| Tag | Content |
|---|
EnhancerAtlas ID | HS060-16721 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:4350490-4351920 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr19:4351537-4351554 | GAGGTCATTGTGCCCTT | - | 6.28 | | ESR2 | MA0258.2 | chr19:4351538-4351553 | AGGTCATTGTGCCCT | - | 6.07 | | GATA2 | MA0036.3 | chr19:4351556-4351567 | ACAGATAAGAA | - | 6.14 | | Gata1 | MA0035.3 | chr19:4351556-4351567 | ACAGATAAGAA | - | 6.62 | | NKX2-5 | MA0063.2 | chr19:4351331-4351341 | CTCAAGTGGT | - | 6.02 | | PPARG | MA0066.1 | chr19:4351379-4351399 | GTGGGCCACTGTGCCCGACT | + | 6.09 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAGCTGGTCC AGGTGAGGGA TGATGGAGTG GCCCAGGCCG ACCATGGAGC AGGGAAGAAG 60
TGGGCAGGTT CCAGGTATTT TTGGAAGTGT ATCCGCCAGA TTTGCTGATA GATCAGATGC 120
TGGAGTCCTG AGCAAGTGGG TGGATCGAGC TGCCAAAATT GGGGGATGTG GGAAGGGCAG 180
ATCTGGGGGT TCAGTGGGGC CCAGCATGGC TGTGTTGAGT GTGACCCTGT GAGTCCCCCA 240
CATGGAGACA TAGAGAGGCA GCTGGGCCCT GAGTCTGGAG CCGGGCGAGG CTTGGGCTGG 300
AGACAGGACT GTGGGCAGTG TCAGGTGTAG ACAGGATTTG GAGCCCTGAG AGGGGATGAG 360
GCCACCTGGG AGGGGTGTGG AGGGAGGAGG CCTGAAAACC CAGCCTGGGG CCAGCAACAG 420
CGAGAGGGGA GGTGAGAGGG AGCCAGGCGA GCGTGGGATC CGGGGGTTGT GTGAGGACCG 480
TGTCCTGGTA GGTAGGAGGC TGTGCTGGGT CAGATGCTGC CGAGAAGGTG ACGAGGACAG 540
AAAGTGAGAT GTGACCCAGA GAGGTCACCT CCACAAGGGC AGTTTAGGAC AGAACTGGAG 600
GAGAGGTTAT TTTTAATTTG TATTTTTGTA GACAGAGTCT CGCTCCGTCA CCCAGGCTGT 660
AGTACAATGG TGTGATCTCA GTTCACTGCA GTCTCCGCCT CCCGGGTTCA AGTGATCCTC 720
CTGCCTCAGC CTCCTGAGTA GCTGGGATTG CAGGTGTTCG CCACCATGCC TGGCTAATTT 780
TTGTATTTTT AGTAGAGATG GGGTTTCACC ATGTTGGCCA GGCTGGTCTC GAACTCCTGA 840
CCTCAAGTGG TCCACCGCCT CAGCCTCCCA AAGTGCTGGG ATTGCAGGCG TGGGCCACTG 900
TGCCCGACTG GGAGGAAAGG TTACTGAAAG ACGTGAAAGC CACCTATGTA TGGTGCTGGC 960
TCGCTCAATG AACGGAGCAT CTAGGTGTAT GCTAAATGCT TTGTGCGTAT GATTTCATTT 1020
CACCCTGATG CCATCCCCGT GGAGTTGGAG GTCATTGTGC CCTTTTACAG ATAAGAATAG 1080
ACTTGGCGGC CGGGCACGGT GGCTCACGCC TTTAATCCCA GCACTTTGGG TGGCCGAGAT 1140
GGGCAAATCA CAAGGTCAGA CGATCGAGAC CATCCTGGCT AACACGGTGA AACCCCATCT 1200
CTACTAAAAA TACAAAAAAT TAGCTGGGCG TGGTGGCACA TGCCTATAAT CCCAGCTACT 1260
CGGGAGGCTG AGGCAGGAAA ATCACTTGAA CCCGGGAGGT GGAGGTTGTA GTGAGCCGAG 1320
ATCATGCCAC TGCACTCCAG CCTCGGCGAC AGAGTGAGAC TCTGTCTCAA AAAAAAAAAA 1380
AAAAAAAGAA TAGAGTTGGC TGGGCACGGT GGCTCACACC TGTAATGCCA 1430
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