| Tag | Content |
|---|
EnhancerAtlas ID | HS133-26619 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:29781570-29782980 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr6:29781808-29781819 | GATGAGTCACC | - | 6.32 | | JUND | MA0491.1 | chr6:29781808-29781819 | GATGAGTCACC | - | 6.62 | | NEUROD2 | MA0668.1 | chr6:29782279-29782289 | GCCATATGGT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 29781738 | 29781880 | | chr6 | 29782615 | 29782769 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I029813 | chr6 | 29781741 | 29781890 |
|
Enhancer Sequence | TGCCTTTTTC TGGCCAATGT CCCAGTGACC TACGAGAAAA CCTTTCCTGC CTACAGGGAA 60
CCAGAACTGA CAATCCCTCT ATAGGAGACA CCGCAGGTGA GAGCAGGAGC AACCACAGAC 120
CTGCACTGCC CGTGCTGTGG TTGCCTCCTG GACGGGGCCC TCTTGCTGCA GGGCAGGGGA 180
TGAACCGTCC CATCTGCCCA GGCCTGAGTG GCCAACTAAC TGTGCAATTA GGTTCAAGGA 240
TGAGTCACCA CCACCTCACT GGCCAGACAC ACGGAAGTGG AGAAATGGCA GAAAGACTCG 300
GGTTTCCTGG ACACCCCAGA CTCTCACTGT CCCCTGCACT GCCTCTGTCT TTGCAGAAAC 360
TCAAAACTTT CTGCTTGCTC TTTTCCTCTC CCCTCAAACA ACCTGACTGT GGGGGAAATG 420
ATTCTGACTG TCTCTTATTG TAAACTTACC AGGCAGCGAC TACACTAAGA ACAAAAACAT 480
TGGCTCAGGA AAGGCAAGGT GAGGCCACAG AGCACAGAAC AAAGCCCAAA AAACAGCCCA 540
CTGGGTACTA TGACCCTCGG GGGCTGGAAA AAGTAACACC TGGACATGGG ATGAAAACAG 600
GGACCACAGC TGCCCTGACA GAGGGCTGGT CCCCACTCCC CAAATAGCCC AGGGACATCT 660
GCTTATCAAC TGGTCCATAT TATCTGCAAG GAAACACAGG GAGACAGGGG CCATATGGTG 720
GGAACCCAGA AAAAGCACGG TCTCGAGGGA CCCAGAGGAC GTGACACCCC TGAGACAGCT 780
CCCAGATGAG GCATATGGGG AGCTGCAAAG TGGACAGAGG ATGGCCATGT GCACTCAGGA 840
CTCTCCCTGT TACAAGGGGA CCTCAAAGGG GCTGTACACA TGGGGGCCCT CATTCTGGGC 900
CTCGTGGGTC TTTTTCTTGA TGTCCTCCTG ATGGCTGGAG AAACAGGGGA GGGGGATGCA 960
GAGAGGAAGG GACTAGAGGC ACCACCTCTC CTTGGATTCC TCTCCAGTTT CTAGCCCTCC 1020
CTAGATCACA TCTGCCTTTA CTATTTGCTC CCTCTGAGAT AGTGATCATC CAGGCCCTCA 1080
GCAATCAGCA CGCAATTCCC AACTCACCCA CCTGGATGCG ACCTGGTAAG CCTGAGAGAC 1140
AGAGACCGGG ATGGGGACAA AGCAGGCACC ACGGCCCTCC CTGCTGCCCA CTCCTCACCT 1200
GCAGCAGGAG GAGGCCACAG CTGGATGTTC GAGGGCCTTG GCCCAGCCCT GGCTTGGGCA 1260
GGACTTAAGG GTGTAAAAAA TAACCTACAT GTGATGGTTC ATTTTCAATT CTATGTGCCT 1320
TAGTATAGGT TTAAGCAGGC CACATGGTCA TAAAGAGATA AAGAAGGAAA ATGTACTAAG 1380
CCACCATCCC CCCTACTTCT TGCTTTCCCT 1410
|
