| Tag | Content |
|---|
EnhancerAtlas ID | HS116-09588 | Organism | Homo sapiens | Tissue/cell | Left_ventricle | Coordinate | chr13:40339850-40341510 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr13:40341492-40341502 | ACCACTTGAG | + | 6.02 |
| | | 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 |
| GH13I039765 | chr13 | 40340001 | 40340539 | | GH13I039766 | chr13 | 40340801 | 40340910 |
| Enhancer Sequence | CATAATCTGG AGCCTAAACT TAATGTAAAA CTCTGAGTTT GGTTTATATC CAATAGCCTA 60
AGGTTTCATA GAATTTTGGT GGTCGGCAAA GGAATTACTG GAATAAAAAT ATCACAGCTT 120
CTGTGCTGTG TGCAGATACT TACTGAGTGT AATGAAGGAA TTACTCTCTA ACCGAGCACA 180
TATTCTGAGC AATTAGGCCA AGTGCCAAAA CCATTAAGGC TCAAATGCCA AGTGCCTGTA 240
GGGAGGGTTC TGTTACAGGA TTTAGCAACC CAACCCTTGG CTCACTTACC AGAGGGTGGC 300
ACTCCAGGCT TCCTGATAAC TGTGCCAGCC TGGCTGAGAC TCAGCAGCTG CCATCCAGCC 360
ACTTCTGGCT TCTGGACCCT CTCCCCAGTA CTGCCTCTGT CTCCACCCTT CTCGCCCATC 420
TGCCCCTCCA TCTGCCTGTC AGTTGAGCAG TGGCTACACA GTTGGGGACA CCTTACATGT 480
TGAGTCATGA CTCCCAGCTA ACACATTGCA TTCACCTTCC CTGTTCCTCC ACCACCTACC 540
AATACTTCTC CCACTTGGCA ACTTGAAAGG AAAGGGTTGC CAATTTCTGT TTCATAACAT 600
TTCAGGGGCT TCCATTCAGA GGCTTCTGGA GTATCCTGGC ACTCAAGGAA ACTGGGCATG 660
GAGGTGGAGT AGGGAGAGCC ACTCAGAGGA TTCTGGGCAT CCAGTCACCC CTGGCCCATT 720
CCCAAAAAAA CCTGGGGGAA CAAGAGTAGC CTTTGTAACT CCAAATTTCA TCAAGATGAG 780
CTGAAATCTG GTTCTGTCAT TTCCCCATCC TACCCCATCC CATACTCCCT CCTAACCCCA 840
TCCCATACTC CCTCCTAACC CCATCCCAAA ACCAGAGCAG TGGAATATCT TAACAATTTG 900
ACTTTTATCC AGAACTGAGG CTCTTTATTT GTTAGAACTA AGCATTTGGT CCAAGATTTT 960
CTAATTCTTT CTGTGGGAAC TTGAATCAGC ACCCCCTCCC CAAGCTCCCA CAGAAGAAGC 1020
AGATGGGGAT CTTGGCAAGG TTTGGAAGTC CAGGACTTGG ACAGGTTGAG AGTTCTATTT 1080
GCCAGGCTGA ATTGCTTGTA ATTAAAAAGC TTATCCTCCT ACTTTTTTGC GCTTCTGAAC 1140
TTATCTGAAG AATCAACAGA GTATTTAATC ATGCATAGAA ACAAATCTGT GCATATAAGT 1200
GAAAATCTGC ATTTAAAGGC AGGTGCTTAC CAGGAGAGAT GAGTCACGTA AGCTGGTTAG 1260
GGTGAAGTTA AGCTCTCTAA TGTTGACTTG ACATGTCTTG TTTTAAAGGG TGATAGGGTA 1320
TGATCAGTGT TTTGTGTACA GGTTAGGGCT GGGGTATGGA ACTCTACCCC CTTCCTTCTC 1380
TATTTGTTTC CTTCATCTCC TTGCCTAAAA AGTGCCTACA ATAAGCACTC TGCATATTTT 1440
GGGTCTTCTT AGTGACACTT ACTGACACCA GATTGTTAAC GTTTATCTGC TTTCTACAAC 1500
AGAAAAGAAA ATAACTCATT AGTCTTGACA TTTTAATGTG TGAGGGTTTT GAGACAAAAA 1560
ATAATTTGGC TCCTTCCGGA CTAAGTTGTG CTAATTGCCA GATTGTACTC ATGTTAGGAA 1620
ATTGAGAACA AAGTGAAGCA TGACCACTTG AGGCTCTTGG 1660
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