| Tag | Content |
|---|
EnhancerAtlas ID | HS165-02820 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr11:119129770-119131410 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr11:119130190-119130202 | AAGTAAACAGTA | + | 6.18 | | Foxq1 | MA0040.1 | chr11:119130086-119130097 | TATTGTTTATT | + | 6.62 | | HES2 | MA0616.2 | chr11:119131095-119131105 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr11:119131095-119131105 | GGCACGTGCC | - | 6.02 | | SPI1 | MA0080.4 | chr11:119130842-119130856 | AACTTCCTCTTTCA | - | 6.03 |
|
| | 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 |
| GH11I119257 | chr11 | 119128485 | 119131878 |
|
Enhancer Sequence | GTTCTTGATT TGATTCTCAG GTTGGTCATT GTTGATGTGT AGCAGTGCTG CTGACTTGTA 60
TACGTTGATT TCGTAACCTG AGACTTAACT GAATTCACTT ATCAAATCTA GTTGTCTTTT 120
GGAGGAGTCT TCGGGGTTTT TTTTAGGTAT GTGATGATAT TATTGGCAAA ACAGAGATAG 180
CTTGACTTCC TCTTCCAATT TGGGTGCCCT TTCTTTCTCT TGCCTAATTG CTGTGCCTGG 240
GTAAGTTGGT AGTCTTATGT GGCTTTAAGT TTCTTGTATT CTGCTTAAGA TACATTTGTG 300
ATTTTTTTCT CCCATGTATT GTTTATTCTT ATGTTTTTCC CCATTTATTG AATATACCTC 360
TGCTTATTTG ACAATACTGA AATTTTGTGT ATTTACTTAT ATATTAGAGC CACTATGCAA 420
AAGTAAACAG TATTTACTAA ATTTATGTGA ATTTAGTAAA CACAGTAAAT ACTATTTACT 480
TTTGCATAGG GGCTCTAATG TTCAAGTTCC ATATAAATAT AAATATTTCT GGTGGGAGAA 540
TTATGATAGA TACCACTGGA TGGGTGTTAG AACTCCCCAA AATTGATAAT TTTTGAGGTG 600
CTAAGATACT AAATGTGTTT TCATCAAGCT TATATAAAAG ATACTGAGAA ACAAAGATTG 660
GGTCTCAAAG AGATGGCATT AGTTTCTGCC TTAGGTGAGA ACAACTAAAA AATTGGCATC 720
GTTTTCTTAT AAATATAGCT CATTTGGGAC ATGGATTGTA TTTCCAAATA CCTGTCACAT 780
GGATTTATTC TGCCTTTTGT AGGAGAAACC TGTAATATTG TTCTTTTGTA TCCTTCCGAT 840
TCTATCTCAC TTACCTCCAC ACTCTTCTCA AAGGGGGAAA CTCAGTTTCA GCTTGATTAT 900
CTTGTACAAG GGCACTAGCA AATGGACCGT TCCATTCCCA GAGATGCCAA CAATCTTACA 960
CAGATTATTC ACAAATCTGT TTTCCCAAGC TACCTGCTAG TTATACTCAT GTTAGTATCT 1020
TCCCACACTC AAAATACCTG AACACTGAAT GTATCCTCTT CATCAGCAAA CCAACTTCCT 1080
CTTTCATGTC CCGTTACTGA GTTAGTACTG TATAATGTAG TGAGTAGTGA TGATGAGCAT 1140
GGATTGATTA TTGGCTTAGC TTCTTTTTTT TTTTTTCTTT TTCTTTTCTT TTCTTTTTTT 1200
TTGAGATGGA GTGTCACTCT GTCGTTCAGA CTGGATTTAG TGGTGCAATC TCGGCTCACT 1260
GCAACCTCCA CCTCCTGGGT TCAATCAATT CTCCTGCCTC AGCCTCCCGA GTAGCTGCGA 1320
CTACAGGCAC GTGCCATCAC GCCTGGCTAA TTTTTGTATT TTTAGTAGAG ATGGGGTTTT 1380
ACCATGTTGA CCAGGCTGGT CGGCTCAGCT TCTTTATGCC TAAATTGTCT CATCTGTAAA 1440
ATGGGGATAA TATTGGAATC TGATGGGATT GTAAGTGAGA ATTAGTTAAA TAACAAAATA 1500
CGTAAAGTGC CTGGTACTTA GTAAGCCCTT AAAAAACATT AGCTTTTACA TTATTACCAA 1560
TATATTATTG GTAATACCCT AGGTTTATCT CCTCTCTTAC TCAGTCATAC TCTTGATTTT 1620
ACTGCTGCAG TCTGTCTCAA 1640
|
