Tag | Content |
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EnhancerAtlas ID | HS187-23494 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr8:11415550-11417080 |
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 | GGTGAAGTAC CAGGTGCAGA GAAAGGGCGG CATGTGCCAC CTGCTGCCCA CAATGGCTGC 60 TCGTGCCTTA CCACCCCATC CTCTCAGCCA GCAGGAGAAG TCAGGGGGTA CTGAAGGCCA 120 CCTTCCTCTA GGCAGATATC CCCAAGGTCA CCCACTGCAC TTGGACTTGC AAACCCTGGC 180 CACTGTGCCT CCTGCCCCAC GCAGCTGTGA GGGAGCCCAG GGAATGGAGC CTTAGACCCG 240 GGCTGCTGTG TTGGAATGAG GCTATTCTGT TCCGAAGGAA GAGAGGGCGA ATGAATGTCA 300 TGGGAAACAC ACAGAGTTAG CAAGAGTTCC ATTGAACCCG GCAGGCAAGT GTGTTCTGTT 360 GTGACCTCAT CTCTTCCTTA GATGGTGCCC ACAAACATCT CCTGTAGGAC TTCCCATCCC 420 AGGGGCCCTC AGCCTTTGCA CAGCCCTGGC GTCGACCCCA GGCTGATGGG CAGGCCTGAG 480 CTACACACAG ATGCCAGGGA CATGACTTCT CTGAGCCCTG GAGGACAGCC CCACCTTCTG 540 CCACCAGGGA ATTGCGAGTG CTGGACCTCC TTGGCTACCC AGGACTGGTC CTCAGTGTCC 600 CTCACGTTCA CATGCAGAAC TTTCTGGACT CCATGGGGTG AAGAGCAGAG TGGAGAGGAG 660 GGTTTTAGCC GAGAGCTCTA GCTGGCAGGA AGCACATCTG GTGGCCCTGT TAAAACTGGA 720 ACTCTCAGCA GAAAAGTTTT GGTCTGTGGT CAGCCTGTGA GGCACACACG TGCGTACACA 780 TACACACACA CATACAGCTG CCACCGAGAG GAAACGCTCC CACCCACCGC CCACATCAGC 840 CCTCCCACCT CGCCCCTCGC CCAGCCTTAC CCAGTAGCGC CGCTGCAGGA ACTGATGCCA 900 CAACGCCTTT TTCCGCTGAG GTGGGCAGAC AGCCATCTGG GCAGGCTGGT TTTGGAAAAT 960 GAGTGCTGGT AACCGGCTTC AAACCCCAGG GCAGTGATAA GCCTGCCCAC TGCTGCTGCT 1020 TCCTTTCCCC TTCCTTCTCT CACCCTCCGC TGTCTCCTAT TCAATCCCCA CTACACCCCC 1080 TTGGGAAATC TCGTGTGACC CAGGGGCAAA GGATGTGAAA AGCCATCGGA GTTTAATACC 1140 TGGATGTAGC CACAGAATCG GGGGTGAGGA GCCAGAAAAT CAGAACTTCC CAGAAGGGCA 1200 GCCTCTAACC ACATGCTGAC CATGCCAATG GCTCTCTAAG CACACATGTA CACACACACA 1260 CTCTCACACA CATAAAAACA CAGACTCACA CACACACGGA CAAACACAAA CACATACACA 1320 GACTCACACA GACACGCAAA CTCACACACA GACAGACACA CACACAGACA CACAGACTCA 1380 CACACACAAA CTCACACAGA CACACAAATA CACAGACTCA GACTCAAACA CAAACTCACA 1440 CAAACACATT TACACAAACT CACAAACTCA CACACACAAA CACACACACA AACACGCAAA 1500 CTTACACACA CATGAGCAGA CACACACCCG 1530
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