| Tag | Content |
|---|
EnhancerAtlas ID | HS116-32490 | Organism | Homo sapiens | Tissue/cell | Left_ventricle | Coordinate | chr7:158908170-158909290 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr7:158908555-158908566 | AAGCACTCAAG | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 158908170 | 158908947 | | chr7 | 158908351 | 158908780 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH07I159115 | chr7 | 158908021 | 158910019 |
| Enhancer Sequence | CAAAACTTGG CAGAGGGGTA GAGAAGGAGC CTCCTCTGAT CTCAGCAGCC TCTCACCCAA 60
AGTCATGGTC AGGGCTTGGC AGGCAAGCCT GGCTGAAACA GGACTTCAAT CTGTCTGCTT 120
TGGACGTCTC ACCTTAATTA GAACACAGCA AGGTGTGTCA CCACTAGTGC TTAGAATGTG 180
TCACCAAAGC CCCTGAGCTC AGGCTTGCTG GCTGGGTCGT CCCTTGGCCT TTTCAGATCA 240
CGCCCCTGAC GTGCTGCCTG CAGCCTCCAA GGTCAGGGTG CTGGGAATGG AGGAACTCAG 300
GCTGGCAAAG CTGGTGTCCG AGCTGCCCCA CGCCCTCTAG CTGCCCTTCT CACCTCCGAT 360
TCCGTTGCTG CTTCTAGTCT TTCCTAAGCA CTCAAGTCAG CTTCCTGGGG CCACGTGCTT 420
CCTTTCATAT ACCAGCTTAG GCTGCGTTTA GCTAAGTAGT CAGGCAGCAG GTGTGAGGCA 480
TCGATTTGTT TGTGAACAGC AAGGTCTCCC AGGGCTGCTG TGAGCTCCAC CCATTGGACA 540
TGGGGTCTTG TCCCCACCCT GCTATGTGGC CCCGTGACCT GTGCTGACCC CTCGGACTGA 600
CAGGCTCTTC CTTCTGGAAG GTGGTCATCA CGGAAGGGCT GGAGCAGTTG GTGGGAGCCC 660
TGGTCGGAAA GGCTGCAGGG AGAAGGCTTA GGCACCTGCT GAATGTAGGA AAGGAACAGC 720
TTGGGTGACG TGGGCAGAAC CTTTTGGGCC AACCTCAGAG CCTTGGGAGG AGCCAACTAC 780
TAATTTTGAA GCCAAGTTTC AGGAGATTTG TGCCATAGCC ACACATAACC AGGAGCAAAT 840
CTTCCTGGGA AGCAAACAGC TGGCAGAGCA GAGTCACATG GGCCCTCCAG AGGGCACTGC 900
AGTGGGTTGG CACCGGCATG GTCAGTGCCC GCATGGTCAG TGCATTTGGG AAAGCAAGTG 960
GGCAGAGTGG GCAGTGACCG GTGGTCAGTC ACAGGGGCTG GTCAGGGGGC TGGAAGCTTC 1020
CAGGCAATGA GTGACTTTTC AATGTAGACT GGCAGTGGTG GCTTCCTAAT TTTTGCTTGA 1080
AAATCAGCTT AGTCTCCTGA AAAAGACACT GTAGACTAAG 1120
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