Variant report

Variant rs529542794
Chromosome Location chr5:92522163-92522164
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:92519600-92522800 Enhancers NHDF-Ad bronchial
2 chr5:92521400-92522200 Enhancers HMEC breast
3 chr5:92521400-92522600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr5:92521400-92522800 Enhancers Osteobl bone
5 chr5:92521400-92523000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr5:92521400-92523600 Enhancers Muscle Satellite Cultured Cells --
7 chr5:92521600-92522400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr5:92521600-92522400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr5:92521600-92522400 Enhancers NH-A brain
10 chr5:92521600-92522400 Enhancers NHEK skin
11 chr5:92521600-92522600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr5:92521800-92522200 Enhancers Cortex derived primary cultured neurospheres brain
13 chr5:92521800-92522200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
14 chr5:92521800-92522200 Enhancers NHLF lung
15 chr5:92521800-92522400 Enhancers HUVEC blood vessel
16 chr5:92521800-92522600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr5:92521800-92528000 Weak transcription Fetal Kidney kidney
18 chr5:92522000-92524600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
19 chr5:92522000-92524600 Weak transcription HSMM muscle
20 chr5:92522000-92524800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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