Variant report

Variant rs10875696
Chromosome Location chr12:48301383-48301384
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:48299600-48301600 Weak transcription Placenta Placenta
2 chr12:48299600-48301800 Weak transcription Liver Liver
3 chr12:48299600-48303800 Weak transcription Adipose Nuclei Adipose
4 chr12:48299600-48303800 Weak transcription Small Intestine intestine
5 chr12:48299600-48304200 Weak transcription Placenta Amnion Placenta Amnion
6 chr12:48299800-48303400 Weak transcription NHEK skin
7 chr12:48299800-48304000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr12:48300000-48301600 Weak transcription Fetal Intestine Small intestine
9 chr12:48300000-48301800 Weak transcription Rectal Mucosa Donor 29 rectum
10 chr12:48300000-48303200 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr12:48300000-48303600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr12:48300000-48303600 Weak transcription HMEC breast
13 chr12:48300000-48307200 Enhancers Rectal Mucosa Donor 31 rectum
14 chr12:48300200-48301800 Weak transcription Colonic Mucosa Colon
15 chr12:48301000-48302400 Enhancers Duodenum Mucosa Duodenum
16 chr12:48301000-48303800 Weak transcription Sigmoid Colon Sigmoid Colon
17 chr12:48301200-48301400 Enhancers Pancreatic Islets Pancreatic Islet
18 chr12:48301200-48301600 Weak transcription Fetal Intestine Large intestine
19 chr12:48301200-48303600 Enhancers HepG2 liver

Quick Search:


  
Input of quick search could be:

what's new

Quick links