Tag | Content |
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EnhancerAtlas ID | HS007-03521 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr11:133814600-133815950 |
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) |
EWSR1-FLI1 | MA0149.1 | chr11:133815306-133815324 | GCCTGCTTCCTCCCTTCC | - | 6.41 | EWSR1-FLI1 | MA0149.1 | chr11:133815310-133815328 | GCTTCCTCCCTTCCTTTC | - | 7.56 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_41022 | chr11:133813916-133827876 | Left_Ventricle | SE_49730 | chr11:133814614-133817993 | Right_Ventricle | SE_54961 | chr11:133814443-133817952 | Stomach_Smooth_Muscle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I133944 | chr11 | 133814473 | 133816011 |
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Enhancer Sequence | GCTGTGAAGA GATGAAAGAG AGAATGAAAA AGTGCCAACA GAAGAGGATG GGTGGGGGGT 60 CTCCAGCGCA CCCGGGAGCA CCTCCATTCA GGCTGAGCAA TATCCCTATC CCAGCAGCAT 120 TTCCAGGACT ACTGGCTCAC CCAGCTTCCC TCTCTAGGGC AGAGGGAAGG CAGGCTGGGG 180 TCCAGGATGC TAGGGTCCCC TCCCAGTCCT GCTGTCAGTG CCAGAGAGAC TATGTATCCT 240 ACCAAAGCCC AGTGACCCCA GGAGATGAGG GCAGCAGGGC CCAGAAGCCT GAGAACAAGG 300 AATGGGTTGG CCATCAGAGC AAACATCCTG GAGGCACCCT TCCTCAGCTC TAATCCCCTG 360 CCCCAGTAGG ATGCCATCTG TGTCTCACAT GTGGCAATGA GGAGGCCAGA GGTGCAGAAG 420 CCTCTTCCAT GACGCCAGCA GGGTGGAGCA GCCCTCGAGG TCGGCCCACC TCACCCGCTC 480 TTAGCTCACC CCTCACCGCA GCCAATATCA CCACACCTCT GCTCTCCTCC TCGTCCTGAT 540 GCTGGCAATC TGCCTAAAAA CTAGACTCTC AAAGCCAACC CTGGCCAAAA AGAGAGCATG 600 AGACATGGGC ACAGGAGCGA AAGAGGGACA GAGACGGAAG CATTCTGAGA AAGGCAGGGC 660 AGACCTCAGA AGCCACCAGC AAAGATGAAA GTGAAGGCAG TGCCCTGCCT GCTTCCTCCC 720 TTCCTTTCAA CCCCAACAAC GCTCGCTCAA TGACACGCAC ACGCACGCAC ACACACACCC 780 ACGCCCTCCT CTCCCGCGGG CTGGGGGGCA GGCAGCGGCA GTGAGTCACG AGGCCTTTGC 840 TGGCAGGAGT AACTGCCAAA CAGGACACAG ACGGGGCCAG GAGAAGGAGA GGACAGCATG 900 ACAAGGAGGC AGACACCAGG CACCTGCAAA CGGTGGGAGG CCAAAGATTC ATCCATACAC 960 TCAGGACGGG AAGGCGCCCC GACTTCAGAG CCAAGAGGAA AGGGGTGGGT GCGGCCAAGC 1020 AGGGAGAGCC GTGCTGGCCC AGGGCTGCCT GACTCAGTCT GCTGTCCTCT CCATCCCACT 1080 CTCCCACCCA GGCCTCTCCA GCTTCCCCTT TGGCTCCCAG CCCTCTCCAC AGCCCAGGCG 1140 GTGCTGTTCA GAAGGCTTTA CCCTGCCCCA CCTCCACAGC CCTCTCCTCC CACCGCTTGA 1200 TTAGAACCAA CAGAGGACAA AGGATGGGAG GAACCAGGCA GAGACTGGGA AACAGAGATA 1260 AAGAGTGGTC AGGACAAGGC AGGGGCCAGA GGGGAACCAC CGAGGAGCTG ACTCCAGCTG 1320 GGGAAGGTGC GGGAGACCGG GTGCCCAGAC 1350
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