Tag | Content |
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EnhancerAtlas ID | HS101-00392 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:15666720-15668230 |
Target genes | Number: 20 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chr1:15668141-15668155 | GAAAGGTAAACAAT | + | 7.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_53278 | chr1:15665531-15667437 | Small_Intestine |
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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: 2 | ID | Chromosome | Start | End |
GH01I015339 | chr1 | 15665681 | 15667375 | GH01I015341 | chr1 | 15667711 | 15669313 |
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Enhancer Sequence | TTCTAGAGGC AAATGAGCTT TACGGGTTAT ATCATTCTGA TAGCTATTGC CATAATAGTA 60 TTATATAATA AACAACCACA AAACTTCAGC GGCATTCAGC AATTGCTATT TACTCCTCAC 120 GTGTCTGGGG TCAGTGGCAA GGCGGCTCTG CTGACCTTGG ATGGGCCCAC CCACTTGTCT 180 GGGTGTTAGC TGGCCTTTGG TTGATCTAGA CTGGCCTCAG CTGGAGTGAC TCAGCTCCCT 240 GTGTCTCTCA TCCCCCAGCA AGCAAGCCTA GGCTGTTCTC ATGGAGACTA CGAGGTATAA 300 AAGAAAGTGG CCCAATCACA TAGTGTTTTT CAACCTTCTG CTTGTGTTAT GTCTGCTAAG 360 ATCCCATTGG CCAGAACAAG TCACATGGCT GAGTTCAGTG TCTGGAGGCA AAATATGGGC 420 GGGCACTGCA AGTTACATAG CCCTAGACAT GGATAGAGTG GGGTAAAGAA GGGACCACCA 480 TGCCAATCAG CCACAGAGGC TTGAGTCCAG GGATTGGCAA CTTTCTCTGT AAAGGGCCAG 540 ATGGTAAATA TTTTATGCTT TGCAGACCAT ATTCATACCT CTTCCACTCT GCTATGGTAA 600 AATGAAAGTA GCCATAGACA ATATGTAAGC AATGGACATG ATAAGCATGG CACTGTTCCA 660 ATAAAACTTT ATTTACGGCG GGCACGGTGG CTCATGCCTG TAATCCCAGC GCTTTGGGAG 720 GCTGAGGCGG GTGGATCACC TGAGGTCAGG AGTTCGAGAC CAGCCTGGCC AACATGGTAA 780 AACCCCATCT CTACTAAAAA TACCAAAATT AGCCAGGTGT GGTGGTGGGC ACCTGTAATC 840 TCAGCCACTC AGGAGGCTGA GGCAGGAGAA TCACTTGAAC CCGGGAGGCA GAGGTTGCGG 900 GGAACCAAGA TTGTGCCCCT GCACTGCAGC CTGGGCGACA GAGCAAGACA CCATCTCAAA 960 AAAAACAAAA CAAAACAAAA ACACCACCTT ATTTACAAAA GTATGCAGTG GGCCCGATTT 1020 GGCCTGTGGG CTGTAGTTTG TCAACCCCTG GTCTAGTCCC TTCTCCTTAT TTTTCAGATA 1080 AGGACAATTT CAGTGTCACA CAGCTAATGG GTGAAGAATC AAGACAAATG TTCAAGCGTC 1140 CTGGCTCCTA CATGACTGCT TTTTTTCCTC ACACCCACCT ACCACTTACT GAACACCTAC 1200 TATGTGCTCA GCACTGTGCT AAAAGCTTTC CATCATTATC TCACTTAATC CTCACAACTC 1260 TAAAAGATCA ATACTGTTAT TAACTTCATT TTCTAAATGA GGAAGCATCT AGAAACAACT 1320 AGAGCTGGGA TTCTTTCTAG ATCCAGAGTC TGAATTCTTA ACCACAGCAT GCTGTAGTGT 1380 TCTGTGATTT TAAGAAACTT TTGGGTAAAC CTTTGTACCC AGAAAGGTAA ACAATTGGTA 1440 AACAAATGGG GAAAGACTCT TTAGTTAGGC CTGTCCCCCA TCAGCATCGG TTTACTTTTC 1500 TCACATTTCA 1510
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