| Tag | Content |
|---|
EnhancerAtlas ID | HS193-21663 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr21:37809280-37810690 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr21:37809948-37809963 | GAGGTCAGGAGTTCA | + | 6.22 | | Stat4 | MA0518.1 | chr21:37809374-37809388 | TGACTTCCTGGAAG | - | 6 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_38121 | chr21:37809145-37811008 | HUVEC |
|
| | 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 |
| GH21I036437 | chr21 | 37809320 | 37810813 |
|
Enhancer Sequence | CATAAACTAC TTCATGTCTG TTGCCTCATG GTCACAAAGT GGCTGCTCAC CTCCAGCATC 60
ACGTTTTTTA GGCACTGTTA AAAAGCTGCT AAAATGACTT CCTGGAAGCC TTGGTAATTT 120
CCACTTACAT TTCACTGGCC AAGATCTAGC TGTAAGAGAG ATTGGGAAAA ACGAATGTCT 180
TTATCTGGGT ACATTGCTCA CCCCAAACAA TACTGGAGTT TTTAAAAGAA AAAATGATAG 240
AAGGGATAAT AGGTATACAA CTAGTAGCAT CTGCCCAGTG TCTCACTGAC TAATTGTTGT 300
AAGATGTTGG GGGAAGAGAG AAACAAGAAT GACATCTGGG CTCTAGGCCC CAGGGACTGG 360
GAAGCCAATG ACACTGTCTA CTGATTTGGA AACATAAGGT TGGGAAATCA ATACTTCTCT 420
TTTAGCCATA TTCAGTTTGA GATGCCTGTG AGATTTCTGA GTAGAGAAAT CAAGGAGACA 480
GTGGAACATG CATACCTGCA GCTCCAGGAT ATACAGATTT GAGAGAGCAG CATATGAATG 540
AAATTTTAAA ACCATGGACT GGATGACATC ACCAGGCAGA GAAGAGGAGA AAGTCTAGGA 600
CAGGCTGGAT ACAGTGGCTC ATGCCTGTAA TCCCAGCACT TTGAGAGGCA GAGGTGGGTG 660
GATCACCTGA GGTCAGGAGT TCAAGACCAG CCTAACCAAC ATGGCGAAAC CCTGGTTCTA 720
CTAAAAATAC AAAAATTAGT CGGGCATGGT GGCGGGCACC TGTAATCCCA GCTACTTGAA 780
CCTGGGAGGC AGAGGTTGCA GTGAGCCAAG ATCGTGCCTC TGCACTCCAG CCTGGGCGAT 840
AAGAGTGAAA CTCTGTCTCA AAAAAAAAAA AAAAAGGTCA GGACAGAGAC CTGGGTCTGG 900
AGGGAGGAAG AGCAAACGAA GAGATTGCAC CAGAACCTGC AGTGTTCCCC CAAGCCCCAG 960
GAGGAAGGTT TCCAGGATGA AGAAGTGGTC AAATATGTGA CTTGGCTGCT GCCACTGTGA 1020
GTAAGATAAG GATAGAAAAC CAGCTGGTGG TTTTGGCAAA ATACGGGCCA TTCGTGTCCT 1080
TGATAAGAAC TTTTACTCAC TGTCTGGTGG ACGTAGCCAC TCCCTTAATG ATGCACACTT 1140
GACTTGTCTT TTTTTTTTTT TTTTTTTGAC CCCCCAGATC CCATAGACTG AGAGTTGTAT 1200
CTTGTTTTCT CTGCTTTTTT GCTAATGAAG GCAATGCTAC AATGAGAATC TTGTGCATAT 1260
ATGTTTGCAA ACCTGTGAAA GTATTTCTTT TGGATAAGGC CTAGAAACCA TTGAGTCAAA 1320
AAGTATGCAT ATGTTAAATT GTAATCCATA TCATCAGATG TCTACTAAAT AGTTATACCG 1380
ATTTACATTC CCACCAGCAG TGTTTTTGAG 1410
|
