Variant report

Variant rs13228635
Chromosome Location chr7:12844881-12844882
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:12839000-12845600 Weak transcription Sigmoid Colon Sigmoid Colon
2 chr7:12841000-12845000 Weak transcription Right Atrium heart
3 chr7:12842400-12845200 Weak transcription iPS-20b Cell Line embryonic stem cell
4 chr7:12842600-12848800 Weak transcription iPS-15b Cell Line embryonic stem cell
5 chr7:12842600-12849200 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr7:12842800-12845400 Weak transcription Hela-S3 cervix
7 chr7:12843000-12845000 Weak transcription HMEC breast
8 chr7:12844200-12845000 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr7:12844200-12845200 Weak transcription Fetal Intestine Small intestine
10 chr7:12844200-12845200 Enhancers K562 blood
11 chr7:12844800-12845600 Enhancers ES-I3 Cell Line embryonic stem cell
12 chr7:12844800-12845600 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr7:12844800-12845600 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr7:12844800-12845800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr7:12844800-12845800 Enhancers Fetal Intestine Large intestine
16 chr7:12844800-12846000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr7:12844800-12846000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr7:12844800-12846000 Enhancers NHEK skin
19 chr7:12844800-12846800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links