Tag | Content |
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EnhancerAtlas ID | HS129-33809 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr7:74024180-74025910 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr7:74024628-74024643 | TGAACTCCTGACCTC | - | 6.22 |
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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 |
GH07I074609 | chr7 | 74023620 | 74025738 |
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Enhancer Sequence | TCCCAAAGTG CTGTGATTAC AGGCAAGAGC CACCACGCCC GGCCTGCCTT AACTCTTTAA 60 ATCCTCCTGC TCCAGTGATT CCAGTAACCT CCTTCCCCCA ACCTCAGCCC CAGAATCCAT 120 CTGTAGGGGA ACTATGACTT GTGCCTCCAT CAGTAGAATT TGCTTTCTCT ATTTCTGGTC 180 ATAAATTGGA ACTCCATAGA AATCCTATAT TTATTTATTT ATTTATTTAT TTATTTATTT 240 ATTTTTTGAG ACGGTGTCTT GCTCTATCAC CCAGGCTGGA GTACAGTGGC ACAATCTCAG 300 CTCACTGCAA CCTCCACCTC CCAGGTTCAA GCGATTCTCC TGCCTCAGCC TCCCGAGTAG 360 CTGGGATTAC AGGCACCCGC CACCACGCCC GGCTAATTTT TGTATTTTTA GTAGAGACAG 420 TGTTTCACCA TGTTGGCCAG GCTGGTCTTG AACTCCTGAC CTCAAGGGAT CCGCCCACCT 480 CAGCCTCCCA AAGTGCTGGG ATTACAGGCA TGAGCCACCA TGCCCGGCCC ATTACGCAAG 540 AACTTTTATG TGCTCTGTTA ATCCTCACAG CCCTGCAAAG TAAATATTAT TTCTTCATTT 600 CACAAATGAA GAATCTGAGG TTCAGAAAGA TGAAGGGCTG AGTCCAGGGT TACACAACTA 660 GAAAAGATGA AGCACCAGGC TTGGCTTCAG AGGAGACCGC CAGACTGACT CAGGCGGCTG 720 AGCACTGCCC CAGGCGAACC CCGCAACTTG GGGCTGGACA GAGCTTCTCT TTCGGTTTCC 780 CTAATGTGTT TGAAAGAGAG TAACAGAGGT ACATTTGAAA AGAAAAACAG AGGGCCGGGC 840 GCGGTGGCTC ACGCCTGTAA TCCCAGCACT TTGAGAGGCC AAGGCTGGCA GATCATGAGG 900 TCAGGAGATT GAGACCATCC TGGCTAACAT GGTGAAACCC CGTCTCTACT AAAAATACAA 960 AAAATTAGCC GGGCGTGGTG GCAGGCGCCT GTAGTCCCAG CTACTCGGGA GGCTGAGGCA 1020 GGAGAATGGT GGGAACCCGG GAGGCGGAGC TTGCAGTGAG CTGAGATCGT GCCACTGCAC 1080 TCCAGCCTGG GCGACAGAGC AAGATTCCGT CTCAAAAAAA AAAAAAAAGA AGAAGAAAAG 1140 AAGAACAGAA ATGGGTCCCG ACGAGTCAGG TTTGCTCAGA CCAGACCTCC CCTGCACAGG 1200 AAAGGGACAT CAGGAAAGAT CTCAGCTGCA AAGACCAGAG AAATACGCGC ACACGCACAC 1260 ACACTCACAC ACACACATTG TGTACACACA CATACACACA GGCACACACA CTTTAATTTT 1320 TTTTTTTTAG TAGAGACAGG GTCTCACTAT GTTGCAGGCT GGTCTCAAAC TCCTTGACTT 1380 AAGCGATCCT CTCGCCTCAG CCTCCCAAAA TGCTGGGATT ACAGGCATGA ACCTCTGTGC 1440 TCAGCCTGCT TTTAAAAAAC AAAACAGGCC GGGTGCGGTG GCTCACGCCT GTAATCCCAG 1500 CACTTCGGGA GACCAAGGCG GGTGGATCAC GAGGTCAGGA GATCGAGACC ATCCTGGCTA 1560 ACAGGGTGAA ACCCCCGTCT CTACTAAAAA TACAAAAAAT AAGCTGGGTG TGGTGGCGGG 1620 CACCTGTAGT CCCAGCTACT CGGGAGGCTG AGGCAGGAGA ATGGCGTGAA CCCAGGAGGC 1680 AGAGCTTGCA GCGAGCCGAG ATCGCGCCAC TGCACTCCAG CCTGGGTGAC 1730
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