| Tag | Content |
|---|
EnhancerAtlas ID | HS043-23366 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr2:111530750-111531900 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxq1 | MA0040.1 | chr2:111531752-111531763 | AATTGTTTATT | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 111530894 | 111531400 | | chr2 | 111531400 | 111531516 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I110773 | chr2 | 111531161 | 111531310 |
| Enhancer Sequence | ACATATATTA TGACTATTAT TTTTATCAGA ATTTTAGGTA ATCTCCGTTT GAGGTATTTT 60
TGTATTTGGA GAAATATCAG GTGGGTGATC AGATCTAAAA TGGAAGAATG TTCTAAGGTC 120
AGCTCACCTT AGAAGGTGTT TGGGAATGCC GGGGAGGGTG GTTACTTTTC TACTCAGACC 180
TTGAGAGAAG AAACAGCCTT TCCTGGGAAG CGTTTACATT TAAGCCCTGA GTGTGTTGTG 240
CAAAAGGAGC TGAGCCAGGA ATCTGCCAAG AGGCTGAGAT GTCTGTCCTG TCCCAGTCCC 300
AACTCACCCA GGCCCCACCC TGTTGCCCAC AACTTCCAGT GCCAGCCCCA GCGAGTGCTG 360
CAGACTGTGA CCGCTGTACT CCCCCACCCA TCCCAGGACT GGCTCCTGAC CGACGGACAG 420
ACTCTGAGCT CTTGGCTCTG CCGCCCTGGC CTTGGCTCCC TCTTGGGCCT CTGGCTTCTG 480
TTTGTACTGG AACCCAGGCT TCTCCTAGTG GGCTGTGACA GGCTCCCCTG GCTCTTAGTC 540
CTATATACTG TCTTTGGCAG GAGTCCCTGT CCCAGCTCCA GCTCCACAGA CTTGGACATT 600
GGCCACTTGG CCAGCACTTT GGTCAGGCCA GCCCTGGCCG CCTGGGATAT CTTGGAGGAT 660
TTGGGCAGAG ACAACAGGAC AGAGAGGTCT GTTTACAGAA GTCCCTCTAT GTAGATTGGC 720
ACCTGAATGC AGTTGTCATC TGTGATAGCC ACAGGGATTA CTTGAAAGCG GGGCATGGCA 780
GGGAGTGAGC TGGACCTGCC CTGGGATTCC AGTGCAGCTG GAATCATGGT GCTATTTGTT 840
TTTTGACACT GCAACCATTC TGCATTAAAA AACACCCTTT TCAATCTAAG CCTTCATTAT 900
TACTCGTGCA GTGAAATACT ATGTAAAAAA CCAATAATTA TTTCTCGCTA CCTTTTGCTA 960
AGTCCCTTCC GTGTGCCAGG TGAGGTGATT CGTTCATTTT ATAATTGTTT ATTGAGCACC 1020
TACAGTGAGC CAGGCATTGC TCAAGGGGCA GTGAACAAAG CAGGCAGAAA TTACCTGTCT 1080
CGATGGAGCT TACATTTTTG TCTGGGAGGA GTCAGACTAT AAACTAATAA ACAAAGTAAA 1140
TTTCTGGTAT 1150
|
| |
|
|
|
