| Tag | Content |
|---|
EnhancerAtlas ID | HS073-06942 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr18:60707070-60709480 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SREBF1 | MA0595.1 | chr18:60707758-60707768 | ATCACCCCAC | + | 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 |
| GH18I063040 | chr18 | 60708131 | 60708610 |
|
Enhancer Sequence | AGCCACTGCG CCCGGCCTAT TTTTACCTCT TTTGAGAAGT ATTCCCTGAA TAACCACACA 60
TCAGATTGAT CGGTCCCTCA CCTTCTCAGC CTATTAACTG ATTCACAAAG CAATTCTTGA 120
GCACTTTCAA GAGACCAGGC ACTGTGGTTA CAGAGGGGAA TTAAAACCTC TGGACTCAGA 180
GTGCCTCATG GTGAGCAGAT AAGGAAACCA GGTAATGTGA TAGATTTCTG GTCAGTGTGG 240
TAGAGGAATG CATGCGAAAC CTCCCCTTTC TAATGCCAAA TATATATTTG ATATATTTAT 300
ACATGGAGAT GATAGAGTAT ATATTTGAAG GATTAAAATA TACAGTCACT AACTTAGCTT 360
CCTGGGGATG TCAGGACAAA AGACCACAAA CAGGGCAGCT TAAACAATAC AGATGTATTG 420
TCTCACAGTT CTCAAGGCTG GAAATCCAAG ATCAGGGTGT CGGCAGGGTT GGTTCCTTCT 480
GGGGACTGTG AGGAAGGCCC GTTCCGAGCT CTTCCCTGGC ATCTGGTGGT TTGCTGGAAT 540
CTTCAGCACT CCTTGACTTG TGGAAGCACC GCCCTGGTGG TGCGCCCTGT GTCTCCTCAC 600
ATTGTCTTCT CTCTGGGCAT CTCTGTTTCC ATAGTTCCCC TTTCGGCAAG GACACCAGTC 660
AAATCCTAGG GTCCACACCC ATGACCTCAT CACCCCACTG ACCTCATTTT AACTTGATTA 720
CCTCTGTAAA GACTCTCTTT CCAAATAGGT CACATTCTGA AGTACTGGGA GTTAGGACTT 780
CAACATATCA TTTTGGGGGA CATTCAACAT ATCATTTCAG CCCATAACAG TCACAGTAAA 840
AATAAAACAA AACAAAAACT AGATGTAAAT CTCTGTGGAC CAGGAGTGGA GACCCCTGTC 900
GTGAGCAGGG GCTGAAGCTC TGGGTGAGCA GCCTGGAAGC CAGCAGTGGT GTGAGAAGAA 960
GTCAACCCTA TGGAGGAAGG GGGCTGGGCC ACCTCCTTGG ACAGTGAGAG TCAATGCCAG 1020
GTGCCCTGCC TGCTGGAAAC TCCAGCCTGT GACCATTCTT TGCCTGTGAA TAAAGCTAGA 1080
AAAGCTCCCC TCCCCCACTG CAAGGTTGCA GTAAGAAACA AGCAGTTTGC TGGGGTGGAA 1140
GGAGGCTCTA GACATGAACA CGTGTCTGCT GGAGCCCTGA TGTGCCCCAG AGAAGACTGC 1200
GCTGAGCTAT TGTGGGCATG AATCCCAGGT CTGACCTGTC CTCCTAGGAG GCTGCACGGG 1260
AGCACTCAGA AACTTCCAGA TACAGAAAGG TAAATGGAGA AGGGCAAGGA AATGTCCATG 1320
CAAGCAGAGT GTGCAAACTT ACCATACAAC AAAACTTACC ATACAACAGG TGGGAAAATC 1380
CAACAGCAGA ACAAAAGAAC CAACAAAGCC AATAGCAGAG GGGAAATCAT GCCTCCCAAA 1440
ATAGAAACCA GAGAGCAACC AGGAAGGGAC TTTCCCAAAG AGAAAGGAGG GGAAGTCATT 1500
CATAAATAGG AACAGGTGTT TACATCAGCA AATCACAAGC CCAAAGATGT TATGTGAAAC 1560
GTATATGCAT CACCTCTCCC TTCTGACACT TCTGATAAAA TAATAGTAAG GAAGTAAAAA 1620
GGAATAAATC CCTAAGGACA AAGAATATAG AAGAAAACAT CAGTAGAGAA GAGAGTTCAA 1680
TGAAATTTTT CAGGACAAAA ATTAGATGGA CAATTGTCAT TGACTTAGCA GAACTGAGAA 1740
AGACACAACC CAAAGTGCAC TTAGAGAATG GAATCTACAG TAAGAAGGTC GTGGTGAACC 1800
CCAAGAGGTC AGAATGTGGG GGTACCAGGA ATGTCAGACA GAGGGGCTGG GATACCCAGT 1860
TGAAAGCAGG GTCTTGCGTG GGGAGTCAGA GAATGTTTAA CCCTCTTCTG CTGTCTCAGA 1920
CAGGGTGCTA GCTGCCAGCC ACTGCTTCCT GGCAGGAGGC TTGAGATCTA TTTTCTGAAG 1980
GAACTGAATT GGAGGAGCTT AGCTTAAAGC CATTCACAAA ATGGAGATGG GGATGAGGCT 2040
GAAAAGAGGG AGAGAATACT CAACGTCTGC CAATGGAATG GTCTTTTAGC CTGAGGGCAG 2100
GTCACAAGTA ACCCACACCT TCTCTTCTCT CCACTTTCAG GAGATGGGAG GATTTCTCCT 2160
CCTTGGATTC CCTGGATAGC TCTAGGGAAA ATATCATTTA GGGGACCCTC AAGGAACCAT 2220
TAACAGATTC CACCTTGCAC ACAGAGCTTC CATTTAGTCT TTGATGATCT TCAATGCCAG 2280
ACAACTGAGG TTTTCCAAAC ACACCAAGAG AACCCTCAAC ACGAGGAGGC CCCAAGTAAA 2340
CAACTGCAAA ATGGAACTCA TGCAGGGAAG AGAGAACATT TAAAAAAATA AAGACCCAAA 2400
TGCTATCCTT 2410
|
