| Tag | Content |
|---|
EnhancerAtlas ID | HS136-05119 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr12:116838020-116839800 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr12:116838693-116838707 | TACTTCCTCTTTCT | - | 6.87 | | SPIC | MA0687.1 | chr12:116838693-116838707 | TACTTCCTCTTTCT | - | 7.52 | | ZBTB18 | MA0698.1 | chr12:116839539-116839552 | GCACATCTGGAAA | - | 6 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I116400 | chr12 | 116838292 | 116839356 |
|
Enhancer Sequence | CCAAGATCCT GACTGAGTCC TTCCTGGTTC CTTTCATTGT TAAGCCTGTT TTCTATCTGT 60
AAAATGGGGT TAACAATGGT CCTATTGGCT GGGCATGGTG GCTCATGCTT GTAATCCCAA 120
CACTTTGGGA AGCCAAGGTG GGTGGATCAC TCGAGGTCAG GAGTTTGAGA CCAGCCTGAC 180
TAACATAGTG AAACCCCATC TCTACTAAAA ATACAAAAAT CAGCTGGGTG TGGTGGTGGG 240
CACCTGTAGT CCCAGCTACT CGGGAGGCTG AGACTGGAGA ATGGCTTGAA CCCAGGAGGC 300
AAAGGTTACA GTGAGCAGAG ATGGCACCAC TGCACTCCAG CCTGGGCAAC AGAGCGAGAT 360
TGTCTCAAGA AACATAAACA GAAACAAGCA ATGGTCCTTA TCTTGTGGGT TTGTCATGAG 420
GATGAATGAA CACATAAAAT TCTTAGCACA TAGTAAATGC TCAGTTAATA CTTTTCACAG 480
GAAACATGTT TGGAAAGATC AGCTAAATGT AAGTTGGTGA CTCCCACGCA GCTAAAATTG 540
TGTACATTGG AGCCTGATTT TCTTTTCCTG GGGCCTCAGA AAGCTGGTTC TACCCAGCAC 600
ATGCCAGATA GATGAGGAAG CTTGGGGAGA GGGGCCTGGG AAGGAAGGTG GGTGATGCTG 660
TCTAAGAAGT CAATACTTCC TCTTTCTCTT TCTTAGAGAA GTACTGCTGC CCAGACCCAA 720
AGAATTACTG GAAACAGAAC TAGTCTGATA TTAAACAGAG TAGTAACCAT GCACTTGAGA 780
TAATTTGAGG GCCACACAGA ATGTCCACCT ACCCCCAGAC TCACCTTGTA TCAGTCTATT 840
CTCACACTGC TATAAAAGAC TACTTGAGAT TGGGTAATTT ATGAAAAAAA GAGGTTTAAT 900
TGACTCTCAG TTCTGCAGGC TATACAGGAA GCATGGAGGC CTCAGGAAAC TTACAATCAT 960
GGGGGAAGGG TAAAGGGGAA GCAGGCATGT CTTCACATGG CGGCAGAAGA GAGAGCAAAG 1020
GGGGAAGTGC TAAACACTTT TAAACAATCA GACCTCGGGA GAACTCACTC ACTATCATGA 1080
GAACAGCAAG GGGGATGTCT GCCTCATGAT CGAATCACTT CCCACCAGGC CCCTCTTCCA 1140
ACACATGGGA ATTACAATTC TACATGTGAT TTGGGTGGGG ACACAGAGTC ACATATCACA 1200
CCCTTAGGTC TATCATTGTG CCTGGGAGTT CCACCATTCA ACCTGCTTCT AAAGGTCCCT 1260
GGGAAATGTA ATTTGTCAGC TTAAACTCAA CCACATCTAT TCAGAGCCTA TTGCATGTAA 1320
TCTGCTCTAG GGGAAAGATC TATAAACGTT TTCTTTATAC TTTACACGGT GCTTTTATAC 1380
AGCTAATTTC ATCACTGCAA TAATGTTATG AGGTAGGTAT TTATGATGAT TCCCATTTTG 1440
CAGAGGAAGA AACTCAGGCC CAGAGAGGTT AAGGGGCTTA TTGGGAGGCC AGGCAGATGT 1500
CAACTGGCAG GGCTAGAAAG CACATCTGGA AAGCACATCT GAAAACTCCA AGTTGTTGGT 1560
GTTTTCTTGC TCATCTCAGC TGCTCTCAGG AAGTTTACAG GAAACAGACA AATCAGCCAA 1620
TCAAGAAATG GTCAAGGCTT TCAAACTGGG TTCCCTAGTA TTCCCCTGAG GTCTCCTGAG 1680
TGTTAAGAGG TAAGAGAGGG TTGGATAGCG TGCGTGGCAG TAGGTCTTGG GCTCCCCAAC 1740
ACACTTTGGC AGGATCTCCT CTTTCTTCTG CCTTTAGAGG 1780
|
