| Tag | Content |
|---|
EnhancerAtlas ID | HS047-12435 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr16:4734160-4735580 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr16:4734473-4734488 | GGGTCACCCTGCCCC | + | 6.83 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 4734554 | 4734610 | | chr16 | 4735495 | 4735579 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I004684 | chr16 | 4734821 | 4734970 |
|
Enhancer Sequence | TGCACCAAAG CCCCTTCCCT CCCTGGGGCC ACATTGGCCA CAGGAGGTGA GAGACGCGAG 60
AGAGGCTGCC TGTGAGAGGA TGGGGTCCTT TTCCCTCTGC CTGCTGCTCA CGCCAGGAGG 120
GCAGATCCGG CCCCACTGGG ATCACCACAT GTTCCCCCAC TCCTGGTCCT ATCGTGGGCC 180
CACAGGCCCC ATGCTGGGTG CCACGTGCGC TCCTGGCAGT GCCTGAGAGC TGCAGACAGA 240
GCAGGAGCAG GTACCACACG CTGTGCTGGG TAGCGGGGGC CCTGGGCCAC AGAGCGCAGG 300
GGCAGTGTCT TCTGGGTCAC CCTGCCCCGG GCCTGACAGA GGCCACCTGA TGCAGCAGCA 360
CATCCCAGGC CAGGCACAGA GGACGGCGGG GGCGCCAGGC GCCAGCGGGG AACAGCAAGG 420
CAGCAAGGCT GGGACAGAGG GTTGCTCTTC TCACCTTTCC CGGAGGCTCG GGCCCCAGAC 480
CCCATCAGCC AAGCACCTTC GTGCTCTGCT CTGCTGGGAT AAGATCCTCA GTTTCGAATC 540
CTAAGCTCTA AAGACCGGGA GGGAATGGGG GCTCTCAGAC TAGTGTCTCA GCACCTGCCA 600
CGAGGCTGTC TGCGGCTCTG GAACTGCGAT AAACAGCCAC GGTGCTTTCA GACATGACCC 660
CAGAGCCACT GCTTAGGGAG TGTGGCTCTT CCCTCGCGGC TGCCAGGCTT CACCCGCTTC 720
CTGGCCCCAG GGCCCACCAT TGCTCAATCC TCCTGAGTCA CCTGGTGACC TGGGCCTGAC 780
ATTGGGTGGT TGTGACGTGC TTTAGTTGGA AAGGGGCTCT TGTGCCCCCG GACTCTGGCT 840
GAGCAGTGGC CTGTGCTCAT GGGCTGGGCG TGACAGGTCG CAGGTGCAGG AGCAGGCACT 900
GCCTCTGGTG CCCTGATGAC CACAGCGGCC TGCCCCGAAC AACTCACAGC AGAAGGTGTG 960
TTTAGGACCA GCTTACCTTA AAGTGACACA GAATTCGAGT AAGGTCTTTC AGAGGATCTC 1020
AAATATTTCA TTCTGATTAA AAACTTGGGG GGTGATCGGG GAAGAGGCCA GAAGGACCTC 1080
AGCTTCTGGG AGCCACGAAC ATGATATCTG ATCCTGCAGG GTGGCCCTGT GGGGGAGCAT 1140
CTCAGAGGCT GCGCCTCCCC TCTGTGGCCA GGCCTGGGAA GGATTGGGAC AGCTACAGAG 1200
GAGGCCCACA CAGAGGAGGC CAGGACTCCG AGTCTCATGC CCCACCCACA GGGGAGGGTC 1260
TCGGGCCTTC TTCAGGCCCA CAGACGGGGG CAGGCAGTCG TCATCTGTGG AGGCGGTAGA 1320
GGAGAGGCCG AGTCTACATC GGGGCAGCCT GAGGTGAACT CCTGGGCCCT GGGCCCCGCT 1380
CTTGGAGTTG GCTGCTGCTG AATGCCAGCA GGTCAGCCTG 1420
|
