| Tag | Content |
|---|
EnhancerAtlas ID | HS092-01136 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:34733580-34734730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr1:34734015-34734026 | TCTGACTCATT | + | 6.32 | | MEF2B | MA0660.1 | chr1:34734668-34734680 | GCTAATAATAGC | + | 6.07 |
|
| | 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 |
| GH01I034268 | chr1 | 34734021 | 34734170 |
|
Enhancer Sequence | ATCACCTGGG GGATACACGA AAAAAAACAA GTGGACCAAG AGTTGGTCAA GCCAAAGTTT 60
GGTCCAACTC TGACATTTAC TAACTATGAA ATTGTCCACA AATCCCACAG TATTGTTAGT 120
GGTTATGAGC AATGATCTAT GGCATCAGGC AGACTTGGGC TCAAATCCTA GCACTGCCAT 180
TTTTGGACCT AAGGCAAGTG ACTGTATCTG TTCCCTTATG TGTAAATGGG GAAAATCATT 240
CTGATCCAGT AGGTTACTGA GAGAACCAAA TGACTACAAG CCAGGAAAAT GCTCAGCACA 300
ATATCTGGCA CAGAGTACAA GAATTCAATT AATGGTAATT AGGATAGCTG TTATTATGAT 360
TGCTCTCCTC TCTGACTCAG TTTCCTTGGG GGTTGGACTG CTTGACTTCC GAGGGCCCTC 420
CCAGCTCCAG CATCCTCTGA CTCATTGGCA TCCTTCTTGT TTCAGGTTTT TTATTAGATT 480
TCCACGACTG ACTCATCTTT CTCCATCTCT CTCCTTATCA TCACCCTCCA TGAAAAATGC 540
ACCCTCCTTC CCTTTGTATT CAGGCCATTG CCCCATCATC TCTGCCCTGG GGGGTCGAAT 600
AATCCAAGCC AGCCAGACCC CTGCATGCCA CTGCCACTTG GAGTCAGATT CCATTGGATT 660
TATGAGGCAC CACAGGAGTA GGTAGTCGAT ATGAATAACC ATTACGTTGG GGAGGGCTTT 720
TTCTTCTCCC TCTGACTGAT GACAGCTAAA TTACTGCTAA ATATAGGCCC TGAATTTGCA 780
TGAATCTGCA GCTTGCCACA GCCAGGCTGG GGGTTTTATT GACAGCTGAG GCACTGGAGG 840
CAGGCAGGCA CCTGCTCCAG TACACCTCTT CCAGAGGAAG CATGGAGTCA GGGAGAGTGC 900
ACCCCTCCCT CACCCCTCTC CAAGAGATGC TCTCTTCTCT CCAAGCCTCC AGCCTTGTTG 960
GTTCCAAGAA AAGAGCTTAG GCATGGGTTT GAATCCCAGA TCTTCCATCT AGCTGTGTGA 1020
TCCTAAGCAA ATTACTTAAC CACTCCCTAT CCGTTCCCCT GCCTCCGTTT CCCCATTGCT 1080
ACAACGGGGC TAATAATAGC TCACTGTTAT CTCACATAAA GTTCTGACAT AGGCTCCTCC 1140
AAGTTTCTAT 1150
|
