Variant report

Variant rs531327
Chromosome Location chr1:193291934-193291935
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:193289200-193292200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr1:193289200-193292400 Enhancers NHEK skin
3 chr1:193289400-193292400 Enhancers HMEC breast
4 chr1:193290400-193292200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr1:193290400-193292200 Enhancers NH-A brain
6 chr1:193290400-193292400 Enhancers NHDF-Ad bronchial
7 chr1:193290400-193292400 Enhancers Osteobl bone
8 chr1:193290400-193292800 Enhancers Muscle Satellite Cultured Cells --
9 chr1:193290600-193292400 Enhancers HUVEC blood vessel
10 chr1:193290800-193292000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr1:193291000-193292600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr1:193291200-193292200 Enhancers NHLF lung
13 chr1:193291400-193292200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr1:193291400-193294800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
15 chr1:193291600-193292000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr1:193291800-193292400 Genic enhancers HSMM muscle

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