| Tag | Content |
|---|
EnhancerAtlas ID | HS047-18544 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:25149160-25150450 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HEY2 | MA0649.1 | chr2:25149907-25149917 | GACACGTGCC | + | 6.02 | | Npas2 | MA0626.1 | chr2:25149907-25149917 | GACACGTGCC | - | 6.02 | | ZNF263 | MA0528.1 | chr2:25149165-25149186 | CTCACCTCTTCCCTCTCCTCT | - | 6.09 |
|
| | 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 |
| GH02I024926 | chr2 | 25149270 | 25150455 |
|
Enhancer Sequence | CCCGCCTCAC CTCTTCCCTC TCCTCTCCTC GATCGGTGCC ATCCACACAG GACGTGGGCT 60
CTGCTGGCTG CCCTCGGGTG CTGTTTCTAG GCCCCTGACG CAGGCAGAGG GAAGCGGGCT 120
GAGGATGCGC AGTGAAGACA TCCAGGCACC CAGGCTGGTG CTGGGCTTGG TTCCGGGTCT 180
TTGCCCCTTG GCAGGTGTGA GCGTCTCCTT GGGAGCAAGG ACCAGGGTCC CTGGTTCCTC 240
CTGCCCAGTA TTTGAAACAG AGTGGCTATT CCACAGTCTG TCATTGAAAT AATGTCACCG 300
GCACACTAGC CACAGTGCCA GTAACACCCA TGGGCCCGAT CCCCAGACAG CGGCAGCAGC 360
TCCCCTTCCT GCGCCCCGCC CTGCAGGCAC CGCGCGCTGC CTTCTTCCCT TTGGTTTCCG 420
CGGTGGGGAC TCCCGGCGTC CCTGTTGTGC GGGTGGAGAA GCGGGAGCGC AGAGACATGA 480
GGTAACTTGC TCCGGCCCCA GCTAGGAAGG GGCGGAGGCC CAGGCTCTGG CCACCCAGAA 540
GTCCGGCTGT ACCAGGAAGG CTCAGGAAGC TTCCTTTGCT TGTCACTGCT TCTCTGTAGC 600
CAAGGGTGCC CTTGACCTCA GGGACTCAGA GCGAATCCTG GAGAGTCACA GCTCCCTGCT 660
GGCAGTTGAA AGAGACTCCA AACACCATTC TGCTGCAGCC CTGGTGGAGA CATTGAGGCC 720
CAGAGGGGTT AAATTTGGGG AGAGAAGGAC ACGTGCCCAC GGAGCGTGAA ACGGCATGTG 780
AATGCTGAGT AATTCCGAGG CCTCTGCGGG ACGTCACGTT TCCAAAAGCG CGCGAGCCCT 840
GCCCCTCCGG CAAGAGGCAC CATAGAAATG TGTGCTAACA AGCCTCCCTG CGGCCTGCGG 900
GGAATAGGAG AGAGCAGGAA GCTTTCAGAA CAACAAGAGT GGCTAGAAAA GGCCCCGGAT 960
GGGAGGAGAC GAACAGCCCA GCCCCACGGT CTTTCTCATG GGTGGAAAGT CACTAGCACC 1020
CAGAAAAGCA AGGCTAAGAG ATCCTGGGGA GCTGGCACAA GTTCTCTGGT CTTAAAGACG 1080
CATGTGATTA GATCTGGCTC ACTGGGATGT TCCAGGAGAA TCTCTCCATC TCGAGATCCT 1140
TCACTTAATC ACGTTTGCAA AGTCACTTTT GCCATGTAAG GCATCATAGT CACAGTTTCT 1200
GGGGGTTAGG GTGGTGACGT TTTGCGTGGA CATGATTCTG CCTATTACGG CAGGCTCCTA 1260
ATGTGATATA GATCCCGGTA GTACTGATTA 1290
|
