Variant report

Variant rs17270384
Chromosome Location chr7:17001683-17001684
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:16988600-17009000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr7:16991200-17002200 Weak transcription Stomach Mucosa stomach
3 chr7:16999600-17002600 Weak transcription HepG2 liver
4 chr7:16999600-17003400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr7:16999800-17002200 Enhancers Muscle Satellite Cultured Cells --
6 chr7:16999800-17002400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr7:16999800-17002400 Enhancers HSMM muscle
8 chr7:16999800-17002400 Enhancers Osteobl bone
9 chr7:16999800-17002600 Enhancers NHDF-Ad bronchial
10 chr7:17000800-17003400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
11 chr7:17000800-17003800 Enhancers Hela-S3 cervix
12 chr7:17001000-17002000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr7:17001000-17002000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr7:17001200-17002000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
15 chr7:17001200-17002200 Enhancers Colon Smooth Muscle Colon
16 chr7:17001400-17003000 Enhancers Fetal Stomach stomach
17 chr7:17001400-17003000 Enhancers Small Intestine intestine
18 chr7:17001400-17025600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
19 chr7:17001600-17001800 Flanking Active TSS HSMMtube muscle
20 chr7:17001600-17005600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links