Tag | Content |
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EnhancerAtlas ID | HS072-01962 |
Organism | Homo sapiens |
Tissue/cell | GM19193 |
Coordinate | chr9:127046720-127049250 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GCM1 | MA0646.1 | chr9:127047496-127047507 | CATGCGGGTGC | + | 6.02 | Gata1 | MA0035.3 | chr9:127049140-127049151 | TCCTTATCTGT | + | 6.14 | ZNF263 | MA0528.1 | chr9:127048546-127048567 | TCCTCCTTTCCCTTCTCCACA | - | 6.16 | ZNF263 | MA0528.1 | chr9:127048346-127048367 | CCCCCCTCCCTGCCCTCCCCC | - | 7.66 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_01861 | chr9:127046506-127049775 | Aorta | SE_02294 | chr9:127046497-127049969 | Astrocytes | SE_03002 | chr9:127046477-127048332 | Bladder | SE_03002 | chr9:127048433-127049834 | Bladder | SE_04593 | chr9:127046574-127049467 | Brain_Anterior_Caudate | SE_06625 | chr9:127043834-127049648 | Brain_Hippocampus_Middle | SE_09789 | chr9:127046591-127050293 | CD14 | SE_23712 | chr9:127046626-127047227 | Colon_Crypt_1 | SE_23712 | chr9:127047265-127049868 | Colon_Crypt_1 | SE_24006 | chr9:127047555-127048089 | Colon_Crypt_2 | SE_24006 | chr9:127048095-127049763 | Colon_Crypt_2 | SE_26169 | chr9:127046463-127049845 | Duodenum_Smooth_Muscle | SE_27460 | chr9:127046556-127049833 | Esophagus | SE_29975 | chr9:127046449-127049606 | Fetal_Muscle | SE_31765 | chr9:127046641-127049905 | Gastric | SE_36996 | chr9:127041377-127050527 | HSMMtube | SE_38009 | chr9:127046644-127050178 | HUVEC | SE_38868 | chr9:127046466-127050685 | IMR90 | SE_42506 | chr9:127043941-127049998 | Lung | SE_44293 | chr9:127046454-127050001 | NHDF-Ad | SE_44809 | chr9:127043918-127049996 | NHLF | SE_45648 | chr9:127040018-127051411 | Osteoblasts | SE_47283 | chr9:127041647-127050279 | Panc1 | SE_47557 | chr9:127046812-127047158 | Pancreas | SE_49326 | chr9:127046669-127049494 | Right_Atrium | SE_50283 | chr9:127046482-127049944 | Sigmoid_Colon | SE_51779 | chr9:127046603-127049889 | Skeletal_Muscle_Myoblast | SE_52726 | chr9:127046633-127049907 | Small_Intestine | SE_54297 | chr9:127046540-127050009 | Spleen | SE_60448 | chr9:127019058-127056389 | DHL6 | SE_63558 | chr9:127046603-127049955 | HSMM | SE_65907 | chr9:127046833-127049972 | 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 | TTTCCTGCTC CCAGGAGTGG AATGGGAGCG TGGCAGCGAC CACGCACACG TTTGTTTAAT 60 GATTATCCAA TGTTGACCCA AAACTATGAG CAAAGCTCCG GGGATTTTCT GGGCGTTCAG 120 CACAAAATTC CCAGTTAATG GGTTCCAGTG TCTTAAAAAG GCAGGACTGA GGCGGTCTCT 180 ATGGAGTTGT TCTGACTGCA GCTGGGCCCT GTCCTTCCAC ACCTGCCCCT GCAGGAATTC 240 TCCGGACGCC TGTGGAGGGA AGAATGTGTG TGTCTGGGGT CCAAGACCAC ATGCACCGCC 300 TGGTGGAACT TTCTCTGCTC TTGCATGTCT GGTGGGAGCT TCCCTTAATG ACACAGGATC 360 TGCCGAGATT CATCCCCAAC TCCAGGCTGG CACCAGTGTT CAAGCCCCTG CCTCTGCTGT 420 CTCCCAGGTC TTCAAATTTA CACCACTCTG ACTCTCAGTT TCCCTATCTG CAAAATGAAG 480 GCAGGAATGC CCACCTCATG GGGTGAGCCA GTGGACCCAA ATACGTGGTG CAGTAGGTGC 540 CACGGAGTAG TGGCACGTGA TTTTGTGGCT GTTAGTGTGA GTATTCCTTA CTTTAGAGAG 600 CAGAGGAAAA CACATCAGCA GATTGTTTAA GCCAAAAAAT GTCTGTTGTT TGAAGAATTT 660 CGTTTTGGAA GGCAAGCCCA GGTTTTGGGT CAGAACCGTA TTCCCTCAGG CACGGCACGG 720 TTGAACGTCG AGGCATATTT TACAGGCTTG GTGACCGCTC AAGCCTTTGA GCCCTCCATG 780 CGGGTGCTCT GAGGTCAGAC TTTTCGGGAA GCCCTCACAC AGCTGGTCTG CTTGTCGCGT 840 TGGTAGCACC GTTTCCACAG AGCAGGCTCT GTTTGGCTAT GAATAGATGT TTTTCTCACT 900 CTTTTCTTGG ATGCCTGAAT GGCAGGCTCC CCTCCTGCAG TCTCAGAGGC CGACCTGCAT 960 GTAAAACTCC AAGCGGACAT CAGAGTGGGT TCGTCTGTTC CTGCTTGGAC TTGAGGCTCT 1020 CAGCAAGGCT CAAAGAGCTG GGTCGATGGC CACCATGACC CAGGGAGCCT CCCGAGAGTC 1080 TCCCAGGCTA TAGTTTCTGA AGGCTACTGA GTGAACTGAA GAAATCAGAG TTCATGGAAG 1140 AGGCAGCAGA TCCGAGCAAC AGCCGAGATT GAGGAGGATG GTTCAGGATC TCCAAACACA 1200 GGCCCGCTGG CTCCACTGTG TCCAAGCCGC AGATGCAAAG CCTGTTAGGA CAGAAAGGAC 1260 ACGAGATAGC AGCCAGGGCC GGCCGCAGGC AGGAGGGCCG GGCCACCAGC AGTTAGGAGT 1320 GTGGGTTCTG GAGCCACACA ACCGGGGTTC AGATCCCAGT TTTCCCACCT CTATTGGGCA 1380 GCATACTGTA AGCCTCAGTT TTCCCCTTCT GTAAAACGGA GATAATAATT TACCTGTCTC 1440 ACAAGGCTGT TATGAGGATT AAAGTAAGTT AACATCACTC AAGTGCATAG AACGATGCTG 1500 GGTACATACT AAATAAATAC AGATAAACTG AGGCCCAGAG AGGGCAAGGG ACTTCGCTGT 1560 GGTCACTCAG CAAGTCATTG GGGCAGCCAA GGCTGAAACT CATGACTCCT AGTCTCGTGA 1620 ACGGTTCCCC CCTCCCTGCC CTCCCCCGCA GTCAGACTTT TTAAACACTG CCTTTTGCAG 1680 AGGAAATCGC GTGACCCTTC AGCCCACAAG AATTCCGACT GCACAGAATG TCTGAAACCT 1740 CTTCGGGCTG GCTGGGGGCC TTGTTGCAAT TCTATTCAGC TGTTAGTTCT TTTTTTCCCC 1800 TCTCTTTCTT TTAAAGCTCT ATAGGATCCT CCTTTCCCTT CTCCACAAAT AGAAAAATTA 1860 ACCTCTTGAC AAAGGAGTTG GAAGACTTGA GTCCCTGCTG TGTGTCCCGG AACCAATCCC 1920 CCAGCCTCAG GTTCCCCGGC TGTGAAATGA GAAGGTGTCC TCTGTTGACA GGGAGGTGGC 1980 CCCACCTGCC AGTCTGTGAT TGCCACAGAG ACAAGCCAGC CAAGAAGTGC CACCCTGGAC 2040 GAAGGTCGGG TGAGTGCTGA TTAAACAAAA TCTGGTGACG CATCCTTCTA AGAAGCGAGG 2100 CGAAACCCAC CAGAGATGCT GCGTGCTTCT GCCCACCTCC TCGTGTCAAA GGTGATTTGA 2160 GTCATCAGCC TGGCCTGCAC TTTTCTCGCT CTCCTGTTTC CTTGCAGTGC TCCTGGGCTC 2220 CTGAGCCACT CGGGGCTGAG GCCCGGGGGC CAGTTGTGTC CCATCTGCAG GCCCCAGGGC 2280 ATTAGACCTG AGGGGCCTGG TCACCTTCTG ATTTCTGCTG GGCGCCCCAG CCATGAGCTC 2340 CAGAGGCTGC CAGCCTAGGG TGTGAGTCTG TCTCCGAAGC TGCTGACATG AGTAGGGACT 2400 TCCCCTCTCT GAGCTTTAGT TCCTTATCTG TGAAATGGGT GCATGAGCCC TGCCTGGCAG 2460 GGTGAGATGA GGTACACAAG CCCTATCCTA CTTCACTCCC CTCTTCCTTC CTGCCCGAAA 2520 GGCCCTGGCT 2530
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