| Tag | Content |
|---|
EnhancerAtlas ID | HS178-00219 |
Organism | Homo sapiens |
Tissue/cell | Skeletal_muscle |
Coordinate | chr1:10735910-10740290 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PLAG1 | MA0163.1 | chr1:10739593-10739607 | CCCCCGCGGGCCCC | - | 6.24 | | ZIC1 | MA0696.1 | chr1:10737869-10737883 | GGCCCCCTGCTGCG | + | 7.01 | | ZIC3 | MA0697.1 | chr1:10737869-10737884 | GGCCCCCTGCTGCGG | + | 6.25 | | ZIC4 | MA0751.1 | chr1:10737869-10737884 | GGCCCCCTGCTGCGG | + | 6.14 | | ZNF263 | MA0528.1 | chr1:10737332-10737353 | GGAGCAGGAGGGGGCAGGGGA | + | 7.4 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_23439 | chr1:10734421-10736602 | Colon_Crypt_1 | | SE_23439 | chr1:10736646-10738355 | Colon_Crypt_1 | | SE_23439 | chr1:10739259-10740980 | Colon_Crypt_1 | | SE_24212 | chr1:10734337-10736492 | Colon_Crypt_2 | | SE_24212 | chr1:10737206-10737677 | Colon_Crypt_2 | | SE_24212 | chr1:10739337-10739842 | Colon_Crypt_2 | | SE_25175 | chr1:10734217-10738863 | Colon_Crypt_3 | | SE_25175 | chr1:10738928-10739864 | Colon_Crypt_3 | | SE_26713 | chr1:10734646-10736359 | Esophagus | | SE_26713 | chr1:10736607-10738272 | Esophagus | | SE_26713 | chr1:10739834-10743868 | Esophagus | | SE_28494 | chr1:10735553-10738837 | Fetal_Intestine | | SE_30102 | chr1:10736768-10740350 | Fetal_Muscle | | SE_31374 | chr1:10732699-10751186 | Gastric | | SE_33519 | chr1:10736191-10741085 | H2171 | | SE_37889 | chr1:10737466-10743900 | HSMMtube | | SE_40607 | chr1:10733336-10741092 | Left_Ventricle | | SE_41555 | chr1:10735242-10738779 | LNCaP | | SE_41555 | chr1:10738952-10740970 | LNCaP | | SE_42099 | chr1:10732695-10754653 | Lung | | SE_48591 | chr1:10736516-10740326 | Right_Atrium | | SE_54510 | chr1:10711383-10754578 | Stomach_Smooth_Muscle | | SE_63296 | chr1:10733447-10756197 | NCI-H82 | | SE_65281 | chr1:10730535-10740589 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 10738626 | 10738847 | | chr1 | 10736682 | 10738250 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I010662 | chr1 | 10722544 | 10750567 |
|
Enhancer Sequence | AGCGGCAAAG TCCTCTTTCC CCAAGGTTTG CAGGGAGCTG GCCTGGCAGG CCGGTCCGGG 60
CCAGAGCTGC CTGGGATGGG CAGGGCTAGG CCTGTTACCC TCAGCCTTGC CTCTTCTCCC 120
TCAAGTTCCA TCCCAGGGGC TCAGACACCT GCCTGCCAGG GATGGCAGAG ACAGTCAGGA 180
TGAACCAGGC GCCCAACCCC AGCAGCCAGG GAGGGGCCCC AGGAAGAGGG CGGGGCTCCC 240
CCTGGACCTA GGCCTGCTCA GAGGCTTGGG GGCCAAGGAA GGAGGGACAG CAGGAACCCC 300
TGAGGGTCAC ACAGAATGTG TGATCTCAGG GTGGTGACAA ACCCATGCCA ACCAAGTGAC 360
AGACACCAAG GCCCTGCTGG ACTGGCCCGG ACCCCCGTCC CCCATGCTGC TTCTCATTCC 420
CTCTCCCGGA AGCCCTGGGC TCCCGCTATT GTCGGCCACG TTGAGGGAGG GCCCCTGCCT 480
GTCCCATGCT CACCCCTGTC CTTCCTCTCC AAGGAGAGCC ACCACAGAAG CAAAGCTCTC 540
ACTCCATCAC ACAGCGTTAG CCCCAAAAGG TGACCTTTCA ACAGAACATC CCCAATGCAG 600
GCTCTTCCCA CCAGGACAAA GAAGACACCA AGAGCCCCCG GGGAGGCCTC TCCACCATCC 660
TCTGAACAAA GGGGCTCTCC TCCTGGGCTC CTCCATCTCT CTCTGTGCCT CTCCATCTCT 720
CTCTGTGCCT CGGTGGACCA ACCTGCCTAG GGGTGCCCTG GGATCCTATT TCCACAGCAG 780
GCCTCCCTCC ACCTTGGTGC CTGCCCTCGA CCAGCCTACA GCTCAGAAAC GAGCCCCTGG 840
CCCGGGGCGA GCAGCCCCAC AGTTTCCTGA CGTGGACGCC TTTGCTGGTT CCTCCACGTC 900
CCAGCCACAC AGGCCAGCAG GAGCCTCTGT GAAGCCTGCA TGGAGAAGAG ATGCTGGGCT 960
GGGCCAGAGA CTCTCTCTAA CATCCTGTCT CCCGGGATCT AGGTCCTGGC AGCTGGCGGG 1020
TATCAAGGGC ATGCACTCTG TCCGGGCTGA ACCCCATACT GCCTGGCTCT GCCACTGCCT 1080
CTCGCTGAGG CCCCTGTGGG CACAGCCAGT CAGGGGGTGC AGGGCCCCAC AGACTTCAGT 1140
GCTGCCTGGG CTCTGGCACG TAGGACGTGA AGGAAAGCCA GCAGCTTTTC TCCCCCTCTT 1200
TCCTGGGCAG AGCCCCCTGG GGCTCCATCG CCCCCCGCCT CCAAGATGAG TGAGTCACGG 1260
TGAGGGCAGA GTGGAGGGTC GAGACAGAGA GAGCTCAGGA GGGGGCAGGT GATGCCTCCC 1320
AAGCCTCCAG CCGCTCTGCT CAGGCTGGAA GGAACGCCAG GAGCTCACAC TCCCTCGCTG 1380
CTGGAGGAGG CAGACGGAGT CACCCAGCGC CAAAGCCTCG CTGGAGCAGG AGGGGGCAGG 1440
GGAAGGCACC TTCAGGGTCA GGGGAAGGAT TGACAGAGGG CAAGGCAGAG GGTGTCTGGG 1500
TGGCACCGAG GAGGGCAGGA GGGGACAGGG GCCTTCTCAT GGGTACGTCT AAAGTGGGCA 1560
AACAGGGAAG CAGCTGCTCG TCCTGACCCA CTGTTTCTAG AACCTGTGTG TGGGGCATGG 1620
CAGGGGTGTG GCAAGTGGCT CTGGCTGGAC ACGGAGCTAA GGAGGGCAGC CTGCACTTAG 1680
GTCCAACGCA CCTTGGGACA GGGGACAGCT ATCAGGGTGG AGGCTGTCCT AGGTGCACAG 1740
AACTTTAGAC CTGGAAAGGG ACCGAGGTCC AAGAGGCTGA GAAACTTGGC AAAAGCCCAG 1800
GCCACTCACT CGTGAGGACT AGGCAGATCC AGGGGCCCAG TTCCCAGTCT GAGCCCTCTC 1860
CGGCCCAGCA AATCCAATGC TACACATTTC TGTTTCAAAG CAGAGCTTTC CGCAGCCTTG 1920
GAGATTGCAC CAGGCCCCTC GGGCCCCAAA TACCACAAAG GCCCCCTGCT GCGGAGGATT 1980
TGAGCCACAC ATGGCCCAGT GGGCAAGGAC CCCAAATGGC TCTGAACCAG CACCTGCGGT 2040
GTGCGAGGCC TGGAAGCCAG GCTCCCCCGT TCTCCAGGGG AAGCAAAGTG GAGGCTGGCT 2100
GCGTGGCCTG GCTGACCCAC CGGAAATGGG TAGGACGTGT GTGGCAGGAG GGGACCTTTC 2160
TCTTGCAGGG ACTGAGACCC TGAGACCTTC CAATGTGTGT TGATGGGGAG ACAGGGCAGG 2220
CGCTCTCTGG GGATGAGAGG GAAAGCCTGG ACTAGAGAGG CCCCGGACAG CAGGCCCAGC 2280
CCAGGAGAGG CGGCGGCGTG GGCAGCAGGT GGCAGAGGAA CACGGGGTGG CACACCACCC 2340
GCCCTCCCTG CAGCCCGTCT CCACAATCCC CTTGCTGAGG CCAGCGACGG CGACCATGAC 2400
GAGGACATGA GGGGACTAAT TTAGGAGTAT TTTTAAAACG GTGGCCCTGT GGAGGGCTTG 2460
AGCAGTTGTC AGCCATCTGG AAGAAGGAAT TACAATCACC TCCCTAATCC TATATTCCCT 2520
AAACCCTAAA GCTGGTTACA GTGTGAGGGA GAGGCAGCAG GTGGGTGGGG GTGGGGGGGT 2580
CTGTTCCAGA GTGGGGCAGA GCCCAGGGAG GTGCCCACAG GGCCGGGGCA GCACCGCCCC 2640
CGCGAGGGGG CCCGAGGCCG GGGCTGAAGA TCCCAGTGTC CTCTGAGCCC ACCCAGCTCC 2700
CCCACCCGTT CACGCACACT CGCTCCCTGG GCCGCGCCGG CTCGCGCAGG GGCCGTCAGG 2760
TAAATTAGAT CTGAAAGCTG ACAATTTCTG ACCATATTTC CTTGATTATT TCAAACAAAT 2820
GCACAGCAGC CGCTGTAAGG AGATTAAAGT GACATAAACG TCCCGAGCGG GAGGGGGGAG 2880
GGCAGAGGAT TCAGGTCACC CCCATCCGTC CCCCGCCTGA CAGACGCTAT ATCGCTATCC 2940
AATCCAATAA AAAATCCCCC CCTTTTGCTT TAATTAATTT TACAGCTAGC TTGCTTAATT 3000
ACTTTCAATC AAAATCCTCC TGCCATCGCA AAATTAGAGA TGGTTGAGCT CCATTAGCCT 3060
AAATTCTTCA TTTCCATATA GAAAAGAGGC TGTCTGCAGA GCCAGCCTGG GCCCCTGGCA 3120
GGACAGACGC CCGTCTGCCC GCCCGCTGTG AGCCAGCCCA CCCCTGGCTT CCGCTCTCTG 3180
GCTATCTCTG GCCTATGCGT GTCCCCTCAC TCTCCTCCAT CACTGCTCCC TGGGCCATGA 3240
AGAGCTGAGG TTCAGGAGGG GTACCCGCTG CCCCGACTTC CCAGGATTCA CGAGGGGACT 3300
GCAGGGCTGG CACAGAGCTC TCCGCCAGGG CCTGCTGCTT TTGATGAAAG CATAGGCTGA 3360
TCCTGGGAGC CTGCTGCCCT GCCAAAGGGC CCCTGCTGCC TCCAGGACAG AGCCTAGTCC 3420
CAAACCTGAG GCAGACAGGT CTCCTGGGCC ATCTGCACCA CATGCCCCAG GAAGCGGTCC 3480
CTCTCCCAGC AGGCGGAAAC ACTCCCAACC CCGGACTTAG GCCCCTGTCA GAATAGACCC 3540
CTGGAGCCAA CGCCACCCAG GGCTCCCTCT GCCGATTCCA GGCTGGAGTC ATTGTTCACC 3600
ATCAGGATGA CTCGGGCCAG CTGTCTCGAT GGTGCTACCA AGCAATGTAG CAGCCCCCAC 3660
ATACTCTGGC ATTCTCCTAG GGCCCCCCGC GGGCCCCTCC TCCCCATACC ATAGTCCTGG 3720
TTCCCAGCCT GCAACAGCTG CACCTCCACC CCCAGCCTGG GTCGAGTGGG TGGTGGGTCT 3780
GGGCTCTGTC CACATCCTGT GCCTGCACGG GCACCCTTCT CCTCCCCTCC ACCTGCCTCA 3840
TCTTCACAGT CCCCAACCCC AACTCTGGAA GCTCCACTTC AGGTTTTCCA TACTACAACC 3900
CCGAGTGTCA CCACAGGGTC CGGCCCAACC TGGGCTCCAG CTGATTAAGG ATCTGCAACA 3960
GGATGTAGGG ATTACAGTAA AACCTGGCTC CGGATCTGCA GGGGCAGCAG GCCAAGTCCC 4020
AGCCCTGGGA CTCCCCTCCC CTACCCTTCC AGCATCCCTA CCCATTACCC GTCCCAAACC 4080
CAGCTGCCAA GTGAGGGAGG AAGGCTGAGC CCCTTGGCCC TTAGGGGACT CCTGGCTGGA 4140
CTCTAGGGGG TCTGGACTGA GAAGGGGTGG CATTAAGGAG CCCAGGCCAG CTCCTGCAGA 4200
AAGGCTGGGG TGGGGCAGGC TGGGGAAGGG GAGTGATGGC TTTATGCCGC CTGGCTTCCT 4260
TCTCAGGGAA CCAATGTGAA GGTGGGGTGT CCTGGGCCTG ACCTCTGGGC AAAGGCTGAG 4320
TAAGCAGGGA AGGAAGTACC CTAAAGGCCA GGAGAGCCCC TTCCAGGCAG AAGGCCTTAC 4380
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