Tag | Content |
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EnhancerAtlas ID | HS129-02982 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:203576160-203576790 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:203576594-203576605 | GATGAGTCACC | - | 6.32 | Foxd3 | MA0041.1 | chr1:203576399-203576411 | AAACAAACAAAC | - | 6.32 | JUND | MA0491.1 | chr1:203576594-203576605 | GATGAGTCACC | - | 6.62 | NFIC | MA0161.2 | chr1:203576579-203576590 | TCTGCCAAGAA | - | 6.02 | RREB1 | MA0073.1 | chr1:203576623-203576643 | GGGCTGGGGTGGGTTGGGGT | - | 6.03 | RREB1 | MA0073.1 | chr1:203576622-203576642 | GGGGCTGGGGTGGGTTGGGG | - | 7.16 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_25758 | chr1:203575191-203577246 | DND41 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I203606 | chr1 | 203575245 | 203577382 |
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Enhancer Sequence | GTGCCAGGCA CCTGTAATCC CAGCTACTCG GGAGGCTGAG GCAGGAGAAT CATTTGAACC 60 TGGGAGGTGA AGGTTGCAGT GAGCTGAGAT CGCACCATTG CACTCCAGCC TGGGCAACAA 120 GAGTGAAACT CCATCTCAAA AAAAAAACAA GAAAGACATT GTTAGATAGC ATTGAGCATA 180 TCACTTAAAT GGCCTTGGCT CACCCCCTGG GGAAATCATG TTCTTTCAAA GACACTATAA 240 AACAAACAAA CAAAAAAAGC AACAGTAGCT ACAGAGTTCC TGCTCCAGCA ACCAGGAGCC 300 TTGAGGCAGC ACAAGGACAC CGGGGCGGGA GCGTGGCCCA AGAAGCAGAG ACAGCAACAA 360 CAACAGGATG ACTTCATTTA CTGAGTTATC AAAAACCACA ATGTCTGAAA ACCACAATGT 420 CTGCCAAGAA AGAGGATGAG TCACCAAGAC CCACAGGAAA GAGGGGCTGG GGTGGGTTGG 480 GGTGGGCAGC ATGGCATGAT GAGAAAAGCA AGTATTTTGA CAGCACACAG ATTCAAATCC 540 TGACACATCT CTGAGGCCTT CAGCTCTCTG GGTCTCAGCT TCCTTTATCT TTAGTTTTTA 600 TTTATTTTTA TTTCAAAAGA AATGAGATGG 630
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