| Tag | Content |
|---|
EnhancerAtlas ID | HS047-17212 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:19620820-19621980 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP1 | MA0079.4 | chr19:19621937-19621952 | CAAGCTACGCCCACT | + | 6.12 | | SP4 | MA0685.1 | chr19:19621937-19621954 | CAAGCTACGCCCACTCT | + | 6.5 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 19620850 | 19621028 | | chr19 | 19621675 | 19621818 |
|
Enhancer Sequence | CTGGGATTAC AGGTGTGAGT CACCACGCTT GGCCGTTTCT TGTCTTTGAA GCATCCTTGC 60
CTCCGGCCTG GGAGCTCATA CCTTCCCCAC AACTCCCAAG TGCCTGGTCT TATGGGCACA 120
GAGCTGGTAG AGAACATGGT AGAAACTGAA CCTCAGCCTG TCCAGTAGCG CGATCTTGGC 180
TCATTGCAAC CTCCGCCTCC CAGGTTCTAG CGATTCTTCT GCCTCAGCCT CCCGAGTAGC 240
TGGGATTACA GGTGCCGCCA CCAGCACGCC CAGTTAATTT TCAGTAGAGA TGGGGTTTCA 300
CGTGTTGGCC AGGCTGGTCT CAAACTCCTG ATGTGATCCA CCGGTCTCAG CCTCCCAAAG 360
TACTGGGATG ACAGGCGTGA GCCACTGCAC CCAGCCACTT TTTTTTTTTT TTTTTTTTGA 420
GATAGGCTCT CTGTTGCCCA AGCTAGAGTG CCTAGAGGCT CTCTGTTGCC CAGGCTCAGG 480
CGATCCTCCC ACCTCAGCCT ACCGTGTAGC TGGGGCCAGA GGCTTGCTAC AGGCATTTCT 540
TGCTTGGCCT GAGAAACATT CCTATGGGGT GCTGTCTCCT GGGCTTGGCT CTTGGTTCCT 600
CGTGAGGCTC TGCTTCCCTG GATTGGGCAC AGGCTTGTCA GTGCAGTTGG GGCAGATTCA 660
AGGGGCGGGT CCTGGGTCAT GGTCTCAAAT AGCCTCTCCA GCTGAGAAAA TGGGACACTC 720
CCCTCGTCCC TGACATCTTG TCCCCGACAT CTCATCCTCT CTGAATTGAG CCTTGGGTCT 780
GTGGCCACAT GGCAGGCAGA GACCCTGACC CCATCTGCTC CCACAGATTC GTCGGTGGAC 840
AGATGGCATG CACTATGCCC TGGGCCCCGG AGATGTGGCA GGAGCTATCC AGACAGAAAC 900
ATATAGCACC TTGAGAGGAG GGCATGGGGT GACATTTTAG GCAAGGCTTG AAGAGGGGAA 960
AAGTGCCAGG AGTGTGCAAA GGCTTGGAGA TAGGAGCCAG CATGGCAGGT CAAGAACAAA 1020
AAGGGCAATG TGGTGGGACT GGGTGGGAAG ACGGGGCAAG GGCGTGGGTT TTAGCTAAGT 1080
GCAGTGGGAG TCTAGGGAAG GTCCTGGGCC CAGTACTCAA GCTACGCCCA CTCTGAAGCC 1140
ATGCCCACTA CCCCAAGGAT 1160
|
