Tag | Content |
---|
EnhancerAtlas ID | HS062-12034 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr4:1748800-1751500 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 | 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 | chr4:1750786-1750799 | 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 |
|
| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_25282 | chr4:1748689-1749125 | Colon_Crypt_3 | SE_25282 | chr4:1750005-1750787 | Colon_Crypt_3 | SE_47504 | chr4:1748386-1749508 | Pancreas |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr4 | 1751277 | 1751400 | chr4 | 1749368 | 1749530 | chr4 | 1750091 | 1750746 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH04I001745 | chr4 | 1747241 | 1752336 |
|
Enhancer Sequence | GACTCCCACC TCTCTTTGCC GGGTCAGCTC TGCTCTGACA AGGTCTCAGG ACACAAGGCG 60 GCTGCCAGGT CCTCCTCCTC ACTCAGCCCT GCCGGTCTGG CCTTCTGGCT CCTCTGACAG 120 CTGCCCAGGG CCCTGTCCCC TGCTGGGGCC TCTCTGAGCC AAGCCGGGAG CCTGCCCGGA 180 GAAGGCCGTG CAGGGCGGCT GAACGTGTCA GGGCACCTGG CCGGGCCTGG GGCCGCGCCG 240 AGGACACCGG CCACCAGGCA GCGTCCTGGG CCGGGAGCCT CTCTCCCAGG ACAAAGGGGC 300 CTTGTGTGGC TGAATGGGTG TTTATCCTGG AGCCTGAGTT AACTCAGGGC TGCGAGGCCG 360 GGCGGGGGCC CTGGCACTGG CCTGCCTGGT AAACATGACC TGAGCTGGGC ACGCAGCCGT 420 GGCCTGGACT TCCGCAGCCC CGGACCCCCT GCACATCCAC GCAGTCGCCT TGTGGGGGGC 480 TCAAGGAAAC AGGAGCTGTC CTGGGGGCTG CCTCCGTGGG AGTCCTCATA CACAGTCATG 540 GAGGCAGCGC TCGGCTCTGC CCTTCCCACA GCTCAGGGCA GGGCTCAGAA ACACCCCCCC 600 GACGTGCCCC ATTGGAAGGA GGGGTGAGGG TTAGACGAGG TCGTGAGGGT GAGGCCCTGG 660 TCTGCTGGGA TTAGTGTCCT TGCGGGAAGG CAGCAGGCCG GGAGAGCACT TTGGAGGAAC 720 TGACCCGCCA GCACCCTGAT GGCGGACTTG GCGCCTCCAG AACCCAGAGA AACACGTGTC 780 TGTGGTGCAA GCCATCTGGT CCCAGGCAGG ATGAGACCCC GCCGTCCGAG GGGCTGTCCA 840 GCCTGGTGCC CACCCACTGC CCAGCTCCCC CTGCAGCCAA TATCCAAATC CCGAGGGGAG 900 TGCAGGGCTC AGCCCACATG GAGAAGCTAG GTCTGTGGGG CACCCCCACC CCTCTAAGGC 960 CACCTAGGAG TGGAACCTGC AGCTGCCTCC CTGGGCTGGT CAAGACCCTT TCAACAGGGC 1020 CGGTGGGGCT GCCCCTCCAA GCTCACTCCC ATGCCCCCAT GCTCTCTCCA GGGGCCGCCA 1080 GCCACCAGGC TGGATGGAAG AGGGGGTGGG GGCGAGGGAG ATAGGCCAGG ACAAGCTGAC 1140 CACAGCCCGA GCGTTCCCTG CCAGGCACCC CTCTGCAGCC CCCACCCTGC CCTACCCAGC 1200 CTGAGCCCCG GGAGAGAGTT CACCCAGCCT GCAGGCAGAC CCAGATCACC CTCCCATGGA 1260 CTCAGGAGCT GTCCCCAGCC CAGGCTGAAC CCCAGACCCC TTTCGGTCCC CAAGGTCCAT 1320 GCCAGTGAGG GTCGCTGCAA GCCCACGTGG TTGCCGGAGG TCCCTCCTCC AGCCCATCAC 1380 TCCACTTTCT GGGAAGGACC CCCGGAGGCC TGGGGACTAA GCCCCGGCGC CGCGCCGGAC 1440 TGCCCTGGTG GGCTGAGCGC ACATCCCTTG TCTCTCTTAG GGAGCTCTGT GAGGGGCAGG 1500 ACCGGGCCAG CAGCCGCTCA GGAAGCTGGA GCACGTGAGG GAAAAGCCCT GTCCCCACAG 1560 GGCTGAGGCT GGACGAGGTC CAAGGAGGGG CTTCTGCCCG AGCCCAGGCC TTCCTTGGGG 1620 TGTGCTCCAG TAGCAGGTGC GCGTGCCACC TGTGCCGTGG GTTGGAGGGG TGGAACGTGT 1680 ACGTCCTGGC TGCCCCCGAG CTCTGGGGAC CCCGAACTCC TGGGGCTTCT GCCTGAGCCT 1740 TTGGACCCCA ACAGCCTGCA GGGGGCGCCA TTGGGCCACC GGAGCCCCTT CTGCAGACCC 1800 GGCGCGACCG CACTCCTGCC AGGCTGTTCC TACCGCCTGG CCACAGGCCT CCAGGAGGGG 1860 CCCCCACCCT GGGGCGACGA GGAGCCACCT GGGCCCGCAC CAGGCCTCCC CACAGGGCCT 1920 CCCCACCTGC CCCCTCCCCA CTGCTCTCCC TCCCCACCGC TCTCCCTCCC CACCGCACCC 1980 CCTCCCCACC ACGCCCCCTC CCCACCGTGC CCCCTCCCCA CCCAACGTGC CCCCTCCCCA 2040 TCACGCCCCC TCCCCACCTG TCCCCCCACC ACGACCCCTC CCCACCTGTT CCCTCCCCCT 2100 GCCCCCTCCC CACCACGAAC CCTCCCCACC TGTCCCCTCC TCACCTGTCC CCTCCCCACC 2160 TCCCCCCTCC CCACTGCGCC CCCTCCCCAA TGCACCCCCT CCCCAACACG CCCCCTCCCC 2220 ACTGCCCCCC CTCCCCAAGG CACCCCCTCC CCAACACGCC CCCTCCCCAC TGTGCCCCCT 2280 CCCCACCATG CCCCCTCCCC ATCTGCCCCC TCCTCACCTG CCTCCTCAGC ATAGCCCCCC 2340 CCACCTCCCC CTTCCCCACT ATGCCCCCTC CTCACCACCC CCTCCCCACC AGCCCCTCAC 2400 TGCGACTTTG CCTCCCCTCT GTTCCCTGGA CCCTGCACAC TCACCAGACC CCTGGAGGTT 2460 TGTGGAGGGC AGGGCTGGGG ACTGGGAGGT TTCAGGCCAT GCAGGGCTGG AGGCAGCACA 2520 CCAGGCACCC TCGCTAGCTG AGGGTCTGGC CTAGCCTGAT AGGGGGACTG CAGGACAGGG 2580 GGGCCCTGGC AAGGCCCAAT CCCTCCCTCC CTACCCAACC CTGCCCAGCT GGGTTCTGGG 2640 AACACACCCT GTAACTGGGT GGCTGGGGAT ATGGCGCTCT ACAGCCTGAA CCACCAGTGG 2700
|