Tag | Content |
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EnhancerAtlas ID | HS129-35085 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr8:23000380-23001960 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr8:23000461-23000476 | CTATGACTCAGCACC | + | 6.34 | Nfe2l2 | MA0150.2 | chr8:23000459-23000474 | CACTATGACTCAGCA | + | 8.07 | STAT3 | MA0144.2 | chr8:23001518-23001529 | CTTCCCAGAAG | - | 6.14 | Sox3 | MA0514.1 | chr8:23000474-23000484 | CCTTTGTTTT | + | 6.02 | Sox3 | MA0514.1 | chr8:23000985-23000995 | AAAACAAAGG | - | 6.02 | TBX20 | MA0689.1 | chr8:23001406-23001417 | TTTCACACCTA | - | 6.14 | TBX2 | MA0688.1 | chr8:23001406-23001417 | TTTCACACCTA | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | AAAGAATCAC AAGAAATTAT CTGTTGTATT CACCTGAATG AAGAAGGGCT GGGGGCTGGA 60 GGAAGTGTTA GGGGACTACC ACTATGACTC AGCACCTTTG TTTTTTTTTT GTTTTTGTTT 120 TTGTTTTGAG ATGGAGTCTG ACTCTGTAGC CCAGGCTGGA GTGCAGTGGC GTGATCTCGG 180 CTCACTGCAG GCTCCGCCTC ACGGGTTCAC GCCATTCTCC TGCCTCAGCC TCCCGAGTAG 240 CTGGGACTAC AGGCACCCGC TACCACGCCC GGCTAATTTT TTGTATTTTT AGTAGAGGTG 300 GGGTTTCACC ATGTTGGCCA GGATGGTCTC CATCTCTTGA CCTTGTGATC CACCCTCCTC 360 GGCCTCCCAA AGTGCTGGGA TTACAGGCAT GAGCCACGGC GCCCGGCCGA CTGAGCACCT 420 TTCTATAGTG TGGCAGATGT GTGGCTCTGC ATTTACCACT TTCAAAAAAT GTGCAGCGCG 480 GCCAGGTGCA GTGGCTTATG CCTGTAATCC CACCACTTTG GGAGGCCAAG GTGAGAGGAT 540 GACTTGAGGC CAGGAGTTTG AGACCAGCCT GGGCAACATA GCAAGATCAG ATCTCTACAA 600 ATTACAAAAC AAAGGTGCAA TGCGATTCAG CAGCGTGGAG TAATTGTTGA TATTTTTTGT 660 TTATTTCCTT ACCTTTTTAT ACTTCCCTTC ATTAAAAAAA ATGGGGTATA GTTATAGGAA 720 AGGAAGAAAA TGGGTGGAAA GTGAACCTTG TCTAGGTAAG TATTTGACAA GTGATCAAAG 780 AGGAGCCAAA AGCAGAGAAA AATAGGAGAA TCAGTTCCTA AACAGGCGTG GAGGAAGGAG 840 ACAGTGACTC ACAACAATTC AGGGAATTCC TCACTTCACA CAGCATCACA AAAGAAATGG 900 CACCTACGTT CCACTGGTGT ATGCTACAAA CCAAATCATT CTTTAAAAGT CCACAAAAAA 960 TTAGGTAGGA TCATCTTATT TTATCCTGAA GGAAAGAACT TAAAAAAAAA CAAATGTGTG 1020 TCCAGATTTC ACACCTACTC AATGTCATAT CAAAACTAGT GAATCGATGT GAATAACTGG 1080 ATGTGTGTGT TTCTGTAATA CAAAAGCACT TCTACACACT GACTCAGAAA TCCTACTTCT 1140 TCCCAGAAGC CTCCTTACAT ACTTGATCAG AAATCTGGAC AAAGATTTAC TGTGAAATAT 1200 GTTCAATGTA GTAAGAATTT TGAAGAACAT TTAAAACTTC CGCTGTTTCA AGCAAGGGCT 1260 CCCTGACTTC TGTTAGGAGC ACACGATGGA GACTGTGCAG CCTTATTCAG TCCTCAGTGA 1320 ACCCTGTGAC ACCCACTCTA TGCCTGTGGA GATCCAGGCT CTGGGGACAC AGCAAGGACA 1380 GGACAGGGAG TAAGAAGCAG ATGTCCTGCA GACTGGCACG GTCACCACCT CAGTGCAGCT 1440 GCTCCGTCCC CTGCAGTCCC CTGTCTCCCA AAGGCTCCAT GTCCCCTTGG GCCAGGAAAG 1500 AGGAGGCACT GCCATGTCCC ACTGTCTACA AAGTCCTGTG CAGGCTGCAC GCCAGGCAGG 1560 GCACAGTCCC TCCTCAACTC 1580
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