Variant report

Variant rs571438432
Chromosome Location chr6:29817628-29817629
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29815800-29817800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr6:29816200-29818000 Weak transcription Gastric stomach
3 chr6:29816600-29818000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr6:29816800-29818000 Weak transcription Esophagus oesophagus
5 chr6:29817400-29818000 Bivalent Enhancer Primary T cells fromperipheralblood blood
6 chr6:29817400-29818400 Bivalent Enhancer Primary T killer naive cells fromperipheralblood blood
7 chr6:29817600-29817800 Bivalent Enhancer Primary T cells effector/memory enriched fromperipheralblood blood
8 chr6:29817600-29818000 Bivalent Enhancer Primary T helper cells fromperipheralblood blood
9 chr6:29817600-29818000 Bivalent Enhancer Primary Natural Killer cells fromperipheralblood blood
10 chr6:29817600-29818000 Active TSS Right Ventricle heart
11 chr6:29817600-29818200 Bivalent Enhancer Primary T regulatory cells fromperipheralblood blood

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