Variant report

Variant rs2389735
Chromosome Location chr7:17175600-17175601
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr7:17172800-17179000 Weak transcription NHLF lung
7 chr7:17173800-17176000 Enhancers Primary T helper memory cells from peripheral blood 2 blood
8 chr7:17173800-17181800 Enhancers Primary T helper 17 cells PMA-I stimulated --
9 chr7:17174200-17175600 Enhancers Primary T helper memory cells from peripheral blood 1 blood
10 chr7:17174200-17178200 Weak transcription Primary T cells fromperipheralblood blood
11 chr7:17174400-17176800 Weak transcription Primary T helper cells PMA-I stimulated --
12 chr7:17174600-17176600 Weak transcription Primary T helper naive cells from peripheral blood blood
13 chr7:17174600-17177800 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
14 chr7:17174600-17178200 Weak transcription HepG2 liver
15 chr7:17175000-17177400 Weak transcription Primary T regulatory cells fromperipheralblood blood
16 chr7:17175200-17178600 Weak transcription GM12878-XiMat blood
17 chr7:17175400-17181800 Enhancers Primary T helper cells fromperipheralblood blood
18 chr7:17175600-17177600 Weak transcription Primary T helper memory cells from peripheral blood 1 blood

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