Tag | Content |
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EnhancerAtlas ID | HS133-22402 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:58026780-58027980 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr3:58026946-58026967 | TTTTGCTTTCAGTATCACTTT | + | 6.7 | RREB1 | MA0073.1 | chr3:58027242-58027262 | CTCCCCACCAACCACCACCA | + | 6.33 | RREB1 | MA0073.1 | chr3:58027246-58027266 | CCACCAACCACCACCACCAC | + | 7.32 |
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| Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
SE_00762 | chr3:58026357-58028180 | Adipose_Nuclei | SE_23194 | chr3:58026684-58027587 | Colon_Crypt_1 | SE_27681 | chr3:58026398-58027802 | Fetal_Intestine | SE_29426 | chr3:58025684-58027847 | Fetal_Intestine_Large | SE_30574 | chr3:58026442-58027846 | Fetal_Muscle | SE_36024 | chr3:58026477-58028276 | HMEC | SE_37989 | chr3:58025669-58040227 | HUVEC | SE_41579 | chr3:58026680-58028166 | LNCaP | SE_45969 | chr3:58026358-58032250 | Osteoblasts | SE_47269 | chr3:58019885-58040171 | Panc1 | SE_56289 | chr3:58026661-58028194 | u87 | SE_64106 | chr3:58026703-58027892 | HSMM | SE_65730 | chr3:58025436-58027838 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I058034 | chr3 | 58020175 | 58032048 |
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Enhancer Sequence | GGAACGGTGT TAATCCCGTT TTGCAGCTGA GGAAACTGAG GCTACATTTA CGGTCACCTA 60 GCTGGCAAGC AAGTGGCTGA GCCTGGAGCA GCAGCAGATC TGGGGAACTC CACAAACCAG 120 ATTTCTGTGT GGTATCCCTG TGGACACAAG GATTTAACTT GATTCTTTTT GCTTTCAGTA 180 TCACTTTATG ATATTACAAT GAGCTTGCAG TATTTATTTT CAGAAGAAAA GCCAGATTAT 240 TCCCATTTAT GAGAGAAGCA GCCAGGTGGG CAGGGATTTC CAGCGCTGAA CCAGCCAGTG 300 TGTGCATTGT CTCTTCCCGC TGAGCGGCCC TGGTGTGCTG GGTTAGTCTG TGAGCCACAG 360 GAAATGTTGT CAGGGCCTCT GGGCTTTTGG ATGTCAGCAG GCCTTCAGTG GTGAGGAGGT 420 TGTGGCTGGA CTCAGAGGAC TCCTTGCTTT TGCTGAACGA CCCTCCCCAC CAACCACCAC 480 CACCACCACC AGTGGGACTA GCCCATGAGC TGTAAGCCAA CCTTTTCCTT CCTAACTTAA 540 TTTTCCAAAG AATAGTAACT TACCCACCAC CACTGCAGTC ACTGGGCCGG GAAGACAAGC 600 ACTCTTGCCT TGAATCCATG CCTTGAGCCA GTAGCCTTGA CCCAGGGTAA AGCAGTTATG 660 TGCTTGGGTC ACCTGGGTCA TGTTTTTGAA ATTGCCTCAA GCCTACCTTA CAAATCCTTC 720 CTGGAACCCT GCTTGGCTTT TCTTTGTGGG CTTCCCTTAG GAGGGAAGCT TCCCGAGCAG 780 CTTGTCTTGA CTGTAGCCAG CTGGGTGGTC CCAGCCACAG AATTTAACTG TCAAACAGCA 840 CCAGAAGGGT TCCTCATCCA GCTGTCTTGC CCCAAGTGCC CTCTTTGCTT TCTTTTTAGA 900 GAGTTCTGAG ACTCATTAGA GAGTTTAGAG ATTTTAGCAT TCTTGAAGTT CTTTCTGTGG 960 TCAGTTTGGT GAACCACTTC ATTTCTAAAG TTTCTCAGTT GACCCCATTC TTCCCCAGCT 1020 TTGCATTCTC CATGAAGCCA CCTGTGTTTG GTGTGTATGG GTTTTCTGCA ACCTAGGTTG 1080 AACAAGTCCT CTAGAATCCT GAACAATTGG TGATTCATGC TGGCCTGGTT TTTCTAATTG 1140 GCCTGGAAAT GTGGCTGTAG TGGACACAAG TGGACTTGGC CTCCTCTTTG ATGCGGGTAA 1200
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