Variant report

Variant rs35727175
Chromosome Location chr3:100416129-100416130
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100414400-100417600 Enhancers HSMMtube muscle
2 chr3:100414800-100416200 ZNF genes & repeats Fetal Intestine Small intestine
3 chr3:100414800-100416800 Weak transcription Fetal Lung lung
4 chr3:100415200-100418200 Enhancers Liver Liver
5 chr3:100415200-100418600 Enhancers HepG2 liver
6 chr3:100415600-100420400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr3:100415600-100420400 Weak transcription NHEK skin
8 chr3:100415800-100418400 Enhancers Fetal Intestine Large intestine
9 chr3:100415800-100420200 Weak transcription HMEC breast
10 chr3:100415800-100420800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr3:100415800-100424600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr3:100416000-100416200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
13 chr3:100416000-100416200 Enhancers K562 blood
14 chr3:100416000-100416400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr3:100416000-100416400 Enhancers Placenta Placenta
16 chr3:100416000-100416600 Enhancers HSMM muscle
17 chr3:100416000-100417000 Enhancers Esophagus oesophagus
18 chr3:100416000-100417800 Enhancers Duodenum Mucosa Duodenum

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