Tag | Content |
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EnhancerAtlas ID | HS050-02112 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:45349690-45350910 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:45350083-45350101 | GGTAGAAAGGAAGGCAAG | + | 6.4 |
| | 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 |
GH01I044884 | chr1 | 45350253 | 45350992 |
| Enhancer Sequence | TGTAGAGGCA AAGTCTCACT ATGTTGCCCA GGCTGGTCTT GAACTCCTGG ACTCAAGCAG 60 TCCTCCCACC TCAGCCTCCC AAAGTGCCGG GATTACAGGT GTGAGCCACC GCACCTGGCT 120 GCCAGTGGTA GTTTTTAAGC AAGAAAGTGA CATGAACAGT TTTATCTCTT ATTAAGGTAA 180 TTCTGGTAGC AATGTGGAAG AAAGCCTGGA ATAAGGAAAC TGAAGAAAGG GAGACCAGTT 240 ACAATATTCT GAGAGATGAG ATAATGAGGC CTGAGAGAGG GGTGAAAGTA TGGGCAGCTC 300 TATAAACCTG ACTTGCTGCA TACTTCCCAC CACCTCTCCC AGCCCCCATT CAAAGCTCTG 360 CATGCTGACA CAAAACCAAA CAGATGGAGT GTAGGTAGAA AGGAAGGCAA GACAGAGGCA 420 GAGGCTGAGG AGGGTAAGGA AAACTATGAA CCCTGGAGCT ACACAGTTCA TAGTTTCTGC 480 AATTTTTAAA GAATCAATTT TGAAAAATTC TGTGTTAAGC TGTGAGCTCT TGTATTGAAT 540 TTCAATGTGA TTTTTCTCCT GATCCTTTGA TGAAGATTTA AAAATTTCCA TGTGAATACA 600 AAGAATGAAG CAACACTTAC TCTTAGCTCT TTTTCTCCCC TTTTAATGCT TCAAACCAGT 660 GTAGGCAGCA AATGTTCCTC CTCCATTGGA AAACAAGTCA GTTCCCTTTG AAGAAGTGAC 720 AAAGCACGGA CAGCTAGGGG ATTTCAGGGC CATGATATTT ACATTACAGA CCAAAAAGAA 780 CTGTCACTGC AAGAGGCAAG CAGACGAGCC TTGGCACATG GCCCCATCAG GCAGAACCTT 840 CGAGAGGATC CATGATTTGA AGAGAGGCTA TGAAACAGCC CTGCCAGGTC CCACCCACCT 900 CTGCTGGAGC TCAACATTAG GTCAATCCCC ATGATGCAGT TGACTTAGAA ACATAATGAA 960 GGAAACAATT ACTCTTCCTG CTTCCTAGTT AAAGTGCAGG CAGCTCAGAG CTGTGCCAAG 1020 AAATGTTACA AAGCTACAGT GAACCATTGT GAACATCCTG GGCCTAGGCC ACTTGCTGGA 1080 TACAGTGCCC TGGTCAACCT TACTTTCTCC TTTCCCTCTT ATACACAGCC TTCCTAGAAA 1140 CACCTGTCTT ATCTCATGAA ATCATAAGCT CTTCTCAAGC AATCACAAAG GAGAACAATA 1200 GACTTGACTA CTAGCAAACA 1220
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