| Tag | Content |
|---|
EnhancerAtlas ID | HS133-01936 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:95044830-95046340 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr1:95045547-95045558 | CTGAGTCATCC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:95044896-95044908 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr1:95044900-95044912 | GTTTGTTTGTTT | + | 6.32 | | JUNB | MA0490.1 | chr1:95045547-95045558 | CTGAGTCATCC | - | 6.14 | | NFE2L1 | MA0089.2 | chr1:95045543-95045558 | ATGGCTGAGTCATCC | - | 6.36 |
|
| | 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 |
| GH01I094579 | chr1 | 95044561 | 95046719 |
|
Enhancer Sequence | TCTACTTTCG ATCTTTGGAG TTGCTGACCT TTGGATGGGG TTTTTGTGGG CCTTTTTGCT 60
TTTGTTGTTT GTTTGTTTGT TTTTCTTTTA ACAGTCTGGC CACTCTTTCA TAGGCTGCTG 120
CAGTTTTCTG TGGGTCCATT CTGGACTCTA GTCACCTTGG TTTTTCCCTA ACCTGGAGGT 180
ATCACCGGTG AAGGCTGTGA AAAAGCAAAG ATGGCAGCCT GCCCCTTCCT CTGGAAGGTC 240
CTCCATCCCA GAGGGTACTG ACCTGTTGCC AGCCTGAATG TGCCTGTAGG AAGTGGCTAG 300
AGATCCCGGT CTTTCAGTCA GGAGGAATGG GATCAGAGAT CTGCTTAAAG AAGCAGTTTG 360
GCTGCTTTTT TGTAGAGCAG CTGTGCTGTG TTGGGGATCC CTTCAGCCCC CAGTTGGTTT 420
AGGTTCTGCA ATATCCTCAG GCTGGACCAG CTGAGATGCC CAAACAGCCA AGGTGTTGGC 480
CTGCCCCACC ACCCCAGGCT CCCCATCCCA GGGAGAAATT AGAACTCTGT CGGCCATAGA 540
ACATGGGCAG GGAAGGCCAA GTCCTCTGCT GGGGGGACCA ACACCTTAGG AGAAGTGGAT 600
CAGGGTTCTG CTTGAAGAAG CAGTCTGACC ATGCCTCAAC AAAACAGCCA TGTTGTGCTG 660
GGAAGCTGCC TCTGCTTCTG TAGACTTGGA CTCTCCAAAG CCTGCAGGCT AGAATGGCTG 720
AGTCATCCAA ACAACCAAGG TAGTGGCCCA CCCTTCCTCC TCAGGCATTC CATCCCGGGA 780
GAGATCAGAT TCCTGCTTAA AGAAGCATTC TGGCCAGGCT CTGGCAAAGC AGCTGTGCTG 840
TGCTAGGGAG ACACCTCCTC ATCTGGACTG TCTGACTCTC CAAAGCCCAC AGTCTGGAAT 900
GGCCAAGTAG ATCAAACAGC AGAGATGGCA CCCGCCCCTC CCCCTAGGGG TTCAGTCTTG 960
TATCAGGCAG GCTCCACCCT GTTGCTGGTG GCTTGCTGGA ATTCCAAGCC AGTGGGTTTT 1020
ATCTTGTGAG GTGCCGTGAA AGTGGGGCCC ACAGACTGAT GCTGCTCAGC CTCCTGGATT 1080
CAGCCCACTT CTTTGGGGTA TGCACGGACC TCCTGATTTG CCTCGTTGCA TACACCTTTA 1140
TTAGAGATCC TGAGGCCAGA GTATGTAAAG CTCCTGGGTC TCTGTGTGTG CCTGAGCAGG 1200
CACTCTGCCA AGACTCCATA CAGCTCCGTG TGTTGAACCT AAGGCCCTGA TGGTGTGGGC 1260
TCACAAAGGG ATTCCCTGAT CTGCGGGTTG CAAAGATCTG TGGGAAAAGC ATGGTTTCCC 1320
AGGGTTGCAC ACTCACTCAC CACTTCCCTT GGCTGGGGGT GGGGGTTCCC TCGACTCTGT 1380
GTCACTCCTA GGTGGGCTGT CACCCCACCC TAGTTTTCTT TATTCTCCGT GCTTTGAGTT 1440
GTTTCCCTGA TCAGTCCCAA TGCGAGTATC TGGATATTTC AGTTAAAGGT GCTGTATTCA 1500
CGCACCTCTT 1510
|
