Tag | Content |
---|
EnhancerAtlas ID | HS043-02968 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr1:166894480-166896300 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr1:166894555-166894567 | AAGTAAACAGTA | + | 6.18 |
| | 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 |
GH01I166925 | chr1 | 166894261 | 166896264 |
| Enhancer Sequence | AATGAGATTT CAAGATTGCC CAGTTCCATG ATCCAGCCCA TGGTTTACTA TGTTCTTCAG 60 GAACAGGACT TCTCAAAGTA AACAGTATTC CTACTTTATC TCTATGCAGT TGTTATAATA 120 TTAACTTGCA GGTTCCAGGA GATCAGGGTT CCAGTTCTGG CACTGGCACT GAGTACTGGT 180 GCTTGTTACT TTCCCTTTCT ACCTTAGTGA AGGGGACGGA TTCAACAACC TCAGAGTCCC 240 TTCCAGCTCT GACATTCTAA AGTCCTACTA GCTAGAAGGC TGTGGTCTCT GAACAGAATG 300 GAGCCATGGA GCCATCCACA TTACAGCCAT GGAGCCATCC ACAGTTTGCC CAAGAGTTTC 360 TTCTGGAAAG ACCACAGGAC TGGGAATCAG AAGAGCTGGA ATCTGGTCCT AATTGTGTCA 420 CCGCATCCCT AGGCTTCTGT TTCCTCACCT GCACACTACA AAGGTTAACC TAGGCCATCT 480 CTAAGACCCC CTTTGACTCT AAGAGTCCAT TACCTTATGA CCATTAAGCC CCTAGAGACC 540 ATTTTAATGA AGTAGAGAGA CAGGAGACAT CACCTAAACC AGAATTCTTC CTTTAGTTTT 600 AACCTTAGCT GTTAACTTTT TCTCTGAGCT GTGAGATTCG CAAATTTCCT GCACAGACTC 660 CTCTGTGGTC CCTGACTCAC TCTGTCTCTG GCCCCTTACA GGGATCCATG ACAACATTGT 720 TACAACTAGC TTGTCAAGTG CAGTGACATC TGCATTCCTG ACATTCCAAT CTGGAAATGG 780 TCTTTTTATA GTCGGTGTGG TGGGAGGATA CAGCAATGGA TACAACGCAG ACAGGATGAA 840 TTTAGAATTG CAAACTGGGT GGAATATGTT GTCCTTAATC TGAATAAAGC TCTTCTAGTC 900 TGGGACTGTT TCCCCAACAA TTCCGTCAAG TCTCTCGTTA GTTCCAAGAA GAGGAGGGTA 960 AAGAGACAGC ATAATGACCT CACTTCCACA CCCGCCAGCA CCCTCTGATA ATGAGCCTGT 1020 CCATGTGGGA CCTGCCCTAT GTTACCTCCC ATGATACATA AGTTGGAATC CACCCCAAGA 1080 ATCAGCTGTG TCAGCTGCAG AGTATCCAAG GGCTGGGGGT GAGTTAAGGG TTGGGGCCCG 1140 GCCACCTCAG ACTTAGTATT CAAAAAGTTC TTTTGACAAG AGGATCAGCC TCTTTGCTTG 1200 CCCCTTAATC TCTGTTGTTT GGCATCTTCG AGGAGCAACA ACCTTTTTTC CAGATTCACG 1260 TGCCAGACTT GTTCTTTCAC TTTCAGGAGG CCTCCATGCA GCGAGTTGGT GGTTGTATTA 1320 TCCAAGGCTA GCACCCTTCA CGTTGGAAAA AACTGATACT TAAGCTTCCA CATCTTAAGA 1380 CATTACTTTG AATATATTTT AAAGGGAGTA GAAGGGAAAG ACTATTTGGA ATGCTTTATT 1440 AAAATAGTCT TTCCCTTCTA CTCCTTTTAA AATATATTCA AAGAAAGTTG GTTCTTTATT 1500 CAAAGAAAGT TTGAATAAAA TATATTCAAA GAATGTTGGT TCTATCCATG GGGCATGGAT 1560 AACACAGCCC CAGAAATACT GACTGCCCCA TGGAGAAAAC CAACATAAAC CAAGATGCTA 1620 CCGAATTGCT CTACTCTTCA CACCAGAAGA CCTTTTTTTC CCCTCTGTGT ACTGAGAGCT 1680 ACTTTCTTCA GTAGTGTCAC CAGCACCCCT GCTAATTCTA AGCCTGCAAG CTCAGGGCTG 1740 CCCAAGTTTG GTGACCCCCA AATCCCCTTT ACACACTAAC TCCTGCATAA TGCACAGATC 1800 ACAGAAAACT AACAGATGCT 1820
|
| |
|
|
|