| Tag | Content |
|---|
EnhancerAtlas ID | HS187-13724 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:102856970-102857940 |
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 | TCAGTATGCA CACACGGAAT GGAAAAAGCT CTGTTCTATG TTATTTGTTC TATTTTGTTC 60
AAGTCTAGCT CAATTTTTCA AAATGCTGGT CACAGCTCGC CAACTTGTTT TAATAACCAA 120
CTTATGCCTT TCCACTGCAA TCTGGAGAGC TCAGCCTCTC AGGCTGCTGG TCCCCCTGTC 180
AATCACGATA CTTTGGCTAC TTTGCTTTCT TCAATCAACA AGGCTTTATC AAGAACTTAT 240
GGCTCTTTTA ATTATCTGAC TTCCTGGTCA ATCAGCTTTG TTTGTGGTTT TAAATGACCA 300
CAGGATAGTA GAAGTGAACA TAATTTCCTG CCTGTGTAAA AGGATGACAT CAAGAGGAAA 360
AGAAAGCAGC TCACTGGGTG AAGGACCTTG AGAAAGAGAT GAACATTTCC TCTCTTGAGA 420
CACAGGACAA ACAAGGTCAC GCCTGAGCTC GGCAAACAAG GACTTCGGTG CCTGCCTACG 480
GCGCCATTGC GCCCTCTAGT GGCTGCTGAG GAACCGCTGT CCAGCCCGAA GCTCACAGAG 540
CCCCGTTCAG GCTGCCGCAA CCTACCTAGG CGGCCAGAAT GGAGACTTAC AGGTGGGCGG 600
GCATCCCGGG GTGCACACAT TACCTTCTCG GGGCTCTCCA ACTTAAGGCC AAGGATATCT 660
TTCTTCTTTT TCGGCTGCTG AGAAGGTGGA GATAGTGCCA TTTTCGAATG TGTTCCTAAC 720
TCTTGGGCTT CTGAGACTGT CGCAGTCTGT CCAAGGGTGG TGAGTGGGGA TCAGCAGGCC 780
CTGTTTACTA TGTGCTCGCA AGAGGGGACT GCGGTCATAG GGATTTCAGA GAGGTGGCCC 840
TGGCGTCGGG CCCCTGGACT CCAGTCACAA CTCAACCACT TGCTGAGGGA GTATGCTAGC 900
TAAATCCCTC TTGCAAGTCA AAAACCCTGT GCCCCAGTTT CTTCCTCTGT AAAAAAGGGA 960
TAATACAATG 970
|
