| Tag | Content |
|---|
EnhancerAtlas ID | HS116-00322 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr1:12045580-12046760 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:12045743-12045758 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_28500 | chr1:12037809-12046747 | Fetal_Intestine | | SE_29466 | chr1:12037756-12047000 | Fetal_Intestine_Large | | SE_40992 | chr1:12038203-12047280 | Left_Ventricle | | SE_42819 | chr1:12045532-12046902 | Lung | | SE_49145 | chr1:12045709-12046770 | Right_Atrium |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 12045959 | 12046248 | | chr1 | 12046299 | 12046451 | | chr1 | 12046023 | 12046196 |
|
Enhancer Sequence | TGGCGAGATC TTGGCTCACT GCAAATTCTA CCTCCCAGGT TCAAGTGATT CTCCTGCCTT 60
GGCCTCTGGA GTAGCTGGGA CTACAGGCAT GCGCCACCAC ACCCAGCTAA TTTTTTGTAT 120
TTTTCATAGA GACGGGGTTT CACCATGTTG GCTAGACTGG TCTTGAACTC CTGACCTCAG 180
GTGAGCTGCC TGCCTCGGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACCGTGCCT 240
GACCCCTGAT CCCTTTTCTA TTCCTTTTGG ATGGCTTTCC TCTTGTGCCT GCCACATCCC 300
CTCTTTCTCG AACAGTCTGA TCTGCCAGGC CATGGCAAGC CTCATTTCAG CGCACTCTCC 360
TTTGCTGCTT TGGAAGAGTG AGAGTAGCAT TTTCTTTGCA GTTTCCTTTC TCAGAGCTGT 420
ACTGTCTTTA AGCCCTGGAC ATATGGCTTC CATGCTGAGA AAACATCTCT CATAGCTGTG 480
GCGTCATGCT GAGGAGGAAT GTAGAAACGG AAGTGGGGTC ACTTCCTTCC CTTGTCTCCA 540
GAGGAATCAT TAACATTGCA CAAGAACTTG TTGGTTTGGG CACACATGTG GGTCCCTATC 600
CCGCTTTGGG TCGGTCTGTC TTCTGCCCAC TCTTTGGGAT GGTTAGTTAC TAAAAGTCCG 660
TTTTGGCATT TGGTCTTCAT GTACCTCTTC CGGGTGTTCT TTCTGCTTTT CAGGACCTTG 720
TGCAACATAC TTTGGCCCCA TTTGGAAGTT TTTCACGTGT GCTTGCTGGG GAGCAACACC 780
TCATTTCCAA TCTAGAGAGA GTGAGCTTAC TGCTGGGTGG AGAACTGAGC AGTAAGATTA 840
GGGTGGCTGG GGAGGCAGTG ACAGACCCAG GCACAGTCAG CTGTGCACAC ACCCCCTCAT 900
CCAGGAGGGC CTTTGCCCTT TGACTTCCTG GGATTGGTGG GCTCTGCTCA AGAAGTAGCT 960
TTCGCCGTGG TGGGAACTCT GAGGGACCTG GCAGGGGTCC ACTTTTGGGG TCGGAATTCC 1020
CAGTCTTACC CTGGGCACTC CTTCTGGTGT GTACGCCTCT TTTTGATCTT TTTTTTTTTT 1080
TTTTTGAGAT GGAGTCTTGC TCTATTGCTC AGGCTGGAGT GCAATGGCGC GATCTTAGCT 1140
CACTGCAACT TCCAGCTCCC AGGTTCAAGC AATTCTCGTG 1180
|
