| Tag | Content |
|---|
EnhancerAtlas ID | HS047-23821 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr3:48935110-48936120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DMRT3 | MA0610.1 | chr3:48935688-48935699 | AATGTATCAAA | + | 6.02 | | HINFP | MA0131.2 | chr3:48936038-48936050 | CAGCGTCCGCGC | + | 6.22 | | HNF4G | MA0484.1 | chr3:48935336-48935351 | TGGACTTTGGTCCCC | - | 6.39 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCTGCCCAAG CTGGCCAAGA GGAAGTGCCC ACAAAACTAT TTCGCTGTGG AAGAAATCTG 60
ACCCAACATC CTAACAAACC CCCTCACATG GGCTTCCAAT CTTTTAAAAC TCATGTCTGC 120
TCCCCACAGG CCCACCCTGG CAATGACTTG TCAATTTCCT TCACGTCTAC GTCTAGAAAA 180
AAAGTGAGAA AACTGGATGC AGCTTCGAGT GCTAAGCCAT GGGGGATGGA CTTTGGTCCC 240
CAAGCAAAGC ATTAATGAAG GTGTTGCAAG GGGAATAGTT GAGATATGAT ATGAGGAAGA 300
CCAGAGAACA ATTCCTGATG AACGTCCTCC CTCCCAAGCC TCAGTCTGAC CATAGCTTCC 360
TCATCTGGGA GTTGTGAGAA TGAGGCTGGC CTTGTGCAAA GCTGATCACC TTGCTTTCCG 420
TGGAAGGGGC TCGGTCACTG AGGTCATCAT TGCTTCTCAC AGGGATGCCT CTGCCCAGGA 480
GGCTGAGCAG GCCACCGTTG GGTGACAGGC CGAAGAGTGT CAAGTATCTC CCCGGGCCGG 540
GAAAGGTGCG AAAGAGATGG GTACTCTTGC CCCAGGGGAA TGTATCAAAG GACACCTCCA 600
GAACAACCGT ACCGCTCTGT CTTTAGTTGT CTTCCTGGGG CAGGCTTTAC AGGGGACCTG 660
TTTCAACCTT AACGATAATA TTAGTGTTGG CTGAAACCAA AACTATGGAG AGACGTTTAT 720
TCCTTCCCAT CCCTAAAGAA GTGGCGCAGG GTCAGAAGAG ACTGCGGGAC AGGGAACTTT 780
ACATCAGAGC TCTTGACAGG CAGTTAGAGG CTGCTCACTT TGCGCCGCCG CCTGGCTCTT 840
TGGGGCGCAA GGTACAGCTT CCTGCCCACC CCTGAAAGAG AGATTCCCTA GACTTCTCAC 900
GGAAGCTCAC ACATGCCCCT CTTCTGCCCA GCGTCCGCGC CTCGCGGGGG ACCATGCTTT 960
CCGCGCCCCG CCCGGGCCTC CTCCCCAAAG CCTGCGACCC AGCCTCCCGC 1010
|
