Tag | Content |
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EnhancerAtlas ID | HS187-04911 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr11:110243140-110245280 |
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) |
Foxd3 | MA0041.1 | chr11:110245061-110245073 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr11:110245065-110245077 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr11:110245069-110245081 | AAACAAACAAAC | - | 6.32 | IRF1 | MA0050.2 | chr11:110243497-110243518 | AAAAAAAAAAAGAAAGTAAAA | - | 7.4 | JUN(var.2) | MA0489.1 | chr11:110244133-110244147 | ATGAGTCATTTTCT | - | 7.64 | ZNF263 | MA0528.1 | chr11:110245192-110245213 | TTTTCTTGCATCTCCTCCTTC | - | 6.17 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr11 | 110243695 | 110244609 | chr11 | 110244062 | 110244430 | chr11 | 110244612 | 110244708 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I110372 | chr11 | 110243104 | 110246347 |
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Enhancer Sequence | TCAGCTCACT GCAACATCCA CTTCCCGGGT TCAAGTGATT CTCCTGCCTT AGCCTCCTGA 60 GTAGCGGAGA TTACAGATGC CCACATCCAA GGTGGCTAAT TTTTTTTTCT TTTTTGTATT 120 TTCAGTAGAG ATGGGGTTTT GCCATGTTGG CCAGGCTGGT CTTGAATTCC TGACCTCAAG 180 TGATCCGCCC ATCTCGGCCT CCCAAAGTGC TGGGAGTACA GACATGAGCC ACCATGCCCG 240 GTTGCCAATT TTAAAATATT TTGTCTTTTC TCCCTGGATA TGAAATAAAA GTGATTAGGT 300 CTTAAGATAA AAAAATTAAA ACACATTTAT TTTCCTGTAA CATGCAAAAA TGCAAAAAAA 360 AAAAAAAAGA AAGTAAAATA AAATAGATAT AATTTTGGAG AAATTGCCTT TGCTCACTGT 420 GGATTCTGGA GGGTGTGAGT GATGGACAGG TCCATCTGTG CATGGAGAAT GGAAAGCCCC 480 TTCTCCAGGA TCACCCTTTA CCTTAGGAGA ACACCTCAGC TCCAGGCACC AAGCAGGAGT 540 ATCATAGGCA CTTAGCTTTA CTCCTATAGA CAAATAAGAG TGGGGAGACT ATGTGGTAAG 600 GAATGATACC CTTACACTCT TTCCAGCCCT TCCCAGTCTT ACAAGGAGTG ACACACTTGG 660 TGGCCTTCAA GCCTGTCACT GCAATTCATG CAGTGGGTGG TAAGAGGACA AAGCACGCTA 720 GGTCCCTGAT CCGACCTCCC AGGGATGACA GGTCTGGCTA CTCCTCAAAC TGAACCTGAA 780 AGAATGCAAA TGGTTCAAGT TTTCACCCTG ATTCTGGCAC ACCCCGAGGC AAAAATAGCC 840 ATTTGCCTTC ATACGAGCTT CTGTGTAGGC TGTGAATAAG GAGGTTTCTA TCTCAGCTTT 900 CTTTTTGCTC ATTTAAAGAC AACTGAGAGT ACGACAGGGT AATTGTTTTG TTTTAAAGCA 960 CTGTAATTTA GTTCCTTTCT GGACCTTCTA TGTATGAGTC ATTTTCTGTA GCAGTACTAA 1020 GAGATGCAAA TAGAAAAACA TTATTTCTGA AAGCTTGAGA TTTCAAGCTG GGCCTTTTAT 1080 TCACATTCTC TTGCTAGTTT TAGTTTTACT TGTGACATTC ATGTTATTAG AAGAATGACA 1140 CAATTTCAAT CACATTTTTG TCCCATGTAC TAATGTAGCA AACAATTTCA CAACCTTCCC 1200 TTTCTTTTAC ATGTGAGTCA TTATCATTTG GTTTTGTTCT CCTTTACTCC TGAACTCACT 1260 ATCTCCTGAT CACATGTATA CACATTTCTC TGATATCCTA GATCTTTATG GGTGATCAAG 1320 ATTTTTGTAT ATTCTGTTTT GTTGCTTTCA TACCCGCTAG TATCCTTTTT AAGTTTGACT 1380 CTTTTATACT TTGGGAGATG CCAAACAAAT ACTTCAGGAG AAAGGAGGCA GTGTGTTGAA 1440 AGGAAGTTGA CAAAGCAAGA AGAAAAGAAG AAGAAGATAT AAGGAGGAAA CGTAGTGGCT 1500 CTTAAACAAA GATCTTGCAT CTTTTCCTTC TTTAATTTTT TTTTTTTTTT TTTTTTTTTT 1560 TGGTTTGAGA CAGAGTGTCA CTCTGTCATC CAGGCTGGAG TACGGTGGTG CAACCTTGGC 1620 TCACTGCAAC CTCCACCTGC TGGGTTCAAG CGATTCTCCT GCTTCAGCCT CCTGAGTAGC 1680 TGGGACTACA GGCGCAGGTT ACCACGCCTG GCTAATTTTT GTATTTTTAG TGGAGGTGGG 1740 TTTCACCATG TGGGCCAGGC TGGTCTCGAA CTCCTGACCT CAAATGATCC ACCCACCTCG 1800 GCCTCCCAAA GTGCTGGGAT TACAAAACAG AATTGCTTGA ACCCAGGAGG GAGAGGTTGC 1860 AGTGAGCTGA GATGGCGCCA CTGCACTCTA GCCTGGGCAA CAGAGCGAGA CTCCATCTCA 1920 AAAACAAACA AACAAACAAA CCAAACCCAA CTTTGAACCC AGAATCAGAA AGCAGATTTA 1980 ATTTGGAACT CTATAGAATG TCTGCACATG AACAGATGCC ATAGCCGTAA CAAAAATTAG 2040 GGCCACAGCC ACTTTTCTTG CATCTCCTCC TTCCTCCTTT TTTCTTTGGC TTTCTTGTAT 2100 AAACCTTAGC ATAAGGCATG GTTGCTTGGT TTACAAAATA 2140
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