| Tag | Content |
|---|
EnhancerAtlas ID | HS083-00239 |
Organism | Homo sapiens |
Tissue/cell | HCC1954 |
Coordinate | chr1:205253860-205254810 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr1:205254178-205254189 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr1:205254178-205254189 | GACAGCTGCAG | + | 6.14 |
|
| | Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
| SE_02431 | chr1:205253201-205255000 | Astrocytes | | SE_03194 | chr1:205253899-205254801 | Brain_Angular_Gyrus | | SE_03963 | chr1:205252695-205257315 | Brain_Anterior_Caudate | | SE_04837 | chr1:205252438-205255709 | Brain_Cingulate_Gyrus | | SE_05801 | chr1:205252449-205257899 | Brain_Hippocampus_Middle | | SE_06736 | chr1:205252450-205256085 | Brain_Hippocampus_Middle_150 | | SE_07799 | chr1:205252396-205255918 | Brain_Inferior_Temporal_Lobe | | SE_11085 | chr1:205251353-205259013 | CD20 | | SE_26974 | chr1:205252457-205257684 | Esophagus | | SE_29391 | chr1:205253543-205255044 | Fetal_Intestine_Large | | SE_32765 | chr1:205252644-205254723 | H1 | | SE_38936 | chr1:205252877-205255818 | IMR90 | | SE_43852 | chr1:205252499-205258684 | MM1S | | SE_46173 | chr1:205253006-205257823 | Osteoblasts | | SE_50327 | chr1:205252697-205257801 | Sigmoid_Colon | | SE_52983 | chr1:205252823-205257708 | Small_Intestine | | SE_54130 | chr1:205252675-205258056 | Spleen | | SE_55645 | chr1:205253025-205256564 | Thymus | | SE_56704 | chr1:205252917-205256555 | u87 | | SE_56879 | chr1:205252970-205254378 | VACO_400 | | SE_58462 | chr1:205242169-205295027 | Ly1 | | SE_58967 | chr1:205242236-205295022 | Ly3 | | SE_60263 | chr1:205242326-205284722 | Ly4 | | SE_60576 | chr1:205242267-205294889 | DHL6 | | SE_61365 | chr1:205242037-205294994 | HBL1 | | SE_61423 | chr1:205183427-205322469 | Toledo | | SE_62465 | chr1:205242393-205294944 | Tonsil | | SE_65493 | chr1:205252784-205254787 | Pancreatic_islets | | SE_67308 | chr1:205252499-205258684 | MM1S | | SE_68815 | chr1:205252846-205254572 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I205283 | chr1 | 205252730 | 205258354 |
|
Enhancer Sequence | CCCCAGCTGC TCTCAGAGCT GTGAGGACAA GAGTGGAAAA CCTGCCCTCA CAGGCCCAGC 60
TGGCCAGAGG GCTTGTCTCT TTCAGTCGCC CTCCCCCAGA GGGAGCAGGA GCAGACAATG 120
GCCACCATGA CTCACCAGTG AGCCATCTTC CCCTCCCCAC CCCTCCAGCC TGGCCCATGA 180
CAGCTTAGCT TGTCCTCCAA GGGAGCTGCA GCCCAGCCTC CCAGGGCCGC CAGCTTCCTC 240
TCTCTTCACC CAACCTGGCT CCCCCCCTGC TTGTGCAACA CCACATCAGA GGGTTGTGAA 300
GTGGAGAGGG AGGAGTTTGA CAGCTGCAGA CCCAGGCAGA CAGAGCAGAC TCCTTTGTGA 360
AGGAGATAGA GGCTGCAGGG GCCCAAGTCC AGCCTGTACT CCCCTGCCCT GACCCACAAG 420
GCATCACCCA GTCTCCCCAA ACCCTAGGGA AGTGGTCATT GTCATTTATT TGTTCCTTTC 480
TTAGATAGAG CTTGGATCCT GTCTGCAATT TATTCCTTCC TGCAAAACCA AGTATGTGAG 540
GCAGAGGAAA GTCCTATTCC ATTCCAGGAG GGACAGGGCT CCCTGTTGGA AAGTATTTCC 600
TTTTGCTAAG TTTCTATCTG CCTCCCGGGT AGACTCCACT AGGCAGTATT TCAAGAAGTT 660
AACGCACTTC CAATCCCCAT CTAACCTATA TTCTTTGCCG CAAGCCAAAT ACCCTTAGTT 720
CTTTCAGTCA TTTCTCCTAA GACATGGATT TAAGACCTTT TGACAGCTTG GCCTGTATCC 780
TCTGGAAACA TTTCCATTTA CCCAAGTTCT TCTTAAAACA TTATGTCTTT GTCCAGGTGC 840
AGTGGCTCAC GCCTGTAATC TCAAAGTGGA GGCTGAGGGA GGAGCATCAG TTGGGTCCAG 900
GAGTTTGAGA TCAGCCTGGG CAAGATGACA AGACCCCATC TCTAGTTAAA 950
|
