| Tag | Content |
|---|
EnhancerAtlas ID | HS133-18389 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:241312710-241314890 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPIB | MA0081.2 | chr2:241314704-241314716 | CACTTCCCCATT | - | 6.18 | | ZNF263 | MA0528.1 | chr2:241313763-241313784 | AGAGAAGGAGGATGGGGAGGA | + | 6.85 | | ZNF263 | MA0528.1 | chr2:241313766-241313787 | GAAGGAGGATGGGGAGGAGGC | + | 7.95 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_37774 | chr2:241311909-241315234 | HSMMtube | | SE_52304 | chr2:241312770-241314688 | Skeletal_Muscle_Myoblast | | SE_64063 | chr2:241312770-241314688 | HSMM |
|
| | 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 |
| GH02I240368 | chr2 | 241307753 | 241314834 |
|
Enhancer Sequence | AGCCATGATT ATGCCACTGT ACTCCAGCCT AGACGACAGA GGGAGACCCT GTCTAAAGAA 60
TTTTGGGGCA ACACAAACAT TCAGTCCATA ATACTCCCCA TGGACAGGCC ACGCTTCTTG 120
CCTCAGCTTG GATCTTCTAG GCCAATGCAG GTCCCAGCCC AGCAGCCTCA GCGGACCGAG 180
TCTCGGGGGC CGGCAGGGGT CTGTACCTGC TTCCCCGGCC CCTTTACCGC CCACCACTCT 240
GCTCAGGTCT CTGGACCTGT GGGCTTTCCA GGCTCCTTAG ACCAAAGCCC ACCAGCCCGA 300
GCCCAGCATC TGCGCAGGTG CTGTGGGGAC CAGGACATGG GTGCTGGGGT GCACGGCCTC 360
TGTGATAATC CGGGACACAG CACTCGGACG GAGCCTGCAC TGTTTCTTAA ACACACACAA 420
GGTGGCCTGG ACACAGATGC TGGAGTGCGC GGCCTCTGTG ACAATCCGGG ACACAGCACT 480
CAGAGGCTGC ACCATTTCTT ACACGCACGG GTGGTAGCCC CTTCGATGGA CAGTACTCAT 540
TCTCAGACTC TGGCTGGGCC CCTGGGGTGC TGGAACCAAG ATGAGGAATC AAAAACAAGG 600
GTCTGGGAAG TAGCCCAGGC TGAGGCTCCT AGGAGGGAGG GCGAGAAGTA CCCGAGTACT 660
AGGGCTAGCT GGACGTGTTG ACCCTGCTTG GCCTCCCCTC CCAAACCCTG GACCTCAGTG 720
AGCCTGGGTA CTGGGGCTAG CTGGACGTGC TGACCCTTCC TGGCCTCCCC TCCCAACCCC 780
TGGACCCAGG TGGACTGGGG TACCAGGGCA AGCTGGGCAT GCTGACCCTG CCTGGCCTTT 840
CTGGTCTCAT TGTGACTCAG GCCTGGGGGT TCCCGAGGCT CCCAGCTTAG AGGCGGACAT 900
GGCTGTGAGG CCCTCGCCCT TTCCCACTCA GCAGGGATGA GTTCAGGGAT GGCCAGGCCC 960
CAGTGATGTC ACCAAGTTGA GCTTCTGAGC TTCTGGTGCC TGTGTGGGAG CTGCAGCCCT 1020
CAGGAAGAAG TGTCCTCCCC TCCTCAAGGG ACCAGAGAAG GAGGATGGGG AGGAGGCCTG 1080
GCCCGAGGTC GTCTGATGCC AGCCTGGGGC CTGGAGCAGC CTGGAGCCAG CATGCGTTCC 1140
AAGGGGAATT CCTGGGGAAT GATGCAGCCG GCCTCGCTAT CACAAGCTGT CATTTGAGGG 1200
AGAGCCGCAC TCGGAACGCC TCCCAGCCCC AGTGCAGGAA TCCATCTGGC AAGTCTGCCC 1260
TCGGACACTC ACAGGACACT CTTCCAGGAT CCCTGGGCCT CGGGGTGGGG CCAGGGTCTC 1320
AGGGGAGGAA GTGCCCAGAT TCCTGGACGC TGGCCCCGAG GAGGGTCTGG TGGCAGCCAC 1380
CTCGGTCAGG ACGAGGACAG AGCGTCCAGC CCCGTGCCAG CTCAGTGGCC TCAGAATACC 1440
ACAGCCACGT CCCTCCTGTC CAAGGCCCAG CAGTCCCCGG GACACTCCAA GAGCCATCCA 1500
CTTTCTAGAT TTGGGCTTCC CCTCCTCAGT GACCCCAGCT CCTCCCCAGA GAGCAAACCC 1560
TGAAGCAGCT CCTCTGGGGG TCTTTAAGAG GAGAATAGGA CTCGTGCTAT GCTCGGGGTG 1620
GACTGAAATC ATGCTCATCA CACTAAAGCA TACTGCAACA TAAAGCCAGG TGTTTGCAAA 1680
TGAAATGCAA ACAGTCACAC AGAGCCAGCA AAGCTACCCT TCACCTCACT TGCCGAATGA 1740
GGCTGTTCGG CTGAAACTCA GTGTCACCGG GCCCTGAGTC TGCACACTCA CGCTCTCAGC 1800
TGCTACAGAA TGATGACTCG GTTTCCCCAC CGCTCTTTGG ATTCAAGCTG CTGCAAAGCC 1860
CTCCCCAGCC TGGGTGTCGA GAAGTTGCTT GGCCCAGTCG CATGGCACGC CCAGGCAGTG 1920
GGGCCCGCAG ACAGCGTGGG CACCGTTTAC GGATGAATCG ACGAGCCCCT CTTCGCCTCC 1980
ATCCCTACGC GATGCACTTC CCCATTCTCC TGACACCGCA TGGGCTGTTT CTGACTTCCA 2040
GCTACCAGGA GCAAGGCTGC CATGACCTCC TGTGTGTGTA CATCGTGCTG CCGTCACACG 2100
TGCCCCGATT TCCGCAGGGT GCCCACGTCC AGGGTAAAGC CGCTGAGTCA GGGAATCTAC 2160
ATCTTCAAGT TGACCAGGCG 2180
|
