Variant report

Variant rs6988241
Chromosome Location chr8:11835911-11835912
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:11833000-11836600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr8:11834400-11836000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
3 chr8:11835000-11836000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr8:11835000-11836000 Enhancers HUES48 Cell Line embryonic stem cell
5 chr8:11835000-11836200 Bivalent Enhancer Fetal Stomach stomach
6 chr8:11835000-11836400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chr8:11835200-11836000 Enhancers HUES6 Cell Line embryonic stem cell
8 chr8:11835200-11836200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr8:11835200-11836200 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr8:11835400-11836200 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr8:11835400-11836200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr8:11835600-11836000 Bivalent Enhancer Fetal Muscle Trunk muscle
13 chr8:11835600-11836000 Enhancers NH-A brain
14 chr8:11835600-11836400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr8:11835600-11836600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr8:11835800-11836000 Bivalent Enhancer ES-WA7 Cell Line embryonic stem cell

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