Tag | Content |
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EnhancerAtlas ID | HS032-00640 |
Organism | Homo sapiens |
Tissue/cell | DLD1 |
Coordinate | chr2:120994240-120996420 |
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) |
ZNF263 | MA0528.1 | chr2:120996281-120996302 | GGAGGAGGACAGGCTGGGAAG | + | 6.06 | ZNF263 | MA0528.1 | chr2:120995484-120995505 | CCCTCCCCTCTCCTCTCCTTT | - | 6.33 | ZNF263 | MA0528.1 | chr2:120995462-120995483 | TCCCCTCCCCTCCCCTCCCTT | - | 6.47 | ZNF263 | MA0528.1 | chr2:120995472-120995493 | TCCCCTCCCTTCCCCTCCCCT | - | 6.9 | ZNF263 | MA0528.1 | chr2:120995466-120995487 | CTCCCCTCCCCTCCCTTCCCC | - | 7.03 | ZNF263 | MA0528.1 | chr2:120995479-120995500 | CCTTCCCCTCCCCTCTCCTCT | - | 7.08 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27989 | chr2:120995243-120998525 | Fetal_Intestine | SE_28776 | chr2:120995138-120998740 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 120995093 | 120995456 | chr2 | 120995461 | 120996023 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I120237 | chr2 | 120994937 | 120998381 |
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Enhancer Sequence | CACATCGAAG CCGTTGTGGG ACACCCAGGA GTCTGAGCTC AGCAGTGAGC TCGGAGCTTG 60 AGCTTGAGCT TGGGTTGCAG AATCCAAAAA TCAATTAATG TGGGGCTTGG GGGGAAATCT 120 GTCTGACCGG TGGTTTGGCA AAATCTTCAA TCACTGTGAG ACAGAAGATG TGTGCTGCGT 180 GCTGTGGCTA TGGTGCGCAT GGCTGCAGCT GCTGCCAAAT AGGAAAGGCC CCCACAGTGC 240 CTCCATCCCC CAGCCCTGCC TTTCCTCCCA AGTGCAGTGG GGGTGTCTTG AGGCGAGGGG 300 CTCTCTAGGC ACTATGCCTC CTCCATAGTC CTCCAGACCC CCTTTACTTG AAGACTAAGC 360 AACTAGCCCT TTGGCAGTCA GTTCTAAGGG TGAGGGGCCT GAAGTGTCAG CAAGGGTCAG 420 AGCCAGGCGC CTGGCAGAGG CTGGAGGGGC AGAGGCAATG GTGATGGGAG CCAGTGAGGC 480 CAGAGCATGA GCCAAATCTC CCCTCTGATC ATTTTGGACC AAGTGCAGTG AGCATGAGTT 540 GGAGGTGTCC TCAAATTGCA ATCCTCTGGG GTCTTCCTCT GTCTCTTCTT TTCGGGTGAG 600 TTTGGCAGCG GATGTGAGGA AGGTGCTCTT CATCAGTCGC TGGGTTCATG AATGGTCCTC 660 ATTTCCTGAA TCCTTCTGGA TCATTCTCTG AATTCAGCAG GGGCATGTCT CCCTGGGCTG 720 ACGGGTGGGG CTCCAGGTGC ATCTGGCTGC AGCACTCTGG GAGGGGGCCC GAGGTGCATG 780 CAGATCTTGA GTGGGTCTCA GAGAAAGAGA CACACAGGCC CCACATGCGT GTGCACACGC 840 ACACATGGGC ATGAATGTGG GTACGAGGCA TGTGTGCTCC ACACGCTGAC TTCACTGGGA 900 ACACTGACCC CAGCTGCAGA GAGACCGGAG CAAGGGCTGA GGGAGGCAGA GTGAAGGAGC 960 GCTCATCCCT GGGAGGGCGC CTGGGAGGAG AAGTGAGTCA TTGACCAGTG GTCATGGTGA 1020 GTTTGCCTTA CGGAGCCATC TCTGGAGCCT GAGGTCACAG GGTCTCTGGA ACTGGCCCTT 1080 CAAGTTCCTG GGAAGGGTTT TGACAGGGAA GTCGTCCACA AGGGCTTTCC CCCACTGGAA 1140 CACTGCCTAG CCTTCTCAGA AACGCCCCAT GTCTGTGGCA GGCTTGGTGT TCCTCCTGCC 1200 ATTCCAGGCT TTCTGCTGCC CCTCCCCTCC CCTCCCCTCC CTTCCCCTCC CCTCTCCTCT 1260 CCTTTCCTTT CCTTTTTTTA AATAGAGATG GGGTCTCCTC ATGTTTTCCA AACTGGTCGC 1320 AAACTCCTGG GCTCAAGCAG TCCTCCCACC TTGGCCTCCC AAAGTGCTGG GATTACAGGT 1380 GTGAGTCACC TTGCCCAGTA ATTTGTGTAA GCATATACCT TGGATTCTCT ACTAAACCGC 1440 CTAGTCTTGC CAGTCACTTC CTAGTCTTTC CTGCCTCCTG GCCTTCCTTT ATCTCAGTCC 1500 CCTGCTGCCT GGAATGCTCT AATTCTCTCT CTTTCTCTCC CTCTTTTGTG TTTGTCAGAA 1560 TCCTCATTGT TTTTTAAGCC CACTCAAGCC TCAAGCTCCA CCTCTCCCAG GAAACATGGG 1620 GGCCTACTTT AGTCGAAGAA GACTCTTAGC TCTGAAGTTC TTTGAAATCA TCTCTTCGCC 1680 TGAGGCTTCA GTTTCCTTAC CTGTAAAAAT GAGACAATAC CATGTCATGG TTTGTTGTGA 1740 ACATTCCCTG TGATGACCTT CATAACAGTG GCCAGCACGC AGTAGGTTCT CAGTGAAATC 1800 CTCATTCCTT TCCTGCTTTA CGCCAGGCAC AAAAATACAG ATGTGAGGTG CACCCCTGGC 1860 TTCTCAGGAG GGAGCAGGGC TGGGGTGGAG GAGGCCTGGG TGAGGGGTTC CATACCTACC 1920 CAGGGAAGGG AAGGGATGGC AGGAAGCCTT TGAGAAGACC TGCTACTGGG CTGGGTTTGA 1980 AGGACAGTTA GAGGCCATCA GGAGCACCCG AGGAGCAGGA GTACGGTGAG GCAGTGGGGC 2040 AGGAGGAGGA CAGGCTGGGA AGATGGGAGA CAGGTGGTGG GAGGGGCTGG GTGCGGGGCA 2100 CTGTCGGGGG CAGCCGGAGA GAAGACGAGA GCCTGGACTT TATGAAGAGG TGAGGAAGTC 2160 ACTGAAGGAG TTGAGGGCGG 2180
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