Tag | Content |
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EnhancerAtlas ID | HS129-30755 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr5:177504700-177506130 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr5:177506018-177506039 | TATTAGTTTTTCTTTTTTTTT | + | 6.18 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 177504847 | 177504951 | chr5 | 177505069 | 177505886 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I178077 | chr5 | 177504801 | 177506014 |
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Enhancer Sequence | GAGCATCTCC CTTTCCCATG GCAGACGCGC ATTTGAAGGA GCTGCCTCCA GGCCTCCCAA 60 CTCCACTGCT CCGGCCTCCA GCCTGGCCCT CTTGGACACA GAGCTTGGAC ACCCAGGTTC 120 CTGTCAGGAC TGAAGTGGCC CAGAGCTGGC AGGGCCTCTA GAGGTCATCC ACCATGCTTT 180 TCCCTCCAGC AGACAGAAAG TGGATGTCAG ACTTCGGCCA CCAGGGCAGG AGCAGAACTC 240 AGGCGTGGCA CTTCACAGTT CCAGAACCCT AGGGTCTCTC AGGCTGGAGT GGGGGTGGGG 300 CACTCACCTT TATCCAGCTG TCTCTGCTAG TCAAGCAAAA GCACTGGGCA GGCTGTTTTC 360 TCTAAATCCT CCTGACAACA CTGGGAGGTG CTCCAAGGAA GACACAGACA CGTGGAAAGC 420 TTCAAAGACG TAACTGGTCT GACCCAAACT CCTTGCTTTT CTGACACTGT ATCACAAAAA 480 AATCTTCTCC TGCCATTCCC ACCAATCAAT TTCATCCTAA GTTCTTCGCT TACACCAGCA 540 GCAGCATCTT CCAGGCTTCC AGGCCAGCAG TGGAGGAGTC ATTTTTAGCT CTTCCTTCTC 600 CTTCACCCTG GCATCCCATT TGTGGGCACA GAGCCCGGCC CTAGAGGGCT GGGAGAAACC 660 GCAGAGGGCA TCCAGTTCAG CTGCCCACGT AACACTTGGA TTTTCTGTAA ACATTTGTGG 720 TGAAGCTGCT GCCCAGGCTC AGCCTAAACA CGGCCCCCAC CTCTGTGCGA GGGAGCTCGC 780 CACTCCCTGA CATGACTGTT GCATCTTGAA ACGGTTATGA TGTTCAAAAG TCTGCCTCAG 840 TTTGAGAGTA AATCTGCCTC CCTGTTGCCT CCTCTCCTCG CTCCCTGCAC GCACGTCCAC 900 TGGTTCTAGT TTTTTGCGGG GGTGGTATAG AACCGATCTG ACCTCTTCTC TGTCTTAGCC 960 CTTTGAATGA GAAAGCCGTG ATCAAGCCCC CAGCGGGTAA ATATTCCCCA TTGCTCCAGC 1020 TGGTCCTCAT ATGACTAGTT TCAAATCACT AGACAGTCTA GTCCCTTCTC CAATCATGCG 1080 TCAGTTCATC TAAACTGGGT GTTGCAAACT CAATGCCTAA GGGGGCCAAG CAAGCGGCAT 1140 GGGTGAGTGA GACGGGTGGA GCGTAGCAAT ACGGAGTGGT GGGGACTGCA GCCAAGAGGT 1200 GTTTCAGCCA ATTGCTGCCA TGCAGAAGTG AGGCCCTGCA TCCCCAGATC CTCTCGTTTT 1260 CGAATAGGAA TCAGTATAAT TTGGGTTTGG ATTTGAAATG TTGATTTTTT GAGTTGGTTA 1320 TTAGTTTTTC TTTTTTTTTT TTTTTTTCTT TTTTTTGAGA CAGAGTCTCA CTCTGTCACC 1380 CAGGCTGGAG TGCAGTGGTG CGATCTCGGC TCACTGCAAC CTCCACCTCC 1430
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