| Tag | Content |
|---|
EnhancerAtlas ID | HS138-02490 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr1:159988300-159989840 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr1:159988914-159988925 | AGTGACTCATC | + | 6.02 | | JUND | MA0491.1 | chr1:159988914-159988925 | AGTGACTCATC | + | 6.32 | | STAT3 | MA0144.2 | chr1:159989244-159989255 | TTTCTGGGAAG | + | 6.02 | | ZNF263 | MA0528.1 | chr1:159988374-159988395 | CTCTCTCTCTCTCTCTCCCCC | - | 6.3 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 159988839 | 159988969 | | chr1 | 159989083 | 159989221 |
| Enhancer Sequence | AGAACAACTT AATATTCATC TTCCCCACCT CATATTCATG CGTGCACATG CATGCGTGTG 60
CACACACACA TATTCTCTCT CTCTCTCTCT CCCCCTTTCT CTCCCCACAC TGCATTCTTT 120
CCAAGTCCTC TCATCACCCT TTGTACTTTT CTCCAGCATC CACCAGGCTG GATTTGTTCT 180
GCCTTGATGT TTTCTCACAG TTCATCCTTC CACTGCATGC TGGGCTCCCA ATATTTGTTA 240
TAAAATTAGG AACCTTATTT ATGTATGTAA AGAGGCCTTC TGCATGCACA ATCAATAAAT 300
GTGAGCTCAA AATGAACCCT TTCTCTCCTA CGAGGCACTC ACTTCCCTTG CCTTTCCTGG 360
GTTATCTTCT ATTTCATTGT CCCTGGTAGC TATGTTCTAA TCACCAAGGC AGGGGTTTTA 420
CTTTTTGGAG GTCAGAGAAC CCTTTGAATG CTACAGACAC ATTTTACAGA AAAAATGCAC 480
ACAAATACAC ACACATTTTG CACACAACCA AGGTTTATGG GCTTCTGATT AAAACCACTT 540
TACCAAGGAA AAGACTTCTG TGACCATCCG CCACCCCCAT ACACACACAC CACTAATTCC 600
TACCCTTCAC TAGCAGTGAC TCATCCATGC CTTTGCTGCC AGACACCAGT AAAATAAACC 660
TGGTTCCTCT CTCCTAATAT TTGTTATGTT GAGAGATAGA AAAACAAAAA CACAAAGCAT 720
CCCCAACAAT TATAGGCAGT TACACTTAAG ACCCATTAAA AGTGTCCCCC ATTAGAACAC 780
TTCCCCAAGG CAAACACTTT ATAATTTCCT AGATTACTAG TTTAATGCAC AAGTTACGTT 840
TTAAATGCTT TTCTTTACAG GGAGGCATTC TTGGACCCTG GCTGAGATTA GGAAACAGCC 900
AAGGCTTAGC AGCACACTTA CCAAGAATTT CTTAGGTGGG TTATTTTCTG GGAAGATTAT 960
CACAGTGAAT AATCTCATCT ATTTTACTGT CAATTTCAGA GGGTGACATT TTTGGCCCTG 1020
TTCTCAGTTC TAGAGATATT GTCAAGTTGA AACTTGCAGC TTCTTATATG CTAACTCTAT 1080
CTTCTAATTA GAAAAGAGGT TAGAAAATGC TGGAGCTTTC TGGGTTGCCT TCCCCAAGCT 1140
AAATTAGAGT CTACTGAAGA AAAGGAAAGG TGGAGAAGAG ACAGAAGGAC CGGGTGGATG 1200
CAGTAGAGTA AGAACCATAC GATCAAAGGC AGGTCAGGGA CTAGACAGAA TAGTCTTTCT 1260
ATCCTACCAA TGCCAGTGGC TCATGAATGG CCCCAAGCCC CTAGGACTTC TCTTAAGCCC 1320
AATCTGACTC CCCATGGGGT CATGGATGCA TTTATTTTGT CTGATGAATT GCTTTTCATT 1380
AGAGTCAACA TGGAATAGAG CAGGATTTCT CAATGTAATA GAATGAAAGT CTGTGTCCTC 1440
CAAAATTTCA AATGTTGAAA ACTAGGATCC CTTTCTTGCC TCCACTTCCT TGTTAGCAGG 1500
GACCCTAAGC TCTACTCCCA TTGCCCTCAG CCACCCACCC 1540
|
| |
|
|
|
