Tag | Content |
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EnhancerAtlas ID | HS038-00101 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr1:8498060-8501000 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELF3 | MA0640.1 | chr1:8498713-8498726 | TTACTTCCGGCTA | - | 6.54 | ONECUT1 | MA0679.1 | chr1:8498368-8498382 | AAAAAATCAATATA | + | 6.62 | ONECUT2 | MA0756.1 | chr1:8498368-8498382 | AAAAAATCAATATA | + | 6.91 | ONECUT3 | MA0757.1 | chr1:8498368-8498382 | AAAAAATCAATATA | + | 7.19 | Sox6 | MA0515.1 | chr1:8499620-8499630 | CCATTGTTTT | + | 6.02 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_00045 | chr1:8497982-8499894 | Adipose_Nuclei | SE_02022 | chr1:8498913-8499948 | Aorta | SE_03947 | chr1:8498778-8499975 | Brain_Anterior_Caudate | SE_04978 | chr1:8498182-8500162 | Brain_Cingulate_Gyrus | SE_07042 | chr1:8498385-8500215 | Brain_Hippocampus_Middle_150 | SE_07921 | chr1:8498882-8500242 | Brain_Inferior_Temporal_Lobe | SE_11329 | chr1:8496575-8500743 | CD20 | SE_25808 | chr1:8497845-8499987 | Duodenum_Smooth_Muscle | SE_28078 | chr1:8498322-8500011 | Fetal_Intestine | SE_29095 | chr1:8498172-8499988 | Fetal_Intestine_Large | SE_29887 | chr1:8497659-8500219 | Fetal_Muscle | SE_31622 | chr1:8498048-8498478 | Gastric | SE_31622 | chr1:8498521-8499967 | Gastric | SE_40658 | chr1:8498953-8499664 | Left_Ventricle | SE_41679 | chr1:8499010-8499949 | LNCaP | SE_41679 | chr1:8500125-8500471 | LNCaP | SE_42166 | chr1:8498911-8499835 | Lung | SE_48103 | chr1:8498317-8498850 | Psoas_Muscle | SE_48103 | chr1:8498931-8499864 | Psoas_Muscle | SE_48600 | chr1:8498898-8499546 | Right_Atrium | SE_51176 | chr1:8497978-8500178 | Skeletal_Muscle | SE_53408 | chr1:8499004-8499850 | Spleen | SE_54752 | chr1:8497250-8500103 | Stomach_Smooth_Muscle | SE_58576 | chr1:8455425-8501956 | Ly1 | SE_60225 | chr1:8480836-8499894 | Ly4 | SE_60758 | chr1:8454848-8500160 | DHL6 | SE_62661 | chr1:8450826-8509851 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I008437 | chr1 | 8497651 | 8500633 | GH01I008440 | chr1 | 8500863 | 8502291 |
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Enhancer Sequence | TTAGAGACAG GGTCTTGCTC TGCCACCTAG GCTACAGTGG TATGATCACA GTTCACTGTA 60 ACGTGGAGCT TCCGGGCTCA AATGATCCTC CTGGCTCGGC CTCCCAAGTA GGTCAGACTA 120 CAGGTATGTG TCAGTTACCA TGCCCAGCTA ATTTTAAAAA TATTTTTTTG TAGAGACGGG 180 GTTCTCACTA TGTTGCCCAG GCTTGGTCTT GAACTCTTGA TTTCAAGCAA TCCTGCTGCC 240 TCAGCCTCCC AAAGAGTTGG GATTATGGCA TGAGCCACTG TGCCCAGCCA GATCTCACTC 300 CTGTAGGAAA AAAATCAATA TAGGATAATT TTCAGTTAAA AAGATGTATA TACATACGAA 360 GAGGGAGACC TACTAAAACA TCTGTTACAA CAGCATATAG TAAGGCAGAA TCTTTGCATT 420 TTCAAAATGT TTTCATAAAC TTTATTTGTT AGAGCAATTT CAGGTTCACA GCAAAACGGA 480 ACAGAAGGTA TAGGGATTTC CCATATAGAT GGGTCTCTGG ATTTTTCAGC TAATTTTGAA 540 AAATAGGGAA AAGAGCAATC AGCATTTTGT GCTCACTACA GTAAACCAGG AACACAGGCA 600 TCAGGAGAGC TGGGCTCTGA TTCAAAGGCC TGATTCTAGC AAGGCCTCAC AGTTTACTTC 660 CGGCTAGCCA TGAACACTCT CTGCGCCTGA GGTTTTCGTG GAAAGACAGC ATCACAAGTA 720 CTCAAATGTA GCGTTTAAAA GTACTAACTT TTAAAATGTT GAATGTTCCA GTAAAACAGT 780 TAAAGAAAAA AAAAGGTAAT AATCCAACTA AGTAAAAATA TTAACTTATA CATATCTGGA 840 TAGATGATAA GCTCATTACA GGCCCTAATT TTATTATTTA AAATGTTTAC AACAAAACTC 900 TCTAATTGAT ATTCTCCCTC TCTCTCTCTT TTTGCCTTGA TATGGTTTCT ATAAACTCTT 960 GGTTTAAAAA AGAAAAAAGG TCCATTTCTG AGGCTTGGGT TTACTGTACT TACAGTTCCA 1020 CCAGTAAATC GTCTCCCAGT CTGGGCTGGA GAAGCGCTGG CCACGGTTTG ATTGCTCCAG 1080 CCCCAGGTTG CCAGGCAACC CACACAAGGG GGAAGTCTGA GAACCGCTGA CAGATAGCCA 1140 AGTGGCTGAA ACAACAGACT TCTCTCTGTC AAAAATGTGT TTGAGAGAGC CACTTGCCCA 1200 CCTCTGCTCT CTGCTAAACA CTACATGATT GTAAAATCAA AATCAAAAGG CCACTGTAAT 1260 AAAAACACAC TTCCTGCTCA ATTACTAATT GTTCTAAAGC TGTGGGGAGG CCCAGATCCT 1320 ACAGTGTATG GCAACAGAAA TGCGATACTG TAAATGAGAT AAAGCCAGCA GCATGCAAGA 1380 AACCTGATCT AAATGCATCT CCGTAGCTTC AAGTCAGGAG AGCTGGTGTG TGGAGGAATC 1440 AACTGCCTAA GAAAACACCA GGAAGAAAAT AATGAATGTC AAGATGTTAA AGAAACAAAC 1500 CAATCAATAA CTACGAAGCT AGAGGTCAAG ACTACTTAGT AATAAAACCA AGAACATTCT 1560 CCATTGTTTT GAAACACAAT CTGGAGGCAA TGAAAGTTTT CTCCCTCAGA TGGAAAGGAG 1620 GAGCAAGAAA GGTCAATGAC CCTTGGGAAC CACACCCCCT GGCGGTTCCA GGTGGATTCC 1680 CTGATACTTG ACTGTAAATG GGATTACAGG AAATAGTAGC ATCCTTAGGA TAATGCAGGA 1740 CAATAACAGG TCTGAGAGTC TAATGCAACA TTTAAAATAC CTATGGTGTG AGCTGGGCAC 1800 AGTGGCTCAC GCCTGTAATC CCAGCACTTT GGGAGGCCGA GGTGGGTGGA TCACCTGAGG 1860 TCAAAAGTTT GAGACCAGCC TGGCCAACAC AGTGAAACCC CGTCTACACT AAAAATACAA 1920 AAAATTAGCT GGGCATGGTG GCAAACGCCT GTAATCCCAG CTACTGGGGA GGCTGAGGCA 1980 GGAGAATTGC TTCAACCCGG GAGGCAGAGG TTGCAGTGAG CTGAGATCGC GCCATTACAC 2040 TCCAGCCTGG GCAACAAGAG TGAAACTCCC TCTCAAACAA ACAAAAACAA AATATCTATG 2100 GTGCATGTAC CAAGCCAGTA ACATTGTGCC CAACACCAAC TCTATGCAGC ATCCTTCCAT 2160 GAAACCACTG TATTGAAACT GTCATCTTGG ACTCTGGAAA CTATTTGTAG TATGTGGAAG 2220 GGGCCAGCAC TGAGTGCACA GTTCTTTATC TCTTCTGTGC CATGGACCCT TTGGCAGTCT 2280 GGTAAAGCCT GACTCCTTCT AAAAATGGTT TATGGCCAGG CACGGCTCAT GCCTGTAATC 2340 CTAGCACTTT GGGAGGCCGA GGCAGGCGGA CATGAGGTTA GGAGATCGAG ACCATCCTGG 2400 CCAATATGGT GAAACCCTGT CTCTACTAAA AATACAAACA ATTAGCTGGG CGTGGTGGCG 2460 CATGCCTGTA ATCCCAGCTA CTCAGGAGGC TGAGGCAGGA GAATCACTTG AACCAGGGAG 2520 TCAGAGGTCG CAGTAAGCCG AGATCATGCC ACTGAACTCC AGCCTGGCGA CAGAGCGAGA 2580 CTCCACCTAA AAAAAAAAAA AAAAAGGCTG GGCACGGTGG CTCCTGTCTG TAATCCCAGC 2640 ACTTTGGGAG GCCGAGGCTG GCGGATCACC TAACGTCGAG TTTGAGACTA GCCTGGCCAA 2700 CATGGTGAAA CCTCGTCTCT ACTAAAAATA CAAAAAAAAA AAAAAATTAG CTGGGCATGG 2760 TGGTACATGC CTGTAGTCCC ACCTACTTGG GGAGGCTGAG GCAGGAGAAT CGCTTGAACC 2820 CAGGAGGCGG AAGTTGCAGT GAACCAAGAC CATGCCACTG CACTCCAGCC TCGGTGACAG 2880 AGGGAGACTC CATCTCAAAA AAAAAAAATA GAAAGTATGC CAGAGTAATA TAACTGCTCT 2940
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