Variant report

Variant rs112641239
Chromosome Location chr2:209087538-209087539
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:209086600-209087600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr2:209086800-209087600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
3 chr2:209086800-209087600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr2:209086800-209087600 Enhancers K562 blood
5 chr2:209086800-209087600 Enhancers NHEK skin
6 chr2:209086800-209088200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:209086800-209088200 Enhancers HMEC breast
8 chr2:209087000-209087600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr2:209087000-209087600 Enhancers Osteobl bone
10 chr2:209087000-209087800 Enhancers Muscle Satellite Cultured Cells --
11 chr2:209087200-209087600 Enhancers NH-A brain
12 chr2:209087400-209089600 Weak transcription HSMM muscle
13 chr2:209087400-209100000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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