| Tag | Content |
|---|
EnhancerAtlas ID | HS133-03429 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:210001520-210002950 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:210001967-210001982 | TGAACTCCTGACCTC | - | 6.22 | | Stat6 | MA0520.1 | chr1:210002727-210002742 | GTTTCTCTAGAAATG | - | 6.31 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_35823 | chr1:209995332-210002113 | HMEC | | SE_38331 | chr1:210000184-210002987 | HUVEC | | SE_46498 | chr1:210000630-210002109 | Osteoblasts | | SE_46498 | chr1:210002403-210006112 | Osteoblasts | | SE_64223 | chr1:209995569-210002089 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I209829 | chr1 | 210002404 | 210006112 |
|
Enhancer Sequence | AAGGGGCGTG GCAGGGCTCC CCAGTCGCCA GAGATGTATC CTCGAGTTTG GTCCTCTGGT 60
CTCCCAGATA GTGCTGCTCC GGCCTTTTCC CACTATTCCC TGGCTCCCGC TGTGCTCGGC 120
CGGGGAGATT CTGGCGCCAT CCCGCCGGGA GATGGAGTGC TTCACGGGCC TTTTTGTTGA 180
GCCTGTAATT TCCTGCTAAG AGGCACGCCC GTTGTGTGGG GGAGGATTTT TTTTTTTTTT 240
TTAAGACGGT GTTTCGCTCT GTCGCCCAGG CTGGAGTGCA ATGGCGCGAT CTTGGCTCAC 300
TGCAACCTCT GTCTCCTCCC GGGTTCAAGC GATGCTCCTG CCTCAGCCTC CCGTGTAGCT 360
GGGATTACAG GCGCCCGCCA CCAAGCCCGG CTGATTTTTT GTATTTTTAG TAGAGATGGG 420
GTTTCACCAT GTTGGCCAGG CTGGTCTTGA ACTCCTGACC TCAGGTGATC CACCCACCTC 480
GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACCGC GCCCAGCTAT GGGGGCGGAT 540
TTTTGTGTGG TCAGAGATCT AGGAATTTTT TGTAGACACA CATATATATA TGTATATATA 600
TAATTTTTTT TTTTTAAGAC AGAGTCTCGC TTTGTCGCCC AGGCTGGAGT GCAGTGGCGC 660
GATCTCAGCT CACTGCAACC TCCGTCTCCC GGGCTTAAGC GATTCTCCTG CCTCAGCTTC 720
CCGTGTAGCT GGGATTACAG GCGCCCGCCA TCACACCCGA TCAATTTTTT GTATTTTTAG 780
TTGAGACGGG GTTTCACCAT GTTAGCTAGG GTGGTCTCGA ACTACTGACC TCGGGTGATC 840
TGCCCGCCTT GGCCTCCCAA AGTGCTGGAA TTACAGGCGT GAACCACCGC GCTTGGCCTG 900
TTTTTATAAT TATTTTTAAC TTACATAAAA TGATTGTACA TATTTGTGGG ATACAGTGTG 960
ATATTTTGAT AACAATACAT GTACCCAATG TGTAATGATC AAATCCGGGT AATTAGCATA 1020
TTCATCATCT CAAACATCAA TTCTTTGCGT TGGGAACATT GAAAATCCGC TCTTCTAGCC 1080
ATTTGAAAAT ATACAATAAA TTGTTAGTTA TAGTCACATC ATATGTTGTG TGTGTTTTTA 1140
AAGAATTTGT TGGGACATCA TTGATCTTTG CAATTACGAT AAGGAACTAA GTGTATTAGT 1200
AGTTGTGGTT TCTCTAGAAA TGTCTAGGTG CAGTTATGAT CTCAATGCTC ATCCCACTAC 1260
TTTGGGCTGC TTTGTCATCA GTTAGGGACA TTCTTTTTTT CTTTTCTTTT CTTTTTTCTT 1320
TTTTTTGAGG CAGGGTCTCA CTTCGTTGCC CAGGTTGGAA TCCAGTGCTG CAATCCTGGC 1380
TCACTGCAGC CACCACCTCC TGGGCTCAAG CGGTCCTCCT GCCTCAGCCT 1430
|
