Tag | Content |
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EnhancerAtlas ID | HS062-11587 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr3:124646840-124648290 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr3:124647643-124647662 | ATGCCACAAGGTGGCGCAG | + | 6.17 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28191 | chr3:124644010-124654710 | Fetal_Intestine | SE_29085 | chr3:124642142-124654716 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 124647550 | 124647768 | chr3 | 124648113 | 124648216 |
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Enhancer Sequence | GAGGAACAAA GATACCAAGT TTGAGGAGAC AGTACATTGA ATAACTAATG GCAGTTACTT 60 AATACTAAAT CATATCCAAC TCATTCTTTT TTTTTTTTTT TTAGAGGTAG GGTTTCCCCA 120 AGTTGCCTAG ATTGGTCATA AACCCCTGGG CTCAAGCAGT CCACCCTCCT TGGCCTCCCA 180 AAGTGCTGAG ATTATAGGTA TGAAGTGCCA TGCCCAGCCT CAACTCATTC TTTTCTGGAA 240 AAATGAAAAT ATATGACTAC ATTAAAAATT AAAATACATG GTTATTTCTA AACACAAAAA 300 ACCCACAATA AATAACATTA AAAATTAAAC AGACAAAACT GGAAAAAATG TTATTGAAAA 360 ATGTGACAAA TAAAGAGTTA ATGTTTATTT ATTTATTTTA GGAATAAGGT CTTGCTCTGC 420 CACCCAGGCT GGAGTGCAGT AGTGTGATCA TAGTTCACTG CAGCCTTGAG CTCCTAGGCT 480 CAAGCAATCC TCCCACCTCA GCCTCCCAAA TAGCTAGGAC TACAGTTGTA ACACCTCCAT 540 GGCTGGCTAA TTTTTTTGTG TGTTTTAGAG ATGAGGGTCT CACTATGCTG GCTAGGCTGG 600 TCTCTTAACT CCTGGCCTCA AATGATCCTC CTGCCTCAGC CTCCCAAAGT GCTGGGATTG 660 CAGATGTGAC CCACCAGTCC CGCAGAAGAG TTAATGTTTT TTAAGTTGAA TACTAAGAAG 720 TAATATTATT TATGCCTGTA GTCACGTAAC TGTAGATCAG GGTTTAATAT ACTTCAGACC 780 ATTCTCAGTG AGGACAATTG AGAATGCCAC AAGGTGGCGC AGTGACTACC CAGAAATGGA 840 CTACTTTTGT CTTTCTGCAC TTTAAGGCAA CTGTCCCATT TTTTCATTAC CTTGATAGAT 900 TGAGGGAGGG AAAGGTTAGG GTTGGGTAAT TTAAAGAATA ATAAAATAAA AATACCTCAT 960 TAAGTGCTTA TTATACTTCT TCCAAAATTT TATTCTAGTA GTGTTTTCCC ATTCACAATT 1020 CTAGATACAT TGACTAAGAG TAAGATGAAT AAGTGATCTT TGCCCTCTGA GCTATGATGG 1080 ATATCAAAGT CGCATTTTCA CAACTTTTAG GAACCCCTGG ACACATGGAG TAGTAAACTC 1140 TAGGGATCCA GTGATCCATT TTCTTCCCCC ACTCTTTTAT TTTATTTTTT TTTTTTAGAG 1200 ACATGGTCTT GTTCTGTCAC ACATGCTGGA GTGCAGTGGT GCCATAATAG CTCACTGCAG 1260 CGCTGAAACT CCTGGGCTCA AGTGATCCTC CCACCTTGGC CGCCCAAGTG TTAGGATAAC 1320 AGGTGTAAGC CACCTTGCCT GGCCCAGTGA TAAGTTTTCT AGAACTTTTC CTTGTCTCTA 1380 AGAACTCTGA CCTTGACAAT AGGTTAAAAA AATTATTGAA AGAAAAAGGT TTAGTGAGGA 1440 AGCAATTTCT 1450
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