| Tag | Content |
|---|
EnhancerAtlas ID | HS133-10977 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:10173390-10175270 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr16:10174427-10174441 | GGGAAATGAGTCAT | + | 6.48 | | RFX1 | MA0509.2 | chr16:10173701-10173717 | GGTTGCTATGATAACG | - | 6.83 | | RFX1 | MA0509.2 | chr16:10173701-10173717 | GGTTGCTATGATAACG | + | 6.84 | | RFX2 | MA0600.2 | chr16:10173701-10173717 | GGTTGCTATGATAACG | - | 6.66 | | RFX2 | MA0600.2 | chr16:10173701-10173717 | GGTTGCTATGATAACG | + | 6.86 | | RFX5 | MA0510.2 | chr16:10173701-10173717 | GGTTGCTATGATAACG | - | 6.46 | | RFX5 | MA0510.2 | chr16:10173701-10173717 | GGTTGCTATGATAACG | + | 6.61 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_56317 | chr16:10172728-10175770 | u87 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I010079 | chr16 | 10173268 | 10175436 |
|
Enhancer Sequence | AGGGCCAAGC CCTCATAAAT GATATTCATG CCCTGATAAA AGAGGCTCCA GAGAGATCAA 60
CGGCCCCTTC CATTACCAAT GAAGAACAAA ACAAAATGAT GACAGCCATC TATGAAAAAG 120
GAAGCAGGCC CTCACCAGAC ATGAATCTTC TGGTGCCTTG ACCCTGGACT TAAGCAGCCT 180
ACAGAACTAT AAGAAATAGA TGTTTGTTGC TTACAAGCTA CCCAGTTTAT GACATTTTGC 240
TATAGCAGCC CAAACAGACT AAGAAAGCAG GAAAGAGCTT GGCACAGGCT GGGAAGAAGT 300
GACAGAAAGA AGGTTGCTAT GATAACGCAA TGGTGTAATC AGTGTGATTT TTATGTGTTT 360
GTATCAGAGA ACCCTGGGTG CAATTCCTGT ATGAAGAATT GCATGAGCAC TTTGTATGAG 420
AATGAGCAAG TTACCCTCTG TGCAATGCTG CTCTCAGCGA GCAAATAAGA ATGATCATGG 480
AACTGAATTG ATGGCACTTT TGTGCATATT AATCAAATTG ATTCATGTAA AGTACTTAAT 540
ACACCACATA CAGTAAGTGC TTAATAAATG CCAATTACTG TTCTTATCAT CTCCCTGCCT 600
GGTTGCCACA ACAGCAGAGT ATATTCAGGG CTTAGCACTG AGATCTGATT TGCCTCTGTA 660
AGGTCCCCTG TTAAGTTTCT TGCTGTGGTT CTCACTCCCA AGGCAGTCAT CAAATATTTG 720
TTGAATGAGC AAATAAATCA ATGAATGGGT TTCCTGATTA CCTTATCTTT AAGCCACCAA 780
AAGGCACCTT TTTATGATTA GGCTTCCTTT GCAAGCAATG TGACTCTGCC AGGCCCTGGG 840
CTTTTGCAGA AAGCGAAGGT GGAAGGGAGA TGGTTATTAG CCACTGTCTC TGCAAACGAC 900
AAGCCATCTG CACCCCGTTA CCTAAGCATA GACCTCTGTG GGTGCCAAAC TTCAGAGCCC 960
AGAAAGTTGG AAGGGATTCC GAGCTTGGAT CCCTCAGGCT AGGCTATTCT TGGAAGCCGA 1020
GCAACACGCC TGCCACAGGG AAATGAGTCA TGCAGAGGCT GAAGGCTTGA TGGATTTCTC 1080
CACGGCAGCA GCTATTTATC AGGGTAGATC TATACACCAC AGAACACAAA GGGAGCGATG 1140
GAGTACAGAT GAGCGCTACT TAAAGCAATA TCACCCTCAC CTTGTATTGC AGATCCTTGT 1200
ATTGCAGCCA GATGACAATG CCTGGGACCC TCTTACCATC CAAACACCCA CCTCAAGGAG 1260
GCCCAGCCCT GTCATATGAC TGTCCCCATT ATACTTGAAC AGCCTTTGAA GGGCTTTCAA 1320
AGTGTTTCCC AGCCACATCT CCACCCTCCA AGCTCAGGTA GCCCATTCCT TCATTCCCGT 1380
CTCAAATGTT CTGCCCCAGT GAATATCTTC GCCTCCCTGT TAGACTCTGA GATCTTGTAC 1440
TGCAGAATCC ACTGTTGCTC ATACAATTCT GAGTTGTACC TGAGGGCAGA ATCAGAGTGG 1500
TCTTTTTGCC TTTTGTGTTT GCAGAGTCCC AACTGCAGAA GAGAGTGACA TGCCATAAAC 1560
AGGTCAAATG TCGTTAATAT AAATATCTAC CATGGGGCAA TTTCCGAGGC TCTTACATGC 1620
TTCGTCCTGA GGTTAGCATG AGGCAACTGC ACTCACTGCT ACGCCTTCCC ACACTTATTC 1680
TAAGGGACAG CCAGCTAGGA TGGAGTGGGA GCTGATGCCC TGGATTAAGG TGCCTGGTTA 1740
ATTCCACTTG CCTGGTTTCC TTTGTTCTCA AACTCTGCCT GGAGATGAAG CTATTGCGAA 1800
GTCAGTCTCA GCTTGTGCTT CTAAGTTCTG CTCCTTACAT ATGCCCCCAG AAAGTTGTTC 1860
CAAGTGAAGG CAGCTTAATT 1880
|
