Tag | Content |
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EnhancerAtlas ID | HS187-15044 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr20:5509640-5510810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
YY1 | MA0095.2 | chr20:5509716-5509728 | CAAGATGGCAGC | + | 6.32 | Zfx | MA0146.2 | chr20:5510046-5510060 | CCCGCCTCGGCCTC | + | 6.01 |
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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 |
GH20I005528 | chr20 | 5509641 | 5509830 | GH20I005529 | chr20 | 5510047 | 5511030 |
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Enhancer Sequence | TGCTCAAAAA GGTTAGAACT CACCCAGTCA GCTAGCGACT CCAGAATAAT CAGATACATG 60 TTCCCCCAAG GTACCACAAG ATGGCAGCAC ATGCACACAG CATTTCAAGC TCCTGCACAC 120 TGAGATGACA GCAATTAATC TGCCCTCTAA TAATGCCTCT GCCATCCTGG AAAGCCCTAC 180 ACTTAAACGG TCATGATGCC TGTTTCTATG ATGATGTGTT GCAAACACAC GCAGCATTTC 240 TGAGGTAGAT GAAGAGATTC AAAGGGTAAC AGGAGATTAT GTAGTTCAGA ATTCTTCACC 300 TTTTTTTAAA AAAAATATTT ATTTATTTAT TTATTTATTT TTAATAGAGA CAGGGTCTCA 360 CTATGTTGCC CAGGCTAGTC TTGAATTCCT GGGCTCAAGC GATCCTCCCG CCTCGGCCTC 420 CCAAAGGGCC GGGATCACAG GCGTGAGCCA CTGAGTGTGG CCAGAATTCT TCACCTTTTG 480 GTGCAGAGTG TGTATGTCGC ACCTGAAGCC AGAAGTCAAC GATACTCGAT GAAAGGGTTT 540 GTTCAGCGCA GATGACCTAC TTGGGTTCAT GGCTTGCATG TGTTATAATT GCTGCTGTTT 600 ATTTCCTGAA AACTTAGACG ATTTGGGGCA CATTATCGAT GCCTTACAGG CATGGTCGCA 660 TTAAACTTTA CTGCAGCCAT CTGTCATAGT GATTATTATC CTCATTTTAC AGATGGGGAA 720 AGAAAGAATT AGACCTTCAG GCACCTTGGT AATGGCACGC ACAGCGAGTA GAGGCAGAGA 780 GAACCTGCTT CCCTGACGGC CCACACTCCC CCGGCACACA AGGCTCCCTC TAGGTGGCGC 840 GCGCGTCTCA GCTTCTACTG CGGAAGTCTC GGTTATGTGA TTATGTATAC GCTCAATCCT 900 ACACCAATTG AGAATGGCCC TTAGCTTGGA ATTAGTAAGA ACAGTAATTA GCAATTTATT 960 GTCAGAAAAA AGTTCATAAG ATTATCGGCC GCAGTCTCTT TGCTGCACAT CTTTCTCATC 1020 TTGACAGGAC AGCCACAGGG AATCCAGGTC TTCTCCACCA CCCCAGGCTC AGCAGTTCAT 1080 GCTTACCCAC CCAGCTCAGG CACAGATGCG ACATTCAGCT TAGCAACATT CAGCTTAGGA 1140 TCGGGTAAAC AGGCAGAGCT TTCTCTCTCT 1170
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