| Tag | Content |
|---|
EnhancerAtlas ID | HS047-19402 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:96738010-96739650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Tcf12 | MA0521.1 | chr2:96738138-96738149 | CAGCAGCTGTT | - | 6.32 | | ZNF263 | MA0528.1 | chr2:96738384-96738405 | AGAGGAGGATTAACAGGAAGA | + | 6.07 |
|
| | 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 |
| GH02I096071 | chr2 | 96736965 | 96738709 |
|
Enhancer Sequence | AAAGCAAGAG AGATGCACAC CAGCTTGGGG CTCGCACTGG AGAACACAGA ACAGCAGGGC 60
AGGGGCTCCA CTGGGTTGGG GCTCTGGTGT CCCCAGGCTA CTGCAGACAC AGCCCTGAGC 120
CCAGGGAGCA GCAGCTGTTG TTTCTGCAGC AGAGCGGAGC AGCCGGGTCA GCTCCAGCCC 180
TCCTGTGAGC TGTGGGAAGT TGCCACAGGC CCACCAGCCC TCCTCACTTC TCCTGTAGCT 240
CCCAGGAACT GTCATCATGA ACCATCTGCA CCCTCACCAT CCCTTAGGGG CTGGGCAGTG 300
CTGGGGCTAT TATTCTCCTT GACCTTGAGA AAACAGAGGA CGCCGGGTGG CCTGGCCAGG 360
GTCCCTCGGA TGTAAGAGGA GGATTAACAG GAAGAAGTTG AGCATGTCCT ATGTCCCAGG 420
CATATGTGGT CTAAGTCTTC ACATACACGA CCTCACCTGC TCACTACCAC AGGCTGCAGA 480
GGAGGAGCTG AGCTCCCATG TTAAGGTGAG GCTCGGAGGC ATTAGGTGAA GTGTCCAGTT 540
CCCCAGCTCT TATGTGACCA GCTGGGCGTT CAGCGGAGAT ATTTCTACCT CTCTAGCTTC 600
CCATCCTCAA GAATGTGGCT GGGCCAGACC TGGACTCTGA GGACATTCAG GGACACTGTG 660
CCTCACCAGC CCTCTGAAGC GCTCAGAACG CGTGTCCTGA CCCAGCTGCA TGCCAGGAAC 720
CGTGCATTGG GAAGTGGGTG GACAGGAGAG ACAAGACATG CTCCTTCCCC CAGAGGAGGC 780
TGCAGGCAGC AAGCGAAACC CTTAGGTAAG ATCGGAACAG CCGTCCACCA CTGGGAGCAT 840
GAGCTGCATC CTGCCTTGGG GGGCCGCTTT GGTGGGAGTG TGCTGGGCAG AGAAGAAGGG 900
AAGGACATCC AGGCAGAGGG GGCTCCTGGG CAAAGGCTCG AAGGTGCAGA GGTGAGAGGC 960
ATTTGGGAGC TGGTGAAGGC ATTGGGGGTG GCCTCCTATT GGGGAGGAAT GAAAGGGAAG 1020
GGCTCCTCTG GCAGGGGCCC CGTACTTTCC CGTGGGGACT TGAGTGGGGC TGGCTCTGCA 1080
CCCCCACCCC TGCCCAGGGA GGGCTCCACT GTCCTGGGCT GACCAGAGAA GCAGTGGGTT 1140
CTGTCAGGAA GGGGAGGCTT CTTTAGCCCC GTTCATGAGG CAGCTGGGGG AGGAGGAGGA 1200
ATGCAGTGGC ATCCCACAGA GTGGCCCCGG GCCACTGACC TGCCCTCTCT GCCCCATTTC 1260
CTCACCTGTG ACACAGAGAC CCACACACCC AAGCCTCTAA TCTGCTTCTA AGAACATTGT 1320
GAGAGCCAGT GATGATCAGA GGACTGCTTA TTGTAAAGCA AAAGCTCCAG AAGGCTGTAA 1380
GTGAACAGGC CTGGGACATG AGAGCTAAAG GGCCCTGGGC TATCTGAGTG TCCAGCCTTC 1440
ATTTAACAGC AGAAGAAACA GACCCAAGGA AGTCAGAGAA TGTGGCCAAG ATGAGCCGAT 1500
GAGTTCGGGC AAAGACAGAA CCCTGCCTTC TCTCCTGCAC CATGCTAGCT CCAGACTGGC 1560
AACCCTTTCT CACCTCTGCC TGCTTCATCC CAAAACATTT CTCCTCAGCC TGGGTGCTGA 1620
ATGGGATCAC ACCATTAGAA 1640
|
