Variant report

Variant rs6685445
Chromosome Location chr1:71172978-71172979
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:71171800-71173000 Active TSS ES-I3 Cell Line embryonic stem cell
2 chr1:71171800-71173000 Active TSS iPS-15b Cell Line embryonic stem cell
3 chr1:71171800-71173000 Active TSS Fetal Kidney kidney
4 chr1:71171800-71173200 Active TSS Pancreatic Islets Pancreatic Islet
5 chr1:71172000-71173000 Active TSS HUES48 Cell Line embryonic stem cell
6 chr1:71172000-71173000 Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr1:71172000-71173000 Active TSS Right Atrium heart
8 chr1:71172000-71173200 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr1:71172200-71173000 Active TSS Fetal Lung lung
10 chr1:71172400-71173000 Active TSS HUES6 Cell Line embryonic stem cell
11 chr1:71172600-71173000 Flanking Active TSS Brain Hippocampus Middle brain
12 chr1:71172600-71173000 Weak transcription Rectal Smooth Muscle rectum
13 chr1:71172600-71173000 Flanking Active TSS Stomach Smooth Muscle stomach
14 chr1:71172600-71173000 Weak transcription HSMM muscle
15 chr1:71172600-71173000 Flanking Active TSS NHDF-Ad bronchial
16 chr1:71172800-71173000 Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr1:71172800-71173000 Flanking Active TSS Muscle Satellite Cultured Cells --
18 chr1:71172800-71173000 Flanking Active TSS Brain Germinal Matrix brain
19 chr1:71172800-71173000 Flanking Active TSS Brain Substantia Nigra brain
20 chr1:71172800-71173000 Bivalent Enhancer Fetal Heart heart
21 chr1:71172800-71173200 Weak transcription Colon Smooth Muscle Colon
22 chr1:71172800-71173200 Enhancers Fetal Stomach stomach

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