Tag | Content |
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EnhancerAtlas ID | HS044-00838 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr1:151913450-151914370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr1:151913717-151913728 | TCAAGGTCATT | + | 6.32 | ESRRB | MA0141.3 | chr1:151913815-151913826 | TCAAGGTCATT | + | 6.32 | Esrra | MA0592.2 | chr1:151913716-151913727 | GTCAAGGTCAT | + | 6.32 | Esrra | MA0592.2 | chr1:151913814-151913825 | TTCAAGGTCAT | + | 6.62 | Esrrg | MA0643.1 | chr1:151913717-151913727 | TCAAGGTCAT | + | 6.02 | Esrrg | MA0643.1 | chr1:151913815-151913825 | TCAAGGTCAT | + | 6.02 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_10113 | chr1:151911730-151920206 | CD14 | SE_23217 | chr1:151913044-151914904 | Colon_Crypt_1 | SE_35018 | chr1:151912751-151921049 | HeLa | SE_36600 | chr1:151912821-151915067 | HMEC | SE_64760 | chr1:151912958-151915082 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 151913574 | 151913780 | chr1 | 151913815 | 151914271 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I151940 | chr1 | 151912796 | 151920351 |
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Enhancer Sequence | TTATTATTCC CAATTTACTG ATGGGGGAAT TAAAACTCAT TGAGGTTAAG TAACTCATCC 60 ATGAAATCAA AGCTAGTAAG TAAAGAAATC AGAATTCAAA CCTAGGCAGT TTGGTGCCAG 120 AGCCTGTGTA AGTAACCATT GCACCCCACT CTGTTATGGT AGAAGCTGGG CAGTCCTGAA 180 TCAGTTCCCC AAAAATACAG TGATTTAAAT AAAATTTATT AGTGTATCCT AAGTGAATCT 240 GACTAAGCCT GTTGCTGGGG AAATCGGTCA AGGTCATTTG ACTCCCTTTC TAGCTGCCCT 300 GCCTGTCTCT CTCTCTCTCT CTCTCTCTCA CACACACACA CGCACACATA CACACACAGT 360 CTTTTTCAAG GTCATTTGAC TCCCTTTCTA GCTGCCCTGC CTGTTTCTCA CTTAAACACA 420 CACACACACA CACACATACA CACACACACA CACACGCACA CACAGTCTCT CTCTCTCTCT 480 CATAGTATTT CTTCCCCTGT CTGGCTCACT GGAAGAAATG ACAATATCAT AGCTGCTCCA 540 GGTCTGTGAA TGATGACAGT AAGGACTGGT GAAAATGAGT CAGGAGCCAT TCATTGGAAA 600 GATTGTGTAA GTGTATGTAT TGTATTTTCA CCACTAATAT AGTAACTTGG TTACAGTTGC 660 TTGGTAACTA TACACTGTTC TAAGTAATCC TTAAAAACTG GCTCTGGTGA ATGCCCACAG 720 AGATTTTTCC ACCTCTTTTT GCAGCCTCTA GTTCTCACTA CTGTAACAGG GCAACAAAAA 780 TCCCATAGTC CTTATGTCAT ACCTTTGCCC ACACTCCTCC TTTGTGTTTG GCATCCACTC 840 ATAGCACTCT TTTGCCAAGT TCTGCAAGTT AGGAATTCGA ACCCATGGCA TGAAAACACT 900 TCTAATAGCT CTTAAAATTA 920
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