| Tag | Content |
|---|
EnhancerAtlas ID | HS129-10771 | Organism | Homo sapiens | Tissue/cell | MCF10A | Coordinate | chr13:98433680-98435110 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr13:98434436-98434451 | ATAGCTGAGTCATAC | - | 6.53 | | Nfe2l2 | MA0150.2 | chr13:98434438-98434453 | AGCTGAGTCATACTG | - | 6.32 | | Nr5a2 | MA0505.1 | chr13:98434795-98434810 | TCTGACCTTGGACTT | - | 6.57 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATAATTTAAA AGGAAGATAA ACAGTTCCAA CATTTAATGG GTAAACAAAT GTGGCAGAAT 60
AATTTATTGA GATATTAATT TGTGATTTTT TGGTCTTGCT CCTGCAGGAG TCTGAAAAAA 120
TATAAAAGTA TTGTCATTTG CCCAGGCAAG AATGTGGGCA TGTTATGAGT CCAAATTCCT 180
TCTATTATTT ACAGTGTCTC ATTTTAAGGC CTGAAAGCAA AGCTGCCAAG CAACCTTCAA 240
AGAGAGAGCT ACAGCTCCAG AGAGTAAGTT ATCAAGGGCC TATCCTAGAG CAGGGCTGGG 300
TCAGGGGAGG ATGGAAGGAG AAGTTCCCCA GGATATCATA AGGGATGGAG TTGGGGTGAA 360
TCTATAAGTG GAAGGGATCC GTTTACCAAA TGCTCACAGA ATTCCAAGAG GTATAGAGGG 420
ACCAGGAATA TCTGAAAAAA AGTAGTCTTC AGGTTTCCCT AAACAGCTTC ATATGGACTA 480
CCTTGGTCAT GAGTAACCAA TGTTGAGAAA CCAATGTTGC AATCTCACTC CCACTCCCAC 540
TGTTACCCTC AGCCATGAGA ATCCGAAACC ATTCTTGGTC TAGGTATCAC TCCCCAGCGG 600
TATGTTTTGC TAAATAATCT TGGGTTTAAT TATAATATTG GTCACAAATT ATTTGCTTTG 660
GCCCATGGGA CACAAGTGGA AACTTGAATA GTGCTTGCTT ATTTTGATTT CATCATTTCT 720
TGCTGCTTCT GGAACACAGT CCCCCAGTAA TCTGGGATAG CTGAGTCATA CTGGACAGAC 780
ATAGCCCTAT TGCCCACACC ACCAGGGCCA ACAACCAGAC ATGTGAGAGA GGTCTGGGAC 840
TGACAAACCC CCAGGTGACC CATCCTGCTA TGGGCTGAAT GTTTGTGTTC CTCCAAAATT 900
CACATGTTGA AACCTAATCT CCAATGTGAT TATATCAAAA GATGGGGCCT TTAGAGGTGA 960
TTAAGTCGTG GGAGCACAGC CTTCGTGAAT GGAATCAGTA CCCTTATAAA TGAGGCCCCA 1020
CAGAGCTAAC AAGCCCCTTC CACCATATGA AGACACAAAA AGAAATTACC ATTTATGAGT 1080
AACAGGCCCT CAGCAGGCAC CACATATGCC AGAGCTCTGA CCTTGGACTT CTCAGCCTCC 1140
AAAATTGTGA GAAATAAATT TCTGTTGTTT ATAAGCCACC CAGTTTGTGG TATTTTTGTT 1200
ATAGCAGCCC AAATGAACTA AGACAGAGAT TGGTACTGAG GAGTGGGGGT ATTGCTACAA 1260
CAAATATCCA AAAATGTGGA AGCAGCTTTG GAGCTGGTTA ATGGGTAGAG ACCGAAAGGA 1320
TTTTGAAATG TATGCTAGAA AAAGCCACAT TGCCACGAAG ATACCTTAAA GGGAGGTTCT 1380
GATGAGAGCT CAAAAGAAGA GGAAGATGTA GAGAAAGCCT CAATCTTCTT 1430
|
| |
|
|
|
