| Tag | Content |
|---|
EnhancerAtlas ID | HS095-06829 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:26445340-26447180 |
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 | chr12:26445571-26445592 | AAAAAAAAAAAGAAAGAAAGG | - | 6.1 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_36295 | chr12:26444818-26447460 | HMEC |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I026291 | chr12 | 26444819 | 26447460 |
|
Enhancer Sequence | AGGCAGGTGG ATCATAAGGT AAGGAGTTCG AGACCAGCCT GACCAACATG GTGAAACCCC 60
GTCTCTACTA AAAATACAAA AATGATCTGG GTGTGGTGGT GGGCGCCTGT AATCCCAGCT 120
ACTTTGGAAG CTGAGGCAGG AGAATTGCTT GAAACCAGAA AGCAGAGGTT GCAGTGAGCC 180
GAGATCGCGC CACTGCACTC CAGCCTGGGC AACAAGAGCA AAACTCTGTC TAAAAAAAAA 240
AAGAAAGAAA GGCTAAATGA ACACCTTGGA GATGAAGCCA ACAGACTTGC TGAAAGATTG 300
GAAGTAAAGA CTGAAGGGAA CAAAGAAGGT AAGTTCATGA CTCAGTTTCT GGTCTGAACT 360
AGTTTTCAGA CACAGATCCC ATTATAAGAA GGAGATGCTT TCCTGGGAGA CAGGACACTG 420
CAACACCACA GCAAACAGTT GGTAATGAGT CACGCAGTCC TTCCCAAAAG GGTCCTACCA 480
TCACTTACTC TGGTAGCCAT GCACTGGAGA AAGGATTAAC TAGGCATTGT GAGGATGGGA 540
GAATGCTAAT ACAACTCATT TAATGGGTGA CATAGGCTTC CAGCTCTGAG ACAGGCCCAG 600
AGCAAGTAAG AGCTCTGTAG CAGGTCCAGA CTGTGGTCCA GGCCACCCTG CTTTTTGGAC 660
AATATGACCC AGCAGACTTT ATAATATCAG AGACATCCAT GGTAAGAAAA GCTGTCATGT 720
GGTGTTTAAG GCAAGACTAG TAGGAGAATC ACAATATAGA CTCCAAGGGT TTTAGATCGA 780
GGCCTACCAT GTACAGCAGA GAATCATACA CCTTTCAAAA GATAACAACT TGAATGCTAC 840
TCGCCCTTGG TAGAGATGAA ATCCCTGACA ATGGAACAGC AAGTGAACAT GTGGTCAGAA 900
TTGCCCATGA TCTGGTTCCT AACAGACTCA CCAAGTCATA AAGTCAGGTG GATCAGCCAC 960
AGTCCATTGT AAGATGGAAA TAGCACATCC AGGATAGGTC ACAAGCAAGG CCAGAAGGAA 1020
CAAGGAAGCC ACACAAGCAG GTGACTTGGA CTCCCATGTC ACCCCCCACT GTCTGGCCAC 1080
ATCTTCTCTC AGCTCACACC TGTGGCTGCA TGAGAGTCCC TTATAACCAA GTGATGGAGG 1140
GAAAAAAAAA AAAGGCTGAG CTTGTGGATG CGAGCCAAAA GTGAATGCTG CTACCTTACT 1200
CAGAGAACAC CTTGAAAGAC AGCAGTAAAT AGAAATCCTC CCAACAGGCA GAGCCTCAGG 1260
TGGTATACCT CGCCAGCTAC TTCATGTGGA AAAGGAAGTG GCCTGCAGTA AGAATACAAG 1320
TGGGTTTATA GACACTAGTA AACGGTTCAG CTGGTTGGTC AAGGGTCTGG AAAGAGAAAG 1380
ATTGAAAGAT TGGACAATGA AATCTGAGAA AGAGGCATGT GAATGGTCTT ATTGGAATGC 1440
ACACAATGTG AAAATCATTG TATCCATACT ATCCACCTAC CAGAGAGCAT TAACCACAAA 1500
CAAAGCACTA AAATATCAAG CAGACAGAAT GACTTAGCCA GTTGACACCA GCAAGCCTCT 1560
CTCATTGGTG AGAGTGCTGG CACAATGGGT GTGTGAATGA AGTACTGTAG TAGCATGATT 1620
GGAAGCTACT CATGGGTTCA ACAGCATAGG CTGCCACCCA CAAAAGCTGA TCTAGATACT 1680
CCCACTGACA ATTGTCAGTC TGCCATCGCC AGGCCCCTGA TATGACCCAG TCCTTCCAGG 1740
AGTTCAACCA ATCACTTGAT GGTAAGTTGA TTACATTTGA TCCCCTCCAC TTGGAAGGAA 1800
CAGTGGCATA TATTCTGGGT ATGGGTTTGT CTTTCCTGCC 1840
|
