Variant report

Variant rs17023966
Chromosome Location chr2:39778628-39778629
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:39762200-39785000 Weak transcription HSMMtube muscle
2 chr2:39770800-39789600 Weak transcription Left Ventricle heart
3 chr2:39775800-39780400 Enhancers HepG2 liver
4 chr2:39776400-39779000 Enhancers Fetal Intestine Small intestine
5 chr2:39777000-39778800 Enhancers Fetal Heart heart
6 chr2:39777000-39779200 Enhancers HUVEC blood vessel
7 chr2:39777400-39778800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr2:39777600-39778800 Enhancers Muscle Satellite Cultured Cells --
9 chr2:39777600-39779200 Enhancers Hela-S3 cervix
10 chr2:39778000-39779000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
11 chr2:39778000-39788000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
12 chr2:39778400-39791800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links