Variant report

Variant rs62173045
Chromosome Location chr2:187600335-187600336
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:187592200-187618600 Weak transcription Osteobl bone
2 chr2:187595200-187602600 Weak transcription Brain Anterior Caudate brain
3 chr2:187596000-187600400 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr2:187596600-187611400 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
5 chr2:187596600-187626200 Weak transcription Stomach Smooth Muscle stomach
6 chr2:187597400-187600400 Enhancers Brain Inferior Temporal Lobe brain
7 chr2:187598600-187621200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr2:187599000-187601800 Weak transcription Ovary ovary
9 chr2:187599200-187601200 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr2:187599600-187601200 Enhancers HUES6 Cell Line embryonic stem cell
11 chr2:187599600-187631000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr2:187599800-187601200 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr2:187600000-187600400 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr2:187600000-187600600 Active TSS ES-WA7 Cell Line embryonic stem cell
15 chr2:187600000-187601200 Enhancers ES-I3 Cell Line embryonic stem cell
16 chr2:187600000-187601800 Weak transcription Cortex derived primary cultured neurospheres brain
17 chr2:187600000-187602200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
18 chr2:187600000-187602600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
19 chr2:187600000-187613200 Weak transcription Pancreas Pancrea
20 chr2:187600200-187600600 Flanking Active TSS HUES48 Cell Line embryonic stem cell
21 chr2:187600200-187601800 Weak transcription H1 Cell Line embryonic stem cell
22 chr2:187600200-187602600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
23 chr2:187600200-187611000 Weak transcription Brain Angular Gyrus brain

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