| Tag | Content |
|---|
EnhancerAtlas ID | HS023-13916 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr2:25139020-25141180 |
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 | chr2:25139334-25139349 | GAGGTCAAGAGATCG | + | 6 | | PPARG | MA0066.1 | chr2:25139822-25139842 | CTGGGTGACAGTGAACCAGT | + | 6.35 | | Zfx | MA0146.2 | chr2:25139312-25139326 | GAGGCCGAGGCGGG | - | 6.01 | | Zfx | MA0146.2 | chr2:25139123-25139137 | CAGGCCCCGGCCCA | - | 6 |
|
| | 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 |
| GH02I024919 | chr2 | 25139891 | 25140364 | | GH02I024917 | chr2 | 25140470 | 25140869 |
|
Enhancer Sequence | TTTTCTGTTT TCTAAGTTTT AGGGTTTTAT GTCTTAGCAA TACTCAAAGG AGAACAATCA 60
TGAGTTTAGA AGTGATCTCC GAGTAGCCAC GTGGTGGGGC ACCCAGGCCC CGGCCCAGCC 120
CTGTGGCCAT ACCTTCTCAG TCCTTTTCCC TGGAAGCTCC AGGAGCCTCA AAATAAGCTC 180
CTTGTCCACC TGAGGAGATG GAGCTAGAGA GACCAGTCAT CCTCAGACCT CAGACCTTAG 240
AACCTGGGAT GCCTGGGCAT GGTGGCTCAC GCCTGTAATC CCAGCACTTT GGGAGGCCGA 300
GGCGGGCGGA TTATGAGGTC AAGAGATCGA GACTATCCTG GCCAACATGG TGAAACCTTG 360
TCTCTACTAA AAATACAAAA ATTAGCCAGG CGTGGAGGCG CGTGCCTGTC ATCGCAGCTA 420
CTCAGGAGGC TAAGGCAGAA GAATAGCTTG AACCTGGGAG GCGGAGGTTG CAGTGAGCTG 480
AGATCGCGCC ATTGCACTCC AGCCTGGCAA CAAAGCAAGA CTCCGTCTCA AAAAAAAAAA 540
GAACCTGGGA CTGGCTAATG CATGGCCTGA AGAGATATGA CTGGTGTTTC CACCTAGTCA 600
ATGACCAGAA ACTCACAGCC CCCTCTACAG AGATTTGGGG TGGGGACGGC AGGGCAGCAC 660
ATAGCCACTG TCTCCAGGAG GTGGGGTGGG AAGCAAAGCT CCTGCTCTCA GGCAGCTCTC 720
AGTGCTCCAA GGAACATACA CAAATGAGCC CTGGGCTGGG GGTCAATGCC TGGGCTCCCG 780
TCCTGTTTCT GCCACCAAAG TGCTGGGTGA CAGTGAACCA GTTATCACTC ATCTCTGTTT 840
CCTCCTCTGT AAAATGGGTA GTCTGGGCTA GATGCCCTGC CAGGCCCTGC CTATGTTAAC 900
ATCCTCTACC CATTTCTAGA ACAAATCAGC AGGATGAGAC ATGAGTGGAG AAATCAGCAG 960
AGGAGTGGAA GATTCTGTCT GTCCACCCTG GGCCTGCACA TAGCACCTGG TCTCCAGGAC 1020
CCAGGCACTG ACCTCCATGG CTGCTAGAGG CTCACGTCAG TCAGCAAGGA TTCTGGGCAC 1080
GCCCTGCCTC TCCTGACACC CAGAAGGTCA CCGCTTCAGA GCTGACTCTA CCCCAGCCCC 1140
ACTAACCACA GAACAGAGCT GGCGTGGGAG TTAAGACATC TCTACCAGAC AGAGCACTGC 1200
AGGGGCAGGA AGTGGGGGAG CCTCTCTTGA CCATCATTGG CACGAGGCTG GCAGGCTGGG 1260
CACCAAACCC AGATGCAGAC ATCTCCGCCT CATTCTCTGG TCACCGGCTT GCTGGCTCCC 1320
CAGGGACACA CACTGCCTAC TGTCCCTCAG GTCCCCTGGT CTCTGCAGCC CCTGAGGGCC 1380
TGGCACTTGG TGGGAACACA ATACTATAAT AGTTAAGCTG AGGCCGAAAT TCCACCCCTT 1440
CCAGTAGAAA GCGTGCTCCA GGACCAGCAG AATGCGTGCT TTAGGACCAG GAGACCCTAC 1500
GTCACAGTGG CCGGCATGAC TGTCCCCATT TGCATCCCCA CACCACACCT TCAGTGGGGA 1560
GACCACCATT CTCCACTTCA TAGAACTCCC CAGGCACCCC GAGCTCCCGG AGGCAGGAAA 1620
TATGACAACT GCGTCTTCCC TCTGTGCAGC CCTTCACGTA TCCTAATGCG CTTTCCCCCA 1680
CATCTCCTGC AATCCTGACA ACAACCGTGT CATGCAGGCA GAGCGGACGT TATCCCCATT 1740
TGACAAAGGG GCACTGAGTC CACACAGCTA GTCAGTGCTG GGGAGAGATG GGAATCAAGG 1800
AGCCCTCTTC CCAAGGGAGG TCCTCCTTGC CAGGGTCACT GACAGGGAAT GGCCAGGACA 1860
ATGCTGCCTC AAGACCAGCC CTGGGTGGGC CTTCCTGTCA CACACTTAGA CTGGGCACAG 1920
GTGAAGAGTG GCCCTGAGGC CCAATGCCCT GACATCCTCC TTTCCCTGGG GCCAAGCACA 1980
GGCAGACTCC GGGTAATGGC ACAGGGGTGA AAAGGCAGGG ACTAGGGAGA GAGGTGAGAG 2040
CCCCGGAGGC CCCCAGGACA CATTTTGACT CAAAGGCAAA GCAAACAGCA ACTCCAACAG 2100
GTCCCAAGTT GGTGAGAGCT GCAGGAGAGG ACGCTGTGGG GGGACAGTGG GCAGGACTCA 2160
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