Tag | Content |
---|
EnhancerAtlas ID | HS043-24975 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr2:234082300-234083650 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr2:234082361-234082376 | GAGGTCAAGAGGTCG | + | 7.26 | TFAP2A | MA0003.3 | chr2:234082757-234082768 | TGCCTGAGGCT | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGCACCGTGG CTTATGCCTG TAATCCCAGC ATTTTGGGAG ACCGAGGTGG GTGAGTCACC 60 TGAGGTCAAG AGGTCGAGAC CAGCCTGGCC AACATGGCAA AACTCTTGTC TCTACTAAAA 120 ATACAAAAAT TAGCTAGGCG TAGTGGTGTG CACCTGTAAT CCCAGCTACT TGGGAGACTG 180 AGACAGGAGA ATCGCTTGAA ACCTGGAAGC AGAGGTTGCA GCGAACCGAG ATGGCGCCAC 240 TGCACTCCTG CCTGGAGCAA GGCTCCGTCT CAAAAAAAAA AACAAAAACA AAAACCATAA 300 ATGCACACAT TAGCCTAGGC TGAAACAGGC TCAGGATGGT CAATGACATT ATCACCCACC 360 TCCACATCTC ATCCCATGGA AGGTCCTCGG GGCAATAACA TGGAGCTGTC GTCTCCTATG 420 ATGACAATGT CTTCTTCTGG TTACCTCCTG AAGGACCTGC CTGAGGCTAT TTTATAGTTA 480 ACATTTTCTT ATAAGTAGGA ATACACTCTA ATGATAAATA ATATCGTAAA CACGGAAATG 540 AGTGACAGTT GTTTATCATT ATCAAATATT ATGTACTGAA CAGAATTGTA CTGTTATGCT 600 TTTACACAGC TGGCAGTGCA GTGGGCTGGT TTGCACCAGC ATCCCCAGAA GCATGTGAGT 660 AATGTGTTGC GCTGTGACGT GATGACAGCT ACAGCAGCAC TACGTGATGG GGATTTTCCA 720 GCTCCATTAT AATTTTGTAG GACCTCTGTC CTATATGCAG TCCATTACTG TGGTACATGA 780 CTATTTGTGG AGCCCCACGG GTAATTCTCA GAGGCAGCTG ATGCCGAGAA CTGCAATGTT 840 AAGAAGTAAC TGTTTAGGCT GGGCACAGTG GCTCATGCCT GTATTCCCAA CACTTTGGGA 900 GCTGAGGCAG GTAAATCATT TGAGGCCAGG AGTTTGAGAC CAGCCTGGCC AACATGGCGA 960 AACCCCATCT CTACTGAAAA TACAAAAATT AGCCAGGTGT GGTGGCGCAC TCCTGTGATC 1020 CCAGCTACTC AGAAGGCTGA GTCAGGAGAA TTGTTTGAAT CCGGCAGACA GAGGTTGCAG 1080 TGAGCTGAGA TTGCCCCACT GCACTCCAGC CTGGGCAACA GAGTGAGACC CTGTCTCAAA 1140 AAAAAAAAAA AAAAAAGGAC TTAACTAACT GTTAGGCAGA ATCAATGAAA ACTAAAAATG 1200 CACCTATTCT ATGATTCAGT AATTCCGCTT TGGTGTGTGT TCAAGAGAAA TTTGTATATT 1260 TGTTCACCAA AAATAGGTAT AAGAATGTTT AGCCGGGCAT GGTGGCTCAC GCCTATAATC 1320 CCAGAGCTTT GGGAGGCCAA AGCAGGTGAA 1350
|
| |
|
|
|