Tag | Content |
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EnhancerAtlas ID | HS026-07881 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr12:53314270-53315640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:53315023-53315041 | CTCTCCTTCCTTGCCTCC | - | 6.25 | RFX1 | MA0509.2 | chr12:53314927-53314943 | AGTTCCCATGGCAACA | - | 6.08 | RFX1 | MA0509.2 | chr12:53314927-53314943 | AGTTCCCATGGCAACA | + | 6.1 | RFX2 | MA0600.2 | chr12:53314927-53314943 | AGTTCCCATGGCAACA | + | 6.3 | RFX2 | MA0600.2 | chr12:53314927-53314943 | AGTTCCCATGGCAACA | - | 6.43 | RFX5 | MA0510.2 | chr12:53314927-53314943 | AGTTCCCATGGCAACA | - | 6.54 | RFX5 | MA0510.2 | chr12:53314927-53314943 | AGTTCCCATGGCAACA | + | 6.59 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_34646 | chr12:53314392-53315691 | HeLa | SE_47304 | chr12:53313962-53322747 | Panc1 |
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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 |
GH12I052920 | chr12 | 53314408 | 53317272 |
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Enhancer Sequence | CTTAAGAGGC TGAGGCAGGC GAATTGATTG AACCCAGGGG GCAGAGGTTG GGGTGAGCTG 60 AGATTGTGCC ATTGCACTCC AGCCTGGGCA ACAAGAGCGA AACTCCATCT GAAAAAAAAT 120 TAAAAATGGA CAGCCCCATG AGGGCAGAGA CCTTGACTAT GTTGTTGACC GTCACATCCA 180 CAGCATTAGA AAGACATCTA ACAGGCACTC CACCAGTATA TGATGAACGA ATTCACAAAT 240 GGCTGAACCA GCCTGCCAGG TAAGCCTGTG CCCAGCCAGG CACAGTGGCT CACACCTGTA 300 ATCCCAGTAC TTTGGAAGGC CAAGGGAAGA TCACTTGAGG CCAGGAGTTC AAGACCAGCC 360 TGGACAACCA GCGACATAGC AAGACCCTGC ATGTGTGCAT ATATGTCTGT AAGACAGAAA 420 ATGAGACAGA GAGACTCTAG AGAGCACGCA GCTCAGCTAA AGAAAAGACC TGCTACCCAC 480 CACTCTGTAA CCAACCTGCC CCCACCCCAT TCCCTGGTCT CTAAGGACTA AGATAACCCC 540 AACTCAGATA CAATGACCCA TTCATAGGCC TTTAGGAAAA TCTGTTGACC TGGATGGTGG 600 GAATGGGCTA AGCCCAGGCC AGCCCAGGCC AGCTTAGCCT CAGGGACCTG TTAGTCAAGT 660 TCCCATGGCA ACACAACTAA TTGTGTGTTT ATGCATTCCC TACAGAACTC CAGGCAGAGG 720 CCATCTATTC CCCAAGGCCA CATTCTACCT TCTCTCTCCT TCCTTGCCTC CCCAAGTTTC 780 CTGGGTGACC ATCCAGGGAA CATTAAGAGA AGCTTAAGTA GCAACAGCAG CCTCCAGAAC 840 ATGGAAGGCA AAGGAGGGAA AGCCTCTCTG AGGGAGAGGA CCAGTACTTC TTGCTCACAA 900 TTGTCCAGCT GCAAAAGTCA AACTCCCTAG TCCTCCTCCT GGACCCACAG TTCTATGGCT 960 TCGATGGCTC CCACATGTCA CCACACTAAA CCTCCACCCC CAGGCCCCCA TGGCCTGACC 1020 CTATCCTACT TGACTGCCAG CTCCTGCACA AACTCCCTCT TCACTTATGC AGTGCACAGG 1080 CCCAGGGCCC CTCCTTCCTC TCTCTTTGTG TCCCTCTAGC CTGGCTCTAC CCCCAAGGAC 1140 TTCCTTCAGG AAGCCCTCCC AGATGGACTA TTCCTCCCAG GCTTCTCCCT CCAGCCCTCC 1200 AGCCTGGAGC CTCTGATTGT GCATCCCCAG CTGTGGCCGG ATCTCCCAGA GCTGGGCATG 1260 GGTTCAGCTA TTCCCCCATG GCCTAGCAGT TTCCTTAAGG TGGTAAAGCT TTTAATTCTT 1320 ACAGAAACTA TAAAATAAGC ATTATCTGCA TTCTAGAGTG GAGAACACTG 1370
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