| Tag | Content |
|---|
EnhancerAtlas ID | HS091-05996 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr10:95048400-95049580 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr10:95048979-95048998 | TGCTGCCATCTTGTGGACA | - | 6.83 | | YY1 | MA0095.2 | chr10:95048980-95048992 | GCTGCCATCTTG | - | 6.32 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_32827 | chr10:95048520-95049016 | H1 | | SE_68917 | chr10:95048319-95049647 | H9 |
|
| | 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 |
| GH10I093287 | chr10 | 95047101 | 95049568 |
|
Enhancer Sequence | ATCTGCCTGC CTCGGCCTCC CAAAGTGTTG GGATTACAGG CGTGAGACAC CGCGCCTGGC 60
CAATTCTACC AATTTCTATT CCTTCAAGTT CCCTGCCACT CCTGTCCGTA TGTACAGCAG 120
AGCCAATATG GACATCCCGT CACAAGGTCT GTTTTCCTTT GCTTAACCTT CAATCCTGTA 180
TTATGACAGT CTGCAGGCTT GTAATTTTTC GTTGCATGAG AGACTCCTTC CTGTGATCTA 240
CCACTGTTTG ATTTGCGACT CGCTATGGGT CATGAGAGCA GGCCCTTCTG TTTTATTCCT 300
TTGCAGGATA ACTGGGATGC GGTAGGCTTT TAGTACATAA TTGTTGAAGG AATGAAGGGG 360
CGAATGAATG CGTGAGTTCC AGCGTTTCCC AAGGCCAGAG CGTTTTTGTC TGTCTAGTCA 420
TAGATTTCCA TAGCATTCCA GAAGGAAGGG CATCGTTTAG ATGCGGTGCT GGTCGCCTTC 480
CACTTAAAAT ATGTCCCAGA GATGCCTGTC TGGGGTGGGG TTCCATGGAA TGCAGACTGA 540
ATGGAATGCC TTTTAGGCCC GGTGAGAACC TGAGGCCACT GCTGCCATCT TGTGGACAGT 600
ATTTGAAACA CAGGAGACGT GATGGCCGTT TCTCCCAAAG AAACCTTGGC TGATTCTATT 660
ACATGATGAA ATATTCTCCT TAGCAGTGCA TTAGGCCATG TTACCAGACC CATCCTTAAC 720
CTATTTGTAT TCCTCTGTTG AAATAATAAT AATATAATAA CAACAACAAC AATAACTCCC 780
ATTTGCTGAG TTTTAGGCAC TGTGCTAGTA AGAGAACCAG GATTTGACCT CATCCCATCC 840
ACTCTGGACC CAACTTTTGG CCATTTCCCC ACACTCTTTC GTTTTTTGAG TTCTTTCTCT 900
TCTTTCCCTT CCAACTCTCT ACTGTGATTA TGTATCAGTC CCTGTAGTCA CATCTTGTCT 960
CAATGATTTG CTTATGTGTT TGCCTTTCCA ACAAGACAGT GACCACCTTG ATGACTGGTC 1020
AGAGCTGTTG AGTACAGGGA TTTCATTGAC CTCTGTGCAC CAACTATGCA CCAGGCCCTG 1080
TGCTAGATTA GGAGTGTGTG AACACACGTC AAACTGGACT GTAGGCCTTC CCAGTGTACG 1140
TGTGCAGGGT GTGTATAAAG CCATGGGAGA GACGTGGAGT 1180
|
