Tag | Content |
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EnhancerAtlas ID | HS183-01535 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr14:105240320-105241270 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr14:105240492-105240512 | CCCCACACCACACACCCCAT | + | 6.05 | RREB1 | MA0073.1 | chr14:105240496-105240516 | ACACCACACACCCCATCACA | + | 6.12 | RREB1 | MA0073.1 | chr14:105240519-105240539 | CCCCACACCATACACCCCCA | + | 6.15 | ZEB1 | MA0103.3 | chr14:105241055-105241066 | CCCACCTGCCC | + | 6.14 |
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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 |
GH14I104773 | chr14 | 105240305 | 105242303 |
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Enhancer Sequence | CAAGGAAGGG GAGCTGGAAC TGCGGCCCCA CAGGCAGGAC GGCAGCCCCG CACCACGCTG 60 CCCGACACCA CGCTGCTTGA TACCACGTCG CCTGATACCA CACCGCCCGT AGCCCCACAC 120 CACACTGCCC GACACCACGC TGCCTGATAC CACACCGCCC GATACCACAC TGCCCCACAC 180 CACACACCCC ATCACACTGC CCCACACCAT ACACCCCCAC ATCACACTGC CCCCATGCCA 240 CGCTGCCCCA CACCACACTG CCCCACACCA CACTGCCTCA TGCCACGCCA CCATCAGGCT 300 GGGCCCCGGC AGCCCCTGAG GTGCCAAGGA GTGTTTGAAA GGTGAGCAAG GTGGCCTGGG 360 CTCAGGTCCT CCAGGGTGAG TTGGGACCTC AGCAGGGGAC AGTGCTCCCA GCACCAGGGC 420 CTTCGCAAAG GGAGGACACA CCCTCCCAGG CGAGACCCAC CCTCCCGCCT TCCACCACAG 480 GCGACTGTGC TTTTAAAGCA AAGGCCCCAT CTGCAGGAGA ATCGTCCCCA AACACAGTGA 540 CCTGGAACTA ACCAAGTGGC TGGACCCTGG CCCCCTTCAC AGTAAATACC TCCTGGGCCA 600 AGTCCCCAGA ACAGGTTCTG CAGGACAGAG CCCGGGCCTC AACAAAAGCC TGGCAGGCAG 660 GGCTGCAGGG CATGGGGAGC TGGGGCCTCC TGGAGCCTCG GCAGAGTGCA AGGAAGACCA 720 GGGCCACCTG CCCCACCCAC CTGCCCGCAC ACGGGAGCAG CGAGCACAGC CCCTAGCCCA 780 CACTGGGCAC CTCCACAGCC TGACCCTCCA GGGCAGGCCT GTCTCACCAG CGGCGGAGTC 840 CACGGTGTGT AAAGCCCTCA CGTGCCCAAG AAGACAGGAC ATCGTCCCCT AGAGACAGCC 900 CCAGGAGTCG CTACCTGGCC CCAGCCCTTC AGCCCCATCT GGGCTCCCAC 950
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