Variant report

Variant rs557486798
Chromosome Location chr8:11408814-11408815
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:11404000-11411000 Weak transcription Muscle Satellite Cultured Cells --
2 chr8:11404600-11418400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr8:11404800-11421800 Genic enhancers Primary B cells from peripheral blood blood
4 chr8:11405400-11409200 Weak transcription Primary Natural Killer cells fromperipheralblood blood
5 chr8:11405800-11409200 Genic enhancers Spleen Spleen
6 chr8:11406000-11417600 Genic enhancers Primary B cells from cord blood blood
7 chr8:11406600-11409400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
8 chr8:11406800-11410400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr8:11407000-11410800 Strong transcription Dnd41 blood
10 chr8:11407400-11409800 Enhancers HSMM muscle
11 chr8:11407600-11410400 Weak transcription Fetal Kidney kidney
12 chr8:11407800-11412000 Genic enhancers GM12878-XiMat blood
13 chr8:11407800-11412200 Weak transcription HUVEC blood vessel
14 chr8:11408200-11409400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
15 chr8:11408400-11410000 Enhancers Fetal Thymus thymus
16 chr8:11408800-11410200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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