Tag | Content |
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EnhancerAtlas ID | HS108-27253 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr22:50363620-50365000 |
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: 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 |
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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 | TCATTCCAGA TGTAGCAGAA ACATGGTGAG GGCTCTTTGG GGCCACTATC ACCATCAGCC 60 TTTGCACAGG TGGGCTCCCC AGTGGGGCCT GGGAGACAGC ACAGGCAGCT CTGCAGAGAT 120 CTGGGGAGAG GGGCTTGGCA GTGGGGCAGC AGGTGCAAAG GCCCTGAGGC AGGCGGAGGG 180 GCCAGGACCA CAGTCCCATC CAGCACTCGC CCTGGGCCCT GCCTCCTGGT CTACTCCATG 240 CCCAGGGTCC CCCTCAACAG TCTGTTCCGT GTGGGATGAG CTGAGGGGAG GAAGCAGGGG 300 TCTCAGAAGC ACAAGGGCCC TGAGCAGAGC CCTGGGGACT GTCTCCTGCT GTGAGACAGG 360 ACTGGGCAGG GGCTGGCAGG CATGTGTCTG GGTGGCCCAT GCCAGCCGTG GAGCAGGCCA 420 GGGGCTGCTC TGATGCCCAC AGGACTGCCC ATTTGCCAGC ACAGGACCTG GCCCTGGAGG 480 GTCCTGGAGT CCCAGCTCTA CCCTGAAGCA GCCACCTCAG TCCTCCCTCT AGAAAGGACC 540 AGCAGGGTCT ACCGGGCCAC CCAGGAATGC AGGCAACTCT TATGATGTGT AGGCACCTGT 600 GTGTCCACAT CTGTACACGT AGAAAAGTGT CGGTGGGTGT GTAAATCTAT ACATGTTCCA 660 AGTGTGTGTG TCTGGGTTTT TGTGCATGTG CATGTGTGTG TGTGCATGTG AATCTCTGTG 720 TGTGCAGGTG TGATTTCCTG TGTGCACGTC TATGTGTATA TGCATGTGGG CACGTGTCTG 780 CCATGTATGT GTGTGCTCCA ATGTGTGTGA TCCTGTGTGT GCACACGTGT GTGTGCATGC 840 ACGCGTCTGC ACCTGGGCAG GACCTGGCCT AGGAAGAGCC TGGAGCCAAG ACTAGCAGTT 900 CTCCCCTCCC CCGCCCCCAA ATGACGTGGC CGCTGCCACC GCGTGACTCA CCCTCCCTTC 960 ACTCAAAGGG CACAGCAGCA CGTGGGGGCG CCTCCTGTGA CTCAGCACCT CCCGGAGGCG 1020 GTGAAGGGGG ACGCTGGTGA CAGGGGAGGA GTCTGGAGCT GAGAGGCGAA CGGAGAGCAC 1080 AGTGGAGCAC ACGGGCCCTG CCCACCCGCC TGTCCTGTCC AAGGATGCTG GGGCCCCGAC 1140 CAGCCGGTCA CAGGCGCNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN 1200 NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN 1260 NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN 1320 NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN 1380
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