| Tag | Content |
|---|
EnhancerAtlas ID | HS167-03038 |
Organism | Homo sapiens |
Tissue/cell | Retina |
Coordinate | chr2:107501540-107502540 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CATCAAAGTA ACCAGCATGG GGTTTTTCAA GTGTGCAGAA AGTTCTCTAA ATACAAAATG 60
TGCTTCCAGC CCACCAAAGA CCCCCCTCAC CCAAGCAGGC AGTCCTCGGC GAGGAGGGTC 120
AGCATGCCCC TTTATGGTCA GAACGGCAGT GGTGCAAAAG ACAATGATTT CAACCAAATA 180
TGGTTTGCCT CTCGCCAAAT TTTTCGCATG TCCAATAAAA ATAAGTTCAC AAAAATCCAG 240
CCAAGCATTA CTTTCCCCCC AAAAGTGCTT CTCAGATTAC AAAACAGCTT TGAAAGTTCA 300
GCCTGACAAA ACAAATATGG TACTAGGAGG AGAGACCTGG AAGGCAATCA CAAAAAGTCT 360
CATTTAAATT CCTGGAAAGC ACAGCTTCTC CAAACACAGC TATTCAGCTC TTTGGAAGGC 420
AGCACTTGCG GGAGCCATTG AGTTTAACTT CACTCAGTCC CCCAACACAG AACCGGCAAA 480
TCCGAATGAG ATGGACGTCA CACTCCCTAC TCAAAAGAAT GCATCAAATA TCCACTCCGT 540
AACACCGCGG AAAGTAAACC CAAAAGCGGA GTTTGCCGCC TGCCAACTAC ATAAGAATTA 600
ACACTCGGGT ATTTAGGATT CTAAAGATCC CTACTACCCC AAACATTATA GCCACAGAGA 660
ACCAGAAATG AACAGAACAC ACTTTAACCT TTAAGAAGTG CAGTTTTGTA CGGGGGTTGG 720
CTGAAGAAAG ACAAAAATCT TCACTCCCTT CCAGAGCCAA AAGAGCCAAA ATAAAAGATC 780
ACCTTTACTG AGCCACAGGG GCACAACTGT ATCCGCCCGT CCCCAAAGCG CAAGCCGTCC 840
TCCCGTTCGC TTCTCCAGAA TTTCCTGCTT TTCCCCAAAC CACCTTCAAC ATTCCCCACA 900
CACGGGTCTC GCTCCTAAAC ACGGAGTGTA ACTCCGCGCA CAGCAGCGCG GAGGCTGCAG 960
CGCCACCAAG AAAGGCGTCG CCAACCCTTA CCCAGTGCCC 1000
|
