| Tag | Content |
|---|
EnhancerAtlas ID | HS187-02195 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr1:204732500-204733590 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBX20 | MA0689.1 | chr1:204733202-204733213 | CTTCACACCTA | - | 6.62 |
| | | 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 |
| GH01I204763 | chr1 | 204732729 | 204733387 |
| Enhancer Sequence | ATCCCCCATT TTACTGATGA GGAAACTGAG GCAATGTATA ACAGGTATAA GTAGCCCAAG 60
GTTATTCAGG CACTAATGTG TAAGGCTGTG ATTCTAAGGC AGACTGACTG ACTACAAAGC 120
TAATGTTCTT AATCCCTAGA TGCTCCCACC TTCCAAATGT CCTGGCTCCT AGAATTACAT 180
CTGTTCTACT CCCTCCATGG CTCCATGGAA CCTGGACATC TCAATTTCCT CCCCAAAAGC 240
TGGAGTTCTC CAAGATGCAG AAGCCAGAGG GCTGATGTTC CTGTGCAGGA AGAAGCAACG 300
CCCAGGCCCA CTGCCCCCAC TCTCTCAGCA GATTCTCATT TTCAGAATCC TGGAAACCAG 360
AGCTAGAAAT CTGCCTCCCT CTGTTTACCC TGAGTTCCAA TGTCACCAAC CCCCTTAATT 420
AATGCTAGGG TGCTGGGTCA TGCATAGCAC GGTCAGCTTG GTCTCCAGTT CTGGCAGCAG 480
CTGCAGCCAA GGTCAAGAAC AACGGGGGCT GGGTTAGCTC TTACTCATCC ACCTAAATGC 540
CACTGCCCAC GCTCTCCGCT CTCGCCCCTC CCGCTGAGCA GTGGCTGCCA GGGCGGCAGG 600
AAGTCCTTCT TCCTGGGCCT GGCGCCCTCC AGCGGTGGGC GCAGAGCACT AGGCTCCAAA 660
ACTAGGAAGC CGGCTCAGCC TGCAGCAGGG CAGCTTGGGC AGCTTCACAC CTAAACCAGC 720
CTCTAAACGG GCGCACCTGG ACAAAACCCA GTAATTTAGA AAAGCCTGTG TTTCTAGACA 780
TCTCGCACTG CCAGCATTCT CCATGAGAAA GGAGCTAATA GGATCAACTT TTCCTATACG 840
CTGGAGACTT AATGAGTCCC TCACCGACCC AAGGCTGACC TGTAATCTGA CAGATGACCA 900
CGAAAAAGAG GCAATTTCAA GCCTAAAGAA AGGACCCCAT TATGTTGACA TTTAGGCATG 960
AGTGTGGGTG GCATTGGGGC AGGAGTCCTA TGTGCTGCTC AAATCCCACC GTAGAGTCAA 1020
CTGGCAGTGT GGCCTCTGTC TGACACAGCT CAGGCTCTCC TGCTCCGAGG GAGTTTAGCA 1080
GAAGGTCCCT 1090
|
| |
|
|
|
