| Tag | Content |
|---|
EnhancerAtlas ID | HS002-02248 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr12:9485980-9488210 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| YY1 | MA0095.2 | chr12:9487508-9487520 | CAAGATGGCTGA | + | 6.04 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 9486561 | 9487257 | | chr12 | 9487525 | 9487585 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I009333 | chr12 | 9485606 | 9488844 |
|
Enhancer Sequence | GTGCCACAGA CTGAAGGGCT TTAACAACAG AAATGCAGTT TCTCACAATT CTGAAGGCTT 60
GAAATTGGAC ATGGAGCTGT GGGCTGCATT GGTTTCTCTG AGGCCTCTCT GCATGGCTAG 120
TTGATGGTCT CCAGCTCTCT CTGGGTCACA GGGCCTTCCC TGGTGCTTCA CTGTGTCCTT 180
ACTGCCTCTC TTATAAGGAC TTTAGTCATA TTGCATTAGG GCCCGCCCTA ATGAACGTAA 240
TCTGTGTCAC CTCTTTATGG ACCACATGTC CAAATACAGT TCCATTCTGA GGCACTGGTG 300
TTAGACATGA ACATGAACTT TGAAGAGTAG ACAAAATTCA TCCTGTAACA TATACTAATG 360
CCTTGCAGAA GACAGACTCC CAGGAAAGGA GTTACTTGGT GAGGAATATG CATACATGAC 420
ATTTTCATGG CTTAGTCAGA TGACTTTCCA AAAGGGCTGT TGTGGATACA TTGCCACCAG 480
CAGTCCTGAA TGTAGCTGCT TCCCAGCATC CAGCCACCCC TGGGTGTCAA GTCTTCTAAT 540
ATTTTGTCAA TCCGGTGTCT GCGTGACAAA TAAAATTCCA TTGATCCTTT CATTTCCAGC 600
TTCCCTGCTG ATATGTGTGT GTCACCTTTC GGCTGTATAG TCCCCACTTG GATTTTCTCC 660
TCCCTGAGTC ATCGCTCAGA TCCGTGGCAC TGTGATGGGC TCTTTCTCCC ACCCAATGAG 720
TCTCCTGGCA TTGGGCCCTT TGCCGGGTCT GCAATTGCGG TAGCTGTTTC TCAAGACTGC 780
CTTTATGTTA AACAAAGAAG CAGTTATTGG CTTTAAGTCC AAAGGGTTCT TCTAGTTTTT 840
TGCTGTGTCA CTGTCTCTAA AACAGAGGAG GAAACAAGGC CTCCCCAGGT CCTTTTCCTC 900
CGTGTCAGCG CAGACCAAGC CTCGGGGAGT TGAGAGGGAA AGTCACACAG TAGTTCCCGT 960
GAGCAGTTTT GGAGCTGCCT TCTTACATCC AAAAGCCTGT GTTTGCTCAT TTCTAAAATG 1020
AGGGTGTGTT TTTGAGGATT TGCTGGGATA ATGCTCTTTA TACAGTCTAT GAATACAAGT 1080
CCCTGCGTGC TAGAAGAGAG GCCCCAGGCA CGCTCAGTTA TCTAGGAAGG TTCTGGTTGG 1140
TGTTCATTCA CTAAACACAC ATATGTTAAG CATTTACTTT GTGCAGGCAC TTTTATAGAT 1200
GACTAGCATA TTTTAACAAA CAAAGCAGAT GCCAACCCCT GGGCCTCAAC TCCATTCTAT 1260
CCAGGGAGTC AGATCCTCAC TGGAGACATC GAAAGCAAGG CACGCCCACA GAGTGGGAGA 1320
TGCAATGCCC TCCTGGCCTC CTCTAGGTAT AAACACTTCC TCCCAGATTC TGAGCAGGAT 1380
GACAGATCCC AGGACCAACT CTAAAGTGGG TGGACTCTGG GTCCAGAAGA AGGACTTCCT 1440
GGGACCCCAA AAGGATGAGG GGATTATACG GCCTGTGGCT GGGGAGAGAC TGACGGAACT 1500
CTGGATCTCA TACACCTCAT AATTCCTCCA AGATGGCTGA GGTCTGGGGC TTCTGCAAGA 1560
GGAAAGAAGT CAAGGTGAGC TGAAGATGGG GCCTCACGTC CTTGTCAAAG GAGAGGGGAG 1620
TTGGAGTCAG AGCCGGCCCC CAAAAGACCC ATGCCCAGCA CAGTCACTTC CCAGCTCTGC 1680
TTGTCCTCCT CCTTCCCACA TCCACCTTTC CCAACCCCAG CACCAGGGGG CCCAGACCTG 1740
AAGCAGTGAC GAGCCACCTG CTCACACGCC TGCCTGGAGC CACAGTCCTG GTGCCCAGGT 1800
ACACGAAGCT GTGTGCCCTG GGCCTACAGG AGGAGAATGT CAGTGGGTAG CTGAGATCCA 1860
CAATTGTCTG TAAAGTCCTG CTCTATGACC AGGTCTGTCC CTGCCAGGAC AGCACAAAGG 1920
GCTTGGACTG GGATGGGGCT GTCCTCTAGA CAGGCAGCAG CACACAGGTG CTGTGGATGA 1980
GCCGTGCTGG AGGAAAGACC AGGCCTCTGA CTCTGATGCC CACTTCCTGC CCCCAGCACC 2040
TTCTCTTTCA TTTTGGCCAC TTGGCCAGAT CAATACTCTG TAGATTTCTC TCAGCCCCCA 2100
AGCTTTCCAT CCTTCAAGCC TAAGGTGACC TACATGTAGG TCAAGTGGCC TGGATCAAAG 2160
CTGCCGCAGC ATCTGCACAT TTTTCTTGCC TGGATGAAGC CTCTGGAGCC CATCAGATAG 2220
AGGGAGAGGT 2230
|
