| Tag | Content |
|---|
EnhancerAtlas ID | HS089-04900 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr16:2211750-2213110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr16:2212781-2212793 | GGGCACGTGGCC | - | 7.22 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_24208 | chr16:2211380-2212020 | Colon_Crypt_2 | | SE_24208 | chr16:2212329-2214258 | Colon_Crypt_2 | | SE_26937 | chr16:2199546-2214313 | Esophagus | | SE_45297 | chr16:2205675-2212123 | NHLF | | SE_58273 | chr16:2212517-2214157 | VACO_9m |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTGGGACATC CTCACCCCAA GCACAATGGC AAAAGGCAAG CCCTGGCCAG CTCTCCCCGA 60
CCTTCCTGCC GGGAGCTGCT GGAGACGGGA TAGACATGTG CCAGGGCAGA GCAGCCTTGT 120
AGACACACCA CGACCACACC TCTGTCCCAG GGCTGACTCC TCTGAGCCTG GCTGCAGGTG 180
TGTGGCACTG CCCACACTCA GGAGCCCCTG CCTCTTCCAC AAGAGAAGTC CCCCGAGAGC 240
CTAGTCTGGG TCACACAGGG CCAAGCCCCT CGAGTCGCAG TGGGGCCTGG GGAAGGCCGA 300
GGGAGGCTTT GGCCAGGCCC CATCTCCCGA GACCATGGGA CGCAAAGATC AGGTGGGGCC 360
AGGTAGCTCG TGGCGCTGCC AACTGCAGGG GCTGAGATGT CGGGTTGAGC CCGAGTCCTG 420
AAGGCTGAGT GGCTCCAGGG TGGGTGGCCT TCCAGGTGGC ATTGGAAGGG ACAGGTGGGC 480
CTGGGCAGCC TAGAGAATGG GAGAGGAGAC AGCAGGAGTG GTAGACAGCC CAGGAGCTCA 540
GGTGCAGGGA ACCAAGGGCT TGAGAGCCAG CCCCTCCCTG CACACCTGTA GGCCGGGCTG 600
GGGGGCCCCA GGCCAGACTG TGGGCACGGT GGTGGGTGAT GAGTGGCATC TTGAAGGCGC 660
ATGCAGGGCG GGCATGGCCA AAGGGACCCA GTCAGGAGGG ACTGATGGAG GAGGTACTGG 720
AGCCAGCTGG GCTCAGTGAT GCCCCCTGAG CTGTGCTCCT GCTGGGTGGG GGCAGAGACC 780
AGCTCCGCCA CTTTGGCCTG GGACTGGGAC TGTCCTGCTC CTCTCAGGCC CCTGGGGCCT 840
TGGTTTGCAG CCCGGCTTCC CCAGGGTGAG AGCAGGGCCG CAGGAGTGGG CTCCCTGCTG 900
CTGCACCGCC CCCAGAGCAA GCTTGTTCTG AGGGCTCCTG CCTTGGGAGC TGAGCCCATG 960
GTGTGTCCTC ATGGGGTGCT GCGCATGGGC CTCGAGGTGG ACAGTGCAGG TGGGCCCGGG 1020
GCAGGAGTCC TGGGCACGTG GCCTTCCTCC CCACAGGGAG CTCAGCTTCA AGCCGGGGCT 1080
CGGCTGCGCT ATCCGCTGCC AGCAGGAGAC AGGGCTGTCC CAGCTGCATT CTGCCAGGCT 1140
CCTGGCTTCC AGGCTGCCCA AGTCCTGAAA GTGGGACCTG CTCGGGAGGA GGGGCGCCTG 1200
CTGACAGAGC CTGGTGCCTC ACGGGGGGAG AGTGGGCGTC ATCCAGCATG GACAGCCCCT 1260
TCCCCGGGCT CTGTCCTGGG TGTGACCTGT TGGCTGGGTC TCTTTTTCTC TCTAATGTTT 1320
ACCTTCCCCT ACTGGTGTCC CTGGGCCTGG CCAGCACTCC 1360
|
