Tag | Content |
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EnhancerAtlas ID | HS095-17793 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr2:233367590-233370090 |
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) |
CREB1 | MA0018.3 | chr2:233367868-233367880 | CGTGACGTCACC | + | 6.32 | CREB1 | MA0018.3 | chr2:233367868-233367880 | CGTGACGTCACC | - | 6.32 | RFX5 | MA0510.2 | chr2:233369420-233369436 | GGTTACTATGGGAACT | + | 6.03 | RFX5 | MA0510.2 | chr2:233369420-233369436 | GGTTACTATGGGAACT | - | 6.17 | ZNF263 | MA0528.1 | chr2:233367630-233367651 | GGAGGAGAGGGGGGCGGGGAG | + | 7.08 |
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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 |
GH02I232500 | chr2 | 233365404 | 233368709 |
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Enhancer Sequence | AGACGGGAGG TTGGGGGGAG TGGAGCGGGG TGGTGTTGGG GGAGGAGAGG GGGGCGGGGA 60 GGCAAGATCA GACGACAAAG AAAGGGAAGG CAGAGGCGGG GGCGGGAGGG AGGTTTATCC 120 GTAGGAGTCA GCCCAGTTGG GTCAAACTAA GGACCCAGTG CAGACCCCGA GGCCCAGAGA 180 CACAGGTGTG CGCACAAACA CGCACTCTGC GGAAGGCCGG GGCGGGCCTG GCCGCTGCGG 240 GACTCCTGGC CCGGCGCCCT TGACGTCAGC GGCTGGGCCG TGACGTCACC TCACCGCCCC 300 CGCCGCGCTC CCGCCCCCGC CCGCGGGCAC TCAGTCTCCG CTAATGGCAG GCGACGGGGA 360 ATGGCACATC TGTCTTGCCG GGAATTAGTT CATTGAATCA GGCGGCCCGA GCTGCGGCAG 420 CGACCTTAGC CCTGGCCCCA GGGAGGGGTC TGGGCGGGCG GCGTGGGGGA GGTTCAGGCT 480 GGAGGGCTGA GTGCGGGGAC GGGAGGAGGG GACTCACCTG GACTCGCGAG GGGGACTGAG 540 CGCTCTCCAA ATATAGGTCA ATGTCCCGCT CAGCCTCCCT CCCCCAGCAC CGTGAGGACC 600 GAGGCCTGGG GCCTGGCGCC CGCCTGGTGG ACCTCGGGGG CAGGCTGGGG ACCGGGCCCC 660 TGCGGGACGC GGCGCGGCAG GACGCTCCCC GCGCCTTTCT TTCTGCACCT GCCCCTCGGG 720 GTGGGTCCCC CTCTTTACCC TCGCTTCCCC CCGCGGGTGC CGATAAAGGC GGCTAATTCC 780 CGAGCCCGGG GAGGGAGGGG GCGACTGTTC CAGTCAACAC TTCCCCGCGC TCTTCCCCGA 840 CCCTCCCAGA GCGTTCCCGC TGCTCAGGGC GAGGAGCAGC TGCGGCCAGT TTGTCCTAGC 900 GGTTTAGGAG GCAGGGAGGT TTCCTCCAGC CTGGAGCTCT GGCTCGGGCC CTCGGGCCCC 960 AACACCTTCC CGCTGAGACC GCGGGCGTTG TCCCTGGGTC TCTCTGCCTC CATTTCCCCC 1020 ACCTCCATTC TGGTTACCCC TTCCCCCCAC TCTTTCCTTC CTAACCCATG AGAGCACTGG 1080 AAAGATGCTA GAAAGTCGGG CTTCTAGAGC CCCAGCCCTG CCTCTTGTTC CTGCGAGACT 1140 GTGGGCAGGT AATTTAGCCT CTCAGCCCCT TTCATCTGAC GCTGGGAAGT AATGAGGAGA 1200 CCCCACTTCT CTGGGAAGTT CAATGATATG CGTAAAGGGC TTAGAATTAG CAGATTCTGG 1260 TAGCCAGTGC GTTACGGTTT TGCACTGGGG AGGCAGAGCT GCCGCGGGAG TGTGGCTTCT 1320 CTAGAAAGAT CCCTGGGCAC TTCAGTGATG AAAGTACCAC AGTGAGGATT GTGGTGATGC 1380 AAAGGGCGGA AGAGTCTGGT GGGGCTGCCA AGTGGGCCAG GCTGGGGTCC CTCGAGATGG 1440 AGTCCCTTGA GATAGGGAGG CTCACCCACA CCAGGGATCC CACCCCAAAC TCAGGCTTCG 1500 CCTCCCTCTG CTTCTACCAG GTTGTGACAC TGACCCACTG GGCTTTTCAC ATTACTTCCA 1560 CACCTTTGCT TGGCCCTTCC CGCTTTCACC CATTGGCAAC TTAATTTTGA ATGCTTAATC 1620 CATGAACAGT ATCATCCCCA TTTCACAGAC AGGAGAAGGT TCAAAGAGGC AGAGGTTCAG 1680 AGAGGTTAAG TGACTTGCCA AAGACCTCAC AGCTATGACA TGGCATAGCT GGGATTTGAA 1740 CCCAGTGCTC TGGCCTCAAA TGTCAACTAC TCTCTAATAC TCTGCCTCAC CTCTGAGAAC 1800 CACTTAGTTG CTAGGAGACA GCAAGCTGGC GGTTACTATG GGAACTGGGC TGATGTGGAA 1860 AGTGGAGAGT TGGTGTCCAG GCAGCAATGA GAAGGCTCCA GGTAGGTTCC ACATCCCTCC 1920 CCTGTCCCTT CCATGAAGGC AGCCCTTGGC ATTCAGCTCT GGGTTCCAGA TGGCACATGT 1980 CCTGATGGGA CCTGAGGGAG GTGCAGTGAT GGTGAGTTAC GCTGGACACT GCCCTGGCAA 2040 GCCAAGAGCC CTGGTGGAGG ATGTGGTCCC AAAGATGGGT CTGAGGGGCG AGACAGGCCA 2100 GAGAACCTCA CGATCCTGCT TTCCGGACAT TTGCTGCAGT CACACCTGCC CTGCAGACAG 2160 TAGTGCAGAG CAGAGCCTTT CCTTGTGAAG TAAGGAAAAG GGAAGGCAGA ACCATGATGG 2220 GGCACAGACC CATGCCAGAG AGTTCTGGAC CCAGGAGAAC ACCTCAGTTC TCTCAACTGT 2280 AAAATGAGGA TGATACCAGC CCCTCTCTCA TAGTGTGCTG AGAAAATTGA CAAAGATACA 2340 AAGCACTATG TCTGACACAT AGACTTCACT GACTGTGTGA CCTTGGACAA GTCACTTAGC 2400 CTCTCTGAGC CTCTGTAAAA TGGGGATATT AATAGGACCT GCTTTATAGG GTTGCTGTAG 2460 GGATTCAACA TGTGCGTACA GGTAAAGGTC CTCCCAGGCT 2500
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