| Tag | Content |
|---|
EnhancerAtlas ID | HS024-03511 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr12:49669700-49672140 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr12:49671810-49671823 | GAACCTTCCAGAA | - | 6.19 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CGCTGGCTAG CCTGCCAGAG GGGATTTTGA GACCTTCCCA GGCCAGGAGA TCTGCTGATT 60
GCCATAGTGC AAGCACTGGA GGAAATGGGA ATGGGACACC CGTGTATGAA AAGGAGCAGA 120
TAAATCACAA AGCTTAGGCG AGTGTGACAC CCCATGACAC CAGCATTTCC CAAGCAGGGT 180
GCCCTGAGAA TAGGATTCAG GGTGCCCATA TAGGATCCCT TCGGCTTTTA GAATGACATG 240
GTGGAAACTG GAGAGCCTGA CTCACCCATC CTCCCTGGGG CCAGTCACCC TGGCCAGGAG 300
TAGCCCCCTC CATTTACCTC TGTACACCTT ACAGATGAAT TATTTTCTAC ATGTGCCAAG 360
ATGTGAAAAA GGTTGGAAAG CTTTAAGCAG CCACAGAGGT CTGGGGTGAA AGAAGGTGAG 420
AGAAAAGTTT AGCTGAGAAG AAATATTCCA GTAGAATAAA GCCTGGGGAA TTGGAAGAGC 480
AAAGTGCCAG TGGTTGGGGG GGCATTTGTC CTTGTAAAGA TGATTTCCCC CTCCTGCGTT 540
GGAGGGAGAG TGAATAGAAG TTAGCCTGCA GCAAGAACAA ATATACCCCA AGGTCTAGGT 600
CACTGCTTTG TGGCTGACAA TCATCTGATC TGCCCTTGAG CACGAATGGA AAGTCTGGAC 660
CCAGAGCTGC GACTGATGCT GATGCTGAGG CCGCTGAAGC TTGATGGGAA TAAATGCACA 720
CAGCCTAAGA GGATTCGGGC TCCTGAGGCT GGCGGCAGCC CCAGGTCCGG CTGTGTGGAC 780
AGAGGGCTTA GTCTGCCCTC ACCTAACCTG GCCAGAGGAG CAACCTGCTT CCCCCCACAG 840
AGGCCGCTGA CCACTGAGAG GTTAGCATGT CTGGGCAGAG GTGTTTTGGG CAGGGATGAG 900
AAGGGGGATA ATGACTTTGA GGGGCTAAGG GCCTGCCTGT CCACCTGTCA TTCTGTGTTT 960
GGGAAGCAGC TGGCAAGTGA CTCTTCTCCA GCAGGAATCT GTCAGGCCAG AGGATGGCCA 1020
AGTGGGTTAT GCAATTACAA ATCAGTCTTC AGGCCTCTGC TGGAAGGTGG TGTGGCAGTC 1080
CTGGGTGAGG CTGAAGGAGG TCAGGGGAGG CGCTGTCAGG GTGGGAGGAA AAGGTGCCTT 1140
CACAGTTTCC ACAGTACCCT GGGAGGTGAT GTTATTATAC CCACTTCCAT AGCTCACAGA 1200
GATTGAATAT CTAGCCTAAG GCTACAGAAT GAGTGGCAGA ACTGAAATTT TACCGCAGAG 1260
CTCTGGCTCT AAAGCCTAGG CTGACTCCAC TCTGTCGTCC AGCCATCGAG GAGCTCCAGA 1320
GGAAATCGGC TCTGCACCTG GCAGCCTTTC CAGTCCTGGG GGGATAGTGC CACCTCCCAG 1380
GACCCTTGGG GCATGAGGTC AACAAGGGCC AGCCCTCACA TGAGCACTGG ATGGAGCTGT 1440
AGTCACAGAG AGATCTCATT ATGCCAGTGA TTGTCAGAAA ACCTCCCAAG AGCCCCGTTC 1500
CTGGGCCCAG GTGGCAGCCC ATTGACCTTA AATAGCAAAG CCAGCTGGTC CCCATGTCCA 1560
GGCTGTAGCT TCCCTAGTGA GGGGGCATTT TTGTCCAGGC CTCCCTCTGA ACTCAGTTCT 1620
CAGGTCACGG GGAGATACAG TGCCCTTGCA GGATGGCTGC TGCCACCTGC CTGGTCTCCT 1680
GCCAACAGGG ACACCAGCTG AGGCACAGGC AGGACAGTGT ACACCTGGAG CCTCGCTCCT 1740
CTATGCTCCA GGGCCAGAGT GGTCAGTGCC CGTCAGCTGA GGCGGCAAGG TGAAGCTGGC 1800
AGAGATGACC CAGGCAGATG GCTCCAGGAG CCCAATGCCA GGGCGACTAT CTAGGAGACA 1860
CAAGGCAGCA GAAGCTGAAG AGAAAATAGA CCCTTGGGTG TGGGGGCTGT GGAGCAGGAG 1920
TGGGCCCTCG CCCCGTGAAA TAGGTCCCCT TTGCTGACAT CTCATTAGCC TGTCACTGCC 1980
CCTTTCATGC CAAGAACCTA GTGCCCCTGA ATTTGTCATT GTCAGCCCCA AGCAGGTTTT 2040
GGGAAAACAG TTCTTTCCTC CTCTACACTC CCTCCGAGTC TACAGCAGGA GAGCAATAGT 2100
CAGAATCAAT GAACCTTCCA GAACTAGAGA CATGTCTGCT TTAGTCATAA TACAAAAAAT 2160
GCTTTTAAAC AGTCGTCTCC CTACTGGACT TTTTTTTCTC TCTCTCTCTT ATTTATTTAT 2220
TTATTTATTA TTTTTGAGAC AGTCTGTCTC TGTCGCCAGG CTGGAGTGCA GTGGTGTGAT 2280
CTCAGCTCAC TGCAACCTCC GCCTCCCGGG TTGAAGTGAT TCTCCTGCCT CAGGCTCCCA 2340
AGTAGCTGGG ACTACAGGCA TGTACTACCA CGCCCAGCTA ATTTTTGTAG TTTTGGTAGA 2400
GACAGGGTTT CATCATGTTG GCCATCTCCT GACCTTGTGA 2440
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