Variant report

Variant rs181775969
Chromosome Location chr1:104066192-104066193
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:104043200-104067400 Weak transcription Aorta Aorta
2 chr1:104050000-104067400 Weak transcription Left Ventricle heart
3 chr1:104054400-104066200 Weak transcription Psoas Muscle Psoas
4 chr1:104059800-104067400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr1:104059800-104067400 Weak transcription Osteobl bone
6 chr1:104060400-104067400 Weak transcription Fetal Heart heart
7 chr1:104060600-104067200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr1:104060600-104067400 Weak transcription HUVEC blood vessel
9 chr1:104061000-104067400 Weak transcription GM12878-XiMat blood
10 chr1:104062400-104067400 Weak transcription Right Ventricle heart
11 chr1:104064200-104067200 Weak transcription Hela-S3 cervix
12 chr1:104064800-104067400 Weak transcription Fetal Adrenal Gland Adrenal Gland
13 chr1:104065000-104067400 Weak transcription Pancreas Pancrea
14 chr1:104065200-104067800 Enhancers Fetal Intestine Large intestine
15 chr1:104065400-104066200 Weak transcription Fetal Intestine Small intestine
16 chr1:104065400-104066600 Weak transcription Skeletal Muscle Female skeletal muscle
17 chr1:104065800-104066400 Enhancers Skeletal Muscle Male skeletal muscle
18 chr1:104065800-104067800 Weak transcription Fetal Stomach stomach

Quick Search:


  
Input of quick search could be:

what's new

Quick links