |
3 | HG01109.hp2 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.235-484C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/12 | chr22 | 37297080 | |||||||
| chr22:37297373 | A | G | 7 | a0002c0003t0007g0044 a0002c0003t0007g0048 a0002c0003t0007g0050 others(4): Show |
7 | HG02280.hp1 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-191A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/12 | chr22 | 37297373 | |||||||
| chr22:37297455 | C | T | 5 | a0001c0001t0010g0019 a0001c0001t0010g0062 a0001c0001t0010g0064 others(2): Show |
6 | HG02622.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-109C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 4/12 | chr22 | 37297455 | |||||||
| chr22:37297720 | A | C | 7 | a0002c0003t0007g0044 a0002c0003t0007g0048 a0002c0003t0007g0050 others(4): Show |
7 | HG02280.hp1 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.353+38A>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37297720 | |||||||
| chr22:37297811 | C | T | 11 | a0001c0001t0001g0052 a0001c0001t0001g0080 a0001c0001t0001g0106 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.353+129C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37297811 | |||||||
| chr22:37297879 | A | C | 1 | a0001c0002t0005g0289 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.353+197A>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37297879 | |||||||
| chr22:37297890 | C | T | 1 | a0001c0001t0007g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.353+208C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37297890 | |||||||
| chr22:37297923 | A | T | 5 | a0001c0001t0010g0019 a0001c0001t0010g0062 a0001c0001t0010g0064 others(2): Show |
6 | HG02622.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.353+241A>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37297923 | |||||||
| chr22:37297960 | C | T | 1 | a0001c0002t0005g0328 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.353+278C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37297960 | |||||||
| chr22:37298093 | G | C | 1 | a0001c0002t0002g0220 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.353+411G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37298093 | |||||||
| chr22:37298101 | G | T | 2 | a0001c0001t0011g0034 a0001c0001t0011g0244 |
3 | HG01109.hp2 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.353+419G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37298101 | |||||||
| chr22:37298149 | G | A | 1 | a0001c0002t0005g0321 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.353+467G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37298149 | |||||||
| chr22:37298182 | C | T | 2 | a0001c0001t0011g0034 a0001c0001t0011g0244 |
3 | HG01109.hp2 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.353+500C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37298182 | |||||||
| chr22:37298236 | A | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(226): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.353+554A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37298236 | |||||||
| chr22:37298323 | C | T | 1 | a0001c0002t0005g0285 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.353+641C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37298323 | |||||||
| chr22:37298354 | G | A | 2 | a0003c0010t0007g0098 a0003c0011t0009g0281 |
2 | HG01243.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.353+672G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37298354 | |||||||
| chr22:37298367 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0033g0104 |
3 | HG01109.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.353+685C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37298367 | |||||||
| chr22:37298372 | C | CA | 10 | a0001c0001t0004g0275 a0001c0001t0005g0297 a0001c0001t0008g0157 others(7): Show |
10 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.353+701dupA | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr22 | 37298372 | ||||||
| chr22:37298538 | G | T | 1 | a0001c0001t0002g0209 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.354-688G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37298538 | |||||||
| chr22:37298547 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.354-679G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37298547 | |||||||
| chr22:37298690 | G | C | 2 | a0001c0004t0019g0299 a0005c0008t0031g0296 |
2 | HG00735.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.354-536G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37298690 | |||||||
| chr22:37298931 | A | G | 5 | a0001c0001t0004g0275 a0001c0004t0013g0067 a0001c0004t0013g0150 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.354-295A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37298931 | |||||||
| chr22:37298949 | C | T | 1 | a0001c0002t0002g0088 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.354-277C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37298949 | |||||||
| chr22:37299017 | G | A | 5 | a0001c0001t0010g0019 a0001c0001t0010g0062 a0001c0001t0010g0064 others(2): Show |
6 | HG02622.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.354-209G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37299017 | |||||||
| chr22:37299062 | G | C | 1 | a0001c0001t0005g0297 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.354-164G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37299062 | |||||||
| chr22:37299075 | G | A | 1 | a0001c0001t0004g0315 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.354-151G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37299075 | |||||||
| chr22:37299165 | G | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0094 others(14): Show |
22 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.354-61G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37299165 | |||||||
| chr22:37299215 | T | C | 213 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(210): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.354-11T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 5/12 | chr22 | 37299215 | |||||||
| chr22:37299367 | G | A | 1 | a0001c0001t0003g0008 | 4 | NA18959.hp1 NA18998.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+61G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/12 | chr22 | 37299367 | |||||||
| chr22:37299371 | C | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0094 others(14): Show |
22 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.434+65C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/12 | chr22 | 37299371 | |||||||
| chr22:37299571 | ATTAC | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0080 a0001c0001t0001g0106 others(1): Show |
4 | HG01891.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.434+268_434+271del others(4): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 37299571 | ||||||
| chr22:37299750 | T | C | 1 | a0001c0001t0006g0144 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.434+444T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/12 | chr22 | 37299750 | |||||||
| chr22:37299764 | A | G | 3 | a0001c0001t0009g0262 a0001c0001t0009g0306 a0001c0001t0016g0058 |
3 | HG02723.hp2 HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.434+458A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/12 | chr22 | 37299764 | |||||||
| chr22:37299818 | A | G | 7 | a0001c0002t0004g0305 a0001c0002t0007g0059 a0001c0002t0007g0101 others(4): Show |
7 | HG01884.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.434+512A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/12 | chr22 | 37299818 | |||||||
| chr22:37300059 | C | CA | 4 | a0001c0001t0001g0052 a0001c0001t0001g0080 a0001c0001t0001g0106 others(1): Show |
4 | HG01891.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.434+755dupA | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 37300059 | ||||||
| chr22:37300207 | T | C | 2 | a0001c0001t0001g0116 a0001c0001t0003g0205 |
2 | NA18612.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.435-700T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/12 | chr22 | 37300207 | |||||||
| chr22:37300364 | G | A | 1 | a0001c0001t0003g0180 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.435-543G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/12 | chr22 | 37300364 | |||||||
| chr22:37300514 | A | G | 197 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(194): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.435-393A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/12 | chr22 | 37300514 | |||||||
| chr22:37300529 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0003g0233 a0001c0001t0004g0260 others(1): Show |
8 | HG00099.hp1 HG00735.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.435-378C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/12 | chr22 | 37300529 | |||||||
| chr22:37300625 | C | T | 5 | a0001c0001t0007g0065 a0001c0001t0007g0093 a0001c0001t0009g0262 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-282C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/12 | chr22 | 37300625 | |||||||
| chr22:37300816 | C | T | 1 | a0001c0002t0008g0057 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.435-91C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/12 | chr22 | 37300816 | |||||||
| chr22:37300865 | G | A | 5 | a0001c0001t0007g0065 a0001c0001t0007g0093 a0001c0001t0009g0262 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-42G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/12 | chr22 | 37300865 | |||||||
| chr22:37300886 | G | A | 1 | a0001c0001t0003g0176 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.435-21G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/12 | chr22 | 37300886 | |||||||
| chr22:37300893 | C | T | 13 | a0001c0001t0009g0036 a0001c0002t0004g0305 a0001c0002t0007g0059 others(10): Show |
14 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.435-14C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 6/12 | chr22 | 37300893 | |||||||
| chr22:37301069 | C | T | 1 | a0001c0001t0009g0036 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.547+50C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37301069 | |||||||
| chr22:37301233 | C | T | 8 | a0001c0001t0001g0127 a0001c0001t0001g0133 a0001c0001t0003g0183 others(5): Show |
8 | HG00323.hp1 HG02040.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.547+214C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37301233 | |||||||
| chr22:37301234 | G | A | 9 | a0001c0001t0001g0079 a0001c0001t0004g0290 a0001c0001t0004g0312 others(6): Show |
9 | HG02055.hp2 HG02647.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.547+215G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37301234 | |||||||
| chr22:37301270 | C | T | 39 | a0001c0001t0001g0023 a0001c0001t0001g0045 a0001c0001t0001g0127 others(36): Show |
43 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.547+251C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37301270 | |||||||
| chr22:37301586 | T | C | 1 | a0001c0001t0003g0171 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.547+567T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37301586 | |||||||
| chr22:37301606 | T | C | 1 | a0001c0001t0030g0318 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.547+587T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37301606 | |||||||
| chr22:37301682 | C | CT | 7 | a0001c0001t0003g0214 a0001c0001t0004g0312 a0001c0001t0010g0064 others(4): Show |
7 | HG01361.hp2 HG01981.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.547+690dupT | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37301682 | ||||||
| chr22:37301682 | CT | C | 171 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(168): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.547+690delT | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37301682 | ||||||
| chr22:37301682 | CTT | C | 38 | a0001c0001t0001g0023 a0001c0001t0001g0110 a0001c0001t0001g0111 others(35): Show |
44 | HG00408.hp1 HG00408.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.547+689_547+690del others(2): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37301682 | ||||||
| chr22:37301682 | CTTT | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0094 others(20): Show |
28 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.547+688_547+690del others(3): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37301682 | ||||||
| chr22:37301682 | CTTTT | C | 14 | a0001c0001t0011g0034 a0001c0001t0011g0244 a0001c0002t0004g0305 others(11): Show |
15 | HG01069.hp1 HG01109.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.547+687_547+690del others(4): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37301682 | ||||||
| chr22:37301682 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0005g0297 a0001c0001t0008g0157 a0005c0008t0031g0296 |
3 | HG02683.hp1 HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.547+680_547+690del others(11): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37301682 | ||||||
| chr22:37301682 | CTTTTTTT others(6): Show |
C | 1 | a0001c0002t0006g0073 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.547+678_547+690del others(13): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37301682 | ||||||
| chr22:37301722 | A | G | 247 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.547+703A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37301722 | |||||||
| chr22:37302219 | T | C | 8 | a0001c0001t0001g0052 a0001c0001t0001g0106 a0001c0001t0004g0242 others(5): Show |
8 | HG01891.hp2 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.548-1035T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37302219 | |||||||
| chr22:37302468 | T | A | 1 | a0001c0001t0003g0179 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.548-786T>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37302468 | |||||||
| chr22:37302626 | A | G | 13 | a0001c0001t0005g0297 a0001c0001t0008g0157 a0001c0001t0010g0019 others(10): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.548-628A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37302626 | |||||||
| chr22:37302755 | C | T | 1 | a0001c0002t0005g0287 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.548-499C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37302755 | |||||||
| chr22:37302792 | G | A | 9 | a0001c0001t0001g0079 a0001c0001t0004g0290 a0001c0001t0004g0312 others(6): Show |
9 | HG02055.hp2 HG02647.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.548-462G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37302792 | |||||||
| chr22:37302927 | C | G | 2 | a0001c0001t0001g0054 a0001c0012t0023g0084 |
2 | HG01516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.548-327C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37302927 | |||||||
| chr22:37302957 | GAGA | G | 173 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(170): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.548-294_548-292del others(3): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37302957 | ||||||
| chr22:37302966 | G | A | 3 | a0001c0002t0002g0043 a0001c0002t0006g0129 a0001c0002t0006g0164 |
3 | HG00140.hp1 HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.548-288G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37302966 | |||||||
| chr22:37303027 | G | A | 18 | a0001c0001t0001g0054 a0001c0001t0001g0079 a0001c0001t0004g0290 others(15): Show |
18 | HG01516.hp1 HG02055.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.548-227G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37303027 | |||||||
| chr22:37303085 | G | A | 1 | a0001c0001t0003g0183 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.548-169G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37303085 | |||||||
| chr22:37303118 | GGCCTCAA others(7): Show |
G | 12 | a0001c0002t0004g0305 a0001c0002t0007g0059 a0001c0002t0007g0101 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.548-132_548-119del others(14): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37303118 | ||||||
| chr22:37303127 | G | A | 221 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(218): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.548-127G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37303127 | |||||||
| chr22:37303156 | C | CG | 222 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(219): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.548-94dupG | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37303156 | ||||||
| chr22:37303221 | G | C | 4 | a0001c0001t0011g0034 a0001c0001t0011g0244 a0001c0005t0006g0158 others(1): Show |
5 | HG01109.hp2 HG02965.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.548-33G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37303221 | |||||||
| chr22:37303238 | G | A | 1 | a0001c0001t0003g0179 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.548-16G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 7/12 | chr22 | 37303238 | |||||||
| chr22:37303435 | C | T | 3 | a0001c0001t0005g0319 a0001c0002t0007g0059 a0003c0011t0009g0281 |
3 | HG00099.hp2 HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.696+33C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37303435 | |||||||
| chr22:37303743 | T | C | 1 | a0003c0011t0009g0281 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.696+341T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37303743 | |||||||
| chr22:37303765 | A | G | 237 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(234): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.696+363A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37303765 | |||||||
| chr22:37303875 | G | A | 1 | a0001c0002t0008g0159 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.696+473G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37303875 | |||||||
| chr22:37303879 | G | A | 1 | a0001c0004t0019g0083 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.696+477G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37303879 | |||||||
| chr22:37303901 | C | G | 6 | a0001c0001t0007g0065 a0001c0001t0007g0093 a0001c0001t0009g0262 others(3): Show |
6 | HG02572.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.696+499C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37303901 | |||||||
| chr22:37304136 | T | C | 237 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(234): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.696+734T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37304136 | |||||||
| chr22:37304203 | G | A | 1 | a0002c0003t0007g0048 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.696+801G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37304203 | |||||||
| chr22:37304396 | G | C | 9 | a0001c0001t0001g0079 a0001c0001t0004g0290 a0001c0001t0004g0312 others(6): Show |
9 | HG02055.hp2 HG02647.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.696+994G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37304396 | |||||||
| chr22:37304559 | G | A | 6 | a0002c0003t0007g0044 a0002c0003t0007g0048 a0002c0003t0007g0050 others(3): Show |
6 | HG02280.hp1 HG02809.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.696+1157G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37304559 | |||||||
| chr22:37304806 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.696+1404T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37304806 | |||||||
| chr22:37304910 | G | A | 1 | a0001c0002t0006g0073 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.696+1508G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37304910 | |||||||
| chr22:37304992 | G | GAAAAAAG others(4): Show |
1 | a0001c0001t0004g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.696+1592_696+1602d others(13): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37304992 | ||||||
| chr22:37305076 | C | G | 1 | a0001c0001t0005g0297 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.696+1674C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37305076 | |||||||
| chr22:37305166 | T | C | 6 | a0001c0001t0001g0052 a0001c0001t0001g0106 a0001c0001t0004g0242 others(3): Show |
6 | HG01891.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.696+1764T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37305166 | |||||||
| chr22:37305228 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.696+1826G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37305228 | |||||||
| chr22:37305332 | G | A | 9 | a0001c0001t0005g0297 a0001c0001t0008g0157 a0001c0002t0002g0192 others(6): Show |
9 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.696+1930G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37305332 | |||||||
| chr22:37305394 | G | A | 2 | a0001c0004t0013g0150 a0001c0004t0013g0151 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.696+1992G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37305394 | |||||||
| chr22:37305481 | C | T | 1 | a0001c0001t0004g0040 | 2 | HG01256.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.696+2079C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37305481 | |||||||
| chr22:37305541 | G | C | 1 | a0001c0001t0008g0105 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.696+2139G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37305541 | |||||||
| chr22:37305607 | C | T | 3 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0004g0267 |
3 | HG00408.hp1 HG00408.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.696+2205C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37305607 | |||||||
| chr22:37305696 | T | G | 1 | a0001c0001t0008g0157 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.696+2294T>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37305696 | |||||||
| chr22:37305935 | TGGGGCA | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0079 others(26): Show |
35 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.696+2541_696+2546d others(8): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37305935 | ||||||
| chr22:37306006 | G | A | 1 | a0005c0008t0031g0296 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.696+2604G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37306006 | |||||||
| chr22:37306047 | C | T | 7 | a0001c0001t0009g0036 a0002c0003t0007g0044 a0002c0003t0007g0048 others(4): Show |
8 | HG02258.hp2 HG02280.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.696+2645C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37306047 | |||||||
| chr22:37306124 | G | A | 3 | a0001c0001t0005g0297 a0001c0001t0008g0157 a0005c0008t0031g0296 |
3 | HG02683.hp1 HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.696+2722G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37306124 | |||||||
| chr22:37306243 | TC | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0106 a0001c0001t0004g0242 |
3 | HG01891.hp2 HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.696+2843delC | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37306243 | ||||||
| chr22:37306662 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.697-2550G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37306662 | |||||||
| chr22:37306706 | G | A | 5 | a0001c0004t0013g0067 a0001c0004t0013g0150 a0001c0004t0013g0151 others(2): Show |
5 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.697-2506G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37306706 | |||||||
| chr22:37306861 | T | C | 3 | a0001c0001t0005g0266 a0001c0001t0006g0119 a0001c0001t0006g0144 |
3 | HG00280.hp2 HG01934.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.697-2351T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37306861 | |||||||
| chr22:37307233 | C | T | 1 | a0001c0001t0009g0036 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.697-1979C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37307233 | |||||||
| chr22:37307234 | G | A | 3 | a0001c0001t0001g0212 a0001c0001t0004g0268 a0001c0001t0004g0269 |
3 | HG02080.hp2 NA18982.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.697-1978G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37307234 | |||||||
| chr22:37307276 | C | T | 1 | a0001c0001t0003g0230 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.697-1936C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37307276 | |||||||
| chr22:37307393 | G | T | 1 | a0001c0002t0005g0037 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.697-1819G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37307393 | |||||||
| chr22:37307430 | C | T | 2 | a0001c0001t0004g0040 a0001c0001t0004g0327 |
3 | HG01256.hp2 HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.697-1782C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37307430 | |||||||
| chr22:37307488 | C | T | 171 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(168): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.697-1724C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37307488 | |||||||
| chr22:37307498 | C | T | 1 | a0001c0002t0007g0059 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.697-1714C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37307498 | |||||||
| chr22:37307522 | G | A | 3 | a0001c0001t0007g0065 a0001c0001t0007g0093 a0002c0003t0007g0071 |
3 | HG02572.hp2 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.697-1690G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37307522 | |||||||
| chr22:37307592 | T | C | 2 | a0001c0001t0003g0189 a0001c0001t0004g0264 |
2 | HG03491.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.697-1620T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37307592 | |||||||
| chr22:37307598 | A | G | 5 | a0001c0001t0010g0019 a0001c0001t0010g0062 a0001c0001t0010g0064 others(2): Show |
6 | HG02622.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.697-1614A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37307598 | |||||||
| chr22:37307832 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0106 |
2 | HG01891.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.697-1380T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37307832 | |||||||
| chr22:37307840 | A | G | 1 | a0001c0001t0010g0064 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.697-1372A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37307840 | |||||||
| chr22:37307916 | C | T | 1 | a0001c0002t0005g0293 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.697-1296C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37307916 | |||||||
| chr22:37308012 | G | A | 1 | a0001c0002t0005g0037 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.697-1200G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308012 | |||||||
| chr22:37308031 | T | C | 1 | a0001c0001t0003g0195 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.697-1181T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308031 | |||||||
| chr22:37308041 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0106 |
2 | HG01891.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.697-1171C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308041 | |||||||
| chr22:37308048 | GACCCC | G | 14 | a0001c0001t0008g0157 a0001c0001t0010g0019 a0001c0001t0010g0062 others(11): Show |
15 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.697-1158_697-1154d others(7): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37308048 | ||||||
| chr22:37308189 | G | T | 238 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(235): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.697-1023G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308189 | |||||||
| chr22:37308249 | C | T | 3 | a0001c0002t0014g0051 a0001c0002t0014g0061 a0001c0002t0014g0114 |
3 | HG02055.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.697-963C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308249 | |||||||
| chr22:37308255 | T | G | 32 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0094 others(29): Show |
38 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.697-957T>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308255 | |||||||
| chr22:37308461 | TAA | T | 20 | a0001c0001t0001g0079 a0001c0001t0007g0078 a0001c0001t0007g0081 others(17): Show |
21 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.697-750_697-749del others(2): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308461 | |||||||
| chr22:37308463 | AGT | A | 32 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0054 others(29): Show |
36 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.697-740_697-739del others(2): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37308463 | ||||||
| chr22:37308540 | G | A | 3 | a0001c0001t0009g0262 a0001c0001t0009g0306 a0001c0001t0016g0058 |
3 | HG02723.hp2 HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.697-672G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308540 | |||||||
| chr22:37308542 | A | G | 1 | a0001c0002t0006g0138 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.697-670A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308542 | |||||||
| chr22:37308542 | ATGTG | A | 4 | a0001c0001t0007g0065 a0001c0001t0007g0093 a0001c0002t0007g0059 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.697-666_697-663del others(4): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37308542 | ||||||
| chr22:37308557 | C | T | 1 | a0001c0001t0008g0108 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.697-655C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308557 | |||||||
| chr22:37308572 | A | C | 1 | a0001c0002t0006g0136 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.697-640A>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308572 | |||||||
| chr22:37308582 | G | A | 2 | a0001c0001t0011g0034 a0001c0001t0011g0244 |
3 | HG01109.hp2 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.697-630G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308582 | |||||||
| chr22:37308586 | A | G | 15 | a0001c0001t0008g0157 a0001c0001t0010g0019 a0001c0001t0010g0062 others(12): Show |
16 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.697-626A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308586 | |||||||
| chr22:37308588 | ATG | A | 5 | a0001c0002t0007g0101 a0001c0002t0007g0140 a0001c0002t0007g0154 others(2): Show |
5 | HG02559.hp1 HG02630.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.697-620_697-619del others(2): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37308588 | ||||||
| chr22:37308623 | T | C | 1 | a0001c0002t0005g0293 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.697-589T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308623 | |||||||
| chr22:37308626 | ATGTC | A | 3 | a0001c0002t0014g0051 a0001c0002t0014g0061 a0001c0002t0014g0114 |
3 | HG02055.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.697-582_697-579del others(4): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37308626 | ||||||
| chr22:37308630 | C | A | 156 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0079 others(153): Show |
191 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.697-582C>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308630 | |||||||
| chr22:37308667 | A | C | 3 | a0001c0002t0005g0294 a0001c0002t0005g0295 a0001c0002t0006g0288 |
3 | NA18940.hp1 NA18969.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.697-545A>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308667 | |||||||
| chr22:37308721 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0094 a0001c0001t0001g0153 others(2): Show |
9 | HG01884.hp2 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.697-491C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308721 | |||||||
| chr22:37308735 | T | C | 17 | a0001c0001t0008g0157 a0001c0001t0010g0019 a0001c0001t0010g0062 others(14): Show |
18 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.697-477T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308735 | |||||||
| chr22:37308747 | T | C | 3 | a0001c0001t0009g0262 a0001c0001t0009g0306 a0001c0001t0016g0058 |
3 | HG02723.hp2 HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.697-465T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308747 | |||||||
| chr22:37308768 | G | A | 3 | a0001c0001t0009g0262 a0001c0001t0009g0306 a0001c0001t0016g0058 |
3 | HG02723.hp2 HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.697-444G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308768 | |||||||
| chr22:37308785 | T | A | 4 | a0001c0001t0007g0065 a0001c0001t0007g0093 a0001c0002t0007g0059 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.697-427T>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308785 | |||||||
| chr22:37308814 | A | G | 1 | a0001c0001t0009g0036 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.697-398A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308814 | |||||||
| chr22:37308835 | TAA | T | 3 | a0001c0001t0009g0036 a0001c0005t0006g0158 a0001c0005t0035g0115 |
4 | HG02258.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.697-376_697-375del others(2): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308835 | |||||||
| chr22:37308871 | TGC | T | 186 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
221 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.697-339_697-338del others(2): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37308871 | ||||||
| chr22:37308873 | C | T | 12 | a0001c0001t0011g0034 a0001c0002t0007g0101 a0001c0002t0007g0140 others(9): Show |
13 | HG02280.hp1 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.697-339C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308873 | |||||||
| chr22:37308888 | G | A | 4 | a0001c0001t0007g0065 a0001c0001t0007g0093 a0001c0002t0007g0059 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.697-324G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37308888 | |||||||
| chr22:37308990 | C | CG | 4 | a0001c0001t0001g0120 a0001c0001t0003g0182 a0001c0001t0004g0276 others(1): Show |
4 | HG00438.hp2 HG01099.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.697-218dupG | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37308990 | ||||||
| chr22:37309005 | G | C | 1 | a0001c0001t0004g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.697-207G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37309005 | |||||||
| chr22:37309006 | C | A | 1 | a0001c0001t0004g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.697-206C>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37309006 | |||||||
| chr22:37309007 | A | G | 1 | a0001c0001t0004g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.697-205A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37309007 | |||||||
| chr22:37309031 | T | G | 3 | a0001c0001t0002g0206 a0001c0001t0003g0089 a0001c0001t0004g0270 |
3 | HG01069.hp2 HG03710.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.697-181T>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37309031 | |||||||
| chr22:37309104 | T | A | 1 | a0001c0001t0003g0186 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.697-108T>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 8/12 | chr22 | 37309104 | |||||||
| chr22:37309446 | G | T | 1 | a0001c0001t0001g0128 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.808+123G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 9/12 | chr22 | 37309446 | |||||||
| chr22:37309567 | G | A | 1 | a0001c0012t0023g0084 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.808+244G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 9/12 | chr22 | 37309567 | |||||||
| chr22:37309898 | G | GAC | 5 | a0001c0002t0007g0101 a0001c0002t0007g0140 a0001c0002t0007g0154 others(2): Show |
5 | HG02559.hp1 HG02630.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.808+576_808+577ins others(2): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr22 | 37309898 | ||||||
| chr22:37309981 | G | A | 5 | a0001c0002t0007g0101 a0001c0002t0007g0140 a0001c0002t0007g0154 others(2): Show |
5 | HG02559.hp1 HG02630.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.808+658G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 9/12 | chr22 | 37309981 | |||||||
| chr22:37310183 | C | T | 6 | a0001c0001t0001g0079 a0001c0001t0007g0078 a0001c0001t0007g0081 others(3): Show |
6 | HG02647.hp2 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-805C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 9/12 | chr22 | 37310183 | |||||||
| chr22:37310263 | T | C | 1 | a0001c0001t0008g0108 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.809-725T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 9/12 | chr22 | 37310263 | |||||||
| chr22:37310431 | T | C | 1 | a0001c0002t0006g0138 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.809-557T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 9/12 | chr22 | 37310431 | |||||||
| chr22:37310571 | C | T | 1 | a0001c0002t0005g0303 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.809-417C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 9/12 | chr22 | 37310571 | |||||||
| chr22:37310584 | A | G | 1 | a0001c0002t0008g0097 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.809-404A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 9/12 | chr22 | 37310584 | |||||||
| chr22:37310769 | C | T | 1 | a0001c0001t0002g0200 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.809-219C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 9/12 | chr22 | 37310769 | |||||||
| chr22:37310908 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0094 others(5): Show |
13 | HG00639.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.809-80C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 9/12 | chr22 | 37310908 | |||||||
| chr22:37311081 | T | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.885+17T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 10/12 | chr22 | 37311081 | |||||||
| chr22:37311099 | C | T | 6 | a0001c0004t0013g0067 a0001c0004t0013g0150 a0001c0004t0013g0151 others(3): Show |
6 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.885+35C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 10/12 | chr22 | 37311099 | |||||||
| chr22:37311104 | C | T | 1 | a0001c0001t0040g0147 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.885+40C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 10/12 | chr22 | 37311104 | |||||||
| chr22:37311172 | T | C | 1 | a0001c0012t0023g0084 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.885+108T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 10/12 | chr22 | 37311172 | |||||||
| chr22:37311328 | A | G | 5 | a0001c0002t0007g0101 a0001c0002t0007g0140 a0001c0002t0007g0154 others(2): Show |
5 | HG02559.hp1 HG02630.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.886-128A>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 10/12 | chr22 | 37311328 | |||||||
| chr22:37311329 | T | C | 1 | a0001c0012t0023g0084 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.886-127T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 10/12 | chr22 | 37311329 | |||||||
| chr22:37311417 | C | T | 1 | a0001c0001t0009g0036 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.886-39C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 10/12 | chr22 | 37311417 | |||||||
| chr22:37311589 | G | A | 1 | a0001c0001t0004g0076 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.957+62G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 11/12 | chr22 | 37311589 | |||||||
| chr22:37311724 | G | A | 3 | a0001c0002t0005g0029 a0001c0002t0006g0134 a0001c0002t0018g0029 |
3 | NA18956.hp1 NA18974.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.957+197G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 11/12 | chr22 | 37311724 | |||||||
| chr22:37311753 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0079 others(8): Show |
17 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.957+226C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 11/12 | chr22 | 37311753 | |||||||
| chr22:37311754 | G | A | 1 | a0001c0012t0023g0084 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.957+227G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 11/12 | chr22 | 37311754 | |||||||
| chr22:37311772 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0004g0248 |
2 | NA18977.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.957+245G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 11/12 | chr22 | 37311772 | |||||||
| chr22:37311859 | CAG | C | 154 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(151): Show |
175 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.958-154_958-153del others(2): Show |
CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37311859 | ||||||
| chr22:37311870 | C | T | 1 | a0001c0001t0003g0171 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.958-150C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 11/12 | chr22 | 37311870 | |||||||
| chr22:37311921 | C | T | 145 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(142): Show |
166 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.958-99C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 11/12 | chr22 | 37311921 | |||||||
| chr22:37311941 | G | A | 6 | a0001c0004t0013g0067 a0001c0004t0013g0150 a0001c0004t0013g0151 others(3): Show |
6 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.958-79G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 11/12 | chr22 | 37311941 | |||||||
| chr22:37311963 | T | C | 154 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(151): Show |
175 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.958-57T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 11/12 | chr22 | 37311963 | |||||||
| chr22:37312402 | G | A | 1 | a0001c0001t0003g0008 | 4 | NA18959.hp1 NA18998.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.1112+228G>A | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 12/12 | chr22 | 37312402 | |||||||
| chr22:37312420 | T | C | 4 | a0001c0001t0007g0078 a0001c0001t0007g0081 a0001c0001t0009g0243 others(1): Show |
4 | HG02647.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1112+246T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 12/12 | chr22 | 37312420 | |||||||
| chr22:37312420 | T | G | 6 | a0001c0004t0013g0067 a0001c0004t0013g0150 a0001c0004t0013g0151 others(3): Show |
6 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1112+246T>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 12/12 | chr22 | 37312420 | |||||||
| chr22:37312606 | C | T | 6 | a0001c0004t0013g0067 a0001c0004t0013g0150 a0001c0004t0013g0151 others(3): Show |
6 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1112+432C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 12/12 | chr22 | 37312606 | |||||||
| chr22:37312626 | G | T | 1 | a0001c0001t0003g0095 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1112+452G>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 12/12 | chr22 | 37312626 | |||||||
| chr22:37312931 | C | T | 1 | a0001c0005t0035g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1113-508C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 12/12 | chr22 | 37312931 | |||||||
| chr22:37313016 | T | C | 8 | a0001c0001t0007g0078 a0001c0001t0007g0081 a0001c0001t0007g0113 others(5): Show |
9 | HG01109.hp2 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1113-423T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 12/12 | chr22 | 37313016 | |||||||
| chr22:37313138 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1113-301C>T | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 12/12 | chr22 | 37313138 | |||||||
| chr22:37313232 | T | G | 3 | a0001c0001t0011g0034 a0001c0001t0011g0244 a0001c0001t0034g0068 |
4 | HG01109.hp2 HG02622.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113-207T>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 12/12 | chr22 | 37313232 | |||||||
| chr22:37313256 | G | C | 4 | a0001c0001t0010g0019 a0001c0001t0010g0062 a0001c0001t0010g0064 others(1): Show |
5 | HG02647.hp1 HG02895.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113-183G>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 12/12 | chr22 | 37313256 | |||||||
| chr22:37313298 | T | C | 13 | a0001c0002t0007g0101 a0001c0002t0007g0140 a0001c0002t0007g0154 others(10): Show |
13 | HG01243.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1113-141T>C | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 12/12 | chr22 | 37313298 | |||||||
| chr22:37313392 | C | G | 1 | a0001c0001t0022g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1113-47C>G | CYTH4 | ENSG00000100055.21 | transcript | ENST00000248901.11 | protein_coding | 12/12 | chr22 | 37313392 |