| Tag | Content |
|---|
EnhancerAtlas ID | HS098-15646 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr13:40810140-40811180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr13:40810848-40810860 | TGCCCTCGGGCA | + | 6.27 | | TFAP2C | MA0524.2 | chr13:40810848-40810860 | TGCCCTCGGGCA | - | 6.52 |
|
| | 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 |
| GH13I040232 | chr13 | 40806390 | 40811154 |
|
Enhancer Sequence | GAGGATTCAA GAATGCAGAG CAAATGTCCA GGAGTCGCAG CCAAATTGGT AGCTTTTCTT 60
GCTCCTTTCC ACTGCATTAG CATGCCCCTA GCCAAAACAA GATGGCACCA TGCCCCGGCC 120
AACTTGATCT CAATGTTCTC CACAGCTGTG TGTCCCCACT GGGGTGAGTA TTGGAGCAAT 180
GTCTCATGTC TAGTCTAGCC AGGAAGATTG TCACTTTGGA CCCTAACCCT TTCTGAGGTT 240
TGAGCCTCCA ATTCACTCAT GTCTGGCCAG CACGAGTCAT GCCATCCATG TATCCTCACT 300
CCCAAAAGAA ATGACACCCT TGGCAAATTC TTGAACTACG TTTTGGAAGC CGCCGCTGAG 360
GTTGCGCAAA CACATTTGGC ACAGGCTTCA GGGACCAAGC AGTTCTCTGG GTTGAATCGC 420
AGAAACAAAA TGTACTTGTC CTGCTTCCGA GATGGTGTCT GAGGACTTGG CTCCCTCGGC 480
CGAGGAACTG CCTCCTCGCT GATGTCATCC TGCCACGGAA AGGCAAACAT CTCTGGGTTC 540
AGCAGTTCAG AACCAGAAGT GAGAAAAGTT GGGGATCCAA AGGGCATCCA CCCAGGCTTA 600
ACTCCATCGG GACAACGTAG AGAGACATGC ACTCAATTCT TAACAACTAA ATCATCTTAA 660
AATAAAATGT ATTGAAGCAG TTTGTGAGGA GGAATCATGC TGCTGAAATG CCCTCGGGCA 720
AGGATTACTG GTCGTGATGC TACCTCCATC CAGTGGGGTT TTGTGGGGCT CCACGTGCTG 780
CCACATGCAC CCCATAGGAG CACAAGTTCC CAGAGGCCCA GGAGAATATT CAACATCCAA 840
CCCTAAGGAA GAAATAATTT CCATGTAGCA CTCGTGCCTC ACATTCATGT CACTGCGTAA 900
TATCTCAGAC ATCCAGTGAC TGCACTTTCC TGGCCAAATT GAGGCGGGTG CTTCTGGAGT 960
CTGGTACATT TCTCAACTCC AGGTTATTTC TCAGCACACA AAGTACCAGG GCTGCTTCAG 1020
TCTCCTCAGA GGAGCCATTC 1040
|
