Tag | Content |
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EnhancerAtlas ID | HS007-07627 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr18:25711720-25712730 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr18:25712454-25712472 | GGAGAGAAGGACGGAAGG | + | 6.71 | SPI1 | MA0080.4 | chr18:25712071-25712085 | TACTTCCCCTTTCT | - | 6.59 | SPIC | MA0687.1 | chr18:25712071-25712085 | TACTTCCCCTTTCT | - | 7.04 | ZNF263 | MA0528.1 | chr18:25712443-25712464 | GAAGGAGGTGAGGAGAGAAGG | + | 6.28 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I028131 | chr18 | 25711917 | 25713318 |
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Enhancer Sequence | ACTATTTTCC ACTAATTTGC AAGCTAGCAT CCCATTTCCA TCTTTCTAAA TTACTTAACG 60 ATGTCATTAA AAATATTTCC ATACTATTCT CTGCAATAGA TATTACTCCC CTTCACCTTA 120 TTTTCTTATT TCTCAATAAA CATCCAAACT TGTGTTCACA CTCATTTAAT CTATCAATGA 180 GTATCAAAAG GCCAGGACTC GTCAGGCATT GTGCTAGGCA TTGGGAATAC CGGGCAAATG 240 TGACAAGGTC CCTGCCTTAC AAAGGTGACC TCCTCTCAGG CTCATTGAAA AAGCACAGCA 300 GTATGGACCC CTTGTTCAAA AAGAAACACC TTTTATTTCT CTCTAAGGTG ATACTTCCCC 360 TTTCTGGCCT TCGCCATGTA CACCAGCCTC TCATTCCCCC AAAGTTATGC AGTCTGCGCT 420 CACATCCTTG CTGAGACCTT CAGTGAAACC CACTATCAGT TAGGATGCAA CTCACTGCAC 480 GGAACAGAAA CTCATCTCAC GCTGCCTTAC ACAATCAATG GTGCTTATCA GCTAACGTGA 540 CTGGAGGCCC AGGGATAGGA AAAGCTTCTG GATTATATTA ATTCAGCAGC TCAATGATTT 600 CATTAAGGGC CAGTTTCTTT CCTTCTCTCC ACTCTGCCTG GAAGTGGATG ATTGACAAGG 660 ATTCTTGAGA TTACTGGCTT CCCTTTCTCC AGTCAAGGAG TGAGAGAACC ACTGAGGGAA 720 AGGGAAGGAG GTGAGGAGAG AAGGACGGAA GGGGGCAAAA GACAGAGGCA ACGGGTGGGA 780 GGGAGCAACA ATTCCCTAAA TGTGATCTCA CTGATCCAAA GGGGTTCCAC TGCAGTCAGA 840 GGAACAGGAC TTTGATGCTT CATCCCTAGA ACCAGAGGTG GACTTAGCCC CTCCTAAAGC 900 TATGGATGGC ACAGGAGCAG CAGGGAGCAG ATACCCAAAC ACTAATTTAA AAAATGAATC 960 TCAGGGGAGG CCACCATAGT GTCCCCTATG CAACTGATTT CACACAAAAT 1010
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