Variant report

Variant rs1680499
Chromosome Location chr3:100381957-100381958
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100370200-100383800 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
2 chr3:100373800-100382000 Strong transcription Fetal Intestine Large intestine
3 chr3:100373800-100385400 Strong transcription Liver Liver
4 chr3:100379600-100383200 Weak transcription Duodenum Mucosa Duodenum
5 chr3:100379800-100384200 Weak transcription Fetal Intestine Small intestine
6 chr3:100381000-100382000 Enhancers K562 blood
7 chr3:100381000-100383800 Weak transcription Primary T helper 17 cells PMA-I stimulated --
8 chr3:100381200-100382200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr3:100381400-100382000 Enhancers Primary T cells from cord blood blood
10 chr3:100381400-100382000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr3:100381400-100382200 Enhancers HUES48 Cell Line embryonic stem cell
12 chr3:100381600-100382200 Enhancers Primary neutrophils fromperipheralblood blood

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