| Tag | Content |
|---|
EnhancerAtlas ID | HS091-33918 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr3:33413220-33414580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr3:33413519-33413534 | CCTGGCCTTGGGCTT | - | 6.16 | | Stat6 | MA0520.1 | chr3:33414145-33414160 | GTTTCTCTGGAAAGG | - | 6.34 |
|
| | 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 |
| GH03I033372 | chr3 | 33414116 | 33414665 |
|
Enhancer Sequence | TGTTGGGTGC AGATATTTTT GTATTCCTAT AAATACTCAG GTTTTGTTCT GGGATACAGT 60
TGACTTAATT GGGAATAGTT CCTGTTAGGT CTTGTTTTTA AGATTTGTTA GGTTGTACCA 120
AAGCAGTGTT TAGGGCTAAT TATGCGCCAC TCCTAAAGGA AGACTATTCT CAATACTCTA 180
CCCAATGCCC CAAGAATTGT GGCATTTTTC ACTCTTGGTT GGTAGAAATG GGCACTATTC 240
CTTGCCCTCG GTGAGCTCTG GCTACTGTTT CCTTTAATGC TTTTTGTTCA TTCTGATTCC 300
CTGGCCTTGG GCTTTGGGTA GTTTCATCAC ATGCATACAT TGATCAGTGT GGTACTGAAT 360
TCTTTTTGTT GTTGTTGTTG TTTTGGAGAT AGAGTCTCAC TGTGTTGCCT AGGCTGGTCT 420
CAAACTCTTG GGCTCAAGGG ATCCTCCTGC TTTGGTCTCC CAAAGTGCTG GGATTACAGG 480
CATGAGCCAC CATGCCTGGC CTGTACTTAA TTCTTGAGGG GCACCCTCCA CAGATCTCTG 540
GAGTTCTCTT TGTGACGTTC TCTCTACTCC AATGCTCTTG CCAGATAACT CCAGCTGCCT 600
TGGTCTTCCT AGAATTTCAG CCCCATTTCT TCATCTCAGA CAGTCCCATC AGGCTTGGTT 660
CCCCCTACCG GTACCAGGGC AGGTTGGAAG GAGCAAATCT CAAAGCTGTA TTTCAGAATG 720
ATGGAGACGA CCTGAGCTAG TCCTTGCTGA ATATGTTAAG CAGTGAGTGG TGAATAGGGC 780
GTTTTAATGT GCTGCTTCTG GCCTTGCTAC CAACCCACAG ATCAATGAGG AAGTTCCTCT 840
TCATGACTGA ATGTCCTCAC CAGTAAAATG AGTGGGTCTT GATACTGATT AACTGCTAGA 900
CGTCTTCTAT CAATCGCCAG AAATGGTTTC TCTGGAAAGG CTCTAGGGTA AGCAAGTGAC 960
AGCATGGCAC AGTACTAGAA GATTTGCCCC CTTGGTTCAA ATTGATTTTT TTGTAGAGCG 1020
GAGGGAGCAG GGAGCTAGGC CTCTATTCTC ATGATTCGGT GATGACTCAC CAAGCTGTGG 1080
GTAAAGGAGA ACTGATTGAT AGGTAGTCTA GGACTCTGCT TCTCAAAACG TGGTCCCTAG 1140
ACTAGCAGCA CTGGCATCAC CTGGGAGTTT CTTTGAACTG CAGACTGTCG AGCCCCATTC 1200
TAGATCTATC ATCAGAATCT GCACTGTGAC AAGAACCCTA GCTGATTGTT ACGCGCTTTA 1260
ATTAAGTTTG AGGGAGCGCT GTTCTAAGCG TGAATGGTTT CATATGCCCT CTAGTGGCTG 1320
TCCAGCAACT TGCAGGGAGC TTTAAAATGT TTTCTCATTT 1360
|
