Tag | Content |
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EnhancerAtlas ID | HS134-47264 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr5:61513840-61515400 |
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) |
Gata4 | MA0482.1 | chr5:61514379-61514390 | AGGAGATAAGA | - | 6.14 | NR2C2 | MA0504.1 | chr5:61514333-61514348 | TGCCCTTTGACCTCC | - | 7.14 | Nr2f6 | MA0677.1 | chr5:61514333-61514347 | TGCCCTTTGACCTC | - | 6.65 | Rxra | MA0512.2 | chr5:61514333-61514347 | TGCCCTTTGACCTC | - | 6.62 | ZNF263 | MA0528.1 | chr5:61514388-61514409 | GAGGGAGGGAGAAGGAGTGGA | + | 6.38 |
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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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Enhancer Sequence | TCCCCTCCCC TTTTCTCTAT ACTTAAAACT CCCTCTACCC CACCCAGATA TCCAAAGGTG 60 TTGATCCTAC CCTCCCAAAG CTCCCACTGT AGCTAGCTCC TCAGAGGCCT CTCAGGGAAG 120 AGCGAAGTGA GCTAATCAAC CCAGCCTAGG CTTCTGTTGA CCCAGAACCA ATTCAAGATG 180 AAGGCCATGC CTTAGACAGC AGCTGCCAGG GAAATACATG ACTTATACAA TGACATCAGC 240 TGAAATTCAC AAAGGTCATT GCATTTAACT CATTCCTCAC CCAAGGTGAT GCAAACATGC 300 TAACCCTTTT CCTCCCAGTC TTCTCTGGAT GATCTTCTCC ACTTGATTTT ACTGGGATGT 360 ACATGAACAA GCTAGAGGAG CAGCCTGTGC CTGTTATCCT CTCCTCCCCA CTGCTGAAGT 420 CACTCTCCAC CCTTCTCATC CTACTCTCTT GCTGGGGACA CTGGACTGTA TGAGTTTCAT 480 CAATGGACTC CCTTGCCCTT TGACCTCCAG TTGGGTTCTG CCAATTAGAG ATCCTTAATA 540 GGAGATAAGA GGGAGGGAGA AGGAGTGGAG GCTGGGGTAT TTATGCCTCT GGCTTGATCC 600 CTGAAGTATT GTCTTGCAGT CATCTCTATG TGATTCTCTC CACCCAGGTT CCAGTAACTG 660 ATCACTCCTC ATATCATTTC TGGTGAGGAG TCGTAACTGA ACTCAGTGGT GCTACACTGT 720 CCTTTATGGA TTCCATAAAC ACTGCTCATC CTTTGTAAAC AGTCCCTTCA TTAAACCTCC 780 CTCCAATTGT TCTAATGCAA ATGGCCCAAC ACATTCCTCC TGGGATCCTG AAATGATTCC 840 TTAAATGATG TGGTCTATCC TATCTCCCCT TCCTGCCTAC AATGGCCTTG GGCTCCGTCC 900 TAACTCTGCT GCCTTTAAGA TTGGTCTACC CTAAACTACA TCCACATAAC CCCAAGATTG 960 TCTCTTCATG CCTAACCCAC AAAGAGAGGT GATAGGAGTT AGGCTGAGGA GTGGGGATAG 1020 GGAAAGACAA GGCTCAGCAT GGTCCCTGAT AACCTCGTAG CTTCCAGGCA GATGAAGTGC 1080 AGGGTGGAGG CAGGCTGCTC TGAGCCCAGC TGGTCGGTGC TCAATCAGAA AGGATATGGG 1140 TTGAGCTCAG AAAGCCTGAG AGCAGTGGCA CTCTGGAGCA GATCAGAAGC CAAGACTCTA 1200 AGAACAACAT GCAAATCTGT GTAGGGAACA TCAGAGGCTC CTGCCCAGGT CTGAGCAAGT 1260 GCAGACAGAC AGGCTGGTTG TCAGGAGGCA CTGATTGACA GGGGAGAGGA GTGAATCAAA 1320 TATGAAGCAA AGCAATAATC AATTAGCTCA GTCTGCAGAT AGAAATAGAT TCCTACAGAT 1380 AGGAATTTAA GTCAGAGTTG CAAGGGGATT TAGAAATCAC ACACTTCAAT CACTTCACTT 1440 TTAGATGAGG ACTACCAGAC TGTAGACACA GGGGTGATGA GTGCAGAACA AAGACAAACA 1500 CCCAGAACTT CTCACTTCTA GATTAAGGAT TTACCTGTGA AACCCATGCC TCTAAAAAGA 1560
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