Variant report

Variant rs2814966
Chromosome Location chr6:34712232-34712233
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:34698000-34714000 Weak transcription Esophagus oesophagus
2 chr6:34706400-34712800 Enhancers HepG2 liver
3 chr6:34708400-34712800 Weak transcription A549 lung
4 chr6:34708600-34712600 Weak transcription Hela-S3 cervix
5 chr6:34708600-34713000 Weak transcription Rectal Mucosa Donor 29 rectum
6 chr6:34708600-34713200 Weak transcription Liver Liver
7 chr6:34709000-34712800 Weak transcription K562 blood
8 chr6:34711200-34712800 Enhancers NHEK skin
9 chr6:34711200-34713200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr6:34711200-34713200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr6:34711400-34714600 Enhancers Placenta Placenta
12 chr6:34711600-34712600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr6:34711600-34715400 Enhancers Fetal Intestine Large intestine
14 chr6:34712000-34712400 Weak transcription Placenta Amnion Placenta Amnion
15 chr6:34712200-34713000 Enhancers Duodenum Mucosa Duodenum
16 chr6:34712200-34713000 Enhancers Small Intestine intestine
17 chr6:34712200-34713000 Enhancers Stomach Mucosa stomach
18 chr6:34712200-34714800 Enhancers Fetal Intestine Small intestine

Quick Search:


  
Input of quick search could be:

what's new

Quick links