| Tag | Content |
|---|
EnhancerAtlas ID | HS059-28613 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr20:32535290-32537100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr20:32536442-32536456 | AACTTCCTCTTTCT | - | 6.7 | | SPIC | MA0687.1 | chr20:32536442-32536456 | AACTTCCTCTTTCT | - | 6.24 |
|
| | 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 |
| GH20I033947 | chr20 | 32535661 | 32535790 |
|
Enhancer Sequence | AGACTCAATT GAGAACTTCT CTCTCATTTC ATAGCCTGTC CAGCCTTTCC AGTTTATAAC 60
TGTATTCCCT ACTCACTCTA AGGTCTGAGT CCAAGTCATG GTGTCTGAGA TCTTAAAAAT 120
AGAATCATCA GAATGACCCG CCTTGCCAGT TTCAGGGTAC AAATATAGCC ACCTTTATTT 180
CAATTTTCCA CTCATTCAAG TTCTCACATA CTTTTTTTAG TGCAAGGTCC CAAGACACCC 240
TCTTTAGGCA TCCACTGATC CCTGGATTTT CAAAGTCTAG GGGATAACTT GGGCTTAGGG 300
CATCAGTGTG GTTCCAATGC CACCTACAGA GAGAACTAGT CTATCAGTCC ACCACCAATA 360
GTCATTGCTC CTCACTGCCA CATGGTGTCG CTGTTGAAGA CTGATTCTGC ATAGTCTCAT 420
GGCTGCTTGT CCATTGCTGC CAGATGTCCT TGCTGGGTTC CTGCACAAGT CACAGTAGTG 480
CCCCCTCTTG GTCTTAGCAT TTATCACAAA TTTAATCACA TATTTGTTTT CCTGCTTATT 540
GTCTGACTCT CCTATAGGAC GTAAGTTCCA TGGGTGCAGT TCCTATATGT GCTTTATTCA 600
GCACTACTGA ATTTGTACCA GAATAGGTAC TTAATAAATA TTGCTGAAAT CAATGAGTGA 660
ATGAAGAAAT GCATGCATGC CTGCATGAAT AAATGAAATA AAGTGTCTGA AGCAAGGGGG 720
AGACAAGACA GAGAAAGTGG TTTCCAGAGA CAGAATCTCA GCCCACCTCT TGAGAGGGAG 780
ATGGCATACT TGTTACATAA ATGCTTCTAC TCCCCACTCC TTTGTCCATG GGGCCACTAA 840
TCAATCACAT CATTCTTTCT CGCTGAGGTT GGAGACAATT TCTAAATCCT CAGTACAGAA 900
GTCCAGCCAT CTCTTGTAAT GAATTGGAGG AGGCAGACAA CAATGGAACG TTTTGTGGTA 960
ACAGGATGCA AGGGAATGTT CTCACTGTGG CAGTTTTAAC ATATAGCCCC CAAATTCTTT 1020
GACATTCCTC TTATTTAATG GTGGGATCCC TGACCCTTGC CCTTGAATCT GGGTTCTGCG 1080
AATGCTTGAC CAATAGACAA TGGCAGAAAT GATGTTCTAT AAGTTTCCAG GAACAGGTAT 1140
TAAGAACCTG GCAACTTCCT CTTTCTGTCT CTTTAAACAT TCATCTTGAA ACCCAGCTGC 1200
CATGCTGTGA GGAAGCCCAA GCTGCTTTGG GAAGAGGCCC ACCTGAGAGA AAACAGCAGC 1260
CAGTGCCAGC TTGCTGGCCT TGTGAGTGAG TCACCTTGGC AACGGACCCT CCAGCCTTAG 1320
TAGAGACATC CCTGGTGACA TTACATGAAC AAAGATGACC TGTCCCCACT GAACCCTGCC 1380
CAGACTGCAG GCTCATGACA AAATAAATGG TCTCTGTCTT ACGCCGCTAA GTTTAGAGTG 1440
TTTTGTTAGG CAGCAGTAGT AACTGGGACA CTCATCAAAC TTCAGCATCA ACTCTGCTAC 1500
CATGGCTCAG TCCTTACAAT CAAGTTCTGT CTCAGTTTCC CCGGCTCCAC ATGCCAGGTC 1560
CCCTTCTGGG CCTGCGGCTT TGAGAGGAAG CTTACATCTT ATCCCATCCA TGGAATGGGA 1620
TAGGAGCTTA TTCTGCTCCC TATATTGCCA GTCATGTAGG GGGATTGCAT AGCCTGCAGT 1680
CACCACCCAC TTGGTCTCTC CAGCAGCCCA TGCTGAGAGC CTGAATATTT CATGATAGGC 1740
TGCAGCTTTT GAGCTTAGGA AGGAACTGCG GGTGTCATTT CGAGCTAGTT CCCATCCCTT 1800
TCATTCCCAT 1810
|
