| Tag | Content |
|---|
EnhancerAtlas ID | HS034-28889 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr8:11499480-11500660 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr8:11500516-11500530 | GGACACGCCCACTC | + | 6.43 | | SP4 | MA0685.1 | chr8:11500514-11500531 | CAGGACACGCCCACTCC | + | 6.46 | | SP8 | MA0747.1 | chr8:11500517-11500529 | GACACGCCCACT | + | 6.37 | | ZNF740 | MA0753.2 | chr8:11500218-11500231 | CCGCCCCCCCCCC | + | 6.64 |
|
| | 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 |
| GH08I011640 | chr8 | 11498236 | 11501093 |
|
Enhancer Sequence | AGTTGGAGTC AGGGTTTTCT AACATTTTTG CAAGCGAACA AGTCTCAAGT GATTCGCTCT 60
ACTGTTTAAA AATGCATATG ATGACGGCAT GTGTGTACCG AGCTGGGGCA GAGGTTAGAG 120
AAATTTAAAA ATGCGTATGA ATAACAGCAT GTCTCTACAG AGCTGGGGCA AAGGTTAGAG 180
AAAGCGATCT ATGTAAACGA GCTGCCAGGC CCGTACACAG TAGGTGCTCC GTGAAGGCTG 240
TCTCCCTGCC CCGTCCTCAA ATATCTGCTT CTTGATCTGG GCTTCAAAGC TGATCCCATT 300
CTCTCTCCAG TCACCTCTCA AACTCCTCCT TCTTTTCTGT TAAGTAGCAA GTCTGGTCTT 360
TCCTTCTTTC CGAGCAGAAC CCAGGCTTTA CAGTTAATAT CCTGCCGCCT CTGATTGCAG 420
CTTTAAGAGG TGTAACATTT GATAAGCTCC ATTTAGCTTG GCTGAGCTGC ATTGTTTAAA 480
TTATTCGAAG ACAGATTGCT CCCTCCCCCT ACCCTGAGGA TTTCTGCTCT ACTGAGCTTG 540
CCCACAGCAA GTTACCAGGA AACACGGCAG GGAAGTCAGC AGGGCAGTTT GTCACCGTGA 600
GGCTGAAAGT CAGTTCCAGC CGCTGTTCTG CAGCCATCAC ACCCCATTAT TCCCTGCTAA 660
TTGCAAGCCT GGTATGCAGG CTAACTCTTT GAGAACAATG CCAGCTTTGA TTGCTGAAGA 720
GGCTTATTCC TCTCCGCACC GCCCCCCCCC CCCGCCCCCG CCCTCTTCTC CCACCGTCCT 780
CAGCTGACTC TGCCTGTCTG GGATTCCAAG CATCTCACAC TGGGGAAGAA GAGTCTGGGT 840
TGGGAAGGAA TCTGAAGTGA AGCCCGTTCC CCAGGCATTC CGATTGGGGG AGGGAAGGAG 900
GGCACTGAGG GGAAGGCTGG GTGGGTCCCA GCCCCCTGAG ACGTGAGCAG CCTCCATTCT 960
AAATGATGTG GAAGAGCCGG CAACCCAGAC ACAGCTGCTC TGCAAGCCCA TCTGCCCAGC 1020
TCAGGGCTCA ACCTCAGGAC ACGCCCACTC CTCCTGGTCC AAACGAGGAT GGAGCCCCTC 1080
GAGCCTGTGC TCATGGGCAC TGTCTCACTC CATCCGAGCA CTGCTTAAAA CACACTGGAT 1140
AAATGCGGAT GGCTGTCAGA CGCTTTTAAT GAGGAAATAT 1180
|
