Tag | Content |
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EnhancerAtlas ID | HS105-59387 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr4:1747610-1751840 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr4:1750551-1750570 | CAGCCTGCAGGGGGCGCCA | + | 7.04 | KLF16 | MA0741.1 | chr4:1750787-1750798 | ACCACGCCCCC | + | 6.14 | KLF4 | MA0039.3 | chr4:1748655-1748666 | ACAGGGTGTGG | - | 6.14 | KLF5 | MA0599.1 | chr4:1748189-1748199 | GGGGCGGGGC | - | 6.02 | REST | MA0138.2 | chr4:1749291-1749312 | GGAGCTGTCCTGGGGGCTGCC | - | 6.53 | RREB1 | MA0073.1 | chr4:1750783-1750803 | CCCCACCACGCCCCCTCCCC | + | 6.03 | RREB1 | MA0073.1 | chr4:1750984-1751004 | CCCCAATGCACCCCCTCCCC | + | 6.4 | RREB1 | MA0073.1 | chr4:1751032-1751052 | CCCCAAGGCACCCCCTCCCC | + | 6.4 | RREB1 | MA0073.1 | chr4:1750767-1750787 | CCCCACCGCACCCCCTCCCC | + | 6.58 | RREB1 | MA0073.1 | chr4:1751000-1751020 | CCCCAACACGCCCCCTCCCC | + | 6.8 | RREB1 | MA0073.1 | chr4:1751048-1751068 | CCCCAACACGCCCCCTCCCC | + | 6.8 | SP3 | MA0746.2 | chr4:1751774-1751787 | GGTGGGCGGGGCC | - | 6.14 | SP3 | MA0746.2 | chr4:1750786-1750799 | CACCACGCCCCCT | + | 6.29 | SP8 | MA0747.1 | chr4:1750787-1750799 | ACCACGCCCCCT | + | 6.52 | STAT3 | MA0144.2 | chr4:1750185-1750196 | TTTCTGGGAAG | + | 6.02 | ZEB1 | MA0103.3 | chr4:1750721-1750732 | CCCACCTGCCC | + | 6.14 | ZNF263 | MA0528.1 | chr4:1751095-1751116 | TCCCCATCTGCCCCCTCCTCA | - | 6.2 | ZNF263 | MA0528.1 | chr4:1750952-1750973 | TCCCCACCTCCCCCCTCCCCA | - | 6.46 | ZNF263 | MA0528.1 | chr4:1751107-1751128 | CCCTCCTCACCTGCCTCCTCA | - | 6.83 | ZNF263 | MA0528.1 | chr4:1751136-1751157 | CCCCCCACCTCCCCCTTCCCC | - | 6.8 | ZNF740 | MA0753.2 | chr4:1751131-1751144 | TAGCCCCCCCCAC | + | 6.19 | Zfx | MA0146.2 | chr4:1748756-1748770 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_25282 | chr4:1747966-1748618 | Colon_Crypt_3 | SE_25282 | chr4:1748689-1749125 | Colon_Crypt_3 | SE_25282 | chr4:1750005-1750787 | Colon_Crypt_3 | SE_34415 | chr4:1747159-1748092 | HCT-116 | SE_47504 | chr4:1748386-1749508 | Pancreas | SE_69102 | chr4:1747149-1748683 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr4 | 1751277 | 1751400 | chr4 | 1751416 | 1751622 | chr4 | 1748791 | 1749189 | chr4 | 1749368 | 1749530 | chr4 | 1750091 | 1750746 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I001745 | chr4 | 1747241 | 1752336 |
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Enhancer Sequence | ACCCTAACCC CATCTCCAGC AGTCCCGTCC TGCGGATCTC AAACTCAGAC AGGCACACTG 60 GAACCCAAGG CAGTTCCAGG AGCCCTTCTG GTCAGGCAGA GGCTTGGCCC AGCTGGGGCA 120 TCCCGGGAAC CTGGGTACCG AGCTGAGAGA TGCTGGTCAC TGGGTTCAGC CATGGCACCT 180 AGGACCCCAG CACCAGCCAG AGGGCCAGGG CCTCCTGAGG GGCCAGGCAA GACCAAGGGT 240 TGACGCTGTA ACCTGTTTCC AGGGGTCGGT GCTGCTGCTG TGCCCAGATC ACGCCGTCCA 300 GAAAAGCCGT TTTCTCCCAT CAGTGAAGAG TGGGGCTCCC CACATAGGGA GGGACCCAGG 360 CCGAGATCTG GCCGCAGTCA CCTGGCCCCA GTAGTGTCTG AGCCTGGGGG TTGCAGTCCC 420 AGGACCTGCT TCCAAGGCTC TGCGAGTCTG CCCCTTGGCC TGGTGAGCAG CACTGCAGTA 480 CTGACCTCGG GTGGGCGCAA CAACACCCCC AGCCGCCGCC AGGGGTCGCT TGCCGCCATG 540 GGCCATGCAG GGACCGGACC AGGTGGGTGA CACCCTGAAG GGGCGGGGCA CGGGTGCCAA 600 GAAGCCGCAT GGACCGCCAG GGAGGCTGAG GGGCGGGCAG GGGCTTCAGC CTGGGTGGCC 660 AGTGGGGTGT CCCCAAGGGC ATGAGGGTGC ATTTGTTCTT AGCACGTTTG GAGGAGGGGG 720 CCTGGCACAG GGATGGACGG CCACAGCGGG CCATGGCCAG TCACGGCTGG GGCAGGGACT 780 GGGCCAGCCT CAGGGGGGCC TGGGGGCCAC TCCCTCCCCC TCCACAGCCC ACCTGTGCTC 840 CTGCGGCACC TCCTGACTGG CTTCCCAGGA CCATCGCGCC CCTCCCTCCC GTGGGCAGCA 900 ACCCCCATCT CAGCCCCGAG CCTGGGTAAC AATAGGGTGT AATCCCTGGC TGAGGGGCCT 960 CTGAGAGCCT TCCGTGGCCC ACTTCACAGA CGAGAAACCG AGGCCCACAG ACCAGTGGCC 1020 ATTGGCCGGG GGAGACGGGC CAAGCACAGG GTGTGGGCCC CCTCTCCTGC TTGGGGTTGA 1080 GGATATGGGG GAGAAGAAGG GCCCTCGAGC CTCCAGAGCT CACCAGCTGC CCTATGGGCA 1140 GCACGGCCCG CCTCGGCCTC CCCGCTGCCC ACAGGCATGT CCGGCCGCAG GACTCCCACC 1200 TCTCTTTGCC GGGTCAGCTC TGCTCTGACA AGGTCTCAGG ACACAAGGCG GCTGCCAGGT 1260 CCTCCTCCTC ACTCAGCCCT GCCGGTCTGG CCTTCTGGCT CCTCTGACAG CTGCCCAGGG 1320 CCCTGTCCCC TGCTGGGGCC TCTCTGAGCC AAGCCGGGAG CCTGCCCGGA GAAGGCCGTG 1380 CAGGGCGGCT GAACGTGTCA GGGCACCTGG CCGGGCCTGG GGCCGCGCCG AGGACACCGG 1440 CCACCAGGCA GCGTCCTGGG CCGGGAGCCT CTCTCCCAGG ACAAAGGGGC CTTGTGTGGC 1500 TGAATGGGTG TTTATCCTGG AGCCTGAGTT AACTCAGGGC TGCGAGGCCG GGCGGGGGCC 1560 CTGGCACTGG CCTGCCTGGT AAACATGACC TGAGCTGGGC ACGCAGCCGT GGCCTGGACT 1620 TCCGCAGCCC CGGACCCCCT GCACATCCAC GCAGTCGCCT TGTGGGGGGC TCAAGGAAAC 1680 AGGAGCTGTC CTGGGGGCTG CCTCCGTGGG AGTCCTCATA CACAGTCATG GAGGCAGCGC 1740 TCGGCTCTGC CCTTCCCACA GCTCAGGGCA GGGCTCAGAA ACACCCCCCC GACGTGCCCC 1800 ATTGGAAGGA GGGGTGAGGG TTAGACGAGG TCGTGAGGGT GAGGCCCTGG TCTGCTGGGA 1860 TTAGTGTCCT TGCGGGAAGG CAGCAGGCCG GGAGAGCACT TTGGAGGAAC TGACCCGCCA 1920 GCACCCTGAT GGCGGACTTG GCGCCTCCAG AACCCAGAGA AACACGTGTC TGTGGTGCAA 1980 GCCATCTGGT CCCAGGCAGG ATGAGACCCC GCCGTCCGAG GGGCTGTCCA GCCTGGTGCC 2040 CACCCACTGC CCAGCTCCCC CTGCAGCCAA TATCCAAATC CCGAGGGGAG TGCAGGGCTC 2100 AGCCCACATG GAGAAGCTAG GTCTGTGGGG CACCCCCACC CCTCTAAGGC CACCTAGGAG 2160 TGGAACCTGC AGCTGCCTCC CTGGGCTGGT CAAGACCCTT TCAACAGGGC CGGTGGGGCT 2220 GCCCCTCCAA GCTCACTCCC ATGCCCCCAT GCTCTCTCCA GGGGCCGCCA GCCACCAGGC 2280 TGGATGGAAG AGGGGGTGGG GGCGAGGGAG ATAGGCCAGG ACAAGCTGAC CACAGCCCGA 2340 GCGTTCCCTG CCAGGCACCC CTCTGCAGCC CCCACCCTGC CCTACCCAGC CTGAGCCCCG 2400 GGAGAGAGTT CACCCAGCCT GCAGGCAGAC CCAGATCACC CTCCCATGGA CTCAGGAGCT 2460 GTCCCCAGCC CAGGCTGAAC CCCAGACCCC TTTCGGTCCC CAAGGTCCAT GCCAGTGAGG 2520 GTCGCTGCAA GCCCACGTGG TTGCCGGAGG TCCCTCCTCC AGCCCATCAC TCCACTTTCT 2580 GGGAAGGACC CCCGGAGGCC TGGGGACTAA GCCCCGGCGC CGCGCCGGAC TGCCCTGGTG 2640 GGCTGAGCGC ACATCCCTTG TCTCTCTTAG GGAGCTCTGT GAGGGGCAGG ACCGGGCCAG 2700 CAGCCGCTCA GGAAGCTGGA GCACGTGAGG GAAAAGCCCT GTCCCCACAG GGCTGAGGCT 2760 GGACGAGGTC CAAGGAGGGG CTTCTGCCCG AGCCCAGGCC TTCCTTGGGG TGTGCTCCAG 2820 TAGCAGGTGC GCGTGCCACC TGTGCCGTGG GTTGGAGGGG TGGAACGTGT ACGTCCTGGC 2880 TGCCCCCGAG CTCTGGGGAC CCCGAACTCC TGGGGCTTCT GCCTGAGCCT TTGGACCCCA 2940 ACAGCCTGCA GGGGGCGCCA TTGGGCCACC GGAGCCCCTT CTGCAGACCC GGCGCGACCG 3000 CACTCCTGCC AGGCTGTTCC TACCGCCTGG CCACAGGCCT CCAGGAGGGG CCCCCACCCT 3060 GGGGCGACGA GGAGCCACCT GGGCCCGCAC CAGGCCTCCC CACAGGGCCT CCCCACCTGC 3120 CCCCTCCCCA CTGCTCTCCC TCCCCACCGC TCTCCCTCCC CACCGCACCC CCTCCCCACC 3180 ACGCCCCCTC CCCACCGTGC CCCCTCCCCA CCCAACGTGC CCCCTCCCCA TCACGCCCCC 3240 TCCCCACCTG TCCCCCCACC ACGACCCCTC CCCACCTGTT CCCTCCCCCT GCCCCCTCCC 3300 CACCACGAAC CCTCCCCACC TGTCCCCTCC TCACCTGTCC CCTCCCCACC TCCCCCCTCC 3360 CCACTGCGCC CCCTCCCCAA TGCACCCCCT CCCCAACACG CCCCCTCCCC ACTGCCCCCC 3420 CTCCCCAAGG CACCCCCTCC CCAACACGCC CCCTCCCCAC TGTGCCCCCT CCCCACCATG 3480 CCCCCTCCCC ATCTGCCCCC TCCTCACCTG CCTCCTCAGC ATAGCCCCCC CCACCTCCCC 3540 CTTCCCCACT ATGCCCCCTC CTCACCACCC CCTCCCCACC AGCCCCTCAC TGCGACTTTG 3600 CCTCCCCTCT GTTCCCTGGA CCCTGCACAC TCACCAGACC CCTGGAGGTT TGTGGAGGGC 3660 AGGGCTGGGG ACTGGGAGGT TTCAGGCCAT GCAGGGCTGG AGGCAGCACA CCAGGCACCC 3720 TCGCTAGCTG AGGGTCTGGC CTAGCCTGAT AGGGGGACTG CAGGACAGGG GGGCCCTGGC 3780 AAGGCCCAAT CCCTCCCTCC CTACCCAACC CTGCCCAGCT GGGTTCTGGG AACACACCCT 3840 GTAACTGGGT GGCTGGGGAT ATGGCGCTCT ACAGCCTGAA CCACCAGTGG TACTCACTGG 3900 GTCCTCCAAC TCTGCAATTC TGCAGGCATG GACCAGACTC CAAGAAACAG CCCCTCGAAC 3960 GCGTCTGCCC CAGCCCGGTT CCAAACACCA GGCTGAGGCT GCACAGTTTG CAAGTGTGTC 4020 AAATGAATGA AGGAACAACT GTGCAGGCTC CAGGAACCCC CACCCCACGG TCCCCGCCCC 4080 CAGTCCCCGC CTCCCTTCCA CTCAGGCCCC TCCCTCCAGG CCAGCAGGGG TGAGGTGAGG 4140 GCTTAGAGCC CCTGCAGACA TCAGGGTGGG CGGGGCCCCT GCCCTGTGTC TCCTCTGTCC 4200 CTCGATGTCC ATTCGCACCC GTCTCCCCAA 4230
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