| Tag | Content |
|---|
EnhancerAtlas ID | HS002-01992 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr11:74397920-74400030 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr11:74398405-74398416 | TCAAGGTCATT | + | 6.32 | | EWSR1-FLI1 | MA0149.1 | chr11:74397934-74397952 | GGAAGGGAAGAAGGCAAG | + | 6.39 | | Esrrg | MA0643.1 | chr11:74398405-74398415 | TCAAGGTCAT | + | 6.02 | | RORA | MA0071.1 | chr11:74398404-74398414 | ATCAAGGTCA | + | 6.02 | | YY1 | MA0095.2 | chr11:74398481-74398493 | CAAGATGGCTGC | + | 6.74 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_46155 | chr11:74397003-74399990 | Osteoblasts |
|
| | 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 |
| GH11I074685 | chr11 | 74397004 | 74399990 |
|
Enhancer Sequence | GGTGTGGAGA AGTGGGAAGG GAAGAAGGCA AGGCAAGGGT GTGATTCAGG CCAAGTCCCG 60
CAGAGGGGAG CTTGACTCAG ACTTGCAGAG GAGCTCCGGA GATCGTGCAA TCACTCCTCA 120
GAGTCATCCA CATCAGCACA AGGGAGCTGG AGGATTGGCA CCTCCATACT CATCTGTCTG 180
AGCTAAGGGC CACCTGGGGT GGAGCGGAGG TGGACATTGT CAGGCTCTTC TGGTTTTCCA 240
TGCTCACTGG CAAAGTGGGC TCAGGCAGCC TAAGGTCAGT GTTCTGACAA AGAGAAGCAG 300
GTGCTGGCTG TTGGGAATGA AAGCTCACTG GAGCTGGTAT GTATGACAAT GGTAAAGGGA 360
TAACAGGCAT TGTGATTGGG TCAATGGCAG TGCCGCTACA GTGGCATAAA CTGCAAGGAC 420
ATCTGTTATT TTCTTAACAA GAAATGTGGA GGTATGTGGT CTCCAGACTG CTTCAGTGTA 480
GGTCATCAAG GTCATTGAGG ACTCAGCTCA GGACAGCCTT CCTCAGCATC CTGGCTTTTA 540
TCATTCTCAG CCTCATGGCC ACAAGATGGC TGCTGCAGCA CCAGGGCTCA TGTCCTTAAC 600
TGATAGCATT TGAGTCTGGA AGAAAAGGGA GGGCTGCAGC AAAAAAACCT TTCGCCTCAC 660
ATGACCCTCC CCTACAGAAG GAAAATCTTC CCTGCTCACT CCACCAGCCC TGGTTCATGT 720
CATCAGTGCG TGTGAAAGGG CTTTATATCC TGCGAAACAC AACAATGCTA ATTTTAATTG 780
CTATTGAAAT CCATGCTTTT TCTTCCCCTT TGCACTGTGA GGGGCTGTGT GTGACTCACC 840
GTGGCTTCTG TTGATTCTGC CCTCTAAATA GCTGGCAATC CCACCCACTT CTCTCCCTCT 900
CTGTTGCCAC ACCCTCATCC AGACTGCCAC CATCTCTGTC ACTGGTAGCT GCAATAACTT 960
ATTAATACTA ACTGATTGCC CTGCTTCCAT TCTTGACTCC TTCCAAGTCT TTCTCCCACA 1020
GAAGCCTCAG GGATCTTTGT AAAACACAAA TCTGTCTGAG TCACTCCCCT GCTGGAAATC 1080
GTTCCAGGCT CAAAAATAGG GGAGATATTC AGAATAACTA CTGATTTGGA ATAGGCCCTG 1140
GGCAATCAGG ATAGGCCCCA GTGTTGACAG CCCTGCCAGC CCATCCTTCC TGAATATCAG 1200
CCCTGTTCTG GTGGCCCTGG GGAAATTGAC CTCTGCTGCC TCTCCAGGCT TCTCTCTAAA 1260
GCCCGTGCCC CTCACCCCCA CTTCCTGCAC CACCTACATC CACTGCCCGA TACTACTCTC 1320
TTGCCAGGCT GAACTTTTTG CTGCTTCCCA GATGTTTAAC ATACAGTAGG TGCTCAATCA 1380
ATGGTTGTTG AGCTCTGGAA TGATCACTGC TACCATTGTT ACTCCCATTA CCACTGCCAC 1440
CACCACCATT ACTGCCTCCA CCACCACCAG TACCACCCCT CCGATTTGCA GGACCCAGGC 1500
AAGAGTGCAA ATGGAGACTA CATATCATAA TATGTAATAG ATCATATGTG ATATGACATG 1560
GAGTCTCCAT TTGTATCCTT GCCTGTCACC ACTTTTGCCT GTTGTGAGGC CTCTGACCTC 1620
CCTGTTTCCT AGGACTGAAA CACGATTTCT CCACTTTCCC TGAATAATTG CTTAACGTCT 1680
CTATTTGGAT GTCTCCTCAT CCAGGAAGCT TCCTCTGACA CCCCTCTCCC CGCTCCCTGG 1740
CCATGGGTTC TCACAGCCAC CCCTGTGCCT TCTTCTGTGT TTGTCACTCT GTTGTCATTG 1800
TTTATGTCTC TCCCTCTCTA GACTGGAGAC TTTTGAGGAT GCAGTTGGAC ACAGAGGACA 1860
ATTACATCCC CTGTGCTGGT AGTAGCAGGG AGCCATGGTG GTAAAGGAGG GCAGGACCAC 1920
CTTTAAGCCC AGGAAAGAGG GACCCCCACC CTGGGCCATG CCCTCTGGAG GGCCCCAGTC 1980
TGACCCACTT TCAGCTGCAC TCCTACCCAC AGCCCAAGGG GTCCATGGGA TTGAGGGTAT 2040
GTGCACCCCA CCTCCTCTCT AGACCACAGT GGGGACCTAG GATCCTGGAA TTCTCTGCCC 2100
AAGCAGCCCT 2110
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