Tag | Content |
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EnhancerAtlas ID | HS129-20514 | Organism | Homo sapiens | Tissue/cell | MCF10A | Coordinate | chr2:132243520-132244760 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Spz1 | MA0111.1 | chr2:132243608-132243619 | AGGGTTACAGC | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 132244223 | 132244349 | chr2 | 132244073 | 132244209 |
| Enhancer Sequence | GCAGGGATAG GACGGCCCTC CTTATGAGTT TCCGGGGAGT TCTTCCTCAG AGAATGAGAT 60 CTTTGCTCAT TCTTGCCTGG TGGTGGTGAG GGTTACAGCG GTGTCATGCT GGGAACTCTG 120 TCAGCTTGTC ACACTTGGCT GAACAAAGAT GGAGTCAGGG TTGCCCTGAG CCAAGGAGGA 180 GCGCAGTCAG GAACACGTGG TGGGTGATGA TTGGCCACCT CAGCCCAGCA GTGACTAGTG 240 AAAAAGGCAC AAAGCAGACA ATAGCCACCA CGCATCTCTT GTGGTACAAA CTGCCATAAT 300 TCTAGTCCCC ACTGACTGGT CAAGGGGCAA GGATTCTGTC TTCCATGAGC AGACGGGACC 360 CACCACCCTG CAGCAGCTCC CACACTGGGC CAGCATCCTC CTCTGAGGCC ACAGTCCCTC 420 TGCAGGCCAG GCCAGACAGT CAGATCTTCT GTAGCCGCAG CCTAATCTGG GTGCTTAGGT 480 GCCCATGCGC TCTCAGCTCC CCACAGCACG CAGCATGGCA GGCCGTGCAC CTAGGCCTGA 540 CTCAGAGTCG GCTTCCCTTC AGTTTGCCGC CATCTGAGCT TCCTCTCCTC CCCTCAGTAG 600 TGACCCAGTC CCTTCTGGAA ACAAGGATGA CAGCGAAGCA GAAAAGAGCA AATAATGCTT 660 TTTTTTTTTT TAAGAGTGGT GGGGGAGGGG GGTTTAGAGA CTGAGTCTTG CTCTGTCACC 720 TGGTCTAGAG CACAGTGATG CAATCACAGT TCATTGCTGC CCGGAACCCA TGGCCTCGAG 780 GGATCTTCCT GCCTCAGCCT CGATGTAGCT GGGACTACAA GCATGGGGCC ACACCTGGCT 840 AATAATGCTT ATCTTTAAAT CTGACAGGGT TGACAAACCC TGGAAATGTG AAACCAACAT 900 AACCGTAAGC CATAACTGAT ATTAAGAAAA TCCTGGAAAT CTTCAGGAAT TGCGTGCTCT 960 CGGGGCTAGT GGGGAGCCCT GTTCAGGCCT CCTCACTTTA TGAAGGATGA GAAGGCCCAG 1020 AATAGAATGG CCTGCAGTGC CTTGCAGTGG GGAAACCAGC TTTGCTTAGC CCTGCTCCCT 1080 CGGGAGGGGC TACTGAGTCA GACGGGCTAG ACAGTGGGAT TGAACCAAGT GTGGCTGCAG 1140 GTTGGGGTGT GAGGGCAGGG TGACTGATGC CCCTACACCT GGTCCCTGGA GGGCCCTCCT 1200 AAACGCCAAA AACAGTCAAT GACCACTGAA TGTTAAAAAC 1240
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