Tag | Content |
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EnhancerAtlas ID | HS197-06442 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr14:35815890-35817410 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF7L2 | MA0523.1 | chr14:35816776-35816790 | GGAGATCAAAGGGA | + | 6.75 | ZNF263 | MA0528.1 | chr14:35816784-35816805 | AAGGGAGGAGGGGGTGGGGAG | + | 6.61 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_23298 | chr14:35816257-35817251 | Colon_Crypt_1 | SE_24327 | chr14:35816552-35817140 | Colon_Crypt_2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr14 | 35816661 | 35817200 | chr14 | 35816552 | 35816667 | chr14 | 35816709 | 35817157 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I035346 | chr14 | 35816026 | 35817319 |
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Enhancer Sequence | TTGCAACTTA TAAATCTTTC ATGGGCTCTG AGTTTCTTGT TTTTATTTTA TTTTTGTAGA 60 CACAGGGTTT CACTATGTTG CCTAGGCTGG TCTCAAACTC GTGGCCTCAA GCTAATCCTC 120 CCACTTTAGC CTCCCAAAGC GCTGGGGTTC CAGGCATGAG CCACCTCGCC CAACATGCTC 180 TGAGTTTCTA AAAGAACATT TAGCAGCTGG GAGGGGTGCA GCAGTGAGAG TGCGGGGCTT 240 GGAGTCCAGC TTTGTTGGCT GTGTGGCCTT GGGCAGGGAG CTTCACCCCT CTGAGCTTTA 300 GTCCCCTCCT CTGTTAGACA GGGTCGACTG CCCCCAGCCT GCTTGCATGA TGAGGGTTTA 360 AGGACAATGG ACACAGCAGA TCCCACACAG TCTTGATACT TACAGATTCT CAATGCCTCG 420 GTGTTACTGT TGTTCCCACG TGCCAGCCTG AACTTAGCAC CCACTGCTGG CTTCCTCCTC 480 CCCTCTCTCG GAATGGACCC AATGGGCCCT GCCTCCGCAG AAGCCATAGA AAGCTTTTAG 540 GTTTCACACA GTCAGTCACA ATTCATGTGT CTGGGGTTTA TCATGTGCGG GGCGCTGTCC 600 TAAACACTTC ACATGAATTA ACAAATTTCA TTCTCATAAC AGCCTCTAGG ATCAATATGA 660 TTATTGCTGG GTGTTCCAGA TCTTGATGCC TAAGGATACC CAGGTAGTCA ATGGTAGACC 720 TGGGCTGTGC ACCCAGGCAG GCTGGCCCCT CAGCCCACAG GCGTGACCAG AGGTCATCCC 780 TCCTCTCCTC CAGCTTTGTG CCCTGGAGGA GCTGCTGTGT GCACTGCATG GACGCCACCC 840 TTGCCCTCTG GCCGCCTTTT GGTCATGGCC AGTGAAGAGC CTAGTGGGAG ATCAAAGGGA 900 GGAGGGGGTG GGGAGTCTGC ATTCATTCCC CTGCAGTCCT CCCCGCAGGG TCGCCCAGGC 960 TGGGTTGGAC CTAAAAGGAA GGTCACGGCC CCACTCAGGC AGCCTCTGTC CCACAGGGTT 1020 CTGGTGCGGG TTTCTGGTGC AGGTGCTGGT GCGCAGTGTT CCTCTTGCTC GCATCCGCCC 1080 CGCATTGCTG CACAATCCCT ACTTCTACGC CCCTCGTGGT TTTGTAAATA GTGTCATTGT 1140 AAATGAGCCA GCCACTCCCC CATGCTGCCT CTCAGCTGCA GGCTGAGCAA AGCTTAGCTT 1200 GTCCTTGAGC CTTACCTGCT TACTGTGTAA TGCCCAACCT CATTTTTACC AATCCTGTTT 1260 TTAGACTCTC CCTTTCCTTT AATCACCCAG CCTTGTTTCC ACCTGAATTG ACTCTCCCTT 1320 AGCTAAGAGA GCCAGACAGA CTCCATCTTG GCTTTTTCAC TGGCAGCCCC TTCCTCGAGG 1380 ACTTAACTTG TGCAAGCTGA CTCCCAGCAC ATCCAAGAAT GCAATTAACT GATAAGATAC 1440 TGTGGCGAGC AATATCCGCA ATTCTCAGGA ATTCGTCTGA TTGATAATGC CCAAAGCCCC 1500 AAGTCTATCA CCTTGTAATG 1520
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