| Tag | Content |
|---|
EnhancerAtlas ID | HS133-11134 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:24711730-24714250 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr16:24713141-24713159 | CCTTTCCTCCTTCCTTCT | - | 6.47 | | EWSR1-FLI1 | MA0149.1 | chr16:24713137-24713155 | CCATCCTTTCCTCCTTCC | - | 6.96 | | Nr2f6(var.2) | MA0728.1 | chr16:24712905-24712920 | TGAACTCCTGACCTC | - | 6.22 | | ZNF263 | MA0528.1 | chr16:24713137-24713158 | CCATCCTTTCCTCCTTCCTTC | - | 6.21 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr16 | 24711784 | 24711831 | | chr16 | 24711901 | 24712770 | | chr16 | 24712879 | 24713390 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I024699 | chr16 | 24711162 | 24714135 |
|
Enhancer Sequence | ATTTTTAGTA GAGACAGGTT TCACCATGTT GGCCAGGCTG GTCTTACGAA CTCCTAACCT 60
CAGATGAGCC TCCCCCCTTG ACCTCTCAAA GTTTTGGGAT TATAGGCATG AGCCACCGTG 120
CCCAGCCTAT GTCTGAATAT TAAATAAATA AGTAAGTGGT GCTCCAGGGG GTTCCCTCAC 180
ACTCTTCTCT TTCTCTTGCT GCACCCCTGA ACCCTAATGA CCTATGGATC TTCGTGGTAG 240
AGGTGCCATA TTGGCTGTGC TCAGTAACTA GGCTCAAAGT GCTGACCGCT GTGCCTGTCT 300
GGCTGTCTTA GCCAGTGAGA TGCTGTCCTT AGGCAATAGC CTACCTATAT GTTTCAGCCG 360
ATCCCTGACC CCACACCTCT AGACATTCTC CACTAGCCAG CATGTTGAAC ATCTTTTCTC 420
TTGCTTCTTT ATAGCAAACC ACTTGTTCCC TGCCACCCCA TGTTCCGCCA TGGCTACCAC 480
GTGGGCTGAC GCCTTCACAG ACATGTTTCT CTCGCTCTTT GGAATTGTCT GTCACTGACC 540
CAATGCAATA AGGCTGCCCA ATGTGCTCTG GTCATCCCAG GCTGAATTAA TCAAAGTATA 600
AGGCCCAGAA CCAGGGAGGT GGACTTGGGT CAGCCCTAGC CCGGGAAGAA CATTCAGTTC 660
TGGGAGGAAG GGTGCCAAAA GGCAGTTAAG TTCAGAGGCA ATTATCCAGA GAGCACGAGG 720
CTCAAAGCCA AAATGTATGA GTAACATTGA AAGAATTGAG GTTGTGTGGA CTGAAGCAGA 780
GATGACTCAG GCGGAGACTA TTCCCAAATG AGGCTGCAGG GGACTGCAGG GGGAGCTTCA 840
GGAGCTGGGG CTCACTGCCA CTAAGAATTC ACTCCTCTGC TGGCATCTGG CTCTTCAATG 900
CTCCCAAGCC TCTCTGAGTC TGAGTTCCCT CTCCCACCCA CCTTACTAAC TTTTTTTTCT 960
TTTTTTTTTT TTTTGAGACG GAGTCTCGCT CTGTCGCCCA GGCTGGAGTG CAATGGCCAT 1020
GATCTCAGCT CACTGCAACC TCCATCTTCT GGGTTCAAGC AATTCTCCTG CCTCAGCCTC 1080
CCGAGTAGCT GGGACTACAG GCGCATGCCA CCATGCCTGG CTAATTTTTG TATTTTTAAT 1140
AGAGATGGGG TTTCACCATG TTGGTCAGGC TAGTCTGAAC TCCTGACCTC AGGCGATCTG 1200
CCCGTCTCAG CCTCCCAAAG TGCTCGGATT ACAGGCGTGA GCCACAGTGC CCAGCCACTT 1260
ACTAACTTGT CTAACCTCCT GGCTTCCGAA ACCCATGGCC CTGCTATCCC TTCTGTCATT 1320
TTCACAAATG ATTCTGCCTC TTTCCTCAGG AAATTGAGGC CAATAAGAAA AACATTCTCT 1380
GCACCATCAA CTAATTGGTA TCTGAACCCA TCCTTTCCTC CTTCCTTCTG GTCTTATGGA 1440
AGAGAGACTG GACTCCTTCC AAGGTTAATT CTTCCACATG GACTTTGGAG TCCATCCATC 1500
AACTTTGTTC CTATTTCTTC CACATCTCAC ACTCCTATAA AGAAGCCTAA GTCTTTCCTG 1560
TACTGAAAAA AAACAAAAAC AAAAAAAACA CGCCTCTCAA TAACCCCACT GATTGCCTCC 1620
TCTTCTATAT GCAGGGACCA TGTGTCTTCT CTTTCACATT TCACATGTAA ACTCTATTTT 1680
CTTTTCTTTT CTTTTTTCTT TTTTTTTTTT TTTTTTGAGG CAGTGTCCAC ATTTCGCGTG 1740
TAAACTCTTT TTTCTTTTCT TTTTTCTTTT TTCTTTTTTT TTTTTTGAGG CAGGGTTTCG 1800
CTCTGTCACC CAGGCTGGAG TGCAATGGCA CAATCTTTCC TCACTGCAGC CTCTGCCTCT 1860
GGAGCTCAAG TGATCTTCCC AGCTCAGCCT CCCGAGTAGC TGGGACTTCA GGCACATGCC 1920
ACCATGCCCA GCTAATTTTT GTATTTTTTG TAGAGATGAG ATCTTGCCAT GTTGCCTAAG 1980
CTTGTCTTGA ACTCCTGGGC TAAAACAAGC CACCCACCTC AGCCTCCCAA AGTGCTAGGA 2040
TTATAGGCAT GAGCCACCAT GCCTGGCTCT ATCAAATCTT CAAACCTTAT CATAGTATAC 2100
CACTGCTATT TAAGCTATTG CAGATTAGAT TGGACCATAT GAAATTGTCA TTTTTTCAGT 2160
AACAGCTTTT TTGAGAAATA ATTCACATAC CCTACAATTC ACACACTTAA AATATACAAT 2220
TTGGCTGGGC ACGGTGACAC CTCTTGAAAC CAGGGGTTCG AGGCTGCAGT GAGCTGTGAT 2280
CATCCCACCG CACTTTAGCC CGGGTGACAC AGTGAGATGC TAACTCTAAA AAAATAAAGC 2340
ATACAGCCAG GCGCAGTGGC TCACGCCTGT AATCCCAGCA CTTTGGGAGG CTGAGGCAGG 2400
CAGATCATGA GGTCAGGAGA TCGAGACCAT CCTGGTTAAC ATGGTGAAAC ACCGTCCCTA 2460
CTAAAAATAC AAAAAATTAG CTGAGCGTGG TGGCGGGCAC CTGTAGTCCC AGCTACTCAG 2520
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