| Tag | Content |
|---|
EnhancerAtlas ID | HS127-08186 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr12:121678670-121680260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr12:121680146-121680167 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | | MEF2C | MA0497.1 | chr12:121678901-121678916 | TTGCCAAAAATAGCA | + | 7.13 | | NFKB1 | MA0105.4 | chr12:121679359-121679372 | AGGGGAATCCCCG | - | 7.04 | | NFKB1 | MA0105.4 | chr12:121679359-121679372 | AGGGGAATCCCCG | + | 7.34 | | Nr2f6(var.2) | MA0728.1 | chr12:121679918-121679933 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_09417 | chr12:121675310-121679936 | CD14 | | SE_28089 | chr12:121673492-121679558 | Fetal_Intestine | | SE_28761 | chr12:121673137-121679628 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 121678935 | 121679219 | | chr12 | 121679311 | 121679629 | | chr12 | 121679801 | 121679870 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I121235 | chr12 | 121673672 | 121679877 |
|
Enhancer Sequence | TCCTGCTCAC CGAACAGAAA ACCAACATTA AGACTCTGAG AAATGCCAGC GAGGCCCTGA 60
GCCAGCTGCT CCCACATCTG GGCCCCCTGC CCAAGTGGGC CGTCGCGCAC CCCCTGGAAC 120
GTGATCTACG TAACCCAGTC TTTGAGATCC TCTCCCCTTT TCCTTGCTCA CATAAATTTT 180
TCAAAGGAGA CTTTGCACGC AGCCCCTCTG TAAATGAAAG ACCAGCATCA TTTGCCAAAA 240
ATAGCAAGGA CCCGTACAAC AGTTCCAAAA CTATGTAACA CCAAAATTCA CTGCACAAAT 300
CCCAAGTAGA AGGCACCCCC CACCCCACGG CGCCTGTCAT ACCAGGTTTT TAGGTACTTC 360
GATCCCCCAC TTAGGCTATG AGCCCTTACA GGGAAGGGAC TGTGACGCTT GTCCTCAGTC 420
ACCAGATGTT GAGTTCCTTG TGTGTGGGGG TGATCAGAGC CTCCCCTGCC TGGCCTGGCA 480
CACAGCTGGC CCTCAAGAAA GGGCAGATGA CAACTGCTCC AGGGATCCTC CCGCCTCAGC 540
CCTCCTGCAG CCAGCCCTGA GGGAGGAGCA CCTCAGACAG AAGAGGAGGC CCCTTCCCTC 600
TTGGAAGTGG GAGGAGGAGA GCCCTTGTTT CCCTGAAGAG CCCAGGCTGG AGCCGCCGGT 660
GTGACAGCGT GGATGGCGTG ACAGGTGCGA GGGGAATCCC CGAGCCTATC CCCTCACCAC 720
CATCACACAG CTCCCCTGTT CTTAGGGAGG TCACTGGGCA TGCCACATGG GTTACTGTCT 780
GTCCTTCCCC CACAACAATC CGTGTCTCCT GTCCAGGAGG GAGACTGTCC TTACACAAGG 840
GAAAGGAAGC GTGATGTCTG GCTTGCTATG TTTCTGATGG AGAATGTGGG TAAGGTCCCT 900
GGGGAGGGGG GCGCTGTAAC TAGACGTTAG GTCAGGCCCT CAGTCTCTGC CCTCGCAGTT 960
GCCTGTTGGT AGGGGTTGGG TCTTACTGCA GACGGCAGGC AGGCCCCCAG TCCAAGACCC 1020
CCAGTGCCTG AATCAGCTCT GTGAGCTCCC ATGACCAAGG CATCCTACCT GCTGGGGGCT 1080
GAGGGCAGGG GATCCCAGGT GAAGAAAGGA AGGGGCAGCA TAGCCCTTTG GGGCCAGTCT 1140
CCATCTGCTG GTGTCTTGCA ATTTTGATCT CATTGAAACG AAGGCCGGGC ACAGTGGCTC 1200
ATGCCTGTAA TCCCAGTACT TTGGGAGGCT GAGGCAGGCA GATCACCCGA GGTCAGGAGT 1260
TCAAGACCAG CCTGGCCAAC ATGGTGAAAC CCCCATCTCT ACTAAAAAAA TACAAAAATT 1320
AGCTGGGCAT GGTGGCACAT GTCTGTAAAC CCAGCTACTC AGGAAGCTGA GGCAGGAGAA 1380
TCGCTTGAGC CTAGGAGGCA GAGGTTGCAG TGAGCCGAGA TCACACCACT ACACTCCAAC 1440
ACTCCAACCT GGGCAACAGT GCAAGACCCT GTCTCAAAAA AAAAAAAGAA AGAAAGAAAG 1500
AAAGAAAGAA AATAGGAAAG AAACCAACAG CAGACTTGCT CAGAGACAGG AGGCAGCCCC 1560
GGTTTGGCAA ACCCTAAAAT GGAGATTGAG 1590
|
