| Tag | Content |
|---|
EnhancerAtlas ID | HS133-21255 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr22:32729350-32731940 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr22:32730298-32730308 | GCCCCGCCCC | + | 6.02 |
|
| | 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 |
| GH22I032335 | chr22 | 32731863 | 32732644 |
|
Enhancer Sequence | AGTAGGAGCT CGCCAAGGGG CCAGAGTGGG GAAACCTGTG AGGTGAATGG GTGTAGGTAA 60
GCACCTCAGG GCAGGGATGG GGACTGATCC ACTCTGTATC CCCAGTCCTG GCCTGGGGCC 120
CAGACTTAGC CCATGCTTTT TAATCCTTAT GAAATGAATG TGTCCTTTAC CTCCAAGGCT 180
GTGTGCACTG TGGCCCTGAT CATCGGCTCC TGGTCCCACA GGCCCTGGTG CCCTTGCATC 240
TCCGTGCTTC CTTCAGCCCG GGCTCTGACC TGACCAGCTT CCATGCATTC TGCATTCCTG 300
GCCCGCCCCT GATGCTGGGG CTGCTTCCCC AACGTCCTTT CTACTGCCCA GGACAGTAAA 360
CATCCACAAT ACACACACGT ACACCATGCC ACACAGACAC CCACAATACA CATAAACACA 420
CACACCATGC CACACAGATC CACACAATAT CACACACACA CACCACATAG ACCCTCACAA 480
TATACACACA CACACCACAG ACACCCACAA TACACATACA CACACACCCC ATGCCACACA 540
CCATGCTGCA TACCCACAAC ATACACATAG ACACACGTCA CACACCATGC TGCAGACCCA 600
CAATATACAC ACACACCATG CAACACAGAC ACACTACACA CACTACACCA TGCCAGATAC 660
ACCATGCACA CACACACACC ATGCCACAGA CTCACACAAT ATACACACAC TATGCCAGAC 720
AACACACACA CACACATCAC ATAGACCCAC ACAATATACA TATACACACC ATGCCAGACA 780
ACACACACAC CCCATGCCAC ACAGACATCA CACAATGCAC ACACCATGCC ACACAGACTC 840
CTGCTCACCT GTGACCTGTC CTAGCCCCTC AGGACCCACC TCTGCCCTCT CCACCTCTCC 900
CCTGGTGCTG GCGTCCCATG GTGGTAACAA TGCACGACCC TGTGCCCAGC CCCGCCCCTC 960
CAGCACTGTC CTTCCTGGTC AGCAGCAACA CCACGTGTCT CTTGGTTCAG ACCCTCGAGT 1020
TGTCCTCGTC CTCAGTGTGC CCCTCCAACA TCCAATTCCT CTGTGGCTCC TGCCTGCACT 1080
ACCTCCAAAA TACTGCCTTG TGTCCCCCCA CTGCCTGGGG CACAGTGATG GCCTCCCCCC 1140
GGGCCTCCCT GCCTCCATTC CTGCTGGTTG GCTGCTGTGA GCTGTGTGGT AGTGGCCTCT 1200
CACCAAAACC CCCACCTGAC CAAGTCCCCG TGCTTCGCTG GCTCCATGTT TCCCTTAAAC 1260
GAACGGAACC ACTCTCCCAT CTCGACAACC CTGCAGACTG GAGTCCCGAA GCTCCCTCCC 1320
TCTTGGATGC TGTCAACGGT GAGATGTCCC AGGGATTGAA TCATGGCTTT GGGGAGGACG 1380
TCAGCGGCAC TCCAGTAAGC GTACACACTG ATCGGGGGAC ACATCTGGGC TTGAGGCCCT 1440
GAAGGGTGAC AAGGACATGT CCCTTAGAAA CAAGTGACAA CAGTATTGGT CAGAGTCCAG 1500
GCAGGGACAC AGCAGCCATG GCTTCATGGA ATAGGGCATT TATGATAAGG ACTTGAGTTT 1560
CCACACTTGT AGGAGGAGCT GGGCAGTGAA GGTCCAGAAG GGACCGTGGA GGCTCAGAGA 1620
AGGGACGCTC CGCAGTGCTG GGCAGGGAGA GAGCGGGGCC AGCTCGCATG GAGGCTGAAG 1680
CCAGGCCCAT CCTGCCTCCA AGAGATCACA GGGAGGGTCA CAGGGTCTGC CAGCCTAGGG 1740
TAGGTGGTCG GGAAGGAGAG CCAGACACAG ATGGAAAACC CAAGGACACT GGGAGCCCTG 1800
GGACACCCCT GCAGCTGTGC TTCTCTGGCT CTGCCCAGTG AGACCACCAG CACCAGTGAC 1860
AGCCGCTTCC GCCTCCCACG TCTCAGACAG CTCAAGCCAG CTCACCGGGA AGCAGATCCT 1920
GGGATACAAC GAGCCCAGAG CAACCAGGCT GGCAACAGAA CCACCTAGCA CAGTATCTCC 1980
TCCTTCTTGT CTGGCTAGAC AAGCTGTGAG TAAGCCCTGA GCAACCTCAA ATGAGGGGTA 2040
AGTGAAGGAG GCACGCTTGG CAGGGACCTC TTTCCACACA CAGAGTGGAC AGAGACAAGA 2100
AAAGAGGATA GACTTTGGGG GTTCTTCCTA TGAGCGGAGT ACGGAGCTAG GCCCTCCCCA 2160
CATCCCCTCT GATTTCATCC CCTTGCCAGG TGGAGCTCAT TTGCTCTCTG TGCCTACATC 2220
CACATGGCAG CCCAGAGAGG TGATGCAACT TGCCCAAGGA CACACAGCTG GGCAGCACGG 2280
AGTCCGGTCC AAGCCCAGCC CAGGCGGCCC CAGAGCCCAT TGTTCCTGCC TGCCCCCAGC 2340
TGCAGCACCC AGCGATTCCT GAAGCCGTAG GTCCCAGCAC ACAGGGTGTG ACAGACTCAA 2400
TCCCAGAGCT CACGGCTGAA GGGGTCAGGT GACAAGTCCC CCTCTCCCCC AGCACCTCTG 2460
GGACCCCTTA GAAGCTACAG GAAGTCCGAT CTGGACGGTG CTTAGGAGGA GCAGGGAGCG 2520
AGCATCCTCC AGCCCACGGG CAAGCCTCGG TTTCCATCAT TGTCACGGGA GCCGAAATGC 2580
CCGTGTTGGG 2590
|
