Tag | Content |
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EnhancerAtlas ID | HS050-35382 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr2:16146020-16147180 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr2:16146957-16146968 | GGCCACACCCA | + | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 16146425 | 16146631 | chr2 | 16146733 | 16146825 |
| | Number: 1 | ID | Chromosome | Start | End |
GH02I016005 | chr2 | 16145800 | 16147640 |
| Enhancer Sequence | GTGACCCAAG ATCACGCCAC TGCATTCCAG CCTGGGTGAC AGAGTGAGAC TCTGTCTAAA 60 AAAAAAATAA AAAAGTTCAT GACTCAACCA TGCCAGAAAG CATGGAGACT GCAAAAGGAG 120 ACAGATGATT AAGAATGTGT ACATATGTAT TGCACTGATT AGCTATGTTA GCACTACATA 180 TCCATATGAT CTTGGTTGAA TACAACAAAA GAAGCAAATA AACTGTCTTG TCCAACCTCT 240 TATATTTTCA GGTGTGGCCC AGAAAAATTG ACCGAATTGT CCCAGGCATT ATGGTTGGTT 300 CCTGGCAGAT CTGAACCGAG AACTCCAGTA TCATTCTCTC CTTCTAGACA GACACACACA 360 CACACACACA CACACACACA CACGCACACA CACATGACAG GGGCACATGT CCCATGCTGC 420 TTTCTATTTA AAAAAAAAAA TGACATCTGC CCAGGAATCA CATTGCACAA TGGCAGTCCT 480 TTCTTTTCCT CTTCCTGTGT TGAGTCATTG CCCTTGCCTG TGAAGTGCCT GCATGACCAC 540 GTTGCCCTAT GGACTTACTC AGAAGAAAGG AGTAATGATC AGCTGATGGG TCAGACACTC 600 AGGGGTACAC AGCCGGCCCC ACTATGGGAA GCAGAGATGT GCTGGGGGTC AGAGCAGCCC 660 TGGCCTTGCT GTCCCTATGT AAGATCTCTT CTTGTCTCTA TAGAATGCAC CAGAGCTCTA 720 AACATAGAGA CTGTTTATAA CCAAAGGTCA TTTTCCTGGT AGAACAAGGA GTCCTCTTTT 780 GCTTTGGAGG CAGATGAGTC TGGGCTGGCT CATAGTGTTT GATGTGAGAT GGCTGTGCTC 840 AAGTTTCCTG GCCAGAAAGT TAAGCTGTGG CCCTTCAGAG TTTTATAGGG CCCAGCACAA 900 TCTTCTTGCC TCCTGCCTGG GCCCCAGTAT GCCCCGAGGC CACACCCACT GTGGCCAAGT 960 GCATGGTCCA GGGAAAACAG GAGCTGCCTT TTCAACTCTG CTTCCTTGAT CATAGGTTTA 1020 ACCAATAAGG CTCATGACAA CTACTCTTTC TGAGCACATT TGATGAGTTC CATATGAGAC 1080 ACATATTATC TAATTTAATG CTTATGATAA TCCTTCAGAG GTGAGATTTC AGCTCCCTTT 1140 TAAAGTCAGG AAACTGAAGC 1160
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