Tag | Content |
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EnhancerAtlas ID | HS130-27856 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr9:110265680-110267860 |
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 | AATAGCTGAG ATTACAGGCA CCCTGTAGTC TGGAACTCCT GACCTCAGGT GATCCACCTG 60 CCTCAGCTTC CGCAAACTGT TGGGATTACC GGCGTGAGCC ACCGCACCTG GCCCTGACAC 120 TTTACTTTTA TGAGCCCATC TACCTTTTGA AACCAGAAGC ATGGACCTCA GAAGAGGGTG 180 AAAACCAACT TTTTTTTTTT TTGAAACGGA GTCTCTCTCT GTCACCCAGT CTGGAGTACA 240 ATGGCACAAT GTCGTCTCAC TGCAACCTCC GCCTCCTGGG TTCAAGCCAT TCTCTTGCCT 300 CAGCCTCCTG AGCAGCTGGG ATTACAGGCG CCCGCCACCA TGCCCGGCTA ATTTTTTGTA 360 TTTTTAGTAG AGACAGGGTT TCACTGTGTT GGCCAGGCTG GTCTCAAACT CCTGACCTCG 420 TGATCCACCC GCCTTGGCCT CCCAAAGTGC TGGGATTACA GGCGTGAGCC ACCGCGCCCA 480 GCCGAGAACC AACACTTTTA GAGAACCTTT AAAAAGCCTG AAACTTCCCC ATATACTTTG 540 CATATGTTAT ACCCAAAATA ATCCTGCAAA GTAGGTATTA TTATTATTAT TTTATTAATT 600 TTTAGAGTCA AGGTCTCACT CCATTGCCTA GGCTGGAGTG CAGTGGCATG ATCATAGCTC 660 ACTGCAACCT CAAATACCTA GGCTCAAGTG ATCCTCCCCT TTCAGCTTCC TGAGCAACTA 720 GGACTTCAGG AAGCCACCAT TAAGCCTGGC TACTTTCAAA AAGTTTTTTG TAGAGATGGG 780 GTCTCGCAGT GTTGCTCAGG CTGGTCTCAA ACTCCTGGCC TCAAGCAATC CTTCTACCTC 840 AGCCTCCCAA AGTGCTGAGA TCACAGGCGT GATTCACTGT GCCTGGCCTA AAGTTTATTA 900 ATTCTATCAC ACAGAGGAGG AAATGAAAGA ACTGGAGATG AAATTGATCA AATTAGTAAT 960 CTCCAGCCAG TCCTGAGGAG ATTTAGCACT GGGCAGTGTT CGAGTTGGAT TTAAGAAGAG 1020 GCAGAGTGGT ACCACCAGTT TGCCCCACGT GGGTAAGGGA GAGATTTTCT GGCAAGACTG 1080 AAGACATTCT GATACCCTCC TCTCCCCTAA CATACACTTA CTCAGGTGTA AGAGTAATTC 1140 AGGCATAAGA GTCAGCAAAA ACACTTTCTC AAGACGCTGT CTAGCTGTCT CAGGATCTTG 1200 TCCTGCTCAG GGTTGAGCAC AAGGAGAACA CAATCCTTGC TGGCCGGGCC CTGTTCTGGA 1260 ATGACTGAGC TGTCCAGCAT GGCCAGTGTG TAAATGTCAA GTAAACACCA AATTCAAGTG 1320 CAATCTAACT ATTGTGCTGG GACTGTTTGT TTTAGATATA ATAGTCAGCA GGAAGGGAGA 1380 AGGGGAGGGA GGGGGAAAGT ATATATCACT TCACAAGGCA AAATTATGAC TATCGTGAGC 1440 CCTCCCTTGG TCAACTTGAA TGTCAAGAAA CCAATATCAA ATAAATAAAG AGCCTGCACT 1500 CCATGCTGCA AAAATAAGCA TGTCCATTTG CTTGAAAAAA AGATTTTTTC AGATGAGGGA 1560 ACATTTTCCA GTCAATCACC CTGCAGCAAA GTCATCCTGT TGAATTTGTG ACTCACAGCC 1620 TCTCTGTGTC AATAGACAGA GTCAGCCCAG AGTTATGACT TCACAGAAAG ATGAAGCAAA 1680 AGCTGGGAGA CGAGGCAGGA CCAGCTTTAA AAGAAGGCTG TAAGCTCAGA CAACAAGTAG 1740 CAAAAGAAAC ACTGACCACT CACAGGCTGG GTAATTGCAT TCGTTGCTTC TTTTTATTTC 1800 TTGCTCGTCT CCTAGAAAAG AACAACTCTG ACTTTGACTT CATCCTTTCA TTGCATTAAC 1860 ATTGACGGGG GACATGGTCA TTGTCAGGGC TATGACTTTG CCTGGTGCTC CATATACATT 1920 GTTATCTCAT TCTGTTCTCA TAGCAATTCT ATAAGGTAGG TGGTATTTGT ATTATTTTAT 1980 TTTATTTCCT TTTTTTTGGA GATGGAGTCT TGCTCTGTTG CCCAGGCTGG AGTGCAATGG 2040 CGCAATCTCA GCTCACTGTG CGAACTCTAC ATCCTGGGTT CAAGCGATTC TCCTGCCTCA 2100 GCCTCCCGAG TAGCTGGGAC TACAGGTGCA TGCTGCCACA CCTGGCTAAG TTTTTGTGTT 2160 TTAGTAGAGA CGGACGGGGT 2180
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