Variant report

Variant rs2901695
Chromosome Location chr1:172961211-172961212
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172959000-172964200 Enhancers HSMM muscle
2 chr1:172959400-172964000 Enhancers NHDF-Ad bronchial
3 chr1:172959600-172964200 Enhancers HSMMtube muscle
4 chr1:172960000-172961400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
5 chr1:172960600-172962400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
6 chr1:172960600-172967000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:172960600-172974000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr1:172960800-172962000 Weak transcription Placenta Amnion Placenta Amnion
9 chr1:172960800-172962400 Weak transcription NH-A brain
10 chr1:172961000-172962400 Weak transcription Osteobl bone
11 chr1:172961000-172967400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
12 chr1:172961200-172962200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr1:172961200-172962400 Weak transcription Muscle Satellite Cultured Cells --
14 chr1:172961200-172962600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung

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