Variant report

Variant rs6980000
Chromosome Location chr7:7188476-7188477
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:7187600-7190800 Enhancers Fetal Intestine Large intestine
2 chr7:7187800-7190800 Enhancers Fetal Intestine Small intestine
3 chr7:7187800-7191000 Weak transcription Primary T helper cells PMA-I stimulated --
4 chr7:7188000-7189400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr7:7188200-7188600 Enhancers K562 blood
6 chr7:7188200-7188800 Enhancers Placenta Amnion Placenta Amnion
7 chr7:7188200-7189000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr7:7188200-7189200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr7:7188200-7189200 Enhancers HMEC breast
10 chr7:7188400-7188800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr7:7188400-7188800 Enhancers Primary hematopoietic stem cells short term culture blood
12 chr7:7188400-7189000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
13 chr7:7188400-7189000 Enhancers Duodenum Mucosa Duodenum
14 chr7:7188400-7189000 Enhancers HSMMtube muscle
15 chr7:7188400-7189200 Flanking Active TSS HepG2 liver
16 chr7:7188400-7189400 Enhancers Breast Myoepithelial Primary Cells Breast
17 chr7:7188400-7189600 Enhancers Placenta Placenta
18 chr7:7188400-7189600 Enhancers Stomach Mucosa stomach

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