Tag | Content |
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EnhancerAtlas ID | HS045-60700 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr6:159074470-159077070 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr6:159075666-159075677 | GGATGACTCAG | + | 6.32 | Foxq1 | MA0040.1 | chr6:159074969-159074980 | AATAAACAATG | - | 6.02 | JUNB | MA0490.1 | chr6:159075666-159075677 | GGATGACTCAG | + | 6.14 | MYC | MA0147.3 | chr6:159075767-159075779 | GAGCACGTGGCT | - | 6.04 | SOX10 | MA0442.2 | chr6:159075965-159075976 | AAAACAAAGAC | + | 6.14 | TCF7L2 | MA0523.1 | chr6:159074899-159074913 | TTCCTTTGATCTGA | - | 6.17 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_02632 | chr6:159074789-159076958 | Astrocytes | SE_09522 | chr6:159073311-159077550 | CD14 | SE_15242 | chr6:159073751-159077595 | CD4_Memory_Primary_7pool | SE_16597 | chr6:159073338-159077176 | CD4_Naive_Primary_8pool | SE_17191 | chr6:159073720-159076873 | CD4p_CD225int_CD127p_Tmem | SE_17563 | chr6:159073699-159077653 | CD4p_CD25-_CD45RAp_Naive | SE_18193 | chr6:159073567-159077729 | CD4p_CD25-_CD45ROp_Memory | SE_18754 | chr6:159073254-159077363 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19401 | chr6:159073669-159077638 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20271 | chr6:159073414-159077584 | CD56 | SE_21839 | chr6:159073574-159076650 | CD8_Naive_7pool | SE_23027 | chr6:159073707-159077482 | CD8_primiary | SE_27252 | chr6:159073769-159074872 | Esophagus | SE_27252 | chr6:159074883-159076609 | Esophagus | SE_42870 | chr6:159074496-159077484 | Lung | SE_45067 | chr6:159074776-159077316 | NHLF | SE_45976 | chr6:159074538-159078465 | Osteoblasts | SE_49358 | chr6:159074392-159076385 | Right_Atrium | SE_50961 | chr6:159073750-159077293 | Sigmoid_Colon | SE_52770 | chr6:159073702-159077572 | Small_Intestine | SE_53918 | chr6:159073569-159077361 | Spleen | SE_62860 | chr6:159062856-159089459 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr6 | 159074587 | 159075256 | chr6 | 159075641 | 159075823 | chr6 | 159076608 | 159076855 | chr6 | 159075400 | 159076800 | chr6 | 159076335 | 159076366 |
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Enhancer Sequence | GAGGTTGTGG TGAGCCAAGA TCGCGCCATT GCATTCCCGC CTGGGCAACA AGAGCGAACT 60 CCGTCTCAGA GAAAAAAAAA AAGAATCTAT GCAAGCAAAA AAGTCATGAG GTTTTCAGGT 120 AAAATTTCAA GGACAATGCA GTCACTCAAC TTTTCCCCTG TGTACGAGGC AGAAAGCATG 180 GTGGCTGCAC GCTGAAGCTG TGAAACTTCT CAAGGAAATA GCTGTGGTAA ACAATACAGG 240 AGCGAGCTGC CGCCCGCTTG AAATGACCTG CAGGGCTGTG GCTTGTGGGC TTTGAGAACG 300 TTCTGTAGTC TTCCCTTGAA AGCGTGTGTG GTGATGACAG TCACATTCAC ACGCACTCAT 360 GCTACCGCAG ATCTCTGCAT TTCCACTCTG GTGACGTTTC CCCCGTACCA GGGAGGGCTG 420 AACATTTATT TCCTTTGATC TGATGACTGA CTGCTCAGAG ACAATAGATG ATTGGATGAA 480 AGAAATAGGG GCCCCTAAGA ATAAACAATG TGTCCCTTTC CCATCCTCCT CATCTCTTTT 540 CTTCATTGGT TTTACTTTTC TTGTACTTTT CCCCTTTCAC CAGATTTAGA AGCCAAAGTC 600 AAGATTTGCT GTTAGGCTGA GGAAAGCAAG CAGGCATTGT TTCAAACTCC TAGTGCATGG 660 CTGACTATTT CAGTCCCCTG GCGGAGCTGT CCCACACGTC TCTCCCTGGG AAGCCCTCCC 720 TGGTCCCACC AGCCCTCTCT GCTCCTGTGT GGAGTGACTC TTGCCTTCTG ATCCTTGGGT 780 TTTGTACTCA TCCCACCATG TTATGAGTTA TTTGTCTGTG TGTCCATGTT CTGGCTGGGA 840 TGGGTCCTTC TTAAATGCAG AGATTGAGTC TCACTTCTTT TTAGATCCTC GATATCTGGC 900 ACGTGCTTGA TACATAGAGG CCAATAAAAT CAGTGTTGAA CTGACACACT CAATGCCGTA 960 ACCAAACTGT GTTTGTCTGG ATGCCGAAGT TCCACTGGGA TACAGCATGA CCAGATAAAG 1020 ACCAATGGAA ACACCTAGAT TGAAGTTTTC CCCATGGCTG CCCGCGTCCC TCCCAATCCC 1080 AGAACAGTGG CTTAACTTCC TACTCTTGGG CCTTCCTGAA GGGGAGATGG AAGGGTAGAA 1140 GAAACCCTTT TGAGTCGGGC TTGCTTTGTT CTGGCTGTTG CTCTAGGGCT GTGCCTGGAT 1200 GACTCAGTGA GTTCCCCAAA CAGCCCTGTG AAGCAGGGAT GGCTCCATGT CACGGAGGAG 1260 GAAGGCCAGT CTCCCAGAGA TGAAGCAGCT GGCCTGAGAG CACGTGGCTG AGTCCTGGCT 1320 GGGTATGAGC CCAGACTGTC TGGCTCCAAA AGTGACACAG AGACAGGATG GCTGAGTGTC 1380 GGGGGGGCTT CTCCACATGG CTGTAGGAGA ATGTTTCCTT CCAGGTGGTG CTGTGGTGTG 1440 GGATTTATTC ATTTTTAATT GCCAGATAAA ATCAGGCTGA TCGATGGAGT GCTGTAAAAC 1500 AAAGACAGGC ACCATTACAA AAATGTAGCA GGGGAGTTAG GAGACTGGAT CTAAGCTCCG 1560 AGCAGGTGAG GACGGTGCCT GACTCAGTGC TTGGGACATC ATAGAGCATT TAAGATCTTG 1620 TTGAGCAAAT GATGGAGTGA CCGAATAAAT GTCATCCTGG GAAAATGGAC CTAGGAGATT 1680 TCCGTATTCA AGCTATGAGA TTGTGAATTC CTGCGTGAGA TGATTAACAT ACAATTTCAA 1740 AGATTCCTGT TAAATTCCAA AATGACTCAG ATTTTTCTAT GCTTTTTGGA TTTCTGAAGA 1800 CTGAGGTTTT CTGCAGTGAG GACTCACTTG CCCCCTGCCC GTCCTTACTT CCTGCTGTAC 1860 TTGAATATGG GCTTCCTGCC CTAGGAAGGA AGTTTGACAT CGGAGTAAAT CTCCGTGTCG 1920 CAATATTCTT CAGGTTTCTC AATTCAAGCC AAACATCAAG TGCCTCCTGG CTGGGTGATG 1980 GGGGAATCGC TGAAATCTGA TATTGTCCCT AGAAGGCAAA CACTCAAGAC AGAATGAAAT 2040 CAGGGTCACC ATCGAAATAT ACAAATTAGA AAGCAGTTAA ATTTGAAGGA GCAATGGATC 2100 TTTATTGTAA ATGAGGAGAA AGTTTCTGAA CTGGGTAGCC TTGATCTGGC CCTTGAAGGG 2160 CTAATAGTAA GAGTGAGGCT GCTCTTACTG TTAGTACCAC GACTGTCAGC CGGCATTAGC 2220 TGAGTGTACT TATGAGCTGA GCACTGTGCT CTAGAGGTCT CCACATGCAT CAGCACGTTT 2280 CGTCATCATA GCACCGCCGT GAAGTGGGTG CTGCACCTGT CTACTTCGTA GATGAGGACA 2340 TGAAGCCCCA GAGGGCTTAA GTAACTTGCC CATCATCAGC TCAACAGCAA GTCGGTGGCA 2400 GAGGCAGCTA CTCACCCACA CAGCCAGCCC CCAGCCCTGG TCTCATGACT GTCCCCATCT 2460 CTTGCCTCAT TGGGCAGAAG GAAGAGTGGG GCCGATGCGT GGAAATGCAG AGCGCATGTG 2520 GTCAGGGAAT GGTCTTGAAT GAGGTCAGTA TGGGAGTGGC GAGCATTCTG TGGGAACTGA 2580 GGATGGAGGA GTCAGGAGAA 2600
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