Tag | Content |
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EnhancerAtlas ID | HS051-13147 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr18:56359720-56361030 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr18:56360661-56360672 | AAGCAATAAAA | + | 6.32 | MNX1 | MA0707.1 | chr18:56360043-56360053 | GGTAATTAAA | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_18939 | chr18:56359056-56361510 | CD4p_CD25-_Il17-_PMAstim_Th | SE_62695 | chr18:56306617-56365029 | Tonsil |
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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 |
GH18I058692 | chr18 | 56359716 | 56360380 |
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Enhancer Sequence | CCCCACTCCC TCTTTGGGCC TCCCTATTCC CTGAGACACA ACAATATTGA AATTAAGCTG 60 ATTAATAACC CTACAATCGT CTCTAAGTGT TCAAGTGAAA GAACAGTGAC ACACAACAAT 120 ATTGAAATTA GGCTGATTAA TAACCCTACA GTGATCTCTA AGTGTTCAGG TGAAAGGAAG 180 AGTCACATGT CTCTCACTTT AAATCAAAAG CTAGAATTGA TTTTACTTAA TGAGGAAGGC 240 ATATCAAAAG CTGAGATAGG CTGAAAAGCT AGGCCTCTTG TGCCAGTTAA CCAAGTTGCG 300 AATGCAGAAG AAAAGTTCTT GAAGGTAATT AAAAATGCTA CTTCAGTGAA CACACGAATG 360 ATAAGAAAGC AAAACAGCCT TATTGCTGAG ATGGAGAAAG TTATAGTAGT CTGGATAGAT 420 CAAACCAGCC ACAGCATGCC CCTAAGCCAA AGCCTAATCC AGAGTGAGGC CCTAACTCGC 480 CTCATTTCTG TGAAGACAGA GAGGTGAGGA AGCTGCGGAA GAAAAGTTGG TTCATGAGGT 540 TTAAGGAAAT AAGCTGTCTC TGTAACATAA AAGTGCAAAG TGAAGCAGCA AGTACTAGTG 600 GAGAAGCTGC AGCAAGTCAT CCAGAAGATC TAGCTAATGC CAGGCATGGT GGCTCGTAAT 660 TGATCATGGT GTCTATAATC CCACCACTCT GGGAGGCCAG GGCAGGAGGA TTGCTTGAGC 720 TTAGGAGTTT GATACCAGCC TGGGCAACAT GGTGAAACCC CGTCTTTGCA AAAAATACAA 780 AAAATTAGCC AGGCACAGTG GCACCTGCCT GTAGTCCCAG CCACTCGGGA GGCTGAGGTG 840 GGAGAATTGC TTACACCTGG AAGGCGGAGG TTGCAGTGAG CGAGATCATG ACACTGCACT 900 CCAGCCTAGG TAACAGAGAC AGACCTTGTC TCAAAACAAA AAAGCAATAA AAGATCTAGC 960 TAAGATAATT AAAGAAAATG GCTATAATAA ACAGATTTTT CAGTGTAGAT GAAACAGCCT 1020 TCTATTGGAA GAAGATGTCA TCTAGAACTT TGATAGCTAG AGAGAAGTCA GTGCCTGGCT 1080 GACTCTTGTT AGGGGCCAAT GCAGCTGACA ACTTTACGTT GAAGCCAGTG CCCATTTACC 1140 ATTCTGAAAA TCCTAGGGCC CTTAAGAATG ATGCTAAGAA ACTGCAAAGT TTTTGTCCTG 1200 AGTAACCAGA TGGATGGTGG TAGGCAGTAA GACTGGTTTA CCATCTTTGA GATGGGGAAA 1260 CTGTGGGGAC TGGCAGAGGA GTAGATTTTG TGTCAGAAGG GATTTGGGAC 1310
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