| Tag | Content |
|---|
EnhancerAtlas ID | HS116-21653 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr21:38966050-38967220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HINFP | MA0131.2 | chr21:38967022-38967034 | CAGCGTCCGCAG | + | 6.02 | | NOTO | MA0710.1 | chr21:38966680-38966690 | GCTAATTAGC | + | 6.02 | | NOTO | MA0710.1 | chr21:38966680-38966690 | GCTAATTAGC | - | 6.02 | | ZNF263 | MA0528.1 | chr21:38966902-38966923 | GGAGAAGGAAGCAGAGGAGGG | + | 6.94 |
|
| | 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 |
| GH21I037590 | chr21 | 38963231 | 38967192 |
|
Enhancer Sequence | AAAAATGCTC ATACTGAGTT CTTTCTGTCT GTCCCCTCTC GACTTGGTTA TCAATTCCTG 60
CACCCCCTTG GGCTCTGTCA GGATTGCATC CTGCCTGCTT TGTACACATG GAACAGACTT 120
CTGGGTTCTT GGCAGCCCTA AGGGATCAGG CTCTAGTGAG TGATCACAGC CAGCGCTGCC 180
TTCCTTTCAG GCCCTGGTGC TTCTCTGTTT ATGTGCCTTA CGGCTTCTGC AGCGCTGCGA 240
TGCCTGGAGG AAGAATTTCC CACTTAGAGG CTTACTGCTC TGTGCACAGA CACGCGAGTT 300
GCAGAATGAG TGTCTAATTT GGCGTGGCCC ATGAAGGGTG AAGGCTCAGC CCCACGTCTT 360
GGTTTACCTT CAGCTGCTGG CAATGGAGGT GAGGGGGAGG GTGGGGCCGT GGGTTTCCAC 420
TTAATTTGTT TCTCCTGGAT CTTTGGCCCT GGCAGCCTCC CTTCAGCATT TCGAGGTACG 480
GATAAACCCC CGGAGAAGGT TTGTTCAGAT TCCATTTGAC ACCAGTTATC TCGGTCACCC 540
TGTGTCTGAG TGCCGGCTAA GTAGCTGTCC GCCTGCATTT CCCACTGCAG TCTTCTCACT 600
TCCAGGACTT GTTAGGGTGC ATTAGCCAGA GCTAATTAGC AGTGAGATTG TTGCTGTGGC 660
TCAGAGGGTT TCATAGGGCG GCTCTTCGTG GCTTCAGCAT GGGTGCACAC CAAGGGATGA 720
CGTGAATAGC GATCCTGACA GTTGTGTTTT CATCAGGGAG CTGCTGTGAC CCTCTCGTTG 780
GAATGCCGTG AATATGATGT GGTTCTGTCT TCCTTGTTGC TACTTTTTGG CGGGGAAGTG 840
ATGTGTGAAT TCGGAGAAGG AAGCAGAGGA GGGCCGGGTG GGCGTTGCCC TGGGCAGGTG 900
CTGTAGAGGG AGGGGACAGT GTGGAAACTG GGCTGAGGGA GTTAACCCCT CTCACCAGGC 960
CCCTTCCCAG CCCAGCGTCC GCAGAAGTGG AAGGGAAATG GCAGTGAGGC CTCATGTGGC 1020
AGGTGGTTTT CCAAAGCTAA CTACAAAGCT GTTGCCACGC CTATGGTCTT CTGTGAACTT 1080
GCCACCCTGT GATGGTGGAG CCTCTGCGTG GTGGAATCCT GGAATCCGAC TGCATGGAGC 1140
ATCGGAATAT GGTGAAAAAT CACTCCGTTC 1170
|
