| Tag | Content |
|---|
EnhancerAtlas ID | HS133-02446 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:154445960-154447910 |
Target genes | | Number: 25 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:154447199-154447214 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_24531 | chr1:154446396-154446923 | Colon_Crypt_2 | | SE_24531 | chr1:154447234-154447729 | Colon_Crypt_2 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I154473 | chr1 | 154446397 | 154446923 | | GH01I154474 | chr1 | 154447276 | 154447677 |
|
Enhancer Sequence | AGGGGTCGAA GGGGAAGAAA GAAAAAAAAG AATGGCAGCT GGGCGCTGTG GCTCATGCTT 60
GTAATCCCGG CACTTTGGGA GGCTGAAGTG GATGGATTGC TTGAGCCCAG GAGTTCGAGA 120
CCAGTCTGGC CAACATGGCA AAACCCTGTC TCTACTAAAA ATACAAAAAA CTAGCTGGGC 180
ATGCTGGCAC ATGCCTGTAG TCGTAGCTCC TCGGGAGGCT GAGGTGGGAG GATCACCTGA 240
GCCTGGGAGT GTGAGGCTGC AGTGGGCTGT GATCACACCA CTGCCTTCCA ACCTGGGTGA 300
CGAGTGAGAC CCTGCCTCAA AAAATAAAAA AAAAAAAAGT AAATAACGGC TACCATTTAC 360
TGCCTCTCCA CCATGTGCTT TATAAACAGG ATATTCTTCC TTAATGTGGC TGCCATGTAA 420
GTATTCTCAC CTGTTTACAG ATGAGGCAAC TGAGGCTTAT ATTGAAGATG GTGGTCCAAG 480
ATGCCCACGC TAGTTAAGAG GCTGAACTAG ACTCCAAACC TGGGCCTGCT GGACTGGAAG 540
GCTGGTGCTC TTTGCTTTTG CCATGGGGCT CCGGCCCCCA GCCACTGGTG ACTACCTCAT 600
GGGCTTCTCT TACCAAGCCC TTTCTCAGGC CAGGTGCCCT CACCCTGTGT GGGGTGGGGC 660
CTGACCCACT CACCCCGGGA GGAGATGGAC CTGGTATCCT CATGTGGTTT GTCACGTTTA 720
TCAGTGTGAG CTGGGGCTGG AGGCTGACCC ATGGGAGTCT GAGCGCACAT ACAAAGGCAT 780
GGCTTGGGGG CTCCCATAGG TGATCCTAAG GCAGTGGCAG CCAGAGATGG GTCTCAAAGG 840
AGAGGGGCAA AACTAGTTCC TGACATAGTT AACTCTCTCT GATCAGGGAC CAAATCAAGC 900
CACTTCCCCT CCATCTATAC CTAGCCACAC CTCTGCACTG CATGAATGGT TTGGTTTTTT 960
CCTGTTGGTT CCTTGGTATA AACTTTGATG AACTTCCTGA AAATTCTCAA ATTGTGCTTT 1020
ATTTATTTAT TTATTATTTT TTAGACAGAG TCTTGCTCTG TTGCCCAGGC TGGAGTGCAG 1080
TGGTGCCATC TTGGCTCACC ACAACTGCCT CCCAGGTTCA AGCGATTCTC CTGCCTCAGC 1140
CTCCTGAGTA GCTGGGATCA CAGGCACACA CCACCATGCC TGGATAATTT TTGTATTTTT 1200
AGTAGAGATG GGGTTTTGCT ATGTTGGCCA GGCTGGTCTT GAACTCCTGA CCTCAAGTGA 1260
TCTGCCCACC TCGGCCTCCC AAAGTGCTAT TACAGGCGTG AGCCACCACG CCCAGCCAAA 1320
TTGTGTTTTA CTGATGGTAT GGAAGCCTTA TTACATCCAC TCCCTCTGAA AGGATGAACG 1380
GTCACCACTC TGTGAGTGGA GCTGCTCTCT GGGTGCAAGA ATTCATTCAA GGAATGTTTA 1440
CTAGGCCACT GTGCTGGGTG TGGGGTACAA GAGGAACCAA TGTCCTCCTC CAGGAGTTGG 1500
CAGTATGCCT GGTCAGCCAC ACAATTAACA AGCAAATGCT GTGTCTGGGA GCAAATGACT 1560
AATCTGGTCT AGGGAGTGAG GGAGCAGAGT AGGAGGGTCT GGGGAGTGGG AGGCCTGCCG 1620
GGGGTACAGG GGAGGGCTGA GGGCAGGGGC CAGGTGGGAG GGAGGCCGCC TTGGATGTCT 1680
ACTATGTTGA GCACCTCTGC AATGTTCTTT TTTCTTTTTT TGACAGAATT TCACTCTTTT 1740
TGCCCAGGCT GGAGTGCAAC GGCGTGATCT TGGCTCACCG CAACCTCCGC CTCCCAGGTT 1800
CAAGCGATTC TCCTGCCTCA GCCTCCTGAG TAGCTGGGAT TACAGGCATG CGCCACCATG 1860
CCTGGCTAAT TTTGTATTTT TTAGTAGAGA CAGGGTTTCC CCATGTCGGC CAGGCTGGTC 1920
CTGAACTCCC GACCTCAGGT GATCCACCTG 1950
|
