| Tag | Content |
|---|
EnhancerAtlas ID | HS133-07898 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:96026670-96028510 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr12:96028112-96028123 | TTCAAGGTCAT | + | 6.62 | | Esrrg | MA0643.1 | chr12:96028113-96028123 | TCAAGGTCAT | + | 6.02 | | Gata1 | MA0035.3 | chr12:96026980-96026991 | TCCTTATCTGT | + | 6.14 | | Gata4 | MA0482.1 | chr12:96028315-96028326 | AGGAGATAAGA | - | 6.14 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_30434 | chr12:96026821-96028331 | Fetal_Muscle | | SE_34205 | chr12:96026020-96029927 | HCC1954 | | SE_38108 | chr12:96026012-96033324 | HUVEC | | SE_39171 | chr12:96026819-96028640 | IMR90 | | SE_46351 | chr12:96025945-96029765 | 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 |
| GH12I095632 | chr12 | 96026148 | 96036716 |
|
Enhancer Sequence | TTTATTTATT TTTGAGACAG GGTCTCACTC TGTAGCCCAG GCTGGACTGC AGTGGCACAA 60
TCTTGGCTCA CTGCAGCCTC CGCCTCCCAG CCCCAAATGA TCCTCCTGCT GCTCTGTCTT 120
CAGCCTTCCA AGTAACTAGG ACCATGGACG TACACCATCC CACCCAGTTA TTTTTTATTT 180
CTATTTTTTG TAAAGACAGA GTCTTGCTGT GTTGCCCAGG CTGGTCTCAA ACTTCTGGCC 240
TCAAACGATC ATCCCACCTT GGCCTCCCAC AGTGCTGGAA TTACAGGCAT GAGCCACTGC 300
CCCCTGCCCT TCCTTATCTG TGTTCATCGC ACTCATCACT ACCTGACATT ATTATGTACT 360
TATTTATTTA TCTATTACCC CTGAGTAGAG TGTAAACTCG GTGAGGACAG CAGTTTTTTC 420
CATTCACTGC TGTATCCCTA GCACCTAGAC CAGTGCCTGG CACACAGTAG CTGCCCAGTA 480
GTACTTGCTG AATCACTGAA TGACTCTCAA CCTCATGAGT GCGGTGCTGT GAGTCACCGG 540
GTTACTACAT CATGCCCAGA CTGGGCAACC TGGGGGCGCT GAAATGGAAT CACCGGTAAA 600
GATCTGCAGC TTCCTCTGTG ATGTGGGTGT GGTGGGAAGA TTTGCATTCT GAATCCATCA 660
TTTCCTTGCT GCCGGACTGT GAGCAAGTTT CTCAACTCTC TGTAGTCTTC GTTGTGTCAT 720
ATGTAAAATG GAGATAATAA TTATTAGATA ATTACATAAT TATCAGATAA TTATGTAGAA 780
TACTGAAAAA GTTATCCAGT TCAAACCTCC TTTTTATGGT AAATCAGAAG TTCCCCCTCA 840
GCTCCATAAA CTTCATTTGC TTTCACAATC CCAGACATCT GATTAGGCAG CCAAGAGCTC 900
TGAGAGGCCT TTGGCCGGAA ACTAAGGATT TATGAGAGCC AATGTTCTCT GTCTCTCCTG 960
TTTGAGCATG TAGATGACAT GGAATAACCT CTCTGATGTA TTGAATTCGT TTCTCCAGTG 1020
TCGTTTATGC TGCCAGATGA TCACTTCCCA GTTTGATAAA AATCACTTCA TAATGGGGAT 1080
TAGATGGTAC CAAAATGACA GTGGTCTCTG CTGGATCTGA CAAATTCTCT CTCTCTCTTT 1140
TTTTAACCCC AAATCTCTAG TATGCCAAAA GTTTGCACAA AGGCTTATTG TTGTTATAAT 1200
TGTCTAGGAC TTAATAAATT AGCTATTGTC CTGAGATAAC CTCAAAACTC CTGGCTAGGA 1260
GGTTAAAAAC GATTTTTAAG GGAGCATAAA TATGGACACA CTGGTAAAAA AGTTTTTCAT 1320
CCCGTGTAGC ATTTTTTTTA GGTTTGAGTG GAAAGTGGTG TGTGACCACA GGAATGTACA 1380
TTAACAAAAG CAGTAAGCTA ATTAAATAAC ACACAAATGT TGTATTGTCT GGGTATTAAT 1440
TCTTCAAGGT CATGTCTTAG TTTATAATGG CAAAGGGAAT TTATTAAGGG AGAATTATTT 1500
GACAGGAATC TTTTTGTTAT TATAAGTTAC ATGCAGGTTA AGATAATCAA CAATATTTTT 1560
TCTATAAGAA CCATAAACAA GAGAAATCCT GCAACATATA CTTCTTGCTT ATTACATTAT 1620
GGTGTTTAGC TTACAGGAAC TTGGGAGGAG ATAAGAAAAA AGAAGAGAAG AGGAGAGGAG 1680
GCAAACACTC ATTGGGCGTT GTATTCGTCT GTTTTCATGC TGCTGATAAA GACATACCCA 1740
AGACTGGGTA ATTTATAAAA GAGGTTTAAT GGACTCACAG TTCCATGTGG CTGGGGAGGC 1800
CTCGCAATCA TGGCAGAACG TGAATGGCAC GTCTTACATG 1840
|
