Variant report

Variant rs9392543
Chromosome Location chr6:452291-452292
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:443200-453200 Weak transcription Right Atrium heart
2 chr6:448000-452600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr6:449000-455000 Weak transcription Primary T cells from cord blood blood
4 chr6:449200-454600 Weak transcription Primary T helper cells PMA-I stimulated --
5 chr6:449400-454800 Weak transcription Primary T killer naive cells fromperipheralblood blood
6 chr6:449800-456400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
7 chr6:450400-452600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr6:450400-456400 Weak transcription H1 Cell Line embryonic stem cell
9 chr6:451600-452400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr6:451800-452600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr6:452000-452600 Enhancers Adipose Nuclei Adipose
12 chr6:452000-453000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr6:452000-453000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr6:452000-453400 Enhancers Osteobl bone
15 chr6:452000-453600 Bivalent Enhancer Fetal Muscle Leg muscle
16 chr6:452000-453600 Enhancers NHDF-Ad bronchial
17 chr6:452000-453800 Bivalent Enhancer Fetal Muscle Trunk muscle

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