Tag | Content |
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EnhancerAtlas ID | HS112-06778 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr18:55869020-55870550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr18:55869711-55869722 | GGTGACTCATG | + | 6.62 | FOSL2 | MA0478.1 | chr18:55869710-55869721 | GGGTGACTCAT | + | 6.14 | JUNB | MA0490.1 | chr18:55869710-55869721 | GGGTGACTCAT | + | 6.32 | JUND | MA0491.1 | chr18:55869711-55869722 | GGTGACTCATG | + | 6.02 | NR3C2 | MA0727.1 | chr18:55869023-55869040 | TGGTACATACTGTTCTG | + | 6.03 | Sox6 | MA0515.1 | chr18:55869203-55869213 | CCATTGTTTT | + | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27800 | chr18:55869040-55870289 | Fetal_Intestine | SE_28643 | chr18:55868651-55870453 | Fetal_Intestine_Large | SE_41571 | chr18:55869281-55870207 | LNCaP |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr18 | 55869037 | 55869309 | chr18 | 55869311 | 55869996 |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I058201 | chr18 | 55868921 | 55870489 |
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Enhancer Sequence | ACATGGTACA TACTGTTCTG AGCCCTGGTT TTCTTTTTTT CACTTAGCGT TGTATACTGG 60 AACTCACTCA ATGTCAGTAT ACAGAGAATT CCCTTGTCTT TTTATAACTC TGTGCTATAC 120 GCTGACGGAA GTTCATTCAG TCAGTCCCCT ATTGATGGAC ACTTGAGTTA TTCTCAGACT 180 TGTCCATTGT TTTGCAAAAA TAGCCCTGGG CATATGTCAT TTGGTATTTT TGTCGAGGCA 240 TTCCAATAAA AATAAGTAAA TTCTTCCTCT CTTGCCTTGA AGATGTGCAG CTCCTCAGTA 300 ACCTTTTATT CTCTAAAGCT CTGTCCTCAT CTTTAATCCC TGATTTAAGA GGTGCAGCTC 360 TTCAGGCCAT AAACCTTTCT TCCTGCCTCA AGTTTTTAAA GCTACAAAGG AACCTAAGAG 420 ATCCCTTGTG TTTTACAGCT AAAGGACCTG AGAGCAGGAA ACAAAGGGAG AGCCGGAAGC 480 CCAGGTCTCC TGTTCCCTGC CTGGCAGGTG ATATTCTTTC TGTTAAACTC TCTTTCCCTC 540 TGCCTATTAT TGGCCAGGCT GTCCTCCAGG ACAGTGCTTG CCAAAGTGTG GTCCATGGGC 600 AGCAGCATCC CCGGAGCTCA TCAGCAATGT AAGATGTCAG GCCCTGCCCC AGAGGGGCTG 660 AGATAGAATC TACCAATTAC TGGATTCCCT GGGTGACTCA TGCAGTCAGG TTGGAGAAGC 720 GCTGGACTGG TGGCTTTCTC CAGAGGAGCA TGCAACAGCG GTTTGCAAAC AGGGATGATG 780 CAGTTCCTTT TCAACACGTG GATTTGCACT TCCTCCTGGT GCGCTCCTCC AGCCTGCCTG 840 TCCTGTTCAC ACCAGCCTCC CCCTGGAAGG GGTTCAGACT TGATCCTTTG GGTGGTAGGG 900 TCTTTCTTGG ATAGCGTAGC CATCCATTCC TGCTGCATAC ATTCAACACA GCCTTCATCC 960 TTCGCCATTT GTCTCTGATA CTTCATACTC CTTTTGTTTG ACAAGTGCCC TAGCTTTATT 1020 TATTTTCTCA TCATTGTTGT TAAGGGCCTA TTGTGCTTGC TAGTATACAC ACCACTATGT 1080 AAGTTACTAG TTCAATTTAT TTGTTTTACT GCTGCTGTGA GGTGTGTCCA TGTGTGCACA 1140 TCTACCTGTG TTAATAACTG ATAATATTGG GCCTCAGTAC ATACTTTTTT TTTTTAAGAG 1200 ACAAGGTTTT ACTTCGTCAC CCAGGCTGAA GGACTGAGAC ACACTTGTAG CTCACTGCAG 1260 CCTTGAGCTC CTGGACCCAA GTGATCCTCC CACCTTAACC TCCTGAGTAG CTGGGACTAC 1320 AGGCACACAC CACCACACCA ACTAATTTTT TTATTTTTTG TAGAGACGGA TTCTTACTGT 1380 GTTGCCCAGG CTGGTCTAGA ACTCCTGGCT TCAAGCCATC CTACCACCTC AGCCTTCCAA 1440 AGTGCTGGGA TGATAGGTGT AAGCCGCCGC ACCTGGCCCT CAGTGCATAC TTAGATATAC 1500 TTAAATAAAA ACTTAATTGC AAATTACTTC 1530
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