| Tag | Content |
|---|
EnhancerAtlas ID | HS068-02077 |
Organism | Homo sapiens |
Tissue/cell | GM18526 |
Coordinate | chr16:27367920-27370230 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr16:27369202-27369223 | CATTTCTTTCGTTTTTTTTTT | + | 6.18 | | Nr2f6(var.2) | MA0728.1 | chr16:27369003-27369018 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_09427 | chr16:27369581-27371016 | CD14 | | SE_17448 | chr16:27364916-27368281 | CD4p_CD25-_CD45RAp_Naive | | SE_17448 | chr16:27369350-27371368 | CD4p_CD25-_CD45RAp_Naive | | SE_18369 | chr16:27369130-27371244 | CD4p_CD25-_Il17-_PMAstim_Th |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I027357 | chr16 | 27369131 | 27371368 |
|
Enhancer Sequence | TGAGCTGGCC AGGGATAAGC AAGATGGAGT CATCCCACAT CCCCTTACAA CGCTGGGTGC 60
CTGGGCAACT GGGGGCATCT GGGGGCATGT GGTAGGAGCC AGAGGAATTT GCGACGATTG 120
CCCTGATGGA GTCAGGAGAC CTGGGTTTGA ATCCTGGCCT TGGAGCTTGG TAGCTGGCGG 180
CCGACAAGTT GCTGAAACCC CTGAGCCTGG GGTTCCTGCT TTGCAGAGTG ACAGTGATGG 240
TGAGAACATA TTTCATCAGC CAGAAGAGGC CAAATCACAG TAAAGGCTGA GGGAGGAGAT 300
GAGTGGCGAG TGGCTGGGAG GTGGTGGAAG GAGCCTCGTT TCCAGAGAGC TCTTGCCAGC 360
CCTTGGAATC ATGGTGTCTC AGAGCCTCAG TCCTCCCATC TCTGAAATGG GACTAGCAAG 420
CTCAACCTCA CTAAGTCAGG ATTAGAGGTG GCTAAGGATT ATTAACATGA TTGATGAAAG 480
TGCCCACTCT TGGCCCAGCA CACACTAGGT AGGCAGGGAA TGCAAATTCC CCTCCATATC 540
TTGTCACTGA TGCCTCCGAG CAACCTTGGA CTGATCGCCT TGCTCTGAGC CTCAGTTTCC 600
CCATCACCTG TACCTCTTCC CACTCCCCAT CACTATATCC CAGCATGCCA GCCTCTTTGC 660
TGTTCTTTGT CTTTGGTTTC TTGTTTTGTT CTGTTTTTTA GACAGGGTCT CACTCTGTTA 720
GCCAGGCTGA AGTGCAGTGG CGCGGTTACG GCTCACTGCA GCCTCCAATT CCTGGGCTAA 780
AGAGATCCTC CCATTTCAAC TTCCAGAGCA GCTGGGACAA CAGGCGCTTG CCACCACACC 840
TGGCTAATTT TCTTATTTTA ATTTAATTTA ATTTTATTTT TTGGGACAGA GTGGAGTCTC 900
AAAAACCAAG CTGGAGTGCA GTGGTGCGAT CTCGACTCAC TGCAATCTCT GCCTCCCGGG 960
TTCAAGCGAT TCTCCTGCCT TAGCCTCCCG ACTAGCTGGG ATTACAGGCG TGTGCCACGA 1020
CACCCAGCTA ATTTTTGTAT TTTTAGTAGA GATGGGGTTT CACCATGTTG GCCAGGATGG 1080
TCTTGAACTC CTGACCTCAA GTGATCCACC CACCTCGTTC TCCCAAGGTG CTGGGTACAG 1140
GCATGAGCCA CTGTGCCTGG CCAATTTTCT TACATTTTGT AGAGACTGGC TGTCACTTAT 1200
GTAGCCCAGG CTGATCTTGA ACTTCTACCC CTTTATCTTT ATTCATGGCA CTTATTACCA 1260
TGAATGAATG ACCTCATATA AGCATTTCTT TCGTTTTTTT TTTTTTTTCT TTGAGATGGA 1320
GTCTCATGTT GTCCCCCAGG CTGGAGTGCA GTGGCGCGAT CTCAGCTCAC TGCAACCTCC 1380
GCCTTCCGGG TTCAAGCGAT TCTCCTGCCT CAGCCTCCTG AGTAGCTGGG ATTGCAGGCG 1440
CCTGCCACCA TGCCTGGCTA AGTTTTGCAT TTTTAGTAGA GACGGTGTTT CACCATATTG 1500
GCCAGGCTGG TCTCGAACTT CTGACCTCAG GTGATACACC TGCCTTGGCC TCCCAAAGTG 1560
CTGGGATTAC AGGCGTGAGC CACCATGCCT GGCCTCATAT AAGCATTTCT GTCTCCATTT 1620
ATCATCCATC TTTCCCTCTT GAAGGTCAGT TTCACCAAGG CAGGCATCTT TGTCTCGTTC 1680
ACTGTTGTGG CCTCAGGGCC AGGCACAGTG AGTCAAACAT AGAAGGTGCT CAATAAATAT 1740
GTGTTTATTT ATTGAAACCA TGGGCAGAGG CTAATTCAGA AGCGGTCTGA GGACCTTACC 1800
TCCCAGTGAT GATGCACCAT GGCCCCAGGC AGGCCAGGAA GAGAGAAGGG TTGTGTTTCT 1860
CCGTAGGTCC CCCAGCTTCC CAGGCCATCC CAGGCCATTC CCTGGTCATT TGCCCTCAGC 1920
TGCTCTGAAA AAGGGATTGT TGAGGGGAAC CTAGAATCCT CTCTCTGCAG TTTGAGTCTT 1980
TCCTAATCCC CTGGGGTCTC ATTCCCACTG AGGACATAGG TGGCCTCCTC AGGAACTCTG 2040
TGCTGGGTAA CAGAATGCGG GAGTGTGAAC CTGGCTCTGC CACCTACCAG CTGTCACTCC 2100
ACCTCCTTGG GCCTCACTCT CCTCATCTGT AGAATAGGGT TAGCAATAGA ATCCATGTCA 2160
CCAGGTTAGA ATGATGAGTC AGTGGTTTGA CCTCCAGAAA CTAATCAGCC TGATCTCTGA 2220
TGCCAAATAA GTATTGGTGA TAACGACCAC TTTTATGGGA GGAGCGTTCA CCTGTCAATA 2280
ATTCAGAGAT CAACACCTTT TCCTTTTGTT 2310
|
