Variant report

Variant rs2786762
Chromosome Location chr1:168735429-168735430
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:168726200-168736600 Weak transcription Placenta Amnion Placenta Amnion
2 chr1:168730000-168735600 Weak transcription Fetal Heart heart
3 chr1:168730000-168737200 Weak transcription Left Ventricle heart
4 chr1:168730400-168743600 Weak transcription Psoas Muscle Psoas
5 chr1:168733000-168737000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:168733600-168736800 Weak transcription NHEK skin
7 chr1:168733600-168737200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr1:168733800-168737000 Weak transcription HMEC breast
9 chr1:168734200-168739200 Enhancers Fetal Lung lung
10 chr1:168735000-168736400 Enhancers HepG2 liver
11 chr1:168735200-168737600 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr1:168735400-168736200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr1:168735400-168736200 Enhancers Stomach Mucosa stomach

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