| Tag | Content |
|---|
EnhancerAtlas ID | HS108-14662 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr16:11961000-11961980 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr16:11961353-11961364 | CATGAGTCACC | - | 6.62 | | JUND | MA0491.1 | chr16:11961353-11961364 | CATGAGTCACC | - | 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 |
| GH16I011867 | chr16 | 11961101 | 11961990 |
|
Enhancer Sequence | CTGTGGCGCA ATCTCGGCTC ACTGCAGGCT CCGCCTCCCA GGTTCACGCC ATTGTCCTGC 60
CTCAGCCTCC CAAGTAGCTG GGACTACAGG CCACGCCCGG CTAATTTTTT GTATTTTTAG 120
TAGAGACGGG GTTTCACCGT GTTAGCCAGG ATGGTCTCGA TCTCCTGACA CCGTGATCCA 180
CCCACCTCGG CCTCCCAAAA AGTGCTGGCA TTACAGGCAC ACGCCTCCAC GCCCAGCTAA 240
TTTTTGTGTT TTTTAGCAGA GACTGGGTTT CACCACGTTG GCCAGGCTGG TCTGGAACTC 300
CTGACCTCAA GTGATCTGCC CGCCTCAGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGT 360
CACCGTGCCT GGCCTGAACC CCTACTTTAA TAGCAAGCTT GGTCCCAAGT TTTAAGCTAT 420
GATTGGTTTA ATGCCAAATA CCTAGAGGCT GACTGCCAAA ACCTCAAAGC GATTCACCTA 480
AAGACAGTTC AAACAGGAAC TTAGTACACA GGAATGAACT GCTGTCATTC AAGTAGCCAC 540
TGTGTATGTT ACCTTTATCA TTAACTTCTT CTTGCCCTTG CACATTGAAT GAAAAGGGCA 600
AGCACTATTT GGTCTCTTGA TCTTTATTAA AAATCCTGAA TGTAGAGGTT CATAGTTCTA 660
ATAATAATTG ACGTTTCCCC CAACTCTACT GTTCACATAA AACCACATAA CTGTGATCTA 720
GTTATTTATT ATTCAGCATC CCTAACTTCC TATAGGGTTC TTATTTTTGT TTCCTAAGGT 780
TGTCGTATAC ATTATACAAA AGACTTGCAT GCCATATGCA AGCAGATGAC GTTTGTGAAT 840
CCCTTATGTG ACAGAGCTTA TTAGATCCAT CCAACAAACC TTTTGGTAGA TGGTTCCAGT 900
ACCTGATACA AAAATAAAAG GATTGTACAA AAAAGGGCAT GGTTTTTGCT TGTTACAACA 960
CAGGTAATTA CAAACGACAA 980
|
