Tag | Content |
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EnhancerAtlas ID | HS187-17057 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr3:46254830-46256010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ONECUT3 | MA0757.1 | chr3:46255905-46255919 | TCTATTGATTTTCT | - | 6 | TBX21 | MA0690.1 | chr3:46255627-46255637 | TTCACACCTT | - | 6.02 | TBX2 | MA0688.1 | chr3:46255626-46255637 | TTTCACACCTT | - | 6.62 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09580 | chr3:46252980-46256536 | CD14 | SE_43623 | chr3:46245420-46257731 | MM1S | SE_67194 | chr3:46245420-46257731 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 46255175 | 46255353 | chr3 | 46255767 | 46255830 | chr3 | 46254966 | 46255200 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I046212 | chr3 | 46254185 | 46255449 |
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Enhancer Sequence | CAGGCCAGTT ACGAGAGTAC AAAATAGAAG CTGTAAAGCA TTTTAAGGCA TAACCTCAGA 60 AGTCACATGA TGCTGCTTTT GCAAGTAAGT CACAAAGCCA AGCCACATTC AAGGAGTCAG 120 GAAATAGAAA CTACCTTTTT TGGAAGAGCT ACAAAGTCAC ATTGTAAAAG GCTGTGTGTA 180 CTCGGCTTGG AGGAGTTTGA GTCCGTAAAT TATCTTCTAC CACAATGCAC AAATTTCCTC 240 TAGTTCCATA GCCAAGTAGT TTCTTGAACT TCATCCCTCT AATGGTCTTG TCTTCCCCAT 300 ACCTTGGTCA CATATGCCCA TGATCATAGC TCCTGAATCT TACTATCACT AATATCTGTA 360 GCTCTTCATA CTTCCTGCTG CCAGCATCCA GCCTCTGACC ACCACCTCCT ACATTTACTA 420 CTCACTGCCT CTAGCACCTC AACTCCAACA GTTCTTTAAC CCCAGTGGGA CCTCCAGTCC 480 ACTGATATTT TAATTTTCCA CTGACCTTCA GCCTCCTCAT GCCCTCACTT CCCATCATCT 540 TAAAAATCCA TGAGCCATCA TTACAGTCTC TCCCTTAAAC ACACCCTCAA TTCCTTTGCT 600 CTTTTCTGAT CCTGTCATGC CCACTTGGCA AAATTTTGGT CCTAGTTAGA TCCAGCTCCC 660 CCACTTGCAT CTGTGAAGTT AAATATGGCC AGAGAAAATC ACACAACCAC AGTGACTAGG 720 GTGGCTCTAA ATGATGATAG CTGTATCCAA AGCATCCTTA ATGCCCATCA ACTGCATTCC 780 CCTCTTTTAG ACATTATTTC ACACCTTTTG CCTTTTCCTT AAACCTCCAA CACCACCTGT 840 TATCCTCATT CTTAGCTGAT GATCTTGTTT CCTATTTCGC TGAGAAAATG AAAGCCATCA 900 GAAGAAACTT TCTACAAGCC CCCACCTCTC ACCTCCCCTG CTACCGGTCA CTTTTTTCCT 960 GGACAGTTCT CTGCCTCCCA CCTGTTACAT GGCTGGATTC TCCATGTTCC TGTCTAAACC 1020 CATCCCTTCC GCTTGTGCAG GATCCCAACC TCTCTCACTC ACTCAAGGAC ATTGCTCTAT 1080 TGATTTTCTC TCATCTTGTC AGTTTTTCCT GCTCTATTGC ATTATTCCTA TCCGAGTTAT 1140 TTAATTTAGC AGCTTCATCT GGGACTCAGG TTCCTCCCAT 1180
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