| Tag | Content |
|---|
EnhancerAtlas ID | HS116-15410 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr17:74413600-74414610 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HINFP | MA0131.2 | chr17:74413894-74413906 | CAGCGTCCGCGA | + | 6.11 | | TCF3 | MA0522.2 | chr17:74413865-74413875 | AGCAGGTGTT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 74413601 | 74413943 | | chr17 | 74414038 | 74414609 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I076417 | chr17 | 74413626 | 74413718 |
|
Enhancer Sequence | TTGTTAATAT GGTCAAAATT CTCTACCCCC TCCTTTTTAT GAGTGTGGAC ACACCCACCA 60
CCAGTGATAA GAGGACATGG ATGGAGGCCA AATGAGAGTG CACTGGGTGG CTGAACTGAG 120
CTGGGTCTTT AGAGGCCATC ACTAAAACCA CCTGGCAGAG AGCACCACGA AGGGCCTTCG 180
ACTACAGGAG GAAAGAATGC TAAGCATGTC CAGGGGCAGG AAACAGCTAT TGCAGGCCCA 240
GGCGAGACAG GAGGAAGGGA AGAGGAGCAG GTGTTTGATG CTGCATGGAT GCATCAGCGT 300
CCGCGAAGAG ACGTCTGGGT GAAGAGATGA ATGTCTCACT GCACCTGCAG AATTGGGCAG 360
AAACTCCTCC CAGTCTCCAT GATGGTGCTG TTTCCGCTGG TATTTGAGTC CTGGCTCACT 420
GCATTTAGAG GAGCTGCTTG CTGCTGTTGT GCCTTGGGAG AAGTGGAGGT GGAGAAGTGG 480
GCAGATGAGG TTCAATGCTC TTCACCACCT CAGGAGGAAG GCGCAGGGGG AGGTCACAGA 540
GCTGGGACAC GTGGAGTGGG CCTACACCCA GTCCCACCCT GGGGTCTGGG ATAGCTGCCC 600
CACACTGCCC TGGGACGCCC TGAAGAAGGG ATAATAGAGA ACAGACACCA ACATGTGAGA 660
CCTGGAACCT CAGCCTTCTG ACAATGTTTT CTATACTATT AGGCAAAAAA CTTCCCTCTT 720
CTAGGAGCCC ACAGCCTCCC GGAGGGCTCT CCAGGCCTCA CACAAAAACT CATTTTATCA 780
CAGTCCTGAA GGAGGTACAC AATTCCTGAA AGTAACAGAC TAAACTGTAC TTGGACTATA 840
GGACACCCTC TTCCAGGAGC CATGCCTTAC AACCAGCAAC TGCGAGGCGC CATTTGGCTG 900
TCTGCACCCT GTGCTGGCCT CTGAAGGGCA ATGGTGGAAG CCAACAGTTG GAGGAAGTTT 960
AGATATTCAA TTCAGCAGTG CTGAAAGCAA AAGACCATGA AGCTGTGGAA 1010
|
