| Tag | Content |
|---|
EnhancerAtlas ID | HS133-03268 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:204056300-204059640 |
Target genes | | Number: 11 | 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) |
| POU2F2 | MA0507.1 | chr1:204057583-204057596 | GGCATTTGCATAT | + | 6.3 | | Pou2f3 | MA0627.1 | chr1:204057582-204057598 | TGGCATTTGCATATAA | - | 6.44 | | SPDEF | MA0686.1 | chr1:204058253-204058264 | TACATCCGGGT | - | 6.62 | | ZNF263 | MA0528.1 | chr1:204057285-204057306 | CCCTCATTTACCTTCTCCTCC | - | 6.47 |
|
| | Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
| SE_01182 | chr1:204056274-204058246 | Adrenal_Gland | | SE_01182 | chr1:204058247-204059454 | Adrenal_Gland | | SE_03017 | chr1:204056278-204058243 | Bladder | | SE_03017 | chr1:204058249-204059534 | Bladder | | SE_04661 | chr1:204056379-204058327 | Brain_Anterior_Caudate | | SE_04661 | chr1:204058370-204059675 | Brain_Anterior_Caudate | | SE_06365 | chr1:204056169-204060053 | Brain_Hippocampus_Middle | | SE_24644 | chr1:204058329-204058842 | Colon_Crypt_2 | | SE_31799 | chr1:204056312-204059529 | Gastric | | SE_41791 | chr1:204056249-204059508 | LNCaP | | SE_42361 | chr1:204054906-204059621 | Lung | | SE_47675 | chr1:204057012-204057426 | Pancreas | | SE_47675 | chr1:204057647-204058068 | Pancreas | | SE_47675 | chr1:204058262-204059202 | Pancreas | | SE_49400 | chr1:204056234-204059271 | Right_Atrium | | SE_50648 | chr1:204056148-204059540 | Sigmoid_Colon | | SE_53078 | chr1:204056234-204059443 | Small_Intestine | | SE_54451 | chr1:204056226-204059533 | Spleen | | SE_65332 | chr1:204054712-204059717 | Pancreatic_islets | | SE_68685 | chr1:204056205-204059260 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 204057041 | 204058591 | | chr1 | 204058173 | 204058362 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I204087 | chr1 | 204056343 | 204060013 |
|
Enhancer Sequence | CGGCCTCCCA AAATGCTGGG ATTACAGGCG TGAGCCACCG CGCCCAGCTT TTCTCCTTCC 60
TTCCATGACT TCTGCAGAGG CAAAAGGGCC AGGCTGCCCA TCACCTGGGT AGATAAGTCA 120
GGCTGGGAGG CCTAGGACTG CTCGCCTTAT ACAGAGGGGT CAGGTGCCTG CCTTCCCAGG 180
GGCACCAGCT GGACCCTGCT GACTCCATGG TGGCTGCAGC TATCTGTTCC AGGACCTTCC 240
TGTAGCTTCC CAGGGCCTGC TCCCTGTGCA TGAGGCAGTA GGCCCCCCTG TCCCACCTTT 300
TCTTATGGGA GCACCCTGAC ATCTCCCCTT TCTGTCTGTG CTGGTGTTTC CGGGAGGTGC 360
TGGGACCACC AGTGCTAAGG CCCTGGTCTA GCTTCTACTG CTAATGGCTT GTATGCCCTC 420
AGGGCTGTCA CTTAGCCACT TGGAGCCTTA CTTCCTCCAT CTGCAACTTG GGAAGGAGCA 480
TTTTGAGTTC TCTTGCTATA AAGTAAGAAT TCTGGTTTGC TGGAAATAGA GTTAGATGAG 540
GATGATGACA ACCACACTGG CAGTTTTTGC TGCAGTTTCA AAGCCCGGAT GTGGAGTCAG 600
ACACTTTGCC ACAGCCCCGC ACAGGATGCT TCTGTGAGGC TTGTCTCGGG TACCTCATAA 660
AACCTTCTAG TTTGGAAGGG CAGGGAGCAT CTACTCCTCA GATTTGGCAG ATGAGGATAT 720
TGGAAATTGT CTAGGTAGTG GGGCTTCCAG AGTCCCACCT GGCTGTGGAT CTGCAGGGAT 780
GAGGCTGGTC TATGCGGTAT GTCTGACTCT GTTCAGAACA AGTGACAGCC CACACTGGGA 840
TCTTGCTTTA GAGTCCCTTG GCCTCCTGCC CTGGCATCTT GCCATTGGTT TTGGGGAAAT 900
GGTGATGGGA AGGGCCCATT GGGTCTCCAG ACAGTCACAG GGAACCATCC TGAGACTGGA 960
TCTGGAAGGA TGTGTGCTTG TAGGGCCCTC ATTTACCTTC TCCTCCCTCA CTTCCCACCT 1020
TGGCTGTGGA CGTAGCCCTG TTTTCTCTTC CCCTGTGGTC ATGTTTCTCA GATAGCCACA 1080
AAGTGGGCTG AGACCAAGGA GAGGCATTGG TGCAAAGGGG ATGCTGGTCG ATTCGGCTGG 1140
GGACACTACT CTGGGTTCTC CTAGCCAGGT GGTCAGATGA CTCCCTACGT AGCCTTGGAA 1200
ACTGCCCAAA TAAGAAAGAG AGCGAGGCAG AAAGAGCAGC AGGGACACTC GGATTTTTCC 1260
AGGGGCTTTG TCCATATTTA CATGGCATTT GCATATAACC AGTACACTAA ACATAATTTT 1320
ATAATCTATC CCCAGGCACA TTCAGATTTG CCTTTTACTC TTGTTCTTTC CAGAGATGGC 1380
TGGTTCTGCC TTTTTGCACC TGTCTGTGCC TTCTCACTCC TGTCCCGTTA CCCCCACTCC 1440
CAGACTGGGG GTAGGTGACT GGGAACAGAG TCAGTGTGGG GTAGGGGTCA TTCCTGCTGT 1500
TGAACTGATC TGATAAGATG AGATCAGACC TGACCTCTCT GGGCTTAGCA CAGACGGCTG 1560
GATGCACAGG CCCAGCCTCC CCTCTGCATC CCACCCCAGC GGCCACCACC TCGCCTCGTC 1620
AGGGATCAGG ACACCATGCC TGGCACTCAG CAGGTACCCA TTAAATGTGA AGTGAAAGCT 1680
CAATTAGAGT TCGGACAAAT ACATACTGTG CAGGCTCCTC GGGACCTGGC TTTTGAGCTC 1740
ATGAAGGGAG ATGCTGGTGG GTTGAGGGGA GCCTCCAGTG GTCCAGAGGG TGGGAGGAAT 1800
CAATTTCCCT CTCAGCGATT GTGACCAGGG AGGCATTTCT TTCTCTGCTT GGCCTTGCAG 1860
GAAACAGTGT TGAGAATGAG AGGAGCAGAA AGGAAGAGCT AGGCCTTGTA TTAATTTGTT 1920
TTTCAGATTG AGTCTCTGTT ACTAGCAATT TATTACATCC GGGTCTCCAG CCAAGCACAT 1980
TCTGTTCTCC AGTGTTGGGG GAAGATGCAT GGGGGGGTGG GGAAGAGGCT GGACAGGAAA 2040
GAGGAGCAGA TCAACAATTT TATGACTGAG TGTGTGGTGT CTTGGCGTGC GCTAGAGGAC 2100
GGTTTTAGCA CAGGGCATTT TGAGCCCAGC CCCGTGTGGG GAGGCACTCC TCTGGACAGC 2160
ATGGCATTCC CATGCGAGCC CAGACAGCCC TGGGGAGCAG GATGAATGGG CTTCCCTCCC 2220
ACTCTCATGC CCGCCGGCCT CAGGGTCCAG ATTTCTCTCT GTGAAATGAG GTCAGGACAG 2280
TGATGCCTGG AACAAAATCA TAGTTTCTTG AGGCAGCGGG GCCTGGGGAG ATCCCTCCGA 2340
GGAACAGGGG AGCAGCTGTG TGAGGGGACC CCGGAAGAGG GGTAGCAGGC AAGGCGGCCA 2400
CCCTGTGGAA AGAATGGTGC ACAAGCAAAA CAACCCCCTC TCTGCAAAAG TGCTGAGCTG 2460
GTGGAATTTC ACTTGGCGGC TGTGAGATCA GGGCAGTAGA TAGAGCCCTG CGGGCACCAG 2520
GGCTGTGTGG GTGCAGGGGG TCCCGGAAGA GAGGGCAGGG GCAGCACCTG TGGCACCCTC 2580
TCCCCTGAGC TGGCCTCCAC ATTGCCCAGG GCTCATCACT GGTCCCCATT CCTGGAGGTG 2640
CGTCCCTTAT CTCTATCCAC CTGTCACGTA AGTTGGTCTC ATTCTTCCCA TTTTCCCTCA 2700
TTCTCTTCCC AACTGTGGCT TTGACTAGAA GTAGCTACAT CATCTAGTCT TCAAGGGGCC 2760
AGCATTGCGT AGAGGGCCAT GGTGCCAGAG GGCAGGGAAC TCTGGTAGGA GGAACTCTCT 2820
CCGACCAGGA TGGTGGTGGC TGAAGCCCCC GGGGCCTCTG CCTTATGGCT GGGCCTCTGG 2880
TGGGAGCCCA GGCTGCTTAG GGGAGAGTGA ACCCTTCGGT AGTGGTTTTT TGCATCCCAG 2940
CCACATCTTC AAGCTGGGTG CCATTGGATG GTTGTTGAAG GGCAGATTCA CTGGAAGGAT 3000
AAGAAGCTCT GGTGGGACTC TGGGTAGAGC CAGCACAGAG AATGTGTGTG TTGGGCAGTC 3060
GGGGAGAGAG GGTGTTAGGC AGGGAGAGCA TGGGCCTGGT TTCCAGCTGT GAGGTTTGAA 3120
CTATTATTAT CCTCCACACT GAGCTGATGG CCACTTAACC CTGAGGCTGG TTACTTGTTC 3180
TCTGTTCTCT GGGTTGACTG CCTCCTCCCT GACTAGCTCA AGACTTCTTC TTCTTCTTTT 3240
TTTTTTTTTT TTTTGAGATG TAGTCTCACT CTGTCACCCA GGCTGGAGTA TAGTGGCATG 3300
ATCTTGGCTC ACTGCAACCT CCGCCTCCAG GGTTCAAGCG 3340
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