Tag | Content |
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EnhancerAtlas ID | HS017-02336 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr1:167625790-167628890 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr1:167626339-167626350 | AAGAGGATTAA | + | 6.14 | EWSR1-FLI1 | MA0149.1 | chr1:167626837-167626855 | ACCTCCTTCCTCCCCTCC | - | 6.28 | FOSL1 | MA0477.1 | chr1:167627946-167627957 | CATGAGTCACC | - | 6.62 | Foxd3 | MA0041.1 | chr1:167627661-167627673 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr1:167627665-167627677 | GTTTGTTTGTTT | + | 6.32 | HES2 | MA0616.2 | chr1:167627804-167627814 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr1:167627804-167627814 | GGCACGTGCC | - | 6.02 | JUND | MA0491.1 | chr1:167627946-167627957 | CATGAGTCACC | - | 6.02 | PPARG | MA0066.1 | chr1:167626723-167626743 | AATGGGGCAAATTGACCTAA | - | 6.69 | RORA(var.2) | MA0072.1 | chr1:167626734-167626748 | TTGACCTAAATTTT | - | 6.25 | ZNF263 | MA0528.1 | chr1:167628296-167628317 | TCCCTCCTCTCTCTCTCCCTC | - | 6.06 | ZNF263 | MA0528.1 | chr1:167626837-167626858 | ACCTCCTTCCTCCCCTCCCCT | - | 6.36 | ZNF263 | MA0528.1 | chr1:167628302-167628323 | CTCTCTCTCTCCCTCTCCTTC | - | 6.73 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_09281 | chr1:167625562-167627191 | CD14 | SE_09281 | chr1:167627488-167634107 | CD14 | SE_10929 | chr1:167583491-167658519 | CD20 | SE_18431 | chr1:167616965-167626664 | CD4p_CD25-_Il17-_PMAstim_Th | SE_18431 | chr1:167627886-167631868 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19445 | chr1:167625731-167626881 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19445 | chr1:167627839-167628615 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_37223 | chr1:167628293-167641530 | HSMMtube | SE_40850 | chr1:167625615-167626820 | Left_Ventricle | SE_51323 | chr1:167628454-167637093 | Skeletal_Muscle | SE_58405 | chr1:167569022-167658109 | Ly1 | SE_61444 | chr1:167568870-167637276 | Toledo |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 167628000 | 167628400 | chr1 | 167628400 | 167628458 |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I167656 | chr1 | 167625563 | 167627191 | GH01I167658 | chr1 | 167628038 | 167629238 |
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Enhancer Sequence | TTTGGTGACA CTGGGCCTTG AATGATCTTT TGAAAAATGA CCCAATGTAA CACAGGTAGA 60 CAGTGGGCTA GAGCTGAGGA ACAGCAGCTC CATTCATTTG GATGGGGACA GGACAGGACG 120 CCTTCCACAT AGTCATTTAC ATTGCCTGCC CACCATCTAA AGGCACTGGA GTTAGCAACG 180 CCTCCTCTAA ATGATGGGAG AGGGAGGCAT GGAAACAAGC TACAAAGCTG GGCCTGGATG 240 AAAATGGGTC TTGCACATTG GGAAGCTCTC CCTTTTCCAT CTGCTCTAAA GGGGGTCATT 300 GCTCCCAAGA GTCAAGCTGC AGTCTCAAAA TAGGAGCTGC TGTTCAGAAT TTACATCACT 360 GACACAGAGT AGAAAGAGAG TTCATAGAAG GGAGGATAGC TGTGTCTTGG TAAGAGTCAG 420 ACTGGGACAC ATTTTGAACC CACCTTCACT ATGCCAGCAT GTGACCCTGG TTGGGAAAGC 480 CACTTTATCT CTATGCTTCC CTGTTAGATG GGACTGATAA TACAATAATA TCTACTTCAT 540 AGGGCAAGTA AGAGGATTAA GTGAGCCAGT GTCCATGATG TGCCTTGCAC ATAGTAAGCA 600 CTCAATCTAT AGATGTTGAT TCCTGTCCTG CTGGTTTTTT TCGAAACTGG TGAATACATG 660 ACTCCTTTGG AGATACAATC TGTTTATCAC CAGGGATATA GATGGATCTA TGCTTGTTTG 720 TCCAAGACCT ACAGAAAATC AGGGGTGTGG GGCCTAAAGA AAATCACCTA TGTTCCCATT 780 CTCTTTCTTT TGTCCTGTGA TTTGGATTTT TAAGAGTATA TGCTGAGATG ACAGGGCCCA 840 TTTTGGCTTC AGATTGATCA TTTGCTTGAG CAGAAAGCAG TTGCCAATAG CAAAGGGACA 900 GCATTTTTAA AAATATGTTT AGGGCTGGCT GCAAATGGGG CAAATTGACC TAAATTTTGG 960 TAAGCCTCAT ACTTCCTAAA AACAGCTTCA AGGTGCATAC ATTTAAATTT AGTAATGAAA 1020 TATCCTTATG GGATTATTAG TAATTTCACC TCCTTCCTCC CCTCCCCTCT GGGCATCTGT 1080 GCCCAGTCCC CAGACACCCA GGACTTGGTT TTGATATGCT GAGCAGATGG ACTGCTCACT 1140 GCAGCGTTGT TTTCCAGGTA TTTGTTCCCC TGCTCAAATC AGACGTCCTG GAGAGCAGAG 1200 CTTAAAATTC TCATTTCAGC ATTAAAATTT TTTTTCTTTA TTTGATGTTT TCCATATTAT 1260 ATATCTTGAC AACTTGCTTC CTTTTCCTTG AAAATATATC GTGGACAGCC CTACAAAATC 1320 AGTTCTAGTT TACTCATGCA CACACACACA CACACACACA CATGCACGTT TTATTTTTGT 1380 TTTAATTTTT TAGAGACAGG GTCTCACTCT GTCACCCAGG CTGGAGTGCA GTGGTGCGAT 1440 CCTAGCTCAC TGCAGCCTCA AGCTCCTGAG CTCAAGTGAT CCTCCTGCCT CAGTCTCTCG 1500 AGTAACTGGG ACTACAGGTG TGCACCACCA CACCTGGCTA CACACACTTT TACATAACTG 1560 AGATGGTATG AGACACACTG GGTTTATGCA GCAGTGCTTT TCTTTTGGTT TGCTTCCACC 1620 AGATCAGCCC CCCTCCCTGT GTCCAGCCTC CAGAAACTTC ACATATACCT TTCTGTAGGA 1680 TACTTTACAT TCACATAACT ATATAAAAAA TTACATATAC ATTGTGAGCA TATGTGTACA 1740 TAGAGATACA CACACAAGGG GTAAGTTTTC TGGTTGTTGA TTTATAAAAC TAGTGTTATA 1800 TAAACTTATC TGCATCTTAC AATTCTCACT TTACAATTTT TCCTGGAAGT TGGAGTTTTT 1860 TTGTTGTTGT TGTTTGTTTG TTTGTTTTTT GAGATGAAGT CTCGCTCTGT TGCCCAGACT 1920 GGAGTGCAAT GGTGCAATCT TGGCTCTCTG CAACCTCCGC CTCCTGGGTT CAAGCAATTC 1980 TCCTGCCTCA GCCTCCTGAG TAACTGGGAT TACAGGCACG TGCCACCACG CCTGGTTAAT 2040 TTTTTTTTTC TTTTTTTTGG AGAGACGGAG TTCCACCATA TTGGCCAGGC TGGCCTAGAA 2100 CTCCTGACCT CAAATGATCC ACCCTCCTCG GCCTCCCAAA GTGCTGGGAT TACAAGCATG 2160 AGTCACCATG CCTGGCCTAG TTCATTCTTT TTAATGGTTT CCTAATAACC TGTTATGTGG 2220 ATGGGCCATA AACCATTTCC CTTTTTATGG TATTTTTTTT TTGTCTCTAG TGTTTTGCTG 2280 CTGTAAACAG TACTGCAGTT AGCCCCCATG GCTGTGTACG CTAGCATTTA TGTCTATGGG 2340 GTAGATTCTC AGGAGTGTAG GGTGAGCTGA AGGGTTTGTG TAATCTAATT TAATCGATGT 2400 TGCCAGATTA CTTTCCCAAA AGGCTGTAAC AAGTCACATT TACTCCAGCA ATATATCAAT 2460 ATATGAGGGT TCCTTATCTC CATTTCCCCA ACCGCAATTG CTATTTTCCC TCCTCTCTCT 2520 CTCCCTCTCC TTCCCACCGC CCATCATCTG ATAAGCATAA AAAGAAATCT TAGTGTTAAT 2580 TTAACTTGCA TTTCCCTGAC AAGTACTATC GTAAGTTTGA GCATCTTTTT ATGTTGATTG 2640 GCGTTTTGAA TTTGCTTTTC TATGAATTGC CTATTTATAT CCTTTGTTAT GTATTGTTCC 2700 TGTCATTATG CGAGAGTGCT TTATATAACA GACATTACCT CATTTTCATC TGTGTTAGAA 2760 TACTTTTCCA GGTCTCTAGT TTTCTCTTTA CTTCTTTGAT AGTATTTCTA TATGTAAATA 2820 AGTTTTACAT TTTCCTTTAT AGTCAGGAGG TTTTGTTTCC TGGGGTTTTA AAATTTTAAT 2880 AGTTTCTGGG AGTTTTCCCT TAGTTAAAAA AGGGAAACAT TTATTTTAAC ACCTTTTTGG 2940 GCACACTCTA CACTCTGCCA CTGCATCCTA TGTTTCAACT AAGTAATCTC AATTTGCCTT 3000 CAGAATGCCA TGAACTGCAG AGCCAGGCGT GGGAATCCAG CAAAGCATGC TGGGAACTGT 3060 GATCACAGGC TCCCCTTGGA CCACGTGTCC ATTCCCTGGC 3100
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