Tag | Content |
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EnhancerAtlas ID | HS050-70816 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:134131080-134132480 |
| Number of super-enhancer constituents: 38 | ID | Coordinate | Tissue/cell |
SE_09361 | chr9:134126808-134138940 | CD14 | SE_10759 | chr9:134130225-134133328 | CD19_Primary | SE_11405 | chr9:134127138-134155283 | CD20 | SE_12146 | chr9:134130208-134133493 | CD3 | SE_13249 | chr9:134131782-134132497 | CD34_Primary_RO01480 | SE_13579 | chr9:134131058-134133449 | CD34_Primary_RO01536 | SE_14464 | chr9:134130006-134133411 | CD4_Memory_Primary_7pool | SE_15482 | chr9:134130757-134132926 | CD4_Memory_Primary_8pool | SE_15960 | chr9:134130241-134133433 | CD4_Naive_Primary_7pool | SE_16450 | chr9:134130517-134133034 | CD4_Naive_Primary_8pool | SE_17086 | chr9:134130919-134132783 | CD4p_CD225int_CD127p_Tmem | SE_17445 | chr9:134129893-134155392 | CD4p_CD25-_CD45RAp_Naive | SE_17921 | chr9:134128949-134133914 | CD4p_CD25-_CD45ROp_Memory | SE_18747 | chr9:134130406-134134742 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19407 | chr9:134130269-134134369 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20268 | chr9:134127140-134134040 | CD56 | SE_20819 | chr9:134130581-134133004 | CD8_Memory_7pool | SE_21594 | chr9:134130488-134133494 | CD8_Naive_7pool | SE_22019 | chr9:134130594-134133078 | CD8_Naive_8pool | SE_22737 | chr9:134130058-134134193 | CD8_primiary | SE_25701 | chr9:134127131-134134558 | DND41 | SE_29891 | chr9:134130804-134132623 | Fetal_Muscle | SE_31045 | chr9:134130157-134132601 | Fetal_Thymus | SE_40648 | chr9:134130930-134132557 | Left_Ventricle | SE_42331 | chr9:134128984-134132556 | Lung | SE_43702 | chr9:134130117-134133808 | MM1S | SE_48088 | chr9:134131013-134133521 | Psoas_Muscle | SE_48582 | chr9:134128933-134132591 | Right_Atrium | SE_49606 | chr9:134131461-134132254 | Right_Ventricle | SE_50385 | chr9:134130947-134132571 | Sigmoid_Colon | SE_51267 | chr9:134128852-134132710 | Skeletal_Muscle | SE_52980 | chr9:134130955-134132577 | Small_Intestine | SE_53628 | chr9:134128994-134133668 | Spleen | SE_55150 | chr9:134130991-134132503 | Thymus | SE_59220 | chr9:134127420-134154306 | Ly3 | SE_61761 | chr9:134100900-134154925 | Toledo | SE_62280 | chr9:134108336-134154785 | Tonsil | SE_67312 | chr9:134130117-134133808 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 134131233 | 134132425 | chr9 | 134131602 | 134132161 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I131251 | chr9 | 134126988 | 134134384 |
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Enhancer Sequence | TTTTTTGTTT CCTGATGAAA CTGTCTTCTT TTGGGCTCCA AGAGGGGCTT TCCTGTTTGG 60 CCTCATGGCC CAGACTACAG CAAGTCTCTG TCCCATTTAA AACAGCCCCA GAGCAGAAGA 120 GGCTCTCCTG AGAAGTGACT TTGAAAGTGG GAGGTGGAGA TGTTATGGGG TCGCTGTGCA 180 GCTGCTTCTC CCAGACCCTG GATGTCTCAG GCAGGTGAGC CTGGCCTGGC CCAGACAGCC 240 GGCTCTCCCA GGCCCAGATC CTGGAGAGGA ACCCGTGACA GCTGGGCAGA ATCTACTGTC 300 TGTGCCTCTT CTCCCAGTCT GGACTTCTAA ATTTCACCTG CTGTCAGCTG GAGAGGCTGG 360 AGGGCTTCCA CTCTGTGACT AAATGCCACT TGGAATCCAC TTTACTCACA ACTCCCTCCT 420 TGTACATTTC CCTCTCGAAA CTGTTACCCA CAGATTCAGC TGCGTCTCCC CATCTCCCGT 480 CTCACTGCGC CTCTGCATGA AGGCTTTGCT CTCCTGAGCT TCTGAAACCC TGCTATCAGG 540 TTAGGCCTGC ATCCCATTCT CTGTACACAC ACACACACAC ACACACACAC ACACACACAC 600 ACACACACAC ACACACACAC ACACACACCA TAGTCTCTCA TGGGCAGAGC TCAGGAGCCG 660 ACTCCACACC GAGAAGCCAA ACCACGACAG TGAACTGCAC CACCCAGGAG CCATCTGCGT 720 GGAGCTCGGC CAGCAATGCC TGTTATGCAA TTTCCTGCTT TGGTGTCTCA GCCCCAGGAG 780 GCAGGATGTG AGCGCCGTTG GTTTGCTGCA ACGTGGAGAA CCCACAGAAG ACCCGAATTC 840 TGATGCCCAG AGTGCATGGG GCCTCCCTGT CCCCGTGGGG GTGCAGAGAA GCCACTGCCC 900 ACCCTGGATG ATGAGCCTGT GTGCGGTGGG TGCAGCAGCC GGCCCCTGCT CAAAGGGAAT 960 CAGATGGGCT CATTGTGGGC CAGAAAGAAC TGACTGCCCC GAGACTTCCG GGGTGGGGAG 1020 GGGGGTGCAC TTCCTGCCCG GGGCACCCAG GATGGGGGAG CAGAGGCCTG GGACCTTCTC 1080 AGTAACAGTC ACCAATGTTA TTGGACACTG CACATGGCCC CACCGTCTCA GGCTCAAGAC 1140 TGAGAGTGCG CTATGGCGAG AGGTGGCTCT GTGGCCAGAG TTCGAATCCT GGCTCCGCCT 1200 TCCCCTAGCT ATGTGGTCTC AGGCAGCTCC TTGGCGTCCA CTCTCCCCGT TCCTTCGTCT 1260 GTGAAATGGG GGTGGCAGTT AACACCTCCC TTGTGGGGTT GTCATGAGGA TTCAATGAGT 1320 TCGCACCCAG AAAGAACAGG GAGTTTCCAC TGAATCCGCC AGGAGGCAGC TCCTCTGAAA 1380 ATCTCCATTT TCTTTTTCCT 1400
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