Variant report

Variant rs10147816
Chromosome Location chr14:35137022-35137023
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:35134400-35139200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
2 chr14:35134600-35137800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr14:35135600-35137800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
4 chr14:35135600-35140800 Weak transcription Primary monocytes fromperipheralblood blood
5 chr14:35135800-35137200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr14:35135800-35140800 Weak transcription Monocytes-CD14+_RO01746 blood
7 chr14:35136000-35137400 Weak transcription Osteobl bone
8 chr14:35136000-35139600 Weak transcription Hela-S3 cervix
9 chr14:35136000-35144600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr14:35136200-35137800 Enhancers Placenta Placenta
11 chr14:35136400-35137400 Enhancers K562 blood
12 chr14:35136400-35137600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
13 chr14:35136400-35137600 Weak transcription HUVEC blood vessel
14 chr14:35136400-35137600 Weak transcription NHLF lung
15 chr14:35136400-35139200 Weak transcription A549 lung
16 chr14:35136800-35137400 Weak transcription Spleen Spleen
17 chr14:35137000-35137800 Enhancers Muscle Satellite Cultured Cells --
18 chr14:35137000-35138000 Enhancers NHDF-Ad bronchial

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