Variant report

Variant rs10102013
Chromosome Location chr8:129801067-129801068
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:129784000-129809800 Weak transcription Dnd41 blood
2 chr8:129797600-129801400 Enhancers NHDF-Ad bronchial
3 chr8:129798200-129801200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
4 chr8:129798200-129801200 Enhancers HMEC breast
5 chr8:129798400-129801800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
6 chr8:129798600-129801200 Enhancers HUES6 Cell Line embryonic stem cell
7 chr8:129798600-129802400 Enhancers ES-I3 Cell Line embryonic stem cell
8 chr8:129798800-129801400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr8:129798800-129801400 Enhancers NHEK skin
10 chr8:129799200-129801400 Enhancers Muscle Satellite Cultured Cells --
11 chr8:129799400-129801200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr8:129799600-129801200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr8:129800600-129801200 Enhancers ES-WA7 Cell Line embryonic stem cell
14 chr8:129801000-129801400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr8:129801000-129805200 Weak transcription HUVEC blood vessel
16 chr8:129801000-129806000 Weak transcription HSMM muscle
17 chr8:129801000-129806600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung

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