Tag | Content |
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EnhancerAtlas ID | HS184-14574 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr18:20045860-20047060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr18:20046683-20046701 | GGAAAAATGGAAGGAATG | + | 6.09 | FOSL1 | MA0477.1 | chr18:20046155-20046166 | CATGAGTCACC | - | 6.62 | FOSL2 | MA0478.1 | chr18:20046156-20046167 | ATGAGTCACCC | - | 6.14 | IRF1 | MA0050.2 | chr18:20046549-20046570 | GTCTTCTTTTACTTTCTTTTA | + | 6.19 | JUNB | MA0490.1 | chr18:20046156-20046167 | ATGAGTCACCC | - | 6.32 | JUND | MA0491.1 | chr18:20046155-20046166 | CATGAGTCACC | - | 6.02 | Myog | MA0500.1 | chr18:20046309-20046320 | GACAGCTGCAG | + | 6.62 | Tcf12 | MA0521.1 | chr18:20046309-20046320 | GACAGCTGCAG | + | 6.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_48987 | chr18:20045421-20049085 | Right_Atrium | SE_65170 | chr18:20045383-20049854 | NHEK |
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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 |
GH18I022465 | chr18 | 20045407 | 20052904 |
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Enhancer Sequence | CTGAAACTCT GGGGTCAAGT CATATGGCTA CGAATGTGGA GCAAAGCAAT ATGGAAACAA 60 TATGTTCAAC TTTATGACTA GTAACTCATT GGCTCATGGA CAGCTTTGTC CCAGCTTCTC 120 TGGGGGTAGT TTTCCTGCTG CATGGCACAC ATTTGAGGAG CACTGGAAGT CCCACAGTTT 180 TTCCCACACT ACAGTATTCT GAGTATTGCA AGTAGAGATG GAACGGAGAG TGGGTTTGTC 240 AAAATAAGCC AGCCCCACAT TGAAAAAGTC ACGTGTGCTT GGTGCTATCC ACAAACATGA 300 GTCACCCAGG GAGGTATGTA GATGCTTGTG ACAAGAGAGG AGAGGCCTAA AAATAACAGT 360 TCCACTGAAG GGTGGAGCTA CAGGCTGCTG GTGTGTCATG TTTGGCTGCT GCTTCTGAAA 420 ATTCCTTCAG TTAAAGTAGC AAGTGGGATG ACAGCTGCAG ATACCTGGCT TTCAGGAGAG 480 AAGTGTAGCA GGTATCCATT GAGGGGGGAT TTCAGGGTCA TGAACTCCTC CTTATTACTT 540 ATTTCCTGAA GCTGATGTGT GAAAATCCAT ACAAGAATCC CACATCTTTA GTTAAAGACT 600 TTGATCCCCA ATAAATCAGA ACGACAGCAC ATTCGGCTGT TCTCAGTGAC ACATTTGAAG 660 GTTGCTGGAG ATACAAGGAT GCTCAGAGTG TCTTCTTTTA CTTTCTTTTA ACTTTCTCCT 720 GCTGTTCCAT ATACTACATG AGGGCAAGGA CCTTGTTTGT CCTGTTTTCA GTTCCATCCT 780 CGGTGTCTTG CACAGAGCAG GAGCTAAATA AATATTTGCT TAAGGAAAAA TGGAAGGAAT 840 GTGTCTAGCC CAGCCCTCTT AGTTTGCAGG CAAGAATACT GAGCAGGGAG AAGAAACTTG 900 CTCAGGATCA TGCAACCTAT CAGCAGGGGT AGGAGGGAAG CCAGCCTCTG ACTCTCCACC 960 CAGTGCTCTC ACCTTTCCAA CAAGCTAGCA ATGACTCAGT GTGGCTAGAA GTGTCTTGTT 1020 GAGGGCAAAG ACCAAACACG AGGTCTCTGG CTACTAGGCT GAGGTGGACA GTATGGGGCA 1080 GCAGTTCTGA GGGGGGCCAA AAGATAGTGA ACTTCACTGG GAGGAGGTGA CAAAGACAAG 1140 GCTTGCCACT GGAGGCTGCC CAGCAAAGTT TCAAGGGCAC AGTGGTGCTC CTTTCTGAGC 1200
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