Tag | Content |
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EnhancerAtlas ID | HS129-01725 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:116810320-116811740 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:116811488-116811509 | AAATAAAAAGTGAAAGCTCCC | - | 6.19 | NFE2L1 | MA0089.2 | chr1:116811016-116811031 | TCTGCTGACTCATCT | - | 6.09 | REST | MA0138.2 | chr1:116811170-116811191 | AACAGCACCAGGGACAGAAAA | + | 6.18 | Stat6 | MA0520.1 | chr1:116810687-116810702 | GTGTTCCTGAGAAAT | + | 6.87 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_33703 | chr1:116808541-116812093 | H2171 | SE_66933 | chr1:116808541-116812093 | H2171 |
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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 |
GH01I116267 | chr1 | 116810481 | 116811570 |
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Enhancer Sequence | ACCGTACCAT GAAAATCGAG ATAAGGTGGT GCTTTCCTCA GTCAGCAGGA GCACCCAGTC 60 AAACAGAGCA CCTGGCCCCC GCCCAGCGAA TGAAGAGTGG TTGATTCATG AAGAGCCTGG 120 AATGGAGACA GCACCTGTCA GAAGAGGTGA TGGGGCATGA GTATGTGTAC CAGGTTCAGA 180 GTTCGGGCTC CTTCAGTCCA ACTGACCAAT AGGAGAAAAC GCTGAAAAGA GACGGTGATT 240 CAGGGCTGGC AGTGAGGAAG TCCCCAACTT TATCAATGTA CCTGAATTAT TGTTTGGTTC 300 TTCCTGTCTT TGGCTTTTGA TAGTTGTGGT CCTCAGCCAA GAAGAGACAG AGGAAATGGA 360 ACAGAGGGTG TTCCTGAGAA ATATGGGGGA GGAAGAAGTT ATTGTCAACT GGCGCTCCCG 420 CCTGCAATTA TTGTGGTGTT GGCGTTCCTC ATACTTCCCA GTGCCGTCCC CACCACTCAT 480 TGTGCTGGCT TGGAGGCACT CGGTTCAGAG TCTTCAAACC CTCCTCCTCA GCCTTGGCCA 540 GGCTGTCTGT CTCCTCAGGG CAGCCAAAGA AGATGAGCTC ATTTCCAGAA CCCAAGAGGT 600 GGCTCTGACC CTCTCTTCCC AGTTATTGCT GAAGTTGGGT GGCTGAAACC AGTCAGGGCA 660 TCATGCTGGC ACCAGGCCAG TCTTGCATCA GGCAAATCTG CTGACTCATC TCTCTCTTCT 720 AAACAAGCTC TGAGAGTTGG CATGCAGGAA GCAGCACCAA GGAGTCTGAT GGCGTGGGCC 780 ACCTGGCAGG GACTGACCAA GGGGAGGCGA GGAGCAGCAG CCACCTGCCA CCCCAATCCC 840 ACATTCTTCT AACAGCACCA GGGACAGAAA ATATGTGCCT ACCCAAGAAT TTCAGGGCCA 900 CAAGTAGAAA CAAGTATATC ATAACAGGGA AGGTTGCAAC ATGAGAAATA TGCTTTCCCT 960 GAGAAAAGTG GATAACTTGA CTTGAATGAT CTTCAAAAAT TATGTTTGGT GTTTGGAAAA 1020 GCTTAGTGGA TTCTTTAAAA AGAGCTACAC ATTAATATTT GCAAATAAAA GATATACAAA 1080 GAATAAAACA AAAAAAATGG CCCATAATCT CCTCTCCCCC AACCTCAGAT AATTGTAGAA 1140 GTACTTGATT AGATAATATA TATGTACAAA ATAAAAAGTG AAAGCTCCCA TCCCCTGACT 1200 TATCCCTCTC TTAAACGCAC ATTTTTACGT GCTTTTTCTT TCTTTCCCAT GGGAAAACAA 1260 TGTATGTATA CCCCTACATT TCCATTTGTC CTTAAACATC TTTAGTGTAC CAAAACCGCC 1320 TCAGGTTTGC ACAACTTCAT GGAACACCAA CCACATTGTA CTTTAGGGTG TCTTGAACAG 1380 GGGCAATATT CCCATAGCAC ACAGTGTGAA TGGTGCCCAC 1420
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