Tag | Content |
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EnhancerAtlas ID | HS170-03119 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr5:147183590-147185010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr5:147184615-147184626 | ATTGCACAATA | + | 6.62 | TFAP4 | MA0691.1 | chr5:147184682-147184692 | AACAGCTGAT | + | 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: 2 | ID | Chromosome | Start | End |
GH05I147803 | chr5 | 147183421 | 147183815 | GH05I147804 | chr5 | 147183964 | 147185425 |
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Enhancer Sequence | CACTTTTAAG GACACTTACC CTGAAGGGTA ATTTTAACTT GCCTAAGATC ACATGACTGC 60 TTTTTCATTG TGAATCACTG TTTCTCTGGG TGAGATGGTC AGCCCAATTT CCCAAACAAT 120 ATTCCAGTCT AGCGTGGAAA ATTGTGACTA GAAAGAGCAA ACAACCTTGG AAAATAGTTT 180 TATTACACAT TATATAAATG AGAGATTCAT ATCTATGTCA GTTAGTGCCA AGCCCAGAAA 240 TCAGAGGTCA TTCTAAATAT TTCAAGCAAA GAGGGATTTA ATGCAGACAA TTGGTTACAG 300 TGCTCTTAGA AACACAGAAA GAACACAAAA AAGAAGAGTG TTATAAAGAC ACTGGAAGCT 360 GCGATTGAAC CTGGACTGAA GCCTAGCTGC CCTTGCCCTC TGTCTGCTGG AGGTGCTGCC 420 ATTGATGCTG AAACTGCATC CGGGCAACTG AGCAGGAAAG TTAGGAGTTT ATCTTCCTGC 480 TGCTGCGGCT GAATGCATGA CTGCTGCTTT TACAGCTGGA TCCACACCAC TGCAGCTGAG 540 CAGGAAATGC AGGAGTTTAT GATCCTGCTG TTGCTGCTGA ATGCATTGCT GCTACTTCTT 600 CAGTTGGATT CATACCATTG CAGCTGAGCA GAAAGTCAGG AGATTACACT TCTACTGATG 660 TTGCTGCCAC ATCTTGATGT ACCATTAATA ATAGAAAATA AAATGGTTTC CCTCTTCTTT 720 TATACTATAT TCTCTCAGAC TCCACTGTCA ATGAAACCTG GAAAAAATGG TTTTCAGGCT 780 CCCATTTCTG CCAGTTATTC AGAAAAGAGC ATTACAGAGT AGGGGTAGAG CTGGCAATTA 840 ATAGACATAG AGTCAACATA GTTCACCTGC TGCTTATACA GTGTCCATTT GCCTCCCTTG 900 TACCCTTATT TAAATTTCAT TCAACAACAA TCACAACAAT ATGGTGCTTT TACCTAACAT 960 AATTAACAAT TTTGCATACA AACAGAAAAG CTGTCACTCT GGATATTCTG TAATTTAAAC 1020 ACTAAATTGC ACAATAGCCA TCATCCCACT TTATATGTAA AATAGGATAA GAAAGGGAAA 1080 GACGAAAAAG GAAACAGCTG ATTAACATAC ACAAATATTG CATAACAGAC GAGGAATAAA 1140 TCATGTGTAA CTGCAGTCAT CATTTCTATG ACTGGTTGTT AACAGATCAT CAGCTTCTGG 1200 TGATAGTTGC AATTTCCTCT TCTGCTTTTC TATGCTTCCT TTTTTTTTTT TTTTTAACGA 1260 TAGAGTCTCA CTCTGTGGCC CAGGCTAGAG TGCAGTGGTG TGAACAACAC AGCTCACTGT 1320 AACCGCAACC TGCTGGTTTC AAGCGATCCT CCCCCCCAGT CCCTCGAGTT GCTGACACCA 1380 CAAGCATGCA CCACCATGCC TGGCTATATT TTTAAATTTC 1420
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