Tag | Content |
---|
EnhancerAtlas ID | HS047-19617 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr2:112677230-112678140 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr2:112678071-112678086 | AGTTAATAATTACCA | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 112677520 | 112677630 | chr2 | 112677749 | 112678135 |
| | Number: 1 | ID | Chromosome | Start | End |
GH02I111918 | chr2 | 112676330 | 112678814 |
| Enhancer Sequence | TGGGGGACAG GCTGAAAGGG ATGATGAGAG GGTACCTAAA GCCCTTTGGG GCCCTTGGGG 60 CTTGCCCTGC TAACATGTGT GTTCAAGGCC AAGCAGAGAG GTACCTCTGC TCATTTTGTT 120 TTTTGATGTT TTTTCTTTTT CTTTTCTTTT TTTTTTTTTT TTTGAGCCAA AAGGAATGTA 180 TTGGGCCAGG GGCAGTAGGA AGGTCACCCC ACTGATAAGC AAGCCCCTTG TGCTTTTGCT 240 CAGATGTCTC AGCCCCTTCA TGCTGCAAGC CTTGGTTCAG AGAGGTTGGA TAGCTTTCCT 300 GGTGTGCCAG GTCCCTGTTT GCCCCTCCAG ACCCACTCTC CATGCTGCTC TAAGCCCCAA 360 GAAGCAGCCT GTGGGAAGGG CAACAATGAA ATCCCTAGTG CTGTGGCTCC AGCTGGTTTT 420 GACTAAATGA TACTAAGTTA TATTTGTTCC TCTAAGTAAA TCCGGGGTGT TCCCATATTG 480 GTTGCTTATC TGAAATTCAG GTGTAAAGGG CTGTACTGTT TTTTATCTGG CAACCCAATG 540 CCAACACCGT GTTTTACAGG CAACTTCACG TTCCTTCCAC CGTGCAGGCA TTTCTGGGCT 600 TTCACTGGCA CTTGGGCTTT TCTCCTCCTG TGGCTGGGCT GTGACCTCTT GGGGCACACA 660 CTGCCCAGCC ATTTACTTCC TTTCCTTCCT GCAAGCGCCA GGCCTGTTCT CTCCAGCACT 720 GACTCAGAGC CAGCCACCCG CTTTCTCTTG CAGGGCTTTG CTACACTTAG GGCAAATGGG 780 TGGCGTGATC GCCTCTTCCT CCTTTAACAT TCTCCAAGTG GCCCAAGGGT CACTCCAGTG 840 AAGTTAATAA TTACCATTTG CAATTTAGGA CTGATCCATC AGGTCAAGTG AGTTCTGATT 900 GAAGGTTGTT 910
|
| |
|
|
|