Tag | Content |
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EnhancerAtlas ID | HS023-09201 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr16:24983920-24985050 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELF4 | MA0641.1 | chr16:24984338-24984350 | CACTTCCGGGGT | - | 6.02 | Gabpa | MA0062.2 | chr16:24984336-24984347 | CCCACTTCCGG | - | 6.02 | HOXA13 | MA0650.2 | chr16:24985000-24985011 | CCCCATAAAAC | + | 6.02 | YY1 | MA0095.2 | chr16:24984062-24984074 | CAAGATGGCAGC | + | 6.32 | ZBTB7A | MA0750.2 | chr16:24984336-24984349 | CCCACTTCCGGGG | - | 6.92 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_11037 | chr16:24983559-25004231 | CD20 | SE_27894 | chr16:24984375-24988067 | Fetal_Intestine | SE_28675 | chr16:24984195-24988697 | Fetal_Intestine_Large | SE_54347 | chr16:24984098-24985653 | Spleen |
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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: 2 | ID | Chromosome | Start | End |
GH16I024972 | chr16 | 24984021 | 24984170 | GH16I024973 | chr16 | 24984537 | 24992604 |
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Enhancer Sequence | TGGTTATGCT GCCTTTCTAA AGGAGGTTAA ATACCTATTA AAGATCAATG CAATAATCAA 60 GACAAATATA TTGTGCAACT CTGGAACTCT AGGAGTCTAT GGAAAAAAAA TAATAGAAAA 120 CTCTATTTTG ACAAGCATCA CTCAAGATGG CAGCTGTAAA TAGTTTTGTG GTTTCCCTAA 180 CCTGACCCCA AAGCCACAAC AATCTTGTTT CCTATGTACA TAAATAAGGA AACTCTGCTT 240 AACATATGGG CTCATTAATC AAGTATCAAC ACTGAACTCC TCCACAGGGA GGGCTTCGTG 300 CTTCCTAGAG GTGAACAGCT TTCTATCATC AGGGATAATT TTTTTTTTTT TTTAAGACAG 360 GGTCTGGCTC TGTTGCCCAG GCTGGAGGTC AGTGACGCGA TCTCAGCTCA CTGCAACCCA 420 CTTCCGGGGT TTTGCCATGT TGCACAGGCT GGTATCGACT CCTGAGCTCA AGCAATCCAC 480 CCACCTTGGC CTCCCAAAGT GCTGAGATTA CAGGAGTGCA GCACCATGCC TGGCCAGGGA 540 TGAATTTTAA ATGCTCTAAA GACTTAATTT GTAAAATGCA TGCCAATCGC ACAAAAAGAA 600 ATAATTCTCT AATCTAATAA TCTATCTTAT CTGACCCACG ACAGTTCTGC CATGTCAATG 660 GTGGCTGGGC TGCAAAGGTC ACCTGCCTCA TGTCTCTCTC TTCCCTTCTA TTCTTGCCTC 720 TTCCCATGCA GGAAGCATGT TATGAGGCCT TTGGGAGGTT CCTCCTGTGT TTTCTAGAGC 780 CCTGGAGACT GCTGCAATTT TCTCCATATT AGTCTTCTCT CACCATTGTT GTGGTAACTC 840 CTCTTCCCAA GTGCAAAGTG TAGGCATCCT CAAAGCCCTG TCTTTGGCAC TTTCGTTTGA 900 CGTTGGAAAA GGAAAGCTAA AGCATTAGGT TTCAGAAATG AGGGCCAAGC ACTTTGCCCC 960 AGCTGCCTGG AATATTCCCA CCACCTGCCA CTAATTTCCC TCCTTTATAG GGCAGACACC 1020 ACCTCCTCCA GGAAGCCTCA CCTAACTACC TCCCTCTTCC TCTGGTACCC ATTCTGGGCC 1080 CCCCATAAAA CCCTGTGCAT GTTTTATTGA GCATCTTGTT TTATAATGAT 1130
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