Variant report

Variant rs2682862
Chromosome Location chr2:187602230-187602231
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr2:187596600-187611400 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
4 chr2:187596600-187626200 Weak transcription Stomach Smooth Muscle stomach
5 chr2:187598600-187621200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr2:187599600-187631000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr2:187600000-187602600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr2:187600000-187613200 Weak transcription Pancreas Pancrea
9 chr2:187600200-187602600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
10 chr2:187600200-187611000 Weak transcription Brain Angular Gyrus brain
11 chr2:187601800-187603400 ZNF genes & repeats Fetal Muscle Leg muscle
12 chr2:187601800-187603800 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell
13 chr2:187601800-187603800 ZNF genes & repeats Cortex derived primary cultured neurospheres brain
14 chr2:187601800-187604000 ZNF genes & repeats Ganglion Eminence derived primary cultured neurospheres brain
15 chr2:187602000-187602400 Weak transcription H1 Cell Line embryonic stem cell
16 chr2:187602200-187602400 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell

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