Variant report

Variant rs2883526
Chromosome Location chr19:40372750-40372751
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:40361200-40374000 Weak transcription Pancreas Pancrea
2 chr19:40366200-40372800 Weak transcription Primary T helper naive cells fromperipheralblood blood
3 chr19:40367000-40373400 Weak transcription Fetal Stomach stomach
4 chr19:40369800-40375800 Weak transcription Rectal Mucosa Donor 29 rectum
5 chr19:40369800-40402600 Weak transcription Rectal Mucosa Donor 31 rectum
6 chr19:40369800-40404000 Weak transcription Colonic Mucosa Colon
7 chr19:40371200-40402800 Weak transcription Sigmoid Colon Sigmoid Colon
8 chr19:40371200-40404000 Weak transcription Primary T cells from cord blood blood
9 chr19:40371400-40391000 Weak transcription Fetal Intestine Small intestine
10 chr19:40372200-40372800 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr19:40372200-40372800 Enhancers Primary Natural Killer cells fromperipheralblood blood
12 chr19:40372200-40372800 Enhancers Dnd41 blood
13 chr19:40372200-40372800 Enhancers HepG2 liver
14 chr19:40372200-40372800 Enhancers K562 blood
15 chr19:40372200-40373000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr19:40372400-40372800 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
17 chr19:40372600-40372800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
18 chr19:40372600-40372800 Enhancers Primary T helper cells fromperipheralblood blood
19 chr19:40372600-40372800 Flanking Active TSS A549 lung

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