| Tag | Content |
|---|
EnhancerAtlas ID | HS077-00998 |
Organism | Homo sapiens |
Tissue/cell | H128 |
Coordinate | chr1:205253000-205255280 |
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 | GCCACCAGAA GGTTGAGGAA TGCGGGCTCT AACCTACATC TGTCGACTCC AAAGCCACAC 60
AGCCGCCCAC ACAAGGTAGC TCTTTTCCTC ACCTCACCCC CTGAGCTCTG GAACACCTTT 120
GTTCTGCCCA AACGAGAATG AAGCAGCAAC GGAGGCAGCG GCAGGGGAAC TGTAAGGTGG 180
CCCCAAACTC AGACTGTCCC CAAGTTGGAG GCCTGCTAGG GCCTGGGAGC ACAGCAGTCC 240
CCCACCAGGG AGTCTTCCCT TCCCCACCTG CCCACTGCAG ACTGGGCACC CCTGCTGCAT 300
GTGTCTGACC TCTGTGAACC TCAGTTTCCC CAACATACAA TAACCCTGAC AGTCTGTCAT 360
TCTGTGCTTC TGTGACGTCA GCCTTAGGAG TTATCAGGGA CCCAAACTTG GGCTTCACAG 420
GGGGCAGGAT GGAGGCCCTG CCACTCGGAC CAGACCAGGT TGTGGTGAGG GGCAAGGGTG 480
GTGCCTCCAG GCACCAATCC AGAGTGACCT CACTCTCTGC AGGCTCCCCT GGGGCCCTGA 540
GGGAGGGTGG GGTGCTGGAC AGGCCTGCTA GATGGGAGCA GGTTTGGAAG GAGGTTTAGG 600
AAGGGTGCGG TGGGGAAGGT GTGCCGCTCA GGTTCAGTGT GATCACTAGA GAGGGGCACG 660
CCTGCCTGCA TCGTCTGCCA TGCCAGACAG GGCAGGACAG CTTCTCCCCC AGCCTGGGCC 720
TTTAGGATCC ACTGTGTGAC CATCCTGAGC CCCTTAGCAA GGTGTGAGCG GGGTTGGACA 780
CCCTCCCCTC AACATCCATC TAATGTCAGC CACCAGCCCT GCCTTGCTGC ATGATGGGAA 840
ATCAGGGTAA GGGAGCCAAA CCCCAGCTGC TCTCAGAGCT GTGAGGACAA GAGTGGAAAA 900
CCTGCCCTCA CAGGCCCAGC TGGCCAGAGG GCTTGTCTCT TTCAGTCGCC CTCCCCCAGA 960
GGGAGCAGGA GCAGACAATG GCCACCATGA CTCACCAGTG AGCCATCTTC CCCTCCCCAC 1020
CCCTCCAGCC TGGCCCATGA CAGCTTAGCT TGTCCTCCAA GGGAGCTGCA GCCCAGCCTC 1080
CCAGGGCCGC CAGCTTCCTC TCTCTTCACC CAACCTGGCT CCCCCCCTGC TTGTGCAACA 1140
CCACATCAGA GGGTTGTGAA GTGGAGAGGG AGGAGTTTGA CAGCTGCAGA CCCAGGCAGA 1200
CAGAGCAGAC TCCTTTGTGA AGGAGATAGA GGCTGCAGGG GCCCAAGTCC AGCCTGTACT 1260
CCCCTGCCCT GACCCACAAG GCATCACCCA GTCTCCCCAA ACCCTAGGGA AGTGGTCATT 1320
GTCATTTATT TGTTCCTTTC TTAGATAGAG CTTGGATCCT GTCTGCAATT TATTCCTTCC 1380
TGCAAAACCA AGTATGTGAG GCAGAGGAAA GTCCTATTCC ATTCCAGGAG GGACAGGGCT 1440
CCCTGTTGGA AAGTATTTCC TTTTGCTAAG TTTCTATCTG CCTCCCGGGT AGACTCCACT 1500
AGGCAGTATT TCAAGAAGTT AACGCACTTC CAATCCCCAT CTAACCTATA TTCTTTGCCG 1560
CAAGCCAAAT ACCCTTAGTT CTTTCAGTCA TTTCTCCTAA GACATGGATT TAAGACCTTT 1620
TGACAGCTTG GCCTGTATCC TCTGGAAACA TTTCCATTTA CCCAAGTTCT TCTTAAAACA 1680
TTATGTCTTT GTCCAGGTGC AGTGGCTCAC GCCTGTAATC TCAAAGTGGA GGCTGAGGGA 1740
GGAGCATCAG TTGGGTCCAG GAGTTTGAGA TCAGCCTGGG CAAGATGACA AGACCCCATC 1800
TCTAGTTAAA AAAAAAAAAA AAAATTACTG ATTCTCACCA AAAAAAAAAA AAAAGCCAGG 1860
CGTGAAGACA TGGGCCACCT ACTTGGGAGG CTGAGGTGGG AAGATCGCTT GAGCCTGGGA 1920
GATCAAGGCT CTTGAGCCTG GGAGATCAAG GCTGCAGTGA GCTGTGATCA CGCCACTGTA 1980
CTCTAGCCTA CGCGACAGAG TGAGACTCCA TCTCTAAAAA AACGAAACTA ACCAACCAAA 2040
AAAAAAAAAA AACCACAAAA AGCATGTTGT TTTGAACAGA GCGCAGTGCT CCAGCTAAGG 2100
TCAGGCCAGC ACAGAGGGTG CTAATGAAAT TCACCTCGCA GGCTCTGGCA CTGTGGTTCT 2160
CATGAGCTCT GTTAGCTTGC CGGTATTTTC AGACCCACAT AGGCATGTCC TTGTTGAGCA 2220
GGTCACTTCG GTTCATGAAT ACGGCCACCA AGGATTTGAG GCCCCTCTGC CTGCCCCCCA 2280
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