| Tag | Content |
|---|
EnhancerAtlas ID | HS133-32886 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chrX:109257830-109259890 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chrX:109259531-109259552 | TTGTATTTTCTCTTTCCCTTC | + | 6.19 | | SNAI2 | MA0745.2 | chrX:109259454-109259464 | TGCACCTGTT | - | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH0XI110014 | chrX | 109257441 | 109260254 |
|
Enhancer Sequence | TGGGCTGGCT CCATGGTGCA AACTCTCTTG AGATTGGTAG TCTAGGAAAC CAGTGAGTTT 60
GTGACAGAAG TATGAAAGGA GTGAGCTTGG GGGAATGGGG TGGGCATAGA CTGGTGAATG 120
GGTTTTTTTT TTTGGTTGTT TCTTTTTTTT TTTTTTTTTT TTTTTACTTT TTCATTTATT 180
TCTTTTGATT AAGGGGAGTG CAACTTTCTC CAGTGCCAAC TATTACCAGA GCTGGGTAAC 240
TGTTGGAAGA GAAAGGGCCA CCCCCAGAGC TCCTGGGTGA AAGGCAGGTT CAAGTGAACA 300
AGTATCTTAG CTGAAGGAGA AGCACAGTAT AGTGGAAACT GTGCTGCTTT CAGGAGAAGA 360
CTTCACTGTG CCTTGGCTTT TTGCATCAGC AAATGGACAG AAAAAAACCA ATTATTCTTA 420
CATCTCCGGG ATATGGTAAT CCTCTCTCCT TAAGACCAGC TCTCCTCCTT TTCAAGACTT 480
TGCTCTGGGG CCTCGTTTTC AAGACTGAGG TCTGGGGCCT AAGCCACCAA TCACTAGAGA 540
AGGATCCCCT TAAGAGCAGC CTTCTGGGGC CTAGACCTTG ATCATGTGAT TTCAGGCCTT 600
GGGATGTGGG GGGTGTGCTG TATCCTGCCA AGGCCATTGG AAGGCCTCTG GGCATATTCC 660
CAAGCATTGT GGGTAAGAAG GCTGTTTCTT AGTCTTGGAG GTGGGAGAAT TGAGAAAGCT 720
AAGGTCATGT TTTCTATAAC CTGGTTCCTG GAAGAGGAGC TGGTTTAGAG GGCATTTCTA 780
AACAAACAGC AACCCAAATA AACAGCAGCG CTTGGAAATT AGTTATGAAA GTTCACACAT 840
TCTAAGACCT AGGGAAGATT GTAACAAAGG GTCCTCTTCA TATCAGCACT TGTTCATTGT 900
TGGTTTGCAT TTGTTAAGAG TTTCCTTTTT TAAGTTCCAG GAACTTGAGT GTGTGTGTGT 960
GTGTGTGTGT GTGTGTGTGC GCGCCTGTCA CTTTATTCTC TGCACCCTGC AGGAATGTTG 1020
CTCAGAGTCA TGTGCACAAG TGCCTCATTA TCAGCAGCGC TTTCACACTT GGTCCCTTGG 1080
GCTGCCACTG CTACTGGCTG CTGCTTCATG TGGGTATTTC TACCTATTTC CTGGAGCCCC 1140
AGCCCCACAG GGAATGTTGG CACCCTGAGG AAAGGGACCG CCTCTACATT TGGATCTCCC 1200
TTCTGCTGCA GGGCAGCTGA CTTTACTCTG CTTTCAAGTT CACCTTTCCT CAGAATAGCC 1260
CTGCAAGCTA GCACCAAGCC AAGGTTATGT TTCCTTGCTT GCATGTGGGG TTTCTGGCCA 1320
GTCAGCCAAG TGAACTGATT GACCCCCAGC CCTGTGGGGA ATTTCAGGGG GGTATTGTCT 1380
TGGTCATCGG AGTCAGGGGT GGCCTTTAGG CCAAGGCTGC ATTAGCTTTG TGGAGAAGAA 1440
TGTGAAGCCC GCCGTGTCAC AGGGTCTGCT GACCGGCTGG GTAGTGTTTG GCCATATCTC 1500
ACAGCCAGTG CTGTGTTTGC TCAGATGGAC GCACATGGAA ACCAGGCTAG GATCATCTTC 1560
CCAAATGTCT TACTCCCTGC TTTGGGTCTG TCCTGAAAAA CAATTTGCAA AGTACATTGT 1620
GGTCTGCACC TGTTGTTTTT TCATCCCCCT TTTCCACAGT CAGTTTGCAG TGAATGGAGG 1680
ATTAATCCTG GCTCTTGCCA CTTGTATTTT CTCTTTCCCT TCTTTCCTTG ACGTTGGGTT 1740
CTTGCTTTTC AGTTATAACT GTCTGTGGAC ATTAAGGACA GCTGGTGCCC CTGATCATTT 1800
AGGACCTCCC TTAGGCCTTT AAAACGCTGG AAATGTGTAA CAGGGCCGGA TGGGCAAAAA 1860
AGAGTCGAAT TTAGGAGAAA ACTCACTATA ATTTCTGGTT ATCTTTGTAC ACTCTCAGAA 1920
AAGTGAGGAG TGGTAGTAAT AACACTTGTA ACATTTTTGA ATACACGTTA ATTATGCTTT 1980
AGGCATGGTG CTTAGTCTAC TGCCTGTGTA TTACCTCATT TGCAGCCTTC CAGAAAGGTT 2040
GTTTTTTGTT TCATGTAATT 2060
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