| Tag | Content |
|---|
EnhancerAtlas ID | HS191-05118 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr10:74777490-74778880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mafb | MA0117.2 | chr10:74777642-74777654 | AAAATGCTGACA | + | 6.62 | | TBXT | MA0009.2 | chr10:74778671-74778687 | TAACACCCAGGTGTTA | + | 6.77 | | TBXT | MA0009.2 | chr10:74778671-74778687 | TAACACCCAGGTGTTA | - | 6.88 | | Tcf12 | MA0521.1 | chr10:74777835-74777846 | CAGCAGCTGTT | - | 6.32 |
|
| | 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 |
| GH10I073017 | chr10 | 74777315 | 74778944 |
|
Enhancer Sequence | GTGACGCACC AAAATTTAAG AAAAATATTT GGTCTGAGTT CAAGTTCCAG CTCTCTTAAT 60
TACAATGTAA CTTTGGATAT CATCTCAGTT TTCTTATTTG TTAAAGTGAA GAGAATGATA 120
CTTAACTCTT TCCCTCAATC ACACAACACA ATAAAATGCT GACAAAATCA AAGGAGAACA 180
TAATTAAGAG TGCTGCTGAT GAAACCAGAA GGAGAATACT GGTGGAACTG GAACTGCTGG 240
AGTGTGTCTT GCTCTGGGGC CAGTAGCCAC AGCACCCCTT CATCCCTGAA GCTAAGCCAG 300
GAATGAAGGC CTACTTGAAG GCCTGACATT CCCAAGCAGA GCTGCCAGCA GCTGTTACAC 360
CCTTCCTGGT GGGGTCAAGA GAGGTGGAAC TGCTCTACCC ACCCCTCCCC CAACTCCCTG 420
AGGCAGGAGC TGCAGCCATG TACTCCCTCC CAAGAAAATA GTACTTTGGC AGAACCCTGC 480
ATCCCATGAG ATGTCTGGGC CACCCAGAAC AGTCACGTCC CCTGAGCCTG AGCTGAAACA 540
GCACATCACC CTTGGGGAAT TGTTGCACTG GCCAAGCTGA GCAGCTGCAC ATCCCAGGGC 600
TGAAGTAGTA CCCAGAGACC CAGGGAAACA GAGCAGTGGC TAAGCTGAGA AATGTGCCCT 660
GCAGGGCAAA TAACTCTAGT ACCCTGCTTC CCTGGAGAGT CTGCGCTGCT GAGACACTTC 720
TCTTTCTAGG GAGTGAAGTC ATTGCTGTGC TGCTCTCTGC CCCACAGGGC CCAAACAACA 780
GGCATGCTTG GCCATTCAGG GGTGCCTGTT CCTGCTGTAC CTGGCCTCAG AGTCTGGGAT 840
CCATCTGAGC TCCACCAATC CAGGTTCTAG AGTGACTACT AGAACCTGGT GCCTCATCCA 900
GGGCACCTCA TCATGGTGCC TCATCCCCAG GGATAGGAGT TGCCACTAAG CCCTATTGGC 960
TCAGGCTCCT AATAGAGCCA AACCCTGCAT CCCAGACTCA AACCTCCAGA GCATCCTCTC 1020
TTCCCTGGAG TTGGGCCAGG GCTGTGCCCT GTCCACCAGG GGTAGACTCA CAGCTACAAC 1080
CTGACACTCT TTTCCCAAGC AGCTAGAGGG TGCCTCAGAG TCACAGATCC TGGCACTATA 1140
GGCAACCTAC ATCCAACCCT GCCAATAGTG ACCCTGTACC CTAACACCCA GGTGTTACAA 1200
TAGTATGCAA GACCCTGAGC CCAGGATCCT AGCCCCATAG CCACTCCAAA CGCTTGCACC 1260
TGGATTGCAG CACCATGGCA GCTGCTTGTA GGATATGTAA GACCTGCCAC CAAGAAGACT 1320
CCCACTGGCT AAAACTCCCT ATTGTGGGGA AAACAAGAAT GGAAGGATTC CAAAAGCTCT 1380
TGCCACTGAA 1390
|
