Variant report

Variant rs733874
Chromosome Location chr11:17531831-17531832
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:17516800-17553000 Weak transcription Stomach Mucosa stomach
2 chr11:17525400-17533600 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr11:17526200-17539400 Weak transcription Pancreas Pancrea
4 chr11:17526600-17536600 Weak transcription Brain Substantia Nigra brain
5 chr11:17526600-17537200 Weak transcription Brain Cingulate Gyrus brain
6 chr11:17527600-17549200 Strong transcription Duodenum Mucosa Duodenum
7 chr11:17528800-17544000 Weak transcription Gastric stomach
8 chr11:17529800-17532400 Enhancers Spleen Spleen
9 chr11:17529800-17548600 Strong transcription Rectal Mucosa Donor 29 rectum
10 chr11:17530200-17533200 Weak transcription Left Ventricle heart
11 chr11:17530600-17532200 Genic enhancers Fetal Intestine Small intestine
12 chr11:17530600-17533200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr11:17530600-17536600 Weak transcription Colon Smooth Muscle Colon
14 chr11:17530800-17532800 Weak transcription Sigmoid Colon Sigmoid Colon
15 chr11:17530800-17533000 Weak transcription Psoas Muscle Psoas
16 chr11:17530800-17539800 Weak transcription ES-I3 Cell Line embryonic stem cell
17 chr11:17531200-17536000 Strong transcription Rectal Mucosa Donor 31 rectum
18 chr11:17531400-17532200 Enhancers Fetal Muscle Trunk muscle
19 chr11:17531600-17532200 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
20 chr11:17531600-17547200 Strong transcription Fetal Intestine Large intestine
21 chr11:17531800-17532200 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
22 chr11:17531800-17532200 Strong transcription Colonic Mucosa Colon
23 chr11:17531800-17552400 Weak transcription Pancreatic Islets Pancreatic Islet

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