Tag | Content |
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EnhancerAtlas ID | HS052-22626 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr2:235243940-235245410 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr2:235245139-235245151 | AAACAAACAAAC | - | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_25541 | chr2:235242801-235245291 | DND41 |
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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 |
GH02I234333 | chr2 | 235242251 | 235245290 |
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Enhancer Sequence | TTCATGTTCT ATATCACCCT TTGGAAGATT CAGGTTTACC TAAATTTTTT ATTAACGGGA 60 CAGCCACCTT CTAAACAGGG ACAGAGTTCT ATAGGCACAA AGGGGTGGGA ATACAGTCCA 120 GGTCTTCTGT TCACATGGAC CTGAGAGAGA GCAAGTAGAA AGTCAGTGAT TCAATTGCTT 180 GGTGGGTTAA TGCCATTTCC CCTTAAGGAG GTATTGCTAG ATCCTTTTTA GGACTCAGAG 240 GAAAATAAGA AATATTGCCT GATGTCTACC CACTCCCTTC CAATTCTGTT TCAATGTTAG 300 AATTTTCCTT TGCTAACATT TAATCTCTGT AGAGGGTCAG CTACTTAATG CAACAATGTT 360 TCATTTCCAT GGAAGCATCT GTTTGCTGAA GACATGGGGG TTCCCACGGC AACCTACTGA 420 CATGGGATTT TGCAGTCCTT CCTCCCGAAT TACCAGGAAG CCAGGGCTCA CGTGTGTGGG 480 TGTCAGAGCT GACAACTGGC CTCGTCGGCG TCCATCTCTT CCTCCACTCC CTCTAATGAA 540 ATTAAGTCCC TGCTGCTGGA CAGCGTCCTG CTAACAGCTC GCAGATTGCC CCACCTCTCA 600 GGGCCTGTCT GGGCATCTTA GCAGCATCTG CTTCCAGCCT GTCACGCTCT AGACTCGTGA 660 TAGCTGTCTG CTGACTAGAT GGCATTCTGA TAAAGGGCAG AAAGGCAGAG CGATGTCTGT 720 TCTGGGGTGT GTGCCAGGCA CAGGGTGCGG GACAGTGGTG ACGCGCTCTG CCTTTCCTCA 780 GCCAAAACCA CAAGCCCTTG TCCCGTGCAG CGTCCTCATG CGAGATGTTC CGCAGAGCCA 840 CTTCATGGTT CTCAGCACAC TCAGAGCACT CACTGTGGCT TTCAGCAGCA CGAAACAGAT 900 GCTTGAATGG GCCAAGAATG GGGGGCAGTG GCTCAGGCCT GTAATCCCAT CACTTAGGGT 960 GGCTGAATCG GGTGGATCTC CTGAGGTTAG GAGTTCAACA CCAGGCTGGT CAATATGGTG 1020 AAACCTCGTC TCTACAAAAA TACAAAAATT AGCTGGGCAT GATGGTGGGT GCCTGTAGTC 1080 CCAGCTACTT TGGAGGCTGA GGCAGGAGAG TCACTTGAAC TCGGGAGGCA GAGGTTGCAG 1140 TGACCCAAGA TTGCACTCCA GCCTGGACAA CAGAGCAAGA CTCCATTTCA AACCAAACCA 1200 AACAAACAAA CCCAAGAATG AATGAAGCAT TTGGGACGTT ACGCGATAGG AGCTGAGGCT 1260 TGGGGGCAGG CACTGTGCTG CATGTTATCC CACTGTTAGT ATCTTAAAGA CAGGGACACA 1320 AGTTTAGGGA ACAAAAGCAA ATTAGGCGAG GTCTGACTCC AGGACCTGAG GCTCAGCCGC 1380 TGTCTGTGAC TCTAATCCCC AAATTGCTTT CCACTGTCAG GAGTCCACAC TCTCAGTAAT 1440 GAAACTTCCT GTACCACTGG CTTCTTTTTT 1470
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