Tag | Content |
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EnhancerAtlas ID | HS176-25916 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr3:37010950-37012140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr3:37011156-37011174 | GGAAGAGAGGGAGGGAGG | + | 6.14 | EWSR1-FLI1 | MA0149.1 | chr3:37011152-37011170 | GGAAGGAAGAGAGGGAGG | + | 6.73 | EWSR1-FLI1 | MA0149.1 | chr3:37011148-37011166 | GGAAGGAAGGAAGAGAGG | + | 7.82 | EWSR1-FLI1 | MA0149.1 | chr3:37011144-37011162 | AGAAGGAAGGAAGGAAGA | + | 8.2 | RFX5 | MA0510.2 | chr3:37011491-37011507 | TGTTGCCAAGGAAACC | + | 6.1 | RFX5 | MA0510.2 | chr3:37011491-37011507 | TGTTGCCAAGGAAACC | - | 6.23 | ZNF263 | MA0528.1 | chr3:37011145-37011166 | GAAGGAAGGAAGGAAGAGAGG | + | 6.11 | ZNF263 | MA0528.1 | chr3:37011201-37011222 | GGAGGAGGAGAGAAGGAGTGG | + | 6.35 | ZNF263 | MA0528.1 | chr3:37011149-37011170 | GAAGGAAGGAAGAGAGGGAGG | + | 6.78 | ZNF263 | MA0528.1 | chr3:37011235-37011256 | GGAGGGGGAGGAGGAGAAGGA | + | 6.7 | ZNF263 | MA0528.1 | chr3:37011226-37011247 | AGTGGAGAAGGAGGGGGAGGA | + | 6.92 | ZNF263 | MA0528.1 | chr3:37011221-37011242 | GGAGGAGTGGAGAAGGAGGGG | + | 6 | ZNF263 | MA0528.1 | chr3:37011241-37011262 | GGAGGAGGAGAAGGATAAAAG | + | 7.18 | ZNF263 | MA0528.1 | chr3:37011192-37011213 | GGGGGTGGAGGAGGAGGAGAG | + | 7.37 | ZNF263 | MA0528.1 | chr3:37011238-37011259 | GGGGGAGGAGGAGAAGGATAA | + | 7.37 | ZNF263 | MA0528.1 | chr3:37011195-37011216 | GGTGGAGGAGGAGGAGAGAAG | + | 7.38 | ZNF263 | MA0528.1 | chr3:37011153-37011174 | GAAGGAAGAGAGGGAGGGAGG | + | 7.61 | ZNF263 | MA0528.1 | chr3:37011198-37011219 | GGAGGAGGAGGAGAGAAGGAG | + | 7.64 | ZNF263 | MA0528.1 | chr3:37011229-37011250 | GGAGAAGGAGGGGGAGGAGGA | + | 9.38 | ZNF263 | MA0528.1 | chr3:37011232-37011253 | GAAGGAGGGGGAGGAGGAGAA | + | 9.68 | ZNF740 | MA0753.2 | chr3:37011184-37011197 | GGGGGGGGGGGGG | - | 6.03 | ZNF740 | MA0753.2 | chr3:37011187-37011200 | GGGGGGGGGGTGG | - | 6.44 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 37010977 | 37011113 | chr3 | 37011163 | 37011850 | chr3 | 37011455 | 37011827 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I036968 | chr3 | 37010223 | 37012549 |
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Enhancer Sequence | TTGAGACCAG CCTAAGCAAC GTAGTGAGAC CTCATCGCTA CAAAAAAACA GAAAAATTAG 60 CTGGGTGTGG TGGTGTATGC CTGTATTCCC AGCTACTTCA GAGGCTGAGG CAGGAGAATC 120 AGTTGAGCCC AGAAGGTGGA AGCTACAGTG AGCCAACAGA GTGAGACCAT CTCAAAAAAA 180 ATTTAAAAAA ATGAAGAAGG AAGGAAGGAA GAGAGGGAGG GAGGGAGCGT GGGCGGGGGG 240 GGGGGGGTGG AGGAGGAGGA GAGAAGGAGT GGGAGGAGTG GAGAAGGAGG GGGAGGAGGA 300 GAAGGATAAA AGGTTACAAG TGGTTGTTAC TAGGAATGGG GGAGAAGAGA AGTGGGTAAT 360 GGCACTGAAG CTTTTTATTA TGTCTTTCAG CATTCTCTGA TTGTTCTTAA ACCATCAACA 420 GATCTCAGTA TGTAGACTAA AAGGGAATAT TTGGTGAAGA GATCTTCTTT CACTATTGTA 480 CACTTGCTAT GGACATGTCC ATGCCTGCTG CCTGGCAGGC ACCATTCATT AAGTAGGCCC 540 CTGTTGCCAA GGAAACCAGC TCTTCACTGA TACCAAAGAT AATGCAGAGG CCTGCCGCTC 600 ACCAAGCAAC CTTCCTCATG AGCTATGCCC CCACCTTCCT GAACTGTCTC TTGCTCCTGT 660 TTGATACTGT CATGCTGCAC GAAGCTTACA CTTGCTATCT CTCACTTCCC TCTTAGTCAT 720 CTGTGATGCT GGCTAAGGGA GCTAGGCCAG TCAGCAGTGA CCTGTTGCCC TTGGTTTATT 780 ATAAGCAAAC TGTTCACAAG AAATGAACTT CTGTTGTTTT ATAAATGATA TGCATCACAG 840 AACACAGAAT AATATCAAAA CCACATTAGT TTTTTCATAC TTGCTTCATT GACCCCAGGG 900 GAAGAGGGGA GAGCAGGGAG AGGACTTTCT CTTTTTTTAA ATACTAATTA TATTGAGGTA 960 TAAAGAACAT ATAGTAAGTT CACAGACCTT AAGTATACAG TTTGATGAGT TTTGGCAAAT 1020 ATGTATACCT GTGGAACCAA CACCTCAGTC AAGATATAAA TACTTACATC AGCCGGGCGC 1080 AGTGGCTCAT GCCCGTAATC CTAGCACTTT GGGAGGCCAA GGCAGGTGGA TCATGAGGTC 1140 AGGAGATCGA GACCATCCTG GCTGTCCACT AAAAATACAA AAAATTAGCC 1190
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