Tag | Content |
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EnhancerAtlas ID | HS113-03509 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:224443190-224444700 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr1:224443252-224443263 | GTCTGTGGTTT | + | 6.62 |
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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 |
GH01I224256 | chr1 | 224443941 | 224445622 |
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Enhancer Sequence | GCCTAAAATG GTGTAGTTTT TAATCCTTTA TCAGATATAT GCTTTGCAAA TATTTTCTCC 60 TAGTCTGTGG TTTATCTTTA TATTCTCTTA TTTGCATTTT TGTAAGAGAC TGGGTCTCAC 120 TACACTGCCC AGGCTGGCCT CGAAGTGCTG AGCTCAAAGG ATCCTCCCAC CTCAGTCTCC 180 TGAGTAGCTG GGTTTACAGG CGTGTACCAC TGTACCTGGC TTATTGGCAC TTTTGAAGAG 240 CAGTTCAGTT TATCTATTTG CTCTTTTATG GTTTACGCTT TTAATATCAT ATAGGAAATC 300 TTTGCTTAAT TCAAGGTAGA AAAAAATTTC TCCAGTGTTT TCTTCCAAGA GTTTTATAAT 360 GTTGTTTTCA ATGGTCTTTG ATTCATTTTG AGTTATTTTT TGTATGTGGT AAAAGGTATG 420 AATTAAGGTT CAATTTTTCT TTTTGCATAT GGATATTCAG TTGCTCCAGT ACCATTGTTG 480 AAAAGACTAT ACATTCTCCA CTGCATTGCC TTTGTGCTTT TTAAATACAT CAACTATCTA 540 GATATGCATA GGAATATTTC TGGATTTTTT TTCTGTTCCT TTTATTTATC TGTCTCAGCT 600 CTATGCCAAT TACCATGCCG TTGAAACATC TTTTAATTTA AACATATAAA TACATGCCAG 660 GCATGGTGGC TCATGCCTGT AATCCCAGCA CTTTGGGAGG CTGAGGCGGG TGGATCACTT 720 GAGGTCAGGA GTTCGAGACC AGCTTGGCCA ACATGGTGAA ACTCCATAAC TACTGAAAAT 780 AAAAAAATTA GCTGAGCATG GTGTTGCATG CCTGCAATCC CAGCTACTCG GGAGGCTAAG 840 GCAGGAGAAT CGCTTGAACC TGGGAAGCGG AGGTTGCAGT GAGCCAAGAT CGTGCTACTG 900 CACTCCAGCC TGGGCAACAG GGTGAGGCTC CATCTAAAAA AAAAAAAAAA AAAAAAAAAC 960 CCACAGAAAA CTCCCCACAA AACACATCTT AAAGCCAGTT CTACATGCCC CAAGGTAAAG 1020 GGGAATACTG ATGATAATTA TAAAGCATTC TTAGTTTGGG AGTCCTATAA TCACTTAACA 1080 TCTCTGACAA ATATCACACT TAATATTATG CAGTTTATTA TTTTAATAAG TTATTTACAG 1140 TAAAAGGCAT TCTGGACACT TTATATAAAT TTTAGTATTA GATGACTTAA ACTACACTTC 1200 ACTAAAGGCT CCTGCAAGAT TCTATGTATT ACATCATTAG AAATGAGATG CTAATCTCTT 1260 CCTAGCTCTT CCCTAAACAG GCCCCTACCA TTGTCTTTCC CGTCTTAGTT AATGTGAACT 1320 CATTCTCCCG GTTTTTCAGG CCCAGACCTT GGAGCCATGC TTGATTCCAC TTTCCCACAT 1380 CCTTAACTAC TCCATTAGCA AATCAGGTCA ACCCTATGAC ACAATATATT CAGATTCCTT 1440 CTACATCCAC AGCTATCACC CGGCTCAAAC CACCACCACC TTGCACCTGC ATTATTCTTA 1500 CAGCTTCCCA 1510
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