| Tag | Content |
|---|
EnhancerAtlas ID | HS092-25976 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr20:3915720-3916790 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr20:3916192-3916204 | GCTATTTATAGT | - | 6.11 | | MEF2B | MA0660.1 | chr20:3916192-3916204 | GCTATTTATAGT | - | 6.74 | | NFIL3 | MA0025.1 | chr20:3916721-3916732 | TTATGTAACAT | + | 6.32 |
|
| | 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 |
| GH20I003931 | chr20 | 3912621 | 3917007 |
|
Enhancer Sequence | CTGAAAGACA AATGCACAAA TGAAGCCAAG TGTCTGTTAA GTACCCTCCC AGGTACAAAG 60
TAGAGTGCAG GCTCCTAAAG GCTCAACCGT TTGAAGGGAC TCATGAGACT CTTATCTTAA 120
AAAAAAAAGA AATGAATGAA TAAATGACTG AAAAGAAACA GGCCAAAATA GATGAATGTC 180
TCCTGCTCTT CCTGTCCCAT ATCTTCAAGG AGGTGGGCAG ATGGGAGAAG ACAGAAAGCA 240
AGAGGCAGCT GCCTTTACTT CAGTGCATCA GAAGTGTGGG ACCGAGGGAG GGTTACTCTC 300
ACATCTGCCA GCTTAGCCTG CTGTCCCTTT CCTGGTGTGC CGAAAGAGCT GAGGCTCTCT 360
GGGTTCTCCA CCTTGTCAGC AGCACAGCCT GGCTCCCAAG CACTCACTGA AAGGGACCGC 420
TCAAGCCCTG GCAATCTTTT CTCCTGTTTT TATGCACAGC TTGCAGTAAC ATGCTATTTA 480
TAGTTCCTGG GGCCTCCCAC TTTGGCACTG TCCTTCTGTC AGTGTCTCTG TCATATAAAA 540
AGTTACTGAA GACTCAGTTA ACTCATGAAC ATGTGCAGAT GGGACCAGGA CTGCTCTCAG 600
CCAATGACTA GTCTCCATGG CTTGGAGAGA GGCCTTTGCC ATCGTACCCA GGGGCTGGGT 660
TCCAACACTT TCCTGGGCAT TCACCAGGGC CCGTGGATAC CATGTGTCAC CACACTGACC 720
CATTTTACCG ATGAGGAAAC AGAAGCTCAG GAAAATAATG TTGCTTGAGG CCATTTAATT 780
GGAGAGTGGC CAGGCCTGGC TGGGACCCAG GTCTGTTGCA CTGATGTGCT GTTGTGCCAT 840
TGCTTTCTCC TGCCCAGTGG TTGAACTCCT TTCTCCCTAC TTGCTTCCCT GTCCATTCCC 900
AAGGATCCTG GTTCAGGCCA TCACCATTTC TAGCCTGGAC TGTTGATGGC TTTGCTGTTA 960
CTAGTTTCTT AACCTATAAC ACGTAACCCA GTCTTCTTAG ATTATGTAAC ATGATCCAGG 1020
CAGGACATGT GGCTCTTGGT GCCCAGTGAA CCGTGCCATG TTGGTTTTTA 1070
|
