Variant report

Variant rs4426564
Chromosome Location chr2:96780986-96780987
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:96772000-96782200 Weak transcription Liver Liver
2 chr2:96775000-96781800 Weak transcription Right Atrium heart
3 chr2:96775600-96781400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr2:96777200-96781400 Weak transcription Esophagus oesophagus
5 chr2:96778000-96781000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr2:96778600-96781600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
7 chr2:96779800-96781000 Bivalent/Poised TSS Skeletal Muscle Female skeletal muscle
8 chr2:96779800-96781800 Bivalent/Poised TSS Fetal Muscle Leg muscle
9 chr2:96780400-96781000 Active TSS Psoas Muscle Psoas
10 chr2:96780400-96781600 Enhancers Right Ventricle heart
11 chr2:96780400-96781800 Bivalent/Poised TSS Fetal Muscle Trunk muscle
12 chr2:96780400-96781800 Enhancers Spleen Spleen
13 chr2:96780400-96783000 Active TSS Left Ventricle heart
14 chr2:96780600-96781600 Bivalent/Poised TSS Skeletal Muscle Male skeletal muscle
15 chr2:96780600-96782000 Bivalent Enhancer Placenta Placenta
16 chr2:96780800-96781000 Enhancers Lung lung
17 chr2:96780800-96781400 Flanking Bivalent TSS/Enh Fetal Adrenal Gland Adrenal Gland
18 chr2:96780800-96781800 Bivalent/Poised TSS Stomach Smooth Muscle stomach

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