Variant report

Variant rs72917322
Chromosome Location chr3:100415803-100415804
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100413600-100416000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr3:100414400-100417600 Enhancers HSMMtube muscle
3 chr3:100414800-100416200 ZNF genes & repeats Fetal Intestine Small intestine
4 chr3:100414800-100416800 Weak transcription Fetal Lung lung
5 chr3:100415200-100418200 Enhancers Liver Liver
6 chr3:100415200-100418600 Enhancers HepG2 liver
7 chr3:100415600-100416000 Weak transcription HSMM muscle
8 chr3:100415600-100420400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr3:100415600-100420400 Weak transcription NHEK skin
10 chr3:100415800-100416000 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr3:100415800-100416000 Flanking Active TSS Duodenum Mucosa Duodenum
12 chr3:100415800-100416000 Bivalent Enhancer Esophagus oesophagus
13 chr3:100415800-100418400 Enhancers Fetal Intestine Large intestine
14 chr3:100415800-100420200 Weak transcription HMEC breast
15 chr3:100415800-100420800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr3:100415800-100424600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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