| Tag | Content |
|---|
EnhancerAtlas ID | HS047-00040 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:1873790-1876020 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr1:1874294-1874305 | AGAGGGTGTGG | - | 6.02 | | MYC | MA0147.3 | chr1:1874008-1874020 | GGGCACGTGGGG | - | 6.07 | | NR2C2 | MA0504.1 | chr1:1874393-1874408 | TGACCTCTGACCACT | - | 6.05 | | SP1 | MA0079.4 | chr1:1875862-1875877 | ATGGCCACGCCCACG | + | 6.22 | | SP3 | MA0746.2 | chr1:1875864-1875877 | GGCCACGCCCACG | + | 6.04 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 1874601 | 1874908 | | chr1 | 1875848 | 1876000 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I001942 | chr1 | 1873910 | 1876089 |
|
Enhancer Sequence | GAAATGAAAT CTGATGAAGA ATTCTTAAAA ATAACCACAT CGAAACGGAA GCACGGTCCT 60
AATGGGCTCT CGGGAACCAG ATGCTTTCCG GGAAGAGCAC CTGCCAGGCA GCCCCTGGGT 120
GCGGGGCCCT GGAGGGGACA TGAGGGGTGG AACCCCTCCC TCCAGGGCTC TGCCCGCCTC 180
CTGCCCAGGG CATCCCCACA TCCTGCAGCT CAAGCACAGG GCACGTGGGG GGCCTGGGAC 240
GGCCACAGGC CTCGGTTATG ACAGCAGCCT CCAACCCAAG ACGAGCCTGA GAGAGCCAAG 300
GTACCCGCCA GTCACCTGGG AGGCCATGCG TCTGTCCGGT CCCTACCTCC GGCTCCCTTA 360
AGCCAACGGC CTCCTCAGGA CCACCTGGAG CCTCCCTGTT CCCACAGTGA AGCCTCCCTC 420
CCCTCCCCCG TCTTGGAGCC TCTGCTAAAC AGTGTTGTGG CCGCCCCGCC ACAGCTGCCC 480
CGGGCAATCC ACGAGGGGGG ACCCAGAGGG TGTGGCAGTG AGAAATCTCC TCCCTCCTGT 540
GCTTCCATGC GACAGTCACC CATGCTGTGG CAGCCTCATC TCCGTCCATC ACAGACCTGC 600
CTCTGACCTC TGACCACTAC CCAGAGGCCA CCCACAGTGC GTCTGGGCAC GCCAGCCTCT 660
GCACCCCTAC TGCTGGGCCC CATGGGAGGC GGGCGCCCGG GTGCTCAGAG ACCGCGCCCT 720
CCCCGTCAGG CAGACGCTGC TCTGCCTTCC GGTTCCCTTA TGGGGCCAGA GTCTATACAA 780
ATGAGCACAC AGCTACACTG AGGTACACAC AACCACAGCC GGAGACCATC CACAGAGCTG 840
GGCCCCACTC AGCCCTCAAT GCCCGACAGA CACGCCTGGG CCCTTTCTGT CAAGTTTCCA 900
AGGCCACTGA GAGGCTGTAG TAGGACGATG CCGGAGGCGA GCAGACTCCA CCGCAGACAC 960
GCCAACACAC GCAGCTGGCT CCCGGGTCAC CGCAGGCTGC ACATTCCCGG CCCATGCCGG 1020
GCCCACAGGA GTCCGACAGC AGGAGGACAG GCGCCGCGGG AGCTGTTCCT ACCCAGGTCA 1080
CCGGGGAGAG GTGGCTGTGC CTGGGGCCGG TGCCCGGGGC CTCTGTGTCC GCACACCCTG 1140
CTCCTTGGTG CTGGTGGCAC AGGGGCTCCG TCATGGAAAC CCCGCAGGCC CAGCCTCGCC 1200
GTCCCTCTGC GCTTTCCCAC CGGCGTGGCT GTTCAGGGCA GGCTGCTTGC TCTGATGTCT 1260
GGAGCCCTTG CCAAACCCTG CAAGTGGAGG CTTCCTCCTC CAGGCTCACC CTGCCTGTGT 1320
CCACGAGGGG CTGAGGACTC TGGCCGGGCC CAGGCGGGCA GTGCGTTTCC TGTGGCTGCT 1380
GAAAGGATTT GCCCCAAGCT TAGGGGCCCC ACAACACAGA GGCACATTCA TTCTCTCCAC 1440
GTCCTGGAGG TCAGAAGCCA AGACGGAGCT AAGGCCAAGG TGCGGGCAGG GCCGTGCCCT 1500
TGTGGCTCTA CGGGACAGGT TTCTCCTCTC CTTTCACAGC CTCTAGAAGC TGCAGTGTCC 1560
CCGGGCTCGG GGCCCTTCCT CCATCTTGGA AGCCGACAGT GCAGTGTCTT CAAATCGGCC 1620
TGACTCTGAC CCTCCTGCCT CCCTGTGACG CCTCCCGTGA TGACACTGGC GCCTCCCAGA 1680
TGATCCTGGA TCACCCCCCA CCAAGGTCCC TCTCCCCAAC CATGTCTGCT AAGCCCCCTG 1740
CTTGCCACAC AGGATGCCGT TCAGGGCCTG GACAGCAGCC GTGGCAGCCC CAGGTGCCAT 1800
GTCCCCGCTG GCCACTGGGG GGCTCACCGC GTGTGCACAG GCAGGCAGCG GCTCACCCCG 1860
TGTGCGTGGG TCACCCCGTG TGCGTGGACA GGAGGGGGCT CACCGCGTGT GCACAGGCAG 1920
GCAGCGGCTC ACCCCGTGTG CGTGGGTCAC CCCGTGTGCA TGGACAGGAG GGGGCTCACC 1980
GCGTGTGCAC GAGCACAGAG TCCTGGTAGA GCCGGTCATA CATGCAGATC TTCAGGTCCA 2040
CGCTGGGCTT CGGCACCCAG ACCGGCACAT CGATGGCCAC GCCCACGACC CTGAAATGCA 2100
GCTGCATATG GACACAGGAG CTCAGCAACA GGAGTTCCTT GGGCACAGCA GGCATTGTTG 2160
GTGAGCACTG ACACAGCTCC CAGGAGGAAC GTTTCATGGG CTTGAGTTTT CTAACTCTTT 2220
GGGACGGCTG 2230
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