| Tag | Content |
|---|
EnhancerAtlas ID | HS047-16783 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:10589280-10590700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF8 | MA0652.1 | chr19:10590616-10590630 | AAGAAACCGAAACT | + | 6.54 | | IRF9 | MA0653.1 | chr19:10590615-10590630 | GAAGAAACCGAAACT | + | 6.22 | | Stat6 | MA0520.1 | chr19:10590046-10590061 | CTTTTCCTGAGAATA | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 10589374 | 10589607 | | chr19 | 10589760 | 10590264 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I010478 | chr19 | 10589121 | 10590829 |
|
Enhancer Sequence | CTGCACCCAG TCTATATTAC TTTTATAATC AGAAAGTTAT TTTATAATCA GGGGAAATGA 60
AAAACATCTG GTATTTATTA TCTGGGAGGC ACAAAAACGT GGTGGATAAG CACACAGATT 120
CTAGATTCAG CTTTCCTGGA TTTTGGCTCC AACTCAGCCA AGTTAATGGC TGGGTTAGTC 180
TGGGCAGGTT ACTGGCCAAG GGGGGAAACC ATGCCTCAGT TTCCCCCATT GTAAAATCCA 240
AATAACAATA GCTTAGGTTT ACCGAGAGGT TGTTATGTGA CAAGCACTGT TTGTTTTACG 300
TAAATCATCG AGGTAAATGC TCACAACAGC CCTATTAAGT AAGTACTATT ATTATAAAAA 360
GGGTCACAGG CATAGGCAGG GAAGGAGGTA GGGCTGGGAG TCGGAGCCCG TGAGCGCCCC 420
CTAGAGTAGG GCTAAGGGGC GGGGGGGCGG GCTACAGCAG AATAGGGACC CAGCGCACTC 480
GCAGAACGAG GGGGGAGGCG AGGCGAGAAC GAGCGGGAGT TTTTTTCCCG ACTACGATTG 540
GCTGGTGTAA TTGTCATCAC TTGAAAAGGC AGCCAATGAG AGGCGCGGTC GCCTCGCTGG 600
TGGAAGCCGA GAGCTGAGCG AAGTGAGGCG TGCGGAGCCA AAGGCGCTAG AGCGATAGCG 660
GGAGCCCCGG ACCCCGAAGC GGTTGAGGGG ATCCAGGCCT CACAACGTCT TGAGAGTGGC 720
CCCAGCGTCG TTCCTAGTCT CTTCGGCAGA CCCCAGCGTC GTCCTTCTTT TCCTGAGAAT 780
ATCCTGACAC CAGTCGCCCG TTCCAGAAGG GGACACTTGG CGTCATCCCT TTTTTTCTGA 840
GTGACCCCAG AGTCGTCCTC ACTTCCTGAG GGGGATCCTG GCGTCATCCG CCCTTCTTGA 900
GGGGACCCTG CTGTCACTAC CCTGTCCTGA TGGCCAGCAC CGCATTGTCC TTTCTTCCCG 960
CGGGAAACCC GGACATCATC CCCTCTTTCT GGCGGGGACC CCCATGCCAT TATCCCCTCC 1020
TGAGGAGACC CCAGAGCCAG AGCCGTCCCC CCTTCCTCAA GGCTCCCCAG CGTTGTTTCT 1080
TCTTCCCGAG AAGGGGCCTG GTGCTGTTCC CCGTTTCCAG AGTGTTTCCT ATCGTTGTCC 1140
TCCCCACACT CAGAAGGCAT CTGTCATCCC CCCTTTTTCT GAGATCAGTC CCTTCCTCCT 1200
TTCCAGTTTA AGGCCGACCC CTGCAAACGC TTCTGTGGCA CCCATAGATA GAAGGCCCAA 1260
AGACCCCCCT GTGCTCCCTT GCCCCCAATT GAGCAGACGG GAAGGCAAAA GACTCAGCTC 1320
ACCCCATGAA GATGGGAAGA AACCGAAACT AGCTGATGAA GGAACTCACT ATGCCACATG 1380
AGAAATCATT TAGGGCCGGG CGCAGTGGCT CACGCCCATA 1420
|
