Tag | Content |
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EnhancerAtlas ID | HS051-19494 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr3:47011990-47013810 |
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 | CACTATCACT GCACAAAGTT CTAGTGAGCA ACACTGCTGC TCTAATCTCT AGAGCCAGGT 60 GACAACCAGG AATTGCTGGT TGCCTGGAAC CTGCAACTTG ACAGCCAGAC CTCAGCCCCA 120 AGGGCTGGTC AGCCAGACAG CCAGTCTCCC TGTCTCAGAG CAGCAAGAGA CAGCCCAATT 180 CAGGGCAATC GCTCAGGAAA GCTTGGCATG TTTATGCCAA GTTAATCATC ACCTTTAGAG 240 AGCCTCCATT TGGCTGCTGA AGAAGAAAGA GGTCAAAGGA GGACAGAGTG GCCTCACACT 300 GCCCTGCCGG ACAGCACTGT AAAGAGATGC CAGAGTTTCA TCCACACAGC CTTGAACTGT 360 TCACCTACTC ACCCAGCCAG GAACTTCTGG ATGAGCATCA GGAAATGAGG TTCAAATACA 420 ATACAGAAAA GTGTGCCCAG GCTGGCTACC ATCCCTGCTG GAAACCCTGG CTCTTGCAAA 480 ACTTGGCTAC CAGAGTACCC CAGTCCAGCA CTTTCAGACT GTACCCCTGC CCCTGTATCA 540 CTGCCAAGTG CTTGCTGTCA AACTCCCTGG AGCATCTCCA CTCTCACCTC TATGCACCTG 600 AATGTTCCCA CCTCTAAAAT GCTCCCTGGG AACACTCTCC TTTCCAGCTA CCTCGATGAC 660 CTTCTCCCAC TTCCCCATCC TCCGTGGCTC AGCTCAAGTT CCATGCTGCC TTCCCATGAA 720 GCTTCCTCAG GCTCTGCCTG GCTTTCCCAG AAAATGAACC CCAGCAGTAC TGTCTTTCTG 780 CGTGTCAACG GGAACTGGCT GACCTACAAG ATGCTGCTTC AGGCAGTGCT GTGTCCTCTA 840 CAGAATCCCC TTCCCCCAGG GGGTCTTGCA TGGGCTGGAA TCCTGGAATC CAGGAGACAT 900 TACTTCCCCT CCTCAGCCTT GGACATCCCA GCTCTCCTCA GCCTCTTGCC TTGCTCCTCT 960 CACTAATAAG TGGCATCAGG TGGGCTGACC AGGACGTCTT TGTAAAACTA CAGCTGCATG 1020 ACTACAAGAG AGTTTTGCGC AGAATAATAC ACGGAAACAT TGCAACCCCT AATCTTGTCT 1080 CTTTCCATCT GCCACAACCT CAGGACCCTG AATTGTCTTA ATATCACTAA ATTATGAGTT 1140 TATAGTCTGG TGAGAGTTAG GAAGAAAGAT AAAACTGTGA GGAAAACCAA CTCCATGCCT 1200 GAAATTCCTA AGGCCTCCAG CAAAACCATG CCCACAGTAA GAACTCAATG AAGGACCTGC 1260 CACTGAGTGC TAGGAAACCA GCAAGATGCC ATCCTCATGG GGCAGACAGG TGCTCTCCAA 1320 GTGCAGGCAG AGAAGGTGCT CAATCCTGGT GTCTGTTGTC ACATCAGAAA CCTGAACTAA 1380 AAATGTGAAG CCGCTTCCTC TCTGAAGGAG GAGACTCAAG GGGTTTTATC TGGCCACAGC 1440 AGGCAGTCAT ACTTCCTCAC CAGACTCCCC ACTTAAAAGG TCCAGCAGAA AGGGCCACAG 1500 GCTGGAAAAT CAACTCAAAG GTTAGACCCT TACCTGTCCT GTCCCCAGGC ATTCACCTTA 1560 ATAAAAAAAA TCACTCAAGA ACTATAGGGA TTAAATATGA CACTAAAAAT ACATGCAACA 1620 AAATCAAAAA CAGATAAATT GAACTTCATC AAATTTTAAA CTCTTTGCGC AGCAAATGAG 1680 ACTATCCACC AGGTGCGGTG GTTCACACCT GTAATCCCAA CACTTTGGGA GGCCAAAGCA 1740 GGAGGACTGC CTGAGGCCAG GTGTTTGAGA TCAGCTTGGG AAACACAGTG AGACCCCCAT 1800 CTCTACAAAA AATTAATTTT 1820
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