| Tag | Content |
|---|
EnhancerAtlas ID | HS187-02126 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:200874360-200875460 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:200875430-200875445 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23181 | chr1:200874081-200874690 | Colon_Crypt_1 | | SE_23181 | chr1:200874811-200875442 | Colon_Crypt_1 | | SE_27435 | chr1:200873387-200874956 | Esophagus | | SE_27435 | chr1:200875065-200878791 | Esophagus | | SE_33981 | chr1:200873398-200878744 | HCC1954 | | SE_50836 | chr1:200873411-200875646 | Sigmoid_Colon | | SE_52641 | chr1:200873442-200875476 | Small_Intestine |
|
| | 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 |
| GH01I200905 | chr1 | 200874082 | 200874690 | | GH01I200906 | chr1 | 200874781 | 200875150 |
|
Enhancer Sequence | GGTAAAGATT TTTTCATTAA ATTGCGGAGC AGGCTGAGCA TGTTGGCTCA AGCTTGTAAT 60
CCCAGCACTT TGGGAGGCCA AGGCAGGAGG ATCTCTTGGG CCCAGGAGTA TGAGACCTGC 120
CTGGACCACA CAGGGAGACC CTGTCTCTAC AAATAACTAA AATAAAAAAA TTGGATAGGC 180
ATGGTTGTGG ACACCTATAG TCCCAGCTAC TCAGGAGTCT GAGGTGGGAG ATTGATTGAG 240
CTCAGGAGGT CAAGGCTGCA GTGAGCTGTG ATCGGGCCAC TGCACTCCAG CCTAGGCAAC 300
ATTGTAACAA CCCATCTTTA AAAAGATGGG TTAAACCTTT GTGGAGCAAA GGTTAACAAA 360
CTTTTCCATA AAGAGCCAGA CAGTACATAT TTTAGTCTTT GTAGGCTCTT TGGTCTTTAT 420
CACAACTGTT CAACTCTGCT ACTTCAGTGC TAAAACAGCC AGACATTACA TAAACAAATT 480
CATAGCCGTG TTCCAATAAA CATTTATTTA CAAAAGCAGC TATTGAACTG GATTTGACCC 540
CTGGGCCATA GTTTGCTAAC CTCTGTTGTA AGGGATTTCA AGATGGTTGG AACTTTTTAC 600
TTTTTTTGAA ACTTCCTGGG CAATGCCCAT GCATTTGAGA TGCAAGCTCA CAGGGGAGAG 660
CCCATAAAGG GTTGTGGTTA AGAGCAGACT CCAGTCAGAC TGTCTGGGTG TGAATTCTGA 720
CTCAACCACC TTTGTTGAAT GTATAACCTA AACCACGTTA CTCAACTCCT CTGAGACGTG 780
GTTTCCTCAA CTGTCACTTG CAGGTGATAA TATCTACCTT ACGTGGTTGT TATGAGAATT 840
ACCTGAATTA ATATATATAA AGTGCTGTAT TTAGAAATGT ATTGGCACAG TAGAAACATT 900
AGCAATTATT ACTTTTTCCT CATCTTCATT CTCAAACACA GTTGAAAATG TTTCGTGAGT 960
TCCATCCAGG TCACTTTAGG CTTATTCTCA AGATCTGAAG GCCTGGCCGG GTGTGGTGGC 1020
TCACGCCTGT GATCCCAGCA CTTTGGGAAG CCGAGGTGGG TGGATCACCT GAGGTCAGGA 1080
GTTCAAGACC AGCCTGGCCA 1100
|
