Variant report

Variant rs2257331
Chromosome Location chr6:31898285-31898286
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:31895800-31901200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr6:31896000-31898600 Enhancers Monocytes-CD14+_RO01746 blood
3 chr6:31896000-31901000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr6:31896000-31903400 Weak transcription Fetal Intestine Small intestine
5 chr6:31896200-31898600 Enhancers Placenta Placenta
6 chr6:31896800-31913000 Weak transcription Lung lung
7 chr6:31897200-31901200 Weak transcription Spleen Spleen
8 chr6:31897200-31911000 Weak transcription Small Intestine intestine
9 chr6:31897200-31913000 Weak transcription Adipose Nuclei Adipose
10 chr6:31898200-31898400 Enhancers Duodenum Mucosa Duodenum
11 chr6:31898200-31898600 Active TSS H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr6:31898200-31899000 Genic enhancers Liver Liver
13 chr6:31898200-31899000 Genic enhancers HepG2 liver

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