| Tag | Content |
|---|
EnhancerAtlas ID | HS133-16975 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr2:61406900-61408130 | Target genes | | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:61407312-61407333 | GATGCAGGGAAGGGAAGAGGA | + | 6.15 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATTTCACCAC CCCAAAACAA AACCCTGGAC CCATGAGCAG TCACTCTTGT TGCCCTCCTC 60
TTCCCCAGTC CCTGGTGTCT GCTCACCCGT TTTCTCTGGA TTGGCCTCTG AACATTTCAC 120
ATAGATGAAT CATGTAGGAT GTGTTTTTTG GTGTCTGCCT TCTTTTACTT CATAATGTGT 180
TCAACGGTCA TCTGTGTTGT GTCAGGTAGC AGCACTTTAT TCTTTTTTAT AGCTGATGAA 240
TATTCCACGG GTGCATATAC TGCATTCTGT TTCTCCATTT ATCAGTTGCC GGGCATTTTG 300
GGTGTGTCCA CTTTTGGGGT CTGTGGGTTC AGTTCTCCAA TGGTGCCTCG ATCCTGGCTG 360
AGCAGACAGC GTGTGCGCAC TCAGTCCTTG TTGAGGGAGC CAAGTCTGTG GAGATGCAGG 420
GAAGGGAAGA GGAGGAGCTA GGGTTTGAGC CTCAGCCCAG GAGTCAGCTC CTATCTGGAG 480
TGTGTGCCCC AGAGCAGTCC AGTGAGTTGG CCTCGAGCCT CTGCCCTGCT GGCTGCCTTT 540
CTCACAGACG AGGGTGTTCA GCCCTTCCCC CTTCGCCTCA GAACAGGCTC AGAACTCCTC 600
TGGCTGGGAG TTTGCCTCTC TTGCAGCCCC CTGTGTCTGC TGCTGTCTGG ATCATAGCAG 660
TCTGGCTCCC TGCCCACTAC CCCAGCACCG AGCCCTAAGG CCTGAGGAAC CTTGTGGGCC 720
TTGTGTCTTT TCCATCTCTC TTGGCTCCTT TGCAAGGATA AGACCCAGCC ACTGCCAGGC 780
AGCAGCCAGA GGACGGGTTG TTAGGGCTTG TCCTAACACC TCCCAGCTGC TCTCCTCCAG 840
CAGCGAGTCT CTAGGGTGGC AACTGGGACC CACTGGGGAG GAGGCAACAC TCTAGTCCTG 900
AGAGAAGTCT ACCTGCCTGG TATCCCCCAC ACAATGCCCT CAAGCCAGAG CCTCCCTCCC 960
CTCCGTGGTC AGAACGTACT GTCCCTTTCT GTCCTTCCAT CGCTTTTGTG ACTGCTTCTC 1020
CCCTTCAGGG TACTCCTTTG TCCTGCTTTG CCCAGGCAAA GAGTACCCTG GGACAAGAAG 1080
AGGAATATGG GTGCACTTGC CCCACACTCC TCTCAGGACG GCGGACTGCT GACTCCTCAT 1140
GCCCTCTCCT TGGCCATGGC CTGCCTGACC TTTCTTCCGT GGCTGCTCAG GGGGCCCTGG 1200
AGTGGTGGAA CCCTGTGAGG GCAGCTGAGC 1230
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