| Tag | Content |
|---|
EnhancerAtlas ID | HS154-18760 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr6:27719840-27721180 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr6:27720876-27720893 | TGGATTCCAAGAAAGCC | - | 6.18 | | Mafb | MA0117.2 | chr6:27720348-27720360 | AAAATGCTGACT | + | 7.22 | | ZNF263 | MA0528.1 | chr6:27720985-27721006 | AAAGGAGGATGAGGGTGAGGG | + | 6.85 |
|
| | 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 |
| GH06I027751 | chr6 | 27719661 | 27722579 |
|
Enhancer Sequence | CAGGGATTCC AGACCAGGCT GGCCCATATA AGAAGCAGCT AACACCCCTA GGGCTGAGGG 60
CTGAGATGGA GCACGCAAGT ATTCTCTTCC CCACCAGGGC TGAGATCCAG ACCTGCATCC 120
AGGTTGGGAG GGTAGAAAAA AAGTGCTCCA GCGGAAGGTG CAGGTCATGT GCCATCTAGA 180
GTACCAAAGA AAAATGTTCA TGGGGAAGTC TGTTACCAGA GATGCTCTAA AGGAGGTTCC 240
CCCAAAGTAC TGCTGGCCAC CATGCACTGC AGGAGGTTCC TACTAGGTAA ACTGCTCAGG 300
CTGTGGGAGC CAGGCCACTG TGCACAGTAA CGCCAAGAGA TTATTTCCTC CAGCAATGTC 360
TCTCCATCGC CCTCTATTGA CAAAATTTAA TATTGAGCTA AACTGCGACA GAAAATATTT 420
AAAGGGCCCA GCTCCGTTCC ATTGTTATGG AGCAAGGAAA AGTGATTTTG CTGCTGAGAG 480
GTAATAAATA GATAACCGGA CAGAAGAGAA AATGCTGACT TTCTTTGGAC TGGTTCGAAT 540
TCAAACACAC TTTTATATCC TTGTCCAAGT GCACAATCCA TGGTGAAAGT TTAAGAGCTG 600
TCAAAAAGTT TGTTTTGGCC GGGCGCGGAG GCTCACGCCT GTAATCCCAG CACTGTGGGA 660
GGCCGAAGCG GGTGGGTTAC CTGAGGTCAG GAGTTCGAGA CAAGCCTGGC CAACATGGCG 720
AAACCCCATC TCTACTAAAA ATACAAAAAT TAGCGGAGCG TGGTGGTAAT CCCACCTACT 780
CGGGAGGCTG AGGGAGGAGA ATCGCTTGAA CCCGGGAGGC GGGGGTTGCA GTGAGCCGAG 840
ATCGTGCCAC TGCACTCCAG CCTGGCAACA ACAGCGAAAC TCTGTCTCAA AAAAAAAAAA 900
AAAAAAAAGT GTTTCCTCTC TGTGCTTCAG CAAAAAAAGA GCAAATCCAA TTCCCCGAAG 960
GGCTCAAAGC GAAGCGCTCT TCCTTAGAAA TCCCCGAGGA AACCCCCTCC ACGAAAAACC 1020
CGCAAGTGCT GCTCTCTGGA TTCCAAGAAA GCCTGTCTCA CCTGCGAGGT GCAGGCGGGT 1080
GGAGTTCTGG GACTCCGGTG CCTATTGGGA TTGACACCAC CGGGGTCACT CAGACGGAGA 1140
TCAGAAAAGG AGGATGAGGG TGAGGGTTCG GCGTGGGGTA GAGAAAGGTG TGACGCGGGA 1200
TTCAGCGCCA CGTCGCTGGG TGACGGAAGG AGTACAGAAG TTGAGGGTTC ACGTGCTCGG 1260
CAAAAAGCAA AGATTCTATT GGTTCAAATG AAAATACTCA AAAACAGAAT TAGCGATAGA 1320
AAAAAAAGCG ACTCTCTTTG 1340
|
