Variant report

Variant rs2981960
Chromosome Location chr6:167706559-167706560
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167704400-167707400 Flanking Active TSS HepG2 liver
2 chr6:167704800-167706800 Flanking Active TSS Fetal Intestine Large intestine
3 chr6:167705000-167707000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr6:167705200-167706600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr6:167705800-167706600 Enhancers ES-WA7 Cell Line embryonic stem cell
6 chr6:167705800-167715000 Weak transcription Liver Liver
7 chr6:167706000-167707200 Enhancers Placenta Amnion Placenta Amnion
8 chr6:167706200-167706600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr6:167706200-167706600 Transcr. at gene 5' and 3' Fetal Intestine Small intestine
10 chr6:167706200-167706800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr6:167706200-167718600 Weak transcription H9 Cell Line embryonic stem cell
12 chr6:167706400-167706600 Bivalent Enhancer Fetal Muscle Leg muscle
13 chr6:167706400-167707200 Enhancers Spleen Spleen
14 chr6:167706400-167707400 Bivalent Enhancer Fetal Muscle Trunk muscle
15 chr6:167706400-167714600 Weak transcription H1 Cell Line embryonic stem cell
16 chr6:167706400-167717400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell

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