Tag | Content |
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EnhancerAtlas ID | HS002-10004 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr9:130307080-130309270 |
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) |
KLF5 | MA0599.1 | chr9:130308845-130308855 | GCCCCGCCCC | + | 6.02 | SP2 | MA0516.2 | chr9:130308841-130308858 | CTCAGCCCCGCCCCATC | + | 6.18 | SP2 | MA0516.2 | chr9:130307978-130307995 | GAGAGGGCGGGGCTGAG | - | 6.34 |
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| Number of super-enhancer constituents: 42 | ID | Coordinate | Tissue/cell |
SE_00872 | chr9:130307100-130309530 | Adrenal_Gland | SE_01693 | chr9:130306961-130309439 | Aorta | SE_02373 | chr9:130307115-130309071 | Astrocytes | SE_02928 | chr9:130307014-130307921 | Bladder | SE_02928 | chr9:130307931-130309075 | Bladder | SE_06387 | chr9:130306787-130309382 | Brain_Hippocampus_Middle | SE_09759 | chr9:130307399-130308808 | CD14 | SE_23282 | chr9:130307005-130309400 | Colon_Crypt_1 | SE_23944 | chr9:130307025-130309323 | Colon_Crypt_2 | SE_25019 | chr9:130306996-130309121 | Colon_Crypt_3 | SE_26215 | chr9:130306862-130308979 | Duodenum_Smooth_Muscle | SE_26528 | chr9:130306979-130309763 | Esophagus | SE_30306 | chr9:130307079-130308183 | Fetal_Muscle | SE_30306 | chr9:130308225-130308976 | Fetal_Muscle | SE_31422 | chr9:130306988-130309744 | Gastric | SE_34381 | chr9:130307293-130309172 | HCT-116 | SE_34621 | chr9:130307025-130309715 | HeLa | SE_36116 | chr9:130306964-130309134 | HMEC | SE_37370 | chr9:130303549-130309613 | HSMMtube | SE_38118 | chr9:130307095-130309348 | HUVEC | SE_41594 | chr9:130306994-130309597 | LNCaP | SE_42140 | chr9:130306957-130309660 | Lung | SE_44201 | chr9:130306954-130309354 | NHDF-Ad | SE_44773 | chr9:130307002-130309462 | NHLF | SE_45705 | chr9:130295920-130309670 | Osteoblasts | SE_46654 | chr9:130307439-130308653 | Ovary | SE_46654 | chr9:130308770-130309105 | Ovary | SE_47421 | chr9:130307032-130309038 | Panc1 | SE_47474 | chr9:130307029-130307910 | Pancreas | SE_47474 | chr9:130307913-130309626 | Pancreas | SE_50184 | chr9:130306967-130309642 | Sigmoid_Colon | SE_52096 | chr9:130306944-130309175 | Skeletal_Muscle_Myoblast | SE_52507 | chr9:130306965-130309353 | Small_Intestine | SE_53712 | chr9:130307483-130308862 | Spleen | SE_54748 | chr9:130301339-130309339 | Stomach_Smooth_Muscle | SE_55718 | chr9:130307336-130308761 | u87 | SE_63440 | chr9:130298563-130342452 | NCI-H69 | SE_63712 | chr9:130306930-130309344 | HSMM | SE_64980 | chr9:130307148-130308824 | NHEK | SE_65259 | chr9:130301019-130309850 | Pancreatic_islets | SE_67516 | chr9:130307336-130308761 | u87 | SE_68760 | chr9:130306962-130308837 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 130307843 | 130308200 | chr9 | 130307429 | 130308679 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I127533 | chr9 | 130295863 | 130309594 |
|
Enhancer Sequence | CCATGGCTGT TATCTTGGCC TTTGGTGCTG GTAGAATCCC TGCCATGGCA CATTCCCTCA 60 TTCATGGGCC AGCCACATAC TCCTAAGAGG CCACTGGACC TGGGAAGGGA CCTCCAAGAT 120 CAAGTCCAAA CTATCTTTTG GACAGATGGG GAAACTGAGG CTGGGGAAAT GGGGAAAAGC 180 TGCCCAGGGT CCCATTGCCC TGTTAGTGTC CCAGCTCCTC TGAGACCATC TTGGGGAGAA 240 ACAGGTGAAT GGGGCTTTCA CACCCAGCGA ACCCAAGCGA ACCGCAACCT CAGCCCCTCA 300 GCTTCCTCCT CAGCGGAGGA AATCTGGCCT CTGGCCTTGG GGTCCCACGT CTACAGTGCC 360 CTCCTAGCGT CCACCCCTTG TGCCTGGCCA ACTCCTCTTT CTCCTCCCCA GGCTCAAGTG 420 CCACCTCCTC GGAACCCTCC CTCCAGACAA GTCCCGGCCT CCCAGGTCTC CACAGCCTCC 480 CTGGCCTCCA CTCCCACAGC CCCTGGCCTG CTCCCCGGCA CTCCCCTCAA CCACAGTTAA 540 TGCCTCATCT GAGACGCTCC CCGGACTGAG ACTGCTCTCC GCTGTCTCCC CAGCACCCAG 600 CTCCCGCCAG GCCCAGGGGG GTGCTTGATA AACAAGTGCC GAACAAGTGT TAGGTCACCC 660 AGCCTCAGGC GCCAAACAGG TCACCAGGGA GGCCATGGTG GGCAGGGACT CAGTCTGAGG 720 GCACAGGCCG TCTGGGTCTC ATCACAGAGG CAGGTCAGGC CCAACAGAGC CAGGAGTCAG 780 CTGGGGTTTT TCACAAGGCT GCCTTGAAAA CTCTTCTCGG TTGGCAAATA TTTAACCAGG 840 GCTGGGCCAC AACAGGTCTG GTGGGGAAGG GTGAGCTTTG AGGCAGGAGG GCTGGGAGGA 900 GAGGGCGGGG CTGAGGCGGG AGCCCAGAGA AATGCACCCA AAAAAACGGG TGACCCAAAA 960 CCCGCCCACT GGGGCTGCCC TTTCCTTTAC ACCTCGAGGC CGCCTGGTGG GAGGAAGTCC 1020 ATTCCCATCT TGACACAAAC AGAAGGAAAC AAAAGCCCTC TCATCCCCTC CTGCCCCCCA 1080 CCCCGCCTGC CTGGCAGCGG CCCCAGCCCA CAGCCCACAG TGGCAGCTTG TTCTGGGAGC 1140 CCAGGATGAG GCATGCCTGC CGTCTGGGAA CACAGATCCT CGCTGGGAGG GCAGCCCAGG 1200 GGGTGCCGAG GCCCCCAGCA GCGTCACCAC CCAGAGCAGG ACCCACACTC CAGGGGGTGG 1260 GCACCCAAGG CTGCCATCCT GCGGCCCCCT GGCCAAGGCC ACGCCCAAGG AGGAGGCTGA 1320 TCTATGACAG TGATTGTGTA GACACGACCC TCCTTTCCTC TCACATGGAG TCACCCTTTC 1380 CTGTTGACTT TTTCTCCACA ATGTCTCTGG CCTTCATTCC TTTCTTGTCA TCCTCACCAC 1440 CCCCACAGGA GCCTGAGCCT TAGCCAGCCA CCTGTCAAAA CTGCCCAGGC CCCAGAGGAG 1500 CATCCCCACG CCTGTCCACA GGTGCTCCTC ATACCCCTTC TCTCAGTCAC GTCCAGGGCC 1560 GAGGCTGGAC TGGGAACCCA GGGTGCTCTG CTGTGGCTCG TGCACATTGG CAGGTGCCCC 1620 CCACGGGCCT GGACACCTGC CCTGGGCCTG AGAACCCACC ACCAATGTTC CCCTCAGCGT 1680 CCAGCCTGGT GTTGGACCTT GAGATATGCA GGAAGAGCCT GTGGTCAAGC CCTTCCCCCA 1740 AGATGTCCGC AGTGTCAACC ACTCAGCCCC GCCCCATCAG ACAGGTCACA ACCACTGGGG 1800 CAGGGCTGAG GACAGGACCC AGCCCAGATC CCATGTCCTC CATCAGCCAG CGCGGGCCAA 1860 GCCAAAATGG CAGATGTCAG GCGAGTCACC AAGTTCAGGC GAGGCTCTGA GGCTTCATCA 1920 CGATGGCCAA GAAAGGGTTT ATGTTGCTCT CACTCATTCA TTCAGCAATC CTGGCCACTG 1980 GGTACTCAGG AGAGAGTACC CTAATGAGGG AGGCAGATTG TCAACAAAAA CTACAATTAC 2040 TAGGAGCCCC AACTGGGAGA AGCACAGGAG GTCACAGGAG CCCAGGAAGG TGACTGACCA 2100 AGCCTGCAGG GTCACGGAAG CCTCCCAGAG GGAGGTAGCA GCTGAGACAC AAAGAGTCCC 2160 TGCTAGGGGA GGGAGGACAC CGGGAAGGGA 2190
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