| Tag | Content |
|---|
EnhancerAtlas ID | HS105-48936 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr20:2129660-2130980 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr20:2129672-2129687 | AGAGGTCAGAGGTCA | + | 8.73 | | Nr2f6 | MA0677.1 | chr20:2129673-2129687 | GAGGTCAGAGGTCA | + | 7.42 | | Rxra | MA0512.2 | chr20:2129673-2129687 | GAGGTCAGAGGTCA | + | 6.88 | | TEAD1 | MA0090.2 | chr20:2129823-2129833 | CACATTCCAT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTCGGTTCCA TGAGAGGTCA GAGGTCAGGT CAGTGGCCTG AGGTTGGTAG CACCCGTGTC 60
CAAAAAGCAA AGGGGTCCAA TCAAGCCAGG CCATCCTGGT TGGGTTGGGA ATGGGAAAAA 120
GAGCACATAG TCCATCTCCC TTTCTGCCTG GGCCAACAAA AGCCACATTC CATGAGGACC 180
AGGGACTGGA ATTTATGAAA AGCCACATGT TTTTGTGACC ATCGTACTGC ATAGCAGGTG 240
TGATGTATGC TCCTCTACGC ATAAGAGAAC TAAAACCCAG AGAAATCAAG ACTGCTGGGT 300
GAGTGCCAGG CGGGCTGGGG AAAGAGCTCC CGCCACTTGC CAGCCGGGAC AGGTAACTGA 360
GCCTCGCTGA ACATCTACTT CCTCAACGAA AGTGGGGGTG ATGACAGCTA CCTTCAGACA 420
AGTTGCAGGC TAAATAAGAA CCTAATATTG GGCCCAGCAC ATAGTAGGCA CTGAAATGGT 480
TTTTTGATTT TCCCAAAGAG ACAGGTTTGG GATTCTTCCG GAGTCTGCTG AGCACTAAGC 540
CCCAACTCCT GGCATCGCGC AGCTTTGGTG AGGCTGCCCA GTCTGGTGAG GGTTGATGTT 600
GACTGTGGAG CCCATCATTC AGGGGCTGTC CCAGGGAGAC CCGGGGAACC CAGGACAAAT 660
ACAACTCCTG CAGGAGGATG GAGTCAGGAC TTAGGAATGT GTAAGTTAGA AGAAAAGAGA 720
AGACTGGCTT GCCTAATCTG CGAGTGAATA AGCTACATTC TGGGCCCAAG AGTTGGTGCC 780
CAGTGGCTGC TGGGGATGGG GCTTCCAGAA AAGGATACTT CTGTCCTTAG CCTGGGCGAT 840
AACCTGGAGC TTGAAGGACA GCCAACAAAT TTGTTTTCTT ATTAACAGAT TTTTTTAGAG 900
AATTCATCCT TCTGAAGAGT GCAATTCAGT GGTTTTTAGT ACATGTACAG AGTTGGGCAG 960
CCATTACACT AGCTAATACC GGAACATCTC CTCAAAAGAA AAAAAAAAAA AAATCCATGC 1020
CTGCTGGCAG TCACTTCCTA GTCCTTCCAT GTTTTTCATT TCCTTGGGTA TATACCAAGC 1080
AGTGGAATTG CTGGGTCATA TAATCACTGT TTAGTTTTTT GGGACCTGCC AGGCTTTTCC 1140
GGAGTGGCTG CACCGTTGTC CATTCCCACC GGCAATGCAC TAGGGTTCCT GTTGCCCCAC 1200
ATTTTTGCTA TATTGTCTTT TTTATTGTAG TCAATTGAGT GGGTGTAAAG TGGTCACAAG 1260
TTGTTATAGG CTAGGTCTAC ACCATTGTAC TACGGGTTAA TAGCGGATAA GGGGAGAATA 1320
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