Tag | Content |
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EnhancerAtlas ID | HS184-01538 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:155101160-155102820 |
Target genes | Number: 33 | 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 | GTAGTAAAAG CGAAGAGCTG GGAGAGGGAG ATCATGGGAA AGCTTCAGAA TGAACAGAAG 60 AGGTTAAAGG GGTTACAGAA GGTTCTGGGC AGGAAGGAGT TAATTTCTCC TGGGCAGGTT 120 TAGGGCTGTG AGGCAAATGG TACTGGGAGG AAGACTCTGT CGGCCCCTTT GTTCTTGCCC 180 TTGAGTTTTC TGAAGTTATG GGAACAATAT TTGAGGGAAT ACAGGAGAGG GTGGTAGGGA 240 GGAGCAGGGA GAGAAGTGGG CAGCTTGGTA TCACGAAAGC CATCTCACCG GCTTAGCCAC 300 TCTCGGCCCT AGCAAGCTTG CCCCCCACTC CCCTTGAGAA ATATGTTGTG CCAGCTTCCT 360 CTGACCCCGT GTCATCGTCT GGTGAGGCAG TCTGTTGTCT GTGGCTTGTT AGGGTGGGGG 420 AGAGAACAGC CAGCTGCCAA CCCCAGAGGG CAATGCCCTC CTGCCCATGG ACGCTGGGGA 480 GGCTCAGCCA GCCCTCCGCC ACCCGCTCCC TGTGCTTTGC CTCCTTGACC TGATGCATCT 540 CGCCCTAGTA TGGGAGAGAG CAAAGTCCCT GTTTATGCCC ATGCCAGGTG TTGACTGGAG 600 GAGGAGGAGG GGACAGGAAG CCATGAGTAG GGAGGGGGGG ACCCTGGCCT TTTCCGTTCC 660 CAAGCTCCCA GGTTTCCTCT CTTTCAGGAA GGAGCCTCTT CCTTACCCAC CTCCCCGCCT 720 TCCCTGACGC CGCTGCCCCC CTTTCCCAGA TGGGGAGCAA GAGTCAAATG AAGGCTAAGT 780 ACAGCAGACT GTACCCCCAG GAGAGGGGGC TGATGGGTGA CCCTCTGGCC ACACACACAC 840 ACACACACAC ACACACACAC ACACGCACAC CCTATCATAC CCAGGACTAA AGAGACGCCA 900 GTCCAGAGTA GAGTCCGTAG GCAGCCAAGC TGGGCCCAGC GTGGGGGCAA ATATGAGGCT 960 ACAATGAACG GGGTAGGTGA GGCTGGCATG GGTGACTCAG GCCAGTGGGC AGCAGCCCTG 1020 GGATCTCCAG GCCTCAGGCG GGGGCAGCAT GCTGAGAAGG GCGCCAGCCT CCCTCATGCT 1080 GGAGGGCAGG CCCCTCATTC TGACCTGCCA GCTCCCTTTG TTTGGAGGAC ACTGTTGGGG 1140 GTGAGTGGGC GCTGTGCCCT CCTGGGGTCC TGGGGGCTGT GCACATTTGA CAAGGTAAGT 1200 TTTCACAAGT TCTCATGAGT GCTGGGGCGG GTAGCAGAGG TGGATGAGGA ATGAGTCAGT 1260 GCCCGTCACG GGAATGAGGG AAAGACGCCA GGCCCAGAGC TGAAATACCT GTTCTGAAAT 1320 GGCTTCTATG TTTATCTCTC CAGAGAGGAA TTTTAAAAGC CTCTCTCTGC TCCTCTCTTT 1380 TCCCCAGGGT GGGGGAGGGG CCTGGTAAGC CCAGTTTGGG CGCTGGCACG CTGCTGCAAA 1440 GCCTGGCCTC TCAGGGGTCA TGCTGATTGG GCAGTGGGTG CCCACCTCCG AGTCCTCTCT 1500 GCCTGACTCC TTCCTCGCCC TCCCAGCCGT GGCCAGGGCT TTCAGTTCGA AGCAACTTAG 1560 CGCTAATTCT GCTGGGTCTC TAGCTGGCAG TGCCTGGGGG AATTAGAGAA ACTGACCAGC 1620 TTGCGGGGTC GGGGGAAGCA CTTTTCCCCC TACTGGGACC 1660
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