| Tag | Content |
|---|
EnhancerAtlas ID | HS108-33397 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr5:176087590-176088870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr5:176087970-176087989 | TTACCACCAGAGGGCGCCA | + | 8.45 | | EGR2 | MA0472.2 | chr5:176087994-176088005 | CCGCCCACGCA | + | 6.32 | | EWSR1-FLI1 | MA0149.1 | chr5:176088799-176088817 | TCCAGGAAGGAAGGAAGG | + | 6.47 | | EWSR1-FLI1 | MA0149.1 | chr5:176088803-176088821 | GGAAGGAAGGAAGGAGAC | + | 7.67 | | Sox3 | MA0514.1 | chr5:176088407-176088417 | AAAACAAAGG | - | 6.02 |
|
| | 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 |
| GH05I176660 | chr5 | 176087901 | 176088202 |
|
Enhancer Sequence | TAAGACTGTC CATCCCTCTA GGAGGGTCCC TGGGCCTTGG GACCAAGGTC ACCTCCCACC 60
GTCTGTTAGG ATGAGATGCA CACTCATCTG TTAGGTAGGG ACAGGTGCAT ACTGGTAGAG 120
ACAGGTGCAC ACTGTCTGGC AGCCTGGGAG TCCCCTGTCT AACCACAGGA GAGGCTGCCA 180
GCAGCTCCCT GATCAGCTTG GTGGGAGGAC ATCCTGTGAC ACCAAGATAC CCTACAGAGA 240
GAGCTGGAGG GACAGAGAAC ACCCAGGCTG GCGAGCTCCT TTATCTCTGG GTGAGGTGGT 300
CATATGGGCT GGAGAGGACG GGCAGGAGCT CCTTCTGGGG AGGCTAAGGC CACAGATGCC 360
TTGGTGGTAG CCACTCCCAG TTACCACCAG AGGGCGCCAA AGTGCCGCCC ACGCAGCTCA 420
GCCGGCTCAG CTCGCGGAAG GAGCTCTGTG TAGAGTCATT GGGGCGACCC CTAGGGCCAA 480
GCAAGCCCAT GCCATCGTTC CAGAGACCCT GGGCCCACCC CGCTGGTGCC AAATCCAGGC 540
CTTACCACCC TCTGCCCTGT CTTCTCTGGG GAGTGGAGCA AATGATGCTG CCTGCCCACG 600
GGTGCCTCTC TCAGTGCTTA CAGGGCCCGA GCCCACTTGC TGGGCTGGGT GGGTGGTGGT 660
GTCCGCCCGA TAGAGCTGGA GAAAGGGGTG AGCGTCACTC TCTCTAGGAG GATGACGCAA 720
TGTGCTCCAC AACCTACACC TCCATTCACT CATTCAGCCA GGGCAGCGGA GCACCCCGTC 780
GCTGCCAGGC ACTGCCGCGG GCACTTACGT GAGGGACAAA ACAAAGGCCC CACCTCGTGG 840
AACTCACAGC CCAGGCCAGG AAGCAGTCGG CTTTGTCTGC CAAAGGTCAA ATATAATGGC 900
AAAAACCGCA ACTACTTTTG CACCAACCTA CTTAAATCCG CTAGGCTGTT GGGCCGTGCT 960
CCCCTTGACT CTGCCTTCAT GGTGGAAAGC AGCTCCGGGT GGGGCTAAGC AGTCTCGTGC 1020
GGGGTGTCCC CATCACATCG TACTTGTGGA CGCTGACGGC GAACCTCGTG TGATTTTCAT 1080
GGGTCGTGAA TATCATCCTC CTTTTGATTT TCAGCTATTA AACAACAGAA AACCATTTTT 1140
GGCTCTTGAG CTCTATAAAC ACAACTAGCG GGTGGGATCC ACCCCGCGGC TGGAGTTTGC 1200
AGACCTGGGT CCAGGAAGGA AGGAAGGAGA CGGTACACAG TGAACATCAT CGCGTGAGCC 1260
TGCCCTGCTG CCAGTGGGGA 1280
|
