Tag | Content |
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EnhancerAtlas ID | HS184-27868 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr7:41187950-41189090 |
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) |
RUNX1 | MA0002.2 | chr7:41188489-41188500 | AAACCACAGAG | - | 6.14 | Sox6 | MA0515.1 | chr7:41188794-41188804 | CCATTGTTTT | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_36910 | chr7:41185127-41190193 | HMEC |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I041145 | chr7 | 41185432 | 41189837 |
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Enhancer Sequence | AGAGGCATAA ATAACATAAA GAATGACACT GAGAAAACAC AAAATGAAGA ACAGAGCAAA 60 ACTAGAAATT CTGTCCCAAG TGGGTCTTAA CTGAACCATA TGCAGTATTA CATATTATTG 120 AACAGTCATG AGTTTCCAAT TCGCTATAAT GTTTTCCTCT GTGCTCACAA GTTGTTTGGT 180 GAAGTCAAGC AAGCTAGCAA AAGGAAGCAC TTATTCAGAG CCCATTTGAA AGAGGAAGAA 240 CCATGAACAG TGAATAAACA GGTGGAGGCA GGTATATTAC AAAACTCTAT GCATTTTGAA 300 GGTTTGTATC AATATGAACA GGGCTTTCTC TCTAATCCCA GGGGCAGGAT TTCAAAACAT 360 AGGCTTGGCT GGAATATTTA TCTAATTTCT CATCACCTGA CTAAAGCCAA ATCCTAACCA 420 CAATAATTGG TCTATTAAAA GATGTAGTTC TAGCAACTCT GGCAGATGAA TCATTCAGAT 480 ACACGCACAC ACATTTATGC TCCTCTTGGC TACACATAAG CAAACAAAAC AAAACAAATA 540 AACCACAGAG AAGGCAGAAT GGGTGTAAGA AATTCCCACT CTACTGGTCC CTAACTCTCT 600 ATCTTTAATA CATACTAAAG GCTAAATTTA TATATATATA GATGGCTGTA AGAAGAGACA 660 AATATCCCGG GAACATTTCC TGCAGAAAGA CTAGTATTTC CTTTGGTATA TAAGTGAAGA 720 GTTTCAGAGG AAATTGGGAG AAGTACTTTC CTTTGTGCAA TTCGTTTCTT GGACTGGCAC 780 TCCCGTTCCC CTGTTTATTT TTGCTTATCA GCCTCCTTAA GCTCCAAGCA CAACCTTTCC 840 TTTTCCATTG TTTTCATTTC TTTGCCACCT TTTTATTGAT ACATCTCATT CTCATTAATG 900 TAGATTATGA ATTATGATCA AGCAGTATCA AGCCCTTTTC AAGATACAAC AATACTGAAG 960 GGTTCTCGAA GAGGGTTAAT ATATACACAC CTAGTGGTAG GGCCAGGGCC GAGGTCTCGC 1020 CACTACTGGG CCCGTTTTTT CCTCACTGCT GCTTTGGGGA CACAGTCCCA CGACAGCCGC 1080 GTGACATCGT CCAAGATGAG AATTTGCTGT TAGCGAAGGT CTTCCAGAAG AGACCAGAAA 1140
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