Tag | Content |
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EnhancerAtlas ID | HS133-06335 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr11:73988620-73990430 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2F1 | MA0017.2 | chr11:73989500-73989513 | CTGGTGACCTTTG | - | 6.21 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I074276 | chr11 | 73987694 | 73991829 |
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Enhancer Sequence | GATGATAATA ATATCTACTT CACAGACTTA TAAAGATTGT GAGAGGCAAT GCTTATGAAG 60 ACACTTTGTG AACTATACAT TAGTGTTACT TTTAAACACA GGAAAATCTC TGCTCTACTG 120 CAAGACAAGC CAGGATAGGG CAAAGGCCAA ACAGCAGAGT TCAGTCTCTT TTCCTGAATG 180 TCTTGTTGAG GTTCTGACAA AGTGGCAACT TTGGAATCAG AATTTACGTC CCTGGGAAGT 240 GAGAAAGTGC TCCCTAAAGC CAGTGGGTCT CCTGGGGAGA CGATAAGGCT CTGAGGGAAC 300 AGCCTTGGCA TGATATGGAA GACCATTTCT TTGCTCTTTG CTTTTGATGG ATTAGTGTGT 360 TCATTCTTTC AAATAGAGTG CAAGCAGAGT GCTATGCCAC ATGCTCTTAG GTTACAGAGA 420 TCCCCAAGAC AGAGCTATTG CCTTCTAAGA GCTCATGGAT TATGGGGGAA AGGACAAACA 480 CAAATATAAC TAAGAACAAA GTAAGGTACA GTGAAAAATT GAGAAACAGA CTTTAAAGTG 540 CTGGGAAGCA CAGAGGAAGG AGAAGTTCAT TCCAGTGGGG CACTCAGGTA AGATAGTGAC 600 ATTTAAGCCA AATTTTGAAG AGTGCATAAA ATTTCAATAG ATGGAAAAGA TGTAGGAGTA 660 TTCCAGCCTG AAGAAACAGC ATAAGCACAG ACATGGAGGT GTGGCAATAA ATTATGAATA 720 AGGAGATAGG AAGAAGTAAC GGGAGATACA GCTGGAGAAG CAGGCTCAGG GCATGACATA 780 GAAAACTGAA AACACTGTGA TATGGAATCT GGACTTTATG GATAATGGGT ACTCAGTGAA 840 GGTGTGTGAG CAGGAAAATG ATTTGGCAAT TAGAAGTTCC CTGGTGACCT TTGGGAGACC 900 AGCTCCAGCG AAGTTGTGAG GACAGAACCA AAAGTCAAAG AGTTGAAGAG TGATGCAAGT 960 GGAGAAAGAA AGTAGTTTCT TGTTCGGAAA AGGGAAGAAA ATACCACCTG CTCCCCTGGA 1020 AGCAATTAAC CCAAGGCTGA ATTTTCTCTC TGACACTAGA ATATCAGAAA GGTTAGAAAA 1080 AGCAATGAGG CTGAGGTCAT AGGGACCTTC CATAGGTTAG AGAATAACTA CTAATATGAA 1140 AGGCCCTTAA TGTACCAGAC CAAGTAAGTT AAGCCAAATG ATTCTGAATC ACAGCTTTCA 1200 TCACTCACCT CCCTTCCCAG ACAGCACAAA CTGATCTCCA TCCTGAGGTC TGGCCTCCCC 1260 CCAAGGATGC TGACGTCACT GTCTCACATG TCTTTGGTGG ATGTAAGTAA AGGGCTGCAG 1320 TGGGGGGTGG GCAGGGCTGG AGGGGTGGGA TAAAGCTGGG CTCTCACAGC TGAATCTGCT 1380 CCTCTACAGA AGCCATCAGG GCCAGAGTCT ATTTGTCCTT CTGGTCTCAT TCTTGGCAAG 1440 TCATGCTTTC AATATGAGTC AGGAGGTGGG AATGGAATCT TGTAAAGTTA AATTACAAAT 1500 GTGGACAGGA CTGTATCTTC TGGAAAAGCA ATCCTGTTTA GGAGAACAAC TATAGACATA 1560 TTTTTTGGTT TAGGGCAGAG GAGCTCTTCC AAGTCTCTCT CGAATGGCCT TCTAGTTAAA 1620 CCCTCAGATG ATCTAACAAC CTGGGAAAGG GGAGTGGAAA CTTCACCCTC TTAAAAAGAA 1680 TGTACAGCTA TAAACGTGAA CTAGGGATTC TCCACCTCTG GAGGTCCCTG AATGGCTGTT 1740 GCTGACTGGC AGTCAGCTAT GCTACGGCCC GAGGGTGGGC AGCAGGTATG ACCAAGGAAG 1800 GGCCCTTCTT 1810
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