| Tag | Content |
|---|
EnhancerAtlas ID | HS133-28124 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:24772050-24773890 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr7:24772650-24772671 | AGAGGAGAGGGAAGAGGAAAA | + | 6.95 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_29454 | chr7:24772110-24774225 | Fetal_Intestine_Large | | SE_36736 | chr7:24772052-24774026 | HMEC |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 24772167 | 24772415 | | chr7 | 24772828 | 24773057 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I024732 | chr7 | 24772073 | 24774150 |
|
Enhancer Sequence | CAACTATCTA TATAAAAAAG CACCTTCATC AGAACCAAAA ATCAGGTGAG CAATCACAGT 60
ACCTGGTTTT GACTTCATTT TGCTGAAAGA GGCACTGAAG AGGGTAGGAA AGGCAGTCTT 120
GAATTGCCAA CACCACCCCT CCCCTATCTC TGGGCAGCAG CCATGTGGCA GAGAGAGAGA 180
AGCCGTGTGC TGTAGGAGGG AGAGCACAGC AACTGTGGGA CTTTGCATGG AACTCAGTGC 240
TGCCAACACC GGGCAGAACT CAGCCAGCGC CCACTGAGGG AGCATGTAGA CCAGCCCTAG 300
CCAGAGGAGA ATCACCCATC CCAGTGGTCA GAACCTGAGT TTTGGCAAGC CTCGCCACCA 360
TGGGCTAAAG TGCTTTGGTG TTCTAAATAA ACTAGAAAGG CAGTCTAGGC CACAAGGACT 420
GCAGCTCCTA GGCAAGTCCT AGAGCTGTGC TGGGCTCAGA GCCAGTGGAT TTGGGGGGTG 480
GGTACACAAC CTACTGAGAC ACCAGCCAGG GTGGCTAAGG GAGTACTGGA TCTAACCCTC 540
CCCCAACTCC AAGCAGCACA ACATGCAGCT CCAAAAGAGA TCCCTTCCTT GTGCTTGAGG 600
AGAGGAGAGG GAAGAGGAAA AAGGACTTTG TACTGTAACC AGAATACCAG CTCAGCCACA 660
GTAGGATAGG GCACCAGGCA GAGTTGTGAG GCCCCCACTG CAGACCCTAG CTGCCAGACA 720
TTTCTAGAAA CACCCTGAGC CAGAATGTAA CCTCCTGCCT TAAGGGAAGG ATGCAGTTGT 780
GACAGGATTC TTGTTCTTCT GACTAAAGAG CCCTGGGCCC TGCATGATCT GCAACAGTAA 840
CCAGGCAATA CATGCCATGA GCCTTGGGTG AGACTCTGAG ACATGCTGAC CCAGCTGTGG 900
TCAGGTGTGA CTCGGCACTT TCACAGCTGT GCTGGCTATG AGGAGAGATT CCTTCTGCTT 960
GAGAAAAGCA GAGAGAAAAG AGGACTTTGT CTTGCAGCTT GGGTACCAGC TAAGCACAGT 1020
GGGGTAGAGC ACCAAGCAAG CCCTTCAAGT CTCTGATTCC AGGTTGTGGC TCTTGGATGG 1080
CATTTCTGGA CCTACCCAGG CCCACAGGGG ACCCCACTGC CCTGAAGAGT GCGTCTCAAA 1140
CCTGCCAGCA TTCACCACAA GCTGACTAAA GAGCCCCTGG CCTTAAGTGA ATATGGGTGG 1200
TGGCCTGGCA GTGCTCCTTG TGGGCCTGTA GTGCTGGTGG ACATGGGTGA GAGTCCTCTG 1260
CCTGGGGAAA GGAGAGGGAA GAGTGAAGGG ACTTTGTCCT GTGATTTGAG TGCCAGTTGA 1320
GCCACAGTAG AGTAGAGCAC CACATAGATT TCTAAGGTTT CCAACTCGAG GCCCTGACTC 1380
CTGGACAGCA TCTCTGGACC CACCTGGGGC CCCAGGGAAA TCACCTCATG TCTGAGGGGA 1440
AGGACACAAG CCTGGCTGGC TTTACCACCT GCTGATTATA CAGCCCTAGG GCCTTGAGCA 1500
AACATAGGCA GTAGCCAGGT AGTGGTTACA ACAGGCCTTA GGCAAGATCC AGAGCTGTGG 1560
TGGCTTCAGT TCTGACCAGT GCAGTCCCAG TGGTGGTGGC CACACAGTTG CTTGTGTCAC 1620
CTCTCCCCCA GGTCCAGACA GCTTAGCATA GAGAGAGACT CTGTTTTGGA GAAAGTAAGG 1680
GAAGAGAACA AGAGTCTCTG CCTGTGATCC AGAGAATTCT TCCAGATCTT ATACAAGACC 1740
ACCAAGGTGG TACCTCTACA AGTCTATAAG AACCACACAG TTACTGGGCT TTGGGTGTCC 1800
TCTAATGCAG ATACAGCTGC AGTGACAAAA AACTTGGATG 1840
|
