| Tag | Content |
|---|
EnhancerAtlas ID | HS092-11678 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:32756340-32757820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr12:32757031-32757042 | GATGAGTCACT | - | 6.02 | | IRF1 | MA0050.2 | chr12:32757227-32757248 | TGTCCTTTTCACTTTCTCTTT | + | 6.51 | | JUN(var.2) | MA0489.1 | chr12:32757032-32757046 | ATGAGTCACTTTTC | - | 6.2 | | JUND | MA0491.1 | chr12:32757031-32757042 | GATGAGTCACT | - | 6.32 | | Nr5a2 | MA0505.1 | chr12:32757333-32757348 | GCTGGCCTTGAACTC | - | 8.25 | | RUNX1 | MA0002.2 | chr12:32756974-32756985 | CTCTGTGGTTT | + | 6.14 |
|
| | 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 |
| GH12I032603 | chr12 | 32756656 | 32758861 |
|
Enhancer Sequence | CGGAGTCTCG CTGCTCTGTT GCCCAGGCTG GAGTGCAGTG GCGTGATCTA GGCTCACTGC 60
AAGCTCCGCC TCCTGGGTTT ACTTAGCCAT TCTCCTGCCT CAGCCTGTTG CTGGGACTAC 120
AGGCGCCTGC CACCACGCCT GGCTAATTTT TTGTATTTTT AGTAGAGATG GGGTTTCACC 180
GTGTTAGCCG GGATGATCTC TATCTCCTGA CCTTATGATC TGCCTGCCTC GGCCTCCCAA 240
AATGCTGGGA TTATAGGCGT GAGCCACCGC GCCTGGCCTT TGTTTCTATA ATGTTTATTA 300
TTTTTTTTTT TTAGAGACAG GGTCTTGCTC TTGTCACCCA GGCTAGAGTG CAGTGGCCCA 360
GTCACAGCTC ACTGCAGCCT TGAACACTTG GGCTTGAGCA ATCCTCCCAC CGCAGCCTCT 420
CAGGTAGCTG GGACTACAGG CATGCGCCAC CACCCTGGCT AAATCTTAGA ATTTTTTTAT 480
AGAAACAAGG TCTGGCTATG TTGCCCAGGC TGGTCTTGAA CACCTAGACT CAGCCTCCCA 540
GAGTGCTGGG ATTACAGGCA TGAGCCACTG CACTCAACCA GTATATGGAG ATCCCCCCCA 600
GCACTTTGAA TATGTCATTC TCCTGCTTTC CGTCCTCTGT GGTTTGAGAT GAGAAGCCAG 660
CCATTGATTG TATTGATACT CCCATGCGTG TGATGAGTCA CTTTTCTCTT GCTGCTTTCA 720
AGATGTTCTC TGTTTTTTGG CTTTCAGCAG TTTAAATATG ATGTGTCTGG GTGTGGACCT 780
TTTTGTATTT GTCCTGGTTA GGGTTGGTTG AGCTTTTTGC ATTTGTAGAT TGATTTTTTT 840
TTAATCATTT TCAGAAGTTT TCAGCCATTA TTTCTTCAAA TATTTTCTGT CCTTTTCACT 900
TTCTCTTTTT TAAAATCTTT TTACTCCCAT TACACAAATT TTGGTGGGTT CCTTTTGTTT 960
GTTTTGGAAA TGGTGTCTTG CTGTGTTGCC TAGGCTGGCC TTGAACTCCT GGGTTCAAAT 1020
GATACTCCCA ATCTTTGTTC TATTATTCAG ATTGTATAAT TTCTACTAGT CTTTCTTCAA 1080
GTTCCCTGAT TCTTCTGTCA TCTCAAATCT GCTGTTGAAC CTATAGTGAA TTTTTCTTTT 1140
CAATTACTGT ATTTTTCACA TCTACAACCA CAACTTCTGG CTAGTAGAGT TATTGGCTCT 1200
CACCTCTCAC TCACCTCAGG GATCTTCACT TCTACTGATG TTGTTGGGTG TGTATGTTGC 1260
CCACCACTCC AAATGAATGA GCCCTTTTCA GCCTCAGCAG AGGAGCTGCC AGTCCTCACA 1320
GTCCGTGCCA CCCTGATGGC CCCTTCATAG TGACTGAGCT GGGAGAGGAA CAGGAGCAGC 1380
CACAGGCTAG AATGCCACAG ATTCTCACCG TTCTTACCCA AAGTTCAACA ATTTTTAAAG 1440
TGTAAACAGA TTTCAGGTTG TTGCATGCCT TTTAATCAAT 1480
|
