| Tag | Content |
|---|
EnhancerAtlas ID | HS089-07136 | Organism | Homo sapiens | Tissue/cell | Hela | Coordinate | chr2:9843010-9844190 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr2:9843978-9843991 | CCTTTGACCTTTG | - | 7.22 |
| | | 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 |
| GH02I009702 | chr2 | 9842226 | 9845172 |
| Enhancer Sequence | TACTTATGGC AACCTTTGAA TGTGGTAGAA TAATTCCCAT TCTTCAGATG AGAACATTGA 60
GGCTCAGAGC GGCGATGTAG CCTGCAAGGG CACATAACTG GAAGCATCAC AGCTGAGATC 120
CAGACCCCAG TCTTTCTGAC TTTAGAGCCC ATGCTCTCCC ACTACAGTCT ACACTGGGGC 180
TCAGTAAACA TTTACTGAGT GAAAGAATAA ATACGTGCAG AACCCAGCCA ACAGAGAGCA 240
TCCCCGGAGG TGGGGCCAGG GCCCCAGGCA CTCAGAGGAG GCAGGCCTCT GGCAGTAGCT 300
AAGCAGATTC CCGTCTCAGA TGTCAGCCCT GCCCACCCTT CTGTGCCCCC CCACCCCCCT 360
GGTTGGTGTT TGTGGGACAG TTTCCACTGT GTTGCCTGGG AAACGAGGCA TCCTGCCACC 420
ACCACTCCCC ACCTCCGGGC TGCCAACACC TACCACGCCC GGCTTGGGGG TTTTGGCTGG 480
TTTCCCTTGT GTCCTAGTCA GCTTGAGAAA CCCTCGGATG CACTCGCCAC TTTTACAGTG 540
TGGCTTTGCT CATCTGGGTG GGAGGTACTG CCTGGGGTGA GCTCATCACC TCTGGTTCCT 600
CAGTGCCACC CACTGATGTC TCTTGGCACT GAGTTCTTAC AACTTGTTCC AGGGGATATT 660
TGGTGGTTGA TGGTCACCAC CCATGTGTCA TGGTCCCTGA GCATCCCCCG CCACCCCACT 720
GCTCCCTATT TTGGCAGTTA CTGTCACCCT CTAGGGATGC AGGGATGCAG TTTACCTATC 780
TAGAGTGCGG TGATCAGGTG GGGAAGTACA AATGGCAATT GACAGCTAGA GAGCTTGAAA 840
CCCTCCCACT TGGCTCTGCT CACCCTGGAC TCTGGGAGAC CTCAGCTGCC CAGCAGTGGA 900
GGCTGGGGCA GCAGAGGGGC CAGACCTGGG AGCCCAGAAG CCTGGATCTG AGTCTGACTC 960
ACTGCTAGCC TTTGACCTTT GGAGGCTTGG GCAAGCTGAG GAACTTCTCT GGTCTTAATC 1020
TCCACCCCCT GCTGGAGTAG GTGAGGTCAA TGAGTGAGCG CATGTAACTT CCTCTTGGTA 1080
AGCCCTGGGT TCCTGGAGAC AGGAGAGGGA GGGTGGTTTT CCAGGGGCAT TTGTTGACAT 1140
TTCTAGAGAA TATCTGAGGC TTCGACAAAA TCAGACCTCA 1180
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