Variant report

Variant rs2804098
Chromosome Location chr10:1360615-1360616
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:1350600-1362200 Weak transcription Aorta Aorta
2 chr10:1354200-1369400 Weak transcription H9 Cell Line embryonic stem cell
3 chr10:1355000-1387800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr10:1358800-1369200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr10:1358800-1370200 Weak transcription Fetal Brain Female brain
6 chr10:1359200-1363000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr10:1359200-1367000 Weak transcription Brain Substantia Nigra brain
8 chr10:1359400-1362200 Weak transcription iPS-18 Cell Line embryonic stem cell
9 chr10:1359400-1362200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr10:1360400-1360800 Enhancers HSMMtube muscle
11 chr10:1360600-1360800 Enhancers Brain Cingulate Gyrus brain
12 chr10:1360600-1360800 Bivalent Enhancer Brain Inferior Temporal Lobe brain

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