Tag | Content |
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EnhancerAtlas ID | HS127-21136 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr3:37010520-37012360 |
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 | AACAATGTAA ATATCAAAGT GAAGCTCACA GAAACCAGAA GGTAGAAGTA GGAAAAGAGA 60 TGGAGGCAAG GGTAGGGGAA AAAAGTCAAG AGACGTTAGT GAAAATTGAC AGAATTAAAA 120 ACAAATAGTT TAAGAACAGA ATCTAAATGT ATAAAAGTAA CCAATGGAAA GAAAACCAAT 180 GATACAACAA AAGTCATGGT AAAAAGAAGA AAAGGAGAAA TGGGGTGGTA TTAATTAGTT 240 AAATCCTTAT TAATCATAAG CAATAAGTAG ACAATGCCTA CAGTTGATAA ATTAAGAATT 300 AGCAATATAC AGAAATATAT ATGAAACCAA AATAACTAAT GAAAGAAAAG GAGGCTGGGC 360 ACGGTGGCTC AGGCCTGTAA TCCCAGCACT TTGGGAGGCA GAGGCAGGCA GATCATTTGA 420 GTCCCGGAGT TTGAGACCAG CCTAAGCAAC GTAGTGAGAC CTCATCGCTA CAAAAAAACA 480 GAAAAATTAG CTGGGTGTGG TGGTGTATGC CTGTATTCCC AGCTACTTCA GAGGCTGAGG 540 CAGGAGAATC AGTTGAGCCC AGAAGGTGGA AGCTACAGTG AGCCAACAGA GTGAGACCAT 600 CTCAAAAAAA ATTTAAAAAA ATGAAGAAGG AAGGAAGGAA GAGAGGGAGG GAGGGAGCGT 660 GGGCGGGGGG GGGGGGGTGG AGGAGGAGGA GAGAAGGAGT GGGAGGAGTG GAGAAGGAGG 720 GGGAGGAGGA GAAGGATAAA AGGTTACAAG TGGTTGTTAC TAGGAATGGG GGAGAAGAGA 780 AGTGGGTAAT GGCACTGAAG CTTTTTATTA TGTCTTTCAG CATTCTCTGA TTGTTCTTAA 840 ACCATCAACA GATCTCAGTA TGTAGACTAA AAGGGAATAT TTGGTGAAGA GATCTTCTTT 900 CACTATTGTA CACTTGCTAT GGACATGTCC ATGCCTGCTG CCTGGCAGGC ACCATTCATT 960 AAGTAGGCCC CTGTTGCCAA GGAAACCAGC TCTTCACTGA TACCAAAGAT AATGCAGAGG 1020 CCTGCCGCTC ACCAAGCAAC CTTCCTCATG AGCTATGCCC CCACCTTCCT GAACTGTCTC 1080 TTGCTCCTGT TTGATACTGT CATGCTGCAC GAAGCTTACA CTTGCTATCT CTCACTTCCC 1140 TCTTAGTCAT CTGTGATGCT GGCTAAGGGA GCTAGGCCAG TCAGCAGTGA CCTGTTGCCC 1200 TTGGTTTATT ATAAGCAAAC TGTTCACAAG AAATGAACTT CTGTTGTTTT ATAAATGATA 1260 TGCATCACAG AACACAGAAT AATATCAAAA CCACATTAGT TTTTTCATAC TTGCTTCATT 1320 GACCCCAGGG GAAGAGGGGA GAGCAGGGAG AGGACTTTCT CTTTTTTTAA ATACTAATTA 1380 TATTGAGGTA TAAAGAACAT ATAGTAAGTT CACAGACCTT AAGTATACAG TTTGATGAGT 1440 TTTGGCAAAT ATGTATACCT GTGGAACCAA CACCTCAGTC AAGATATAAA TACTTACATC 1500 AGCCGGGCGC AGTGGCTCAT GCCCGTAATC CTAGCACTTT GGGAGGCCAA GGCAGGTGGA 1560 TCATGAGGTC AGGAGATCGA GACCATCCTG GCTGTCCACT AAAAATACAA AAAATTAGCC 1620 AGGCATGGTG GCACATGCCT GTTGTCCCAG CTACTCAGGA GGTTGAGGCA GGAAAATCGC 1680 TTGAACCCGG GAGGCAGAGG TTGCATTGAG CCGAGATAGC ACCACTGCAC TCCAGCCTGG 1740 GCAACAGAGA GAGACTCCGT CTCAAAAAAA CAAAAAACAA CAAAAAAAAC CATACATCGA 1800 CCCAGAAAGT TCCTTCTGTC AGTAGCAGTT CACCCCCCCA 1840
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