Tag | Content |
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EnhancerAtlas ID | HS117-00480 |
Organism | Homo sapiens |
Tissue/cell | LHCN-M2 |
Coordinate | chr1:153584280-153585420 |
Target genes | Number: 18 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr1:153585282-153585297 | AGTTAATAATTACCA | + | 6.02 | NFIC | MA0161.2 | chr1:153584721-153584732 | TCTGCCAAGAA | - | 6.02 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_23345 | chr1:153579766-153590628 | Colon_Crypt_1 | SE_26764 | chr1:153579284-153592276 | Esophagus | SE_34771 | chr1:153579759-153587524 | HeLa | SE_36428 | chr1:153579895-153590703 | HMEC | SE_38418 | chr1:153578867-153585763 | HUVEC | SE_42913 | chr1:153579237-153590776 | Lung | SE_50824 | chr1:153579813-153590695 | Sigmoid_Colon | SE_52793 | chr1:153579948-153590590 | Small_Intestine | SE_57408 | chr1:153584104-153586101 | VACO_503 | SE_64441 | chr1:153580204-153590871 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | CCACAAGGCC CTCTCCAGGA ACAGCTCCCG GAGCATAGTG GGGCCTGCTT GGCCCTGCCT 60 CACCCCTTAC CATCCTCACA GGATTCTGCG TCTAACTCTC TTTGTCTCTC TCTCACACAC 120 ACACACACAC ACACACACAC ACACACACCG AGCAAGGACC TCGGCCATTC CTGATCCCCT 180 CTGCTTGGGT GACCCATCAC CCTTCCACTC ACTTCAGTTC TTGGAGCAAG AAGCCAGCCT 240 CTGAAATTTT TCCAGGCAAG TGAAGTTGGA GGAGTTCAGT GTGGATCTTG CCCCCGCCTC 300 CCCCAACACA CACACAGCTA CCCCAGCCTC AACAACACTT ACTAGAATGT GGGGAAAGGC 360 AGAGCCAGCT CCCCAGCACC CCTGCCCTCA CCACCATCCC CACTGGGCTG GGCAGGGGAA 420 GGCTCCCATA GTGCAGGTGG CTCTGCCAAG AAAAGCAGCT CAAGCCGGGG CCTGCCTGGG 480 TCCTGAGGTG GAGGAGCTGC CGAGGTTCAG CCCCCCTCTC TCTATCTTTC CCTCTCCCAG 540 GGAGCTTGCA GGCTCCCCAC AGCCTCACTC GGGTTCCTCC CAGATCTCAT CATCCCTCTC 600 AAGGAACAGC TCCTGGAACA CAGTGGGGTC TGCTTGGGTC GTGAGGTAGA GGGGACGCCA 660 CCTCAGCCCC CGCCTCCTCT TCTCGGAATC TCAGGCTCCC TGGAAACTGC CTGGTTCCTT 720 CTGGACCCCA TCACCTCCCC TAGGACACAG CTCCCAGAGC CCAGCAAGGC CTGTGTCCAA 780 GCTCTGACCA CCCCCAACCC AGACCAACAC GCATTTGTCC TCTCCTTTTG GGGAGGATCG 840 AGTAGCTGTG GTCAAAGCTT CCAAATACTC TGCCCCTGGA GAGGAGCTCC GTCAGCTGCT 900 GCGGCAGGGA GGGGGTCTCA CCATCCCATC CATCCCTCTA AAGGCCTCAC CCAGCCCCCA 960 ACCCCCCAGG ACTCCCCATT CCTAAACTGG CCTGTGGGAG AAAGTTAATA ATTACCAAAA 1020 TCTTCCTGCC TGCTCTCTGG CAGGCCCCTC TCCCCAGGCC CCCTTCACTG CCCCTTCTCC 1080 TGGCCTCCCA ATACTGTGGG GCCCTCCGGC AGCCGAAGAC CTCCCAGGCC GGGCCCAGGG 1140
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