Variant report

Variant rs1723245
Chromosome Location chr7:14788239-14788240
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr7:14786800-14788400 Enhancers Brain Substantia Nigra brain
4 chr7:14787000-14788400 Enhancers Brain Angular Gyrus brain
5 chr7:14787000-14789000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr7:14787200-14788600 Enhancers NHDF-Ad bronchial
7 chr7:14787200-14788600 Enhancers Osteobl bone
8 chr7:14787200-14788800 Enhancers Muscle Satellite Cultured Cells --
9 chr7:14787400-14788400 Enhancers HMEC breast
10 chr7:14787400-14792200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
11 chr7:14787400-14801400 Weak transcription Brain Cingulate Gyrus brain
12 chr7:14787800-14788400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr7:14787800-14788400 Enhancers Brain Anterior Caudate brain
14 chr7:14787800-14788400 Enhancers Brain Germinal Matrix brain
15 chr7:14787800-14788400 Enhancers Brain Inferior Temporal Lobe brain
16 chr7:14787800-14792000 Weak transcription Cortex derived primary cultured neurospheres brain
17 chr7:14788200-14789600 Enhancers HUVEC blood vessel
18 chr7:14788200-14793600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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