| Tag | Content |
|---|
EnhancerAtlas ID | HS133-06238 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr11:70089740-70091160 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr11:70090183-70090194 | GATGAGTCACT | - | 6.02 | | JUND | MA0491.1 | chr11:70090183-70090194 | GATGAGTCACT | - | 6.32 | | ZNF263 | MA0528.1 | chr11:70090889-70090910 | AGAGCAGATGGAGGAGGAGGA | + | 6 | | ZNF263 | MA0528.1 | chr11:70090904-70090925 | GGAGGAGAGGGAAGGAGGGGA | + | 7.63 | | ZNF263 | MA0528.1 | chr11:70090895-70090916 | GATGGAGGAGGAGGAGAGGGA | + | 7.83 | | ZNF263 | MA0528.1 | chr11:70090901-70090922 | GGAGGAGGAGAGGGAAGGAGG | + | 8.89 | | ZNF263 | MA0528.1 | chr11:70090898-70090919 | GGAGGAGGAGGAGAGGGAAGG | + | 9.79 |
|
| | 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 |
| GH11I070242 | chr11 | 70088752 | 70092972 |
|
Enhancer Sequence | ACCGCGCCTG GCCTCCCCCC AAATTTCTAC CAGAAAAATT CTTACCTTCC TGAAAAGTTG 60
AAAGACCAGT ACCACAAACA CATTTTCTTC TACCTAGAGT CAACAATCAT TGATATCTCC 120
AGCTTTGCTC TCTCAAGACA CAGCAAAGTG GGTGGATTTT CTTTTTCTGT ACCATTTGAA 180
AGTCAGTTTC AGACATGGTG ATGCTTCACC CTGAGCTGCA TCTCCTGAGA ATGAAGGCAT 240
TTTTCTCCTG AATCGCAGAA CCAGTATCGC ACCTCGGAAA CACAACAGGA GTGACGTCTG 300
CTGCCCAGTT TGTGTCCAGA TGGATGGCCT TTCATGGTTG GGTTTTTGTT TTGAGAGCCG 360
GGGTCCCATC AAGATGCCAG CGTCGCATTT GGTTGTCTCT TTAGTCTCCA AGAAAGACTC 420
TGGAGGTGGA ATGTGTAGGG CTTGATGAGT CACTGGGTTT CAGGGGTGGA GGGCAGGGAG 480
GATCCGGGCG ATGACCGGGT TCTGGTTTGG GCAGCCAGTG GTGCAATCCT TGGCATGAGG 540
AATTCTGGAG AGGGAACAGA TCTCAGGGGA GAGTGGGTTT TGGAAGGGCC GAGTGTGAGG 600
AATTGTCTGG CTGTCAGGTG GGAAGCTCAG GAGATGGTAG CGAGATACAG TGAGGGCTGT 660
GTTAGCTTCC TGGGGCTGCC AAACAAATGA CCAGAGATGG GGTGGCTTAA AGCAACAGAA 720
ATGTGCTTTC TCTTAGCTCT GGAGGCTGGA AGTCCAAAAT CAATGTGTCA GCAGAATCCT 780
GCTTTTCCCA AGGGCTCAAG GGAAGAATCC TTCCTTGTCT CTTCTAGCTC CTCGTGGTTT 840
TCGGCAGTCA TTGGCGACGC TGCGCTCCAA TCTCTGCCTC CGTTTTGGCA CATGGCCACC 900
TTTCCTCTTG TAGTTCACAT GGCCCTCTTA TAAGGACACC AGTCATTAGG TTTAGGGCAT 960
ACCTTCCTGC ACTGTGACCT CATCTTAATT TAACTAATTA CATCAGCAAA GACCCTGTTT 1020
CCAAATAAGC TCACGTTCTG AGGTTCCTGG TGGACACCAA ATTTGGGGGG CACATTATCC 1080
AACTCAGTAT ACGGTCAGCA GCATCTAAAT GGTGACTGAG ACAGCAGGAA TGGCTGCAAC 1140
TAGCCAGGGA GAGCAGATGG AGGAGGAGGA GAGGGAAGGA GGGGAAGGGG CCCTAGAAAA 1200
GAACCAGGGG GCTTAGTCAC AGTCTGGAAG GGAGGAGGGC GTGGCTCTAC AGGGTCAAGT 1260
GCTGTGGGGT GTCAAGTAGA GAAGGGCTGA GCCGCATGCA GCCTCTGGAT TCCACGATGA 1320
GCTGGCCGGA GACTTTGGCA AGAGCAGTGT CAGGAGACCG CTTGGGGAAA ACCCAGACTG 1380
CATGGAATTT TGTTTTTACA TTTCAGACCC TGGCCTCATA 1420
|
