| Tag | Content |
|---|
EnhancerAtlas ID | HS133-17695 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:152048160-152050580 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA13 | MA0650.2 | chr2:152048583-152048594 | CCCCATAAAAC | + | 6.02 | | NFYB | MA0502.1 | chr2:152048304-152048319 | CTGATTGGTTCAAAT | - | 6.47 | | Nr5a2 | MA0505.1 | chr2:152049559-152049574 | CAGTTCAAGGCCACC | + | 6.64 | | Znf423 | MA0116.1 | chr2:152049299-152049314 | GCCACCCTGGGTTGT | - | 6.21 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AATTCATGAT TTGGTGGCAT TTTCAAAAAT GGACTTTCAA AATTATTTTC GTTTTTTAAA 60
ATTGCACTAC CAGATGCAAA TTTAGTGATC ATTAAGCCTA CTCTTCTCAT TTTACTGATT 120
AGAAAGGAGA CCCGGAAACA CCAACTGATT GGTTCAAATC AGGCAGCCAT CTAAGGTAGA 180
ACCAAGACCA AAATCCAGCT TTCCTGCTTC CTTATGTCTC TTTTCAAAGG AACAGAAAAA 240
GGACATGAAA AACAGAAGGT CTAGAGAATG CTGATTCTCT CATGAAAGAC ACGGCCTCCC 300
AGGTGACTGG CTCCTATAAG CCTGGCAAAA GCTGCCAGGG GAACAGTCAG TTGTCCATCT 360
GAACGGAAGG AGGCAACTTA AAAGATGAAA GAATCATGAA AGACCCCTGC TCCAGCCCCA 420
GCCCCCCATA AAACTGTTAA GTTTTTTAAG TTTTATAGGC ATATTTGGCT TTAAAGAAAA 480
TCTGAAACAT AAAATCAAAA TTTATAGATC AGATATGTCT GGAAGCACGG TTTATGTTAC 540
AAAAAAATGG AATTTTTGCT TTACTAAACT CTTCACTACA GTTTTCTCTG AAATAATGAC 600
TTCCCTTATG ATTAATAAAT ATCCCATTCA GGTGCAATAT CAGGGCTATT TCTATGGCAT 660
TAAGCAAGGT ACACCTCTGC ACTGTTGACT CCACTAAATT TAGCTTACTT TCTTATTGTA 720
ATTGGGAGGA AAACTCATAG TGTGTGATGC CCACAGACAA TGGTCTGCTG GTGCCAGGTC 780
ATGCCCACTC ACAAGAACCT ATTGTGGGCC TGTCTTCCCA ACTCTGCATT CAGTGGTTAA 840
GGGGTCTGAT AGTTGGTCCT TGGTGGATGA ACACAGTAAG GAATGGAGAA GGCATGAGAC 900
TGTGAAGCAG GTTCGCTGTG TACCAGTTGC CAACTTGTCT GAGTCTAGTG ACAAAACACA 960
TTCATATGCA ACAAGTTCCA GGAAGCAGAG GTATTACTTA CAGATAGGCA GCAAGGAACA 1020
AAAGAAGCAT GAGATCCATG GTGAGCCAGT TCCCCAAGGC TCAAGAAAGC TGCCCAGGCA 1080
GGATGGAATC TTGACTGCAT GTGCCCCACT TGCAGCACAG CTGAGGACCC TGAAAGGCAG 1140
CCACCCTGGG TTGTATACCT CAGGGGCATG TAATTCACTG GGCTAAAGAA CATCTTGCTC 1200
CCAGGGGAGA AAGGAACAAA GCCCAGACTG ACCCATGAAG TTCCTGCCTA ACTCAAGTGT 1260
TACATCCGCT AGGAAGGACA CAAACAAGGC CTAGACTGTT TCAGGCAGCT CCTCCCTATC 1320
TCAGCTACTG CTTTCCCAGC ACATTCTATA GTTATATATA TAGAACTACA GAAACTACAA 1380
AAAGCGGGCA GAACTGAGTC AGTTCAAGGC CACCTAAAAA ACTGTTCTTC AAAAGCAAGC 1440
TTGTTTAAGT TCCATAAGTT GCTTAGCACA AAAAATAAAG GATCATACAG AAATAAATGG 1500
TCCAGGGCCC TGGTGGGATT CCATGTAGCA TGGAGTCTGG GCCTTAGCAG CTTAACTCCC 1560
TGCAAAAAAA AAAAAAAAAA AAAAAAAAAA AGAAAAGAAA AGGGAAGTAT ACCCTACTGG 1620
GGAATGGAAG TTTAGGGAAG CCATTCCAAA GGCCTCAAGT TCTGAGCCAG CCACAGAGAC 1680
CATGGCCCAG GCGATGTGCC AGCATCAACA GGGCAATGAC AGTGACACAG AGCAGCCAGG 1740
ACTACGCTGG GCAGGGGATG CCTGGACTTC ATGTCCGCAG GTGTACCCAT AAAAGAGGAG 1800
TGACTGGGGC CATCTCACAG CTACCACCTG GAATCTTAAA AGCCCATGGA ACTATGAGAG 1860
AGGACAATTG GTGGGAACAA GTAGGAAAAA AGATACATCT GCACCTCTAA GCTAGTGTCA 1920
TCAGGAGACA TCTGGTAAGT GGAGCATAAG AGATGGGAAA ACACTAAATG AAAGCTACTG 1980
CTTTGGCCTA ATTGGCCCAG ACCTGTCCTC CTAACAATCA AATTTCATTT AGCCTGAATT 2040
ATTTGGTCTC AAAGCCTTAA TGACAGAACA AAGACCTGAA TCGAGAAACA CGCACATCCT 2100
CCACCCACCA GGTAGGGGTC AGTAGTCACT GAGACTATTT GTGTGTGGGA GTAATCACCG 2160
GACTCACAGG ATGTTAATGA CAATATTTAA TGAGGTGCAC TATTTCGCTC TAGCAGAGAC 2220
TAGAAAGTAT TTATAATTAG CAAAGTTCTA ATGGATTTTA TACTGCAATT GGTGCTTATG 2280
TGGGGAATAG CATATTTAGG GTCCATTTAG CATCATTATA TTCCTTATGG CCTCTTTTGT 2340
GATCTTTACC CACCTAACCC AGGAGTAGGG TGATACGAAC CTATTGAACT GTTTGTTATC 2400
TCTTGCTAAA CATAATTGGC 2420
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