| Tag | Content |
|---|
EnhancerAtlas ID | HS116-31642 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr7:75535050-75536000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX2 | MA0600.2 | chr7:75535378-75535394 | GGTTGCTTTGGCAACA | + | 6.08 | | RFX5 | MA0510.2 | chr7:75535378-75535394 | GGTTGCTTTGGCAACA | - | 6.63 | | RFX5 | MA0510.2 | chr7:75535378-75535394 | GGTTGCTTTGGCAACA | + | 6.8 | | ZNF263 | MA0528.1 | chr7:75535494-75535515 | TGGGGAGGAAGAGGGGGAGAA | + | 7.54 | | ZNF263 | MA0528.1 | chr7:75535497-75535518 | GGAGGAAGAGGGGGAGAAAGG | + | 8.27 |
|
| | 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 |
| GH07I075905 | chr7 | 75534525 | 75537500 |
|
Enhancer Sequence | CCTCAAGTGA TCCACCTGCC TTGGCTTCCC AAAGTGCTGG GATTACGGGC TTGAGCCACC 60
ATGCCTGGCC TAATTTGACA TTTCTAACAA GTTCCCAGGT GAGGCTGCTG CTCCTGGTTT 120
GAGAATCACT GAACTAAACC AGTACTGGCT GGGATGTGAG TCAGCCTGGA GACTCCCAGC 180
CCCTGGAGGC CAGGGATCAG CTCTCATCAA CTTCCATTTC TGCTAAGTGA CTGCTCAGAG 240
GCACAGGCAG GTGTCCTCCA CAGCACTGTC TGAACAGTTC GTGGAAGCCA GGCAGGCTTC 300
TCTTCATCGG CCCTTGCACA ATGGTGCTGG TTGCTTTGGC AACAGCCAGC AGCAGCCAAG 360
CAATTTTGAG CACAGAATCC TGGGGCTTGT GTCATACTGG GGAGACAGGG CAAAGGTTCT 420
GGCCCATTGG CATGTGAACG CGAATGGGGA GGAAGAGGGG GAGAAAGGGC GTGGCTTCCG 480
AGGCCCCCTC TCACCCGAAC ACCCTCTCAT TTCCCCAGAA GCTTGCTCTG GCTCCCGCAT 540
GCAAACCCAG AAGAGCTGAA ACTTTGATTG CGTAACAGAG GGGAACAAAG GATGGAGTGA 600
AACTGGGGCG GGTATGCGGG CAGTAGGAAG GAGAAAGAAG CCATCCTGGG CTCTGAGAAC 660
CGCTGGGTGC ACCAGGCCAT GTCACACACA CAGCAACTCA TTTAATCCTC ACGCAACTGC 720
CTGGGTCCGT GTGCCCAGGA CCCATCCATG GCCACACAGC TAGCCGGAAA CCTGATCTGC 780
TGTAGCTAAA GGCCATGTTT GCTTTCTCAG TTCAGGGCCG CCTCTTTGAA ATGCCTCTTT 840
GGCCGTGTTA GGAAGACCCA GGGGTTTGGG GCAGCAAGGA GGCAGGAAGA AGGTCTGGGG 900
GAGTTATTTG GACAATGAAG AGAGCCAGGC GGGTCAACCA TCCTCTTGGC 950
|
