| Tag | Content |
|---|
EnhancerAtlas ID | HS073-05634 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr16:84640030-84642730 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFKB1 | MA0105.4 | chr16:84640676-84640689 | TGGGGATTCCCCG | - | 6.34 | | NFKB1 | MA0105.4 | chr16:84640676-84640689 | TGGGGATTCCCCG | + | 6.41 | | SNAI2 | MA0745.2 | chr16:84640116-84640126 | AACAGGTGCA | + | 6.02 |
|
| | Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
| SE_09246 | chr16:84625458-84646481 | CD14 | | SE_10600 | chr16:84639048-84644362 | CD19_Primary | | SE_11114 | chr16:84621939-84652116 | CD20 | | SE_12322 | chr16:84640295-84642247 | CD3 | | SE_12322 | chr16:84642443-84645023 | CD3 | | SE_14767 | chr16:84632378-84644428 | CD4_Memory_Primary_7pool | | SE_15740 | chr16:84639803-84643728 | CD4_Memory_Primary_8pool | | SE_16608 | chr16:84640065-84645566 | CD4_Naive_Primary_8pool | | SE_17292 | chr16:84640235-84640876 | CD4p_CD225int_CD127p_Tmem | | SE_17292 | chr16:84640962-84644320 | CD4p_CD225int_CD127p_Tmem | | SE_18003 | chr16:84625951-84646438 | CD4p_CD25-_CD45ROp_Memory | | SE_18985 | chr16:84638624-84646326 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19809 | chr16:84639565-84644252 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_21255 | chr16:84639240-84643622 | CD8_Memory_7pool | | SE_31867 | chr16:84640146-84641887 | Gastric | | SE_32646 | chr16:84637938-84644281 | GM12878 | | SE_53279 | chr16:84640371-84643362 | Small_Intestine | | SE_53428 | chr16:84629488-84645031 | Spleen | | SE_58632 | chr16:84618716-84691095 | Ly1 | | SE_59422 | chr16:84582392-84644442 | Ly3 | | SE_60919 | chr16:84626327-84654674 | DHL6 | | SE_61298 | chr16:84618328-84643462 | HBL1 | | SE_62422 | chr16:84609550-84652864 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 84641438 | 84641605 | | chr16 | 84641200 | 84642196 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I084592 | chr16 | 84626261 | 84644894 |
|
Enhancer Sequence | GTTCCCAGCG CTGCCAATAC TGCAGAGAAC AAAGCTGACC TGGTTGCCCC ACGGGGCTTG 60
GATGCTCCCA GGAAAGTCAC AAGATAAACA GGTGCATAAC TGCACATGTG GCTATGATCT 120
TAGGCACTGC TAAATGCTGC AAGGAGATGC TTTTTGACTC CTTGTCACCT TCTCCAAGGC 180
CATGTCTGGT TTCAGTGGTA GTGGGCGTAG CCACTTGGGT ACACCATGAC ATCCTGCCAC 240
GTCTAGCTGC TCAACCTCAC AGAGGCACAG CCTGGAGTGC AGAAACCCTA AAGCCCCTAA 300
AGGACCCCTC AACCAATGGG GGATAAGAGT CGGTGGCTAC GTGCCCCCGC CTCCCAGGGC 360
TGCACCCTCC ATGTTCCTCT TAGGGTCCCT GAGGGATTCT GTCCCAGGTG CCCACAGCAG 420
TAACTGTAGG ATTCTGTCCC AGGCGCCTAC AGCCCATAAG AAGTAGAGCT GAAATTTGAA 480
CCCAGGCATT ACGGGTTCTC TTCTATAAGC AAGAGACAAA GGAGTGGACA GCCAGCACGT 540
GCTGGGAAAA GCCTATGACC CAGGATTCAG CCCATGACTT GGGCCCACTC AAGGGAGCAA 600
CACACCCATG GGGGAAAGAG ATTGGCAGCC ATCTAACCAT GAAGGATGGG GATTCCCCGC 660
CAAGGATACC ACCACCAAAG GGACAAAGTC CCTCTCTCCA GGAGGACTTC GCCAAGGAGT 720
TGAAGAAACA GACATGCACA CGACCACCAT ACGGGACACC AACACCACAA AGACAAGGAG 780
GGCATCCGAG CAGAGGGAAC ATTCACACCG GGCCTTGACG GGTGTGTAGG AGTCCTCCAG 840
GAAGGCGAAA CAGATGAAGA CAGTGCAGGC AGAGGGAAGA GAGTCCACAG GCCTAGGGAA 900
GCGGGAAGGC AGGCCAGCGC GGCACAGGGG AAGAGCTGAG AGCCTCGGAC ACAGATCTGG 960
ATTCAAAGTG CAGTTCTTCC CAACTGCAGC ATCTCCAGCA AGCGACTCTG GCTCTCCAAG 1020
GAAAATGTCA GGTTCCTCCT CAGTGAAGTG GGGATAATTT CTACTTGTGG GTGTCACTCT 1080
GCTCATTACT CCCTCAGAGA GAAGATAAAT TAGATAAACT AACACACGCA GAGCTCCTAC 1140
GTAGGGCCTG GGACTTGGGC ATCCCTAAGG TCAGCATCGT GTGTGTTGGG GACACACACT 1200
GGAGGGGTCG GCTGGCCAGC ACCTGTCATA AAGGGCACCC CATGTCATGT CTGAGCGTTT 1260
GGACCTTATG GAGAAAAGGT GTTGGAAGTG GGAGGCGGGG GAGCAATCTG ACCTGAAGGT 1320
TAGAAAGCCA CCCCTAGCCT GGACTGCAAG CTCACTGGGG TCAGGGAAAG GACTCAACTC 1380
AGTACTTGGC AAAGGGCTTG GGGCATAGTA GATGCTCGAG AAATGTCCCG GAGAAGACAA 1440
GGTCATGATC AAGGGTGGAG CCCTAAGAAA CGCCTAGACT TATCGGGCAG GAAGCAGAAG 1500
CAGCAGCAGA AGGAAGTGAG AATGACAGGA GAGAGACATA AAAGGAGAAC TAGGCAAGTC 1560
TAGCCACGCA GAAGCAGAAG CACAAGCGAG GGGGACTATC TTTTCAGGAG GTGCTGGCCA 1620
CTGGCAAATG CTGGAGGGAG GTAAAGTGGA TCAGAGACAA AGAAATGACC ACTAAATCTG 1680
GCAACTGGAA TATTTACCAA AGACCTAGAC ATAGAGCTCC ATGCTCTGGG TGTGGGTGGG 1740
CACCAGAATG AAATGGGGTA AAGAAAGGAT GGGAGACAAG GAGGTATTTA TAACACCTAT 1800
AAAATCTGTA AGGGATGCTT TCAAAAAGTT TGCATTAACT TCTGAATATT TTCAAGGGAC 1860
AAAAACCCAA TTCACCTAGT GTTTAGGGAA TGCTTTTTTT GAACTTGAGA CACTGTACTT 1920
ACCAGGAAGA TACACATCTA TCATCCTTCA TCATTTTCTG TTTGTGGTGA CACAGCCACA 1980
AACAGAAAAG AAAGCACAAA CATCACCATG CAGTAGACTG AAAGAGCTAC CACAAAGCCC 2040
ACGCCCCTGT GGACACACAA AAAAGCTATG CAGCGTGGCT CAGGGCCTCC CAGCAACAGA 2100
TCTGTGGGCA AAGAAGGCAA TGGGAGACTG GATAGTGCAG AAAATTACAA AGGTAATGTT 2160
TTCGCAGCCC TTCAGGGTAC CACTTAAAAA CAAAAACCCA GCCGGGCGGG GTGGCTCACG 2220
CCTGTAATTC CAACACTTTG AGAGGCCAAG GCAAGTGGAT CGCTTGAGCC CAGGAGTTCG 2280
AGACCTGCCT GGACAACATA GTGAAACCCT GTCTCTACAA AAGATACAAA AATGAGCCAG 2340
GCGTGGTAGC AGGCGCCTGT AGTCCCTGCT ACTGGAGACG CTGAGGTAGG AGAATCGCCT 2400
GAGCTGGGAG GCAGAGGTTG CAGTGAGCCA AGATCGTGCC ACTGCACTCC AGACTGGGTG 2460
ACAGGGCACG ACCTTGTCTC AAAAATTAAA TTAAATTAAA AACCCAACAT TGTTTCTGGA 2520
GCAAAGTAGG AACCCAATAA AATGTTTGTC GCATGCATTA ACGGACAGAC TGTTCAGCAC 2580
TTTATAACTG CCCAAAGCCC TGTCACAGAT TTGGAGCTTC TTTTTGATGT CACATTCCCT 2640
TAGACCTTAG GAAAGAAAGC AATTTCTCTC CTTCCCTTCT CGCCCAAATT TCTGAAACCC 2700
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