| Tag | Content |
|---|
EnhancerAtlas ID | HS133-17938 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:198491570-198493890 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:198493336-198493357 | AGAGAGAAAGAGAAAGAGAGA | - | 6.65 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr2 | 198491710 | 198491800 | | chr2 | 198491800 | 198492570 | | chr2 | 198493370 | 198493740 | | chr2 | 198492726 | 198493190 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I197627 | chr2 | 198492044 | 198493754 |
|
Enhancer Sequence | TGACCTCGTA ATCCGCCCAC CCCAGCCTCC CAAAGTGCTG GGATTACAGG CGTGAGCCAC 60
CATGCCCAGC CATAATCATC TTTACCTCAC AGGTTGCTGT GGGGACTAAA TGAGTTAATG 120
AATGCAAAAT GCTTAGCACA ACGCTGGTGT ATAGCAAGTA CAAAATAGAT GTTAGCTGCT 180
GTCATTGCAT TCTTCCTGTT TAGGACCCTG TAGGGACTGG CTGCTGCCTA CCTCTTCCAT 240
TGTGTCCAGA GCCATACTGT TGCTTGCCTT GCTCCAGAAA CACAGACCTT TTCCCAGTTC 300
CTCTTTCCTG CCCTAAGGTC TTTGTACATT TAGATGTGTT TCTCCGGCCT AGAATGGCCT 360
ACCTCTGGTT CTCACAGGTC TGCTCCTCTC CAGCTGCCCA GTCTCAGTGT GATTGCTGCC 420
TTCTCAGAGG GGACCTCCCG ACCACCTCTT TAAGTGAGTT CTTCCCTGGT ACTCTCGCCA 480
TAATATCCTC TATGGTCATG TTACACAATT TTCTTAGTTT TGAAATTAGA TATATATGTT 540
TTGACACTTT CACTGCCTGA CTGCCCGATG CCATACGGCT AGCGCCTTGT AAGTAGGGAA 600
GAGTATTATA AACCCAGTGC TTGGCATGGG TCCTGGCATA TATGAAATGA GTTTCAATGT 660
TATAACTCCA TCCTCACTCT TCATTGTGCT ACCTCTCCTC TACTAGTGCC ACACAAACAT 720
TTTTATAGGA GTGGAAAGAT TGAAATGAAT AACAAGTGAA GTCTGAAAAG AATTCTTAAA 780
AAATCAAAAT GTAGCCTTAA GATGTGGTAT CCTAAGGTGG GGAAAGACTA TGCTCTGGCG 840
GTGGTGGGGC ATTTGGAGGC TGGGGAAGTG TAGGAACCTC GAGGCTAATT GTGTGTGTGT 900
CCCAGGGTGT GCTTCACAGC AGAAAAGGCT GTTAGAGTGA GTGTGGAGGG ACACTGAGAA 960
GGAATTTCAC AGATCTTACA ACTTTTACAC TCTGCTGAAG TAGAAAACTT TTTGAACATC 1020
TGTCCCCCGC CCCCCCGCCC CCCCGTGTTT CTGGAAGGAG GTATTTTATT CAGCGTGATT 1080
TGTGGGGTAA TATATTTAAA TTTCTGAGCG CTGTCTGGTT TTGTTCTTCC ATTCCTCATG 1140
GTGGGCTAAC TTCTGACAAT ATTTTGGAAG AGGACAGAAG CAAGACCAAA CAAAATATGC 1200
ATTGTCTGCC CCCACCACCC TCCCCATGTG CTTTAGATGT CAGGCATCAA ACATACCAAA 1260
ACAAAGCGAC CAATTCAGCC CTGCTTCCTC TGAATGCTTC TCACAGTGAC ACAGATATTG 1320
GTCACAATTT CCCCTTGGCA ACTTCCCTGT GTACTCCCAG GAAAGTCCCA AATGACATGC 1380
TCAGTTGCCA GACCCCATAG ACTGACGTGG CTTGTGAGGG GCTTGCCATA GCCTGCAATG 1440
TCAAATGTCT AATGAGACAT TCCAGAGCTG CTGAGAGGGG AAGATTCTGC ACCCCCGTCT 1500
CCGTGACCCC CTCCACCCCA TGAGCTGCTG AGAGAGGGAG TCTCCCTGGG GCTCTCTAAA 1560
TAGCTTCTGA GGCTTTAAGA ACAAAAGCCA CACAGAGCCT GGCTGGCAAC TGCTGTGGCT 1620
AATTTTATTT TCATCAGGCA AGACCCAAGG CAGGGATGCC TGAGAGAGAT TGTGAAAAGT 1680
GTATGTTTTG TTTTTCTGTT CAGCAGTTAG TCACACACCA AAATTTGAAA TGGCTTCAAC 1740
TAAACTTTTT GGAGAGAAGA GAAACAAGAG AGAAAGAGAA AGAGAGAGAG AGAGAGATAT 1800
TATGAAGCAT AAACCAACCT CTAAATAGAT GATCCACACT AAAAGTACTG TAATTGCACA 1860
TAACAAGTGG CAGGAAAGAA AACTAACACC AGAAAATGAA CTCTGACTGT AGGCTAGGCA 1920
TTCTGGGAGT CACTTTACAT TTATTATATC TTGTTACATC ATCACAACAG AAAAAGTAGG 1980
AGTATTTTTA TTCCTCTTTA AGAAACTGAG ACTCAGTGAG CTCAACTAAC TTCCGAAGAT 2040
GACACAGCTA ATAAGTAGAA GACATAGGAT TTAAACCTTG GTCTGTCTGA TTCTAAAGCC 2100
CATGTCCTTC CTATGAAACT TTGCTATTGC TATAAAAGAC CAAGTGGATG GGACCGTAAA 2160
CTAGTTCAAC CATTGTGGAA GACAGTGTGG CAATTCCTCG AGGATCTAGA ACTAGAAATA 2220
TCATTTGACC CAGCCATCCC ATTACTGCGT ATATACCCAA AGGATTATAA ATCATGCTGC 2280
TATAAAGACA CACGTACACG TATGTTTATT GTGGCACTAT 2320
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