Tag | Content |
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EnhancerAtlas ID | HS129-32465 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr6:139854120-139855530 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr6:139854421-139854434 | GAAGGTTCTAGAA | - | 7.12 | SOX10 | MA0442.2 | chr6:139854588-139854599 | TGCTTTGTTTT | - | 6.02 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH06I139532 | chr6 | 139854086 | 139856366 |
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Enhancer Sequence | CTCAAAGTGC TGGGATTACA GGCGTGAGCC ACCCAGCCCA GCCTTAACCT TGTCTTTTAA 60 AGGCAGGGTT TGACACATAC TTGGTATGAG AATGAAGGGT AGCGTGAATA AAAAGGAATA 120 AGGGCCTTCC ATTCAGAGGG ACTGATTCTA GACTTTTGTA ATGACTGCAT TTTGGGTGAA 180 ACCTTTGTAA ATTGAGACAA AAATGCCTGA GTTTGTCTTA AAAATTTTTA TTTATTTTAA 240 AAAATTCACC TCGATATTGG AAAAGATAAA GGTGTTAATG TGTACTACTC CAGCAGTGAG 300 GGAAGGTTCT AGAATGCTCC CTGGTTGTTG CCCTCATACT TTGGGATGTT ATGCTGATCC 360 CTGCACCTTA AGTTCAAATT CCAGTTTCCT TGCTCAACTT GAACAACATG CAAGAGTTGG 420 CTGTAAGGGC TGTTTTTTTA TTTTTTATTT TTCTGCTTGG TTTTGTTTTG CTTTGTTTTT 480 TAACCACGTA ATTAAAGAAT TGTGGATATA GATTAACTTC TCGCCCACTC TATCCCCTCC 540 CGTACTGTTT TAACTAACAG GGACTAAGCA CCATGGTCCT TTGATGGATT TCCTATTTTG 600 ATGGTAAAAT CCTTGTTTTT CTTACAAAAA ATATCTTCTC TGCTTCTGAC AAAACTCTAA 660 TCTTGCCCTT CTGACTCCGA GTCCCTGCAT GCCTCTCTTC CATGTTTCAG GAAGGAACAA 720 TTAGGCAATC CTGCCATGTT TCTTCTGAAA GTAGCAAAAA CAGTGACTTC AAGAGCCCTT 780 ATGCTGAATC ATGACATAGA TATTTTTTTC TACACCACCC GGAACACTTT GAATTAAAGC 840 AGGAAGCCTG ATTCTAAGCC ACTATTGCAC TAAGCCCTGG AAAGAAAGAA GTGTGGAAGA 900 AGGGAAGAGG ATGGAAGAAA AACAACCTTT TCTGAGTAAA AAGTTTAGTC TTTCTTCCAG 960 TGTACAGTTT AAAAATGTGG GCTCATTGGA ATGAATTTGA AGGTTAGGTT ACAATTTGCT 1020 TACAGCAGAT TTTACGATTA AACTCATTGA ATCAGCCTTT TTTTAACCCG TTAAGTGACG 1080 TATACATGGG ATTAAACAGA ATGAAATTCA GTTGTTTCTC AACTCACTCT CCTAGCCTCA 1140 CATCTGTCAA AATCATTGCT GTTTGATTTT CTTTTCTGCA AAGGCCCCCG AGACACATTT 1200 GCCTTTAAGC GCTTGGGCAC TGGTGGGAGC TGCGTGTTCT GGGTGTCTTT AAGTGCACTG 1260 GGCTGGGCTA GGCAACGCAG CTCGTGTGTC CCGGGAAAGC TGCAGTCTGC TGAGTGTAAG 1320 ATACACACCC AGACCACACC TTCAGAGCCA TGCAAAGCTG GAAGGAGACA GAGATAAGGT 1380 ACACTGAAAG GAAGAAAGAA ACTCCTCTCT 1410
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