| Tag | Content |
|---|
EnhancerAtlas ID | HS092-21474 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr18:6780530-6782880 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6 | MA0677.1 | chr18:6781235-6781249 | TGAGCTTTGACCCC | - | 6.1 | | Rxra | MA0512.2 | chr18:6781235-6781249 | TGAGCTTTGACCCC | - | 6.46 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH18I006780 | chr18 | 6780532 | 6783397 |
|
Enhancer Sequence | AATCCCCCTC AGATGCTGAG GGATGCCTGT ATAACATTTA AGCAATGGAG GCTGAGAAAA 60
AAAATCAGTC TCTTAGGCCA GGTGCGGTGG CTCATGCCTG TAATCCCAGC ACTTTGGTAG 120
GCCAAGGTGG GTGGATCACC TGAGGTCAGG AGTTCGAGAC CAGCCTGCCC AAGATAGCAA 180
AACCCCGTCT CTACTAAAAA TACAAAAATT AGCCAGGCAT GGTCGTGGCA GGCGCCTGTA 240
ATGCCAGCTA CTCACGAGGC TGAGGCAGGA GAATCTCTTG AACCCGGGAG GTGGAGGTTG 300
CAGTGAGCCG AGATCACGCC ATTTGCACTC CAGCCTAGGC AACAAGAGCA AAACTCCGTC 360
TCCAAAAAAA AAAAAAAAAA TTCAATCAGT CTTGTAATGC CCATGAATTT CACAGTCACA 420
GAATGTAATT TTCTTTATTT CTGGTAATAA AATTTATATT CTAACTCTGA GCCCCCACTT 480
CTGACGGACA GCAGAAAAGC TCCATCTAGT CACAGCCACA GCCAGTCGAC TTGATCCAAT 540
TTAGCACTTT CTAAGTTGCT TCTGGTTAAA ATTCAGGAAT ATTCAGAATA TTTCCCTTTG 600
ATTCCCCTCC TTTCCTTCTA TTGCTGCTGG AAGCCATTGC ATCTGGAGAG GCAGTCGGGA 660
CAGTCAGGGG GACCTGTGTT GGTGACTCAG CCTTCCTCTG CTGTCTGAGC TTTGACCCCA 720
GGGGATTGGA CACAGTGCTG CTGGGATGCA AGAGTGGATC TATGGGGTGG CTCCCACCTG 780
GGTCTCTGAT ATGAGTTGAG CCTTCGTCCT GTTCCAGTTT CTGGAAGGAA CTGTTCACTC 840
TGCAGCCCCT GCCACGGGGA TCCTTATCTC CAGCCAGGCA CGTCTGTCAG GCTCTGAGAA 900
TCAATCAGTC TCTGTCTGCT TCCTTTTCTC TCTCAGCTAA AGTGGGCACC CCTCAGGCTG 960
TGCAGGGAAC TCCTGACCCC ATCACTCCCC AGCGGGAGCG GGAGCTGCTG TCTCTGCCCA 1020
TTCTTCTTGC CCTGGTGACA TGGGATGTGT CTCTGAGGCT GCTTCCTTAA TCACAAAAGA 1080
AGGGAAGCAG GAAGCAAGTG TCTTCCTAGA TCCTCCCAAA CTTCGTGGAG AAGCCTGTGA 1140
GGGCCCCAGC TCCCACCTGA CACACTGTGG CATTGTTCTG GGGGTGGGAC ACCAAACACA 1200
TGGCCTCTAA TTGCTCATAA TGATTTTTTC CTCTGCAAAT TCTTTCCTTC TCCCTAGTTT 1260
GGATGGGGTG GTAAAAAAAA CTTGTTTTGC CAGTTGATAT CTCTTTTCAA AACTATTTTT 1320
GTCTCTCTTT TGAACTAGAG CCAAGATTCT GGAATCTGTT TGCTGTTTTT ATTTTTCTTC 1380
CTGACAATTC TCCCTGGGGC AAGTGGTAAA CTGGCCAGCC CATATCTCTT GGAATATGGG 1440
TTTAGGGATG GGGACAGGGC AGTGGAGAGA GGGGCACATC AGTCAACAAG CTATCATATT 1500
ATCCTGGCAG AGAGCACCCA GATCTGATTC ATCAGTCAAG GCCCAAGCCA ATTTCTCACT 1560
TCCTGGAGAT TCCAACTGGT TTTTTTTTTA GCTGCCTCCC CAGCCTTGGG AAGGTCTGCT 1620
GTGCTTAGCC ACTGCAACTG ATGAGGAGCA GAGCATGTCC TTGGTTTAGG GAGTGGGGGG 1680
TTGAGGGGGT GAGATAACCT TGTTTTCTAG GGTGAATGGG TAGAAGAGTG TTCACTGTTT 1740
TTTAGCACGT TGAAAATCCA AATATGAGGT TATTCTTTCC ATCTTTTAAT GTTATTCCTA 1800
ACAGCCTCGA TTAGAGTATT AATGAGGAAT CCCTTGAAAT ATACATATAT GTCACTATCT 1860
GTTATATATA ATGTCAAGAC ATTAATTATT ATTATTATTA TTTTGAGATA GAGTCTCACT 1920
CTGTCACCCA GGCTGGAGTG CAGTGGCACG ATCTCGGCTC ACTGCAACCT CTGCCTCCTG 1980
CATTCAAGTG ATTCTCATGC GTCAGCTTCC TGAGTAGCTA GGATTACAGG CACCTGCCAT 2040
CACGCCCAGC TAATTTTTGT ATTTTTTTTT TTTTTTTTTT TTTTTTTTTT TTTTTTTTAG 2100
TAGAGACGGG GTTTCACCAT GTTGACCAGG CTGGTCTCAA ACTCCTGACC TCAGGTGATC 2160
CACCCACCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACCAC ACCCAGCCAA 2220
GAGATTAATT ATATATCATA TTTTATATAC AATTATATAA TTGTATATAA TGTGTGCCCA 2280
TATGTATTTC TCTAACAAAC TTCTGATTGG ATCTTTTTAG GAGCTGGCTA TTTGGTCTTG 2340
GTGCTTACTC 2350
|
