| Tag | Content |
|---|
EnhancerAtlas ID | HS184-05626 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:61393920-61396310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr11:61394345-61394357 | TCTATTTATAGT | - | 6.22 | | MEF2B | MA0660.1 | chr11:61394345-61394357 | TCTATTTATAGT | - | 6.37 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I061625 | chr11 | 61393045 | 61396713 |
|
Enhancer Sequence | CACCCACTAA CTCGTCATCT AGCATTAGGT ATATCTCCCG ATGCTATCCC TCCCCCCTCC 60
CCCCATTGTG TGTTACTCTT AACTCCTCAC CACAAAACCA GAACGGCCCT GAGACCAAGA 120
CTCAGGTCTC CAGAACAAAG CCCTTAGCCT GACATTCAGG GCCCTTGGCC ACTGGGTCTC 180
AGGAACTGCC GCAGTCCCTT GCAGCCTGTG TCCAGCCTCT CAGAGCCACC TGCCTGCTCC 240
ATTCCTTGCT TCCCCAGACT GTTCCTTCTG CCTGAATGGC CCTCCTGGAC CTCCAATGCC 300
AGGGGCACTC CTATCCAACC TCGAAGAGAT TGCTCTGTCA GTGCAGCCTT GCAGGGCCTC 360
GCTGGGGGAG AATCAGAATT CCTTTCTCCT GCCCTCCCTT GGGCTTCCGG AGCCTTCCGT 420
CATCCTCTAT TTATAGTTCA AGTCAGGTGC CCCTGGACAT GTTGCTGGGA GGGAAGGGCC 480
TCAGCTGGGA GAGCCGGTTC TGTGACCTGC TGGGGAAGGG CTGGGATTTT CCAGGATGCC 540
TCCTCTAGCC CTATAGTCCC CTTGGCTACC TCTGTCTACG GGGAAATGGA GCCCCCTACC 600
TGGACAGCCT TAATCCGGTG CACCTGGTGG CTGCTTGTCT CCTTGGCTTT GCTGTGAGCC 660
CTGGGGCCTG GGGATGGGCT TCTCTCCAGC CCTGGGCCTG CTCCTGCCTC TGCTGTGGTG 720
AGGTGACCTG AGTAACGGGT TGGGTTAGGT GGTCTCTATG TTGGTAGGGG TCTCAGTAGG 780
GTCAGGCTTG CTCTAGGAGA GAGTCACAGT TGCTAGAGTT GAGTATAGAG GGCAGGAACC 840
AGCTGTAACT TTGCAAAGCT CTGTCCTGGG ATGCTCGGCT TCCCTCCTGT TGTCCTCCAC 900
CTTCCAGAAA GCCCAGCAGG GAGAGATGAG CACTGTGTCC CCAAACTCAA TGTCACTGTC 960
ACCTCCCCTC ACCCAGCCCA GCCACTCCCC GTCAGCTCCA GACCAACTCG GAATACTCGG 1020
GAAGGTTGAT CCTTCGACTT CCTCAAGCCA TTGCTCAACA TCCCCCAATC ACAGCCTCCC 1080
CAACTCCCAT CTCCAAAGGC CTCCTTCCTC CCCAGATCCC CGGCTGTCAC CATCCTCATT 1140
CTTCTAACAA GCTGACAAAC TTGAATTCTG AGCGAGCATG ACCTGGGGTC TTGGGCCTGA 1200
GCCGCAGCCC TCTGCCTCCA CCCCATCCCC CACTTACATG CCCACTTTCA GATACAGACA 1260
CGGACCCTGA TGCCAAGGAC ATCCACTGGC TGAATGCCTC CTCCTGCCCT TTCACGAGCT 1320
CCCATGCCTG GCCCTGACTA CCTGCACGCA GCCCTGGACC CTCAAGTGAC TGTAGGAACC 1380
CCCTCTACGA GACTCAGCCC TTTTGCCACC AGTGGGACTT GCAGGCCCAG CTGACCAGCA 1440
CCTTCTTGCC TGCTGTGGGC CATGTGACCG ACGGAATCCC ACCACATCTG CCGTGAGCCT 1500
CGCCTGAATC AGGACCAAGT TTAGGTTTTC AGAATCAGAC GGACGTGACT ATGTGACCTG 1560
GGGCAAGTGA CTAACCCTCT CTGAGCCTCT GACATTTATA GCTGACTCCA ATCTGATACA 1620
TGGGCTCCCC AGGGGCCTGA GGAGGGAAGG TTTGAAACCT CACTCTTCCC TCCCTTGCCC 1680
TTGGAAGGTG AGAGCAGGAG GCTCCTTCAT GGAGGTGGCT AGGATGGGGA GGGAGGACCA 1740
GGAAGCTTCC TGACCTTGCC CCAGGAGCTG GCAGCCCCCA GTCCCACCTT GTCCAGAGAT 1800
CACTCAGGGG AAACCACTCT GGCTGAGGGA TTCAGGTGCT GGTGCCAACT AGGAGAAGCA 1860
GTCTAGGGCG CCTCCCAGTG GACACCAAGG GAACGTCTAT TCTGGCTGGC CCTTGGTCCA 1920
GCCCTGTGAT TTTAGCCCTT GGCATGCAGT CAGGCTCCAG TACTGACCCC AGCACCAGCA 1980
GTGGCAAATT GCACCTCATT TGAGGAATCT CAGTTTCCTC TTCCACAAAA CGGAAATAAT 2040
GATAACATCA CCACACAAGA CCACAGTGAG GCTTCCTTCG GACGACCTAG GCGACCCGCC 2100
TTCCACACTA ATGTTTTCCA GGTCTAGAGA GGCCAGGGCT TGCCTGGGGA CCACAGTGAG 2160
ATGTGGTGAG GAGCCAGGGG TTCAGGCTCT CAGGCTCCTG GTCCACTGCT CTTTCCACTG 2220
CTGGGAGGTG CCTCAATGTA ACCTTGGACT CTCCAGGCCT ATTAACTCCT CCGTGTAGCT 2280
CTGGAAGTTT TCAGATGTTT TAGTGCTATT AACATGCCTG TCCCAGGAAC AAGCTTACAA 2340
ATGCATCCAA TTAACCTTCT GCCAACAATT CTGGGACGTG ATTTCTTTTC 2390
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