The 2.0 version of rSNPBase

Variant report

Variant esv2210020
Chromosome Location chr7:48294193-48294195
allele n/a
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:48289000-48295200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr7:48290400-48299000 Weak transcription iPS-15b Cell Line embryonic stem cell
3 chr7:48290600-48294600 Weak transcription NHEK skin
4 chr7:48290800-48294200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr7:48290800-48299000 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr7:48291000-48294200 Weak transcription Fetal Adrenal Gland Adrenal Gland
7 chr7:48291000-48294200 Weak transcription Osteobl bone
8 chr7:48291200-48294400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
9 chr7:48291800-48294200 Weak transcription NH-A brain
10 chr7:48292000-48294800 Enhancers Primary neutrophils fromperipheralblood blood
11 chr7:48292200-48294200 Weak transcription GM12878-XiMat blood
12 chr7:48292200-48308600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr7:48292800-48295000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
14 chr7:48293000-48294400 Weak transcription iPS-20b Cell Line embryonic stem cell
15 chr7:48293200-48294400 Weak transcription HMEC breast
16 chr7:48293400-48298800 Weak transcription HUES48 Cell Line embryonic stem cell

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Last update: Aug 31, 2015