| Tag | Content |
|---|
EnhancerAtlas ID | HS182-03688 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:46513250-46514400 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:46514119-46514140 | GGAGGTGGGAGGGAGGTAGGG | + | 6.02 |
|
| | 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 |
| GH11I046491 | chr11 | 46513223 | 46514666 |
|
Enhancer Sequence | TCTCCTAATG GCATTCTGCA TCCTTTGATA GATTTTCTCA GATTTCACAT CTGTAAACAG 60
CTGCCCACTG CAACACAGCC CCTATATTCA AAGGCATCCA TAAGTGTAAT TAGGCCATTT 120
GGGGTCAGAC CACAAGGCAT AAAGTAGGAA ACAGGAAATT GAAGTAAGGA GGTCTTGGAG 180
GCAAGGCAGA AAAAAACAAC ATACAGCTGT TCCCCCAAAG CTAAATGCCA AGGAAACAGA 240
GATCTGCCGG CAGTAGAGAA GCAGGAGGTG CTGTATGGGG TGGTGGAGGC AGATGTCTGG 300
AACAAAGAAG GGTGGAGAAG AGCTCTAGAG TATTGTCTGG CAGCAAGTTA TTATCTGCCA 360
GTGAAAAAAG CTTTAACGTG CCTTCGGTTA AGCCACACAG AAGTGCCAGG CAAGGAGAGG 420
CACGGACCAC AGCATCTGTT TTACAACTAG GGCCAGAGCC TCCTCAGATG AGGCTGTCAG 480
GAGATTGTGG TATAGTCTGC TCTCCTGCCA GGCCAGAGCC TATGAAGTCC TGGTGTCTGA 540
CAGAGAAACC ACTGAGGTTT CTGGAATTTC TAAGCATTGA TGTTGGATCA AACATACTAT 600
TTAGGAAAGG CCAGATCCCA TGGCCTTGAT GCTGTCACAG CAGCTTGGTT AGAAATCATA 660
AGATAAAGCT TGTAACATTC TCACAGTCAG ACAGTGCCAC TGCCTCAGTA GATCCCTCCC 720
CACCTTTAAC CATCACATGG CCCAGATTCT CCAAAACAGA ATGTCATTTT AAAACTTTTA 780
ATAAAGATGC TTATTAAAGA TACCTCTAAA TGTGGCTTGA TTTTTATACC TTTTATGCAT 840
TTGCATTCAT AAATTTATAA GTCGGCAGTG GAGGTGGGAG GGAGGTAGGG AAAGACTGTG 900
ACAGGGAAAC AACCTTTGCC ACATATAAAA ATGGAATTCT GCTTTACTTC CTTCTCTAGA 960
GACTGACCAG AAGCAATAGC ACACACAACG TCTCAGAACA CAGTCACGTC ATGCCTCACA 1020
GCCGAAAAAC ATCTGTCACT AAGCTATTCA ACCATCATAA AACTGCTGGC CAGGCACAGT 1080
GGCTCACGCC TGTAATCCCG GCACTTCGGG AGGCTGAGGC AGGCAGATCA CGAAGTGAGG 1140
AGATTGAGAT 1150
|
