Tag | Content |
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EnhancerAtlas ID | HS062-10647 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr22:20810070-20811430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr22:20810148-20810159 | TCTTCCCGCCC | - | 6.14 | SP2 | MA0516.2 | chr22:20810775-20810792 | CTAAGCCCCTCCCACAA | + | 6.49 |
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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 |
GH22I020457 | chr22 | 20810621 | 20810830 | GH22I020456 | chr22 | 20810881 | 20811030 |
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Enhancer Sequence | AAATACACTA GCACGTAGAG CCACAGTGCA TGCGCTGCTA GAAGACCACC CAAACAAAAC 60 ATGCTTATGA GTAACACCTC TTCCCGCCCA TTTATGAATA ATCATGTAAG CCTCCTGTAA 120 GGGAGGTTTC CCATGCCAGT TGGGGCGATC TTATTCTGGA GCAGCCTGCT CTGACTCGGC 180 CTTCAGAATG TACCTTCACT TTTGCAATAA ACTGCCTTAC ACTTATCTTC GTTAATGCAT 240 GTCTCTTGCT TAAAGTCTTA ACCAAGAAGA CAAGAACCGA GGACACATTC CCAGTAACAT 300 TTCCTCCCTC TGTAAATGGC AGGTCTAATT GACATCTCCT CAGATGGACA TTCCCCAAAA 360 AGTCCCTCTA GATTCATCCT ACCAGAGCCC CCTCCCTGGA AATCCTCCAG TTCAGCCCCC 420 TCTTCATTTC ACTTACCATA ATTGTAACCA CTTTACTGAT CTGTTTTCTG GTTAAGAGTG 480 GTTTCTCCTA CAAGGCTGTA AACACCATGG AGTGGGGAGT CTTTCTCATT TCTTGTCACC 540 ACTGGATTCC CAGGACTTGG TACATGGTGC TTAGTAGTTG CGGAATGAAT GCGTGCATGA 600 AGGAACACCG GCAGCCACGA TGCAGCTGGT TGAAAGCCAA GGCTGCCCCT CTGTGGCCAA 660 GCTGGAGAAC TGCTGCTTCC CCAGCTGCCG CAGACAAAGA AACTGCTAAG CCCCTCCCAC 720 AACACCCACC TAGGAGGCTT CCCCCAACAC CCTTCCTGGA ACAGAACCCA AGAGCCCTCC 780 TTGTCCACTT GGTCTCAAGG ACCTCCTGAT CTTCTCCATG CAAAATCTGC TCCTTTCCCC 840 AGGATGGGGG TACGGAGTGT CCTTCCAAAG AGGCTTCCTT CTCCCCAAAG AAGCTGAGAG 900 CAAGGAGCAG GCCACAGCTT GCAGCTCACA GCTGCCCAAG AGACAGAAAT CTGTGTGGGC 960 TGTGTGAATG ACCTGGATAA AGAAGAGCTG GATCCATTGA GGAGACACTA GCCCTGACCC 1020 CTGAAGTCAA AGTCTAAGTC CCTGGGGGAA TTGGGGGTCA TGAGAGATAC TGGAAAGAGG 1080 CTTACAAAGG CCAGAGCTCT TGCTAAACTC CCTGAGGCAG TGCAGGTAGA ACCTGCCCCC 1140 CATACCATCC TCTGCCTCTC AGGTGCTCGG TTATCCCCAA AGGTGTACCT GGCCCATAGC 1200 AGGTGCTCCA CAAATGCTAT GCCAGTACTA GCGGGGTGCC CTGCTAGGGT ACCCCTAGTA 1260 CTGCTAGGGT ATGCCCTGTT CTCGGAGGCT GAGACCCAGG AAGTAGGGGG CCAGCAAGGC 1320 CTGTTCCTTC CCTGGGATCC CATGTCTGGT TGTTACACCA 1360
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