The 2.0 version of rSNPBase

Variant report

Variant rs61773762
Chromosome Location chr1:76651399-76651400
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:76636600-76652800 Weak transcription Primary B cells from cord blood blood
2 chr1:76643800-76651800 Weak transcription Fetal Kidney kidney
3 chr1:76644800-76653200 Weak transcription H9 Cell Line embryonic stem cell
4 chr1:76645400-76652600 Weak transcription HUVEC blood vessel
5 chr1:76646600-76652600 Weak transcription Brain Hippocampus Middle brain
6 chr1:76646600-76658000 Weak transcription Fetal Stomach stomach
7 chr1:76646800-76652800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr1:76646800-76653200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr1:76647000-76665600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr1:76649000-76652600 Weak transcription Brain Cingulate Gyrus brain
11 chr1:76650800-76651800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr1:76651000-76651400 ZNF genes & repeats Fetal Lung lung
13 chr1:76651200-76651600 ZNF genes & repeats Aorta Aorta

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Last update: Aug 31, 2015