| Tag | Content |
|---|
EnhancerAtlas ID | HS139-26316 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr19:16476290-16478390 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr19:16477854-16477865 | TTTTATGGCTC | - | 6.14 | | Hnf4a | MA0114.3 | chr19:16476296-16476312 | CTTGGACTTTGAGCCT | - | 6.22 | | MEF2A | MA0052.3 | chr19:16477656-16477668 | TTTATTTTTAGC | - | 6.04 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_10209 | chr19:16475292-16484487 | CD19_Primary | | SE_11315 | chr19:16474290-16485342 | CD20 | | SE_11937 | chr19:16473771-16485687 | CD3 | | SE_14609 | chr19:16473598-16485678 | CD4_Memory_Primary_7pool | | SE_15445 | chr19:16475158-16485044 | CD4_Memory_Primary_8pool | | SE_15848 | chr19:16475046-16485222 | CD4_Naive_Primary_7pool | | SE_16360 | chr19:16475218-16485623 | CD4_Naive_Primary_8pool | | SE_17083 | chr19:16475450-16484473 | CD4p_CD225int_CD127p_Tmem | | SE_17319 | chr19:16468964-16489910 | CD4p_CD25-_CD45RAp_Naive | | SE_18015 | chr19:16473227-16488773 | CD4p_CD25-_CD45ROp_Memory | | SE_19662 | chr19:16473512-16478578 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20143 | chr19:16473448-16485693 | CD56 | | SE_20988 | chr19:16475387-16484302 | CD8_Memory_7pool | | SE_21494 | chr19:16475691-16485519 | CD8_Naive_7pool | | SE_21927 | chr19:16475508-16486069 | CD8_Naive_8pool | | SE_22683 | chr19:16473350-16485641 | CD8_primiary | | SE_31861 | chr19:16477431-16478097 | Gastric | | SE_50928 | chr19:16475528-16478306 | Sigmoid_Colon | | SE_53383 | chr19:16475646-16485667 | Spleen | | SE_55459 | chr19:16476277-16478310 | Thymus | | SE_61491 | chr19:16432573-16510994 | Toledo | | SE_62295 | chr19:16434424-16512260 | Tonsil | | SE_66507 | chr19:16475752-16476848 | Jurkat | | SE_66507 | chr19:16476878-16478277 | Jurkat |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 16477143 | 16477842 | | chr19 | 16477247 | 16477817 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I016362 | chr19 | 16473350 | 16485630 |
|
Enhancer Sequence | CTTGATCTTG GACTTTGAGC CTCTAGAACT GCGGGACAAT CCATGTCTGC TGTTTAGGCT 60
GAGATAGAGC AAGTGTGAGC AGGGAGCCAC CAAAGCCACC GGCAGGGGCA CCCTGGGGGA 120
CAGTGTGACA GTGTCCTGCA CCCCAGCCTG TGGGTTTGCA GGGGATAGGG ACAGTGACCT 180
CAGCCAGTCC CTCGAGCCCC TGCCTGCTTC TGCCCAGCTT CTCCCTCCAC GGGAAAGCCC 240
CCCCTCCCCC AGGGTCCCTC ACCACTCTGC TTCCCGTGGC ACTGGCCTCT GGCACGGCTG 300
AGGGTCAGCT CTGTGAAAAG CGGGCCCAGC ATACCACAAA TGCCAGCCAA TACTGCCCCA 360
TGTCCCTGGT GCCCTCCAGC CCAGGGCTCG GCACACAGTG GGCTTCAGGA GGTCCTGGTG 420
AACCAGGTGC CACCTGTTAC AGATTCCACG GGTCTCCAGG GACCTGGGGC CCTTTGGAGC 480
AACACCCTGG GGAGCGAGAA GGGAATAAAG GCATCTGCCC TTCCTGGTTT GCAGGAAACA 540
GCAATGTTAC TGTGCATGCT TGGGTATTTG ATTTTTCCTC GAATACCTAT GTGATATGGA 600
TCAAATAGCA AGATTCTAGC AGAGGAAACA GTTAAGTGTT TCCAGGGGAG AAGCTCAAAG 660
TCCCAGGACA CGGTGTAGCC CCCTGGGACG GGCAGCAAGT CCAGGGTGGA CACTGCTTGA 720
TTTCTCGAAG CCGTTCCTGC AGGGAGTGAT CACCTGAGGC AGATTTGCAA GAATGTGGAG 780
GGAGGTGTAA AGGGAGGACG CCCCAGCCAG GCCCCCAAGA GCGACTGCCA CGGTACAGAA 840
GGTTCAAATA AATCAGTCAT TTTTGAGCTG CTTTTCTTCT TCTTTTCAAT GAAGATCTTC 900
CTCCCTTGGT TTGGGGGGTT TAAAAAAAAG AAATTGGTTT TTGGGAGGAG CGGTTAAGAA 960
TTCTGCCTGC TACCATTTCA AGCTGAGGTT TCTGATGCGC AAAGAGATGT TCAGAGAGAT 1020
GAAAAGCTTC GTTCACACCA AGAACTGCCT GTGCCTGGTT TTGCTCTGTT GCCGAAACCG 1080
TTGTTATTTA GAAATCATGA CTATGGTAAT ATGAAACCAG GGCACATCAA CTGCTGGCCT 1140
CTTGTTTTCA GAAGGAACAT CAACAACAAC AACGGTTTTT TTCTCAGTTG TTAGTGTTTG 1200
TGCTTTGGTA AGAGAGGAGA TTTTGGACCT GACACGTGTG AGGTCAGCCG AGTGCCCGGT 1260
CCAGCTCTCG ACCTTGCTAA TGACCAGACG CTTTGAGCAA AGAAAGCCCC CGGCATCACT 1320
GTAGGGCCAC GGCCCTCAGC CCAAACTTCC CACTTTTGCT CAGCGATTTA TTTTTAGCGG 1380
CTGTATTTTT CAAACCTTCT AGGTCTAGTT CCTGCTTTTA TGTAACCACT TCTGCTAACT 1440
CCTTAATCGT TTTTTCCGAT TTTGTGAGGT ATAGCTTATC TCAAACGTGA CAAAGTAACT 1500
TTAATCTGCC TCCAGGCCCT GAAGCAAAAG CTGCCACGCG CACCCACGCC AGGGTTTTAT 1560
ACTTTTTTAT GGCTCCAGAA AACATGAGTA AGGAGAGAGC TTTACTGACG CGCATTTCAG 1620
AAAAGGGGAT GGAAATCATG AAAACAAAAC CCAAAAAAGT GGGTATAGAA ACATCTGGGA 1680
ATGATGGCAT CAAACCAGGT GCCAGGCATC ATCCTGGCAC CTGGTTCGAT GCCATCAATC 1740
CTAGATATTT GCAGCGGGAA CTACCGGGGA CCACAGCAGA CGGCAGTGAA TAAAGACAAA 1800
TGAAATTAAA GACCCTCTTG GGTGTGCTGA CTGCCTACCG CAGGGAGACT TCATTAACAG 1860
GGGGCAAGGG ATACAAGACT GAAGAAAACA CAAAATAGAA CTTATTTTCA AACCACAGCA 1920
GTTTCAACAG TTACCCAAGC GGTGTACCGA AACCACACAC AGGACTGACT TTAGCAAAAA 1980
CAATATGAAC CAAATGGTTT ACCACAGTAT GTGCTGTTAA AAAAAAAAAA AAAAAAAAAA 2040
AAAAAAACTT GGTGGCCGGC TCCACCCTGA TAGAAATTTC TTTAATTCTC CTATTTCTCA 2100
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