| Tag | Content |
|---|
EnhancerAtlas ID | HS133-11689 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:68701680-68703900 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr16:68702082-68702100 | TTTAGGCTTTCATTTTCC | - | 6.93 | | RUNX1 | MA0002.2 | chr16:68702520-68702531 | AAACCACAGAG | - | 6.14 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_34047 | chr16:68697743-68703782 | HCC1954 | | SE_35835 | chr16:68697045-68704759 | HMEC | | SE_64307 | chr16:68697315-68703904 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I068663 | chr16 | 68697209 | 68703920 |
|
Enhancer Sequence | CTTGGCAGGA TGATCTTTAG AGAGGAGCTT TGAACATAGG CCAGAGACTC CTGGTTTCCA 60
TTGGATGTCT TCTATCGAGT GCAGATACAT AGAGCTCTGG CTTTTTTGTT GTTAATTTCT 120
CTTTTTATTT ATTTTTACCT ATAATGTGTC CTATGATATT AATTGTTAAT TTCTCTAGAA 180
GCAGCCTCAG GTTACTGATT CCCTTTTTCC CTTCCCCGAC AGTATTTTAG GGAATGTACA 240
TTTAGGCTCA GTGCTAAAAG CTGTCCATTT ATATTGGTAG AGCAGGCACC TCTTCATCAG 300
GTTCATTGAC CTTGTAATTC AGAATCCTTG TGGGAGAAAC TGAGGCTAAT GCGGTCAAAT 360
GACTGTCTGA AGCCCTGGAT GGGTGTGGAA GAAAGAGCTA TGTTTAGGCT TTCATTTTCC 420
AGCCTTAAAT TCTGAACTAT TGCCCCATGT GCTCATCATC AAGTTGCCCC AGAAAGAGTT 480
TGATGCAAGC CCATTCATGC CCCCGTGATT TGGCCAAGAT GTGTGGCCTT GTGGAACCAT 540
GCTGCAGTTA GGAACAGGAG TCAGTTTACT TCGCTGACTA TTAAAAGATG GGGTAAAGGA 600
GGGATGAGTG ATGATGAGAC CTGGTTTCGT ATCAGTTTCA TTATGAAACT AGTGATACAA 660
GCCAGTGGTG CCAGGAAGCA TCTGGGAGGA AATTGTAATG ATCTGCCCCA GGGCTTACCA 720
TTTACTATGT CTTGACTCAT AGCTTGCAGA GAAGACTACT CATGTTCCTA CATGTGCCTA 780
GCAAGTTTCC CTAGAAAGGC CAGCTTTTTC ATGAAATCTC CGTCTTCTGC TTCCTCTGGT 840
AAACCACAGA GGACCCCTAC AAAACAGCCC TCTCCAAATG CAGACTGAGC CAGTTCCCTA 900
TTGTGCCCTC TGGTCCCATG TGTCACCATC TTTGATCAGC TTCATCCGTT GAGTAAAGCA 960
TACAGCTGTA GCTAACTTCT TCCCACTTTG AGAGAGAATT TTTCGATGGT ATACATAGAA 1020
AGAGGCCAGG ATGTGGATGT CAGAAGCCTA GGTTAATTGT AAGTAGTCTA AGGTACCTTT 1080
TTATTGAGAG CTTACCTTAC TTACTCTGGG CCAGGCACAG TATTCAGTGC TGTTTGAACA 1140
CTATCCCATT TAATCTTCCT AATAACCTGA TGAGGTAGGT ATTGTTTCAT TTTCCAGATG 1200
AGGAAACTGA GCTTCTATAT AATCATACAA TTTGCCCAAT CATGTGATAG ATAAGTGACA 1260
TTATAGGGAT TGGAATCCAA GTCTTCTGGA CTCCAAATTT CGTATTCTTC ATTATTTCCC 1320
TGCCTTCAGG ATTTGAAACC TGATCTTGCT GCTTCCTGGG GCAGTTCAAC CCCTGGCAGC 1380
CTCTTGTTTC CTGAGTTGTC AGATTGGGAG AAGTAATACC ACATTGCAGG TTATTTTGTG 1440
AGGATTTGGG TAGGAAAACA CTTAGCTGGG TATCCTGAGC AGAGTGGGTG TTTGAAGCTT 1500
ATTCCTATCA GTCTGGACCA TTGCCCCTTG GTTGTGCTCT GTACCCAACT CAAAGCAGTT 1560
TAGAGCTGAT GGGGCCAGCT CCTCAGATGT ATCTGGAATA TGCACCCTGA GTGGGAGGCA 1620
CATACACCTA TAATACATGA CCGTTGGCTT CCCCTTGATT ATTGACACTG TCCCTTCTAC 1680
AAATAGATGC ACAGCCCAGA TACTGTGCTA CAAATATGTG GAACCATGTA ACAGTGGAAA 1740
TATGCCAGAA GACAGGGTAG TAGAGTGAGT TGTACACTCT AGTGGGAAGC AGATTTTGTA 1800
GACAGCGGGA AGAGGATTTC TAGCTCCTGG TGGGGTGGCG GGGGGGGTGG GCGGTAGCAG 1860
CTCTCAGAGT TTTGGGGATT AAGTCTTCTG AGTAGTAGGG GAGTCAATCC ATTAGCCTCC 1920
TTCTGGGTTA CCTGGTGGGA GAGGATTGGA GTCATTGAGT CTCTCCTTAA AGGAAATAAT 1980
TGACAGAATT GTCTGGTTAG CCCTTTACTG GCTAAAGATC TTCCCTTAGG AAGAGGGCTG 2040
TTTTAGGATT GAGAAAAGTG GCCAGGCACA GTGGCTCATG CCTGTAATCC CAGCACCCTG 2100
GGAGGCCAAG GTGGGAGGGT CACTTGTGCC CAGGAGTTCT AGACCAGCCT GGGAAACAGC 2160
AAGACCCTGT ATCTACCAAA AAAATAAAAG TGACCTTTAG TCACTCACTT TGGGAGGCCA 2220
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