| Tag | Content |
|---|
EnhancerAtlas ID | HS073-11996 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr6:395940-397100 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr6:396176-396187 | CTTCTGGGAAA | + | 6.62 | | Stat4 | MA0518.1 | chr6:396176-396190 | CTTCTGGGAAACAG | + | 6.01 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_59283 | chr6:376365-448765 | Ly3 | | SE_61254 | chr6:346354-405900 | HBL1 | | SE_61604 | chr6:353480-406085 | Toledo | | SE_67293 | chr6:388844-396716 | MM1S | | SE_67293 | chr6:396927-400791 | MM1S |
|
| | 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 |
| GH06I000396 | chr6 | 396261 | 396410 |
|
Enhancer Sequence | GTGGAGGGCA CTGGGCTCCC TGAGGGCGAG GCTGTGTGGG CCAGCTGCCC ACATGGCCAG 60
AGAACCACAG CAGCCCAGAC AGCAGAACTT GCCATTTGCT ATGGCTGCTC CAACAGCCCA 120
GAAAAACCCC AGGTCACTGA ACGAATGTCT CACTTTCCAC ACGGTGCTGC CATTGGTGTG 180
GATTTTAAGT TGGGGAGGGT CGGGCGTGTC CGCCTGTTGG AATATGCTTC TCAGGTCTTC 240
TGGGAAACAG ATGTTTTGTG GAAGTGGAAG ATTTTGGAAG TAGTGCCTTA TCATGTGAAA 300
CCACAGGGCA GCTGATCTCT TCAGGCTTTC TTGATGTGAA TGACAGCTTT GTTTCATCCA 360
CTTTGGTGGG TAAAAGAAGG CAAATTCCCC TGTGGTACTT TTGGTGCCAG GTTTAGCCAT 420
ATGACGAAGC TTTACATAAA ACAGTACAAG TATCTCCATT GTCCTTTATG ATCCTCCATG 480
AGTGTTTTCA CTTAGTCTGA TGAAGGGTTC ACTCCAGTCT TTTCGGATGA TAAAATGCTT 540
CGGCTGTCAG TCTAATAAGG GATTCCCTGA GGAGTTTGGA GGCTGTAAGA GCACCCCCCG 600
TCTCAATGCC AGTGCTTCTT ATCTCAGCCT CTCCTGCACT CCTTTACCCC CGTCTCGATG 660
CCAGTGCTTC CTATCTCAGC CTCTCCTGCA CTCCTTTACC CCCGTCTCGA TGCCAGTGCT 720
TCCTATCTCA GCCTCTCCTG CACTCCTTTA CCCCCGTCTC GATGCCAGTG CTTCTTATCT 780
CAGCCTCTCC TGCACTCCTT TACCCCCGTC TCAATGCCAG TGCTTCCTAT CTCAGCCTCT 840
CCTGCACTCC TTTAACCCCG TCTCGATGCC AGTGCTTCTT ATCTCAGCCT CTCCTGCACT 900
CCTTTACCCC CGTCTCAATG CCAGTGCTTC CTATCTCAGC CTCTCCTGCA CTCCTTTACC 960
CCCGTCTCAA TGCCAGTGCT TCCTATCTCA GCCTCTCCTG CACTCCTTTA CCCCCGTCTC 1020
GATGCCAGTG CTTCTTATCT CAGCCTCTCC TGCACTCCTT TACCCCCGTC TCGATGCCAG 1080
TGCTTCCTAT CTCAGCCTCT CCTGCACTCC TTTACCCCCG TCTCAATGCC AGTGCTTCTT 1140
ATCTCAGCCT CTCCTGCACT 1160
|
