Tag | Content |
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EnhancerAtlas ID | HS002-04656 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr18:29092780-29094190 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Esrra | MA0592.2 | chr18:29093945-29093956 | GTCAAGGTCAT | + | 6.32 | Esrrg | MA0643.1 | chr18:29093946-29093956 | TCAAGGTCAT | + | 6.02 | Gata1 | MA0035.3 | chr18:29093603-29093614 | ACAGATAAGGA | - | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_64603 | chr18:29089530-29094276 | 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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| Number: 1 | ID | Chromosome | Start | End |
GH18I031509 | chr18 | 29089614 | 29094612 |
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Enhancer Sequence | TTATTGCTCT TATCAAAACC TGGTCTGTCT TTGTCTCCCC AGTATGTAAG CATCCAACAG 60 GGTAAGAATA TTGTGTTACT TAACATATCC TACAAGCTCA GGAAATTGAG GGTATGAATT 120 AATTCAAACT TGCAGAAATT TTAAGATAAG GACCATGCAA AACTTAGAAT TGAGGAAATG 180 TCTCATAAAT TCTGTTTATT GAATGCCAGT CACTGCAATA GTTACATTTC ATATATTTCT 240 TTAATTTGCA CATCAGCCCT GCAAAATGGA TGTATCCTAG TTAGGTGGCT TTCAGATGCA 300 AGTAACAAAA CCCAACTAAA ACTAGGTTAA AGAAAAGAAT GTTGAATATC AATCGTAAGA 360 AAAAGTTTAG AGAGAGAGTT GGTCCAAATT TGAACGATTC TGTAACTTAA AGCCTTTATG 420 GTTTCAGTTT GGCTTCTCTA GCATTTCATT AGCTTTCCCC TCATGGTCAC AGCATGGCTG 480 TAGCTATTCC AAATGTCACC TCCTCACTCA ACAGTCTCCA GAGGCACTTA AATAGGAAGG 540 TTATGCATGT GCTTCTCTTC TAATCAGTGA GGAGAATCTT TTGTAGGGTC TCCTGATACC 600 TCATTGACCA AAATTCTCTT ACACATTTAT GCCTAAACCA GCCAATATCA AAGTAAATGG 660 GCATACATAC CATGCTTTGT CATGCCAGTC ATTCAGCTCC ATGAGCTAGG CAGGGTCTAC 720 CTGAGAGTAC AAAGTAGAGT TTTATGAACA CTGAAGATGA GAGAAAATGC CAATAAGCTA 780 GACAATTGAA AATGTCTGCC ACAGTATGTA TTACTCTCCT GTTACAGATA AGGAAATTCA 840 GACTAAAGCA TCTTGTCTGG CAGGATCTCC TCCCCGCTTC CCTCTGCCCT GAGGATGGGT 900 TAGACTTAAT GACTCACTCC CAAAGAATGG AATAGGGACT GGGAAAAATA GTAACTTTAC 960 AACGGAGAAA CTGCAATCAG TACCTTAGCC AGTGGTGTCA TGTGGCTATT GCACACCAGC 1020 TAGTATGGTG TGACAGAAAG GGCACTTCAG CTCTGTGATG TTCTTTCCAA AAATGCATAA 1080 TACTGATCTA ATCGTGAGAA AAACAACAGA TAAACCCAAA TTGGAGGACA CTGTGCAGGA 1140 TACTCAGCCA GTATTCCTCA AAACCGTCAA GGTCATGAGA AACAAAGACT GGGAAAGTGT 1200 CAAAGACCAG AGGATATAAA GGAGAAGTGA TCACCAAATG CAATGTGGAA TCGTAGATTG 1260 GATCCTGGAA CAGCAAAAGA ACATTAGTGG GGGAAATGGT AAAATCAGAA TAAAGTATGG 1320 AATTTAGTTA ACAGTGCATT AACTAAATGC ACCAATGTTA ATCTCTTAAT TTTGACAAAT 1380 GTACAGCAGC TATTTAAGAT GTTAACATAT 1410
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