| Tag | Content |
|---|
EnhancerAtlas ID | HS095-06238 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:118562100-118564260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr11:118562896-118562907 | CTGAGTCATCC | - | 6.32 | | JUNB | MA0490.1 | chr11:118562896-118562907 | CTGAGTCATCC | - | 6.14 | | Myog | MA0500.1 | chr11:118563420-118563431 | CTGCAGCTGTC | - | 6.62 | | Tcf12 | MA0521.1 | chr11:118563420-118563431 | CTGCAGCTGTC | - | 6.14 | | ZNF263 | MA0528.1 | chr11:118563166-118563187 | TTTCTCTCCTCCTACTCCTCT | - | 6.37 | | ZNF263 | MA0528.1 | chr11:118562607-118562628 | GGAGGAGGAGAGGGAGGGAGG | + | 9.66 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr11 | 118562675 | 118563898 | | chr11 | 118562658 | 118562793 | | chr11 | 118562463 | 118563803 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I118691 | chr11 | 118562342 | 118564020 |
|
Enhancer Sequence | AGTAGCTGGG ATTACAGGCG TGCGCCACCA TGCCCGGCTA ATTTTGTATT TTTCATAGAG 60
ATGGGGTTTC ACCATGTTGG CCAGGCTGGT CTCGAACTCC TGACCTCAGA TGATAGCTCC 120
CACCTTGGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACCGTGCCC AGCTGTTTTT 180
CTTCTATTAT TATTGTTCTT GCAGGAGCTG GTAAAGTGGC TGATGTGGCC ACAGCTCCAT 240
AAATCCATGT GGAACGAAGG GTGGACATCG CCTGAGTCCA GGAGACAGGA CAGGGTCACT 300
CATCTCTGTC CCTGGTGATG GAAACTCAGG CTCAGGAAAG AGCCTTGACC TGCCCTGGGT 360
CACAGAGAGA ATATTAGGGT CAGGGCTTGA GCCCGGGTGC TGTGGTCAGG CCCTTAGGCC 420
GCCTCTCACA CCCAGACTAG GAAGCTGGAG CAGAAAGTTT GCTAGAACAA TCCTGAGAAG 480
AGGCCTGCAC AGTTCAAGGG GCAGCTTGGA GGAGGAGAGG GAGGGAGGAC CGGCTCTGGC 540
CAGTGGGCTC TTGGACCTCA GGCCAGGCTC TGGCAGCTGC ATCTGGTATC AGGCCTGCAG 600
GTCCAGTGCC TATTATGGGG CCTATTATGA CTGCACAAGG GGCCTCAAGT TCATTCAGGC 660
CAAGCCTCTC ATTCTGCAGA GAACCACACA GTGGTTGCCG GGATTTGCCC AAGGCTGGTG 720
GGTTGGTCAT GAGGGCAGGC CCGAACTCAT CTCTATTTTC TTGCATTCCG GCTCTCCTGA 780
TGTTCCAGGC CCATCTCTGA GTCATCCTTG GACAGGAGAG ATCCCAGAGG GTAAACAGGA 840
CATGAGCCTG CAGTGAGGGG AGACAGAGGA GGAGAGAACT CCCTGAAACA AGAGGAGAGG 900
AGGAGCTGGT GGGGAGGACA CAGGTAGGGC AGCGGGCAGA CCACCAAGGG GCAGGCTTGC 960
TGTTTCGCAG CCTGACCCCC AGCCTGTGTG CCTCATTGCC GCCTCCTCCT CCCAGAGCAG 1020
GGCCTACGCC TCAACCAGAG CTTGGAGCAA GACAAGGAAG GCTCCATTTC TCTCCTCCTA 1080
CTCCTCTACT CAAACCACAG CCATCTGTAC ATCAGAAACT TTTTTTTTTT TTTTTTTAGC 1140
CCTCAGCTGC CTGATGCCCA TGGTTGGGGT TTGGGCTGAG TCACCGAGGG CTGCCTGCAC 1200
ACACCAGGGA GGGCTCCTGA GCACCCACTC TCAGGCTTTG CACGTTTCCG AAATTCTGCA 1260
CACGACAGCA ATTTTTGCAG CAAGGGTGTG GAGGGTGCCT GTGGGCCAGT CACCAGCCTG 1320
CTGCAGCTGT CCGTGGTTGC CTCTGTCTGC CAGGGCTGCA CGACCTCTGG TTTTCACCTC 1380
AACCACTGCG GCTTCCTCTC TCCCCGTGGG AACAGGGCAT GGGGTGAGGG AGCTACCATG 1440
CCCAGACAAC TAGGCATCTC CCTGCCAGGC CAGGAGTTCC ACTGCCACAG CCCAATACCA 1500
GCAAATTCAG ATGCAACCAA GTGACCCCAA CTCAAGTTAC ATTCCCTTTC TCCCCCACAG 1560
GCTCTGCAGT CCCAGGGATT CGCAGTGTTA GTTGATCTCC GGGGACACTA GTTCCCAAGA 1620
GACCCCACTG AAGGCCTGGC TGTACCATCA TAGGCTGTGT GCCCTTGGGC AAGAACCTCT 1680
ACCATTCCTC GTTGCCTGTA TATAAATTGA AGGCTTTGCT CTAGGTCAGT GTTGCAAACT 1740
CAAATTCCAG TAATAGGAAT GTGCAAAATA TGTTGGGGAT AAGGGAGCCA ACAGTGCAAG 1800
GGGGAAGTGA GTGTTGGGGA CCTAGTCTTG GGGTGACGGG AACTGGGCTG AACCGGAAGC 1860
GTATTCCTGT GTAAGGGAGG CCACTGCTCA GAGGGTGGCT GCTATGGGGC TGGGGGATCC 1920
TGATTTGTCA AAGGAAGGTG GAAATTTATA TTTCAGCTCA CACGCTCCTG TTTTTAAAAT 1980
GTCTCAATGT CTCTAATTCT GACTGTAAAT CTAAGAGTGA TTCCTGTGTG GGTACGGTTA 2040
GGAGGAGTCT GACCTCCACC AAAGGGGCTT TGTGGGCTGG GACTTCGTAC TCCTGCAGAG 2100
CGCAGGACCG CACCCCTGAA TGCAACCTCA GCCTGGAATG TTGACACAAT CATTTGGTGT 2160
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