Variant report

Variant rs12473749
Chromosome Location chr2:37385993-37385994
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:37384800-37386000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr2:37384800-37386000 Enhancers Brain Hippocampus Middle brain
3 chr2:37384800-37387200 Weak transcription Esophagus oesophagus
4 chr2:37385000-37386000 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr2:37385000-37386600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr2:37385000-37386600 Enhancers Brain Angular Gyrus brain
7 chr2:37385000-37386600 Enhancers Brain Cingulate Gyrus brain
8 chr2:37385000-37387200 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
9 chr2:37385000-37388400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr2:37385200-37386000 Bivalent Enhancer HepG2 liver
11 chr2:37385200-37386200 Weak transcription Primary T helper 17 cells PMA-I stimulated --
12 chr2:37385400-37386000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
13 chr2:37385800-37386000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
14 chr2:37385800-37386000 Enhancers Ovary ovary
15 chr2:37385800-37386200 Enhancers Cortex derived primary cultured neurospheres brain
16 chr2:37385800-37389000 Weak transcription Primary neutrophils fromperipheralblood blood

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