Variant report

Variant rs368407258
Chromosome Location chr19:41340076-41340077
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:41330200-41349400 Weak transcription Right Ventricle heart
2 chr19:41333600-41349400 Weak transcription Left Ventricle heart
3 chr19:41336400-41340200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr19:41336400-41340800 Enhancers Fetal Intestine Large intestine
5 chr19:41336600-41340800 Enhancers Fetal Intestine Small intestine
6 chr19:41337200-41340200 Enhancers Placenta Placenta
7 chr19:41337400-41340200 Enhancers Primary monocytes fromperipheralblood blood
8 chr19:41337400-41340200 Enhancers Primary hematopoietic stem cells short term culture blood
9 chr19:41337400-41340200 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr19:41338600-41344000 Weak transcription A549 lung
11 chr19:41338800-41341000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr19:41339600-41349400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr19:41339800-41340200 Flanking Active TSS K562 blood
14 chr19:41340000-41340800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --

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