Tag | Content |
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EnhancerAtlas ID | HS034-06921 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr12:53261210-53262140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr12:53261603-53261614 | GCCACGCCCCC | + | 6.62 | MYC | MA0147.3 | chr12:53261635-53261647 | GCCCACGTGCTC | + | 6.27 | SP1 | MA0079.4 | chr12:53261600-53261615 | CACGCCACGCCCCCC | + | 6.2 | SP3 | MA0746.2 | chr12:53261602-53261615 | CGCCACGCCCCCC | + | 7.22 | SP4 | MA0685.1 | chr12:53261600-53261617 | CACGCCACGCCCCCCAT | + | 6.14 | SP8 | MA0747.1 | chr12:53261603-53261615 | GCCACGCCCCCC | + | 6.44 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_23067 | chr12:53260969-53262039 | Colon_Crypt_1 | SE_23945 | chr12:53260964-53261976 | Colon_Crypt_2 | SE_26564 | chr12:53260695-53274096 | Esophagus | SE_64566 | chr12:53260752-53261867 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr12 | 53261473 | 53261693 | chr12 | 53261248 | 53261948 | chr12 | 53261995 | 53262128 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I052867 | chr12 | 53260806 | 53262242 |
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Enhancer Sequence | GCATGCATCA GTGTGCAAGG GTATGTGTGA GAAAGACAGA AGCTAGGCAT GTGTGTATGG 60 GGGTGTGTTA TAAATGTGCA GGTGCGGGTG TGTGAAGGTT GTGTGTGAAT GTTCACCTTC 120 CCCACCTCCA CCCCAAACAC ATATCTCTTG GTAAGGGGGC TTCAACAGAG ACAAAAGTAC 180 CCCAGGCTGA GAGAACAGTG TTCCTGACTC TGGAACAAAC GATATTTTTC TCTTTCAAAG 240 CTTTCAGATT TCCTGAAGAA GAGCTGCTAG CTCAACCAAG CTCAGCCTTA AACCCGCCCC 300 TCTGATCGAA ACTAAGGAAG GAAACCAGCA CCAGCCACCC CCGCCCTGCA CCCCCACCCC 360 TGCCAGGGAA TGCTCTATGC CAGCAGAACG CACGCCACGC CCCCCATTTC TCCCTCCCCG 420 CTTGGGCCCA CGTGCTCTCC CCAGCCACTC AGGGTGCCCA GGGCAGCTCC CAACCACCAA 480 CAGAAGTTTA AGCCCCTCTC CAGGCTTTGG GAGCACTTTG CTACCTGCCC AGGCAGGCAC 540 TACCCTAGGG CAAGCAGGCC ACTCCCTGCC AGGGGGAACT GAGAGGTGGG GGGTAGGGGG 600 TGGCAGCTTC AGAACACACA ACCAACCCCC TTCCCGGGAG GCAGGCACTC CACCCCACCC 660 CGCATCTCTT CAAGAAGACA AAATCAGGAA AGAGGGCTGG GTGGGGAGGG CATCTCAGGA 720 GGAAAGGGTC ACTTAGAGGC AGGGTTTGAA TGTCAAGAAT GTCCCTTCCT TTCATTCAAG 780 GGTCCCAAAG AAGACCATTC TTCCAGGAAG TTGTCTCAGT TGTCAGTAGT ATTATATGTA 840 TCAAGAATAA TTAGGCCAGG TGCAGTGGCT TACGCCAGTA ATCCCAGCAC TTTGGGAGAC 900 CAGGGCAGGT GAATCTACTT GAGCCCAGGC 930
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