Tag | Content |
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EnhancerAtlas ID | HS042-48692 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr9:130307030-130309110 |
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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH09I127533 | chr9 | 130295863 | 130309594 |
|
Enhancer Sequence | CCTCGGCCTC CCGAAGTGCT AGGATTACAG GCATGAGCCA CCGCACCCGG CCATGGCTGT 60 TATCTTGGCC TTTGGTGCTG GTAGAATCCC TGCCATGGCA CATTCCCTCA TTCATGGGCC 120 AGCCACATAC TCCTAAGAGG CCACTGGACC TGGGAAGGGA CCTCCAAGAT CAAGTCCAAA 180 CTATCTTTTG GACAGATGGG GAAACTGAGG CTGGGGAAAT GGGGAAAAGC TGCCCAGGGT 240 CCCATTGCCC TGTTAGTGTC CCAGCTCCTC TGAGACCATC TTGGGGAGAA ACAGGTGAAT 300 GGGGCTTTCA CACCCAGCGA ACCCAAGCGA ACCGCAACCT CAGCCCCTCA GCTTCCTCCT 360 CAGCGGAGGA AATCTGGCCT CTGGCCTTGG GGTCCCACGT CTACAGTGCC CTCCTAGCGT 420 CCACCCCTTG TGCCTGGCCA ACTCCTCTTT CTCCTCCCCA GGCTCAAGTG CCACCTCCTC 480 GGAACCCTCC CTCCAGACAA GTCCCGGCCT CCCAGGTCTC CACAGCCTCC CTGGCCTCCA 540 CTCCCACAGC CCCTGGCCTG CTCCCCGGCA CTCCCCTCAA CCACAGTTAA TGCCTCATCT 600 GAGACGCTCC CCGGACTGAG ACTGCTCTCC GCTGTCTCCC CAGCACCCAG CTCCCGCCAG 660 GCCCAGGGGG GTGCTTGATA AACAAGTGCC GAACAAGTGT TAGGTCACCC AGCCTCAGGC 720 GCCAAACAGG TCACCAGGGA GGCCATGGTG GGCAGGGACT CAGTCTGAGG GCACAGGCCG 780 TCTGGGTCTC ATCACAGAGG CAGGTCAGGC CCAACAGAGC CAGGAGTCAG CTGGGGTTTT 840 TCACAAGGCT GCCTTGAAAA CTCTTCTCGG TTGGCAAATA TTTAACCAGG GCTGGGCCAC 900 AACAGGTCTG GTGGGGAAGG GTGAGCTTTG AGGCAGGAGG GCTGGGAGGA GAGGGCGGGG 960 CTGAGGCGGG AGCCCAGAGA AATGCACCCA AAAAAACGGG TGACCCAAAA CCCGCCCACT 1020 GGGGCTGCCC TTTCCTTTAC ACCTCGAGGC CGCCTGGTGG GAGGAAGTCC ATTCCCATCT 1080 TGACACAAAC AGAAGGAAAC AAAAGCCCTC TCATCCCCTC CTGCCCCCCA CCCCGCCTGC 1140 CTGGCAGCGG CCCCAGCCCA CAGCCCACAG TGGCAGCTTG TTCTGGGAGC CCAGGATGAG 1200 GCATGCCTGC CGTCTGGGAA CACAGATCCT CGCTGGGAGG GCAGCCCAGG GGGTGCCGAG 1260 GCCCCCAGCA GCGTCACCAC CCAGAGCAGG ACCCACACTC CAGGGGGTGG GCACCCAAGG 1320 CTGCCATCCT GCGGCCCCCT GGCCAAGGCC ACGCCCAAGG AGGAGGCTGA TCTATGACAG 1380 TGATTGTGTA GACACGACCC TCCTTTCCTC TCACATGGAG TCACCCTTTC CTGTTGACTT 1440 TTTCTCCACA ATGTCTCTGG CCTTCATTCC TTTCTTGTCA TCCTCACCAC CCCCACAGGA 1500 GCCTGAGCCT TAGCCAGCCA CCTGTCAAAA CTGCCCAGGC CCCAGAGGAG CATCCCCACG 1560 CCTGTCCACA GGTGCTCCTC ATACCCCTTC TCTCAGTCAC GTCCAGGGCC GAGGCTGGAC 1620 TGGGAACCCA GGGTGCTCTG CTGTGGCTCG TGCACATTGG CAGGTGCCCC CCACGGGCCT 1680 GGACACCTGC CCTGGGCCTG AGAACCCACC ACCAATGTTC CCCTCAGCGT CCAGCCTGGT 1740 GTTGGACCTT GAGATATGCA GGAAGAGCCT GTGGTCAAGC CCTTCCCCCA AGATGTCCGC 1800 AGTGTCAACC ACTCAGCCCC GCCCCATCAG ACAGGTCACA ACCACTGGGG CAGGGCTGAG 1860 GACAGGACCC AGCCCAGATC CCATGTCCTC CATCAGCCAG CGCGGGCCAA GCCAAAATGG 1920 CAGATGTCAG GCGAGTCACC AAGTTCAGGC GAGGCTCTGA GGCTTCATCA CGATGGCCAA 1980 GAAAGGGTTT ATGTTGCTCT CACTCATTCA TTCAGCAATC CTGGCCACTG GGTACTCAGG 2040 AGAGAGTACC CTAATGAGGG AGGCAGATTG TCAACAAAAA 2080
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