Tag | Content |
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EnhancerAtlas ID | HS197-10522 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr19:18569140-18572380 |
Target genes | Number: 27 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr19:18570799-18570810 | TTTTATGGCTC | - | 6.14 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_01013 | chr19:18570706-18572741 | Adrenal_Gland | SE_06012 | chr19:18566890-18569673 | Brain_Hippocampus_Middle | SE_06012 | chr19:18570472-18572983 | Brain_Hippocampus_Middle | SE_08139 | chr19:18566951-18569590 | Brain_Inferior_Temporal_Lobe | SE_23216 | chr19:18570560-18571677 | Colon_Crypt_1 | SE_23893 | chr19:18569895-18570354 | Colon_Crypt_2 | SE_23893 | chr19:18570880-18571579 | Colon_Crypt_2 | SE_23893 | chr19:18571685-18572129 | Colon_Crypt_2 | SE_26168 | chr19:18570408-18572157 | Duodenum_Smooth_Muscle | SE_26932 | chr19:18570667-18573176 | Esophagus | SE_31681 | chr19:18570731-18572664 | Gastric | SE_41123 | chr19:18570485-18573111 | Left_Ventricle | SE_41560 | chr19:18569881-18570405 | LNCaP | SE_41560 | chr19:18570655-18573168 | LNCaP | SE_42344 | chr19:18570637-18572709 | Lung | SE_44495 | chr19:18570573-18572419 | NHDF-Ad | SE_46271 | chr19:18569670-18572362 | Osteoblasts | SE_47511 | chr19:18570846-18571845 | Pancreas | SE_48120 | chr19:18566935-18573376 | Psoas_Muscle | SE_48694 | chr19:18569737-18570446 | Right_Atrium | SE_48694 | chr19:18570515-18572905 | Right_Atrium | SE_50125 | chr19:18569695-18570438 | Sigmoid_Colon | SE_50125 | chr19:18570516-18573140 | Sigmoid_Colon | SE_51145 | chr19:18566712-18574014 | Skeletal_Muscle | SE_52434 | chr19:18569863-18570520 | Small_Intestine | SE_52434 | chr19:18570522-18572360 | Small_Intestine | SE_53541 | chr19:18570544-18572320 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 18569684 | 18570327 | chr19 | 18570598 | 18571706 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I018458 | chr19 | 18569759 | 18572635 |
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Enhancer Sequence | TGCAAGACAG AGCCAGCCAT CACTTTGTGG GAATCCTGAG AGAGACGGGG GACTAGAGAA 60 AAAAGATCTG ATAGTGGGTT TGGGAGGGTG TGCAGAGACA GTGGGAGACA GACAGAGACA 120 GAGGAGAGGA AAGAGGATGG CCCACTACCG ATCCGTGATG TCTCCCACCC CCAGTTCCCC 180 CGCACACAAT CCTCAGGGTG CAGAAGGGAT AATGAGGGTC ATGAAGGCAG GTCCAGACTC 240 AACTGTCTTA GAGGTGCTGG GGCCAGGCTG GCTCCAAAAA GGGGAGGGCT ACCACCTGCA 300 GTACTGAGAC CCCATCACCT GCCCCCTGGC CCCTCTAGCC TGCTTTTTTT CCTTTTTTGA 360 TACAAGATCT TAGCTCACTA TAGCCTAGAC CTCCTGTGCT CAAGCGACCC TCCCACGTCA 420 GCCTCCCAGG TAGGTGGGGC CACAGGTGTG CACCACTATA CTCCAGCTAA TTTTTTTTAA 480 GAGATGGGAT CTCGCTATGT TGTCCAGGCT TGTCTTGAAC CCCTGGGCTC AAGCGATCCT 540 CTGATCTCAG CCTCCCAATG TGCTGGGATT CCAGCCACCA CACCTGGCTC CTATTTCTTC 600 CAGGCTGGAG TGCAGTGGTG TGATCAAGGT TCACTGTAGC TGCAAACTCC TGGGCTCAAG 660 CGATCCTCTT GCCTCAGTCT CCCAAGTAGG TGGGCTATAA GCATGCACTA TCATACCCAG 720 CTAATTTTTT GTATAGATAG GATCTCAGTA TTTTGCATAG GCTGGTCTCG AGCTCCTGGC 780 CTCAAGGATC CTCCCACCTC AGCCTCCCAA AGTGCTGGAA ACAGGCGTGA GCCACCGCGC 840 TGGGCTCCAC CCCATTTCTG ATCACAACTC CCAGGGAAGA GTCAGCCACG GCTGGGGATG 900 CTGGGTGAGG GGTACCTCTG GGGCCACGTC TGAGCCCACC TTCCCTACAA CCAGCCTGCC 960 TTGCTGTTGC CGGTTGACCA AAGCTAAGTT CGTCTCCCAG ACTGCTAACA AAGATGGATT 1020 CAGAACGTCT GCCTTAGAGG GATCTGAGGA AGCTCCAGGT CACTGCCCTG AGTGGGTGCT 1080 GCGTGCTGGC CTACAGGGCA CTCTGGTCTC CATCTTGCTG CAGGCATAGC AGTCACTGTT 1140 TTCTGCTGCA TCTGACATGG CTCTGCGTCA CAGCGTATCC CATGGGGAGC ATTTTTTTTT 1200 TTTTTTTGAG ATGGAGTCTC GCTCAGTTGC CCAGGCTAGA GTGCAATGGC GCTATCTTGG 1260 CTCACTGCAA GCTCCGCCTC CCGGGTTCAC GCCATTCTCC AGCCTCAGCC TCTGGAGTAG 1320 CTGGGACTAC AGGCACCCGC CACCACGCCC GGCTAATTTT TTTGTGTGTG TATTTTTAGT 1380 AGAGATGGGG TTTCACCATG TTAGCCAGGA TGGTCTCGAT CTCCTGACCT CGTAATCCAC 1440 TTGCCTCGGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CCACCGCGCC CGGCCCATGG 1500 GGAGCATTTT TAACAGTTGA GTAATATCCC ACCCCCAAAC TGCTGCCAGT TTCTCTGTAG 1560 CATAAACAGA CATTACTGTG TGCAGTTTTT TTCAGGTTGG CAACAGTTTC CTTCGACGGG 1620 ATTCCCAGAA GCCAGATTAG TAGGTCAAAG GCTGAATATT TTTATGGCTC ATGACAGGCT 1680 TTGCTAAATA TTACTCAGCC GTCAACACCC CTCCCCTTGA AGGATAGGCT TGCGGGTTTC 1740 CCTGGGGCTC AGCCAGTCCT AGAGGTGGAC ACCTTCCATC TCTGCTCTAG ATTTTTCCAC 1800 AGAGGGAGGG CCAAGCACCT TTGAGGCATG CAGTTTTGTC ACTGCCATTC CTCAGCATGT 1860 CTGAGGGCCT GTGAGGGGCT GGAAATGACC AGTCTGGGTG AGGCACATCC CCCTCCTCTT 1920 CTACAAGCCA ACAGTGTCCT GCTGACCCCC ACAGCTGCTT GGGGGGAAGC AGCTGCATAA 1980 TGAATATAGA AGCAAGAAGC AGACGAGCTG TCCAGGGGAA GTCACAGTGG CACAGGAAGG 2040 GACAATCTGC CTGCAGATGC TGGCCAGGCC TGCTCCCAGG AGGCACTGAA CCAAAGTCAC 2100 CTGGAGAAGC CAGGCACCAG CACAGACACC TCCTGGCCAG GCCAATGCAG GTCCCACATC 2160 TGATGACTCC ATCGAGCTCC CTTCAGCAAC TCCTGCTGGC ACCATGCCAG CCCTAGCCTT 2220 GGGAGCAGGA TGGGGGTGGA CGAGGGCCAG GCTGACATCC TCCCAAGGAA TGTGGAACAG 2280 GGTCCCACCA GCCGCGCACC CGAGAGGGAC GCCTATGAGG AGCTCCGTAA ACATGGAAGA 2340 ACGTCCTTTA TACAGCTGCT ATCCCGGCAT GCCACAGCAT GTGCTTTTTG CTGCAGGCAT 2400 CACCTGTGTT CCTGAGGTGC TGGATGTGAC CCCGAACATC CCACTTCCAT CATCCTAAAA 2460 GGTGCAAGAG GCTCAGCCAT GTCTCTTCCT CCACCACAGC AGCGATCCGA GGAGACCCAT 2520 CCTCAGTTCA CCTCAAGGCT GCATCTGCAT AGCCTGGCTA ATGTTCTGAA GCCAGTGCGA 2580 GTCACTCCCC TTCCCAGGGA CCCCAGGAAG CCAAGGTGGA GCCTCAGGAA CCTCCATGGG 2640 TGAGGGGGGT GGAAGGCAGT CAGGGCCATC GCACCTGCTC CAATGCCCGG GGTGTTTCTC 2700 AAGAGCAGGC TCCACTCGCC AGCACCACAT TCCAGATGGC CTAGCCTCCA ACCCCAGGGA 2760 GGGGCACTGC AGGTCACAGA TGGAAGCCTG ATGGTCTGAG ACGTGAAGCC CCTCACCCGG 2820 AGGCGCAGGT GGAGGGCGGC AGGCAGCTGA TTCACACTGA GGCCTGCCAG GCTCTGCCAG 2880 GCACGTGTAG ATTCCTTCCC CAGGCCTTGA GTCCACAAAT CGTCTGCAAC TGAAGCCTGA 2940 ATCCACTGTG CCAGGCCCCA CGGCCCGTGT GTCAGCAGAC AGTGAAGGAG GGCCTGGGCT 3000 CCATGCTGAG TCCACCTCTC AACCCTGGAC AGTCGGGGCC ATGCCCAGAA ACGCATCCAT 3060 GGCCCCCTAA GCTTGTTCTA ATCCAGGAGG CCCTGGCTCT CAGGCAGGTT CTGAACCTGT 3120 GAGAGACCCC AGGAAGGGCT CTTCCTTGCC AGTCCCAATC CCAGTCTCCA TGCTCTGGCC 3180 CATCCCACCC GCACAAGACC ATCTGCGGAG ACCACTGGTA AAGACAAGAC ATCGGGGCGG 3240
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