Tag | Content |
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EnhancerAtlas ID | HS069-00892 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr1:246861760-246863400 |
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) |
MEF2A | MA0052.3 | chr1:246862526-246862538 | GCTATTTATAGC | - | 6.32 | MEF2B | MA0660.1 | chr1:246862526-246862538 | GCTATTTATAGC | - | 7.22 |
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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 |
GH01I246698 | chr1 | 246861721 | 246863190 |
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Enhancer Sequence | TTTACTGATT CCTTAGGTAA CCCTTCACCT GTGCTTAGAC CACCAAGGGT GGGCACCAGG 60 AAACCCCATC TTCCTTTCCC ACTCATTCAG TCTCCACTCT CCCAGCTTCC CTCCCACAGC 120 CTTCTGTGTT TCATTTGCCT TGGACCCACA GATACCTCAG GGAGGAGCAC CACGAAGGCA 180 AACCAACCTC TTTCATATCA ACATCCATTG CCACCTGTTA GTAAGTGTCA AATGGTGTTC 240 TGCATGCTAG AAGATCTCCC TCCCACGGGG TGCCTGTGAG CCTCCTGCTA TAGGAGACAG 300 AATTCTGTAT GGCCCATCCA GGGAGGAGCA ACCGAAGGAA AAACAGCAAC TGTGGTTCTC 360 TGTGCCTATA TTGGATTATG TCCCATAGAT GCCCCTTACA TCTTCTAATG AGGGAGTGGC 420 TAGTGGGGCT CCTATTTGCT AGATGTTTCT GCTGCTGGGC TAAAAACCGC TTAGGTGGCC 480 GGGCGGGGTG GCTCACGCCT CTAATCCCTG CACTTTGGGA GCCGAAGTGG GAGGATTACT 540 TGAGTTTAGG AGTTTGAGAC CAGCCTGGGC AACATAGTGA GACCCCCATC TCTACAAAAT 600 GAATAAGTAG AGTTTAAATT AAAAAGAGAA AAAGAAACAT GCTTAATCTA CTTCTGAGAA 660 TGATCTCAGG AAGAGAGTGA AACAGATGGG CTCGGTCTCC TGAGGGAGAC AAACAGGGCT 720 TCAAGCAGGG CTTAGGCTGG GGACGCTGTG TGGAGCAGAG TCACTGGCTA TTTATAGCCC 780 AAACAGTAAG AAGAGTCGTT ATGAAAATGC CCAGAGGTGC TTTGATCCGG GAAGTACACA 840 AGCCAATCAA AATACGCCGC CTTCGGGCAA GAGGAGCCGG AGAGCGCCAT CTAGTGACCC 900 CACAAGTTCC CTTCCTGAAG GAAGTATTCA GTCCGGAGAA ACCAAGACCC ACCTCACAGC 960 GAGGACCAGA GAGACACCTT GGTAAGAGGC CCTGGAAACG AAACACAAAG CGAGGAAGGA 1020 CAGTGCACGG GCCTCAGACG CGAAAAACAG GGGTCGGAGT GCCCATCCTA CAGGTTGTTT 1080 GATAATTAAA TGAGATATTT CCTTTTTATA TGAAATGTTT TATGTTCATA AAGATGACAA 1140 CTAAATAATC TTCATTAACT TAGGAATCCA GCCCTTACTA TGTGACACAG TGTGTGCCAA 1200 TGTATTTATC ATTTTGTTTT ATGAGTTGTA TCTTTTTTTT TTTTTTTTTT GAGACAGGGT 1260 CTCACTTTGT CACCGAGGCT GGAGTGCAGT GACACAATCT CGGCTCACTG CAACCTCTAC 1320 TTCCCAGGCT CAAGTGATTC TCCTGCCTCA GCCTCCTGAG TAGCTGGGAC TACAGGCGTG 1380 CGCCACCACG CCCAGTTGAT TTTTTGTATT TGTTTTGTTT TGTTTTGTTT TGTTTTAGTA 1440 GATATGGGGT TTTGCCGTGT TGGCCAGGCT TGTCTCGAAC TCCTGAGCTC AGGTGATCTG 1500 CCTGCCTCGG CCTCCAAAGT GCTGGGATTA CAGGCGTGAA CCACGGCGTC TGGCCAACTT 1560 GTATCATTTT TGTTATTATA GAATATTTAT TTGAAATGTT CTAGTTTGCA GTAATTTGTG 1620 GGAGTTTTGT TCTTACTAGG 1640
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