Variant report

Variant rs12971036
Chromosome Location chr18:13177395-13177396
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:13173000-13177400 Enhancers Fetal Thymus thymus
2 chr18:13174000-13182600 Enhancers HepG2 liver
3 chr18:13176200-13181800 Weak transcription Gastric stomach
4 chr18:13176600-13177400 Active TSS Colonic Mucosa Colon
5 chr18:13176600-13177400 Enhancers Fetal Intestine Small intestine
6 chr18:13176600-13177400 Flanking Active TSS Rectal Mucosa Donor 31 rectum
7 chr18:13176600-13177600 Flanking Active TSS Duodenum Mucosa Duodenum
8 chr18:13176800-13177400 Flanking Active TSS Primary T helper 17 cells PMA-I stimulated --
9 chr18:13176800-13177400 Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr18:13176800-13177400 Active TSS Rectal Smooth Muscle rectum
11 chr18:13177000-13177400 Flanking Active TSS Primary T cells fromperipheralblood blood
12 chr18:13177000-13177400 Enhancers Primary T cells effector/memory enriched fromperipheralblood blood
13 chr18:13177000-13177400 Active TSS Duodenum Smooth Muscle Duodenum
14 chr18:13177000-13178600 Weak transcription Small Intestine intestine
15 chr18:13177200-13177400 Active TSS Primary T regulatory cells fromperipheralblood blood
16 chr18:13177200-13177400 Flanking Active TSS Liver Liver
17 chr18:13177200-13177600 Active TSS Rectal Mucosa Donor 29 rectum
18 chr18:13177200-13178600 Weak transcription Thymus Thymus
19 chr18:13177200-13182600 Enhancers Fetal Intestine Large intestine

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