Tag | Content |
---|
EnhancerAtlas ID | HS108-33769 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr6:10101640-10103100 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr6:10103013-10103028 | TGAACTCCTGACCTT | - | 6.04 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACCTGCCTAT ATTTTTGAAT TGAGGTTTTC CTTCTCACAG TCACTCAAAG GGATAATACT 60 AATGTTTACA GCAACGAAGT CGGAAGGAGC CTTCCTCCCA GATCAGCTTC CTGGAAAGAC 120 CTGGAAATTC CTCCTCCTAA GTTTCCTTTA TACCATGTAG GCATTGTTCC TATCTCCTCT 180 CCCCCTGCTT TTTAGTTACT CCTCATATTC CCAGCACTAC TCTTCTACCT TGCACGCCTT 240 TGCACCTTCA TCTCTGAAAG TCTTCCTAAA ACTTCCTCTC TGAGGTTTTC CATGACTAAG 300 GCAGAGAGAC CGAGGAAGCC ACAGCTGGAG CTGCACCCAT TTGCACAACA GCACATACAT 360 GTGGTCTAAA ATAAGCAATC CAGAAACCAT CTCTTTCACC CACCTGCCAA GCTCCCCTTC 420 CCTCAATGGA GAGAGAAAAT TATCTGGAAG GCCTGAGTTC TCAGAGACTG GTTCCACATG 480 AATGCTCGCT TGTATTTGCA TGGTACCTCT CTTGCAAGGT GCCCAAAGTG CTATGTAAGT 540 GGCTCACACA TTTTTCACAA CTGCTCTTTG ACATAGATTG TCAACAAACA CCATTATTCC 600 TAGACAGTAG TTGAAGGTGA CTGAACTTTA GGGAAGTCAG GCAGCTCCCA AAGACAGAGC 660 AGGACTGAGA CCTTGCACTA AACTACACTT ATCAGAGCAG GCCAGGCACG CAGCAGAGAC 720 TCAACTGAAA CACAGTCAGG CCAAAACCAA ATACAGTTTT TAAAAACTCA AACAGGAGAA 780 ACCACTTTCT GAACCACTAA TAATCTCTGA ATAACTTTAA CATGGATCCA AGGTGATGGT 840 TAATAAAATA GACGCCAGTG TAGACACTGT TTGCATGGGA GGCAGGATCT AGGACATTGG 900 CAACTGATAA ATAAAGGAAA GGACAGAGAG AAAAAAGACA AAGTTGTACA ATGCCAGCCG 960 TGGGACTCAA TGGGAAGACA CCATTTAACT TACCTGAGAC TTCTAGACAC AGGTCACTCT 1020 GTTTTTGCCA ACAACAGGAA CCAATCTTTG GAACTTTTTG AACAAAGGGG AGGGGATATT 1080 GCCTTCATGA CCTTTATCTC TATGAGACCA GACAGAAAGT TATGGTTACA AACTAATCCC 1140 AAGTCATTCT CGCCTTTTCT TTTTTTTTTT TTCGAGATGA AGACTCGCTC TGTCGTCCAG 1200 GCTGGAGTGC AGTGGCGCAA TCTTGGCTCA CTGCAACCTC CACCTCCCGG GTGCAAGCAA 1260 TTCTCTGCCT CAGCCTCCCT AGTAGCTGGG ATTACACGCG CCCGCCACCA CACCCAGCTA 1320 ATTTTTGTAT TTTTAGTACA CACGAGGTTT CACCATCTTG GCCAGGCTGG TTTTGAACTC 1380 CTGACCTTGT GATCCACCCG CCTCAGCTTC CCAAAGTGCT GGAAATACAG GCGTGAGCCA 1440 CCGTGCCCAT CCCATTCTCA 1460
|
| |
|
|
|