| Tag | Content |
|---|
EnhancerAtlas ID | HS091-16877 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:28515370-28518100 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr16:28516458-28516475 | GGGCACACCATGTTCTG | + | 6.16 | | Hnf4a | MA0114.3 | chr16:28516207-28516223 | ACTGGATTTTGACCCC | - | 6.3 | | STAT1 | MA0137.3 | chr16:28516977-28516988 | TTTCCTGGAAA | - | 6.62 | | Stat4 | MA0518.1 | chr16:28516974-28516988 | TGTTTTCCTGGAAA | - | 6.14 | | ZNF263 | MA0528.1 | chr16:28517126-28517147 | TCTCCCTTCTCTCCCTGCCTC | - | 6.7 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCTGGAGAGA TGGGAAGAGG GTGGCAAGAC AGGGAGAGAG CTTGAGAAGG AAGGGAACAT 60
GCCTTTTCTG AGCCTGTGCT AGCTGTGAGC ACGGTGCAGG CACTTTGACC AGCATCATTC 120
CTCTGCCTCC TCAAAACCAC AATGGAGGCT GGGTGCGGTG ACTCACACCT GTAATCCCAA 180
CAATTTAGGA GACCGAGGCG GGCGGATCAC CTGAGGCCAG GAGTTCAAGA CCAGCCTGGC 240
CAACATGGCG AAACCCTGTC TCTACTAAAA ATACAAAAAT TAGTTGGGCG TGGTGGTGCA 300
TGCCTGTAAT CCCAGCTACT CAGGAGGTTG AGGCAGGAGA ATCGCTTGAA CCTGGGAGGC 360
AGAGGCTGCA GTGAGCTAAC ACCACTGTGC TCCAGCCTGG GCGACAGAGC CAGACTCTGT 420
CTCAAAAAAA CAAAACAAAA CAAAACAAAA CAAAACCCCA CGATGCAGCC AGCACGGCCC 480
CCATATGGCA TCTCCGCATG GTGTGCCCAC TTTTGCAAAA AGACCAGAAG CCTGATCCTT 540
TTTTTTTTTT TTTGAAACAG AGTTCTGTTC TATCACCCAG CCTGGAGTGT AGTGGTGTGA 600
TCACAGCTCA CTGTAGCCTT GAACTCCTAG GCTCAAGTGA TCCTCTCGCC TCAGCCTCCC 660
AAGTAGCTGG GATCACAGGG ACACACCACT GTGCCTAACT GTTTCTATTT TTTTGTAGAG 720
ACAGGGTCTC ACTATGTTGC CCAGGCTGGT CTTGAACTCC TGGCCTCAAG AGATCTTCCC 780
GCCTCAGCCT CCCAAATTGC TGGGATCACA GGCATGAGCC ACTGTGCCGG GACAGAGACT 840
GGATTTTGAC CCCCATAAAC TCCCTTGGCC AAATGCCTTT TTCAGTGAGC AACCTGCACA 900
ACCACGTGTG GCAGCCTCAG TGCTATTGTT CTCCCCAATT TGCAGGTGAG GCTCAGTGAG 960
GTTGACTTGC CCAAGGTCAA ATAGCCAGAA GGTGGGAAGC CAGGACTGGA TTCCAGGTTT 1020
TTCCAAATGC AGAGCCCATG GGTTTTCCCC AGAGAATGCA GAGGGAGGCA GCCATCTGCC 1080
CCAGGAGTGG GCACACCATG TTCTGGCAAG GATTCTTTGG GCTCAGCCAA GCGGCTCTGA 1140
TGGCTTGAAC TGGCCATGAG GTCCCCAGGG ATGGGCTGGC AATGCCAGAG GCTCTATTCC 1200
AGGGAGTCAA AAGGACAGGT TTGTCCAGTT TCCACCACGG CAGGTGGATC CTAGCAGGGT 1260
AACCTGCCTG GGGCGAATCC ACAGTATGGG AGCTTTTTTT TTTTTAAGAC AGATTCTCAC 1320
TCTGTCACCC AGGCTGCAGT GCAGTGGCGC GATCTCGACT CACTGCAACC TTCACCTCCC 1380
AGGTTAAAGC AATTCTCCTG CCTCAGCCTC CTGAGTAGCC ACCACGCCTG GCTAATTTTT 1440
ATTATATTTA GTAGAGAGGG GTTTTGCCGT GTTGGCCAGG CTGGTCTCCA ACTCCTGACC 1500
TCAGGTGATC CGCCTGCCTT GGCCTCCCAA AGTGCTGGGA TTACAGACAT CAGCCACTGC 1560
GCCCAGCCCA GAATGGCTGA ATTCCGAGTG TGCTTCCTGA CCTGTGTTTT CCTGGAAAGA 1620
GGGGCAGCGG ATGGGCGCTC TAGGAAGAGG GCAGCATTCA TCAATTTCCC CCTCAGGGAG 1680
AGGAAATCTA GCAAGCACAA GAGTTACACA ATTCTCCTCG AAACACAAAC CAAAACTGGC 1740
CCGAAGTCCA TCCTGCTCTC CCTTCTCTCC CTGCCTCTTC CCTGTCCTCT CTCAATCTCT 1800
AACCCCTGGG CTCTGCTCTT CGAAATGTCC CCTGATAAAG GTGAAGGGGA GCTTCTAGGG 1860
ACATCTACCT CCCTCGTGGG CTTGCAGATG TGGTGGGCGA TGCCTAACGT AAGATCTCTG 1920
GCATTCAGAC TCCCTGGTTT TGGGGCCACT CGGACCCTCT GACATCCTGG AGACTTAAGG 1980
CAGAGTGGGG TTCTTCCTAG CTCAATGTTG GGGACAGGGT GGGTGCCCCC AGGCCCTGGT 2040
GGATCAAGCC CAACCGTAAG TGAGCTGTGC CATCTCCAAC CTGACCTCTG GAGACCCCAG 2100
ACCCCCTCCT TACCCTCTGC AGCTGATCCT GGGTCATTGG CTCTGGCCTT TGAAGGCTCT 2160
GTCTCCATCC TCCAGCCTTT GGTCCCTACC TGCCCTACGT GGCATGTTAC CTTCTCCACT 2220
GCCTACTGCT CTGGTTCTAG CCCCTGAGTT CTGCAGCCAC CAGCCGCAGA TTGGACCTCT 2280
TTCCAACATC AAACTAAAGA CCTTTGACCC AGTGAGGCTG CTGACATCTT GGTCCCAGTG 2340
CTCCACTTGT GCCAGCACCT CGTTCTGCTC TTCCTCCAGC CGGCCCCATT CTCAGTCTTA 2400
GCCAAGCTGT TTGGCTTCTG CTTATTCACT CCAAACTCTT CATTTATCTG CCTAGACCTG 2460
GTCCTTGTCA AATTGCTGGT CCAACCCTCC CCATTCCCAC TAGCCAAGGC CTCCTTCTCA 2520
TCCTCTGCCC AGCCCTGGGT CAGACCACCA CCCCACTGCC CCAGGCCCCC ACCCAGTCAT 2580
GCCAGCCTCC CTTCCCATGC AGCAGCCAGC CGAATCCTCA GTCTTGGCCA AGTTGCTGCT 2640
CTCAGCTCTC GACCCCCCAT CTGCACCAGC CAAGCTCGTC CATTCTCTGC CCAAACTCAA 2700
CCAAGCCCCC CACCCCTGGC TTCAAACTCA 2730
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