Variant report

Variant rs3813662
Chromosome Location chr2:96779695-96779696
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr2:96775400-96780400 Weak transcription Spleen Spleen
4 chr2:96775400-96780800 Weak transcription Lung lung
5 chr2:96775600-96780400 Weak transcription Left Ventricle heart
6 chr2:96775600-96781400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr2:96776200-96780400 Weak transcription Right Ventricle heart
8 chr2:96777200-96781400 Weak transcription Esophagus oesophagus
9 chr2:96778000-96780000 Bivalent Enhancer Fetal Muscle Trunk muscle
10 chr2:96778000-96781000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr2:96778600-96779800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr2:96778600-96781600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
13 chr2:96779000-96779800 Bivalent/Poised TSS Skeletal Muscle Male skeletal muscle
14 chr2:96779400-96780800 Bivalent/Poised TSS Fetal Adrenal Gland Adrenal Gland
15 chr2:96779600-96779800 Bivalent Enhancer Fetal Muscle Leg muscle
16 chr2:96779600-96780200 Enhancers Brain Inferior Temporal Lobe brain

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