Tag | Content |
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EnhancerAtlas ID | HS104-19478 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr14:77427040-77429160 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr14:77428491-77428512 | CTTTACTTTCACTTTCTAGTC | + | 7.7 | IRF2 | MA0051.1 | chr14:77428490-77428508 | GCTTTACTTTCACTTTCT | - | 6.22 | SP2 | MA0516.2 | chr14:77428148-77428165 | AGGGGGGCGGGACAGAG | - | 6.28 | TBX20 | MA0689.1 | chr14:77427532-77427543 | CTTCACACCTT | - | 6.32 | TBX21 | MA0690.1 | chr14:77427533-77427543 | TTCACACCTT | - | 6.02 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_01254 | chr14:77427828-77429221 | Adrenal_Gland | SE_08284 | chr14:77427720-77429238 | Brain_Inferior_Temporal_Lobe | SE_24529 | chr14:77427815-77429058 | Colon_Crypt_2 | SE_27091 | chr14:77426354-77429307 | Esophagus | SE_29618 | chr14:77427506-77429165 | Fetal_Muscle | SE_31928 | chr14:77427265-77429271 | Gastric | SE_32994 | chr14:77427618-77428287 | H1 | SE_32994 | chr14:77428378-77429199 | H1 | SE_34422 | chr14:77418557-77429646 | HCT-116 | SE_34742 | chr14:77415823-77429622 | HeLa | SE_37233 | chr14:77415973-77429404 | HSMMtube | SE_38430 | chr14:77419198-77429214 | HUVEC | SE_41258 | chr14:77419224-77429300 | Left_Ventricle | SE_41987 | chr14:77427895-77428623 | LNCaP | SE_42676 | chr14:77426329-77429253 | Lung | SE_44184 | chr14:77427235-77429338 | NHDF-Ad | SE_46080 | chr14:77427116-77429322 | Osteoblasts | SE_46723 | chr14:77427822-77428631 | Ovary | SE_47949 | chr14:77427780-77429166 | Pancreas | SE_48706 | chr14:77427612-77429247 | Right_Atrium | SE_49653 | chr14:77427823-77428586 | Right_Ventricle | SE_50880 | chr14:77427538-77429325 | Sigmoid_Colon | SE_53991 | chr14:77427468-77429327 | Spleen | SE_55769 | chr14:77427013-77429370 | u87 | SE_65382 | chr14:77427384-77429616 | Pancreatic_islets | SE_67544 | chr14:77427013-77429370 | u87 | SE_68739 | chr14:77427162-77429357 | H9 |
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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 | CGTTACAGGC ACCTGCCACC ACATCTGGCT AATTTTTTGT ATTTTTAGTA GAGACGGGGT 60 TTTGCCATGT TGGCCAGGCT GGTCTCGAAC TCCTGGCCTC AAGTGATCCG CATGCCTTGG 120 CCTCCCAGAG TGCTGGAATT ACAGGCGTGA GCCACCACGC CCAGCCAGAA TTTTTTTTAA 180 AAAAAGGAAA TAGAAGAGAA TGTAAGAATA GAAGTGCAGG TTAAAAGGAA CGTTTAATTT 240 CATAAAGTTT TTGCCTCAGG GTAGTATGCT TGTCTGAGTA ATGGGTTGAG ATAGGAACGC 300 ATTTCTTAGT GCAGGTCTTG ATTTCAAATG TTCGAAAGCC ACTGCTCTGG AAAATAGAGG 360 AGTGGAGACC AAAGTGTGCC CTTTGTGTAT GTGTCGGCAG TGGGGTGGGG GTGGGGGTCT 420 CTGTCCTAGC ATTTGGTTGC AGCACCCCAG GAGTGCCTGT AGGGGAACCA CTGACCTCCA 480 CTTTTCCATA CGCTTCACAC CTTCACACCG AAATGTGCTC CATTCCCTTT GCTATTTTTT 540 TTTCTTTTCT TTTTTTTTTT TTTAGACAGA GTCTAGCTCT GTCGCCCAGG CTGAAGTGCA 600 GTGGCACGAT CTCGGCTCAC TACAACCTCT GCCTCCTGGG TTCGAGTGAT TCTCCTGTCT 660 CAGCTTCCTG AGTAGCTGAG ACTATGCCTG GCTAACTTTT GCAGTTTTAG TAGAGACGGG 720 GTTTCACCAT GTTGGCCAGG CTGGTCTCAA ACTCCTGACC TTAGGTGACC TGCCCACTTC 780 AGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACCTC ACCCAGCCTG CTATTTTCAT 840 TAGGAGGAAA AGAGGGATGG TAGCTTTCAT CCAGATCCCC CATCTTCAGA ATGTTTTCAA 900 CTTTCCCCAG AACCTCCACA GCGTTAAGTC AGTCAAAATC CTTGGATGGA CCCTTCCAAG 960 TAGCAAGGGC CACCCTGTCC CCTTTCCCCT GGCCATGAGA CCACGCAGAG CGCAGGGGCC 1020 GGAGTCAGAA AGGGCAGTTT GGCCCCTGGG CAGTCTCCTG AGAGTCTTTC TCCTCCCAGT 1080 TTCTACTATT TGGCGGAACC TTGAATGCAG GGGGGCGGGA CAGAGAAAAA ACTAGAAAGC 1140 TCGACTTCTG CCTGCGGGGC CGGAAGCCCC GCTGCGGCCC CAGCCCGCGG TTAGCCCCTG 1200 TTTGTCATTT TGCAAATCTG GTCAACCCAC CTCCGGTGAA AACTCCCAAC CTCACCCCAG 1260 GGGGCAATGA CTAATTACAA AACACATTTT CTCTCGTTTT CGTCAAGCTC GCTGTCCCGC 1320 CCACACATCC CCCGCCTATC CCGGCACCCG TCGGCTTCCT CAGGAGCCTC ACTCAACTGT 1380 GTTGAATGAA CTCTTGGCCT GGTCCCTCCC CCAGAGACTT CACACCGTGG GGTTCTTTCC 1440 TCCCTGCTCA GCTTTACTTT CACTTTCTAG TCACTCTCAC TTCTCTGTCA GCTTCAGCTT 1500 CTCACCCTAG AGCTTGAGCC CTGGTCCTTT CTTAAGGCAG GGGCTATTGC CCAAGTCCTG 1560 GGCTGCACCC AATTCGTCAA AAGTCTCGAT TCATCAATAG TCAAAAATAT TTATCAAATG 1620 CATTCTGTTC CAGGCTCTAG GAATGCAGTG CAAGACAGGC AAGGTTCTTG CTCATACAGA 1680 GCTTCTAGAA ACCTGGGATA CAGAGATGCA ATCAAGTGAT AAAACACATG GATGAAGGCT 1740 CTGCCATTGA ACACATGGTT CTTGACAAGC CCACAGAGAG GCACAGCTAA GCCAGCCCTG 1800 GGGAGCCAGG GAGGGTTCCC TGGAGGGAGA GAAGCTGGAT CCAGGTCTGA AAGATGACTT 1860 GAAGTCAGCC ATGAGCAAGG AAGAGATTTT CCAGGCCAAG CGAACAGCCT GTGAGTGGTG 1920 CCATTTGGGT GAGGCTGGCT GGAGCTCACA GGGTGGGAGG GAGTGCAGGG AGCTGGGGTC 1980 CCCAAAGGTG GAAAGAAGCC AGACCCAAAA GGACTTTGAA ATTCTGCTCA GCCATTTGGA 2040 TTTTGTCCTG AGGGTGATGG AGATTTGTGA GCCCCAAATA TCTGAGACAG GTCCCAGTCC 2100 CTTTAGAAAG TTTATTTTTG 2120
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