Tag | Content |
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EnhancerAtlas ID | HS003-47103 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr9:110265570-110267980 |
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 | chr9:110267052-110267073 | AAGGGAGAAGGGGAGGGAGGG | + | 6.38 | ZNF263 | MA0528.1 | chr9:110267055-110267076 | GGAGAAGGGGAGGGAGGGGGA | + | 8.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_23179 | chr9:110266233-110267128 | Colon_Crypt_1 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I107503 | chr9 | 110266177 | 110267869 |
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Enhancer Sequence | TTTTTTGAGA CAGAGTCTCT ATCGCCAAGG CTGGAGTGTG GTGGCTTTGT CTCGGCTCAC 60 TGCAACCTCT ATTGCCCGAG TTCAAGCAAT TCTCCTGCCT CAGCCTCCCT AATAGCTGAG 120 ATTACAGGCA CCCTGTAGTC TGGAACTCCT GACCTCAGGT GATCCACCTG CCTCAGCTTC 180 CGCAAACTGT TGGGATTACC GGCGTGAGCC ACCGCACCTG GCCCTGACAC TTTACTTTTA 240 TGAGCCCATC TACCTTTTGA AACCAGAAGC ATGGACCTCA GAAGAGGGTG AAAACCAACT 300 TTTTTTTTTT TTGAAACGGA GTCTCTCTCT GTCACCCAGT CTGGAGTACA ATGGCACAAT 360 GTCGTCTCAC TGCAACCTCC GCCTCCTGGG TTCAAGCCAT TCTCTTGCCT CAGCCTCCTG 420 AGCAGCTGGG ATTACAGGCG CCCGCCACCA TGCCCGGCTA ATTTTTTGTA TTTTTAGTAG 480 AGACAGGGTT TCACTGTGTT GGCCAGGCTG GTCTCAAACT CCTGACCTCG TGATCCACCC 540 GCCTTGGCCT CCCAAAGTGC TGGGATTACA GGCGTGAGCC ACCGCGCCCA GCCGAGAACC 600 AACACTTTTA GAGAACCTTT AAAAAGCCTG AAACTTCCCC ATATACTTTG CATATGTTAT 660 ACCCAAAATA ATCCTGCAAA GTAGGTATTA TTATTATTAT TTTATTAATT TTTAGAGTCA 720 AGGTCTCACT CCATTGCCTA GGCTGGAGTG CAGTGGCATG ATCATAGCTC ACTGCAACCT 780 CAAATACCTA GGCTCAAGTG ATCCTCCCCT TTCAGCTTCC TGAGCAACTA GGACTTCAGG 840 AAGCCACCAT TAAGCCTGGC TACTTTCAAA AAGTTTTTTG TAGAGATGGG GTCTCGCAGT 900 GTTGCTCAGG CTGGTCTCAA ACTCCTGGCC TCAAGCAATC CTTCTACCTC AGCCTCCCAA 960 AGTGCTGAGA TCACAGGCGT GATTCACTGT GCCTGGCCTA AAGTTTATTA ATTCTATCAC 1020 ACAGAGGAGG AAATGAAAGA ACTGGAGATG AAATTGATCA AATTAGTAAT CTCCAGCCAG 1080 TCCTGAGGAG ATTTAGCACT GGGCAGTGTT CGAGTTGGAT TTAAGAAGAG GCAGAGTGGT 1140 ACCACCAGTT TGCCCCACGT GGGTAAGGGA GAGATTTTCT GGCAAGACTG AAGACATTCT 1200 GATACCCTCC TCTCCCCTAA CATACACTTA CTCAGGTGTA AGAGTAATTC AGGCATAAGA 1260 GTCAGCAAAA ACACTTTCTC AAGACGCTGT CTAGCTGTCT CAGGATCTTG TCCTGCTCAG 1320 GGTTGAGCAC AAGGAGAACA CAATCCTTGC TGGCCGGGCC CTGTTCTGGA ATGACTGAGC 1380 TGTCCAGCAT GGCCAGTGTG TAAATGTCAA GTAAACACCA AATTCAAGTG CAATCTAACT 1440 ATTGTGCTGG GACTGTTTGT TTTAGATATA ATAGTCAGCA GGAAGGGAGA AGGGGAGGGA 1500 GGGGGAAAGT ATATATCACT TCACAAGGCA AAATTATGAC TATCGTGAGC CCTCCCTTGG 1560 TCAACTTGAA TGTCAAGAAA CCAATATCAA ATAAATAAAG AGCCTGCACT CCATGCTGCA 1620 AAAATAAGCA TGTCCATTTG CTTGAAAAAA AGATTTTTTC AGATGAGGGA ACATTTTCCA 1680 GTCAATCACC CTGCAGCAAA GTCATCCTGT TGAATTTGTG ACTCACAGCC TCTCTGTGTC 1740 AATAGACAGA GTCAGCCCAG AGTTATGACT TCACAGAAAG ATGAAGCAAA AGCTGGGAGA 1800 CGAGGCAGGA CCAGCTTTAA AAGAAGGCTG TAAGCTCAGA CAACAAGTAG CAAAAGAAAC 1860 ACTGACCACT CACAGGCTGG GTAATTGCAT TCGTTGCTTC TTTTTATTTC TTGCTCGTCT 1920 CCTAGAAAAG AACAACTCTG ACTTTGACTT CATCCTTTCA TTGCATTAAC ATTGACGGGG 1980 GACATGGTCA TTGTCAGGGC TATGACTTTG CCTGGTGCTC CATATACATT GTTATCTCAT 2040 TCTGTTCTCA TAGCAATTCT ATAAGGTAGG TGGTATTTGT ATTATTTTAT TTTATTTCCT 2100 TTTTTTTGGA GATGGAGTCT TGCTCTGTTG CCCAGGCTGG AGTGCAATGG CGCAATCTCA 2160 GCTCACTGTG CGAACTCTAC ATCCTGGGTT CAAGCGATTC TCCTGCCTCA GCCTCCCGAG 2220 TAGCTGGGAC TACAGGTGCA TGCTGCCACA CCTGGCTAAG TTTTTGTGTT TTAGTAGAGA 2280 CGGACGGGGT TTCACCGTGT TGCTCAGGCT GGTCTCAAAC TCCTGAGCTC AGACAATCCG 2340 CCCACCTCGG CCTCCCAAAG TGCTGGGATG ACAGGCAGGA GCCGTTGCGC CTGGACTTTA 2400 TTTACTTTTA 2410
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