| Tag | Content |
|---|
EnhancerAtlas ID | HS116-01231 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr1:53370760-53372190 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP2 | MA0516.2 | chr1:53372152-53372169 | CCTAGCCCCACCCCCTG | + | 6.08 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I052904 | chr1 | 53370498 | 53372058 | | GH01I052906 | chr1 | 53372081 | 53372230 |
|
Enhancer Sequence | AGCTGCTCAG ATAGAACAAA GTGAGGCCTC CCTCCCCCAT CCGGTCCCCC AGTGCTAATC 60
CCGGGGGCCA CAGCTGCCTC TGCTGTCTAC TCGCCCCTCT AGCCACTTGC CCCATGGTCT 120
GGCCACAGCC AGGCCTCTCC AGACTCTGCC TTTGGAAGAG CCCTAGCCCA GAAGTCAGGA 180
GCCCAGGCCC TTATTTCACC ATGCCCCTTT GATGGAGTTG TAAGTCACCA GCAAGTCTCA 240
CCCTTCCCAA GCCTCAAAGG TGGAAGAAAG ATGGCTGGCC CTCTTCTGTC TGCTTCAGAG 300
AGCCGCTAAG GATCACACGA GGTACGACGC TTGGAACAAG GAGAGTTCCT AGGAGGTGCC 360
CCATATCTAT TTGTGGATTA CTATTAATAG GTTCTCTGGC TTAGCCCTGG CCTGGCCTAG 420
AATGTCAGTG ACTCCTGCTC CTGCTACAGT CGTCCGTTCC AGCTTTGTCA CAGCCTGAAA 480
TTGCCCTGAC TGTTCCAGTC CATGTCCTCC TGAGTTCTGC TTCCTTCCTT CGAGAAACTT 540
GCCTTGACTG ACGCACCCCC CCGGGTCTGT CTCCTTTTCT GAATTCCCTC AGCATGGACC 600
ATGTGAACGT GGGCAGAAGG GAGTGGGTTT TACATTCACT CCGTCTTAGT CTTCCCCAAA 660
ACCCTGTGAG TTAGTTGCGT GAACGTGGGC ATGTGAGAAG GAGAGTTGGG GCTAGACCAG 720
CCTGGTATTT TGGTGCCTGG ACACCTGGTC AGTTCCTTCT CTTTGACCTG CATTGTGTAG 780
ACAGAAGCTA CTTTCATGCC TGGAGCTACA CATTTTTATA TGTTGCTCCT GGGGTGGCAG 840
GAGAGAGCGG TGGGGGGAGA AGGGAAGACA TTCAGACTTT GCCTAACTGC ATCCAAGAAG 900
GCTGCTCCTA ATCACCAGGT CAGTCACCTG AGAAAATGAT CAGTTATCTT CTTTATCCCC 960
TCCCATTCTT CAAACAAAGC TCAATTGCTC AGAACAAGTA ATGCAAATTT GGCTGGTGCC 1020
AGTATTCCTG CCCAGGCACC TTTGTGATTA GCTCAGCCAT TGACAAACTA TCCCTGAGGC 1080
TCACCTTTTT CCGAAACATG GTCGATAAAT CTGACTTGGA CAGAATGGGA AGACTGGACA 1140
TTGCTCTTTG ACCTCCTTGG CTCGTAACAG CAATTGCTCT GAGGTTGGTC AAATATTCCC 1200
AAAATGAAGG AAGCAGGTTC TGACAGGTCA CAGATACTAC AGCAGCTAAT GGCTGCACCA 1260
GGAGGGGAAG CAGCTTCTGC CTGAGCACCC TCTGTGCTCT GCCTTGCCTT AGTTTTGCTT 1320
TTGGTTGGAA GCCAAGAACA GTGGCTGACT GCAGAATGTC CAGACTCACC CTGTTTCACT 1380
CACCCCTGAC TCCCTAGCCC CACCCCCTGC CCCCAGTCCT GGCCCAGTAC 1430
|
