Variant report

Variant rs11722584
Chromosome Location chr4:187055207-187055208
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:187039200-187065000 Weak transcription Fetal Brain Female brain
2 chr4:187040600-187058200 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr4:187045200-187058400 Weak transcription Rectal Mucosa Donor 31 rectum
4 chr4:187047200-187063200 Weak transcription Fetal Stomach stomach
5 chr4:187050600-187065000 Weak transcription Gastric stomach
6 chr4:187054000-187055600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr4:187054200-187055600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr4:187054200-187055600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr4:187054200-187055800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
10 chr4:187054200-187057800 Weak transcription Pancreas Pancrea
11 chr4:187054200-187058400 Weak transcription Fetal Lung lung
12 chr4:187054200-187065000 Weak transcription Fetal Kidney kidney
13 chr4:187054400-187058400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr4:187054400-187065000 Weak transcription Fetal Intestine Small intestine
15 chr4:187054600-187055600 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chr4:187054600-187055800 Weak transcription H1 Cell Line embryonic stem cell
17 chr4:187054600-187055800 Weak transcription HUES48 Cell Line embryonic stem cell
18 chr4:187054600-187056000 Weak transcription HUES6 Cell Line embryonic stem cell
19 chr4:187055000-187056200 Enhancers Primary B cells from peripheral blood blood
20 chr4:187055000-187065000 Weak transcription Fetal Intestine Large intestine
21 chr4:187055200-187056000 Flanking Active TSS GM12878-XiMat blood

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