Tag | Content |
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EnhancerAtlas ID | HS129-02325 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:156895830-156896990 |
Target genes | Number: 23 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:156896349-156896369 | CTCCACCCCACCCCCCACCT | + | 6.03 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 156896077 | 156896303 | chr1 | 156895882 | 156896378 |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I156926 | chr1 | 156895977 | 156896091 | GH01I156927 | chr1 | 156896900 | 156898011 |
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Enhancer Sequence | CATGGGAGCA AATTTTTACA TAGCGTCATT TCTAGCCATT AGTTCAGTTT TTGCTGTGAC 60 TTAGAAAAGG ACCTCCATTC TTACAGCACT GTTAGAGAAG CAACTGCCAT GTGGAGGCTC 120 ATGTTGTAGT TATCTCTTGC TGTGTGACAA ATTAACCCCA AGATTCAGTG GCTTAAAAGG 180 ACATACATTT ATGATCTCAT AGCTGCTGTG AGATGACCTG GGGGTGGGCT AGCTGAGTGC 240 TCTGGCTCAG GGTTTGAGGT TGCGGTACAG CTGCTGACTG TGGCTGCACT TACCTCAAGG 300 ATCAACTGTG GTGGAGAATC TGCCTCCAGG CTCACTTATG TGGCTGCCTG GGCCTCTCCA 360 CAGGCTGCCT GAGTGTCCTT ACCACATGGC AGCTGGCCAG CTGAGAGAGT GCCAGAGAGC 420 ACTCAAGACG GAAGCCACCG CCTTTGTAGC CTAAACCTGG AGGTGCTGTC CCATCTCTTC 480 TGCCATGTTC TGTTCATTAG AAGTGAGTCA CTTATTTCCC TCCACCCCAC CCCCCACCTC 540 TTCTTTTTTT TTTGGAGACA GAGTCTTGCT ATGTCGCCCA GACTAGAGTG CAGTGGCACA 600 ATCTTGGCTC ACTGCAACCT CCGCCTCCTG GATTCAAGTG ATTCTTCTGC CTCAGCCTCC 660 CAAGTAGCTG GGATTACAGG TGCACGCCAC CATGTCCCGC TAATTTTTTG TATTTTTAGT 720 AAAGACGGGG TTTCACCCTG TTGCCCAGGC TGGTCTCGAA CTCCTGAGCT CAGGCAATCT 780 GCCCGCCTTG GCCTCAAAAA GTGCTGGGAT TACAGGCGTG AGCCACTGTG CCTGGCCAGA 840 AGTGAGTCAC TTCTAATGTG AAGTCCACAC TCAAGGGGAA GGAATGACAC AGGGGCATGA 900 GTTCCAGGAG GTGGGGACCA CTGAAGGCCA TCTTAGGGGC TACCCTACCA TGGGTCACCA 960 ACTTTGGGGA GCAGTCCCTT CACAATGGGC ACATCTGTGA ATTTTTAGTC TGGGGAATTG 1020 TCACATATAT TTCCTATATT GGGGGGGCAA TCCTTTGACT CTACTTCCTA GCTGCTTCCC 1080 AGAGACGCAC ACTTCCTCTC TGTTCCCTTC CCTTACCTGG CCTCAGTGGT ACCTTCTGGT 1140 TCTCAGATCT CCCCTGCCCT 1160
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