| Tag | Content |
|---|
EnhancerAtlas ID | HS099-19139 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr6:18346580-18348010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr6:18347724-18347735 | CATGAGTCACT | - | 6.14 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_36128 | chr6:18346638-18354129 | HMEC | | SE_59493 | chr6:18324545-18366590 | Ly3 | | SE_64561 | chr6:18346709-18348691 | NHEK |
|
| | 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 |
| GH06I018346 | chr6 | 18346390 | 18349073 |
|
Enhancer Sequence | AAGGTAATGG TGTCGAGTTT TTTGTGTTTA ATGTCATACA CTCATCATCT AAGGCCGGTA 60
ACAACTTGGG ACAACATAAA AAAATGAGGT TGATTCAAGT CACAGAGAGA AAGTTTAAAT 120
GGAGAGAGCC TGAACTATGT TGCTGATTTC TTTTCTTTTC TTTCTCTCTG ATGGAGTCTC 180
ACTCTGACTC CCAGGCTGGA GTGCAGTGGC ACGATCTCGG CTCACTGCAA GCTCCGCCTC 240
CTGGGTTCAA GCGATTCTTC TACCTCAGCC TCCTGAGTAG CTGGGATTAC AGGTGCCTGC 300
CACCACACCC AGCTAATTTT TGTATTTTTA GTAGAGACGG TGTTTTGCTG TGTTGGCCAG 360
GCTGGTCTCA AACTCCTGAT CTCAGGTGAT CTGCCCGCCT CAGCTTCCCA AAGTGCTGGG 420
ATTACAGGGG TGAGCCACCG TGCCCAGCTG CTGATTTCTT AATCTGTGGC AAGGACTACT 480
AGTTGCCTTT CCAAATTCCA TTTTCAACTT TTCCTTTAGC AACAGAACAT TAGCTTAGTT 540
AAAGGCTATA CTCAGCCTCC TTTGCGGTCA AGCTGATGTA AGTCAAAGTG TTGTGGGAAG 600
CTCCAGAAAG GCTATTGAAC TTGGCCCTTT AAGAAAGGGT AGACATTTTG TTTCTTTCTC 660
CTTTCCTCTT TCTGCTGGTC TCAGATGTAA TGGCTGGGAT TCTAGCAGGC ATCTTGGACC 720
GTGAAGTGAT ATTGAAAATA GAAGCCTGAC GTGAGATCAC AGAGCAGGAA GACAGAATAA 780
GCTCAAATCC TGAGTGACTC AAGCAACTGC AAGGCATGCA TGATTGTGTG CAGACTTGAA 840
AAGTTTATTT ATTTAAAAGC TTTATTTATT TATTTTTTGA TACAAGGTCT ACTCTATTGC 900
CTGGGCTGCT GAAGTGTAGT GGTGCAATAA TAGCTCACTG CAGCCTTGAA CTCCTGGGCT 960
CAACCGATCC TCCTACCTCA GCCTCCCTAG TAGCTAGTAC TACAGGCACA CAACACCATG 1020
CCCAGCTAAT TTTTGTATTT TTTTGTGTAG AGATGGGGTG TTGCTATGTG GCTCAGGATG 1080
GTCTCAAATT CCTGAGCTCA AGTGACTCTC CTGCCTTGGC TTGTTAAAGG GTTGGAGTTA 1140
CAAGCATGAG TCACTGGGCC TCGCCAAAAT TTTTTTAATA TGAAAGAGAA ACCCCTCCTA 1200
TCTTAAGACA CTGTTCTTTT TTTTTTTTTC TTCTGAGATG GAGTCCTCTC TGTCACCCAG 1260
GGTGGAGTGC AGTGGCACGA TCTTGGCTCA CTGCAAGCTC CACCTTCTGG GTTCACGCCA 1320
TTCTCCTGCC TCAGCCTCCC GAATAGCTGG GACTACAGGC GCCCACCACC ACGCCCGGCT 1380
AATTTTTTGT ATTTTTAGTA GAGATGGGGT TTCACCATGT TAGCCAGGAT 1430
|
