Tag | Content |
---|
EnhancerAtlas ID | HS176-14767 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr16:11177570-11179830 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr16:11178536-11178550 | ATGAGTCATCTCCA | - | 6.52 | MEF2C | MA0497.1 | chr16:11178367-11178382 | TTTCCAAAAATAGAC | + | 6.57 |
|
| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_25367 | chr16:11177333-11195892 | DND41 | SE_33447 | chr16:11177254-11183743 | H2171 | SE_45167 | chr16:11177315-11180359 | NHLF | SE_62880 | chr16:11169251-11234543 | Tonsil |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH16I011082 | chr16 | 11176659 | 11180248 |
|
Enhancer Sequence | CCTGGCCCTA AGCCCCAGTC CTCTCCTGAA CTGGGGCAAG CCCTCCACTT CCAGCCTCCT 60 GCTGCCTGTG GCGCTCCCCT GTCCGCTGGG AGGCAGGGAG GCTGGCCCAG GGGGACCTGA 120 CATGAAGAGT CTGTCTTACA GGGCTCAAGG GGATGGCTGT GGTCTCCCCT TGCCTGTGTG 180 TGTTCTACCC GGAATGGAAA CCAGCTTTTC ACCTTGTCCA GGAGGTTGGG AACCTGAGGG 240 AACACAGCAC TGCCTCTGTC CCAGCCCCCC ATTGCTGGTT TTCTCTCCAC CAGCAGAGTC 300 CAAGCCCAAG CCGTATGGGC CCCAGCAGGA CCACACTGAG CCCTCTCTCC AGCCCCGCGG 360 CCTGGCTCTG GGATGTACCC ATACCACCCC TTTTAGTCCC CTGCTTGCTG AGTGTGTCCC 420 CTTCAGCTCT GGGCCTTCAT ACAGGCCCAT CCCTCTGCTT GGGATGCTTA TTCCTGCCAC 480 CATGGTCCCC TGTGTTTGGC CAACTCCCTG ACACCTTCAA CTCTGCAGAC AGCTTACTTC 540 CTAGCAAAAT CTTCCCTGAC CACCAGATCT CTCTCTGTTC ATGGCATTTC CCACTGTGTG 600 TGATTTTCTA TTTTTATGTG GTTCTTTGGT TCATGTGGGT ACCAAGCTGC TTGGGGGCAG 660 AAACCCCAAT TCTTATTCAA AGTTGGATCC CAGGGCCCAC AGTGTAGCAG GTACTCAGTG 720 AAGACAGGCC AGATATGAAT GAATGGAAAT GCGAGTGGGT TAGGGTCCGA GCCCACAAAT 780 GAGGACATTG GCCTTGTTTT CCAAAAATAG ACCATGACTC CAGGGCCCTA GAGGAAGCCT 840 GTAAACCTCC TGGTCTGACA GACATCTGAC ACACTTTGCG TGGGTCTCTT TCTCCACAGA 900 GAAGTTGGAA TAAGATCAAG ACTTAATTCG CAGGCCCAGC ATTAGTCTTC TGAACTCGCC 960 GGCTATATGA GTCATCTCCA CTGTGGAGGG AGGCAATTTT AAACTGGAAA GGTCAATCGA 1020 CATGTCAGAA TATCTAGTAA ATCATTCGCG TTCCACCTGG TGCCCCTTCC ATTCCCCTGA 1080 AAAAGCCTGC CCTTGTTCAG CGCCTCTCGA AGACACTGTG GAGAAAGAGG TAGCCGGGGC 1140 TGGGTGGTGA TTTACCTCGA GGAAAATTAA TATGGTGCCA TCAATTCTGA AGGCAGAAAG 1200 GGCCCATGGC CAGAAGGCTG CACGCAGGCT GGAATAACTC ACGGCCCATG AGGGCCCTGA 1260 GTTTGGGGAG GCCTCTCCTT GGCCCTGGAT ATAAATCAGC AGCCCTTTTG CAGAGAGAGA 1320 GTCGGAGTTT TGTCAGGCCT GGGGGAAGGG AGCCAGCACC AGAAGCCCCT CTTCCCCAGG 1380 AGCCTGTCGT TGTCTGAAGG GTTGAAAGGC ACCTCTGTGC CACCCTTCTC GGCCAGCACC 1440 AAGCACTGGA CTCATTTACA GACGAGGCCA TGAAGCCCCC ACCCTGGGTT CCAGGAGGAT 1500 CACGGGAAGG GGGCTTTCAG CCTGGCTGTC AGAGAAGAAT GTGACAGGCC CATTTTCACT 1560 CCACAGGCCT TAATTGGATG GTCAGAGGGC ACATCTGTGG CTTATAAGAA ACAGATGGCG 1620 GGATGGGTTA GTGAAGGAGA AAGCACGCTT GCTTCAGGTT GAGTGCCCGT GGAGGTGCTG 1680 GGGCAGCACG CTGGCAAGCA GGCAGACTCG GCCAAGACCC AGCTTTGTCA CGTGCGTGAG 1740 GCCTTGGCTG TCCTCTTCAT CTTTCTGCGT GTCTGTTTCT TCAGCTGTAA AATGGAGATG 1800 ATGAGGCCCA ACAACATAAC ATAGGAGGAT TTGGTGAGAA AATGCATTTG AAATGGCTGA 1860 AGACAGTGCC GTGTGTTATA AGTGCTTGGT AGTTGTTATT GTCCTGTGGT AGCCTTGGGT 1920 CTCTAGAGCC AAGAACAGCC TCCTGTCTGG ATCTGAGTGG CTTCATCCCA CTGTGTGGGA 1980 CTCTGGTCCC AAGTGTTGTA TGTGAGTAGC TGGGACCACA GGTGTGCGCC ACCACACCCA 2040 GCTCATTTTT GTATTTTTTG TAGAGAAAGG GTTTCATCTT GTTGCCCAGG CTAGTCTCAA 2100 ACCCCTGGGC TTAAGTGACC CTCCCACCTC AGCCTTCCAG AGAGCTGGGA TTACAGGCGT 2160 GAGCCACTGT GCCTGGCCGG GAATCCCATT TCAACCTGAG ATTGGGCGGG GACAAACATC 2220 CAAACCATAT CAGTACCTGT GGGAAGTGAC TTGGAGGCCT 2260
|