Tag | Content |
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EnhancerAtlas ID | HS095-28800 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr7:142493970-142497020 |
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) |
RREB1 | MA0073.1 | chr7:142495587-142495607 | GGCGGGTGGGTGTTAGGGGG | - | 6.06 | ZNF263 | MA0528.1 | chr7:142495317-142495338 | GGAAGAGGGAGGGGGTGGGGA | + | 6.67 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_02778 | chr7:142493717-142496872 | Astrocytes | SE_10458 | chr7:142493711-142499724 | CD19_Primary | SE_10992 | chr7:142490229-142511921 | CD20 | SE_11861 | chr7:142491838-142509385 | CD3 | 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 | chr7:142492574-142509454 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19996 | chr7:142490747-142509282 | CD56 | SE_20831 | chr7:142492309-142500862 | CD8_Memory_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_25347 | chr7:142493902-142514183 | DND41 | SE_30895 | chr7:142491858-142516124 | Fetal_Thymus | SE_39429 | chr7:142493774-142509301 | Jurkat | SE_49938 | chr7:142494048-142506653 | RPMI-8402 | SE_50773 | chr7:142493655-142498088 | Sigmoid_Colon | SE_53139 | chr7:142493705-142500292 | Small_Intestine | SE_55099 | chr7:142493654-142508314 | Thymus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 142494676 | 142496039 | chr7 | 142496464 | 142496800 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I142798 | chr7 | 142495885 | 142497684 |
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Enhancer Sequence | GGGGGCGGAC CCATGGGAGG GGCTGTTTTT GTACAAAGCT GTAACATTGT GGGGACAGGG 60 TCCCTAGCGG GCCAGAAACT CCTACAATGA GCAGTTCTTC GGGCCAGGGA CACGGCTCAC 120 CGTGCTAGGT AAGAAGGGGG CTCCAGGTGG GAGAGAGGGT GAGCAGCCCA GCCTGCACGA 180 CCCCAGAACC CTGTTCTTAG GGGAGTGGAC ACTGGGCAAT CCAGGGCCCT CCTCGAGGGA 240 AGCGGGGTTT GCGCCAGGGT CCCCAGGGCT GTGCGAACAC CGGGGAGCTG TTTTTTGGAG 300 AAGGCTCTAG GCTGACCGTA CTGGGTAAGG AGGCGGTTGG GGCTCCGGAG AGCTCCGAGA 360 GGGCGGGATG GGCAGAGGTA AGCAGCTGCC CCACTCTGAG AGGGGCTGTG CTGAGAGGCG 420 CTGCTGGGCG TCTGGGCGGA GGACTCCTGG TTCTGGGTGC TGGGAGAGCG ATGGGGCTCT 480 CAGCGGTGGG AAGGACCCGA GCTGAGTCTG GGACAGCAGA GCGGGCAGCA CCGGTTTTTG 540 TCCTGGGCCT CCAGGCTGTG AGCACAGATA CGCAGTATTT TGGCCCAGGC ACCCGGCTGA 600 CAGTGCTCGG TAAGCGGGGG CTCCCGCTGA AGCCCCGGAA CTGGGGAGGG GGCGCCCCGG 660 GACGCCGGGG GCGTCGCAGG GCCAGTTTCT GTGCCGCGTC TCGGGGCTGT GAGCCAAAAA 720 CATTCAGTAC TTCGGCGCCG GGACCCGGCT CTCAGTGCTG GGTAAGCTGG GGCCGCCGGG 780 GGACCGGGGA CGAGACTGCG CTCGGGTTTT TGTGCGGGGC TCGGGGGCCG TGACCAAGAG 840 ACCCAGTACT TCGGGCCAGG CACGCGGCTC CTGGTGCTCG GTGAGCGCGG GCTGCTGGGG 900 CGCGGGCGCG GGCGGCTTGG GTCTGGTTTT TGCGGGGAGT CCCCGGGCTG TGCTCTGGGG 960 CCAACGTCCT GACTTTCGGG GCCGGCAGCA GGCTGACCGT GCTGGGTGAG TTTTCGCGGG 1020 ACCACCCGGG CGGCGGGATT CAGGTGGAAG GCGGCGGCTG CTTCGCGGCA CCCGGTCCGG 1080 CCCTGTGCTG GGAGACCTGG GCTGGGTCCC CAGGGTGGGC AGGAGCTCGG GGAGCCTTAG 1140 AGGTTTGCAT GCGGGGGTGC ACCTCCGTGC TCCTACGAGC AGTACTTCGG GCCGGGCACC 1200 AGGCTCACGG TCACAGGTGA GATTCGGGCG TCTCCCCACC TTCCAGCCCC TCGGTCCCCG 1260 GAGTCGGAGG GTGGACCGGA GCTGGAGGAG CTGGGTGTCC GGGGTCAGCT CTGCAAGGTC 1320 ACCTCCCCGC TCCTGGGGAA AGACTGGGGA AGAGGGAGGG GGTGGGGAGG TGCTCAGAGT 1380 CCGGAAAGCT GAGCAGAGGG CGAGGCCACT TTTAATCTTT TTTCTGGGGT GTTTAGAGAG 1440 AAGGTGAACG ATGGAGGAGA GGATTTGTTA GGACTCTGGG AGAGGCGAGA CTGGAGAGGA 1500 CGAAGGGAAA TCCTGGTTTG GGGAATGGGT AGGAGTGGGG GTAACTGCTA TTCGTAGGCA 1560 AAAAGAGCTG AGCAGGCTGG GAACAGCGCG GGTGGGCAAG GGTCAGCACT GCGGGCAGGC 1620 GGGTGGGTGT TAGGGGGCAG AAATCCTGCA GCCGAGGGTG CAGTAGAACA CAGAAGAAAA 1680 AGCCTGCCAA ACAAAAGTGG AACAGAGAAG CCAAAAAGGG AGATGAACAT GAGTCAGTGA 1740 AGAAAAGAAT GAAAGTTTAC TGTTTAGCAG TGTGGATCTC TAATCCGACT TAAAACTCCT 1800 TGTTCCCGAT TCCTATTCCT CCTAAGCCAG AGATCCCTGG GTCCAGGGTG AGGGCACGGC 1860 ATTCATGCTT ACCCACGGGC TGGTCAACAA AGAGGTGCTG ACCTGAGAGT AGGGCACATA 1920 ACCTCAGCCA CTGGGGTACA CTTACCACCC CCGCCCCCGT GTAGCTCCCT CCCCTATCCT 1980 GAAATCTCCC TTAGCACACT AAGTATTCTA GGTTAAACAG CCCAGATGTT CAGGGAGTTC 2040 ATTCGCCACA AACACACATT AAAATGCAGA CAATTTGCCT GTGAGATGAG GAAAATTCTC 2100 TGGAAGATTT AGGCCCTGAG AGCTGAAAAG GGACCCTAAA CATTACCTGG TGACAACTGC 2160 CCTGAGGCCA GAGAAGAGAA CTCACAATAT TGGTATATTA ACCGGTACCA TTTGTAGTTA 2220 GGCTGTCATT AATCTGGGTG TAATGGGGCT CAGCTACAGA GAAGCGTATC CAGAGGAAAT 2280 GTGGGGTTCC TGCAGTCAGC TGGGGCACCG AAAAGACCCA GACTTTAGAA CCAGATAAAG 2340 GCTGAGTTCG AACCTCTGGT TCTTTTGTGA TGTGGTGACC TTGGGCAAAT TAATGTGTGA 2400 ACCTCAGTTT CCTCAACTAT AAAATGTAAT GAACAATACC TACCACTTAC TATTGCTGTG 2460 AGGAAGAAAA GAGAGTCAAC ATGTACCGTG TACAGATTAT TGATGTAATT CAATGGTTCT 2520 TTTCCCCATC CTCCTAGGAG GTCACTGGGG AGACAGGGGG CAGGGTCAGC CCAGTGCCAA 2580 AGGATGGGCA GGATCTGAAG TGTGGAAATG GAGTAAGGCT GTGTCTGTGT CAGAGGTGGG 2640 TTGGGAAGAT GTGAGACAAA CATCACAATT TTGCCTAAGG TGAATCCAAC CCACAAGTAG 2700 AGCACAGGCC AACAGCAGCT CACTAGTACA CATACTTACA CCAGCAGCTC ACTAGTACAC 2760 ACACTTACAC CAGACGCTCA CTGGTACACA CTCACACCAG AAGCTCATTA GAACACACAC 2820 ACCGTCAGCT TGCTAGTACA CACACTTACA CCAGAAGCTC ACTAGTATAC ACTTACACCA 2880 GAAGCTCACT AGTACACACA CTTACTCCAG AAGCTCACTA GTACACACAC TTACACCCAC 2940 AGAGACAAGC CCCACACCAC ACGGACTCAC AAATGCAGAA GAAGAGTTGA CCCTGCCCTC 3000 ATGTACAGAT AGTATGCTGG TGTGTAGTGA GAGGCGGCTA GTGTTCGCCA 3050
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