| Tag | Content |
|---|
EnhancerAtlas ID | HS150-01250 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr1:205252950-205254300 |
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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I205283 | chr1 | 205252730 | 205258354 |
|
Enhancer Sequence | ACTGTCACTT CACAGATGGG AAATGAGATC TAGGCAACTC TCAGGGTCCA GCCACCAGAA 60
GGTTGAGGAA TGCGGGCTCT AACCTACATC TGTCGACTCC AAAGCCACAC AGCCGCCCAC 120
ACAAGGTAGC TCTTTTCCTC ACCTCACCCC CTGAGCTCTG GAACACCTTT GTTCTGCCCA 180
AACGAGAATG AAGCAGCAAC GGAGGCAGCG GCAGGGGAAC TGTAAGGTGG CCCCAAACTC 240
AGACTGTCCC CAAGTTGGAG GCCTGCTAGG GCCTGGGAGC ACAGCAGTCC CCCACCAGGG 300
AGTCTTCCCT TCCCCACCTG CCCACTGCAG ACTGGGCACC CCTGCTGCAT GTGTCTGACC 360
TCTGTGAACC TCAGTTTCCC CAACATACAA TAACCCTGAC AGTCTGTCAT TCTGTGCTTC 420
TGTGACGTCA GCCTTAGGAG TTATCAGGGA CCCAAACTTG GGCTTCACAG GGGGCAGGAT 480
GGAGGCCCTG CCACTCGGAC CAGACCAGGT TGTGGTGAGG GGCAAGGGTG GTGCCTCCAG 540
GCACCAATCC AGAGTGACCT CACTCTCTGC AGGCTCCCCT GGGGCCCTGA GGGAGGGTGG 600
GGTGCTGGAC AGGCCTGCTA GATGGGAGCA GGTTTGGAAG GAGGTTTAGG AAGGGTGCGG 660
TGGGGAAGGT GTGCCGCTCA GGTTCAGTGT GATCACTAGA GAGGGGCACG CCTGCCTGCA 720
TCGTCTGCCA TGCCAGACAG GGCAGGACAG CTTCTCCCCC AGCCTGGGCC TTTAGGATCC 780
ACTGTGTGAC CATCCTGAGC CCCTTAGCAA GGTGTGAGCG GGGTTGGACA CCCTCCCCTC 840
AACATCCATC TAATGTCAGC CACCAGCCCT GCCTTGCTGC ATGATGGGAA ATCAGGGTAA 900
GGGAGCCAAA CCCCAGCTGC TCTCAGAGCT GTGAGGACAA GAGTGGAAAA CCTGCCCTCA 960
CAGGCCCAGC TGGCCAGAGG GCTTGTCTCT TTCAGTCGCC CTCCCCCAGA GGGAGCAGGA 1020
GCAGACAATG GCCACCATGA CTCACCAGTG AGCCATCTTC CCCTCCCCAC CCCTCCAGCC 1080
TGGCCCATGA CAGCTTAGCT TGTCCTCCAA GGGAGCTGCA GCCCAGCCTC CCAGGGCCGC 1140
CAGCTTCCTC TCTCTTCACC CAACCTGGCT CCCCCCCTGC TTGTGCAACA CCACATCAGA 1200
GGGTTGTGAA GTGGAGAGGG AGGAGTTTGA CAGCTGCAGA CCCAGGCAGA CAGAGCAGAC 1260
TCCTTTGTGA AGGAGATAGA GGCTGCAGGG GCCCAAGTCC AGCCTGTACT CCCCTGCCCT 1320
GACCCACAAG GCATCACCCA GTCTCCCCAA 1350
|
