| Tag | Content |
|---|
EnhancerAtlas ID | HS133-32357 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr9:132004540-132006140 |
Target genes | | Number: 23 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr9:132005828-132005849 | ATCAGTGCCTGGGACAGTGCC | + | 6.08 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 132005480 | 132005830 | | chr9 | 132005135 | 132005862 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I129242 | chr9 | 132004868 | 132005869 |
|
Enhancer Sequence | AGACCCGAGA CCAGAGAGGG ACCGTGACTG CCCAAGGTCA CATAGATCTT TGGCCTAACT 60
TGACACAGCA TTCATTCACA GCCTGAGCAC CGCTCTACGG AGCTCCTGGA CAGATCTGCG 120
TGTCCCCTCC TGGGAGTCCC ATCCACTGGA GCCGCAGAGT GGGGGCAACA CTGGACCCTG 180
CATGCTGGTT GGGAGGGGAA CTGGAAGAGT GGGCTTCATT CCACGTATAG GGGGAGCCCC 240
AAAGAGTCTG TAGCCAAGGA AGTGACAGGG TCTGATTTGC TTTTAGAGGA TCTCTGAGGC 300
TACTGGGAGG AGAAGGCGTG GAGCTGGGTG AGAATGGAGG CAGGGAGGCC TAGGAGGGGC 360
TGGCGGTGAT GAGGCTGGGG TTGAGGAGGA GGCCGCAGGA AGGGAGACAA AGGGAGGCAT 420
TTGGAAAGCA TCCAGAAGTC GCGTGGCTGG GACCTGATAA CAGGTGTGAG CCAGGGGCTG 480
AGAGGCAGGG AGGACTTAAG GTATGCAAGG ACAGCTGAGG GAGGATGGGT GTCATTCGCA 540
GATTGGAGGA GCCCTGGAGG AGGAGCCAGT CTGGCTGGGG TGCAGGAGGG CAGGGTGACA 600
AAGATCCAGT TTTGGCCAAG GTGCCTTTGG GTCATGAGTG GGGACATGCA GTGTCTGTGA 660
GGGTGGCTGG GATTTCGGGG CAGCCATGAT CCAGTCGAAG CCCTTCCCCA GCCCCTGGCC 720
TCCAGCAAAA TCAGGACTTG GGGCCTGTTC CTTGGGGCCT CGGGAACACG CAGATCTCAT 780
TCCCCGCCCC AGTTTCTCTG GAAGGAAAAC ACCCAGGGCC TCGGTGGAAC CGGCATTAAT 840
TTCCCCTGTT CGGCTCATCA TTCCATCATC ACGAGAGAGC CAAACAGATG ACCATTTCGT 900
CATTGCATAT GCCCATGCGG GGCTTCCGTA ATCTGATCAC TTAATCACAT GCTTATTCCA 960
TGAGGACGGA GGCACGGGCA AGCTCTGGGG CCCACTCCTT GGGCAGCGCA TTTTGGACCA 1020
AGTCCCTTAG CGTTCCTGGC TGCCTCTGTT TCTCTGCCTG CCTTGGGAAT CCAGACAGCC 1080
TCATGACAAG AGGAGATGAG GCAGTGGTTG CGGAAGAGCC TGGTCTCTCA GCCACAGCAG 1140
CCACGAGGTG CTGGCAAGCT CTCTGCAGCC TGTGCTGCTG GGAGGTAGAG GCTTCGGCAG 1200
CTTGTCCTCC TTGTGGCCTA ACACACGCTG CCCGTCTCCC CACTTGCATG GAAGCCCCAG 1260
GAGGACACGC AGTTTGTCTC TTTGGTTCAT CAGTGCCTGG GACAGTGCCT GGCACATGAG 1320
GGAGCTTAGG TGAAGTTTAT CGAAATTTCC CATTTGTCTT TTTGTTTTGT TTTGTTTTTA 1380
AGACAGTGTC TCGCTCTGTC GCCAAGGCTG GAGTTCAGTG GTGTGATCTC AACTCACTGC 1440
AACCTCCGCC TCCTGGATTC AAGCAATTCT CTGCCTCAGC CTCCCAAGTA GTTGGGACTA 1500
CAGACACACG CCACCACACC CAGCTAATTT TTTTTTTTAA GAGATGGGGG TTGTACCATG 1560
TTGGCCAGGC TGGTCTTGAA CTCCTGGCCT CAAGTGATCC 1600
|
