| Tag | Content |
|---|
EnhancerAtlas ID | HS095-11000 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr16:11960870-11961980 |
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 | CACACTCAGC TAATTTTTGT ATTTTTAGTA GAGATGGGGT TTCACTATAT TGGCCAGGAT 60
GGTCTCGATC TCTTTTTTTT TTTTTTTTTT TTTTGAGACG GAGTCTCACT CTGTCGCCCA 120
GGCTGGAGTG CTGTGGCGCA ATCTCGGCTC ACTGCAGGCT CCGCCTCCCA GGTTCACGCC 180
ATTGTCCTGC CTCAGCCTCC CAAGTAGCTG GGACTACAGG CCACGCCCGG CTAATTTTTT 240
GTATTTTTAG TAGAGACGGG GTTTCACCGT GTTAGCCAGG ATGGTCTCGA TCTCCTGACA 300
CCGTGATCCA CCCACCTCGG CCTCCCAAAA AGTGCTGGCA TTACAGGCAC ACGCCTCCAC 360
GCCCAGCTAA TTTTTGTGTT TTTTAGCAGA GACTGGGTTT CACCACGTTG GCCAGGCTGG 420
TCTGGAACTC CTGACCTCAA GTGATCTGCC CGCCTCAGCC TCCCAAAGTG CTGGGATTAC 480
AGGCATGAGT CACCGTGCCT GGCCTGAACC CCTACTTTAA TAGCAAGCTT GGTCCCAAGT 540
TTTAAGCTAT GATTGGTTTA ATGCCAAATA CCTAGAGGCT GACTGCCAAA ACCTCAAAGC 600
GATTCACCTA AAGACAGTTC AAACAGGAAC TTAGTACACA GGAATGAACT GCTGTCATTC 660
AAGTAGCCAC TGTGTATGTT ACCTTTATCA TTAACTTCTT CTTGCCCTTG CACATTGAAT 720
GAAAAGGGCA AGCACTATTT GGTCTCTTGA TCTTTATTAA AAATCCTGAA TGTAGAGGTT 780
CATAGTTCTA ATAATAATTG ACGTTTCCCC CAACTCTACT GTTCACATAA AACCACATAA 840
CTGTGATCTA GTTATTTATT ATTCAGCATC CCTAACTTCC TATAGGGTTC TTATTTTTGT 900
TTCCTAAGGT TGTCGTATAC ATTATACAAA AGACTTGCAT GCCATATGCA AGCAGATGAC 960
GTTTGTGAAT CCCTTATGTG ACAGAGCTTA TTAGATCCAT CCAACAAACC TTTTGGTAGA 1020
TGGTTCCAGT ACCTGATACA AAAATAAAAG GATTGTACAA AAAAGGGCAT GGTTTTTGCT 1080
TGTTACAACA CAGGTAATTA CAAACGACAA 1110
|
