Tag | Content |
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EnhancerAtlas ID | HS050-35820 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:28629210-28630800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr2:28629427-28629442 | TGACCTTTGGCCCTG | - | 6.24 | Nr2f6 | MA0677.1 | chr2:28629427-28629441 | TGACCTTTGGCCCT | - | 6.56 | RARA | MA0729.1 | chr2:28630208-28630226 | AAATGGCCTCATGACCTC | - | 6.21 | Rxra | MA0512.2 | chr2:28629427-28629441 | TGACCTTTGGCCCT | - | 6.18 | ZNF263 | MA0528.1 | chr2:28629779-28629800 | TGAGGAGGTGGGGAGGGGAGG | + | 6.56 |
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| Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
SE_00532 | chr2:28629101-28630654 | Adipose_Nuclei | SE_00936 | chr2:28629184-28632689 | Adrenal_Gland | SE_01852 | chr2:28629267-28632704 | Aorta | SE_02435 | chr2:28629255-28632743 | Astrocytes | SE_02920 | chr2:28629297-28630420 | Bladder | SE_09457 | chr2:28612393-28639628 | CD14 | SE_16603 | chr2:28628975-28630568 | CD4_Naive_Primary_8pool | SE_18763 | chr2:28628985-28635955 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19338 | chr2:28629101-28634999 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20015 | chr2:28628855-28637205 | CD56 | SE_21406 | chr2:28628991-28630860 | CD8_Memory_7pool | SE_22508 | chr2:28628988-28635261 | CD8_primiary | SE_23078 | chr2:28629286-28630800 | Colon_Crypt_1 | SE_23736 | chr2:28629559-28630196 | Colon_Crypt_2 | SE_24706 | chr2:28629455-28630072 | Colon_Crypt_3 | SE_25842 | chr2:28629221-28630926 | Duodenum_Smooth_Muscle | SE_26550 | chr2:28611854-28633926 | Esophagus | SE_31386 | chr2:28629008-28632746 | Gastric | SE_34659 | chr2:28629036-28633683 | HeLa | SE_37130 | chr2:28626786-28632931 | HSMMtube | SE_38066 | chr2:28627427-28634298 | HUVEC | SE_42329 | chr2:28629209-28631251 | Lung | SE_45875 | chr2:28629087-28633041 | Osteoblasts | SE_46832 | chr2:28629542-28630137 | Ovary | SE_48773 | chr2:28629275-28630717 | Right_Atrium | SE_50076 | chr2:28629205-28632736 | Sigmoid_Colon | SE_51112 | chr2:28629001-28630827 | Skeletal_Muscle | SE_52349 | chr2:28629259-28632737 | Small_Intestine | SE_53354 | chr2:28628992-28634013 | Spleen | SE_54732 | chr2:28629288-28630742 | Stomach_Smooth_Muscle | SE_56154 | chr2:28629101-28630614 | u87 | SE_62927 | chr2:28581266-28660518 | Tonsil | SE_63825 | chr2:28629203-28630715 | HSMM | SE_67698 | chr2:28629101-28630614 | u87 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH02I028404 | chr2 | 28627764 | 28634922 |
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Enhancer Sequence | GAGCCACCGC GCCCGGCCAC GCTCTCCATT CTCTTCTGGG CCTACCTCAC ACCAAATTTA 60 GAAATTTGTA TCCAGAGGGA CTTTGGAGAC CATCTTTTCT CATTTTCCCT TTATACCCAT 120 TTTACAGACA AGGAAACGGA GACCCAGAAA GGTGAAGGGC CCTGTTAGAG TCTCACAGTG 180 AATTAGTAGC AGAGCCAGCA CTGGAACCCA CTTCTCCTGA CCTTTGGCCC TGTGGTTTTC 240 CCACCACACC ACCTAGGCGT GCCTCATACA ATCTGTCTGG AGAGTTTCCT TCCTTTTTTG 300 AGAGGGAGGG AGAGAACAAG GAGCATTGTA TCCCACATCA GTTGGGAATT CACACATCTC 360 CCAGCAGCTT TAAGGAAGCC TGGGCAGTGG CAGCCTAGAA CTTTGGCTGT TCAGGTTGCC 420 AGCCCTCAGG GCTTTGCTCT GAAGCTTACT CCGGCCGTCC CCAGCCTCCC CCAGCCTCCC 480 TGCTAGGGAG GAGCCTGCCT CCGGAGCCGG CCTGGTGCCT CATAGGCCTC CTCTTGGGAG 540 GTTCCCTCTG TGCCCTGTGG CGGCGACTCT GAGGAGGTGG GGAGGGGAGG GTGTGTGTGG 600 CTTGTGGGTG GGTACATGGT GCTGCTGACA CACTCAAGCT GGAACCATGT TGATCTCACC 660 GCCCCTGAAC ACTTCCTATG TTGACAGCTC CCACAAGTTG CCCCACACCT CACCAGTCAG 720 GGGAGAGACT TCTAGGTCAG TCAGGAGGCC AAAAGTTGTC CAGAAGCAGC CAAGGGGGAA 780 GGAGGGCTTG AACTGGGTCA AGGCCAGCCT CCTTCTTTTC TGCCTCTCAT TAGCGAGGGA 840 TCTAGGGGGC TTCCTGGGCC TTAAGGGGAG CCCTGGTGGC CCTTTCAGTG GTGAGCCCTA 900 AACCCAGGCC TGCAGCAGGG CCATAAGGCT TTCTTGGCAA TTCTGCTGGG CTCAAGACAA 960 GACAGGTTTA GGAGCAGGAA GTATTCAGGG CCTTGGCCAA ATGGCCTCAT GACCTCAGCC 1020 GGGCTGTGGA CTTCCCTCTG TGTGACAGGC ATGGGATTGT CCTCTCTGGT GCTGTGATGA 1080 TTGTCCTCTC TTTGCTGTTC AAAACATCAC AGCAACAGAC CTCCAGGGCT AAAGGGAGCA 1140 TTGTGGGACT CTGACTTGGA CCCAACCAGG ACAGTGGCTC TTTCCTTCAT GGGGTGACCT 1200 GAAGTCCAGG CAGTATCCCT CCTTGGGGTA GCTTCTCCCT GCTCCTCCAA AAGTAGCTTT 1260 GATTTTGCCC CCAGGTGTCC CGTGAGAGCT GACCCAGGTC TTATTCCCCT TGAGATCTTC 1320 TAAGCTCCTA GTGTAGCACC GGGCAGTTAG TAGGTGTGCA GTCAACGTCT GATAACTGAA 1380 TGGGTGGGCT TTCCCTTTGT GTTGCTTTCT GCTTTGGCCC ACAGCCGTCT CCTTGTGTCA 1440 CCTCTGCCTG AGAGAGGCAT TGGGGTCACA GCTCTGCAGG GCTCTGTAGA ACCAGAGCAT 1500 TTGCCCTGCT CAGTAGAGCA GAGTTCATGC TTTCCGGTAT GAGTGACAGA TTCCTAACTG 1560 TCTCACTGGA AGAAGCTAGA TCCTAAGCTC 1590
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