Variant report

Variant rs9261300
Chromosome Location chr6:30040185-30040186
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:30035600-30041000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr6:30036600-30040600 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr6:30036600-30040800 Strong transcription NHEK skin
4 chr6:30036800-30042400 Weak transcription Hela-S3 cervix
5 chr6:30037200-30040600 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr6:30037800-30040600 Strong transcription HMEC breast
7 chr6:30038000-30041200 Weak transcription Pancreas Pancrea
8 chr6:30038000-30041200 Weak transcription Rectal Mucosa Donor 31 rectum
9 chr6:30038000-30041400 Weak transcription Primary T killer memory cells from peripheral blood blood
10 chr6:30038000-30041800 Weak transcription Ovary ovary
11 chr6:30038400-30044000 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
12 chr6:30038600-30042000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr6:30038800-30041200 Weak transcription iPS-20b Cell Line embryonic stem cell
14 chr6:30038800-30043400 Weak transcription Dnd41 blood
15 chr6:30039000-30042000 Weak transcription Lung lung
16 chr6:30039600-30041000 Genic enhancers Breast Myoepithelial Primary Cells Breast
17 chr6:30039600-30042200 Weak transcription Right Atrium heart
18 chr6:30039800-30040400 Enhancers HepG2 liver
19 chr6:30039800-30041200 Weak transcription Esophagus oesophagus
20 chr6:30039800-30041800 Weak transcription Gastric stomach
21 chr6:30040000-30040200 Bivalent/Poised TSS Foreskin Melanocyte Primary Cells skin01 Skin

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