| Tag | Content |
|---|
EnhancerAtlas ID | HS098-10271 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:64683250-64684430 |
Target genes | | Number: 34 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr11:64683973-64683988 | GGGGTCAAGAGGTCA | + | 8.07 | | Nr2f6 | MA0677.1 | chr11:64683329-64683343 | AAGGTTAGAGGTCA | + | 6.06 | | RARA | MA0729.1 | chr11:64683973-64683991 | GGGGTCAAGAGGTCAGGG | + | 6.56 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCCTGGGCAA CATAGCGAAA TCCTGTCTCT ATAAAAATAA AAAAGGGGCA GCCTAGAGAC 60
GGCCTTAGAG GCTGAGGCTA AGGTTAGAGG TCAGAGAGGG CTTCCTACAC CAGAATTCAC 120
AGACAGCAGG CCACTGGGGG GTGCCCCCAG TTCAGGGCCC ACGATTATCC TACCCCACAT 180
TTGCTCACCA GGGCCTGGCC TACCCCCAAA GCCTAGCTCT TCTGCCCAGA TTAGCAGCCC 240
CCTGAGTCCA GCCACAAAAC TGAGAAGTCC CTGCCTCCAT GCCCACCCCT GCTGCTCTGG 300
ACCTGGTGGA TCGACCAGGA CGCGCCTCTA ATTGGTGGCT CCTTCAAAGC TCCCCAGGTC 360
AGCTGAGCTG TGAGTCAGGG CTCCTCACCG TTCCCAGCCT CAAGCCTCTG ACCTTACACC 420
TCTTGGCCTC CCTAGCATCT CCCTTGGCCT CCTCCCGGCT TGAAGCCAGA TCTCCCCACC 480
TTTCCTCCAG GGCCTCCCTC CAGGCAGGGA CACTGAGCCG GGGGGGTCGG TGGGAGATGT 540
AGGTGGGGGC CATCCAGTCC CTCCCTAGAC ACCCACTTGG CCCATCCCAC TCTCCCAAAA 600
GCAGGAAGTA GGCAGCGACC CAGGCACACG AGGTGTTGAT CAACACTGGT ACTGACGTAC 660
TGACGCGGTT GTTGACATAC ACATCCGGTG GTTTGTTGAT CCCACCTACG GGCTCAGGAC 720
CGTGGGGTCA AGAGGTCAGG GCACATGATC CACAGGTGTC CTCGCCAGGG CTCCGGACCC 780
CTACCAGCTT CCCCCACCAG CTGCGCAGGC CCAAGTCTGT CACTGCCCTG GCCCAGCTCA 840
GTTCCTACGC TCCCTCCCCA GCCCCTCCTC AGCCCGAGAG CCAACCTCCT TAACTCAGCC 900
CCCAAACTCG ACGAGTTTGT CTTGCATTCT CCAGACAGGT GATCTTGCCC TCTCCAGCCT 960
CAGTTTCTCC TCCCGTGGAG ACAGAAACCC CTTCCCGCTC AGTTTCTGGC TCTGGTAAGG 1020
AACTGAAGAG GCCAGCCGGG GTGCCTCTGA CGCCTGGAGA GGGCAAGATT CCCCTGGCCT 1080
CTCTACGCCC GGTGCCTGAT CCCCCAGCCC GATCCTGCCG CAGGGAGCCT CAGGTCGCTG 1140
CGCTCCCACC CTCCGCACCT TCCTGGACTC GGGCCTGGCT 1180
|
