Tag | Content |
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EnhancerAtlas ID | HS051-06190 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr12:53260880-53261950 |
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: 4 | Chromosome | Start | End |
chr12 | 53261473 | 53261693 | chr12 | 53261124 | 53261227 | chr12 | 53260892 | 53261046 | chr12 | 53261248 | 53261948 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I052867 | chr12 | 53260806 | 53262242 |
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Enhancer Sequence | CCTGGATCTC CTCTTGCTCT CACTGTCATC TGAGGACAAC CATCCCTTCT GGCTCCCTGA 60 GATGAGAGGG GAAGAGACAG AGAGAAAGAA AGAAAATGTG TAGGGACAAG GGTATACAGG 120 GAGCTTGTAA GATGTGTGTA AATAAATGGG GGGGGAGCAT GAGTGCGAAG GTGCAGAGAT 180 CATCTATGAT CATGCAGGGG CATGTGCGGG CCAGTAAAAT CACAGGGGCT ATGAAAGTGA 240 CACAGTTATG TGTGAGTGCG CCAGGCATCG GTGTATGTGG AAGGGTGGGG TGGGAATGTG 300 TACCTTCTGG GATGGGTATA GTGGATGCTT GCATGCATCA GTGTGCAAGG GTATGTGTGA 360 GAAAGACAGA AGCTAGGCAT GTGTGTATGG GGGTGTGTTA TAAATGTGCA GGTGCGGGTG 420 TGTGAAGGTT GTGTGTGAAT GTTCACCTTC CCCACCTCCA CCCCAAACAC ATATCTCTTG 480 GTAAGGGGGC TTCAACAGAG ACAAAAGTAC CCCAGGCTGA GAGAACAGTG TTCCTGACTC 540 TGGAACAAAC GATATTTTTC TCTTTCAAAG CTTTCAGATT TCCTGAAGAA GAGCTGCTAG 600 CTCAACCAAG CTCAGCCTTA AACCCGCCCC TCTGATCGAA ACTAAGGAAG GAAACCAGCA 660 CCAGCCACCC CCGCCCTGCA CCCCCACCCC TGCCAGGGAA TGCTCTATGC CAGCAGAACG 720 CACGCCACGC CCCCCATTTC TCCCTCCCCG CTTGGGCCCA CGTGCTCTCC CCAGCCACTC 780 AGGGTGCCCA GGGCAGCTCC CAACCACCAA CAGAAGTTTA AGCCCCTCTC CAGGCTTTGG 840 GAGCACTTTG CTACCTGCCC AGGCAGGCAC TACCCTAGGG CAAGCAGGCC ACTCCCTGCC 900 AGGGGGAACT GAGAGGTGGG GGGTAGGGGG TGGCAGCTTC AGAACACACA ACCAACCCCC 960 TTCCCGGGAG GCAGGCACTC CACCCCACCC CGCATCTCTT CAAGAAGACA AAATCAGGAA 1020 AGAGGGCTGG GTGGGGAGGG CATCTCAGGA GGAAAGGGTC ACTTAGAGGC 1070
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