| Tag | Content |
|---|
EnhancerAtlas ID | HS062-06636 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr16:88750600-88752730 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr16:88751712-88751731 | TGGCACCCCCTGGTGGCAG | - | 7.21 | | EWSR1-FLI1 | MA0149.1 | chr16:88752334-88752352 | CCCTCCTTCCCTCCCACC | - | 6.03 | | ZNF263 | MA0528.1 | chr16:88752162-88752183 | AAGGGAGGTGGGGGAGGGAGG | + | 6.33 | | ZNF263 | MA0528.1 | chr16:88752165-88752186 | GGAGGTGGGGGAGGGAGGGAG | + | 6.92 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCACTGGGGG AGCCCCAGGT TTCCCGGCTT TGCTGGGGCC TCTCTGCAGG AAAAAGTCAC 60
CATTTCTTTT TTCCATCTCT AAGACATGGC CACCTTTCTG CCTCCAGGTA TTGTCACAGA 120
GCCAGGACCC TGTTTGTGGG CCCAGTGGCT GAGCCCAGAG GCAGGACGGG GCAAGAGACA 180
GTCTCGCCCC GTCAGGCTGA CCATGTGTTT CTGCTGGGAT TTTAAATGCT TTCCCCATAC 240
TCTCTGGGTT TTGCTTGCCT TTTTATTCAT GCTGCGGTCC AGATCCTGGG GAGAAGACAC 300
TGTTTTGTTT TGTTTTGTTT TGAGACAGAG TCTCGCTCTG TCGCCCAGGT TGGAGTGCAG 360
GGGCGCGATC GTGGCTCACT GCAACCTCCA TCTCCCGGGT TCAAGTGATT CTCCTACCTC 420
AGCCTCCTGA GTATCTGGGA TTATAGGCAC CCGCCAGCAC ACCGGGGTAA CTTCTGTATT 480
TTTAGTAGGG ACGGGGTTTC GCCATGTTGG CTGGTTTCGA ACTCCTGACC TCAAGTGATC 540
TGCCGTCCTC GACCTCCCAA AGTGCTGAGA TTACAGGCAT GAGCCGCCAC ACCCAGCTGA 600
AGAGACTGTT TAAGTACCTT GCTGGCTTCA GGGGTTCCCT GGGGAGCCAT AGGAGCCATT 660
TATTTAAAAG GAGAGATTGA GGGGCCCCAA ATCCCAGCAC CTCAGGTCTA TCCTGGGGTA 720
ACATCTTGGC AGAAAGTTGC CAGGGCCCCC TGGCTGTCAG AAAGCCAGGC AGCTGGGGCT 780
ACAGTGAGGA GGGGAGCGGG GGCGGGGAGC AGAGAGCACT GCGGGGCAGC ACGGCTACTC 840
ACGACAGTTG CCCACTGGGC CCAGCACAGC TACCCAGATT TGCACACTGG GATGGACCCT 900
AAGCAACACT TTGAAACTTG CAACTATTAC CCATGTAAAT TCCGCACACA TGTGTAGTCA 960
CATGCGCATC CACATACACA TAACAGAAGC CAGTGTCCTT CACCATGAGC CAGGCACTCC 1020
GGCAGTTTCT GCTCTATTTT ATTTTACAAA ATTGCTGGGG GTGACTGATG AAACTGATTT 1080
CAAAATGCAC ATTTGAAAAG CATGGTCCTA GCTGGCACCC CCTGGTGGCA GCCCGGGCCT 1140
CGGGTGTGGG TCCAGGTGGG ATCCCCCCCA TCCCCAACTC TGGGTTCTGA GCTGGGATAA 1200
AGGCCTCTTG GCGGTGTTGC TGGGGGCCAC AGCCCCAACA GCGCCCTTCC TGCTCTCCCC 1260
CACCGGCCAC AGAGCGTGAG TCCCGACCAC CGCGTCCGCC GGCGCCCCTC AGTGGGCCTT 1320
TGTCCCAAGA AGCTGCCAAG CCAGGTGGGG ACTGCTCTCA CCGCCCGTGT GGCAGGCTGT 1380
CCTCTGAAGG ACAGAGTCCT CTTCTCTCGT GTCCCTAAGC CTAGCAGGCA GTGGGAATGA 1440
ACGGGCAGCC CGGTTGCTGG GCACCCATCT CCCCAGCCTA GCCGGTGTGT GGAGGATTGC 1500
AGCCCTTTAG CCCAGCCTGC CCAGGCAAGC CTGCCGGGGT GAGCAGGAGG GCTTCTGGGG 1560
TGAAGGGAGG TGGGGGAGGG AGGGAGACCA CGGGCGGAGG CTCACCTGAA CTGAATGCAG 1620
GAGGGGCAGT GCCTTTGCAC CAGAAAGAGC CCATGTGTCC TTCTCACCAT CCCCTGTGCT 1680
TACACCCCCA GTCAGCATGC TCCGGGGGTC CCTGAGCCGG GCCGCCCCAG ACGGCCCTCC 1740
TTCCCTCCCA CCCACCACCC CGCGACCCCT CCCAAACGTG TGCGCCAGGA AGATGACTCC 1800
AGGGTGCCTT TAGCTGGGGC TGTAGTGGTT GGGACGGGCG GCTGTATATC AGGGGTGAGT 1860
TCCAGGGAGA CTTGGGGGCT TAGAAAACTT AGAAAACTTC TCCAAGTTGG GAGAGAATCC 1920
CGCCCGCCCT GCCGGAGGCG GGGCTCAGTG CCCTGAAGTG GAGGCGCCCG TGGGCCACCT 1980
CCCTCCCTGC AGCCGCAGCC GCTGCGCAGA GGCGCTGGCT CCTTCTCCTC CCACCTGGGA 2040
CAGGTGTCTC CCCAGCCCCC GCTCCCAGGG GCCTCTCTCT CTCTCCCGCC CCTCAGGGTC 2100
GAGTCCCGGC AGGGGCTCGG GGATCGGGTA 2130
|
| |
|
|
|
