Tag | Content |
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EnhancerAtlas ID | HS108-34691 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr6:41690630-41693240 |
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) |
RARA(var.2) | MA0730.1 | chr6:41691548-41691565 | TGACCCCAGCCTGACCT | - | 6.85 | ZNF263 | MA0528.1 | chr6:41690673-41690694 | AGATGAGGAAGCAGAGGAGGA | + | 6.16 |
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| Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
SE_01517 | chr6:41690972-41692916 | Adrenal_Gland | SE_03162 | chr6:41690020-41691233 | Brain_Angular_Gyrus | SE_03162 | chr6:41691372-41693461 | Brain_Angular_Gyrus | SE_03890 | chr6:41689883-41693577 | Brain_Anterior_Caudate | SE_04788 | chr6:41686998-41693888 | Brain_Cingulate_Gyrus | SE_05789 | chr6:41686984-41693922 | Brain_Hippocampus_Middle | SE_06686 | chr6:41686810-41693790 | Brain_Hippocampus_Middle_150 | SE_07757 | chr6:41689786-41693648 | Brain_Inferior_Temporal_Lobe | SE_10407 | chr6:41689903-41693737 | CD19_Primary | SE_10977 | chr6:41658732-41703851 | CD20 | SE_20329 | chr6:41689981-41703529 | CD56 | SE_24100 | chr6:41691488-41691862 | Colon_Crypt_2 | SE_27512 | chr6:41690300-41692001 | Esophagus | SE_27930 | chr6:41686945-41704088 | Fetal_Intestine | SE_28789 | chr6:41686934-41704233 | Fetal_Intestine_Large | SE_32569 | chr6:41687122-41693433 | GM12878 | SE_40921 | chr6:41690021-41693217 | Left_Ventricle | SE_42065 | chr6:41690065-41691404 | LNCaP | SE_42065 | chr6:41692452-41692943 | LNCaP | SE_42849 | chr6:41690562-41693465 | Lung | SE_47896 | chr6:41692170-41692494 | Pancreas | SE_48161 | chr6:41687013-41693572 | Psoas_Muscle | SE_48786 | chr6:41690011-41693397 | Right_Atrium | SE_49598 | chr6:41690896-41691874 | Right_Ventricle | SE_50457 | chr6:41690005-41693468 | Sigmoid_Colon | SE_51489 | chr6:41690441-41693523 | Skeletal_Muscle | SE_53720 | chr6:41690176-41693495 | Spleen | SE_58883 | chr6:41671378-41704020 | Ly3 | SE_59865 | chr6:41670633-41703769 | Ly4 | SE_60547 | chr6:41671030-41704212 | DHL6 | SE_61043 | chr6:41671264-41704230 | HBL1 | SE_61929 | chr6:41668086-41703943 | Toledo | SE_62316 | chr6:41671424-41703890 | Tonsil | SE_65465 | chr6:41689674-41693735 | Pancreatic_islets |
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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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Enhancer Sequence | AGAACTCACA AGGTGGGCAC TATAACTGTC ATCTCCATGT TACAGATGAG GAAGCAGAGG 60 AGGATAACTT GCCAGCATCA TGAAACTGCA AAACGACAGG GCCAGGATTC AAGCAGGTGG 120 ATGTAGAGCA TATGCTCCCA GCCCCTAATG TAAATGGGTA TTCACTGTGG CCTGGCCAGT 180 GACATGCTAA GCCCATCCTG CCCATGACCT TCTCACTCGA CCCTTGAAAT AAGCCTGGAG 240 AGATGAGGAA ACTGAAGCAC AACTCTGGCT GACTCCTGAT TTCCCACGCT GTCCAACCTG 300 CACTCCAGAG CTTGGCCACC TTCTTCCCCA TTCTTTCCCT CACCCCAGCC TTGGCCATGC 360 TCAGAGACCC CCACCCCTCC CCAAAGACAT CCCAATGCCA GTGCAGCCTG AGGGGCCTCA 420 TCCCTACCCA CCCACCTCCC CAAAGACACC ACACGCATGC ACATACACTC ACACAGATGC 480 ACACAGGCTA ACACACATGG ACACACATTC ACACACATGC TCACACACAT GCACACACTC 540 ACACACATGC ACGCGTGTGC TCTCATACCT TCGAGAGGGC AGCCCCCTGG AAGGAGGCCC 600 CTGGAATGCT CAGCTCCTCC AGGGGCCGGA GCCCAGGGCC GCACCCCAGC CCCAGGGCCG 660 GGCTCAGTTT CCTCATTTCC CCGGCGGCTG CTGTTTCTCA CCCAGCCCCC TGCACCTCAG 720 CTGGAGAGGA AGTTGCACAA TCCCCTGGGA GCTGCAAATG CGGCCGAGGA TTACTCACAG 780 CACAGAGGGA ACTGCGCCCC GACGGCACAG TCCCACACCG CAGCCTACCC AACACAGACT 840 GCTTCAATCT CACCCGCCCG GCTCCAGGCG CCCACAGCGC TCCTTGGTCC TCCCACAGGA 900 GGCCTCTCAT GGCCGCCCTG ACCCCAGCCT GACCTCAGAG GGCCCTAGGC AGATGGAGAG 960 ACACAGAGCA GCAAGAATTT CGCCAGAGTC CCAATCCCAC CAGGTCCAGG GTGGGCCTAA 1020 CCCTAACCCC AGCCCCGCTT CCTAGAGACA TGTGTCCTTC TAGCCAGAAG CCCCACAGCT 1080 CACCATCTTC CTGACTGGCC ATACACCTGC AGTCTTGGCC TTGGGCCTTC CCAGGGCCTC 1140 CAGACACCCA GGTCGAGGCC GTACTACAGC CCACCTTGAA ATGGAGCCTG AGATCAAGCA 1200 GAGCCCTGGG CAGCTCCGGG AAGATCCACA CCACCGCACA CTTTTCACTT GTGCAGAAAC 1260 TGTTCTTGAT ACACATGCAA GTTCAGTGGT TCCTCAGCCC CCCAGCACTT TTTTAGCAGC 1320 CTGCCAAAGA GACTGGGCAG AGATTTCACT TAGTGCTTCT TTCTGGTGGC CAAGGGATTC 1380 CCATCGTTGA TAAGCAAATA CCCTGTATTA AGAAAGGTTA AGCTATTATC GGTCGTCTGC 1440 GTCTCAGGGT GGATGAGTTT ACTGGGCCCT TTCGTGAGTG CAGGTTTCAG GAAGGAAGCG 1500 GGCAGCAGAG AGGAGATGAG GCAGGCCGTG GCTCCTGGAG AAGGCAGGAG ATGCCAGCAA 1560 TGTGAGGGAA GCCCAGAACA GTGAGGCCAG AGAGGCCCAG GGAGGATGGA CCCAGACTCT 1620 GGTCCAACCC TGGGCCTCCC TGGGCTGGCA AATTCTGGAA GGACACAAAG GATGAGTAGG 1680 AGCCAGGCCT GGGTGTGCAG AGCCCCCAGG GAGGACCTCT GGCTCCCGCC CCTTGCCGCC 1740 CGAGACCTGC AATGGGGCCT CAGATAAGGA ACATGATAAA TACCTCTTAT CACCCCCACA 1800 ACCTTGGACT CCCATCCAGC TAAGGACAAA GTTGGAAATG TTTTTGTCCT GGGCCCCAAG 1860 GCTCCCAGAG AACCCCTCAT TTCTGCAGCC CTCATCAAAA GGCTGGGGCC CGCAGGGACT 1920 GTGGGGGAAG CGCCTCACAG CCCCTGCAGC AGCACGAACC AGGACTGAGG TTCACAGCGG 1980 TCACCTGATG CCTCCAGCTT GGTGGACAGG GAACACAGTC AAGGAAGAAG GGCCAGTGCT 2040 GAAAAGGCCT GGCTCTACTG GAACGCAACA GCCACAAGGC CCCTTTGCAG GGACGCCTCC 2100 CCCAAAATGC CTGCACATTC ACCATCTCCC CCATCCTGAC AAGAGCCCCA TGAAGGGGAA 2160 GGGCAGCAAC GCTTGCTATC CGTTTTTCAG ATTCCAAGGA GGCTGAGGCT CAAATCACTT 2220 AAGTGACTTC CTCGAGGCCA TGCAGCAAGT TTATGGCAAA TCTGTTTCCT GGCTCTTTTC 2280 CTAGATCAGA GTTTCTCAAC CTCAACACCA GACACTCAGG GCCAGGTAAT TAGTTACAGG 2340 GGCTGTCCTG TGCATTTTAA GATGTTTAGT GGTATCCCTG GCCAATATCA TCAGACATTG 2400 GCAAATGTCC CCTAGGGGGA CAAAATCACC CCTAGTGGAG AACTACTGCC CTAGAAGCAC 2460 CTAAAAGATG GGCACCTGCC AATTCCAAAT TGAACGGTAC ACCTGCTGAG GGCTCTAGCC 2520 TGAGAGTCTC CCCCTCTCCC CCACCAGATG TGCTAGGCAA GAGGGCCTGA AGGGTGATGG 2580 GTACTCTGTG GTTCAGTACC CTCTGGGAAG 2610
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