Variant report

Variant rs35111299
Chromosome Location chr4:149182594-149182595
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:149171000-149183600 Weak transcription Primary T helper cells fromperipheralblood blood
2 chr4:149175600-149195000 Weak transcription Rectal Mucosa Donor 29 rectum
3 chr4:149176400-149186400 Weak transcription Fetal Intestine Small intestine
4 chr4:149176400-149188400 Weak transcription Right Atrium heart
5 chr4:149177200-149184400 Weak transcription Pancreatic Islets Pancreatic Islet
6 chr4:149177200-149194800 Weak transcription Small Intestine intestine
7 chr4:149177400-149184600 Weak transcription HUVEC blood vessel
8 chr4:149177400-149184800 Weak transcription Sigmoid Colon Sigmoid Colon
9 chr4:149180000-149194600 Weak transcription Left Ventricle heart
10 chr4:149181200-149194800 Weak transcription Rectal Mucosa Donor 31 rectum
11 chr4:149182200-149182800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr4:149182400-149182600 ZNF genes & repeats Esophagus oesophagus
13 chr4:149182400-149182600 Enhancers Gastric stomach
14 chr4:149182400-149182600 ZNF genes & repeats Lung lung
15 chr4:149182400-149182800 ZNF genes & repeats Duodenum Mucosa Duodenum
16 chr4:149182400-149182800 Enhancers Placenta Placenta
17 chr4:149182400-149182800 ZNF genes & repeats Pancreas Pancrea
18 chr4:149182400-149183000 Enhancers Rectal Smooth Muscle rectum
19 chr4:149182400-149183200 Weak transcription Colon Smooth Muscle Colon
20 chr4:149182400-149183600 Enhancers Fetal Stomach stomach
21 chr4:149182400-149184000 Enhancers Fetal Kidney kidney

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