| Tag | Content |
|---|
EnhancerAtlas ID | HS024-00266 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr1:17890070-17892630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:17891101-17891116 | TGGGTTCAAAGGCCA | + | 6.53 | | MYCN | MA0104.4 | chr1:17891089-17891101 | AGCCACGTGGCC | + | 6.37 | | MYCN | MA0104.4 | chr1:17891089-17891101 | AGCCACGTGGCC | - | 6.37 | | ZNF263 | MA0528.1 | chr1:17891863-17891884 | TTCCCTTCTCCCTCCTGCTTA | - | 6.14 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_00612 | chr1:17885040-17898127 | Adipose_Nuclei | | SE_01537 | chr1:17887238-17903710 | Aorta | | SE_03096 | chr1:17890604-17891914 | Bladder | | SE_06186 | chr1:17884729-17903611 | Brain_Hippocampus_Middle | | SE_23081 | chr1:17890473-17892557 | Colon_Crypt_1 | | SE_23747 | chr1:17890421-17891202 | Colon_Crypt_2 | | SE_23747 | chr1:17891217-17891794 | Colon_Crypt_2 | | SE_24767 | chr1:17890329-17891818 | Colon_Crypt_3 | | SE_26139 | chr1:17891743-17893168 | Duodenum_Smooth_Muscle | | SE_26573 | chr1:17889896-17898099 | Esophagus | | SE_31687 | chr1:17890278-17892487 | Gastric | | SE_34117 | chr1:17890518-17891819 | HCC1954 | | SE_40808 | chr1:17889889-17894001 | Left_Ventricle | | SE_43031 | chr1:17890076-17897872 | Lung | | SE_46963 | chr1:17890621-17891038 | Ovary | | SE_46963 | chr1:17891953-17892681 | Ovary | | SE_47562 | chr1:17890635-17891305 | Pancreas | | SE_47562 | chr1:17891307-17891921 | Pancreas | | SE_47562 | chr1:17891929-17892571 | Pancreas | | SE_50079 | chr1:17890152-17892462 | Sigmoid_Colon | | SE_52601 | chr1:17890706-17892409 | Small_Intestine | | SE_54767 | chr1:17885171-17898261 | Stomach_Smooth_Muscle | | SE_65277 | chr1:17890222-17891588 | Pancreatic_islets | | SE_65277 | chr1:17891654-17892888 | Pancreatic_islets | | SE_68684 | chr1:17890304-17893069 | H9 |
|
| | 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 |
| GH01I017564 | chr1 | 17890529 | 17892478 |
|
Enhancer Sequence | TCAGAACAGG ACTTGGCTCA TGGAGGTGCT TAATAAATGT GGGTTGAATG AATGAATGGT 60
TGGATGAATG AATGAATATT ACCTAATTGG GTCTCAGGAG TGTCATGACA CCCAGTTTGC 120
AGATGAATAA ACTGAGGCTT AGGGAGGTTA AGTTGCACAT TTGCTAGGTT GTGGAGCTGG 180
GATTTGGAGT CCCCACTGTC TGACTCCAGA GCCGGTGCAC AGACCCACCC ATCTATTAGG 240
ATCCTCAAGG AGGAATTCTT TCTGTGGCTG ACAGGTTGGA TTTCAACCTC TCAAAGACCC 300
CTCCGTCGTC TGAGAGCGTC TGATTGTGGG AAGAAACAAA ATGACCCAGA CAACAGCTGG 360
GTCAGTGCTG CAAGTGACAG CAGATGGCTC CTGCCACTAA CTCCTGTTCT GATCAGTGGG 420
TGCCCTTTCA AGGAGCCAGG TTGGGAGAGA GATGGATGCT GCCAGCCCCA AGGAGGCCCT 480
TCCAGGCTTG GTCTGACATC ATCGTTATCC TCAGCCACAG AGCGGGAGGG TGCTGGCTCT 540
GGCACAGCTG GCACATAGTG CTTGCTCTGG CCTGCACAGT GGGGCCCGTG TCTCAGGTCA 600
CCCCTGCCTG GGTGCATCTC CAGGGTGGTG GCTAGATGGC CTGGGTGAAT CCCAGGTGTT 660
CACGGGGACA TGTGCCTGCC CTCAGCCCCC AGGTGGTTCT GGACCAGAAT GCCCAGGAGC 720
TTAGGGCTGG GACCCAGAGA GACTTGGAGG GGGGCTGCTT TGAGAGGCTC TGTTAGGGGC 780
AGTGCCGCTG CAACACTTCA GGGGGGCCAC TGGTCTTGGG CACTTGATCT GAGTCCCCCA 840
AGTTCTCCTC CTGATGTGCT GTCCCACTGG GGCCCTGTCC TACTTGCTCC CATGGGTGGA 900
GGCTTCATGG TCCCACCTGA GTGTACCCCA GCAGCACAGG AGCCCAGCTG ACTGGTGGCT 960
GGCTCGTGGC TGAGGTTTTA ACCTGTAAAT ACTGTAGGGG CTCAAGACAC AGGCTCTGCA 1020
GCCACGTGGC CTGGGTTCAA AGGCCAGCGC TCTCATTTAT TGACTATGTG ACCTCGAGCA 1080
ATTTTCTGAA CCTCTCTATG CCTCTATTTC CTAACCTGTA AAAGGGAATG AGAGTGGCCC 1140
CTGTCTCAGA GGGTTTTTAG GAGGAAATTA TAGGAGCTGT AGGAGTAAAG GGCTTGGATT 1200
AGCACTGGGC CCTTAGCACG CAGTTAACAC GTGTTCGGTG TCTGATGTTG ATTTTGGCAC 1260
TGACATTGGG CAACCCAAGG AGCCACTGCA TTTCTGCTGT GCCCTGTGGC TGGCACCTGG 1320
ATTCCACTTC CTCAGTAATG CTTGTCATGA ATGGGCCAGG TCAGCAGGGA CAAGAAGAGC 1380
AAAGGCAGCA CCCGGGCACT TCACTCCCAC CCAAGGCCCC ATTCGGGCAG CTGTAACGAA 1440
ATGCCGTGAC TCTTACCAGC AACAGGCAGT TATTTCTCAA AGTTCTGAAG GCTGGAAGCC 1500
CATGATCAAG GCAACAGCAG ATTCGGTGTC TGGTGAGGGC CTGTTCCTTA TAGATGGTAC 1560
CTTCTCACTG TGTCCCTGCG TGGTGGGAGG GCCTAGCCGG GGCCTTGTTT ACAAGGATAC 1620
TAATCCCATT CACGAGGGCT CTACCCTCAT GACCTGATTA CCTCCCCAAA GCCCCACTGC 1680
CTAATCCATC ACCTTGGGGG TGAGGTTTCC GCATAGGAAT TTTAGGGGGA TAAAAACATG 1740
CAAATACTGT GGGGCTCAAG GCACAGGCCC TGGAAGCCCT CATTTCTACC TTCTTCCCTT 1800
CTCCCTCCTG CTTAACATTT GCTCCTTGCT GCTGCATCCC AGGCATTGCA GACGAACTAT 1860
CCATGCTTTT GGTCACCCTT TCAAGGAGCA CTAACTGGTG GACGGCCCCC CTCCAACTCC 1920
TCATTGCCTG AATCTAGGCT CAAGTCTGCT CTCAGGAGTT TCTGCAGCCC CCAGGTCTCC 1980
CGAAGGGAAG CCCAGCTGCT ATTGTCAACA CTGTTCAGTT CTCCTTCCCC TTCTGGACCG 2040
CCAGTGGCTG TGTCTTTCTC ACCACAGCAG GGGATACTTG ATGAATATGC ATAGAGGGTT 2100
GAGCCATGCG CTAGGCTCCG GGACACAGGG CAGGAGGGTG CAGCTCCTGG CCTCGGAGAG 2160
CTCGGCAGTC TGGTTGTTTA TTTACTAACT CGGGTACCAG GACCGTGGCT GGGCACTGAG 2220
GACATGGAGA GGCAAAAGAT GCAGTCCCAC CTTAAAGAGG CGGCTGTACA TATTCCCCCT 2280
CCCTCCCTGG CTGCCTCCTC TCCCCACCTC CTGTATTGCG GATGCTGGGC CAGGTGGTGC 2340
AGATACAGAC ACAAGTAGGT CGTGGTCTCT GCCCCCACAG TCTAGCGGGG AGAGGCACAA 2400
AAACAAGTAC TGTAGCAGAA TGCAGTTTCT TTAGATACTT GTAGCCTGGT GTTTGTCTGC 2460
CATGGAAACC AGTGGCAATG GCTTTGGTCT TTGTATTCCT GTGACTAGTA ATGGTGACAC 2520
AACCCTGCAT TAACAGGCCA GCGTCTGCTA TAGATCCCCA 2560
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