Variant report

Variant rs57801137
Chromosome Location chr2:183084959-183084960
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:183061000-183085000 Weak transcription Brain Cingulate Gyrus brain
2 chr2:183065800-183087600 Weak transcription Aorta Aorta
3 chr2:183065800-183087600 Weak transcription Duodenum Smooth Muscle Duodenum
4 chr2:183071600-183086800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr2:183083200-183085800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
6 chr2:183083800-183086800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr2:183084000-183086400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr2:183084200-183085000 Enhancers Fetal Brain Male brain
9 chr2:183084200-183086200 Enhancers Cortex derived primary cultured neurospheres brain
10 chr2:183084200-183086200 Enhancers Brain Germinal Matrix brain
11 chr2:183084200-183086200 Enhancers Fetal Brain Female brain
12 chr2:183084400-183086200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
13 chr2:183084400-183090600 Weak transcription Fetal Kidney kidney
14 chr2:183084400-183095200 Weak transcription Left Ventricle heart
15 chr2:183084800-183085800 Enhancers Brain Substantia Nigra brain
16 chr2:183084800-183086400 Enhancers Brain Angular Gyrus brain

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