| Tag | Content |
|---|
EnhancerAtlas ID | HS133-02740 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:161677130-161678540 |
Target genes | | Number: 11 | 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) |
| FOXC1 | MA0032.2 | chr1:161678396-161678407 | ATATTTACATA | - | 6.62 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_58760 | chr1:161674084-161711741 | Ly1 | | SE_59497 | chr1:161674276-161714796 | Ly3 | | SE_61570 | chr1:161674449-161712145 | Toledo |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGGGTAAGTA AAATATTTGA ATATTGGTGT GGGAATGGAG CTTTGCTTAC CTTGGGAGAA 60
AGGACCAGAA GGAAAGAAAC ATGGACTAAT TCTGGCCCTC CAAAGAAGCA GTATTCAGGT 120
GGAATAAGAA GGGTAGGTAT AAGAAAGTTT GGTGTACAGG ATTGAATTAC TTTCTGAATA 180
TAAAAATCTT CCATCCTGAA AGTCCCCTCT GATCATGATA TCCTCTCTAG CTCTAATCTC 240
AACTCTTTTC TTTCACTTGT GAGACAAGTT TTCTTAAAAG AATAGTTTGC ACTTGCTATC 300
TCCACTTCCT CACTTCTCAC ACGCTCCTCA ATGCTTGCAG CCTGGCTTCC ACTGGAATTG 360
GTTTTGTCTA GGGCACAACG ATCTCTATAT TGACTGGGTT ATGGCATGCT TTTCAGTTCA 420
TATCCTGCTG GACTTCTCTG CTGCACTGGG CTCTGTTGAT CACTTACTCC TTCTTGCATT 480
CTCTACTACC CTGGCTTCCA TGGCACCATT TTCTCCTTGT ACTACATGGA CTTCTCTTGA 540
TCCCTTAATA GCTTCTCTTC TCTTCCCCTT AAACACTAGT GTTCTCTATA GTTATAGCCT 600
TGCCTCTGTA CTCCTCTTTC TTTACACAAT CTCCTTCATG AGCTTATTTG TCTGTTTAAT 660
TTTTGCCACT ATAACTCTGT ATTTAAGAGT CCCAAATCAT ATCCCCAACC CTAACCATGC 720
TTTTGAGCTT CACATTCAAA TATCAAGCTT CATACCAGAC ATATCTACCT ACATATCTCA 780
CAAGTGTCTC TGCACCATGT GACTAGAGTT GAACTTATCT GTCCTTTTGG CCCCTGCCTC 840
ATCTAATTCA TTTTCCACTT TCTGATCTCA GCTAATGACA CCAGCATCTA CCCTTACAAG 900
GCCATAAACC TCAGAAACAA CCCAGACTCT TCCTTCTTTT TCATTCTCTA AATCTGATCA 960
ATCATTAGGT TTGGCCAATT TTACCTTCTA AATTGTTCAT AGAAGCAGTC CCTTGCCTGG 1020
ATCATCACTA ATGTCTTAGG ACAAGCCCTC ATCCTCTATG ACTTGGGCTA TTCCAGTAAA 1080
TTCCTAACTA ATCTCCTCGT CCAAACCTTG TGTTCTTGAA ATGAATTCTG TACCCTGCAG 1140
ACAGAGTAAT TTCTAAAACT CAAGTTTACC AGCCCAAATT CTTTATCATG GCACAAAAGG 1200
CCAAGCAGCC TCTACTTTTA CCCTCTCAGC CTTGTAACTT ATGCTCTAAT AAATCTCAAT 1260
CAGTTCATAT TTACATACTC ACACACCAGA CTCTTGCCTG TCTCTAAGGC TTTGCTTATA 1320
CCACTATCTC TACCTGAAAT GAGTTCTTTC CATGGCACCC TACTCTCCTT CTCCTTGCAA 1380
ATGTGTAGGT ACCCCTAAAG ACTCAGCTTA 1410
|
