| Tag | Content |
|---|
EnhancerAtlas ID | HS047-13655 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr16:89418420-89419610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr16:89419349-89419361 | AAACAAACATAC | - | 6.37 | | Nr2f6(var.2) | MA0728.1 | chr16:89419533-89419548 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_07656 | chr16:89416756-89419443 | Brain_Hippocampus_Middle_150 | | SE_09347 | chr16:89418184-89420957 | CD14 | | SE_26651 | chr16:89418608-89419289 | Esophagus | | SE_31628 | chr16:89418524-89419380 | Gastric | | SE_41566 | chr16:89418541-89419026 | LNCaP | | SE_47827 | chr16:89418932-89419268 | Pancreas | | SE_65322 | chr16:89418276-89419258 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH16I089352 | chr16 | 89418609 | 89418808 | | GH16I089354 | chr16 | 89419209 | 89419570 |
|
Enhancer Sequence | CAATTCTCAC GCCTCCGCTG AAATGACAGG CACAAGCCAC CAGGCCCAGG TAATTTGTGT 60
AGAGGCGGGG GTTTCAACAT GTTGGTCAGA TTGGTCTCAA ACTCCTGACC TCAAGTGATC 120
CGCCTGCCTC AGCCTCCCAA ATGCTGGGAT CACAGGCGTG AGCCATTGCA CCTGGCCGAT 180
TATCTTCTTT GAAAAGCATG AGACACGTTT CCCTAGGGAT GGAATGCTGG ACACGAGACA 240
AGACTTGTCC TAAGGACTGG ATCTCACAGT GGCCAGGTAT GCATCACGCC ACGCGGTGCA 300
GAGCCCTGGG GGAAGGCAAG TCAAGAAGCC AGGGGTCTAG GCACCGCAAT GTCTCAAGGC 360
AGCCCCCCAA GAAAACCAAG CAGAAGGCCA CAGTGACGCC CTCCTGCTCT CAGGTCAGTG 420
GCAGGAGGGC ACTTGCTGAT GCTGGGCACA GAGGAATGTC AGGGCAGATC TTCAAGGCTC 480
ACACCCTTCA GAGCTTCTGG CAAGCTCAAC ACAGTGAGCG AGCCCTGCCC CCAAGAGTGA 540
GGCCCCTGTC AGGGCCACTT CCTCTCGCCC TGGCCCATCC AGATCTCACA CACACTGTGG 600
TAGATCTTTG AAGGGTAAAA GCTCTGTCCG CTCCACTCAT CAGCACCAAA GTGTTCTGTG 660
CCTGGCCCTT CTCCACCCAA TTCACCAGTT TATTGAAGCC TCAGCTGGGT GAGTCCCGCT 720
TGCCTCTGAA AATGTGTGTG CTCAGCCAGG CAGATTCTTG AGTGCGTTTC CTATGTGCTG 780
CTGCCCTCCT TCAAGATGAC CACATGGGCC CCCAAGCAGG GCCCCTACCT GCTTTGTCAG 840
CATCTTGTCC TTTCCCTCTT TTCTCTCACG GCTTGTTCTA CTTCACGGCA TGTTTAAGCA 900
AAGGGGGTCA CTACAACAAA ATTATTTTAA AACAAACATA CTTCAGAAAA GTTTATGGAA 960
AACATTAAAC CTTGAATATA TTAACTTTAC AGGATCCATT TACTTCACCC TAACACTGAG 1020
TTAAAATTAT AACAAGAGAA AGTAGGGCTG GGCGCGGTGG CTCACGCCTG TAATTAATCC 1080
CAGCACTTTG GGAGGCCAAG GCAGGTGGAT CATGAGGTCA GGAGTTCAAG ACCAGCCTGG 1140
CCAATATGGT GAAACCCCGT CTCTACTAAA AATACAAAAA TTAGCCGTGC 1190
|
