Variant report

Variant rs10147236
Chromosome Location chr14:69107143-69107144
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:69095600-69107400 Enhancers Fetal Stomach stomach
2 chr14:69095800-69107800 Weak transcription Fetal Brain Female brain
3 chr14:69100800-69107800 Weak transcription Primary B cells from cord blood blood
4 chr14:69105000-69107200 Weak transcription NHEK skin
5 chr14:69105000-69121600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr14:69105600-69113000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr14:69105800-69113200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr14:69106000-69117000 Weak transcription Fetal Intestine Large intestine
9 chr14:69106200-69112800 Weak transcription H9 Cell Line embryonic stem cell
10 chr14:69106200-69115600 Weak transcription Esophagus oesophagus
11 chr14:69106400-69118200 Weak transcription Placenta Amnion Placenta Amnion
12 chr14:69106400-69118400 Weak transcription Spleen Spleen
13 chr14:69106600-69107400 Weak transcription Duodenum Smooth Muscle Duodenum
14 chr14:69106600-69107600 Weak transcription Colon Smooth Muscle Colon
15 chr14:69106600-69111000 Weak transcription Fetal Heart heart
16 chr14:69106600-69111800 Weak transcription Rectal Smooth Muscle rectum
17 chr14:69106800-69116000 Weak transcription Ovary ovary
18 chr14:69107000-69107200 Enhancers Small Intestine intestine
19 chr14:69107000-69110600 Weak transcription Right Ventricle heart

Quick Search:


  
Input of quick search could be:

what's new

Quick links