Variant report

Variant rs10026482
Chromosome Location chr4:1051128-1051129
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr4:1050600-1051600 Bivalent Enhancer Fetal Muscle Trunk muscle
14 chr4:1050800-1051400 Bivalent Enhancer Rectal Mucosa Donor 31 rectum
15 chr4:1051000-1051200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
16 chr4:1051000-1051200 Flanking Bivalent TSS/Enh HepG2 liver
17 chr4:1051000-1051400 Bivalent Enhancer Colonic Mucosa Colon
18 chr4:1051000-1051400 Bivalent Enhancer Sigmoid Colon Sigmoid Colon
19 chr4:1051000-1052800 Bivalent Enhancer Stomach Mucosa stomach

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