| Tag | Content |
|---|
EnhancerAtlas ID | HS133-06542 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr11:111319950-111322130 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr11:111321826-111321837 | GGTGACTCATG | + | 6.62 | | JUND | MA0491.1 | chr11:111321826-111321837 | GGTGACTCATG | + | 6.02 | | MAX | MA0058.3 | chr11:111321093-111321103 | ACCACGTGCT | + | 6.02 | | Tcf12 | MA0521.1 | chr11:111321392-111321403 | AACAGCTGCTG | + | 6.32 | | ZNF263 | MA0528.1 | chr11:111320249-111320270 | CCTTCCTGCCCCTCCACCCTC | - | 6.2 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_58284 | chr11:111214563-111322309 | Ly1 | | SE_60973 | chr11:111229476-111322231 | HBL1 | | SE_61456 | chr11:111234062-111326162 | Toledo |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 111321278 | 111321652 | | chr11 | 111320088 | 111320168 |
|
Enhancer Sequence | CCATTTCCAA AAGGGTCACA GCCAAAAACC TGGGCATGGT TCACCACAAC GAAGTATTAA 60
CCAACCAACA TGAACCAGCA CTCCTCCCTC CCCCTCCCCG CCCCCAGCCC AGTGACAGTC 120
GGTACCCCTG CCTCCCGGGC CACCGAGACT TTGGAGAGCC AATGGGCTGT GTCCAGTGGG 180
AACACAGGAG CTGCAAGGAC GGAGCCACTG GAATCAGGAG GGGCTATGTT TGACCAAGGC 240
TCAGTGGAAT GACCACTGTG CCCACGAGGT AGGAGAATGC CCATCTATTA TGTCCTTGGC 300
CTTCCTGCCC CTCCACCCTC CCATTCAAAT GTCCACCATT CCAGCCACTG GGCTCATTCC 360
ATTGCCCCTC TCTGGAAATA TAGAGGTCAG TACTTTGCAC TCTCAGGCAG TTCCTAGAAG 420
CAGCTGGAGA GAATGAGGAA GAGCTTCCCC AGGGAGGTGT CCCCAAGAAG TTTGAGTCTT 480
TGTGCAGGTG TGTGCCACAC CAGGAGATGC CCATGGACAT GACCCAAGCC CTGGGGCTCT 540
GCCTGTGCTG GGGACAACAG TCAAGCAGAA TGTGCAGCCC TCTGTGCCCA GAGAGACAGA 600
GACACATCTT GCAGCTCAGC TGCCCTGATG GCATCCCACA GATTTCTGTC ACTGAAGGCA 660
TGGGGAGTCA GGTACAGTAC TCTGAGGTCC TACCTCATGC AGAGCCAGGG CCTGTGACTT 720
CTGCCTCCAA AGAGGGAGCA TGCAGGACAT GCCTATGTGC AGGGTCCAGA GGCTGCTGCT 780
GCCTGGCCCA CATCACTGGC ACCTCACCAA CATCAGAGGC TCAGAACCAG AGCAAGGCCC 840
CTTTGTTGAT TTTATTTCAT CCTACAAAAC TCCTTGAATA AGAGGTCATT GTGTTCATGA 900
AAGAAGAGGG ACACTGTCCA AGAGGTCATG ACTCCAGGCT GCCCCTGCCC CATGGAGTTC 960
TTGGAACTAT TCCCACCCCC ACCTCCCTTG TGTCCTTTCA GGACACTCAG ACACAGCTCA 1020
GGGAAGGGGC TGTGTTCGCC CTCCCTTCCT ACTGGGCAAG TGTGTGACTC CGTGTCTTGA 1080
GGGAAGATCT GACACTGCCT CTTTTCGTTT CCAGGATTTT TACCTTCTGG ACCAGCCTTC 1140
CCCACCACGT GCTGTGGGCC ATCCCTGCAA CTTGGACTTA GGGCAGAAGT CTGTCCCCCT 1200
CTATGTGGTC AAGATGGATG GTAAGAGAGC TGGACAGATG GAGGCCACAG GGAGGCCTGT 1260
GGCTCGGGAC CACACACATG CAAGCCTTGT CCTTACCAGG GCGTGTGCTC TGTCCCATGA 1320
CCAGAAGCTG AGGTTTGACA GGGCAACCAC TCCCCTAGGG AGGGCTCCCT GAGAACTGCA 1380
TGCAAATTCT GACCCCCCTC AATGTTTCAG AAAGTTGAAG CTACCACGTG CAAACCAGGC 1440
TGAACAGCTG CTGATTATAT ACATGCTCTT GGGAAAACTC TTACCCCGGT CCCTGCAGGG 1500
TCAGAGGGAA TCCCTGCTTG TTCTAGCGCT TGGCTTCCTG GGCCTGACCT GACCAGATGG 1560
TGAGCTACTA CACTCCCTAG GCCTTCCCCT CGGGGATCCC AGGTGTCCAG ACCAGGATCC 1620
AGGTGGGCAT CGCAGCTCAC CTGTTGCCCC TCCTATCCCT CCCCTACCCT TCCCAGGTCC 1680
CAGCACAAAC CCATCTGAAG AGTGGCAGCT CTCCCTCATT CTCTGAATCT TACCTAGGAA 1740
AGTCTAGGGA AGGACATCTG GACTCTTCTT GGTCACTGAG CCTCAACTCC ACACATCTTG 1800
GGGATCTGCT GCCCCCAGAG CCAGGCATCC GAAACCCCAC AGTCTGCCTC CAAGTCAATG 1860
ATACCCTGGC CTTCCTGGTG ACTCATGAGC ATTACCCAGA GTATGACCTG TGAGTGTCCA 1920
GAGACCACAG CCCCATCATC ATGGAGGCCC TAGAGAGGAA ATGCCCCTGC ATCAGCCACC 1980
ACTCCCAAAG GCAACGTATT CCCTCCTTTC TCTCTCCTCA GGGGCCACTT CTATAACACA 2040
CTGGAGCAAT ATGACTGGCG GCGCTTCCGG GCCCTGGCTG AGGAGTCCCA GCTCTATGAG 2100
CAAAGCCTCA GCCTCTTTCT GCAGCAGTTC CAAAAGCCGG GCATTTATGT CTTTCGTCTG 2160
AGCAGCAACC GACATCGGAA 2180
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