| Tag | Content |
|---|
EnhancerAtlas ID | HS047-18428 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:16499260-16501570 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:16499903-16499924 | AGTCACTTCCTCTTTCTGTTT | + | 6.16 | | SPI1 | MA0080.4 | chr2:16499906-16499920 | CACTTCCTCTTTCT | - | 6.51 | | Stat6 | MA0520.1 | chr2:16500626-16500641 | AGTTCTCTGGAAAAA | - | 6.75 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 16499732 | 16499985 | | chr2 | 16500147 | 16500473 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH02I016317 | chr2 | 16499238 | 16501050 | | GH02I016319 | chr2 | 16501201 | 16501350 |
|
Enhancer Sequence | AATCCCCTCT GGTTGGAATA ACCTCTCACG GCTCCTGGGT CCTCTCTGGA CCCCGAATGA 60
TTCAGGTCAG CTCAACCTGG GGAAGACCTT CTTGGGAAAG TGACAAAGCT GAGAAGTGGA 120
GAGTGAACAG GACACAGCCA GGCAAAGAGA GAAGGGAGAG TGCGGCAGGA AGAAGGAAAA 180
GGGTGTGCAA AGGCTCTGCG GTGTGAACAC ACTTCTGCCA TTACAGGAGC CGTGAAAAGG 240
CCTCTGCAGC TGGAGTGGGG GCAGTGTGGC ACCTGATGAG GCTGAAGGGG TGTGCTGAGG 300
GGAGCCTCAT AGGCAGGGCC TAGCCATGGT TGTATGTGGG GTGCCCTGTC TTTCCTAGGG 360
TGGTGCCATG GCACGAATGA CCTCTCTGAA GGTGTGTCAT GCAGTTCCCT TGCCTGTGGG 420
TCACAGAAAA CATTGGATCT AATCTCAAGA GTAGTGGATT TTGAATGGGA GAGGTGCAGG 480
GTGTGATTTG TATTTGTAAA GGGCAACTTT ACCTGCTGTG TAGAGAACAC ATTGCAGCGA 540
GGCCAAGTGG AACTGGAAGT GGTTGTAGCA GTTTGTGCAG GAAGAGATAG GGAGGAATGG 600
GGCCGGAGCA GCATGGGGCT CCCTGGCTCT CTGACCTGGA GGCAGTCACT TCCTCTTTCT 660
GTTTAACCAG CTATAAAAGG AGGAGGCTGG GCCAGGGCAA GGATTTTTCA GCTGGAGTCT 720
AAGTCCTCTG AGGGGGGTCT ATGGATGGGG GTCAAGGGGT GGGAGAGACT CTGAGATTGT 780
ACACAAATGG TTGGACCTAT GTCCACAGAT GCCTTTTTCC CTCAGGGAAA AGGGTTCTTG 840
ACTTTCAGCA CATTCTCTGT GAGGTAACAG CCACAGAGTT TTAAGCCACT CATCTAACAA 900
TCTGGAAAGG CACTTGCAGC TCAAATTGCC AATGGCTTGC GATTCTGGAC CTTCCCAGTG 960
AGTCATGCAT TCTTAAAGTG TTCCTGCTGG CTGTTAAAGT TTGTGAGGAA GGGGAGGGGA 1020
CCCTGACACC ATCTGGAGGC AGGGTGACAT GCCCATGGAG CTGCTCCAAG CACAGGTACA 1080
GAGGTAATCC ACTCATGGTG GCCTTTCTGA GCAGCAGGCT GGAGGCACCA TTTCACTTGA 1140
TCATTGACAC AACCCAATGA GGCAACAGGC ATTGACACCC ACTTCGTTAC CTGTGCAAAG 1200
GCTCCCCGAG GCCACCACGC CACCCTACTC TCTCACATCA CAGCCAGGGC TGCCTTTAGG 1260
AGCGCCCCAT GTTTGCCTTC TGCCATCCCC ACCTTCCAGC GCTCCTCGCC CCTGACCAGT 1320
GCCCTCTGAC ACCTCTTTCC ATCTCCCCTC TCTTCGGAAA CAACGGAGTT CTCTGGAAAA 1380
ATAAAATGTA AAATCAGACT CACTCTCAGT CACACGAATT GGGGTCACTG TGTCCAATTT 1440
CCAAAGGGAA ATGTTAGCTT CATGCTGCAG TGAGACTGGA AATGCCATTC CTTTCTGAAA 1500
AAGTGGGTCA GGCACCAGAA CATGTTACAG GGACTGGGGT CTTTACAGGG CGCCCCTGGA 1560
ATCCCTGAGG GCAGGGCCAC AGCTGGCTCT CGCATGCGTG CCCACCCTGT GCTGCCGGCC 1620
CAGCCCACGG GCTCCATCCT CCAACCCAGG CCAAGGCAGA AAACCAGATG CCTTTCCTAT 1680
GTCTCCAGCG TGTCCCATCT TGCTAGGATT TTTCACATTT TTCTGTGGAA GCCCTTTATG 1740
GTCTGTGACC CTGGCCACTG CTGAGCCAAA AAGACAACAG ATTTATGGCA GGCCTGGAGA 1800
GCAACAATCC ATGGATGCAT TTTCCCTGCT TTCAGTCAGT AATTTATTTT TAAATGATCT 1860
TTCTGTTATT TATGGGTCTC GCTGACTCCG ATGGCCAGGG TGAACTGCAT CTTATCAGAC 1920
TAGCAAAACT AACTGGATTA AAGGGCATCC CTCACATGTC ATCAAAAGGA GGACTAAGAA 1980
CCCCGATGTC TCAGAAGTGC AGCTGAACTG GTTCATCTCC TTTTGTCCCT GAACAGCGAT 2040
GTGAGCTCAG GCCAATGCCT TTGGGCCATG GGGTCAAACC TTCGCGGCTC CTCAGTGTTG 2100
AGGGCACAAG GCATGACAGC CGACTTCCTG CCTTGTAAAG TGGGGCTCAG GACACCCGCC 2160
ACAGACGCTT ATAGTGACAG TAGGGGAAGT CGTAGGGAAC ACCTGGTACA TCTAATACTC 2220
AATAAATGCT ACCTGTGTGA TTATTATGGC CTTCTTTACC TTGTCCTCAT CTCCCCTCTG 2280
GGAATACACC ACTCAGAACC CAGGATGAAA 2310
|
