| Tag | Content |
|---|
EnhancerAtlas ID | HS133-15731 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr19:43685180-43686660 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr19:43685264-43685277 | ATGGCATCATCAT | - | 6.01 | | Zfx | MA0146.2 | chr19:43685848-43685862 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr19 | 43685547 | 43685800 | | chr19 | 43685800 | 43686600 | | chr19 | 43685470 | 43685863 |
|
Enhancer Sequence | TAAGTTTGTG TGAATTAGGA AGAATCTAAG TGAGATGCCA ATGGCTCGTG TGTCTCCCCA 60
CACGTAGAAC TCCAACTTAT GAAAATGGCA TCATCATGAG GAAACAGTTT TATGTGGCAC 120
AGGCAGTAAA ACCATTAGAT AGCACACACC TGGCCACCTC CAACTGGTCC CCAAAACCAC 180
CAATATTCAC ATTACGTGTA TCTGACAGCC TTTGCAGTTG TCCACAACTA CAAAATTTAA 240
AAATTGCTAT TGCCAAAACA AAATATTAAA TGTGAAGTTG AATGTGTTGT TCCACTTTTT 300
TTCCCCCACT CTTATTGAAC TTTCCTTTTT CAGTTTTGGA AGTTTCTATT GACACATCCT 360
CAAGCCAGAG ATTCTTTCCC CAGCTGTGTG CAGTCTACCA GTAAGCATCA AAAGCATTCT 420
TCATTTCTCT AACAGCATTT TTTTTTCTGA GACAGAGTCT CTCTCTTTCA CCCAGGCTGG 480
AGTGCAGTGG CATGATCTCA GCTCACTGCA AGCTCCACCT CCTGGGCTCA CGGCATTCTC 540
CTGGCTCAGC CTACCAAGTA GCTGGGACTA CAGGCATCCG CCACCACGCC CAGCTAATTT 600
TTTGTATTTT TAGTAGAGAC GGAGTTTCAA CATGTTAGCC AGGATGGTCT CCATCTTCTG 660
ACCTTGTGCC CGCCTCGGCC TCCCAAAGTC CTGGGATTAT AGGCATGAGC CACTGTGCCC 720
AGCCATCTCT GAGGGATTTT AATGAGTTGT TGACTTTTGA GTTTGTTCAA CTTTTTACTT 780
ACTGTTAGAA CCGAGTGACA AATTTCAAGC TTGTTATATG CCTGACAGGA AGCCAGAAGT 840
CTCTAAGAAG TGACAGGAGA ATGTGAGCTC CATAGTAGTT TGAGGATGGA GTCACGAGTG 900
AAACAGTTGA AATGAGTCCA TGGGCATTGG GGACTGCAGG CCTGTCCAGC CTCTGACACC 960
CTGGTGAGTC AGTCCATACA TTACAACAGT GACAGCAAAG TAGCATGTCT GACTCCATCT 1020
GGCATCTAGT CTCTGGCTGG CTATCCTCAC TCATTCCTGG GCATAGGCCA GGCTAACCTT 1080
GGGAGGAATT TAATTTATGG TTTGACTTTG AAGCAAGAAT CACAAAACTT CCTCCATGAA 1140
ACTAACAACC TTACTTTGCC CAGGGATGGC CTTTGTCAAA CTAGTGAAAG ACCATGAGAT 1200
TAAGATTATA GGAGGGAACT GAATTCTGCT AAAATGTTGG CACAGTTTCT ATAATTCCTG 1260
ACTGCTGCAA TGTTGTTTGG CCAGAGTTTA CAAAATTTGT AACTAATTGC TCCTATAGAT 1320
AACATCACTA TTGTAGAACA TGAGATTGGT CTTTTGAGAT GTTTCTCATT CTTTTGCATT 1380
CTGGCAACCG GCTGACCTCA TTCATACCTA TGACTAATGG CTCAGCCAGT CATGTGGTCC 1440
CTACCTGGAG GCAGATTCGA GCACAAACAG ATCATTTCCC 1480
|
