| Tag | Content |
|---|
EnhancerAtlas ID | HS118-02643 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr10:90923040-90924380 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CEBPA | MA0102.3 | chr10:90924201-90924212 | ATTGCACAACA | + | 6.14 |
| | | 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 |
| GH10I089163 | chr10 | 90923021 | 90924357 |
| Enhancer Sequence | TTATTATTCT CATTTCACAG ATGAAGCAGT TGAACTCAGA GTTAATGAAG CTGCCAAAGA 60
GACTGAAATT ACATGACCTA AACTCAGGCT GTAGTAACCT TGGTGCTGGT GGCTGAGGCA 120
GGACTGGCCC TGGATAGAAT GTAGTAAGTG TGGGTCTCAG CTTGGCACTT CTCAGAGGCA 180
GCTTTCTATT CTCCTCCCTG GTAAGGCCAA TCTTAGTGGT TACCTTTATG TAAAGTAGAA 240
CTATGTCCTG TGCCAAGCAA GATAAGCAGC TCTATGCATG TCCCTAAGAA GCTAAAATAG 300
ATGCTCATCA TCCCAGTCTG CAAATTAAGC CAAAATTTCA GTGTCACTAG CAGTCAACTC 360
TCCAAAGACA AATAGGTTGT AATCTAGTTT CAGAAAGGAA AAAGTGACTA GTTGTCTGAA 420
AGAACTGACA TCACCTGCAA GCTAAGTACC TTTTCCTGTA TCTGTGGGCT TTCTGCTCAC 480
CCTGGCTGTC TTGCTGTGCT CACTTGTACC AGATGGACGG CGAAACAAGA CTTGCCAGGA 540
AACTGAAACT TGCAACCAAA CGAGAGAGAC CAATTGCCAG ACAGCGTGTC TCAACACTGC 600
TCCGTCAGCA CACAACTTAT GTAATCGCCT GTTTATGCAA CAGAGTACAT GAATTTTAAT 660
TGATAGCACT GTTAGGTTTG ATTCAGTGTC ATCTAGTAGA GAGTTCTTCA CTGGAAATTC 720
TACTTGTGGT TCTACCACTA AATTTGTGGT ATTAGGGGGT GGGAGGAAAA GTCAGAACCA 780
GCTCTGTTTG CAATAATGCA ACTCAATGCT GTATTCAAGG AGAAGTGGAG TGAACAGAGG 840
GATGCTTCTT CAAAGTTGAA CACATTGGAA AAAATGAAGA ATTTGTAGCA GGGTTAGAGG 900
AAATACAATA AGATATCAAG AACCTTATAA CGTCTAAGTA ACCAAAGCTG AGACAAGAGT 960
GTTAGAAAAA GGAAGCTGTG TCTTTAGAAC TAACAGTAAG TATAAAGCTC TCCACAGAGG 1020
AAGCATCTGC GCGCTTAGGT CTCACTTTAA ATATCAGATC CTCTAGGAAG CCTTCACTAC 1080
TTCCCCTACA CCCCAAAACT GACTTAAAGA GTCATTGTGT GTGTTCAAGT AGCACCTTCT 1140
CTTCCACCTG TTATAGCCTG CATTGCACAA CATCCTAACC AATGGCTTAC TTGTCTCTCT 1200
TTCCACAAGT GTCAAAAATT TACCAGGACA GTGCTGGGAC CTCATTCACT GTCATGACCC 1260
TTGCACCAAG CTCAAATCCT GGTATGTAAT GAGCACCTCG GAAGAATTTG TTGAATTAAT 1320
GAATAAACAG TGTCCCATGT 1340
|
| |
|
|
|
