Tag | Content |
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EnhancerAtlas ID | HS073-14203 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr9:4814230-4816460 |
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 | chr9:4815873-4815891 | TCTTCCTTACCTCCTTGC | - | 6.01 | FOXA1 | MA0148.4 | chr9:4815246-4815262 | ATTTGTTTGCTTAATG | - | 6.53 | REL | MA0101.1 | chr9:4814989-4814999 | GGGGATTTCC | + | 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 |
GH09I004815 | chr9 | 4815101 | 4816011 |
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Enhancer Sequence | GTGTTCTTTC TATACCTAAC GTAAGAGTTT TTATCATGAG GGGGTTTTGA AATTTAAAAA 60 AATTTTTTTT AGAGATAGGG TCTGACTTTG TTGCCCACGC TGAAGTGCAG TGATACAAGC 120 ATAGTTTACT GCAACCTTGA ACTCCTGGGC TCAAGCAATC TTTCCGGCCT GGTCTCCCTA 180 CAGGTGTTTG CCACCATGCC CGGCTTTTGT ATTTTTTGTA GAGATGGCGG TCTCGCTTTG 240 TTGCCCAGGC TGGTCGCCAA CTCCTGGGCA TGATCATCCT CCTGCCTTGG CTTCCCAAAG 300 TGTTGGGATT CTAGGCATGA GCCACAGTAC TTAGCCTCCT GTCCTTATAA AAATTGTTTT 360 CTGGTTGATT CGTGTCTCCT TTTTTTCTTC CCGTCTTATT GTTTGTCATT GCAGTTTGAT 420 GGTTTTCTAT AGTGATAAGG TTTGATTTTT TTCTCTTTGT CCTTTGTGTA TTTGTTCTAC 480 CAGTGAGTTT TATACTTTCA TGTTTTTTCA TGGTAGTGAT TATCATTTTT TCATTTCTAG 540 ATGTAGGACC TTCTTGAGCA TTTCTTGTAA GGCCTGGCTA ATAGTAATGA ATTTCCTCAG 600 TTTTTGCTTG TCTGGGAAAG ACTTCATTTC TGAAGGATAG CTTTTTTGGG TATAGTGTTT 660 TTGGTTGACG TTTTTTTTTT CTTTCAGCAT TTTGAATATA TCATCTTATT CTCTCATGGT 720 CTATAAGGTT TCTCTGGAGA AATCTGTTTT TAGTGTAATG GGGATTTCCT TGTATTAACT 780 TGATGCCTTT TTCTCTTGCT GTTTTTAGAA TTCTCTTTTT ATCTTTCACT TTTGACAGTT 840 TAACTATTAA TATGCCTTGG GAAGACCCTT TTGGGTTGAA TCTATTTTGG AACCTTTGAG 900 CTTCCTAGAT CTGTATGTTC ATACCTCTTA TCAGCCTTGG GAGCTTTTCA CCTATTTCAT 960 TTGGCAGGCT TTCTGTGCTT CCTTTTTTCT CCTCCTGGAA CTTTCATAAC ATGAACATTT 1020 GTTTGCTTAA TGATTTCCTG TAAGTCTTGT AGGTGTTCTC ATTTCATTTT CATTCTCATT 1080 TCTTATTTCT TTGAGTAGGT AATTTTGAAA GACTTATCTT CAAGTTCAGA GATTTGTGTC 1140 TTATGCTTGA TCATGTCTGC TATTTTAGTT CTATTATATT TATTTCATTC ATTGAAGTCT 1200 TAAGCTGCAG TATTTTTCTT TTCTTTTTTT TTTTTGCAAC TGCAAATTTT AAAATTTATC 1260 CAGGAAGCAT CAGATCTGGC CCAGTGGGGT GGGGTAGGGG TAGGTGGAGT GGCTCCATCT 1320 TCATTTGGCA CCATGCTGAA AGGTACAGTA GCCGCTTAAA GCTCGGCTTG AGGATGTTGG 1380 GCCACTGGTC TAGGGTGTAT CCTCACGGGA AAAGGGGAGT TTTTGCTGCT TGCTCCTGGA 1440 GCAAGACACA CTCCAGCCAT AGTTCTAATT CCAGGATAGT GTAGCGCAGG CCACAGGGAG 1500 CTGGGCACGG TGTTGACTCC TTCTCTGTGG GGAGCACAGC TACGTATGTA TACTCCAGGC 1560 AGCTTAGGCC TATGAGGACT GCAGGGTTCC TCAGTGGTGA GGTCTGTAAG TGTCTAAGGT 1620 ATTGATAGGG ATCGCTAGGA TCCTCTTCCT TACCTCCTTG CAGCAGGGAG AAGTCCTTTT 1680 GGTTCCCAGC TGATCCTGAT TGGGGATTGG GGTGATAGAA GCTTGGCATT TCCTTCTGCT 1740 CTCTCTGTGG TCATCTCGAG TTTCTTTTAT AAACTCTTCT GATGCACTCT GGCACCCTTC 1800 CTCAGTTATT TGTGTTAAAG TCTAGTTGTT TAATTGTTGT TTTGGCCGTC TTTGTGAAGG 1860 ATTTCTAGCT GGCCATCTTG ATCTGAGCAC CTTTTCTTTG ATGTATTGGT CAGTTGGATA 1920 TCCTCTTTTA TGAAGTCTCC ATTCAGATAT TTTGCTCATT TTTCTGTCTT TTTCTTATTT 1980 AATTGTTGAT TCATTGGTAT ATTCTGGATA TGTTAAAGGA TTGCACATAT GTTATTCCAC 2040 TCTGACTTGT CTTTTGACAC TTTCAGTGTA GTCTTTTGAT AAACAATACT TCATAGTTTT 2100 AATATCCAAT TTATAAATCT TGCCTATCCT TTTACCATGA AGATACATTC TCTGTGAACT 2160 TTAAAGTCTT CTGTTTTAAA ATATAAACTC TGTGTTACAT TTAGCAAACT CATTTGCCAT 2220 TCTTTTTAAA 2230
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