| Tag | Content |
|---|
EnhancerAtlas ID | HS133-23434 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr3:187768870-187771220 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr3:187769889-187769900 | GTCTTTGTTTT | - | 6.14 |
| | | 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 |
| GH03I188050 | chr3 | 187768755 | 187771673 |
| Enhancer Sequence | AGGAACTAAG TCCATGATGA CTAGAGGAGC ACTGGTTAGC TGAAGGTCTG CCAAGCTTGC 60
TGTAAAAATA TTTCAGCTTT AGGTGAGGAG CTGCACTGGC CAACCTGCTT CCTTGTAGCT 120
CCAGGGTTTC ATGCACGGGG TCTATGAATA GCCAAAGCAA AAGGCCACAC TAAGCATCTT 180
TTCTGCTCCT ATCCCCAATC TTGAGTTCAG AAAGATCTGC TAGGGATCAG TGCTTTAAAT 240
CATCTCTCCT CACTCCCTGT AGAAAAGCCC TCCTTCCAGG AGCTGACTAA TGCTTACTGT 300
CCTTTCCCAA GGAGCACTTT TTTTTTTTTT TTTTAGACAG ATTGTTGCTC TGTCACCCAG 360
GCTGGAGTGC AGTGGCGCGA TCTGGGCTCA CTGCAACCTC TGCCTCCCGA GTTCAAGCAA 420
TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATTACAGGC ACACACTACT ACGCCCAACT 480
AATTTTTGTA TTTTTAGTAG AGACGGGGTT TCACCATGTT GGTCAGACTG GTCTCCAACT 540
CCTGACCTCG TGATCCACCC TCCTTGGACT CCCAAAGTGC TGGGATTACA GGCGTGAGCC 600
ACCGCGCCCA CCCCAAGGAG CACTTTCTGT TGCTTTCTGG GCAGGCTGTG TTTTTACCCT 660
GTGCCCATCT CTCTCTCCCT GGCCCTCTGG TCTGCCCGGC ACAGGTAAGG AGTCCGAGAG 720
TCACCCTTCT CCTATGAGTA TTCCGGTGGC TGCTGCTCTA CCCTTGGGAG GTGGAAAAGG 780
CACCAGCACA AGGCTTCCCC CGCCCACTCA TCTCAGCTTC TTGCTTTCTG CACTGGGCCG 840
TGTGGGGTGC TGGGAGTTTC GTGATCACAA GGAAAAGAGA TGCGGGCGCC AGGCAGGGAA 900
GGAGGACAAA GAGCAATCCC CTTATTCATG CATTCTTCAG GAAAAAGAGA GAATTTGACC 960
TGAGCCTATT TTCCGAATAA TTCGGCATCA AACAGCAATG AGGCCTGGGA CTTTGCCAAG 1020
TCTTTGTTTT GTTTTGTTTT TTTCCTTTCC TCCAATCAGC CCAAGGCAAT GGGGAGTGGG 1080
AGGGGGTGGA GGGGTGGGGG CTACACGCAC ACTGGGGCTG AGAGGGAATG CTGAGCCTGC 1140
AGAAGTGGCC CATTGACAGC TCCTGCTCAC AGCAGAGGGG CGGGTGGCAC CCCCAGCCTA 1200
CCACCACAAG GGCAGCTCTG TCCTGTGGGC ACAGGGCTCC ATCCCAGCCC CACCGGCTGG 1260
GAGAGAACAA CATTTCCTTA TAAGGCCCCG ACCGCTTTGC CAAGGCTGGA TGGCTCCAAC 1320
AGACTGTAGC TTTCCATTCT CCTCGTCAGC TCCAGTGCAG GCCTTGAATG TAGCCCTTGT 1380
TGTCAGGCTC CTCCTCTCCT CCACAGCCCC CACCTCACCT ACTTCCACTC CCTGCCAGAG 1440
CTAGCCCCAC TGGCGCAGGA TAAACAGCCC AGAGGCCTCT CCCACGCAGG GCCTGCCTCG 1500
GTTCAGGCCT GCTGGAGGCA GCACAGGGTA GCAAAAGGAA CGTGGGAGTC ACAGTTTCGG 1560
CTGTCCCTGT GCGAAGGGAA GGCCCTTTTC CTCATCTGGA AGATGGGGCT CTAATGGCCA 1620
TGGGGTCCAA ATTCTTTGCA TTGTATTCAA AGTCCTTCCC AGTTAAGCTG CAGGTTAACT 1680
TCACTGTTTA ACTGCCTTTC CATACCTTGA AGGCCAGATT TCCCCTAGCT CTTCCTGTTT 1740
CCCCCAAACG CACCTTGCTC ACACAGGCCT CCACTGCTTC GTGCACGTGT TTTTCTCTAC 1800
CTAGGTATTT ATCTGCCTAG GTCACTCATC CTGCAGGCCC CACGGTAGGT ATGCCTTCCT 1860
CCCCTCCCCA GGAAAAAGGA ATCATTGCTT TCACTTCGCT GCTCAACATT TGTTTGCACC 1920
TCTCTTACAG CTTTTCTGTT TTGCAATTGC AATGATTTCT TTACCTGCCT GTTTCCTCTA 1980
TAAGATGATG AGCTCCTCCA GGCTCACATG CTCTCCTCTT TCTTTATGTC CATGAGCTCA 2040
ACCCACAGTA CCAGGCACAT AATCCAGCTT CACAAAAGAT TGCTGCACAA ATGCCTGAGC 2100
ACACAGTGTT GCGTAAGTTC AAAAGAGACA ACTATAGTGC AAATACTTGT AAACTATAAA 2160
GTGCTGTTAA CCCATGAAAT GTAAAACTTT ATCTTGCTAC CCTCCACTCT AATTCTACTG 2220
TTTGTCACAC TGTTACAGCC CTTTTCCCTG TCTGACCAGT TCTGTATCCA GAATTCCAGG 2280
CTCACTGCAA CCCCTCAGGA GGTTAACATC TATCACTAAG CCATTACTCA TCTTTAGAAT 2340
CCCAGTGTTG 2350
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