Tag | Content |
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EnhancerAtlas ID | HS108-25398 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr20:47654090-47655500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata4 | MA0482.1 | chr20:47654696-47654707 | TCTTATCTCTT | + | 6.02 | HES2 | MA0616.2 | chr20:47654652-47654662 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr20:47654652-47654662 | GGCACGTGCC | - | 6.02 | RUNX1 | MA0002.2 | chr20:47654726-47654737 | AAACCACAAAC | - | 6.02 |
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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 |
GH20I049037 | chr20 | 47654338 | 47655337 |
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Enhancer Sequence | TAACTTTTTA AGTCTAGGGT CTGGCATGGT GGGAGGATTG CTAGAAGCCA GGAGTTTGAG 60 ACCAATCTGG GGAATGTAGT GAGACCCTAT CTCTACAAAA TAATAATAGC AAGTGTGGTG 120 GCACACGCCT GTAGTCCCAG CTACCCAGGA GACTGGGGTG GGGAGGACTG CTTGAGCCCA 180 GGAGGTCGAG GCTGCAGTGA GCTTTGTTTG TGCCACTGCA CTTCAGCCTG GGTGACAGCC 240 TGTCTCAAAA AAACAAAAAC CAAAAAAACC TTCTGGCCAC AAAGCAAAAA GTTGCATAGC 300 CACGGTAAAG ATTTAGTTGG TTATAAAGTT GTAGTTATTG CCACTTTAAG CTAATACTTC 360 GTTTTGGAGC TTTTATACAC AGTATTTTTG TTAGGGATCA CAGTTCTGCA ACCTCTGCTC 420 CAAAAAGAAT GAGTTTTCTT AAAGGGAGCT TAACTTCTGA AGTCTTAGTG ATTCATAGGT 480 GTGCATAGAA TGTGTGATTC CACATCCCAG GTGGAAAGAA AGCAATCTTT CCACCTCAGC 540 CTCCCAAAAT GCTGGGATTA CAGGCACGTG CCACCATGCC CAGCTAGGTT TTTGCTGAGG 600 TTAACCTCTT ATCTCTTGTC CCTCCCTCCA CCACAAAAAC CACAAACAAA AAACACTTCT 660 ACAGCTTCCT TCTTCTTGGC TGTCTTTGTC AATGTTTCCA ATTTTTTTTT TTAAGAGACG 720 TGATCTTGCT TTGTCACCCA GGCTGGGGTG AGTGGCCTCA TTGCAGCTGA CTGCAGCCTC 780 AATTTCTCGT GCCCAAGCCA TCCAAAGTTC TTTGTTCTAT TATGTGGACA GACACGAAGG 840 GCATGGCATT TGTTAAGTTC TGTTAAAGTC TTCTCTGCCT CTCTCATGTC TGTATTTTTG 900 TGGCCCATGT CTTCTATGTG GTTGAGTTGT TCCCCTTGTT TATCCAGTAT TGTGATGATC 960 TTGATTCCTG CATCCTGAGA CTCAATGGCT AAACCCAGGA TTCTCCTTGT ACTTTCTAGA 1020 GACTCATCAG CAACTTGGTG AACCCTCAGA TGAATTCTTT TTGATTCAGG ATCTTGCTGT 1080 GGCTCCCAGG CTGGAGTGCA GTGGCAGTGG CACCATCATA GCTTACTGCA GCCTCAAATT 1140 CTTGGGCTCA AGCAATCTTC CTGCCTCAGC CTCCCCAGTA GCTGGGACTA CAGGCACACC 1200 TCACTATGCC CAGCTAATTT TTTTAAATTT TATTGTAGAG ACAGGGTCTT GCTACGTTGC 1260 CCCAGCTGGT CTCAAACTCC TAGGCCCAAG TCATCTTCCC ACCTCAGCCT CCTAAAGTGC 1320 TGGAATTTAC AGGCATGAGC CACTGGACTT GGCCCTGAAT TTCTTTTAAT GACAGATTAT 1380 CCATGATGAA TCAAAACTAT CAGGCATGGG 1410
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