Tag | Content |
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EnhancerAtlas ID | HS187-12275 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr19:36443820-36445210 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr19:36444555-36444565 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr19:36444555-36444565 | GGCACGTGCC | - | 6.02 | STAT3 | MA0144.2 | chr19:36444917-36444928 | CTTCTGGGAAG | + | 6.14 | Sox6 | MA0515.1 | chr19:36444967-36444977 | CCATTGTTTT | + | 6.02 | ZNF263 | MA0528.1 | chr19:36444051-36444072 | CCTCCCCTTCCTCCCTGCCCC | - | 6.41 | ZNF263 | MA0528.1 | chr19:36444044-36444065 | TCCCCCACCTCCCCTTCCTCC | - | 8.02 |
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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 |
GH19I035952 | chr19 | 36443788 | 36445345 |
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Enhancer Sequence | TGAGCCACCT CACCAGGCTA CAACCTCCAT ATTTCCATCC TCAACCCCAG CATCTCTCCT 60 AAGTCCAGAC CTGGCTTACC TCAGTTTCCC GGACCCCTCT TCCTGGACAT CCCCTGGGGC 120 CCCTCACACC CACTGGATCC CACACCCACC TCGGCTTCTT CTCGGACCTA TGCCTCCTTC 180 TAGGTCCTGT CTGGGAGAGC AACCCCCATG CAGCCTCCTG AATGTCCCCC ACCTCCCCTT 240 CCTCCCTGCC CCGGCCCCAT CCTGGGCTAG TTCTGGCCTC ACCCATCTGG GTCCTTGCAC 300 TGGGCTCCTG GCCTCAGTCT CTTCTCTGGT CCAGGATCTT CCTAAAGCCA AACCCTCCTC 360 TGTATAGGCA CCCCCATGGC TCCCCAGGGT TCCTGGGACA GTCTGAGCTC CTCAGCCTCT 420 AGCATCCCAG CCCTTCCCAC GCCATCCCTC TTCCCCAGCT CTGTTTCTAG CACATATGTT 480 TGTTCCCCAC CTCAGGCAGG AAGGAAACAC TAACCACATC CTCTGCTTGT GATGAAGGAG 540 GATCTTAAGC AAGTGACAGA TGAAGCTATT GAAGGAAAGT GGGTTCCAGC TGGGCGTGGT 600 GGCTCATGCC TGTAATCCCT GCACTTTGGG AGGCCGAGTT GGATAGATCA CTTGAGGCCA 660 GGAGTTCGAG ACCAGCCTGG CCAACATGGT GAAACCCTGT CTCTACTAAA AATACAAAAA 720 TTACTTGGGC GTGGTGGCAC GTGCCTGTGG TTCCAGCTAC CCCGGAGGCT GAGGCAGGAG 780 AATCGCTTGA ACCCAGGAGG CGGAGGTTGT AGTGAGCCGA GATCGCCCCA TTGCACTCCA 840 GCCTGGGCAA CAGAGTGAGA CTCTGTCTCA AGAGAAAAAA AAAGAAAGAA CATGGGTTGC 900 TTCTTGAATG CTCCCCTTAT TCCTCCCACC AAAGGTAACG TTCTGGGGGA GAAGGAGGCC 960 TGGGTGCAGC TACTAGCATC TGGGGGAGAG GCAGTTGGTA ACTGTACCCA GGGTCCCTTG 1020 CTTCTCCATT TCTGGAGATC CATCCTTGCC CTCCTCTCCG AGATCCTCCT AGAAGGCTGT 1080 AGCTCCATTG TTCTCAGCTT CTGGGAAGCC GAGAGGACGT TCTGGGAAGA AGAAAGTGAT 1140 GTATAGGCCA TTGTTTTCTC ACGGGAACCT CTGTCCCCAA ATCCTCCAGA CCTCCACATC 1200 CAGGCACCTG GTGCCCTCTC CTGCCTCTGT CTCTGGTCAC TTCCACAATC CAGGAGCCCA 1260 GGCGTCTAGC TTCCTCCTTC CTCAGGAGTT CAGGTCTGCA GTCCCCTCCT TCCTCAGGCA 1320 CAGAAGCCCC ATCTCCACTC CCCTCCATCC TCAGAACACA GGCTCCCGGC CCCCTTCCTA 1380 GGATCCTCAA 1390
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