Tag | Content |
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EnhancerAtlas ID | HS145-01636 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr1:155101070-155102730 |
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: 1 | Chromosome | Start | End |
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Enhancer Sequence | CCCTCACTAG GGGTCTTTTG GGGTGGCATG AGTGAGGCAC ATGCTGTGCA TGGGTAGGCT 60 GAGGGAATCA CCTGTTTATG GGGCTCTCAA GTAGTAAAAG CGAAGAGCTG GGAGAGGGAG 120 ATCATGGGAA AGCTTCAGAA TGAACAGAAG AGGTTAAAGG GGTTACAGAA GGTTCTGGGC 180 AGGAAGGAGT TAATTTCTCC TGGGCAGGTT TAGGGCTGTG AGGCAAATGG TACTGGGAGG 240 AAGACTCTGT CGGCCCCTTT GTTCTTGCCC TTGAGTTTTC TGAAGTTATG GGAACAATAT 300 TTGAGGGAAT ACAGGAGAGG GTGGTAGGGA GGAGCAGGGA GAGAAGTGGG CAGCTTGGTA 360 TCACGAAAGC CATCTCACCG GCTTAGCCAC TCTCGGCCCT AGCAAGCTTG CCCCCCACTC 420 CCCTTGAGAA ATATGTTGTG CCAGCTTCCT CTGACCCCGT GTCATCGTCT GGTGAGGCAG 480 TCTGTTGTCT GTGGCTTGTT AGGGTGGGGG AGAGAACAGC CAGCTGCCAA CCCCAGAGGG 540 CAATGCCCTC CTGCCCATGG ACGCTGGGGA GGCTCAGCCA GCCCTCCGCC ACCCGCTCCC 600 TGTGCTTTGC CTCCTTGACC TGATGCATCT CGCCCTAGTA TGGGAGAGAG CAAAGTCCCT 660 GTTTATGCCC ATGCCAGGTG TTGACTGGAG GAGGAGGAGG GGACAGGAAG CCATGAGTAG 720 GGAGGGGGGG ACCCTGGCCT TTTCCGTTCC CAAGCTCCCA GGTTTCCTCT CTTTCAGGAA 780 GGAGCCTCTT CCTTACCCAC CTCCCCGCCT TCCCTGACGC CGCTGCCCCC CTTTCCCAGA 840 TGGGGAGCAA GAGTCAAATG AAGGCTAAGT ACAGCAGACT GTACCCCCAG GAGAGGGGGC 900 TGATGGGTGA CCCTCTGGCC ACACACACAC ACACACACAC ACACACACAC ACACGCACAC 960 CCTATCATAC CCAGGACTAA AGAGACGCCA GTCCAGAGTA GAGTCCGTAG GCAGCCAAGC 1020 TGGGCCCAGC GTGGGGGCAA ATATGAGGCT ACAATGAACG GGGTAGGTGA GGCTGGCATG 1080 GGTGACTCAG GCCAGTGGGC AGCAGCCCTG GGATCTCCAG GCCTCAGGCG GGGGCAGCAT 1140 GCTGAGAAGG GCGCCAGCCT CCCTCATGCT GGAGGGCAGG CCCCTCATTC TGACCTGCCA 1200 GCTCCCTTTG TTTGGAGGAC ACTGTTGGGG GTGAGTGGGC GCTGTGCCCT CCTGGGGTCC 1260 TGGGGGCTGT GCACATTTGA CAAGGTAAGT TTTCACAAGT TCTCATGAGT GCTGGGGCGG 1320 GTAGCAGAGG TGGATGAGGA ATGAGTCAGT GCCCGTCACG GGAATGAGGG AAAGACGCCA 1380 GGCCCAGAGC TGAAATACCT GTTCTGAAAT GGCTTCTATG TTTATCTCTC CAGAGAGGAA 1440 TTTTAAAAGC CTCTCTCTGC TCCTCTCTTT TCCCCAGGGT GGGGGAGGGG CCTGGTAAGC 1500 CCAGTTTGGG CGCTGGCACG CTGCTGCAAA GCCTGGCCTC TCAGGGGTCA TGCTGATTGG 1560 GCAGTGGGTG CCCACCTCCG AGTCCTCTCT GCCTGACTCC TTCCTCGCCC TCCCAGCCGT 1620 GGCCAGGGCT TTCAGTTCGA AGCAACTTAG CGCTAATTCT 1660
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