| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00335 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:11939750-11941890 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:11940950-11940968 | CCATCTTTCCCCCCTTCC | - | 6.03 | | KLF5 | MA0599.1 | chr1:11940623-11940633 | GCCCCGCCCC | + | 6.02 | | ZNF263 | MA0528.1 | chr1:11940934-11940955 | TCCCTCCCTCCCGCCTCCATC | - | 6.01 | | ZNF263 | MA0528.1 | chr1:11941840-11941861 | TGAGGAGGCAGGGGTGGAAGG | + | 6.62 | | ZNF263 | MA0528.1 | chr1:11940931-11940952 | CTCTCCCTCCCTCCCGCCTCC | - | 6.87 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_40948 | chr1:11939367-11944310 | Left_Ventricle | | SE_49584 | chr1:11939603-11941132 | Right_Ventricle | | SE_49584 | chr1:11941144-11942679 | Right_Ventricle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 11940227 | 11940565 | | chr1 | 11940714 | 11941660 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I011879 | chr1 | 11940022 | 11944112 |
|
Enhancer Sequence | TCTGACGGAG GTGCTCCCCA GTGCAGGCAC CGCGTGGCGT GGCCCTGCTA CGACAGCTGC 60
CCCTGACCCC AGCCTGATGC TATCTCACTT CTGCTGGAGG AGCTGCAGAG GCTGGAGACA 120
GAGCTGGGCT AATGCCCTCA GTGATGGAAG GACACCTGGG ACCAGGTGAA GGCTGCACAG 180
CGCCTGGAAG GCTGGCCAGA CGGAAGTGGC ACCCCTAGCT CCCTTCTAGT GTCCACTGCA 240
CCCCACCACC ACCGTTCCTG GGTGTGTGAC TGCCGGAGGG GCCCGTGGGC TCCACCCTGA 300
GCCTCAGCCT GGACAGCGAC CAGAGTAGTG GCTCGACCGC TTCTGGCTCC TGCCAGGCTG 360
CCCGCCACAG CACCAGCACC CTGTGCAGCC AGTTCCAGAG AGCTGAGAGT GAGAACGGGT 420
CCAACGAGGG CACTCTGTAG AAGAAGGAGG CCTTCATGAA GCCTTGGAAG GCCCGCTGGT 480
TCATGTTGGA CAAGACCAGC ACCAGCTGTG CTACTGCAAC CACTGTGTGG ACACAGAGTG 540
CAAGGGTGTC ATCGACTGGC GGAGGTGGAG GCTGTGGCAG GGGCACGCCC TAAGACCATG 600
GATGAGAAGG CTTTCTTTGA CGTGAAGACA ACACTTTGCG TTTACAACAT CTGTGCCCAG 660
GATATGCCCT TGGCCCAGCA GTGGGTGGAC GGGATCCAGA GCTGCCTGTC AGACACCTGA 720
GCCTCCCGGC CCCGCCCAGC TGCTCTGCTT CCGGTCGTTA CTGACCACTA GGGGTGGGCA 780
GGGCTGCCCC AGCCATCTTT ACTGCCCCAG CCCTCAACAA TATTGAGGCC CTGAGCCCCC 840
AGCACATGGT GCATACAGCC CCTGCCCCAT CCCGCCCCGC CCCACCCAGC TGGCCCTAAC 900
TTATTTTGGG GTCACAGCTG AGCACTGTCC CTGGAGGTGA CCAAGGTACA GCCCGCAATG 960
GGCCTGTAAA TAGCCCAGCC CTGTCAGCGT GTGCTGGTCC AGCCAGCCGG CTGCAGGCGA 1020
GTTGTTTCTA GAACCAGAGT CTATATAAAC AGAGAGCTAA TGCCAAAAAA AAATAATAAA 1080
TACATAAAGA AATCATACAG AGCAAGACAA ATCATCCAGA AATCACCTCC AGGGAACTGA 1140
AGCACTTATT CCAGGACATT TGACCCTGCA GCCTGGTCCC TCTCTCCCTC CCTCCCGCCT 1200
CCATCTTTCC CCCCTTCCAT CTTCTGTGTT CAGATAAACA CCAAGAGCCT TCAAAGAGCC 1260
CCCGGGAAAT AACTCAGTTT CTTGGGCACA TATCAGCTGC CATGAATGGT TCTACACACT 1320
GAAGTCCATT ATCTCAGTGA CTGCGAGGAC TGAATGAGCA CAGCCTGGAG CTGAGTCAGT 1380
GTTCCATAAA AGTTGGCTCT TATTTTTATT ATACTGGACA CAGAAAGGCC AGATGCCTTC 1440
CCCAAAGCCC CTCCCTGTGG GTGGCAGTGG CCCAGGAAGT CTGGCACTAA TGTCAGTGCT 1500
GTCACCTGCC ACTCTGTCCT CAAGGGCCTC TGGGACATGC TGGGAAGGCA GGCCGTGAGC 1560
CAGATGTTGC AGAGCTGGGC CCTGAGACGC TGTCCCTTCA GTGACCTTTC CTGTCCAGGG 1620
CCCACAGCGG AAGCTGACAT GTGTGCTGCC CCTCCCCTCC GCTCCCCTCC CCTCCCCACC 1680
CCATTCTACT CTATGGGCTT TGGTGGGAAA AAAACCAGGG CCCCATCCCC TGAGGCCTAG 1740
GCCAGTGCAG ACATAGACCT CGAACTCTGC CCAACATGGA TGGCCTCTGC CCAGGTGTGG 1800
GAGAACAAAG GCAAGGAAAG GCTCAAGGAA CGTTCCAGGC ATCAGGAAGC CAGGCTTCCC 1860
CTTCAGGGCT GTCGAGTGCT CAGGTTTCTA TGCCTGTCAG TCACCAACAC TTTTGCAGTG 1920
GGCAGCTACT ATGTGCCAGG CACAAAGGGT AACTGGGCAC ACCTCTTTTC TTGGAATGGG 1980
TCAGAGGTTG TCATCAAGGA GGTGATGTTT AAACTGAGCT CAGGGGAATA AGGAGGAGCC 2040
AGGGTTCGGG GAAGAGCATC CCAGCAGAGG ACAGAGCCAA AGCCAGCGCT TGAGGAGGCA 2100
GGGGTGGAAG GAATGTAGTG GTTTGAGGAG CCCTGGCAGG 2140
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