| Tag | Content |
|---|
EnhancerAtlas ID | HS136-08832 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr18:10304460-10305550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr18:10304570-10304581 | TTAATTAAAAT | - | 6.62 | | ZBTB18 | MA0698.1 | chr18:10305118-10305131 | CAACATCTGGCTG | - | 6.25 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH18I010304 | chr18 | 10304724 | 10305630 |
|
Enhancer Sequence | GGAAATGATT TGGCCCAGCT CACACGTGCA CCAACAGGAG AGTCATGGCT GAAACTCAGT 60
GTTCCCCCAC CTCTGTTCTG CTCTGACCAG TGGACTGACC TTTTGGGGAG TTAATTAAAA 120
TGAGAAAGTC CAGTTTTCAT GAGTCTCTGT TGCTCAGTTA AGAATGCAAA TAGCTTCAGG 180
GAGGAAATGA AGACTAATCC ATGCAATGAG ACAGAAATCA TAAAAAGATG TCCAAGTCCC 240
AAAGCTCTAG TTTCTGAAGG TCTTAAAATC CATAGGAAAG ACCCATTTAA GCTGCTGTGA 300
ACTTGTAGTA ACAACTCTTA TATAAGAGCT TGACCAGCAC AGATTGTGCT GTCTGTCCCC 360
AGGGAGCTCT CCACCCAGTG GCAAGTTCCA GGGAAAACCA GCAGGAAGGA GCCCCCAGGC 420
TCCCTGGGCC CAGCCCCCAA ACTTTGAAAT TCATGCAGAA CCACAGATAC CCAAGGAAAG 480
AGGACTAGGG GTCCTGCTTG TATGAGCTGG TGCTCATGAT TCATTCCTAC AACAAATGGT 540
CCATGACTAA TTTGGCACAG CACATGAGAA GAACTAATTT TGCAATGTTT GATGTCCTTT 600
GTGTCTACTG TCTTTCACAT GGCTTGCCAT TTCACATCGT GCGAGCATGT TGCATAAGCA 660
ACATCTGGCT GGGCACACAA AGTCACTTTT CCACACAAGA GGCAAAAGTA ACCCTGAATG 720
CCTTCCAGGG CCTCCATCCT GCCCTGAACC ACGGGGAACA GATGGGGCAC ACAATGAGCA 780
TATGTCATGA ACAGCACACT TCCCTCTTCC ATGAGAAAGT ACAGGAAAGG AGAAAGTACC 840
TGTGTTGTGA ATTTGGAGTA CATTGAACGA AAATTCATTT ATGATGCAGC CACTGTGAAC 900
AGGCACTACA GATGCAATGG TGAACAAAAC TCACGTCCTG CCTTCTTGGC ACTTGTAATT 960
TTGCAGAGAA CCTATGGGAA GCCTGATTCT GGTCCTTTGT TCTGATCATG TACAGCCCTC 1020
AGTTGGATGG CTCAGGGCTC TCAGGCCCCA AAGCCTGGTG CTGAGGCCTC GAACTGCCTC 1080
CCATCTCCTG 1090
|
