| Tag | Content |
|---|
EnhancerAtlas ID | HS023-09680 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr16:67927280-67930010 |
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 | chr16:67929530-67929545 | TGAACTCTTGACCTC | - | 7.64 | | RARA | MA0729.1 | chr16:67929527-67929545 | TCTTGAACTCTTGACCTC | - | 6.45 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CGGCCCGGCC CAGGACGACG GCCCGACGGG CGGGAGGGGC AGCCGAACTG TGGTCGTGGT 60
CGCTTTCTGG CGCTCCGGGG CCTGCCCCTG GTCAGCCTGC AGCGTCGGCC CGTGCCCCGT 120
GCGCCAGGGC CTACAGGGTT GGAGAGCAGG CCGGGCGATG GCTGCTCGGG TTCCCGGCGT 180
CCGAGTCTGG ACTGGCCTCG GAACGTGCTG TCGTGCTGGA TAGCCCGTCT CCAGGCCCGC 240
TTGGGCCTGG TGGACGTGGT CGGTTGCCCT GCCTGCTTGC TGTTCAGCCG CCCCGCGTCC 300
AGAGCGGGTC AGGTTGATCC AACCTGGTTG TCCTTGTCCT TACTGCCTTC TCGCGCCCGG 360
CGCCTACTCC ACACCCCTCC TTTGCGTCTG CCAGGGGCCG GCGGGGCAGC TGATCGCTTC 420
CTTGTGCAGG CTGGGAAATA GCAGGTCTGA GTCCAGCTGG GTTGCTTGCT TGGCAAGCTT 480
GTCATTCCTC TACCTGCAAG GGGAAGCCTA GTCCCCCACA CTTAGTCCCC CTCCATAAAG 540
CGGCTGAAGT GATAATTCCC ACCTGAAAAT CTGAGTAAGT CCTTCACTGC CTGAAACTAG 600
TTCCTTAGTG CCTTCAGGAC AAAGGCCGCA CTTCTTAGCA AGGCATTCAG GGCTCTTCGT 660
AATCTGGTGA AGGTTTAACC AGCCAATCAA CACCGGAGCA CTTCTGTGCT CCCTTTACGT 720
AGTTTATTGT TGTTAAAACG TGTGGCGCTC CTGTTAGCTC TGGTTTCATA CCTTTGTGTT 780
TTAGTATTAC TAATTTTGAG ACAAGGCCTC TATTGCCCAA GCTGGAGTGC AATGGCTCAT 840
TCATAGCTCA CTGCAGCCTT GAACTCCTGG ACTCAAATGA TCCTCCCGCC TCAACCTCCC 900
GAGTAGCTGA GACAAGAGGC ACTCCCCTCC ACGCCTGGCT AAGTTTAAAA TTTTTTGTAG 960
AGCCAGGGAG TCTGGCTTTG TTGCCAGAGC TGGCTTCAAG AGACCCTCCT GCCTAGGCTC 1020
CTAACATATT GAGATTATTA ATACAAGCGT GAGCCACTGT GCTTGGTCCC CTTGTGCTTT 1080
AGATAACGCA GTTTTCTCAG TTTGCTATAC ACTGCCTTCC ACCCCACCGA CCACCTACCA 1140
GTGTTGGAAA CTTACATCTG TCCTATAAAA TCCACCTGAG ATGTCACTTC CTAGGAAAAA 1200
AATCTACCTT GCTTGGCATG TAACCATTAA CTCCTCTATA TCCATGCTGC TACTATTGAG 1260
TACATCCTGT TGTGTCACAT GGTGGTCTTC TGTCTGCATA TGTCTGGCTC TGTGCCTGGC 1320
ATAAAATAGG GGCTAGCCTC CAGTAGCATT TGCTGAATGC TGACTTATGA ATGGATAGAT 1380
TCAACTGTAT TTTTGAGCAC CTATCAGGGC TAGGATCTAA GATGAGCACA GCAAATGCCA 1440
GCGTATGTGT GTGGTAGGTA GTACAGCCTC TTAATCCTGG ATAGTCCAAA ATCTCCTGGG 1500
ATAATTTTGT GATACAAAAT CAAGAGCCTT ACTGTCTGAG TTAGTTTTTT TTTTTTTTTT 1560
TTTTTGAGAC GGAGTTTTGC TCTTTTTGCC CAGGCTGGAG CAATGGCGCG ATCTTGGCTC 1620
ACTGCAACCT CTACCCCCCA GGTTCAAGTG ATTCTCCTGC CTCAGCCCCC AGAGTAGCTG 1680
GGGTTACAGG CAAGCACCAC TATGCCCAGC TAATTTTGTA TTTTTAGTAG AGATGGTGTT 1740
TCACCGTGTT GGCCAGGCTG GTCTCGAACT CCTGACCTCA GGTGATCCAC CTGCCTCGGC 1800
CTCCCAAAGT GCTAGGGTTG CAGGCATAAG CCACTATGCC TGGCTGAGAT TTTTTTTTTT 1860
TTGTTTAAAC AGAGACGAGG TCTCGCCATG TTGCCGAGGC TGGTGTCGAA CTCCTGGGCT 1920
CAAGCAGTCC TCCCACCTTG GCCTCCCGAA GTTTTAGGGT TACAGGCAAG AGCCACCACA 1980
CCTGACCCAC TCTTTGAGAT TTTGATGAAG AAGATCTGGG GTAGGAATCT GTATTTTTTT 2040
TTTTTTTCTG AGATGGAGTC TTGCTCTGAC ACCCAGGCTG GAGTGCAGTG GTGCGATCTC 2100
GGCTCACTGC AACCTCCGCC TCCCAGGTTC AAGCGATTCT CCTGCCTCAG CCTCCCGAGT 2160
AGCTGGGATT ACAATCACGC ATCACCACGC CCAGCTAATT TTTGTATTCT TAGTAGAGAC 2220
GGGATTTCAT CCTGTTGGCC AGGCTGGTCT TGAACTCTTG ACCTCGTGAT CCACCCGTCT 2280
CAGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCA TGTCTGGCCA GGTATCTGTA 2340
TTTTGAGAAA ACTTCCCAGG TAACTTTACT GTGCTTCCTC ATTGAAGATC TTTGTCATTG 2400
CCTAAGAAAA CTGTTGTCTC CTTTGTCCAG TGAGAAGGCC TTGCCTTGTG GACTCCTGTT 2460
GTGGTCTCAT GCCTAGAAGC ATGGGCTTTG GTGTCAGAAA GACCTGGATT CAGTTTCTGG 2520
CTTTTCTGAA ATCTTGAGGT TCTCTAAGTC CTAATTTCCT TATTCCAAAA TAGGAATCAT 2580
CGTGCCTACT ACATGTGCTT GTAGAGAGGA GTGAGATGGT ACATATAAGA TCCTTAGCAA 2640
AGTTGGCACT CAGTTAATGG AAGCCACTTT TATTACTAAT GGCTCCTCTT CCCAGAGTTT 2700
CCCTTGTCAA AAGAAGGTCT TGTCTTCTTT 2730
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