Tag | Content |
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EnhancerAtlas ID | HS105-15294 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:76474280-76475750 |
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) |
NFYA | MA0060.3 | chr11:76475356-76475367 | TCTGATTGGTT | - | 6.62 | Nfe2l2 | MA0150.2 | chr11:76475287-76475302 | CACCATGATTCAGCA | + | 6.82 | Nkx2-5(var.2) | MA0503.1 | chr11:76475244-76475255 | CTTGAGTGCCT | - | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_26826 | chr11:76473940-76476097 | Esophagus | SE_33832 | chr11:76474085-76476157 | HCC1954 | SE_34932 | chr11:76474172-76475929 | HeLa |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr11 | 76474777 | 76474856 | chr11 | 76474549 | 76475408 | chr11 | 76475426 | 76475558 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I076763 | chr11 | 76474293 | 76475698 |
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Enhancer Sequence | TCCTTCCTTC ATCCATTCAT CAGATAGCCC CTGACAGCAT CGCTGTGCTG GCACAGGAGT 60 AATGCAGGGA TGACGGAACA GCCCCTGTAG GTTCCCCAGT CTGTTTCACT TTGATGGCAT 120 TACCTGTTAA GCACCCAACT TCTCCACCAG CCCGGACCCA GGTGAGGCTG GAACCAGGTG 180 AAACAGGACC CAGGTAAGGC TGGACCCAGG TAAGGTGGGA CTCAGGTGGC ACAGGGCATG 240 GGAGGTACTC TCTAAATAGT TGTTCAATGT TAAAGGAATG GATGAACAAA TGAATGAATA 300 GCCAGGTCCA CAGGAATACT TTGGTAACAA GATGCTTACT GCTTCAAAGG AAGCCCATTT 360 TCCTAAAGGT TGGAGGTGAC AGACCCAGGC TGAGGCAGGC ATAGCTGGCC CAAGATCTCC 420 TTCTGACATG GGAGGTGGAA TCCACTGGAG AAGCCGCTGC TACCCAGAAC CTTCCCATAC 480 GTGCCTGGGC TCCAAACTGG GAGCTGGCGG ATTCCCCAGG CCTGGAAACC CCCAGTAGGG 540 TTGTCTGACT CCACCCACAC CCCACAAGGC TGGTCATTCT CAACCCTGTT TCTTGGAAGG 600 AGAAACTGGC TCATGATCAG ACGTTCTGGA ATTCACTACA GGAAGTGGCC ATTGAGTGAG 660 AGGAAAGGCC CCTGGTTAAA TGAGCCAAGA ATTCTGCATT TTGATTCCCA CTCCAACATT 720 TAAAGCCATG GGATGCAGGC TCAGACGGAC CTGGGTTCAA CTCCAGTTCT GCTGTTTAAG 780 AGCTGCCTGG TTTCTGGAAA GTTACTTACT TCACTGAGCC CTGGTTTCCT CTTTTGGGAA 840 AGGGATTATA GTATCTGCCT CAACAGGTTC TTGTGAGGAT TCTAAGAGGA ACCTGTAGGG 900 CTGATACTCA GCTGGCATGC AGATTCTAAC TTACTGCTTG GTAAACAGCC ATGACTCAGA 960 GCCCCTTGAG TGCCTCTGCC ATGCAACCCA GCATCCCCCA ACCTTCCCAC CATGATTCAG 1020 CAACCAAGGG GTTAATATCT AGCCCCTCAG AAGGTCCTCA AGATCCTGGC AACCCTTCTG 1080 ATTGGTTGCT GCCCATACTG AACTAAATGG GTGCCAATAA ATGCTCTGTA AACTACAAAG 1140 TGCTGGCTAA CCCCAGATCC ACACTTCCAG CTCCAATTTA TCTCCTGGAG GCTCTTCACC 1200 CACCTCCCGG CCCTTCCACC TTCATACTTC ATGCAAATGG CACTCTCACA ACTCCCAAAT 1260 TGAACTGAGT TTCTCCAGTT AAACTCATCC CAGGGACTGC CTCCACCTCT GCCTGGCAGA 1320 CTCCTTCATT ACCCAGTCTC TATCTGGCAG TGCTGTTTCC TCTATGTCCC CTAGCTCTGT 1380 CCCTCCTTCC TGCCCCCACC CACCTGGTGC CTTCATCATT TCTCTGCTAA ATCACAACTA 1440 CCTTCCCACT GGCCTCTGGA CTCCAGTGTG 1470
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