Variant report

Variant rs6558520
Chromosome Location chr8:1697573-1697574
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:1692600-1707400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr8:1694400-1702400 Weak transcription HUES48 Cell Line embryonic stem cell
3 chr8:1694400-1702400 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr8:1695200-1703400 Weak transcription HSMMtube muscle
5 chr8:1695200-1703400 Weak transcription NH-A brain
6 chr8:1695400-1702800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr8:1695400-1703000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr8:1695400-1703000 Weak transcription Placenta Placenta
9 chr8:1696600-1700000 Weak transcription Pancreas Pancrea
10 chr8:1696800-1697800 Enhancers Fetal Brain Male brain
11 chr8:1697000-1697600 Enhancers ES-I3 Cell Line embryonic stem cell
12 chr8:1697000-1697800 Enhancers ES-WA7 Cell Line embryonic stem cell
13 chr8:1697000-1697800 Enhancers Stomach Smooth Muscle stomach
14 chr8:1697200-1700000 Weak transcription K562 blood
15 chr8:1697400-1697600 Bivalent Enhancer Fetal Intestine Large intestine
16 chr8:1697400-1697600 Bivalent Enhancer Fetal Muscle Trunk muscle
17 chr8:1697400-1697800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links