Variant report

Variant rs17040825
Chromosome Location chr2:50785178-50785179
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:50766200-50791800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
2 chr2:50780000-50791400 Weak transcription Brain Germinal Matrix brain
3 chr2:50783200-50785800 Enhancers Hela-S3 cervix
4 chr2:50784000-50785200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr2:50784000-50785200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:50784000-50785200 Enhancers NH-A brain
7 chr2:50784000-50785600 Enhancers Fetal Heart heart
8 chr2:50784200-50785400 Enhancers NHEK skin
9 chr2:50784400-50785200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr2:50784600-50785200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr2:50784600-50785400 Enhancers HUES64 Cell Line embryonic stem cell
12 chr2:50785000-50785200 Enhancers HMEC breast
13 chr2:50785000-50785400 Enhancers iPS-15b Cell Line embryonic stem cell
14 chr2:50785000-50785800 Enhancers iPS-18 Cell Line embryonic stem cell

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