| Tag | Content |
|---|
EnhancerAtlas ID | HS133-13473 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:75859170-75860610 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PRDM1 | MA0508.2 | chr17:75860220-75860230 | TCACTTTCAC | + | 6.02 | | REST | MA0138.2 | chr17:75860508-75860529 | GGCAGCACCATGGCCTGGGCC | + | 6.24 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_20722 | chr17:75859212-75861867 | CD56 | | SE_33705 | chr17:75859589-75863133 | H2171 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I077863 | chr17 | 75859411 | 75862009 |
|
Enhancer Sequence | TTAACCTCTC TGTGCCCTGA TATCTTCAGT CTATAGAATG ACGATAATGT CAATACCACC 60
TCATTGCATT ATTGTGAAGA GTGAATGGGA AGACACATAC AGTCACTAGC ACCGTGCCCA 120
AGTTGTTAAT AATGAAGATA TTGCTGCCAT TTTATTTACA GTGTACTAAA TAGTGAACAA 180
TATGATTCTA TTTACAGCAA ACCGTGACGA ATGGATGGCA TGGGCTCAAT GCCAGCTTCC 240
AGCCCCAGTC ACTAGGCTGC AGTTCAGCCC GCCTTGAGGT AAGGCTAAGG GAACTCGAGG 300
CCCTGGCTCA GGCCTGGTCT ATGCCTTGTC TTCTTGCTCC ACGTCCTTGG ATGCCGTTGC 360
ACACCCCACC CTGGGCTCAC TGGGTTTTTC CCTTGGCCTC CACCTGCAGT TCCCAGGTTC 420
AGATCTCAGG ATATGTATCA AAGCTCAAGG AACAAGTTTC CTTCTGGGGC TGCCCATGTC 480
CCCCAAGAAT GGGCTGTCCC CTGGAAGAAC CAGGGGAACA CTCATCAGTC CTCTAGACCG 540
TCTGAATCTG GTTGCTGGTG AGCCCAGAGA GGGGAAGCAA CCTGCCCCGA GACACACAGC 600
AAGGCAGCGG CAGGAGGCTC CCAAGGCTCT GAGCTCCAGC CTCTCACTCC ACCACCAGAC 660
AAGTTTACAA TGGAACTAGC TCACGCCCCA ATGACATGGA AGGGAGAATG AGCCCTTGGT 720
AAATATGAAA AGCCACCTCC TCCCTCCTGA AGTCTCCACC ACCAACAGCT GCTCATACAC 780
TTCCTGCTAT CTTCATGCTG TGGTCAAGGC TGACCTCTCT TCTCCGCCCT TCAGGAAGAG 840
AAGACATTAA AGCATGTGAG AGAGGGGAGG GCCCTGGGGA CGGGGAGCCG GCAGAGCCGC 900
CAGCCTCGCT GAGTGCAGTG ACAGAAAGCA GCCACTCCCG CCTTCAGTGT GGAGCCCAGG 960
CCGCACCCAG CCTGGAGTCC GGGGCCTCGG GCAAGCTGCC TCCCTTCCAG GCCGGCGTGG 1020
GCCACTCCAG GACCCCGGGA CTCCCTGCCC TCACTTTCAC AGAGGCAGCT GGGTGTTCTG 1080
GGTGCACAGC TCCTGTCAGC AGAGCAGGCT CGGGAGCCCA CTCGGCTTCA GGCAACCGTC 1140
AGCAAAAAAC AGTAACAGCA CGATCCCTCC TGCTCACAGG CACCTTCCAT GCCAACAAGT 1200
CCTGCAGGAA AAGCCCAGAT GACTCCAGGA TGGGCCCCTG ACTTCGAGGC AGGCCAGCCC 1260
CCTCGTTTCT TCACTTTTTT GACCCATGAG GAAACAGAAG CATTCATTAG CCAGAAGCAT 1320
GTGGACGTCC ATGCAGCCGG CAGCACCATG GCCTGGGCCA GCAGGGGCCG AGAACAGGAC 1380
ATCTGATTCT TTCCTCACCT TCCCTCAAGG ACAAGGTCAG CCAACAGAGC ATGGGGGCGA 1440
|
