| Tag | Content |
|---|
EnhancerAtlas ID | HS017-26948 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr5:138410460-138411920 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr5:138410732-138410747 | TGAACTTCTGACCTC | - | 6.38 | | RARA | MA0729.1 | chr5:138410729-138410747 | TCTTGAACTTCTGACCTC | - | 6.88 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH05I139075 | chr5 | 138410890 | 138411794 | | GH05I139076 | chr5 | 138411861 | 138412010 |
|
Enhancer Sequence | CCCTTCATCC CCTCTTGCCT TCAGAACTAA GCATCTCTTT CTCTCTCTGT CTTTTTTATT 60
TTTATTTTTT TTGAGGCACA GTCTTGCTCT GTCACCCAGG CTGCAGTGCA ATGGCACAAT 120
CTTGGCTCAC TGCACCTCCG CCTCCCGGAT TCAAGCGATT CTCCTGCCTC AGCCTCCTGA 180
GTAGCTGGGA TTACAGGCAC ATGCTACCAT GTCTAGCTGA TTTTTGTATT TTTAGTAGAG 240
ATGGGGTTTC ACCATGTTTG CCAGGCTGGT CTTGAACTTC TGACCTCATG ATCTGCCCGC 300
CTTGGCCTCT CAAAGTGCTG GGATTATAGG CGTGAGCCAT CGTGCCTGGC CAGAATCTCT 360
TTTTATGAGG TTATGTTTAA TACTAAACAC CCATTATGAC TGAGAAGCAG AAATTACCAA 420
CCAGAGTCTG AAAGCACTAT CCACAGAAAC CTCTGAAAGA AGAGTGTCCT AACCAACCTG 480
GACAGGGTTC AGTGCAGTTC TGCCTGGAGG CAGATGGATG GAAGCATGAC ATTTTAAAAA 540
CTCCCATCCC CTAGAACTTT ATTTTCCCTC TGCAGCAGGA GATATCTCAA AACAAGGACA 600
TTAGTCCAAA CTACTCTATA GAGGAAAAGC AATAATCCAA GGACTTTTCT GAGTATGTAG 660
CAACCACTGA GATGCATGAA AATGATACGT GTGCCTAGTT TTTATGTCTA CTCCTACTAA 720
CTATGCAAAA CTGAAACTAG TTCCTTAAAA ACAAACTGCT CCTGGACACC CTACACAGTC 780
GCTGCCGCCT CCCTGACTCT GCAGACATCA GTAACAGAGC ATGTCATAGG GAATAAAACA 840
CAATCATAAG GTAATGCTAC ATAAACGCTA GTGTGTTTAT GGGGAATAAA TGTCAAGGTA 900
AAGCAGGAAT ATCTATTTTC TATGTGGGAG ATGGTGATTC TGTGTGTCAA TGCCCCATTA 960
TACTGAATTG ATTTTAGTTT TGCCAAATCA CTAAAATATT TCACAATCTC CTTTTGGAGG 1020
CTGTGGCTGT CATAATGACA GAATCTGCAA TGACCTTTCA CAAGGTCTAC TTTCCAGGCA 1080
TCTGGACTTC ACAATCTCCT CCATTCTAAG GTTCCATTTT CCCAGGAAAG AGGCACAGTA 1140
GGGCATGGAA AGCTGGCCAG TTGTGATTCA TTCCCAATAC GATCTGCCAA GCAGGCCCAT 1200
CCATGCTCTT GGTATCTTGA AATTCCAGAG AAGCTAGACT TCAAGTCCTT CCCAAGACCC 1260
TAATGTCCTG TCATTTAGTC CCTTCTGAAA GTTGCTTAAA GTGACATAAG GGAAGCAGCT 1320
AATTTACAGT CCTATTCTTT TAATCTTGGT CAGCCAGATT TTCACAGACA TCAGTTTATT 1380
TCACTTTATA ATATATTAGA CAAAACAACA GTACCGGAAT CAGTTCCAAG GCAGCAACTC 1440
ACTCTCAGGG GTTCTGCTGA 1460
|
