Tag | Content |
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EnhancerAtlas ID | HS062-15422 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr7:142490300-142493280 |
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) |
CTCF | MA0139.1 | chr7:142491303-142491322 | GGCTGCCCCCTGCTGCCCA | - | 6.25 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_10458 | chr7:142490667-142491364 | CD19_Primary | SE_10992 | chr7:142490229-142511921 | CD20 | SE_11861 | chr7:142491838-142509385 | CD3 | SE_14462 | chr7:142490594-142491283 | CD4_Memory_Primary_7pool | SE_14462 | chr7:142491771-142511449 | CD4_Memory_Primary_7pool | SE_15402 | chr7:142491881-142500323 | CD4_Memory_Primary_8pool | SE_15813 | chr7:142491658-142500550 | CD4_Naive_Primary_7pool | SE_16301 | chr7:142491721-142501237 | CD4_Naive_Primary_8pool | SE_16869 | chr7:142491830-142509475 | CD4p_CD225int_CD127p_Tmem | SE_17317 | chr7:142490561-142513566 | CD4p_CD25-_CD45RAp_Naive | SE_17799 | chr7:142490662-142511579 | CD4p_CD25-_CD45ROp_Memory | SE_18273 | chr7:142490551-142512240 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19176 | chr7:142490652-142491343 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19176 | chr7:142491838-142492519 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19176 | chr7:142492574-142509454 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19996 | chr7:142490747-142509282 | CD56 | SE_20831 | chr7:142492309-142500862 | CD8_Memory_7pool | SE_21462 | chr7:142490759-142491436 | CD8_Naive_7pool | SE_21462 | chr7:142491654-142509656 | CD8_Naive_7pool | SE_21921 | chr7:142491616-142509527 | CD8_Naive_8pool | SE_22327 | chr7:142490622-142510498 | CD8_primiary | SE_30895 | chr7:142490690-142491802 | Fetal_Thymus | SE_30895 | chr7:142491858-142516124 | Fetal_Thymus | SE_39429 | chr7:142490652-142491302 | Jurkat | SE_39429 | chr7:142492108-142492590 | Jurkat | SE_55099 | chr7:142491943-142492302 | Thymus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH07I142784 | chr7 | 142491839 | 142492590 | GH07I142782 | chr7 | 142490769 | 142491830 |
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Enhancer Sequence | AACTCCAGTC TCCCACACAG TCTGCTCTGG GTGAATTACT CTTTCTCTAT GTCAATTCCC 60 CTGTCTTGAT AAATCGGTTC TGTCTATACA GCAGGCAAGG TGAACCTATT GGGCAGTTAC 120 GATATCTCTC TGAAAACAAG TCACTATTTT TTGTTTGTTT TTGTTTTTGT TTTGTTTTTG 180 AGACAGAGTC TCTCTCTGTC GCCAGGCTGG AGTGCAATGG TGCGATCTCG GCTCACTGCA 240 ACCTCCGCCT CCCGGGTTCA AGCTATTCTC CTGCCTCAGC CTCCCAAGTA GCTGGGATTA 300 CAGGCAAGCG CCACCACGCC CGGCTAATTT TTTGTATTTT TAGTAGAGAC AGGGTTTCAC 360 CATGTTAGCC AGGCTGGTCT CGAACTCCTG ACCTCAGGTG ATCCACCCGC GTCCGCCTCC 420 CAAAGTGCTG GGATTACAGA CGTGAGCCAC CGCGCCCGGC TTCAGTCACT AACATTTTTA 480 CTGACTCTTC TGGCACCATG ATTAACCCCG ACACGCACTA TCGCATGCAA TTCTCACAAC 540 CCCATGAGGT AGGTATTATT ATTGCTCCTA GCTTACAGAT AAAGAGACAG AGTTTAAGAG 600 GTTTAGCCAC GCTACGGGGC TGCTGGGAGC CCGGCAGTCT GGCCACAGGA GGTCGGTTTC 660 ACGGAAGGGC AGGATGTGGC GGCATCTCCT GAATTTAAGG AGTCTTGGGG GCGCGGTGCT 720 TCTCTGTCAT TGGGCAACTC ATTTTAGCCT CTTGGGGTTT CAGTTCCTCA ACTGAGAACA 780 AGGAATTTAG GTTGAAATGA ACATGCTGGA AAGCTTTCAA GAATTGCACA CGTGAAATGC 840 TCTTTGCGTG TCTCCCGGTC TCCCACCCGC CCCCGACACA GAGGCGCAGG AGTAACCCTG 900 CTCCCTTCCG CGTCCTCGCC CCACCACGAG CTGCGCATTC TTCTCGCCCC CTCAAGTGGC 960 CGAGCTCAGA TTGCAGTTAC TTAGGTCTAA AAAAATAAGG AAAGGCTGCC CCCTGCTGCC 1020 CACATGGATG CATGACCCCA ACCTGATACC TGCCTAACTG GTCTTCCTAG CTTTTATGGA 1080 AAAAACGCTG CATATGAGCT TGGGCATACC GTCCAGAGAG GCAAAACTGG GACAAACTCC 1140 ATCGGAATTC TAAAAAACCA TGATGCCAAG ACAGAGTGGC ATTATTATTT ATAAGGCCAG 1200 TAGGGATGAG GGCCCCCACT AGGTGATTAA AAGACACTAA CTTAGAGGAT GAATTATTGA 1260 TAAGTAAACG AGGTGAGTAA GGCAGGAAAA CATGCAGAAA TAGATCAAAA TAAACTGAAT 1320 ATTTCAATTA GGAAAGGTAC TGGCAAGAGG CTTTGACACA ATCCAATGGA TGAAAGCAAT 1380 CAACTTTTTT TTTTTTTTTT TTTTGACAGA GTCTCACTCT GTCGCCCAGG CTGGAGTGCA 1440 GTGACTCAAT CTCGGCTCAC TGCAACCTCC ACCTCATGGG TTCAAGCGAT TCTCCTCCCT 1500 CAGCCTCCCG AGTAGCTGGG ACTACAGGCG CACACCACCA TGCCCGGCTA ATTTTTTTGT 1560 ATTTTTAGTA GAGACAGGGT TTCACCGTGT TAGCCAGGAT GGTCTCGAAC TCCTGACCTC 1620 ATGATTCGCC CTCCTCGGCC TCCCAAAGTG CTGAGATTAC AGGCGTGAGC CACTGCACCT 1680 GGCTGCAATC AACTTTTTAT GCAGGCATTT GGTAGCATGT TGCGAGGTCC ATCACTATTA 1740 ATGCCGTGAA TATACCAAAT CCTCTTTTTC TTTCTTCCCT AAGTTCTAAG GGCCATGCCC 1800 TGGCACCAAA CTTATGGCAG TCCTAGACTA CCCTCTGATG TTCACCATGG CTTACCTCTG 1860 CCCTGTTCTA GTTGGGGACA AGCTGTGGGT CCCAAGCCTG GCATTGTAAC AGAAACGCCC 1920 AGGGTAATTT TCTGTTTGTT TATTTAAATA AATAAATAAG TAAACTCAGT CTTGGAGATT 1980 TTAACTCAAT AGGTCATGAA GACTACTCAG AAATCTACAT TTTTCACAGT TGTCCAAGTG 2040 ATTAAGTCCT CACTGAGCAA ATTCAGGACA AGGAAACAAC TTCTTACATA AATTCTACAT 2100 AACTTCATAC ATAACTTCAC ACATAAACTT CTTTGGCAAA AAAAATGACT TTGTAAATTA 2160 AACAAGTAGG TTTTTAAAGT AGCATATTTT ATTTAAAGCC AAATTTTCTT GATTTTTAAA 2220 ATTAACTTAA GTTTGACTTT CAATAGACAA TAGAGCTATA TGACTCTAAA ATGGAAACAA 2280 CCCAGTAACG TTGACACTGG GAAATGTAAC TTTTACTTCC GCTCTGTTTC TGTCTACTCC 2340 ACCCATTCTT TCTTTTCTTT TTTTTTTTTT TTTTTTTTTT TTTTGTTTTG ATAGAGTCTC 2400 ACCGTGTCGC CCAGGCTGGA GTACAGTGGC GTGATCTTGG CTCACTGGAA CCTCCGCCTC 2460 CTGGGTTCAA GTGATTCTTC TACCTCAGCA GCCTCTCAAG TAGCTGGGAT TATAGTCACC 2520 TGCCACCACG CCCAGCTAAT TTTTTTTTTT TTTTTTTTTG TACTTTCAGT GAAGATGGGG 2580 TTTTGCTGTG TTGGTCAGGC TGGTCTCGAA CTCCTGGCCT CAGGTGATCT GCCTGCCTTG 2640 GCCTTCCAAA GTGCTGAGAT TACAGGGGTG AGCCACCGCA CGTGGCCTAC TCCACTCATT 2700 CTTAATAGGT CATCACTCTT GTCAGTTTCT GTTGTATCTT TACAGTGTTT CTGTATACAA 2760 AATGTATACA AAATCAAGTA AATACAAAAG TATAATTCTT CTTTTCCCCC CTCTGTTAGA 2820 CAAAGGTGGC ATCTAGTTAT GCTATTCTGA GACTTTCTCT TTTCTGGGTT AATAATGTAT 2880 CTTAGAGAAT TTTCCATAGC AATATAAAAT ATTTTGATTC TTTTTTTAGC ATTGAATATT 2940 ACTCCATTGT GTGAACATAT CACAGTTTAT CCAGTCCCTT 2980
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