Tag | Content |
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EnhancerAtlas ID | HS127-20466 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr22:37364210-37367520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:37364869-37364887 | TTTTCCTTCCTTCCTTTT | - | 6.4 | EWSR1-FLI1 | MA0149.1 | chr22:37364784-37364802 | CCTTCCTTCTTCCCCTCC | - | 6.84 | EWSR1-FLI1 | MA0149.1 | chr22:37364810-37364828 | CTCTTCTTCCTTCCTTCC | - | 7.39 | EWSR1-FLI1 | MA0149.1 | chr22:37364776-37364794 | TTTTCCTTCCTTCCTTCT | - | 7.52 | EWSR1-FLI1 | MA0149.1 | chr22:37364780-37364798 | CCTTCCTTCCTTCTTCCC | - | 8.13 | EWSR1-FLI1 | MA0149.1 | chr22:37364818-37364836 | CCTTCCTTCCTTTCTTTC | - | 8.57 | EWSR1-FLI1 | MA0149.1 | chr22:37364814-37364832 | TCTTCCTTCCTTCCTTTC | - | 8.73 | Foxd3 | MA0041.1 | chr22:37367138-37367150 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr22:37367142-37367154 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr22:37367146-37367158 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr22:37367150-37367162 | GTTTGTTTGTTT | + | 6.32 | IRF1 | MA0050.2 | chr22:37364848-37364869 | TCTTTCTTTCTCTTTCCTTCT | + | 6.6 | SPI1 | MA0080.4 | chr22:37365962-37365976 | AAAAAGAAGAAGTT | + | 6 | ZNF263 | MA0528.1 | chr22:37364787-37364808 | TCCTTCTTCCCCTCCTCCTAC | - | 6.02 | ZNF263 | MA0528.1 | chr22:37364730-37364751 | CTCTCTCTTCCACCTTCCTCC | - | 6.04 | ZNF263 | MA0528.1 | chr22:37364790-37364811 | TTCTTCCCCTCCTCCTACTCC | - | 6.06 | ZNF263 | MA0528.1 | chr22:37364726-37364747 | CTCTCTCTCTCTTCCACCTTC | - | 6.28 | ZNF263 | MA0528.1 | chr22:37364796-37364817 | CCCTCCTCCTACTCCTCTTCT | - | 6.55 | ZNF263 | MA0528.1 | chr22:37364802-37364823 | TCCTACTCCTCTTCTTCCTTC | - | 7.03 | ZNF263 | MA0528.1 | chr22:37364793-37364814 | TTCCCCTCCTCCTACTCCTCT | - | 7.35 | ZNF263 | MA0528.1 | chr22:37364784-37364805 | CCTTCCTTCTTCCCCTCCTCC | - | 8.94 | Zfx | MA0146.2 | chr22:37365698-37365712 | GAGGCCGAGGCGGG | - | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I036969 | chr22 | 37365841 | 37366000 |
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Enhancer Sequence | AAGAAAGAAA GAATGATTCC CTCTTCGCAC AAGAAGAAAG TTCTGATGCT TTTGGTATCA 60 TGGGGTCTTA GGTTCAATGT GTAGTGAGAG CTAACTAAGA CAATTTTTAT TTGTTCCTCT 120 GAACACTTCT GTATTCCTAT GACTACGTCA TGCTTTTCCA GTTGCTATAA CTTATGGAGT 180 GTTTTGATAT TTGGCATCCT CACTCATTAG TCTTCCTTTT CAACATTTTA TTGGACACGA 240 TTACGCTATT ATTCCTCCAA ATTATTGTTA GAATCAATTT ATCAAGTCAT AAAAATGTCC 300 TCTTAGAATT TTTATTGGAA TTGCGCTAAA TTTAATTCTT AATTTGGGAA GATCTGACAG 360 TTTTGACAAC TTTGTAATAC TGGCTCTTTT GATCCAATAA TTATGGATTT CCACTTATTT 420 TGGGAATTTT ACTTCAGCAA ATTTTAAAAG CTTTTTCCTA GGTTCTTATT AGATTCATCT 480 CCAGGATTTT AAGATTTCAG TGCCAGCCTA CCTTCTCTCT CTCTCTCTTC CACCTTCCTC 540 CCACCTCTCT CTCTTTCTTT CTTTTCTTTT CCTTCCTTCC TTCTTCCCCT CCTCCTACTC 600 CTCTTCTTCC TTCCTTCCTT TCTTTCTTTT TTTTTCTTTC TTTCTTTCTC TTTCCTTCTT 660 TTTCCTTCCT TCCTTTTTCT TGCTTGCTTG CTTGCTTTCT TCATTTTCCT CTTTTGTGGC 720 CAATATCTTC CCAACCTATC TTATTGCAAA TGATTATTAT TAGTGCAAAG AAAAGCTACG 780 GATGTTTGTG TAATGAGTTT ATACCCAGCT CCTTCTCGAA GTCTTGTTCG TTGAATAATT 840 CTTATTTAAA TCTTACATGC TTTCTAGACA TACAAGCCTA TCTTCTTCAA ATTATGAGCT 900 TTGTCTCTTA TTTTTAATAG TTATTTTACA TATTATTCCT ATTCAATCAC AATTGCCAGA 960 AAGTTCAAAA CTATGTTGAC AAATTCCTGG TGTTGCACAC ACCTGTCTTC AGAGAGATTG 1020 CATAGAGAAT GCCAAATGCT TCACCATTCG AGAGACTTAG CATCGCTTCC TGAAAAGTCA 1080 TCTTGATCCT ACTAAAAAAA TATTCTACTC ATGACAGCAG GCATTCACCT CTCAAGGGTC 1140 TATGTCCAGG GAAATGTTTC TGCCTCCATC TCCAAGTGGC CATGTGAGGC GTTTTAATAA 1200 AATGAGCCTC CGACTAAGAC CACACCAGAA GGCTCCTGTG GTTGGGCACC AGTGGCAGGT 1260 GACAGAGAGC TCCAACCAAA ATGCCCTTAA AGTTCTCCTC AGCTTGGTTT GACTTCAGAT 1320 GGCTTCTCAT TGAGTCTAGG CCCTGACCTC CCTTATTTTA GAGCATCTTC TTTAGAAAAT 1380 TTGTCATTGA AAATGATTTC TCTGTCCCTT TGAGATGTTG GTAAATCTTT TCAAAAGCCT 1440 CTTGCTGGCC AGGCACAGTG GCTCACACCT GTAATTCCAG TACTTCGGGA GGCCGAGGCG 1500 GGTGGATCAC CTGAGGTCAG GAGTTTGAGA TCAGCCTGGC CAACATGGTG AAACCCCGTC 1560 TCTACTAAAA ACACAAAAAT TAGCCGGGCA TAGTGGTACA TGTCTGTAAT CCCAGCTACT 1620 CAGGAGGCTG AAGCAGGAGA ATTGCTTGAA CCCAGGAGGT GAGGCAGAGA TTAGCCGTGA 1680 GCCAAGATTG CACCACTGCA CTCCAGCCTG GGCAACAGAG CAAGACTCCG CCTCAAATTA 1740 AAAAAAAAAA AAAAAAAGAA GAAGTTCAAG GCTACAGTAA GCTGTGATCA CACCACTGCT 1800 CTCCAGCCTG AGTAACACAG CAAATCCCTG TCACTAAAAA ATAAAAAGGG AAAAAGAAAA 1860 ATAAATAAAA AGAATTGTTT TACACTTAGA TTTCAAGATT TAAAAAGCTG TCAAATACCA 1920 TATATTCAAA AATTCTGGTA TCGTAAAAAG AGAACAGTAG AGATCTCTTA ATGCTGCAAT 1980 TATCCACTGA GGTTTCACAG TTTATGAATA TCATGCTTTT TTGTAGAAAT CTGCTAAGCT 2040 TACTGTTGAA TCATTTATGT ACACTGACTA ATTTTTGAGC CATCATCAAT TTTCATGAAT 2100 TATGTAATTT AGCCTCAGCA ATGTATCACA TGCATTTGAA ATAATTAAAC TTTTCAAAGA 2160 GACTTAATAC ATGCAACAAT GAGTAAATTA ACGCTTTTAT TAACATCAGC AGAGTTCTTT 2220 TTTTTTTTTT TTTTTCTGGG AGACAGGAGT TTAAGTTCAG GTAAAGCGAC ACTCTTGGCT 2280 TTGAGGCTTT TCTCTAGCTT TAAACTCTAG CCTGCAACTG TTTCTGATTA GCAGCTAGGT 2340 GACCTTCGTT GTACAAAGAG GCATCATCCT CTTGATCTTG GGTTTTCTTT CTAAAGGGCC 2400 TTGTGTGTTT TCATCCCACA TTTTAAGATA TAATAGCTGC ATTGAACGAA TTGGGGGATA 2460 TTCCTTCCAT CTTTATCTTT CCATTGGTAT TATTTAAATA ACATGAGGAT TATCTGTTAC 2520 TTAAAAAGTA ATCTGCCTTG TAAGAACTTA ACATCTTAAA TGAGCTTAAA AACAAAAGAG 2580 CTTGCCTGTT AAACTGTCTA GGCCTGATGC ATTTATAAGT GATTATTAAA TACACTTCTC 2640 CACTTTTTCT ATAATTATTC TATTCTTTAG TATTTTACCA TTTAAAAGGA GACTTCTTGC 2700 TTTCTGAAAA CACTCTTTCT TTTTCTACAT GTCTGCTGGC ATTCACCTCT CAAGGTTCTG 2760 TGTCCCAGGC AAATGCCACT CCAAGATGCC AGGCCTGTCT CTGCCTTCAG TCAACTTCCA 2820 CGTGGGTTTC CAAAGCTTAG TATTAAATTG GGTATCAGGT TAAAATAAAC ATCAGAAACA 2880 TTCTCATCTT TTTTCTTTCT CACTAGCATT TCTACTTCCT TTTGTTTTGT TTGTTTGTTT 2940 GTTTGTTTGT TTAAGAAATA GGGTATTGCT CTGTCACCCA GGCTGGAGTA CAAAAGCATG 3000 ATCATGGCTC ACTGCAGCCT TGACCTCCCG GGCTCGAGCA ATCCTCCCAT CTCAGCCTCC 3060 TGGGTAGTTG ATACTACAGG TACACGTCAC CAAGCCTGAC TATTTATTTG TTTTTTGGGG 3120 GGTTTTCTTT GTTGTAGAGA CAGAGTCTCA CTATGTTGCC TAGGTTGGTC TTGAACTCCT 3180 GGGTTCAAGC GATCTGCCTA CCTTGGCCTC CCAAAGTGCT GGATTACAGG CGTGAGCCAA 3240 CGTGCTCAGC CTCTATTTCC CGTTGAACTG GTTTTGGTAA GATATTTTAC AGGCTAACTG 3300 TGTATTTCAT 3310
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