Tag | Content |
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EnhancerAtlas ID | HS023-12658 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr19:17217900-17222210 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN | MA0488.1 | chr19:17218618-17218631 | ATGACCTCATCCT | - | 6.23 | JUND(var.2) | MA0492.1 | chr19:17218617-17218632 | CATGACCTCATCCTA | - | 6.25 | NR2C2 | MA0504.1 | chr19:17221878-17221893 | CGACCTCTGCCCTCA | - | 6.14 | SRF | MA0083.3 | chr19:17218657-17218673 | TTTCCAAATAAGGTCA | + | 6.01 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_01070 | chr19:17217900-17219642 | Adrenal_Gland | SE_01070 | chr19:17220228-17222170 | Adrenal_Gland | SE_01695 | chr19:17217904-17219751 | Aorta | SE_01695 | chr19:17220056-17222186 | Aorta | SE_07171 | chr19:17217875-17219856 | Brain_Hippocampus_Middle_150 | SE_07171 | chr19:17220087-17222286 | Brain_Hippocampus_Middle_150 | SE_09204 | chr19:17217853-17225810 | CD14 | SE_11414 | chr19:17210931-17224728 | CD20 | SE_32165 | chr19:17217911-17219588 | Gastric | SE_32165 | chr19:17220100-17220936 | Gastric | SE_32165 | chr19:17220946-17222157 | Gastric | SE_32675 | chr19:17215550-17218465 | GM12878 | SE_32675 | chr19:17219903-17222227 | GM12878 | SE_42559 | chr19:17217842-17219831 | Lung | SE_42559 | chr19:17220086-17222209 | Lung | SE_44945 | chr19:17217893-17219831 | NHLF | SE_45910 | chr19:17217694-17219939 | Osteoblasts | SE_45910 | chr19:17220005-17221204 | Osteoblasts | SE_50282 | chr19:17217887-17219656 | Sigmoid_Colon | SE_50282 | chr19:17220077-17222207 | Sigmoid_Colon | SE_52769 | chr19:17217885-17219586 | Small_Intestine | SE_52769 | chr19:17220064-17222195 | Small_Intestine | SE_53370 | chr19:17217871-17219778 | Spleen | SE_53370 | chr19:17220038-17222391 | Spleen | SE_59337 | chr19:17188995-17222500 | Ly3 | SE_62772 | chr19:17177847-17247718 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 7 | Chromosome | Start | End |
chr19 | 17220489 | 17221449 | chr19 | 17218539 | 17219391 | chr19 | 17218276 | 17219491 | chr19 | 17221570 | 17221897 | chr19 | 17220741 | 17221250 | chr19 | 17220155 | 17220353 | chr19 | 17221934 | 17222043 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I017106 | chr19 | 17217795 | 17222204 |
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Enhancer Sequence | CCAGGCATGG CAGTGCATGC CTGTGGTCTC AGCTCTCAGG AGCTTGAAGT GGGAGGATTG 60 CTTGAGCCCA GAAGTTCAAG ACTGCAGTGA GCTGTGATCA CACACTGCAC TCCAGCCTGG 120 GTGACAGAGC AAGACCCTGT CTCAAAAAAA TAACAAAAAA AATTTAGTAG GTGAATGAAT 180 GAGAGGGTAG ATCCAACATT TACCATGTCA GACATTTTGC CAAATGGGAC TAGGCAGGTG 240 GGTAAATGCC TGAGCCCCGC AGAAATGACA CGCCCAGCCC CAGGGTCTCA AAGTGGCACG 300 GCCAGGAGGC AGGATTGCCA CCTAGGTCTC AGTTCAGGGT CCATGTCCTC CCCACCACGT 360 TGCTGCCTCC ACAGCGCCAT CTCACTAGGA CCCTCCAGGG CGTGGACAAG TTTCCTGTTG 420 CTAAGTGTTA GGGGCAAGGG AGTCTCCAAC AACAGGGATT AAGGCTCTCA TGGTCCTGGA 480 GGCCAGAAGT CTGAAATCAA GGTGTCCACG GGGCCGCACT CCCTCCCGGC TCTGGGGGAG 540 GATGCTTCAG GCCTCTTCAG CTTCTCTGGT GGCTGCAGAT GTGCCCTGGC CTGTGGCCAC 600 GTCACATCAG TCTCTGCCTC TGTCGTCAGG GGCGTTCTTC CTGTGTGTCC ATGTCTTCAC 660 GTGGCTTTCT TATAACAAGG ACACCACTCA TGGGATGTAG GGCCCATCCT ACCCCGGCAT 720 GACCTCATCC TACCTAATTG CATTTGCAAA GACCCTATTT CCAAATAAGG TCACATACAC 780 AGTTTCTGGG GGTGAGGATG TGGATATAAT TTTGGGGGCG GGGGGCTCAA GTCAGCCCAC 840 AGCATCCCCC ATACAGCCCC ACCTGGTCTG CTTCAAGTCC TACCTGGCCC CTGGCAAGTC 900 CCACTTGGTG ACATCTTGTG CCTGGGTCCT TGAGGGCTGC CCCAGATCCG CGATTGTCCT 960 GGGGACCGGT AGTTCCTCCC CGGATGCCAG CAAAGCTCCC TCCAGCCTCC ACGCCTGCAC 1020 AGTCTCCAGT ATGCCTTCAA CAGCCATTAG TCACCCTCTG TGAGTCAGAC CCCCGGTCCT 1080 GCCAGGCCAA CCTGCTTGGG GCCTCAGCAG CGGGGGCTGG CGAGGCCAGT TTTCTCCAGC 1140 GGTTCTAAGC CGCTCGAGGG TGGTGCCCAC GCCGGCTTCC AAAACAGGCT TGAGCCAAAT 1200 CCACGTCATG GCAATAAACG TGCTTCCTGG GGCGACTGTT TGCAAAGGGA TGTGATTGTC 1260 TTCACTGAGA GCTGGATTTC TCAACCTGGC TCTGCTGACA TTCAGGGCCG GATCGTTCTC 1320 TGGGGAGGGA GTCATCCTGT GCATTGAAGG ACATTGAGCA GCATCCCTGG CCTCCACCCA 1380 CCAGATGCCA GGAGCACTCC CCACCCCGCA GGTGTGACAC CCAGAAGTGT CCCCAGACAT 1440 TTCATTGATT AGAGAGGTAT TAACAAAATA GCTTCCCGTT GTCCCCTGGG GACAAATCAC 1500 CCCCTGGGAA TAGAACAGCT GTCTTTGAGT TCTTCCCATA AGACCCAATC ACTGTTCATT 1560 GCAGCCACTG AGCTTTTAGA AATTATCTGT GAGTTCTTTC TGTTCTGTGC TAACTTAAGA 1620 GTCATTTTCT TTTTTTCTTT TTTTGAGATA GAGTCTTGCT CTATCGCCCA GGCTGGAGTG 1680 CAGTGGCACG ATCTCGGCTC ACTGGAACCT CTGCCTCCTG GGTTTGATTC TCCTGCCTCA 1740 GCCCTCCCGA GTAGCTGGGA CTACAGGCGC CCACCACCGT GCCCGGCTAA TGTTTGTATT 1800 TTTAGTAGAG ACGGGTTTCA CCATAGTGGC CAGGCTGGTC TCAAACTCCT GACCTCAAGT 1860 AATCTGCCCT CCTCAGCCTC CCAAAGTGCT GGGATTATAG GCGTGAGCCA CCATGCCTGG 1920 CCCCAAGAAT CTTTTTTTTA ATTTTATTTA TTTATTTATT TATTTATTTA TTTATTTATT 1980 TATTTATTTA TTTTGAAACA GAGTTTCTCT CTGTCTCCGG GCTGGAGTGC AGTGGCGCGA 2040 TCTCGGCTCA CTGCAAGTTC TGCCTCCCGG GTTCGTGCCA TTCTCCTGCC TCAGCCTCCT 2100 GAGTAGCTGG GACTACAGGT GCTCACCACC ACACCCAGCT AATTTTTTGT ATTTTTAGTA 2160 GAGATGGGGT TTCACCGTGT TAGCCAGAAT GGTCTCGATC TCCTGACCTC GTGGTCCGCC 2220 CACCTCAGCC TCCCAAAGTG CTGGGATTAC AAGCATGAGC CACTGCGCCC GGCCATCATT 2280 TTCTAATAAG AGGAATAAGA CCTCAGGCCC ACTGGGTATC AGGGTTTGGG CTTCGTGATT 2340 TTCCTCCATC ATCTCTAATC CCTCACGGCA GCTCTGCCCA TTTTAAAGAT GAGGAAACTG 2400 AGCCCCAGAG AGACACGTGG ATGTGTGAGT TTCCTGAGGT GTCTATAACA AAGTATTACG 2460 GGCTGGGAGC CCTCAAACAG CAGGGGTTGA TTCTCTCACA GTTCTGGAGG CCAGAAGTTG 2520 AAAATCAAGG TGTGGGCAGG GCTGGGTCCC TCTGGAGGCT CTGAGGGAGA ATCTGTCCCA 2580 GGCCTCTCTC CCGGGTTCTG GTGGCTTCAG CCATCCTTGG AGCTCTGGGC TTGTGGCCGC 2640 ATCACTCTGC CCTCTCCCTC CGTCGTCACC TGGTCTTCTC CCCTGTGTGT GTCCAATCTC 2700 CCTTGCCTTT CTCTCATGGG ATCACCTCAT CTCAAAATAC TTACCTTCAT GACATCTGCC 2760 AAGACCCCGT TTCCAGATAA AGCCACAGTC ACAGGTTCTG GGGGTAAGGA CTTAGACATG 2820 TCTTTTTTGG GAAGCCACAA GTCAACCCAC TGCAGGTAGA TTCCCCAGGC CACACCGCAG 2880 AGAGCCAAAG CCTAACCCGG GGTTTGAACC CGGCCTGAGC CCCAGCCCCC CGTTCAGGCT 2940 GCCTCTCTGC TCTCCCCTCT CTCGCCCGGG CTGCAGAAAG CCGGAGATCA GCACAACTCG 3000 CTGCATCGAT TGGGGATTTT TTCTCAGCTC CCCGAAAGGA GAAGTTGAGC TGTTTTGAGG 3060 TTTGAGTGTC GCTGGATGCA CCCCCTGACC CCCGCCCCCC GCGAGGGTTG CAGCCTCGCT 3120 GTGTAATGCT GACCAAAAAA CAGGAAGGGA GCACTGTGGA AAGCCGGTTC CAATCAGCTG 3180 ATCTGCCCGC CACTGCAGTT AACTGTTGCC ATCACCTTTC ACCAAGTCTA GGGGCTGCAG 3240 AAGCCATGAG TCTCCCCATC TTCCACATGG CCTCTAGCCT CCCAGTGCAG GCGCCCGTCG 3300 ACAGCCCAGG GGCTGTGGAT AGAGCACCTT ACAGCATCGG CCATGGGGTC TCGCCGCAAA 3360 GCACACCCAG AACACGCTCC TCTCCCTTTG CCCACAGCCT CAGATCCACC AGGCACTCGC 3420 CTCGGTGCCC TTCTGAGAGC AGGCTGAGTC CAGGGGGCCA AAGGCTGGGG TTCCCTTCAT 3480 CTGTCCTGAA CTGTAGCAAG TGCAGCTGGC AGCTGGCAGC GTGCATGGGG TTTTCATTCT 3540 GAAAGCAGAA ATAAAATAAG GATCCTTGCT TGTCAGGCTG TTGTCCCAAG GGTCCCTGGA 3600 CTCCATGGAG CCCCTGTGGC CCGGCCCACA GTGGGACACG GTGACAGTGA TGGGCTGCAG 3660 GGCGCAGAGG GACGCCCCCA GCTGGTGGAG CCAAGCTCAC CCGAAGTTGT GCCGATGCCC 3720 AGGACATTCC AGTGAGGGAC TGAGGAAGGG TCCTGAACGT GCCACTGCCC CAGACCCCCC 3780 TCTTGGGGCA AAGGAACCTA GGACTCGTAC CCACCTGGAC CGGGTCCTGA GCTCCTCCTT 3840 AGGGGCCCTA CAAACCCAGT CTCATGTTTC CCCCAACTCC CCCAGCCCCT CTGCCATCAG 3900 CCAGGCCACT AGCTCTGTTC CCCCACCCAC AGTCAGCACT GGGGTAGGTC ACCTAGACCA 3960 CAGTGCCATT ATCCACTTCG ACCTCTGCCC TCAAGGACAC CTGCCTGGGC CACGTCCTTT 4020 CCCCCTGAGT CTGTCGGGCA AGACACAGTT GGATGCCAGC CTCCACCCAG CATTGGGGGC 4080 GTCATCTCAT ACGTCCTCAC CACATCCTGA TGTGGGCAGA CTGACCACCC CCACCTGACA 4140 TGTGAGGAAA CTGAGGCACA CGAGCTGCTC AGCAAGGGTG GCAGAGATAG AAGTTTCTGG 4200 AACCAGGTGT GTGTCAACTC TCATGCCTCT GAAGTTGAGG TTCCTGTTTA AGAGCTTATG 4260 GAGATATAAT TTACCTATTT ACTTATTTAT AAATAGATAC CTTATATTTA 4310
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