| Tag | Content |
|---|
EnhancerAtlas ID | HS059-23093 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr19:33896880-33898290 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:33897912-33897931 | CACTGCCCTCTTCTGGCCA | - | 7.35 | | EWSR1-FLI1 | MA0149.1 | chr19:33897757-33897775 | GGAAGGAGGGGAAGAGGG | + | 6.2 | | EWSR1-FLI1 | MA0149.1 | chr19:33898076-33898094 | GGAAGTGAGGGAGGCAGG | + | 6.35 | | RREB1 | MA0073.1 | chr19:33898048-33898068 | CCCCCCTCCAACCCCCACCA | + | 6.67 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_24617 | chr19:33897247-33897881 | Colon_Crypt_2 | | SE_25205 | chr19:33896322-33898427 | Colon_Crypt_3 |
|
| | 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 |
| GH19I033406 | chr19 | 33897574 | 33898385 |
|
Enhancer Sequence | ACTGGCATTG CCATTTTATG CATGACATGG ACAGAGGCAC GGCACCAGTG AGGGGCCCCG 60
GGTCCCAGAA GAGCACTGTG GGGTGCCTCG TCCAGAGGTG GGTGAGACAC AAGGACAGCT 120
GCCAGGAAAG CACAGTGGGG TGAGGCCCGG GCGTCAGGGC AGTGGCCTTG GCAGGCGGGA 180
GGGAGAGTCA CACGCGCAGC ACATGCTGTA TTTTGCTTTT TTTGGTGACC AGTGTCTCAT 240
GATGTCTGGG AGCACCCAGG ATGTCTGGAC AAGTGCTGTT CAAACTGTGG GTCATGACAT 300
CAGCTGAGGA GGGTGCAGCC ACGAAGCACA AACAAGAGAC AAACCGAAAA CGCGTGGGCA 360
GGTGTCTGCT CATAACCAGG CCTGTCCATG TGTATGAGGA CGGGTGAGAA TGGAGAGCAC 420
GCTCCTAACT GGGATGGGAT GGGACGGCCA TGCCTGTGGG TCTGGACCCT CCTGAGGGCG 480
TTCTGTGGCC CCAAGAGCAT GTCTTTAAGA CCGCAGAGTG CTCAGGGCAG GGCTGGCTGG 540
TGACAACAAG TCTCCCTCGG AGGAAACAGC AAGGTGGTGG GGGAGAGCTG GGCTGGGACA 600
GGCAGCAGAG AGCAGGCCTG GGGGCAACGC TCTACCCTGG AGCTCACCAA AGCATTGGGC 660
CCCAGGTGGA GTGGGGCAAG GGGGTCCCCA GGAGCTTGTC ACCCATGGGG TCCGCAGCGC 720
GATGGTGGCA GACAGACTCA GGCTGAGTAG ACAGCAGGAG TAGGCTGGCC GCATCCCAGG 780
CTGCAGGGCC CATGTGAGGC CAAGGTGGCT GCTGAGGTCC TGGGTGAGCG GGCACCCCAT 840
GGCCTGCAGG GTCGAGGTCT CGCCATTATC TAGCCAGGGA AGGAGGGGAA GAGGGCACTG 900
GTGGCTGCTG AGTGTGAGGG CTGGGACAGG TCTCTCCTCC TAGCCAGGCT GGCCACCCAC 960
CCCCCATGCC CAGGAGCAAC ACAAAAGACC AGGCCCAGCA GGGGTGAGGC CTGGCCCATC 1020
GTCCTGAGAC AACACTGCCC TCTTCTGGCC AGTTCTGGAA GGACAGGCTT GCTGCCCACC 1080
AGCTGCATCC CGACTGGGAC AACCAAGGCC TGGGGCATCC TGGGACACGT GCTCTAGAAA 1140
CTCTGCGAGG GGCCACAGTA GATTAAGGCC CCCCTCCAAC CCCCACCACC TGATCGGGAA 1200
GTGAGGGAGG CAGGAGGAGT GTCCCAGCTG CTTTCCCAAC CAGAGCCCTC CACCTCTGCC 1260
CTGTGGGGTG AGCCTCTCCA GGACCTGGGG CGGCCTCAGG CCCGGAGTGC TGCAAGGGAT 1320
GGTCCCTCTC TGGGCGCACT GCTTCCCAGA ATCGTGGACC ATGCGCCCCC TGCCCTAGCT 1380
GCGAAGCTTG CTGGCCTGCA GTGGCTCTGG 1410
|
