Tag | Content |
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EnhancerAtlas ID | HS108-09445 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr12:49407990-49409880 |
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) |
Zfx | MA0146.2 | chr12:49409602-49409616 | CCCGCCTCGGCCTC | + | 6.01 |
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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 |
GH12I049015 | chr12 | 49408921 | 49408951 |
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Enhancer Sequence | TTTACTCCAT TCTGATGAAA TTCTACCTCT CTGGAATCAC AGAAGAGAAG AAACCAATAC 60 TGCTACAATA TTGTGCCTTC CAGAAATGCT TCTATCCACT TCTGAGCTGA ACGAGCATTA 120 TCTGCAAAGC TCATGTTCTT GTACACTATA CTGCCTAATG AAACACTAGG TCCTAAAAGC 180 TAAGACTAAA GATCTGAGCT TAGGGCTAAC CCCTACAAGA TTCTCACAGA TCTACTTTAT 240 TAAAACATGG AAGCCAGAGA GACAGCATTG TCTTCCCCAA ACACAGACAC TCACTAGGCA 300 TAGTTGTAGG CACTAGAACC ACAGACACTG GTTCCACCAT TGTCTAGCTC CATGGCAGAG 360 AGAGAGCCAC AACTGGGGAG GATCCCAGTA GCTGACTGTC AGCCAGTCAA AACCTGAATG 420 ACTGAGAGGT GGATAAGGAA CACGAATGTA CTGAAACTGG GAACTTGAGT CCACTCAGCA 480 CCCTTGTGAG TCAAAGGCTG CTATAGCCAG GGGATGCTGG TTTTCCAAGT TTCCCTTCCC 540 AAGATAGTCT GAGATTAGAG AGTGCTTTGA CTAGACAAAA CTTAGAACCA TTTCTGTGCT 600 CCCTCAAGTG GGAACATTTG GAAATGCCAT TGTTATTTAG GAACCCAGAA GGGATCACAA 660 CAATTTTCAT CTGCTAGCAT CAACAGTCTT GGCTCCATTT TCTCTGGGTG ATATCTCCAA 720 AATAAAACCA TACTTCATCC CCATAGCTTC TGTAGTAACA TGACATTAAA AACTTCAACC 780 TGGGAGGTTG GCTGACAAAC TTCCTAAACC AGGGAAGTTT AAGACAGCCC TAAACTTTTC 840 TCCCTTAATG GGCTAGGGGA GAGTGCAGGG AGTAAGGGGG ATAATCTCCC TCTTCCCACT 900 GGACTGCATA AGACTGTCAG CTTGGCCTGC CATTTTGGCA AGACTATCAG AACAACAGCC 960 TCATCACTTA TAAGTGGGAG AGAGGGCTGT GATAAAGATA GACACATGAT ATATCAGAGT 1020 CTCACAAAGA TCTACACAAA GGCACAAAAA CAGCTACTTC TGTAGAATTT ACCCATCATA 1080 TGATATATAC TGTACTGTGC TACAGTTATT TTGTTCATTA TCTATCCAAA CAGATTATAA 1140 ATTCCTGGAA ACCTAGAACT ATCTTATACT TTGTATCTCC CATACCACCA AGCACAGGGT 1200 TTTGCATATA ATTCACAGTT GTTTTGTTTT TTAATTCTCA AAGAATGATG CACACTGATA 1260 TGAACAGATA TGCCCAAGAC TAAGTTACAG AGGGAGGAAA GAAACATAGA GCTAACTAGA 1320 GATACAGATA CCAACATAAG AGAGTCAAAC ACAACTGCAT ATGTGACTTT TTTTTTGGGC 1380 GGGTGGGCAG AGTCTCGCTG TGTCTCCCAG GCTGGAGTGC AGTGATGCGA TCTTGGCTCA 1440 CTGTAATCTC CGCCTCCGGG GTTCAAGCGA TTCTCCTGCC TCAGCCTCCC AAGTAGCTGG 1500 GACTACAGAT GCCTGCCACC ACGCCCAGCT AAGTTTTTTT TTGTATTTTT AGTAGAGACG 1560 GGGTTTCACT ATGTTGGCCA GGCTGGTCTT AAACTCCTGA CCTCGTGATC CACCCGCCTC 1620 GGCCTCCCAA AGTGCTGGGA TTACAGGTAT GCGCCACCGA GCCTGGCCGT GACTTTTAAC 1680 TTTCTGCCTG TTTCACCATA TCAGAGGGGG GATTATGTAA TTACATCTAC TCCTTTCTAC 1740 CTTTTTTTTT TTTTTTGAGA CAGGGTGTCA CTCTGTCATT CAGGCTGGAG TGCAGCGGCA 1800 TGATCACAGA TCACTGCATC TTCAACTTCC CCAGCTTCTC CGACTTCTGC CTCCCGGGCT 1860 GCTGGGACTA CAGGAACATA CCACCAGGCC 1890
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