Variant report

Variant rs1937356
Chromosome Location chr1:151707920-151707921
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:151700800-151709800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr1:151702200-151709800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr1:151702600-151709600 Weak transcription Right Atrium heart
4 chr1:151702800-151712200 Weak transcription Stomach Mucosa stomach
5 chr1:151707200-151708000 Enhancers A549 lung
6 chr1:151707400-151708000 Enhancers ES-I3 Cell Line embryonic stem cell
7 chr1:151707400-151708000 Enhancers Hela-S3 cervix
8 chr1:151707600-151708000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
9 chr1:151707600-151708000 Enhancers Placenta Amnion Placenta Amnion
10 chr1:151707600-151709800 Weak transcription Liver Liver
11 chr1:151707800-151709400 Weak transcription Fetal Intestine Small intestine
12 chr1:151707800-151710200 Weak transcription Skeletal Muscle Female skeletal muscle
13 chr1:151707800-151712200 Weak transcription Pancreas Pancrea

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