Tag | Content |
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EnhancerAtlas ID | HS184-05126 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:17007940-17009820 |
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 | chr11:17008409-17008427 | GGAAGGGAGGCAGGAAAG | + | 7.67 | IRF1 | MA0050.2 | chr11:17008138-17008159 | TATTTATTTCACTTTCACTTT | + | 6.96 | PRDM1 | MA0508.2 | chr11:17008146-17008156 | TCACTTTCAC | + | 6.02 | SNAI2 | MA0745.2 | chr11:17009563-17009573 | TGCACCTGTT | - | 6.02 | ZNF263 | MA0528.1 | chr11:17008941-17008962 | GCTCCCTCCTTTTCCTCCTTA | - | 6.37 | ZNF740 | MA0753.2 | chr11:17008805-17008818 | CCACACCCCCCAC | + | 6.03 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_23209 | chr11:17006345-17010079 | Colon_Crypt_1 | SE_24588 | chr11:17006954-17010047 | Colon_Crypt_2 | SE_27642 | chr11:17005603-17011510 | Fetal_Intestine | SE_28618 | chr11:17005858-17011943 | Fetal_Intestine_Large | SE_31464 | chr11:17005871-17010093 | Gastric | SE_42048 | chr11:17006935-17008802 | LNCaP | SE_42048 | chr11:17008809-17010048 | LNCaP | SE_48027 | chr11:17007452-17009993 | Pancreas | SE_50712 | chr11:17006304-17010109 | Sigmoid_Colon | SE_52571 | chr11:17006346-17010116 | 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 | CGAATGAGCC CAGACACATT TTGAGTACAT AAGAAAAGTG CAGCCCCACC AGAGCCCTCC 60 TGGGAATGCT GCAAAGCTGC TGGGGAGATG CCAGCAGAAC CATGTCACAC CTTGCCCACA 120 GTCACCAAAG TGGGGACCCT ACTGACTGGC TGGAGGCAAG GAGGAAGTCA GGGGAGAGAA 180 ACCATAAAAA TTGCTCACTA TTTATTTCAC TTTCACTTTG AGCACACAAG TGGGGAGAAG 240 ACGCCCTGGC CCAGGAGTAG AGAAACCTGG CTGGAGTCCC AGCTGTCACC AACAACCTGA 300 GTAACCTTGG GCAGGTGACT TCACCGCTGG GGCTCAGCTT CCCCATCTAT AAACCAGAGC 360 TTCCACCATG AGCCCCACCT CTACCAACAT CCTGGAAAGG CCCCAATCAG ATAAGTATCA 420 GCTCTGCATA GCTTTATGTA GCACCTACTA TATGATCTTC CTTGTACCAG GAAGGGAGGC 480 AGGAAAGGGG CAGGCCGAGC CCCTGCCCAG AGAAGGTTTT AACAAGGTGG TCCAAGCAGG 540 TACTGCAGAA CACCGGCAAG GGCATTTCCA GCCACATTCT CCAGCCAGTC TTACTGCCCA 600 GCCCAACCCA GCCCAGGGAA GGCGGAGAGG AAGCAGTGAG CTGTTTTACA ATCCATCAAA 660 TTAATTGCCC CAAATGGGAA ATTTGCAGGC CTCCTACAGC CTCCTGTGTA TTCCATAATC 720 TCCCATGGCC CTAATCTGCT GAGAAAGAAT GTGTGGGCTG TAATCTTTTC AGCCCACTGT 780 TCACAGGGGC AATGCCTTGG AAAAACCTCA GTCCCCACCA GTGATCACTC CCTCCCAACC 840 AAAAGCCTCC CCGACCTCCC ATCCCCCACA CCCCCCACTG ACCTGGTGGC CAGCCAAGGC 900 CTGGCTCCGC CCCCCAGAAG CCAGCTAGGC CAACCTTGGC CTTGACTTTG ACCTCGGAAA 960 GGAGACCTGC CCAACCAGCT CCTTTGGTAA ATACAACTTT TGCTCCCTCC TTTTCCTCCT 1020 TAAGACAGAA CAGCCTGGCA GGAGGCAGAA CCAGGAGAAA TGGCTTCCGA GTAGAGACGC 1080 ACCCTTGAGG CGTGGTGAAA ACAGCCCCAG GTGAGGTGCT GGGCATTGGT TCTAACCTTT 1140 GCTTACCCTA TCCCTGCTAG GAAACCCACT TCCCATCTCT GGACCTCATC TTCATTTGAG 1200 AAATGAAGGG AATGTAAAAC AGCCTCCCAG GAACTCCTTA CCCCACCCCT TTAAACAAGT 1260 TGCTTCTTTG CTTCTGCTGT AACCTTTGCC TGCTCCTTTT CCTGCATAAT GAAGCCTCTG 1320 TCTAGGCCCA ACTCAAATGT CACTTTCCCC ACGAAGGCTT CCTGGATCCC TCCCTTCTCA 1380 ACACCTGTCC CAAACTCTTT CTGCCTCCTA CACTCAACTA GCCTTGAGGG CAGAGGATTC 1440 TTTTACTCAT TGCTACTGTC AGGAAACTCA TTTGATAACA TATTTCAGAG AGCTCTGGAC 1500 AAACCTAGGG CCAAAACCTA TTTCATTCTC TAAAATACCT GGCATGGCAC AGATCCTGGG 1560 TCACCACCAC TGGGTGAAGT TTTCTCAGAC AGTGTGTGGA AGGCCAGGCT CCCTGAAGTT 1620 GACTGCACCT GTTAATAACC AGTGTCTGTA CCCTCTCTCC TTAACAAAGT GCTTTCCTAC 1680 TCACTACCTC ACCTACAGGG GAAGGACTGA TGTGATCCCC TTTCACAGAG AAGGCAAATG 1740 TCTTGCCCCA GGTCAGGCAG CTGTAAGGGG CTAAGCCAGG ATCCAAACCC AGGTCTCCTA 1800 ATTCTGGTTC TAACTTTGTG TTCCTCCCAC CGTACCTGAG GGAACATGCA AAGCTGAGCC 1860 TATTGAGAAG ATCTGGGCTT 1880
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