| Tag | Content |
|---|
EnhancerAtlas ID | HS052-00279 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:12045540-12046710 |
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 | AAGAGAGAGA CTTCGCTCTG TCACCCAGGC TGGAGTACAG TGGCGAGATC TTGGCTCACT 60
GCAAATTCTA CCTCCCAGGT TCAAGTGATT CTCCTGCCTT GGCCTCTGGA GTAGCTGGGA 120
CTACAGGCAT GCGCCACCAC ACCCAGCTAA TTTTTTGTAT TTTTCATAGA GACGGGGTTT 180
CACCATGTTG GCTAGACTGG TCTTGAACTC CTGACCTCAG GTGAGCTGCC TGCCTCGGCC 240
TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACCGTGCCT GACCCCTGAT CCCTTTTCTA 300
TTCCTTTTGG ATGGCTTTCC TCTTGTGCCT GCCACATCCC CTCTTTCTCG AACAGTCTGA 360
TCTGCCAGGC CATGGCAAGC CTCATTTCAG CGCACTCTCC TTTGCTGCTT TGGAAGAGTG 420
AGAGTAGCAT TTTCTTTGCA GTTTCCTTTC TCAGAGCTGT ACTGTCTTTA AGCCCTGGAC 480
ATATGGCTTC CATGCTGAGA AAACATCTCT CATAGCTGTG GCGTCATGCT GAGGAGGAAT 540
GTAGAAACGG AAGTGGGGTC ACTTCCTTCC CTTGTCTCCA GAGGAATCAT TAACATTGCA 600
CAAGAACTTG TTGGTTTGGG CACACATGTG GGTCCCTATC CCGCTTTGGG TCGGTCTGTC 660
TTCTGCCCAC TCTTTGGGAT GGTTAGTTAC TAAAAGTCCG TTTTGGCATT TGGTCTTCAT 720
GTACCTCTTC CGGGTGTTCT TTCTGCTTTT CAGGACCTTG TGCAACATAC TTTGGCCCCA 780
TTTGGAAGTT TTTCACGTGT GCTTGCTGGG GAGCAACACC TCATTTCCAA TCTAGAGAGA 840
GTGAGCTTAC TGCTGGGTGG AGAACTGAGC AGTAAGATTA GGGTGGCTGG GGAGGCAGTG 900
ACAGACCCAG GCACAGTCAG CTGTGCACAC ACCCCCTCAT CCAGGAGGGC CTTTGCCCTT 960
TGACTTCCTG GGATTGGTGG GCTCTGCTCA AGAAGTAGCT TTCGCCGTGG TGGGAACTCT 1020
GAGGGACCTG GCAGGGGTCC ACTTTTGGGG TCGGAATTCC CAGTCTTACC CTGGGCACTC 1080
CTTCTGGTGT GTACGCCTCT TTTTGATCTT TTTTTTTTTT TTTTTGAGAT GGAGTCTTGC 1140
TCTATTGCTC AGGCTGGAGT GCAATGGCGC 1170
|
