Tag | Content |
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EnhancerAtlas ID | HS130-28963 | Organism | Homo sapiens | Tissue/cell | MDA-MB-231 | Coordinate | chrX:135332180-135333440 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chrX:135332395-135332409 | CAATCGTAAACAAT | + | 6.92 | HINFP | MA0131.2 | chrX:135333167-135333179 | CCGCGTCCGCGG | + | 6.04 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATCTAAATCA CTGAAATAAA CCAGTGCCTG AGAGCCACAG GTACCAATAA GCAACACAAT 60 TTATTGGAGA CTGTCTTTCT AGGTGAACCA TAAGTATAGA CACGGAAGGA AGATTCTTTT 120 CTCCCTAATG AATGGTGAAA GTGTATGTAG TATATGCTTC TGACACAGTC TTTGGAGAGC 180 TGATTCAAAG TCTTCTCAAG TAACATATAG CTTCCCAATC GTAAACAATC TAACTTTTTA 240 ATTGCAAATG CAAAAAAACC CCTAAGAAAT TCAATTAAAA TTAATAAAAT CGTTTTATTC 300 GCGCTCATAG CAGAGGGAAC TAGTCTAACA GGCTAAAAGC AACCTCCTGA AAGGAAGAAA 360 TCCTATCTCA GGTAGTGGAG CAGTCTCCTG GACCAAGCAA TGTGCTGTCA AATTGTATAA 420 GATTAACGGT TTTCGAGGAG GGAAAAACGT TTTGGCGATG GGACTAGTTG AGGAAAAAGC 480 ACTCTGAAGT GCTGATTCCC GTTCAGTTCA GCCTAGAGAC TGCAAGATGT CCCACAGAAG 540 ATGACATCTT GTTGAAGTCA TGTGCTACAG CAGGCAAATC AGGAGATGCA AAGAGCCAAG 600 TTTCATCCCA ACTTTTAAAG CAACTTTTAA GCATCCCCAC CCTCACCCAG CTTCCTCCCT 660 GGACCTTGAC CGGGAGGGTG CAGGAGGTAA GCCTTTGGGA GAGGCAAGGA CTGCGACAGT 720 AAAAGCGCCT AAACTCGCCC ACGACCCGGG CTGGGGGATA ACTCAAACTT TCCGTGCCTG 780 GAAAGGCTGC CTGGCGGCGG AGGCGGCGCC GGCGCGCGGA GTCCCTGCGG GCGCCCGCAC 840 ATCCCAGGCA GCTGTGCGTT CGTTGGGGCG GTTGCGCGGG CGGCCACCGC CCCCCAAGGG 900 CAGATGGGGC ACGGGGCGGT CCGCGGGGTC CGGCTTCCAG CCGCCCCCGC CCCGCCCGTC 960 GAAGCAGAGC CCGTGAGTTG CCTCGCGCCG CGTCCGCGGG GCTCAGACCG TTGGCAGCGG 1020 CAGTTCGACC GTTGGCGGCG GGACTCAGGC GGCTCGCGGC GTCGGCTGAC AATTTCAACC 1080 CCCCGCCCCC GCCCCTGTCC CATCCCAGGG CACTCCGGCG GGGGTGAGGG GAGGACCAGA 1140 TAGCACGAGG CGACTCCAGG GAAAAGTTTT GTGGCGCCCG CTGCGCCGCT CCGACGGCCC 1200 GGGGACTGCG GGAACCCTGC CTCCCACGCG GGCCCGAACC ACCCCCGGGA GCCACCCGCC 1260
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