| Tag | Content |
|---|
EnhancerAtlas ID | HS127-12868 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr17:18078750-18080520 |
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 | | Nr2f6(var.2) | MA0728.1 | chr17:18078823-18078838 | TGAACTCCTGACCTC | - | 6.22 | | ZNF263 | MA0528.1 | chr17:18079171-18079192 | GCCTCCTCTCCCACCTCCCCC | - | 6.64 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 18078829 | 18078982 | | chr17 | 18080276 | 18080356 |
|
Enhancer Sequence | CATGCCACAA TGCCTGGCTA ATTTTTGTAT TTTTAGCAGA GATAGGGTTT CACCATTTTG 60
GCCAGGTTGT TCTTGAACTC CTGACCTCAA GTGATCCATC CACCTCAGCT TCCCAAAGTG 120
TAGGGAGGGG CGTACATGTG TAAGCCACCA CTCCTGGCCC CCTAGACAAT CTCTAAACGT 180
TGCTGAGTCT GGGTCTCTCC CCAGGGCACC CTGTCTGATA CTGAGGCTTT CAAAACCATG 240
TCTACCATCA CAGCATCCAT ACTTCTACCT CCTGCCCAGA CTACCTGAGC TCCAGGCTCC 300
CTCAGCATCC CCCTTGGAGA CCAACAGTCC TCTCCAGCTT TCCTCCCGAT CCTCCCAGGC 360
ACTCAGGCCC CAAATCTGGG AGTCCTTCCC ATCCCTGTCC CTTCCTCCCA TGACCTTTGT 420
GGCCTCCTCT CCCACCTCCC CCATCTCTGC TCATTCCTCC AGCCACCCTG GCTCCCTTGT 480
GCTGAGCTTG TTCTCCCTGC CCTGGGCCCT CTGCCCTCAC TGTCCTCTCC ACCTGGAATG 540
CTCTTCCTTG ATCCATCACA GGGCCCATTC TCTCCCTTTA TTTGGGTTTC AGCACAAATA 600
TCACCTTTTT CTAGAAGCTT TCCCTAACCT TCCTCCCTAA GAACTCACGA TCCCTGCCCC 660
CATAGCCCTA CTTATGGCTT GGAAATCATT TAGTTATTTG TTTATGTATT GTCTCCTTAT 720
ATTAGTCTGT TTTACGTTGC TATAAAGGAA TATCCGAGGC TGCATAATTT ACAAAGAAAA 780
GAGGTTTATC TGGCTCACGG TTCTGCAGGC TGTGCAAGAA GCGTGGCACC AGCATCTGCT 840
TGGCTTCTGT GGAGGCCTCA CGAAGCTTTT ACTCAAGGCA GGAGGCAAAG GGGAAGCAGG 900
CACATCACGT GGCAAGAGAG GGAACAAGAG AGAGAGGGCC CAAACAGCCG TCTCTCGTGT 960
GAACTATTAG AGTGAGGACT CACTCATTAC CTTGGGTAAC CAAGCCATTC ATGAGGGATT 1020
TGCCTCCATG ACCCAACACC TCCCACCAGG CCCTGTCTCC AACATTGGGG ATCACATTTC 1080
TTCTCTTTTC TTTTTTTTAC TTTTCTTTTT TTTTTTTTTT TTTTTTTTAC TACAGTGTCT 1140
TGCTCTGTTG CCTAGGCTGG AGTAATCTCG GCTCACTACA ACCTCTGCTT CCCCAGTTCA 1200
AGTGATTCTT CTGCCTCAGC CTCCCAAATA CCGGGATTAC AGGCATGTGC CACCATGCCC 1260
GGCTATTTTT TTGTATTTTA GTAGAGACGG GGTTTCACCA TGTTGGCCAG GCTGGTCTCA 1320
AACTCCTGGC CTCAAGTGAT CCACCCGCCT TGGCCTCCCA AAGTGCCGGA ATTACAGGCA 1380
TGAGCCACCA TGCCTGGCTG GGCATCACAT TTCAACACAA GATTTAGAAG GGACAAATAT 1440
CCAAACTGTA TCATTCCCCC ATCAGAATGT CAGCTCCAAG AGAGCAGGAC CGTATCCATC 1500
TTGTTCATGC TGTGTCCATA ACTCAGCGCC TGGCACATAG TAGATGCTCC ATACATATTT 1560
GTTGGTTGCA TGGGTGGGTG GGTGGATAGA TGGATGGATG AAGGCCTCTT TGCTTTTCCC 1620
ACTTCCTTGC AGCACCACCT GACCTCCTTA TGCTGCCCTC TCTGCCTCTG GCCTGTATGT 1680
GTCAGGGGCT ACATTCATTC ACTCATTCAG TATAGATCCA CTGAGCATCT CTGTGTAGCA 1740
AAGATACTGA AGTGACTGAG ACCCCCTCAG 1770
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