Tag | Content |
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EnhancerAtlas ID | HS175-16787 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr20:2279260-2280750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr20:2279955-2279969 | ATTCCCAGGGGACC | + | 6.25 | ZNF263 | MA0528.1 | chr20:2280300-2280321 | GACTCCTCCCCTGCCTCCTTC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 2280063 | 2280323 | chr20 | 2280034 | 2280402 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I002299 | chr20 | 2279981 | 2283245 |
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Enhancer Sequence | CTGTACCATT CCCAGCGTCT GGGTCTACCA CCAAACCGTT CTCCTTGGAG CTGGGACACC 60 AGTCGCCCCT CCTCCCATGG AAGCGGTCAG GAATTGCTCT TGGGTTCTGG CCTCCTTCTC 120 TTCTGTAAAT CTTCTAGGTG CTTCCTGGAC CCTCCTCATA TTTTTGTGTC TGGCACTGGG 180 ACCAAGGCAA TATCTACTCT CTCTCTCTCT GAAAAGGAGA TGGCCCCTCT GGGCTCAGAG 240 TCTTGTGACT CCAGCTGCTC ATTGTTTGAA ATGAGGACCA GCTGCCTCCT GTCTGCCCGG 300 CTCCATGGCC TTCTTCCACC TGGGACAGCG GCTACTCCCT GTTCCTTAGA GACAGCCCAT 360 GAGCAGCTTC ATTCCACCGG GAATGACAGC TGCCCGTATT TCAGCGTTTG TTCCTGTAGG 420 ATTCCTTACA GGATAGCTGA TGGGTTAAGA GTGCAGGTTC AGAGGTGCTC TCTGGATCAA 480 GGCTCCACTC TGCCCCTTAC GAGAAGAGTG GTCTTGGGCA GGTCACTTAA CTTGTGTGTC 540 TCAGTTTCCT CATCTCCAAA ATGGGGTTAT TGCAGTATCC ACCTCATGGG TGCTTACGAT 600 TACCTGGAAA TTTTTTCATG AGCCTGTTTT CTCCTTGTCT TGGGGGGACT TAAGAAAAAC 660 CCTATGAGAG GAATTACATT TTCTAATCAG GGGCGATTCC CAGGGGACCC TCTCCATTAA 720 GCGCCTCAGC ACAAGTCCTC CCCACTCCCG CTTCATCCAT TCCCAAGTCC AAAGTCCTCA 780 TGCCTGAGCA CTCCCCTTGT TCACCTCAAG TAACTTCATG CGGCTCCACC CCGCAGGGCT 840 GTCTCTGCAG ATGGAGCAAT CATTCTCCTC CCCAGGGCCC ACGTGCCAGG CTGGGGTGTG 900 TGCTGAAGTT AGGAAATCTC GCTTAGCAGT GGAGGGCACA AGGCCCTAGG ATCTTGGTAG 960 GAGCTGAGAG ATGGGAGTCA GAAGGAGTCA GCCTTCCCCT CCCTCAGCCT GATTTTCCTT 1020 ATTTGTAAAA AGAGGACAGC GACTCCTCCC CTGCCTCCTT CCTATAGCTG CCGGGTGGCT 1080 CTGGTCAGGT AATTTATGTG AAGGAGCTTT TATAAGTGTA GATGATAAAC GGGCCTAAGG 1140 TAGTGAGGTC TCAGTCCCTG CTGCACATTA GAATCACCAG GAAAGCTTTA AAGAAAATGC 1200 TGGCCGGGTG CAATGGCTCA CGCCTGTAAT CCCAGCACAT TGGGAGGTCA AGGCGGGTAG 1260 ATTATCTGAG GTCAGGAGTT CGAGACCAGC CTGGCCAATA CGACAAAATC TCATCTACTA 1320 AAAATACAAA AATTAGTGGG ACATGCTGGC ACGCACTTGT AGTCCCAGCT ACTTGGGAGG 1380 CTGAGGTTAC AGTGAGGCAA GAGAACTGCT TGAACCCAGG AGGCAGGGGT TGCAGTGAGC 1440 TGAGATCACA CCACTACACT CCAGCTTGGG CAACAGAGAG AGACTCCATT 1490
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