| Tag | Content |
|---|
EnhancerAtlas ID | HS133-18777 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:25845680-25847200 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr20:25846226-25846246 | AACCCAACCAACACCATCCC | + | 6.06 | | ZNF143 | MA0088.2 | chr20:25847163-25847179 | TTCCCACAATGCCAAG | + | 6.18 |
|
| | 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 |
| GH20I025865 | chr20 | 25846075 | 25847036 |
|
Enhancer Sequence | TGATGCTAGA AAAGAGGCTG CTCAGGATGA GGATGAGATT TCAATTGCTC CAGGACCGAC 60
GCATCTCCTC ACGTGGGCCA GGCCTTCACA CACCCAAAGC GGATCCGCGG CCGCGAAAAC 120
GATTGACAAC CGGCCTCATG ACCCAGGCAA AGATGCAGAA AGAGGCTCAC CAAAGACAGG 180
CCGCCATGCG AGAAACCGCT TTGTGGCACA CAGGGCACAT TCGGCCAAAG ACACACATGG 240
ACACGGGCAC ACACACACAA ACCCACAGAG AGAGGGAAAG AAACTCACAG AGATTGAGAG 300
ACAGAGAGAG AAGAGAGAAT GGGAGACACA CACACAGACA CACAGATACA CACACACACA 360
CACACACACA CACACACAGA CACACACACA GAGTCATACA GCAGAGGCAT GAAAACACAC 420
ACCCCCAGGC AACCCCTGAG GCTGCGGGGT TCTGCTGTCG ACCCTCTGGT GAGAGAGCAC 480
CCTAGGGGCA CGCATTCCAA CCTGTCTTCG AGATCTCTGA CGGCGGCACG ACTTTTGGGG 540
AGACTCAACC CAACCAACAC CATCCCGGCA GGCCTGAGGC TGGGATGCCG TGCTGCTTCC 600
CCAGGACTCC GCCTGGGGTT TCCTCATCCT GGTCGGCCCT TTGCGACTCC TGGCATCCGG 660
AAACCTTCCC GTCGACCCCG TGGAGAGGTC AGGCCGGAGC CTCAGAGCCC CGACACACAA 720
GCACTGGCAC AGAGGGCTCC TGCTTTGCCG AGCCTCAGAG ACTGGTTTCT AAGACAACTG 780
TGGGAAGCAC TGTGACGGGA GAAGCCGCTC GCACCTCACG CATGCGCATT GGCTGGGCCG 840
ACTCGCTCTC CGCTCCTGGC AGGCAGGCTG CGTCCTCTTT AAATAATGCC ACCGCTGCGC 900
AGCGGCTGGA TCCGGGCTCC AGTTTGGGGC GGCGTGGGAG AGGCGACCGC GGGTGTCTTG 960
TCCTGTCCCA GGGCCAAACC CCCAGGTGTC CTGTCCCCAG GACCTCCTTG AGCTGACTTC 1020
CACCTTGGGA GGAAGGGGGA GCTTCAGGAC GCCTGCTGTG TTCTCAGGAC TCCCCTTCAG 1080
ATCCCATTTT GGCCCACTCC GAGTGAGATA GGATGGGCTC GCCACATCTG GTGAGGCAGG 1140
CAGGGCCTCG CTGCAGCACA GAATGATCCC ATAGGTCTCA AGGCCTAGTG TCAGCTGCAA 1200
ATTCACTGAT CCATCAGCCC TCTGCCTCCC TCCTCCTTTG AAAGAGCAGT GGCCTGCCCA 1260
GCTTCTAAAA GCCCTGGTGC TCCGGAAAGC CCACCATGCT TTACAGGACA CTTGCAGGCA 1320
GGAACCAGGG CAAATCCGAT GTGGAGACCA TGTGACCACG CGTGGCACTG GCGTATCCCA 1380
CAGCAGATGG TGTGAATGTG TGTCACCGGA GGCATACGGA GCGATGGCGA AAGAAACGGT 1440
GGTGTCCAGG CATGTGCCGG TGGAAGGGTG GAACGAGTGA ACTTTCCCAC AATGCCAAGG 1500
AAAATCGAAG AACACCTGGG 1520
|
