Variant report

Variant rs1639241
Chromosome Location chr7:14791572-14791573
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:14785800-14792200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr7:14787400-14792200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr7:14787400-14801400 Weak transcription Brain Cingulate Gyrus brain
4 chr7:14787800-14792000 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr7:14788200-14793600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr7:14788400-14794200 Weak transcription HMEC breast
7 chr7:14788600-14793800 Weak transcription Osteobl bone
8 chr7:14788600-14794400 Weak transcription NHDF-Ad bronchial
9 chr7:14788800-14793600 Weak transcription Muscle Satellite Cultured Cells --
10 chr7:14790600-14791600 Enhancers HUVEC blood vessel
11 chr7:14790600-14791800 Enhancers Primary hematopoietic stem cells short term culture blood
12 chr7:14790600-14793000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
13 chr7:14791400-14793800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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