| Tag | Content |
|---|
EnhancerAtlas ID | HS047-05289 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr11:1457410-1459290 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr11:1458831-1458841 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr11:1458831-1458841 | GGCACGTGCC | - | 6.02 | | NR2C2 | MA0504.1 | chr11:1459201-1459216 | TGCCCTCTGCCCTCT | - | 6.62 | | ZNF263 | MA0528.1 | chr11:1458011-1458032 | GCCCCCTCCTCTCCCTTCCTC | - | 6.07 | | ZNF263 | MA0528.1 | chr11:1458012-1458033 | CCCCCTCCTCTCCCTTCCTCT | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 1458380 | 1459278 | | chr11 | 1457510 | 1458121 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I001436 | chr11 | 1457517 | 1460257 |
|
Enhancer Sequence | GGGGAATAGC ACAGGGGTGG GAGCCAAGGT TGTGGGGACC TGCGGTGCTG GATGCGGGTG 60
GGGGGGCGGG CCCTGCAGGC TCCTGGGCCG CCACACCCCT GCTGGTCCCC TGGTAGGGTG 120
CCTTTGCTCT TGCTCCTCCC TCCAGCCCTG CCCACCTTTC TCCTGCCTCC AAGCAGAGTG 180
GGCACCCCTG AGGGGACAGG CTGCAGCTGG GCAGTTCAGT TGCTGCAGGA CCTGCTGTGC 240
TAGCAGGCGG GGCTTCAGTG TTCCCAGCTA GAATGGAGAG GAGTTCCCTG CCTCAGAGCA 300
CCCCTCTCCT ACCAGGGCAC AGCTTGGCAG AGGGGAGCTG CACCTTCCTC TTCCACTGGG 360
GCCTGGCCTC CGTCGGCTCC ATCCGGTGGT GTCTGGTCAC CATGGAGACC AGGCAGGCCC 420
CCTGGGTGGA GGGTTTCTGG GCTGTGACCC ACCTCTCAGT GGGGAGGGGG CGGCCCCGGC 480
TGCTGGGAAG CCTGACCCTG GGTGTAGAGG AAGAGGCTGG GGCTCCCAGC TGCTCCGGGT 540
CCCACCCACA GTGGGACCTG GGCTGGCAGC GTGCGACCCT CCCAGCACTG GGGCCAGTCG 600
AGCCCCCTCC TCTCCCTTCC TCTCCATTCG CTCCTTGGCA TGCAGGGCTG CGGGTGGGGC 660
AGGACCCGGG GACGAGGCCA GTGGGAGTGG CCAAGAGAGG GGAGGCTTGT GGAAGGTGCT 720
AAGGGTTGGG GACTGTGACA TGTTGGGCAC CCCCCAGCTG CTGGGGTGTG GAGGAATTAA 780
CCAGACTAAA CTGGGGAGGC CTGGGGACCC TATGGGGAGG TGGGGGTGGG GTTAAGGGCT 840
GCTGAGGGCT GCCTGGATGG GGCTGGCAGG GTCCCACCCT GCCTTGGAGG AGAAACAGAG 900
GCCCTGGGAG TGATGGGGCC AGGACAGCGC CTGGCAGAGA GATCCAGTGC GGGGCGTAGC 960
TGGGGAGAGT CCCATGCTGA ATTTGGGAGG TGCCTGTGAG CCCCGACTAA AGGAGGGCCT 1020
GGGGATGCGG GAAAGGGGAG GTGTCCCTGT CACCTGCAGG CGCTGTGCAC AGATGTCCGC 1080
CTGGGAGGGA AGGACTTGGG GACAGGCTGG CCAACTCGCC AGGGCTGGGA CCCCATCACA 1140
AGACTGGCCC TAGCTCCAAA GCCTGGTCCA CGCTGGCTCC TGAGGGCTGG GACCCCAGGC 1200
CGTGGCCTCA CTGGCCCCAC CACTGACACG GCCACTTCTT TGTGCTGGGC GGAGCACCAG 1260
CTGCCCGTGG CCAGGCTTGC ATGTCTGAGG GAGGGGGCCC TGCCCTTACC TCGGAGCAGG 1320
ACTGGGTGTC CTGAGTCAGG TGCCCTCTGG GGTCACTTCT GCCCCTCCCT GGGGCCCTCC 1380
CCACTTGGGG GACAGTACCA GCTGGGAGCC TGTGGATGGG GGGCACGTGC CCTGCCCACG 1440
GCCTGCACAC CTACTGTATG TCCCACACAC AACAGGATGC CTGCCCCCAC CTCATGGGGC 1500
CCACAGAGGC CTGTCCCGGC CCCTCCTCCT GTGAGGCCTC CACCGTAAGG AAGGGCGGAG 1560
CCCAGGCACA GCCTGCCTGG AAGGGCCCTG CATCCGACTG GCTGGGAGCC TGGGAGGCCT 1620
TATCTCCAAC AGCTCCAGGC CCCATTCCTG AGGCTGGGCT CACAGAGAGG CCCAGGCTGC 1680
CTGCCTTCCT GGGCAGTGTG GGGAGGGGCC CTCCTGCTCC AGGGGCCCCC AGTCCTCAGC 1740
CCTACAGGCT GGTGTCAGCC CGGCGGCCTG GGCTCCCTCC ACTGAGGCCC CTGCCCTCTG 1800
CCCTCTCCAC CAGCCAGGGC CCCAGCTGAG CAGCCCACGT CCCTGCATCC CCCACAGCTG 1860
GCACCAAAGG CCCCTGCGTC 1880
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