| Tag | Content |
|---|
EnhancerAtlas ID | HS017-28573 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr6:45649340-45650750 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx3-2 | MA0122.3 | chr6:45649465-45649478 | TTAACCACTTAAT | + | 6.98 | | RARA(var.2) | MA0730.1 | chr6:45649891-45649908 | TGACCTCCAGCTGACCC | - | 6.64 |
|
| | 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 |
| GH06I045681 | chr6 | 45649382 | 45650302 |
|
Enhancer Sequence | AATATCTAGG ATATTATTTT TATAATTTTA AAACATGCAA TCATACTGCT GGGACATGAC 60
TCTTTAAACA GCAGATCTTT GAGTGAATGT GAATGTGATA AACTCTGCTT TCTAGAGAAT 120
CCTTTTTAAC CACTTAATGC CTCTTTTAGC TACTAGGTCT AAGAATCTAT AGAGAGGGGA 180
TATGGCAGAG TGTAGAAATG ACCCTAATTA TTCATCCCTC CTGTATCTAT GTCCTTCACC 240
ATACACATCT GTATTGCTGT CCAATGCTGT TTCTGAGCCT AATCATGGAC CTGTTTTGGC 300
CAACAAGGTA AAGTGTAAGT ATCAGTTCCA CATATAGAAC TTCAGAGACT GTGTGTGTTT 360
CCTTTTGCTG TCTTGTGTAT CTGCCATTGC CATGACAACA CGCTCAAGCT AGCCGGCTGG 420
AGGAAGAGAA ACTGAGCAGC AGAGCTGAGC CATCTCTGTT GCTCCAGTCA AAGCCAGTCT 480
AGATCAGCCA ACTGCCAGCC GACTCTCACA CATATGAGTA AGCCCAGCCA AAATTAGCAG 540
AGCCACTTAG CTGACCTCCA GCTGACCCTA GATGTTTACT GTTGCATGTC CCTGAGGTTT 600
TTTTACTGCG AGGGAGCATT ATTGTGGAAG TAGATGACTG ATTTAGGGAA TTGCCTCATA 660
TGCTTTTTTT TTTTTTTTAA TCACTCCTTT TCCCCTTGTT TCAATCAACT TGTCACAAAT 720
ACATCTGAAC ATTGTTAGGT GTCTACCCAA TATCCACTCT CCTGCTTTTT CTTACTGCCA 780
GAACCACATG CCCAGCTAAA AACCTACATT CTCTGGCTTC CTTTGTAGAA AGGAGTTGTC 840
ATGTGACATT CCTTTGGCCA ATGAGAAGCA AGTGAAATAT TGAGTAGTTC CTTGAAGGAG 900
GATGGGGAGT CCTTTTGCCC TTCTCCTTCT TCCTTTCTGG AATAAAAATC TGATGCTGGA 960
AAATATTATG GCCCCAAGGA GCCAGCACAA GCTGAGAATG ATTGAGAGGA AAGCAGAAAG 1020
AGCTTGGGTC TCTGATGGTA TGACTACAGT ACCAGCCATG GGCTGCCTCC TTTTTCACTT 1080
CTAGCTACAT GTGAAAAAAA TAAGACTTCT CAACTAATTA TGCCACTGTT TTTTTTTTTT 1140
TTTTTTTTAA TTCTTTTACT TGCAGTTCAT TGTAATTCAT TTTCTTCTTT TTTTTATTTG 1200
TGACAGAGTC TCACTGTGAT GCCCAGGCTG GATTGCAATG GTGCGGTCTC AGCTCACTGC 1260
AACCTCCGCC TCCTGGGTTC AAGGGATTCT CCTGTCTCAG CCTCCCGGGT AGCTGGGATT 1320
ACAGGCATTT GCCACCACAC CCAGTTAATT TTGTTTTTTT AGTAGAGATT AAGTTTCTCC 1380
ATGTTGGTGA GGCTGGTCTT GAACTCCCGA 1410
|
