| Tag | Content |
|---|
EnhancerAtlas ID | HS118-19093 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr9:34606550-34607710 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr9:34607103-34607116 | CAAAGGTCAATAG | + | 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 |
| GH09I034606 | chr9 | 34606695 | 34607722 |
| Enhancer Sequence | TGAGTTATCC ACAATCTCCT GCATCCTTCA TCTCTTTCCC TACTGGCTTC TTCGTCTGTC 60
AGCCTATAAA CATGCTCAAG TCTCTGCTAG TATATTAAAA ACTACAACAA CAACAACAAC 120
AAAAACAAAA TCCAACACTC TCTGTACTCC ACATTCCTCT CCTGCTATCT ATCACCCCTT 180
TCTACCCATT CACAATCCAA TTTCTTGAAA GAGCTGTCTC TACTTCCTTA CCTTTTGTGC 240
CAAGACGTGA CCTTATGGTG GCAGAAGCCA CATTGCAGTG AATTAAGGAG AAAGTGGACA 300
GAACTAGACA CAACTCTTGT GCTCTCTTGT AAAGCTGGTC AGCCTTTCTG ACTCCAAAGG 360
GCTCATGCCT CTGGTCCCCT CCCTGCCATT CCTCCTGTAG GCCCCAGCTG GGCCCCGTAG 420
AGACCAAAGA TGGAGAGAAA ATGCCCCTCC TGGGACTCCA GAGCTCGCAA TGCCACCTTC 480
AGCACAGATC ACCATAATTA TTATATGTGA TCCCTCCACC CTGGCCATCA GCAGATGGGA 540
TGAGATCATC AGCCAAAGGT CAATAGTCTG CAAGGTGGCC TGGCCTCAAA GCTCTGGAGT 600
TCCAATGATA CTCAGAGAAC TGCTGATGGC AGAAGACACA CAAGTGAAGA TGTTCAGAGA 660
AAAAGCGGTA TGCAGAAGCT GAGAGGGAAC AAAATTCCTG AATTAGCTGC AAGGAGAATG 720
GGGGAAGTCA GTCAGTTGCT GGCAGCAAGA CACCTGAGTC ACTGCCACTG CAGCCATAAT 780
TGCCTTTAGG AGTGTTTTAG ATGCTTCACG ACCCTGTGCA TTTGAGAGAC CTGCTCGGCA 840
GCCACTGAGG TTTTCTCTCC TAATCTCCTC TGAATCCCCA TCACCTACCC CTCCCCCAGG 900
GTCCTCCACA TCACTCAGAG CTAACCTATC TTTGAAAGCA AAGGATGCAG TATTTACAGT 960
TTTGAAAACT GCCTGCTGGC CCTGTGGTCA CCTCACCCCT CCTCTAAGCC CTTATCAAGG 1020
GCTTCAGTCC TCCAATTCCC TCTCCTTCTC AATCCCTCCT GCCTGGTCTC AGTTAAGTAT 1080
CACTGCAACA TCCTTACATT GCTGGGCCCA TTCTACTACA ATGTGAGCCC AGAAGAACCC 1140
CAACCTTCTG CTTTCCTCAT 1160
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