Tag | Content |
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EnhancerAtlas ID | HS129-27900 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr4:87897900-87899330 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr4:87898595-87898616 | CCATGGAAAGTGAAACTGCAG | - | 6.03 | NFAT5 | MA0606.1 | chr4:87898546-87898556 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr4:87898546-87898556 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr4:87898546-87898556 | ATTTTCCATT | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_28924 | chr4:87897693-87900600 | Fetal_Intestine_Large |
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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 |
GH04I086976 | chr4 | 87897502 | 87900366 |
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Enhancer Sequence | AACCTAAAGT AAAAGTTAAG AAAAAGAAAT GGGCTCTGGA GCCAGAACTG GGTGCCTACC 60 TCGGTGTCTC ACATGCCCAT ACCTGATGTC TAGGGCAAGG TTTGTAACTC TTTGTGCCTC 120 AGTTTCCTCA TCTGTAACAC TGAAATGATG ATAGCACCTA CCTTGTCAGG TTATTGTAGT 180 GATTAAGTAA CTTAATACTT AGGAAATTCT TGGAACAATG TCTGGCACAC AGCAAGTGCC 240 CAATAAATGC AGGTGATGGT GCCTGTGGGC ATTTTATTGC ATGGAAATAA TCTTTGACCT 300 GTTGGAAATC CATGAAGGCC TATTTGCAGT GGAATAACTT GATCATGTTT CTGTTTTTCA 360 AATACAGTAA GTAGTCCCCC CATATGAGAC AGATACATTC TAAGACCCCC AGTGAGTCCT 420 GAAGTCACAG ATAGTACTGC ACCCTATACA CTATATAGTA TGTATTTTCA ATCTCATAAC 480 TGAAACAGCT ACTGAGTGAC TTACAGGTGA GTAGTATCTG TAGTGTAGAT ATACTGGACA 540 AAGGGATGAT TCACGTCCCA GGTGGGACGG AGAGGACAGC GAGAAATTTC ATCACACTAC 600 TTAGAATTGT GTGCAATTTA AAACTTATGA ATTGCTTATT TGTGGAATTT TCCATTTAAT 660 ATTTTTAGAC CTTGGATGAC TGTGGGTAAC TGAAACCATG GAAAGTGAAA CTGCAGATAA 720 GGGGGGCTTC TGTATTGTTT TAGAGGGAGT GTGAGCATGT GTGTTAGGAG GGGGCTGGAA 780 TTGCATTTCT GTGGATTCTC CAACCTCACC TTTTTCCCTC ACCCCCTGCA TAATTACCTG 840 TTCCTTCACC TGTGTTCCCA TGGTGTCTTA TCTCTGCTGT GGCGTTTTCC TATTGTATTT 900 TATAGTCTGT GTTTCTCATA CTAGACTGGG TCCCCTCAGG GTGTTAAGGA CTATGTGTTA 960 CTCATCTTTA CATCCCATTG CCAAGAATAG TACCTAACAC TGGCACATAC TGGGCACTCA 1020 ATAAATGTTT GTTGAATTGC TTTGAAAGGT TTACCAGGGA GTTGCCCTAA CATAATTCTG 1080 GAGAAAGGTC CTCCCATAGA AGAGTCTGGG CACGTTGCTA TGGGAGAGTG TTTTCTTTGT 1140 TTCACACACC AAGTATTTAT CGAGTGCCTA CTGCACACTG TGCTGTGAGG GGATACATAG 1200 ATGAGTCAGA CGTGTACTCT GCCCTGGGTT GTGTTGACTT AATCGTGGGT GGAAGGAAGA 1260 TGGTAAATGG TTGCTGATAG GTTTAATGAG AAATAAGCTA TGATGTGGTT TAGTTGTATT 1320 TGGGCTTTTG TTTAGAAGCA TAATTATTTC AATCAAAGAA TGTTAGAATT TTTTTAAAAT 1380 GATGTCTCAT TGATGGTAGC TTACTTCTCT TACTTCTCAT TACATTCACT 1430
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