| Tag | Content |
|---|
EnhancerAtlas ID | HS146-02725 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr11:47968230-47969240 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nfe2l2 | MA0150.2 | chr11:47968672-47968687 | TGCTGAGTCACTACT | - | 6.04 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_34924 | chr11:47967098-47970362 | HeLa |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 47968538 | 47968912 | | chr11 | 47968255 | 47969183 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I047945 | chr11 | 47967137 | 47970036 |
|
Enhancer Sequence | TGGGTGACAA AGTGAGATTG TGCCTTAAAA AAAGAGAGAG AGAGAAGGGA GGGAAAAGAA 60
AACAACAAAT GCAAAGGCCT TAAAGTGAGA CCAGGTGTGT TAGAGGAACC CCATGGACAT 120
GCCACATACT ATTCTAAGTT TTCTCACTCC TAGGAGGGAG ATACTATTAT TGTTCCCATT 180
TACAGATGGG CAAATTGTGA CCAGAGATGA TAAGAAACTT GCTCCAGGTT GCATAAGAGG 240
CAGAGGTAGC TGCTGAGGAA GGCAGAGTTT GTGCTCTTAA ACACTAAGCT ATTAAATCAT 300
TAAATAAATG ATTTCATTAG CCTGGGTAGA CCCAGGTACC AAAGATTTAT ACCTCCAGCT 360
CCCAGTGAAC TTTCCAAGCC CTTAAGGAAA ACCCCGGGTG TGGTTGTAGG GGAGGGAGTG 420
ACTCAGGCCT TGGCTGGCTT CCTGCTGAGT CACTACTCCT GGGCCCAGGA GGGAGGCTCA 480
ATCCTCATCT CTTCGCAGTG GCAGGTTCCT GCCTTTTTGG GGGAAATGTC TGGCGCCAGG 540
TCTTAACCGC ACACCATCGG TGGATGAATT TGTCTGACTT TCCTAACAGC TTCGTTGTGA 600
AATTGTGGGT GCGCTCCATT TCCTAATGTG ACCCTTCAGC CAGCAAGAGG GAACTTTCTG 660
CCCAGCCTAG CACTTCATTC TCCAAGGTGT CCTCGATGGA CAGGTTCTGC CCCTTGACAG 720
GCTGGCTGGC TTCCATCTCA GGTCAAACAG CTGTGTGCTT GGCACGCTCA AGACAAAGTT 780
GAGCAAGATG CCAAGGGAGC CACACGCATT ATCCTGGGCC TGGTGATGCT CACTCCAGAC 840
ACATTCACAG ATACAGCAAA GAAGAAATGG GTAAGGACTG TGATGTGGAT GCCAAGTGCC 900
ATGCACCAAG TTGGTTAATA CTTCAAACCA AGAGTCAGCC AGGCATGGTG GTGTGTGCCT 960
GTAGTCCCAG CTACTTGGGA GGCTGAGGCA GGAGGATCAC TTGAGCCCCG 1010
|
