Variant report

Variant rs1764594
Chromosome Location chr1:215013468-215013469
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:215002000-215019600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:215010400-215014200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr1:215010400-215017400 Enhancers NHDF-Ad bronchial
4 chr1:215010600-215013800 Enhancers Osteobl bone
5 chr1:215011000-215013600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr1:215011000-215013800 Enhancers NHLF lung
7 chr1:215011000-215014200 Enhancers Muscle Satellite Cultured Cells --
8 chr1:215011400-215014400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr1:215012000-215016000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr1:215012400-215019400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr1:215012600-215016400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr1:215012600-215021000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr1:215013000-215014200 Enhancers HSMM muscle
14 chr1:215013000-215015400 Weak transcription NH-A brain
15 chr1:215013000-215016600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
16 chr1:215013000-215021000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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