Tag | Content |
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EnhancerAtlas ID | HS136-13346 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr3:37010600-37012300 |
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 | AAAAGTCAAG AGACGTTAGT GAAAATTGAC AGAATTAAAA ACAAATAGTT TAAGAACAGA 60 ATCTAAATGT ATAAAAGTAA CCAATGGAAA GAAAACCAAT GATACAACAA AAGTCATGGT 120 AAAAAGAAGA AAAGGAGAAA TGGGGTGGTA TTAATTAGTT AAATCCTTAT TAATCATAAG 180 CAATAAGTAG ACAATGCCTA CAGTTGATAA ATTAAGAATT AGCAATATAC AGAAATATAT 240 ATGAAACCAA AATAACTAAT GAAAGAAAAG GAGGCTGGGC ACGGTGGCTC AGGCCTGTAA 300 TCCCAGCACT TTGGGAGGCA GAGGCAGGCA GATCATTTGA GTCCCGGAGT TTGAGACCAG 360 CCTAAGCAAC GTAGTGAGAC CTCATCGCTA CAAAAAAACA GAAAAATTAG CTGGGTGTGG 420 TGGTGTATGC CTGTATTCCC AGCTACTTCA GAGGCTGAGG CAGGAGAATC AGTTGAGCCC 480 AGAAGGTGGA AGCTACAGTG AGCCAACAGA GTGAGACCAT CTCAAAAAAA ATTTAAAAAA 540 ATGAAGAAGG AAGGAAGGAA GAGAGGGAGG GAGGGAGCGT GGGCGGGGGG GGGGGGGTGG 600 AGGAGGAGGA GAGAAGGAGT GGGAGGAGTG GAGAAGGAGG GGGAGGAGGA GAAGGATAAA 660 AGGTTACAAG TGGTTGTTAC TAGGAATGGG GGAGAAGAGA AGTGGGTAAT GGCACTGAAG 720 CTTTTTATTA TGTCTTTCAG CATTCTCTGA TTGTTCTTAA ACCATCAACA GATCTCAGTA 780 TGTAGACTAA AAGGGAATAT TTGGTGAAGA GATCTTCTTT CACTATTGTA CACTTGCTAT 840 GGACATGTCC ATGCCTGCTG CCTGGCAGGC ACCATTCATT AAGTAGGCCC CTGTTGCCAA 900 GGAAACCAGC TCTTCACTGA TACCAAAGAT AATGCAGAGG CCTGCCGCTC ACCAAGCAAC 960 CTTCCTCATG AGCTATGCCC CCACCTTCCT GAACTGTCTC TTGCTCCTGT TTGATACTGT 1020 CATGCTGCAC GAAGCTTACA CTTGCTATCT CTCACTTCCC TCTTAGTCAT CTGTGATGCT 1080 GGCTAAGGGA GCTAGGCCAG TCAGCAGTGA CCTGTTGCCC TTGGTTTATT ATAAGCAAAC 1140 TGTTCACAAG AAATGAACTT CTGTTGTTTT ATAAATGATA TGCATCACAG AACACAGAAT 1200 AATATCAAAA CCACATTAGT TTTTTCATAC TTGCTTCATT GACCCCAGGG GAAGAGGGGA 1260 GAGCAGGGAG AGGACTTTCT CTTTTTTTAA ATACTAATTA TATTGAGGTA TAAAGAACAT 1320 ATAGTAAGTT CACAGACCTT AAGTATACAG TTTGATGAGT TTTGGCAAAT ATGTATACCT 1380 GTGGAACCAA CACCTCAGTC AAGATATAAA TACTTACATC AGCCGGGCGC AGTGGCTCAT 1440 GCCCGTAATC CTAGCACTTT GGGAGGCCAA GGCAGGTGGA TCATGAGGTC AGGAGATCGA 1500 GACCATCCTG GCTGTCCACT AAAAATACAA AAAATTAGCC AGGCATGGTG GCACATGCCT 1560 GTTGTCCCAG CTACTCAGGA GGTTGAGGCA GGAAAATCGC TTGAACCCGG GAGGCAGAGG 1620 TTGCATTGAG CCGAGATAGC ACCACTGCAC TCCAGCCTGG GCAACAGAGA GAGACTCCGT 1680 CTCAAAAAAA CAAAAAACAA 1700
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