Tag | Content |
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EnhancerAtlas ID | HS095-19952 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr22:50363380-50364880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HEY2 | MA0649.1 | chr22:50364388-50364398 | GGCACGTGTC | - | 6.02 | Npas2 | MA0626.1 | chr22:50364388-50364398 | GGCACGTGTC | + | 6.02 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_00426 | chr22:50354389-50365028 | Adipose_Nuclei | SE_01044 | chr22:50353163-50364855 | Adrenal_Gland | SE_10057 | chr22:50363395-50364983 | CD14 | SE_17909 | chr22:50362716-50365069 | CD4p_CD25-_CD45ROp_Memory | SE_19477 | chr22:50362118-50364919 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_23129 | chr22:50363042-50364827 | Colon_Crypt_1 | SE_23738 | chr22:50363659-50364809 | Colon_Crypt_2 | SE_24687 | chr22:50363517-50364841 | Colon_Crypt_3 | SE_26808 | chr22:50363561-50364843 | Esophagus | SE_29459 | chr22:50363708-50364757 | Fetal_Intestine_Large | SE_31381 | chr22:50340030-50364844 | Gastric | SE_34375 | chr22:50362078-50364952 | HCT-116 | SE_35007 | chr22:50363379-50364948 | HeLa | SE_35554 | chr22:50363866-50364772 | HepG2 | SE_41142 | chr22:50352558-50364901 | Left_Ventricle | SE_41617 | chr22:50363670-50364696 | LNCaP | SE_42159 | chr22:50339996-50364887 | Lung | SE_48365 | chr22:50351987-50364883 | Psoas_Muscle | SE_49074 | chr22:50351981-50364875 | Right_Atrium | SE_50117 | chr22:50362880-50364872 | Sigmoid_Colon | SE_52469 | chr22:50363083-50364861 | Small_Intestine | SE_53398 | chr22:50363456-50364874 | Spleen | SE_56937 | chr22:50362431-50363537 | VACO_400 | SE_56937 | chr22:50363556-50364515 | VACO_400 | SE_56937 | chr22:50364605-50364826 | VACO_400 | SE_61206 | chr22:50315437-50364432 | HBL1 | SE_61985 | chr22:50315627-50364432 | Toledo | SE_62450 | chr22:50318672-50364388 | Tonsil | SE_65335 | chr22:50354738-50364978 | Pancreatic_islets | SE_68380 | chr22:50327316-50364640 | TC32 | SE_68381 | chr22:50327316-50364640 | TC32 | SE_68382 | chr22:50327316-50364640 | TC32 |
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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 |
GH22I049968 | chr22 | 50362640 | 50364777 |
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Enhancer Sequence | ATGCCAGGAT TGAGTCTCAG GCCACATGTA CAACCTGCTG GCCAGGTCCC CACAGAGGCA 60 GCCCTATCCC ACGGAGCATC CCAGAGGGGC CACCCCAAGA CTCCCAACCC TCCACTTGCC 120 CCTGTCTGGT TTTCTGCTTA CCAAATCCTC CCACTTTTCA CTCAGGAGGG AACCAGACGT 180 TCCTGAGCCT GGGGGCTCAC CCCTGCCTGA GAGGCATGAC CAAGACCTAT GTGGGCGGGA 240 TCATTCCAGA TGTAGCAGAA ACATGGTGAG GGCTCTTTGG GGCCACTATC ACCATCAGCC 300 TTTGCACAGG TGGGCTCCCC AGTGGGGCCT GGGAGACAGC ACAGGCAGCT CTGCAGAGAT 360 CTGGGGAGAG GGGCTTGGCA GTGGGGCAGC AGGTGCAAAG GCCCTGAGGC AGGCGGAGGG 420 GCCAGGACCA CAGTCCCATC CAGCACTCGC CCTGGGCCCT GCCTCCTGGT CTACTCCATG 480 CCCAGGGTCC CCCTCAACAG TCTGTTCCGT GTGGGATGAG CTGAGGGGAG GAAGCAGGGG 540 TCTCAGAAGC ACAAGGGCCC TGAGCAGAGC CCTGGGGACT GTCTCCTGCT GTGAGACAGG 600 ACTGGGCAGG GGCTGGCAGG CATGTGTCTG GGTGGCCCAT GCCAGCCGTG GAGCAGGCCA 660 GGGGCTGCTC TGATGCCCAC AGGACTGCCC ATTTGCCAGC ACAGGACCTG GCCCTGGAGG 720 GTCCTGGAGT CCCAGCTCTA CCCTGAAGCA GCCACCTCAG TCCTCCCTCT AGAAAGGACC 780 AGCAGGGTCT ACCGGGCCAC CCAGGAATGC AGGCAACTCT TATGATGTGT AGGCACCTGT 840 GTGTCCACAT CTGTACACGT AGAAAAGTGT CGGTGGGTGT GTAAATCTAT ACATGTTCCA 900 AGTGTGTGTG TCTGGGTTTT TGTGCATGTG CATGTGTGTG TGTGCATGTG AATCTCTGTG 960 TGTGCAGGTG TGATTTCCTG TGTGCACGTC TATGTGTATA TGCATGTGGG CACGTGTCTG 1020 CCATGTATGT GTGTGCTCCA ATGTGTGTGA TCCTGTGTGT GCACACGTGT GTGTGCATGC 1080 ACGCGTCTGC ACCTGGGCAG GACCTGGCCT AGGAAGAGCC TGGAGCCAAG ACTAGCAGTT 1140 CTCCCCTCCC CCGCCCCCAA ATGACGTGGC CGCTGCCACC GCGTGACTCA CCCTCCCTTC 1200 ACTCAAAGGG CACAGCAGCA CGTGGGGGCG CCTCCTGTGA CTCAGCACCT CCCGGAGGCG 1260 GTGAAGGGGG ACGCTGGTGA CAGGGGAGGA GTCTGGAGCT GAGAGGCGAA CGGAGAGCAC 1320 AGTGGAGCAC ACGGGCCCTG CCCACCCGCC TGTCCTGTCC AAGGATGCTG GGGCCCCGAC 1380 CAGCCGGTCA CAGGCGCNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN 1440 NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN 1500
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