| Tag | Content |
|---|
EnhancerAtlas ID | HS179-00194 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr1:10735920-10740280 |
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 | TCCTCTTTCC CCAAGGTTTG CAGGGAGCTG GCCTGGCAGG CCGGTCCGGG CCAGAGCTGC 60
CTGGGATGGG CAGGGCTAGG CCTGTTACCC TCAGCCTTGC CTCTTCTCCC TCAAGTTCCA 120
TCCCAGGGGC TCAGACACCT GCCTGCCAGG GATGGCAGAG ACAGTCAGGA TGAACCAGGC 180
GCCCAACCCC AGCAGCCAGG GAGGGGCCCC AGGAAGAGGG CGGGGCTCCC CCTGGACCTA 240
GGCCTGCTCA GAGGCTTGGG GGCCAAGGAA GGAGGGACAG CAGGAACCCC TGAGGGTCAC 300
ACAGAATGTG TGATCTCAGG GTGGTGACAA ACCCATGCCA ACCAAGTGAC AGACACCAAG 360
GCCCTGCTGG ACTGGCCCGG ACCCCCGTCC CCCATGCTGC TTCTCATTCC CTCTCCCGGA 420
AGCCCTGGGC TCCCGCTATT GTCGGCCACG TTGAGGGAGG GCCCCTGCCT GTCCCATGCT 480
CACCCCTGTC CTTCCTCTCC AAGGAGAGCC ACCACAGAAG CAAAGCTCTC ACTCCATCAC 540
ACAGCGTTAG CCCCAAAAGG TGACCTTTCA ACAGAACATC CCCAATGCAG GCTCTTCCCA 600
CCAGGACAAA GAAGACACCA AGAGCCCCCG GGGAGGCCTC TCCACCATCC TCTGAACAAA 660
GGGGCTCTCC TCCTGGGCTC CTCCATCTCT CTCTGTGCCT CTCCATCTCT CTCTGTGCCT 720
CGGTGGACCA ACCTGCCTAG GGGTGCCCTG GGATCCTATT TCCACAGCAG GCCTCCCTCC 780
ACCTTGGTGC CTGCCCTCGA CCAGCCTACA GCTCAGAAAC GAGCCCCTGG CCCGGGGCGA 840
GCAGCCCCAC AGTTTCCTGA CGTGGACGCC TTTGCTGGTT CCTCCACGTC CCAGCCACAC 900
AGGCCAGCAG GAGCCTCTGT GAAGCCTGCA TGGAGAAGAG ATGCTGGGCT GGGCCAGAGA 960
CTCTCTCTAA CATCCTGTCT CCCGGGATCT AGGTCCTGGC AGCTGGCGGG TATCAAGGGC 1020
ATGCACTCTG TCCGGGCTGA ACCCCATACT GCCTGGCTCT GCCACTGCCT CTCGCTGAGG 1080
CCCCTGTGGG CACAGCCAGT CAGGGGGTGC AGGGCCCCAC AGACTTCAGT GCTGCCTGGG 1140
CTCTGGCACG TAGGACGTGA AGGAAAGCCA GCAGCTTTTC TCCCCCTCTT TCCTGGGCAG 1200
AGCCCCCTGG GGCTCCATCG CCCCCCGCCT CCAAGATGAG TGAGTCACGG TGAGGGCAGA 1260
GTGGAGGGTC GAGACAGAGA GAGCTCAGGA GGGGGCAGGT GATGCCTCCC AAGCCTCCAG 1320
CCGCTCTGCT CAGGCTGGAA GGAACGCCAG GAGCTCACAC TCCCTCGCTG CTGGAGGAGG 1380
CAGACGGAGT CACCCAGCGC CAAAGCCTCG CTGGAGCAGG AGGGGGCAGG GGAAGGCACC 1440
TTCAGGGTCA GGGGAAGGAT TGACAGAGGG CAAGGCAGAG GGTGTCTGGG TGGCACCGAG 1500
GAGGGCAGGA GGGGACAGGG GCCTTCTCAT GGGTACGTCT AAAGTGGGCA AACAGGGAAG 1560
CAGCTGCTCG TCCTGACCCA CTGTTTCTAG AACCTGTGTG TGGGGCATGG CAGGGGTGTG 1620
GCAAGTGGCT CTGGCTGGAC ACGGAGCTAA GGAGGGCAGC CTGCACTTAG GTCCAACGCA 1680
CCTTGGGACA GGGGACAGCT ATCAGGGTGG AGGCTGTCCT AGGTGCACAG AACTTTAGAC 1740
CTGGAAAGGG ACCGAGGTCC AAGAGGCTGA GAAACTTGGC AAAAGCCCAG GCCACTCACT 1800
CGTGAGGACT AGGCAGATCC AGGGGCCCAG TTCCCAGTCT GAGCCCTCTC CGGCCCAGCA 1860
AATCCAATGC TACACATTTC TGTTTCAAAG CAGAGCTTTC CGCAGCCTTG GAGATTGCAC 1920
CAGGCCCCTC GGGCCCCAAA TACCACAAAG GCCCCCTGCT GCGGAGGATT TGAGCCACAC 1980
ATGGCCCAGT GGGCAAGGAC CCCAAATGGC TCTGAACCAG CACCTGCGGT GTGCGAGGCC 2040
TGGAAGCCAG GCTCCCCCGT TCTCCAGGGG AAGCAAAGTG GAGGCTGGCT GCGTGGCCTG 2100
GCTGACCCAC CGGAAATGGG TAGGACGTGT GTGGCAGGAG GGGACCTTTC TCTTGCAGGG 2160
ACTGAGACCC TGAGACCTTC CAATGTGTGT TGATGGGGAG ACAGGGCAGG CGCTCTCTGG 2220
GGATGAGAGG GAAAGCCTGG ACTAGAGAGG CCCCGGACAG CAGGCCCAGC CCAGGAGAGG 2280
CGGCGGCGTG GGCAGCAGGT GGCAGAGGAA CACGGGGTGG CACACCACCC GCCCTCCCTG 2340
CAGCCCGTCT CCACAATCCC CTTGCTGAGG CCAGCGACGG CGACCATGAC GAGGACATGA 2400
GGGGACTAAT TTAGGAGTAT TTTTAAAACG GTGGCCCTGT GGAGGGCTTG AGCAGTTGTC 2460
AGCCATCTGG AAGAAGGAAT TACAATCACC TCCCTAATCC TATATTCCCT AAACCCTAAA 2520
GCTGGTTACA GTGTGAGGGA GAGGCAGCAG GTGGGTGGGG GTGGGGGGGT CTGTTCCAGA 2580
GTGGGGCAGA GCCCAGGGAG GTGCCCACAG GGCCGGGGCA GCACCGCCCC CGCGAGGGGG 2640
CCCGAGGCCG GGGCTGAAGA TCCCAGTGTC CTCTGAGCCC ACCCAGCTCC CCCACCCGTT 2700
CACGCACACT CGCTCCCTGG GCCGCGCCGG CTCGCGCAGG GGCCGTCAGG TAAATTAGAT 2760
CTGAAAGCTG ACAATTTCTG ACCATATTTC CTTGATTATT TCAAACAAAT GCACAGCAGC 2820
CGCTGTAAGG AGATTAAAGT GACATAAACG TCCCGAGCGG GAGGGGGGAG GGCAGAGGAT 2880
TCAGGTCACC CCCATCCGTC CCCCGCCTGA CAGACGCTAT ATCGCTATCC AATCCAATAA 2940
AAAATCCCCC CCTTTTGCTT TAATTAATTT TACAGCTAGC TTGCTTAATT ACTTTCAATC 3000
AAAATCCTCC TGCCATCGCA AAATTAGAGA TGGTTGAGCT CCATTAGCCT AAATTCTTCA 3060
TTTCCATATA GAAAAGAGGC TGTCTGCAGA GCCAGCCTGG GCCCCTGGCA GGACAGACGC 3120
CCGTCTGCCC GCCCGCTGTG AGCCAGCCCA CCCCTGGCTT CCGCTCTCTG GCTATCTCTG 3180
GCCTATGCGT GTCCCCTCAC TCTCCTCCAT CACTGCTCCC TGGGCCATGA AGAGCTGAGG 3240
TTCAGGAGGG GTACCCGCTG CCCCGACTTC CCAGGATTCA CGAGGGGACT GCAGGGCTGG 3300
CACAGAGCTC TCCGCCAGGG CCTGCTGCTT TTGATGAAAG CATAGGCTGA TCCTGGGAGC 3360
CTGCTGCCCT GCCAAAGGGC CCCTGCTGCC TCCAGGACAG AGCCTAGTCC CAAACCTGAG 3420
GCAGACAGGT CTCCTGGGCC ATCTGCACCA CATGCCCCAG GAAGCGGTCC CTCTCCCAGC 3480
AGGCGGAAAC ACTCCCAACC CCGGACTTAG GCCCCTGTCA GAATAGACCC CTGGAGCCAA 3540
CGCCACCCAG GGCTCCCTCT GCCGATTCCA GGCTGGAGTC ATTGTTCACC ATCAGGATGA 3600
CTCGGGCCAG CTGTCTCGAT GGTGCTACCA AGCAATGTAG CAGCCCCCAC ATACTCTGGC 3660
ATTCTCCTAG GGCCCCCCGC GGGCCCCTCC TCCCCATACC ATAGTCCTGG TTCCCAGCCT 3720
GCAACAGCTG CACCTCCACC CCCAGCCTGG GTCGAGTGGG TGGTGGGTCT GGGCTCTGTC 3780
CACATCCTGT GCCTGCACGG GCACCCTTCT CCTCCCCTCC ACCTGCCTCA TCTTCACAGT 3840
CCCCAACCCC AACTCTGGAA GCTCCACTTC AGGTTTTCCA TACTACAACC CCGAGTGTCA 3900
CCACAGGGTC CGGCCCAACC TGGGCTCCAG CTGATTAAGG ATCTGCAACA GGATGTAGGG 3960
ATTACAGTAA AACCTGGCTC CGGATCTGCA GGGGCAGCAG GCCAAGTCCC AGCCCTGGGA 4020
CTCCCCTCCC CTACCCTTCC AGCATCCCTA CCCATTACCC GTCCCAAACC CAGCTGCCAA 4080
GTGAGGGAGG AAGGCTGAGC CCCTTGGCCC TTAGGGGACT CCTGGCTGGA CTCTAGGGGG 4140
TCTGGACTGA GAAGGGGTGG CATTAAGGAG CCCAGGCCAG CTCCTGCAGA AAGGCTGGGG 4200
TGGGGCAGGC TGGGGAAGGG GAGTGATGGC TTTATGCCGC CTGGCTTCCT TCTCAGGGAA 4260
CCAATGTGAA GGTGGGGTGT CCTGGGCCTG ACCTCTGGGC AAAGGCTGAG TAAGCAGGGA 4320
AGGAAGTACC CTAAAGGCCA GGAGAGCCCC TTCCAGGCAG 4360
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