Tag | Content |
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EnhancerAtlas ID | HS191-25806 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr3:47000720-47003300 |
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: 39 | 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_47478 | chr3:47002902-47003205 | 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: 3 | Chromosome | Start | End |
chr3 | 47001323 | 47001648 | chr3 | 47001666 | 47002342 | chr3 | 47000781 | 47001063 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I046952 | chr3 | 46993692 | 47003318 |
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Enhancer Sequence | GCTCAGCATA TGGAAAGGTT GAGAAAGCAG AACCACATGA GGAGTCAATA CCCAGCACTA 60 ACAACTGTGT ACTGTGGTAC TCTGGGCCAG TTTAGCTTCT CAGAGCTGCA GTTTCTTCAA 120 CTGCTAGATG GCATGACTTA AGGGTACGCA TGTGAGTGAC AGCCCTACAC TGTGGCTGGC 180 ACAGAGTACG TCCTCAGTCA GTAGGCGCCA ACCACAGTGA TGATGATGGT GGAGCCTGAG 240 ACTCTCACCT GTGTCTTCGG GGTGAGGCCC TCTCATCCCG TGACAAAGGG GTCACATAAC 300 AGATCCCCAC ATTCATGCCT TGTTCCTTCC CTCAGTTCAC CCAGAGCAGC CATCAGTGTC 360 ACCCGGAGGA AGCCCCAGCC CTTGCCCTCG AGCTACCACA GTTGAGAAGA GCAGACCCTA 420 CACGTGTGCA GAGAATATGA ATCCAAGTCA GAAAACGCTA GCCAGTGTGG GGGGACAGGG 480 AGGTGGCAAG GAAGAAGGGC CTTCCACAGA TCATCTTCCC AAATTCAGAC CACCTCCATG 540 CCTGCCTGTT CTGCTCCTGC CCCTCCTCTG CCTAAAATCC CTCCACCTCT TTCACACCTG 600 GAAACAGCTA TCACTCTCCA TGCCATCCAC TCAATCCCTC AAGTGTTTTC TCAGCACCTC 660 TACCAGCTCA GGCTCTGTCT TGTGAGTTAT GCAGCCTGGG ACAAAGCCCA AATGGGGACA 720 CTACTCATAA GCCAACCAAT GAGATAAAGC AGGGTATGTA TATCGATACT GGGTTGAGCG 780 CTCTCCTCCA CGCGACATGC ATGCAAGTGT TGTCCCCCAT CCCCTGTCCA TGCCCTCCCT 840 CCAAGACACT GACAGCTCTC CTCTGCCCCT CCTCCGTGGA TGGCAGTATA CAGTATTATA 900 CCTGGGGGTA CACAGATCAG CCTTCCCACA GGGCCCCAGC CTGACCGTGC TTGAGGCAAG 960 GGCCAGCCTC ACTGACCCCA TTTCCCACCC AGGCTCTGTG CACAGAGAGG CCTCAACAAT 1020 AACACTTGTA ACAGCCAGAT GTGGAAACTG ACTCCTCACC CCAGACACAG CCCAGCATTC 1080 ACTCTCACTT CCTACATAGA TGGAAGCTGC CTGAGTCATG GACTCCTGGG CCCAGGACAG 1140 GAAAGTCCTG CTTTAACCAG ATGATGTCAA ACACAGGTGC TTTTTCTTCA GGATTCAAAT 1200 TACCCTGCAA GAAATCTAGT GGTGCCCTGC CCTGAAAACA ATGGGAGGGG GGCTGTCCTT 1260 GAAAGGACAA ATGTTTTCTG CTCCAGCCAC TCACATTTTC TCTAGACAGA GCAGCTCTTT 1320 AGAGCCCTGA ATCAAAACAG CCCAGGAGTG TGGATGTTAC TGCCACAGGG CACCGTTGCC 1380 GAAGCAACTG TTTTTCCTCT TGGAATTCTT TCAAGGATAC AAGCTGTTGC TTCCCTCCAA 1440 AACAAAACCA GGGAGAAGCC AGGGCCCCAG AATTTAAGGG AAAGCTCCGA AGGAAGGAAG 1500 AGGGCCAGGC ATGACTGAGC CTTATCAAGC TCGCTATGGG GTCTCCCAGA TCTCCGAACA 1560 ACTGGCTTAG AAACAGCAAG TCCGTCTCAG CTGCTGAAGG TGTATGTGTA GGGAAAGGCA 1620 AATTGTGGGT ATGGAGGTAT AAAGGTGGTG CTGCTTATGT GTGTTTTGAG GTGTGTATGA 1680 GATATGTATT GGTGTAAAGG GGTTGGGGTT TGTAGGTGTG GGTTGGGGGC ATGTGGAGGG 1740 GTGCTGTGGA GTGTTGGAGG TGTGCAGGGA ATGGGAGGGT GTGGGGAGAA GGGAGGTACT 1800 ATTGTGGGGG GAAGTGTGTG GGGTAGGGCC TGGGGTGTGT GGTGGTGTTG TGAGGTTAAG 1860 GGAGTGTAAG GAGGTGGGAT GCACTGTAGG CAGGGGGCTG GGTGTGGAGA GTACATGCTG 1920 TATGTGCATG TGTATATGCG CTGGAGGTGG GTTGGAGGTA TGTGGGATAG GTTACAGAAA 1980 ATATTCCAAG ATGATATATG AGACATCTTC TCCAGAAACA AAAATATGAA TTGCATTTCA 2040 TTTCTGTATT ACAATTCTTA GTGCTACAGA ATCACATGCT GCTCCCAATG TCTGCAGGGT 2100 CAATGGAAGA GCCAAAAACC ATTTAAAACA TACAGCCCCA GTTTGAAACA ACTGACCCTG 2160 AAGCAACTAT CGGAGGTAAC ACATATTTCT AGTCAGAACA CCCCTGGCTC GGTAGGTCCA 2220 GAGTATGGAC AGAGTCTGGC TAGCAGGTCA GGAGGCCAGC ACTGGAGGGC CTGGCTCAGC 2280 AGGTCCTTGT CTTCCCTGGG AGTCCATGTT GTCTTTTCTC TAGTGCACAA AGCCTAAGGG 2340 GCTCAGAGTC ACAGGACGCA GCATACCCAC TACAGTGCCA TGGGGCACCC AGGAAATGTC 2400 TGAATGTTTT GTTAAAATAA GTTTAAGAGT TGTCTCTGCC TACAAGGAAC TGCCTGTCCA 2460 CTGAAGGGGT GGCATGAATT GGGACTTAGA AGCATGAAAA AACAAATATA TTTTAGCAGC 2520 TACCACTGCT ACTACTACTA CTACTATATG TACAATGACA ATTATCAGGA TGTTATGGAA 2580
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