| Tag | Content |
|---|
EnhancerAtlas ID | HS197-10481 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr19:17790190-17792890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ATF3 | MA0605.2 | chr19:17792494-17792506 | AATGACGTCACC | + | 6.07 | | ATF3 | MA0605.2 | chr19:17792494-17792506 | AATGACGTCACC | - | 6.18 | | EWSR1-FLI1 | MA0149.1 | chr19:17792149-17792167 | GGAAGGGAGGAAGCATAG | + | 6.42 | | IRF1 | MA0050.2 | chr19:17791643-17791664 | CTTTTCTTTTTCTTTCTTTTC | + | 6.15 | | JDP2(var.2) | MA0656.1 | chr19:17792494-17792506 | AATGACGTCACC | + | 6.44 | | MEF2A | MA0052.3 | chr19:17791179-17791191 | GCTATTTATAGC | - | 6.32 | | MEF2B | MA0660.1 | chr19:17791179-17791191 | GCTATTTATAGC | - | 7.22 | | ONECUT3 | MA0757.1 | chr19:17792752-17792766 | ATCATTGATTTTTT | - | 6.07 | | REST | MA0138.2 | chr19:17792561-17792582 | GGCGCTGTCCACGGTGCTGAA | - | 11.12 | | SP2 | MA0516.2 | chr19:17791229-17791246 | AGGGGGGCGGGGATGAG | - | 6.23 | | ZNF263 | MA0528.1 | chr19:17791470-17791491 | TCTCCTTTCTCCTCCTCTTCT | - | 6.22 | | ZNF263 | MA0528.1 | chr19:17791480-17791501 | CCTCCTCTTCTTCCCTCCTCT | - | 6.29 | | ZNF263 | MA0528.1 | chr19:17791473-17791494 | CCTTTCTCCTCCTCTTCTTCC | - | 6.31 | | ZNF263 | MA0528.1 | chr19:17790515-17790536 | TGTCTCTCATCTCCCTCCTCC | - | 6.32 | | ZNF263 | MA0528.1 | chr19:17791486-17791507 | CTTCTTCCCTCCTCTTCCTCC | - | 6.67 | | ZNF263 | MA0528.1 | chr19:17791476-17791497 | TTCTCCTCCTCTTCTTCCCTC | - | 7.36 | | ZNF263 | MA0528.1 | chr19:17791467-17791488 | CCCTCTCCTTTCTCCTCCTCT | - | 7.58 | | ZNF263 | MA0528.1 | chr19:17791464-17791485 | CTTCCCTCTCCTTTCTCCTCC | - | 7.6 | | ZNF263 | MA0528.1 | chr19:17791489-17791510 | CTTCCCTCCTCTTCCTCCCTC | - | 7.92 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_69003 | chr19:17790307-17791462 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr19 | 17791017 | 17791370 | | chr19 | 17790400 | 17791527 | | chr19 | 17792244 | 17792636 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I017679 | chr19 | 17790410 | 17791634 |
|
Enhancer Sequence | AGAGCAAGAC TCTGTCTCAA AAAATATATA ATAATAATAA TAATAATAAA AGAGAGAGGG 60
GGAAAGATTT CCACTAGGGA GGGCAGGCAG GTGGAGGAGA CACTGGGGAG AGGAGAGGCA 120
GTTGGGGGAG AAAAGTAGGG ATGCATATGG GGGTGGGAAA GTGACAGGCT CTGGGGGGTG 180
ATACAAGGGG CTCACTGGGG TCTAGACTGG GCTGGGCTCA CTTGAAGCTC CTCCAACTGT 240
GCCCTGTTTT ATAAACCATG GATTTAGGCT CAGCGGGGAG CCCAGTAGCT CCTTGATCTG 300
TTCTCTCTCT CTCTTTCCCA ATCCCTGTCT CTCATCTCCC TCCTCCCCGT TCTATTTCTC 360
TCCACTCTGG TCGTCTTCTT TTGGTCTCTG TTCTCTCCTT CTCTCTCTCA CTGTCTCTGC 420
CCTTCTTGTG CCCCTCCCTT GGTCAGTCCG GCTCCTCTTC CCTAAGCCTC AGCTCCTTCC 480
TGCAGCCTCT CTTGGCTAGA GGGGAATGGT CTCCGTTGGG GTCCTCAGGC AGTGGGGGAC 540
CGGCTGGAGG GCTGTACCCT CTGATAGCTG AAGCCAGGCT CCTGCACTTA GCTCCCTGCC 600
GAGGTCCAGG TTGAGGACAT CCATGATTTT TCATCACTGG GGCTCCCAGT GGGAGAGGGG 660
TCTCAGAGGG AAAAGGGGAC AGGAAAGGGG GCCGAGAGTG GCGAGGGGGT TCTCAGGAGG 720
GAAGGGTGTT CGCGGTGAGG GAGGGGATTC GGGAAGGGGG ATGGGCGCAG AGGGGAGGGT 780
GGTATCGGGG GAGAGGCTTG GAGGAGGAAG GGGGCTCAGA GAAGGAACCC AGTCTCTCTC 840
CCTGTCTTCC CCGGTCAGTA AATGGTCCCT GAGTCACCGT CTTCGTCGTC ACATCCCGCC 900
ACCTCCCCGC CTGCGCCGGG TTGCTGTATC AGGGTCAGCG GGGCGGAAGC GCCACCCTTC 960
CCCAGCGGGC TTCGGGTCAC ACGCATGAGG CTATTTATAG CGTGGGCGCG CGGAGGGCGT 1020
GGGAGGCGCG CCGGCGGACA GGGGGGCGGG GATGAGGGGG GTGCCCACTG CTGTCCCCAG 1080
CGACGAGCGG GTGAAGACAC CGCGTCATGC GGCCTCAAAG GTCTTTGGGG CCCCCAGAAG 1140
CGCTGACTGA TGAATGTAGT GGCCGTACCC GGGGAGGCTG AGGCAGGAGT TCAGGCTGCG 1200
GGACACCCCT GCAGCCTGGC TTCGCGCCTC CGTTTCTGCA TCTGGAAAAT GGGGAGACGG 1260
AGTGGCTGAT CTCCCTTCCC TCTCCTTTCT CCTCCTCTTC TTCCCTCCTC TTCCTCCCTC 1320
ACCCCTTCTG CAGAATGATT ATAGTGTCAT TTATACTATT ATTATTATTA CTGATATCTT 1380
TACTGTTTTT ATTATTTGGT TGTGTTCTAA AGGTGTCCCT GGCCTGGATT CTAGGATTTG 1440
AATACCCTGG ATTCTTTTCT TTTTCTTTCT TTTCTCTTCT TCTTCTTCTT TTTTTTTCTT 1500
TTCTTTTCTT TTTTTTTTTT TTTTTTTTTT TGACAGGGTC TCTCTCTGTT GCCCAGGCTC 1560
CAGGCTGGAG GGCAGTGGTG TGATCATGGC TCACTGCAGC CTCGATCTCC CAGGTTCAAG 1620
CGATCCTCCC CACTCAGCCT CTCGAGTAGC TGAGACTGCA GGTGCGCATC ACCATGCTTG 1680
GCTATTCCTT TTTTTTTTTT TTTTTTTTTG TAGAGATGGG GTCTTGCTAT GTTGCTATGG 1740
CTGGCTTCAA GGCTCAAGCC ATCCCCTCGG CCTCCCAAAG TGTTGGAATT ACAGGCGTGA 1800
ACCACATGGC TGACTGACCC TGGATTCTAA TTAGGGGGGA CTGCAGTCTT GGGGCACTGG 1860
CTCCCTGACC TGCCACGTGG GATGGGGTGG GGAGACAGGA GGTGGAGATC CAGCCGTCTA 1920
GGGCTTCTGA AAGCCCACCC GCCCCAGGAT TAGCTTGGGG GAAGGGAGGA AGCATAGAGA 1980
ATCCAGAAAT AGATTATAGG AGATTTGATC GTTTTGTGTG TGATGTTGGT GGAGGGCATT 2040
TCAGCGGGAG ATGGATGGGC TTTAGGATAA AAGACCTCAG CTGTGCTGGT TTCGCATCTG 2100
GGAGACACTA AATGAGGACC CTTATCCTCC GTTGACACAA ATAGACCAGA GCCAGACTGA 2160
GCCTTCAGTG TAAAAAACAC CAAGAACCTG GAGTTCCAGA GAGCTTCGGG AATAAGGGAT 2220
TTGTGTGTGT GTTGTTTACC ATGAACCACT TAGAAGTAGG CCTAGCCTAT AGTAGGTGCT 2280
CATTAAATAG TAATTCACGG AAGGAATGAC GTCACCTCCT CCATTAATCC TGGGAGGCTG 2340
AGCTAAGAGC TGTCCCCCAG AGGCGCGGGC AGGCGCTGTC CACGGTGCTG AATGCTCGGT 2400
CCCACCCGTG TACCCTCAAC GAACTAGGCT CCCTCCTGGA GTGGCCCTGG GGGACCCCTC 2460
TTGGAGCGCT CCTCGGGCCC CAGAATGCAG TGGACTCTCA GAAATGTCCT GCACTCAGAA 2520
CCGCCTTCCA GAAAGCTTTT AGTCTCCATT AATAAAAACA TCATCATTGA TTTTTTTTTT 2580
TTTTTTTTTT TGACGGAGTC TCACTCTGTA GCCCAAGCTG GAGTGCAGTG GCGCGACCTC 2640
GGCTCACTGC AACCTCCGCC TTCGGGGCTT AAGCGATTCT CGTGCCTCAG CCCCCTGAGT 2700
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