Tag | Content |
---|
EnhancerAtlas ID | HS103-15293 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr22:50363550-50364780 |
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 |
|
| Number of super-enhancer constituents: 31 | 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 | chr22:50363556-50364515 | 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 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH22I049968 | chr22 | 50362640 | 50364777 |
|
Enhancer Sequence | AACCAGACGT TCCTGAGCCT GGGGGCTCAC CCCTGCCTGA GAGGCATGAC CAAGACCTAT 60 GTGGGCGGGA TCATTCCAGA TGTAGCAGAA ACATGGTGAG GGCTCTTTGG GGCCACTATC 120 ACCATCAGCC TTTGCACAGG TGGGCTCCCC AGTGGGGCCT GGGAGACAGC ACAGGCAGCT 180 CTGCAGAGAT CTGGGGAGAG GGGCTTGGCA GTGGGGCAGC AGGTGCAAAG GCCCTGAGGC 240 AGGCGGAGGG GCCAGGACCA CAGTCCCATC CAGCACTCGC CCTGGGCCCT GCCTCCTGGT 300 CTACTCCATG CCCAGGGTCC CCCTCAACAG TCTGTTCCGT GTGGGATGAG CTGAGGGGAG 360 GAAGCAGGGG TCTCAGAAGC ACAAGGGCCC TGAGCAGAGC CCTGGGGACT GTCTCCTGCT 420 GTGAGACAGG ACTGGGCAGG GGCTGGCAGG CATGTGTCTG GGTGGCCCAT GCCAGCCGTG 480 GAGCAGGCCA GGGGCTGCTC TGATGCCCAC AGGACTGCCC ATTTGCCAGC ACAGGACCTG 540 GCCCTGGAGG GTCCTGGAGT CCCAGCTCTA CCCTGAAGCA GCCACCTCAG TCCTCCCTCT 600 AGAAAGGACC AGCAGGGTCT ACCGGGCCAC CCAGGAATGC AGGCAACTCT TATGATGTGT 660 AGGCACCTGT GTGTCCACAT CTGTACACGT AGAAAAGTGT CGGTGGGTGT GTAAATCTAT 720 ACATGTTCCA AGTGTGTGTG TCTGGGTTTT TGTGCATGTG CATGTGTGTG TGTGCATGTG 780 AATCTCTGTG TGTGCAGGTG TGATTTCCTG TGTGCACGTC TATGTGTATA TGCATGTGGG 840 CACGTGTCTG CCATGTATGT GTGTGCTCCA ATGTGTGTGA TCCTGTGTGT GCACACGTGT 900 GTGTGCATGC ACGCGTCTGC ACCTGGGCAG GACCTGGCCT AGGAAGAGCC TGGAGCCAAG 960 ACTAGCAGTT CTCCCCTCCC CCGCCCCCAA ATGACGTGGC CGCTGCCACC GCGTGACTCA 1020 CCCTCCCTTC ACTCAAAGGG CACAGCAGCA CGTGGGGGCG CCTCCTGTGA CTCAGCACCT 1080 CCCGGAGGCG GTGAAGGGGG ACGCTGGTGA CAGGGGAGGA GTCTGGAGCT GAGAGGCGAA 1140 CGGAGAGCAC AGTGGAGCAC ACGGGCCCTG CCCACCCGCC TGTCCTGTCC AAGGATGCTG 1200 GGGCCCCGAC CAGCCGGTCA CAGGCGCNNN 1230
|