Variant report

Variant rs12755391
Chromosome Location chr1:168721591-168721592
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:168711200-168724200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr1:168720000-168721600 Enhancers Colon Smooth Muscle Colon
3 chr1:168720000-168721600 Enhancers Hela-S3 cervix
4 chr1:168720000-168722000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr1:168720200-168721800 Enhancers Rectal Smooth Muscle rectum
6 chr1:168720400-168722000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr1:168720600-168722200 Enhancers Rectal Mucosa Donor 31 rectum
8 chr1:168720600-168722600 Enhancers Fetal Lung lung
9 chr1:168720800-168722000 Flanking Active TSS A549 lung
10 chr1:168720800-168722000 Bivalent Enhancer HepG2 liver
11 chr1:168720800-168724000 Weak transcription Fetal Heart heart
12 chr1:168721000-168723600 Weak transcription Fetal Kidney kidney
13 chr1:168721000-168723800 Weak transcription Placenta Amnion Placenta Amnion
14 chr1:168721200-168725400 Weak transcription Pancreatic Islets Pancreatic Islet
15 chr1:168721400-168722000 Enhancers Stomach Mucosa stomach
16 chr1:168721400-168725200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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