| Tag | Content |
|---|
EnhancerAtlas ID | HS108-26229 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr21:45789230-45791130 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr21:45790325-45790339 | AGATAATGAGTCAT | + | 6.03 | | KLF14 | MA0740.1 | chr21:45790074-45790088 | GAGGGGGCGTGGCC | - | 7.52 | | KLF16 | MA0741.1 | chr21:45790076-45790087 | GGGGGCGTGGC | - | 6.62 | | SP1 | MA0079.4 | chr21:45790075-45790090 | AGGGGGCGTGGCCAG | - | 7.26 | | SP3 | MA0746.2 | chr21:45790075-45790088 | AGGGGGCGTGGCC | - | 6.82 | | SP4 | MA0685.1 | chr21:45790073-45790090 | GGAGGGGGCGTGGCCAG | - | 8 | | SP8 | MA0747.1 | chr21:45790075-45790087 | AGGGGGCGTGGC | - | 6.92 |
|
| | 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 |
| GH21I044368 | chr21 | 45788471 | 45791547 |
|
Enhancer Sequence | GTGCGGCCCC CTAGGGAGGG GAGCCTAAGA CCAGGGGTGT GGGTGAGGTC TGACTGGGCG 60
CTGTGGGGAG CAGGTGGAGT GTACGGGGGC CGGGGTGTGG GTGACGTCTG ACCGGGCGCT 120
GTGGGGAGCA GGCGGAGTGT GCGGGGGCCG GGGTGTGGGT GACGTCTGAC CGGGTGCTGC 180
GGGGAGCAGG TGGAGTGTGC GGGGGCCGGG GTGTGGGTGA GTTCTGACCG GGTGCTGCGG 240
GGAGCAGGTG GAGTGTGCGG GGGAGGCGGG GTGTGGGTGA CGTCTGACCG GGTGCTGCGG 300
GGAGCAGGTG GAGTGTGCGG GGGAGGCGGG GTGTGGGTGA CGTCTGACCG GGTGCTGCGG 360
CGAGCAGGTG GAGTGTGCGG GGGCCGGGGT GTGGGTGAGT TCTGACCGGG TGCTGCGGGG 420
AGCAGGTGGA GTGTGCGGGG GAGGCGGGGT GTGGGTGACG TCTGACCGGG TGCTGCGGGG 480
AGCAGGTGGA GTGTGCGGGG GAGGCGGGGT GTGGGTGACG TCTGACCGGG TGCTGCGGGG 540
AGCAGGTGGA GTGTGCGGGG GCCGGGGTGT GGGTGAGTTC TGACCGGGTG CTGCGGGGAG 600
CAGGTGGAGT GTGCGGGGGA GGCGGGGTGT GGGTGACGTC TGACCGGGTG CTGTGAGGAG 660
CAGGTGGAGT GTGCGGGGGA GGCGGGCACA CTCAGGAGAT TGGGTGCAAC TCCCGGCCCA 720
CCCCTGACCC AGGTGACCCC GGACAAACGG CTAACTTGGC TGGACTCTGG TATCTCCCTC 780
AAGGTTGTAA GAGGGGTCCA CGTGACAGTC ACTCGCTGCG AGGGTTCCGC TAACAGAGCA 840
GAGGGAGGGG GCGTGGCCAG CAGGCAGCTG GGTGGGGCTG AGCCAGGGCG ATCCGACCCC 900
GAACCGGAGC TTTTAGCACT TTGAGTCCCT GTACTCAGAG GTCTCCTGCA GCCGGGAATC 960
CCACTGTGCT GTGGTCCCTG GCAGCCAGCA CCCACCCCCA GCTTCTCCGT CAAGGTTGAG 1020
GACGGAGCAC TCCTGCCTCT GATTAACTGG ACGCAGGAGA AGCAGTTGCT TTAATCCGGA 1080
GCCTTGAGTT GGGACAGATA ATGAGTCATT CAACCAGATT TTCCAAGGAC ACACTAACTT 1140
TGGTATGATG CGTGTGTGCC CCTGAATCCA CGTGGTCAGG AAAGCCCAGG GAACACTGGC 1200
CTGTGACTCA CTGAGCAGGT TCCCTTGTTA CCCCGAGGGG TGATTTACTC CTCTGACAGT 1260
GACACGGACA CTGTGCGTCC ATTCCCCGGG CGGGCAGAGG ACACTCCCAG ATGCCCACGA 1320
GGGGCCCAGC AAGCACTGGC CAGCCCCAGC CCGGCCTTCG CCTTCCTTTG CGTCAGAATC 1380
ATGAATGTGT CCGGCGGGGT CGGACTGGAC CAGCTGTTGG GCTTTGTTTG CTCTTTTTAC 1440
GAATTGAAAA ACTGAAGCCA GGAGCGGCTG GGTGACGTCC CAGGTCACTC CTTACTTTCC 1500
TCCCCACGCT GAGCTCAGAC GACTTCCCGT GACACCACTG TTGGTGGCGG AATGGGACTG 1560
TGGCTGCTTC CGCTCAGCCA CGCTCCCTCT CTGTGGACGG CGGAGGGTGT GTGTCCCAGC 1620
CCGGCTGCCG CCCTCCCTTA GGTCTGTCTC CCGGGGCTGC TGTAACCCAG GCTCACAAAC 1680
CTGGTGGCTT AAAGCAGCAG AAACTTAGTC TATCAGATCT GGAATCCGCG TCGATTGGCC 1740
ATCATCCAGC CATCGGTGTT GGCGGGGCCA CCTCCCTCTA GGGCCTAGGG GAAGAGCATT 1800
CCTTGCTGCC TCCAGCGTCT GGGTGCTGAT GGCATTCCCT GGCCAGTGGC CACCTCCCTC 1860
CAGTCGCTGC CTCCGTGTCC CATGGCCGCC TCCCTCCAGT 1900
|
