| Tag | Content |
|---|
EnhancerAtlas ID | HS154-06147 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr14:20895300-20896460 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr14:20896137-20896147 | ACCACTTGAG | + | 6.02 | | SPIC | MA0687.1 | chr14:20895990-20896004 | AGAAAGAGGAAGCA | + | 6.04 | | ZNF263 | MA0528.1 | chr14:20895933-20895954 | GGAGAAAGAAGAGAAAGAAAA | + | 6.03 | | ZNF263 | MA0528.1 | chr14:20895930-20895951 | GAGGGAGAAAGAAGAGAAAGA | + | 6.42 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28028 | chr14:20895260-20896705 | Fetal_Intestine | | SE_29051 | chr14:20895241-20896718 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 20895383 | 20896384 | | chr14 | 20895931 | 20896136 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I020426 | chr14 | 20894921 | 20897612 |
|
Enhancer Sequence | CCTGCACATT GGGCACATGT ACCCTAAAAC TTAAAGTATA ATAATAATAA AATAAAATAA 60
ATTAAAAAAA AAAAAAGAAA AAGAAAATTG ACCTAAACAC ACACAAAAAA ACTGACCCTT 120
TTTTGCTCTC AGCTGTCCAG TAGGCAGAAA TGGAAAGAGC AGACAGGAAG GATAGAGGTG 180
AGTCATAGAG GGCGGGAATA CACAATCATT AAGTGAAAGC CATTATCCTC AGGAAGGCTC 240
CAGAGAAGAG AGTAGGTGGC AAGAGCAGCA GAATTATCTG AAAAGCCTCT GGAATACCCA 300
CTTCCTCTTT GCTATGGAGA AACAGGGCAT GGCATGCCCC ACTTCTTTCT GTTTCAAATG 360
CATTCCCCCT TCTCTAATGG GTGAGACTCT AGGCAGCCTT TAAGATCCAG TTCAAAATAC 420
ACCCATCGGA TGACACCTTT CCTAACAGAA GCCTTCCTGA GCAGAGTTCA CTGCTCTATC 480
CTCTGGGCTC TCGCAAGACT CGTCCATACA TGTAAGTCCA CTCAAAATTT GTATTTGTTT 540
ATGTCTATCT GCTGGTCAGG AGCTCTCTGA CCTCTGTATC TTGGTGCCTC CTACAGTGCC 600
TGCCACACAG TAGGTAATTA ATAACTGTGT GAGGGAGAAA GAAGAGAAAG AAAAAAGAGA 660
GGCAGTGGGG AGAGCAGGAT GGGGGAAGAG AGAAAGAGGA AGCACCTGAC TACCTTCCCT 720
GGCCAAGATA AAGGGAAATG GATTTAAAAA TAACTCTGGG GGAAAGGAAC TGAAAGGGGG 780
AAATGACTTT TCTGAGTCTT GTCTGCTTCT CACTCTTCTC TCCCCCCACA TCCTCTCACC 840
ACTTGAGACC TCAGGCAACA ACGGTCTCAT TTTCACTCCT GATTCCTCAG TTTGCCCAAA 900
AGAAAGAAGG CACACAGGCT TCTGACTTCT TCCACCCCAT CTCCTTAAAC CTCAGATCAT 960
CTGTTTTTCC ACTGTGGGCC TCTCCCTCCT TGGCCTCTGC CCCCATCATC TTTCCCACAC 1020
AACACTCCTG CCACATGGCC CTGGGGGGCC CGTCAGGCCT CTCAGGCCCC TGTGCCGTGC 1080
ATGTCCATGT GGGAGCTTCT GCCTCAGAAG GAAACCAAGA GGTTCTCAGG GGCAGCCTGT 1140
GGTGTCTCGC TGGGAAACGC 1160
|
