| Tag | Content |
|---|
EnhancerAtlas ID | HS133-01958 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:98402550-98404840 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr1:98403696-98403710 | ATGAGTCATTTTTT | - | 7.52 | | POU2F2 | MA0507.1 | chr1:98402647-98402660 | GTCATTTGCATGT | + | 6.08 | | SPI1 | MA0080.4 | chr1:98404076-98404090 | GAAAAGAGGAAGTT | + | 7.14 | | SPIC | MA0687.1 | chr1:98403927-98403941 | AGAAAAAGGAAGTA | + | 6.2 | | SPIC | MA0687.1 | chr1:98404076-98404090 | GAAAAGAGGAAGTT | + | 6.31 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I097937 | chr1 | 98402563 | 98404495 |
|
Enhancer Sequence | TAATACTTCT TCTCCCATTC ACCTAGAGTT TCTTCTAAAT TTAGGGGGTA GCAAAGTGCC 60
CATATTTCAG GCAGGAGAGT GAGGCACCTG GGCCCTAGTC ATTTGCATGT TCCAGTGTGG 120
TGACTGATGA GATGAGCATC ACCCATTCTA TTCGCTGGTC CATCTGCATG AGTACAAGAA 180
GCTTCTGTTT CCTAAAGAAA AGACTCTCAA AGCGTTGTGT TCTCTCTCAG TTGCTGCTGT 240
GCCAGTGTGG GCCTCATATT CTGCTCTGAA TGTGTCAAAG ATGGGGTGCT GGCAAGGGGA 300
TGTAAAACAT CAGGGCTCAG ATTCTTTTCT CAGAGTCCCA GTAGTGACTA GTTTTTTTCC 360
CTTGATAGGG AGGATAGGAA GTGTAGAAAT TGGCTGATTG CATATTCTCC CAAATCTTAC 420
AATGTACCGT AACTTCAGGT TTTGAAATCA AGAGGCTAAA ATTTGACTTT TCTAAAACTT 480
GTCTTCTGTT TTAATAACTC TCAGCTGAAG CTATAATCCC GCTGACTGAG TAGAGGCAAA 540
AATGAGGAAA AAAAGTTGAA AAATGCATAC CTTTCATCAA AATATCATTC TATGAAAGAG 600
ATACATATAT ATGTTTGTGT ATGTAAATGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT 660
GTGTGTGTGT GTGTATTTGT TGTTGTTGTT CACATTGAAA GAGATAATGC TGCCTACCAA 720
ACTAATAAGT CCTTTCTTGG AGAAATTGCC AAACCTGCTG ACTAACTACT CAGGTTTCCT 780
GTGGGTAAGG TGGTCATCTT CTGCACCATG CAACTATATT ATCTAATAAA ACCTGACTAT 840
CCAGTGTTTA TTTGCAATCC CAGAGCCAAA ATTCTTCTTT AATAATATGC ATCCCAATCA 900
TATTCTTAAC TTAGTATTTT ACCTGGAGGC TTAGGTGTTC CCAGAAATAC ATTTTTAAAA 960
TGTATTTTAG AGGTGGTGGT GATGGGATAG GGGATTATTA TTTGTATGCT CATTTGTTGG 1020
TTAGCTGTGG CTTTAGAAGA GCCATTTTGT CTGTCATTGG AGGAAGGTGA CTCACTAGTT 1080
GTAAATGTAA TTCCCTCCCT TTCTACATCC AGTTTCCAAG AAGGAAGACT TGCCACTGTG 1140
TTTCTAATGA GTCATTTTTT AATCATGCTG CCCATCAAGC AAAGACAGAT GAATAGATTA 1200
TTTTTTCATT TTTGTGGATA GTTTTGCAAC CCAATAAGCA CTTCTTCTTG AGACATTAAT 1260
CCACTTTATG AGAGAGAACA GGACCAGGAT AGTGGAGGGT TTATGTTTTG GGAGGCAGTT 1320
GGAGTGGGTA GGGTTAATGA GAGAGTTTCC TGATTGGGAA ATGGGAAGGA GAGGAAAAGA 1380
AAAAGGAAGT ACAAGTTCCA CAGAGTAGAG GCCCCCTGAA TATGTAGGTT CATAGAAGGA 1440
GAAGCCTCTG TGGGTCCCTG TAAAGACTTA GCACTCAATT TCGCTGTTTC AAGGATCTTG 1500
GCGAGTGTCT CTCACAACTA AGCCAGGAAA AGAGGAAGTT CATCTTCCAC GGGAGCCACA 1560
GCCATCATAA AATGTTAGAG TGGAATGACC AGTGAATGAG TGGAAAATGC AGTGGAAGAG 1620
TAAAGTTTAA TAGTGACAGT GTATAATCCC TAGACGATCC CTCTACTTTT AACAGACTTT 1680
TAATTTTAGA ATAGTTTTAG ATATAGAGAA AAGTTTCGAA GATAGTACAG AGAGGTCCTA 1740
TTCATCTCAC ACTCAGTTTC CATTATTGTA CCTTCTTACA TTAGTATGGT ACGAATATTA 1800
CATTCATGAT CCAATGTTAG TCCATTATCA TTAACTAAGT TCCTACCTTA CTCAGGTTTC 1860
CTTGGCTTTT ACCTAATAGT TTTCACTCGT GCAGGATCCC ACCAGTGTAC CATACTACAT 1920
TTACTGGACA TGTCTCTTTA GGTTCCTTTT CACTGTGGCA GTTTCTCAGA TTGTCCTTGT 1980
TTTTGATGAC CTTTGAGTAG TACTAGTCAG ATATTTTGTA GAATCCCTTA ATTAGATTTG 2040
TCTGGTATTT CTTAATGATT AGATTGGCTA AAGATTTTTA GGATGAAGAC TTCAGAAGGA 2100
AACTTCCATT TTTATCCCAT CATAATACAA GTGTGTGCTA GCAATATGAC TTATCACTGT 2160
TGATATTAAA TTTGTTCACC TGGCTGAGAT ATTGTTTGTC AGGTTTCTCC ACTGTAAAAT 2220
TACTCTCTTC TTCTATTTCT TTTCATAGTG TATTTTTTAG AATGAAGTCC CTTATGAGAA 2280
GACCACATAT 2290
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