Tag | Content |
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EnhancerAtlas ID | HS098-22726 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr16:87668660-87670530 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr16:87669270-87669289 | GAGTGACACCTGCTGGCGG | - | 6.17 | FOXA1 | MA0148.4 | chr16:87669959-87669975 | TTTTGTTTACTTAATC | - | 7.54 | FOXP2 | MA0593.1 | chr16:87669960-87669971 | TTTGTTTACTT | - | 6.62 | KLF4 | MA0039.3 | chr16:87669490-87669501 | CCACACCCTCC | + | 6.32 | Klf1 | MA0493.1 | chr16:87669488-87669499 | AGCCACACCCT | + | 6.02 | REST | MA0138.2 | chr16:87668853-87668874 | GCATCTGTCCATGGCCCTGAG | - | 6.79 | SREBF1 | MA0595.1 | chr16:87670189-87670199 | GTGGGGTGAT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 87670268 | 87670506 | chr16 | 87669315 | 87670076 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I087635 | chr16 | 87668633 | 87670751 |
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Enhancer Sequence | GTAGTGGGAG CCTGGGTGGG GGCTTTTGCC TGCCAGAACT CATGGGTCGG GGCCGCACAT 60 GAGTGAGTGT CTCCTGGGCA GGGCTGTGGC CATGAGCTCA GGTCTTTAGT GGGCTCCTTG 120 CTCCTCCCAG CAAAGCGTTC ACCTTGCCCC ACCCTGGGAC CTCTCAGGTG CTCTTTGGAG 180 GTGTTGACCT GGGGCATCTG TCCATGGCCC TGAGGAGGTG GAGCACCTGG TGAGGGCTGC 240 GCTCTCTCCA GCTGGGACCC CGGGCTCCGA AACTAAAGTT TTGGGAAGAG TGTCAGCTGA 300 CGGGTGGGGC TTCAGAGGAG GAAAAGAAAC AAGGGTGTGA GATGTGCAGG CCCTGGTGAG 360 AGACAGGCAG CAGCAAGAGC CTGCCAGCCA TACTTACCCA CAAGGCCGGC TGAGGGGCTG 420 TGCTGGCCCA GGGCTCTGGC TTTCGGACCC AGACAATGCT GCTGACCAAG CAGGCCAGGC 480 GCTGAGTGAC TGTCCCAGCG GATCTCCGAG CAGGGTCCCT TGAGCATTAG GAATGCAGCT 540 TCTCAGGCCA TGCCAGCCTG GCAGAACAGG AAGGGAGGGG TACAGCCCTG TGGGGACGCA 600 GCTGTGGCTC GAGTGACACC TGCTGGCGGC CTCATCTCAT CCGCTCTCTG CGAGTCTGTG 660 GTGGTTCTAG TCGGCGTTTC ACGGGCAAGG TTTAGGGGGT TTGTTCCTCA GCTGGGGTCC 720 ACCCACGTCT TCCGACTTCC TCTCTCAGTG TTTGGGCCAT CGGTGGGTGA GGTGGCTGCA 780 GCAGAGCCGG GGGCTCCTGT GTGCGGAGGC AGCACCGACA TCCACTGCAG CCACACCCTC 840 CTGAGAGGGT CTGGAAGGAA GCAGGGCACC CTGCGAACCC ACCTTCCTCT GGGGTGTCTT 900 CCGGGGCCCC AGGGCCAGGG CAACTGGAGC AGACAGGACA TTATCTAGCT CTGGGGGCCG 960 TGCTGACCGA GCCAGACCCT CGCGGCGGCC CACAGAGATG GGCAGCTTGC GGGGCAGCTT 1020 TGTCCCCCCG ACACTGGGTC CTGTCTTCAT GCACACAAGC CGCCTGTTCT GCAGGTGACC 1080 AGTTAGGTTC GATGGGACAG GCTTTGGGAA TCAGCGGCTT GGGTTTGCCC CCCACAGCCT 1140 TGGATCTTGA CCTTGGGAGA GGCCTCCACC ACGTGCCCTG GGGTGGGGTG GGGGCGGGGG 1200 CGTCCTGCAT CTGCGCCGTT CAGCTCAGTT GCCCTCAGCC GCGGTTGGCC GCCAAGCACT 1260 AGGGTGTTGC TGGCACAGCC AAGGAACTGA GCCCAGACTT TTTGTTTACT TAATCAAGCA 1320 TAAATGCAAA GGGCTGGGGG TGGCCGAGCT GATGGTGCAG GCGTGTGCGC TCAATAGCTC 1380 CGTCACAGTG GCTGTCGCTT TATTGAGCAA CCGAGGGAGC GAGGGAGAGG AGCAACTGCG 1440 GCGAGCGTGG AGGCCCAGCC CGCAGAGCTC CCGTCTGGGG GAAGCCCTGT CCCTCACTGC 1500 CTGTTCCCGG CGCTTTGGTG CCCTCTGCTG TGGGGTGATG AGGTCAGGCT ACGCAGGCAG 1560 TCACGGCAGA ACTGAAGGCC GTGTGCTTTC GTGTAGCCAA ACCCCTTTTC TTACTGATAT 1620 CAGTTATAAA ATCAGAGCTA TGTTCCCACC AGGGGCAAAA ATCCAACACC GTGCAGTTGC 1680 AAACACGGGG CAGGAAAGAC TCCGGCGACC CTCATTACAC TGTGCCGGGA GGCATGGCCA 1740 GAGCTCCGTC AGTTCATGCG TCGCTTAAAC CTAGAGGTGG GTGCGATTGT CACCCTATCT 1800 TACAGGTGTG GAAACTAACT CAGCTCCGAG ATGTGACTGA CCTTCCCCGG CCATAGTACG 1860 CGCAGCGCAG 1870
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