Variant report

Variant rs74121387
Chromosome Location chr1:168769673-168769674
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:168755600-168772800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr1:168768800-168770800 Enhancers Fetal Intestine Small intestine
3 chr1:168769000-168769800 Flanking Active TSS A549 lung
4 chr1:168769000-168771600 Enhancers Duodenum Mucosa Duodenum
5 chr1:168769000-168772000 Weak transcription ES-WA7 Cell Line embryonic stem cell
6 chr1:168769000-168773800 Enhancers Fetal Intestine Large intestine
7 chr1:168769200-168770000 Enhancers Pancreatic Islets Pancreatic Islet
8 chr1:168769200-168770200 Flanking Active TSS Liver Liver
9 chr1:168769200-168772600 Enhancers HepG2 liver
10 chr1:168769200-168774600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr1:168769400-168770000 Enhancers Fetal Kidney kidney
12 chr1:168769400-168770600 Enhancers Stomach Mucosa stomach
13 chr1:168769400-168773000 Enhancers Hela-S3 cervix
14 chr1:168769600-168770000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr1:168769600-168770000 Enhancers iPS-18 Cell Line embryonic stem cell
16 chr1:168769600-168770400 Enhancers Gastric stomach
17 chr1:168769600-168770600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
18 chr1:168769600-168770600 Enhancers Pancreas Pancrea

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