| Tag | Content |
|---|
EnhancerAtlas ID | HS098-10247 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:64225060-64226960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr11:64225671-64225681 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr11:64225671-64225681 | GGCACGTGCC | - | 6.02 | | KLF5 | MA0599.1 | chr11:64226668-64226678 | GCCCCGCCCC | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCATGGCGTG ATCAGGCCAT GGCAACCAGG GCCTCAGACC CCTCAGGGAT GAGAGTCTGG 60
GTCGCCCCAC CAGGCAAGGC CCCAGCCCAG CAGAGAGTAA GGGAGGAGTC AAGGGGGCCG 120
ATGGCATGGA TCAGTTAAGG CCTTGGGGTC AGTGGCAGCA ATGGGGTCCC TAGTCCTTCG 180
CAAGAGCCTG CCTTGTGGCG GTTTCCCCAG GGAGGGTTTC TGACCGTCCT GGAGAAGCTG 240
GGCCTGCACA GAGTGGACTC TATGCGAGAA GCAAACAGGT CTGAATGGTG CAAAGGGTGG 300
GCTGTAGTGG ACAGTCTGGT GCCTGGCCCA GACCCCTTCA CCTGGCCAGG GCACATGTCC 360
GTCCATCAGC AGCTGCAAGA GGGACTGCTA GTGGCAGGGA GTTTCCCGTC TTCTCCACAC 420
TTGACCTCAG CCAATGGAGC TGCTCTTCCT GCGGTGTAAA GTCCCCTTCT CACTGCAGTG 480
ACAGGCCACA GCCAGTGGCT GAGGAATCAA GGGGACAAAA GACCAGCTCC ATTGCTTCAA 540
GCTGGGACAG CCCTGCAGTG GGGTTTACTC TTTAGAGCCT CCTCGGATCA GAACCTGAGA 600
CTCAACTTGA GGGCACGTGC CTGCCTGGCC TGCACCCCTC CCTCATCTGC TTCCCTCACT 660
TCCTGAGAGC TTCTCCTGCA GAGCGGTCCC TGGTCAATGA CCAGAACAGG AAGATCCAGA 720
GACAGAGCCC ATTGATGGAG CCTGGGCGGA GCCAGTGGGG AATAGGGAGT GATGCTGAAT 780
AGGTATGAGG TTTTCTTTCA GGCAAGGAAA ATGTTTTGGA ACTTGATAGA GGTGGTGGCT 840
TTAAAACATC GTGAGGGTAC TAAATGGCAC AGAAACAGTA CACTTTAAAA TGGTTAATTT 900
TATGTAACAC GAATTTCACC CCAATTTAAA GAAATAGATA TAAGAAAAAA AAGGACCTCC 960
CCCTTCGTCC CCGGCAGCCA CTGCCAGCTT CTTTCTTGCG GTGGGCTGAG CCTCAGCCTT 1020
TAGTGAGATG GAGAGTTGGA TTCTCACCTG GTCTTGGGTG TCATAATTAC TGAGCCAAGG 1080
CTGTTCTTGG ATCTAGAAGT GAGGACATGA CTTACATTGC CTGGGACCAT GTGCCTGCCT 1140
GAGATTTATC TCAAGCGGGG GTGGGAGAAA GGAGCCCCAC AGACTGAGGA CAAAGCAATA 1200
TCACCCTGTC CTGCACCTTG CCTGTCCTGT TCTTCCTCAG GACTGGCCAC GCTGAGGTGT 1260
CACTTTTCTT CCTAAAATCC TCTGCAGCGT TGGAGACAGC ATCCCCAACC CCCCAAAAGA 1320
AAGTAAACAT AATGCTTACT TTCTTTCTTG TGAATACTAA TCCTGGCTAA ATTATTCACT 1380
TCTTTTTAAA CCCCTATTTT TTTTTTTAAA CAAAGCTTTT CTTTATTAAC TGAGAAGGAT 1440
TTACCCCTCA GAATCCAGGC ATCTCTCTCA GCCCCATGGA GAAGGGGGAG ACGGGATCGA 1500
ATGTGTTGGG AGCTGAGCAG TAAGAAGGGA ATCTCAGGAA ATCCCACTGG TGCTCAGACA 1560
TGGGATCACA TCACCCTCTC AAAGAGGCTC CCCTGGGCTC TCTGTCCCGC CCCGCCCCGC 1620
ACCCCCACCC CCTTTCCATT TCCTGTATTT TCTCTGTAAC ACGATGGTTC TGGGATGACC 1680
TCACTTGCTG ACTTTTCTTC CACTGGAAGT CGGCCCCATG AGCGCAGGGA CCTCATTTTT 1740
CTTGCTTGCC AGAGCATCTG CCTCACCCCA GAACCTCATC TGCCACACCG AGGTGCGCAG 1800
GAAGTGTTCA CTGCACAACT GCACAGTGCT TTCTAGGTTA ATACATGTTT ATCCATTCCT 1860
TGCCTTTAAA AAAAATTGTG GTAAAATGTA TATAACATAA 1900
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