Tag | Content |
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EnhancerAtlas ID | HS060-28070 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr5:133828720-133830860 |
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) |
FOXA1 | MA0148.4 | chr5:133830741-133830757 | CATTATGTAAACAAAA | + | 7.71 | FOXP2 | MA0593.1 | chr5:133830745-133830756 | ATGTAAACAAA | + | 6.14 | IRF1 | MA0050.2 | chr5:133829862-133829883 | AAGAAGAAAGAGAAAGAGAGA | - | 6.52 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 133829417 | 133829567 | chr5 | 133830545 | 133830641 |
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Enhancer Sequence | GCACCAGGGG TTGTGTTGTC ATCTTTACAG TCCTGTGTTC ACCAAGAGTC ATCCAGGTTG 60 GGCAAATGGT GACATGTGTA ATCCATGAGG AGGAAGAGAA CTGGAGTTAC CCTGTGCGGC 120 CTCTCCCTTA AATCTCCCCA GATCCTGCTG GCACACCTGC AGTAACAGGG GGCTTCCTAC 180 CTGGTGAGGC AGCTCCCCTT GTGAGAAAGT TCTTCCTTGC CTGGGTTCCC ACTTGCCTGT 240 TGTAGGTCCG TCCCACCTAG TCCAGGGTTC TGGTCTTAAC TCAGAAATCA TTACATTGCC 300 TGAGCTTGGG CCAGTCTCTA AGCCTCAGCT TATTCATCTG AAAAAAGTTG TCCTACCTCA 360 AGGATTTCTA ACTGCAAGTA ACAGAAAATG GCTCTTAACT TAGGCAGATT GACTAGCTGA 420 CTTAAGGAGA AAAATAATAA AGATATTGAG CAGCTCAGAG AATCTCTGGA CAGAGCAGAA 480 AAAGCAGACC CAGGGACTAC ACAGCAATGA GCAAGGCCCC AGATCACACT GAAGAACTGG 540 TTTAGTCAGG GCCTTGCTGC CATCATGGTC ATCACCGACA CCATGCTCTA GACTCTGCAG 600 GCTAGGCTGC AGGGACCATG TCCGTGCCCT CAGGTGCCAC CACCTCTACC ACCCTGAGGA 660 CGCCAGCCTG CTACACCCAC AGTAACCATT AAGGAGAGTT CTCTGTGTTC TCTGCTTCCT 720 GGGGTCATTA GCTCTTGGGT TAGTCTGGAG CTTGTGTGGT TGATTGTGAG AGCCTAGGTC 780 TTGTGCCCTT ACCCAGCCAC TGGGAGGCTG GCAAAAGAGT GCACATGGTA CTTGCAGCCT 840 CTAAAGAGGG AAATGGGCTC TGTCTCAGAG TGAAGGTAAT TTCCCAACAC AGGAAGAGGG 900 CTCAGATCCT GGGTAGCCAA AAGAAAGAAC AAAGAATCAA ATAAGATATA GATGTTAAAG 960 AGGTTTTAGA ATATATTAAG CTTGGGGGCT GGACGCCATG GCTCACACCT GGAATCCCAG 1020 CACTTTGGGA GGCTAAGGCA GGAGGATCAC TTGAGGCCAG GAATTGGAGG TTGCAGTGAG 1080 CTATGATCAT GCCACTGCGC TCCAGCCTGG GCAACAGAGC AAGACTTTGT CTCAAAAAAA 1140 ACAAGAAGAA AGAGAAAGAG AGAGAATATC AAGCTCTACA CACCTGCCAA AGATTATTCT 1200 TATTCATTCA TAAGTATTTC TGCAGATATT AAAAGGGCAA AGTTGTGGTC CTTACCCTCA 1260 AAGAAAACAC AGTACATTCA GGGAGTAAGA AGGCATGGGT CAGATGACCC CCGTTCCAGG 1320 CAGAGGGTGA TGACTCTTGT GGATTCTGAA TGTCCAGATT ACATGGTGAT TAACTATGAA 1380 ACACTAGGTC TCAGAGGGGT GGGCAGTATC TGGAGGCTTC TGGGACAGCC CAACATTTTC 1440 TTGGAGTTGG GTGGTATGTC ATATGCTCTC TGTATCCTGT GCATCAGTAC ACCGATGTCC 1500 TATATAGACC CAGACCAGAA GAATCCTGCC CATACATGAC TGTTTCCTAT TGATAGCTGT 1560 TGTCATTTCT CTGCTTAGTA CCCACTCCCC CTCTTCTGGT AATAGCACCC CAATTTTACC 1620 TGGGGAACTA CTCTTGTCAT TTTCAGCTCA TGTACTTCAG GTGGAATTAA TTCCATGGCG 1680 TAAGAGTCAC AGGTGAATCA AGCCTGGCTA ATCAGAGCTG TATAGCGCAT TATGCACTAT 1740 GCAGAGCTGC ACAGTGGTTG GTTTAGGGAT GGGCATGGGA CCCAAGCCAA GCCATGAGGT 1800 CCAATCAGAG CGAATATCAG ATATTCAAGT GGACAGAAAA AGATGCTCTT CTTTCTCTTG 1860 GACTTGGAGA TGTGAGAGCA TCAGCAGCTG CTGACAGCTG TCTTGCCACC AGAGTCTGAG 1920 AACAAGGCCA ACTCTAAAGA AAGCAGAAGT GAAAAATGGC CTGGTCCAAT GATATTTTTG 1980 AGCCCCTGGA TCAAACTGTG CCTGAAGCCC CAGAATATTT CCATTATGTA AACAAAACCA 2040 ACCAACAAAT AAATAGGTCT CTTGCTTAAA CCAATTTGGA TGAGTTTTAT ATCACTTGCA 2100 GCTAAAAATG TTCTAATTGG CTCTCACCCA CACACCCTGT 2140
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