| Tag | Content |
|---|
EnhancerAtlas ID | HS098-27095 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr19:10512880-10514050 | 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 | GTAATGCAGG CACACTCATT TGGGGTAGCA GGAGGTTAAA CCTTTAAGTC TTAGTCATCC 60
CATTGGCTCG TGAGCACTGA GAGGGTGGTG GGACATGGAT CACCCAGGCT TGGGATTCTG 120
GGGTCTGGAT TCGGGACCTC TGTTGTGGTC AGATAGAAGA AGGGGTGGTG AATTTAGAAT 180
CAGACCAGGA GAGTCCCTGG ATAAGAGCAG GGACAATTTG GGTCACAGAG TAGCTAACAG 240
GCTGGGGACA AAAGGTGGGG TGGGTTTGGG GTTCTGGGCT TGAGTTAGGG GAGAGTTTCC 300
AATGCTGGCT GAGGCTCATA CAGGAAGCCA GTCTGGGAAG TGGGTGGTGA CAGGGTCTGC 360
AATACCAAGT AGGAGCAGGG GCTCTGGCTA GGCCGGAAGC CACGTGGGCA GGATTTCCTG 420
GTATAATGGG AAATGGGTCT ACCGGAGGCC AAAGGAGAGG CTGGAATGTG AGGCTCTATC 480
GGGTTGGAGC TGGTAGTTAG ATCCAGAGGG GAACCAGATT CCAAAACCCA AGTACTCGGT 540
GAGACTAAGG ATCCTGAAGG GGGACGGTTC TACACTCTAG GAAGGGGGTC CTGGGTGTGG 600
GCAGGGACAG GAATATCAGA GTAGCACAGA GTTCCTTGTT CCGTTTAGAA AAGGAGTGGC 660
GACTCCGGAT CTGAATGGGA ACCCCGGATC AAGATCCCGG AAAGTAGATC CCGGGACAGA 720
CCAAAGTATT GGGGGTCCAG ACTACGGAGG TGGGGGGGCG ATGGGAGATC CCAGATAGGA 780
AGTGAATACC CGAATAGGAT GAGGGATCAT CTAGAAGAAT TTGGGGTCCA AACTTTGAGG 840
CAGAGTTCTG GGTATAAATG TTAACTGCCG AACAGAATTA GGGAGAACCC CCAAGACTCG 900
TCTAGGGGAC TCCAGACTAT GAAGAAGTTC TAGGGGGTGA ATAGGGAATC CCACGCAAAA 960
ATCGGAGCAG GGAGTGGGGG AGCGGAGATC CAGGGCAGGG ACTCAGGGTC CCAATGGTAC 1020
TGGGGTCCCG GAGTTGAATC GAAGCTCCTG AAAATCCAGA CTGGGGGGGT GAGAATCCTA 1080
GGTGTGAACA GCGGGGTCCC TGGGCAGTAT CGGGGATCAC AACTCCGAAG CGGGGTCCGG 1140
GAGTGGGGAA AGGGATGGGC GCGCGCGCCT 1170
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