Tag | Content |
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EnhancerAtlas ID | HS060-24223 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr3:47000530-47002910 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr3:47002493-47002504 | GGAGGGTGTGG | - | 6.32 | RREB1 | MA0073.1 | chr3:47002555-47002575 | TGTGTGGTGGTGTTGTGAGG | - | 6.32 | Sox6 | MA0515.1 | chr3:47001954-47001964 | AAAACAATGG | - | 6.02 |
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| Number of super-enhancer constituents: 38 | ID | Coordinate | Tissue/cell |
SE_00943 | chr3:47000636-47003247 | Adrenal_Gland | SE_02008 | chr3:47000692-47002741 | Aorta | SE_11155 | chr3:46999721-47003820 | CD20 | SE_14564 | chr3:47000278-47001837 | CD4_Memory_Primary_7pool | SE_16650 | chr3:46999983-47001584 | CD4_Naive_Primary_8pool | SE_18708 | chr3:46999601-47003619 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20061 | chr3:46999416-47002518 | CD56 | SE_20061 | chr3:47002557-47003528 | CD56 | SE_22640 | chr3:46999598-47002488 | CD8_primiary | SE_22640 | chr3:47002498-47003619 | CD8_primiary | SE_23114 | chr3:47000575-47002747 | Colon_Crypt_1 | SE_23749 | chr3:47000733-47001255 | Colon_Crypt_2 | SE_23749 | chr3:47001324-47001875 | Colon_Crypt_2 | SE_23749 | chr3:47002233-47002725 | Colon_Crypt_2 | SE_26114 | chr3:46999989-47002735 | Duodenum_Smooth_Muscle | SE_28630 | chr3:46998170-47003223 | Fetal_Intestine_Large | SE_30558 | chr3:47000885-47002668 | Fetal_Muscle | SE_31407 | chr3:47000683-47003179 | Gastric | SE_32585 | chr3:47000613-47001820 | GM12878 | SE_38780 | chr3:47000232-47003616 | HUVEC | SE_40617 | chr3:46999813-47003535 | Left_Ventricle | SE_41619 | chr3:47000640-47002043 | LNCaP | SE_41619 | chr3:47002075-47002794 | LNCaP | SE_42118 | chr3:46999822-47003340 | Lung | SE_47478 | chr3:47000658-47001925 | Pancreas | SE_47478 | chr3:47001962-47002754 | Pancreas | SE_48306 | chr3:46999915-47003370 | Psoas_Muscle | SE_48684 | chr3:47000717-47002767 | Right_Atrium | SE_49453 | chr3:47000756-47002110 | Right_Ventricle | SE_49453 | chr3:47002144-47002748 | Right_Ventricle | SE_50160 | chr3:46999961-47003286 | Sigmoid_Colon | SE_52388 | chr3:46999875-47002632 | Small_Intestine | SE_53507 | chr3:47000017-47003202 | 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 | SE_64772 | chr3:47001706-47002732 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr3 | 47001323 | 47001648 | chr3 | 47001666 | 47002342 | chr3 | 47000781 | 47001063 | chr3 | 47000667 | 47001400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I046952 | chr3 | 46993692 | 47003318 |
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Enhancer Sequence | CTGAGAAGTA AAGGTAAGAC AGCTGTCTGC TCTCTGGTGT GATCTACAAG TGATAAAAAT 60 CCTAATTAAA CCAAATTTAA ACAAGTCAGA ACTGGCACAT TTTTTTGTGG GGGGAAATAC 120 TGCTTCACAA GGTCTTATCC CCACCTACAC ACACTTCCTT TAGCTACAAA GCGTTTTTAA 180 AAATCCACAT GCTCAGCATA TGGAAAGGTT GAGAAAGCAG AACCACATGA GGAGTCAATA 240 CCCAGCACTA ACAACTGTGT ACTGTGGTAC TCTGGGCCAG TTTAGCTTCT CAGAGCTGCA 300 GTTTCTTCAA CTGCTAGATG GCATGACTTA AGGGTACGCA TGTGAGTGAC AGCCCTACAC 360 TGTGGCTGGC ACAGAGTACG TCCTCAGTCA GTAGGCGCCA ACCACAGTGA TGATGATGGT 420 GGAGCCTGAG ACTCTCACCT GTGTCTTCGG GGTGAGGCCC TCTCATCCCG TGACAAAGGG 480 GTCACATAAC AGATCCCCAC ATTCATGCCT TGTTCCTTCC CTCAGTTCAC CCAGAGCAGC 540 CATCAGTGTC ACCCGGAGGA AGCCCCAGCC CTTGCCCTCG AGCTACCACA GTTGAGAAGA 600 GCAGACCCTA CACGTGTGCA GAGAATATGA ATCCAAGTCA GAAAACGCTA GCCAGTGTGG 660 GGGGACAGGG AGGTGGCAAG GAAGAAGGGC CTTCCACAGA TCATCTTCCC AAATTCAGAC 720 CACCTCCATG CCTGCCTGTT CTGCTCCTGC CCCTCCTCTG CCTAAAATCC CTCCACCTCT 780 TTCACACCTG GAAACAGCTA TCACTCTCCA TGCCATCCAC TCAATCCCTC AAGTGTTTTC 840 TCAGCACCTC TACCAGCTCA GGCTCTGTCT TGTGAGTTAT GCAGCCTGGG ACAAAGCCCA 900 AATGGGGACA CTACTCATAA GCCAACCAAT GAGATAAAGC AGGGTATGTA TATCGATACT 960 GGGTTGAGCG CTCTCCTCCA CGCGACATGC ATGCAAGTGT TGTCCCCCAT CCCCTGTCCA 1020 TGCCCTCCCT CCAAGACACT GACAGCTCTC CTCTGCCCCT CCTCCGTGGA TGGCAGTATA 1080 CAGTATTATA CCTGGGGGTA CACAGATCAG CCTTCCCACA GGGCCCCAGC CTGACCGTGC 1140 TTGAGGCAAG GGCCAGCCTC ACTGACCCCA TTTCCCACCC AGGCTCTGTG CACAGAGAGG 1200 CCTCAACAAT AACACTTGTA ACAGCCAGAT GTGGAAACTG ACTCCTCACC CCAGACACAG 1260 CCCAGCATTC ACTCTCACTT CCTACATAGA TGGAAGCTGC CTGAGTCATG GACTCCTGGG 1320 CCCAGGACAG GAAAGTCCTG CTTTAACCAG ATGATGTCAA ACACAGGTGC TTTTTCTTCA 1380 GGATTCAAAT TACCCTGCAA GAAATCTAGT GGTGCCCTGC CCTGAAAACA ATGGGAGGGG 1440 GGCTGTCCTT GAAAGGACAA ATGTTTTCTG CTCCAGCCAC TCACATTTTC TCTAGACAGA 1500 GCAGCTCTTT AGAGCCCTGA ATCAAAACAG CCCAGGAGTG TGGATGTTAC TGCCACAGGG 1560 CACCGTTGCC GAAGCAACTG TTTTTCCTCT TGGAATTCTT TCAAGGATAC AAGCTGTTGC 1620 TTCCCTCCAA AACAAAACCA GGGAGAAGCC AGGGCCCCAG AATTTAAGGG AAAGCTCCGA 1680 AGGAAGGAAG AGGGCCAGGC ATGACTGAGC CTTATCAAGC TCGCTATGGG GTCTCCCAGA 1740 TCTCCGAACA ACTGGCTTAG AAACAGCAAG TCCGTCTCAG CTGCTGAAGG TGTATGTGTA 1800 GGGAAAGGCA AATTGTGGGT ATGGAGGTAT AAAGGTGGTG CTGCTTATGT GTGTTTTGAG 1860 GTGTGTATGA GATATGTATT GGTGTAAAGG GGTTGGGGTT TGTAGGTGTG GGTTGGGGGC 1920 ATGTGGAGGG GTGCTGTGGA GTGTTGGAGG TGTGCAGGGA ATGGGAGGGT GTGGGGAGAA 1980 GGGAGGTACT ATTGTGGGGG GAAGTGTGTG GGGTAGGGCC TGGGGTGTGT GGTGGTGTTG 2040 TGAGGTTAAG GGAGTGTAAG GAGGTGGGAT GCACTGTAGG CAGGGGGCTG GGTGTGGAGA 2100 GTACATGCTG TATGTGCATG TGTATATGCG CTGGAGGTGG GTTGGAGGTA TGTGGGATAG 2160 GTTACAGAAA ATATTCCAAG ATGATATATG AGACATCTTC TCCAGAAACA AAAATATGAA 2220 TTGCATTTCA TTTCTGTATT ACAATTCTTA GTGCTACAGA ATCACATGCT GCTCCCAATG 2280 TCTGCAGGGT CAATGGAAGA GCCAAAAACC ATTTAAAACA TACAGCCCCA GTTTGAAACA 2340 ACTGACCCTG AAGCAACTAT CGGAGGTAAC ACATATTTCT 2380
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