| Tag | Content |
|---|
EnhancerAtlas ID | HS002-00062 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr1:9006940-9008690 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr1:9008150-9008164 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAACCTCTGC CTCCTGGTTT CAAGCGATTC TCATGTCTTA GCCTCCCAAG TAGCTGGGAT 60
TACAGGCACT CATCACCATG CCTGGCTAAC TTTTGTATTT TTAGTGGAGA TGGGGTTTTA 120
CCACGTTGGC CAGGCTGTTC TCAAACTTCT GACCTCAAGT GATCCGCCCA CCTTAGCCTC 180
CCAAAGTGCT GGGATTACAG GCGTGAGCCA CCGCGCCAGG CCCCAAACCA GACTTTTAAA 240
ATGTGAAATG TAAAATCCTG GCATTCAACA TGGGTTCTGG TCCACATGTG AGCCAAAGCT 300
AGAAGGCCGT GTCTGTGGAC TTTGTGGACA CTAAACAGCC CTTTCCAGGG GCAGTGAGGA 360
GAGCTTCTTC CCGCATCCCC CTTCTTTCCA TACGGGACCA TGGATTGGGG CCCATGAGGA 420
GGCTGGTGGC CGCTGGCTGA TGCAGGAAGT GAGACAAACA TCTGCTTCCT GCAGAGTCTG 480
CCCCAGTTCA GCTGCTCCGG AAGCATTCCT TCAGGGTGAA CGGGATGATC TGTTAAGTCA 540
AGGGCAACGG AATTAGGGAC ATCCTGGGAG GTTCAGAAAG TCCAGCCAGC TCTGAACAAC 600
CGCTCTGTTC CTGAGGACAG TGATCTTACA CATGGCAGTG CCTCGGAAGC CTGGGGCATT 660
CTGCTTCACT TGGCCAAGCA GTGCAGGCAG GTGGTTCAGA GGTGAAGGAA GAGAGAATTC 720
AGACAATGAA GTCCTTGTCC TTCCCAGGCT CTGCCCAGCC TCTGAGACAG TGGGCTTCCT 780
GGGAAACTAC TAGGGGCTCC AGGAGAACTT GAGAGTAGCT TTTGTAAATG CCTTCCAGGG 840
AAACCTGAGA GATGTTCCAG TATTGACAGT GCCCTGGGCC AAAGCATCTT GCTCTGAGAA 900
GGCGTTGTGC TCCAGGCCAA TTGCCTTGAT TACAAACCAA AAAGCGGTGA GGGCCCTAGT 960
ACAGACACCT TTTTTTTTTT TTTTGAGAGT TTCACTCTCG TTGCCCAGGC TGGAGTGCAG 1020
TGGCGCGATC TCGGCTCACC GCAACCTCTG CCTCCTGGGT TCAAGTGATT CTCCTGCCTT 1080
AGCCTCTCAA GTAGCTGGGA TTAACGGCAT GTGCCACCAT GCCCGGCTGA TTGTTTTTTA 1140
TTTTTAGTAG AGATGGAGTT TCTCCAGGTT TGTCAGGGTG GGTCTCGAGC TCCCAACCTT 1200
AGGTGATCCA CCCGCCTCGG CCTCCCAAAG TGTTGGGATT ACAGGCATGA GCCACCGTGC 1260
CCAGCCACAA ACACCTGTCT TAAAACAAGC TGTGTACTCA CCACACAGCT ACCCCCGAAC 1320
AGGGAACAGA GGTGGGATTC TCCATGTCAC ATGGCTGACT CCAAGCTCCA CAGCTGTATG 1380
GGAGCCAAGT CACCATGATA ATCACTCACC TATGTTACTC TGTCCCCTAC GATTATCAAC 1440
CCTCTCTGAA AAGATAAACT TTCTCCTTAT GAATTTTAAA AAAGTACTCA TTCTAGGTTG 1500
TCCTGGAACC TGATGCTTCC TTAGTTTCCC TGAATCCATA AGTGTAGACA CCTAGATGGT 1560
CTTTACCATA CGGGAATCCA TAAAAGGGGC TGGAGCAAGA AAATAGTGGT GGGGGGTTCC 1620
TGCAGCATGG GGAGGTGGGG GCTGTGTTCC TGTTGGGGGC ATGGAAGGAC AACTGGGCCC 1680
TTGGGAGGAA ATGAGGAAGA GGCCCCAGGA GCAGCACAGG AAGAGCAAAG CCAAGGATCC 1740
CTCCATGCAT 1750
|
