| Tag | Content |
|---|
EnhancerAtlas ID | HS133-03904 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:236065950-236067120 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE40 | MA0464.2 | chr1:236066088-236066098 | ATCACGTGAC | + | 6.02 | | TFEB | MA0692.1 | chr1:236066088-236066098 | ATCACGTGAC | + | 6.02 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_09146 | chr1:236065813-236067182 | CD14 | | SE_33905 | chr1:236065835-236067159 | HCC1954 | | SE_36048 | chr1:236066057-236067198 | HMEC | | SE_47207 | chr1:236063644-236067246 | Panc1 | | SE_64439 | chr1:236066051-236067148 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I235902 | chr1 | 236065625 | 236067083 |
|
Enhancer Sequence | TCATGATGGC CTGAGTATAC AATTTGTTCT TAAATAGAGT GACTTGCTAA ATGCATAAAT 60
GCATTTGATT TAATATTTAT TCCTTTGTAA ACTTCTCATA GAAATAAATT CACAAATAAT 120
TAAAACATCC TTTTGCAGAT CACGTGACTG AATTTTGTCA GCAAATATGG CCGGCACGCC 180
AATCAGGCTC TGGCTGTAAA TGCAATCAAT CCATTACTGC TTAGCTAAAA AGGCAAAGTT 240
GCTGGTTCAA GTCCTACTGT GTGTACCTGC AGGGGAACTA AGGTCTCCAC TGTGGGGTGT 300
GTGTGAGTCT GAATCTAAAT TGCAGGCTGG GAAGCTGACT TTAAACAGCA TGCTTCTTTA 360
AAGTTCTGAG AGTAGGTTCC TTGCTCCAGG CCTTGAAATG AAATCAAAGC TGGCTTTGGC 420
CTTGGTTTTA GCTTTGGTCT AGTAATAGCC TGATAGGTAC ATCTACAGTA GCTTTTTTTT 480
TTTTTTAATA ACTCTTTCTC TTTAAAGACA GGAACACTTG GTATTTCTCG GTGTCTGTGA 540
GGTGAGTCAT GCATTTTATA GGCGCAGAAA TTGAAAGAGG AGTGACTTGC GTATGGTCAG 600
AGAGCAAGTC CAAGACTACG GTGAGTCCAG CACCACAGGG CCACCCAGAA CTACTTGGCC 660
TGCTGCCCAT CCTCTTGTCT CTCCACTGCA CTAGGCATAA ATGTCAGTAA AGAAAGCAAG 720
TGTGGCCCAT TGAGAGAAAA TGTGGCACAA GCCAAGAGTT CACAGCACTT GAAGTGGTAA 780
AGGCAGATCC AGGTTGAGGC TCTGTTCTGC CCAGTTTATG ATGAAATACT GATAGTGGAT 840
TTCTTCCTTT TCACCTGTTC CTGCCCCACT TGCCTGTCAA AGTCAGCCAG CACACTTTCC 900
TCAGCAAATG GGTGGTAGGT TCTGGGCAAA ACAATGTTAT AATAAAAACA GAAAAGGTAA 960
ACCATGCCAT TGGCTCTGAC TGCCTTAAAG GGTTTTTGTC TCTAAGCTAG AAGACATGCT 1020
TTCTTGTACT TTCCCTGTCG AGATGGAGGC ATTTCACTTG TCATCCATAG AAATTCTCCT 1080
ACTTTGGGGA GTGTAAATTA GTTCAACCAC TGTGGAAGAC AGTGTGGCAA TTCCTTAAGG 1140
ATCTAGAACC AGAAATACCA TTTGACCCAG 1170
|
