| Tag | Content |
|---|
EnhancerAtlas ID | HS187-00107 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:8978240-8979950 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:8978669-8978684 | GAGGTCAGGAGTTCA | + | 6.22 | | SOX10 | MA0442.2 | chr1:8978453-8978464 | TGCTTTGTTTT | - | 6.02 | | Zfx | MA0146.2 | chr1:8979057-8979071 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | 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 |
| GH01I008918 | chr1 | 8978060 | 8978659 |
|
Enhancer Sequence | CCAGCCTGGG TGACAGAGCG AGACTCTGCC TCAAATACAA AAACAAAAAC ATAACAAAAA 60
TTCTGCACAG TATTTTTCTG ACCACTGGGT GTCATGAGCG TACAATAAAT GCTTCAGCTG 120
GAAAAACTGC ATATTTACAG GACTGCCTTC AATATGGTGG TGGTTCTCCT GACTGCAGGG 180
GATGCGGCAG CAAGTAATAA ACCCTTCAAA AGTTGCTTTG TTTTTGCAAG CAAGACATTG 240
AGAAGCAGAG AAAATGTAGA CAGTTGAAGA TAAACAAAAA CACAGCACTG GCTGCTTCTT 300
TGCGTTTTCC AGAATATTTC AGTGGAGCAG CTGTTACGGG AGGAATATAA AAATCTAAAG 360
TAAGGCTGGG AGCAGTGGCT CACTACTGTA ATCTCAACAC TTTGGTAGGC TGAGGCAGGA 420
GGATTGCTTG AGGTCAGGAG TTCAAGACTA GCCTGGGCAA TATAGCAAGA CTCTGTCTCT 480
ACCAAAGCCA GAAAAAAAAA ATCTAAAATA AAGTATTCTT AGGGACACCT CTCAAGAATT 540
GTAACTAAGA GGTGGGCAAG GTGGTTCCTG CCTGTTGTTT CAGCTACTGA GTTTCAGGCT 600
GCAGCGTGCT GGGATAGCAC TTGTGAATAG CCACTGCTCT CCAGTCTCGG CAACATAGCA 660
AGACCCTGTC TTTAAAAAAA AAAAACAGTT CTGAAAGAAA AATGAGCAAC CTTGAACCCT 720
TTGGCCTCAG ACAGTACAGG GCTTGCTCAC CTAGAAAGTT AAAATAAAGA AAGTGGGCCG 780
GACATGGTGG CTCACGCCTG TAATCCCAGC ACTTTGGGAG GCCGAGGCGG GTGGATCACC 840
TGAGGTCAGG AGTTTGGACC AGCCTGACCA ACATGGTGAA ACCCCATCTC TACTAAAAAT 900
ACAAAATTAG CCAGGCATGG TGGCACGTGC TTGTAATCCC AGCTACTCAG GAGGCTGAGA 960
CCAGAGAATT GTTTGAACAC GGGAGGTGAA GGTTGCAGTG AGCCGAAATT GTGCCACTGC 1020
ACTCCAGCCT GGGCATCAAG AGCGAAACTC CTCAAAAAAA AAAAAATAAA TAAATAAAAT 1080
TAAAAAAGCA AGCAAGCAAG TGGTTGCTTA TTGTCACTAT TTATATCCCA ATGACTGGTC 1140
TTTTAATTTT ACTAGAGAGC AACTTCCTTG TCAATTGCCC TGAACAGAGT TGATCTCACT 1200
TCAGAGCAGT ATGATTATGA ATTTTCAGCT CTACCAAGTT TTGGCATCAG CATTTCCTCA 1260
TTGATAAAAG TACTCTTGAT TTCTTCTCTC AGCTGGGGTA GCTCAGAGAG GCCTGAATGT 1320
GCAAACCAGT ACCTTTATTT ATTCTTCTTG GCTGTGGAAA ATCGTCCATT ATAGGAATAT 1380
TGTTAACATT TTTTTTGGGG TGGTGGGGGT CGGAGTCTTG CTCTGTTGTC CAGGCTGGAG 1440
TTCAGCGGCA TGATCTCGGC TCTCTGCAAC CTCCGCCTCC CAGGTTCAAG TGATTCTCCT 1500
GCCTCAAGCT CCTGAGTAGC TGGGATTACA GGTGTCTGCC ACCATGCCCA GTTAATTTTT 1560
GTATTTTTAG TGGAGACGGG GTTTCACCAT GTTGGCCAGG CTGGTCTCGA ACTCCTGACC 1620
TCAAATGATC TACCCACCTC AGCCTCCCAA AGTGCTGGGA TTACAGGTGT GAGCCACCGT 1680
GCCCGGCAAC GTTTTTTTAT ATAATGTTTT 1710
|
