| Tag | Content |
|---|
EnhancerAtlas ID | HS092-21670 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr18:24049860-24051300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr18:24049888-24049900 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr18:24049892-24049904 | AAACAAACAAAC | - | 6.32 | | INSM1 | MA0155.1 | chr18:24050843-24050855 | TGTCAGGGGGCA | + | 6.92 | | RAX | MA0718.1 | chr18:24050607-24050617 | GTTAATTGGC | - | 6.02 |
|
| | 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 |
| GH18I026469 | chr18 | 24049541 | 24050979 |
|
Enhancer Sequence | CAAGATCGTG CCACTGCCCA TCTCAAAAAA ACAAACAAAC AAACAACAAA CAAACAAAAA 60
GGCCCTGCCT GCAAGAACCT TATAATGCAG CAAGGAAGTG AAGATATATA CACAAAATAT 120
CCAGAGTCCA AACATCAGAA AGTAGATCAG CAGGTTTCAG ATGAACTGGT GGGAACAAGA 180
GCCTAGTTTG CATGTTAGCC TCACTCCATT CATCTATTTA CCCATCCATG CGTTCATTCA 240
CTCACGCCAC AAATATTTAC ATGCTTAATA TGTGGCAGGT GCTGAGCATG TGGGACAGAT 300
GCTGCTGGCT AGCTTCCCCA ACAGCTATTT CAACCTCTTT CCCTTGCCTA TTTCTCTTAC 360
TACAGAGGCT AAAAATAAGC GAAGAAAAAA AAATCCCTTT CTCAGCCACC AAGGAGAGGC 420
TCCGTTCTGG CCAATGAGCC ACAAAGGGAA AGCCTTCTGT GGGATCGTCT GACAAGGACA 480
GAGTCTTGTG AGTTGAAAAG CTGTCTGTCC CTTTATCCTG CCTTGACTGA GGATGTGACG 540
CCTGGAATGG TGATGCCTGG TGCCGTGATG CAGTCACCAT ATAATCTTGA GGTGACAGGC 600
ATGAGGCCAG AACGTCAACA CTGAGGATGG CAAAACAGAA AGACAGAAAG CTTCCTGGTC 660
CTCGATAACA TTGCTGGGCA GATACCTCTG CCACAGGCCT CTGACTTCTC ACGTGAGAAA 720
AACAAATCTC CTATAGTGTA AGCCGCTGTT AATTGGCTGT TCCCACTCTC GTAGCTGGAA 780
GCGTCCCTAC CTCACAGCTG CGCAGATGGT GCTGCACAGT GAGTGATAGA TGCACTGCGT 840
GTGACCACGG AGAGTCAGGG GTACAGGTGA GCCTAAGCTA CACCAGGCCC AGGTAGGTTT 900
GCTGGGGGAT GTGGTGAAAA AGATGACTCC TGAATTCCAG TAAAGGCCAG GGGAATGGCT 960
GCATAGGCAC ACAGAGGGGC AGTTGTCAGG GGGCAAGAGG AGGGTGTGTC TGAGGGACCA 1020
AGAGAAGTCC TGTAGGGACA TGTGGAGGGC AAGAGTGGGT GAGGTGGGCA GGGGCCAGAG 1080
CTTTCTGGGC CTTGTGGGCT CTGACAGGGA TGTGGTGCTT TGCTCTGTGA GACAGAAGAA 1140
TGAATGGAAG AAGCCATGGC TGCTCATTTC TGCTTGACCC TCTGACTCTG GGAGGACGTG 1200
CAGGTCTCCA GGAAAATGCC TTGAAGACAC AACAAAGCCG AGTATACAGC CCCCCCAGGT 1260
CTCCTGCCTG AGTCACTACA TTCCTTAAGA GATACATGAC CCTAGTCTTT GCCTTTTCTT 1320
CCGTATGAGA TAAAGTCTGA CAGGTTGGTG ATGACGCTTC TGTAATCTAT AACACGCTGT 1380
ACTCTTACAC CCAAAGCTCG ATGTATTCTG CTTGTAGCGT CTGAGCAAGT GTGATGTGAT 1440
|
