| Tag | Content |
|---|
EnhancerAtlas ID | HS098-42597 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr4:89537260-89538270 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F3 | MA0469.3 | chr4:89538173-89538189 | TTTTGGGCGCCAGAAT | - | 6.04 | | E2F3 | MA0469.3 | chr4:89538173-89538189 | TTTTGGGCGCCAGAAT | + | 6 | | Foxd3 | MA0041.1 | chr4:89537824-89537836 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr4:89537828-89537840 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr4:89537832-89537844 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr4:89537836-89537848 | GTTTGTTTGTTT | + | 6.32 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_36035 | chr4:89536997-89538389 | HMEC | | SE_41502 | chr4:89537307-89538571 | Left_Ventricle | | SE_64313 | chr4:89531463-89538891 | NHEK |
|
| | 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 |
| GH04I088615 | chr4 | 89537021 | 89539257 |
|
Enhancer Sequence | TGTTAAGGGA GAGTTTATAT TATGTTCATT TTTATTTTAG GTTTTAAAGG ATAAGTCTAT 60
TTTCTTTATT GTTAATTTTT GCAGTTCTTT ACTTTATTGT TCTCATGAAA AGTACCTTAC 120
ATATGTTGGG TACACTGTAA AACTGATTAT CCACATATGG ACATGCATAC ATACATCTTC 180
TCTCTATGCA ATTGTTACCA TTACTTCCAG CATTCTCATC CAAAATGGCA AAGATAAGGG 240
AATCAAATTA GGTCGCTGTG GGCACTGTGG TACACCAGGG ACTACTTTAT GGTGCTCCTG 300
AAAGTCTTGT AGTGGTTTGG CACCAGTTAG CTGGGTAGTA TGATCTTGTC ATAGGCTTAG 360
TAAATAGAGT GCAATCCACT GGCTCCTAGC CCAGCTGAAA TCTTTGGGCA GTTACTGTAG 420
ACTTCCAGTT AGCTGTGATG GGGGTGAATC TTTGGATGGA GAGATAAATG ACCTGAAAGA 480
ATGCAAGTGA TTTTCCTTTC TGCATCCTTC AGTTGCCTAA GAAGAGCTCA CTCTGGAGTC 540
TAAACCTACA TGATCTCTGT TTTTGTTTGT TTGTTTGTTT GTTTGTTTTA GTGGTAATGT 600
ATTAGTCGCT ATGCTTGCAG TTTCAAGTAA CAACAGAATG CTAAGCTGTG TCATGAACAA 660
TGAGTAAAAT TTATCATCTC ACATGAGAAG AGGTATTTCT AGGATAGGCT AAGTCAGTAG 720
CACAGTTGCC TCATGTGTTT CCCATCTTTC TGTTCTGGAG TGGAATTTTG TAGTGATGCA 780
GAGATTTATT CTTCCTGCCA AATCTCTAGC CTACTAGTGT GGGTGTAAGA TTTTTCTGGG 840
CCTCATTTAA AGCCTGCATA TATTCCCCAA GTGCTTTACC AGCCAGGGTC AGCCTTGCCA 900
CTATGCCATG TTTTTTTGGG CGCCAGAATT GGCTTGTTAT GTTGAAAGTA TTATTTTCTC 960
TCATGATATT TTTCTCCTTT AGTACGCTTC ACTATTGAAA TGCCTGTAGG 1010
|
