| Tag | Content |
|---|
EnhancerAtlas ID | HS047-01043 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:39512590-39514010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr1:39513769-39513780 | GGATGACTCAT | + | 6.62 | | JUN(var.2) | MA0489.1 | chr1:39513771-39513785 | ATGACTCATCTTCC | - | 6.3 | | JUNB | MA0490.1 | chr1:39513769-39513780 | GGATGACTCAT | + | 6.62 |
|
| | 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 |
| GH01I039046 | chr1 | 39512253 | 39514624 |
|
Enhancer Sequence | AGTCACATGG CACTGTGGCC AAGGAGAAGG ATGATGTTCC AGGCCAAACA CATCTGCAAA 60
TGTGTTGAGC TGGTGTCCTT GATGACAAAT CAAATTGTTT TGTGTTTGGT TCCCCAGAGG 120
CCTGAGTACC TCAGAGAAGC CAAGGTTCCT GCAGGAACCT CGTGCCTGCT GTCCACGTTG 180
GGCTTCATTT TATCAAAATA CAGCAAAGAG CTCATCATTT CTCAGCTCCT GTCGGAAGCA 240
ACAGTGGCTG TTCCTGGACA CAGAGCTGCA GACAAGGAGT GGTGAGGATT CAGGCAAGAG 300
AAGATGGGCA GCTTCCCCTT CATGCTTCCC TCTCAGGAAG AAGCCAGGGT GCCTGGGATC 360
AAAGAGGCTA GGAGGCTGGT GAGGCCTCCT GTCCCTGAAA GCGGTCAGTG AACCCAAAAG 420
TTGAAAAGCC TCTGCTTTGA GAGTGGTTCT GCTGCCCTAC TGGTGCTGAC AGTTTTAGAA 480
ACTGACATGG CAGAGCTGAC CAGGCAGACT ATATTTTTAG GACTCTGCTG GGGCCTATTG 540
AAACGTCCAC ATTACTCAGA TCACCAATCT GGCTGGAGCT ACCAACACAG CATTCTTTGC 600
TGTTTTAGAA TACAAAGCTA CCTCCCCTCG GGGCTTCACT TTGCAGCCAC TGAGAATCCA 660
AGGCTTCGCT AAATTACACG TTTCCATGGT CCCACTGGCT TGCTTTGCAG GGCTTCCACA 720
AGAATGGGCT GGGAGCGTAA CTGAGTAACT GAGTCATGAT TAGGGGTTAA TTAAGAGGAG 780
AAATGGGCTA GCTGTTTCCT AAGATAAGGG AGGGGAAGTT TTTTTAAAAA CTGTAACTGC 840
TCAGAACAGT ATGTGCTAAG GCAGACTTTC TGTGCTGGGA GACAGAACAC TTCTGCAGTG 900
ATGTAGCAGA ATCCTTAAAG GATCCTGCCA ATGACTCTTT TTTTCTGGTG TCACATCCAA 960
TCTTTGCTGC AGCCAACACT TCCTGGAGAT GAAACACAAC TTCAATACAG AGATAGCAAG 1020
TTCACACTCT GGCAGTCATG CAAGGATGAG TGATGCGGGC CTTTTCTAAG TGAGTATGAA 1080
CGGGTGGGAC CTACGGTAAA TTCAATGCAG TATAATCCGT CTACGGGGCA GTGGGCACCC 1140
AGCAACAGCC AACTGTTACC AAATCAAAGT GCAGGCCCAG GATGACTCAT CTTCCAGCAT 1200
TTCATGAGCA ACCAGAAGTC TACATTTCTT TGAGAAAAAA AATTTTTTTG AGACGAGGTC 1260
TTACTCTGTT GCCCAGGCTG GAGTGTGTAG CTTCTACCTC CCGGGGCTTA GGTGATTCTC 1320
CCACCTCAAG TCTCCCAAGT AGCTGAGACT GCAGGCATGT GCCACCACGC TGGCTAATTT 1380
TTTTTTTTTT TTTGAGTCGG AGTCTCGCTC TGTCCCCCAG 1420
|
