| Tag | Content |
|---|
EnhancerAtlas ID | HS133-15326 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr19:19690030-19691710 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr19:19690980-19690995 | GGCCCACCCACCGTG | + | 6.13 |
| | | 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 |
| GH19I019580 | chr19 | 19691361 | 19691510 |
| Enhancer Sequence | GCCTGTAATC TCAGCTACTC AGGAGGCTGA GGCAGAAGAA TCGCTTAAAC CTGGGAGGCG 60
GAGGTTGCAG TGAGCCGGGA TTAAGCCACT ACAGCCTGGC AACAGAGTGA GACTCCGTCT 120
CAAAAAAAAA AAAAATCACC CAGTCTGTGG CATTTTGTTA GGGTGGCCTG AGTAGACTAA 180
GACAGTAACA TAACCCCAAG TTGCTTTAAT TTTTCTCCCC AGGAACAAAG ACGTGGGGAA 240
AAGCAGAAGG CTCAGAGGGA ACCCTCCTTT GCCCTGACTT CCCCAAGCTG CTCACCTGCC 300
CCCTCACCCA CTCAGCAGTG CTCTCACTTG GCAGCGGGCT GTGCTCCCGC CTCCTTCCCA 360
CAGCAAGTGG GAACCATCTC TGGGACCCCA GCCCCATAGG GAGAAGGCTA ACCCATGGAT 420
TAAATCAGAT GCCCTGACTG ACCCCTCGGG TCTGCCACTT TCCAGTCATG TGGCTGTCAG 480
TGGTCACTCC GCTGGCCGCA AGCCCCAGTT GTGAACGGAG CTGCCCCAGG CAACTGACTG 540
GATGGAATTA CATAGAACCG CAGGCCCGGC CCAGAGCCCA TCAGGGTATG GGACTAAGCA 600
AAACACTCAC CTCACGCTCT CCCTGCTGTC TCAAATCAGC AAGAAGCTGG CCCCTCAAAA 660
GCAGAGGCAG GGCCTCCTGT GCCAATCAAT CGATCGTGGA GGCTGAGCCT CCTCCCCATC 720
TCCCCCCACC ATCCACAGCC GGAATGAGCG TTGGAGACGG ATTAAACTGT GGAATCTGGG 780
ACAGAGGGTT GACGCCTGGT GAGAGGCGGC CAAATCTCTC TTTGAGGAGT CCTTTGGTGA 840
CAGAGAGCCA AAGCCTAGTG CGCCGACCTG AGTTGCAATG AGTACCTATA GTCACAGCTT 900
GCTCTGATCA CACAGGCGCA GGCGCAGACA AGCATGTCCG CCTGCCCTCG GGCCCACCCA 960
CCGTGTCTGG AACTGACAGT GCCGGTGACT CTGCACAGGT GAGAATCGAC ATGAAGGAGA 1020
AAACATGGGG ACTTCCTGCT TTCTAGAAAC CTTTTGAGGC TTTTTCAGTC ACTTACTGAG 1080
CACCTACTGA GTGCTGGGCC TGAGCTTTGA GGATGACAAG TGGCTGCTGC TTGCCCTGGG 1140
GGGATAAGAA CCAGGGTCTT GCTGCTGCTA CCGGGGTCTC CTATGCTACT GGCCTCCTGA 1200
CCAGTGACCC TTAGAAAGAA CGGGGCCACT GGCCACAGTT CTGCCGGTGG GACCCAGCGT 1260
GGTAACTGGG ACCTGGGCTG AGGTTAACTT TCCTGTTCCA GTTTTCAGAA GGAGAGCTCA 1320
ACTTCCATCA GCTCCAGCTT ATCTTGTAGT CAAAGAGCCA AAGGTAATAA GGAAATGAGT 1380
TCTACAAGGC ATTCTGGCAA GGTGCTCACC AGGAGCCACT TTCATTTGTA GTGAGAGTGT 1440
TTCCTCCCTA AACAAGGCCT CTGATATTGG AGGACAGGGA TAGGGGAGGC AGGTGGTAAA 1500
TAACCTTCTG TACTTAGACC TCAACTGCTT AAAAGAAAAA ACACCAGCTA CTGGGGAGGT 1560
CACTCAGGCA GGAGTGCAGT GGCACGCTGC AGCCTTGACT TCCTGGGCTC AAGTGATCCT 1620
CCCGCCTCAG CCTCCTGAGT AGCTGGGACT ACAGGCATGC GCCACCCTGC CCAGCTAATT 1680
|
| |
|
|
|
