Tag | Content |
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EnhancerAtlas ID | HS042-49348 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chrX:9895210-9897040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chrX:9895671-9895692 | ACAAAAAAAGTGAAAGTGATT | - | 6.95 | Myod1 | MA0499.1 | chrX:9896301-9896314 | AGCAGCTGTCTCC | + | 6.21 | PRDM1 | MA0508.2 | chrX:9895680-9895690 | GTGAAAGTGA | - | 6.02 | SCRT1 | MA0743.1 | chrX:9895694-9895709 | AAGCAACAGGTGCAT | + | 6.41 | SCRT2 | MA0744.1 | chrX:9895694-9895707 | AAGCAACAGGTGC | + | 6.82 | SNAI2 | MA0745.2 | chrX:9895698-9895708 | AACAGGTGCA | + | 6.02 | SREBF1 | MA0595.1 | chrX:9895893-9895903 | GTGGGGTGAT | - | 6.02 |
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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 |
GH0XI009927 | chrX | 9895609 | 9896869 |
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Enhancer Sequence | AACCCCATCT CTACAAAATA ATTTAAAAAC TAGCCAGGCC ATAGTGGCAT ACACCTGTGG 60 TCCCAGCTAG TCAGGAGACT AAGGCAGGAG GGTCACTTGA GCCTGGGAGG TCGAGACTAC 120 AGTGACCCGT GATCACGCTG CTGCACTCCA GCCTGGGCAA AACAGCAAGA CCCTATCTCT 180 GTCTCCAAAA AAAAAAAAAA AAAAAAAAAA AAAAAAAAAG TAGGTGAGGA GGACCCTGTG 240 GTGTGTGTTC CTTAAGTCAT CTGCAAGATT CAGAAATTTT CCCATCCTCC TTGCTAAAGA 300 TAATTGTTAA CCCTATTCAG AAAACAGTGG TGGATTATTG ATTACAGAGC AGTTCAAAAC 360 TGTTTAGTTG TGTTGGGAAC ATTCACACAC AAGGTCCTTT CACGGAGAAC TTAACCATGG 420 TGTCTTGAAA AAATGCAGCT TCTCACCTTT TAAAATTCCG CACAAAAAAA GTGAAAGTGA 480 TTGAAAGCAA CAGGTGCATT TACATTGTGT TCAAGTGAGG GCATAACATG ATGCATGTAA 540 TAAATATTTG CTTGCAAGGC CCTGAAGGAA ATAGCCCAGA TCCCTGCCCT CTGTAGAGGT 600 GCTTTCAGCC CAGGGAGGAG CGTGGAGGCA GGTGAGCAAT GGGATGATTT GAGAGAGTCC 660 CCTTGCTGGG GCGTGACCTG GAGGTGGGGT GATGTCAGGG CAGGACTGGG GGAGCTGAGG 720 GCTGTGTGGA GGCAGGGGCA GTGCAAGGAG ACCTTGCATT CAGACATGGG GCTGGCTGTC 780 TCGTCGTGGA AGCAAAAATA GAGTAATGCC AGCAGGATCT CTAGAGTGTT TGTTTTTTTC 840 CTAACAGTGG TTTCGGTCCT GTCATAGCAT GCTGGGTGAC TGAGTACACT AATGGTGGCC 900 CTTCCTGCAG GTTTGTCCCC TTCATATAAG TTCTGTTTGG CTTTGAGGTG CTGTTTTAGA 960 GCTTCATGCT CTGTCTCCTT CAGTGGCGGC CAGCCCAGGG AGAATGGCAG GGCCGTGGGC 1020 TCCATGTAGC AGATCTCTGA AGCCACTGCT GCTTGGAGCC TGCCGGCCCT CTCCCCTCTG 1080 GGAACTGTGC AAGCAGCTGT CTCCTTGGGA ACGTGGCATT AGCATGTTTT GCATGAGAAT 1140 GAACACCAAC CAAGGCTGAA TATCAATTGG ATCCTAGAGT GCAGCTGCCT TTGAAATGTT 1200 CCTTTGTGTG GCCGAACTTC CTGCTGCAGT TGATTCCTGG AGCTTGTGCG AAGACACAAA 1260 GTCTTAAGTC ATCTTAGTGC CTTGCTTACT CTATCTCTGG ATCTTGCTGT CACCATTTAT 1320 TTTATCCTTA GAAGTATGGC AAAGAGAAAT GCATACATAT ATGCAGAGAC ACATGTCTAC 1380 ACACAGGCAC AACAGAGACA CACGTACCTA CACATGCACA CAACATATAC AACCCGGGCA 1440 CACACTCACA ACATGCATCT CCACACAGAC ACAACACAGG CACACATACC CACACACGCA 1500 TACAACGCAC AACACAGGCA CACACATACA ACACACATGG ACACAGAGAC ATGCATCTAC 1560 ACACATACAC AACCCAGGCG TACACATACA ACATACATCT ACACACAGAC ACATGTGTAC 1620 ATTCAGACAC AACCCAGACT CCTACATCTA CACATGCAAA CAACCAGACA TACACATACA 1680 ACGTACATCT ATGCAGAGAT ATACATCTAC ACACATACAC AGCGCAGGCA CACACACAGT 1740 GTACATATAG ACAGACAGAC ATTTATACAC ATACAACATG CATCTACACA CACAAAACAT 1800 AGACACAGAC AACATCTACA CATAGATCTG 1830
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