Tag | Content |
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EnhancerAtlas ID | HS047-15639 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr18:8029030-8030540 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr18:8029580-8029598 | AATTCCTTCCTTCCCTCT | - | 6.11 |
| | 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 |
GH18I008029 | chr18 | 8029241 | 8029290 |
| Enhancer Sequence | CCCTATGCAA TGGCTTACTG CCTGTATATC CTACATGGAG GCTGTGGTAA CTTCCTGTCT 60 GGTTCATTCA TATGGGTTCT CTCACCTCAA GATCAGTTTG ACCACCCTGA CATACCTGCC 120 TGCCTGGAGT TCCCTCCCTC ATACCTGTCC TGCCTGGAGT GCCTCTCCTC CACCTGTCCT 180 GCCTGGAGTG CCCCTCCCCC ACCTGTCCTG CCTGGAGTGC CTCCCCCACA CCTGTCCTGT 240 CTGGAGTGCC TCCCCCACAC CTGTCCTGTT TGGAGTGCCC CTCCTCCACC TGTCCTGCCT 300 GGAGCACCCC TCCCCCACAC CTGTCCTGCC ATCAGTGCCC CTCCCTAACA CTTGTCCTGC 360 CTGGAGTGCC CCTCCCCCAC CTGTCCTACC TGGAGTGTCT CCCCCACACC TGTCCTGCCT 420 GGAGTGCCCT CTCCTCATGC TTGCTTGGCC ACTTTCTGTC TACTCTTCTA GTCTTAGCTG 480 GAGTGTCACC TCTTTTGGGA AACCATCCTG TGCTGGCTCC CTGCCACCAT CCTCCCACAT 540 CCCCACTAAG AATTCCTTCC TTCCCTCTGT GTACTCTTTT GTATCTTGTA TATGCCTCTA 600 TCACTGTCCT GATAAACATC TGTCATTCTC AGCAGTTTAC ATGTCAGTCT TCCCCACCAA 660 TGTGAGCTCC TCGAGAGTAG AGATTGTGTC TTATATACTT ATTCAGTTTA GTATCTCCTG 720 CATCAGTATA GTGCCTGGCA CACAGTGAGC CTGCAGGAAA TACTGGCTAA ATTGAGTGTT 780 TTCCTCCTGA TGTCTTCCCA ATGTCCACAG GATGAGATTG AAACTTTCCT GCCCCCTGTG 840 TGATCTGACC ATCCGTGTGG CTGAGGTGGC CTGTCTGCAT GCCTCGGCCC TGTGATCCAG 900 TTGCATTCCG TGCACCGCAG CCTTTTGCTA CTGATGTTAT CCTTGCCCAG ATGTGTTCCT 960 TCTTTTTCCC TGCGAAGTAA ACAGCGCAGA CCAATCCATT CCTTTAAGCA AGAGCACAGG 1020 TGCCACCATC TTTAAAAAGC GCACACAAGT CGATGCCAAT CTGTGTTATG TCTCTCTTCT 1080 CAGAACCTTC AAGGAAGATA CTGCATATGC TTTGTACAAT ACAGTGTGGA CATCATATGC 1140 CATCTTTATT CACATAGTCC ATGTAGATTA CATTCATGCC TACCATAAAA GAAGACACTT 1200 TTTGAGCATA AAAGTTGTAC CTTATACGTC TTTAATTTTC CCAGCAGCAC TGAACATAGT 1260 TTGAGGTCTT AAGCTGGGTA ACAAGTAATT GTTGCTGTAG GCAGAAAGGA GTGGAAAGTG 1320 ATTTGAAAGC CTAGGCCCTG AAACTGGTTT CTCAACATGA CTTCAAGGGA GTGTCCAATA 1380 GTTCTTCCCT CATCATGGTC CGTCAGTGTG AGAATTTGCT CAAAACCATG CATAAGGAAT 1440 ACTATGTCAA AGTGACTGTG TTAGTGGCAT TTCTTAGTGC GTGTTCCGAT AGTAATAGCC 1500 TGTGGACCTT 1510
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