Tag | Content |
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EnhancerAtlas ID | HS007-11136 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr3:37010810-37012020 |
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 | ATTAAGAATT AGCAATATAC AGAAATATAT ATGAAACCAA AATAACTAAT GAAAGAAAAG 60 GAGGCTGGGC ACGGTGGCTC AGGCCTGTAA TCCCAGCACT TTGGGAGGCA GAGGCAGGCA 120 GATCATTTGA GTCCCGGAGT TTGAGACCAG CCTAAGCAAC GTAGTGAGAC CTCATCGCTA 180 CAAAAAAACA GAAAAATTAG CTGGGTGTGG TGGTGTATGC CTGTATTCCC AGCTACTTCA 240 GAGGCTGAGG CAGGAGAATC AGTTGAGCCC AGAAGGTGGA AGCTACAGTG AGCCAACAGA 300 GTGAGACCAT CTCAAAAAAA ATTTAAAAAA ATGAAGAAGG AAGGAAGGAA GAGAGGGAGG 360 GAGGGAGCGT GGGCGGGGGG GGGGGGGTGG AGGAGGAGGA GAGAAGGAGT GGGAGGAGTG 420 GAGAAGGAGG GGGAGGAGGA GAAGGATAAA AGGTTACAAG TGGTTGTTAC TAGGAATGGG 480 GGAGAAGAGA AGTGGGTAAT GGCACTGAAG CTTTTTATTA TGTCTTTCAG CATTCTCTGA 540 TTGTTCTTAA ACCATCAACA GATCTCAGTA TGTAGACTAA AAGGGAATAT TTGGTGAAGA 600 GATCTTCTTT CACTATTGTA CACTTGCTAT GGACATGTCC ATGCCTGCTG CCTGGCAGGC 660 ACCATTCATT AAGTAGGCCC CTGTTGCCAA GGAAACCAGC TCTTCACTGA TACCAAAGAT 720 AATGCAGAGG CCTGCCGCTC ACCAAGCAAC CTTCCTCATG AGCTATGCCC CCACCTTCCT 780 GAACTGTCTC TTGCTCCTGT TTGATACTGT CATGCTGCAC GAAGCTTACA CTTGCTATCT 840 CTCACTTCCC TCTTAGTCAT CTGTGATGCT GGCTAAGGGA GCTAGGCCAG TCAGCAGTGA 900 CCTGTTGCCC TTGGTTTATT ATAAGCAAAC TGTTCACAAG AAATGAACTT CTGTTGTTTT 960 ATAAATGATA TGCATCACAG AACACAGAAT AATATCAAAA CCACATTAGT TTTTTCATAC 1020 TTGCTTCATT GACCCCAGGG GAAGAGGGGA GAGCAGGGAG AGGACTTTCT CTTTTTTTAA 1080 ATACTAATTA TATTGAGGTA TAAAGAACAT ATAGTAAGTT CACAGACCTT AAGTATACAG 1140 TTTGATGAGT TTTGGCAAAT ATGTATACCT GTGGAACCAA CACCTCAGTC AAGATATAAA 1200 TACTTACATC 1210
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