| Tag | Content |
|---|
EnhancerAtlas ID | HS116-23663 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr3:49684850-49686690 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr3:49686669-49686684 | AAGGGCCAAAGGTCA | + | 6.73 | | MEF2A | MA0052.3 | chr3:49685349-49685361 | TTTATTTTTAGC | - | 6.04 | | Nr2f6(var.2) | MA0728.1 | chr3:49686669-49686684 | AAGGGCCAAAGGTCA | + | 6.05 | | Nr2f6 | MA0677.1 | chr3:49686670-49686684 | AGGGCCAAAGGTCA | + | 6.56 | | RELA | MA0107.1 | chr3:49685965-49685975 | GGGAATTTCC | + | 6.02 | | Rxra | MA0512.2 | chr3:49686670-49686684 | AGGGCCAAAGGTCA | + | 6.18 |
|
| | 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 |
| GH03I049647 | chr3 | 49685234 | 49685433 |
|
Enhancer Sequence | AGGAACTGGA CAGAGGGAAT GAGGCAGAAG TAGTCATCAG AGCCACCCCA TTATCCATCC 60
CCTGCCCTTT TGTCAAAGAG GCCAGGCGAA GGGGTAAGCA GGCAGCACTT TCCCAAGGAC 120
TGGAGCTGGC ATGGGCTGAG TGAGGCAGAG TACGAGAGGG CTGTGCAATG AATGGATGGC 180
TGAATGAGGA ATGAACACTG AAATTGCGGA ATGGAAACGA GCGGAAGAAT AAGGGAATGA 240
ATGATTGGGA TGGAGGTAGG GGTATGTTGG GGTTGGAGAA AATGAGAATA GAATGAATAA 300
AGGAATTGGG ACCCCAGCTG TCCCAGCCCC CAGGCACAGA GATTCTACAT GGCCTGCCTT 360
CCACCCGATT CTCATTCCCC AGAAGACTTG GGCCTGGGCC AGGTCTCCCC TGGCTCTACT 420
CCTACCAGCC CCAGTGCCCT GTACCCTTCT TCCCCACTCC CAGAGGGCTT GTGAAGGGCC 480
TCCAGCAGCC AGGTCAATGT TTATTTTTAG CCCTTACTTC ACACGCCTCT TCCTGCCTGC 540
TCTCCCTTCC TCACTGCCTA CTATAGCAGA GCCAGGAGCA AGAGGGCCTG CCAGGCAACC 600
TGCAACCTGG CTGTCTCCAT GAATAAATGT GTGAAGGAGC AAAGCACCAG GGAGCATGTG 660
ACCACAGGTA ACATCTCTGC TGAGAGCTGG GCCTCTGGGC TCAGGCAAGC TGGCCTCTCC 720
AGCATTTGGT CAGAGCACTT AACATTAGGT CTGCTTCCTC CATCCAGACT ACCCTTCCAA 780
GGTGACTTGC TTCATTTAGA CTGTTGCTTC TGTGTGGGGT TCGCAGGCCA GAGATGGGGT 840
TAGGAGTTTG CCAGGCCACC AAGGTGGGCC AGGGCAGATA TCCAAACTTT GAGAGGCCTA 900
ACATGGGATG GGTGTGCACA GGGCTCCAAA GTGGAGTTAG GGCAGCATTG CCTTGGGCCA 960
GCCCACTGGG CCTAGATCCT AAACCCATCA TGCTGACCAT AGGGCTGGGG AAGGGGCTGT 1020
TTGATCATTT CCAGAGCTCT CTCTCTTGAT CTCTGCCTAT AGCCCTGCCA TCTCTCCAGG 1080
GTCATTTTGC CATCTCACAG TCCTTTCTGA CATGGGGGAA TTTCCATTGT GTACACAGGT 1140
GATGCTGGGG GCATGTGAGC TAGGGTTCCT GGATCAGGCT CTGTGCTCTC CCATGTCCTG 1200
TTCATCTGGG GCTCGGTCTC AACCTATCTG TATTTTCCCC AGGCACCTCT GGGGGTGCAC 1260
CCTGCCAGGC CAAGTGAGCC CAGGGCCTGG CCAGTGGCCA GCACTTACTG CCTTGTGGGG 1320
TTTTGTGTGG AGACACATTG AGCATCAGAT AAGGTTCAAG GGAGTCAGTA GTGGTGTTAG 1380
GGCTGGGCTG TGCAGAGAAC AGAGTGAGTA TATGTATGTA GGGCATCTAA AGGGTCCCCC 1440
TCCACAGCTG GGCCACTGCC CCATTCCTCT GCCTGGGACT TGTGCATGAG GTTGGGCCTC 1500
GGGGAAGAGC AGAAGCTCCA GTGGGAGAGA AGCAGTCTCG ACCCTGAGTA ACCAGCCTGG 1560
GGAGCAGGCC TGTCCCTCAA CACACACCAA GGCCCTGCCA CCTGCCCAGC CTAGCCTCTG 1620
CTGAAGCCCA GAGCAGAGAA GTGGAGTGTA GCTCTCTGTG GACAGCAAAC CAGGGCAGAA 1680
TCATTGACAT GTTATCTGCC ATGGTGGCCC TAGGATGCCA GGCTAAGGGC AGGCACCCTG 1740
GGGGTACCAG GCTTCCAAGG CTGCCAGAGG CAGCATGTGA AGTGAGGGTA CTGAGGTTGT 1800
CAGCCTTCCT GGGGGTGGCA AGGGCCAAAG GTCACCTCCT 1840
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