| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00038 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:1489140-1491550 |
Target genes | | Number: 47 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:1490566-1490581 | GGAGGTCAGAGGTCT | + | 6.26 |
|
| | 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 |
| GH01I001554 | chr1 | 1489709 | 1491347 |
|
Enhancer Sequence | CAGCCTGGGT GGCAGAGCGA GACTCCGTCT CAAAAAAAAA AAAAAAAAGG CACCCAGGCT 60
GACAGACGAA CTGGAGCAGG CCGCATCTGA AGGATGTCAC CAGTGTGACA TTCTCTTGAC 120
AATGCAGCTG AACTGTCTAC TGAAAAAAAC GGAGGATAAA GACCTCATCC AGAGGAGGCC 180
AGTGGTCACT ATGGACTGTC TCAAGCAGGG ATCCTCCTGG GGACCACCAG ACTACGTCAG 240
TGGTGAGAAC TCAGCAGGTC CGGGGGACGT CAGGTGGCCA CGGAGACCAC GTGTCAGTGG 300
CCAGGGCCTC TAAAGAGAAA CGAGGAGGAA GTGCAGCTCC AGGGAGTGGA GCGGTTGTGA 360
GATTCACCAT CAGCAAAAAG TGAAGCTGAG CACGAGGCGG ATCCGGACCA CTAAGGGGTC 420
CCCACGAAGC TGAGCACGAG GCGGATCCGG ACCACTAAGG GGTCCCCACG AAGCTGAGCA 480
TGAGGCGGAC CCGGACCACT CGGGGGCCCC CACGAAGCTG AGCACGAGAC GGATCCGGAC 540
CACTCGGGGG TCCCCACGAA GCTGAGCATG AGGCGGATCC GGACCACTCG GGGGTCCCCA 600
CGAAGCTGAG CATGAGGCGG ATCCGGCCCA TTTGGGGGTC CCCACGAGCC CTCGCTGACC 660
ACCCACACCC ATTTGATGTG GTTGCTCTCA GGATAAACCA CCCAGGGCCC CAAGGTGCCA 720
GGACATACCA GGAAACGCCC CAAACACAGC TCGGTTTTCC TTACCAAGGT TTTCTCTTTT 780
CACTCCCTAG GGGCCTTAGT GGGACCAGAA CATCCCGGGG AGTTAGAATG AGCGCAGCTG 840
CCCATCCCAC AGGAGAACCG AGAGGCCAGG ACCACACTAC CCTGCTATGA GTCACCAGGG 900
ACTTGAAAGG GAACCCACAG GCACTGCCAC GCCAGTGTGG CTGGCACCAG GGACCGCACT 960
CTCCCACCAC GGCCTGGGAA AAAGCCATGT CAGGTGCAGC ACGCTGGCCA CAGGCACTGG 1020
AGCCACGAAA GCAACAGCCC TGGGCAGCCC AGCACCATCC TGGGTTCCCT GCTGCCGGCG 1080
CCAGCCCCAC GTACCCCCGA CCACCTCAGC TCCTGGCCCT CAGCCTCTCC TTTGCAAACC 1140
GTGGCTGGCA GCAGAGACTT CCTTGACGTC AAGTCTCCTG AAGGTGTTGA TGCTCCGTGG 1200
AAGCCTTGGT CCTTCCCCGG AAGGCCACAC CATCTTCCCT GCACGTATGA CTCATCCCAG 1260
AGCATGCTAA GTGCTGCTGC CCTGACAGAC ACACCCACGA GGGGGGCCAG CTATCACCTT 1320
ATTGGCCAGA TTGTCCCGGT AACTGAGTGA CGGGACACAC AGGAACACTG CAGAGCCTGA 1380
CAGCCATGCC CCTGCCACAC ACACAGAAGA CTCCCCACAT CAGAGGGGAG GTCAGAGGTC 1440
TCAAAGGTCA GGTTAGAGCT GGGTCAATCC GTTTCCATGG CAAAACTCAA AGCACCGACA 1500
CAGGAGGCTC CGGTATCTGT GCTCCTGGTG CATGGCGGGG ATGAGACAGC CTCGGCGGCG 1560
CTGGTGGAGC TCCTGGGAGC CTCGCTCCAG CGAGGACAGA GCTGCAGCTC AGCACAGTGA 1620
CTGCCCAGGG CTCTGACCCA GATGCCAACA GCCTGGGCAG TGGCACCTCG GCCAAGAAAG 1680
GAGGAACCAG TGCTGCAGGG GCCAGGTGGC GGCTGTGGCA GGCATGTCTG GAGGGAGTGT 1740
CGTGCATGTG GGTGACAAGA ACAGCCGAGT GTGCCACAAG CGTGGACGGC AGCTCCGTAC 1800
TCAGAAGGGC ACGGTGAGAA GAGCAGGTGA CACCGACACG GCTGTGCACA GCACGATGCT 1860
CTGGGCTCCC GGGATGGACT GGGATCCACT CACCACACTA TGCCACAAGC TTGCCAGCTA 1920
CCACTTCCAT GTCAACGTAT CAAGAAATAC ATCTGGGCCG GGCACAGTGG CTGACACCTG 1980
TAATCCCAGC ACTCTGGGAG GCCAAGGCAG GCAGACTGCT TGAGTTCAGG AATCCAAGAC 2040
CAGCCTGGGC AACAGGGCGA AACCTCATTT CTACTAAAAA TAAAAAAATC AGGCCAGGTG 2100
GGGTGGCTCA TGGCTGGAGT CCCAGCTACT CAGGAGGCTG AGGTGGGAGG ATTGAGCCCA 2160
GGGACATAAG GCTACAGGGA GCTATGATGT TACCACTGAA CTCCAGCATC AAAGTCAGAG 2220
CGAGACCGTC TCGAAAAAAT AAATTCACTT TGAGGCTGGG CATGGTGGCT CACTCCTGTA 2280
ATCCCAGCAC TATGGGAGGC CAATGCGGGT GGATCACTTG AGGCCAGGAG TTTGAGACCA 2340
GCCTGGCCAA CATGGCAAAA CCCCATCTCT ACAAAAAATA CACAAAGTTT GGCCAGGCAC 2400
GGTGGCTCAC 2410
|
