| Tag | Content |
|---|
EnhancerAtlas ID | HS134-33500 | Organism | Homo sapiens | Tissue/cell | Mesendoderm | Coordinate | chr2:210169430-210171040 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TEAD1 | MA0090.2 | chr2:210170002-210170012 | CACATTCCAT | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH02I209307 | chr2 | 210169861 | 210169990 | | GH02I209305 | chr2 | 210170440 | 210170878 |
| Enhancer Sequence | AAAAAGCTCC CCCACTGAGC ACCTTGCGAC CCCCACTCCT GCCCACCAGA GAACAAACCC 60
CCTTTGACTG TAATTTTCCT TTACCTACCC AAATCCTATA AAACGGCCCC ACCCTTATCT 120
CCCTTTGCTG ACTCTTTTCG GACTCAGCCC GCCTGCACCA GGTGATTAAA AGCTTTATTG 180
CTCACACAAA GCCTGTTTGG TGGTCTCTTC ACACGGACGC GCATGAAAGA TATGTCAATC 240
ATGTGTTTTT AAAAAATGAC TATTTCATAA AATGATGAAT AGCTAATATG TACCATGAAG 300
TATATATAAT TCTTGGGTAA TTTTCAAGAA CTGGTTCTCA TCTTCAGAGC CAATACTTTC 360
CTTTTAATTA TTCATCTGAA TTAAATATAT TTAAATTTAA ATCTTTAGCT TGAAGGGGAA 420
AAAGAATCCT GTGTACTGCT CTAGCTGTGA CCAAGCCAAT TATGCTAACA TCAGCATCCA 480
ACGATCACAG CAGGAAACAT ACTGTCTTCT TTACATGCAT GGGCTGACTG AATTCTTACA 540
AAATCTCCAT GAGGTAGGCA TCACTATACA TTCACATTCC ATAGGTGAGA ACAATTTGAT 600
GTTAATTAAC CTCCTCAAAG CTATATAATT CTCTAAGAAC TGAATCAGAA TTCAAATAAA 660
ATCTTTCTGA CTCCAAAATG AATGTAAAAC ATACGTAATG TAGCCCCTTC TAAAGGATAT 720
TTCTCAGAGC TTCAAGGCTG TTCTTACAGA TCAGACACCT TTGTAGAATA TTCTAAGACC 780
CACATCTAAA CATATTTCTG TGAAGTATCT AAGGAAATAC CTAAAATTCA TCTTTCAAAT 840
GGTAGTATCT GGTTTAAGGA TTGCTCCTTA TTTCACATAA CCCTTAGTGG GTGTAATAGT 900
TCATTCTTAT GCTGCTGTAA AGAACCACCT GAGACTGTGA AATTTATGAA GAAAAGAGGT 960
TTAGTTGACT CACAGTTCTG CAGGCTTAAC AGGAAGCACG ACGGGAAGCC TTCAGGAAAC 1020
TTAAATCATG GTGTCAAGGA ATCTTTGGGG TGTTGCTTTT CCAGCTGGAA ATTCTGTGGC 1080
CAGTGGCACC TTTGCCTAAG TATTGCTCAG GCCTGCTGGG CTCATTCCAC CCACTCGGCC 1140
TGGCAGGCTG TGCTCAGCTG TGCCACTGGC CTGGATCCCA CACCTGCCAA GGGAGAGTCA 1200
GGCATAGAGC AGTGAGGAGT GTGTGAGCAA GCGTGGGATC TGGCCACTGC CCACAGCCAG 1260
GCATGCCAGC TGCGGAGAGG TGGGGAGCTC CAGGCACCAG CACGGGTGCC GGCTCTTTGT 1320
GAGGCTGTGG CTGGACCAGG CATACCACAA GTAGATTTCA CTGTGAGCAC CATGGAACTC 1380
GGGGCACCTG GACCCTTGGA GACACCAGGA ACCGCAGACC CCCAAAGAGG GTGTCACTGC 1440
CCTGGCTCAG AGGGCCCCTA GGTCTGGGCT CCTGAAAGAA CTGCAGCTCT TCTCTCTTTC 1500
CCATTGAGAG ACAGGACTAG CTGGATTTCC TAGGCCGACT AAGAATCCCT AAGCCTAGCT 1560
GGGAAGGTGA CGGCATCCAC CTTTAAACAC AGGGCTTGCA ACTTAGCTCA 1610
|
| |
|
|
|
