Tag | Content |
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EnhancerAtlas ID | HS043-36976 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr6:76484690-76485870 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr6:76484729-76484744 | TGAACTCCTGACCTC | - | 6.22 | TEAD1 | MA0090.2 | chr6:76485650-76485660 | ATGGAATGTG | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGTAGAGATG GGGTTTCACC ATGTTGGCTA GGGTGGTGTT GAACTCCTGA CCTCAGGTGA 60 TCTGCCCGCC TCAGCCTCCC AAAGTGTTGG GATTTCAGGT GTGAGCCACC ACGTCCGGTG 120 AGAAATTATT TTATGTATAC AAGATTATCC TTTGATATTA TCATTTATAC ATTGTAAAGA 180 AGGTGCCGTT TTTGCAGTGC CAGTAGTCCC AATAGTACAG TGAGTTCTCT CCATTAAGTA 240 TAATCCTCCC GGGATTTGGG ATTTGTGGTT GCCATGTTGC CACTGGTAAG GTTAGAGTCT 300 TCATAATAGC CGAGCTGAGC AAATTCTTCC ATAGCAGGCA CAGAAGAAAT TGTGCAGGTC 360 ACCTCTGGGT CAAGAACTTA TACAGAAGAT AATGCTGCCT TGGCTTCTGG CACTGGGGGG 420 TTGGGCTGGC CCTTGTCTCT GGATGCTTCA AATGAGATGC ATTGGCAACT GTCCAAATTG 480 GAAATAAACT TCTCAGGTTC CAGGCCTCCC TTGGCTCTGA GGCCTGTGTA CGGGAGACAG 540 CAGCATCTGG GGTGGATGCC TGCTTTACCA AAGATCAGTC TCCAACCTTG AGGGCTGTGC 600 TGCTTATCTG TTGACAGTTG GGGAGCAGAT TGCCAAATAC AGGTCAGGAG GTGTATATGA 660 CCTATAAAAG GGTCTTCTCC TTTTCCAGTT AGGCTGCTCA GGGCTTCAGC TTTATTCAGT 720 TGTTCAATTT TATTTTGTTA TTGTTTAACA ATTCTGATGT CTAGTTAAAG TTTAGTAATG 780 CATTGGTTTG AGGGAATATG GTCTGAGTCA CAAATCCATA GAGCTACTAT TATGCAGGGA 840 TGGAAAGTGG CTTTTTAATG GAGTTGACCA ATCTGTTCCT AATATGAGTA ATTAGTGATA 900 TTTACAAGGT AGCTTGAATC CTGATAGGCA GAGCACACTG GTGTTTTTCG TTTTGTTTTC 960 ATGGAATGTG TAGCGTATCA TTTCTTTAAG ATTTTATCCT ACTCATCTTT TAATACTCCA 1020 TTCAAAATGG AGTTCCTGTG TCCTGGTCCT TGTCCTTCAC TGCTCCCCCG AGCACCATTT 1080 CTAGGACTAC TTTATGTCAG TACTATAAAT ATTGCTGTAC ATTGTGGTGT ACTTGTCTTT 1140 CTCCTTTTGT AAGTTGTAAA CGCTTGATTT TATTCTTGTG 1180
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