Tag | Content |
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EnhancerAtlas ID | HS145-03882 | Organism | Homo sapiens | Tissue/cell | NHBE | Coordinate | chr11:1212640-1213710 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2F1 | MA0017.2 | chr11:1213563-1213576 | CCGGTGACCTCTG | - | 6.11 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN 60 NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNC 120 AGCACAACCT CTGCTCCTAT AACCGCATGA CCTCTGGTCC TGGAACTACT CCCAGCCCTG 180 TTCCCACCAC CAGCACAACC TCTGCTCCTA CAACCAGCAC AACCTCTGCC TCTACAACCA 240 GCACAACCTC TGGTCCTGGA ACTACTCCCA GCCCTGTTCC CACCACCAGC ACAACCTCTG 300 CTCCTACAAC CAGCACAACC TCTGCCTCTA CAGCCAGCAC AACCTCTGGT CCTGGAACTT 360 CTCTCAGCCC TGTTCCCACC ACGAGCACAA CCTCTGCTCC TACAACTAGC ACAACCTCTG 420 GTCCTGGAAC TACTCCCAGC CCTGTTCCCA CCACCAGCAC AACCTCTGCT CCTACAACCA 480 GCACGACCTC TGGTCCTGGA ACTACTCCCA GCCCCGTTCC CACCACCAGC ACAACCCCTG 540 TTTCAAAGAC CAGCACAAGC CATCTTTCTG TATCCAAGAC AACCCACTCC CAACCAGTCA 600 CCAGTGACTG TCATCCTCTG TGCGCCTGGA CAAAGTGGTT CGACGTGGAC TTCCCATCCC 660 CTGGACCCCA CGGCGGGGAC AAGGAAACCT ACAACAACAT CATCAGGAGT GGGGAAAAAA 720 TCTGCCGCCG ACCTGAGGAG ATCACCAGGC TCCAGTGCCG AGCCGAGAGC CACCCGGAGG 780 TGAACATTGA ACACCTGGGT CAGGTGGTGC AGTGCAGCCG TGAAGAGGGC CTGGTGTGCC 840 GGAACCAGGA CCAGCAGGGA CCCTTCAAGA TGTGCCTCAA CTACGAGGTG CGCGTGCTCT 900 GCTGCGAGAC CCCCAGAGGC TGCCCGGTGA CCTCTGTGAC CCCATATGGG ACTTCTCCTA 960 CCAATGCTCT GTATCCTTCC CTGTCTACTT CCATGGTATC CGCCTCCGTG GCATCCACCT 1020 CTGTGGCATC CAGCTCTGTG GCATCCAGCT CTGTGGCTTA CTCCACCCAA 1070
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