Tag | Content |
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EnhancerAtlas ID | HS105-08274 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr10:3709800-3711180 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr10:3710701-3710712 | TGTTGTGCAAT | - | 6.14 | KLF5 | MA0599.1 | chr10:3710975-3710985 | GCCCCGCCCC | + | 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 |
GH10I003667 | chr10 | 3709730 | 3711884 |
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Enhancer Sequence | AAACCATTTG GACAGACACT TGGTTTTTCT GTTCTCAGAA TTTTTTCTGC TCTACCCAAA 60 CTAGGGGTTG GCGTTGCATA GGTACCATGG GCACTTGGGG AATGCCTGTT TCGTTTCATT 120 ACATTGAGCG GTGATAAGAA GATTCAGACA CTAATTGGCA TTTTCCCCTA AATCTCCATG 180 GAAATGCAGT CTCTATTCCA GGGCACCATG TACTGCGAGG ACTTTATACT CGCCCTCCGA 240 GTGAAAGGAG AATGAAGGAA TGAATACAGA GGTGGACAGG GTCATTTCTG TCCCATAACT 300 GCATATTGTG GACATTTTTC TTTTCTGAGA TGGAGTCTCG CTCTGTCACC CAGGCTGGAG 360 TGTGGTGGCA TCATCTCAGC TCACTGGAAC CTTTGCTTCC CGGGTTCAAG TGATTCTCCT 420 GCCATGACAG GCACCCACCA CCATGCCCGG CTAATTTTTG TATTTTTAGT AGAGACGAGG 480 TTTCACCGTG TTGGCCAGAC TGGTCTTGAT CTCCTGACCT CGTGATCCAC CCACCTTGGC 540 CTCCCAAAGT GCTGGGATTA CGGGCGTGAG CCACCGTGCC CAGCCTTTTG TGGACATTTT 600 AAACAGCAGG GAAATTAATC CTGAGCAATA AAAAATAAAT AAATAAATAA ATAAATCATG 660 GTTTTTATTT GAATCTTAAA AAAACAAAAC GAAACATGTT TTCACTTTTT TTTTTCCTTA 720 TCTAATTTGG CTACTGCTTC ACTTTCTCTG CCACCTCTCT TACTGCAGTT TCAACTAAAT 780 GACTAAGCAA ATTAGATCTT GAGTTGCTTT TCTGGAATGC GGAGAGTTGG AGAATCAGAT 840 AAAAGTCGAG GTATCTCTCT CTTCAGCAGC TTCCAGATCG GGGGCTGGAG CTGAGCGGGG 900 GTGTTGTGCA ATCCCGTACT GTTGTCGAGC AGGCTTCAGT TCAGGGAGAC CAGGCAGGCT 960 GAGGCCCAGG AGAGTGCCCC CTTGCATCTG CCCTGGGGGA AACTCTAGAA GGGGTAGAGA 1020 AAATCCGAGA AGAAAGGATA TTTTTACACG GTAGGATTGT ATTTTTATCC CCGGAGGCTT 1080 GCTGAACGCA AGTTTCTGGG TAAGTTACAC AATACAGGAA AAGTAACTGT TTAGCGTATA 1140 GGTGATACGT GTTGGAGGCC AGAGCGCTCT GCAAAGCCCC GCCCCTGTGT GTGTTGTGTG 1200 GTCTGAAAAC AAAGAGCAGG CATCACCTTC TGGAGGTGAG GCTGGCCCGG GACTCAGATG 1260 GCTCTAACTC TGCGGGTCGC CTGCCCAGAG GCTGCACTTC AGCCGGCGGG GAAGCCAGGA 1320 TGGATCTTAA GTCATTCGAT TCTCAGGCCA TAGGTTGTTG CCAAACTGCA GCCTGGAAAA 1380
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