| Tag | Content |
|---|
EnhancerAtlas ID | HS133-05708 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr11:61370100-61371340 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr11:61370787-61370798 | CTGAGTCACCC | - | 6.02 | | JUN(var.2) | MA0489.1 | chr11:61370481-61370495 | GGAAAATGAGTCAT | + | 6.3 | | JUNB | MA0490.1 | chr11:61370787-61370798 | CTGAGTCACCC | - | 6.02 | | SREBF1 | MA0595.1 | chr11:61371039-61371049 | ATCACCCCAC | + | 6.02 |
|
| | 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 |
| GH11I061598 | chr11 | 61366337 | 61371586 |
|
Enhancer Sequence | ACTACCAAGG ATCCTGATGG TCCTCCCAGT TCTAGGAAGG GGCAGCCATG CAGAACAAGT 60
CTCAAAAGCC AGCAGGAGCA GGAGAGGAGG ATTGAGAACC CCCAAATTGA TAGGCAGCCT 120
GGGGCTGGGT GGGGCAAAAG GTACTGGAGG TGGTGCCTCT GCCCTTTCCC CTTCCACTGC 180
ACCCCGTCCA CACTCCATAG AAGTCAGCAG TTCAAGTGTC CTGTAATGCA CCCCACACCC 240
CAACACACAA CACACAGGAG CCCCAGGCCT CAGATGGGAA AAACACTGTC TGGCACTAGG 300
TCTGGTTGAC TGGAGAAGTG GGGAGGGAGC CAGGCAGTCC TTCCATCATG CAGATGGAGA 360
GACCTAGAGT CTCAGGCGTT GGGAAAATGA GTCATTTAAC ATCCATCAGG ACCCAAGCCT 420
CCTGAGCCCC CAGCCTGGAC CCCTGCACCC CCTCTAGGGA GCAGAGTGAG ACACAGAGCT 480
CCCTAACACT AGACCAGGTG TCCCTTAGCT CCGCTCTTCT AGGAGGCTCC CTGAGCACAC 540
CCTCTGCGGA GCCTGACTCC CACAGGAGAA GCAGATGGTG CCAGAGTCTG CTGGGAACTG 600
GCTGTCCTGG AGCCCAGCTG TTGCACAGAT GTGAGGGGGG AGGGTGGAAT GGGGGTTGCG 660
AAGGCAGGAA CGCTTGACAG CTCATGCCTG AGTCACCCAT CAGCTCCGGG AGTGGTAATG 720
AGCAGATTAG GGTTATTACA GCCGAATGGC TCAGAGCGCA CTTGCTCACC CGAGCAACCA 780
TCGGCGAACG GCTGATCGCC CACGACTGCC ACGGCCGTCA TGCCAGGCCC GCCTCTCCCT 840
TGCCCTCTCA TTGACTGTGC CGCTGCCAAG GCAGCCTCTG TGGCCTTCAC ACGCCTCATT 900
AGAGCTGCTG GGGCATGCCC ACCAGCCCAT GGCCCAGACA TCACCCCACC CACTCCTCTT 960
CCCAGGTGTG TCAAGGGGGA CACAGGAGTC TGACCTGGGG CCTCGATAAG TGGGCACAGT 1020
GATCCCTGAC TAGGGAAACA GGTGTATAGT TCCCCACCCA CCTAGAATTG GGGCAAGGAC 1080
AGGTATGGCA GGGATCCAGC CTCCAGGGCC AGTCCTTGTC TGTCTGGTCA CCTAGCAGGG 1140
GTCTAAAACC AGTGAGGTCC CTCTAGGTCT GGGCCAGGGA CACGTCAATC TCCAGGGAGG 1200
GCGGCTCCTC CTTCCCCATT GGGCCCATGT TGTCCCCTCT 1240
|
