| Tag | Content |
|---|
EnhancerAtlas ID | HS098-10380 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr11:66346470-66347630 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:66346567-66346588 | AGAGCAGGGGAGTGAGGGAGG | + | 6.1 |
| | | 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 |
| GH11I066578 | chr11 | 66346401 | 66347107 |
| Enhancer Sequence | CGTGCGCCAC CGCGCCCGGC CTACCTCTTT CTTTTGAGGC CACCCCTTCT TCCCACCGCT 60
AAGCGTTCCA GAATCCACAG TGATTAATTC GTCCGAAAGA GCAGGGGAGT GAGGGAGGAC 120
TGGATTCTGA GGGTGCTGGC AGAACAACTG GAGTCGGGGG TCCACGGCGG TCATGACTAT 180
CGACACACGG TGGCGCTGTT GAGGCTCGGT CCTGCGCATT CCCGAGTGTC AGGAGCCCTG 240
GAAGAAGTTG CAGGCTTCTC ACCTCCCACG CAGCCACTGC ACTCCGAAGC GCAACCACTG 300
AGTCAGGGAG GCAGGGCCAG AGAGGAGTTT GGCATCACCG GATAAAAATC AGCCGTAATT 360
TACATCCCCT ACGTGTGGCT AAAAGTTAAA ATGGACAGAT CTGGGTCCTG CGCTTCACAC 420
CACCTACATA GCATCAACGC CTGGATGTCA AACTTAGCCA GAGCTGCGTA TTGTTTTCAT 480
CCTCACCCGT CCTCAGGAAT CTCCCATCCC AGCATATGGC ATCACTATTC CCCCAGCTCT 540
TCAGTCCAGA GAATTGGAAA TGTCATTGAT TCTTCCTTTG CCTTCATGCC GCACGTCTAG 600
CCCATCTCCA AGTGCCCTGG AGTCCAGCCC TCCCCCCAAT ATCTCTCCAA TCTGTCCACT 660
TCTCCCCATT CCCGTAGCCG CCGCTTATGA CCAAGCCCTC ACCATTGCTT GCCTGACCGA 720
ATCCACTCCT GCCTCCAACA AGCTCCTCTG CAGGCCACAG CTGGAGGGAC CTCCTTAAAC 780
ATAAACCGGC CGGCACGGTG GCTCACGCCT GTAATTCCAG CGCTTTGGGA GGTCAAGGCA 840
GGTGGATCGC CTGAGGTCAG CAGTTCAAGA CCAGCCTGGC CAACATGGTG AAACCCTATC 900
CCTACTAAAA ATACAAAAAT TAGCTGGGCA TGGTGGCGCA CACCTGTAAT CCCAGCTACT 960
GGGGAGGCTG AGGCAGGAGA ATTGCTTAAA CCCGGGAAGC AGAGGTTGCA GTGAGGGGAG 1020
ATCCTGACAC TGCACTCCAG CCTGCACAAG AGAGCAAAAC TCTGCCTCAA AAACAACGAT 1080
TGCCGGGCAC AGTGGCTCAC TCCTGAAATC CCAGCACTTT GGGAGGCCGA GGTGGGCGGA 1140
TCACGAGGTC AGGTGTTTGA 1160
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