Tag | Content |
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EnhancerAtlas ID | HS073-04951 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr16:1763610-1764530 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PAX6 | MA0069.1 | chr16:1764226-1764240 | TTCACGCATGAGCG | + | 6.37 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_10840 | chr16:1762013-1765879 | CD19_Primary |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH16I001712 | chr16 | 1762281 | 1765040 |
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Enhancer Sequence | ACAGGAGAAA ATATTGTGAG ATGGGAAAGT GGATGCCAGC AACAGGAAAC AGCAGAGAGG 60 GGCTGAAGTT CTCGAAAGGC CAAGAAGAGC CTGGTGGGAA ACCGCTCGCA CCTCAGGACT 120 GCCTGTGCTC AGGGCACAGG ATCGACTTTT TCGCCTTGGG CTGCTTTTTG TTTTCTTTCT 180 GTGGGTAACA ATTTTATTGC AGTATCATTG ACATACACTG AACTGTACAT ACTTAAAGAG 240 TACAATTTGA TGAGTTTTGA AATACGTATA AACACCAGAA GCCATCCCTG CAGTCCAAGC 300 AGCGTAGACG CCCGGACCCC AGAGTTCCCT GTGTCCTATG TAATCCCCCT CCGACCCCTC 360 CTTGCCCCAC CTGTCCCCAG GTAACCACTG ACCTGCCTTC AGTCACTGTA GGTTAATTTG 420 CATCTTCTAG AGCTTTGCAT AATGGCCTCC TGCAGTGCGT ACGTGGTTTC CTCTGACATC 480 TTCCACTCGG TACAGTGATT CGGGGACTCA CCCAGGCTGT GTGTGTCCTT CCCCCATGGC 540 CAAGCAGGGT CCCAGCAGTG CCGTTTGTCC ATCCGCCTGC CTGCAGGGGA GCTGGGCGGC 600 TTGTTTTTAC GTAACCTTCA CGCATGAGCG GTTTGTAAGC CCGCTCACCC CGTTGGCAGG 660 GTGTTGGGCC AAGCACTGCT CTGGGGCAGG CTGGCAGTGA AACCCAGAGA CTAGAATCCG 720 CTTATGAGGG GGGTGCGTCT TTGCGGAGAC CCTTAGAGCC CACAGCATCA TTACTCTGGT 780 GCATTTTCTT TTGAGCCACT GTTACGGCAA GAGATCCAGG GCGTGCCACG TGAAACGCGA 840 CAGGGCCTTT CCTCAAGACC TCTCCTCCGT GTGGTGCGTT TCTCACACAG GGTCTAGGAC 900 ATTTCAATTC TTGTTATCAA 920
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