Variant report

Variant rs4927306
Chromosome Location chr1:56613052-56613053
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:56604400-56613600 Weak transcription HUVEC blood vessel
2 chr1:56605800-56622600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr1:56610800-56613600 Weak transcription Fetal Intestine Small intestine
4 chr1:56611000-56613600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr1:56611200-56617600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr1:56611400-56613600 Enhancers Fetal Kidney kidney
7 chr1:56611400-56613600 Enhancers NHDF-Ad bronchial
8 chr1:56611400-56613800 Enhancers Fetal Stomach stomach
9 chr1:56612000-56613200 Enhancers Muscle Satellite Cultured Cells --
10 chr1:56612000-56613400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr1:56612600-56613600 Weak transcription Rectal Smooth Muscle rectum
12 chr1:56612600-56615600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
13 chr1:56612600-56616000 Weak transcription Psoas Muscle Psoas
14 chr1:56612800-56616400 Weak transcription Fetal Muscle Leg muscle
15 chr1:56612800-56616800 Weak transcription Fetal Lung lung
16 chr1:56612800-56618600 Weak transcription Fetal Thymus thymus
17 chr1:56613000-56613400 Weak transcription Fetal Intestine Large intestine
18 chr1:56613000-56616000 Weak transcription Adipose Nuclei Adipose

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