Variant report

Variant rs3923232
Chromosome Location chr8:49063360-49063361
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49051800-49065800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr8:49056200-49066000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr8:49058000-49064800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr8:49060200-49064200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr8:49061200-49064200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr8:49061400-49064200 Enhancers Muscle Satellite Cultured Cells --
7 chr8:49061600-49064200 Enhancers HSMM muscle
8 chr8:49061600-49064200 Enhancers Osteobl bone
9 chr8:49061800-49063600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr8:49061800-49064200 Enhancers NHDF-Ad bronchial
11 chr8:49061800-49064200 Enhancers NHEK skin
12 chr8:49061800-49064400 Enhancers HMEC breast
13 chr8:49062000-49064400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr8:49062200-49063400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
15 chr8:49062200-49064400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr8:49062400-49063800 Enhancers Fetal Intestine Small intestine
17 chr8:49062400-49064400 Enhancers Fetal Intestine Large intestine
18 chr8:49062600-49063600 Flanking Active TSS HepG2 liver
19 chr8:49062600-49063800 Enhancers NH-A brain
20 chr8:49062800-49064200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
21 chr8:49063000-49064000 Flanking Active TSS Liver Liver
22 chr8:49063000-49064400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
23 chr8:49063200-49064400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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