Variant report

Variant rs17545292
Chromosome Location chr7:47818118-47818119
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:25 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:47814400-47823200 Enhancers HepG2 liver
2 chr7:47815000-47818600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr7:47815000-47821600 Weak transcription Aorta Aorta
4 chr7:47815800-47818800 Weak transcription Osteobl bone
5 chr7:47815800-47821600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr7:47815800-47821600 Weak transcription NHLF lung
7 chr7:47816200-47818400 Weak transcription HSMMtube muscle
8 chr7:47816200-47818600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr7:47816200-47826000 Weak transcription Right Atrium heart
10 chr7:47816400-47821400 Weak transcription Muscle Satellite Cultured Cells --
11 chr7:47817000-47819000 Enhancers HMEC breast
12 chr7:47817200-47846600 Weak transcription Left Ventricle heart
13 chr7:47817400-47818400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr7:47817400-47818800 Enhancers Liver Liver
15 chr7:47817400-47819000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
16 chr7:47817400-47819000 Enhancers NHEK skin
17 chr7:47817400-47819400 Enhancers Fetal Intestine Large intestine
18 chr7:47817400-47819400 Enhancers Fetal Intestine Small intestine
19 chr7:47817600-47818600 Weak transcription Duodenum Mucosa Duodenum
20 chr7:47817800-47818400 Enhancers A549 lung
21 chr7:47817800-47821600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
22 chr7:47817800-47824600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
23 chr7:47818000-47818400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
24 chr7:47818000-47821600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
25 chr7:47818000-47821600 Weak transcription NH-A brain

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