| Tag | Content |
|---|
EnhancerAtlas ID | HS108-38947 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr8:27319270-27320490 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr8:27319499-27319517 | CACATGCCCAGACCTGTC | + | 6.45 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCTGTGGGGA AGACAGCACA CAGTGACAGG GGCCAGGCCT GGGAAAGGGA TGTGTTCCCC 60
CCATTCACAG CCCCTGCACA GGCGGCCACT GGGGGCAGCA GCAACTGCCC CACAGAGACC 120
TTGGGGAGCA AAGGTCAGCA CAGGGAGCGG GGTGAGTGGA AGGGAGGGAC GGGCTGTTTC 180
AAGGCTCCAG TAAGCTCCAC TGATGATTCC CCTCCCATCC CAGCCCCTCC ACATGCCCAG 240
ACCTGTCCAT ATTATGCTCC TAGACTATAG GTAAAGGAGG CTAGAGGGAC GCAAGGAGGC 300
GGCACGACCA CCCAGGGGCA TGGGCCCTTC TAGGGGGCCT GCAGTGACTT CAATGCAACA 360
CCAGACTTTG CTGCTCACAG GTTGCCTCCT CACCCACCTG CTGGAGCTGG GGAGAGGGAA 420
ACAGGCGAAG GTGGTTGGGA CCCCAGGCAG GCTGGGGGTG GGGCGGGGGC TTTGTAGAAC 480
TTGGGCTCAC AGCCCAGACA AGGGAGCCTG GATTCTCCAC TGCTCCTGGA TGACATCATG 540
ATTAATTTTC TTGTCTGTTC ATCAAGGCCA CTCAGTAATA ACCTCCCGGC CTTTCATCCT 600
TCCCTAGGCT TAGTAGAATT TTGTGCTAGA GTAGCGGCCT GCTCAATGGC AGACAGGAGC 660
TGGGGCAGGG GTCAGGGTGG GGCCAATGCC ATGGCAGGGG CGGGGGAGCG GAGTCCACCT 720
GGCACAACCA AGAATCTGCA GGGTTTATGG TTGAAGAGTG AAGTTTGCAA GATCCTCAGG 780
AGCCCATGAA CAAGGAGGCG GAGGAAGAGA CCATCCAAGA CAAAAGACAA AGGCTGACAC 840
TGCAGCAGCT GACTTTCTGG GTCTCTCCTG AAATGCTCCC CCTGCCTGCC GCCACCTCCA 900
AGGCAATGGT GGGAGCTGGC GGCGTGAGGG AGGCACGGGG TTCAGCATCT GGGATCCTCC 960
CTCTCCGGCT CTCAGGATCC CTGTTAGGCT GAGCTGCTCA TGCCTGACTC CGTGGTGTGT 1020
AACATGCCAC GTGCCAATAA ACGTCCTCAA AGCGGCCAGC TACATGTGCT CTCTTGCTAT 1080
TTATTCCATC TAAGGACCAT GACTGAGGAA AGTGGGCCTT CACGAGAGGG GCCTGGGCTG 1140
CCCAAGCTCA CACTCTGCGG TAAGGTGGTT CCCCGCTAAG TTGGTGGGGC CACCCAGGCT 1200
GGCGCCTCTC CCAACCCCAA 1220
|
