Tag | Content |
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EnhancerAtlas ID | HS034-16936 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr2:107501500-107502540 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6 | MA0463.2 | chr2:107501906-107501922 | AATTCCTGGAAAGCAC | - | 7.42 | BCL6B | MA0731.1 | chr2:107501904-107501921 | TAAATTCCTGGAAAGCA | - | 7.48 | ESR2 | MA0258.2 | chr2:107501655-107501670 | GGGTCAGCATGCCCC | + | 6.3 |
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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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Enhancer Sequence | GTTGGCAAAA AATGTTGATC AGAATTTCAA AAAAGGGAAG CATCAAAGTA ACCAGCATGG 60 GGTTTTTCAA GTGTGCAGAA AGTTCTCTAA ATACAAAATG TGCTTCCAGC CCACCAAAGA 120 CCCCCCTCAC CCAAGCAGGC AGTCCTCGGC GAGGAGGGTC AGCATGCCCC TTTATGGTCA 180 GAACGGCAGT GGTGCAAAAG ACAATGATTT CAACCAAATA TGGTTTGCCT CTCGCCAAAT 240 TTTTCGCATG TCCAATAAAA ATAAGTTCAC AAAAATCCAG CCAAGCATTA CTTTCCCCCC 300 AAAAGTGCTT CTCAGATTAC AAAACAGCTT TGAAAGTTCA GCCTGACAAA ACAAATATGG 360 TACTAGGAGG AGAGACCTGG AAGGCAATCA CAAAAAGTCT CATTTAAATT CCTGGAAAGC 420 ACAGCTTCTC CAAACACAGC TATTCAGCTC TTTGGAAGGC AGCACTTGCG GGAGCCATTG 480 AGTTTAACTT CACTCAGTCC CCCAACACAG AACCGGCAAA TCCGAATGAG ATGGACGTCA 540 CACTCCCTAC TCAAAAGAAT GCATCAAATA TCCACTCCGT AACACCGCGG AAAGTAAACC 600 CAAAAGCGGA GTTTGCCGCC TGCCAACTAC ATAAGAATTA ACACTCGGGT ATTTAGGATT 660 CTAAAGATCC CTACTACCCC AAACATTATA GCCACAGAGA ACCAGAAATG AACAGAACAC 720 ACTTTAACCT TTAAGAAGTG CAGTTTTGTA CGGGGGTTGG CTGAAGAAAG ACAAAAATCT 780 TCACTCCCTT CCAGAGCCAA AAGAGCCAAA ATAAAAGATC ACCTTTACTG AGCCACAGGG 840 GCACAACTGT ATCCGCCCGT CCCCAAAGCG CAAGCCGTCC TCCCGTTCGC TTCTCCAGAA 900 TTTCCTGCTT TTCCCCAAAC CACCTTCAAC ATTCCCCACA CACGGGTCTC GCTCCTAAAC 960 ACGGAGTGTA ACTCCGCGCA CAGCAGCGCG GAGGCTGCAG CGCCACCAAG AAAGGCGTCG 1020 CCAACCCTTA CCCAGTGCCC 1040
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