Tag | Content |
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EnhancerAtlas ID | HS060-07248 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr11:133764430-133766320 |
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) |
IRF1 | MA0050.2 | chr11:133764796-133764817 | GAAATAAAAATGAAAGCATTT | - | 6.37 | JUN(var.2) | MA0489.1 | chr11:133766037-133766051 | ATGACTCATTCTCT | - | 6.69 | RELA | MA0107.1 | chr11:133765342-133765352 | GGGAATTTCC | + | 6.02 | ZNF263 | MA0528.1 | chr11:133764656-133764677 | GGATGAAGGGAGAGAGGGAGG | + | 6.04 | ZNF263 | MA0528.1 | chr11:133764653-133764674 | AAAGGATGAAGGGAGAGAGGG | + | 6.45 |
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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 |
GH11I133896 | chr11 | 133764941 | 133765170 | GH11I133895 | chr11 | 133765181 | 133765330 |
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Enhancer Sequence | CCAAACTTCC ACTAATAAAA GTCCTGGCAT TGCTCAGCAG GGTTCACAAG TGCCATTTCC 60 TAGACCCAAG GGGCTGCATG ACCTCACTTG GGGAACACGG GTGTCCTGGG ACTGTGTCAT 120 GTGGACCTGA AAGGAGGCCT AAGGGAAAAA GTACTGGGCC TCATTTTTAT TTTCTAGGCA 180 ACTTCCTGCT GCCTTAAAGC CTTTGAGCAG CAATGAGGGG AGGAAAGGAT GAAGGGAGAG 240 AGGGAGGCAG AGAGAAGAAG CGAAGAAGTG AAGGGCCATC GATTGGCTCA TTCATTGGTT 300 CTGACCAAAA GAGAGATAAA TCAGACCTAT TTTACTTAAT CTGTGAGGTT ATCTTGAGCA 360 TCAGATGAAA TAAAAATGAA AGCATTTCTT CAAGTATGGA GCACCTGAAT TTAGGCCCAA 420 TCTTAAAAAG AGGCAAAAGT CTCTTAAATC TAACAGAGAC GGTCCTCCTG ACCAAAATTA 480 TTTTTTTCTC ACTACTTTTT TAAAATTTAG CTTTGCCAGA GAGCCTGTGA ATGTTACAGG 540 ATTGTGAGGT CAGCCAGCTG CTCCTGTAGA ATGCCGACGG CATGCTGGGA ATGCAGTACC 600 GCACTGCCCA CAGCCTCGGG GATGAGCTGA GAGCTGGCTC TCACAGGGTG GGGTTGGCAA 660 CTTTGGCCAC ATTCACCTAT GCATAAGAAA GAGACTGCGA GACACTCCAT GCATCTGCTT 720 TTACAAATTA AGATCAAATG TAGAAGAGAC ATCAAAAAGA TTTTCATCAT GGCCTGCTAA 780 GAGCAGGGGA GGGCAGAGGA AAGAGCGAAT GCAAACTAGG GAGGAAAGAG AATCGTGGCA 840 GATCACTGAA GCAGAGGAAA GCTGTGCGGA CCCAGGGCCC GCCAGGCGGA ACAGCCCATC 900 TCACAGCTGT TAGGGAATTT CCCATGGCAG AGGTTTTTTC ATGTATAGAT GGGCCTATTT 960 TTCTGTCCGT TTGCTGGTTT TATCATTTGG CTGTTTTCTC CTCTTGGTAC GCATAAACAG 1020 GAATATCGTA TTTTGGCATC TGATCTCCAC CTAAATCCCA AATAAAATGA GAAGGCAGCC 1080 TAGTAGGTAT TGCTAGGGAA CCAGGGGAGC ATTGCCTACA TCCAGCATGA GAAGGGGAGG 1140 ACGAGGACGG GCCAGGGCAG GAAGTCAAGT CCCCAAACTC AACCCTGGAG GAGACAGAGT 1200 GAGATGCCGA AGCCTGACCA TCCCTCCCTC TCGGGAAAAA GAAAGGCTGA GACAGAGGGG 1260 CCATCACACC CGACTCTTGC ATGAGATTTT GCCGAGGGCC AGCAGGACTT GCTGGCAGGA 1320 GACTCGTTTA GACAAAGATA GAGTCCAACC AAAAAATTAC CATCATTGCA TAATTGAAGA 1380 GCCACTGCAA AGAGCCTACA AAGTAAAAGA GAAGTGTGTG CATTCACCAG ACAAGCCACC 1440 CCCTTTCTGC TTTTGCTCCA GTGCTGCCTC CCGCTGAGAC CCTCTCTGAG CACTCTAAAA 1500 TAGCGCTCTA AACCGCAGCC CCCTCCTTCC TTCTGTACGT CAGCTGCCCC TTACCCTGCT 1560 CCTTTTTTTT GCCTTATGCC ATTCGATGTC ATTTTCTTAG TGCAATAATG ACTCATTCTC 1620 TGTCCCTATC ACTAGAATGA AAGCCCTCCA GGAGCAGGAG CCTTGTCTGG CCTATTCACT 1680 TGTGCACCCC AAGTGAACTA AACAGTGACT CACACACAGT ATACCCTCAG TACATGTGTG 1740 TTCAATGAAC GAAAGGCAAC CTCTTCATCT CCCAGCCGCA AACCATTTCA GAATCATGTT 1800 GAGTCGTGAG TTTAAAGTGG GTTGATTAGG GAGACCTAGG GCCAGGGGTG AGACAACATC 1860 AGGAAGCACT CCCTAGGTAC ACAAAAAAAT 1890
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