| Tag | Content |
|---|
EnhancerAtlas ID | HS191-08279 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr11:133097430-133098870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx3-2 | MA0122.3 | chr11:133098275-133098288 | ATAAACACTTAAC | + | 6.08 | | TCF3 | MA0522.2 | chr11:133098177-133098187 | AGCAGGTGTT | - | 6.02 |
|
| | 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 |
| GH11I133228 | chr11 | 133098421 | 133098570 |
|
Enhancer Sequence | TGAGCTCTTT AATACCGAAA CTTTAAATAT ACCGGTGGCT GTGAAGCACA GCCAGCAACC 60
TAAGAATTGC TCAGAAAATC ACAGGATTTT AAATCAAGGA AAGAAAAAAA AAGGCCGTTC 120
CATTCTCCCC CTCAGGCTGG ATTCCCTGTT TCTTTGTCTG GAAATGCAGT GGCCCTCCAG 180
GGTGAAGGGC ATCTGCAGAG CAAAGCCAGA CAGCAGCCAG GAGGCCACCT GCCTCCCCAG 240
AGAGTGCCTT TTCATCGCCA GGAGCTGCAG TTACAGTCTC CTAGGGGTCC CAGCAAAGAA 300
GCATTCGACT TAATCGCTAA GATGCCCTGC GGTGCAAACG CTGGGCCCTG TGACCACATG 360
CAAAAGGAAG TTGGGTCAGG CTTTGGCCCA GAGCGCGACA TGACCAGTGT CCATTTCCTG 420
AGCAGCAGTG GAGTGCCCCG ACCAAGTCTG GGAACCTGGG GACTCTGCCC TGAGAGCTGG 480
GGCTGGGTTG ATCCAACTTC TTAGGTGAGG TTTTCATCTT TATTGGGAGA CCTTTGTCCT 540
TGGGATGGGA GATGTCCCAT TCATTAATTA TTGTGCTGGC TCTGAATAAT TGCGGCCAGA 600
GACTGCTATG CTGGGCAATT TCCAGTTCTA CCGTGGCTGC TGCCGTGACA CTGTATACGT 660
CTTTCACTGG TACCGCACTG CATTTTACAA GACATGGTCC CTTCACCCGC TCAGCTGTTC 720
CCCATAATAA CATGAGGAGG TGAGCATAGC AGGTGTTCAC ACCCCGGTTT TACAGACAGA 780
AACAGTTGGA AACCTGGAGG CCGAGGTTCA TAAAGGTTAA ATGTGGTGAA GGTCACACAG 840
CATACATAAA CACTTAACAA AACAGGACTA GATTCCTAGT TTTCTGCTTC TAATTCCAGT 900
TCTTTCCGCT ATAGCTCATG GAAACAGAAT CTCAGAGAGA GTTTTCAAAC TCATCCACAG 960
TCCCTTCAGC ACCTTCGCGG GCCAGCCACA AGCCGAGGTG CCCGCTGGTG CTCAACAGCG 1020
CCAAAGCGTG TGGCCCCTCC CAGGACGCTG CGCCCTGCCG GGCCTCCCCG TCCTAGAGCT 1080
CTGCTTCTTG CCACCTGCCC CCGCTTGGGC TGCCCCTCCT ACTGCTCTCG CTGCCAGGCA 1140
GCTTGGGGCC TCCCACGAAT TTATGGAAGG AGATTGGCTC CTGCAGAGCC CCTCAGCACG 1200
GGCCCAGGAG GCTTCGCATG AAAAATGATT GCACCGCACA CGCGGAGGCT GTTTAAACCT 1260
GTCACTTTAA AATATCCCTT CTCCTCTGCC CAAGCTGGGC CAAGAGGAGC AGGTCCAGGA 1320
AAAGGAAATC AGTTTAAAGT GACAGCCCTT AATTTCTGAA GCCAAACCTC AGCATTTGTG 1380
GCAGACTTTT TATGTGCTGA GGTCTCAATT TAAAACCAAA GTGTCCCAGT GGCACCGCGT 1440
|
