Tag | Content |
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EnhancerAtlas ID | HS060-05837 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr11:60699600-60701010 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZEB1 | MA0103.3 | chr11:60700987-60700998 | CCCACCTGCCC | + | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_59489 | chr11:60677061-60704111 | Ly3 |
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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 |
GH11I060932 | chr11 | 60699581 | 60699730 |
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Enhancer Sequence | TGAGTGGCAG GTGCCCAGCT CATGTGAGTC TGCATTTGTG TGGGCACAGT TACGCACACA 60 CACCTTTCCT CCTTCCTCAT GTGGGTCCCC AAGAGAACAG CTTCTTCTTG AGACGAGAAA 120 CCTCATGGGA GGAACCACAG CTTCAACTTC TTTTGTTCCA GCCACCTCTC TCCCGAGTCA 180 AGTAACCCTA ACAGCCCCCC GACCTTAGAC ACTTTCACGC TCATTATTGC ACTGGCAAGT 240 GCGCTGGCCT GAGAGAGTCG AGAGCACATA CTCTGGGATC AGAAAGTTTT AGTTTGAAAC 300 ACATCTTTGT TGTCAACCAG CTTTGTGATC ATGGGCTGGT CTCTTAACCT CTCTGAGCCT 360 CGTTACCTAA ACTTTAAAAT GAGAACATAT CTTCGGGTTG TTGTAAGAAT TAAAAGCACT 420 TTAAGACAGT ATTTAGCAGA TAGCAGGGGC TGAAACAATG GCAGTTATTG CTGTTATAAT 480 ATGATGTAAT AATTATACAA TGGTAAAAAT TATTATTATT ATTATTACCG GTGATTGTGA 540 AGTGAAATAA AAGGGAGGGT GGTAGAGCAA CTTCCTCTAT CTTGAAGTTC TAAGAGGGGA 600 AGCATGGAGT CTGCATGTAT GCAAATCCCA GCCACCTGAA GGGGGAAGGT GCCTTTCCCC 660 ACTTGTGGTC CTTTGCTCAA ATGTGTGTGG TTCCTGCTGG AGGGCCTTGG TGGGAGATCT 720 GCTTTGTCCC ACCTCTGCCT ACCTGGCTGT AGCTGGTTGC CAGGTGGCTC CAAGAGCAAT 780 GTCAAAGGCC AGCATGAATA AGGAGCCAAA GTTTTGGGTT CACACCCCTG CTCTGCCAGG 840 AGGAAGACTG GTATGCAATG GCCAGTTCCC CTGACTGAGC CCCAGGGAAC CTCAAGGAAT 900 GGCCCCTACA GTAAAATCTT AAACAAAGAA CAGGGGCTTA ACCAACAATC CTGCTGCAAC 960 ATGCATTCCA GTGACACACA GAGCTGAACT CAGTGGGAGC CCGTCCTACG GCCTGAGGTC 1020 AGGGCTGCTC TCTTCTGGCC CATGCCTTTT TTTTTTTTTT AATCTATTTA TTTTGAAACA 1080 GAGTCTCACT CTGTCCCCAG GCTGGAGTGC AATGGTACAG TCCGGCTCAC TGCAGTCTCA 1140 GCTACCCAGG CTCAAGGGAT CCTCCCACCT CAGCCTCCCC AGTAGCTAGG ACTACAGGCA 1200 TGTGCCACCA CACCCGGCTG ATTTATTGTA TTTTTTGTAG AGAGGGAGTT TTGCCATGTT 1260 GCCCAGGCTG GTCTCAAACT CCTGGACTCA AGCGATCCAC CCACCTCGGC CTCTCAGAGT 1320 GCTGGGACTA CAGGCATGAG CCACCCACCC GGCCCAGCCT CACACCTGTC TTTAGTGGCT 1380 TAGCCCGCCC ACCTGCCCTC TGCCCTTCCA 1410
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