Tag | Content |
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EnhancerAtlas ID | HS051-11780 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr17:40211850-40213040 |
Target genes | Number: 23 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr17:40212462-40212473 | CCACACCCTGC | + | 6.62 | MEF2C | MA0497.1 | chr17:40212727-40212742 | TTCTATTTTTATTTT | - | 6.21 | RREB1 | MA0073.1 | chr17:40212222-40212242 | CCCCCACACACCCCACATCC | + | 6.9 | ZNF263 | MA0528.1 | chr17:40211958-40211979 | TCCTCTCCCCACACCTGCTCC | - | 6.16 |
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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 | GCTAGTCTCA AACTCCTGAC CTCAAGTTAT CCTCCTGCCT CAGCCTCCCA AAGTGTTGGG 60 ATGACAGGCG TGAGCCTCCG CACCTGGCCC TGGAGCTGTG GTCTTTTCTC CTCTCCCCAC 120 ACCTGCTCCC TTCATCTTGG TGTGGTGGGA TTGGGAAGGG AGGAGCTTTT ACCACAGGGA 180 CCGTTGCCCA GGAAGTAAGA CCTGAAGAGG CTGTGTTACA AGAGGAACAA AGACCAGACA 240 ACATCCTCAG CCACAGGACT GGCCTTCCCC ACTCAGTGTC AGCCCTCCAT TTCTGTCTCC 300 CTCTCAGCAC CCCCTTTCTG ATAACTGAGC TGCCCTCTGT GGCACTGCCT AAGCTAGAGG 360 TGTCCGTGGC ACCCCCCACA CACCCCACAT CCCATTGGCC ACCAAGTCTT GACAGTTCTG 420 CTAAAGAAAA GGCTCCAGAA TCTATTTCTC CATTTCACCT CACTTTCCTT CTTATGTACC 480 CTCGAGCCAG AGACACCTAA AAACACTAAC TGCTCCTGCT CAAACCGCTT CTGCAATGCC 540 CATCACCTTC AGAACAAAGG TCAAAGCCCA GCCTGGTGGC AAGGCTCTTG CAGGTGGCTC 600 CCGCTGTCCT CTCCACACCC TGCACACTCC CTGCACACAC CCAGCACACT GATGGCCAGT 660 GACTTCACAG GTCTGATTTA ACAATCTGGA CTGGAGTACC AGGCCTCATG TCTCCTGATG 720 ACCCCTAAGA TGGTGCCCCT CCCCACCCAA AGAGCCATGG GCTTGCAGGC CTCAATGCCT 780 TTGCTCCGGC TGCTTCCCTG CCTGGGATCC TCTCTTTGTC TCCAGTATCC ACGATCAATG 840 TCACTTCCCA TGTCAGTTTG CCTCTCCCTC CTCTGACTTC TATTTTTATT TTATTTTTTT 900 TGAGACAGGG TCTCCCTCTG TTGCCCCGGC TGGAGTGCAA TGGTGTGATC TCAGCTCACT 960 GCAGCCTCCA CCTCCTGGGC TCAAGCAATT CTCGTGCCTC AGCCTCCCAA GTAGCGGGGA 1020 CTACAGGTGC TCACCACCAC ACCAGGCTAA TATTTTGTTT TTTTAGTAGA TGAGGTTTCG 1080 CCATGTTGCC CAGGCTGGTC TCGAACTCCT GAGCTCAGGC AATCTGCCCG CTTTGGGGTC 1140 CCAAAGTGTT GGGATTACAG GCGTGAGCCT GGCCCCTCCT CTGACTTCTT 1190
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