Tag | Content |
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EnhancerAtlas ID | HS120-00465 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr1:155101200-155102820 |
Target genes | Number: 34 | 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: 2 | Chromosome | Start | End |
chr1 | 155102278 | 155102800 | chr1 | 155102800 | 155102816 |
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Enhancer Sequence | AGCTTCAGAA TGAACAGAAG AGGTTAAAGG GGTTACAGAA GGTTCTGGGC AGGAAGGAGT 60 TAATTTCTCC TGGGCAGGTT TAGGGCTGTG AGGCAAATGG TACTGGGAGG AAGACTCTGT 120 CGGCCCCTTT GTTCTTGCCC TTGAGTTTTC TGAAGTTATG GGAACAATAT TTGAGGGAAT 180 ACAGGAGAGG GTGGTAGGGA GGAGCAGGGA GAGAAGTGGG CAGCTTGGTA TCACGAAAGC 240 CATCTCACCG GCTTAGCCAC TCTCGGCCCT AGCAAGCTTG CCCCCCACTC CCCTTGAGAA 300 ATATGTTGTG CCAGCTTCCT CTGACCCCGT GTCATCGTCT GGTGAGGCAG TCTGTTGTCT 360 GTGGCTTGTT AGGGTGGGGG AGAGAACAGC CAGCTGCCAA CCCCAGAGGG CAATGCCCTC 420 CTGCCCATGG ACGCTGGGGA GGCTCAGCCA GCCCTCCGCC ACCCGCTCCC TGTGCTTTGC 480 CTCCTTGACC TGATGCATCT CGCCCTAGTA TGGGAGAGAG CAAAGTCCCT GTTTATGCCC 540 ATGCCAGGTG TTGACTGGAG GAGGAGGAGG GGACAGGAAG CCATGAGTAG GGAGGGGGGG 600 ACCCTGGCCT TTTCCGTTCC CAAGCTCCCA GGTTTCCTCT CTTTCAGGAA GGAGCCTCTT 660 CCTTACCCAC CTCCCCGCCT TCCCTGACGC CGCTGCCCCC CTTTCCCAGA TGGGGAGCAA 720 GAGTCAAATG AAGGCTAAGT ACAGCAGACT GTACCCCCAG GAGAGGGGGC TGATGGGTGA 780 CCCTCTGGCC ACACACACAC ACACACACAC ACACACACAC ACACGCACAC CCTATCATAC 840 CCAGGACTAA AGAGACGCCA GTCCAGAGTA GAGTCCGTAG GCAGCCAAGC TGGGCCCAGC 900 GTGGGGGCAA ATATGAGGCT ACAATGAACG GGGTAGGTGA GGCTGGCATG GGTGACTCAG 960 GCCAGTGGGC AGCAGCCCTG GGATCTCCAG GCCTCAGGCG GGGGCAGCAT GCTGAGAAGG 1020 GCGCCAGCCT CCCTCATGCT GGAGGGCAGG CCCCTCATTC TGACCTGCCA GCTCCCTTTG 1080 TTTGGAGGAC ACTGTTGGGG GTGAGTGGGC GCTGTGCCCT CCTGGGGTCC TGGGGGCTGT 1140 GCACATTTGA CAAGGTAAGT TTTCACAAGT TCTCATGAGT GCTGGGGCGG GTAGCAGAGG 1200 TGGATGAGGA ATGAGTCAGT GCCCGTCACG GGAATGAGGG AAAGACGCCA GGCCCAGAGC 1260 TGAAATACCT GTTCTGAAAT GGCTTCTATG TTTATCTCTC CAGAGAGGAA TTTTAAAAGC 1320 CTCTCTCTGC TCCTCTCTTT TCCCCAGGGT GGGGGAGGGG CCTGGTAAGC CCAGTTTGGG 1380 CGCTGGCACG CTGCTGCAAA GCCTGGCCTC TCAGGGGTCA TGCTGATTGG GCAGTGGGTG 1440 CCCACCTCCG AGTCCTCTCT GCCTGACTCC TTCCTCGCCC TCCCAGCCGT GGCCAGGGCT 1500 TTCAGTTCGA AGCAACTTAG CGCTAATTCT GCTGGGTCTC TAGCTGGCAG TGCCTGGGGG 1560 AATTAGAGAA ACTGACCAGC TTGCGGGGTC GGGGGAAGCA CTTTTCCCCC TACTGGGACC 1620
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