| Tag | Content |
|---|
EnhancerAtlas ID | HS116-04866 | Organism | Homo sapiens | Tissue/cell | Left_ventricle | Coordinate | chr10:93441160-93442360 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr10:93441771-93441788 | AAGCTCAGTGTGACCTT | - | 6.34 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACCAGGTGGT GGGTAGGCTC ATTGTCTGCT CCAGGCAAAA CACATTAGAA ATGTAGGGCG 60
CTCAAACGTG CTACCTTGAC GTGGGTAATT TTTTTTCCTG CAGGAAGAGA AACCAGGAAT 120
ATAATTGCCC TAGAAATAAC TCAATCAATG GGCATCCTAC GCCCAAACCT CTCCAGGGGC 180
CCACGCTTGC GAGGCATAAA GTAATGGCAT GCTTGCCAGC AGCTAATGAT GCACACCAGC 240
CCCCCAGAAG GCTTCAGTAA AATGTCTCCT CACAGCCACT GTAATGATTT GGAATGTTTT 300
GCCAAAACTA AATGCCTTCC TCTCATTTGC ACTTCATGCC TTTAAGCTCC CAAGGTGCCA 360
CTGCCCCTGC CACTGGGTGA AGAGTGGCAG GGATTTTGCA GGAATGCTCC CCAGTAGCAC 420
AGGCCTAGAA ACACAGAGCA GCCGCCCACA CACTTCTGCG TTGTGACTGC CGCCTCACTG 480
CTGCTAGGCA AGATAATTGG TGGTGCTGGA ATGTGGCCAA GATTTGGCAG GATGCAGAGC 540
AGGCATCTAA ATTGGGGTGT TGGTGCCAGC ATCAAAGCTC TGACCATGGG GTAGGAGCCA 600
AGGTCACCAC GAAGCTCAGT GTGACCTTGG AGGAGAGGAC ACCCCTCCCT GTCTGTGCCC 660
TGAGTCCCAC TCACTCAGCT TCCATGCCAG TTTTGTGCCA CTCTTCCTAC ATACCAGGCT 720
TTAGCTAGGG CAGCAGCGGG AAGCTGTTAG GTGACACATG AATCCTGTAA GGTATGCAGG 780
TGGCGACAGC ATACCACCCA CAGGTTGGAT GGTGACAGTC ACAGCTATAT ATAGGGAAAG 840
GGATTACCAC AGCCCTCTGT GGATACTGCA AGTACTGATA CATGGGCCCT TTGCATTGTG 900
CCATGGAACC TGTTAGCAAT GTAAAATTTG TTCTGTGCCA ATTGGACACA CGATCACTTT 960
TAATATTAGC AGGAGGGAGA ACAGAATCTG ACATTTAAAG AGAAAGAAAG AGTCACACCC 1020
TGGTGATCAG CTGAATGATT GAATCCAACA ACTAGTGTGT CTACAGCTTT TGTCGGAGGT 1080
TCACCCTCAC CACCCTGACC TTAGTCACTG AATTTTCATC CCGAAAGCCC AGCCACAGCC 1140
CTACTCCTGA GGTTGTATGC CACTGGGGGC AGGGAGGGAG CGCTCCCTTG AGTGGAAGAT 1200
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