| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00706 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:25192950-25195370 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
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 | chr1:25193083-25193104 | ACAAGGAAACTGAAACCCAGG | - | 6 | | IRF9 | MA0653.1 | chr1:25193085-25193100 | AAGGAAACTGAAACC | + | 6.66 | | NKX2-3 | MA0672.1 | chr1:25193653-25193663 | TTCAAGTGGT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGGAGCAACC ACTTTGGTAG TGAAAATATT TTAATATCCG CATGTGCATA AAGTGACACG 60
AATAACAGTT CCCGTTTACT GGGCTCTGAT GCTGTAGCAG GCTGTGGGGA TGGCTACTGT 120
GCTCATTTTA CAGACAAGGA AACTGAAACC CAGGCAGGCG AAGTGGCTTG CCCAGGCTCA 180
CACAGCCAGA ACGGGATGAA GCAGGTTCTG ACCTCCAAGC AAGACTGACT CCAGTGGGGA 240
ATTATGGGTT CCCAAATGAC ACTGATCACA GCAACAACGG GCAGGACAGG ACAGGTGACT 300
CAGAGCAGAC TCCTCATGCA AGGGGAGATG TTGCCCAGTG CCGAGGGCAC CGGGGCAGGG 360
TTCATGCCTT CCCCTGGGAG AGCAAGAGGT TCAGAGTCAG AAAGACTGGG GCTTGTGGTC 420
CCAGCTCTGC CACTTTCTGG TTGTGTAACT TCTGCCAAAT CCCTTCACCC CTCCGAGCCT 480
CAATGTGCTC ATATGCAAAA GGGGCGAGTA ACCACCTACC TTGCAGGCTT GTGTGGACTG 540
AGTGTGTTAC GGCCATGAAA ACACCATGTG CTCTATAAGG TGCGCTTTAT TCATTCCTGA 600
AGTGAGCATT TATCATGCAC CCACGTTCAT GCCAAGCCCT TCTCTGGGAT CTGGGGAGAC 660
AGCAGCAAAC ACAGCAGATG AGGTCCTGGT CCCTGGAGTT ACTTTCAAGT GGTTGGAGCC 720
AGATAATCAA CCGAGAAAGC CTGACACAGT TCAGACGGCG TTGAGTGCCG TGGAGAACCC 780
ACGCCGGACA GCGTGACGGA GCGGCCTCGG GGCTGGGCTA CTGAGCAAGG GAGGGGCCTC 840
TCTGACTTTG TGATGTCTGC ACAGAGGCTG AGCGGTGTGG TGCAGGTCAG TGATGGAAAG 900
CTGTTTATGG GAAGTGTCAA GGGATAGCCC CAAGGAAGGG AGGAGCTACA GCGGGTGAGG 960
AACAGAAGGC TAGGGCAGGG AGAATGGGCA AGGGGCCCAC CGGGCAGTGC CTGTGCACTA 1020
GAGGTGGTCT CTAGAGGTGG GAATGTCTTT GTGGACACGT GTCCTTTGCT TAGGACAGCG 1080
GAGAGAGGCT TCCAGGTCTG GGTGGGTGAG AAAGAGGGAG GAGCTGTCAG GCAGAACCAT 1140
GGAGGTAGGT GGTAGGAGGT AGGAGGTAGG TGGGAGGGTG AGGCACCTGC TCTGAGCCCC 1200
TTCTCCCTGG GCAGGAATGG GGCATGTGGG CAGAGCAGAG GGAAGCAGCG GTGCAGGAAT 1260
GGCCCTGACC TGCACAGATG TGGGAGGAGG TCCGCACGCC CAGAGAGGGG CTGAGATCAT 1320
ACCACCAGGG ACCTGGTGTT GGTTCCACAA GAGGCTCAGG GACACACTTC CAGAATTTTG 1380
AGAGCACCCC TAGCAGAGGC AGGGACTTGG ACTGGTTGAC CTGGCTTTCC CACACCCTCA 1440
AAACCTCAAA ATGTCCAATG TCCATCCACT GATCATGATG GGTCTTTCTA GAATGTCATT 1500
TTCTCCCCAG TGCAGTTGGT GAGAGGCATT CTCACCTCCT CCCTGGAGAG TGGGGTTCCT 1560
CCTTACCATT GCCTGGTGGT TGAGCTCTAG TCCTTCTGTC TGGCTGGCCG TGTAGCCTTG 1620
GGCAAGCCGC TCCATCTCTC TGTGCCTCTG TTGCCTGGGC TGTAAACAGA AGTGAGCTAA 1680
AGGCAGGCAG ACCGAGGTCT GTGACCACGT AATAACTCAT ACTCAGTTCC AGAAATATTC 1740
ACCCACAGAA GTGTCTGGGA CAAGCCTGGA AGGCTGATCA CACCAGCCCT CCGGGTGCTG 1800
CTCGTGGCTG AGAGAACAGA AGGGAGCCCT GTCCACCATG GGAAGCTGCT GTTTCCATCA 1860
CCAGCCTGGG CTGTGGTGCA GAAAGAAGGA AGGGGAGTCT GGGTGGGGCG AGGGAGGCAG 1920
CAAAGGGCCT GGACCTTCGT GGGAGCACGG ACACACAGGA CAGCCATTGT CGAGCTTGGA 1980
CTGACCCTAC TTGGTGACGT TAAGTTCTCA AGCTCCAAGA AACAGCATCT GAGTTCTTGA 2040
GCTCAATCTT CCCACCAAAG AAAATCATAC ACAAGTCCCG GCGCAGGGGC TTCACAGCTC 2100
AAAGCATGGT CTGTGTCCAC ATTTCCTGTG GTGGGTCAGG CCCCACTGCA GTCCTGAGCC 2160
AGCTCTGCAT TCCCACCAGA GCCCCAGGAG ATCAGATGCG GGGTGAACTC TGAGAAGCGC 2220
TGCTCTAGGG CACAGGTAGG CTCATTGCAG CCTTGTCCCC AGCGGGAAAA CGCGGTGGAC 2280
CTGCAGCAGT CAGAGGCAAG GCACACTGCA AGCTCCAGGA ACAGGCAGGA CCCGAGAAAC 2340
GTAGGTGGGT GGAAGCAGGA AGAAGGAGAA CCCAGCGCAA AACTGATGAT GCATATTAAA 2400
AACATGCACA TGGCGGCTGG 2420
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