Tag | Content |
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EnhancerAtlas ID | HS087-13096 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr20:37677380-37679510 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELF1 | MA0473.2 | chr20:37678854-37678866 | GACTTCCGGGTC | - | 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 | 37677736 | 37677945 | chr20 | 37678805 | 37678873 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I039049 | chr20 | 37678021 | 37679470 |
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Enhancer Sequence | CTATAATCCT AGCACTTTGG AAGGCTGAGG CTAGAGGATG GCTTGAGGCC AGGAGTTTGA 60 GACCAGCCTG GGCAACATAG GCCCTGTCTA TACAAAAAAA TAACAATTTA AAAAATTAGC 120 CGAGTGTGGT ATGTGTGCCT CCAGCCCTAG CTACTCATGA GGTTGAGGCG GAAAAGTCAC 180 TTGAGCCCAG GAGTTTGAGG CTGCAGTGAG CTGTGATCAG TTGTACCACT GCATGTCAGC 240 CTGGTCAACA CAGCGAGACC TTGTCTAAAA AAAAAAAAAA TAAAAATAGA TGGACTGGTG 300 CCGTGCCTTT TTTTTTCCCC CCACAGATTC TTTGACATGC CTCCCATGCA GAGGTGGGGT 360 CTATGTCCCT CTCATGAATC TGGCCAAGTT GGTAGTGGTT TTGACCCAGG GTTGTGTGAA 420 GTGATGTGGT GTGACTTCTG AGGCTGGGTC ACGAAAGGCC ATGCAGCTCC TGCCTGGCTT 480 GCTGGGACAC TGCCACCCGA GCAAGCCAGC TACCTGATAA CCAGGATGCT GGAGAGGCTA 540 CTCATGGGCT GTGGTTCATG ATGCCATCTG AGAAGTGGGT CCTCTGGCCC AGCTCTTCCA 600 GGGCCCAGCC TTCTGGGTCA CTGTCAGCTG AGGCCCAGAC ATGCAGGAGT ACAGACAAGC 660 TGTCCCTCCT GTGCCCTGTC CCAATTCCTG ACCTGGCTTC TGGAGCTTGG TTTGGAGATG 720 GAGCCCACCT TGACAATGCT GTTTCCCTGG GAGAATGGGC CCCCTCTTGG CTGGCTTGCA 780 GGAGCTCTGG GAGTCTCCTT CCCCTGTGAC TCCTAGGGGC TTGGTGGCTC TGAGCTGGGC 840 AGCTCCACAT TCTCTCAATT TCATTCTGTC TGATCCATGT TAGTTTTATT TACTTTTTAT 900 GTATTTTTTA TTTTTCTGAC ATAGAATCTC GATCTGTTGC CCAGGCTGGA GTGCAGTGGG 960 GATCATGGCT CACTGTAACC TTCAACTCCT GGGCCCAAGG GATCGTCCAG CCTCTGCCTC 1020 CCAGAATCCA TGTTCGTTTT AATATGAAAG CAACGTTTTA TGCGACAACC AGGAGCTCTG 1080 AAGGGTTTTC ACGTGGATGA GCCACACGCC GGGATTTGGA ATTGCGGGAA GTGCCCAGCG 1140 AGTAGGGTAG GAGGAATGTT GGGGGTGGGA CTGGACTAGA AGGGAGGCTG GGACGTCGTC 1200 GAGAACGAGA TTGCAGGGAC GCTGCGGTGG GAGAAGTCGA ATTCCCACCC TGTTCGTCCT 1260 CCGCAAAGAG TGACTGAGGC TCAAAAAGCC ACAGCCTTGC CCAAAACGGA TGCAGCGGGC 1320 GCAGGCACGG TCCACACCCC GAAGCTTGCC GATGCCCTCG GCGGCAGCCC GTCCTGCAGA 1380 GCCGCGTTCC CTGCGCCCAA AGCAAGGTCG GACCCCCACC GGGATTCCCG GAACCGGGTG 1440 TCCCGCGCGT CCCCAGCGCA GGCAGAGACG GCGAGACTTC CGGGTCGGCG TTGCACACGG 1500 CGGCCGGCAG GCGGCGCTGG AGCCCCGCGT TTGGGCAGCC AGGACGCCCT TGCGCTGCTT 1560 CGGGTCCTGC GAGCGCCCAG GGAGGGGGTG AGTGCGGGGA GGGGTCAGAC CCGTGTCTTG 1620 CCCGGTGCGA GCTCACCGCC TGCCCACCGG GCACGTCCAC AGCAGCTCAG TCCCGGTCTG 1680 AGCGCATCGG AGTGAAAACA GCCCCCGCAC CTCTCGTGAC GGTGTCCCCT TCTCTGTCCA 1740 CGTTGCAAGA AGCTATACTG TACTCACCAA GTCTTTAAAT CTTGACCACT TCACCAAGGA 1800 AGGTATGAAC CTCTCCATTT TACAGGCCCA GTTCAAAAAG CAACGACAAA AATCAACACC 1860 AGCAAACCTT TATGGAGTTC TAATTATTGA CCTGGCCTGC CAGGGTCCTT CAGAGTGGAG 1920 TTGGGGTGGG TGCGGGAGAG GGGTCAAAAG CCAGCCCTCA GGAGGGGGCC ACCCGCGCAG 1980 CCCTCTCTCC ACCATCAGGG CTCTTGCAGA CCCAAGGGCC TGCCAGGAGA AGCAGATGGG 2040 CCATGGTAAA TCTGAGGGGC CATTGGGATG CCCAGACTGT CCCAGGTCAC CCCATTTCTG 2100 CATTTTTGTT CATTTTGTTC AGGTGGCCCT 2130
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