Variant report

Variant rs6506906
Chromosome Location chr18:28850277-28850278
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:28847600-28850400 Enhancers Fetal Intestine Small intestine
2 chr18:28847800-28850800 Enhancers Fetal Intestine Large intestine
3 chr18:28848200-28854800 Weak transcription iPS-18 Cell Line embryonic stem cell
4 chr18:28848800-28850800 Enhancers Liver Liver
5 chr18:28849200-28853800 Weak transcription A549 lung
6 chr18:28849400-28854200 Weak transcription HMEC breast
7 chr18:28849400-28854800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr18:28849400-28854800 Weak transcription Hela-S3 cervix
9 chr18:28849400-28854800 Weak transcription NH-A brain
10 chr18:28849400-28855000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr18:28849600-28853800 Weak transcription HepG2 liver
12 chr18:28849600-28854200 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr18:28849600-28854200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr18:28849600-28854200 Weak transcription Rectal Mucosa Donor 31 rectum
15 chr18:28849800-28854200 Weak transcription NHEK skin
16 chr18:28849800-28855000 Weak transcription HUES6 Cell Line embryonic stem cell
17 chr18:28850000-28855000 Weak transcription Fetal Heart heart
18 chr18:28850000-28855000 Weak transcription Small Intestine intestine
19 chr18:28850200-28850800 Weak transcription GM12878-XiMat blood
20 chr18:28850200-28854800 Weak transcription Duodenum Mucosa Duodenum
21 chr18:28850200-28855000 Weak transcription Stomach Mucosa stomach

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