Tag | Content |
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EnhancerAtlas ID | HS195-00426 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr1:155100990-155102820 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr1:155102149-155102160 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr1:155102149-155102160 | GGGTGACTCAG | + | 6.02 | ZNF263 | MA0528.1 | chr1:155101397-155101418 | GGAGGAGCAGGGAGAGAAGTG | + | 6.54 | ZNF263 | MA0528.1 | chr1:155101759-155101780 | GGAGGAGGAGGGGACAGGAAG | + | 7.15 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_06471 | chr1:155096466-155104728 | Brain_Hippocampus_Middle | SE_07527 | chr1:155096600-155104005 | Brain_Hippocampus_Middle_150 | SE_23168 | chr1:155096831-155104699 | Colon_Crypt_1 | SE_23913 | chr1:155096865-155102477 | Colon_Crypt_2 | SE_23913 | chr1:155102493-155103155 | Colon_Crypt_2 | SE_25038 | chr1:155096824-155103109 | Colon_Crypt_3 | SE_26314 | chr1:155097879-155104734 | Duodenum_Smooth_Muscle | SE_26817 | chr1:155096813-155103510 | Esophagus | SE_27749 | chr1:155096773-155104848 | Fetal_Intestine | SE_28639 | chr1:155096730-155104902 | Fetal_Intestine_Large | SE_31531 | chr1:155096816-155104839 | Gastric | SE_34608 | chr1:155099429-155103501 | HCT-116 | SE_35043 | chr1:155095845-155105030 | HeLa | SE_36485 | chr1:155099148-155103878 | HMEC | SE_40872 | chr1:155098208-155104773 | Left_Ventricle | SE_41746 | chr1:155096958-155103454 | LNCaP | SE_42320 | chr1:155096778-155104870 | Lung | SE_47900 | chr1:155098283-155103087 | Pancreas | SE_49199 | chr1:155097092-155104701 | Right_Atrium | SE_49607 | chr1:155100275-155103472 | Right_Ventricle | SE_50340 | chr1:155096805-155104715 | Sigmoid_Colon | SE_52513 | chr1:155096836-155104823 | Small_Intestine | SE_56988 | chr1:155096855-155103515 | VACO_400 | SE_57550 | chr1:155099144-155103474 | VACO_503 | SE_58142 | chr1:155097801-155103164 | VACO_9m | SE_65093 | chr1:155099051-155104035 | NHEK | SE_65444 | chr1:155096946-155105042 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 155102278 | 155102800 | chr1 | 155101105 | 155102178 | chr1 | 155102800 | 155102816 |
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Enhancer Sequence | TGGAAGGACC TCTCAGGAGA GAGCTGGGCT GTAGGCATTC ATTATGCATT CACCCTGTAT 60 TTAAAGCAAA CCTGGAAAGT CCCTCACTAG GGGTCTTTTG GGGTGGCATG AGTGAGGCAC 120 ATGCTGTGCA TGGGTAGGCT GAGGGAATCA CCTGTTTATG GGGCTCTCAA GTAGTAAAAG 180 CGAAGAGCTG GGAGAGGGAG ATCATGGGAA AGCTTCAGAA TGAACAGAAG AGGTTAAAGG 240 GGTTACAGAA GGTTCTGGGC AGGAAGGAGT TAATTTCTCC TGGGCAGGTT TAGGGCTGTG 300 AGGCAAATGG TACTGGGAGG AAGACTCTGT CGGCCCCTTT GTTCTTGCCC TTGAGTTTTC 360 TGAAGTTATG GGAACAATAT TTGAGGGAAT ACAGGAGAGG GTGGTAGGGA GGAGCAGGGA 420 GAGAAGTGGG CAGCTTGGTA TCACGAAAGC CATCTCACCG GCTTAGCCAC TCTCGGCCCT 480 AGCAAGCTTG CCCCCCACTC CCCTTGAGAA ATATGTTGTG CCAGCTTCCT CTGACCCCGT 540 GTCATCGTCT GGTGAGGCAG TCTGTTGTCT GTGGCTTGTT AGGGTGGGGG AGAGAACAGC 600 CAGCTGCCAA CCCCAGAGGG CAATGCCCTC CTGCCCATGG ACGCTGGGGA GGCTCAGCCA 660 GCCCTCCGCC ACCCGCTCCC TGTGCTTTGC CTCCTTGACC TGATGCATCT CGCCCTAGTA 720 TGGGAGAGAG CAAAGTCCCT GTTTATGCCC ATGCCAGGTG TTGACTGGAG GAGGAGGAGG 780 GGACAGGAAG CCATGAGTAG GGAGGGGGGG ACCCTGGCCT TTTCCGTTCC CAAGCTCCCA 840 GGTTTCCTCT CTTTCAGGAA GGAGCCTCTT CCTTACCCAC CTCCCCGCCT TCCCTGACGC 900 CGCTGCCCCC CTTTCCCAGA TGGGGAGCAA GAGTCAAATG AAGGCTAAGT ACAGCAGACT 960 GTACCCCCAG GAGAGGGGGC TGATGGGTGA CCCTCTGGCC ACACACACAC ACACACACAC 1020 ACACACACAC ACACGCACAC CCTATCATAC CCAGGACTAA AGAGACGCCA GTCCAGAGTA 1080 GAGTCCGTAG GCAGCCAAGC TGGGCCCAGC GTGGGGGCAA ATATGAGGCT ACAATGAACG 1140 GGGTAGGTGA GGCTGGCATG GGTGACTCAG GCCAGTGGGC AGCAGCCCTG GGATCTCCAG 1200 GCCTCAGGCG GGGGCAGCAT GCTGAGAAGG GCGCCAGCCT CCCTCATGCT GGAGGGCAGG 1260 CCCCTCATTC TGACCTGCCA GCTCCCTTTG TTTGGAGGAC ACTGTTGGGG GTGAGTGGGC 1320 GCTGTGCCCT CCTGGGGTCC TGGGGGCTGT GCACATTTGA CAAGGTAAGT TTTCACAAGT 1380 TCTCATGAGT GCTGGGGCGG GTAGCAGAGG TGGATGAGGA ATGAGTCAGT GCCCGTCACG 1440 GGAATGAGGG AAAGACGCCA GGCCCAGAGC TGAAATACCT GTTCTGAAAT GGCTTCTATG 1500 TTTATCTCTC CAGAGAGGAA TTTTAAAAGC CTCTCTCTGC TCCTCTCTTT TCCCCAGGGT 1560 GGGGGAGGGG CCTGGTAAGC CCAGTTTGGG CGCTGGCACG CTGCTGCAAA GCCTGGCCTC 1620 TCAGGGGTCA TGCTGATTGG GCAGTGGGTG CCCACCTCCG AGTCCTCTCT GCCTGACTCC 1680 TTCCTCGCCC TCCCAGCCGT GGCCAGGGCT TTCAGTTCGA AGCAACTTAG CGCTAATTCT 1740 GCTGGGTCTC TAGCTGGCAG TGCCTGGGGG AATTAGAGAA ACTGACCAGC TTGCGGGGTC 1800 GGGGGAAGCA CTTTTCCCCC TACTGGGACC 1830
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