Tag | Content |
---|
EnhancerAtlas ID | HS073-04282 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr14:95677480-95678910 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TEAD1 | MA0090.2 | chr14:95677529-95677539 | ATGGAATGTG | - | 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 |
GH14I095212 | chr14 | 95678392 | 95679788 |
|
Enhancer Sequence | GACCAACTGT ATAGACCATT CCTTGTATCA GTGACATTGA AAACATAACA TGGAATGTGC 60 TGTGCCATAA AAATGGAACC AGAAAGACAC AAGTTTGTAC CTCAGCTGTC CCCTCTATGC 120 TTCTAGTGCC ATGGCCTTGG GCAAGTCACC TACCTCTCTG AGCCTCAAAC TCCACACAGT 180 GAACTTGCTG GGGCTTTTGT GGGGAAAGTC GAGCCTGGCC CCAGAAGAAC GGCCAAGTCA 240 TAGGGTCAAC CTAATATACA ACGTTGGGAG CCCAAGAAAG CCACTCACTA ATGACAGCTA 300 CTATTATCAG TAATAGAAAT AAAAGCACCA TTGTAAAAGT GAGGGGCAGA GAGCTTTCAC 360 TCTATTTTGT AGAATGGAGG CTACCTCAAC TTTTTAAAAG TAAAAGTGAA GGACAAAAGA 420 GGAGAGAATC TTGCCAGGCA CTAATTTCCT GTAGAATCTA TCCTGAGACT CCACCAATCT 480 CTCAACCGTG GTCAATAAAC GCTCTTAAAA AAAAAAAAAA AAACCAAAAA CAACCAAGTA 540 CCTTTTTATT TGGAAATCAT TTAAGACCCA AAAGAAGTTG AAACACAGTA CAGAGAGTCT 600 CTACTCTTTC CCCAGCTTCC TCCAGTGACA GCATCTTATG CTACCAGGGT GCGTTATCCA 660 AACCAGAACA CCAATACTGG TCCAAGACAA TTATTAATCA AGCTATAGAC TGCATTTGAA 720 TTTCACATTT TCACAGGTGT TACTTTTCAT GGCGGTGGTG TACAGATTAA TGTAACCACC 780 ACAATAGAGA AACAGAACTG TCCTATCACC CCAAGACACT TCCTCTCCCA TACATCACAC 840 CCCCCTTCTA CCCTAACCCC TGACAATGAA CTTTTTTTTG GTTGATATTT ATGTAAACAA 900 CATTTAATGG TGGTTCACAT TTGTCAATTT CAATCTACCA CGCTTGATCT CTCAATCAAA 960 ACTCTGAAGA TCCAACCTCT CTTCCCTCTT TTATTTCCAC ACACAGGGGA TAAAGGAATC 1020 AATATTTGTG AAGTGCTTAA TATGGGCTGG CACTGTGCAA GGTGCTCTTT CATGGATTTT 1080 ATTTAATTTC ACCTAATTGT CCTGGAAGGC AGTGTGTGAT AGGATACTAT TTGCAGTTGG 1140 GGCTTGGAAA GGTAAATGAT TCACCAGGAT CTCAACCAGT CTGTACGCTG AGGAGCTGGG 1200 GCGGCCCCGA GTTGGTTTGG TTTCCACCAC ACTGGTCTGG CATTTGTGCC CATGGTCCAG 1260 GGGCTGTGGG CCTGCTGCTG GTAAAAAGGC CTGATACAAA ACTGCTAAAA TCACTCTGCT 1320 GCCGGTGTGG GGTGAAACAG GGCCGGAACT TGGCTCCAGT TCCCGTCTCG ATTTTGGAAG 1380 GTCCGACCTA ACTTTGAGTA TGTTACAGCC TTTATTATTA CTATTTTTAA 1430
|