Tag | Content |
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EnhancerAtlas ID | HS074-00662 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr1:93498460-93499930 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:93499505-93499526 | AGTTTCTTTCCCTTTCAGTTC | + | 6.29 | NFE2L1 | MA0089.2 | chr1:93498750-93498765 | AAATGACTCAGCAAT | + | 8.07 | Nfe2l2 | MA0150.2 | chr1:93498748-93498763 | CAAAATGACTCAGCA | + | 7.82 | ZBTB18 | MA0698.1 | chr1:93498583-93498596 | GCACATCTGGATC | - | 6.41 |
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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 |
GH01I093032 | chr1 | 93498529 | 93500070 |
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Enhancer Sequence | GCATTTGCAA TTTTAATTTA CAAACTACCT TTCTATCCAT TTATTCTGAT GCTCTGCTGT 60 GCTTCTTAGA GAGGGTTAGG AGGTTGAAGA GCTTTGTATC AGACCTCTCT TGGTTTACCT 120 GATGCACATC TGGATCAGAT GCATGCCCCG TTGAGCTACA TGCATGCCCC ATGCTCCCAG 180 CAACATCCAA CTGCTCAACC CCTCCCCTGT TCCCTGTCAA CCACAGGCCC TCTTGGGGGT 240 TAAAACCTTT TGAACAGGGC CATCTGTTCT TCACTTCGAC AAGTTGAGCA AAATGACTCA 300 GCAATTCACT CTTCTAGTTT TTTAAGTCAG GACAGGATAA GGGAGAGATG AAAACATCCA 360 ATTCAATTCC AAGAACTTGC CAAACAATAC GTCATTTGCT CAAAGTCACT CAGTTGGGAA 420 GAAAGATTAG AACTCAAGAA ATGTTATGCC CTCAGATGCA CTGCTTATCC AAAAATGTAT 480 CTAAAATGAT TTAGAAATCT CGTATTTCAA TCAGCGTTGG CTTCACAGGT GTGCAACCTG 540 TGCAATCACA CAGGGTCCAC TCTCAGAAGA GCTTTGCACT TGGTTGAATG CTCTGCTGTC 600 TCCATTTTGA AATTCTTAGT TATTTTACTT TTGAACTTAT ATTTTGTAAG TGATGTTCAA 660 TGGGACAATG GCATGAGCAG AGAAGATACA TGAGTGCCTT CCAGTCTTTG TTACTAAATC 720 TGTCTGCATA TGGCTCTCCA GATTTGCTCC ATGAACACAG AATTCCACTA CAGACCCACA 780 ATGCCTAGAA ATGTAGCAGA CACAAAGGAA GTACATGATT AGCATGTATG TCCACAAATA 840 AGTAGGCACT GACAGTCCTG AGAGGCCATG TTTTCCATTC AAACCGGAGC CTGTTTTGAC 900 TGCAGAGAGA AAGCAAAGGC ATCCTAAAAA AAATTATCAA AGGAATCATG TCATATTCAT 960 TCTTGCTTAT GTTGCTTCCC TGTATTAGCC AACCACTTAC ACAGAAAATG ATGCCCTATA 1020 AGGAAAGGGA AAGATAACAG CTCTTAGTTT CTTTCCCTTT CAGTTCCTCC TTACTCATCA 1080 GTAAGCTGAA GATAGTGCTA GGAGGAACAC GTGCAATCAA GAAGTGAAAT AAAAACAGTT 1140 GAGTTAGTTT TGTGCAGTGT TTCTACTGTT CTAGTAAGAA CAAAACATAT GTGTGTGTAT 1200 AAGCTACAAT ATACAAATTG TGTAATTTTG TTGATTCTGC ATGAGTTAAA TACTCTGATA 1260 TTTTCATTTA AAACCGGCAT TGCACAACGG AAAGATGAAC ATTAAAATTC ATGGTAATAG 1320 TTTTAAATTT AAATTTTTCT TTATTCAGAA AAACATTAAA TAGCAAATAA AAAATACCAC 1380 TGCAAATCCA GGAAGAGCTC AGAAGAAAGG GAAAAGCTTT ATATTTTAGC ACTTTTTAAA 1440 AACAGCTTTA CTGAGATATA ATTCATATAT 1470
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