| Tag | Content |
|---|
EnhancerAtlas ID | HS177-18703 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr5:153902740-153904110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr5:153903757-153903770 | TTCTGGAATATTC | + | 6.48 | | Tcf12 | MA0521.1 | chr5:153902838-153902849 | CAGCAGCTGTT | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 153902800 | 153904090 | | chr5 | 153903267 | 153903411 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I154522 | chr5 | 153902321 | 153905099 |
|
Enhancer Sequence | CACAGCAGTG ATGGAACTGG TATCAGAAAG GGAAAGCAAC CAGCTCAGCA GAGCCAGGCA 60
TGTCTGTGCG ACTCCAACAC TCAACCGCAC GGCAGGCTCA GCAGCTGTTC TCTGCTTATA 120
AAGCACATGG CGCCTGGCAC ATTGGTCACC CTCAATCCAT GGCATTGGAT CTTTGTCACC 180
TGACTGTCAT CATCCCTTCT GACTCTCAGT CCCTCCTCTG AACAACAGCT GTGTGTTGGC 240
CCCATTCATG TCCCACCAAT GCCCAGTCCT TTAGGGGGCT CCCCAGCTAG CCAAGGTGAC 300
CCCATGCTAA CATTTCCCAA GCTCTTTCCT CAAATTTTAT CTCCATCATC AATGACCAAC 360
TCCTCTGTGT CAGAGGCAAA CAGCTCCCAC CCGTATTTAT TTCACCCCAG CTTTGTCTAT 420
TTATAGGAAG CTGGCTTGTC CTGACGCTGT TTCTGTTAAC AAGGCAGGCA TCTCAGCCAA 480
CTGGGCAGAA AAGCAGCAGA AACCTTCAGT CCTGCCCATA AAGGCCCCAG AAATGTCTCT 540
GCCTCCAGAG GTTTTTGAGA AACTGCTGCA AGGGGAATTA TGAGTGTAAA CTTGCCCCCT 600
CCCTCTGCCC GCCCCCCAGC CCTCTCATCT GGACAATAAC AGCTCCCATC TCATCTCTGA 660
GAAACCATTC CCGAAGGTTC CAGCTGAGTG CAGGATTAGG CCTCAGGGTG GCAATTAGCT 720
GATAAGGCGA TGACTTCACC CAGAGCAGAG AGAGCCTGGC TAGCTGGAGC CTGTCCCTGC 780
AGGACACCCT GCCCTGGGCC TCTCTCCCTG GACTTAGAGA CAGGAACCCT GGCCCAAGGC 840
TTGGGGAAGT CTCTTCCCCT CTCTGGACCT CTGATTGCCC CTGTGTGAAA TGGAGCATGT 900
TCTGACCTTC ACAGGCTTGT GGGAAGCTCC AGTAAAATAA GAAATAAGAT CTTGCTCAGA 960
AAGAATCCCT GGCAGCAGTG CATTGCTGAC CATAGACAAC CATAGAACTG GAGCCTTTTC 1020
TGGAATATTC CTGAAGGAAC AAAGAAAAGA GGCACTGGCC AGGGAATCAG GTGGACCTGA 1080
GTTTCTGAGC ACAGGCCCTG TGTTCACCAG CTGTGTGCTC TCAAGCAGGC TGCCTCCCTT 1140
TCCTCTCTGT AAAATGGGAC AGTGTTTGTG CCTTGTCTTC CTCGCACATG GTTTTGAGAT 1200
GCAGAGATAA CTGAGGAAGG AGAGCTGAGC GGATAAGATC ACAGGTTTCA GAGCATGTGG 1260
GCCTGGCTTC GAGTGCCTGT TTGACCCCTT ACTAACTGTG TGCCTTTATG TTGATGGCTT 1320
GTATAAGACC TCGGTTCTTG TCTTCTTAGT TTAAAAGAAT TTAAACAAGA 1370
|
