| Tag | Content |
|---|
EnhancerAtlas ID | HS080-02916 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:205253020-205255350 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr1:205254178-205254189 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr1:205254178-205254189 | GACAGCTGCAG | + | 6.14 | | ZEB1 | MA0103.3 | chr1:205253262-205253273 | CCCACCTGCCC | + | 6.14 |
|
| | Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
| SE_02431 | chr1:205253201-205255000 | Astrocytes | | SE_03194 | chr1:205253181-205253866 | Brain_Angular_Gyrus | | SE_03194 | chr1:205253899-205254801 | Brain_Angular_Gyrus | | SE_03963 | chr1:205252695-205257315 | Brain_Anterior_Caudate | | SE_04837 | chr1:205252438-205255709 | Brain_Cingulate_Gyrus | | SE_05801 | chr1:205252449-205257899 | Brain_Hippocampus_Middle | | SE_06736 | chr1:205252450-205256085 | Brain_Hippocampus_Middle_150 | | SE_07799 | chr1:205252396-205255918 | Brain_Inferior_Temporal_Lobe | | SE_11085 | chr1:205251353-205259013 | CD20 | | SE_26974 | chr1:205252457-205257684 | Esophagus | | SE_29391 | chr1:205253543-205255044 | Fetal_Intestine_Large | | SE_32765 | chr1:205252644-205254723 | H1 | | SE_38936 | chr1:205252877-205255818 | IMR90 | | SE_43852 | chr1:205252499-205258684 | MM1S | | SE_46173 | chr1:205253006-205257823 | Osteoblasts | | SE_50327 | chr1:205252697-205257801 | Sigmoid_Colon | | SE_52983 | chr1:205252823-205257708 | Small_Intestine | | SE_54130 | chr1:205252675-205258056 | Spleen | | SE_55645 | chr1:205253025-205256564 | Thymus | | SE_56704 | chr1:205252917-205256555 | u87 | | SE_56879 | chr1:205252970-205254378 | VACO_400 | | SE_58462 | chr1:205242169-205295027 | Ly1 | | SE_58967 | chr1:205242236-205295022 | Ly3 | | SE_60263 | chr1:205242326-205284722 | Ly4 | | SE_60576 | chr1:205242267-205294889 | DHL6 | | SE_61365 | chr1:205242037-205294994 | HBL1 | | SE_61423 | chr1:205183427-205322469 | Toledo | | SE_62465 | chr1:205242393-205294944 | Tonsil | | SE_65493 | chr1:205252784-205254787 | Pancreatic_islets | | SE_67308 | chr1:205252499-205258684 | MM1S | | SE_68815 | chr1:205252846-205254572 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 205254805 | 205255191 | | chr1 | 205253892 | 205254222 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I205283 | chr1 | 205252730 | 205258354 |
|
Enhancer Sequence | TGCGGGCTCT AACCTACATC TGTCGACTCC AAAGCCACAC AGCCGCCCAC ACAAGGTAGC 60
TCTTTTCCTC ACCTCACCCC CTGAGCTCTG GAACACCTTT GTTCTGCCCA AACGAGAATG 120
AAGCAGCAAC GGAGGCAGCG GCAGGGGAAC TGTAAGGTGG CCCCAAACTC AGACTGTCCC 180
CAAGTTGGAG GCCTGCTAGG GCCTGGGAGC ACAGCAGTCC CCCACCAGGG AGTCTTCCCT 240
TCCCCACCTG CCCACTGCAG ACTGGGCACC CCTGCTGCAT GTGTCTGACC TCTGTGAACC 300
TCAGTTTCCC CAACATACAA TAACCCTGAC AGTCTGTCAT TCTGTGCTTC TGTGACGTCA 360
GCCTTAGGAG TTATCAGGGA CCCAAACTTG GGCTTCACAG GGGGCAGGAT GGAGGCCCTG 420
CCACTCGGAC CAGACCAGGT TGTGGTGAGG GGCAAGGGTG GTGCCTCCAG GCACCAATCC 480
AGAGTGACCT CACTCTCTGC AGGCTCCCCT GGGGCCCTGA GGGAGGGTGG GGTGCTGGAC 540
AGGCCTGCTA GATGGGAGCA GGTTTGGAAG GAGGTTTAGG AAGGGTGCGG TGGGGAAGGT 600
GTGCCGCTCA GGTTCAGTGT GATCACTAGA GAGGGGCACG CCTGCCTGCA TCGTCTGCCA 660
TGCCAGACAG GGCAGGACAG CTTCTCCCCC AGCCTGGGCC TTTAGGATCC ACTGTGTGAC 720
CATCCTGAGC CCCTTAGCAA GGTGTGAGCG GGGTTGGACA CCCTCCCCTC AACATCCATC 780
TAATGTCAGC CACCAGCCCT GCCTTGCTGC ATGATGGGAA ATCAGGGTAA GGGAGCCAAA 840
CCCCAGCTGC TCTCAGAGCT GTGAGGACAA GAGTGGAAAA CCTGCCCTCA CAGGCCCAGC 900
TGGCCAGAGG GCTTGTCTCT TTCAGTCGCC CTCCCCCAGA GGGAGCAGGA GCAGACAATG 960
GCCACCATGA CTCACCAGTG AGCCATCTTC CCCTCCCCAC CCCTCCAGCC TGGCCCATGA 1020
CAGCTTAGCT TGTCCTCCAA GGGAGCTGCA GCCCAGCCTC CCAGGGCCGC CAGCTTCCTC 1080
TCTCTTCACC CAACCTGGCT CCCCCCCTGC TTGTGCAACA CCACATCAGA GGGTTGTGAA 1140
GTGGAGAGGG AGGAGTTTGA CAGCTGCAGA CCCAGGCAGA CAGAGCAGAC TCCTTTGTGA 1200
AGGAGATAGA GGCTGCAGGG GCCCAAGTCC AGCCTGTACT CCCCTGCCCT GACCCACAAG 1260
GCATCACCCA GTCTCCCCAA ACCCTAGGGA AGTGGTCATT GTCATTTATT TGTTCCTTTC 1320
TTAGATAGAG CTTGGATCCT GTCTGCAATT TATTCCTTCC TGCAAAACCA AGTATGTGAG 1380
GCAGAGGAAA GTCCTATTCC ATTCCAGGAG GGACAGGGCT CCCTGTTGGA AAGTATTTCC 1440
TTTTGCTAAG TTTCTATCTG CCTCCCGGGT AGACTCCACT AGGCAGTATT TCAAGAAGTT 1500
AACGCACTTC CAATCCCCAT CTAACCTATA TTCTTTGCCG CAAGCCAAAT ACCCTTAGTT 1560
CTTTCAGTCA TTTCTCCTAA GACATGGATT TAAGACCTTT TGACAGCTTG GCCTGTATCC 1620
TCTGGAAACA TTTCCATTTA CCCAAGTTCT TCTTAAAACA TTATGTCTTT GTCCAGGTGC 1680
AGTGGCTCAC GCCTGTAATC TCAAAGTGGA GGCTGAGGGA GGAGCATCAG TTGGGTCCAG 1740
GAGTTTGAGA TCAGCCTGGG CAAGATGACA AGACCCCATC TCTAGTTAAA AAAAAAAAAA 1800
AAAATTACTG ATTCTCACCA AAAAAAAAAA AAAAGCCAGG CGTGAAGACA TGGGCCACCT 1860
ACTTGGGAGG CTGAGGTGGG AAGATCGCTT GAGCCTGGGA GATCAAGGCT CTTGAGCCTG 1920
GGAGATCAAG GCTGCAGTGA GCTGTGATCA CGCCACTGTA CTCTAGCCTA CGCGACAGAG 1980
TGAGACTCCA TCTCTAAAAA AACGAAACTA ACCAACCAAA AAAAAAAAAA AACCACAAAA 2040
AGCATGTTGT TTTGAACAGA GCGCAGTGCT CCAGCTAAGG TCAGGCCAGC ACAGAGGGTG 2100
CTAATGAAAT TCACCTCGCA GGCTCTGGCA CTGTGGTTCT CATGAGCTCT GTTAGCTTGC 2160
CGGTATTTTC AGACCCACAT AGGCATGTCC TTGTTGAGCA GGTCACTTCG GTTCATGAAT 2220
ACGGCCACCA AGGATTTGAG GCCCCTCTGC CTGCCCCCCA TGGAGGGAGC CCTAGGGCTC 2280
AGATGGTGGC TCTTAACAGA CCTCAATGGT CTGATGAAAA CTCTGCATCC 2330
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