Tag | Content |
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EnhancerAtlas ID | HS184-05125 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:17003050-17004350 |
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) |
KLF16 | MA0741.1 | chr11:17003184-17003195 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr11:17003185-17003195 | GGGGCGGGGC | - | 6.02 | SP3 | MA0746.2 | chr11:17003183-17003196 | GGGGGGCGGGGCG | - | 6.11 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_23209 | chr11:17003257-17004864 | Colon_Crypt_1 | SE_24588 | chr11:17003742-17004100 | Colon_Crypt_2 | SE_27642 | chr11:17003136-17005460 | Fetal_Intestine | SE_28618 | chr11:17003274-17005242 | Fetal_Intestine_Large | SE_31464 | chr11:17002653-17005643 | Gastric | SE_42048 | chr11:17003270-17005276 | LNCaP | SE_48027 | chr11:17002785-17003245 | Pancreas | SE_48027 | chr11:17003359-17005490 | Pancreas | SE_52571 | chr11:17003359-17004845 | Small_Intestine |
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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 |
GH11I016978 | chr11 | 17000394 | 17011590 |
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Enhancer Sequence | CAGGATATCT CCCAGCCCCT CCAGCCCCCT ACCCTCTCCC TTTCTCTCAC TATTTCCAGT 60 CAGCCCAGTG CAAACCATGC CCTGGCTAGA AACACCATTT TCCCCCAAGA GGCTGCTAAT 120 AGTAGACGGG GTTGGGGGGC GGGGCGGGGA AGGAGCTGCA ATAACTTGGC TCTTGAGTTG 180 CAAAGAGAAA AATGAAGGAA TGAGGAGGAG TGGGCCACCA GATCCCCACA GATTCCAGGG 240 TGGAGAATGT CCAATTAAAA TGCATTCTGC CAGAGCCCAG CAGCAGCATT TCAACAGAGC 300 CACCATTGTC TCCGTCTGAA CTGCTGCTGC CCACAGCCCA GCAAGTGGCA ACCAAACAGG 360 CTGTCGTCAT GGAGCCGGAA TGCAGGGTCC TGGCCCTCCC CGAAGGCACC AGAAACACTG 420 CTCTGTTTAC CCACGTTGCC CTTATTTAAA AACAAAACAA AAAACCCCAC TCCACCCTCG 480 GCCCTTCGGC ATGCAAGACA CCAGGAAGGA CAGACGGTGG TGAGAGGACA CTCCATATGC 540 CAGCAGCGTG AGGCAGGTCT GCCAGAAGGT TCCCAATGAT CTGGCCAGGC TGGGGGGAAC 600 AAGTCTCCCC CAGGAAGCTG GGAAAGTACT TTGGAAATAT ATAAAAATCA GATACAAATA 660 GATATCTGAA TGGGGCATAA AGAAACTGTT AATGCCCTGG AAGGGCCCCA AGCCCCTTTA 720 CAAAAGCTTT ATGCCCAAAG AATTTGGCCA AGGGCAAATG CAGGCTCCCT GCATAAATCA 780 GAAACCTTGC AGGGCAGAGA CAGACCTGTG TGTCCAGCCA CCTCTGGGAC ACAGGCAAGC 840 TTGAGGCGAG CCAGTTGCCC CTGGCTACAG CACCTGGCCC CCACCCCAAC CCAGGAAAGG 900 GGTGCAGGGG CTGAAAGCCT GGCTCATCCA GTGCTGAGCC CAGAAACAGA ATGTCCAGGG 960 TGACTAGCAC ATTCAAAGTG CTTACTGTCC CTGTCCCACT CTACAGAGAT CTCAAGGACA 1020 GGTTTAATCA GGAACCCTAG ACGAAAGCAG GAAGCAGAGT CAGTGGTGCT CAGAAAGCCA 1080 TTCATCAGCT CTAGGCCAAT GTGAAACCCG TGGTACCGGA GCCCCAAACA AACCAGTTCT 1140 AAAACCCGTC CTCCTGTGCA GCTCTCTGAC CTCTGCCACC TGTGTCCACG ACCTGACCCA 1200 GGCACAGGTG GCCCTCCATG CTTTAGCTTG GGTCTACCTC TCTTACCTCT CAGACTTCAC 1260 CTCCCTCACT ATCCCCTACA CACACACACA CACACACACA 1300
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