| Tag | Content |
|---|
EnhancerAtlas ID | HS133-24628 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr5:1068090-1070270 |
Target genes | | Number: 19 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GCM1 | MA0646.1 | chr5:1069620-1069631 | GCACCCGCATG | - | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I001067 | chr5 | 1067761 | 1068190 |
|
Enhancer Sequence | CCGGAGGACA ACTTTACGAG CGGGGAGCAA GAACACCAGG GCCTTAGGAC CCCTTTTATG 60
CCAATCAGTG CCACACAGAA CAGAGCACAA GGGCGCGCAT GAGCCTCCCT GGCGACTGCA 120
TGAGTCACGA AGCTGCACGC TTCTTAGAGA AATGTCCATG CTTTACAGCC TTGCCCAGAC 180
AGGCTGCCGT GGCTCACACC TGTAATCCCA GCACTTTGGG AGGCCGAAGC AGACGAATCA 240
CTTGAGCTCA GGAGTTCGAG ACCAGACTGG CCAATGTGGC GAAACCCCGT CTCTACTAAA 300
AATACAAAAA TGAGCCGGGC GTGGTGGTGG GCACCTGTAA TCCCAGCTAC TGGGAGGCTG 360
AGGCAGGAGA ACTGCTTCAA CTCGGGAGGT GGAGGTTGCA GTGAGCTGAG ACGGCGCCAC 420
TGCACTGCAG CCTGGGCAAC AGAGGGAGAC TCTGTCTCAA AAAATAAATA AAAATTAAAA 480
AACAAATAAA TAAAAAAGAT TTGCCCAGAT TTCTCTAATT TCACACTAAC ATAGCCACGA 540
TGGAGGAGAA TACGGCTCCC CAGGGCAGTG CAGCCCCAAA GGCAGCCAAG GGAAGGCGGG 600
GCCTGCGGCT GGCTCCAGCC CTCGCAACCA ATGCAGCTAA GTCACAGCCA AAGGCTCGCT 660
GAGAGCAGCG GGGGCAGGGT GCGCTCGTCC TCCCGTCCGC AAGAGCGGGC TCCTGTCTGA 720
GGCTGCCCCA GACCCCCCAG CCGAAGGGCT GTCGGACGGA GAGGATCTGC CTGTGAGCTC 780
CGTTAACGTG AGAGTATAAG TGAGCGCAGC TCTTCCCATG GCCGTGAAGA CTGTGGCAGA 840
GCGTGGCAGG GGGTCCCGTC ATCCCCCAGT CACTGCAATC CCTGCCCTGT CCCTCGTGCG 900
CACAGACGCG CCCTCACACA CCTCCAGGGA GGCCAGGCAG TGCCAGGATT CTTAGAATCC 960
ACGCCAGCAG GGCAGTTCCA ACTCCGGGAT TCCTCCTAAG AGCATTCCAG CATGGGATAA 1020
GGAACACGGA AAGGGACATA TGGGGACCAG GACCGTGAAC ATCCCCCCGA AAACCACGAT 1080
ACCTAAATCC ACGGGTTCAC AGTCAATAGC AGCTAACGCC TGAACCCGTG GTGAGCCATG 1140
ACGCCGCCGT CAGGGAAAGG GAAGGCCCAG AGCATCTCCT GTCTTCCCTG GGAAGGCGAA 1200
CCTGTGCAAC AGCCTGAGAA GGTGGCCATC CACGTGGCCA ACGTGGCGGG AGCGGCGGGG 1260
GCCATTTTTT ACCTCCATGG GATCCTGGCC CTAGGCCACA CCACCTGAGG CTGCTACCAT 1320
CCACGTGCCC ACAGCCCTCT TGAGCAGGGT TCCCACCCCT AGGCTGACCG GCCCAGACCT 1380
GGACGGGCCT CAGTGCGGCT GTGGTTGTGC AGAGAAACGG ACCGGGGAGG CGGTGGGGGG 1440
CGGCTGCAGA TGCCTGGACA CACCCACAAG GTCCCAGTGG GGGCCTGGCA GCAGGGAGCT 1500
GGCTCCCAAC CCACAGCAAG GACAGAGGGG GCACCCGCAT GGGAGGGACC TCGGACACAC 1560
ACCACTGCAA CAGGCACGTG GTATAGGCCC CACAGACTCC CACACACATG AGGGGGAAGG 1620
AGGAGGCTCG AGGCGCCCAC GGCAGCCAGC CCTGCCTGGG AATGAGGTGC CCTTGGCATG 1680
AAAATCACGC AGGTGGGCAC TCAAAAGCTC CCTGCTTTAG CAAGAAATAC AGAAGTAACT 1740
CCAGGTGACG TGACGTGACG TGACGTGATG GGACCCCACA GGCTTTCATC GTGTCATCAT 1800
TCCGTTTCTG GATAGTGTGA AGCTTCCCAT AAGAAGTTTG AAAATCAGAG AAATGAAGAC 1860
ACAAAGTCTC AGACCCCGAT GTCCTGGGGC AGCCGACTGC AGCAGCAGGG CTCAGAGCTG 1920
GCACCAGCAT GCTACACGCC CGGGGCACTC ACCCGTCCCT CCCCACAAAG CTCTGAGTGG 1980
GCAGAAATTC AGCAGCACAC GGCATCACAC TTAACGCAGC CCCCAGTGAG CCCCCAGCAC 2040
ACGGGCATCA CACTTATGCA GCCCCCAGTG AGCCCCCAGT GAGCCCCCAG CACACGGGCA 2100
TCACACTTAT GCAGCCCCCA GTGAGCCCCC AGCACACGGG CATCACACTT ATGCAGCCCC 2160
CAGTGAGCCC CCAGCACACG 2180
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