Tag | Content |
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EnhancerAtlas ID | HS108-31776 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr5:53309190-53310410 |
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) |
MAFF | MA0495.3 | chr5:53309590-53309605 | AGGCTGACTCAGCAC | + | 6.18 | MAFF | MA0495.3 | chr5:53309590-53309605 | AGGCTGACTCAGCAC | - | 6.19 | MAFK | MA0496.2 | chr5:53309588-53309607 | ACAGGCTGACTCAGCACAC | - | 6.05 | NR2F1 | MA0017.2 | chr5:53309421-53309434 | CAGAGGTCACAAG | + | 6 | Nfe2l2 | MA0150.2 | chr5:53309589-53309604 | CAGGCTGACTCAGCA | + | 6.34 | RREB1 | MA0073.1 | chr5:53309672-53309692 | CCCCCACCCAACAAACTACC | + | 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 |
GH05I054013 | chr5 | 53309002 | 53310130 |
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Enhancer Sequence | TGTCCTCACT CATTCCCAGG CACAGGCCAA GCTAACCATT GGAGAGATTT AGTTTAAATT 60 TTAACTTTGA AACAATGATG ATGCTAGTTG CTCCCTAAAA TTGACACTTT CCTTGTTCAG 120 GGACTGAAAC TGCCTCTGTA AGATTAATTT TGAAAAGCCA CAAGATTAGA ATTATGGGAA 180 GGGCCTGAAT TCTGGTAAGA TGCAGGCATA GCTTACCTTC CTATAAGGCA CCAGAGGTCA 240 CAAGATTTGT GACTTCCCCA CTTGCTACTA TAAATAACAT CACTATTGTA GAACTTAAGA 300 TTGGTCCTTT GAGATATTTC TTCATCCTGC ATCCTGGCAA CTGACTGACT CCATCTAGAC 360 CTGTGACTCA TGACTCAACC AGTTCTGTGG CCCCACCCAC AGGCTGACTC AGCACACAAG 420 GGCTGTTCTC CACACCCCTA TGATTTCACT TGTAATCAAT CAGCAGCACC CATTCCCTTA 480 CCCCCCCACC CAACAAACTA CCCTTGAAAA GCTCTAACCT CTGAACCTCT GAGGAGACAG 540 ACTTGAGTAA TAACTCCCAT CCTTCCACTA GGCTGCCTTG CAATAATTGA ACTCTTTCTC 600 TAATGCAATA ATGCTGTCTC AGTGAATTGG CTTCATCTGC ACAGTGGGTA AGAAGAACCC 660 ATTAGGTGAT TACAAAATCT GAAATATTTC AAAATCTGAA ACTTTTTGAG TGCTGACATG 720 ACACTCAAAG ATCATGCTTA AAGTTAATGG TTATTGGAGC ATTTTGGATT TCAAATTCTC 780 AGATTAGAGA TGTTTAACAA ACAAATGAAG GATCATAGGG AACTTCACCC CAAAACACTA 840 CTCCCTGGTA TAATGAGTAT TTTGAATTAA AGGCTCTTGG AGAACAACAG ACACTGGAAG 900 AGATTTTTTC CCACTCTACC TAAAGATCCA AGGGAATCAC AAGGAGAACA ACTGTTTTTC 960 TTCTCCTCCC TGTTATCTTG TACCTATTGC AGAAAAGAAG ACCAAGAATG TAAGGACACC 1020 TGAGCAGACC CAAAGAGAAC TATTTACAAG TTAATCTCTG TTCTTCATCC ATTAATTCTC 1080 CCAAGTAATC ATTTATTGCC CTTCATCAGA ATTCCTCTTG TCCCCCATCC CATAACCTGT 1140 TTTGCCAGGA CCCAAGTCCC CATTCTTTTT TTTTTTTTGA GCTAGAGTCT TGCTCTGTCG 1200 CCTAGGCTGG AGTGAAGTGG 1220
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