Tag | Content |
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EnhancerAtlas ID | HS064-05813 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr16:84627290-84630110 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr16:84628767-84628780 | GAACCTTCCAGAA | - | 6.19 | IRF1 | MA0050.2 | chr16:84627848-84627869 | TGACTGAAAGTGAAAGCTACA | - | 6.5 | IRF2 | MA0051.1 | chr16:84627852-84627870 | TGAAAGTGAAAGCTACAA | + | 6.24 | RFX1 | MA0509.2 | chr16:84628239-84628255 | TGTTTCCATGGTAACC | - | 6.73 | RFX1 | MA0509.2 | chr16:84628239-84628255 | TGTTTCCATGGTAACC | + | 6.75 | RFX2 | MA0600.2 | chr16:84628239-84628255 | TGTTTCCATGGTAACC | - | 7.08 | RFX2 | MA0600.2 | chr16:84628239-84628255 | TGTTTCCATGGTAACC | + | 7 | RFX5 | MA0510.2 | chr16:84628239-84628255 | TGTTTCCATGGTAACC | - | 6.97 | RFX5 | MA0510.2 | chr16:84628239-84628255 | TGTTTCCATGGTAACC | + | 7.07 | SREBF2 | MA0596.1 | chr16:84627809-84627819 | ATGGGGTGAT | + | 6.02 | ZNF263 | MA0528.1 | chr16:84628809-84628830 | GGGGGAGCGGGGTAAAGAGGG | + | 6.25 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_09246 | chr16:84625458-84646481 | CD14 | SE_10600 | chr16:84626481-84629446 | CD19_Primary | SE_10600 | chr16:84629515-84636021 | CD19_Primary | SE_11114 | chr16:84621939-84652116 | CD20 | SE_12322 | chr16:84627347-84629561 | CD3 | SE_14767 | chr16:84627217-84632267 | CD4_Memory_Primary_7pool | SE_15740 | chr16:84627227-84629504 | CD4_Memory_Primary_8pool | SE_16608 | chr16:84627008-84629863 | CD4_Naive_Primary_8pool | SE_17292 | chr16:84627276-84629678 | CD4p_CD225int_CD127p_Tmem | SE_18003 | chr16:84625951-84646438 | CD4p_CD25-_CD45ROp_Memory | SE_18985 | chr16:84625856-84637709 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19809 | chr16:84627254-84636010 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_21255 | chr16:84626979-84629864 | CD8_Memory_7pool | SE_31867 | chr16:84627346-84635991 | Gastric | SE_32646 | chr16:84626311-84630293 | GM12878 | SE_53279 | chr16:84627290-84629422 | Small_Intestine | SE_53279 | chr16:84629459-84632344 | Small_Intestine | SE_53428 | chr16:84627266-84629436 | Spleen | 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 |
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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: 1 | ID | Chromosome | Start | End |
GH16I084592 | chr16 | 84626261 | 84644894 |
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Enhancer Sequence | GTATTTTTAG TAGAGACGGG GTTTCACCGT GGTCTTGATC TCCTGACCTC GTGATCCGCC 60 CACCTCGGCC TCCCAAAGTG CTGGGATTAC AAGCGTGAGC CACCGCGCCC GGCCATTTTA 120 ACCACTTTAA AGCATCCAAT TCAGTGGCTT TAAGGACACT CACAATGTTG TGCCATCATC 180 GCTACTATCT AATTTCACCA CTCCAACGAG AACTCCCGTC CTCAAGAACA GTCACTCCCC 240 ATTCTCCACC CCATTCCCCC AGGCCCTGGC AGCCACTCTT CCACTTTCTG TCTCTATGGA 300 TTGGCCTGTG CTGGACATTT CATTGAAATG GACTCATATG CTATGTGGCC TCTGCGGTCT 360 GGCTTTCACT CAGCGTCACA TCTCCAAGGA TCATCCCTGC TGCCGCATGT GCGGGTCACC 420 ACTTCATTCC TTTTATGGCT GAACAGCACT CCATTGCATG GAGAGAGCAC ATTTTGCTTA 480 TCAGTGCATC AGTTGATAGA CATTTGGGAT CCTTCCAAAA TGGGGTGATT TCACGCCTCC 540 CTTATCAGTT GACCATGATG ACTGAAAGTG AAAGCTACAA AACCCACCTA GCCCATCAGG 600 GTGGAACCTC CAACCTAAAG CTCCTGACAC AGGGCGGGGC TGCCAGGTGG CCACAGCGCA 660 CAGGAAACGA GACTGGTGCA AGAGATGGCA GTTCCTCACT TGTAAGGTGC AAAGTGCGCA 720 GCCACAGGCG GCTGGTGCAG ACTTGGAGTG TGGGGGAGCA GCGCTTTAGC TCGAGAGCAT 780 TTCTCAGCAG TCCCCGTGGT GTCTGGGAAG CCAGGGCTCT GTTTTGAGGA GTGTCGTCAG 840 AGCATCAACA CCAAAGTGCT TAATTAAATG GCAGCCTTGA CCTGAGGGGG AGGAGGGGCT 900 GAACATCCGC CTCCGACTGC ATTTCACAAG CAAAAGAACA CGGTGAGTGT GTTTCCATGG 960 TAACCGCTCT CGGGTTCCCA TTTCCACATT GGTCAGCCCG GACTTGGATC CAAACTACCC 1020 ATCCCTGGCC CAAGCCTCCA TGGAGGTAAG TTACCAGCCC TGCTTTGGGC CAACGCAGTT 1080 TTTGGGGACC TCAACCATGT GTTCAGCCCA TGGCCAAGGC TTCGGGCTGA GCCAGCTCTC 1140 CCAGCCTCTC TCTCTTCTCA GTGTCGCCCC CTCCCACGGC TCTGGCTGGC TCCTCTGCGG 1200 AGCTCCATGG CTTTTCCAGC GTCTGCCCTC TCTGCTGGCT GCCAAGTGCC TCCACATGCC 1260 GGCCATGCTC TGCGCACCTC CAACCCTCCA CATCCACCCT TCCCCTCTTT CAGACCTCCC 1320 CAGGTCTACC TTGGGCAACA CCCTTTGCCC CCGGAGGGTC ACAGATTCTT GTTGAAGAAC 1380 CACAGGCATT GTCCCTGTGT CCCAAGTACC AGCCCAGGGC CTGGCACAAG ATAGATGTAC 1440 AATAAGTAAG TTACACCCAC AACCCCAAGG ACACTGGGAA CCTTCCAGAA CCACAGCCTG 1500 ATGTCATTTA AATGATCGTG GGGGAGCGGG GTAAAGAGGG ACGTGGTTTG CTAGGTGACT 1560 GCTGCGTGCT TATCCGACAA TGGTTTGGTC AACAAGATTG CTGACAGGCC TGTTTTTGAA 1620 AATCCGAGTC ACGTTATGCT TACAAATGTT TGCTGCTAGA GATCTGGCAC GACAGTGACG 1680 GGTCAGCTGA GTCGGAGACG GAAAACCTGT TGGTCTGCGC ACCGTTTTTG CAGCTGCCCG 1740 GCAGACTGGA GGCCTCTCCC CAACCCTGCT CACCCTGAAG GAGGTTCTCG GTCCCTTTTG 1800 ACCTCACACT GGGCAGTGGA AGGGGAATCG CTAGTTCTTC ATCCCTGGTT TAGTTACTTT 1860 CCCTCTTCTG AACAAATTGG GTCCACAAAC CCCAGTGGCA GTCACAGCCC CACATCAGCA 1920 GTGGGGAGCC CTAGGCTCCC TCGTCTATGT CGGGCTATTG TCACTCCTGT ACGCGGGAAC 1980 ACTGGCATAT CTACTAAAGG GCACAGAGAA ACGCTGTCCT GTATATATTA GTGTGATATG 2040 TGTGTGCGTA TATATTTGTG TATGTGTATA TATACATATA TTTGTGTGTA TAATATGTGT 2100 CTATATGTGT ACAGGTGTGT TTGTATATGT GTGTATATAC ATACATTTGT GAGTACAGGT 2160 GTATATATGT GTGTATATAT ATTCATGTAT TTGTGTATGT GTGTTATATA TACATGTATG 2220 TGTATGTGTG TGTTATATAT ATACATGTAT GTGTATGTGT ATGTGTGTTA TATATACATG 2280 TATGTGTATA TGTGTGTGTG TATGCACTAA GACGGCAAAA CTGCCCAGAA GAAGGTTGGT 2340 ACCTGGGCTT TCCATCACCC TCACTGTGCC ACTTGGTCCC CAACAGGGCC AATGGTCCAT 2400 CTCTTCAAAC TGAAGCTGAG AGTCCAGGTC TACGCAGAGG AGACAGGGAG ACTGGGCAAC 2460 CCCAGTGGGG GACGGGGGAC CCAGGACTTC ACCCAAACAC AGGTACCAGA GACAGATGCC 2520 ATGAGCTCCT TCTGCTGGAG CCCTCAGCAC AGGGGAGTGG TCTATACCCT TAACCTTCTC 2580 TGCAATGTCC AGGGTGCAAG TTCAAATTCC AGAATCCTTT AGAAACTTAC CCCCACATGT 2640 ACTAGCCTTG TGACCCAGCC CAGAGTCCTG AATGTCTCTA AGCCTCAGTT TCCTCATCCA 2700 CAAAATGGGT CAAATACTTA CCTCATAAAG TGGTTGGGAG GATTACATGA AAAAGAAATG 2760 AGATCTGAAG GGTTGGCTGA TGGGAATCAT TGCTGATTTT TGACCCCCAA CACCTCTCCA 2820
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