| Tag | Content |
|---|
EnhancerAtlas ID | HS044-10918 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr5:176521230-176522300 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr5:176522000-176522018 | GCTTCCTTCCTTCCTTCC | - | 10.05 | | EWSR1-FLI1 | MA0149.1 | chr5:176522004-176522022 | CCTTCCTTCCTTCCTGCT | - | 7.69 | | MAFK | MA0496.2 | chr5:176521408-176521427 | ATATCCTGTGTCAGCATTA | + | 6.2 | | ZNF263 | MA0528.1 | chr5:176522003-176522024 | TCCTTCCTTCCTTCCTGCTCC | - | 7.23 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_30460 | chr5:176520882-176523067 | Fetal_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I177093 | chr5 | 176520362 | 176528755 |
|
Enhancer Sequence | GCTCCTGACC CTGGCAAGTG ACTTCTGAGC CTCAGTTTTC CCTTGTGTCA TATGGGGTAG 60
ATAACAGTCC CTACTCCCAG CCCAAGGATT GTGGAAAGTG CCTGGCTCAT AGTCAGGGCT 120
CAATAAATCT TCACCACTGG GGTGATGATG ATGAGAAGAA TTTGGTGTGA CAGGCTTGAT 180
ATCCTGTGTC AGCATTAGTC TGTGTCAGCT TTGACTTCAC ATCTCCTTGT CAGCCTCACA 240
GGCCCTCTAC CTCCTTCCTT ATGGTTCCCC CCAGACACAC CCTCAGCCTC CCTTGGACCC 300
TCCCTAGGTC TGCCCCCCAC GTCCACTGCT GTAGGAGGAC AGCCCTTCTG CTTGCACCCA 360
GGCCCAGCCC CGGGGTGCTC TTGCTGGGCA CTCCTGCACC CCACCCATCA GGGCCTCTCC 420
TTGCAGTTCC CCAGCCCCCT CTGCAAGAAT GGCCTCCACT GCTCTTCTGC TCCTCCCCTC 480
CTCTCTACAC AGCTGGGGCC ACCTGGTGCT CCCTGGGAGG CAGGGATTGA GAAATGCACA 540
TTGTGTCATT GGCCCAGGGC CACAGGTCAG CCCCAGGGGC TCAGCCAGAG AAGCCAAAGC 600
AGCCTTCTTC CCAAGCTCCC CGGCTGCACC CGGCCTGCCG CCAGCTCCCT GAATTCCCAG 660
GCCAGTTGGA AGCCAGGCCC TGGTCAAACA GACCCCAGGG CGCCAGCCTG CTTTCCGCAC 720
CCAGAAGCTC TGACCCCATG CGGGGACTAC CGCTGACCCC TCCAGCGGCA GCTTCCTTCC 780
TTCCTTCCTG CTCCGAGCTC TTCCCCTCTC TCCTGTGTCC TGGGCCTGCC CGCTGGAAGG 840
CCTGCCTCTT AGATCCTTGA TACAGTTGCA TCCTTGCAAC TGCTGTGACA GGCAGGGTGT 900
GACCCACTGC TCTGTTTCCC ACAAGACGAA CCTGAGGTTC AGAGACGCTA GGAGACTTTT 960
TCAAGGCCAC ACAGCCTAGC AAGGATTCAG CCCTAGACCT ACGTAGCCCT GGTCCAGTGC 1020
TGCTTGTCCT GCACCTGCCT CTGCATGCTC CCTCGTGCAG TTGGAGGGCA 1070
|
