| Tag | Content |
|---|
EnhancerAtlas ID | HS183-03154 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr3:169579600-169581080 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr3:169580949-169580960 | CATGAGTCACC | - | 6.62 | | IRF1 | MA0050.2 | chr3:169580660-169580681 | TTTTTCTTTCTTTTTTTTTTT | + | 6.59 | | JUND | MA0491.1 | chr3:169580949-169580960 | CATGAGTCACC | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCTGTGTGAT AAGCATAAAA AAGAATTTGC TGTTAATGAT GGATGTATTA AAGATGCATA 60
ATGACCACAA TCAGACAAGT GAAAAGACTG CATAACTCTG AATTGCTCTT TTATAAAAAC 120
CTCAACTCAG AGGCAGAGCC ATTTACTAGG GACAAAGCTT AACTAACCAC TGTTCCTGCC 180
GCCAGGTGCC CAGACACTGC TTCAGGAGCC TGAGGAACGC AGTGGCTTTT CTATCATGAC 240
CTGACCTGGG CTTCTCAGCA TGAAGACAGA GCTGCATTCC TGGGTGAGAA GTAAACCTGT 300
CAGCCCGGCT TTTGAGATGC TTGCTTACTT GAAGGGCACG CATATCTTTG GTGGATGCAA 360
CTGCTAGGGA GGAAGCAGAG ATACTTGCCT CCTCAAACCA AACAGGTGAA GAAGGGAAAG 420
CGTTGAAATC ACCATCAAGG AGCTGCAAAT GGCCACACGG AGTAAGTGGA ATTCTTGCCG 480
GTCAGTTTCT AGACCATTCA ATTGGCAAAC ACAAATCCAG AGAAACTAGG CCTGGGAGAG 540
CTTTTGCTTT TTCTCAACTC CTGCCAGAAA GTGAATTTGG AAAGCCTCGT CTGTCCTCCT 600
TGTTATTAGG GACTACTGTG GCACCCTCAC TAGCTTCCTC TGTAATAACA CTGTAATAAC 660
ATGCTAGTGG CTGGGCACGG TGCCTCACAC CTGTAATCCT AGTACTTTGG AAGGCTGAGG 720
CGGGTGGATC ATGAGGTCAG GAGATCAACA CCATCCTGGC CAACATGGTG AAATGCTGTC 780
TCTACTAAAA TACAAAAAAT TAGCCGGGCG TGGTGGTGCA CACCTGTAGT CCCAGCTACT 840
CAGGAGGCTG AGGCAGGGGA ATATCTTGAA CCCAGGAGGC AGAGATTGCA GTAAGCTGAG 900
ATTGTGCCAC TTCACACCAG CCTGGCAACA GAGAGAAACT GCATCTAAAA AAAATAAATA 960
AATAAATAAA AAAGATAGCA CTATAATAAT AAAAGCTATC ATTTTATTGA GCACCTGTTA 1020
TGTACTCGTT CTTTGCCTAC TTGCAGGTGC CAGCATTTCT TTTTTCTTTC TTTTTTTTTT 1080
TGTTGGGGGG GATGGAGTCT CACTCTGTCA CCCAGGTTAG AGTGCAGTGG CACAGTCTCA 1140
GCTCACTGCA ACCTCCACCT CCCAGGTTCA AGCAATTCTC CTGCCTCAGC CTCCCGAGTA 1200
GCTGGGACTA CAAGCGCCTG CCACCACGCC CGGCTAATTT TTGTATTTTT AGTAGAGATG 1260
AGGGGTTCGC CATGTTGGCC AGGCTGGTCT CGAACTCCTG ACCTCAGGTG ATCCACCTAC 1320
CCGGCCTCCC AAAGTGCTGG GATTACAGGC ATGAGTCACC ATGGCAGGCC AGGTGCCAGC 1380
ATTTAAGACA TACATAAAAC ACATCATACT TTTCTAAGGA AAAATGAATA TACATGTACT 1440
GACAGTGATT TTAAAGTGAT TTTGTAAGTG AAATATACAA 1480
|
