Tag | Content |
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EnhancerAtlas ID | HS062-04094 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr12:104502510-104503620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr12:104503128-104503147 | TAGCACCCCCTGGTGGCAT | - | 6.68 | MEF2C | MA0497.1 | chr12:104503200-104503215 | ATTTTAAAAATAGCT | + | 6.08 |
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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 |
GH12I104109 | chr12 | 104503041 | 104503210 |
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Enhancer Sequence | GTGAAGGTTA CAGAAGTATT CCTTATTTAC TGATTTTAAT TTGCTTGTTC AAAAGATATT 60 TGAAGAGTGC CTAGAGATGT CAGGGTGTTT ACCTATAAAA GAGAAGAAAG TATGAATTGG 120 TGGCATATCA GATATGGAAG ATGTCACAGA GAAGGAAACG TCCCCCCCCA CCACCACCAT 180 TCTACCCACT TCCCCTTCAT GGTCTTCTTA CCCCCGCAAA GATACGAAGC TAAAAGATCC 240 ATCATTCCTG AGCATGAGAA TTGAGGAAGG CACAAGATGA GCCCTTTGGT ATGAGCACAT 300 ACAGGTTAAA AATAAAAGGT AGCAGCTAGT GTTTGTTTTT GAACATAGAA AAACCATGTC 360 CACTAGTAAA TTATACTCCA ACAAATGTCC AGCTCCAACC AAAAAGATTA TCCATTCCTC 420 CTACTGAGAA GATAGAGTAG ACGTTCTCTG AGAATTTAAG AAGAGTTACC TCCTTTTCTC 480 TTTCCATATT GGGGAAGGGG CAAAAAGCTA CAGCCATAAT GTTTATCATC CGCTGTAACA 540 AAGCATAGCA TGTAAGAGAG TGGGCAGAGA TCTGAAGATA AAACTGCTTG ATTCACAATC 600 ATCCTGCCAG TTGCGATTTA GCACCCCCTG GTGGCATTGT CCAGCCCAGC TTACATGTGG 660 ATAAGATTCT AGGTCTTGTA GCTGCCTAGG ATTTTAAAAA TAGCTACAGC AATACCTGGA 720 GCTTTCTGGT GAGTTGGCAA TCCTGTGTTA GACCCAGTTG GAGAGAATGG ACCTGGAGAA 780 TATACTTTCT ACTTTCCTGC AACTTCCTAA CCCAAGATAA TAACTTTAAC CTGCCCTGTT 840 TAGATACAGG GACACACTGA TTATTTCAAG ATCCATTTAA TTTTTGAGGA TTTTTAGATT 900 GTTTATCAAA ATTTCTAGCT AGTTTTCTGA ATCAGGAGAA ATTGCATCTT AACTATGTCT 960 TTTTAAGTCT ACATAATGGC ACTGACATTG ATAACCTTGG TAAAGACGTG ATTGCAAAAT 1020 TGTTATAACA TTTGTGTGAT CAGCAAGGCA CCTGTTATTG AGCAATGTGG AGAAACGGTC 1080 AGTTGCTGCC ATACACTTTC CATATTTTTG 1110
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