| Tag | Content |
|---|
EnhancerAtlas ID | HS098-41645 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr4:6841050-6842420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr4:6842035-6842047 | GGCCACGTGCCT | + | 6.07 | | NFYA | MA0060.3 | chr4:6842028-6842039 | TCTGATTGGCC | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_09487 | chr4:6841580-6844050 | CD14 |
|
| | 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 |
| GH04I006839 | chr4 | 6841395 | 6842425 |
|
Enhancer Sequence | TTTCAGAGTG AGAGTTGGTG CTAATGATGG GTACACAAAT TCCTATACTT CCCAAGACAC 60
CATTAACACT TTTTGTGTGT GTAAAATGTT CTCATGGAAT AGAGAAGTTT TAAATATAAA 120
TATCCCATGT TTTAAAACTG ACATTTCTGC TTTTATGTGC AAATGTGAAT GCATCAATAC 180
AGAGAAAACT AGGGATGGTC CCTGAGTGAC AACTGCCAGT TTAGGAATCA CCTTGAAGGA 240
AGAATAAAGG AATAGTGTGT ATAAAGGAAT AGTGTGTACA AAGACACAGA AATAGGAGGG 300
GCCTGATGCT GTAAGGTCAG AAAAGAGTAT GCTGAGGAGG GGGTAGTCGA AGGTCAGAGT 360
GGGGCAGGCC CGCAGGAAAC AGACCCTGAA GAGACTGATG TGCTGTGTGA GGGCATTTCT 420
AGTTATGTCC TAGAGACAAA AGACCTGTAG ATCGAGTTTA GCCAGCAGGA CTTAATGGCA 480
TGGCAGTGGG CAGACAGGTA GGTCAGTGAG GAGGTCATCA CTGTGGGCTG AAGACCTAGT 540
AGGAAAAACA GGAATATAGT TAACCTGAAA TTATGCTTGT TTGATTGGAG CGGCTCATTT 600
TTTAGGGGCA AATAGGGGTT ATTTTGAGCA ATATATCAGT GGATTTATTA CTGAATGCTC 660
TCCTCAGAAT CTGACTGTAT CTCATTCACA AGCAACCCAA AGTTTGGCCT AAATTGGCTT 720
ACGGGGGAAA AAAGACTCAA ATAACTAAAA GTCCAGAAGT TGGGCTGGCC CCTGTTAGGT 780
TTGATTCAGA GCTTCCCAGT GTCATTCAGG CTTCTGCTCT GCCTCTCTGC CTACCTCTTT 840
TTGTCAGCTT GGTTTTGCAG CCAGCTCCTT GTAGGGTAAA GGGTGGTGAC AATGAGCATG 900
CTTCTGGGAT CATATTCTCA CACACTGTCC AGAGGTCATG TTCCCCGCAT TCCCAGCAAG 960
GACCATGAAA TGTGCATTTC TGATTGGCCA CGTGCCTCTC TCTGAGCCAA TCTTTGTGGC 1020
CAAAGGGATG ATGGGGGTAG TGTTAATCCC ATGCAGACAC ATTGTGGTTT TGGTCATTTA 1080
GGCACTGTGA GGCAGGGGCG TATGCTCAGC AGCTAGCCTC CAGTGACTGC TGGTGTATTT 1140
CCAAGTGGCG TGTGCTTTTT CTCCCCCAGT TCCCAATCTC CCTTTTGATA AAGACAGCAT 1200
GGAAAAGTCA ATCAGAACTC TAGCCTTACG TGACCTCCCT GTAGTGTCTA GAAAAGTACC 1260
TGATAATAGA CTCTCATGCT GGGGAGTTCC TTAGTTGTAT CTGCTTTTGG TACTTGATAA 1320
TTATGTTGTT TCTTTAAGAT TAGGACTGAG TAACTATTTG ACAAATGTCT 1370
|
