Variant report

Variant rs6788891
Chromosome Location chr3:100417574-100417575
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100414400-100417600 Enhancers HSMMtube muscle
2 chr3:100415200-100418200 Enhancers Liver Liver
3 chr3:100415200-100418600 Enhancers HepG2 liver
4 chr3:100415600-100420400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr3:100415600-100420400 Weak transcription NHEK skin
6 chr3:100415800-100418400 Enhancers Fetal Intestine Large intestine
7 chr3:100415800-100420200 Weak transcription HMEC breast
8 chr3:100415800-100420800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr3:100415800-100424600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr3:100416000-100417800 Enhancers Duodenum Mucosa Duodenum
11 chr3:100416200-100419600 Weak transcription K562 blood
12 chr3:100416400-100418600 Enhancers Fetal Intestine Small intestine
13 chr3:100416800-100418000 Enhancers Fetal Lung lung
14 chr3:100417000-100418800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
15 chr3:100417000-100423600 Weak transcription Esophagus oesophagus
16 chr3:100417200-100417600 Flanking Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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