Tag | Content |
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EnhancerAtlas ID | HS184-21205 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr3:149118940-149119860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chr3:149119042-149119056 | CTTGTTTACCTTTG | - | 7.03 | Lhx3 | MA0135.1 | chr3:149119706-149119719 | AATTAATTAATTC | - | 6.29 | Lhx3 | MA0135.1 | chr3:149119705-149119718 | AAATTAATTAATT | + | 6.92 | MEF2C | MA0497.1 | chr3:149119336-149119351 | TGTTATTTTTAGAAA | - | 6.17 | POU6F1 | MA0628.1 | chr3:149119707-149119717 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr3:149119707-149119717 | ATTAATTAAT | - | 6.02 | TFAP4 | MA0691.1 | chr3:149119330-149119340 | ATCAGCTGTT | - | 6.02 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_27098 | chr3:149118857-149119346 | Esophagus | SE_27098 | chr3:149119605-149120202 | Esophagus | SE_28499 | chr3:149118460-149120176 | Fetal_Intestine | SE_32147 | chr3:149118866-149119456 | Gastric | SE_32147 | chr3:149119595-149120590 | Gastric | SE_33885 | chr3:149118040-149120708 | HCC1954 | SE_34635 | chr3:149118220-149120867 | HeLa | SE_38218 | chr3:149118769-149120838 | HUVEC | SE_45806 | chr3:149118827-149120740 | Osteoblasts | SE_47116 | chr3:149118550-149120863 | Panc1 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I149400 | chr3 | 149118137 | 149120952 |
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Enhancer Sequence | AAGACTGGAA GTAAACCTAT GTTTCCAATC CTAGTACCTT TTCTCTCCTA ATATATCATA 60 CAGTTTCTAA GATAATTATG AAAGGTGATT GACTTGAAAT CACTTGTTTA CCTTTGAAGA 120 GAGATTTTCT TTCCAGATCT CCAGTTGCCT GTCACTACCC TCTGTCAAGA CCCTTGGAGT 180 CATGACTAAC AGGAAGGGAG CAGGTGGCAG CGTGGCCACC TGCCATGCAG AAAGACTGGG 240 TCACTTCCTG TTGGTAAAGG GTTTCCTGGT TCAGGTTTGT TAGGCATTCT AAAATGGAGA 300 GAAAAACAAA TGCACCTCTA AAGTACATGG AAAAATAAAC ACCAAAGTCA ATGTTTTTGT 360 GTTCCAAATG AAAATGTCAC TCTAAAGAGA ATCAGCTGTT ATTTTTAGAA AGAAAGAATA 420 AAATTTCAGC TCTGTATACC AAAACTATAG CCTCATCCAT TAGGGACACT GATGTAGAAG 480 CAAGTAGAAA CTATCCAAAG TCTGCAGTTC CTACCTGACT AGGTAATGCT TAAATAAATA 540 ATCAGTTCTC ATCATGCAAC TCAATGTTTA GCTGAGTCCA AACATACTGC TGCCAACATT 600 TTAAAGTCAA CAACGATATC TAAAATAAAC ATAGGCTGAC TAACACACAC TGGTACTTTA 660 ATGAAAATAT ATTGTGAAAT AGCTCCTTGC CAATAGAAGT TCTTGCGCTC CTTCTTTGGA 720 TAACTGTGGA CTATTCAACA GAATGTTAAG CCACCTATAT TTTTTAAATT AATTAATTCA 780 ACAACCTCCC CCCTTTTTCG AGCACTTACT CTTAAGAATT TGAAGGATCT GAGATTTTAG 840 CTTATTTTAT CCTATTTTGA AGCTATTTGT TAGCTTGCCA GTTTCAAAGG AACTGGTAGA 900 AGTCATGAGA TTCTTGGGTC 920
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