Variant report

Variant rs6746501
Chromosome Location chr2:209435825-209435826
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:209431200-209438000 Weak transcription Fetal Intestine Large intestine
2 chr2:209433800-209436000 Weak transcription Fetal Heart heart
3 chr2:209434800-209436200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
4 chr2:209435200-209437200 Flanking Active TSS K562 blood
5 chr2:209435400-209436000 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
6 chr2:209435400-209436000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr2:209435400-209436200 Enhancers HUES48 Cell Line embryonic stem cell
8 chr2:209435400-209436200 Enhancers Fetal Adrenal Gland Adrenal Gland
9 chr2:209435600-209436000 Flanking Active TSS Colon Smooth Muscle Colon
10 chr2:209435800-209436200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
11 chr2:209435800-209436200 Flanking Active TSS Duodenum Mucosa Duodenum
12 chr2:209435800-209436200 Enhancers Rectal Mucosa Donor 29 rectum
13 chr2:209435800-209436200 Enhancers Rectal Mucosa Donor 31 rectum
14 chr2:209435800-209436400 Active TSS ES-I3 Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links