Tag | Content |
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EnhancerAtlas ID | HS060-25000 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr3:124402540-124404800 |
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) |
ESRRB | MA0141.3 | chr3:124404295-124404306 | TCAAGGTCATA | + | 6.62 | Esrra | MA0592.2 | chr3:124404294-124404305 | GTCAAGGTCAT | + | 6.32 | Esrrg | MA0643.1 | chr3:124404295-124404305 | TCAAGGTCAT | + | 6.02 | Klf1 | MA0493.1 | chr3:124404055-124404066 | AGGGTGTGGCT | - | 6.02 | Nr5a2 | MA0505.1 | chr3:124404291-124404306 | GAGGTCAAGGTCATA | + | 6.36 | RELA | MA0107.1 | chr3:124402705-124402715 | GGAAATTCCC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr3 | 124403308 | 124403810 | chr3 | 124403831 | 124404003 | chr3 | 124404078 | 124404324 | chr3 | 124404471 | 124404702 |
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Enhancer Sequence | CTGGCCTCAT CCACAACACA GACTAAGTGC AGACGTTATC CTCAGTCATA TACCAGCCAC 60 CAGATATTTA GCTTGGGGAG TTAAAAACAG TGTTGGGATC TTCTGGGAGA GGGCTCTGAA 120 AGATTAGAGA GAGAAAGCAC TTGGGAAGGT GAAGCTGATT TTGGAGGAAA TTCCCCATTG 180 GAGTAAGAAT CACACTTTCA GAATAAACAG AACCTGGGAA ACATTTAGTT AACCTCTTCA 240 TTTATTTATT TTTATGTTTT GTAGTAAAAT ATACATAACA AAAATTTACC ATTTTAACCA 300 TTTTTGAGTG TGTGGTTCAA TGGCATTAAG TCCCTTCACA ATGTTATACC ACCATCACCA 360 CTATCCATTT CCAGAACGTT TTCATCATCG CAAACAGAAA TTCTTTAGTG GACCCAGTAA 420 ACAACTCTCT ATTCCTCTCC ATCCCTGCAG CCCCTTCACC TTTAACAGAG CCACAGGAAC 480 TTGTCCTTTT CTGTTTGAAA ACTGGAAGGT GCTCTAGTTT CTGAGGCAGC TTCTGGTTTT 540 TCTGCTTGCT ATTCCCCCAC CTACACCATC CTGCGGCCAC TTGGTACCCC ATCTCCAGGT 600 TGATTTTAAC CTAAAACACA GATCCTGGCA GACGAGAAGA CCTAACTCCT AGTGCCAATT 660 TTTGTGTATA AGTGTGTTAT TCCATTTTCC AGCTCAATAA AAAGGAATAT CATTTCTGCC 720 CATCTTGGCT TTCCGAGGCT GAAGTGTAAC TTAAACAAAA ACCACAAAGG CAGTATCACA 780 TGGAAAACTG GAACAGGAGT CAAAAACCTG GATTCTAGTT TGGATACCGC CAGCTATGAG 840 ACTGCTGGCC AGTTAGCCTT TCTGAGCCCC AAGTTCCTCT GGAAAGTTGC ACAGCTCCAA 900 GTGTACAGGT GTTTATACAG TGATGTGTAA CCCTTTGAGC ACCATGCACG TCTAAGGTGT 960 GCTAACAAAG GACTTTGCTC TCCAGCACTT CTGACTTTGA AAACATTGAG ATCCCGACCG 1020 AAGAGGACGT GGAAGATTCT GTGCTTTGGC CAGCAATTCA CTTTTCAGGG GGTGTGGCGG 1080 GAATGGCCTG GGCAGATTTC CTTCTGAGAC TCAACTGGAG TGTCCACTCC TGGCTCTGGG 1140 AAGTTTGAGC GGCCAGAGCT GGTACTTTTT TCCTTCCTCA AACCTACAGT TCCCTGGCCC 1200 GCCTTTCATG TCCTCAGATC TGAAGAGCCA GCCTACTCCC CGCACCCCAC TCCCCGCCAA 1260 CTACCACATC AGCTACTCTG GCCTCCTTAT CCTAGAGCTT CAAAATAACC CGGCCAGACG 1320 GATTGAAGGA AACTTTTACA CCCCCAGCCA GGTGACCAAC CTCCTGGCAT CCCCAGTGTG 1380 TGTCCACTGA TGCCTGGTTC CGCATTTTAT AAAAAGAATT TTTTCATGAA AAGAACCCTT 1440 TGGATGAAAA GAAAGTGAAG CATCACATTC CTGTCGTTTT ATTTTTGCAA AATATTTTCT 1500 TTGTAATATA TCTGAAGGGT GTGGCTTGAA GACTTCCTGC CTGGCTTTGT TCTGACTCTC 1560 CATGCAGACC GATTTATATT CCGCCACCAA GAGAAGGGAG CTGAGCTTAG TGGCTGCTTC 1620 CCTCTCCTGG GAGAATTTTA AGAAGATCGT CCACAGCAGA TTCACATCTA TTATGCTTTT 1680 TGTTCCTTGC AATTGCCCTG TGAAGTAAGT AGGGTAGAGT TTCTCACCCT CCTGGGGGAA 1740 ACATGTTCAG GGAGGTCAAG GTCATACAGC TAATAAAAAG AGCAAGTCTT GATGGTGGTG 1800 CTTTGAGAGA CCAAACTTAG CATGTGCTGT AGAGGAAGTC TACTCGTATG GCTCAAGTAC 1860 TTTCTTAACA AGGGTCAGGC TCAGGCCCTC TTTTGCTGCA CATCTGTTTT AGGAGGAGAA 1920 TTTCTTCAAC AACTTTTCAA ATCTCTTGAC TATTGGGATA ATTACTTGGC CTCACCCACG 1980 CCCTTTCTCA ATGACTCAAG AGCCCAGCCA GAGCAACCAA GAAAGGAAGT CCAATTACAT 2040 GAGTTGGAAA TGTCTGAACT GGTTTCTCAG GTCAACATAG TCACTCAGCA CGCCCTGTCA 2100 TGCATGTTCC ATCGCACCCT CACCCTAGAC TGGGGGCCTA ACCCGTTTCG TTTACGTTGT 2160 ACACTAATGA GATTACAAGG TACCATTGAC CCAGAAGTTC CTCTAAGAGC CTGCTATTGA 2220 AGAAGCAAAG ACCATCACCC CCCAACCCCA CCCCCATGCT 2260
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