| Tag | Content |
|---|
EnhancerAtlas ID | HS133-08004 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:110199800-110201680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr12:110201108-110201119 | CATGAGTCACC | - | 6.62 | | JUN(var.2) | MA0489.1 | chr12:110201109-110201123 | ATGAGTCACCTACT | - | 6.04 | | JUND | MA0491.1 | chr12:110201108-110201119 | CATGAGTCACC | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65301 | chr12:110195186-110201910 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I109762 | chr12 | 110200581 | 110201676 |
|
Enhancer Sequence | TTCACCAACC CCCCAAGACT ACCTTCCATC AACCATCCAC ATGGCTCCTT TGCCCACCTC 60
CCTCCAATCT GTACTCCAAA GCCACATTAT CAGAGGAGGC TTCTTTGCTG ACCACCCTGT 120
CCAAGCTAGG TGCCGCTGCA TCTTGCCACT CATAGTCCCA TGCCCTGCTG TTCTGGTTAC 180
TGTAGCTGTG TACTAACCCA AAACCAGCAG TGCCAAACAG CCAGTCATGC TCGGGAATAG 240
GGGCCGGGCA CAGTGGGGAG GGTGCAGCTG CCCTGTGATG TCCTGGTGAT GGTAGGGGCC 300
ATGGAAATCT TCTGAAGACC TGCATGCTCA CATGTTAGGC CTCAGCTTCG TCAGAACGCA 360
GTGGCCAGGT TCCAAGGATG GAGGTCCCAA GAGAACATAT TCCAGGTGGA AGGCACATTG 420
CCTCTTACAA CCCAGCCATG AGAGTCACAC GGCGCCACTT CCATGGCATC CTATTTATTT 480
GATAGAATGG AGTCACGAAG CCGCAGGCCC CCTCCCCACC ATCCTTGCCA CTGCTGAGAA 540
GCCTGTCCCA GCCCGCTGGC TCACCCACTT CCTTCATGTA AGACCTTTTC CTGTCATTAC 600
ATTTACCAAA ACGGGACTGT GCAATTGCAC TAAACACTCG CAGCTGGGCC CACTTTCAAG 660
GGAGAGTCTA GAGCCTTCAC CAAGCTGGGG TCAGGGCCCC AAGTAGTCTG GGACCCCAAG 720
CCACCTCCAT TGCTACTCTG GTGGAACAGG TTGGGTTTGA GGCACCCATG GGTGAGCTCA 780
GGAAAGTCCT TCAGGGAACA AGATGTAAAG GAGGAGCTGC AAACCCATTG GCTTCCAGGG 840
GCCACCGGAG CACTGTGGCC AGGCCAGGCT TCAGACAGGG ACTCCAGTGA CCTGGAGGCT 900
CATGCCCCAC CTGAAGGCAC TCACATTCAA AGCACGTTGA AGCACTGAGC AGCTCCCCCA 960
AGCCCATCTC TAAGAGGGAC TGGGGCTCAG GGCCACCAGC TGGAGGTTGC TAGGTGCCAG 1020
GCAGAAGCCC AGGGCAGGTG TGAGAGCTGC CTCCCTGGGT GGCCTCCCTG CCTCCTTGAG 1080
CCTCTAGGCT GACTCTGTGG TCCCTTCTCA GGACTGTCCT CCTCCTGATT CTAGGGAAGA 1140
GGAGGGCCTC ATGAAGCCCC TGGCTTTGCC CTGCCTCAAG GTGGAAGTAG GGTGAAGACA 1200
GCCTGGAAAG CAGACAGACT GGGCCTGAAT CTCAGCTCCA CCCTTTGCTG ATTGCATGCT 1260
CTTGGGAGAC TCTGAGCTTC CACTTCCTGC TCTGTACAGC GGGAACTGCA TGAGTCACCT 1320
ACTGCCGTGT GACAAGTAAA ACTCAGTGGC TTAAGGCAGC AACAGTCATT TAATATTTCT 1380
CATGGTTTCT GTGGCTTAGG AAGTTGGGAG CAGCTTGGCT AAGTGGTTCT GCTCAGGGTC 1440
TGTCATGAGG TTGCAGTCAG GATATTGGCC AGGGCTGCAC TCTCATCCAA AGGCCTGACT 1500
GGGGCTGGAG GATCTGCTTC CAAGAAGTCT CACATGGTCT TCTTGGCTGA AGGCTGCAGT 1560
TCATGGCTAC ATGGGCCTCT TTCTCCATGG GCTGCTTCAG TGTCCTGGCA CAACAGTGGC 1620
TTCCCCCAGA GCAAGTGGTC TGAGAGAGCG AGTGAGGAGG AAGCCACAAC TACTTTTATG 1680
ACTGAGCCCT GGAAGCCATA TTCTTTCACT TCCAGAGTAT CATACTAGTT ATACAGGTCA 1740
GTCCTGTTTG GTGTGGGTCC CAGGGACTGG ACAAGGGCAT GAATACCAGG AGGTATAAAA 1800
ATCATTGGAG TGAGTGGCAG ATCATGGAGG CCAGCTGCCA AATGTCCTAA CTTGTCTGTT 1860
TCCTCATCAG TAAAACAGGG 1880
|
