| Tag | Content |
|---|
EnhancerAtlas ID | HS047-18543 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:25101090-25103560 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr2:25101909-25101920 | GGGCGGGAAGA | + | 6.14 | | HSF1 | MA0486.2 | chr2:25101320-25101333 | GAAGGTTCCAGAA | - | 6.33 | | Sox3 | MA0514.1 | chr2:25102973-25102983 | AAAACAAAGG | - | 6.02 | | ZEB1 | MA0103.3 | chr2:25102761-25102772 | GGGCAGGTGGG | - | 6.14 | | ZNF263 | MA0528.1 | chr2:25101501-25101522 | GGGGCAGGAAGGAGGAGGGGA | + | 6.92 |
|
| | 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 |
| GH02I024877 | chr2 | 25099999 | 25102914 |
|
Enhancer Sequence | TGATAAAGTG TTTCTAATAT CCCGGCTCAG AACGCAACCA TGAGAACATT CCTTTACAAA 60
ATCCTCCCTC CTGGAAGTTT ACGCATCGCA AGATCCTTCA CGTTTGCTAA CAACCCGTAG 120
GGAAATGGGG CTGCTCTAAG TGGGACTGTC GAGTGGAAGT CACCCCACTG GAGGCGGTTT 180
GGTGGCTCTC TTGCCCAAAC CAATCTCTTC CTATAAGCTC ATTCCAGCCT GAAGGTTCCA 240
GAACACTCTG GAACTGTGGA GAAGAAGCTG AGCAAGAGAA AGCTGCTCAG GGTGCAGTGT 300
CCGTGTCGCC CACAGAGACC TATGACGTTC TGCGGCTGGA GGCCAGCCGC ACGGGAAACT 360
CGTCATTAAA ACTTACTCAG ATGCTTTAGG AAAAAGTCTC CTAGCAGCCA TGGGGCAGGA 420
AGGAGGAGGG GAGGTGGCCC CTCCAAAGGC AACCAGCCTT CTCCCACCCA AGGAGGCCCA 480
GCCAGAGCCT GTGAGGCCGC CACTCAGCAC AGATGGGTCC CACTTCTGGG GCCACTCTCG 540
CTGCAGACGC CTGTAGAGGC TGCTGCAGTG GCTCCTTAAG TCCCTATGAA ATGTCCCTAC 600
CCCTCAGAGG CCTTCCCTGC CCACCCCTAC TCATTCTCCA GTCCTGCTTT GAGGCCCAGC 660
ACAGAATGTT CTGCACTTGC CCTTCTCTGT CCTCACTCCT TCGCCTCGTC GCCTGGAAAG 720
CAAACTCCAT GCAGCCGGGA CACGGGTTGT TTCCCTGCTG GCTCCCCAGC ACCCGGGACT 780
GGCACATAGA AAGCCATAGG CAACAACTGG CAGATGGAGG GGCGGGAAGA GGTCAGGCCT 840
CGCAGTCACA TAGACCTGCA CACGGCTGCC CGCAGGCTGT GTGCCCTGGA GCAAGTCGCC 900
TGCCTCTCTG ACATGGCTCC TCACCCTTGC AGTAACCCCA CAGGCTGTTC CAGTAAGACT 960
GAAAGACTGG GCCGGGCGCG GTGGCTCATG CCTGTAATCC CAGCACTTTG GGAGGCCGAT 1020
GTGGGCAGAT CACAAGGTCA GGAAATCGAG ACCATCCTGG CTAACATGGT GAAATCCCGT 1080
CTCTACTAAA AAAAAATGCA AAAAGTTAGC CAGGCGTGGT GGGCAGGAGG CTGAGGCAGG 1140
AGAACGGCAT GAACCCGGGA GGCGGAGCTT GCAGTGAGCC GAGATTGCGC CACTGCACTG 1200
CAGCCTGGGC GACAGAGCGA GACTCTGTCT CAAAAAAAAA AAAAAAAAAA AAAAAGACTG 1260
AAAGACTGCA CATACCTCAC ACAGGGCTTG GCACAAAATA CCCCTTTCAT GACTTTTTCT 1320
TTGCTTCCAT TGAAGGCAAA TTAGTAACTA ATAATAACAC TTTGAGGACG TTTTACAAGA 1380
ATCTTCATGT TCATCATTCT ATTTGTTTCT CACAACAAGA GGAGGCAGGG CAGAGTTTTC 1440
TTATTCTCAT TTTGCAAGAG ACTTAAAGTC AGAGAAATAA GCTTCCGAGC CCCTAGTCTC 1500
CCAGCAGCGC TGAGACCGGA ACCCAGACCC CCTTACCCCG GGGCCAGGGC TCCCCTCCCT 1560
CAATACGATC ACCTTAGCTG AACTGTGATG GGTGTCTGCC AAGGCGGGGC TACAGCCGCG 1620
GCACAGGGGG CTCCCCAAGA GCTAAGGATC CAGTTAGGAC CTGGAACATC TGGGCAGGTG 1680
GGAAGGAGGA GTCATAAGGT CTGCAGACAG TGAGTGACTC TCCCATGCTG CCTTGGGCAA 1740
ATTCTAAGCA TCGCTGCACC AAGAGAGACT CTGAGATCTC CAATAAATGC AACCTTAATC 1800
AATACAACAC GAGGCTCAAG CCTGGGGTGC TGCTGCCATG CCCTTCCGAG CTGGGTATCT 1860
GCCAAGTTTC CACCATGTGC CTCAAAACAA AGGGGCCTCC AGAAGCTTTC TGCTTATAAC 1920
TTGTGCATGC CTTTGGTAAG AGATGTTCAA AGTCTACCCT CTTCCAAAAC AAAGAGGACT 1980
TCCAGAATAG GCATCCAGCC CATCTGACAT GTTAGGCCAG GTCCCTCATG ATCTGCCAGG 2040
CAGCTAGAGC AGCTTCTCAG GTTGCGCACT GCCAGGGGTG CCACTACACA GATCTGTCGT 2100
GATGGCTTCC CCAGACACGG AACATGGCGG CCTTGGCCCC AGGCTCTACT GTCTTGACTC 2160
TGGTTGCTCC TCAACAGGCT CCCCTCCCTC CAATCACAAT GGGCCTCTCT CCAGTCCTCC 2220
CTATAAGATG TGCTATTTCA GGGATCCAAG GCTCCAACCA AAACAGCCTG CCTCTGCTGC 2280
CTGTGGAGGT CCACATGTTA TGACGAGTCT GTGACCTTAC CCTTGTCAAG CTCTTAGCAG 2340
AAATAATATT TCAAATGTAA GCATATCAGA GCTCAAAAGA GAATAAAAGT GGTAGAAAGT 2400
GACTAGGTAG CTGCTTTAGA TGAGGTCTGA GGAAGACAGC TGGCCCTAGT TCTTCACTCC 2460
CCCGCAAAAG 2470
|
