Tag | Content |
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EnhancerAtlas ID | HS042-29971 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr22:26843060-26844210 |
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) |
NFYB | MA0502.1 | chr22:26843098-26843113 | GATCTGACCAATCAG | + | 6.06 | RREB1 | MA0073.1 | chr22:26843210-26843230 | TTAGGTGGGGTGGTGGGGGG | - | 6.08 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 26844024 | 26844074 | chr22 | 26844138 | 26844192 |
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Enhancer Sequence | CTCAGTCCTT GGGTCTCCAG GGCTGGGCCC ATGATCCAGA TCTGACCAAT CAGTCTTCCA 60 AACTCTGGGC CACTGAGAGA TTGGGTCAGG GCTGGACACG TGATCCAAGT TCTTTTTCTG 120 GGACGACTGT GAAAGAGAGG CCACTTTTTA TTAGGTGGGG TGGTGGGGGG AGGTGAAGGG 180 AAAGAAGCTG AGAGAGAAAC CCACGGAGGC AAGCGGGGCC TGCGCTGTGG AGATCACGTG 240 AGTCCTGAAC GCAGCTCTGC CGAAAACCAG CTCTACCTCT GGACTTTTCT GTTACATGAG 300 CCAATAAGTG CGCCTTTTAT TCGTAAGCCA AGTTTGAGTT GTGGTTTCTA TCCTTGCCAC 360 CAAAAGTCCT AATCCACTCT GTGAGTGTCA AGTGAGGTTT TGGTAAGATG CTATTATGTC 420 GTGGTCTGGG TGGATGGGAG AGGTGCTCCA TACACATTGT CAGGATGTAA ATATGAGTAG 480 CAGAGGCTAA GCACAGAATG AGGTTTTTGA GGACCGTCAT GCCTGCTGCC AGCAACCTTC 540 CATAACATTT AACTCCCCAG CCGAATCTTG CTAACCAGAT GTAAACACAG GGAACAGGAC 600 AGAATAAGGC CACATATTTT AGAACTGCTG ACAGATGGCA GGGAAAACAC TCAAGCAGAT 660 TGCAGCATTA GGAGGCAGGA GGGAGCACAC ACAGGGATTG GTTTACTTTC CGCCTCTTTC 720 CCAGGCACAC ACGTTGCTTC TAACTTCTGG GTACCTGCCC TTCCCCATAT CTCCCCGCTT 780 CCCATACATT AGCCACCCCC ACGTTCGAGG TGAGGGCACC TGCTTCTTTG AGCATGGAGA 840 GCACTGTGCA CCCTACGAGG TTCCTTCCCC TACCTCATCC TTGTCAATTG CACATTTAAC 900 ACATGAGGAA ACAGGCTCAG AGCGGGCAGC TGACATGAAC AAGGTCACGC AGCCAGCTGC 960 AGGGCGAGCT GGAATTGGAA GCCGAGTATC CAGGCTCGCA GCACAGCGCA TCTTCTGAAG 1020 TCTGGACACA CATCCAGGAC TCACTTCCTC AACATGCAGA AGGACCACAC CCCTCCGGCC 1080 CCCAGGTCCT TCTCCCTGTG CTGGGAGGCC ATTTGCCTTC TCAGAACACT CAACAGGACC 1140 CTCCATTTGC 1150
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