Variant report

Variant rs1724988
Chromosome Location chr1:56616981-56616982
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:56605800-56622600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr1:56611200-56617600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr1:56612800-56618600 Weak transcription Fetal Thymus thymus
4 chr1:56615000-56617400 Enhancers NHDF-Ad bronchial
5 chr1:56615200-56618600 Weak transcription HUVEC blood vessel
6 chr1:56615400-56617600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr1:56616000-56617400 Enhancers Adipose Nuclei Adipose
8 chr1:56616000-56617600 Enhancers Psoas Muscle Psoas
9 chr1:56616000-56618800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
10 chr1:56616400-56617000 Enhancers Fetal Muscle Leg muscle
11 chr1:56616400-56617400 Enhancers Fetal Stomach stomach
12 chr1:56616600-56618000 Enhancers Fetal Intestine Large intestine
13 chr1:56616800-56617200 Weak transcription Fetal Adrenal Gland Adrenal Gland
14 chr1:56616800-56617400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
15 chr1:56616800-56617400 Enhancers Fetal Intestine Small intestine
16 chr1:56616800-56617400 Enhancers Fetal Lung lung
17 chr1:56616800-56617400 Enhancers NHLF lung
18 chr1:56616800-56617600 Enhancers Liver Liver

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