Variant report

Variant rs2014498
Chromosome Location chr2:37386076-37386077
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:37384800-37387200 Weak transcription Esophagus oesophagus
2 chr2:37385000-37386600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr2:37385000-37386600 Enhancers Brain Angular Gyrus brain
4 chr2:37385000-37386600 Enhancers Brain Cingulate Gyrus brain
5 chr2:37385000-37387200 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
6 chr2:37385000-37388400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr2:37385200-37386200 Weak transcription Primary T helper 17 cells PMA-I stimulated --
8 chr2:37385800-37386200 Enhancers Cortex derived primary cultured neurospheres brain
9 chr2:37385800-37389000 Weak transcription Primary neutrophils fromperipheralblood blood
10 chr2:37386000-37386200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr2:37386000-37386200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr2:37386000-37386200 Enhancers Breast Myoepithelial Primary Cells Breast

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