Variant report

Variant rs371856103
Chromosome Location chr6:185882-185883
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:178400-192200 Weak transcription Right Atrium heart
2 chr6:179600-191800 Enhancers Primary B cells from peripheral blood blood
3 chr6:180200-186600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr6:180200-190800 Enhancers Primary B cells from cord blood blood
5 chr6:180800-186800 Weak transcription Primary hematopoietic stem cells blood
6 chr6:181000-194800 Weak transcription Spleen Spleen
7 chr6:181200-194400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
8 chr6:181400-188800 Weak transcription Primary T killer naive cells fromperipheralblood blood
9 chr6:181800-188800 Weak transcription Primary T helper cells fromperipheralblood blood
10 chr6:183200-187800 Enhancers Fetal Thymus thymus
11 chr6:183600-188000 Enhancers Thymus Thymus
12 chr6:184600-188800 Weak transcription Primary T cells from cord blood blood
13 chr6:184800-186400 Weak transcription GM12878-XiMat blood
14 chr6:184800-188800 Weak transcription Primary Natural Killer cells fromperipheralblood blood
15 chr6:184800-190600 Weak transcription Primary hematopoietic stem cells short term culture blood
16 chr6:184800-193200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
17 chr6:185600-186000 Bivalent Enhancer HepG2 liver
18 chr6:185800-188000 Enhancers Fetal Intestine Large intestine

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