Tag | Content |
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EnhancerAtlas ID | HS098-53986 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr8:11415620-11416880 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr8:11416735-11416746 | CTTCCCAGAAG | - | 6.14 | ZNF263 | MA0528.1 | chr8:11416569-11416590 | TTCCTTTCCCCTTCCTTCTCT | - | 6.1 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_10360 | chr8:11414658-11417348 | CD19_Primary | SE_10873 | chr8:11346156-11419244 | CD20 | SE_32678 | chr8:11415415-11416637 | GM12878 | SE_60985 | chr8:11340629-11417326 | HBL1 | SE_61717 | chr8:11381066-11417450 | Toledo | SE_62774 | chr8:11381386-11422544 | Tonsil |
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| 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 |
GH08I011557 | chr8 | 11414894 | 11417288 |
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Enhancer Sequence | CCACCCCATC CTCTCAGCCA GCAGGAGAAG TCAGGGGGTA CTGAAGGCCA CCTTCCTCTA 60 GGCAGATATC CCCAAGGTCA CCCACTGCAC TTGGACTTGC AAACCCTGGC CACTGTGCCT 120 CCTGCCCCAC GCAGCTGTGA GGGAGCCCAG GGAATGGAGC CTTAGACCCG GGCTGCTGTG 180 TTGGAATGAG GCTATTCTGT TCCGAAGGAA GAGAGGGCGA ATGAATGTCA TGGGAAACAC 240 ACAGAGTTAG CAAGAGTTCC ATTGAACCCG GCAGGCAAGT GTGTTCTGTT GTGACCTCAT 300 CTCTTCCTTA GATGGTGCCC ACAAACATCT CCTGTAGGAC TTCCCATCCC AGGGGCCCTC 360 AGCCTTTGCA CAGCCCTGGC GTCGACCCCA GGCTGATGGG CAGGCCTGAG CTACACACAG 420 ATGCCAGGGA CATGACTTCT CTGAGCCCTG GAGGACAGCC CCACCTTCTG CCACCAGGGA 480 ATTGCGAGTG CTGGACCTCC TTGGCTACCC AGGACTGGTC CTCAGTGTCC CTCACGTTCA 540 CATGCAGAAC TTTCTGGACT CCATGGGGTG AAGAGCAGAG TGGAGAGGAG GGTTTTAGCC 600 GAGAGCTCTA GCTGGCAGGA AGCACATCTG GTGGCCCTGT TAAAACTGGA ACTCTCAGCA 660 GAAAAGTTTT GGTCTGTGGT CAGCCTGTGA GGCACACACG TGCGTACACA TACACACACA 720 CATACAGCTG CCACCGAGAG GAAACGCTCC CACCCACCGC CCACATCAGC CCTCCCACCT 780 CGCCCCTCGC CCAGCCTTAC CCAGTAGCGC CGCTGCAGGA ACTGATGCCA CAACGCCTTT 840 TTCCGCTGAG GTGGGCAGAC AGCCATCTGG GCAGGCTGGT TTTGGAAAAT GAGTGCTGGT 900 AACCGGCTTC AAACCCCAGG GCAGTGATAA GCCTGCCCAC TGCTGCTGCT TCCTTTCCCC 960 TTCCTTCTCT CACCCTCCGC TGTCTCCTAT TCAATCCCCA CTACACCCCC TTGGGAAATC 1020 TCGTGTGACC CAGGGGCAAA GGATGTGAAA AGCCATCGGA GTTTAATACC TGGATGTAGC 1080 CACAGAATCG GGGGTGAGGA GCCAGAAAAT CAGAACTTCC CAGAAGGGCA GCCTCTAACC 1140 ACATGCTGAC CATGCCAATG GCTCTCTAAG CACACATGTA CACACACACA CTCTCACACA 1200 CATAAAAACA CAGACTCACA CACACACGGA CAAACACAAA CACATACACA GACTCACACA 1260
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