| Tag | Content |
|---|
EnhancerAtlas ID | HS086-02214 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr11:64683350-64684430 |
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 | | 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 | CTTCCTACAC CAGAATTCAC AGACAGCAGG CCACTGGGGG GTGCCCCCAG TTCAGGGCCC 60
ACGATTATCC TACCCCACAT TTGCTCACCA GGGCCTGGCC TACCCCCAAA GCCTAGCTCT 120
TCTGCCCAGA TTAGCAGCCC CCTGAGTCCA GCCACAAAAC TGAGAAGTCC CTGCCTCCAT 180
GCCCACCCCT GCTGCTCTGG ACCTGGTGGA TCGACCAGGA CGCGCCTCTA ATTGGTGGCT 240
CCTTCAAAGC TCCCCAGGTC AGCTGAGCTG TGAGTCAGGG CTCCTCACCG TTCCCAGCCT 300
CAAGCCTCTG ACCTTACACC TCTTGGCCTC CCTAGCATCT CCCTTGGCCT CCTCCCGGCT 360
TGAAGCCAGA TCTCCCCACC TTTCCTCCAG GGCCTCCCTC CAGGCAGGGA CACTGAGCCG 420
GGGGGGTCGG TGGGAGATGT AGGTGGGGGC CATCCAGTCC CTCCCTAGAC ACCCACTTGG 480
CCCATCCCAC TCTCCCAAAA GCAGGAAGTA GGCAGCGACC CAGGCACACG AGGTGTTGAT 540
CAACACTGGT ACTGACGTAC TGACGCGGTT GTTGACATAC ACATCCGGTG GTTTGTTGAT 600
CCCACCTACG GGCTCAGGAC CGTGGGGTCA AGAGGTCAGG GCACATGATC CACAGGTGTC 660
CTCGCCAGGG CTCCGGACCC CTACCAGCTT CCCCCACCAG CTGCGCAGGC CCAAGTCTGT 720
CACTGCCCTG GCCCAGCTCA GTTCCTACGC TCCCTCCCCA GCCCCTCCTC AGCCCGAGAG 780
CCAACCTCCT TAACTCAGCC CCCAAACTCG ACGAGTTTGT CTTGCATTCT CCAGACAGGT 840
GATCTTGCCC TCTCCAGCCT CAGTTTCTCC TCCCGTGGAG ACAGAAACCC CTTCCCGCTC 900
AGTTTCTGGC TCTGGTAAGG AACTGAAGAG GCCAGCCGGG GTGCCTCTGA CGCCTGGAGA 960
GGGCAAGATT CCCCTGGCCT CTCTACGCCC GGTGCCTGAT CCCCCAGCCC GATCCTGCCG 1020
CAGGGAGCCT CAGGTCGCTG CGCTCCCACC CTCCGCACCT TCCTGGACTC GGGCCTGGCT 1080
|
