| Tag | Content |
|---|
EnhancerAtlas ID | HS133-13169 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:66392300-66393700 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr17:66392376-66392391 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_34349 | chr17:66392265-66393724 | HCT-116 | | SE_34637 | chr17:66393100-66393786 | HeLa |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I068396 | chr17 | 66392717 | 66393683 |
|
Enhancer Sequence | GCCCATGCCA CCATGCTCAG CTAATTTTTG TATCTTTAGT ATAGGTGAGG TTTCACCATC 60
TTGACCAGGC TGGTCTTGAA CTCCTGACCT CAAGTGATCA GCCCGCCTTG GTCTCCCAAA 120
GTGCTGGGAT TACAGGTGTG AGCCACTGTA TCCGACCTGC AGCCTGTTCT TGACCAAGCA 180
GACCTTGGCA ATGGCTCTGG GCTTCCACTT CCCAGCATCA CCTCCTCAAT GTCCCCTGTT 240
TGCACTCTGA AGCACTCATT GGCAGTGACA GCCAGGAAAT GTCAGGCCTC ATGGCCTTTC 300
CTTGTCTTTT CCCTGTGTTT TCCTTTCACC AAAAGGAAGA GGAAGCAGGA GGAGGCAAGG 360
AGGCGGAAGG AGCACAGAGT CCCCTCTGCA ACGCCCTACA AATGCATGGC TTCTTGGTGA 420
GGGACCCACA CATCAAAGGG TCTATTTGTG TCTTTGCTAA GGGTCACATG GAAGTGACTC 480
AAATGTACAG AAGTGTCCTG TGGCTGGTAG TTACCAAAGC TGCCCTTCCC ACCCAGCCTC 540
CCCCAGCAAA CCAGAACATG GGTCTTCTAT GGGCCATCGG TTCTTCTGTG CACATTAATG 600
CAGTTTTTAG GGGTTGTTGG ATGAAGCCTG AGAGGTGTTC TGAAGTCCTG CTTCTCCCCA 660
GAATATCTGC CCCCTAGAGC TGCAGACCCT TCCAGGCCTA GCCCTTCTCC CTAAGCAGGA 720
GCAGCCAGGC AGGAAGATGG TTTCCGCCTT GAGGTTGGAA GTTAGCAGTA TGTGACCCTG 780
GAGGGTTGTC ACAGACGTCA TTGGAGAGGT GCTCCGGAGT GTTTATTACC ATGGCTGCTA 840
GGAATAATTG GGGTCATCAG GAAGTGCTTC AAGGACTGTG CTCTCCTTGA CGTTGTCGGT 900
ACTGCCTGTG GGAGCCAGCT CCTTCATGTA CTAACTTCCT TTCTCAGACG GGAGAGCTCT 960
GCTCTTGCTC TAACTGGAGT TTTGCGCAGG CTCGTAGAGA CCCCATCCTA ACTAGTGCCC 1020
AGCAGGGTTA GGCCCAGGAA CCAGATTGGA AAACCAGATA CAAGTCACAG CATCGTCACG 1080
GGGAGGTATG ATGGCGTGGT TAATGCAGCT GGAGTCAGGA CTGATTTGCT CCCTAACCAC 1140
ACCCCATGGC CCAGAAAGAA ACAGCCATGC TTACTGCTTG TGGGAAGCAG CTGATGGTAT 1200
CTTCAAGGTT AAGAGCACAC GGGGCTGGCA CCTGTGGGTC ACACTCAGTC TCCCAGAGCA 1260
TGCCTGCAGT GTCAGTGAAG ACACTTGAGA TAAGATTCTG AAGTTTGAGG ACAACATGGG 1320
TAGTTGCTGG ACCTGAATTT GGGTTTGGTC TTCTCTAGTC AGTCCTCTCT ATCAAAGCAA 1380
AGTCATAGAC CTAAGGAAAT 1400
|
