Tag | Content |
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EnhancerAtlas ID | HS187-05321 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:8188940-8191940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:8191446-8191464 | GGAAGGAAGGAGGGAGGA | + | 7.16 | MEF2A | MA0052.3 | chr12:8191504-8191516 | GCTATTTTTAGC | - | 6.44 | MEF2B | MA0660.1 | chr12:8191504-8191516 | GCTATTTTTAGC | - | 6.92 | MEF2C | MA0497.1 | chr12:8191503-8191518 | GGCTATTTTTAGCCA | - | 6.49 | Nr2f6(var.2) | MA0728.1 | chr12:8189468-8189483 | GAGGTCAGGAGTTCA | + | 6.22 | SPIB | MA0081.2 | chr12:8189826-8189838 | AATGGGGAAGTG | + | 6.18 | ZNF263 | MA0528.1 | chr12:8191447-8191468 | GAAGGAAGGAGGGAGGAGGAG | + | 6.24 | ZNF263 | MA0528.1 | chr12:8191451-8191472 | GAAGGAGGGAGGAGGAGGGCG | + | 6.51 | ZNF263 | MA0528.1 | chr12:8191458-8191479 | GGAGGAGGAGGGCGGAGAAGG | + | 7.73 | ZNF263 | MA0528.1 | chr12:8191461-8191482 | GGAGGAGGGCGGAGAAGGGGA | + | 8.29 |
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| Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
SE_14898 | chr12:8190621-8192238 | CD4_Memory_Primary_7pool | SE_17604 | chr12:8184138-8189601 | CD4p_CD25-_CD45RAp_Naive | SE_17604 | chr12:8189608-8192202 | CD4p_CD25-_CD45RAp_Naive | SE_18144 | chr12:8189540-8192482 | CD4p_CD25-_CD45ROp_Memory | SE_19091 | chr12:8184165-8189422 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20630 | chr12:8190976-8192004 | CD56 | SE_22745 | chr12:8189552-8190570 | CD8_primiary | SE_30471 | chr12:8190711-8192162 | Fetal_Muscle | SE_32302 | chr12:8188658-8189499 | Gastric | SE_32302 | chr12:8189501-8190262 | Gastric | SE_32302 | chr12:8190351-8191980 | Gastric | SE_41288 | chr12:8184380-8192117 | Left_Ventricle | SE_42951 | chr12:8184354-8192076 | Lung | SE_45441 | chr12:8190770-8191495 | NHLF | SE_49321 | chr12:8188710-8192801 | Right_Atrium | SE_53794 | chr12:8189392-8190524 | Spleen | SE_53794 | chr12:8190890-8191784 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr12 | 8190343 | 8190568 | chr12 | 8189665 | 8190127 | chr12 | 8189748 | 8190200 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I008036 | chr12 | 8189241 | 8191996 |
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Enhancer Sequence | ATCCAGGATC GGTCTTTCAC TCCGAGAATG TCTATGTGTC TGTTTTTCTC TGCCTTTCTC 60 CCAGTTCTGT AGTCTTCATT AGACGTCGTG TGGATGTGAT GGACCCTGCC CTTTGGCTGC 120 CTTTCCCAGC TTCTATGGGT ATTTCCTTTC AGTCTTCCAG CACACAGAGA AGAATGTGGC 180 CTGACTCAGG TTCTGCCCAA GCCCCGTGGC ACAGGGCCCT GGAGAGAGAG GTCTGGGTAA 240 CTAGGTTGGT TGGACTGAGA AATGGAAGTA CCTCTTGTTT GCCTTTCTAA TAATAGCCCT 300 GAACATTAGC CTCGTGCCAT TATTTTGGGG AGCGTGGAAT GTGTGGCAGC CACCAGCTCA 360 TTAAGTTTCA TTCACTTCCC TCCAGGGACG ATGCTTTGGC AGGGTTTATG GGTTCATCTC 420 TTTTATGGAA GGGGGAAACT GAGGCATCAA GACTTCACTG GGGGCCAGGC ATGGTGTTTC 480 ACACCTGTAA TCCCAGCACT TTGGGAGACC GAGATGGGTA GATCACCTGA GGTCAGGAGT 540 TCAAGACCAG CCAGGCCAAC ATGGTGAAAC CCCACCTCTA CTAAAAATAC AAAAAATAGC 600 CGGGTGTGGT GGCGTGTGCC TATAATCCCA GCTACTCGGG AGGCTGAGAA AGGAAAATCG 660 CTTGAACCTA GGAGATGGAG GTTGCAGTGA GCCGAGATCG CGCCACTGTA CTCTATCCTG 720 GGCCACAGAG CAAGGCTTCG TCTCCAAAAA GACAAAACAA AACAAAACAA AAACAAAAAA 780 CACTTCATCA GAGAGGCACG GATGGTTAGG GACAGTCCAG CAGGATTTGG AATAGAACCA 840 AGGAACCTCA GTCTCTGAGG CTCTACATGC TGGGCTGCCC TTCACAAATG GGGAAGTGAA 900 GAGGGTGAGG AAGTGGGATG GGTCAAAGGA GAACGGTGCG GAAAGATCAA AAGAATCAGA 960 TGCTACAAGC TGCTTGTAGC TGGTGAGATT TGAATATATT TTGAGTGCTG GGGGCTGTAT 1020 CTGGAGGGCT GACTGGAAGG GGGCTGGAGA AAGGTTAAAT TTAACCTCAG TGTCCTAACC 1080 TGGTGCTAGG GTAAGGGTAG GGAAGGGCGT AGAACAACTT GCAAAAGGCT GAGAGTGCTT 1140 CCCTTTCAGG AACTCACTGT GATTGGCATG TGCCAAATGG GTTCTTCTGT AAGCCCTCTA 1200 AACACTTTAA ATCCACTCTC ATGCCCCTGT CCAATGCTGG GAAAGTTGTT TCAAATGAAC 1260 ATCAACTGAA GGCCTCCGTG CTCTTAAGAT GAAATTTCCT AGGGATCTTT AGAAGGAGAT 1320 AAATAGGGAA TAGGGCAGAA GTACTTTAGG GACCTCCCCA TCTGGGGAGG ACCCAGGAGG 1380 ACCCTGGTCA TTGGAAACCT GCTCATTGGC ATGCCACTCT TCAGCTCAGA TGACCCAGCT 1440 ACAGGACTGT GATCCTGCTA CAAGTATACA AGTATATATG TGATCTGCTA TAGCCCAGGG 1500 ACTGGGGTGT TTTGACTTAG TAGTATTGGA AGGTGTGAGG TTCCTGGAAT GATTAAGTGT 1560 TCCTATTAGT TTCCAAGTTT CCATGGTTAG GGCAAGGTGG CAGTGGGATG AAGAGGATAG 1620 TGGGAGAGAA GCTAAGGATA AAGGGGAAAC CCTTCATGAC GCTATTTATA AACATGCCAG 1680 CCCCCCTCGC TCCGCCCCTT TTCTCCTGTC AAACAATTCT TGGGTTAGAG TTGCGTCTCT 1740 TGCTGCCCCC GCCCCTGAGG CACTAAGGTG TTTCCTTCAG CCTTGTGGAG TGAGTGTGTT 1800 GCTGGTTAGG AGCTGGGTAC TTGTGCACAC ATGCAGATTG CCATCTGCGT GGGTGGGACC 1860 TTGGGGAGAG GGGAGTAAGT CAGAATGCTG ACCCCTAGGA GAAAGGCTTA AGGGTCAAGG 1920 GCAGAAGAAT CACTACCTAG GATAGAAGAG GGAGCTGAGA CCCTGAAGGA TGTGTTGGAG 1980 TCAGGAGAGA GGGGGACATG GTCCTATCTG CTGTTGAGCT TTGGCCTGCA AAGTGTGTGG 2040 ATCTGTTGTA TTTTATGGAT ACGCTTGTGC ATATATCTGG CTGTGGATTT AGAGATCACT 2100 TACATCATAC GTTTCTGTTC AGGATTCTGA ACTTTGAGGC AATCTAGTCC TGGCTCCTCA 2160 GGAGAAGTGC CCTGGTGGGA CTGAGGAAGA CAATGTTAGC TGGCATCTGG CGGCTGTGCA 2220 GGCACAAACC TGCTAGGCAG CAAGTGCTTA GGGGGTTGCT GGCATCAGCT CTAGGGGAGT 2280 GCCAAATGGC TACCTAGGGG TTCCTGCCAG CCTTTCTAGA CCCTGCAATA CAGATATCAC 2340 CCATCGTTCT TCACCTTCCC TCGCAAGATG TCACTAGCTA TACCTCTCTG CTGGCAAGAG 2400 TGCCCAGGCA GTGTGGGTGG CAGCAGGGCG TGCAAGCATC AGGCGTAGGC GGTCTGGCAG 2460 CTCCAGGAGT TTGCATGGAG GTGCAGCGAG CGTGCCTGCC TGGCTGGGAA GGAAGGAGGG 2520 AGGAGGAGGG CGGAGAAGGG GAGCCAGCTC CGAGCTCCAG AGTGGCTATT TTTAGCCAGG 2580 CTATCTGATT GTTACCGGTA GGCACACAGC TGGGTGTCTC CCTGGCTCGG TGAAGCCCAG 2640 CAGGCTGAGA GGTGGGAGGT CCTTGTGGAT GACTTCTTCC TGGTGTTGGT GTCTGTGGGC 2700 GGGAGCGTGC AAGGGGTAGC TTAAAAAGTG TGAGGGCAGC TGTGTACTTC AGGATGTGTT 2760 GCTTCTGTGT GTGACTTTGT CCTCTGGTGG TAATGTATGC TGTATATGTA ATCGTGATCT 2820 CTGTGTATGT GCTTCACTGT TTATGAGTCT GTCTGCTGGT TGTCATGTAT ACTTTATGCC 2880 TGGGATATAT CTAATATGCC TCAGGTGCAC ATGTGTGTGG GATAAAAAGG GCAAGTGCTC 2940 GTAATGCATC TAGTAGGAAA CATCTTTAGA CGTGTTGGTG TGTGCTTCAT CCGTGTATGT 3000
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