Variant report

Variant rs3010541
Chromosome Location chr6:167706949-167706950
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167704400-167707400 Flanking Active TSS HepG2 liver
2 chr6:167705000-167707000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr6:167705800-167715000 Weak transcription Liver Liver
4 chr6:167706000-167707200 Enhancers Placenta Amnion Placenta Amnion
5 chr6:167706200-167718600 Weak transcription H9 Cell Line embryonic stem cell
6 chr6:167706400-167707200 Enhancers Spleen Spleen
7 chr6:167706400-167707400 Bivalent Enhancer Fetal Muscle Trunk muscle
8 chr6:167706400-167714600 Weak transcription H1 Cell Line embryonic stem cell
9 chr6:167706400-167717400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
10 chr6:167706600-167707000 Enhancers Right Ventricle heart
11 chr6:167706600-167707400 Genic enhancers Fetal Intestine Small intestine
12 chr6:167706600-167707400 Enhancers Fetal Muscle Leg muscle
13 chr6:167706800-167707200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr6:167706800-167707400 Enhancers Fetal Intestine Large intestine

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