Variant report

Variant rs1357990
Chromosome Location chr7:17174023-17174024
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17170800-17177400 Weak transcription Dnd41 blood
2 chr7:17171000-17176600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr7:17171000-17182400 Weak transcription Stomach Mucosa stomach
4 chr7:17171200-17182200 Weak transcription Rectal Smooth Muscle rectum
5 chr7:17172600-17182200 Weak transcription Fetal Kidney kidney
6 chr7:17172800-17174600 Weak transcription Fetal Intestine Small intestine
7 chr7:17172800-17179000 Weak transcription NHLF lung
8 chr7:17173000-17174600 Enhancers HepG2 liver
9 chr7:17173800-17175000 Enhancers Primary T regulatory cells fromperipheralblood blood
10 chr7:17173800-17175000 Flanking Active TSS GM12878-XiMat blood
11 chr7:17173800-17176000 Enhancers Primary T helper memory cells from peripheral blood 2 blood
12 chr7:17173800-17181800 Enhancers Primary T helper 17 cells PMA-I stimulated --
13 chr7:17174000-17174200 Enhancers Primary T cells fromperipheralblood blood
14 chr7:17174000-17174400 Enhancers Primary T helper cells PMA-I stimulated --
15 chr7:17174000-17174600 Enhancers Primary T cells effector/memory enriched fromperipheralblood blood

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