Variant report

Variant rs11590691
Chromosome Location chr1:173095554-173095555
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:173091400-173096400 Weak transcription Small Intestine intestine
2 chr1:173092800-173096400 Enhancers Liver Liver
3 chr1:173092800-173097800 Weak transcription Pancreas Pancrea
4 chr1:173093000-173095600 Weak transcription HUES6 Cell Line embryonic stem cell
5 chr1:173093000-173096400 Enhancers HepG2 liver
6 chr1:173093000-173096600 Weak transcription A549 lung
7 chr1:173093000-173097400 Weak transcription Duodenum Mucosa Duodenum
8 chr1:173093000-173097400 Weak transcription Rectal Mucosa Donor 31 rectum
9 chr1:173093000-173097800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr1:173093000-173097800 Weak transcription HMEC breast
11 chr1:173093000-173101600 Weak transcription Placenta Amnion Placenta Amnion
12 chr1:173093000-173106600 Weak transcription HSMMtube muscle
13 chr1:173093200-173096200 Weak transcription Fetal Intestine Large intestine
14 chr1:173093200-173097600 Weak transcription NHEK skin
15 chr1:173093200-173097800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr1:173093400-173097800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr1:173093800-173096400 Weak transcription Fetal Intestine Small intestine
18 chr1:173093800-173096400 Weak transcription Stomach Mucosa stomach
19 chr1:173095200-173095800 Enhancers iPS-18 Cell Line embryonic stem cell

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