Tag | Content |
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EnhancerAtlas ID | HS108-28083 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr3:49497740-49500850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr3:49498071-49498084 | AGGAGCAGCTGCT | - | 6.11 | Myod1 | MA0499.1 | chr3:49498528-49498541 | AGTGACAGCTGCT | - | 6.64 | Myog | MA0500.1 | chr3:49498531-49498542 | GACAGCTGCTG | + | 6.14 | Nr5a2 | MA0505.1 | chr3:49497947-49497962 | GCTGACCTTGAACAA | - | 6.3 | REL | MA0101.1 | chr3:49499461-49499471 | GGGGATTTCC | + | 6.02 | Tcf12 | MA0521.1 | chr3:49498531-49498542 | GACAGCTGCTG | + | 6.02 | ZNF263 | MA0528.1 | chr3:49499288-49499309 | TCCTTCTCCTCCTCCTCCTCC | - | 10.48 | ZNF263 | MA0528.1 | chr3:49499285-49499306 | CCCTCCTTCTCCTCCTCCTCC | - | 10.85 | ZNF263 | MA0528.1 | chr3:49499291-49499312 | TTCTCCTCCTCCTCCTCCTCC | - | 10.92 | ZNF263 | MA0528.1 | chr3:49499298-49499319 | CCTCCTCCTCCTCCTTGCTCC | - | 6.06 | ZNF263 | MA0528.1 | chr3:49499648-49499669 | TTCCCCCCTTCCCTCTCATCC | - | 6.22 | ZNF263 | MA0528.1 | chr3:49499651-49499672 | CCCCCTTCCCTCTCATCCCCT | - | 6.28 | ZNF263 | MA0528.1 | chr3:49499279-49499300 | CTCCCACCCTCCTTCTCCTCC | - | 7.23 | ZNF263 | MA0528.1 | chr3:49499294-49499315 | TCCTCCTCCTCCTCCTCCTTG | - | 7.96 | ZNF263 | MA0528.1 | chr3:49499282-49499303 | CCACCCTCCTTCTCCTCCTCC | - | 8.27 | Zfx | MA0146.2 | chr3:49500595-49500609 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_24508 | chr3:49498611-49499462 | Colon_Crypt_2 | SE_29912 | chr3:49495837-49500398 | Fetal_Muscle | SE_32208 | chr3:49498405-49500051 | Gastric | SE_33330 | chr3:49497617-49500120 | H1 | SE_35228 | chr3:49496612-49501770 | HeLa | SE_37405 | chr3:49495927-49500745 | HSMMtube | SE_43253 | chr3:49498344-49499963 | Lung | SE_49188 | chr3:49498321-49499858 | Right_Atrium | SE_51340 | chr3:49498910-49500084 | Skeletal_Muscle |
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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 |
GH03I049458 | chr3 | 49495981 | 49501626 |
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Enhancer Sequence | GCGCACCTGC TTGTGCACAC CCAGCCCTTG GGGCCTTGAC CCTGGGTAAG ACCTTGACTG 60 TGACAGCAAG TGGGCCTGGG CATCCCTGAG CTCTGCCTCC TGTGAGCTCA GTGGGGCTTA 120 CTAGAAACAA GTCTGTTCCC AGTGGTTGTA GGTGTCCTGA GGAGGCCTGA GATTTCCCAC 180 TTCTCTGCCG GCCAGGGCCT CAGTGCTGCT GACCTTGAAC AAATTGCTGA GAGCCCCAGG 240 CAGCAGAGTG AGTATAGGGG GGTTTTGGGC AGAGGAAGAA TAGGGGGTCA GCTGAGACCA 300 GGCTTTCTCC CTGGGATTTC CCCAAGGTAG GAGGAGCAGC TGCTGGGCCC TGGAGCAGCC 360 TTCCTCACAC CTACATGTCC TCACCTTTAT ATCAGCTGCT ACATTCTTTT AAGTATCCCA 420 GGGCATGGAG ATGATGAAAT ATTTCTTTTA ACCTTTTCTA GAAAAACCCT CCACACACCA 480 TGAATGGGTT TTTGTATGGC ACTGGGGACA TGTGAGTGCC TCTGCAGAGA GCCACTACCA 540 TGCTATAGCC AGTCATGCCC ACCCCTGAAG GCCCACAACC TGGGCTTCAA GCTGGGGTCT 600 CTCTCTTTCT TACCTTAAAC GCCAGTTCTG AGCTCAGCCC CTAATACTTC CCACTCCAGG 660 CCTTCCTAGT CCCTGGGGTC CCCTGCCAGG TCCAGCATAG TTAACTCATC TGATGGACAT 720 AGACCTTTTC CTGAGGGTCA CACATATTCG TGGGCGACCC CAGCCAGAAA TTCTGTCCAG 780 CTTGGTTAAG TGACAGCTGC TGGGAGGGAC GTTTGAGGGT CACCGGCCCA GAGCATCCCA 840 GAGATGGATG GGACAGCTGG CCTGGGCTTT GTGCCTACCA GGTGACCCTA CACCTGTCCT 900 GAAGGCCTCC AGCATGCTTG TGTCAAGCAG TAGCTCTGGG GGAGGTAGGT GGGGGTTTGC 960 CCTGGAATCC ATCTTAAGGC AGGACCTTCC CCAACTGCTC CCTGCTCCCC AGCTACCCTC 1020 TCCTCTCCAC TCTCTCCTTT CTCCCACCTC TGCCATTGGC CCAGTCCATG GGTTTCCTTT 1080 CCCCAGGCAG TTGACGCTGG GCCCTCTCTG ATGGGCCATG CTGGGTCTCC CCTGAAGTCC 1140 TTACATACTG AGTATACCAG GAGTATATCC AGGCCCAAGG GAGCCCTTCC TCCACCATGT 1200 CCCTTCCCCT TTGACCTTTC TCTCCTGGGG CTGGAAGGAG GGGAGTGGCC TCTCTGCATT 1260 CCAGGGAAGG TGGAGGAAGG ACAAGTGAGA AATTTTCTCT CTAAATGCTT GTTCTGACTT 1320 GACTTCCCTG ATGCCTGTTG CCCCTCCTCC ACATGACCCC CATCTCTGCC TCCACTCTGC 1380 CTGCTCTCTC CTCCCCAACC CCTCCTCTGT GCTCCCACCT TTCTTTTCCC ACCTACAGGG 1440 GAAAGAAGGG CTGCAAGCCT GGAGCTCAGC TGCTGTCCCC TCACCCCTCA CCCAACTGCA 1500 TTCCTTCCTG GAGGCCTGAG GGCACTGCCT GCCCTGGCCC TCCCACCCTC CTTCTCCTCC 1560 TCCTCCTCCT CCTTGCTCCC ATCTTTCAGC TACCATGCCC CTTGCTCCTG GGATCCTACC 1620 TTTCTGGCAA AGCCCAGCCT GGTTAAATAT AGTGCTGGTG CCTGCTCTCC CATCTGTTGC 1680 TTTCTCTCCT TTATCACCAC TCCATTCACT GCTCAGGCCT TGGGGATTTC CAAGATCTTT 1740 CAGGCCTGCC CTGCCCACTT TCTCCTAAGC CTTCACTGTG GCCTTTCTCT AGGCTTATTC 1800 CATTCACTCT CCAGAAAACC CCAGGGTTTC CTCCGTGTTC ACCTCCTATA GGCTCTGCCT 1860 TCAAAGAGTG GATTTCTCAA ATGTTCTGCA CCACACAGTA CACCCTGGTT CCCCCCTTCC 1920 CTCTCATCCC CTTTGTAACT ACCTGATTAT TACATTTGTA TTTACTTATT TTATTTACTG 1980 TCTTATTTGT CTGGAATTTG GGCTCCACAA GGGAAGGGCT TGTCCCTTTT ATTTCTTCCT 2040 GTGTTCCTAG CATACAATAG ACTCAGTAAA TATCTGTGGA TTCAACAAGG CATGGATGGA 2100 TGTTTCACCC TGGCCGTGAC TCAGTCACAT AATCTGGTCT TCTGTCATTT TTAGTGAGCA 2160 GACAGGGCCA CAGCCCACAT ATGAGGTCAC TTGATGATGA GGTGACCAAG GGGCTTAGAG 2220 AGGGCAAGCA GCTTTGCAAA GTCATACAGT GAACTCGGCT CTGAGTCTCA GCAGGGGCTT 2280 ATTCTTTTTT TTTTTTTTTG AGACGGAGTC TCACTCTGTC GCCAGGCTGG AGTGCAGTGG 2340 CATGATCTCG GCTCACTGCA AGCTCTGCCT TCCGGGTTCA CGCCATTCTC CTGCCTCAGC 2400 CTCCTGAGTA GCTGGGACTA CAGGCGCCCG CCACCACGCC CGGCTAATGT TTTGTATTTT 2460 CAGTAGAGAC GGGGTTTCAC CGTGTTCCGT GTTAGCCAGG ATGGTCTCGA TCTCCTGACC 2520 TCGTGATCCA CCCTCCTCTG CCTCCCAAAG TGCTGGGATT ACAGGCGTGA GCCACCGTGC 2580 CTAGCCAGCA GGGGCTTATT CTTTATTCTT TTTTTTTTTT TTGAGATGGA GTTTCGCTCT 2640 TGTTGCCCAG TGCCCAGGCT AGAGTGCAGT GGCGTGGTCT CGGCTCACTG CAACCTCTGC 2700 CTCCTGGGTT CAAGCGATTC TCCTGCCTCA GCTGCCCAAG TAGCTGGGAC TACAGGGATA 2760 GGCCACCACG CCCGGCTAAT TTTGTATTTT TAGTAGAGAC AGGGTTTCTC CATGTTGGTC 2820 AGGCTGGTCT CGAACTCCTG ACCTCAGGTG ATCCGCCCGC CTCGGCCTCC CAAAGTGCTG 2880 GGATTACAGG CATGAGCCAC CACACCTGGC CAAAAAACAC CTTTCCCCGT GGGTGGACAT 2940 ACATGTCCAA TGCCCCCTCC CTTAGCTACA TTCAGCTCCC TGCTGGCTCT GGGATAAGAT 3000 AGTCCCCCAA GACTGACTTT GCATGGCTAT TCCCAAAACA CTGTGTCTGT GGCCTTGAGC 3060 GCTGGACTAA ACACTAGATT AGGTTTAGTC TAGCCAGGCA GTCAGTGGAA 3110
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