Tag | Content |
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EnhancerAtlas ID | HS108-20859 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr19:49240180-49241330 |
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 | chr19:49241195-49241207 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr19:49241199-49241211 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr19:49241203-49241215 | GTTTGTTTGTTT | + | 6.32 | KLF5 | MA0599.1 | chr19:49241056-49241066 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr19:49241073-49241083 | GCCCCGCCCC | + | 6.02 | NFIC | MA0161.2 | chr19:49240953-49240964 | TACTTGGCAGA | + | 6.62 | SP2 | MA0516.2 | chr19:49241052-49241069 | ACAAGCCCCGCCCCACC | + | 6.08 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29817 | chr19:49239566-49242174 | Fetal_Muscle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 49240759 | 49240894 | chr19 | 49240439 | 49241327 |
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Enhancer Sequence | CTATTCGGGA GGCTGAGGCA GGAGAATTGC TTGAACCGGG AGGTGGAGGT CGCAGTGAGC 60 CATGATCGTG CCACTGCACT CCAGCCTGGG CAACAGAGCA AGACTCCATC TCGAACAACA 120 ACGACAACAA CAACAAAAAA ACAAAAAGGA AAATGTGTGG CCTACACCAG GTGCTCAATG 180 GATACTTTGT CGAGGGGGTG GCGGAGACAA TGCTTATAAT CGTCATTCTT TATTAAGCAC 240 CTACTCTGTG CCAAGCCCTG TGCTAGGCCC TTTATATACA TTGAATATAT TATCCCATTG 300 AATCCTCACC TAGGATTTTA CTGAGATTAA CTGGCACAGA ATGGGTTGGA ATTCAAACCC 360 CAGTTCAAAG CCCATCAGTT GAATTGCTAC AACATTCTAT CTCCCAAAAG GAAGCTCAGA 420 TACAGAAAAG CGTTTAGAAG GCTCCCTGAG CAGACCCGTG CTTTCAATGC GCCAGGCCCC 480 ACCCCTGCCA GGCGCGGTCC ACCACCAGCT GTTTGACCAT TGACTCTACC TTCTGTTCCA 540 GGCCTTCCTT CGCCTCTACA GTGATATCTT CCTTCAGCCC CTTCCTTTCC CATGTGATCC 600 CACTTGGCAG CCAACCCAGC CTAAGGCCGT CTTATCCAAG GCCGGCCCCT CAGCGGCTCC 660 GCCCATCTTA GTCCCAGCAG GCCTGATCTA GGAACCTGTA TTCACTCACT CTGCAGGTGT 720 CGCCCCCTTC TATACTCCAC CCACATAGGC CCTGCTCAGT AGCCACCTCA ACCTACTTGG 780 CAGAGCTGCC TCCTACCACA GAGACCCATG CTCACCACAT GCCACCACTC CTCGCGGGAC 840 CCAACAGTTT TTGCCCCAGA CCACGCTTTT CCACAAGCCC CGCCCCACCA CAGGCCCCGC 900 CCCACAACAT GCCCCGCCCA TCTGCTCTGC ATCGCTCCCA AGAACATTGT CCGTGCTTAC 960 TCTTCCGGCT CCTAGGTCTC CAATTCCTTT TTCTTTTTCT GGAGGACAGT TTTTTGTTTG 1020 TTTGTTTGTT TGTTTTTTCG AGACGAAGTC TCGCTCTGTC CCCCAGGCTG GAGTTCAGTG 1080 GCGCGATCTT GGCTCACTGC AGCCTCTGCC TCCTGGGTTC AAATTATTCT CATGTCTCGG 1140 CCTCCCGAGT 1150
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