Variant report

Variant rs11727136
Chromosome Location chr4:1051804-1051805
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:1042200-1052200 Weak transcription Gastric stomach
2 chr4:1049600-1054600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr4:1049800-1056200 Weak transcription Right Atrium heart
4 chr4:1050000-1052200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr4:1050000-1052200 Weak transcription Esophagus oesophagus
6 chr4:1050000-1052400 Weak transcription Left Ventricle heart
7 chr4:1050000-1052800 Weak transcription Spleen Spleen
8 chr4:1050000-1054600 Weak transcription Pancreas Pancrea
9 chr4:1050000-1055400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr4:1050200-1052400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr4:1050200-1054200 Weak transcription Primary mononuclear cells fromperipheralblood Blood
12 chr4:1050400-1055600 Weak transcription GM12878-XiMat blood
13 chr4:1051000-1052800 Bivalent Enhancer Stomach Mucosa stomach
14 chr4:1051200-1052400 Bivalent Enhancer HepG2 liver
15 chr4:1051800-1053400 Enhancers Fetal Heart heart

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