| Tag | Content |
|---|
EnhancerAtlas ID | HS182-22462 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chrX:46436600-46437760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chrX:46436946-46436967 | AAGGGAGGAGAAGAGAGGGGG | + | 6.18 | | ZNF263 | MA0528.1 | chrX:46436942-46436963 | AGAGAAGGGAGGAGAAGAGAG | + | 6.25 | | ZNF263 | MA0528.1 | chrX:46436949-46436970 | GGAGGAGAAGAGAGGGGGAGG | + | 7.35 |
|
| | 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 |
| GH0XI046577 | chrX | 46436666 | 46437171 |
|
Enhancer Sequence | AGTACTGGCT GGGGTGAAGC ATTAAAGAGA ATAGAGAGGA GGGTAGAGGA CAGTCTTTGC 60
CCTCTAGGAG GTTAGAGTCT GTGTGGGTGA CAGTGACTGT GAGGGAAGAC ACTGGTGTTG 120
CTGTTTGGAA GGCCGATGGG GCTTCCTTTG CAGGGCTGCA GGGACATCTG GGAGCAAGCT 180
TTAGGCTCTT CCAGACTTTA GTGACTGAGT CCTTCCTCCC GCATTGGGCA CTTACCACCA 240
ATCAGTGGGT TGATTACAGT GCTTGTATTC TTGGTTCCTA GGAAGATAAC GTTACTGCCG 300
ACTCACTGAT GGGTTTTCCA AAAGTTTGTC ACACTCTATT CTAGAGAAGG GAGGAGAAGA 360
GAGGGGGAGG GATCCTTACT GAAGGGCTAT GTGTCATGCA CTGAGTTAGG CATTGTACAT 420
ATATCATTAT TTATACCAGT TTTCCAGATG AGGAATCCGA GACTCAGAGA AGTAATTTGC 480
CCAAAGTCAT ACCTGGGCTG GTGAGGGTGG AACAGTGTTT GGTGTTAGAC TCCAGAGCTC 540
ATAATCCTCT CTTTTATACC TCACCTGGCC CCTGCCTTGG CATTCCCTGG CAGCACCCTG 600
ATACTCCAGC TAGGCTAGTA TGAGGTGGAA AACACACTCA GCTTTATTAC TAATATGTCC 660
CAACCACTGA ACAAATAAAA TATCCCTGAG CTGCCGACAG TGCCTACACA GGAAAGCCGA 720
CAACTTTACA GCCATCCTCC CCACAGGGCA TCTCAGGGTG CCCTCAGCTC AACTGAGGAG 780
AGAGGCCACA TGTGAATTAA CCTGAGTAAC TTCTGGATGG TCCATACCCA ATGGCCAGGA 840
TTTGGCAGTG AGGGAGTCAG TGAAGTTTTT TCTGGTCTGG GTAGGGGCCG TAGCACCCTG 900
AACCAAGTCA CCAAGGACCT AGGCCCTTTC TATCTTTTAC ATCTTGGCTT TCATTCACTG 960
GCTTATCTTC CCACTGTAAC AAGATGGTAG CCACAGCTCC AAGCAAAACA TCTTCACACA 1020
ACGACACAGG GTTATTAAAA TACAGAAAGG AAGGAAGCTA TCTAGCCAGT AAGGGGTGGA 1080
GGGGTTTTTC CTCCTGCCAT GCTCTTTTTT TTTTTTTTTT TTTTTTTTGA GTGGCAGCTC 1140
TTACTCTGTC ACCCAGGCTG 1160
|
