| Tag | Content |
|---|
EnhancerAtlas ID | HS155-02681 |
Organism | Homo sapiens |
Tissue/cell | Ovary |
Coordinate | chr11:68120480-68123290 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr11:68121263-68121275 | GTGCACGTGGCC | - | 6.22 | | Myod1 | MA0499.1 | chr11:68123263-68123276 | AGGAACAGCTGCA | - | 7.34 | | Myog | MA0500.1 | chr11:68123266-68123277 | AACAGCTGCAG | + | 6.02 | | Tcf12 | MA0521.1 | chr11:68123266-68123277 | AACAGCTGCAG | + | 6.62 | | ZNF263 | MA0528.1 | chr11:68120907-68120928 | GGGAGAGGGAGAGGGAGAGGA | + | 6.53 | | ZNF263 | MA0528.1 | chr11:68120905-68120926 | GAGGGAGAGGGAGAGGGAGAG | + | 6.5 |
|
| | Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
| SE_01084 | chr11:68120238-68123276 | Adrenal_Gland | | SE_01626 | chr11:68117738-68123478 | Aorta | | SE_23171 | chr11:68122194-68122741 | Colon_Crypt_1 | | SE_23847 | chr11:68121803-68122147 | Colon_Crypt_2 | | SE_24963 | chr11:68121832-68122798 | Colon_Crypt_3 | | SE_26848 | chr11:68118376-68123358 | Esophagus | | SE_28000 | chr11:68120995-68122668 | Fetal_Intestine | | SE_28937 | chr11:68120260-68122935 | Fetal_Intestine_Large | | SE_30440 | chr11:68120529-68122975 | Fetal_Muscle | | SE_31879 | chr11:68119764-68123038 | Gastric | | SE_41339 | chr11:68118685-68123382 | Left_Ventricle | | SE_41686 | chr11:68120735-68123366 | LNCaP | | SE_42205 | chr11:68117678-68123483 | Lung | | SE_47270 | chr11:68119431-68123424 | Panc1 | | SE_47593 | chr11:68120880-68122853 | Pancreas | | SE_48658 | chr11:68117684-68123263 | Right_Atrium | | SE_52526 | chr11:68119518-68123360 | Small_Intestine | | SE_54745 | chr11:68118516-68123521 | Stomach_Smooth_Muscle | | SE_56733 | chr11:68121542-68123099 | VACO_400 | | SE_65630 | chr11:68121109-68123518 | Pancreatic_islets | | SE_68821 | chr11:68120613-68123171 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr11 | 68121765 | 68121884 | | chr11 | 68121174 | 68122354 | | chr11 | 68120787 | 68122152 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I068352 | chr11 | 68119993 | 68123322 |
|
Enhancer Sequence | AGGTACTTGG TGCTTGGTTG GGAGATGCTG GGCCCTTGGT TGGGAGTAGT CTTTCCCATG 60
CTCAGATCTG AGCTGGCTTT GCCTGCATCA TCTCTGCGAG CCAACTGTCC CTGTTTGGCT 120
CTGGCTTTTC TTAACTATTT GAAATGGTTC CTTTACATGC TTGCCTCTGA ATTCTCTCCC 180
AGAAGCCCTC CCCAGGATCA CACCTGTGGC TGTTCACTCC CACCCCTGCC CCTGGGGCAA 240
AGTTGACCTT AGTGTTGATT CCTGGGCCTC TCCCCACACC TTCCCTTTGC TCCAGTCATT 300
TGAATGAGAG AGTGAAAACA GTGAGATGCC GGCTCCCACT CATCAGATCC AGTGATGCTG 360
ATGACGCCAG CCATGGTCCT ACCCTGAGGT GCTGACTCTG TCCCTGTAGG CTCCATGTCT 420
CCGGAGAGGG AGAGGGAGAG GGAGAGGATT CCAGCCTGTC ACAGCGCCCG CGGCAGCAAC 480
CCCTGCTCGC CAAATACTGA CTTGAATAGT GGTCCTCAGG CATAAGTGTG GGCGCTGAGT 540
CCTGGGGCAG GACTGCTGTC CTGAGAGTGG GGACAGTGGA GGGTGGGTTT GTCCTCTGTC 600
CTGGCCACAG GCACACGGTT GCGAGGAGCA TCTTGGCCTT CCTCCCGGCC CTGCTAGAGC 660
CCCCGTCATC TCCTGTGCCC TCCTGCAGTG CTGTCCCCCA CCAGGGTCCT TCCTCAGAGG 720
AGGGGGTTCC TGCCCCGGCC ATCATCAGGA AGGGGGTCTC TGGGTCCGAG CGTCCACCTC 780
AGTGTGCACG TGGCCAAAAG GATCAAGAGC CCTGCAGCCA GGGGGGCCCC TCCTGAGACT 840
CGACTTCGTT GCAGTTTCAG CAATGCAGGT GGCCCCGTGC GGACATCCAG GCAGGGTTGA 900
GGGAAGGCAC ATCCCTCCCA GGCCCAGGGT ACCCATGTGG GTGGCAGAGC GGGCTCTGGG 960
GATGACCCTC TGGCCCCTGA GGATCTGGGG CCAGAAAGAC ACTGGCTTAG CATGGGAGGA 1020
GTCCCCGGCC TGTACCAGCC TGACAAGGGG CTGCAGTGGC CCCCGGGTCT CAAATTAAAG 1080
CCAGGGTGAA ACCCAACCCC CTCTTTAAAA TGCAAAATGG CCCTTCCCTA AAATAACACA 1140
CAACCACAAC CGCAGCTGGC TCTGCACGAA GGCCATGCTG CAGCTCTTTT CTTCGGAAGT 1200
CGATTTTCCT CCGTGGAATT TGGCTGGGCT TGTGGTAGCG TTTGAGACTC TGCAAGAGCA 1260
CGTCCACGCC AACCAGTCTC TGGTCACCGA CTGGCTCGCA AATTCCCCAT TTAAGGAAAC 1320
CAGCAGGCCT CTGTTATGAA ACTCGGGGAA GGAATGTGAA TTATGCTCCA TGCGGAGGCT 1380
CCTGCTCCTG CACGTTTTCC AGCCTTTTCC ATGGGCCACG GTGGAGCATT TGGGGAAGGC 1440
CTGTGTGGAT TCCCCCCCAA GTCCAGACTG ATGCCCCTGA TACCTTCTCA GGAGGTGGCG 1500
GAGGGTCTGG GCTCTGTCCA GGCTCCTAGG GGTGGGGACG TGCAGGTAAA GCAAGGCGTC 1560
TGCCGCAGGC ACGCGGGAGC CTTCCCTGGG CTGGCTGCCA GCACCTTGGA GTCCCAGGCT 1620
GCCAGGAAAA GTTCACCCAC ACCCGGGCTT TGCTGGCGAA GGGTGAGTCA TATGATGGCC 1680
GGGCTCGGGC CCTCAGCAGA CACCAAGTGT GTTCCCAGAG CAGCCGCTCA GCGCCTGTAA 1740
CCTGGAACAG GCCAGCCTTT CGGGGCCTCA GTTTTCTCAT CTGCCTAATG GGAATAGCAA 1800
TTCCCACCTT CCCTTTGTTG GTTGGGTTCT CACTAGATGC ACAGGAGACA GCAGCTTGAG 1860
AGGGACTGTT TGGAGAGCTG TTCCATGTGA CACCCCTCTT ACCCTGTCCC CACGGGGCCG 1920
GAGGAGCAGG GGCTTGGTGA TAGCAGCTGG GCGCAGTCAG CCTCTGCAGG GAAGAGGGCA 1980
TGTTTGGTTC GAGGCTCCTA TGCCCTCATT CTTGTTGATC TTGTCACAGC CCCTCTGGAA 2040
GGTGGAGATG GTACTCGCTC AGGAACGATA CCACTCAAGG AAGCATGGCC CCCTGGATGG 2100
GGTGGCCCTT GGTGCACCTG AGGCTCCTGA GGCTGCAGAG CACCATGGTG GGGGAGGAGG 2160
CGGCTGTGTG TCTGTCATTT GCCTCTTCTG CTGAATGGAG ACCCCCAGAG GGCAAAGCGG 2220
GGCTTGTTCT CCCTGTGTCC CGGGATCACT CTCATGCCTG GCTTGGGCGA GCTGCCTGTT 2280
TCTAAATCAC TTGCTAAGGC TGAGGGGAAT GGGGTTTGCC GCCCACCCCA GGAAGAAGGG 2340
AGCAAGGGAG TCAGCACCAT TTTACAAGGA CCAAGAGTGG GAGGAGGCTC CTCAGAGGAC 2400
ATTCTGGGCA CTGTCCCCTT TCTCTGCTGT GAAGGGTGGA CAAAACACAA TAGGTCTGCC 2460
AGCCCTTGTG TCCTGTGGCT CATCCCAGCT GGCTGGGATG GGAACTGAGT CCTCCAAGCT 2520
GGTGTGGTTC CCCTCTGGTC TCCGCTGAGA GTCACGCCCA GCCTCTGGGC ACACACCCTG 2580
TGGTCACCTC CAAACAGGGC ACACTGGGCA CTGGTGGGGG TGGGACCTGC CATCCCAGAC 2640
CTGGTGTCTG CTCACTTTGT CTTGGTTCAT TGGCCAGAGA TCACGTAAGG GCGCCCTGAG 2700
GATGTGCTTG TTTCTCATGG ATGGGTGATG CTTGTCTCTT GGGAACATGG AGAAGCAAAG 2760
CCACGTCGCC CACAGACCTA CCCAGGAACA GCTGCAGCTG CAGGTTCAGG 2810
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