| Tag | Content |
|---|
EnhancerAtlas ID | HS133-06392 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr11:77740760-77742460 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:77741939-77741960 | CTCTTCCCCTCCCTCTGCTCC | - | 6.38 |
|
| | 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 |
| GH11I078029 | chr11 | 77741041 | 77743350 |
|
Enhancer Sequence | TACTAGGGTT TTTTAATAGG TTTTGATGGA ACTCAGTTCC ACAAGGAATC TCAGACAAGA 60
CTTTTTTTTT TTCTTTTTTT TTTTTGAGAC GGAGTCTCGC TCTGTCCCCC AGGCTGGAGT 120
GCAGTAGCGC AATCTCGGCT CACTGCAAGC TCCACCTCCC AGGTTCATAC CATTCTCCTG 180
CCTCAGCCTC CCAAGTAGCT GGGACTACAG GCGCCCACCA CCACGCCTGG CTAATTTTTT 240
TTGTATTTTT TAGTAGAGAC AGGGTTTCAC CGTGTTAGCC AGGATGGTCT CGATCTCCTG 300
ACCTCATGAT CCACCTGCCT CAGCCTCCCA AAGTGCTGGG ATTACAGGTG TGAGCCATCG 360
CGCCTGGCCT TTCTGTGAGA AAATTTCTTT AGAGCAAGAG CTCTCTCTGT CTCCATTCCT 420
GGACAGGAAT ATAAAACCTG CTTGCTTCTT TTTTCCCCCC CTCCAATTGC ATGTTCTTTC 480
TTTGCCACCA ATGCAAAGTA GGAAAAAAAC TCAGTTTTCC AGTGACATTA GCACATTTGA 540
CCCTGGCAGT TCAAAATAGG CATTAGCACC TCCATTTTCT ATATGAGGAC CCCAAGGCTC 600
CCAGAGATGA AGCACCTCTT TGAGTCAGTC AGACCAGGAG ACGAGAGAGC AGGGCTCTAG 660
TTTCGGCTCT GCCACCAGTT TGCAGTACCA CCTTAGACAC GTCCCTGCCC CTCTCTGGGC 720
CTCAGTTCTC CACCTGTAAT ATGGTGGGGG TTTGTGTATT TTCTGAGATG GTCTCTGTGA 780
TCCTGCCTTG CTTGATGCTA TGGCAACAAA AGAATTCAAA CAGCCCCTTG CTATTGCCTA 840
TCACTGGATC TTGTTTCCCT TTGGCCTGAC TCCAAGAGCA AGCACTGCTT CCTTCTGCCC 900
TCCCCTCACT CACTCCCCTC TGTTCTTCAG GAGACAATGC GGCCAGCCCC TCTCCCCTCC 960
AGGCGGCTGG GCTTTAGGCC AGCCAGCCAA ATGGCAGCTG GGACTCAGAT GAAAGGGCCC 1020
TCAGAAGGCT GCTTGTGGCA GAGTGCCCAG CCTAGCCCAG CCCAGGCTTG GCAGCCTGGG 1080
GCTCAGCTGT GCCACGAGGC ATCCTGTCCA CCCGCTCCCA TACAAGGCTC CCTCTGTGAG 1140
TCCTGCAGAG AAGGAGACCC CTGCCAACCC ACAAGGACCC TCTTCCCCTC CCTCTGCTCC 1200
ATACCTGCTT GAGAAATATG CAAGTCTGTA GAGAATGGTC CAGGACTACA TCAGATTGAT 1260
CTGACTGTGC CAGGCACTTT GGAGAGCTTT ATCCCATTGA CTCTTCAGAA TAACGCTGAT 1320
AGCAAGTAAT GGTTTTTTTT TTTTTTTTTT TGAGACAGAA TCTCACTCTG TCACCCAGAC 1380
TCTAGGCTGG AGTGCAGTGT CACTAACATA GCTAACTGAA GACTCGACAT CCTGGAATCA 1440
AGCAACCCTC CTGCCTTAGC CTCCCAAGTA GCTGGGATTA CCGCTAACAC CCAGCTAATT 1500
TTTTTTACTT TTTTGTAGAG ATGGTGTCTC ACTATGTTGC CCAGACTGGT CTCAAACCCC 1560
TGAGCTCAAG CAATCTTTCT ACCTTGGCCT CCCAAAGTAC TGAGATTACA GGTGTGAGCC 1620
ACCATACCTG CAATCTCTTT TTATTTATTT GTTTATTTTT TAAAATTTAT TTTATTTTTT 1680
TTGAGACAGG GTCTTGCTCT 1700
|
