| Tag | Content |
|---|
EnhancerAtlas ID | HS136-07178 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr16:11670140-11671880 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr16:11670772-11670785 | GAAAATTCCAGAA | - | 6.17 | | IRF1 | MA0050.2 | chr16:11670422-11670443 | AGAGAAAAAGAGAAAGGAAAG | - | 6.19 | | NEUROG1 | MA0623.2 | chr16:11670915-11670925 | GACATATGTC | + | 6.02 | | NEUROG1 | MA0623.2 | chr16:11670915-11670925 | GACATATGTC | - | 6.02 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_10082 | chr16:11670345-11671514 | CD14 | | SE_20221 | chr16:11670210-11671339 | CD56 | | SE_22505 | chr16:11670258-11671321 | CD8_primiary | | SE_61608 | chr16:11668804-11735966 | Toledo | | SE_62803 | chr16:11650953-11682137 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr16 | 11670548 | 11671169 | | chr16 | 11670600 | 11671200 | | chr16 | 11670817 | 11671132 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I011574 | chr16 | 11668452 | 11671606 |
|
Enhancer Sequence | ATGGTGAAAC CCCATCTCTA CTAAAAATCC AAAAATTAGC TGGGCAAGGT GGTGCATGCC 60
TGTAGTCCCA GTTACTCCAG AGGCTAAGGC ATGAGAATTG CTTGAACCTG GGAGGTGGAG 120
GTTGCAGTGA GCTGAGATCG CACCACTGCA CTCCAGCCTA GGCAACAGAG CAAGACACTG 180
TCTCAAAATA AATAAATAAG TAAATAAATA AATAAATTCC CATATTCCCC TCTCCTTTCT 240
TACAATCTGC AAAAAAAAAA AAAAAAAAAA AGAGAGAGAG AAAGAGAAAA AGAGAAAGGA 300
AAGGAAAAAT GCTTGTGTCC ACATCTGTGG TTCTACACGG TCCCAGGCTG CCAACAGTCC 360
AACATGGGGC TGATGGCGGC TCCATCCCAC CAACACAATT TGCTACTTCA AAGCCTCTGA 420
GGACTTGGAC ACCAGCAGAA CCCAGCGTGC AAGGACTCTG TGTAAAGTAA GAGTTCATAG 480
TTGCCGTGGG CGCCTCCTCT GAGTGAGGTA AACAGGCTTG GGCATCTGCT TTGATGATAA 540
ATATATACCT TATTTGGGAG TCTTCTATTT GCTTACTTCC TTTGTTCTGG CCAAATTCCA 600
GATGACTGCA GGTAGTCCAA CTGTCTGTCT TTGAAAATTC CAGAAAACAG CAATCTTGCC 660
TTTAGCAAGA CTTACGGATA ATGTGGGAAC AGGGTGGTGG TGGACATTGC CTGTCAAGCG 720
CTTTTCATGC CTGTTTCACA TCCCCTGGCT GACACCACAT GATCTAGCCC TTGATGACAT 780
ATGTCTTCCT CCTGCATCCT AATTGCTTCC TGTCTGCAAG TTAGCTTCTA TTAATATTTC 840
CCTAACTGGA CCATATTACG TTACTCTCTG CCCACCCCAG GGGAAGGGAT GTGATCTATA 900
TTTCCCCACG AGGGCTTGAG AAAGCCAAGT GCATCTGACA TCCTTGCACA GCTGAGGTCT 960
CCTGTGCCCA TATGGCACAT CTATCCCATC TATGACAGGG TATCTATGGC ATCAGCTCAT 1020
TAGAAGTGTC TATTTTTTTT TTTTTTTTTT TGAGACGGAG TCTCCCTCTG TTGCCCAGGC 1080
TGGAGTGCAG TGGCACAATC TCGGCTCACT GCAAGCTCCA CCTTCCAGGT TCAAGCAATT 1140
GTCCTGCCTC AGCCTCCCGA GTAGCCGAGA TTACAGGCAC CCACCACCAC GCCCGGCTAG 1200
TTTTTGTACT TTTAGTAGAG ATGAGGTTTC ACCATGCTGG CCAGGTTGGT CTCGAACTCA 1260
TGACCTCAAG TGATCTACCC ACCTCAGCCT CCCGAAGTGC TGGGATTACA GGTGTAAGCC 1320
ACCACACCTG GCCAGAAGTG TCTATTTTTT AAACAAGAAA AGACAAATCT TCCTCACTGA 1380
CAAATTCCAA ATAGTATGAG TAGATACTCC CTCTCCAGGG GATGCACTTT TATTTTATTT 1440
TCTTTTTTTG AGACAGGGTC TCACTCTGTC ACCCAGGCTG GAGTGCAGTG GCACCATTGG 1500
CACCATCATA GCTTACTATG GCCTCAGCCT CCTGGGCTCA AGCGATCCTC CTCCCTCAGC 1560
CTCTCGAGTA GTTGTGACTG CAGGTGTGCA TCAACAAGCC CAGCTAATTT TCTATTTTTT 1620
GTAGAGATGG GGTCTTGCTC ATTCCACTAT TTCCAGGCTG GCATGCAATG GCTTGATCGT 1680
AACTCACTGC AGCCTTCAAC TCCTGGGCTC AAATGATCCT CCCACCTCAG CCTCCTGAGT 1740
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