| Tag | Content |
|---|
EnhancerAtlas ID | HS060-04999 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr11:258800-259830 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arid5a | MA0602.1 | chr11:259790-259804 | CCAATATTGATACA | + | 6.22 | | DMRT3 | MA0610.1 | chr11:259795-259806 | ATTGATACATT | - | 6.62 | | KLF4 | MA0039.3 | chr11:259133-259144 | GGAGGGTGTGG | - | 6.32 | | Klf1 | MA0493.1 | chr11:259135-259146 | AGGGTGTGGCC | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 259499 | 259612 | | chr11 | 259613 | 259757 |
|
Enhancer Sequence | TAGCTACTCG GGAGGCTGAG ACAGGAGAAT TGCTTGAACC CGGGAGGCGG AGATTGCAGT 60
GAGCTGAGAT TGTGCCATTG CACTCCAGCC TGTGCGACAG AGCAAGACTC CATCTCAAAA 120
AAAAAAAAAA GCTTGAATAC CATCTTCATG TCACATAAAA ACTTTGATAC TTCACACTAT 180
TTTCTTCAAA ACTGAATGAC CACTTCCAAA AAATTAAGCC AGATACTAAG ACTTGGCCCC 240
TTCCTTTCAT CTAAAAAAAC ACATTTCCAC TAAGTACCTT GTAGATTTAG TAGAATTTAC 300
TGAAACTTTG GGATTCATGG GAAGAGATCC TGTGGAGGGT GTGGCCCTCT GCCCTCCACC 360
CCACCCCTGT GCACACCCCT CGTCGGGAAC TCAGCTTTGA CCCAAGCCCT CTTCACATGG 420
AACCTGCCCG TTCGGGACTC TGGTGTCAGT CGACAGTCTC AGCATTGCCC AGCGCTGACG 480
GTTTCGATGG TGCTGTGTGT CAGCTTGACT GGGCCGTGGT GCCCACGTTT GGTCAAACAT 540
TATTCTGGAT ATTTCTGCAA AGGTGTTTTT TGGATGAAAT ACTAACCTTT AAATTGGTGA 600
ACTTTGAGAA ACGCAGAAGA CCCTCCATGA TGTGGTGGGC TTCATCCAAT CAGTTGAAGA 660
TCTTAGGAGA ACAAAGACGG ACCTCTCCTG AGGAGGAAGA AGGAATTCCA CCTCCAGATG 720
GTCCTCGGGC TCCGCCACAG CATCAGCTTT CCTCGGGGCC TCCAGCCACC TGGGCTCCTC 780
TATCAGATTC CGGGCTTACC AAGCCTCTAC AATCACATAA ACAGTTCCTC AAAATAGATC 840
TCTCTCCACA TATATGTGTG TTGGGGATGG GTGGGTACAC ACACACACGC ACGCGCACAC 900
ACACACACGC ACGCACACAC ATCCTGTTGG TTCTGTTTCT CTGGAGAATG CTAATACAAT 960
ATGTATAATA CATTTGTCAC AATTAATGAA CCAATATTGA TACATTAGTT ACGAACTTCA 1020
TGAAGTCCAT 1030
|
