| Tag | Content |
|---|
EnhancerAtlas ID | HS133-26106 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:2521900-2524080 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr6:2522149-2522164 | TGAACTCCTGACCTC | - | 6.22 |
|
| | 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 |
| GH06I002521 | chr6 | 2522154 | 2524150 |
|
Enhancer Sequence | GTTTTCAAAA TATTTTAGTG GTGGTTTTAC TTTATTTATT TATTTTTTGG GATGGAGTCT 60
CGCTCTGTCA CCCAGGCTGG AGTGCAGTGG CATGATCTCG GCTCACTCCA GCCTCTGCCT 120
CCCAGGTTCA AGTGATTCTT CTGCCTCAGC CTCCCAAGTA GCTGGAATTG CAGGCATGTG 180
CCACCACGTC TGGCTAATTT TTGTATTTTT AGTAAAGACA CGGTTTCACC ATGTTGGTCA 240
GGCTGGTCTT GAACTCCTGA CCTCAGGCGA TCCACCCACC TCGGCCTCCC AAAGTACTGG 300
GATTACAGGT GTGAGCTGCT GCACCCGGCC CTGTTTATTT GTTCTCTAGT TTCTAATTTT 360
ATTATTGACT TCTTATTTTA TTGAATTATG ATAAAAATGT TTGTACATTT TAACTTAAAA 420
ACAATTGATG TTTTCTCTCT GCCTGACTTA GTCCATTTTT ATGACTATTA CTGGATCATT 480
TGGGAAAAGG ATTCGTTCAT TCTCTAATTT GAGAGTATAG CATCTGACAT ATAGCAATTA 540
GATCCGTTTC ATTACTGGTT TAGGTCTTGT TTTTTTACAT TGTATGTGTG CACATGTGCT 600
TGATCTAACA TGAACTGAGT TTCCTATTGT CGGTGAATTT CTGCATATTT CTTCTTGCAT 660
TTCCTGTGGG TTTTACTCCA TCAGTGTTGG TGCTGTGCTG TACGGCGCAA ATTCATAACA 720
ATTATATCAC TATTGGGGAT TGCAAACTCC AGCATTTTAA AGTGTGTGTC TTTGTGAATT 780
CTATGATCCT ACCACTTAAA GCACATGTGT TTGAGGGCAT ATTTTTATAG CACAGCTGTT 840
CTGAAAACAC AAACCAACCA AGGCCAAGGA AAGACAAGAG CCTGATTCTT TTAAATTTAT 900
GATGATAACA CTAAAATTCC TTCTACAAAG CGAGCTTCCC GGCCTCAGAA AATGGCTTCA 960
GTTCAAGTAG TAGGATCTTT CACAAAAAAA TTCTCTGTCT ACACATATTT GAACCTTTCT 1020
GACCAACAGC AACAACAAAA AACATAACAC AACAATGTAA AGAGCACATT ACTCATGACT 1080
AATCATCTAA CCACAGAGGG AACTTCACTT CCTTCCTTCT TCACCACGTC CCCTTTTCCT 1140
CCCCAACCTC GCCCCCCTCT ACCTTCTCTC TTGCTGTCTC CTGACGTGTA TCCCTTGAAT 1200
AAATGTGCTT TTTCCAAAGA AGATCGCTCC TGGCTCCTGC TCTCTCGCAG CTACTGACCA 1260
GTTGAACTCA GGGCGCTGGG TCCACTGGTG ATTATGTGTG GGCTCCCACA GGTGACAAAA 1320
AGCCCATCTG GACTGCAGGG TCTTTAAACC CCAACGCTTC ACACGTTCAA CTTCTCACCC 1380
TTGAGAGTCT GTCACTTAGA GTTTTATTTT TCTACTCCCA CTCTGTGCCA CTCTATCCTG 1440
TAGACTCATT TTACAAAAGC AGCAAAATCT AAGTCTGACA GGTAATCCCA TCTCTCCAGA 1500
TTAGATGAGC TGGAAGCAAC TTCTTGGCCC TGACATGTTG TGCAGAGGCA CACAGCCAAC 1560
CTTTGAAAGA ACAAATGGGG GAAATTTGGA AATAGAGAAA GAGTGATGTC TCATGACTGT 1620
TACTATGATT TAGATTAACA CATCTTTGGC CTGGGCCCCG GAAGTTGGAT TTTCTTACAA 1680
GGTGGACATG TATCAACACA GAGCCTGCAG AACACGTAAC TGTACAAGGC ATACAGTGAC 1740
CAGGAAGGGC AAAGACTCGC TAGTAGGCAA CACTTTATCC TAGGGCACAT AAGTATCAGA 1800
GAAAGAGGAC AGAGCAGTCC TGGAGTCTTT CAAGTTGGGT CAGATCACCA TAGATTTTGA 1860
ACAAAATTAG TATCTTGGAG TTTATGATGA CTGGGTTATG AATGCACCTA TTAGGAAAAT 1920
AGCCTATAAT TTTTAGAAAC CAGAAGCAAT TGACGATTAT GGATGTTTTA GTATTTTATT 1980
ATGAGATATT ACCTATTGGA ATTTTTTGTT TGGGGAATTT TAGCAAGATA TTAAATCAAG 2040
AATAGATAAA CATCCAGATT ATTGGAAAAC CTTGGTGATG TAATTTCAGG GTCACTTTGC 2100
TACGTTAACT CATGGAGCAT CATCACAGTA CTACCAGAAG CAGGGAGCTG GGCAAGGTCC 2160
TGCTTGTTTA CTTGCCTAAG 2180
|
