| Tag | Content |
|---|
EnhancerAtlas ID | HS133-05168 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr11:1212720-1213750 | 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 NNNNNNNNNC AGCACAACCT CTGCTCCTAT 60
AACCGCATGA CCTCTGGTCC TGGAACTACT CCCAGCCCTG TTCCCACCAC CAGCACAACC 120
TCTGCTCCTA CAACCAGCAC AACCTCTGCC TCTACAACCA GCACAACCTC TGGTCCTGGA 180
ACTACTCCCA GCCCTGTTCC CACCACCAGC ACAACCTCTG CTCCTACAAC CAGCACAACC 240
TCTGCCTCTA CAGCCAGCAC AACCTCTGGT CCTGGAACTT CTCTCAGCCC TGTTCCCACC 300
ACGAGCACAA CCTCTGCTCC TACAACTAGC ACAACCTCTG GTCCTGGAAC TACTCCCAGC 360
CCTGTTCCCA CCACCAGCAC AACCTCTGCT CCTACAACCA GCACGACCTC TGGTCCTGGA 420
ACTACTCCCA GCCCCGTTCC CACCACCAGC ACAACCCCTG TTTCAAAGAC CAGCACAAGC 480
CATCTTTCTG TATCCAAGAC AACCCACTCC CAACCAGTCA CCAGTGACTG TCATCCTCTG 540
TGCGCCTGGA CAAAGTGGTT CGACGTGGAC TTCCCATCCC CTGGACCCCA CGGCGGGGAC 600
AAGGAAACCT ACAACAACAT CATCAGGAGT GGGGAAAAAA TCTGCCGCCG ACCTGAGGAG 660
ATCACCAGGC TCCAGTGCCG AGCCGAGAGC CACCCGGAGG TGAACATTGA ACACCTGGGT 720
CAGGTGGTGC AGTGCAGCCG TGAAGAGGGC CTGGTGTGCC GGAACCAGGA CCAGCAGGGA 780
CCCTTCAAGA TGTGCCTCAA CTACGAGGTG CGCGTGCTCT GCTGCGAGAC CCCCAGAGGC 840
TGCCCGGTGA CCTCTGTGAC CCCATATGGG ACTTCTCCTA CCAATGCTCT GTATCCTTCC 900
CTGTCTACTT CCATGGTATC CGCCTCCGTG GCATCCACCT CTGTGGCATC CAGCTCTGTG 960
GCATCCAGCT CTGTGGCTTA CTCCACCCAA ACCTGCTTCT GCAACGTGGC TGACCGGCTC 1020
TACCCTGCAG 1030
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