| Tag | Content |
|---|
EnhancerAtlas ID | HS099-04707 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr11:118562400-118563740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr11:118562896-118562907 | CTGAGTCATCC | - | 6.32 | | JUNB | MA0490.1 | chr11:118562896-118562907 | CTGAGTCATCC | - | 6.14 | | Myog | MA0500.1 | chr11:118563420-118563431 | CTGCAGCTGTC | - | 6.62 | | Tcf12 | MA0521.1 | chr11:118563420-118563431 | CTGCAGCTGTC | - | 6.14 | | ZNF263 | MA0528.1 | chr11:118563166-118563187 | TTTCTCTCCTCCTACTCCTCT | - | 6.37 | | ZNF263 | MA0528.1 | chr11:118562607-118562628 | GGAGGAGGAGAGGGAGGGAGG | + | 9.66 |
|
| | 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 |
| GH11I118691 | chr11 | 118562342 | 118564020 |
|
Enhancer Sequence | CATCTCTGTC CCTGGTGATG GAAACTCAGG CTCAGGAAAG AGCCTTGACC TGCCCTGGGT 60
CACAGAGAGA ATATTAGGGT CAGGGCTTGA GCCCGGGTGC TGTGGTCAGG CCCTTAGGCC 120
GCCTCTCACA CCCAGACTAG GAAGCTGGAG CAGAAAGTTT GCTAGAACAA TCCTGAGAAG 180
AGGCCTGCAC AGTTCAAGGG GCAGCTTGGA GGAGGAGAGG GAGGGAGGAC CGGCTCTGGC 240
CAGTGGGCTC TTGGACCTCA GGCCAGGCTC TGGCAGCTGC ATCTGGTATC AGGCCTGCAG 300
GTCCAGTGCC TATTATGGGG CCTATTATGA CTGCACAAGG GGCCTCAAGT TCATTCAGGC 360
CAAGCCTCTC ATTCTGCAGA GAACCACACA GTGGTTGCCG GGATTTGCCC AAGGCTGGTG 420
GGTTGGTCAT GAGGGCAGGC CCGAACTCAT CTCTATTTTC TTGCATTCCG GCTCTCCTGA 480
TGTTCCAGGC CCATCTCTGA GTCATCCTTG GACAGGAGAG ATCCCAGAGG GTAAACAGGA 540
CATGAGCCTG CAGTGAGGGG AGACAGAGGA GGAGAGAACT CCCTGAAACA AGAGGAGAGG 600
AGGAGCTGGT GGGGAGGACA CAGGTAGGGC AGCGGGCAGA CCACCAAGGG GCAGGCTTGC 660
TGTTTCGCAG CCTGACCCCC AGCCTGTGTG CCTCATTGCC GCCTCCTCCT CCCAGAGCAG 720
GGCCTACGCC TCAACCAGAG CTTGGAGCAA GACAAGGAAG GCTCCATTTC TCTCCTCCTA 780
CTCCTCTACT CAAACCACAG CCATCTGTAC ATCAGAAACT TTTTTTTTTT TTTTTTTAGC 840
CCTCAGCTGC CTGATGCCCA TGGTTGGGGT TTGGGCTGAG TCACCGAGGG CTGCCTGCAC 900
ACACCAGGGA GGGCTCCTGA GCACCCACTC TCAGGCTTTG CACGTTTCCG AAATTCTGCA 960
CACGACAGCA ATTTTTGCAG CAAGGGTGTG GAGGGTGCCT GTGGGCCAGT CACCAGCCTG 1020
CTGCAGCTGT CCGTGGTTGC CTCTGTCTGC CAGGGCTGCA CGACCTCTGG TTTTCACCTC 1080
AACCACTGCG GCTTCCTCTC TCCCCGTGGG AACAGGGCAT GGGGTGAGGG AGCTACCATG 1140
CCCAGACAAC TAGGCATCTC CCTGCCAGGC CAGGAGTTCC ACTGCCACAG CCCAATACCA 1200
GCAAATTCAG ATGCAACCAA GTGACCCCAA CTCAAGTTAC ATTCCCTTTC TCCCCCACAG 1260
GCTCTGCAGT CCCAGGGATT CGCAGTGTTA GTTGATCTCC GGGGACACTA GTTCCCAAGA 1320
GACCCCACTG AAGGCCTGGC 1340
|
