Variant report

Variant rs7067690
Chromosome Location chr10:1350605-1350606
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:1329200-1352600 Weak transcription Right Atrium heart
2 chr10:1340200-1352800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr10:1344200-1351400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr10:1350400-1350800 Enhancers HSMMtube muscle
5 chr10:1350400-1351600 Enhancers iPS-18 Cell Line embryonic stem cell
6 chr10:1350400-1351800 Enhancers iPS-20b Cell Line embryonic stem cell
7 chr10:1350400-1352000 Enhancers ES-I3 Cell Line embryonic stem cell
8 chr10:1350400-1354000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr10:1350400-1354400 Enhancers H1 Cell Line embryonic stem cell
10 chr10:1350400-1354400 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
11 chr10:1350600-1350800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr10:1350600-1350800 Bivalent Enhancer Fetal Lung lung
13 chr10:1350600-1350800 Flanking Active TSS NH-A brain
14 chr10:1350600-1351200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
15 chr10:1350600-1351400 Enhancers HUES6 Cell Line embryonic stem cell
16 chr10:1350600-1352200 Enhancers H9 Cell Line embryonic stem cell
17 chr10:1350600-1362200 Weak transcription Aorta Aorta

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