Variant report

Variant rs1639236
Chromosome Location chr7:14788837-14788838
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:14784400-14789400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr7:14785800-14792200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr7:14787000-14789000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr7:14787400-14792200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr7:14787400-14801400 Weak transcription Brain Cingulate Gyrus brain
6 chr7:14787800-14792000 Weak transcription Cortex derived primary cultured neurospheres brain
7 chr7:14788200-14789600 Enhancers HUVEC blood vessel
8 chr7:14788200-14793600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr7:14788400-14789200 Weak transcription Brain Germinal Matrix brain
10 chr7:14788400-14794200 Weak transcription HMEC breast
11 chr7:14788600-14793800 Weak transcription Osteobl bone
12 chr7:14788600-14794400 Weak transcription NHDF-Ad bronchial
13 chr7:14788800-14793600 Weak transcription Muscle Satellite Cultured Cells --

Quick Search:


  
Input of quick search could be:

what's new

Quick links