| Tag | Content |
|---|
EnhancerAtlas ID | HS029-01239 |
Organism | Homo sapiens |
Tissue/cell | CUTLL1 |
Coordinate | chr1:200874220-200875530 |
SNPs | | Number: 4 | 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 | TTCAGTAAGA GGGGGTCTCT TTAATTGAAC CCTAAAGCAA AGGCTACTTG TGAGCCAAGC 60
AAAGCATGGG CTGGCTGGCT ACTCAGGAGT CAAGCCCAGC TCCTGGTACC GTATGTCCTA 120
GAAATCTACT GCCTGCTCTG GGTAAAGATT TTTTCATTAA ATTGCGGAGC AGGCTGAGCA 180
TGTTGGCTCA AGCTTGTAAT CCCAGCACTT TGGGAGGCCA AGGCAGGAGG ATCTCTTGGG 240
CCCAGGAGTA TGAGACCTGC CTGGACCACA CAGGGAGACC CTGTCTCTAC AAATAACTAA 300
AATAAAAAAA TTGGATAGGC ATGGTTGTGG ACACCTATAG TCCCAGCTAC TCAGGAGTCT 360
GAGGTGGGAG ATTGATTGAG CTCAGGAGGT CAAGGCTGCA GTGAGCTGTG ATCGGGCCAC 420
TGCACTCCAG CCTAGGCAAC ATTGTAACAA CCCATCTTTA AAAAGATGGG TTAAACCTTT 480
GTGGAGCAAA GGTTAACAAA CTTTTCCATA AAGAGCCAGA CAGTACATAT TTTAGTCTTT 540
GTAGGCTCTT TGGTCTTTAT CACAACTGTT CAACTCTGCT ACTTCAGTGC TAAAACAGCC 600
AGACATTACA TAAACAAATT CATAGCCGTG TTCCAATAAA CATTTATTTA CAAAAGCAGC 660
TATTGAACTG GATTTGACCC CTGGGCCATA GTTTGCTAAC CTCTGTTGTA AGGGATTTCA 720
AGATGGTTGG AACTTTTTAC TTTTTTTGAA ACTTCCTGGG CAATGCCCAT GCATTTGAGA 780
TGCAAGCTCA CAGGGGAGAG CCCATAAAGG GTTGTGGTTA AGAGCAGACT CCAGTCAGAC 840
TGTCTGGGTG TGAATTCTGA CTCAACCACC TTTGTTGAAT GTATAACCTA AACCACGTTA 900
CTCAACTCCT CTGAGACGTG GTTTCCTCAA CTGTCACTTG CAGGTGATAA TATCTACCTT 960
ACGTGGTTGT TATGAGAATT ACCTGAATTA ATATATATAA AGTGCTGTAT TTAGAAATGT 1020
ATTGGCACAG TAGAAACATT AGCAATTATT ACTTTTTCCT CATCTTCATT CTCAAACACA 1080
GTTGAAAATG TTTCGTGAGT TCCATCCAGG TCACTTTAGG CTTATTCTCA AGATCTGAAG 1140
GCCTGGCCGG GTGTGGTGGC TCACGCCTGT GATCCCAGCA CTTTGGGAAG CCGAGGTGGG 1200
TGGATCACCT GAGGTCAGGA GTTCAAGACC AGCCTGGCCA ACCTGGCAAA ACCCCGTCTC 1260
TACTAAAAAT ACAAAAATTA GCCAGGCATA GTGGTGTGTG CCTGTAATCC 1310
|
