Variant report

Variant rs559966124
Chromosome Location chr6:167312482-167312483
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167297800-167320400 Weak transcription Primary B cells from cord blood blood
2 chr6:167298200-167320800 Weak transcription Primary T cells from cord blood blood
3 chr6:167302000-167314800 Weak transcription Gastric stomach
4 chr6:167307600-167317200 Weak transcription Primary B cells from peripheral blood blood
5 chr6:167312000-167314800 Weak transcription H9 Cell Line embryonic stem cell
6 chr6:167312200-167312600 Enhancers Pancreas Pancrea
7 chr6:167312200-167312800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
8 chr6:167312200-167315800 ZNF genes & repeats Placenta Placenta
9 chr6:167312200-167316800 Weak transcription iPS-18 Cell Line embryonic stem cell
10 chr6:167312400-167312600 Enhancers Spleen Spleen

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