| Tag | Content |
|---|
EnhancerAtlas ID | HS133-31923 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr9:96918510-96919920 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr9:96919510-96919531 | TATTCCTCCTCCACTTCCTCC | - | 6.17 | | ZNF263 | MA0528.1 | chr9:96919513-96919534 | TCCTCCTCCACTTCCTCCACT | - | 7.24 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_02202 | chr9:96918355-96919648 | Aorta |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I094156 | chr9 | 96918705 | 96920074 |
|
Enhancer Sequence | TAGGTGCTCT TGTCAGCACG TAGTCACAGG ATGGCTGTCC CATATAGGCA TCCTGTCCAT 60
GATCCCGGCA AAGGGAAAGG GAAGGGTCAA GACTGGTCCC AGGGGCACAT GCCCACTTTT 120
AAGCAGCTTC CTAAAAGCCC ACCTGACTGG ATTCTACTTC TGCTTCCATT GCACACCTGG 180
TTACTCCCAA TGTCAAGGGA AGCAGGAAAT GAATGTAGTA TTTTTAGCTG CCCACATTGG 240
TTCCCCCAAA GAATCAGAGT TCTTTGGGTA GAAAAGTGGT GAAAAACGGG TAGTGGGCTG 300
GCAACCAGCA GTGTCTGCCA GGCCTGGGGC CTCCCTGCCT CAGGGTGGAA GCCCGGGCAG 360
AGCAGAACCT GTGGGCTGGA GGGCCTCCCT GCAGGGCTTG CCTAAGTGTG TGTTAGTGCT 420
CCCTTGGCAG GACACAGAGA GGCTCATCAG ACCTGTCCAC CAGCACCACC AGCACAAGGA 480
CCATGATCAA AACCATCGGA AACTGCCTGA TCAGCGGCAT CCACAGCCGC AGCCACATGG 540
TTACCTCAAA GCAGGAGCTG GAGCATGCCT CCGAGTTGGA GAGGCTGCAG TGGGTGGCCT 600
GGGACCTCAC AGTCCCCCGC CAGCTCTGCC ACCAGATGCT GAGGCTCCTG CAGCAGCACC 660
AGAATGCGAT ATAGTTTCTG CGAGAAAGGA CAAAAAGTTC AGGACGGAGA TGAAGAGGCT 720
CATGCACGAT GGCATGGTCC CCCAGGTCCC TGAAAAGGAC AACATGTCTA TCAGGCACTA 780
ATTTCAAGAG CTCATTAAAG GAATAGATAT TGCTGACTTG GTCCTGCCTG AGTTAGCCCA 840
GGCGCTGGCC ACCGTGGCCA GGCTGCCCGA GGCCTGCAGG ATGGGCAGGG CCACGCAGAG 900
CGAACTGTTG GAACAAACGC TCCAGGAGAT TTTATGCAAG TCAGAGTTGG GCTTGCTGCC 960
AAAACCGAAC AAAGAGGCAA AGCTTCCTGG GGACCCATGT TATTCCTCCT CCACTTCCTC 1020
CACTGGTGTG TTCTCCACAC AAGGAAGTGG GCTTAAGTCT AGGGAATCAA CAGCGTAAAG 1080
TCATATTTTG GCCTCAAAAT GTCAAAAACT TTGATCATTT TGCCTGTAAT TTGAAAGTTG 1140
CTAGACTTCA CTTCTTAAAA AGAAAAAAAA AAAAAAAACT TTCCACATTG TGATCTCTCT 1200
CTTGATTTGG GTTATTCTGC TGCTAATTAA TCATCCAAAG TTTTTTTTTT TTTTCCATTT 1260
TTAATGGAAA CCTGCTTTAA AAGCTTGTTG CTGAAAGCTA ACATAGGAGG GCTTTAACTA 1320
GTGGGAGATG CTGAGCTTGG CTGGGCTGGA GGTGGTGCAG GAGGTGAGTT CTTGGCACAA 1380
CTGAACAGAA CAGCATCGTG CTCTGATGAC 1410
|
