Variant report

Variant rs16961607
Chromosome Location chr18:28852955-28852956
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:28848200-28854800 Weak transcription iPS-18 Cell Line embryonic stem cell
2 chr18:28849200-28853800 Weak transcription A549 lung
3 chr18:28849400-28854200 Weak transcription HMEC breast
4 chr18:28849400-28854800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr18:28849400-28854800 Weak transcription Hela-S3 cervix
6 chr18:28849400-28854800 Weak transcription NH-A brain
7 chr18:28849400-28855000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr18:28849600-28853800 Weak transcription HepG2 liver
9 chr18:28849600-28854200 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr18:28849600-28854200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr18:28849600-28854200 Weak transcription Rectal Mucosa Donor 31 rectum
12 chr18:28849800-28854200 Weak transcription NHEK skin
13 chr18:28849800-28855000 Weak transcription HUES6 Cell Line embryonic stem cell
14 chr18:28850000-28855000 Weak transcription Fetal Heart heart
15 chr18:28850000-28855000 Weak transcription Small Intestine intestine
16 chr18:28850200-28854800 Weak transcription Duodenum Mucosa Duodenum
17 chr18:28850200-28855000 Weak transcription Stomach Mucosa stomach
18 chr18:28850400-28853800 Weak transcription Fetal Intestine Small intestine
19 chr18:28850800-28853200 Weak transcription Fetal Intestine Large intestine
20 chr18:28850800-28853800 Weak transcription Liver Liver

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