Tag | Content |
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EnhancerAtlas ID | HS176-11304 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr13:46912600-46913790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPI1 | MA0080.4 | chr13:46913401-46913415 | AAAAAGGGGAACTA | + | 6.39 | Zfx | MA0146.2 | chr13:46912951-46912965 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_09573 | chr13:46911853-46917306 | CD14 | SE_11021 | chr13:46911294-46921293 | CD20 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr13 | 46913143 | 46913601 | chr13 | 46913374 | 46913400 | chr13 | 46913400 | 46913693 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I046338 | chr13 | 46912598 | 46916454 |
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Enhancer Sequence | GCCCTAAAAG TGGGGTTGAG ACCACAGGGC AGGGGATTCT GTCTGGGGCT CCATTTGATC 60 TAACAGGAGG GGTGGGGGCT TTGGGTGCGC TTGCCCTTTG TCTCCTCACC AATGGGGATG 120 TACGTAGCCC GAGGAAGGCC AGAGCAGGGC CTCTTTCCAG GATGAAAGGG CAGTCCTGAT 180 CCCAGGCAAG GGATGCAAGA AGAACAAGAC CATGGAGGCA GGAACACGGC AGGACTAGAA 240 AAGAGGGGGC AGCCCTGGGG AGAAAGAAGC CTGGAAGCAC AAGCAGAGGC CAGAAAATGT 300 TCAAGGAAGG GCTGGGCGCG GTGGCTCACA CCTGTAATCC AAGCACTTTG GGAGGCCGAG 360 GCGGGTAGAT CACTTCTGAG ACCAGCCTGG CCAACATGGC GAAACCCCGT CTCTACCAAA 420 AACAGAAAAA AATTAGCTGG GCATGGTGGC ACATGCCTGT GGTCCCAGCT ACTAGGGAAG 480 CTGAGGCAGG AAAATCGCTT GAACCGGGAA GCAGAGGCTG CAGTGAACTG AGATCACGCC 540 AACTGCACTC CAGCCTGGGC GACAGAGCGA GACCCTGTCT CAAAAAAAAA AAAAAAAGTG 600 CAAGGAAAAA TACACAATTT GCTTAACCTA TGTGGTTAAG CTCTTCAATC CTCAGTCCCC 660 TTGGCTTGGA GAGCTGCCCA GATATGCGAG GATGCAAAGG TTCTCGATTT CTCATGTTTG 720 TGCTGAAGCT TCCCAATTGT GTCTGCAGCC TGCTACCTCA GCATTACTCA TAAAAGTATT 780 GTTTTAGTTT CTAGTGAAGT GAAAAAGGGG AACTACGGTT TTCCTTCCCA TACCAGTTGA 840 GAAATTATTT AAAGACAGAG ATCCTTAAAT GCTTGTTTTA AGGAAGCACG CTTCTAAAAA 900 TGACACACTT CACCCTCCTT TGGCGATGAG TTCAGGAAGG CTTCCTGCAG GTAGCATCTG 960 ACGGTGGCTA AGCCAGCCAT GCAGGCTCAG ACCTGGGGGC AGAAACTGAA TGTCAAACCC 1020 CTTCCTGACA TGTCTACCAC GTTCCTTCCA GCAGGTTTGA ATTCCGAAGT CTCAGACAAA 1080 TGACCACACT CTGGGTGGTT TAAAACAACA GGGTCAGGCG CAGTGGCTCA GGCCTGTAAT 1140 CCCAGCACTT TTGGAAGCCG AAGCAGGCAG ATCACCTGAG GTCAGGGGTT 1190
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