Tag | Content |
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EnhancerAtlas ID | HS184-01330 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:120308160-120309480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:120309361-120309379 | GCTCCCTCCCTTTCTTCC | - | 6.25 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28136 | chr1:120307995-120312773 | Fetal_Intestine | SE_29167 | chr1:120307961-120313155 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 120308828 | 120309174 | chr1 | 120309259 | 120309370 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I119766 | chr1 | 120308041 | 120308190 |
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Enhancer Sequence | TTATAACATG CATAATTGGC TTGTTGTAAT CTTACTTAAA TTAATACTTA TCTTACTTTT 60 GGAACACTGC AAAAACTTTA GGTTGACTTT ATTTACTCTC TGCATCCTTT TGAACCATTA 120 TTGTCATATA CTTTACTTCT ACATGTTATA AGCCCTTATA GGGCATAATT ATACAATCTT 180 TACTCATTTT AAAAGTGTAC CTCTAATTAC ATGTCTTTCT CCTTTCTTTT TTCTACACAA 240 GAACATACCC ACTGTTTTCC TACTTTTAAG TAAGTTTTCT GCTAGCTGAT TTTTCTGATA 300 GGGCCTTCCA ATGTTTATTG AGCACACCCA ACACAGTTCT AGTCCAAATA CACAGCAGTG 360 AATAAGACAT GCATTGTGCC CATAAAGAGA GCACAGCCCA GTGAAAGAAG CAGACATTTT 420 ACAGCTAAAT ATGCAGGGAA CACAGACAGC AGAAAGAGCA ATTCTAAACG AGAGCAGAGG 480 AAAAAAGGAA GGGGAAGGAG TCAGCAGAAG AAGGGAGAGA TGATCTATTT CTTTTCTGGA 540 CCAATTCACT TCTCTTTAAC CCAGATTCTT AATATCCCTG GCGAAAATCT GTGTTCCCTT 600 TTGTATGGGA GCATACTGGA GGTGAACTTG GTGATCTCTG TACTGCTCCC ATACAAAAGT 660 ACTTTATACC TTCTGTTCAC TTTAGCAACA TTCTTCATTT TATAGTTAGT GAAACCAAGG 720 CACACACTGG TAAAGTGATG CACTCAGGGT AACTTCATAG TTTCTCACGT GTTAGAAATA 780 CTCTGTCCCT TCACTGCCCT GGGTGCCAGG CTTATAAATT TAGCTCCATT CTACGGGAGC 840 TGGAACTCAG ATTGAATGTG TCTATCAATC ATCTTTGGGA TTCTGAGCCT CTGGTAGAAT 900 TCTAGAGCCT CTCCCAGCAG CAAGGTCACT TCTAAGGACA GCTGTGAGGC AAAAGTGGAT 960 CATATGATCA CAAGATAGTG AGGCAGAATG ATAAATACAC ATTATATCTG ACAGGAGAGG 1020 TTTGGAGTTT ATTTATCTTC CCTATTTATT TGACTCCCTC CAAATAACTG GAGTTTGTAC 1080 TCTCAAATAT TTACGGAGGA GCTTCCCCAG TACCCGGGAG CTAATGGTTA AGCCAGCGCT 1140 TGTCCTGCCA GCTTGGCTGC CTTTCTCTCA GCCTCATTCT CGCTCTGACT TCTCTGGGCT 1200 GGCTCCCTCC CTTTCTTCCC AGTTAGAAAT CAAAGCTTGC AAGAAGAAGC TTAGAATGGG 1260 TCAGTTGGTA ACTTTTGTAG CTGTCTTGGT GGGGAGCTAT TTCTAGAAAT GGATTATAAA 1320
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