| Tag | Content |
|---|
EnhancerAtlas ID | HS133-07008 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:7061340-7063960 |
Target genes | | Number: 51 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:7063039-7063057 | CCCTCCTTCCCCCCATCC | - | 6.18 | | ZNF263 | MA0528.1 | chr12:7062408-7062429 | GCCCCCTGCCCTTCCTCTTCC | - | 6.09 |
|
| | Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
| SE_09821 | chr12:7057722-7072113 | CD14 | | SE_10294 | chr12:7057787-7072648 | CD19_Primary | | SE_11246 | chr12:7051570-7075651 | CD20 | | SE_11874 | chr12:7057290-7072000 | CD3 | | SE_13696 | chr12:7059354-7064308 | CD34_Primary_RO01536 | | SE_15448 | chr12:7059390-7063771 | CD4_Memory_Primary_8pool | | SE_15935 | chr12:7059481-7063047 | CD4_Naive_Primary_7pool | | SE_16424 | chr12:7057934-7063850 | CD4_Naive_Primary_8pool | | SE_16892 | chr12:7057515-7065729 | CD4p_CD225int_CD127p_Tmem | | SE_17385 | chr12:7051304-7075645 | CD4p_CD25-_CD45RAp_Naive | | SE_17804 | chr12:7051451-7075926 | CD4p_CD25-_CD45ROp_Memory | | SE_18513 | chr12:7051903-7072452 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19322 | chr12:7057416-7072760 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20105 | chr12:7057420-7072350 | CD56 | | SE_21550 | chr12:7059066-7064151 | CD8_Naive_7pool | | SE_22026 | chr12:7059039-7066905 | CD8_Naive_8pool | | SE_22431 | chr12:7051483-7072746 | CD8_primiary | | SE_32571 | chr12:7058059-7071909 | GM12878 | | SE_50217 | chr12:7059210-7076065 | Sigmoid_Colon | | SE_53937 | chr12:7057924-7072654 | Spleen | | SE_55163 | chr12:7059653-7064143 | Thymus | | SE_59538 | chr12:7045399-7071773 | Ly3 | | SE_59972 | chr12:7045722-7069352 | Ly4 | | SE_62072 | chr12:7045612-7071479 | Toledo | | SE_62347 | chr12:7051577-7074891 | Tonsil | | SE_66670 | chr12:7059219-7064681 | Jurkat | | SE_67220 | chr12:7057771-7064582 | MM1S | | SE_68053 | chr12:6999072-7081180 | TC32 | | SE_68054 | chr12:6999072-7081180 | TC32 | | SE_68055 | chr12:6999072-7081180 | TC32 | | SE_68056 | chr12:6999072-7081180 | TC32 | | SE_68057 | chr12:6999072-7081180 | TC32 | | SE_68058 | chr12:6999072-7081180 | TC32 | | SE_68059 | chr12:6999072-7081180 | TC32 | | SE_68060 | chr12:6999072-7081180 | TC32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 7061503 | 7061663 | | chr12 | 7062635 | 7063280 | | chr12 | 7061911 | 7062149 |
|
Enhancer Sequence | GTGAGGGCTC CGCACCCCCG CCATTCCCAA GCAGGGATGA GCCGGCTCCC ACCCTGAACA 60
GCCAGGGAGG CAGGGAGACT GGCAGCCGGC GCTGCCTACC CTCCATCCCC TCCCCTCCCT 120
GCACCAGCTG GGGCTCTCAA TGTCCCTCCT CCCTGCTGTC CTGGGACCTG GTGTCTCAGA 180
GCCTAACCTA CCACCCTTTC CACCTAACCC CGAGGAAGCC ACAGAAAGCT GCCTCGCCCT 240
ACTCCGGGAG CCCTGGCCGC TGCAACCCAG GTCCCACTGG AGACAGGGAG GCCACTGCTG 300
GTGGCCAGCA TGTCGTGCAG GCCAGCTCTG TTGTTAGAAA GCTCTTCTTC CTCTGGAATC 360
GAGCCTGCCT TCCTCCGTCT GCCCCTCACC CCAGCACATG TTAGGACAGT GAGGAGCTGA 420
CACTGGGGTG AAGATGGGGA TGAATGCTTG CCAAGACACT TGATGCCTTG TCCCAGCCGC 480
CCCGTGGGGA TGGGTCTGTC CTGTGGGGTC AAATAGGTCT CCGGCCCAAA CAGAGATCAT 540
TGAGAGCACG ATGTGAAGTG TTCACCTGTG TAAAGTGTCT CACGCTGTCC CGGGCACAGA 600
GTAATACTCC AGGCATTTCC TTCCTGTGGC CTCCCCGACT CCTCCTGTGG TCTCCCAAAG 660
GCATGGGCTG GGGGCTGGGG GCTCTGAATG CTCCTCATGA CACCATGGCT CCTTTCAGCA 720
GCCGCATCTC AATGCCAGAT CCCCTTAGAG TAAAGGGCAG CGGAATAACG CTAGGGGGTT 780
TTCACATGCA CCCCTGGGCC AAGCCGACTT GCCCTTGCCG TGGATCCCTG CATTCATGGA 840
TCGGTTATTG AAATGATCGG GAACCTTGCT CCTGCCAGCT TGCAGCCTCT CTGAGATTCG 900
GGCCTCCAAA CTGCATCAAT ATTTTTGGTC AAGGCACTGA TTGAAACTTA GAGCTGGATT 960
CGGTCACGGT GCAGCCCTGT GGCCCACCTG GGAGGCCTCC TTTCCTGGAT CGGCCTCCTT 1020
CAAGGCCTTC CCTCTCTCTG TGAGCCTCAC ATGGCTGGCT CCGTGTCTGC CCCCTGCCCT 1080
TCCTCTTCCC CACCGCAACA CTCAGGGGGC TTTTGGCACC GAGACCCTCT AAAGCTCATG 1140
TCCTCTCTTT CTCCTTGCCT CCAGCCAGGA GAGGAGGACG GGCTGACCAG TGCCTGGAGG 1200
TGGAAGAGAG GAGCAGGGCC CCAGGAGGCC CCTGCAGAGG AGGCTGAGGC CTGGGTTCAA 1260
GGAGAAGAGA GAAGAGAGAG AAGGAAGGGA GGGCAGTGCC GGGGCGGGAG GTTAAGACCA 1320
GGGAAGCCGC ACTGGAGGCC CTTTTGGGTG ACCCGTCCCA GGAGCCAGTG TCACCCCTGA 1380
GCCTGGGAGT GTGTGAGAGG CTCTTTCTCC CAGGTTCTGC TGTGTCCTCT GCCTTGTCTG 1440
TGCGCCTCCT CCTCTGCGAG AATTTGCATC TGTCCCTCGG TGGCTCTGCG CTTCCTGTGG 1500
TCAGCCTGAC ATTTGCATGG AGACTTCCTC ATCCTGGGGC CTGAGGGAAG GGGCTCAGCC 1560
CCCTCCCCGC TACCTGGGGT CCTAGCCTGT CCCCAGGCGG TGGGCTGAAG TAGCCCAGTG 1620
GGGTTAGGAG GCTCTGGGGG TCTCTCGGCT GGAGTCACCT CCGGGCAGGG GTGAGATGGG 1680
TTGGGACAGA CTGGTCCTCC CCTCCTTCCC CCCATCCCTG CGGTTGGAAA ATTTGCCCGC 1740
CCTCCCCTCG TCCCTGGGCT GAGGAAACCT CACAACCTCA CTTCTCACTC TCTCCCCAGA 1800
AGGAGTTTTG TGTTTTTTCC ATCACGTGGT TTCCTGTGGG GCTGGGCTTT GTGGGGCTAC 1860
AGTTTCCTCC TGGGAAAGGG GTGTGCTTCG GGGAAAGGGC TTAGTTCTGC TTTCTGCCCT 1920
GACAGCCCCT TCAAATCCGT TTGAACCCTG GGCTCCCCTT CAGTGACATC ATCCAGGGCA 1980
CCCCAGAACC CCCTACACCA CTCTTTCCCC AGTGGGGTTG TCTTCCCCGC CTCCCTGGCG 2040
GAGCGCACCC CATCCGCCTT CCTTGTGACT TGAGTCTGTG TGTCCATCTC CCACCACTCC 2100
CTGTGGTGTG GCCTCGGTCT GCGTTTCTCT TTGCCTCTGG TCTCTGCTGG GGCACAGTCC 2160
CATCCTTCAC GGAGATTCAT CCTTAGCTTC TCTCCTCCAA ATATTTTGAA TATTGCCAGC 2220
CTTTCTGCCT TTCAGAGGTG GGCTCTGGGT TCGAAGCCCG GTTAGAACTC TGGAGGCTAG 2280
GATGGCTTGA ACCTGGGAGG TCGAGGCTGC AGAGAGCTGT AACCGCGCCA CTGCACTCCA 2340
GCCTGGGCAA CAGAGCTCTG GAAGCTTGCC CTAGAGTCAG TCAAGGGCCC TAGGCCAGTG 2400
AGTAACAGCT CAGCGTCAGT TTCCTCATCT ATAAAATGGG GGTAATATCA TACCTAGCTC 2460
TCAGCATGTT TGTGAGAGAC CTAAATGAGG TGGTGGATTT GGAAGCATGT AGCGCAGTGC 2520
CTGGCACACA GTAGGTGCTT GATTTCCGGC CCCTCTCTGT GAATGTCTCT GCTCAGCGCC 2580
TTCCCCTGTG GCCTGGGTCT TACCTTCCCT GACGCTGCCT 2620
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