| Tag | Content |
|---|
EnhancerAtlas ID | HS133-26426 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:16635630-16637140 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFF | MA0495.3 | chr6:16636646-16636661 | CTGCTGAGTCATCAG | + | 6.16 | | MAFF | MA0495.3 | chr6:16636646-16636661 | CTGCTGAGTCATCAG | - | 6.1 | | NFE2L1 | MA0089.2 | chr6:16636645-16636660 | GCTGCTGAGTCATCA | - | 6.42 | | Nfe2l2 | MA0150.2 | chr6:16636647-16636662 | TGCTGAGTCATCAGG | - | 6.36 |
|
| | 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 |
| GH06I016635 | chr6 | 16635702 | 16637201 |
|
Enhancer Sequence | CACCCTAGTC TGTGGAAAAA CTGTCTTCCA TGAAACCAGT CCCTGGTGCC AAAAAGGTTA 60
GGGACCACTG GTCTAGAGAG AAGGAGCTCT TCTTACACAC TGCCCAGAAA CTGAGGATGT 120
GACAGAAGTT CAACGAGAGC TAACTAAACA ACTAAGTAGC AACCTGACAA GGGCTCAGAC 180
AGCTCCAACT AAACCTACAC TGCTGCTGCC GCTTACAAAA GCTCATTCAT ATGTGTGAGT 240
TCAGGCAAAA ACACAGTCGT TATCTGATTC TTTAGGCAGG ACATTGACCA GATAAATAAA 300
TATGTCTGAA TCTGCAGAGA AATAATTTCA AAAGGGCTTC AGAAGGAGAA GGAAAATCCA 360
CTGTAGCCAG AAGCATCCAA AAGCATCCTG AAAACATGAG TGGAGGAAGG CTGAGCAGGT 420
GTGGGCTGGG GAGGCAGGCA ACCCCGCACA GCAGCCAGCA CAAACACAAA GCGACGACGC 480
CCACTGTGCT GGGGAAGCAC AGGCAGCACA GTCCGTGCAA GGGAAACGCG GCTCCCTACA 540
AGGTGTTTTC AAGGTTCCGG TTTCCCCAGA GCACAACCCT AACCTCAGGC AGTGCACAGT 600
TCTCCCAATA AAAGTCACTC GCCCGTGGAG ATCACCGAAC ACCTGAATTG ACACCACGGG 660
CACTTCCAAC CTGTGTTCCT GACCACCCTC CCCATGACCT GCCTCCCTTA CATCATTTCT 720
GTTTTCCTTT CCCATGGTCC TGTGACTTCT CTTACTCTTT CAAATGCAAA ATGTCACAGC 780
TGAAGGGAAG GAACCTCCAA GGATGATCTG GGCTACTGCT TTCTTCTTCA TAGGGGAGGA 840
AACTGAGATT CCAGAGAGGT TGGTAACTTT CCCAAGGTTA CAAAATTAGC AGTGCAGCCG 900
GAACTGAAAC CTACATTGTG TGACCACTCT CCTCCTCCCA AAGCAATTTA GTTTCCAACT 960
GGACCTCATC TGCCTACTTG TTTCTCCCCC AGCCCCCAGG CAGCCCTTCA CTGTGGCTGC 1020
TGAGTCATCA GGATGAGCTT TGTTCTCAAG CAAGCCACTG GGACAGGCCC TCATGTCTTG 1080
AGTAGGACAA AGTATATTTG GCCACTCCCC ACTTTGTGGT CACCCTGCTC TGCCTGATGC 1140
ATGGGCACCT TCTGCCCATG ACAACTGTCA TTCGCCCTGA ATAGTCTATG CCATCACACC 1200
TCCTTATGGC TACTAACATA AAAGGTAAGT GACTAATAAA TGGTATCATG AATTAATATG 1260
AAACCTTTTA TACAGACAAA TATTTGATTC CTCAGTTATA TTTTCTTGGG ATCTTTTCTT 1320
CCCAGGTCAT AGCAGTGCTG TTTCAACAGG AAATGTCATA GCTTGAATGC CAGGTGCACT 1380
TTAAAAAATA ATCTAAACTA AATTAGCTTT TACACCTAAC GACGGCCTGG GAATAATAAA 1440
GGAACTCTTT GAAAAAGGAA GAAAGTGGAG AAATAGGAAC ACTTTTACAC TGTTGGTGGG 1500
CCTGCAAACT 1510
|
