Variant report

Variant rs34096229
Chromosome Location chr7:17070748-17070749
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17050600-17071800 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
2 chr7:17063000-17074800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr7:17066000-17070800 Enhancers Primary T helper 17 cells PMA-I stimulated --
4 chr7:17068000-17077800 Weak transcription Placenta Placenta
5 chr7:17068400-17071800 Weak transcription Fetal Lung lung
6 chr7:17069000-17071000 Enhancers Primary hematopoietic stem cells short term culture blood
7 chr7:17069600-17071000 Enhancers HUVEC blood vessel
8 chr7:17070200-17073000 Weak transcription Adipose Nuclei Adipose
9 chr7:17070200-17077600 Weak transcription Duodenum Mucosa Duodenum
10 chr7:17070400-17071400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr7:17070400-17071400 Weak transcription Primary Natural Killer cells fromperipheralblood blood
12 chr7:17070600-17071600 Weak transcription Primary monocytes fromperipheralblood blood
13 chr7:17070600-17071600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
14 chr7:17070600-17072200 Enhancers Monocytes-CD14+_RO01746 blood
15 chr7:17070600-17081000 Weak transcription Primary T regulatory cells fromperipheralblood blood

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