| Tag | Content |
|---|
EnhancerAtlas ID | HS098-10888 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:85436450-85437520 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr11:85437141-85437155 | ATGACTCATTTCCT | - | 7.28 | | RARA(var.2) | MA0730.1 | chr11:85436787-85436804 | TAACCTTTGGATGAACT | - | 6.24 |
|
| | 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 |
| GH11I085725 | chr11 | 85436056 | 85438034 |
|
Enhancer Sequence | CTGGAAAGCT GGGAAGTTGG ATCCAATGGA TGAGAATCTT CTGCAGCCAT CTGAATCAAA 60
TTCTGTGTGC TTAGCTGGCA CTCACCACTT TCAGCTTTCT TGAGGAGAGC TGTATTTCCA 120
AAAGTTTCAT CTCTCACTGG AAAAGGAGCT AGTATTTCTC TCTTATCAGC TGAAGTATTG 180
TGACTCTGTT CTATCCCTTT TCCAAAAAAT CTCCCCTCTT CCAGCTTAGA GTTGGTTCCA 240
GTGATAACAG GCGCCAACTT GGCTTGCAAG GGAGAGGGTG AAGTTCCAGT TGCTTCCTTC 300
AGGAGTTTGT CTAGACTAGC AGTCAAAGAG TTCCGTTTAA CCTTTGGATG AACTACTGTT 360
TTGTCAACAT GCTCATTAAT GATCTTCTCA GGTCCTTTGA CTTCTTCCTC AGTATCAGCA 420
AAATCTGTTT TTTGAGGCCA TGTCCTATTT TCAGAAACAC TTGGTTCAAG CACTTGTTTT 480
CCATGAACTT TTCCACCAGA GGGTTGAATT GCTGGTGTTG AGGTTTCTGA AAGCAGTTTC 540
TGCAAGCTGT CATTAAAAGT GTCTTTGCAG TCTTTAGACA AAACATTGGT TTTTATTATG 600
GATTCTTGAA TCTCTTGTTC TGAGTAATCC TTTTCTTCCT TAAACACTGG AGTAACAATC 660
CCTTCCGTAT TCTTTTCCAC ATTTTCCTTT GATGACTCAT TTCCTGGCAA CTGATAAGTA 720
TACTTTCTAA GTGGACTCAA AGGAAATGTG ATTTCATCTG GTAGCACCTG GAGTATGCCC 780
TTTGAATTTA ATTTCTCCAT TTCCTCTCTT GCCATAACTT TTTTTGGGCT TAGAAGCACC 840
TCTGCTTCAT GGGTATTTTT ACCTGATAAT TTAATGTCGC TGAATTCCTT GTGTTTCTGC 900
CTATTAAAAG GTGCAGAATT TTTTTGGCTT GTGGTGGTAA TATTCTTGTC ATTATCCTTA 960
CTGTTTGAAT TAGCTTCTAA GTCCCAAAAC TTTCTCAAAT TCTCAAACTG AGAGGGATTA 1020
TAGACCTGTT CTGCATTGGG TTCATCCATT CTTTCTTTTA GGGACATAAC 1070
|
