| Tag | Content |
|---|
EnhancerAtlas ID | HS043-44309 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr9:131048310-131049540 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr9:131049507-131049522 | AAGGTCAGGAGTTCA | + | 6.04 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGTGAGTAG TTGGGACTCC AGAGCCACAA GCAGGCATCA TAGGGTGTCG TCTCGCCTAG 60
GGGTGTTGGG TTTTGCTCCT GGGCCTCCCA GCTTGCCAAC CGTCACACCC TCAGCAGTTG 120
GCCTGCTCCT AGGCTGCCCC AGCCCCTCTC CTGACCAGCC TCTGGTCTCC CTGGCCACCT 180
AGGTTTGTTC CTCAAGTACA GAACCTGCTT TGGAGCCGCA GCCAGGTTTG AGCGGGGCTT 240
GCCCATCTGC CAGACTGAGA ACTCAGGGTC TCCCCAGTCT TCTGGGACCT ACTCAGAGTG 300
ATCAAGATAC CGTCCATGCC TCAAGTGGCT AGCTTGCTAA AGAGGCTGCA AGTGCAAGGG 360
TGACCCTTTG TGTCTTAAGG AAGTATTTTG TTTCCTCCCT GAACAAAATC TTGCTATCTA 420
GAGGGCTTTA GCCGAGGCAC CAACACCTGT ATGTCATGCT GGCTAGGACA GCCTACCTTG 480
GAGGTGAGGA AATGTGCAGG CGGCCCCTAC AAACCCTTCA GTTCCATCCC CTGGCTTGGA 540
GTGCTGGGTA CTCTGATGTT CAGCAGCCAG TGACTGCTGG GGTAGTGTTC AGAGCTGGGC 600
TGTCTGCCCA GTTGCTGCGT GAGTTTTGGC ACTTGTTGCA GAAATGCCTT CAGCATCCAG 660
GATTCCACGG CAGGGAGGGC TTCTCTGTGT TTCACTGGAC GATGGGCCCC AGAGGAGGAG 720
AGGAAAAAAC TGGAGGTGGG AACTATAGAT GGATGAAAAG AGCGGGGTGA TCAGGGCCCA 780
AGAAGATGGG GGTGTGAGGG GAGTGTAGCC TAGTGGTTAA GAACACAAGC TCAGCCGGGC 840
GCAGTGGCTC ACACCTGTAA TCCCAGCACC GTGGGAGGCC GAGGTAAGTG GATCACCTGA 900
GGTTGGGATT TCAAGACCAG CCTGACCAAC ATGGAGAAAC TGTCTCTACT AAAAATATAA 960
AATTAGCCAG GCATGGTGGC ACATGTGTAA TCCCAGCTAT TTGGGTGGCT GAGGCAGGAG 1020
ACTCGCTTGA ACCCGGGAGG CAGAGGTTGT GGTGAGCTGA GATCATGCCA TTGCACTCCA 1080
GCCTGGGCAA CAGGAGCGAA ACTCCATCTC AAAAAAAAAA AAAAAAAAAA AGGCCGGGCT 1140
CGCTGGCTCG CACTTGTATC CCAGCAGCAC TTTGGGAGGC CGAGGCAGGT GGATGACAAG 1200
GTCAGGAGTT CAAGACCAGC CTGGCCAACG 1230
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