| Tag | Content |
|---|
EnhancerAtlas ID | HS133-03225 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:203371140-203372950 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr1:203371952-203371962 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr1:203371952-203371962 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr1:203371952-203371962 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr1:203371952-203371962 | AACAGCTGTT | - | 6.02 | | SPI1 | MA0080.4 | chr1:203371847-203371861 | TCCTTCCTCTTTTT | - | 6.06 | | SPIC | MA0687.1 | chr1:203371847-203371861 | TCCTTCCTCTTTTT | - | 6.38 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I203400 | chr1 | 203370108 | 203373079 |
|
Enhancer Sequence | AAATAATTAT TTGTCATTTA TCTGAAATTA AAGTTCAAGT GGGCATCATG TATTTTATGT 60
GGCGGTTCTA ACAGGTTAGC GTGTGGACTT CTCTCCCAAA CAACTTGTCT GGGAAGAAGA 120
GCTGATTGCT AGAGCCATAG CTAGAAAGGG ACCCCAGTCA ATGGAAAGTT GTATTTAGGA 180
TGGGATCATC TAAGCGTGTA GCCCAGGCAG CACTTTCTGT AGCCTGTTTG TAGGCCGAAG 240
AGAAAGAAGG AGAGGCTAAA GACACAGTTG GGAGAATGCT AGATTATTGA AACCATGGGC 300
CTCTAATCAG GACCAGCAAT CATTTCACTG GATCCACCCA TAAAAAGCAG AAAGTCCCTC 360
CCCAACACTC CATTCCACTA AAAGCTCAGA AAAATGCAAA TTTCCAACAT TGATTTGCAA 420
GTGTATTCCC GCTCCTGCAA ACTGCAGGAT TGTGGATTTC ATACAAACTC TATCCAGTAG 480
ATTTTTGTTT CTTTTGTTCT TTTGTTCTTT TTCTTGGTGT TTTAATGGAC CACCATAGCT 540
GAAAATATTT TGCTAAATAG AGCAATCCAC TTTGCCAACT TCAGCATTTC TTAAAATTCT 600
GTCACCAGAT AGAACCATTT TTAATAGCTA GATTCCATAA CCAGTTCAGG CCTCAAGCCT 660
AGGTCTTTTA AAGCGAATGA ATCAGATTAG TGCTGAAATC GAGCTCCTCC TTCCTCTTTT 720
TCTATTTTTA CTCTTACTGC TAATGGCGAA GTTATCAAAG CCTCTTTTGA TGATGAAATA 780
ATTGTATCAT TGAATCATCA CATGACTGAG TCAACAGCTG TTTTTCTTCC TCATCACACC 840
AGTTTCCAGG GTCACATCTG GCTTGAGAAA CTTGAAGTCT GGTGTCCTTT TGTTTATTTT 900
TGTTCCTTTT CCTCTAATTC CTTAGATTTC TGCCAGATTG GGAGCCTTCA TTAGTGTTTT 960
GTTTCTGTGT TCGTGAGACA GAAAGGCAGA CAATGGTTTT TTTCCCCTTT CCACAAATGC 1020
TAACTTGAAG TCTTGTTTTG TTTTCATTCA CTTTTGAGGC AGAGTCCAGC CCACCAAGTC 1080
GAATTCTTTG CTCAGTTTTA GGCATGTAGA CCCCACAGCA GAAGCAGTGC TGTGGCTTCC 1140
GCTGTCCTTC CTAAGAATGT CCCTGGCTGC TAACTGTTTG GATGTTCCCC TCCTTCACTA 1200
GGGACTTTGA GACTGTTAAT AAGAAAAAAA TAACAACATT GGGCTACACC AATTTCCCTT 1260
CTCTCAAATT GCTTGTTCTA TGTTAGTTTC AAAACAAGAG TTTGCCACCT TGGTTTTAAA 1320
GAGAGCACTA ATGGACTGCC CCCAGTGCTA CCTGTTCTGT TTCTAATCTG CTCCAGGATC 1380
CGACAGAATC CATATAAGGT AGAGGACAAT TGCTTTGAAC AGACATCCTC AAGATAGTTC 1440
ATAATTTTGC CTTTGGTTTT CTCATTTGTA GCACTCAGGA TAGAGCTTGG TCTTCTTTGG 1500
TGCCTGAGAT TTAGGATTGG GCAGGAGGAG GTTATGTTTG GGATCTGCTT TCAAGTAAAA 1560
TATCTCTACC AACTAATGAG TAATTTAAGA TTCTCTCTCT ATATGGTACT TATCCCAAGA 1620
GGTAGACAAG TACAGACGGG GTGTAGCTAA AGCTGGGGCC ATGGCGGGAC AGGAAAGTTT 1680
CTTTATGGGT CAAAATACTT GCAGTGTTAA ACAGGCATGT TACCAAAACA GGTTCCCTCA 1740
GGGTGATGGC TCTTCGTCTG CTAGGCTGAC CAGGGGGCCC AGATGGTGTG CCTGATATCT 1800
GGGAGGACGT 1810
|
