| Tag | Content |
|---|
EnhancerAtlas ID | HS047-07376 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr12:6854400-6855810 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr12:6854576-6854587 | AAACCACAAAC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 6854826 | 6855400 | | chr12 | 6854629 | 6855601 | | chr12 | 6854848 | 6855156 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH12I006745 | chr12 | 6854237 | 6855929 |
| Enhancer Sequence | AGTTAAATGG ACTTGGAATA TGCAGGCAGC AAGACCAGAC TGCTGGGTTC TGTGGGCCAG 60
CTTCTGGTTC TCTGGGTCAC CTGTTCATGT GACTTGGACA TGAGGTAGAG GGTGGAGGAA 120
AAAGGGTATT ATTACTAGGG CCTGAGGCCA TTACAATAGA AAGGGGGAAA AATCCCAAAC 180
CACAAACAGG GCAGGGGGAG AGTGGCCTCA GACATTTGTT TCTCTTTGCT GACCTGTGGG 240
GCTAAGGTCT GGAGAGAGTG AAAGATGACA GCCAGGAGCT GGGAGGGTGA ACGGCTGGGA 300
GCTGTTCAAG ATCAGTAGGA TGAGATCCAG ATCGTGTCTG GAAGTATTTT AGGGGTCCTG 360
AGGATGGAGT GGGGGATGAG GGACCACCAG AGAACCCTGA AGGAGCAAGG CAGGGAGAGA 420
GTGATCAGGG AGAAATACTA GCATGGAATG GTCATTTGTA TCCCATGTGC ATGTCAGACT 480
CTCTGCACTC ACTCAGGTCT CAGTTCTGAG GTATGACTCC ATAGTCACCA GTGCCTAGAA 540
AGGTTCATTT TACAAAATGG GGAACTGATG TTGCGAGAGA GGAAGTCTTT CCCACAGTGC 600
AGCTGAGTGG TGGAGCCAGG TCTTGCTTGT GCGTGTGCAT CCTGTCTCCC TCCTCTGTGT 660
TATTCTGCTT AGTCACACAC CTAGTGTCAG CCTCTTCCAA CCTGTAATGT TCTGGGGTGG 720
AGAAAATAAC CTGAGGCGTT TGCCCATGTC CTCTGGATAC TCGCTGGGCC GGTGGCTGAG 780
GGGTGGCTGT TGTGTGAGGC TGGGCCCAGA TGGAGAGCTG ACCGGAAGTA GAGTATCTGT 840
GTCCCTCGGG AAAGTTCCTT TCCTCTTCCT CTCCCGTGGC CCTTACCCCA GTGGCAGACA 900
GGTCAGGACG TGCTAGGGGG CTGGTTCTTG AGCATCTCAC TCTACTGATG CTAACACCTC 960
ACTTCCCACA ACATATCCCT GCTGAGAACT AGTCACAGGC CCCAGGAGTA AGTGCTGGGC 1020
TGAAGGGTGG TCCAAACCCT ACAGCAGGGA GCAGGAGTAC AAATCAGTTC ACATGTCTAA 1080
AGGCTGGGAC CTGAACAGGG GAGTCCCTGA AACACTGGAC TGACTCACCT GGACTGAGGT 1140
CAGGGCAGCC TTACTCTGCC GCAGTCACAC TCAAGACTAC ACATGCGCGT GTGGGCACTG 1200
GAACTAAAAT CCGGGTTGAG AGGCTGGGCC TGATATTTTG TGGCTAGAAG GGCCCCACAT 1260
AACTCAGGTC CAGGGAGGTG AGTGACCTGC CCAAGACCAC AAGGCTGTCA GTGGCCGAGC 1320
TAAGGACTGA GGCTCCTTCA ACTCCAGGTT ACCTTGCTGC CTTCTCAGGA GAGTGAAGAA 1380
AACGACTCCC TTCTCAGAGG AAACAGTCGT 1410
|
| |
|
|
|
