Tag | Content |
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EnhancerAtlas ID | HS047-04790 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr10:104494370-104495280 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr10:104494945-104494966 | CCCTCTCCATGTTGCTCCTCC | - | 6.03 | ZNF263 | MA0528.1 | chr10:104494981-104495002 | CCCTCTCCATGTTGCTCCTCC | - | 6.03 | ZNF263 | MA0528.1 | chr10:104494901-104494922 | TGCTCCTCTCCCTCCTCATCC | - | 6.97 | ZNF263 | MA0528.1 | chr10:104494908-104494929 | CTCCCTCCTCATCCCTCCTCC | - | 6.98 | ZNF263 | MA0528.1 | chr10:104494904-104494925 | TCCTCTCCCTCCTCATCCCTC | - | 7.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I102734 | chr10 | 104494588 | 104495375 |
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Enhancer Sequence | CATGGGCTGG GTGCTTTACA TACATATCTC ATTGAATCCT CACAGTAACC CTGCAAAGTA 60 GGCACTGCAA AGTGGTCTGC AGTAGCCCTA AAAAGTAGGT TGTCCTCCCT CTGTGTCTCT 120 GAGGTAACTT GTCCAAGATG GCACAGCTAG TAAGTGGTAA AACTGGGATA CCAACCCAGG 180 TCTGTCAGAG TCCCGCGTCC TGTAAGACCT TGCCTCCCAA ACCCTGGTCC ATGCCAGCAT 240 CGTTGGCATC CTCTGATAAC TTGTTAGAAG TAAAGACTCT GAAGTCCTTC CCCAGACCCC 300 CTCAGTTGGC ACCTGGCATT TTAATAAGCT CCTGAAGTTA TATGCACAGT GAAGCTGGAG 360 AAACTGCCTT TCACTGTGCT CTGACAGCCC AGGTGTTCAA CCAATAAAGA AGCAGGTCTC 420 AGAATCCACA GACTCACTCC TCCCCCTCCA TAGTGCCCCT CCCCCACTCC AAAGTGCCCC 480 TCCCCATCCT GGTCACTCCT CCCGATACAA GTCAATCCTC CCCCTCCAAG TTGCTCCTCT 540 CCCTCCTCAT CCCTCCTCCC CTCTGTGTCC TTCCTCCCTC TCCATGTTGC TCCTCCCCTC 600 CATGTCCTTC TCCCTCTCCA TGTTGCTCCT CCCTGTCCAA GTAGTTCTTC CTACTCCAAG 660 TAGTTCCTTC CCTCCAAGTC ACTCCTCCCC CTTCAAGTCG CTCCTCCCCA TCCAAGTTGC 720 TCCTCAACCT CCAAGTCATT CTTCCCTCTC CAAGTCGCTC CCCACCCTCC ATGCTGTTCC 780 TCCAAGTTGC TCCTGTCCCT CCATGTCGCT CCTCCCCCTC CATGTCCCTC CTCTCCCTCC 840 ATGATGCTCC TCCCCTCCAT GTCGCTCTTC CCCCTCCATG TTGCTCCTCC CCCTCCAAGT 900 TTCTCCTCTC 910
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