Tag | Content |
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EnhancerAtlas ID | HS059-48601 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chrX:2243000-2244140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
YY1 | MA0095.2 | chrX:2243252-2243264 | CAAGATGGCGGC | + | 7.22 | YY1 | MA0095.2 | chrX:2243301-2243313 | CAAGATGGCGGC | + | 7.22 | YY1 | MA0095.2 | chrX:2243350-2243362 | CAAGATGGCGGC | + | 7.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH0XI002324 | chrX | 2242842 | 2243935 |
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Enhancer Sequence | TAGTAGAGAC GCGGTTTCAC TGGTCAGGCT CGTCTCGAAC CCCTGACCTA ATGATCCACC 60 CGCCTCAGCC TCCAAAAGTG CTGGGATGAC AGGTGTGAGC CACTGCGCCC GGCAGCTTTT 120 CTCTTTAACG AAAAGCAGCC CCAAGTCATT TTCTAACAAT GAACAGCCTG TCAAGTCGAG 180 CTGCAGACAT ACACAAGCCA GCTGGGAGCT TGTACGGGTG AATGTCGGGA GGACCTAGGG 240 ACTAGACACG TTCAAGATGG CGGCTCCATC TTCCCGGGAG GAACTAACGA CTAGACACGT 300 TCAAGATGGC GGCTCCATCT TCCGGGCAGG AACTAGGGAC TAGACACGTT CAAGATGGCG 360 GCTCCATCTT CCCGGCAGGA ACTAGGGACT AGACACGTTC AAGATGGCGG TTCCATCTTC 420 CCGGCAGGAA CTAGGGACTA GACACATTCA AAACGGCGGC TCCATCTTCC CAGCAGGAAC 480 TAGAGACTAG ACACGTTCAA GACAGTGGCT CCATCTTCCC TCCTCTTTGT CAGCCACATG 540 TAAAGTAAGA AAAACAGGAC CGAGAGCCCC GACCAACTAC AAAGCCCATT TGCATAACCG 600 ATTAGGGTGG GCAACCAGCC TTTCCTGTGG GCTATGTAAA TGTCATGCTT GATGGAACCA 660 ATCTCTCGGA GAGCCCCGAC CAACTACAAA GCCCATTTGC ATAAACGATT AGGGTGGGCA 720 ACCAGCCTTT CCTGTGGGCT ATGTAAATGC CATGCTTGAT GGAACCAATC TCTGAGCTCT 780 ATGTAAATGA GACACCGCCT CCTCAAACTG GACTATAAAA TCCATCACAT TTGGTGCCAG 840 CTGGTCCTTT CCGCTCGGAG ACCCCTTTCT CTATAGAGAA AACCATTTCT CTTTCTCTTC 900 TCCTGATTAA ACTTCCACTC CTAAACTCCT CGTGTGTGTC TTTGTCCTAA ATTTTCCTGA 960 TGCCCAATGA CGAACCCCAG GGTATATACC CCAGACAACG TAGCCACTTC ACTAACATGT 1020 AGAGAGCTTG CGCATTTTAA TTCCTATCCT CACAATAGGC AAAGAGCAGA ACATACTGAA 1080 AATCAGCAAC TCTGCGATCC ATCAGAAAAT AGAGATCACA AGACGAAATG CTGCCTGAAG 1140
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