| Tag | Content |
|---|
EnhancerAtlas ID | HS161-03186 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr11:95974390-95977640 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr11:95974465-95974476 | CTTCTGGGAAG | + | 6.14 | | ZBTB18 | MA0698.1 | chr11:95977312-95977325 | GTTCCAGATGTTT | + | 6.04 | | ZBTB33 | MA0527.1 | chr11:95976669-95976684 | CAGACCTCGCGAGAG | - | 7.29 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_00421 | chr11:95973587-95977998 | Adipose_Nuclei | | SE_02492 | chr11:95975619-95977693 | Astrocytes | | SE_09528 | chr11:95974025-95977884 | CD14 | | SE_10685 | chr11:95975506-95977701 | CD19_Primary | | SE_11167 | chr11:95975121-95983264 | CD20 | | SE_12380 | chr11:95975921-95977191 | CD3 | | SE_15173 | chr11:95974985-95978232 | CD4_Memory_Primary_7pool | | SE_16197 | chr11:95975909-95977207 | CD4_Naive_Primary_7pool | | SE_17498 | chr11:95975244-95978855 | CD4p_CD25-_CD45RAp_Naive | | SE_18301 | chr11:95974974-95977994 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_30644 | chr11:95974968-95977668 | Fetal_Muscle | | SE_31211 | chr11:95974041-95977421 | Fetal_Thymus | | SE_36675 | chr11:95975745-95977186 | HMEC | | SE_38420 | chr11:95975400-95977617 | HUVEC | | SE_44431 | chr11:95975606-95977612 | NHDF-Ad | | SE_45599 | chr11:95974103-95978312 | Osteoblasts | | SE_50559 | chr11:95974188-95975430 | Sigmoid_Colon | | SE_50559 | chr11:95975503-95977558 | Sigmoid_Colon | | SE_53120 | chr11:95975523-95977493 | Small_Intestine | | SE_54051 | chr11:95974319-95975423 | Spleen | | SE_54051 | chr11:95975534-95977634 | Spleen | | SE_57212 | chr11:95976030-95976842 | VACO_400 | | SE_57212 | chr11:95976983-95977504 | VACO_400 | | SE_58447 | chr11:95917840-96001635 | Ly1 | | SE_61108 | chr11:95917662-96027831 | HBL1 | | SE_61760 | chr11:95940172-96001818 | Toledo | | SE_62369 | chr11:95920962-96006907 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 95976157 | 95976737 | | chr11 | 95974669 | 95975000 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I096241 | chr11 | 95974312 | 95977896 |
|
Enhancer Sequence | ATTTAGTGCT TTAGCAGAGA AACCAACTCT GAAATGAGGA CTTTGAGACT GGCTTTTATT 60
TCCTACTAGG TGGTCCTTCT GGGAAGATCA GTGCACAGCT TCTCTTTCCA ACATCTACTA 120
AAAAATCCTT TTGAAACAAT GTGGGAGGCT GACGACTATT CCCCTATTGC AGTGGTCCTT 180
GACAGGGGGT GATTTGGCCC CCCAGGAGAC ATTTGGCAAT GTCTGGAGAT ATTTTTAACT 240
TTTGTAACTG GAGGGAGGGG TCTACTGGCA CCTAGTGGGT AGAGGCCAGA GATGCTGGTA 300
AATATCTTAT AATGCACAGG ACAGCCCCAT ACAAAAAGGA CTTAGTCCAG AAAGAAAATA 360
GTGCCACGGG TAAGAAACCT TGCCCTATTG GCTTCTCTGT CAACATAACA GGTATTGCCT 420
GTGAACATTT GTTGCCAGAG TGAGTGTCCC TGGGACAGTG TTGATTGCGG AAGTCAACAG 480
AGGAGGAGAA TTTAAGTCCT CCACTTCCTG CTGGGCTCTC ATAAAACGAT GCAAACCAAT 540
GGGCCCTTGG TTTGTTTTAG GTTAGACTTG TGGAAGTTTT CGAAATTCTA GTTTTGCTCT 600
GTTCAATCAT TTTAGAAAAT ATCTAAGTAT CGTTCTGGTT TGAATTAGTT TGTTTGGTCT 660
ATTTTTGAAC ATATTTTGCT TCAGTTACAA CATTAATATT TGGGTTTTAT TCAGTTCAGG 720
GTTCAGCAAA TTAGCAAAAT TACAGCTTTG GGTTATGGTT ACTTGTTATA TATCTTTGCA 780
TGAGAGCCCA TGCAAGTGTG ATTGGAGCAG AAAGCTAAGG TTCATCACAA CCATGGCCAC 840
TAGAGCTTTC TATGATCCAA GGAAGTTAAT TCACTTTTTT ACTTTGTTTC TCAAGAGGAT 900
TCAACAATGC AAGCACCAAA CCAAGTGGAT GCCCCTCTTT CTGTTGCTTG GTTTAAAATT 960
AAAACCCTTG ATGAATAAAG TGATTTATTT CATATTATAT TTATGAAAAG GTAGAGCACT 1020
CTCAATGTTT TGAGTATTCC TGAAACTGTT TACTTAATTA TACAATGAGA AACAAGACAG 1080
GAAAAAACTT CATAAAAATC ACTAGGGATT TTAAAAAAAT GCCCATGTAC TCTTATTTTG 1140
CAATGGCTCT GGTTGTGAAA TCATCAGACT GAAAAATACT GGAGGAGTGG TGAGGGTGGA 1200
TTTTAGTGAC AAGATTTCCT TAAGGCTGTA AATAAACCAG ATTCAGTAAG AGAAACAGAG 1260
ATGGCAGTTT TCATCATAAA AGGGGGAAAA CATTTTCCAG TTGAATTATA GGTACAGCAC 1320
AAAACAGTTG TTCCGTTTTT AAAAACTTTA GTTTCTGCAG GCTGAAACAG AGCATTTCAT 1380
TTGGCTCAGT TCATGAAAGC CATCTGCACC TGCTCACGAA ACAGCTTAAA GAGAAAAAAA 1440
AAGTGTGCAC CAAGGATTTT AACTTACACA GACAATAAGG GATAGACTCT GGCACTCAAG 1500
CACTGAAAAA GCAGGAGCAT GATAAAGGGG AAAGGATCAT AATTTTATGA AGTGCCAATA 1560
AATAATAACC CCAAATCAGC TTACAGCATC ACTTAGGTTT ACCTGTGGAA GCTACACTTG 1620
CCTGTTCTGG TTGCATGTTT AAAAGTTAAG CAATTAAACC TCAATTATAT AGGTTTTTCT 1680
TTTATGTAGC CTAGGGTTGA ATGCATTACT GGCAGGAAAC TTTAGCTCAT GAATTCAATC 1740
AAAAATCCTT TCATTTGTCA GAACTGCTTC CTGCTGCCTC CTTTAAACAT CTGCTTCTCC 1800
AGTTCAGGGA CACACACACA CACACATACA CATACACACA CACCCCCTCT TTGTTAAAAT 1860
AATAAGCAAT CTACCAACTT CCCTTGCAAA AGTTACATTC TCTCTTACAC ACACACACAC 1920
TTGTTCCCAG TAGAGTTTAT TTAATGTGTC TTTTATAGCT TCCTTGTCCT TCTCTCTTCC 1980
TTTCCGCTTT TAAATTCTGG AAAACCTCAA GCTGACAAAA GAAGACATTT TAAAAATGCG 2040
AGGATAAGGC CCGGCCGGCC TCCAGACCAA TGAGAAGGAA GCAGAGCAAG GAGGCGGGGG 2100
AGGCGGGGTT GGCTGTCGGG AATTGCCTGC ACTCCTTAAA CGGCAGGCAC TTCCTGCTAG 2160
AGGAGGCCAG CTCTGAACAG ACAGAAATCG GGTGGAAAGC TAGCAGGAGG CGTTGCTCAA 2220
GTTCAAAACA ATCTGTGCGT GTCCAGGCAC GCGCGGAGCC AGACCCCAGC CGCGCGGCTC 2280
AGACCTCGCG AGAGCCATCA CCTGAGAAAT CCACAGCCTT TTCTCATCAG GCTTAGACTG 2340
TTTTTCCCAT ACCTCCAAGA AGGAAGACCC ACATGTTAAA ACTATGAGAA AAGCTGAAAG 2400
TGCCTTCTGA ACAGTCATCC TTCTTTTTCT TTTTTTTTTT TTTTTGAGAC GGAGTCTCGC 2460
TTTGTCGCCC AGGCTGGAGT GCAGTGGCGC GATGTTGTCT CACTGCAAGC TCCGCCTCCC 2520
AGGTTCATGC CATTCTCCTG CCTCAGCCTT CCGAGTAGCT GGGACTACAG GCGCACGCCA 2580
CCACGCCTGG CTAATTTTTT GTATTTTTAG TAGAGAAAGG GTTTCACCGT GTTAGTCAGG 2640
ATGGTTTGTC GTGATCCGCC CATCTTGGCC TCCCAAAGTG CTGGGATTAC TGGCGTGAGC 2700
CACCGCGCCC GGCCCAGTCA TCCTTCTTTA ACCACGACAT AGGTACTCAG GTCCGCTGGC 2760
CTTCCTCTGC ACTGATGGAC TTTTCTTTGT GAAACTGATT CAGAGGCGGA CCTCAAGTGG 2820
CTTATTCCTT CGCCTAAAAA TCGTGCTGCT TTTTCCTCTA GTGAAGTCTG GAGTACAAAT 2880
TAATAAAAAC TTGGGGCTGT GCGGCCTAAT GGCTCAAACC GTGTTCCAGA TGTTTTGAAA 2940
TATTATTACC CCTTTTGAGA GCCTCAGTGT CTCCCTGGAG GGTAAGACAT CTGCCTTAAG 3000
GGCACTTACC AAGAAACTAC AAACATTTGA CTGCACACAA CAATGGTATC TTAATAAGAC 3060
AAGGTGCTTA ATACAACTGG CTGCCCTATT ATGACGTGTA AGAACGTTTT CATATGTAAG 3120
CTATGCTTGC AATTCTATAA GTAGATAAGG AAGCTTGTGG TTGTTACACT TCTAATATAT 3180
GGATAGAAGA GCTTAAACTC TAATGATTAG AAAATTACTG GTATTCTGAA GTGTATTACA 3240
ATCAATGCAT 3250
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