Tag | Content |
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EnhancerAtlas ID | HS047-12079 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr15:90691500-90693680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr15:90692275-90692293 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr15:90692267-90692285 | GAGAGAGAGGAAGGAAGG | + | 6.25 | EWSR1-FLI1 | MA0149.1 | chr15:90692287-90692305 | GGAAGGAGGGAAGAAAGA | + | 7.33 | EWSR1-FLI1 | MA0149.1 | chr15:90692283-90692301 | GGAAGGAAGGAGGGAAGA | + | 8.2 | EWSR1-FLI1 | MA0149.1 | chr15:90692271-90692289 | GAGAGGAAGGAAGGAAGG | + | 8.32 | EWSR1-FLI1 | MA0149.1 | chr15:90692279-90692297 | GGAAGGAAGGAAGGAGGG | + | 9.72 | FOXP2 | MA0593.1 | chr15:90692759-90692770 | TTTGTTTACAT | - | 6.14 | IRF1 | MA0050.2 | chr15:90692485-90692506 | TCACAGTTTCATTTTCTTATC | + | 6.08 | IRF1 | MA0050.2 | chr15:90691515-90691536 | TTTTTGTTTTACTTTTTCTTT | + | 6.74 | IRF1 | MA0050.2 | chr15:90691521-90691542 | TTTTACTTTTTCTTTTTTTTT | + | 6.8 | NKX2-5 | MA0063.2 | chr15:90692020-90692030 | ACCACTTGAG | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr15:90692027-90692042 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr15:90692272-90692293 | AGAGGAAGGAAGGAAGGAAGG | + | 6.58 | ZNF263 | MA0528.1 | chr15:90692280-90692301 | GAAGGAAGGAAGGAGGGAAGA | + | 6.76 | ZNF263 | MA0528.1 | chr15:90692284-90692305 | GAAGGAAGGAGGGAAGAAAGA | + | 6.94 | ZNF263 | MA0528.1 | chr15:90692288-90692309 | GAAGGAGGGAAGAAAGAAAGA | + | 6.99 | ZNF263 | MA0528.1 | chr15:90692276-90692297 | GAAGGAAGGAAGGAAGGAGGG | + | 7.24 | Zfx | MA0146.2 | chr15:90693434-90693448 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_31744 | chr15:90692171-90693595 | Gastric | SE_43178 | chr15:90692245-90693106 | Lung | SE_47838 | chr15:90692397-90693547 | Pancreas | SE_50260 | chr15:90692154-90693592 | Sigmoid_Colon | SE_52615 | chr15:90692191-90693510 | Small_Intestine |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr15 | 90691714 | 90691800 | chr15 | 90693011 | 90693063 | chr15 | 90693477 | 90693531 |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I090148 | chr15 | 90691728 | 90693506 |
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Enhancer Sequence | ACAAACCACG TTTTCTTTTT GTTTTACTTT TTCTTTTTTT TTTTTGAGAT GGAGTCTCGC 60 ATTGTTACGA TCTCAGCTCA CTGCAACCTC CGCCTCCCAG GTTCAAGCAA TTCTCCTTGC 120 CTCAGCCTCC CAAGTAGCTG GGATAGACAA GCCACATTTC AAGTGCTCAG TAGGTACTGT 180 GGCTGATGGC TACACTATTA GATGCAGCTG TCTAAGTGCT TTAGCTGTGT TAGTCCTCAC 240 AACTGTGCTT TTGTTATCCT CATTTTACAG ATGAGAAAAT TTACACAGAA AGTGCTTCAG 300 CACTTTGCCC ATTGCTACCC AGAAAGAAAA GGGCTGAGCT GGAATCTGAG CCACCAAGGT 360 CAGCCAACTG AGGGTCCACA GTCTGGTGTC CTAACAACTG TGCTATGCTG TCAGCTTCAC 420 AAATCTCATC TCCCATAGGA GGTCATCAAA AAGCTGCTTG CAGCTGGGTG CAGTGGCTCA 480 CACCTGTAAT CCCGGCACTT TGGGAGGCCG AGGCAGGCAG ACCACTTGAG GTCAGGAGTT 540 CAAGACCAGC CTGGCCAACA TGGTGAAACC CCATCTCTAC TAAAAATACA AAAATTAGCC 600 AGGTGTGGTG GTGCGTGCCT GTAGTCTCAG CTACTTGGGA GGCTGAAGCA GGAGAATCTG 660 CTTGAACCCT GGAGGCGGAG GTTGCAGCAA GCCAAGATTG CGCCACTGCA CTCCAGCCTG 720 GGTGACAGAG CAAGACTCTA TCTCAAAAAG AAAGAAAGAA AGAAAGAGAG AGAGAGGAAG 780 GAAGGAAGGA AGGAGGGAAG AAAGAAAGAA AGAAAACAAT AATCCAATAT ATAGGCAAGA 840 GCCCTTACTT CTCTACTACT TACAGTCTAG TGTTCAGAGA ATGTAGGAGT GAGCCCAGAG 900 AGCTTCCCAA GCCTACCATG TCGTCACTGC CTACAAGAGT CCCTGAAGAT GGCCACACAA 960 AACCCTGGGG CTTACTCATA CATGTTCACA GTTTCATTTT CTTATCATAT TGGTCAGTTT 1020 CATCTACACT GGAACGTGGT TCCACCTATC TTTCTGTTCT CTGATAAGCT TCAGCTCAAG 1080 GGGAAACATT TCTGGGGCCA CAGGTTCTGT TGCCTGCCTC TGCAAAGAGC ACATTACGCA 1140 AAGCAGATGT TCTGTGCCCA ATTCAGTCTC TGCTATCAGA AAAGCTGTGT TCAGAGCCAC 1200 ATGGAGCCTG CAGCCTCCTG CTTTGCGGGA ATGTTTGTGT AAAGGTTCCT GGCTTTCTCT 1260 TTGTTTACAT CTGACTGTTT ACCTTTCAGT CCCATCTCGT CTTCTGCTCA GTGAACAGTT 1320 TTTGCACTGG CAGGAGCCAG GTCGAACAGT TCCATAAACT GCTTTTTTAT GGTTCTCAGT 1380 AGAGCAGAGG TTTGAAATTA GAGAACCTGA ATGTTGGCTC AAGGAGGACA CAAACTCCCT 1440 GAATTAGTGT CCAAATCTAT GTGTGTGTGT GTGTGTGTGT GTGTGTGTTT GTGTCTTTCT 1500 AGGGGGTGGT TCCTTATTCT CATTGGATTT CCAAAGGGGT CTGGAACCCA CAACAGGGTC 1560 AGAACACCTG GGTATATGGT GGGCCCCAAG GGGCCACCAA ATGGAACGTT CTGCCGTCTG 1620 CTCTTTGGAA TATTCTTCTG GCCAAGAGCC ACCACTTCCC TGACTCCGGC CTTTCTCTTC 1680 CCCACTGTCA CCAACAGGGG ATATAGGCTT TCTATTGGGC ACCACTCCTC ACTGAGAACT 1740 GCTCTCAGGG CTTTCTGAGC CTGTTGGTGT GACTGCGGTG GTGGCAGCTT GCAGGAGAGA 1800 CACCTCACTC TTTGCTTTGT GGGATCCTCT GCTTGGTCCC TGACTCACAG ACTGAAGCTC 1860 AAATTCTAGC CACGCACCAA AAAGTGACCG ACAGCCGGGC GCGGTGGCTC GTGCCTATAA 1920 TCCCAGCACT TTGGGAGGCC GAGGCGGGCG TTTCACCATG TTGGCCAGGC TGGTCCCAAA 1980 CTCCTGACCA TTGCATTTGT TTGCAATGTA ATTTGCAAAC AAATTTGGTA GGCTGCCATA 2040 ACAAAAGTTC CACAGACTGG GTGGCTTAAA CCGTAGACAT TTAGCTTCTT ACAATTCTAG 2100 AGTCCAGAAG TTCACAATCA AGGTGTCTGC AGAGCTGATT TATTCTGAGG TGTCTCTCTT 2160 TGGCTTGCAG ATGGCCATTT 2180
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