| Tag | Content |
|---|
EnhancerAtlas ID | HS060-15466 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr17:74213830-74214560 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr17:74214017-74214032 | AATTAATGTTTAACA | + | 6.15 | | HNF1B | MA0153.2 | chr17:74214018-74214031 | ATTAATGTTTAAC | - | 6.04 | | NEUROG2 | MA0669.1 | chr17:74213847-74213857 | AACATATGTC | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTTGCTAACG GGAAAAAAAC ATATGTCACT AGTAGATAAA CTTCGAGTGT TTCATTATTA 60
GTGAGCTATA ATTTATTAAT CAAAACTCAT ATTCAGAATT CTTTGCAGGC TTTAAAAAGT 120
CACATCATAC ACATATCTCC AAGATTATAC GTAAACCGTA AGGTATGAGT GGGAAGGAGA 180
AAGGGGAAAT TAATGTTTAA CAAGTACATA GTTTTAGTTT TATAAAATAA AAAAGTTCTA 240
GACATCTGTT GCAAAACAGA GTGAATATAT GTAACACTAA TGAATGCTTA AAAATGGTTA 300
CTATGATTAA ATTTAACGTT ATGTGTTTTT TTGCCACAAT AATAAACACA TAAATATCAA 360
GAAAAAAAAC CAAAAGGTAT GAGCCAGAAT GATCAACACT AAGACAAGTT CAGTAAAATG 420
ACTGACCTTT AAAGAAAGAA AGGCACCCAG GCAAAAAGTC AAAATTCTAG AGGGGAAGAA 480
AATCGGTGTC ATCAGACTTT TCAACAGAAA CACTTTATGT CAGAAGACAA GGGAGTAACA 540
TTCTAAGGTA GTCAAAGAAA GAAAAGCCCC TGAGCTCATC TGAGGAGTCT ACTAAGGAAT 600
AAGCTTCCAG GCCAAGCCCA GTGGCTCACG CCTGCAATCC CAGTACTTTG GGAGGCCAAG 660
GCAGGAGGAT TGCTTGAGCC CAGAAGTTCA AGATCAGCCT GGGCAACATA GCAAGACCTC 720
ATCTCTACAA 730
|
