Variant report

Variant rs565203917
Chromosome Location chr18:28976790-28976791
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:28972800-28976800 Weak transcription Fetal Kidney kidney
2 chr18:28973600-28989400 Weak transcription Esophagus oesophagus
3 chr18:28975000-28983400 Enhancers Fetal Intestine Large intestine
4 chr18:28975400-28977000 Enhancers HepG2 liver
5 chr18:28976200-28983600 Enhancers Fetal Intestine Small intestine
6 chr18:28976400-28976800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr18:28976400-28977000 Flanking Active TSS Rectal Mucosa Donor 31 rectum
8 chr18:28976400-28977800 Enhancers Left Ventricle heart
9 chr18:28976600-28976800 Active TSS Adipose Nuclei Adipose
10 chr18:28976600-28977000 Enhancers ES-WA7 Cell Line embryonic stem cell
11 chr18:28976600-28977000 Flanking Active TSS Rectal Mucosa Donor 29 rectum
12 chr18:28976600-28977400 Enhancers Right Atrium heart
13 chr18:28976600-28977600 Enhancers Liver Liver
14 chr18:28976600-28977600 Enhancers Duodenum Mucosa Duodenum
15 chr18:28976600-28977600 Enhancers Stomach Mucosa stomach
16 chr18:28976600-28978400 Enhancers Small Intestine intestine
17 chr18:28976600-28979400 Enhancers Sigmoid Colon Sigmoid Colon

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