Tag | Content |
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EnhancerAtlas ID | HS026-10908 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr14:99711140-99713920 |
SNPs | Number: 3 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr14:99711295-99711305 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr14:99711295-99711305 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr14:99711295-99711305 | AATGGAAAAT | - | 6.02 | ZNF263 | MA0528.1 | chr14:99713488-99713509 | TTTCTCTCTTTCCCCTTCTCC | - | 6.09 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_11814 | chr14:99693534-99716361 | CD3 | SE_14377 | chr14:99690022-99739643 | CD4_Memory_Primary_7pool | SE_15389 | chr14:99695467-99715852 | CD4_Memory_Primary_8pool | SE_15799 | chr14:99705572-99715750 | CD4_Naive_Primary_7pool | SE_16278 | chr14:99705226-99740428 | CD4_Naive_Primary_8pool | SE_16850 | chr14:99695406-99738869 | CD4p_CD225int_CD127p_Tmem | SE_17293 | chr14:99643170-99741315 | CD4p_CD25-_CD45RAp_Naive | SE_17758 | chr14:99686176-99741294 | CD4p_CD25-_CD45ROp_Memory | SE_18246 | chr14:99687262-99741476 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19101 | chr14:99687731-99741353 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20278 | chr14:99705154-99716331 | CD56 | SE_20747 | chr14:99705359-99716423 | CD8_Memory_7pool | SE_21907 | chr14:99688394-99716606 | CD8_Naive_8pool | SE_22287 | chr14:99687661-99737071 | CD8_primiary | SE_27017 | chr14:99707370-99714771 | Esophagus | SE_30991 | chr14:99707037-99712624 | Fetal_Thymus | SE_30991 | chr14:99713077-99715706 | Fetal_Thymus | SE_50515 | chr14:99711229-99713066 | Sigmoid_Colon | SE_50515 | chr14:99713126-99715674 | Sigmoid_Colon | SE_52605 | chr14:99707386-99716235 | Small_Intestine | SE_55119 | chr14:99712026-99713352 | Thymus | SE_55119 | chr14:99713511-99714735 | Thymus | SE_62255 | chr14:99650017-99741519 | Tonsil | SE_64343 | chr14:99705335-99712247 | NHEK | SE_64343 | chr14:99713117-99714247 | NHEK | SE_68017 | chr14:99696519-99741711 | TC32 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I099239 | chr14 | 99705529 | 99717033 |
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Enhancer Sequence | TGACGGTGCC GTTTACACAA TACTCGCCTT GAGAGCCCAG CAAGTGTAAC ATACTATTTC 60 ATATTATAAG TATATAGGTA TACGCATATT TTTAATACTA CCTTGACTCT TGTTATAGCA 120 AATCAATTCT GCCTGGTTTA GATTTATTTC TGAAAAATGG AAAATAGAGA TGTGGGTCCA 180 ATCCTAGCCT GGAAAAGCTG TCACAGTGAA GGTAAACTTT TAATCGGCTA CAGGCGAACA 240 GTATACAGTT TTATTTCCAG AGTAACAGCT TTGGGAAAAT GTTTGAACAT TTTCTTAAGA 300 GCTTTGTGGT GGACAGGCTG GGCGTCCAAC CACTGCTTTT CTGGGCCTTT AAGGGCCTGT 360 TGAAGTGCTT TAAACAATTG GAGGCCAATT TTTAACACAC AAAACTAGAG ACTCCTAGCA 420 AGGTGACGAT TTGCATACAA ATTCTTGTTG GAAGAGGTTA TCCTAAGAGA AGTCAGGCTG 480 AAAGGAGGAC TGACATTAAA TCCCTGTAAT TCCAGGAGCT TCGGTGTCCC ACTCCAGTGG 540 AGGGTTCCAT TCCCACACAA TTGGGAAAAC ACTTTTGTCC TTGAGAAAAG CGGGCTTACT 600 CTTCTCCCAC TCGGAAAGAA ACTAAGGTCC CCACGAAATC CCCACTTTGA GATGGGGCTG 660 TTGCCCCTGG ATGATCACAT TTTTGTACAA GGGAACTCCC GGAGGCTCCT TCCGTCCCGG 720 CCTCACCTGG ATCCCGGGAA CCGCCCGCTC TGTCCCGCCA AGGTGGGCTG AGGAAGACGG 780 CGCCACTCAT CAGGGCAATG GCGGCGGGCG GAAGAGGGAT CCCCGTGCGC CCCCAGCACC 840 CGGGACGAAT GCCACCCCGG CGAAGCGACC CGACCGGCGC GCACGGTTTC GGGGAGGGGA 900 CCACTTCCAC ATTCCCCATG CCCGAGAAGG TCACCCACCC GGGAGAGCGC CCAAGGGCCA 960 GAGAGGAGGC GACTGGTGGA GGAGGGGCGG CCCCGTGCGC ACAAAGGGGC CCGGGGCCGG 1020 CAGGCTCCCC GCCCTTGACC TTGGGTCTCC GCCTCCATCC ATCTCCGCCG GCTGCCAGGG 1080 AAGGGGGCTG GCCCGGGGCC AGAGGCGTGC TCGCTGGGCT GCTGCTGGGC TGGGGACCGA 1140 CGGGGGCGGG GGGGAAAGGA GCCGGGAAAA AAGACTCCAG GGCTGCAGAG TGCTCCGAGG 1200 AAGCCTGCAT TCCACCACCT TCAGGAGCCG GTCCCGAGGC GGCTCCGATT CACTGCATGC 1260 CCCCCGCCCC CCAAAGCAAA AGTTGCACGG ATGCACGAGG GAAACCCCTT CCCAAAGCTA 1320 GCCCTTCGAC TCGCCCACCC CCCGCCTTCC TCGGACCCAG GCCGAGTGGG GGAGGGGAGT 1380 GTCAGGGGAG GAAGAAAGGA GCGCGCCTTC CCAGCGAGGC CAGACGCGGG CTGGGTCAGC 1440 TGCGCCTCCG CCCGCCCCTC GCCGCCCGGC TCAGGCAGCT GCTCCATTAA GCCCCCGAAT 1500 TATGCATGGA CCTTGAGCCC TCTCGGCCCT CCCGCCCCAC CAAGGCACAA TCAACGTGCG 1560 CAGCGGGCGC GGGTCAAAGA GAGAGGGAAG GAGGTGGACG ATGGGCGCAA GGCCGTGGGC 1620 GAATCAGAGG CCGGCGGCCA GGCGGGGGCC AGGCGCGCCC GCAGGCCTGG GAACAGTGCC 1680 GAGGAGCCTC CCGACCCGGC CAGGGCCAGC CGGGAAAGGG GCACCGCTCG CAGGGGAGGC 1740 CCCCGCGCAG TTTTGAAGTT GCCAAAGTGT CCGCGCCGTG CCGGGTGCGG GGTCCGGGAG 1800 ATGCAGCCGC CCCCGCGGAG CTCTGCGCCC CTGGCCTCGG GGAAGGCCAT TGTGTTCTCC 1860 TGTGTGGCAA TGAAGGGGGC TATGGACCCC AACCATTGAG CCCTTGGAGG GAGGGGCCTG 1920 AAGACCCCTC GGGCAGGGCG GGGGAGGCTG TCTTGCGGGC GGCGGAGAGG ATGGGTATGA 1980 TTTGCTCGGG ATAGGCACCG TCGCGGGGAG GGGAGGAGGC CAAGCTTGAG GAGGGGCTGC 2040 TGGAGATGGA AGGAAGTGAG AGGAGACTTG CAAGTTGCAA ACGTCGGGGA AACCGGAAAA 2100 TTGCAGTAGC GGGGAGGCAG GTGGCGCCCA GAGGTTCGAA AGCAGAATTG GGAGGACTTC 2160 GATGTCCACC TCGCAGACAG TGACCCAGGC CCCAGAGGGC TCCGCAGCCT GGAGCCTCGC 2220 GTCCCGCCTC CCCGCAACAC GCTGTTTTCA GCGTTCCAGA CCACAGCGCT GCAGTCTACG 2280 CTGCCCTGAC GCTGGAGTGT GGACCTTGTT TTGCTCCTCG GGGCCCGTCT GTTTCTGGAA 2340 ATGACTTCTT TCTCTCTTTC CCCTTCTCCC CAAAGCAAAG GCCAGGTCAG GAAAATTATA 2400 TACTTCGTTT TCCCAACAAA TAAAGTCGCC TAGTTTGCAG GGAAAGTTTT ACAAGCCAAT 2460 GATGCAGAGA GAAGACCACA CTGTTTAGCT TTCTTAATTG GCTGGCTTTG AACTTGAGGT 2520 GGGAGGAGAA AAGAACCCGC TCCAGCCCCA GGAAAACTTA GTTTTGCTGG GTTTACCAAC 2580 TCCAACAGTT TTTAGCCAGC TGCTGAAGGT GGCAGGGAGT CACTGAAGGT TTGTCCCATT 2640 TTCTCCCGAA CAGAGAAGAA TTCAGACAGT TGTTGTCTCT CTGAGCCCAG GACAGCCAGT 2700 CTCTGCCCTC AAACCCCAAG GGAGGAGCCT GGAATCCCTG GTTGGCTGGC TACACTCTCC 2760 AGGAGGTGTG CTCTACCCTG 2780
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