Variant report

Variant rs4434022
Chromosome Location chr2:151086666-151086667
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:151083200-151091200 Weak transcription Fetal Brain Female brain
2 chr2:151085600-151086800 Weak transcription Stomach Mucosa stomach
3 chr2:151085600-151090600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr2:151085800-151090400 Weak transcription Fetal Lung lung
5 chr2:151085800-151090800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr2:151086000-151087600 Weak transcription Fetal Adrenal Gland Adrenal Gland
7 chr2:151086000-151088000 Weak transcription HUVEC blood vessel
8 chr2:151086000-151090400 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr2:151086200-151089600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr2:151086400-151088000 Weak transcription Brain Germinal Matrix brain
11 chr2:151086400-151089600 Weak transcription NHDF-Ad bronchial
12 chr2:151086400-151090400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
13 chr2:151086600-151088200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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