| Tag | Content |
|---|
EnhancerAtlas ID | HS062-13724 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr6:11143960-11145480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr6:11144766-11144785 | TGACCACGAGGTGGCGACA | + | 6.59 | | NR2F1 | MA0017.2 | chr6:11144721-11144734 | CAAAGGTCAAAGG | + | 7.22 |
|
| | 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 |
| GH06I011143 | chr6 | 11143373 | 11145232 |
|
Enhancer Sequence | TTTTCTCTTA TCGTTACCGA GAATGAGCTT TTCACAACTC AAATTTGTCT TCTTGCTTAG 60
AACATGTGAA TAGGTTCCCA TTGCTCCTAG AAAAAAGGTA GAAAAGCTTC GACATGCCGG 120
TGACATGCTG CACGGCTTCA TTTGCTGCCT CGTCATCCTC TTACTCTACA TGCTCATGGC 180
CACATGAGTC ATCGTTCAGT TGCGCAAACA TGCTGTCCTC ACTCAGACAT CCCCACCCTA 240
CTCACTGGAT CCTTCCACTG GCCGTGCCCC TCACTCACAA ACTTGCCTTC TCTCTCCTTA 300
TCTTCCAGTC CTTCTTTCAA TTTCAGCACA CAAATCACTT TCTCAGGGAA GTGTTCTTTG 360
AACACAGCCC CCTTTCCAGA CAAAGAGTTT GTCTGGAAAG ACAAACTGTC ACAGAGAAGT 420
CTTCCTTTCC CTCAGTGGCC TGATCCCAGA CAAGAATTGA ACATTTGTTG GTGGATTTTT 480
TTAAATTAAG TGCCACCATT CCCACTATGT TGAATTAATT AAACAATATT TCAATATAAA 540
GTAGAACTTA TATCAAAATA ACATTTTAGC CTGCAATCTT TTTATTGGAA TCTGAGAGTG 600
TAAAATATAA AAGATGCCTT ATTCCTGCCT AATGAGAATC TCCTGAAAGT GGCGATTTTC 660
TTTAATCAGC AAACACAAAA GTGTATGTTA ATGAGATACA TATTTTTCAA GCCCCCTAAT 720
TCTGCATCTT CTGTGTCCAT TTCACTCCTT CATCTCTTCT GCAAAGGTCA AAGGATCCTG 780
TCCAGTGCTG CTGGAACAGC AGCTTGTGAC CACGAGGTGG CGACAGTTTT CAAGAGTTGG 840
CAGGTGAGGA CGCCTTCTAT TCCGGTCTGG TCAGGGGTGT GCTCCTTTAG AAGGGTGTCA 900
CTGGATGGAA ATTTGTTTGG TAATTATGTG GCACCCTGTT TTGTGTCATA GGCATTTTAC 960
CTAGCCTTCT TTACCTAAAG CGGCTGGGGC GAGCATAGAA GCTGTTGATC AAACTGGAGC 1020
ACTTGAGAGT GAATGGGAGG AGAGTGGACT ATACATCATT GGGCCAGGAC AACAGATACA 1080
AACCAGGATT GTTCTGGCCA CACAGGGGCA TCTTTTTTCT CCCTCTAAAG CCAAGTCAGG 1140
GGACAATATT TACAGTCTCT CTGACACCTA CTGATGAAGG CTTGAAGTTG GAGAGAAAAG 1200
GAGCGCTCCC AAATAGCATT TGAATTTTAT CTCCCTGTGT AGAACTCCAG AAAGCAAATC 1260
ATTTCAGAAA ATGAGTGAGG AGAGGATGAT TGATTCAAAG GCTCACATAT TTATTTGTTG 1320
GAGTCAGAGA AACCCTACCT TTGGTGAGAT GTTTTGAAAA TAATAAAGTT TATTTTTTTT 1380
TTTTAATTTT GTTTTGAGAC GGAGTCTTGT TCTGTGCCCA GGCTGGAGTA CAGTGGTGTG 1440
ATCCTGGCTC ACTGCAACCT CCACCTCCCA GGTTCAAGTG ATTCTCCTGC CCCAGCCTCC 1500
AGAGTAGCTG GGACTATAGG 1520
|
