Tag | Content |
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EnhancerAtlas ID | HS191-23236 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr20:34019250-34020170 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr20:34019901-34019912 | TTTGTTTACTT | - | 6.62 | RREB1 | MA0073.1 | chr20:34019386-34019406 | TGGAGGTGGGTGGCTGGGGG | - | 6.94 |
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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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Enhancer Sequence | TTTTGAAAGT GTGCAGCCTT CAGAGCTGAG TGACCATGGG TGGAGAGTGT TTGTGAACTC 60 TCAAGTATGA TAGATGCCTT GTACCCTTTG GGGCAAGAAT GAACAGTACC AGTTTGCAGC 120 TTGTTATGGT TGCGGTTGGA GGTGGGTGGC TGGGGGAGAG TGTTTTCCAA GGAGGCAGCT 180 GAACAGATCC TGTGGTTAGG ATGGGTGACC TGATCACATC CCCAGAGTCT GGGTGGGAAA 240 ATGCAGGAGG GTCCACAGTC TGAAAGAGAG CCCTAGGGCA GGTTGTGGTG GTAGAGGAAA 300 CTCCTAGCGT GTCAATCCAA ACAGTCCACT GGGAGCCCAG GCCTTCAGTA GGAGGGGCAT 360 TGTGGCTCAG ATGACATGAA CCTCTCTGAC TGGGCTAAGG CAGAGAGAAG CTCCAGTTCG 420 GTCAGAACTT TCCAAGAAAC CAGGGACACG CAGCCCAGGA AATAATACCT GTGGGAGTCA 480 GCCCCACCTG TGACCCATTC ATCTTATCTA TCTGCCCTTG GGTTTCTGGC CCCCCAGTTT 540 CTACACTGCT CTCCCTGGAT CCCCAGCCCA CTCCTTGGCT TCCCCAGCAC CTCCCTTCCA 600 GGCCCATTCT CCCCTCACAC ACACCACAGC TCTGTCTGCC ACGGCAGCTC CTTTGTTTAC 660 TTCCAGAGCT GCCAGGCCCA CCACTAGCCA AACACAACGA AGCCCAGCCA GTGAGGGGAG 720 GCTCCAGGCT CAGTCTGTCC CCTCAGAGAG AGGTAATAGC CTCCAGACCA AGGAGGCAGC 780 TCAAAGGTAG GCTGCCCCCG CACTGTGCCC AAGCTTCAGG CCTAGAGGGA AAGGGCACAA 840 GGTCTGCCCA TAGCTGGGTA GGAATCCCTA CTGTTGAAGC AGCTTTGGTG AGGAGCCCCA 900 GGAATCAAAG ACCCAGCTGG 920
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