| Tag | Content |
|---|
EnhancerAtlas ID | HS184-05697 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:63728140-63730440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr11:63730402-63730413 | CAGCAGCTGTC | - | 6.14 | | REST | MA0138.2 | chr11:63730404-63730425 | GCAGCTGTCCAGGGTGATAGA | - | 6.32 | | SP2 | MA0516.2 | chr11:63729420-63729437 | CTCTGTCCCGCCCCCTC | + | 6.4 | | Tcf12 | MA0521.1 | chr11:63730402-63730413 | CAGCAGCTGTC | - | 6.02 | | Znf423 | MA0116.1 | chr11:63729262-63729277 | GGAACCCTGGGGTGC | + | 6.42 | | Znf423 | MA0116.1 | chr11:63729262-63729277 | GGAACCCTGGGGTGC | - | 6.57 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 6 | Chromosome | Start | End |
| chr11 | 63729600 | 63729651 | | chr11 | 63728338 | 63728400 | | chr11 | 63728876 | 63729179 | | chr11 | 63728931 | 63729786 | | chr11 | 63728294 | 63728505 | | chr11 | 63729474 | 63729600 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I063960 | chr11 | 63728399 | 63730471 |
|
Enhancer Sequence | TCCCAAAGTG CTGGGATTAC AGGCGTGAGC TCCCAAGCCT GGCCCTGCTG TGGAGTGTTA 60
ATTCTATTAA GGTGAACATT TAATAGTCCC TACGGACTGG CAGGGCTGGG GCTGAGGTCA 120
CATCATGTGG CGCTGGTGCT TAGTGCAGGC CACCCCAGTG CTGGAGGGAG GAGGCCCTGA 180
GAAATGGGAC CAGGCTGGGA GCCCCCTAAG GGGTGGAGGC TGTTTGACTC AGAGCAGGGC 240
TTGGTAGGCC ACAGCTGGGA GATCGGGAGC AGGGTGAGAG CCAGCTGTGG CTGATTTGGC 300
TGTTGAAAGC CAGGCCCTGC ACCTCTCTGG GGTCATGCTC TGATACAGGA TGGCTCTGTT 360
GCAGCAGGTG AGGCTGACGG GTGGCCTGGA CACTAGTGGC TCCTGTCCGG CTCCCTGGCC 420
CTGAGCCCCT CAGTGGTGAC AAAGGACTAG GCAGCCACGT CCACTGAGGA TCGTAGTGAG 480
GTCTCAAGCC GCCAAGTGCA GGCACTGTGG ATGGCGTGGG GCAGCACATG CCCTTGAAGT 540
TGGTCATGAT GTGGAACTGC CCCCGTGCCT AGCTCGATGC CTGGCAGGTG GGCCACACGG 600
GTGTCACATG TGGGAGCTGT GGGGGGACCG CTCCTGTGGC GGCCCCTCTC CTGAATGTTG 660
GATATATGGG ATGGGGAAAG GTGGGGTATG TGGCTGGAGG GGTCCAGGGA TGGGGCACTC 720
AGGCTAGAGC CCTCTGAGGG TCCTGGCAGT GAGATTGGTG TCCAGGAACA TGAAAAGGAG 780
TGGGGACCTG CCCTAAGCTG ATCAGGGGTC CAGAAACAAG AGAGGCCCAT GGGTATTGGA 840
GCTATGAGCG CAGGCTAGGG GCTCAGAAGG CAGAGGGGCC TGGATGTGGT TCCAGCCTGG 900
TAGGGGTGAG TCTGGGGGCC AGCCCATGAT GGAGGGAAAC GTGGCCTGAG AAGCCAGTCT 960
TCACCAAGCT GGAGCCACCG TCCCACATGG GTGCAAATGC GGTGATCTCG CCCTTACCAC 1020
ACAGGGCTGC TGGCTGTGGA CTGCGTTCCG GAAGGGGTTA ACCACCACAG GCTCTCGGCA 1080
GGCCCGCCCA GCCCTCAGCT TGCACCCTTC CCTCCCGCTG CTGGAACCCT GGGGTGCCCC 1140
AGCCAGTACA GCTGTGCCTG CCTAGAGAGC AACCCCTCCA CCCCCAACCC CGCCCCCGAC 1200
AGCTGTGTCT GGGCCTGTCC CCTGGATGCC TGGCAACAGC TGTATCCCAG GAAGAGCAAA 1260
CACTCCTCTA AGATCCTTGT CTCTGTCCCG CCCCCTCCCT TGACCGTTGC CTGGTTAGGT 1320
TTCCCAAACT AGCTCTTCCA GTGATGCCGT CTCTCCCTCC ATCTTCTCCT GGAGTTTGCA 1380
TTAGCGCCCC CATTTTGCAG ATGGGGAAGC TAAGGCCCAC GGAGGGAAAG GTGCATTCTC 1440
GAGGTACCCA GCACCCCAGT GTTAGGCCTG TATCTCCTTC CCCGAGGCCC TTGTTCACCC 1500
TCCACCTCTG GGCACTGGGC CCTTCCTGCA GCTTCACTAG AGTCTCCTGC TGCTGCCGTC 1560
ACCCCAAGAG TCATTCCCCA CCCACAGGCA GATGAAGAGG CCCCAGCTGC CCTCTGAAAG 1620
CACAGGGCTG GCTTCTTTGC ATCCTCACCA TGCAGCCCTC CTGGCCAGCC CCAGGGCTCA 1680
GTGCCTGGCA CCCACCTGAT GTGCCAGGAG GAGAGACCAG GCCAGGTAGG GAAACTGGAT 1740
ACCCAAAGCT CAGGTTCTTA CCAGCTCCAG ATCAGATGCT TTGGGAGGTG GCAAGCTCTA 1800
GAAAGTGTGC AGAGGAGGGG CAGCTGAGGG TTCTTACCTG CTGGCCCCTC AGGACTGGGG 1860
TGCAGCTCCC TCCCCAGGCC TCGCAGTTCC ATATTTGGAC AAGAGCAGCT GCTGGTCCAG 1920
AGCCTTTCAT GGGGAGAGGG CCAGGCCTGG GGTGGGGAGA CCCAGTGTTT GTCCAGGCCA 1980
TGTGTAAGCA GTGGGTCTGG GGGCCGCCTC TGGGGTGGGG CACCTGGTAT GACAATCAGT 2040
GACAGGAAGC CTGGACCAGC TCCCCTACCC ATCGCCAAGG CTTGGGATCT ATTCCTAGTG 2100
CCCCACTCAG GAGGGAACAG GTTGAGCCCG GGGATCAGAG AGACCAAGGG CTCAAGAGAT 2160
TTAGGTCTCA CCCCTTAGTA GGGAGGGACT CCCTAGCAAG CAATCGGAGC GTGGGGGCAG 2220
TCCCAGGCGG GGGAACTGAG CTCCCCGTCT TTGCAGGCAG CACAGCAGCT GTCCAGGGTG 2280
ATAGAGGGGG TCCCTGTCCT 2300
|
