Tag | Content |
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EnhancerAtlas ID | HS088-27152 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr19:17217310-17221240 |
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 | Nr2f6(var.2) | MA0728.1 | chr19:17217656-17217671 | GAGGTCAAGAGTTCG | + | 6.24 | 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 | chr19:17215286-17217817 | CD14 | 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_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: 3 | Chromosome | Start | End |
chr19 | 17218539 | 17219391 | chr19 | 17218276 | 17219491 | chr19 | 17220155 | 17220353 |
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| Number: 2 | ID | Chromosome | Start | End |
GH19I017104 | chr19 | 17215694 | 17217623 | GH19I017106 | chr19 | 17217795 | 17222204 |
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Enhancer Sequence | AGCTCTGAGA CTCAGCCACA GTGAAACTGC CAGTGGCCCC AGTGTCCTCC CAGCAGGTGG 60 CCAGGGGGCT CAACGGCTCT CCAGGCCAAA ACATCAGTGC CTGGCATCCA CACCCGAGAT 120 AAAACAGTGA TCTTGAAAAT TCAGCATGTG TGGCACACAC CTGTAATCCC AGAGTCAGGA 180 GGCTGAGTCC TGAGTCAGGA GGATTGCGTG AGCCTAGGAA TTCCAGACCA GCCTGGGTAA 240 CATTGCAAGA CCCCATCTCT ACCAAAAAGT TTAAAAACTA GGCTGGGTGC AGTGGCTCAT 300 GCCTGTAATC CCAACACTTT GGGAGGCCAA GGCAGGTGGA TCACCTGAGG TCAAGAGTTC 360 GAGACCAGCC TGGCAAACAT GGTGAAACCC CGTCTCTACT AAAAATACAA AAATTAGCCA 420 GGTGTGGTGG CGAGCGCCTA TAATCCCAGG TACTTCGGAG GCTGAGGCAG GAGAATGGCT 480 TGAACTTGGG AGGTGGAGGT TGCAGTGAGC CAATATCGCA CCATTGCACT CCAGCCTGGG 540 CAACAAGAGC GAAATCTGTC TCAAAATTAA AAATAAAAAT AAAAAATTAG CCAGGCATGG 600 CAGTGCATGC CTGTGGTCTC AGCTCTCAGG AGCTTGAAGT GGGAGGATTG CTTGAGCCCA 660 GAAGTTCAAG ACTGCAGTGA GCTGTGATCA CACACTGCAC TCCAGCCTGG GTGACAGAGC 720 AAGACCCTGT CTCAAAAAAA TAACAAAAAA AATTTAGTAG GTGAATGAAT GAGAGGGTAG 780 ATCCAACATT TACCATGTCA GACATTTTGC CAAATGGGAC TAGGCAGGTG GGTAAATGCC 840 TGAGCCCCGC AGAAATGACA CGCCCAGCCC CAGGGTCTCA AAGTGGCACG GCCAGGAGGC 900 AGGATTGCCA CCTAGGTCTC AGTTCAGGGT CCATGTCCTC CCCACCACGT TGCTGCCTCC 960 ACAGCGCCAT CTCACTAGGA CCCTCCAGGG CGTGGACAAG TTTCCTGTTG CTAAGTGTTA 1020 GGGGCAAGGG AGTCTCCAAC AACAGGGATT AAGGCTCTCA TGGTCCTGGA GGCCAGAAGT 1080 CTGAAATCAA GGTGTCCACG GGGCCGCACT CCCTCCCGGC TCTGGGGGAG GATGCTTCAG 1140 GCCTCTTCAG CTTCTCTGGT GGCTGCAGAT GTGCCCTGGC CTGTGGCCAC GTCACATCAG 1200 TCTCTGCCTC TGTCGTCAGG GGCGTTCTTC CTGTGTGTCC ATGTCTTCAC GTGGCTTTCT 1260 TATAACAAGG ACACCACTCA TGGGATGTAG GGCCCATCCT ACCCCGGCAT GACCTCATCC 1320 TACCTAATTG CATTTGCAAA GACCCTATTT CCAAATAAGG TCACATACAC AGTTTCTGGG 1380 GGTGAGGATG TGGATATAAT TTTGGGGGCG GGGGGCTCAA GTCAGCCCAC AGCATCCCCC 1440 ATACAGCCCC ACCTGGTCTG CTTCAAGTCC TACCTGGCCC CTGGCAAGTC CCACTTGGTG 1500 ACATCTTGTG CCTGGGTCCT TGAGGGCTGC CCCAGATCCG CGATTGTCCT GGGGACCGGT 1560 AGTTCCTCCC CGGATGCCAG CAAAGCTCCC TCCAGCCTCC ACGCCTGCAC AGTCTCCAGT 1620 ATGCCTTCAA CAGCCATTAG TCACCCTCTG TGAGTCAGAC CCCCGGTCCT GCCAGGCCAA 1680 CCTGCTTGGG GCCTCAGCAG CGGGGGCTGG CGAGGCCAGT TTTCTCCAGC GGTTCTAAGC 1740 CGCTCGAGGG TGGTGCCCAC GCCGGCTTCC AAAACAGGCT TGAGCCAAAT CCACGTCATG 1800 GCAATAAACG TGCTTCCTGG GGCGACTGTT TGCAAAGGGA TGTGATTGTC TTCACTGAGA 1860 GCTGGATTTC TCAACCTGGC TCTGCTGACA TTCAGGGCCG GATCGTTCTC TGGGGAGGGA 1920 GTCATCCTGT GCATTGAAGG ACATTGAGCA GCATCCCTGG CCTCCACCCA CCAGATGCCA 1980 GGAGCACTCC CCACCCCGCA GGTGTGACAC CCAGAAGTGT CCCCAGACAT TTCATTGATT 2040 AGAGAGGTAT TAACAAAATA GCTTCCCGTT GTCCCCTGGG GACAAATCAC CCCCTGGGAA 2100 TAGAACAGCT GTCTTTGAGT TCTTCCCATA AGACCCAATC ACTGTTCATT GCAGCCACTG 2160 AGCTTTTAGA AATTATCTGT GAGTTCTTTC TGTTCTGTGC TAACTTAAGA GTCATTTTCT 2220 TTTTTTCTTT TTTTGAGATA GAGTCTTGCT CTATCGCCCA GGCTGGAGTG CAGTGGCACG 2280 ATCTCGGCTC ACTGGAACCT CTGCCTCCTG GGTTTGATTC TCCTGCCTCA GCCCTCCCGA 2340 GTAGCTGGGA CTACAGGCGC CCACCACCGT GCCCGGCTAA TGTTTGTATT TTTAGTAGAG 2400 ACGGGTTTCA CCATAGTGGC CAGGCTGGTC TCAAACTCCT GACCTCAAGT AATCTGCCCT 2460 CCTCAGCCTC CCAAAGTGCT GGGATTATAG GCGTGAGCCA CCATGCCTGG CCCCAAGAAT 2520 CTTTTTTTTA ATTTTATTTA TTTATTTATT TATTTATTTA TTTATTTATT TATTTATTTA 2580 TTTTGAAACA GAGTTTCTCT CTGTCTCCGG GCTGGAGTGC AGTGGCGCGA TCTCGGCTCA 2640 CTGCAAGTTC TGCCTCCCGG GTTCGTGCCA TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG 2700 GACTACAGGT GCTCACCACC ACACCCAGCT AATTTTTTGT ATTTTTAGTA GAGATGGGGT 2760 TTCACCGTGT TAGCCAGAAT GGTCTCGATC TCCTGACCTC GTGGTCCGCC CACCTCAGCC 2820 TCCCAAAGTG CTGGGATTAC AAGCATGAGC CACTGCGCCC GGCCATCATT TTCTAATAAG 2880 AGGAATAAGA CCTCAGGCCC ACTGGGTATC AGGGTTTGGG CTTCGTGATT TTCCTCCATC 2940 ATCTCTAATC CCTCACGGCA GCTCTGCCCA TTTTAAAGAT GAGGAAACTG AGCCCCAGAG 3000 AGACACGTGG ATGTGTGAGT TTCCTGAGGT GTCTATAACA AAGTATTACG GGCTGGGAGC 3060 CCTCAAACAG CAGGGGTTGA TTCTCTCACA GTTCTGGAGG CCAGAAGTTG AAAATCAAGG 3120 TGTGGGCAGG GCTGGGTCCC TCTGGAGGCT CTGAGGGAGA ATCTGTCCCA GGCCTCTCTC 3180 CCGGGTTCTG GTGGCTTCAG CCATCCTTGG AGCTCTGGGC TTGTGGCCGC ATCACTCTGC 3240 CCTCTCCCTC CGTCGTCACC TGGTCTTCTC CCCTGTGTGT GTCCAATCTC CCTTGCCTTT 3300 CTCTCATGGG ATCACCTCAT CTCAAAATAC TTACCTTCAT GACATCTGCC AAGACCCCGT 3360 TTCCAGATAA AGCCACAGTC ACAGGTTCTG GGGGTAAGGA CTTAGACATG TCTTTTTTGG 3420 GAAGCCACAA GTCAACCCAC TGCAGGTAGA TTCCCCAGGC CACACCGCAG AGAGCCAAAG 3480 CCTAACCCGG GGTTTGAACC CGGCCTGAGC CCCAGCCCCC CGTTCAGGCT GCCTCTCTGC 3540 TCTCCCCTCT CTCGCCCGGG CTGCAGAAAG CCGGAGATCA GCACAACTCG CTGCATCGAT 3600 TGGGGATTTT TTCTCAGCTC CCCGAAAGGA GAAGTTGAGC TGTTTTGAGG TTTGAGTGTC 3660 GCTGGATGCA CCCCCTGACC CCCGCCCCCC GCGAGGGTTG CAGCCTCGCT GTGTAATGCT 3720 GACCAAAAAA CAGGAAGGGA GCACTGTGGA AAGCCGGTTC CAATCAGCTG ATCTGCCCGC 3780 CACTGCAGTT AACTGTTGCC ATCACCTTTC ACCAAGTCTA GGGGCTGCAG AAGCCATGAG 3840 TCTCCCCATC TTCCACATGG CCTCTAGCCT CCCAGTGCAG GCGCCCGTCG ACAGCCCAGG 3900 GGCTGTGGAT AGAGCACCTT ACAGCATCGG 3930
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