| Tag | Content |
|---|
EnhancerAtlas ID | HS133-26185 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:4351000-4353600 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr6:4352741-4352752 | GACAGCTGCGG | + | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_41322 | chr6:4350299-4353636 | Left_Ventricle |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I004350 | chr6 | 4350367 | 4353458 |
|
Enhancer Sequence | AGGAAGCCTG GGCTCAGCTC CAGCACTAAC CAGCCGTGCA CCCCAGGAAA TGACAGCAGC 60
TCTCTGAACT CAGCTTCCAA CACCTGGAAA TGGACAGGGA GGGGTGGGAT GAGGTGATCT 120
GGCAATTCAC TAGTGTTCTC ACATGCAGCC CTCCCCTTTT AACGTAACAC AACATTTGCC 180
ATTTTAGTCA TTTTTAGGGG TACAGTTTAG TGGCATTAGG AAAATTACAC TGTAAGAGTG 240
AATGAGGCAT CACCCAACCC TCAGGAGCTG TCCAGAGAAG GAGGTGGAGT TTGTGCATGG 300
GGAAGATACA AGACATACAA TAGTAAGTGG TATTGGATGC CACAGTATCC ACTAGATGGA 360
TGTTATGCAC CCATCACCAA CATCCATCTT CAGGACTTTT TCATCTCCCC AAACGAAAAC 420
TCTGTCCGCA TGAAACACCA ACTCCCCATT TCCCCTCCTT CCCCAGCAGC TCCTGGCCCT 480
TCTCATGCTA CTTTCCGTTG TTATGATTTT GACTACTCTA GTACTGCATG TACGTGGAAT 540
CACACAGTAT CTGTCCTTTT GTGTCTGGCT GATTTCACTG AGCATAATGT TCCTCCATGT 600
TGCAGTGTGT CAGAATTTCC TTCCTTTTCA AGGCTCAATA ATATTTCATT GTGTAGATGA 660
CCACATTCTG TTTATCCATT CATCACTAAG AGACACTTGG ATTTCTTCCA CCATTTGGCT 720
GTTGGGAATA ATGCTGCCAT TAACACGGGG GTGTAAATAT CTCTTCCAGA TCCCGTGTTT 780
GATTCTTTGG GGTGTATACC CAGAAGTGGG ATTGTTGGGT CACACGGTAG CTTGCTGTTG 840
TCTAAGCAGC GCTTTCCCAA ACTTCCCAAC AGAGCAGCCA CACAGCCACT GTAAATGAGT 900
GCAGGAACTA GTAACCGTCC AGTAGTGGCC AACATATCAC GCTCTATTTT ACGAATTCAC 960
CCAGATTCAG CATTCTGCAT CACATCATAT CCTTGTTTGT TTATAAAAGT GTTGCTTTAT 1020
ACTACATTCC AGTGTAAGGA ACACTTTGCT CTGCAGAGTC CAAAAAGCCC TGCTTCTCCT 1080
GTGGCTTCCC CGGGCTGGGC TGTGATGGCA GTGCCCAGCT GGACGAGCAC CCAGAACAGG 1140
GTTGCAGTTA AGATCCCGTC CAGCTCTGAC ACTCTCTGAC TTAAAGCAAC ACCCCTCCCA 1200
GTGGCTTCTT CATTTTCAAC AAAAGTGAAG TGAGCTCAGG ACTCTTGCTG CCGAGCCAGG 1260
AGGCGTGAGT CACTAGCCAT GGGAATTTCA GGCATCTGCG TGTGTGCGAT GGCGGCTGGA 1320
AATGGAGAGG GAGCATTTCT AGAGCTGAAA TGTCGCAGAG GCACAGCCCC CAGTGGGTCT 1380
GGCACAAAAG CAGCGTTATA TCGAGAGGCC TGGCAGCGCT GCCTGGGCTT GTTTCCCAGC 1440
TCTTGCAGCT CTCGGGGGGT TCTAGAAGAT CGTCCAGACT ATGACTCATT CCTGTGTTAC 1500
TGTAATAGAG AAAGAAGTAG GTGGCAGTGT GACATGGATT TCACGGAGAA TTAGTGAGAA 1560
ATCTGTGTCC ACTCAAGCAC ATTTTATGTT GTCTGAATGT GAGGATTCTC CTTTGGGCTG 1620
TTTATGGGCA GGGTGGGAGA GAGATCGCAG AGGTGCAGTC ATGGGCTTCC AGAGGCTTTT 1680
TACAATTCTG TAGTGGCCAT GCTGGGAAGA CGCCCTGAGA AGACACTGCG ACTGTCCATG 1740
TGACAGCTGC GGGAGTGAAA GCCATTGGAA ATTCCTCCAA ACCCATTGAG CCAAGGCTGC 1800
CACTGCCATG TCCCATCCAG GTGAGGCTTT GGCCAGAGCT GGCTATGGAC TGGTTTGCAT 1860
TTCCCTGCTT TTGATTTCCC TGACAGTCTA CGGTGGAAAT GCCCATGGGG AGTGAGGAGA 1920
TGGAAGAGAA CACAAAGGCA GACAGGAAAG GCTGAGAAGG TTCTCCCATT GGACACATAG 1980
TCCTCAGATG CATGAACTGT CCCTTGAGAG AGAGGAGTGG GACTGTAGGT CTAAATTCAC 2040
ATCACTGTAA ATTCCATTTG TATCTTCACG GGATGTGACG AGGACCATAA TGTCAACGCT 2100
CTTGAGACGT CTGCCCACAG GTGCCCTCGT GCTGAAGCTT TCCCTCCCAG CTCCCATTTC 2160
AGGAATGAAG TGTTTCTTCC CCTAGCTGCA GCAGATGTCA CCAGTGGACA GTCTTCAGTG 2220
GACAGCTCTC TTCTGGAAAT ACCCTAGCTG AAGGGAGCCA GTCTAAGCTG CACAGCTCTT 2280
CCTGATGCAG ACTATACACC AGCCATGATG CCGAAGTCAA CTTGCAAGTG GAGAGAGAAG 2340
GAATTCAGAC CAGAAATGGA CTAGGGTTCA CAGCTGAAAA ATACCAGTAG TGGCCATGAG 2400
GTAGGTTGTG TGAGCCACAG ACCTGAGAGA CACCGTGGGC AGCAGCAGGA GAGGCGGTGG 2460
TGACAGAGGC CAGCACCCCA GGCCCCTGGT CTGCAAACAC CTCCAGTGAA GCCAGGGCAG 2520
AGTGGTGACC AGGCGCCATC CTCCTCCACT GTCATGACAG CAGGTGAGAC CTGGAATGTG 2580
TGTGCAACCC CACAGGGAGC 2600
|
