Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9266 |
| ensemblid | ENSG00000105443.17 |
| hgncid | 9502 |
| symbol | CYTH2 |
| name | cytohesin 2 |
| refseq_nuc | NM_004228.7 |
| refseq_prot | NP_004219.3 |
| ensembl_nuc | ENST00000452733.7 |
| ensembl_prot | ENSP00000408236.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 48469369 |
| end | 48482314 |
| strand | + |
| ver | v1.2 |
| region | chr19:48469369-48482314 |
| region5000 | chr19:48464369-48487314 |
| regionname0 | CYTH2_chr19_48469369_48482314 |
| regionname5000 | CYTH2_chr19_48464369_48487314 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 399 | 365 | 90 | 72 | 157 | 8 | 36 | 112 | CYTH2_chr19_48464369_48487314 | CYTH2 | MEDGV others(394): Show |
chr19 | 48464369 | 48487314 |
| a0002 | 0/0 | 399 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | MEDGV others(394): Show |
chr19 | 48464369 | 48487314 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1197 | 338 | 77 | 69 | 148 | 8 | 34 | CYTH2_chr19_48464369_48487314 | CYTH2 | ATGGA others(1192): Show |
chr19 | 48464369 | 48487314 | ||
| a0001c0002 | 0/0 | 1197 | 23 | 12 | 3 | 7 | 0 | 1 | CYTH2_chr19_48464369_48487314 | CYTH2 | ATGGA others(1192): Show |
chr19 | 48464369 | 48487314 | ||
| a0001c0003 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | ATGGA others(1192): Show |
chr19 | 48464369 | 48487314 | ||
| a0001c0004 | 0/0 | 1197 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH2_chr19_48464369_48487314 | CYTH2 | ATGGA others(1192): Show |
chr19 | 48464369 | 48487314 | ||
| a0001c0005 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | ATGGA others(1192): Show |
chr19 | 48464369 | 48487314 | ||
| a0001c0006 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | ATGGA others(1192): Show |
chr19 | 48464369 | 48487314 | ||
| a0002c0007 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | ATGGA others(1192): Show |
chr19 | 48464369 | 48487314 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4445 | 134 | 38 | 26 | 54 | 2 | 14 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0002 | 1/0 | 4443 | 86 | 3 | 9 | 63 | 2 | 8 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4438): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0003 | 0/0 | 4445 | 42 | 3 | 18 | 9 | 3 | 9 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0006 | 0/0 | 4327 | 6 | 1 | 4 | 0 | 0 | 1 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4322): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0007 | 0/0 | 4443 | 5 | 5 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4438): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0008 | 0/0 | 4444 | 5 | 5 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4439): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0009 | 0/0 | 4445 | 5 | 0 | 5 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0010 | 0/0 | 4443 | 4 | 4 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4438): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0011 | 0/0 | 4443 | 4 | 4 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4438): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0012 | 0/0 | 4445 | 4 | 1 | 1 | 1 | 0 | 1 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0013 | 0/0 | 4443 | 3 | 0 | 0 | 3 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4438): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0014 | 0/0 | 4445 | 4 | 4 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0015 | 0/0 | 4443 | 3 | 2 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4438): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0016 | 0/0 | 4444 | 3 | 0 | 1 | 2 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4439): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0017 | 0/0 | 4443 | 3 | 0 | 0 | 3 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4438): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0018 | 0/0 | 4443 | 3 | 0 | 0 | 3 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4438): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0019 | 0/0 | 4445 | 2 | 0 | 2 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0020 | 0/0 | 4443 | 2 | 0 | 0 | 2 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4438): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0021 | 0/0 | 4444 | 2 | 0 | 0 | 2 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4439): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0022 | 0/0 | 4445 | 2 | 0 | 0 | 2 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0023 | 0/0 | 4444 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4439): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0026 | 0/0 | 4445 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0027 | 0/0 | 4443 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4438): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0028 | 0/0 | 4444 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4439): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0030 | 0/0 | 4445 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0031 | 0/0 | 4445 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0032 | 0/0 | 4445 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0033 | 0/0 | 4444 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4439): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0034 | 0/0 | 4409 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4404): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0035 | 0/0 | 4445 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0037 | 0/1 | 4444 | 1 | 0 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4439): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0038 | 0/0 | 4445 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0039 | 0/0 | 4443 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4438): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0040 | 0/0 | 4445 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0001c0001t0041 | 0/0 | 4445 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0001c0002t0004 | 0/0 | 4444 | 14 | 7 | 0 | 6 | 0 | 1 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4439): Show |
chr19 | 48464369 | 48487314 |
| a0001c0002t0005 | 0/0 | 4444 | 7 | 4 | 3 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4439): Show |
chr19 | 48464369 | 48487314 |
| a0001c0002t0024 | 0/0 | 4443 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4438): Show |
chr19 | 48464369 | 48487314 |
| a0001c0002t0029 | 0/0 | 4444 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4439): Show |
chr19 | 48464369 | 48487314 |
| a0001c0003t0036 | 0/0 | 4444 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4439): Show |
chr19 | 48464369 | 48487314 |
| a0001c0004t0001 | 0/0 | 4445 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0001c0005t0025 | 0/0 | 4444 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4439): Show |
chr19 | 48464369 | 48487314 |
| a0001c0006t0001 | 0/0 | 4445 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4440): Show |
chr19 | 48464369 | 48487314 |
| a0002c0007t0013 | 0/0 | 4443 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | AGCGC others(4438): Show |
chr19 | 48464369 | 48487314 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 93 | 17 | 17 | 46 | 2 | 11 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0005 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0002 | 1/0 | 53 | 0 | 7 | 38 | 2 | 5 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0003 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0003g0001 | 0/0 | 35 | 2 | 16 | 9 | 2 | 6 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0006g0006 | 0/0 | 6 | 1 | 4 | 0 | 0 | 1 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0007g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0008g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0009g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0009g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0010g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0010g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0010g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0011g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0011g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0011g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0012g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0012g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0012g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0013g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0014g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0014g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0015g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0015g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0015g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0016g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0016g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0017g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0017g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0018g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0019g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0019g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0020g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0021g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0021g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0022g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0022g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0023g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0026g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0027g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0028g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0030g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0031g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0032g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0033g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0034g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0035g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0037g0001 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0038g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0039g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0040g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0001t0041g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0002t0004g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0002t0004g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0002t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0002t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0002t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0002t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0002t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0002t0005g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0002t0005g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0002t0005g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0002t0024g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0002t0029g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0003t0036g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0005t0025g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0001c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| a0002c0007t0013g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0065 | EUR | GBR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00408 | hp1 | a0001 | c0002 | t0029 | g0092 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00438 | hp1 | a0001 | c0002 | t0004 | g0015 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00544 | hp1 | a0001 | c0002 | t0004 | g0094 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00544 | hp2 | a0001 | c0001 | t0020 | g0002 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00597 | hp2 | a0001 | c0001 | t0021 | g0076 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0006 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00642 | hp2 | a0001 | c0001 | t0009 | g0004 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00673 | hp2 | a0001 | c0001 | t0018 | g0011 | EAS | CHS | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00738 | hp2 | a0001 | c0001 | t0019 | g0069 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0006 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0004 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01167 | hp2 | a0001 | c0002 | t0005 | g0017 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0006 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01169 | hp1 | a0001 | c0002 | t0005 | g0017 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01169 | hp2 | a0001 | c0001 | t0006 | g0006 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01243 | hp1 | a0001 | c0002 | t0005 | g0016 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01255 | hp1 | a0001 | c0001 | t0019 | g0001 | AMR | CLM | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01257 | hp2 | a0001 | c0001 | t0012 | g0001 | AMR | CLM | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01261 | hp1 | a0001 | c0001 | t0009 | g0004 | AMR | CLM | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01346 | hp1 | a0001 | c0001 | t0016 | g0013 | AMR | CLM | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01361 | hp2 | a0001 | c0001 | t0038 | g0001 | AMR | CLM | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01433 | hp2 | a0001 | c0001 | t0015 | g0032 | AMR | CLM | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0039 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01884 | hp2 | a0001 | c0002 | t0004 | g0008 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01891 | hp1 | a0001 | c0005 | t0025 | g0042 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01891 | hp2 | a0001 | c0001 | t0026 | g0014 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01928 | hp2 | a0001 | c0001 | t0035 | g0004 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01952 | hp1 | a0001 | c0001 | t0009 | g0004 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01952 | hp2 | a0001 | c0001 | t0009 | g0057 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02015 | hp2 | a0001 | c0006 | t0001 | g0001 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02027 | hp2 | a0001 | c0002 | t0004 | g0088 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02056 | hp1 | a0001 | c0001 | t0013 | g0002 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02071 | hp1 | a0002 | c0007 | t0013 | g0002 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02074 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02080 | hp2 | a0001 | c0001 | t0039 | g0009 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02129 | hp2 | a0001 | c0001 | t0012 | g0046 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02145 | hp2 | a0001 | c0001 | t0011 | g0084 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02155 | hp2 | a0001 | c0002 | t0004 | g0015 | EAS | CDX | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02258 | hp1 | a0001 | c0001 | t0010 | g0036 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02451 | hp1 | a0001 | c0001 | t0014 | g0001 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02572 | hp2 | a0001 | c0002 | t0024 | g0093 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02615 | hp1 | a0001 | c0001 | t0011 | g0012 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02630 | hp2 | a0001 | c0002 | t0005 | g0010 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02683 | hp1 | a0001 | c0001 | t0012 | g0001 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02723 | hp1 | a0001 | c0001 | t0023 | g0022 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02735 | hp1 | a0001 | c0001 | t0041 | g0001 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0043 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0041 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02818 | hp2 | a0001 | c0001 | t0027 | g0035 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0012 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0008 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0018 | AFR | ESN | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02970 | hp1 | a0001 | c0001 | t0014 | g0083 | AFR | ESN | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02976 | hp1 | a0001 | c0001 | t0023 | g0022 | AFR | ESN | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0037 | AFR | ESN | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0089 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03041 | hp2 | a0001 | c0002 | t0005 | g0010 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03130 | hp1 | a0001 | c0001 | t0011 | g0081 | AFR | ESN | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0018 | AFR | ESN | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03195 | hp1 | a0001 | c0001 | t0028 | g0019 | AFR | ESN | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0008 | AFR | MSL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | MSL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0008 | AFR | MSL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03453 | hp2 | a0001 | c0002 | t0004 | g0090 | AFR | MSL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0040 | AFR | MSL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03516 | hp1 | a0001 | c0001 | t0014 | g0001 | AFR | ESN | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03516 | hp2 | a0001 | c0002 | t0004 | g0008 | AFR | ESN | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03579 | hp2 | a0001 | c0001 | t0015 | g0034 | AFR | MSL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03654 | hp2 | a0001 | c0002 | t0004 | g0095 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0059 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03834 | hp2 | a0001 | c0004 | t0001 | g0001 | SAS | BEB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | BEB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG04115 | hp2 | a0001 | c0001 | t0006 | g0006 | SAS | STU | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | STU | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | STU | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CHB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18942 | hp1 | a0001 | c0001 | t0017 | g0029 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18945 | hp1 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18952 | hp2 | a0001 | c0002 | t0004 | g0091 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18956 | hp2 | a0001 | c0003 | t0036 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18963 | hp2 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18964 | hp1 | a0001 | c0001 | t0017 | g0024 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18966 | hp1 | a0001 | c0001 | t0017 | g0029 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18977 | hp1 | a0001 | c0001 | t0030 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18978 | hp1 | a0001 | c0001 | t0033 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18978 | hp2 | a0001 | c0001 | t0020 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18985 | hp2 | a0001 | c0001 | t0034 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18990 | hp2 | a0001 | c0001 | t0018 | g0011 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19001 | hp1 | a0001 | c0001 | t0021 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19005 | hp2 | a0001 | c0001 | t0018 | g0011 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19010 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0038 | AFR | LWK | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19043 | hp1 | a0001 | c0002 | t0005 | g0016 | AFR | LWK | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19063 | hp1 | a0001 | c0002 | t0004 | g0015 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19066 | hp2 | a0001 | c0001 | t0022 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19086 | hp1 | a0001 | c0001 | t0022 | g0063 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA19240 | hp2 | a0001 | c0001 | t0012 | g0012 | AFR | YRI | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0030 | AFR | ASW | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | TSI | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA20805 | hp1 | a0001 | c0001 | t0032 | g0001 | EUR | TSI | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | TSI | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | GIH | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | GIH | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02109 | hp1 | a0001 | c0001 | t0031 | g0001 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03471 | hp1 | a0001 | c0001 | t0014 | g0001 | AFR | MSL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0033 | AFR | MSL | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG06807 | hp1 | a0001 | c0002 | t0005 | g0010 | AFR | USA | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | USA | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | USA | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | LWK | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| NA21309 | hp2 | a0001 | c0001 | t0040 | g0001 | AFR | LWK | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0037 | g0001 | REF | REF | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0002 | REF | REF | CYTH2_chr19_48464369_48487314 | CYTH2 | chr19 | 48464369 | 48487314 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48470493 | G | A | 1 | a0002 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.160G>A | p.Glu54Lys | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 2/12 | 299/4443 | 160/1200 | 54/399 | chr19 | 48470493 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48470468 | C | T | 1 | a0002c0007 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.135C>T | p.Ser45Ser | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 2/12 | 274/4443 | 135/1200 | 45/399 | chr19 | 48470468 | |||
| chr19:48472429 | C | T | 1 | a0001c0006 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.339C>T | p.Asp113Asp | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 4/12 | 478/4443 | 339/1200 | 113/399 | chr19 | 48472429 | |||
| chr19:48473932 | C | T | 2 | a0001c0004 a0001c0005 |
2 | HG01891.hp1 HG03834.hp2 |
synonymous_variant | LOW | c.462C>T | p.Pro154Pro | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 6/12 | 601/4443 | 462/1200 | 154/399 | chr19 | 48473932 | |||
| chr19:48474186 | G | A | 1 | a0001c0003 | 1 | NA18956.hp2 | synonymous_variant | LOW | c.552G>A | p.Thr184Thr | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 7/12 | 691/4443 | 552/1200 | 184/399 | chr19 | 48474186 | |||
| chr19:48474222 | C | T | 2 | a0001c0002 a0001c0005 |
24 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(21): Show |
synonymous_variant | LOW | c.588C>T | p.Asn196Asn | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 7/12 | 727/4443 | 588/1200 | 196/399 | chr19 | 48474222 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48469483 | T | C | 12 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0010 others(9): Show |
44 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
5_prime_UTR_variant | MODIFIER | c.-25T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 1/12 | 25 | chr19 | 48469483 | ||||||
| chr19:48479305 | T | G | 1 | a0001c0001t0019 | 2 | HG00738.hp2 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*95T>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 95 | chr19 | 48479305 | ||||||
| chr19:48479392 | G | C | 1 | a0001c0001t0030 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*182G>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 182 | chr19 | 48479392 | ||||||
| chr19:48479435 | C | T | 1 | a0001c0001t0041 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*225C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 225 | chr19 | 48479435 | ||||||
| chr19:48479493 | C | G | 1 | a0001c0001t0008 | 5 | HG02922.hp2 HG03139.hp2 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*283C>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 283 | chr19 | 48479493 | ||||||
| chr19:48479644 | C | A | 1 | a0001c0001t0007 | 5 | HG01884.hp1 HG02818.hp1 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*434C>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 434 | chr19 | 48479644 | ||||||
| chr19:48479739 | G | A | 1 | a0001c0001t0031 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*529G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 529 | chr19 | 48479739 | ||||||
| chr19:48479800 | GGAAGAAC others(106): Show |
G | 1 | a0001c0001t0006 | 6 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*591_*703del | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 591 | chr19 | 48479800 | ||||||
| chr19:48479811 | C | T | 2 | a0001c0001t0001 a0001c0001t0016 |
8 | HG00423.hp2 HG02071.hp2 NA18945.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*601C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 601 | chr19 | 48479811 | ||||||
| chr19:48479862 | C | T | 1 | a0001c0001t0023 | 2 | HG02723.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*652C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 652 | chr19 | 48479862 | ||||||
| chr19:48479916 | G | A | 1 | a0001c0001t0006 | 6 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*706G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 706 | chr19 | 48479916 | ||||||
| chr19:48479917 | G | C | 1 | a0001c0001t0006 | 6 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*707G>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 707 | chr19 | 48479917 | ||||||
| chr19:48479919 | TAAG | T | 1 | a0001c0001t0006 | 6 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*711_*713delAGA | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 711 | INFO_REALIGN_3_PRIME | chr19 | 48479919 | |||||
| chr19:48479923 | A | G | 1 | a0001c0001t0006 | 6 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*713A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 713 | chr19 | 48479923 | ||||||
| chr19:48479925 | G | A | 1 | a0001c0001t0006 | 6 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*715G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 715 | chr19 | 48479925 | ||||||
| chr19:48480122 | C | G | 1 | a0001c0001t0040 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*912C>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 912 | chr19 | 48480122 | ||||||
| chr19:48480169 | G | C | 2 | a0001c0001t0015 a0001c0002t0024 |
4 | HG01433.hp2 HG02572.hp2 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*959G>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 959 | chr19 | 48480169 | ||||||
| chr19:48480211 | C | G | 1 | a0001c0001t0014 | 4 | HG02451.hp1 HG02970.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1001C>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1001 | chr19 | 48480211 | ||||||
| chr19:48480211 | C | T | 2 | a0001c0001t0008 a0001c0001t0023 |
7 | HG02723.hp1 HG02922.hp2 HG02976.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1001C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1001 | chr19 | 48480211 | ||||||
| chr19:48480268 | C | A | 1 | a0001c0001t0023 | 2 | HG02723.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1058C>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1058 | chr19 | 48480268 | ||||||
| chr19:48480272 | C | T | 1 | a0001c0001t0039 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1062C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1062 | chr19 | 48480272 | ||||||
| chr19:48480380 | C | G | 1 | a0001c0001t0023 | 2 | HG02723.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1170C>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1170 | chr19 | 48480380 | ||||||
| chr19:48480413 | C | T | 1 | a0001c0001t0022 | 2 | NA19066.hp2 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1203C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1203 | chr19 | 48480413 | ||||||
| chr19:48480438 | C | G | 1 | a0001c0001t0018 | 3 | HG00673.hp2 NA18990.hp2 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1228C>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1228 | chr19 | 48480438 | ||||||
| chr19:48480439 | C | T | 1 | a0001c0001t0038 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1229C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1229 | chr19 | 48480439 | ||||||
| chr19:48480442 | C | T | 2 | a0001c0002t0004 a0001c0002t0029 |
15 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1232C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1232 | chr19 | 48480442 | ||||||
| chr19:48480499 | C | T | 1 | a0001c0002t0029 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1289C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1289 | chr19 | 48480499 | ||||||
| chr19:48480639 | C | G | 2 | a0001c0001t0013 a0002c0007t0013 |
4 | HG02056.hp1 HG02071.hp1 NA18945.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1429C>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1429 | chr19 | 48480639 | ||||||
| chr19:48480641 | C | T | 3 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0028 |
10 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1431C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1431 | chr19 | 48480641 | ||||||
| chr19:48480715 | G | A | 1 | a0001c0001t0023 | 2 | HG02723.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1505G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1505 | chr19 | 48480715 | ||||||
| chr19:48480803 | A | G | 4 | a0001c0001t0003 a0001c0001t0019 a0001c0001t0030 others(1): Show |
46 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1593A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1593 | chr19 | 48480803 | ||||||
| chr19:48480921 | G | C | 30 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(27): Show |
248 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*1711G>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1711 | chr19 | 48480921 | ||||||
| chr19:48480970 | C | T | 1 | a0001c0001t0027 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1760C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1760 | chr19 | 48480970 | ||||||
| chr19:48480987 | G | A | 1 | a0001c0001t0032 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1777G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1777 | chr19 | 48480987 | ||||||
| chr19:48481126 | C | T | 2 | a0001c0001t0009 a0001c0001t0035 |
6 | HG00642.hp2 HG01109.hp2 HG01261.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1916C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1916 | chr19 | 48481126 | ||||||
| chr19:48481156 | G | A | 1 | a0001c0001t0017 | 3 | NA18942.hp1 NA18964.hp1 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1946G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 1946 | chr19 | 48481156 | ||||||
| chr19:48481373 | C | T | 1 | a0001c0001t0015 | 3 | HG01433.hp2 HG02809.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2163C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 2163 | chr19 | 48481373 | ||||||
| chr19:48481478 | A | AT | 27 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(24): Show |
239 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(236): Show |
3_prime_UTR_variant | MODIFIER | c.*2276dupT | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 2277 | INFO_REALIGN_3_PRIME | chr19 | 48481478 | |||||
| chr19:48481491 | G | GT | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0009 others(17): Show |
207 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*2292dupT | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 2293 | INFO_REALIGN_3_PRIME | chr19 | 48481491 | |||||
| chr19:48481496 | T | G | 2 | a0001c0001t0011 a0001c0002t0024 |
5 | HG02145.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2286T>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 2286 | chr19 | 48481496 | ||||||
| chr19:48481553 | C | T | 1 | a0001c0001t0020 | 2 | HG00544.hp2 NA18978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2343C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 2343 | chr19 | 48481553 | ||||||
| chr19:48481828 | T | C | 1 | a0001c0001t0023 | 2 | HG02723.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2618T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 2618 | chr19 | 48481828 | ||||||
| chr19:48481858 | C | T | 1 | a0001c0001t0023 | 2 | HG02723.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2648C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 2648 | chr19 | 48481858 | ||||||
| chr19:48481894 | TGGCAGGT others(29): Show |
T | 1 | a0001c0001t0034 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2685_*2720delGGCA others(32): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 2685 | chr19 | 48481894 | ||||||
| chr19:48481919 | C | T | 1 | a0001c0001t0023 | 2 | HG02723.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2709C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 2709 | chr19 | 48481919 | ||||||
| chr19:48481921 | TA | T | 30 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(27): Show |
250 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*2713delA | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 2713 | INFO_REALIGN_3_PRIME | chr19 | 48481921 | |||||
| chr19:48481971 | C | A | 1 | a0001c0001t0035 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2761C>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 2761 | chr19 | 48481971 | ||||||
| chr19:48482199 | T | C | 1 | a0001c0005t0025 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2989T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 12/12 | 2989 | chr19 | 48482199 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48469633 | C | T | 10 | a0001c0002t0004g0008 a0001c0002t0004g0015 a0001c0002t0004g0088 others(7): Show |
16 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.19+107C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 1/11 | chr19 | 48469633 | |||||||
| chr19:48469697 | A | G | 1 | a0001c0001t0002g0087 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.19+171A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 1/11 | chr19 | 48469697 | |||||||
| chr19:48469817 | C | G | 2 | a0001c0001t0001g0014 a0001c0001t0026g0014 |
3 | HG01346.hp2 HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.19+291C>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 1/11 | chr19 | 48469817 | |||||||
| chr19:48469839 | G | A | 31 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(28): Show |
43 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.19+313G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 1/11 | chr19 | 48469839 | |||||||
| chr19:48469885 | G | A | 1 | a0001c0001t0002g0021 | 2 | NA18985.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.19+359G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 1/11 | chr19 | 48469885 | |||||||
| chr19:48469886 | G | T | 1 | a0001c0001t0002g0086 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.19+360G>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 1/11 | chr19 | 48469886 | |||||||
| chr19:48470090 | T | C | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.20-263T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 1/11 | chr19 | 48470090 | |||||||
| chr19:48470121 | C | G | 1 | a0001c0001t0015g0043 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.20-232C>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 1/11 | chr19 | 48470121 | |||||||
| chr19:48470274 | C | T | 1 | a0001c0005t0025g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.20-79C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 1/11 | chr19 | 48470274 | |||||||
| chr19:48470521 | C | T | 1 | a0001c0001t0017g0029 | 2 | NA18942.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.167+21C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 2/11 | chr19 | 48470521 | |||||||
| chr19:48470748 | G | A | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.234+79G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48470748 | |||||||
| chr19:48470826 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.234+157T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48470826 | |||||||
| chr19:48470982 | A | G | 9 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(6): Show |
10 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.234+313A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48470982 | |||||||
| chr19:48471003 | A | G | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.234+334A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471003 | |||||||
| chr19:48471035 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.234+366G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471035 | |||||||
| chr19:48471042 | A | C | 31 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(28): Show |
43 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.234+373A>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471042 | |||||||
| chr19:48471125 | G | A | 1 | a0001c0001t0012g0046 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.234+456G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471125 | |||||||
| chr19:48471146 | G | C | 1 | a0001c0001t0001g0045 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.234+477G>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471146 | |||||||
| chr19:48471166 | T | TTGTGTGT others(3): Show |
1 | a0001c0002t0004g0088 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.234+502_234+511dup others(10): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 48471166 | ||||||
| chr19:48471166 | T | TTGTGTGT others(11): Show |
1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.234+511_234+512ins others(18): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 48471166 | ||||||
| chr19:48471166 | T | TTGTGTGT others(13): Show |
3 | a0001c0001t0008g0030 a0001c0002t0005g0016 a0001c0005t0025g0042 |
4 | HG01243.hp1 HG01891.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+511_234+512ins others(20): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 48471166 | ||||||
| chr19:48471166 | T | TTGTGTGT others(15): Show |
3 | a0001c0001t0008g0031 a0001c0002t0005g0010 a0001c0002t0005g0017 |
6 | HG01167.hp2 HG01169.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+511_234+512ins others(22): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 48471166 | ||||||
| chr19:48471166 | T | TTGTGTGT others(17): Show |
5 | a0001c0001t0008g0018 a0001c0001t0008g0033 a0001c0001t0010g0036 others(2): Show |
6 | HG01433.hp2 HG02258.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+511_234+512ins others(24): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 48471166 | ||||||
| chr19:48471166 | T | TTGTGTGT others(19): Show |
7 | a0001c0001t0015g0034 a0001c0001t0015g0043 a0001c0001t0027g0035 others(4): Show |
9 | HG00408.hp1 HG00438.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.234+511_234+512ins others(26): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 48471166 | ||||||
| chr19:48471166 | T | TTGTGTGT others(21): Show |
7 | a0001c0001t0010g0019 a0001c0001t0010g0037 a0001c0001t0028g0019 others(4): Show |
11 | HG00544.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.234+511_234+512ins others(28): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 48471166 | ||||||
| chr19:48471166 | T | TTGTGTGT others(23): Show |
4 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(1): Show |
5 | HG01884.hp1 HG02897.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+511_234+512ins others(30): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 48471166 | ||||||
| chr19:48471166 | T | TTGTGTGT others(25): Show |
1 | a0001c0001t0007g0041 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.234+511_234+512ins others(32): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 48471166 | ||||||
| chr19:48471181 | A | T | 29 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(26): Show |
41 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.234+512A>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471181 | |||||||
| chr19:48471198 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.234+529A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471198 | |||||||
| chr19:48471247 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0016g0013 |
3 | HG01069.hp1 HG01071.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.234+578C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471247 | |||||||
| chr19:48471320 | T | G | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.234+651T>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471320 | |||||||
| chr19:48471395 | G | A | 1 | a0001c0001t0002g0047 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.234+726G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471395 | |||||||
| chr19:48471409 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.234+740C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471409 | |||||||
| chr19:48471447 | T | C | 32 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(29): Show |
45 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.234+778T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471447 | |||||||
| chr19:48471480 | T | C | 1 | a0001c0001t0007g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.234+811T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471480 | |||||||
| chr19:48471656 | G | T | 1 | a0001c0001t0011g0084 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.235-669G>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471656 | |||||||
| chr19:48471666 | C | A | 9 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(6): Show |
10 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.235-659C>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471666 | |||||||
| chr19:48471758 | A | G | 6 | a0001c0002t0004g0015 a0001c0002t0004g0088 a0001c0002t0004g0091 others(3): Show |
8 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(5): Show |
intron_variant | MODIFIER | c.235-567A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471758 | |||||||
| chr19:48471773 | G | T | 1 | a0001c0001t0014g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235-552G>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471773 | |||||||
| chr19:48471915 | G | A | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.235-410G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471915 | |||||||
| chr19:48471940 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.235-385C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 3/11 | chr19 | 48471940 | |||||||
| chr19:48472489 | C | T | 36 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(33): Show |
50 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.353+46C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 4/11 | chr19 | 48472489 | |||||||
| chr19:48472550 | C | T | 32 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(29): Show |
45 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.353+107C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 4/11 | chr19 | 48472550 | |||||||
| chr19:48472583 | T | G | 1 | a0001c0002t0005g0017 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.353+140T>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 4/11 | chr19 | 48472583 | |||||||
| chr19:48472761 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.353+318A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 4/11 | chr19 | 48472761 | |||||||
| chr19:48472990 | C | T | 4 | a0001c0001t0001g0078 a0001c0001t0002g0009 a0001c0001t0002g0079 others(1): Show |
6 | HG00673.hp1 HG02080.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.354-308C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 4/11 | chr19 | 48472990 | |||||||
| chr19:48473240 | T | C | 32 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(29): Show |
45 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.354-58T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 4/11 | chr19 | 48473240 | |||||||
| chr19:48473390 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.434+12G>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 5/11 | chr19 | 48473390 | |||||||
| chr19:48473405 | G | T | 1 | a0001c0001t0021g0076 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.434+27G>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 5/11 | chr19 | 48473405 | |||||||
| chr19:48473425 | G | A | 1 | a0001c0001t0003g0048 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.434+47G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 5/11 | chr19 | 48473425 | |||||||
| chr19:48473455 | C | T | 1 | a0001c0001t0003g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.434+77C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 5/11 | chr19 | 48473455 | |||||||
| chr19:48473484 | A | G | 7 | a0001c0001t0008g0018 a0001c0001t0008g0030 a0001c0001t0008g0031 others(4): Show |
8 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.434+106A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 5/11 | chr19 | 48473484 | |||||||
| chr19:48473513 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG03239.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.434+135C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 5/11 | chr19 | 48473513 | |||||||
| chr19:48473541 | C | T | 1 | a0001c0001t0002g0003 | 9 | NA18947.hp2 NA18953.hp1 NA18979.hp1 others(6): Show |
intron_variant | MODIFIER | c.434+163C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 5/11 | chr19 | 48473541 | |||||||
| chr19:48473544 | C | T | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.434+166C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 5/11 | chr19 | 48473544 | |||||||
| chr19:48473597 | T | A | 1 | a0001c0001t0001g0049 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.434+219T>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 5/11 | chr19 | 48473597 | |||||||
| chr19:48473646 | C | T | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.435-259C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 5/11 | chr19 | 48473646 | |||||||
| chr19:48473692 | G | A | 6 | a0001c0002t0004g0015 a0001c0002t0004g0088 a0001c0002t0004g0091 others(3): Show |
8 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-213G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 5/11 | chr19 | 48473692 | |||||||
| chr19:48473712 | A | G | 5 | a0001c0001t0008g0018 a0001c0001t0008g0030 a0001c0001t0008g0031 others(2): Show |
6 | HG01433.hp2 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.435-193A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 5/11 | chr19 | 48473712 | |||||||
| chr19:48473762 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
267 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.435-143C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 5/11 | chr19 | 48473762 | |||||||
| chr19:48474125 | T | C | 32 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(29): Show |
45 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.548-57T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 6/11 | chr19 | 48474125 | |||||||
| chr19:48474133 | C | G | 1 | a0001c0001t0002g0054 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.548-49C>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 6/11 | chr19 | 48474133 | |||||||
| chr19:48474134 | T | C | 1 | a0001c0001t0003g0026 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.548-48T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 6/11 | chr19 | 48474134 | |||||||
| chr19:48474444 | C | T | 14 | a0001c0002t0004g0008 a0001c0002t0004g0015 a0001c0002t0004g0088 others(11): Show |
24 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.696+114C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 7/11 | chr19 | 48474444 | |||||||
| chr19:48474458 | C | T | 5 | a0001c0001t0008g0018 a0001c0001t0008g0030 a0001c0001t0008g0031 others(2): Show |
6 | HG01433.hp2 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.696+128C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 7/11 | chr19 | 48474458 | |||||||
| chr19:48474548 | T | G | 1 | a0001c0001t0001g0055 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.696+218T>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 7/11 | chr19 | 48474548 | |||||||
| chr19:48474567 | G | C | 32 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(29): Show |
45 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.696+237G>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 7/11 | chr19 | 48474567 | |||||||
| chr19:48474627 | G | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0074 |
9 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.697-211G>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 7/11 | chr19 | 48474627 | |||||||
| chr19:48474764 | C | T | 9 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(6): Show |
10 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.697-74C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 7/11 | chr19 | 48474764 | |||||||
| chr19:48474777 | C | G | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.697-61C>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 7/11 | chr19 | 48474777 | |||||||
| chr19:48474981 | C | T | 1 | a0001c0001t0008g0033 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.808+32C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48474981 | |||||||
| chr19:48475068 | T | C | 31 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(28): Show |
43 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.808+119T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475068 | |||||||
| chr19:48475114 | C | G | 1 | a0001c0001t0002g0079 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.808+165C>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475114 | |||||||
| chr19:48475149 | C | A | 1 | a0001c0001t0002g0056 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.808+200C>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475149 | |||||||
| chr19:48475283 | C | A | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.808+334C>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475283 | |||||||
| chr19:48475325 | C | A | 4 | a0001c0002t0004g0008 a0001c0002t0004g0089 a0001c0002t0004g0090 others(1): Show |
8 | HG01884.hp2 HG02572.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.808+376C>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475325 | |||||||
| chr19:48475336 | G | A | 1 | a0001c0001t0009g0057 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.808+387G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475336 | |||||||
| chr19:48475354 | T | C | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.808+405T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475354 | |||||||
| chr19:48475380 | G | A | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.808+431G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475380 | |||||||
| chr19:48475442 | A | T | 31 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(28): Show |
43 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.808+493A>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475442 | |||||||
| chr19:48475532 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.808+583C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475532 | |||||||
| chr19:48475555 | G | C | 1 | a0001c0001t0001g0058 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.808+606G>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475555 | |||||||
| chr19:48475560 | A | G | 4 | a0001c0001t0008g0018 a0001c0001t0008g0030 a0001c0001t0008g0031 others(1): Show |
5 | HG01433.hp2 HG02922.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.808+611A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475560 | |||||||
| chr19:48475632 | A | G | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.808+683A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475632 | |||||||
| chr19:48475654 | A | G | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.808+705A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475654 | |||||||
| chr19:48475702 | G | A | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.808+753G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475702 | |||||||
| chr19:48475710 | C | T | 1 | a0001c0001t0002g0025 | 2 | HG02738.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.808+761C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475710 | |||||||
| chr19:48475784 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.808+835C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475784 | |||||||
| chr19:48475796 | A | G | 2 | a0001c0001t0015g0034 a0001c0001t0015g0043 |
2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.808+847A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475796 | |||||||
| chr19:48475805 | C | A | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.808+856C>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475805 | |||||||
| chr19:48475819 | A | G | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.808+870A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475819 | |||||||
| chr19:48475868 | A | G | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.808+919A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475868 | |||||||
| chr19:48475891 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.808+942G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475891 | |||||||
| chr19:48475929 | C | A | 26 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(23): Show |
37 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.808+980C>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48475929 | |||||||
| chr19:48476168 | G | C | 1 | a0001c0001t0003g0059 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.808+1219G>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48476168 | |||||||
| chr19:48476244 | C | T | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.808+1295C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48476244 | |||||||
| chr19:48476399 | C | T | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.808+1450C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48476399 | |||||||
| chr19:48476407 | T | TAAAATA | 38 | a0001c0001t0001g0044 a0001c0001t0002g0027 a0001c0001t0002g0056 others(35): Show |
57 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.808+1462_808+1467d others(8): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr19 | 48476407 | ||||||
| chr19:48476564 | G | T | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.809-1505G>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48476564 | |||||||
| chr19:48476767 | T | C | 4 | a0001c0002t0004g0015 a0001c0002t0004g0088 a0001c0002t0004g0091 others(1): Show |
6 | HG00438.hp1 HG00544.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-1302T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48476767 | |||||||
| chr19:48476805 | G | A | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.809-1264G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48476805 | |||||||
| chr19:48477029 | A | T | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.809-1040A>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48477029 | |||||||
| chr19:48477093 | C | T | 1 | a0001c0001t0018g0011 | 3 | HG00673.hp2 NA18990.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.809-976C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48477093 | |||||||
| chr19:48477190 | G | A | 1 | a0001c0001t0002g0050 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.809-879G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48477190 | |||||||
| chr19:48477231 | G | C | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.809-838G>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48477231 | |||||||
| chr19:48477242 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.809-827A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48477242 | |||||||
| chr19:48477277 | T | C | 31 | a0001c0001t0006g0006 a0001c0001t0007g0020 a0001c0001t0007g0038 others(28): Show |
48 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.809-792T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48477277 | |||||||
| chr19:48477305 | G | T | 1 | a0001c0001t0003g0071 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.809-764G>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48477305 | |||||||
| chr19:48477357 | C | T | 11 | a0001c0001t0006g0006 a0001c0001t0007g0020 a0001c0001t0007g0038 others(8): Show |
17 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.809-712C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48477357 | |||||||
| chr19:48477372 | T | C | 21 | a0001c0001t0001g0061 a0001c0001t0002g0060 a0001c0001t0007g0020 others(18): Show |
27 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.809-697T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48477372 | |||||||
| chr19:48477906 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.809-163C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48477906 | |||||||
| chr19:48478026 | C | T | 1 | a0001c0001t0019g0069 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.809-43C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 8/11 | chr19 | 48478026 | |||||||
| chr19:48478152 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp2 | splice_region_variant&intron_variant | LOW | c.885+7G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 9/11 | chr19 | 48478152 | |||||||
| chr19:48478182 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.885+37C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 9/11 | chr19 | 48478182 | |||||||
| chr19:48478185 | A | G | 3 | a0001c0001t0002g0024 a0001c0001t0017g0024 a0001c0001t0017g0029 |
4 | NA18612.hp2 NA18942.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.885+40A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 9/11 | chr19 | 48478185 | |||||||
| chr19:48478226 | G | A | 1 | a0001c0001t0022g0063 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.886-49G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 9/11 | chr19 | 48478226 | |||||||
| chr19:48478354 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG01099.hp1 | splice_region_variant&intron_variant | LOW | c.957+8C>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 10/11 | chr19 | 48478354 | |||||||
| chr19:48478416 | G | A | 1 | a0001c0001t0001g0007 | 5 | HG02258.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.958-22G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 10/11 | chr19 | 48478416 | |||||||
| chr19:48478605 | T | TCCTGGGT others(29): Show |
4 | a0001c0002t0005g0010 a0001c0002t0005g0016 a0001c0002t0005g0017 others(1): Show |
8 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1112+19_1112+20ins others(36): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478605 | ||||||
| chr19:48478612 | C | CCTGATGG others(65): Show |
1 | a0001c0001t0001g0067 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1112+83_1112+84ins others(72): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478612 | ||||||
| chr19:48478612 | C | T | 32 | a0001c0001t0001g0044 a0001c0001t0007g0020 a0001c0001t0007g0038 others(29): Show |
45 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1112+20C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478612 | |||||||
| chr19:48478653 | T | C | 19 | a0001c0001t0001g0044 a0001c0001t0015g0032 a0001c0001t0015g0034 others(16): Show |
30 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.1112+61T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478653 | |||||||
| chr19:48478657 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1112+65G>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478657 | |||||||
| chr19:48478676 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.1112+84T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478676 | |||||||
| chr19:48478677 | G | A | 15 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(12): Show |
18 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1112+85G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478677 | |||||||
| chr19:48478689 | T | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
258 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.1112+97T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478689 | |||||||
| chr19:48478701 | T | A | 17 | a0001c0001t0001g0044 a0001c0001t0015g0032 a0001c0001t0015g0034 others(14): Show |
27 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.1112+109T>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478701 | |||||||
| chr19:48478713 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0009g0004 a0001c0001t0009g0057 others(1): Show |
9 | HG00642.hp2 HG01109.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1112+121G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478713 | |||||||
| chr19:48478713 | G | T | 15 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(12): Show |
18 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1112+121G>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478713 | |||||||
| chr19:48478713 | GCCTGGGT others(139): Show |
G | 1 | a0001c0001t0011g0081 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1112+145_1113-241d others(2): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478713 | ||||||
| chr19:48478735 | G | GC | 4 | a0001c0002t0005g0010 a0001c0002t0005g0016 a0001c0002t0005g0017 others(1): Show |
8 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1112+144dupC | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478735 | ||||||
| chr19:48478735 | G | GCAGGGGG others(31): Show |
3 | a0001c0001t0015g0032 a0001c0001t0015g0034 a0001c0001t0015g0043 |
3 | HG01433.hp2 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1112+144_1112+145i others(40): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478735 | ||||||
| chr19:48478736 | C | CA | 10 | a0001c0001t0001g0044 a0001c0002t0004g0008 a0001c0002t0004g0015 others(7): Show |
16 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.1112+144_1112+145i others(3): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478736 | |||||||
| chr19:48478737 | T | A | 14 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(11): Show |
16 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1112+145T>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478737 | |||||||
| chr19:48478737 | T | G | 17 | a0001c0001t0001g0044 a0001c0001t0015g0032 a0001c0001t0015g0034 others(14): Show |
27 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.1112+145T>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478737 | |||||||
| chr19:48478749 | T | G | 32 | a0001c0001t0001g0044 a0001c0001t0006g0006 a0001c0001t0007g0020 others(29): Show |
49 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1112+157T>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478749 | |||||||
| chr19:48478771 | G | GC | 12 | a0001c0001t0001g0044 a0001c0001t0001g0066 a0001c0001t0015g0032 others(9): Show |
20 | HG00423.hp2 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1112+180dupC | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478771 | ||||||
| chr19:48478771 | G | GCCGGGGG others(142): Show |
5 | a0001c0001t0010g0019 a0001c0001t0010g0036 a0001c0001t0010g0037 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1112+180_1112+181i others(151): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478771 | ||||||
| chr19:48478771 | G | GCCGGGGG others(179): Show |
4 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(1): Show |
5 | HG01884.hp1 HG02818.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1112+180_1112+181i others(188): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478771 | ||||||
| chr19:48478771 | G | GCCGGGGG others(322): Show |
1 | a0001c0001t0002g0060 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1112+180_1112+181i others(331): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478771 | ||||||
| chr19:48478773 | A | AG | 5 | a0001c0002t0004g0015 a0001c0002t0004g0091 a0001c0002t0004g0094 others(2): Show |
7 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112+185dupG | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478773 | ||||||
| chr19:48478773 | A | AGGGGCCT others(139): Show |
1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1112+192_1112+193i others(148): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478773 | ||||||
| chr19:48478773 | A | AGGGGCCT others(30): Show |
1 | a0001c0001t0027g0035 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1112+192_1112+193i others(39): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478773 | ||||||
| chr19:48478773 | A | AGGGGCCT others(67): Show |
4 | a0001c0001t0008g0018 a0001c0001t0008g0030 a0001c0001t0008g0031 others(1): Show |
5 | HG02922.hp2 HG03139.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1112+192_1112+193i others(76): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478773 | ||||||
| chr19:48478773 | A | AGGGGGCC others(31): Show |
1 | a0001c0002t0004g0088 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1112+185_1112+186i others(40): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478773 | ||||||
| chr19:48478773 | A | G | 21 | a0001c0001t0001g0066 a0001c0001t0002g0060 a0001c0001t0007g0020 others(18): Show |
30 | HG00423.hp2 HG01167.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.1112+181A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478773 | |||||||
| chr19:48478785 | A | C | 21 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(18): Show |
27 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1112+193A>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478785 | |||||||
| chr19:48478785 | A | G | 10 | a0001c0001t0001g0044 a0001c0001t0023g0022 a0001c0002t0004g0008 others(7): Show |
17 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(14): Show |
intron_variant | MODIFIER | c.1112+193A>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478785 | |||||||
| chr19:48478785 | A | T | 2 | a0001c0001t0002g0060 a0001c0001t0027g0035 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1112+193A>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478785 | |||||||
| chr19:48478797 | C | T | 1 | a0001c0001t0003g0065 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1112+205C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478797 | |||||||
| chr19:48478809 | C | A | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1112+217C>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478809 | |||||||
| chr19:48478822 | C | CCCTGGGT others(30): Show |
7 | a0001c0002t0004g0008 a0001c0002t0004g0015 a0001c0002t0004g0089 others(4): Show |
13 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(10): Show |
intron_variant | MODIFIER | c.1113-256_1113-220d others(39): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478822 | ||||||
| chr19:48478822 | C | CCCTGGGT others(67): Show |
1 | a0001c0002t0004g0091 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1112+238_1113-220d others(76): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478822 | ||||||
| chr19:48478822 | C | G | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1112+230C>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478822 | |||||||
| chr19:48478822 | C | T | 13 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0008g0018 others(10): Show |
18 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1112+230C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478822 | |||||||
| chr19:48478835 | G | A | 5 | a0001c0001t0002g0052 a0001c0001t0011g0012 a0001c0001t0011g0084 others(2): Show |
6 | HG02056.hp2 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1112+243G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478835 | |||||||
| chr19:48478844 | GC | G | 2 | a0001c0001t0001g0044 a0001c0001t0023g0022 |
3 | HG02723.hp1 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1112+254delC | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478844 | ||||||
| chr19:48478847 | G | A | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1112+255G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478847 | |||||||
| chr19:48478847 | G | T | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1112+255G>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478847 | |||||||
| chr19:48478859 | T | A | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1113-264T>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478859 | |||||||
| chr19:48478859 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1113-264T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478859 | |||||||
| chr19:48478859 | T | G | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1113-264T>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478859 | |||||||
| chr19:48478871 | CGGAGGAG others(67): Show |
C | 1 | a0001c0001t0001g0055 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1113-226_1113-153d others(76): Show |
CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 48478871 | ||||||
| chr19:48478896 | T | C | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1113-227T>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478896 | |||||||
| chr19:48478904 | G | C | 2 | a0001c0001t0023g0022 a0001c0001t0027g0035 |
3 | HG02723.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1113-219G>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478904 | |||||||
| chr19:48478908 | G | C | 2 | a0001c0001t0023g0022 a0001c0001t0027g0035 |
3 | HG02723.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1113-215G>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478908 | |||||||
| chr19:48478941 | C | G | 10 | a0001c0001t0007g0020 a0001c0001t0007g0038 a0001c0001t0007g0039 others(7): Show |
11 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1113-182C>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478941 | |||||||
| chr19:48478945 | G | C | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1113-178G>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478945 | |||||||
| chr19:48478971 | G | C | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1113-152G>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478971 | |||||||
| chr19:48478978 | C | G | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1113-145C>G | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478978 | |||||||
| chr19:48478982 | G | C | 1 | a0001c0001t0001g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1113-141G>C | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478982 | |||||||
| chr19:48478991 | G | A | 1 | a0001c0001t0002g0051 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1113-132G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48478991 | |||||||
| chr19:48479030 | C | T | 1 | a0001c0001t0023g0022 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1113-93C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48479030 | |||||||
| chr19:48479031 | C | T | 1 | a0001c0001t0002g0023 | 2 | HG02015.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1113-92C>T | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48479031 | |||||||
| chr19:48479032 | G | A | 2 | a0001c0001t0006g0006 a0001c0001t0023g0022 |
8 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113-91G>A | CYTH2 | ENSG00000105443.17 | transcript | ENST00000452733.7 | protein_coding | 11/11 | chr19 | 48479032 |