Tag | Content |
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EnhancerAtlas ID | HS161-14118 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr7:76635090-76638230 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr7:76638115-76638136 | TTTTTCTTTTTTTTTCTTTTT | + | 6.07 | IRF1 | MA0050.2 | chr7:76638109-76638130 | TTTTTCTTTTTCTTTTTTTTT | + | 6.09 | IRF1 | MA0050.2 | chr7:76638125-76638146 | TTTTTCTTTTTCTTTTTCTTT | + | 6.17 | IRF1 | MA0050.2 | chr7:76638131-76638152 | TTTTTCTTTTTCTTTTTCTTT | + | 6.17 | IRF1 | MA0050.2 | chr7:76638153-76638174 | TTTTTCTTTTTCTTTTTCTTT | + | 6.17 | IRF1 | MA0050.2 | chr7:76638159-76638180 | TTTTTCTTTTTCTTTTTCTTT | + | 6.17 | IRF1 | MA0050.2 | chr7:76638165-76638186 | TTTTTCTTTTTCTTTTTCTTT | + | 6.17 | IRF1 | MA0050.2 | chr7:76637731-76637752 | TTTTTCTTTCTTTTTTTTTTT | + | 6.59 | IRF1 | MA0050.2 | chr7:76638091-76638112 | CTTTTCTTTTTCTTTCTCTTT | + | 6.59 | IRF1 | MA0050.2 | chr7:76637725-76637746 | CTTTTCTTTTTCTTTCTTTTT | + | 6.5 | IRF1 | MA0050.2 | chr7:76638137-76638158 | TTTTTCTTTTTCTTTCTTTTT | + | 6.68 | IRF1 | MA0050.2 | chr7:76638143-76638164 | TTTTTCTTTCTTTTTCTTTTT | + | 7.26 | IRF1 | MA0050.2 | chr7:76638097-76638118 | TTTTTCTTTCTCTTTTTCTTT | + | 7.4 | KLF5 | MA0599.1 | chr7:76635756-76635766 | GCCCCGCCCC | + | 6.02 | MEF2C | MA0497.1 | chr7:76636440-76636455 | CTACCAAAAATAGAA | + | 6.43 | Myod1 | MA0499.1 | chr7:76637516-76637529 | TGCAGCTGCCCCT | + | 6.22 | Nr2f6(var.2) | MA0728.1 | chr7:76637971-76637986 | TGAACTCCTGACCTC | - | 6.22 | ZNF263 | MA0528.1 | chr7:76636262-76636283 | CTCCCCTCCTCCCCCACCACC | - | 6.55 | ZNF263 | MA0528.1 | chr7:76636265-76636286 | CCCTCCTCCCCCACCACCTCC | - | 7.23 | Znf423 | MA0116.1 | chr7:76637626-76637641 | GGAACCTAGGGTGTA | + | 6.07 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_24154 | chr7:76633438-76636379 | Colon_Crypt_2 | SE_24154 | chr7:76636993-76637737 | Colon_Crypt_2 | SE_26739 | chr7:76630193-76636864 | Esophagus | SE_26739 | chr7:76636958-76637946 | Esophagus | SE_68923 | chr7:76631414-76636453 | H9 |
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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: 2 | ID | Chromosome | Start | End |
GH07I077000 | chr7 | 76630194 | 76636864 | GH07I077007 | chr7 | 76636999 | 76637725 |
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Enhancer Sequence | CGGTGGGTGG TCCCCACCGG AGCCCTGGGA CTGGGGCTGT GCTTGGGGCG GACGCATTGC 60 TGGGACCAGG GATGCTCTCT CTAGCATCTT TCCAGGGAGG GGTCCCCCGA CCCCGGTCCT 120 CCCCTTGGCA AGCCCGGGCT CCTTCCACTG TAGAGTCAGC AACAGTGCTC ACCCCCGCTG 180 GGGCCGGGCA AGGCCCAGGA GGAGCGGGTG GGCACCTTGG GGAGGCGGGA TCTTAGTCAA 240 GGTGGGAGGG GGCAGCTTCC CCAAAGTCTA GGCCCCTGTC CCCCACCACG GGCAGATCTG 300 GCAGGAAACT CGGGGGCCGA GTTCAGACCC AGTCTCGTCG GTATTAGGCA GGGAGCAGGA 360 GAGGTGGCTC CTACCCGCTC TTACAGATGA GGAAACTGAG GCACAGGAGG TCAAGTGGCC 420 TGCCAACATC GGGGTGGAGC CGGGATGGGG AAGCAGGCAG TGTGTCCAGG TCAGGACTGT 480 CTGGACACAG GAGGAGGCGG GGTGACCTCA GGAAGACCAG GCCCAGGGGA AGCCGGGAAG 540 GCAGGGCGTG GTGAGGCTGG AACAGCACCC CGCTCCGCCC AGCCCCCTTC TGCCCTCTCA 600 CCCACTCTCC AGGTCCACCC TCTGCCCTCC CCGCTGCCTC ACCCTGGCTC AGCCTTCCAG 660 CTCCATGCCC CGCCCCATCC CCCGCAGCCA CTCTTTTCAA TGCCAACCTG CCAGGTCCTT 720 CCCCGCTTCC CAGGCCTTGC AGAGCTCCCA GCCCTGCAAA GAGACAAACC GAGCCCCTCT 780 GCGGGGCTCC TGGTGCCCTG GGTCCTCAGG CTGCTGGTGA TTGAGCCCCC TGCCCCCCGG 840 CTACTGCTGC CCCTCCGGGA GGCCTGTGAC CCCTGCCCCA TGTGCCCTGC TAAGCCACCT 900 TCACCTGCTC TTTTGGCTTG TGACATTTAG GAACCAGGGC CCCTAAACCA GCATCCCCGG 960 CCCAGGTCTG GTGTCTGGAG AGCAATTGCT CGGGGGGATG AGGGGTGGTG GCACAGGCCA 1020 AGTGGCTGGA GACATCTGAG GGGGATTCTC AGAGCAGGGC CAGGCCATGG GCTGCTGCTC 1080 TTGACGGCAC CCCCACTCCA CATCCATGGG AGGGCCCCAG AGGAGCTGCC TGGAGCTTGG 1140 CCCTGCCCAG GGTGGTCCCG GCCTCTGAAG CTCTCCCCTC CTCCCCCACC ACCTCCCATC 1200 CCCAGGGTGA AGTGATACCC TGTCTTGAAC GAACAGGCCA GGCGCAGTGA CTCACACCTG 1260 TAATCCCAGG ACTTTGGGAG GCTGAGGTGG GCAGATCACT TAAGGTCAGG AGTTAGAGAC 1320 CAGCCTGGCC AATGTGGCAA AACCCTGTCT CTACCAAAAA TAGAAAAATT AGCAGGGCAT 1380 GGTGGTGGGG GCCTGTAATC CCAGCTACTC GGGAGGCTGA AGCAGGAGAA TCACTTGAAC 1440 CCAGAAGGTG GAGGTTGCAG TGAGCCGAGA TCTTGCCACT GCCCTCCAGT TTGGGTGACA 1500 GAGCAAGACT CCGTCTTCAA AACAAAACAA AACAAAACAC ACAAACAAAC AAAAAAACCC 1560 CACCACGGTG GAGCCCAGGT CCCTCTGCCT GGAACTGAGA GAGAGTTAAC AGACGGGCTT 1620 GGTGTCTCAT GCCTGTAATC CCAACTTTGG GAGGCCAGGG CAGGCGGATC ACTTGAGGTC 1680 AGGGGTTTGA GAGCAGCCTG GCCAACATGG TGAAACCCTG TCTCTGCTAA AAATACAAAA 1740 ATTAGCCTGG TGTGGTGGTG GGTGCCTGTA ATCCCAGCTA CTTGGCAGGC TGAGGCAGGA 1800 GAATCACTTG AACCTGGGAA ACGGAGGTTG CAGTGAGCCG AGATCGTGCC ACTGCACTCC 1860 AGCTTGGACG ACAGAGCGAG ACTCCAACTC AAAAAAAAAA AAAAAAAAAA AGACAGAGTT 1920 AAAAGACCAC CTCCCTGTCA GTGACTCTTC AGCAGAGACT GTCTCACGCT GTCCTATCCG 1980 GACCCAAGAC AGTTGGCTAG GGGCCCGGCC CCAGAGGGGT ATGACAGGGA GAAGGAGGGG 2040 GCCGTTGGTG TTTGCTGTGT GAAAAGATGA ATTAATCCTC CCAGGGTTCA AGGACCAGCT 2100 AGGAGCAGGA TTGCCATGGC TTTTTTGTTT TTTTTTTAAC GTGGAGTCTC ACTCTGTTGC 2160 CCAGGCTGGA GTGCTGTGGC GCGATCTCTG CTCACCGCAA CCTCCACTTC CCAGGTTAAA 2220 GTGATTCTCG AGCCTTGGTC TCCTGAGTCG CTGGGATCAC AGGTGCCTGC CACCACACCC 2280 AGCTAATTTT TGTACTTTCA GTAGAGATGG GGTTTCGCCA TGTTGGCCAC AGGCTTTTGC 2340 ATGTCCTGCG GCCCTTCTGT GTTTGTTCTT AATGTCACAA TCCGTGCTGA TGCCAGGCGC 2400 AGCGCCAGGG ACTTCCCATG CGAGCCTGCA GCTGCCCCTC CCTTCTGCAC AGCCTCTCTG 2460 AGCCCACTGA GGAGCTGCCG TCACCCTCAG GAGCCGCCTG GAACTTGACT TTGGAAACAC 2520 CCTCTAAACA GATCTTGGAA CCTAGGGTGT AAAGACTGAA TCATAGTCCA GGAGCCCAGG 2580 GGAGGCTACT GGCCCCCACT GAGAGCCAGG GGGGCTTCCT AGGGGTTCTT TCTTTCTTTT 2640 CTTTTTCTTT CTTTTTTTTT TTTTTTTTTT TTTTTTTTTG AGACCGAGTT TTGTTCTTGT 2700 TGCCCAGGCT GGAGTGCAAC AGTGCGATCT CAGGTCACTG CAACCTCTGC CTCCTGGGTT 2760 CAAGCAATTC TACTGCCTCA GCCTCTGGAG TAGCTGGGAT TACAGGCGCC TGCCACTACA 2820 CCCAGCTAAT TTTTGTATTT TTAGTAGAGA TGAAATTTCA CCATGTTAGC CAGGCTGGTC 2880 TTGAACTCCT GACCTCAGGT GATCCATCTG CCTTGGCCTC CCAAAGTGCT GGGGTTACAG 2940 GTATGAGCCA CCACGCCTGG TCCCTGGGGT TATTTCTGAG CTGACTCTTT TTTTTTCTTT 3000 TCTTTTCTTT TTCTTTCTCT TTTTCTTTTT CTTTTTTTTT CTTTTTCTTT TTCTTTTTCT 3060 TTCTTTTTCT TTTTCTTTTT CTTTTTCTTT TTCTTTTCTT TTCTTTTCTG ATGGAATCTT 3120 GCTCTGTTGC CCAGGCTGGA 3140
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