Variant report

Variant rs373681221
Chromosome Location chr6:167312633-167312634
allele lengthTooLong
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 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 chr6:167312200-167312800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr6:167312200-167315800 ZNF genes & repeats Placenta Placenta
8 chr6:167312200-167316800 Weak transcription iPS-18 Cell Line embryonic stem cell
9 chr6:167312600-167313200 Active TSS H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr6:167312600-167313800 Weak transcription Spleen Spleen
11 chr6:167312600-167314000 Weak transcription Pancreas Pancrea

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