Tag | Content |
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EnhancerAtlas ID | HS176-03307 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:203576100-203577200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:203576594-203576605 | GATGAGTCACC | - | 6.32 | Foxd3 | MA0041.1 | chr1:203576399-203576411 | AAACAAACAAAC | - | 6.32 | JUND | MA0491.1 | chr1:203576594-203576605 | GATGAGTCACC | - | 6.62 | NFIC | MA0161.2 | chr1:203576579-203576590 | TCTGCCAAGAA | - | 6.02 | RREB1 | MA0073.1 | chr1:203576623-203576643 | GGGCTGGGGTGGGTTGGGGT | - | 6.03 | RREB1 | MA0073.1 | chr1:203576622-203576642 | GGGGCTGGGGTGGGTTGGGG | - | 7.16 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_25758 | chr1:203575191-203577246 | DND41 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 203576120 | 203576183 | chr1 | 203576282 | 203576863 | chr1 | 203576404 | 203576703 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I203606 | chr1 | 203575245 | 203577382 |
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Enhancer Sequence | CAGAGTGAAA CTCCATCTCA AAAAAAAGAA AGACCTTGTT AGATAACTTA GCTAGGCATG 60 GTGCCAGGCA CCTGTAATCC CAGCTACTCG GGAGGCTGAG GCAGGAGAAT CATTTGAACC 120 TGGGAGGTGA AGGTTGCAGT GAGCTGAGAT CGCACCATTG CACTCCAGCC TGGGCAACAA 180 GAGTGAAACT CCATCTCAAA AAAAAAACAA GAAAGACATT GTTAGATAGC ATTGAGCATA 240 TCACTTAAAT GGCCTTGGCT CACCCCCTGG GGAAATCATG TTCTTTCAAA GACACTATAA 300 AACAAACAAA CAAAAAAAGC AACAGTAGCT ACAGAGTTCC TGCTCCAGCA ACCAGGAGCC 360 TTGAGGCAGC ACAAGGACAC CGGGGCGGGA GCGTGGCCCA AGAAGCAGAG ACAGCAACAA 420 CAACAGGATG ACTTCATTTA CTGAGTTATC AAAAACCACA ATGTCTGAAA ACCACAATGT 480 CTGCCAAGAA AGAGGATGAG TCACCAAGAC CCACAGGAAA GAGGGGCTGG GGTGGGTTGG 540 GGTGGGCAGC ATGGCATGAT GAGAAAAGCA AGTATTTTGA CAGCACACAG ATTCAAATCC 600 TGACACATCT CTGAGGCCTT CAGCTCTCTG GGTCTCAGCT TCCTTTATCT TTAGTTTTTA 660 TTTATTTTTA TTTCAAAAGA AATGAGATGG AGTCTTCTCT GTTGCCCAGG CGGGAGAGCA 720 ATGGTGCAAT CTTGGCTCAC TGCAACCTCT ATCTCCTGGG TTCAATTGAT TCTCCTGCCT 780 CAGCCTCCCG ATTAGCTGAG ATTACAGGTG CATGCCAGCA CACCGGCTAA TTTTTGTATT 840 TTCAGTAGAG ATGGATTTTA CCATTTCGGC CAGGCTAGTC TCGAACTCCT GACCTCAAGT 900 GATCCACCCA TCTGGGTCTC CCAAAGTGCT GAGATTACAG GTGTGAGACA CCATGCCCAG 960 CCCTCAGCTA CCTTATCTTT AAAAATGGGA AAGAGCCAGG CACAGTGGCT CACATCTGTA 1020 ATCCCAGCAC TTTGGGAGGC CAAGGCAGGT GGATCACGTG AGGTCAGGAG TTCGAGACCA 1080 GCCTACGTGG TGAAACCCCA 1100
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