Tag | Content |
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EnhancerAtlas ID | HS037-20152 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr2:107501650-107502540 |
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 | GAGGAGGGTC AGCATGCCCC TTTATGGTCA GAACGGCAGT GGTGCAAAAG ACAATGATTT 60 CAACCAAATA TGGTTTGCCT CTCGCCAAAT TTTTCGCATG TCCAATAAAA ATAAGTTCAC 120 AAAAATCCAG CCAAGCATTA CTTTCCCCCC AAAAGTGCTT CTCAGATTAC AAAACAGCTT 180 TGAAAGTTCA GCCTGACAAA ACAAATATGG TACTAGGAGG AGAGACCTGG AAGGCAATCA 240 CAAAAAGTCT CATTTAAATT CCTGGAAAGC ACAGCTTCTC CAAACACAGC TATTCAGCTC 300 TTTGGAAGGC AGCACTTGCG GGAGCCATTG AGTTTAACTT CACTCAGTCC CCCAACACAG 360 AACCGGCAAA TCCGAATGAG ATGGACGTCA CACTCCCTAC TCAAAAGAAT GCATCAAATA 420 TCCACTCCGT AACACCGCGG AAAGTAAACC CAAAAGCGGA GTTTGCCGCC TGCCAACTAC 480 ATAAGAATTA ACACTCGGGT ATTTAGGATT CTAAAGATCC CTACTACCCC AAACATTATA 540 GCCACAGAGA ACCAGAAATG AACAGAACAC ACTTTAACCT TTAAGAAGTG CAGTTTTGTA 600 CGGGGGTTGG CTGAAGAAAG ACAAAAATCT TCACTCCCTT CCAGAGCCAA AAGAGCCAAA 660 ATAAAAGATC ACCTTTACTG AGCCACAGGG GCACAACTGT ATCCGCCCGT CCCCAAAGCG 720 CAAGCCGTCC TCCCGTTCGC TTCTCCAGAA TTTCCTGCTT TTCCCCAAAC CACCTTCAAC 780 ATTCCCCACA CACGGGTCTC GCTCCTAAAC ACGGAGTGTA ACTCCGCGCA CAGCAGCGCG 840 GAGGCTGCAG CGCCACCAAG AAAGGCGTCG CCAACCCTTA CCCAGTGCCC 890
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