| Tag | Content |
|---|
EnhancerAtlas ID | HS136-07985 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr17:18078950-18080400 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr17:18079156-18079169 | CCCATGACCTTTG | - | 6.48 | | ZNF263 | MA0528.1 | chr17:18079171-18079192 | GCCTCCTCTCCCACCTCCCCC | - | 6.64 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCAGGGCACC CTGTCTGATA CTGAGGCTTT CAAAACCATG TCTACCATCA CAGCATCCAT 60
ACTTCTACCT CCTGCCCAGA CTACCTGAGC TCCAGGCTCC CTCAGCATCC CCCTTGGAGA 120
CCAACAGTCC TCTCCAGCTT TCCTCCCGAT CCTCCCAGGC ACTCAGGCCC CAAATCTGGG 180
AGTCCTTCCC ATCCCTGTCC CTTCCTCCCA TGACCTTTGT GGCCTCCTCT CCCACCTCCC 240
CCATCTCTGC TCATTCCTCC AGCCACCCTG GCTCCCTTGT GCTGAGCTTG TTCTCCCTGC 300
CCTGGGCCCT CTGCCCTCAC TGTCCTCTCC ACCTGGAATG CTCTTCCTTG ATCCATCACA 360
GGGCCCATTC TCTCCCTTTA TTTGGGTTTC AGCACAAATA TCACCTTTTT CTAGAAGCTT 420
TCCCTAACCT TCCTCCCTAA GAACTCACGA TCCCTGCCCC CATAGCCCTA CTTATGGCTT 480
GGAAATCATT TAGTTATTTG TTTATGTATT GTCTCCTTAT ATTAGTCTGT TTTACGTTGC 540
TATAAAGGAA TATCCGAGGC TGCATAATTT ACAAAGAAAA GAGGTTTATC TGGCTCACGG 600
TTCTGCAGGC TGTGCAAGAA GCGTGGCACC AGCATCTGCT TGGCTTCTGT GGAGGCCTCA 660
CGAAGCTTTT ACTCAAGGCA GGAGGCAAAG GGGAAGCAGG CACATCACGT GGCAAGAGAG 720
GGAACAAGAG AGAGAGGGCC CAAACAGCCG TCTCTCGTGT GAACTATTAG AGTGAGGACT 780
CACTCATTAC CTTGGGTAAC CAAGCCATTC ATGAGGGATT TGCCTCCATG ACCCAACACC 840
TCCCACCAGG CCCTGTCTCC AACATTGGGG ATCACATTTC TTCTCTTTTC TTTTTTTTAC 900
TTTTCTTTTT TTTTTTTTTT TTTTTTTTAC TACAGTGTCT TGCTCTGTTG CCTAGGCTGG 960
AGTAATCTCG GCTCACTACA ACCTCTGCTT CCCCAGTTCA AGTGATTCTT CTGCCTCAGC 1020
CTCCCAAATA CCGGGATTAC AGGCATGTGC CACCATGCCC GGCTATTTTT TTGTATTTTA 1080
GTAGAGACGG GGTTTCACCA TGTTGGCCAG GCTGGTCTCA AACTCCTGGC CTCAAGTGAT 1140
CCACCCGCCT TGGCCTCCCA AAGTGCCGGA ATTACAGGCA TGAGCCACCA TGCCTGGCTG 1200
GGCATCACAT TTCAACACAA GATTTAGAAG GGACAAATAT CCAAACTGTA TCATTCCCCC 1260
ATCAGAATGT CAGCTCCAAG AGAGCAGGAC CGTATCCATC TTGTTCATGC TGTGTCCATA 1320
ACTCAGCGCC TGGCACATAG TAGATGCTCC ATACATATTT GTTGGTTGCA TGGGTGGGTG 1380
GGTGGATAGA TGGATGGATG AAGGCCTCTT TGCTTTTCCC ACTTCCTTGC AGCACCACCT 1440
GACCTCCTTA 1450
|
