Tag | Content |
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EnhancerAtlas ID | HS127-00109 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr1:8498160-8500030 |
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: 26 | 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_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: 1 | ID | Chromosome | Start | End |
GH01I008437 | chr1 | 8497651 | 8500633 |
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Enhancer Sequence | CTCCCAAGTA GGTCAGACTA CAGGTATGTG TCAGTTACCA TGCCCAGCTA ATTTTAAAAA 60 TATTTTTTTG TAGAGACGGG GTTCTCACTA TGTTGCCCAG GCTTGGTCTT GAACTCTTGA 120 TTTCAAGCAA TCCTGCTGCC TCAGCCTCCC AAAGAGTTGG GATTATGGCA TGAGCCACTG 180 TGCCCAGCCA GATCTCACTC CTGTAGGAAA AAAATCAATA TAGGATAATT TTCAGTTAAA 240 AAGATGTATA TACATACGAA GAGGGAGACC TACTAAAACA TCTGTTACAA CAGCATATAG 300 TAAGGCAGAA TCTTTGCATT TTCAAAATGT TTTCATAAAC TTTATTTGTT AGAGCAATTT 360 CAGGTTCACA GCAAAACGGA ACAGAAGGTA TAGGGATTTC CCATATAGAT GGGTCTCTGG 420 ATTTTTCAGC TAATTTTGAA AAATAGGGAA AAGAGCAATC AGCATTTTGT GCTCACTACA 480 GTAAACCAGG AACACAGGCA TCAGGAGAGC TGGGCTCTGA TTCAAAGGCC TGATTCTAGC 540 AAGGCCTCAC AGTTTACTTC CGGCTAGCCA TGAACACTCT CTGCGCCTGA GGTTTTCGTG 600 GAAAGACAGC ATCACAAGTA CTCAAATGTA GCGTTTAAAA GTACTAACTT TTAAAATGTT 660 GAATGTTCCA GTAAAACAGT TAAAGAAAAA AAAAGGTAAT AATCCAACTA AGTAAAAATA 720 TTAACTTATA CATATCTGGA TAGATGATAA GCTCATTACA GGCCCTAATT TTATTATTTA 780 AAATGTTTAC AACAAAACTC TCTAATTGAT ATTCTCCCTC TCTCTCTCTT TTTGCCTTGA 840 TATGGTTTCT ATAAACTCTT GGTTTAAAAA AGAAAAAAGG TCCATTTCTG AGGCTTGGGT 900 TTACTGTACT TACAGTTCCA CCAGTAAATC GTCTCCCAGT CTGGGCTGGA GAAGCGCTGG 960 CCACGGTTTG ATTGCTCCAG CCCCAGGTTG CCAGGCAACC CACACAAGGG GGAAGTCTGA 1020 GAACCGCTGA CAGATAGCCA AGTGGCTGAA ACAACAGACT TCTCTCTGTC AAAAATGTGT 1080 TTGAGAGAGC CACTTGCCCA CCTCTGCTCT CTGCTAAACA CTACATGATT GTAAAATCAA 1140 AATCAAAAGG CCACTGTAAT AAAAACACAC TTCCTGCTCA ATTACTAATT GTTCTAAAGC 1200 TGTGGGGAGG CCCAGATCCT ACAGTGTATG GCAACAGAAA TGCGATACTG TAAATGAGAT 1260 AAAGCCAGCA GCATGCAAGA AACCTGATCT AAATGCATCT CCGTAGCTTC AAGTCAGGAG 1320 AGCTGGTGTG TGGAGGAATC AACTGCCTAA GAAAACACCA GGAAGAAAAT AATGAATGTC 1380 AAGATGTTAA AGAAACAAAC CAATCAATAA CTACGAAGCT AGAGGTCAAG ACTACTTAGT 1440 AATAAAACCA AGAACATTCT CCATTGTTTT GAAACACAAT CTGGAGGCAA TGAAAGTTTT 1500 CTCCCTCAGA TGGAAAGGAG GAGCAAGAAA GGTCAATGAC CCTTGGGAAC CACACCCCCT 1560 GGCGGTTCCA GGTGGATTCC CTGATACTTG ACTGTAAATG GGATTACAGG AAATAGTAGC 1620 ATCCTTAGGA TAATGCAGGA CAATAACAGG TCTGAGAGTC TAATGCAACA TTTAAAATAC 1680 CTATGGTGTG AGCTGGGCAC AGTGGCTCAC GCCTGTAATC CCAGCACTTT GGGAGGCCGA 1740 GGTGGGTGGA TCACCTGAGG TCAAAAGTTT GAGACCAGCC TGGCCAACAC AGTGAAACCC 1800 CGTCTACACT AAAAATACAA AAAATTAGCT GGGCATGGTG GCAAACGCCT GTAATCCCAG 1860 CTACTGGGGA 1870
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