Tag | Content |
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EnhancerAtlas ID | HS133-00394 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:15748700-15750400 |
Target genes | Number: 13 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_01247 | chr1:15749283-15749804 | Adrenal_Gland | SE_09666 | chr1:15747120-15748970 | CD14 | SE_09666 | chr1:15749256-15758688 | CD14 | SE_20093 | chr1:15749236-15750196 | CD56 | SE_23176 | chr1:15749307-15751816 | Colon_Crypt_1 | SE_23801 | chr1:15749329-15751792 | Colon_Crypt_2 | SE_24853 | chr1:15748794-15749155 | Colon_Crypt_3 | SE_24853 | chr1:15749289-15751821 | Colon_Crypt_3 | SE_31522 | chr1:15748784-15749167 | Gastric | SE_31522 | chr1:15749273-15754890 | Gastric | SE_50367 | chr1:15749258-15754549 | Sigmoid_Colon | SE_52537 | chr1:15749196-15754549 | Small_Intestine |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I015422 | chr1 | 15748785 | 15749167 | GH01I015423 | chr1 | 15749251 | 15754774 |
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Enhancer Sequence | GCCTCAGCCT CCCAAGTAGC AGGGATTACA GGTGCCTGCC ACCATGCCCA GCTAATTTGT 60 GTATTTTTAA TAGAGACAGG GTTTCACCAT GTTGGCCAGG ATGGTCTTGA TCTCCTGACC 120 TCATGATCTG CCTGCCTCAG CCTCCCAAAG CGCTGGGATT ATAGGCGTGA GCCACCGTGC 180 CCAGCTGGCC AGGTCATTCT TTGCGGTGGG GCCACCCTAT GCGCTATAGG AGCTTCCCTG 240 GCCTCCACCC ACCAGATGCC ACTGGCATCC CCCCCACCTC CGCCGCCCCA GGTATGACAA 300 CCAAAAACAC CTCTAGACAT TGCCAGATGT CTCCTGGGGG GCACATGCAC CCCAGCTTAA 360 GAGATGCTGC ATTTTGGCCA GGTGCGGTGG CTCACACCTG TAATCTCAGC ACTTTGGGAG 420 GCCGAGGCGG ACGGATCATG AGGTCAGGAG ATCGAAACCA TCCTGGCTAA CACGGTGAAA 480 CCCCATCTCT ACTAAAAATA CAAAAAATTA GCCGAGCGTG GTGGCGGGCA CCTGTAGTCG 540 CAGCTACTCA GGAGGCTGAG GCAGGAGAAT GGAGTGAACC CAGGAGGCAG AGCTTGCAGT 600 GAGCCAAGAT TGCGCCACTG CACTCCAGCC TGGGCGACAG AGCGAGACTC CGTCTCAAAA 660 AAATAAAAAT AAAAAGAGAT GCTGCATTTT GTGGCTGAGG AGCCCAGGCA ATTTGGCTTC 720 AGAGCCTGAC TGTCATCGCT GACCTTGGGA GCCCAGGGTC AGAAAGCGGC AGGGCTTTGC 780 TTTCCTGGGG GGCACTGAGG AGGGGAGTCC TCGTGACTTG GCTCAGGAAA GACTGAGTCC 840 CTCACCAGGT GCTCCTGCAC AGCCCCACGG TCATGTGGCG CCCGCCCAGC CCTCTACCAG 900 GCAGCAAACA GGGACCAGAG ATGGCAGGAG GCGCCTCCGC TGTGCCCCCC AGAACCCCTC 960 CAGCTCCAGG TGGAGGCTGG ACCACAGCAG CTTTGGCCTG CCTGACCCTC TGAGTCCCAC 1020 ACCTTCTACT GTCACAGAGG TGGCCACTGC CCACAGGGGC TGCTGGCCCA TCCACCTCCA 1080 CCCCAACCCT CATCCATCAG TGGGGCAGAA GCCGCAGGAC CCTGTGTTCC CTCCAGGGCT 1140 CCCAAGACCC ATCTTTGCTG TGTCACTTTC AACCACTGAC TCACTGGCTC GTGAACTATT 1200 TATACCCCTC GCACAAATGC TCCCCTTGTG CTCCAGGCAG CCGTCTGTGT TCTGCAGCAG 1260 CCCCAGGACA CGTTGGGGAG GGGCTGGGTA CAGAGCAAAT GTGCAAGTTT ATGAGCCCAG 1320 CAGATCAAGT CTGGAAGCCC AGCTCCTTCC TTACTGCTGT GTGACTGTGG GTGGGTCACT 1380 TAACCTCTCT GAGCCTTGGT CATAAAATAA GGTTATTAGG AAAATTAAGT AAAGTAAGCA 1440 GTTCCCAGCA TAAAGACAGA TCTCAGTACA TGGTTGCTAT TAGGTGTTCA AAGTACACCT 1500 AACTAGAGAA GGCGAAAGGA GCTGGGGAGC CCGTAAGAAG GTGCAGAAAT GAGACATATT 1560 CATGCAGAAG CTCAAGCGCC CGGGACATAG GGTTCTGGAA CACATCCACC TGTGTTGCGC 1620 TGCTGTCACC AGCACTGTCA CCCAGCCAGT TCAAGGCCTG GGGGACTGCA CAAGCCTTCT 1680 TTAGGTGCAG AAAAACCCAT 1700
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