Tag | Content |
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EnhancerAtlas ID | HS031-15403 |
Organism | Homo sapiens |
Tissue/cell | Denditric_cell |
Coordinate | chr3:47012120-47014180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT1 | MA0137.3 | chr3:47012732-47012743 | TTTCCCAGAAA | - | 6.02 | STAT3 | MA0144.2 | chr3:47012732-47012743 | TTTCCCAGAAA | - | 6.32 | ZNF263 | MA0528.1 | chr3:47012652-47012673 | TCTCCCACTTCCCCATCCTCC | - | 7.23 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_00943 | chr3:47011823-47013610 | Adrenal_Gland | SE_11155 | chr3:47006228-47021706 | CD20 | SE_13638 | chr3:47012190-47014336 | CD34_Primary_RO01536 | SE_16650 | chr3:47013004-47014113 | CD4_Naive_Primary_8pool | SE_18708 | chr3:47011981-47014192 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20061 | chr3:47012241-47014117 | CD56 | SE_22640 | chr3:47012989-47013833 | CD8_primiary | SE_23114 | chr3:47011818-47013099 | Colon_Crypt_1 | SE_23114 | chr3:47013149-47013444 | Colon_Crypt_1 | SE_23749 | chr3:47011867-47013045 | Colon_Crypt_2 | SE_28630 | chr3:47011456-47013166 | Fetal_Intestine_Large | SE_31407 | chr3:47011864-47013611 | Gastric | SE_32585 | chr3:47012045-47013761 | GM12878 | SE_40617 | chr3:47009514-47013782 | Left_Ventricle | SE_41619 | chr3:47011859-47013106 | LNCaP | SE_41619 | chr3:47013118-47013549 | LNCaP | SE_42118 | chr3:47006473-47013770 | Lung | SE_47478 | chr3:47011837-47013097 | Pancreas | SE_47478 | chr3:47013259-47013604 | Pancreas | SE_48306 | chr3:47011163-47013545 | Psoas_Muscle | SE_48684 | chr3:47011649-47013186 | Right_Atrium | SE_49453 | chr3:47011900-47013041 | Right_Ventricle | SE_50160 | chr3:47011783-47013586 | Sigmoid_Colon | SE_52388 | chr3:47011775-47013545 | Small_Intestine | SE_53507 | chr3:47011625-47012444 | Spleen | SE_58746 | chr3:46966845-47032612 | Ly1 | SE_59747 | chr3:46966600-47033537 | Ly4 | SE_60850 | chr3:46965041-47030117 | DHL6 | SE_62445 | chr3:46966331-47033109 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 47013284 | 47013477 | chr3 | 47013189 | 47013256 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I046969 | chr3 | 47011422 | 47014580 |
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Enhancer Sequence | AGCCAGACAG CCAGTCTCCC TGTCTCAGAG CAGCAAGAGA CAGCCCAATT CAGGGCAATC 60 GCTCAGGAAA GCTTGGCATG TTTATGCCAA GTTAATCATC ACCTTTAGAG AGCCTCCATT 120 TGGCTGCTGA AGAAGAAAGA GGTCAAAGGA GGACAGAGTG GCCTCACACT GCCCTGCCGG 180 ACAGCACTGT AAAGAGATGC CAGAGTTTCA TCCACACAGC CTTGAACTGT TCACCTACTC 240 ACCCAGCCAG GAACTTCTGG ATGAGCATCA GGAAATGAGG TTCAAATACA ATACAGAAAA 300 GTGTGCCCAG GCTGGCTACC ATCCCTGCTG GAAACCCTGG CTCTTGCAAA ACTTGGCTAC 360 CAGAGTACCC CAGTCCAGCA CTTTCAGACT GTACCCCTGC CCCTGTATCA CTGCCAAGTG 420 CTTGCTGTCA AACTCCCTGG AGCATCTCCA CTCTCACCTC TATGCACCTG AATGTTCCCA 480 CCTCTAAAAT GCTCCCTGGG AACACTCTCC TTTCCAGCTA CCTCGATGAC CTTCTCCCAC 540 TTCCCCATCC TCCGTGGCTC AGCTCAAGTT CCATGCTGCC TTCCCATGAA GCTTCCTCAG 600 GCTCTGCCTG GCTTTCCCAG AAAATGAACC CCAGCAGTAC TGTCTTTCTG CGTGTCAACG 660 GGAACTGGCT GACCTACAAG ATGCTGCTTC AGGCAGTGCT GTGTCCTCTA CAGAATCCCC 720 TTCCCCCAGG GGGTCTTGCA TGGGCTGGAA TCCTGGAATC CAGGAGACAT TACTTCCCCT 780 CCTCAGCCTT GGACATCCCA GCTCTCCTCA GCCTCTTGCC TTGCTCCTCT CACTAATAAG 840 TGGCATCAGG TGGGCTGACC AGGACGTCTT TGTAAAACTA CAGCTGCATG ACTACAAGAG 900 AGTTTTGCGC AGAATAATAC ACGGAAACAT TGCAACCCCT AATCTTGTCT CTTTCCATCT 960 GCCACAACCT CAGGACCCTG AATTGTCTTA ATATCACTAA ATTATGAGTT TATAGTCTGG 1020 TGAGAGTTAG GAAGAAAGAT AAAACTGTGA GGAAAACCAA CTCCATGCCT GAAATTCCTA 1080 AGGCCTCCAG CAAAACCATG CCCACAGTAA GAACTCAATG AAGGACCTGC CACTGAGTGC 1140 TAGGAAACCA GCAAGATGCC ATCCTCATGG GGCAGACAGG TGCTCTCCAA GTGCAGGCAG 1200 AGAAGGTGCT CAATCCTGGT GTCTGTTGTC ACATCAGAAA CCTGAACTAA AAATGTGAAG 1260 CCGCTTCCTC TCTGAAGGAG GAGACTCAAG GGGTTTTATC TGGCCACAGC AGGCAGTCAT 1320 ACTTCCTCAC CAGACTCCCC ACTTAAAAGG TCCAGCAGAA AGGGCCACAG GCTGGAAAAT 1380 CAACTCAAAG GTTAGACCCT TACCTGTCCT GTCCCCAGGC ATTCACCTTA ATAAAAAAAA 1440 TCACTCAAGA ACTATAGGGA TTAAATATGA CACTAAAAAT ACATGCAACA AAATCAAAAA 1500 CAGATAAATT GAACTTCATC AAATTTTAAA CTCTTTGCGC AGCAAATGAG ACTATCCACC 1560 AGGTGCGGTG GTTCACACCT GTAATCCCAA CACTTTGGGA GGCCAAAGCA GGAGGACTGC 1620 CTGAGGCCAG GTGTTTGAGA TCAGCTTGGG AAACACAGTG AGACCCCCAT CTCTACAAAA 1680 AATTAATTTT TAAAAAAATG ACACTACTAA GAGAATGAAA AGATAATCCA GAGAATGGGA 1740 AAAAATATCA CTAATCTCAT CTCTAATAAT GATTTAATAT CCAGAATATA TGAACAATTC 1800 AATGACAACT CAATAACAAG AAAAAGAGCC CAATTAAAAA TATGGGCAAA AGGAATCTGG 1860 ATACTTCTTC AAAGAAAATA TATATACAAG TGGCAAACAA GCATATGAAA GGATGTTCAA 1920 CATCACTCAT CACTGGGGAA ATGCAAATCA AAACCACAAT GGGATACCAC CACTTCACAC 1980 CCATTAGGAA GGTTATAATT AAAAAAACGA AAAAAGAAGA TGGCTGGGCT TGGTGGCTCA 2040 CACTTGTAAT CCTAGCATTT 2060
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