| Tag | Content |
|---|
EnhancerAtlas ID | HS085-01535 | Organism | Homo sapiens | Tissue/cell | Heart | Coordinate | chr19:10512850-10514050 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr19:10513843-10513864 | GGAGCAGGGAGTGGGGGAGCG | + | 6.17 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAAAAAAAGG AATACAACAG ACACTGGTAT GTAATGCAGG CACACTCATT TGGGGTAGCA 60
GGAGGTTAAA CCTTTAAGTC TTAGTCATCC CATTGGCTCG TGAGCACTGA GAGGGTGGTG 120
GGACATGGAT CACCCAGGCT TGGGATTCTG GGGTCTGGAT TCGGGACCTC TGTTGTGGTC 180
AGATAGAAGA AGGGGTGGTG AATTTAGAAT CAGACCAGGA GAGTCCCTGG ATAAGAGCAG 240
GGACAATTTG GGTCACAGAG TAGCTAACAG GCTGGGGACA AAAGGTGGGG TGGGTTTGGG 300
GTTCTGGGCT TGAGTTAGGG GAGAGTTTCC AATGCTGGCT GAGGCTCATA CAGGAAGCCA 360
GTCTGGGAAG TGGGTGGTGA CAGGGTCTGC AATACCAAGT AGGAGCAGGG GCTCTGGCTA 420
GGCCGGAAGC CACGTGGGCA GGATTTCCTG GTATAATGGG AAATGGGTCT ACCGGAGGCC 480
AAAGGAGAGG CTGGAATGTG AGGCTCTATC GGGTTGGAGC TGGTAGTTAG ATCCAGAGGG 540
GAACCAGATT CCAAAACCCA AGTACTCGGT GAGACTAAGG ATCCTGAAGG GGGACGGTTC 600
TACACTCTAG GAAGGGGGTC CTGGGTGTGG GCAGGGACAG GAATATCAGA GTAGCACAGA 660
GTTCCTTGTT CCGTTTAGAA AAGGAGTGGC GACTCCGGAT CTGAATGGGA ACCCCGGATC 720
AAGATCCCGG AAAGTAGATC CCGGGACAGA CCAAAGTATT GGGGGTCCAG ACTACGGAGG 780
TGGGGGGGCG ATGGGAGATC CCAGATAGGA AGTGAATACC CGAATAGGAT GAGGGATCAT 840
CTAGAAGAAT TTGGGGTCCA AACTTTGAGG CAGAGTTCTG GGTATAAATG TTAACTGCCG 900
AACAGAATTA GGGAGAACCC CCAAGACTCG TCTAGGGGAC TCCAGACTAT GAAGAAGTTC 960
TAGGGGGTGA ATAGGGAATC CCACGCAAAA ATCGGAGCAG GGAGTGGGGG AGCGGAGATC 1020
CAGGGCAGGG ACTCAGGGTC CCAATGGTAC TGGGGTCCCG GAGTTGAATC GAAGCTCCTG 1080
AAAATCCAGA CTGGGGGGGT GAGAATCCTA GGTGTGAACA GCGGGGTCCC TGGGCAGTAT 1140
CGGGGATCAC AACTCCGAAG CGGGGTCCGG GAGTGGGGAA AGGGATGGGC GCGCGCGCCT 1200
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