Tag | Content |
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EnhancerAtlas ID | HS038-08867 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr17:44855060-44856960 |
Target genes | |
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) |
EWSR1-FLI1 | MA0149.1 | chr17:44856525-44856543 | GGAGGAAAGGAATGAAGA | + | 6.05 | Nr5a2 | MA0505.1 | chr17:44855680-44855695 | GGGTTCAAGGTCACT | + | 6.32 | RFX1 | MA0509.2 | chr17:44855470-44855486 | GGTTGCTATGGTTACG | - | 6.67 | RFX1 | MA0509.2 | chr17:44855470-44855486 | GGTTGCTATGGTTACG | + | 6.69 | RFX2 | MA0600.2 | chr17:44855470-44855486 | GGTTGCTATGGTTACG | + | 6.79 | RFX2 | MA0600.2 | chr17:44855470-44855486 | GGTTGCTATGGTTACG | - | 6.8 | RFX5 | MA0510.2 | chr17:44855470-44855486 | GGTTGCTATGGTTACG | - | 6.25 | RFX5 | MA0510.2 | chr17:44855470-44855486 | GGTTGCTATGGTTACG | + | 6.29 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 44856471 | 44856521 | chr17 | 44856579 | 44856686 |
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Enhancer Sequence | CAACTCTGGG AGGTGGGCAT TGTTATCCCC ATTTTGCAGA TGAGGAAACT GAGGCATGGA 60 GTAGTTGGGC GACTTATGCA AGGAAGTGGC TGAGCCAGAA TTCAAGCCCT GAGTTTGTCT 120 GACTCCCAGT GTGATGTCCT CTGAGAACAA TTCCTGAGCC TCAGTCATGA TGAGCTGTTT 180 TCCCTCTTTC CACCAAACCC TGTCTCCTTC CTGTTGCCCA GGTCCCACCA ACTGTGGACC 240 TGGGAGCCAT GGTGCCAGGG TCCCATCCAG CTCTACCACT TCCTAGCTGC TGATCTCAGC 300 AATTTTCTTA ACCTCTATAC CTCAGTTTCT TTATCGGTAA AATAGACACG ACAGGAGGAA 360 TAAGTGACAC AATCCAGTGC ATGGCACGTG GGGAGCCCTT GCTAGATGGT GGTTGCTATG 420 GTTACGGTGT GTGTGGAGCT GTCCCCAGCA CTTTGTTCCC TGCCTTGTCA CCAACCTCAT 480 TTCTCCCATC CTTGCATCCC TGACTTGGTA GAACACATCA GAAATCTCAG CCCCTTCCTA 540 TCCAACACTG GAAAGGATGC CTGGATCAGA CCTCAGTCCT CACAGGGGTG GCAGAACAAA 600 GACAGTTGTG ATCTGGATGA GGGTTCAAGG TCACTCAAAG AGTGCAGGCA AAAGGACATT 660 TTCAGGATGC TCCATTCAAA GGCTTCAGTT CAGATGGGGT CATCCTGCGA GTAATTAGCA 720 AGGCCTCTGG CGATGGGGCT TAGCTCCTGG GCCAGTGTCG GAGACTAAAG AGGCTGTGGC 780 CATGGGATTG ATTTCTGCAG GATGGCTGCC CTTCCCCAAA CATGCCCGGC CACCCCCACC 840 CTGAGCCTCC TGCCCGCACA CTGCTGAAAT TCCACCATCG CAGACACATT ACTTTAACTC 900 GCCACTCCTA TTCCCCATTA TTGAAGTACA CGTTCCACTT CGGGAGGCGG CACAGTGACT 960 CTCATGCTCC TCGATTCTTT GTGCCAAAGT GTGCGTGGCT TTGACGGATT TGCCTAGCCA 1020 GCTGAATGAC TCCAGCGGGG CTGTTTCACA CTTCTGCACA TTTGCACATG CTGAGCCCTC 1080 GGCTCGAAGC ACCTCTCCAC TGCCCGGCCC CCGGCAACCA TTCTACACCA TCCTTTGAAA 1140 CCTGATTCCT AGGTCACCAC CATTCTAAAG CCTTCTGTGA GCTCCAGACA GAAGTCACCT 1200 CTCCTCCGCC TGAATCTTTC CTGTACCTAA TTCAAACCTT CTTATCCCAA AGTGCTGAAC 1260 TGATTTGTTT CCAATTCCAT CTGGCTATGC CAGTCTCAGT CTCCAAGAAG AGAGGTAGTG 1320 GTAGTGTTTT CTCCAGTTAT TCCCCGGTCC CTACCCCATC ACACACACAC ACACACACAC 1380 ACACACACAC ACACACACAC ACACACACAC CCCAGCCCAC TCGGCCTTCC AAAGGGCCGG 1440 GCACATGCTA GGTATTCATG ATTCTGGAGG AAAGGAATGA AGAACTCTTC CAAAGGACGA 1500 GCCTGATGCC CCTCACTCGC CAGACCTCCC GGCATCCGGA GCTTCCGCCT ACACACAGGA 1560 CAAGACTCCT TGGTTCCGCT GAGGAAGTTC CTACGTTTAG GATCTGAGAT GATGGCCAGG 1620 CTCCCAAGGG GGATAGAGAC CTGCCTGGCA CTGACAGCTG GTGAGGGGGA GGGCGGAGGA 1680 CCCTGCCAGG CCTTCGCAGC TGGGCCAGGG GCTATTTATA CCCAGCTCCT GGCCCGGCCC 1740 TTCCCTTCCC TAGGACCCTG CCACCCTCCT CCTGAAGCCG GCTCATCCTC CACTCCGACC 1800 ACCCACTGCC CAGCTGGGCC GAGGACACAC ACGGGCAGCC AGGCGGATGG GCTGCGGGTG 1860 CCCTGCACAA CAGGCTGCTT GTGGAAACTT TGGTGTTGAC 1900
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