Tag | Content |
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EnhancerAtlas ID | HS092-16403 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:70103890-70105610 |
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: 30 | 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_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 | chr14:70104003-70105324 | 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 | CTCTTTCTGC TCTGTCTGGC TAATACCTTC TAAAGCCAGG TATCAGCTTA GACTGCCGCT 60 TGCCCCATAC TTGTGTGGGT GCCTCTCCTT GGTGCTGGCA TTACACCCTG TGCTCAGTAC 120 TTACCGCACC ATATTACCGT CTGTTTCCTT GTTCTTCCTG ACCTTACCTG AGCTTCTTGA 180 GGGCAGAGAC TGTCTGCTAT CACCACTGTA TCCCTCATTG CTGGTGCAGC GCCTGGGATG 240 TGGTATATAC ACAGCAAATG TTGAAGGAAT GAATGTCCCC CCCTAACCAG GGTCAGCATA 300 CCCCAGTGCG CTCTGGGAAC TGTTCTCTGA CCCTCTCCAC CCTTACCCTG CCTAAGGCTC 360 TCTCTTTCTG AGCTGTGTGT GGGTGCTGGA GAGCCTTGGA TAATGCTGAG TTGTTTTTGA 420 AGTGTGTCTC ATTGTGGCAA AGCATTGGGT GATGTTGCCA TCCCCACCCC CAGGACACTC 480 TTGCAAGAAT TGCTTCCACC AGGGATGGGC ATTGACTTTG ACCTGGTCCT CCTCATCTCC 540 AGCCCTGGAG GAGGGGCAGG CAAGCACGTG CAGATTGCTG TCCTCTGACC AGCTGCCCAG 600 GGCTGGGCCA TCTGCTGCTT GTGACAGCGG GTGGGGTGAG AGGGGTGAGT GACCTGTGCA 660 GGGGAGGGAG TGTGGGGCAG CAGCATAGTC ACTTCAGTGC ACTGACTGCA TGACAGAGTC 720 CAGCCCCCCT TCTCCCCACG TTCTATCTTC TTTTCCAGTG CTCAGTTATG CTATGCTTCA 780 TCCAGGTCTT GGTTTTGTTC CAGCTGCTGC CCCCCACCAC TCTGCTAGGA GAACTCTTGC 840 TGTGTTTTTG TTAACTCTGT GTGTGTGCTT TGCCCTTTTG CCTATGCCTC CAAGAATCTT 900 TATGTTACAT AAGACAGCAG CAGCAAAAAA CAGAAACAAA AACAAAAAAT GTTAGAAATG 960 AAACTTTGGA CCCTTGTTAT TCTCTGTTCA GATGCAAATG ATGAATCTCT TTCCATCAGA 1020 GTTTATACCT TTCTGTTTAC CACCCCGTTT TCTGTCCCTC CTCCTGGAGA GCCTTTGAAT 1080 GGCAGGGATG GGCTGAATCA CTCACTTGGA AGGACTGTAA TTTAGCTTGT GCTTCAAACC 1140 TTGCCTCTTT CTGGCCTTGT AAGGACCTAA GAAAGACGCA AAAAGGAAGT AATCTACCCC 1200 CATCACTCTT GGTGTGAGTT TGAAGGTTCT GAACTGGGGT GGGGTGGGGA GTGTGTGTGT 1260 GTGTGTGTGT GTGTGTGTGT GTGTGTAATT GTGTGTGTGT GGGATTGAAG GATGAGGGTT 1320 GTGGACAGTC TTAAAAGCCA CCTTTACCAA ATGAAGAGGT GACAAAGCAG GGACTGGAAG 1380 GGCAGCATAC CCTAACCAGG ACTTCCCCAA ACTTTAACAT GCATATGAAT CACCTGGGGA 1440 ACCTTACTAA AATGCAGATT CTGATTCAGT AGATCTGGGA TGAAGGCTGA AATTCTTCAT 1500 TTCTAACAAG CTCCCAGGTG CTGCCAGTGC TGCTGTTAAT GGACCATACT TTGAATAGTA 1560 AGGCTGTGTC CTTCCTATTC CACCTTTTAA TAGTTGATTT AAAAGACTGA CCTAGGGAAG 1620 GCAAGACAGG GGCTAGTCAG GACTTGCGTA ATTTAAACCC AAGGTCCTGG GCTGGCTTCT 1680 CAGCCAGTGT CTACAGAGCC TTTTAGGCGG GCCCCTCTTA 1720
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