Variant report

Variant rs374849040
Chromosome Location chr4:187851439-187851440
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:187837200-187863800 Weak transcription Right Atrium heart
2 chr4:187840000-187853400 Weak transcription Fetal Kidney kidney
3 chr4:187842000-187852400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr4:187842600-187852200 Weak transcription HMEC breast
5 chr4:187846200-187851800 Weak transcription Osteobl bone
6 chr4:187846400-187853400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr4:187849000-187852000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr4:187850400-187852200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr4:187850600-187851800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr4:187850600-187852000 Weak transcription NHDF-Ad bronchial
11 chr4:187850800-187852200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr4:187850800-187852200 Weak transcription Muscle Satellite Cultured Cells --
13 chr4:187851200-187851800 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr4:187851200-187851800 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr4:187851400-187854000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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