Variant report

Variant rs141441041
Chromosome Location chr10:1418158-1418159
allele -/CG/GC
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:1404800-1419600 Weak transcription Right Atrium heart
2 chr10:1412200-1420000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr10:1412200-1421800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr10:1412400-1421400 Weak transcription iPS-15b Cell Line embryonic stem cell
5 chr10:1417400-1418200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr10:1417400-1421800 Weak transcription H1 Cell Line embryonic stem cell
7 chr10:1417800-1418200 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr10:1417800-1418200 ZNF genes & repeats iPS DF 6.9 Cell Line embryonic stem cell
9 chr10:1417800-1418200 Enhancers Gastric stomach
10 chr10:1417800-1418400 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr10:1417800-1418400 ZNF genes & repeats H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr10:1417800-1418400 ZNF genes & repeats H9 Cell Line embryonic stem cell
13 chr10:1417800-1418400 ZNF genes & repeats Pancreas Pancrea
14 chr10:1418000-1418200 Active TSS Brain Substantia Nigra brain
15 chr10:1418000-1418200 Bivalent Enhancer Fetal Brain Male brain
16 chr10:1418000-1418200 ZNF genes & repeats Fetal Kidney kidney
17 chr10:1418000-1418200 Bivalent/Poised TSS Fetal Lung lung
18 chr10:1418000-1418400 Enhancers Brain Inferior Temporal Lobe brain

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