Tag | Content |
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EnhancerAtlas ID | HS129-00253 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:10311260-10312340 |
Target genes | Number: 14 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:10311379-10311400 | TTTTCCTTTCTTTTTTTTTTT | + | 6.36 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 10311478 | 10311596 | chr1 | 10311863 | 10312077 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I010250 | chr1 | 10310859 | 10316097 |
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Enhancer Sequence | AAGATATAAG TTAGGAAAAT CTATTAGTTT CAGAAGCTTT AAAAGTCTGG GAGAAAGGAA 60 TATTGAAGAA GAGGAAAAGG ATTTCATGTG AATTGAGGAA GTTAACTCAT TGGTGTAGTT 120 TTTCCTTTCT TTTTTTTTTT TTTTACTAAG GAAAAGAGAA CAAAGCGATA AAATCTGAGT 180 AGTCTTTCAG TCATTCTTGG TAGAATTGGT AGCTAAAAGG CTGAGTGAAA TATGGCTTAA 240 AAGCTTTATT GGCTGGGCGC GGTGGCTCAC CCCTGTAATC CCAGCACTTT GGGTGGCTTA 300 GGTGGGTGGA TAACCTGAGG TCAGGAGTTT GAGAACAGCC TGACCAACAT GGTGAAACCC 360 TGTCTCTACT AGACATACAA AATTAGCCAG GTGTGGTGAT GCATGCCTGT AATCCTAGAT 420 ACGTGGCAGG CTGAGGCAGG AGAATTACTT GAACCCAGGA GGCGGAGGTT GCAGTGAGCT 480 GAGATCCTAC CATTGCACTC CAGCCTGGGC AACAAGAGCA AAACTCCGTC TCAAAAAAAA 540 AAAAGCTTTA TCATTTATTT TTTGGCCCTG TCTTATGGTG CAGAGGCTTA AAAGTTTTTT 600 GACAGCAAAT TTTCTAGAGG CTAGGAGTGT TTATTATAAC CATGTTTTTG AGCGGTGAGG 660 ACTACCTCAG AGGGCATGCC TTGTGTCATC ATTGTTCTTA TTGCTGAGCT ACCGAAACCT 720 AGAATCTGAC TCACACAATA TGACACTTAT TTCCGTTTTC TTGGTAGAGT TTGTGTGGTC 780 ATTCATCTTT TAGATCTTTT AGAAACTACA GTCCTCCTAG TTCCCACTTT TATATTTATT 840 TATTTATTTA TTTTTGAGAT GGAGTCTTGC TCTGTTGCCC AGGCTGGAGT GCAGTGGTGC 900 AATCTCGGCT CACTGCAACC TCTGCCTCCC AGGTTCAAGC AATTCTCCCG CCTCAGCCTC 960 CCAAGTAGCT GGGATTACAG GTGCGTGCCA CCATGCCTCG CTAACTTTTG TATTTTTTGT 1020 AGAGACGGGG TTTCACCACG TTGGCCAGGC TGGTCGCAAA CTCCTGACCT CAAGTGATCA 1080
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