Tag | Content |
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EnhancerAtlas ID | HS108-38689 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr8:8830450-8832130 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr8:8831685-8831700 | TGGCCTCTGACCCCT | - | 6.81 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 8830695 | 8831121 | chr8 | 8830469 | 8831572 |
| | Number: 1 | ID | Chromosome | Start | End |
GH08I008973 | chr8 | 8830847 | 8830920 |
| Enhancer Sequence | ATCATTTTAT ATTTGCTGAG AGCTTTTCCT TTGAACATAG ATTGGGGGAG GCAGTTTCAT 60 GGATTTCCAT GTTCATAACT GGATCTGTCC CCAGTCTTTT TCTGGCATTC CCAGCCTTGA 120 ACCGCGTCTT GTTAATCCTC CTCCACAAAA GCCCATACTA GCTTTTATTT ATTTTCTCTC 180 AGAATATTCC ATGTCTATAA TTTCTGTTGA TTTATGCTCT ATAAATACTA ATTCCAGACT 240 TGTGTAGCCA GCACTTTCTG GCCCCAAGCG CTCCACAAAA TGGACTCAGA TTGTCTTCTT 300 GTATAACGCA CAGTCTACCA GTTTGGTGAA AGGTGATAAA GTGATCTGTG GAGCTCAGAT 360 GGAAAGAAGC GTCTGGGAGA GCCAGGCTCC TAATCACTTA AATCCTTTCC AAACGTGGGG 420 AGGGGGGTGG TGCGAGGGAG AATGAGAGCA GACAAAGCTG GCTGTCATTG CTATGATTAG 480 GCTTTCGCTC TAAGCCTCCA GAGAGTTGTG AGCTGGGGTA AATGATGTGA AGGATTCATT 540 TCGCCTGGAT AGAGATAGGC TCAAGGAGCT GCACCAGTAA AAGTGGGATG AACGGCGTCT 600 TAGACTCCCT TTCCTCTAAG CCCAGCGCAA GCCACAGCCT CGTGAACAGC TCAATGTAAT 660 AAGACAAATC CAAGGAAAAA GAAGGAATAC GCTTCCTCCT GAGAGCTAGA TTGGAGTGTC 720 TCTAATCCCC TCAAACTGTT ATCTGTCAGG AATCTTATTT GTGAGCAACA GAATCCAACT 780 CCAATAACTT TGGAAGGAAG AAATTTAGCA GAAGGCTATT CAGGAGCTCC GGCTCGTGCT 840 GAGCAGATGG GAGAAGCAGG CTTAAAGTCA AAGCTTTGGT GGCAGGCAGG AGCAGAAGTC 900 AGTCAGTGAG GACACCAGTG CAGTGGGCAT TGGACACAAG ACCACAATGC TCACCATGGC 960 TGATGCTGGC ACGAGATAGT GGTTGCTGAT GCAGGCATCG CTACCTCTGC ACTTGGGAAC 1020 TTGCCAGTAC TCCCCCATCT GCCACCAACC ACCTATCCGT GGTTTCGCCA CCACCCACCT 1080 ATCCGTGGTT TCTCCACCAC CCTGCTTCCT GGGATGCAGC AACCCCCAAA CAGATGCAGT 1140 TTTGGGCCAG CGTTATGGAA GAGAAAGCAA ATCCCCCAAA TGTCTGAATC ACAAACACAG 1200 AGACCTCACC CCCGTGACAG TGGAAACAAA TGCCCTGGCC TCTGACCCCT ACAGATCCGC 1260 GTTCCTGCCC CTAAACGGTG CAGTGAGGGG AGAGCTGGGC TGCAGAACAG GTGGAGAGAA 1320 GAACGTGGTG TGTCCCCTAG GGGTCAGTGC TAGGACATAT TGTCTCCAGG GTCTCGTGCC 1380 TTTCTGTTTG GTTGAGGGCA ACATTTCTCA GAAGTATGTG GATACCTGGG ATTTTAAGAG 1440 GGTATCATGG CAACTCTTTC ACTCTCTAGT TTTAGAGGTG ATCTTGACAA ATGTCTCTCA 1500 CCTGAGAGCC TTTGAGTATG TACCAACTAA CCATATGGAG CAATTGGGGG ATCAGATAAA 1560 AAGGCTGATG ACACGGTCAC TCTATTGAGT TAGCACCAGC TGAGCACAAC AGCCCACCAT 1620 GTTGTCTCTG ACTACCATGG AGCATGGCAG GCTGCTTGTT GTCACCCCAC ATCCATTTTC 1680
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