| Tag | Content |
|---|
EnhancerAtlas ID | HS140-00327 |
Organism | Homo sapiens |
Tissue/cell | Namalwa |
Coordinate | chr1:205253730-205256240 |
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 |
|
| | Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
| SE_02431 | chr1:205253201-205255000 | Astrocytes | | 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 | ACTGTGTGAC CATCCTGAGC CCCTTAGCAA GGTGTGAGCG GGGTTGGACA CCCTCCCCTC 60
AACATCCATC TAATGTCAGC CACCAGCCCT GCCTTGCTGC ATGATGGGAA ATCAGGGTAA 120
GGGAGCCAAA CCCCAGCTGC TCTCAGAGCT GTGAGGACAA GAGTGGAAAA CCTGCCCTCA 180
CAGGCCCAGC TGGCCAGAGG GCTTGTCTCT TTCAGTCGCC CTCCCCCAGA GGGAGCAGGA 240
GCAGACAATG GCCACCATGA CTCACCAGTG AGCCATCTTC CCCTCCCCAC CCCTCCAGCC 300
TGGCCCATGA CAGCTTAGCT TGTCCTCCAA GGGAGCTGCA GCCCAGCCTC CCAGGGCCGC 360
CAGCTTCCTC TCTCTTCACC CAACCTGGCT CCCCCCCTGC TTGTGCAACA CCACATCAGA 420
GGGTTGTGAA GTGGAGAGGG AGGAGTTTGA CAGCTGCAGA CCCAGGCAGA CAGAGCAGAC 480
TCCTTTGTGA AGGAGATAGA GGCTGCAGGG GCCCAAGTCC AGCCTGTACT CCCCTGCCCT 540
GACCCACAAG GCATCACCCA GTCTCCCCAA ACCCTAGGGA AGTGGTCATT GTCATTTATT 600
TGTTCCTTTC TTAGATAGAG CTTGGATCCT GTCTGCAATT TATTCCTTCC TGCAAAACCA 660
AGTATGTGAG GCAGAGGAAA GTCCTATTCC ATTCCAGGAG GGACAGGGCT CCCTGTTGGA 720
AAGTATTTCC TTTTGCTAAG TTTCTATCTG CCTCCCGGGT AGACTCCACT AGGCAGTATT 780
TCAAGAAGTT AACGCACTTC CAATCCCCAT CTAACCTATA TTCTTTGCCG CAAGCCAAAT 840
ACCCTTAGTT CTTTCAGTCA TTTCTCCTAA GACATGGATT TAAGACCTTT TGACAGCTTG 900
GCCTGTATCC TCTGGAAACA TTTCCATTTA CCCAAGTTCT TCTTAAAACA TTATGTCTTT 960
GTCCAGGTGC AGTGGCTCAC GCCTGTAATC TCAAAGTGGA GGCTGAGGGA GGAGCATCAG 1020
TTGGGTCCAG GAGTTTGAGA TCAGCCTGGG CAAGATGACA AGACCCCATC TCTAGTTAAA 1080
AAAAAAAAAA AAAATTACTG ATTCTCACCA AAAAAAAAAA AAAAGCCAGG CGTGAAGACA 1140
TGGGCCACCT ACTTGGGAGG CTGAGGTGGG AAGATCGCTT GAGCCTGGGA GATCAAGGCT 1200
CTTGAGCCTG GGAGATCAAG GCTGCAGTGA GCTGTGATCA CGCCACTGTA CTCTAGCCTA 1260
CGCGACAGAG TGAGACTCCA TCTCTAAAAA AACGAAACTA ACCAACCAAA AAAAAAAAAA 1320
AACCACAAAA AGCATGTTGT TTTGAACAGA GCGCAGTGCT CCAGCTAAGG TCAGGCCAGC 1380
ACAGAGGGTG CTAATGAAAT TCACCTCGCA GGCTCTGGCA CTGTGGTTCT CATGAGCTCT 1440
GTTAGCTTGC CGGTATTTTC AGACCCACAT AGGCATGTCC TTGTTGAGCA GGTCACTTCG 1500
GTTCATGAAT ACGGCCACCA AGGATTTGAG GCCCCTCTGC CTGCCCCCCA TGGAGGGAGC 1560
CCTAGGGCTC AGATGGTGGC TCTTAACAGA CCTCAATGGT CTGATGAAAA CTCTGCATCC 1620
TCTTCCAAGA AAAACGCATC TACTCAAAAA TTCTCTATAT GACACCAGGA CTCCCTGCAG 1680
ACCATCCTCA GACCCCAGGT TAGGAATTTC CATCTGGAAG CTGATACTCA AAAATAAATT 1740
CTGAGGCAGC CTCCCTATTC AAACTGTGGG GCTCAGGGCA AATTCAAAGT AATAAAGTAA 1800
TAACCTCTCA CACGAGTGCT GTGCTCGACA ACTCACAATA CACGTTCACG TACATTGCTG 1860
GGATAGACCC TAGGGTCTGG ATTATAATCG AATAAAGGAG GTCAAGGCCC AGAGAGGTCC 1920
AGTGACTTGC TCAAGGTCAC ACAGCCAATC TGGGCAAAGT CACTCCAGAC TCTCTTACCT 1980
TCATGGGGCC TCACAGAAGC CCAACACAAT TTGCCCACCA GTGGGGAAGA TGCAATGGAG 2040
AACAGGTTGC ATTTGGCCCC TGGGGAAACT GGTCCTGGCT GTGTTCAGCC GGCTCCTGCC 2100
GCTGCTCCAC AGAGGCACAC CCAGCTTGGC CTCTGTGGTG AGCTGTGGTG AGCTGTGGTG 2160
AGCTGTGGTT TGAGCAGCCT CCCTCCTAAC GAAGGCAGAG AGAAGGCCAG GTTGTCAGGC 2220
TGTGTCTTGT GAGAAGGAGG GAACCAGAGG AGGGGCAACG GCAGAAACCA GACCTGAAGC 2280
CTGAACCCCA GGAACCCAGG GGACAAAGAC TCCCTGGCCA CCACTTGTCC CAAGACTGCA 2340
GACACCTCAC TGGCCAGGAG CATACAAGCA GGAGTATACA ATGTGGCCGG GGGTGCATAG 2400
GAGTCAGGAT ACAGAGCCAT GTTCTGTGTG TATGATGTTC ACATACAGGA GCCAGACTTG 2460
ACCATGGGAG ACCAGTTTTT AAGTTTCCAA GGAATTCTTG CTCCCTAAAC 2510
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