| Tag | Content |
|---|
EnhancerAtlas ID | HS175-05494 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr12:7061440-7063760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:7063039-7063057 | CCCTCCTTCCCCCCATCC | - | 6.18 | | ZNF263 | MA0528.1 | chr12:7062408-7062429 | GCCCCCTGCCCTTCCTCTTCC | - | 6.09 |
|
| | Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
| SE_09821 | chr12:7057722-7072113 | CD14 | | SE_10294 | chr12:7057787-7072648 | CD19_Primary | | SE_11246 | chr12:7051570-7075651 | CD20 | | SE_11874 | chr12:7057290-7072000 | CD3 | | SE_13696 | chr12:7059354-7064308 | CD34_Primary_RO01536 | | SE_15448 | chr12:7059390-7063771 | CD4_Memory_Primary_8pool | | SE_15935 | chr12:7059481-7063047 | CD4_Naive_Primary_7pool | | SE_16424 | chr12:7057934-7063850 | CD4_Naive_Primary_8pool | | SE_16892 | chr12:7057515-7065729 | CD4p_CD225int_CD127p_Tmem | | SE_17385 | chr12:7051304-7075645 | CD4p_CD25-_CD45RAp_Naive | | SE_17804 | chr12:7051451-7075926 | CD4p_CD25-_CD45ROp_Memory | | SE_18513 | chr12:7051903-7072452 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19322 | chr12:7057416-7072760 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20105 | chr12:7057420-7072350 | CD56 | | SE_21550 | chr12:7059066-7064151 | CD8_Naive_7pool | | SE_22026 | chr12:7059039-7066905 | CD8_Naive_8pool | | SE_22431 | chr12:7051483-7072746 | CD8_primiary | | SE_32571 | chr12:7058059-7071909 | GM12878 | | SE_50217 | chr12:7059210-7076065 | Sigmoid_Colon | | SE_53937 | chr12:7057924-7072654 | Spleen | | SE_55163 | chr12:7059653-7064143 | Thymus | | SE_59538 | chr12:7045399-7071773 | Ly3 | | SE_59972 | chr12:7045722-7069352 | Ly4 | | SE_62072 | chr12:7045612-7071479 | Toledo | | SE_62347 | chr12:7051577-7074891 | Tonsil | | SE_66670 | chr12:7059219-7064681 | Jurkat | | SE_67220 | chr12:7057771-7064582 | MM1S | | SE_68053 | chr12:6999072-7081180 | TC32 | | SE_68054 | chr12:6999072-7081180 | TC32 | | SE_68055 | chr12:6999072-7081180 | TC32 | | SE_68056 | chr12:6999072-7081180 | TC32 | | SE_68057 | chr12:6999072-7081180 | TC32 | | SE_68058 | chr12:6999072-7081180 | TC32 | | SE_68059 | chr12:6999072-7081180 | TC32 | | SE_68060 | chr12:6999072-7081180 | TC32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 7061503 | 7061663 | | chr12 | 7062635 | 7063280 | | chr12 | 7061911 | 7062149 |
|
Enhancer Sequence | CTCCATCCCC TCCCCTCCCT GCACCAGCTG GGGCTCTCAA TGTCCCTCCT CCCTGCTGTC 60
CTGGGACCTG GTGTCTCAGA GCCTAACCTA CCACCCTTTC CACCTAACCC CGAGGAAGCC 120
ACAGAAAGCT GCCTCGCCCT ACTCCGGGAG CCCTGGCCGC TGCAACCCAG GTCCCACTGG 180
AGACAGGGAG GCCACTGCTG GTGGCCAGCA TGTCGTGCAG GCCAGCTCTG TTGTTAGAAA 240
GCTCTTCTTC CTCTGGAATC GAGCCTGCCT TCCTCCGTCT GCCCCTCACC CCAGCACATG 300
TTAGGACAGT GAGGAGCTGA CACTGGGGTG AAGATGGGGA TGAATGCTTG CCAAGACACT 360
TGATGCCTTG TCCCAGCCGC CCCGTGGGGA TGGGTCTGTC CTGTGGGGTC AAATAGGTCT 420
CCGGCCCAAA CAGAGATCAT TGAGAGCACG ATGTGAAGTG TTCACCTGTG TAAAGTGTCT 480
CACGCTGTCC CGGGCACAGA GTAATACTCC AGGCATTTCC TTCCTGTGGC CTCCCCGACT 540
CCTCCTGTGG TCTCCCAAAG GCATGGGCTG GGGGCTGGGG GCTCTGAATG CTCCTCATGA 600
CACCATGGCT CCTTTCAGCA GCCGCATCTC AATGCCAGAT CCCCTTAGAG TAAAGGGCAG 660
CGGAATAACG CTAGGGGGTT TTCACATGCA CCCCTGGGCC AAGCCGACTT GCCCTTGCCG 720
TGGATCCCTG CATTCATGGA TCGGTTATTG AAATGATCGG GAACCTTGCT CCTGCCAGCT 780
TGCAGCCTCT CTGAGATTCG GGCCTCCAAA CTGCATCAAT ATTTTTGGTC AAGGCACTGA 840
TTGAAACTTA GAGCTGGATT CGGTCACGGT GCAGCCCTGT GGCCCACCTG GGAGGCCTCC 900
TTTCCTGGAT CGGCCTCCTT CAAGGCCTTC CCTCTCTCTG TGAGCCTCAC ATGGCTGGCT 960
CCGTGTCTGC CCCCTGCCCT TCCTCTTCCC CACCGCAACA CTCAGGGGGC TTTTGGCACC 1020
GAGACCCTCT AAAGCTCATG TCCTCTCTTT CTCCTTGCCT CCAGCCAGGA GAGGAGGACG 1080
GGCTGACCAG TGCCTGGAGG TGGAAGAGAG GAGCAGGGCC CCAGGAGGCC CCTGCAGAGG 1140
AGGCTGAGGC CTGGGTTCAA GGAGAAGAGA GAAGAGAGAG AAGGAAGGGA GGGCAGTGCC 1200
GGGGCGGGAG GTTAAGACCA GGGAAGCCGC ACTGGAGGCC CTTTTGGGTG ACCCGTCCCA 1260
GGAGCCAGTG TCACCCCTGA GCCTGGGAGT GTGTGAGAGG CTCTTTCTCC CAGGTTCTGC 1320
TGTGTCCTCT GCCTTGTCTG TGCGCCTCCT CCTCTGCGAG AATTTGCATC TGTCCCTCGG 1380
TGGCTCTGCG CTTCCTGTGG TCAGCCTGAC ATTTGCATGG AGACTTCCTC ATCCTGGGGC 1440
CTGAGGGAAG GGGCTCAGCC CCCTCCCCGC TACCTGGGGT CCTAGCCTGT CCCCAGGCGG 1500
TGGGCTGAAG TAGCCCAGTG GGGTTAGGAG GCTCTGGGGG TCTCTCGGCT GGAGTCACCT 1560
CCGGGCAGGG GTGAGATGGG TTGGGACAGA CTGGTCCTCC CCTCCTTCCC CCCATCCCTG 1620
CGGTTGGAAA ATTTGCCCGC CCTCCCCTCG TCCCTGGGCT GAGGAAACCT CACAACCTCA 1680
CTTCTCACTC TCTCCCCAGA AGGAGTTTTG TGTTTTTTCC ATCACGTGGT TTCCTGTGGG 1740
GCTGGGCTTT GTGGGGCTAC AGTTTCCTCC TGGGAAAGGG GTGTGCTTCG GGGAAAGGGC 1800
TTAGTTCTGC TTTCTGCCCT GACAGCCCCT TCAAATCCGT TTGAACCCTG GGCTCCCCTT 1860
CAGTGACATC ATCCAGGGCA CCCCAGAACC CCCTACACCA CTCTTTCCCC AGTGGGGTTG 1920
TCTTCCCCGC CTCCCTGGCG GAGCGCACCC CATCCGCCTT CCTTGTGACT TGAGTCTGTG 1980
TGTCCATCTC CCACCACTCC CTGTGGTGTG GCCTCGGTCT GCGTTTCTCT TTGCCTCTGG 2040
TCTCTGCTGG GGCACAGTCC CATCCTTCAC GGAGATTCAT CCTTAGCTTC TCTCCTCCAA 2100
ATATTTTGAA TATTGCCAGC CTTTCTGCCT TTCAGAGGTG GGCTCTGGGT TCGAAGCCCG 2160
GTTAGAACTC TGGAGGCTAG GATGGCTTGA ACCTGGGAGG TCGAGGCTGC AGAGAGCTGT 2220
AACCGCGCCA CTGCACTCCA GCCTGGGCAA CAGAGCTCTG GAAGCTTGCC CTAGAGTCAG 2280
TCAAGGGCCC TAGGCCAGTG AGTAACAGCT CAGCGTCAGT 2320
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