Variant report

Variant rs553921884
Chromosome Location chr8:42907016-42907017
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:42901800-42910600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr8:42905200-42910400 Weak transcription Skeletal Muscle Male skeletal muscle
3 chr8:42905400-42910600 Weak transcription Pancreas Pancrea
4 chr8:42905800-42907400 Enhancers Fetal Intestine Small intestine
5 chr8:42906000-42910000 Weak transcription Gastric stomach
6 chr8:42906200-42910200 Weak transcription A549 lung
7 chr8:42906600-42907200 Weak transcription Fetal Intestine Large intestine
8 chr8:42906800-42907200 Bivalent Enhancer HepG2 liver
9 chr8:42906800-42910000 Weak transcription Duodenum Mucosa Duodenum
10 chr8:42906800-42910600 Weak transcription Primary neutrophils fromperipheralblood blood
11 chr8:42907000-42910600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung

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