| Tag | Content |
|---|
EnhancerAtlas ID | HS138-35218 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr6:30058970-30060400 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr6:30059675-30059693 | TCTCCCTCCCTCCCTTCC | - | 6.25 | | EWSR1-FLI1 | MA0149.1 | chr6:30059683-30059701 | CCTCCCTTCCTTCCTCTC | - | 6.88 | | EWSR1-FLI1 | MA0149.1 | chr6:30059679-30059697 | CCTCCCTCCCTTCCTTCC | - | 8.13 | | ZNF263 | MA0528.1 | chr6:30059684-30059705 | CTCCCTTCCTTCCTCTCCTCT | - | 6.3 | | ZNF263 | MA0528.1 | chr6:30059678-30059699 | CCCTCCCTCCCTTCCTTCCTC | - | 6.74 | | ZNF263 | MA0528.1 | chr6:30059679-30059700 | CCTCCCTCCCTTCCTTCCTCT | - | 6.81 | | ZNF263 | MA0528.1 | chr6:30059675-30059696 | TCTCCCTCCCTCCCTTCCTTC | - | 7.48 |
|
| | 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 |
| GH06I030090 | chr6 | 30058573 | 30060526 |
|
Enhancer Sequence | TGGTGGGAAG GGGCTGACTT CTGGACGTGA GTTACTGCAT TGGTTGTGGA GTGTGAGAGC 60
AAAGGAGGAG GCAGGAAGCT CTAACGAATT TGGCCCCACC ATGGGGAGGA TGGAGCTGCC 120
AGTGACTGCA GTGGGAAGAA CTGTGAGGAG CTGGCCTGGG CAGGAATATC AGGGGTGGCA 180
TGTTGGACAT GTGAAGCCAG GAGGCCTGTG GGCCATCCAA CAGTGCTGTG AACTGTGCAG 240
CCCGATGTAA GCATATCTGA CATTAGGAGT GGTGGAGAAA CAAAAAGAAC AAGGATAGTT 300
CATTTTAACA CAGTAATAAT TTTATAATTT TATAATTTTC AAATCATTAA AGATTTTACT 360
ACTTTCTTAA CTACTCCAGG AGCCTGTGTC ACATTCCAGT CACAGGGAGG AAACTGGGGG 420
CCATGCAGGA TAAAGGTCAA AGCCTGCATG CTGGGACTCA AGTGCTTCCT CCCCAACAGT 480
ATTAGAACAC CAACTCCCAG GAGCACAGAG ACTTGAAGAG AGTGTCCGGG TCGTGGACTA 540
TGAGTCAGAG AAACCAAGCC AGGGGCATGC AAGGCAGCAC GAGGCAGAGC AGGGAAACCC 600
AGCAAGGGAG GTGGCAACGC ACAGTGACCT AGAAAAGCCT GATGAGCTGA GAGCCAGCCG 660
ACAACAGGCC CCATGTGCCT CTGTGTCTTG GTCCACATGA TAGACTCTCC CTCCCTCCCT 720
TCCTTCCTCT CCTCTGGTGA CCAGTAGCTA AAACATCACT GGCACGCTGC TGGCATCCAG 780
CCTGCCAATT AGTTCAGGAG CCACTCCCTC TGACTGCCTC CTGAGCCTCA GATGTTACCT 840
CCCCTGTCTC CCAAACACAC CCCTCCAGCT CTGTCCTGCC TGCCCTGAAT CTCTGGAAGG 900
AAAACTTGCC CTGGGACCTG CCTTGGACTC TCTGGTTCCC CTCATCCAGC CCCTCCCTGC 960
GCAGAACATG GCATCTCGTG CCCTTTTATC TGCCATTTCT GGCCACCTTT GCAAGCGTCC 1020
TTGAAACCAG CGCTTGGTAG AGTTATCCAC GCCCATGTGA GGCTCCCCTG CCCCCTGGGT 1080
GGTGTATGTG GCAGGAGGAG CAGGGAGGAG CTTCAAGGAA GCAGAGGGAA AGGAACCTAT 1140
AAGAGTTCTT GGGATGGCTT CCAGGAAGCT GTGAGGACAG AGCTATGCTG AAAGGAGAAA 1200
GGCAAAGGCT ACAGAAAAGT GAACACTGAA GAGGAATTAG GCAAGAACAA AGCCTACCAA 1260
GTTAGAAGAA GGGAATGAGA GGGCGAAACA ACAGCACCAG AAAGGAATGA GGTTGCCGGG 1320
CACGGTGGCT CATACCTGTA ATCCCAGCAC TTTGGGAGGC CGAGGCAGGC GAACCACCTG 1380
AGGTCGGGAG TTCGAGACCA GCCTGACCAA CATGGAGAAA CCCTGTCTCT 1430
|
