Tag | Content |
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EnhancerAtlas ID | HS118-05917 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr14:70103300-70105850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIL3 | MA0025.1 | chr14:70104791-70104802 | ATGTTACATAA | - | 6.32 | REST | MA0138.2 | chr14:70103968-70103989 | GTGCCTCTCCTTGGTGCTGGC | - | 6.27 |
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| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_00199 | chr14:70099323-70104596 | Adipose_Nuclei | SE_01046 | chr14:70102157-70105863 | Adrenal_Gland | SE_04035 | chr14:70101898-70104377 | Brain_Anterior_Caudate | SE_06072 | chr14:70101632-70105993 | Brain_Hippocampus_Middle | SE_09201 | chr14:70101242-70106825 | CD14 | SE_10433 | chr14:70101569-70106019 | CD19_Primary | SE_10939 | chr14:70097782-70144384 | CD20 | SE_12430 | chr14:70102367-70104019 | CD3 | SE_13224 | chr14:70102353-70103977 | CD34_Primary_RO01480 | SE_13365 | chr14:70102301-70104103 | CD34_Primary_RO01536 | SE_14528 | chr14:70101259-70106068 | CD4_Memory_Primary_7pool | SE_18280 | chr14:70100327-70106944 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19536 | chr14:70101084-70106090 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20540 | chr14:70101529-70105909 | CD56 | SE_22932 | chr14:70101176-70106858 | CD8_primiary | SE_25838 | chr14:70101397-70105923 | Duodenum_Smooth_Muscle | SE_26683 | chr14:70102086-70105953 | Esophagus | SE_27827 | chr14:70102878-70107051 | Fetal_Intestine | SE_28670 | chr14:70102819-70107800 | Fetal_Intestine_Large | SE_31172 | chr14:70101683-70103635 | Fetal_Thymus | SE_31172 | chr14:70104003-70105324 | Fetal_Thymus | SE_31600 | chr14:70102121-70106556 | Gastric | SE_32500 | chr14:70101246-70105916 | GM12878 | SE_40959 | chr14:70101832-70105973 | Left_Ventricle | SE_42217 | chr14:70101998-70106034 | Lung | SE_50082 | chr14:70101582-70106026 | Sigmoid_Colon | SE_51685 | chr14:70101681-70105423 | Skeletal_Muscle | SE_52366 | chr14:70101738-70106890 | Small_Intestine | SE_53514 | chr14:70102062-70105872 | Spleen | SE_58413 | chr14:70076448-70170966 | Ly1 | SE_59839 | chr14:70072682-70121076 | Ly4 | SE_60579 | chr14:70076514-70162614 | DHL6 | SE_62292 | chr14:70076365-70194637 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 70104251 | 70104682 | chr14 | 70105047 | 70105358 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I069634 | chr14 | 70101235 | 70107288 |
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Enhancer Sequence | ACTCACAGAG CCTATCTCCG GTACTGCCAT GTGTGCTTTC TGCCTCCTTT CCAGAAGAGG 60 CAGGTAGCCA GTCTTTTTTT CTCATGAGCT GTTCCTACCT TGTTGGAGTT CCTGGAGGCT 120 AGTGCTGCTG GACCTCCAGT CTGGCAGAGG CCTGGACGAG AGCTATTCCT TGGGTTCTCA 180 GAACAGACCT AGCCTAGTGG AGAACAGTTC TGGGCCTGGC TCTGTGTCCA GAAGGGCTCA 240 GTCAGTGGTC AGATTCTGAT TGGGAGATAT ATGAGGAAAC TTTGTTTGGT GAGAGTTAGG 300 AGAATGGGGT TCTGGTTCAG CCATTCTCTC AAGAAGTCAT GATCATTTGA TAGGCCTCAG 360 TTTTCCTCTC CTAAAATGGG TAGATTGGAT TTTATAAGAT GATCCCAAAG TTCCTTAAGG 420 CAGTAATGTG TTAGGATTCC GTGACAAACC CGGGAGTCTG CCCCTGGTCT AGGTGACCAA 480 AGTTAGCAAA GGCTGGGACA GCACAGATTG CAGTTCCCAG GTCTCTTTTG CCTCCCAGCT 540 TTTTGATGTG TTTCTTCTCC TTGGAATGCC CCACCACTCC CTGTACCCAC CTCTTTCTGC 600 TCTGTCTGGC TAATACCTTC TAAAGCCAGG TATCAGCTTA GACTGCCGCT TGCCCCATAC 660 TTGTGTGGGT GCCTCTCCTT GGTGCTGGCA TTACACCCTG TGCTCAGTAC TTACCGCACC 720 ATATTACCGT CTGTTTCCTT GTTCTTCCTG ACCTTACCTG AGCTTCTTGA GGGCAGAGAC 780 TGTCTGCTAT CACCACTGTA TCCCTCATTG CTGGTGCAGC GCCTGGGATG TGGTATATAC 840 ACAGCAAATG TTGAAGGAAT GAATGTCCCC CCCTAACCAG GGTCAGCATA CCCCAGTGCG 900 CTCTGGGAAC TGTTCTCTGA CCCTCTCCAC CCTTACCCTG CCTAAGGCTC TCTCTTTCTG 960 AGCTGTGTGT GGGTGCTGGA GAGCCTTGGA TAATGCTGAG TTGTTTTTGA AGTGTGTCTC 1020 ATTGTGGCAA AGCATTGGGT GATGTTGCCA TCCCCACCCC CAGGACACTC TTGCAAGAAT 1080 TGCTTCCACC AGGGATGGGC ATTGACTTTG ACCTGGTCCT CCTCATCTCC AGCCCTGGAG 1140 GAGGGGCAGG CAAGCACGTG CAGATTGCTG TCCTCTGACC AGCTGCCCAG GGCTGGGCCA 1200 TCTGCTGCTT GTGACAGCGG GTGGGGTGAG AGGGGTGAGT GACCTGTGCA GGGGAGGGAG 1260 TGTGGGGCAG CAGCATAGTC ACTTCAGTGC ACTGACTGCA TGACAGAGTC CAGCCCCCCT 1320 TCTCCCCACG TTCTATCTTC TTTTCCAGTG CTCAGTTATG CTATGCTTCA TCCAGGTCTT 1380 GGTTTTGTTC CAGCTGCTGC CCCCCACCAC TCTGCTAGGA GAACTCTTGC TGTGTTTTTG 1440 TTAACTCTGT GTGTGTGCTT TGCCCTTTTG CCTATGCCTC CAAGAATCTT TATGTTACAT 1500 AAGACAGCAG CAGCAAAAAA CAGAAACAAA AACAAAAAAT GTTAGAAATG AAACTTTGGA 1560 CCCTTGTTAT TCTCTGTTCA GATGCAAATG ATGAATCTCT TTCCATCAGA GTTTATACCT 1620 TTCTGTTTAC CACCCCGTTT TCTGTCCCTC CTCCTGGAGA GCCTTTGAAT GGCAGGGATG 1680 GGCTGAATCA CTCACTTGGA AGGACTGTAA TTTAGCTTGT GCTTCAAACC TTGCCTCTTT 1740 CTGGCCTTGT AAGGACCTAA GAAAGACGCA AAAAGGAAGT AATCTACCCC CATCACTCTT 1800 GGTGTGAGTT TGAAGGTTCT GAACTGGGGT GGGGTGGGGA GTGTGTGTGT GTGTGTGTGT 1860 GTGTGTGTGT GTGTGTAATT GTGTGTGTGT GGGATTGAAG GATGAGGGTT GTGGACAGTC 1920 TTAAAAGCCA CCTTTACCAA ATGAAGAGGT GACAAAGCAG GGACTGGAAG GGCAGCATAC 1980 CCTAACCAGG ACTTCCCCAA ACTTTAACAT GCATATGAAT CACCTGGGGA ACCTTACTAA 2040 AATGCAGATT CTGATTCAGT AGATCTGGGA TGAAGGCTGA AATTCTTCAT TTCTAACAAG 2100 CTCCCAGGTG CTGCCAGTGC TGCTGTTAAT GGACCATACT TTGAATAGTA AGGCTGTGTC 2160 CTTCCTATTC CACCTTTTAA TAGTTGATTT AAAAGACTGA CCTAGGGAAG GCAAGACAGG 2220 GGCTAGTCAG GACTTGCGTA ATTTAAACCC AAGGTCCTGG GCTGGCTTCT CAGCCAGTGT 2280 CTACAGAGCC TTTTAGGCGG GCCCCTCTTA TCTAAGCTGC TGGCTTCTCT GAGCTCCTTT 2340 GGTCCAGTTT GGTTTCCAAG GTATAAGAAC CACAGCCCTT CAGAGGGTGT GTGTGCTTAC 2400 TCACAACAAG ATTGGGTCCT TGCCCGTTTC TCTTTGGATC ATTAGAAGTA GATAAGGCCA 2460 GGCCGGGTGC AGTGGCTCAC GCCTGTAATC CCAGCACTTT GGGAGGCTGA GGCGGGTGGA 2520 TCACAAGGTC AGGAGATTGA GGTCTCGATC 2550
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