Tag | Content |
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EnhancerAtlas ID | HS145-16998 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr3:47000960-47003480 |
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 | 47002951 | 47003388 | chr3 | 47001666 | 47002342 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I046952 | chr3 | 46993692 | 47003318 |
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Enhancer Sequence | ACTCTCACCT GTGTCTTCGG GGTGAGGCCC TCTCATCCCG TGACAAAGGG GTCACATAAC 60 AGATCCCCAC ATTCATGCCT TGTTCCTTCC CTCAGTTCAC CCAGAGCAGC CATCAGTGTC 120 ACCCGGAGGA AGCCCCAGCC CTTGCCCTCG AGCTACCACA GTTGAGAAGA GCAGACCCTA 180 CACGTGTGCA GAGAATATGA ATCCAAGTCA GAAAACGCTA GCCAGTGTGG GGGGACAGGG 240 AGGTGGCAAG GAAGAAGGGC CTTCCACAGA TCATCTTCCC AAATTCAGAC CACCTCCATG 300 CCTGCCTGTT CTGCTCCTGC CCCTCCTCTG CCTAAAATCC CTCCACCTCT TTCACACCTG 360 GAAACAGCTA TCACTCTCCA TGCCATCCAC TCAATCCCTC AAGTGTTTTC TCAGCACCTC 420 TACCAGCTCA GGCTCTGTCT TGTGAGTTAT GCAGCCTGGG ACAAAGCCCA AATGGGGACA 480 CTACTCATAA GCCAACCAAT GAGATAAAGC AGGGTATGTA TATCGATACT GGGTTGAGCG 540 CTCTCCTCCA CGCGACATGC ATGCAAGTGT TGTCCCCCAT CCCCTGTCCA TGCCCTCCCT 600 CCAAGACACT GACAGCTCTC CTCTGCCCCT CCTCCGTGGA TGGCAGTATA CAGTATTATA 660 CCTGGGGGTA CACAGATCAG CCTTCCCACA GGGCCCCAGC CTGACCGTGC TTGAGGCAAG 720 GGCCAGCCTC ACTGACCCCA TTTCCCACCC AGGCTCTGTG CACAGAGAGG CCTCAACAAT 780 AACACTTGTA ACAGCCAGAT GTGGAAACTG ACTCCTCACC CCAGACACAG CCCAGCATTC 840 ACTCTCACTT CCTACATAGA TGGAAGCTGC CTGAGTCATG GACTCCTGGG CCCAGGACAG 900 GAAAGTCCTG CTTTAACCAG ATGATGTCAA ACACAGGTGC TTTTTCTTCA GGATTCAAAT 960 TACCCTGCAA GAAATCTAGT GGTGCCCTGC CCTGAAAACA ATGGGAGGGG GGCTGTCCTT 1020 GAAAGGACAA ATGTTTTCTG CTCCAGCCAC TCACATTTTC TCTAGACAGA GCAGCTCTTT 1080 AGAGCCCTGA ATCAAAACAG CCCAGGAGTG TGGATGTTAC TGCCACAGGG CACCGTTGCC 1140 GAAGCAACTG TTTTTCCTCT TGGAATTCTT TCAAGGATAC AAGCTGTTGC TTCCCTCCAA 1200 AACAAAACCA GGGAGAAGCC AGGGCCCCAG AATTTAAGGG AAAGCTCCGA AGGAAGGAAG 1260 AGGGCCAGGC ATGACTGAGC CTTATCAAGC TCGCTATGGG GTCTCCCAGA TCTCCGAACA 1320 ACTGGCTTAG AAACAGCAAG TCCGTCTCAG CTGCTGAAGG TGTATGTGTA GGGAAAGGCA 1380 AATTGTGGGT ATGGAGGTAT AAAGGTGGTG CTGCTTATGT GTGTTTTGAG GTGTGTATGA 1440 GATATGTATT GGTGTAAAGG GGTTGGGGTT TGTAGGTGTG GGTTGGGGGC ATGTGGAGGG 1500 GTGCTGTGGA GTGTTGGAGG TGTGCAGGGA ATGGGAGGGT GTGGGGAGAA GGGAGGTACT 1560 ATTGTGGGGG GAAGTGTGTG GGGTAGGGCC TGGGGTGTGT GGTGGTGTTG TGAGGTTAAG 1620 GGAGTGTAAG GAGGTGGGAT GCACTGTAGG CAGGGGGCTG GGTGTGGAGA GTACATGCTG 1680 TATGTGCATG TGTATATGCG CTGGAGGTGG GTTGGAGGTA TGTGGGATAG GTTACAGAAA 1740 ATATTCCAAG ATGATATATG AGACATCTTC TCCAGAAACA AAAATATGAA TTGCATTTCA 1800 TTTCTGTATT ACAATTCTTA GTGCTACAGA ATCACATGCT GCTCCCAATG TCTGCAGGGT 1860 CAATGGAAGA GCCAAAAACC ATTTAAAACA TACAGCCCCA GTTTGAAACA ACTGACCCTG 1920 AAGCAACTAT CGGAGGTAAC ACATATTTCT AGTCAGAACA CCCCTGGCTC GGTAGGTCCA 1980 GAGTATGGAC AGAGTCTGGC TAGCAGGTCA GGAGGCCAGC ACTGGAGGGC CTGGCTCAGC 2040 AGGTCCTTGT CTTCCCTGGG AGTCCATGTT GTCTTTTCTC TAGTGCACAA AGCCTAAGGG 2100 GCTCAGAGTC ACAGGACGCA GCATACCCAC TACAGTGCCA TGGGGCACCC AGGAAATGTC 2160 TGAATGTTTT GTTAAAATAA GTTTAAGAGT TGTCTCTGCC TACAAGGAAC TGCCTGTCCA 2220 CTGAAGGGGT GGCATGAATT GGGACTTAGA AGCATGAAAA AACAAATATA TTTTAGCAGC 2280 TACCACTGCT ACTACTACTA CTACTATATG TACAATGACA ATTATCAGGA TGTTATGGAA 2340 GGTTAACAGC ATGATCATAA ACAGTGCATG CCAATTAAGT CACGGGAAAC TCTTCTAAAA 2400 CACAAATGTC AAATATCAAA TAGTGCCAAG TCACTGATAC CCATATGGGG AGAAAAAGAA 2460 TCTTGATCCC TACGCACACC ACACAAAAGT AAATTCGAGA TGGGTTAGAG GTCTAAAGGT 2520
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