| Tag | Content |
|---|
EnhancerAtlas ID | HS116-19052 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr2:102856910-102857820 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:102857456-102857475 | TTGCGCCCTCTAGTGGCTG | - | 7.46 | | RUNX1 | MA0002.2 | chr2:102857249-102857260 | GTTTGTGGTTT | + | 6.02 |
|
| | 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 |
| GH02I102238 | chr2 | 102854507 | 102858977 |
|
Enhancer Sequence | CAAGGCTTTC ATATTTTTAA AACTTTGAAG TACAGTGAGA AACATAATTT AGTAAGCAAC 60
TCAGTATGCA CACACGGAAT GGAAAAAGCT CTGTTCTATG TTATTTGTTC TATTTTGTTC 120
AAGTCTAGCT CAATTTTTCA AAATGCTGGT CACAGCTCGC CAACTTGTTT TAATAACCAA 180
CTTATGCCTT TCCACTGCAA TCTGGAGAGC TCAGCCTCTC AGGCTGCTGG TCCCCCTGTC 240
AATCACGATA CTTTGGCTAC TTTGCTTTCT TCAATCAACA AGGCTTTATC AAGAACTTAT 300
GGCTCTTTTA ATTATCTGAC TTCCTGGTCA ATCAGCTTTG TTTGTGGTTT TAAATGACCA 360
CAGGATAGTA GAAGTGAACA TAATTTCCTG CCTGTGTAAA AGGATGACAT CAAGAGGAAA 420
AGAAAGCAGC TCACTGGGTG AAGGACCTTG AGAAAGAGAT GAACATTTCC TCTCTTGAGA 480
CACAGGACAA ACAAGGTCAC GCCTGAGCTC GGCAAACAAG GACTTCGGTG CCTGCCTACG 540
GCGCCATTGC GCCCTCTAGT GGCTGCTGAG GAACCGCTGT CCAGCCCGAA GCTCACAGAG 600
CCCCGTTCAG GCTGCCGCAA CCTACCTAGG CGGCCAGAAT GGAGACTTAC AGGTGGGCGG 660
GCATCCCGGG GTGCACACAT TACCTTCTCG GGGCTCTCCA ACTTAAGGCC AAGGATATCT 720
TTCTTCTTTT TCGGCTGCTG AGAAGGTGGA GATAGTGCCA TTTTCGAATG TGTTCCTAAC 780
TCTTGGGCTT CTGAGACTGT CGCAGTCTGT CCAAGGGTGG TGAGTGGGGA TCAGCAGGCC 840
CTGTTTACTA TGTGCTCGCA AGAGGGGACT GCGGTCATAG GGATTTCAGA GAGGTGGCCC 900
TGGCGTCGGG 910
|
