Tag | Content |
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EnhancerAtlas ID | HS133-28463 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:47477770-47479080 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr7:47477961-47477979 | GGAAGAGGGGAAGGATGG | + | 6.33 | Gata1 | MA0035.3 | chr7:47478401-47478412 | ACAGATAAGGA | - | 6.14 | NFYA | MA0060.3 | chr7:47478549-47478560 | GGCCAATCAGA | + | 6.02 | NFYB | MA0502.1 | chr7:47478544-47478559 | CAAGGGGCCAATCAG | + | 6.24 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_00125 | chr7:47477988-47488491 | Adipose_Nuclei | SE_23979 | chr7:47478151-47478413 | Colon_Crypt_2 | SE_31448 | chr7:47477663-47478250 | Gastric | SE_31448 | chr7:47478293-47479287 | Gastric | SE_52619 | chr7:47477701-47479116 | Small_Intestine | SE_65257 | chr7:47477694-47478494 | Pancreatic_islets | SE_65257 | chr7:47478568-47480491 | Pancreatic_islets |
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| Number: 3 | ID | Chromosome | Start | End |
GH07I047440 | chr7 | 47477664 | 47478250 | GH07I047439 | chr7 | 47478301 | 47478450 | GH07I047438 | chr7 | 47478569 | 47480491 |
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Enhancer Sequence | CAGCAAGCCC TGTTTATGAC AAGGGGGGGC GCTGCTTTGT GACCCACAGT TCATTTCTAA 60 CCCTGCACAA GAAAAAGATC CCTGCCATAG CCATTTTGCA GGGAGAGCTC TGGCCCTGAC 120 AAGGCCCCAC AGACAGGTGC TGGCCAGGGC TCCAGGCCCT CTGCATGGTC TCTTTGGGGA 180 AGGGGGACTG GGGAAGAGGG GAAGGATGGC CAGAGAGGAG ACTCAGGATG CGCTGACCAG 240 CCTGGGAGTG GCTTCCAAAG GAAGGAGCCA TGGTCCTGCA GAGCACACCG CCTCAGTGAT 300 GAAGGAGGAA GCCCTGAGGA GGAGAGGGCC CCTGGTGAGA GGCACCACCA TCAAATGGGG 360 CTTGGCCACC ACTTCCTGTC CACTGCCAGG TCACAGACAA GACGGGCTTC AAGACCAGAA 420 AGAGGCAGGA GCCTGAGTGA ATCAAGGATC GGGGAGGGGT CAGGACCCAG GTAGCACCTG 480 GGCCAGGGCT GCTCTGGCAT CAGACGGAGG CCACATCCTA CTCTGCCACT TGGGTCCACC 540 TCTCCCAGCC ACTGGTGCCC CAGTCATTGG AGCAGACCAG CAAGGAAGAC AATGAACACC 600 TTGTAGGTTT GCAGGGCAGA TTAGCTTTAC CACAGATAAG GAGGCCTCCT TACTAGAGAT 660 AACAAGGCAG GTAGAGAGAG GGTGCCAGGG AGCTGTCATT CAATCCCATT AGTGACTGTT 720 GACAGCAGAA GGAAGTCAGC CTCCACCTGG GCTACCAACC ATGGGAACAG AAAACAAGGG 780 GCCAATCAGA GGGTGAGAGA TGGTGAGAGG CTGTTCTGTA TTATTCCTCA GATGTGGCTC 840 CACCATCAAC TCGACAAGTG TGTTTTGAAA ATCAAGCTGT CTCCTTGTCT CCAGGGCAGC 900 CCCTGGTTTC TTGGGTGCCC ACCTAATTTG TCTTCCTAAT TTCTGGCTCA GGAGGAGAGT 960 CACAAGTTTG TCTCTTGATA CGAGGGATGC AGCATGGGAG CGCAAGGGTG GCTGGCTGGG 1020 GACATGTCCC AAGGCACTGG GGAGCCAGCC TCACTGATGA GTGCAGGACA AGGCAACAGC 1080 CATCCCTGCG GTCAGCAGTC GTGTGTCCCT GAAAGCTACC TACAGAGACA CATAAGTCTC 1140 CTCCCCAGGC GTGGCAGCAG AGAGACAGAG GACGAAGGCG CCACGGACAG CTGTGTGAGC 1200 CCAGGCCCTT GAGCTTCTCC CTCATGTGTA AACCAGTGTT CTGTGAGTGC CCATCCCTAC 1260 ACAGTGCCTG CTGCAGAGCC TGCCCAAAGG CTCCCAGAGC CGCCCACCGC 1310
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