Tag | Content |
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EnhancerAtlas ID | HS044-06652 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr19:45945590-45948610 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLIS2 | MA0736.1 | chr19:45947643-45947657 | GCCCCCCCGCGGTG | + | 6.03 | HSF1 | MA0486.2 | chr19:45946029-45946042 | TTCCAGAACCTTC | + | 6.3 | KLF16 | MA0741.1 | chr19:45946863-45946874 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr19:45946863-45946873 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr19:45947706-45947716 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr19:45947711-45947721 | GCCCCGCCCC | + | 6.02 | Klf12 | MA0742.1 | chr19:45946100-45946115 | CAGCAGGGCGTGGCC | - | 6.07 | Nr2f6(var.2) | MA0728.1 | chr19:45948492-45948507 | TGAACTCCTGACCTC | - | 6.22 | SP1 | MA0079.4 | chr19:45946860-45946875 | CAGGCCCCGCCCCCG | + | 6.11 | TBX21 | MA0690.1 | chr19:45947162-45947172 | TTCACACCTT | - | 6.02 | TBX2 | MA0688.1 | chr19:45947161-45947172 | TTTCACACCTT | - | 6.62 | ZIC1 | MA0696.1 | chr19:45947643-45947657 | GCCCCCCCGCGGTG | + | 6.44 | ZIC4 | MA0751.1 | chr19:45947643-45947658 | GCCCCCCCGCGGTGG | + | 6 | ZNF263 | MA0528.1 | chr19:45946310-45946331 | GGGGGAGGAAGGGGAGATGCA | + | 6.13 | ZNF263 | MA0528.1 | chr19:45947514-45947535 | CCCCATTTCCCCCCCTCCCCC | - | 6.58 | Zfx | MA0146.2 | chr19:45947703-45947717 | CAGGCCCCGCCCCG | - | 6.18 | Zfx | MA0146.2 | chr19:45946860-45946874 | CAGGCCCCGCCCCC | - | 6.19 |
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| Number of super-enhancer constituents: 45 | ID | Coordinate | Tissue/cell |
SE_01498 | chr19:45945990-45948338 | Adrenal_Gland | SE_02108 | chr19:45945621-45948446 | Aorta | SE_02406 | chr19:45945923-45948427 | Astrocytes | SE_03036 | chr19:45946113-45947549 | Bladder | SE_03036 | chr19:45947662-45948256 | Bladder | SE_06640 | chr19:45945482-45948650 | Brain_Hippocampus_Middle | SE_09930 | chr19:45945246-45948642 | CD14 | SE_11261 | chr19:45945267-45948885 | CD20 | SE_12309 | chr19:45945679-45947635 | CD3 | SE_12309 | chr19:45947717-45948397 | CD3 | SE_13038 | chr19:45946864-45947547 | CD34_Primary_RO01480 | SE_14395 | chr19:45945395-45948823 | CD4_Memory_Primary_7pool | SE_16220 | chr19:45946614-45948594 | CD4_Naive_Primary_7pool | SE_16563 | chr19:45946127-45948539 | CD4_Naive_Primary_8pool | SE_17214 | chr19:45946144-45948458 | CD4p_CD225int_CD127p_Tmem | SE_19219 | chr19:45945599-45948281 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20014 | chr19:45945529-45948761 | CD56 | SE_20748 | chr19:45945638-45948676 | CD8_Memory_7pool | SE_21766 | chr19:45946179-45948391 | CD8_Naive_7pool | SE_22333 | chr19:45945577-45949075 | CD8_primiary | SE_23143 | chr19:45945796-45948504 | Colon_Crypt_1 | SE_23745 | chr19:45945894-45948357 | Colon_Crypt_2 | SE_24769 | chr19:45945851-45948444 | Colon_Crypt_3 | SE_26771 | chr19:45945693-45951267 | Esophagus | SE_29756 | chr19:45945483-45949108 | Fetal_Muscle | SE_31887 | chr19:45945791-45948464 | Gastric | SE_34472 | chr19:45945763-45948329 | HCT-116 | SE_35967 | chr19:45945746-45948665 | HMEC | SE_38090 | chr19:45945582-45948662 | HUVEC | SE_39922 | chr19:45945609-45949180 | K562 | SE_41239 | chr19:45945482-45948430 | Left_Ventricle | SE_44217 | chr19:45945560-45948393 | NHDF-Ad | SE_44830 | chr19:45945750-45948454 | NHLF | SE_45809 | chr19:45945565-45948608 | Osteoblasts | SE_47661 | chr19:45946589-45947589 | Pancreas | SE_47661 | chr19:45947675-45948228 | Pancreas | SE_48343 | chr19:45945492-45948437 | Psoas_Muscle | SE_49047 | chr19:45945509-45948452 | Right_Atrium | SE_50737 | chr19:45945627-45948452 | Sigmoid_Colon | SE_51420 | chr19:45945567-45948657 | Skeletal_Muscle | SE_52836 | chr19:45945622-45948434 | Small_Intestine | SE_53558 | chr19:45945612-45948448 | Spleen | SE_57973 | chr19:45946871-45947657 | VACO_9m | SE_64393 | chr19:45945900-45949160 | NHEK | SE_65504 | chr19:45945622-45948578 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr19 | 45947600 | 45948600 | chr19 | 45946690 | 45947113 | chr19 | 45945937 | 45946679 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I045442 | chr19 | 45945379 | 45949057 |
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Enhancer Sequence | AAAGAAAAAA AGTTTTGGTA ACTACAAAAG GGTATACCTT GGAAAAGTAA ATTTCCCTCC 60 CACTCTGATC CCCACTTCTC AATATTAACT ATTTTTTATG TATCTTGGCC AGTAGGATTC 120 ACTGAGCTCT CACGATGTCC CTGGCCTATG CAAAGCCCAT CACAGAAATG AAGTGGCTGG 180 AATCATTCAG CACTCAGTGA GTAGGCCAGA CCCCATTGCT ATGCCCATTT TAGAGATGGG 240 AAAACTGAGG CTTGGAGAGG TGCAAGGATG TGTCCTTTTG AGGGCCCGGT TCTGAAGGCT 300 TTTCAAAGTT GAGGCAAGGA AGTGGATGAG ATCAAAGAGG CAAGGTTCAG GCCAGGATAC 360 AAATCCCAGG GAGGGTGACA GGGGTGGGGA GTCAAGGAAG GCTGCCTGGA AGAAGACTAA 420 GGGTAGCCAG GAAGGCATCT TCCAGAACCT TCTGATGGAG GGCTTGGATG GAAGTAGATA 480 ACTCTGTTTG GCAGGCTGAG GAACCACCAG CAGCAGGGCG TGGCCCCTCC TCAGACCCAC 540 AGCACCCCAG AGGTATGTAT AGAAGAAGCA GGCTGCTTAA TGACATCTCA GGGACACATC 600 TCGGTGATAG CACAGCCGGC TTAGTTATGA CGTCTGAGTG ATTTGCCAAC TGCCTTAAGA 660 CCAGCATCCC TAGTCATGCC CCGCGGGGGG GATGAAGATA AGAGGAAGTG ACAGGCCATC 720 GGGGGAGGAA GGGGAGATGC AGTCACACAC AGACCAGGGA CTCAGGAGCT GAGGGATGTG 780 TGGTGCCCTC TGCACTAGGG AGGGGTCTCC CAGCTGCCTG GATGTGAGGG TCCATCTTAT 840 TGATTTGTCT AGTGAAGGAG GCCAGGCTCC AAGGAGGTAT GGCTGTAGTC AGTCACACTC 900 AGTTTGGGAT GGGGTCCGCC CAGGGGCTGC AAGGATCAGT CACTGCTGTG TCCCCATCAC 960 CTAAGGCAGT AACTGGGACA CAGCCGGCGC TCCATACATC TTACTGAATG AATGAATCGA 1020 ATGAAAAGGG TCAGCACCGT CTGGGACTCA GTTTACCCTC GCGGTCATTG GGCTGCTTCA 1080 ACCAAGGGGA TCGCTAAGAA CACCCCTCCC CACCTTGGGT CCCAGATCCC AGATCGCCAG 1140 TGAGTAAGAA AACGGGTTCG CGCCGTTGGT GGACTCCGCC CACTTGTGAC GTCACGAGCC 1200 GCTCCCCCAG GATCCCGACC CAGGCGTCTC CCTTGGGATG GGGGCGGAGA GGAACCCGGG 1260 AGTCCAGACT CAGGCCCCGC CCCCGGGAGC AGGCGGGCCG GGCAGGGTTA CACAACCCGT 1320 CGTCGCGTCC CGAGGGAAGT CGCCGGATGT CCTGGCCGGG CCGGGGACAA TGGGCAAGGA 1380 GGGCCCCTCC CGCAGGAACC TGGAAGTGGC AGGGGCTCCC CCTCTTCTGA TTCACCCTTG 1440 TTTCCGGCCC GGTTTAGCCT CCTTCTCCCT GGGGATCCTA TCTCCTCCCA ACTCTACCCT 1500 CCTGTGGCCC TGCAGTTCGG TTCTTTCTCC GAACCGGCAA ACCTCTCTCC TCTACACCCC 1560 GTACCCCGTC CTTTCACACC TTCCCAACGC CCCCCGAAAC TCTCTGCCCT CACACTCATC 1620 GCTTGTAATT CCCGAATCCC CTAAACTTCC AGTGTCCCCG GTCCTTCCTT CACTCATCCA 1680 TACCGGGCCC CTCTTCCCAC CCCCTCAACT ACCCCCACTA TCCTGCCCAG GCCCTCCCAA 1740 TCCCCTCCCC GGGCTCCCCC AAGCTTTCCT CAATATCTCC CAGCCCTCCC TAGCCCCCGA 1800 CTCACCCGCT TCCCTCCAAC TGACCCCAAT ACACTCTCTT GTCCTCCTAA TCCCAGCCTC 1860 CCGCAGTTCC CTCCTGTCTC CTCGAACTGC CCCATGTCCC TACCTCATCT CCCCAAATCC 1920 TGTTCCCCAT TTCCCCCCCT CCCCCAGCCA GCCGCTTCGC CCCCCACCCC GGAGCCCCTC 1980 CCCGCCCCTA GGCCCAAGGC CGGCCCGCGC CCCTCCCGGG CGCGCTCCCA CGCCCGGCGC 2040 GGGTTCCCAG GCCGCCCCCC CGCGGTGGCC CAGAGACCCA GTTTGCTGCG GCAAAACACT 2100 GGTCTCCAGG CAACAGGCCC CGCCCCGCCC CAGGGCCGCC AGATGAGGCT GGGCGGTCAG 2160 GAGGCCACCG GGCCGGGACG GAGCACCCAG GCCTGCGCGC CAAACCCTCG GCCTTGGCCC 2220 CCAGAGGCCT CAGGGCGCAG AAACCCGGAG ACTGAGGCGC AGCAAAGAGG AGATACAGAG 2280 ATCAGGGCCC CGGAGCAAGA AATTCGGAGA CATGCGTGGA GGCCGAAGCA ACAGGGAACT 2340 GTCGGGGCGC AGAGATATAA GGAAAGACCA CGCGACAGAT CGAACAAGGA CGGGGCCCAG 2400 AAATAAGCAC AGAAATAATG CAGTTACACA CGGGCAACAC CGAGGCCGGC AGGGACGCCC 2460 CTGATGGCAG AATAATCCAT CTTTAGTCCT CAGGACCTTT GCACTCAGTT CGAGGGACTT 2520 CCCCTCTCTG ACTCTGTTTC TGTATTTGTA AAATGGGGAC ATTAATACGC AGCGCTTAGC 2580 AAATCAGGCT GTTCTGACGA TTCAGTGAAT TCGCAGACCC AGAGCTTGTA GCACAATTCC 2640 TGGCATGTAC ACTCATCATT CATTCATTCA ACCGATTTTT TGTTGTTGTT GTTATTGTTG 2700 TCTGAGAGGA GTTTCGCTCT GTGGCCCAGG CTGGAGTGCA ATGGTACCAT CTGGGCTCAC 2760 TGCAACCTCC GCCTCCTGAG TTCAAGCAAT TCTCCTGCCT CAGCCTCCCA GGTAGCTAGG 2820 ATTACAAGCC TGTGCCTCCA CGCCCAGCTA TTTCTTGTAT TTTTAGTAGA GACACGGTTT 2880 CACCATGTTG GCCAGGCTGG TCTGAACTCC TGACCTCAAG TGATCCACCC ACCTTGGCCA 2940 CCCAAAGTGC TGGGATTAGA GGTGTGAGCC ACGGCACCTG CCCCAATCAA CAGGTATTTA 3000 TTGAGCATCT ACTATACGCC 3020
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