| Tag | Content |
|---|
EnhancerAtlas ID | HS138-03288 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:206653900-206655040 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PLAG1 | MA0163.1 | chr1:206654093-206654107 | GGGGCCCATGGGGG | + | 6.71 | | ZNF263 | MA0528.1 | chr1:206654792-206654813 | GGAGCAGGGAGGAGGAAGAGG | + | 6.39 | | ZNF263 | MA0528.1 | chr1:206654786-206654807 | GGTGGAGGAGCAGGGAGGAGG | + | 6.59 | | ZNF263 | MA0528.1 | chr1:206654789-206654810 | GGAGGAGCAGGGAGGAGGAAG | + | 6.91 | | ZNF263 | MA0528.1 | chr1:206654783-206654804 | GGAGGTGGAGGAGCAGGGAGG | + | 7.17 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 206654677 | 206654826 | | chr1 | 206654444 | 206654508 | | chr1 | 206654628 | 206654823 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I206480 | chr1 | 206654141 | 206655107 |
|
Enhancer Sequence | GGGACCTCTC AGCCCTGCCT TGTCTGCTCC TCACCCTAGA TACTTCCAAC AATGCACCTC 60
TTCTCCCCAA GCCAGGGCTA CTGCCTTCCC TGCCCTCCTA GAATAGAGGG CACCCGCACC 120
CTATCCCTTA TCCCCACCTC ACCAAATAAC TGCAATGGCT CCCCCAAAAC CCAGTCCCTC 180
ACCTGCAGGG GAAGGGGCCC ATGGGGGCAC AGACTCTCCA GGTACCAAGG TGGCCTCCCT 240
ATCCCAAGAA GGGGCTTGTG TCCTGCCAAG TCCTTCTCTG AATGATTTAG AGTGCTCACC 300
CTATGCCAAG TGCCAGCAGA ACTCTAGGGG GAGGACACAC ACCCACGCAC AGTTCCTGGA 360
TGTGACCAGG GATGGAGATC CAGGTGGTCT CGTTCTCCAT GCCTCATCTC CTGCTTTCTC 420
TGAGTCTTCA ACTTATCCTT GCCTTCCTTG GGTTCCCTGC CCCAATCTTT GGAACCCCAC 480
TCCCTCCACT CCCTTGTCTT GGGCTAATAA GGGGGGATGG GTTGGAAAAA GAGAGAGACC 540
GGGCAGGAGG AAGCCAAGTG GAAGGGTCTG GAGATGGGGA ATGTGGGAAG ACTTCATTGG 600
CCAGAGCACG ATTGAGAAGT AGGCACAGCA CCCCAAATCC TGGAAGGCAC GAGGCCATGG 660
TACGGGTGAG GGTGGGAGCT CTGCAGCCTA GGGATGCCAC TGGTGACAGG AGTCTTTGGG 720
AACAGAAGAT CAGAGACTGC CCATATGCCT GAAGGCCCCC TCCTCCCGCC ACCCCCAGCC 780
CTTGTCCTCA GGGAGCTCCA GGGAGTTTCC CAGCTGTGGG CTGACTCATG CAGCCCCGCG 840
TGCCTCCTGC TTCGCAGCAG CAACTCAGTT GATGGGGCAG CTGGGAGGTG GAGGAGCAGG 900
GAGGAGGAAG AGGAGCATCT CCAGATAACA GGGATGGAGT CTCCATCCAG ACTGAGCCCC 960
TCTCAAATGG TGACAGAGAG TAGGGTTCAG TCAGCAGAAC TGCAAGTGAA TCTCCTTTGA 1020
GCAGAGCTCT GTCCAGGGCA CAGAGGGGGC TCCAGGGGTA GATGTGGCAT CCTGTCATTC 1080
AGAGAGGCCC ATGCTTCCTC CGGAGCAGCT AGCCCTTCCT GGACATGTGA GGGCTGATGG 1140
|
