Tag | Content |
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EnhancerAtlas ID | HS108-42324 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chrX:44342750-44345070 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYB | MA0502.1 | chrX:44342937-44342952 | CTGATTGGTTAGGTC | - | 6.28 | SPIB | MA0081.2 | chrX:44343513-44343525 | AAAGGGGAAGTG | + | 6.07 | SREBF2 | MA0596.1 | chrX:44343790-44343800 | ATGGGGTGAT | + | 6.02 | STAT1 | MA0137.3 | chrX:44344570-44344581 | TTTCCGGGAAA | + | 6.32 | Stat4 | MA0518.1 | chrX:44344570-44344584 | TTTCCGGGAAAGGG | + | 7.22 | ZNF410 | MA0752.1 | chrX:44344991-44345008 | TGCACCCCATAATATAC | + | 6.11 |
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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 |
GH0XI044484 | chrX | 44343681 | 44343830 |
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Enhancer Sequence | AGTAGAGACG GGTTTCACCA TGTTGGCCAG GCTGGTCTCG AACTCCTGAC CTCAACTGAT 60 CCATCCGCCT CGGCCTCCCA AAAAAGTGCT GGGATTGCAG GTATGAGCCA CTGCGCCTGG 120 CAAGGGAGCA GAGTTTTTAA GGACAACTTG GTGGGGTGGC GGTGGGGGAG CTAGTGAGCT 180 AGGAGTGCTG ATTGGTTAGG TCAGAGATGA AATCATAGAG AGTCAAAGCT GTCTTCTTGA 240 ACCGAGTCCT GCGTGGGTGC CACAAGATCA GATGAGCCAG TGTATCGATG TGGGTGGTGC 300 CAGCTGACCT ATCAAGTGCA GGGTCTGCAA AATATCTCTA GCACTGATCT CAGGAGCAGT 360 TTAGGGAGGG TCAGAATCTT GTAGTCTCTA GCTGCATGGC TCCTAAACTA TAATTTTCAA 420 TCTTATGGCT AATGTTAGTC CTAAAAAGGC AATCTAGTTT CCAGGCAAGA AGAAGGTCTG 480 CTTTGGGAAA GGGCTGTTAC CATCTTTGTT TTAAACTATA AACTATAACT AAACTTCTTC 540 CAAAGTTAGT TCAGCCTACG CCCAAGAATG AACAAAGACA GCTTGGAGGT TAGAAGCAAG 600 ATGGAGTCGA CTACGTTAGC TCTCTTTCGC TGTCTCAGTC ATAATTTTGC AAAGGCAGTT 660 TCAATCGCAC ACAGGTACAG GGCAGAAGTG GATCTAGAGC ACAAGTAGTG ACTCTGGACC 720 ATAGTGCGCC CACACTGTAA GTCCAAAAGA TTAGAATAGT CTGAAAGGGG AAGTGGAGGC 780 AGCTCTCCTC AGGAGGAAAG ATGGGGCCGT GAGGAGCCAG CTCTTTATGT TATCACACAC 840 AAATTTCTTA CTGAGATGAA TCAGCAAAAA ACAAAGTCAA GAGCTCTTGC TGGGAGAGCA 900 GGGGCCTTGC CCTTTTCGGC ATGCCTGATT CATTGTGTAC TCACAAGAAA CTCCCCTTGA 960 TTATGATCTC CTGTGGGCCA TGGGCAGGAC TTATTCCATT AGATGGGAAT GAACCCTGAG 1020 CACCTCTCCT AATGGAAGCT ATGGGGTGAT TTCCCTCTAG GGGATGAGCC AAGCTGACAG 1080 GTTCAATGTA GCCTCAGCCC AGATGCGGTT GATGTTGGAG CCTGGGGCTC TGGTCTATCC 1140 TTCCCAAGTA TCCTTCCTAA CAGGTTCAGC TTCTCGAAAT CCCTCTTGTA CTGAGGCCCC 1200 TGTCTCCCAC ACTCTCCCTT TATTTCTTCC CCAAGTCCTG AAGTTCGGAA AGCAGAGTTG 1260 GAGGGAGAAG CTGTTGCCTG GGGCCTGAGA AGCTGAGTTT CTGGCCATTG ATAAAATTAT 1320 CCTTCCCCTC AGTACACCAG GGCTCCTTGA CATGGCTGTC CCTGCTTGTT TTCCCTCCAC 1380 TAGCTGCTCC TAAGCTTCTC ATGCTTTCTT ATCTGGAGGG GAGGAGTAAT AGGGTTATCA 1440 GCTGACACCA ACACTCTGCC ATTTCATCAT CACTCATCAT TGCACATGTA GTTACCACTT 1500 ATTGAGAACC TGCTGTGTAC ATGTCAAGAT CTGCATTCAG CGATTTACAT GTTATTTCTC 1560 AAAAACTGAA GGGCTGAGAT TTTACCCTAC TTACTGTTGC TGGAAAGGGG TCCTGATCCA 1620 AACCCCAAGA GAGGTTTCTT GAATCTCGCG CAAGAAAGAC TTCGGAGTGA GTCCATAAAG 1680 TGAAAGCAAG CTTATTAAGA AGGTAAAGGA GTAAAAGAAT GGCTACTCCA TAGGCAGAGC 1740 AGCAGCATGA GCTGCTGGTT GGCCATTTTT ATGGTTATTT CTTGATTATA TGCTAAGTAA 1800 GGGGTGAGCT ATTCATGAGT TTTCCGGGAA AGGGGTGGAC AATACCCATA ACTGAGGGTT 1860 CCTCCTCTTT TTAGACAATA TATGATAACT TCCTGATGTT GCCATGGCAT TTGTAGACTG 1920 TCCTGGCTCT GGTAGGAGTG TCTTTCAGCA AGCTAATGAA TTACGATTAG TGTATAATGA 1980 GCAGTGAGGA TGACCAGAGG TCACTTTCAT CACCATCTTG ATTTTGGTGG GTTTTCCCGG 2040 CTTCTTTACC ACAACCTGTT TTATCAGCAA GGTCTTTATG ACCTGTATCT TGTGCCAACC 2100 TTCTGTCTCA CCCTGTGACT TAGAATGCCC AACCTTCTGG AAATACAGCC CAATAGGTCT 2160 CAGCCTTATT TTACACAACC CCTATTCAAG ATGGAATCAT TCTGGTTCAA ATGACAACAT 2220 TATGAAGGAA ACCAAACTGA TTGCACCCCA TAATATACTT CTTTGGCATA TTTCAAGATG 2280 GCTATTCAGA GGGGCTGCAA ATGGCCGGGT GAGGTGGCTC 2320
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