Variant report

Variant rs41290007
Chromosome Location chr9:140055703-140055704
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:140052400-140055800 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
2 chr9:140054800-140057600 Weak transcription K562 blood
3 chr9:140055200-140056200 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr9:140055400-140055800 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
5 chr9:140055400-140056000 Strong transcription Right Atrium heart
6 chr9:140055400-140058800 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
7 chr9:140055600-140055800 Bivalent/Poised TSS H1 Cell Line embryonic stem cell
8 chr9:140055600-140055800 Bivalent/Poised TSS iPS-18 Cell Line embryonic stem cell
9 chr9:140055600-140055800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
10 chr9:140055600-140056200 Bivalent Enhancer A549 lung
11 chr9:140055600-140057000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
12 chr9:140055600-140057200 Enhancers Pancreas Pancrea
13 chr9:140055600-140058200 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
14 chr9:140055600-140058400 Enhancers Gastric stomach

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