| Tag | Content |
|---|
EnhancerAtlas ID | HS133-17331 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:97649660-97651970 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:97651183-97651204 | CCCTCCCCGCTTCCCTCATCC | - | 6.1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GATGAGCATT TGAGTTATTT CTTGTTTCAA GGTATTATGA ATAAATCTGC TATGAATTTT 60
TTTTTCCAAG ACAGTTTCGC TTATTGCCCA GGCTGGAGTG TAATGGCACA ATCTCGGTTC 120
ACTGCAACCT CCGCCTCCCG GGTTCAAGCG ATTCTCCTGC CTCAGCCTCC TGAGAAGCTG 180
AGATTACAGG TAGGTGCCAC CACACCCAGC TAATTTTTAG TAGTGATGGG GTTTCACCAT 240
GTTGGCCAGG CTGGTCTCGA TCTCCTGACC TTGTGATCTG CCGCTTCAGC CTCCCAAAGT 300
GCTGGGATTA CGGGTGTGAG CCACTGTGCC CTGCCAAAGT GGTACATAAA AACTTTCACT 360
CCGCCACCAG GAAGACAATT TGCCCAACCT GTTCAATACA GTTCCCGCTC AACAAACCCC 420
AATTTAGCAT CTTCTATGTG TCAGGCAGTA TGCTGAGCAT TGGGACCTCA AGGATGAGGA 480
AGATGCAGTC TCTGCCCTAG AGGAGCTTAC AGCAGCAGGA AGTTTCTGTC ATAGGACAGA 540
CCCAGGGCTC ACCAAGACTC AAGCAGATGA TGAAGCCTGG GGCTCACTGG CCCAATCAGC 600
GTATTCAGAC TGGCTGGCTG CTTATGAGGC TCTTGGGCCA GGGCTGCCTG CTCAGTGGGC 660
AGCTGACTCT AGCTGCTGCA AAATGCCTTT CACTCAAAGG TGCTATCTAC CAGTGATTAT 720
ATGGCATTCC AATTTTACCT GGAAGGGAGA TGCAGCTACC AGCTGTTTCT TCCCTCTCCC 780
AACCACAAAG TAACACATTT TTCATTTGTC TATCTGTTGT TTCCAGGTTT TTGCTTTTGC 840
CAATCCCCTC CCTCACATGC CTTGAAACAA GCACTTTCAA AGACAAAGAC ATAAACAACA 900
AAAGGGTGCA GGCTGAGGTG GGTCATCTTC TCTGCCTGCG TCTCCAACTC TGGATCCTGC 960
AGTTACTGGA CTCAGGCCAT GGCTGACTCC TTCATCACAG CTAAGATGCT GCTGGGTTTA 1020
AGGCACTGTG ACTTTCTGTG CCACTAAGAC CGACAAAAAG CTGCCAAGTG AACGATGACA 1080
CAAAGAAAGA CACAAACTGT GGGACCCAGC CCAACTTCAG AGCTGCTAAA ATGTGAACAA 1140
AAATGCATCC CGGAATGGAT GGAAACCGAT CATTCTAGTT GGTGTGACCT GCTCCAGTGC 1200
CTACAGTACG TGTCCTGACA GCGTGGGAGG GGATATGAAG GCCCCCCAGT CAAACAGGAG 1260
ACAGCGTTAG TCTCCAAACT TAACTTTGTT ATCTCTTTCC CTCCTGGGGC CCAATACCCG 1320
CCAGCCAGGA CCTGTTTCTC CTCCATCTCA CATTCTTTCC AGGTTCAGGA CTGAAGTCGT 1380
CTTGTTCAGC TCCTTGACTT GGCCATGCTC ACTCTACAAT GCAGCCCATG GATGGCGCCC 1440
CCTCTGCCCA GCACATCCCT CTGCCTGGGC TCTTGTCTCC CCGAATCCTG CAAACCCCAG 1500
CCCCAGCCTT TAGCGTTCAG CCGCCCTCCC CGCTTCCCTC ATCCTCCCTC GCGTCCTCGC 1560
AGTGAGATTT CAACATGTCA TCTCAGTTTT TTTGTTCTTT TACTTTCCTG ACTACAAGAA 1620
AAATAAAATA ATCTGTCTTA AAGTGTAGCA TGAGGCCAAA TAATTACGGA ATCCCAAGTG 1680
CTTTGGGCCC TGATGTCAAA AGAGCCAAGA TGAATTCAGA ATATTACAAT GGTGCTGTTT 1740
CTGCGAATAC TGCTTTTTCA AGACGCCTTA TTCCTAACAT CATGTTTTAT ATCCATCCTT 1800
TTAAACAAAT ATTTAATAGC TTGGGAATGC TGGCGAGAGC AGCGGCTCCT GTCAGCAAGG 1860
ACTGAGCTCA CAATTTGAAA GATGAAAGGA GATGCGTTCT ACCCACAAAG AAAACGGTCT 1920
CCAGCATCAT AAACTCCACA TCCATCAAAC CGGGCAGGGG CTGGGAATAG AAAGCCTTTC 1980
TGGAAAGAAA ACACCAGCTA CCCTTTGCAC CCTGGGGAAC ATTAAAAATC AAAACAAAAC 2040
ATGCCACATC AACCAAAACA TAAACCAGTT CTCAAACCAA TCTAAGGTTC CACCCCACCA 2100
AGGCCGGCCG CGCAGTGGCC TGTGGAGAGG AGGGCCCGGC TCACGTCGGA ACCCGAACCA 2160
CGCGGGGTCG CAGGAACCTG AAAAGCGCCA GAGTAGCCCG GCGGCCGCAC CGGGGCTGAC 2220
CTGCAAGGCC TGGACCAGCC AGGAGTCCCA GGGAAGTCGA GTGCTCTCTG AGCGCTAACC 2280
ACGCGCCCCT GCGGTTCCTC GGCCTCAGTT 2310
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