| Tag | Content |
|---|
EnhancerAtlas ID | HS116-17092 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr19:18569680-18572380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr19:18570799-18570810 | TTTTATGGCTC | - | 6.14 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_01013 | chr19:18570706-18572741 | Adrenal_Gland | | SE_06012 | chr19:18570472-18572983 | Brain_Hippocampus_Middle | | 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 |
|
| | 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 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I018458 | chr19 | 18569759 | 18572635 |
|
Enhancer Sequence | CTGATCTCAG CCTCCCAATG TGCTGGGATT CCAGCCACCA CACCTGGCTC CTATTTCTTC 60
CAGGCTGGAG TGCAGTGGTG TGATCAAGGT TCACTGTAGC TGCAAACTCC TGGGCTCAAG 120
CGATCCTCTT GCCTCAGTCT CCCAAGTAGG TGGGCTATAA GCATGCACTA TCATACCCAG 180
CTAATTTTTT GTATAGATAG GATCTCAGTA TTTTGCATAG GCTGGTCTCG AGCTCCTGGC 240
CTCAAGGATC CTCCCACCTC AGCCTCCCAA AGTGCTGGAA ACAGGCGTGA GCCACCGCGC 300
TGGGCTCCAC CCCATTTCTG ATCACAACTC CCAGGGAAGA GTCAGCCACG GCTGGGGATG 360
CTGGGTGAGG GGTACCTCTG GGGCCACGTC TGAGCCCACC TTCCCTACAA CCAGCCTGCC 420
TTGCTGTTGC CGGTTGACCA AAGCTAAGTT CGTCTCCCAG ACTGCTAACA AAGATGGATT 480
CAGAACGTCT GCCTTAGAGG GATCTGAGGA AGCTCCAGGT CACTGCCCTG AGTGGGTGCT 540
GCGTGCTGGC CTACAGGGCA CTCTGGTCTC CATCTTGCTG CAGGCATAGC AGTCACTGTT 600
TTCTGCTGCA TCTGACATGG CTCTGCGTCA CAGCGTATCC CATGGGGAGC ATTTTTTTTT 660
TTTTTTTGAG ATGGAGTCTC GCTCAGTTGC CCAGGCTAGA GTGCAATGGC GCTATCTTGG 720
CTCACTGCAA GCTCCGCCTC CCGGGTTCAC GCCATTCTCC AGCCTCAGCC TCTGGAGTAG 780
CTGGGACTAC AGGCACCCGC CACCACGCCC GGCTAATTTT TTTGTGTGTG TATTTTTAGT 840
AGAGATGGGG TTTCACCATG TTAGCCAGGA TGGTCTCGAT CTCCTGACCT CGTAATCCAC 900
TTGCCTCGGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CCACCGCGCC CGGCCCATGG 960
GGAGCATTTT TAACAGTTGA GTAATATCCC ACCCCCAAAC TGCTGCCAGT TTCTCTGTAG 1020
CATAAACAGA CATTACTGTG TGCAGTTTTT TTCAGGTTGG CAACAGTTTC CTTCGACGGG 1080
ATTCCCAGAA GCCAGATTAG TAGGTCAAAG GCTGAATATT TTTATGGCTC ATGACAGGCT 1140
TTGCTAAATA TTACTCAGCC GTCAACACCC CTCCCCTTGA AGGATAGGCT TGCGGGTTTC 1200
CCTGGGGCTC AGCCAGTCCT AGAGGTGGAC ACCTTCCATC TCTGCTCTAG ATTTTTCCAC 1260
AGAGGGAGGG CCAAGCACCT TTGAGGCATG CAGTTTTGTC ACTGCCATTC CTCAGCATGT 1320
CTGAGGGCCT GTGAGGGGCT GGAAATGACC AGTCTGGGTG AGGCACATCC CCCTCCTCTT 1380
CTACAAGCCA ACAGTGTCCT GCTGACCCCC ACAGCTGCTT GGGGGGAAGC AGCTGCATAA 1440
TGAATATAGA AGCAAGAAGC AGACGAGCTG TCCAGGGGAA GTCACAGTGG CACAGGAAGG 1500
GACAATCTGC CTGCAGATGC TGGCCAGGCC TGCTCCCAGG AGGCACTGAA CCAAAGTCAC 1560
CTGGAGAAGC CAGGCACCAG CACAGACACC TCCTGGCCAG GCCAATGCAG GTCCCACATC 1620
TGATGACTCC ATCGAGCTCC CTTCAGCAAC TCCTGCTGGC ACCATGCCAG CCCTAGCCTT 1680
GGGAGCAGGA TGGGGGTGGA CGAGGGCCAG GCTGACATCC TCCCAAGGAA TGTGGAACAG 1740
GGTCCCACCA GCCGCGCACC CGAGAGGGAC GCCTATGAGG AGCTCCGTAA ACATGGAAGA 1800
ACGTCCTTTA TACAGCTGCT ATCCCGGCAT GCCACAGCAT GTGCTTTTTG CTGCAGGCAT 1860
CACCTGTGTT CCTGAGGTGC TGGATGTGAC CCCGAACATC CCACTTCCAT CATCCTAAAA 1920
GGTGCAAGAG GCTCAGCCAT GTCTCTTCCT CCACCACAGC AGCGATCCGA GGAGACCCAT 1980
CCTCAGTTCA CCTCAAGGCT GCATCTGCAT AGCCTGGCTA ATGTTCTGAA GCCAGTGCGA 2040
GTCACTCCCC TTCCCAGGGA CCCCAGGAAG CCAAGGTGGA GCCTCAGGAA CCTCCATGGG 2100
TGAGGGGGGT GGAAGGCAGT CAGGGCCATC GCACCTGCTC CAATGCCCGG GGTGTTTCTC 2160
AAGAGCAGGC TCCACTCGCC AGCACCACAT TCCAGATGGC CTAGCCTCCA ACCCCAGGGA 2220
GGGGCACTGC AGGTCACAGA TGGAAGCCTG ATGGTCTGAG ACGTGAAGCC CCTCACCCGG 2280
AGGCGCAGGT GGAGGGCGGC AGGCAGCTGA TTCACACTGA GGCCTGCCAG GCTCTGCCAG 2340
GCACGTGTAG ATTCCTTCCC CAGGCCTTGA GTCCACAAAT CGTCTGCAAC TGAAGCCTGA 2400
ATCCACTGTG CCAGGCCCCA CGGCCCGTGT GTCAGCAGAC AGTGAAGGAG GGCCTGGGCT 2460
CCATGCTGAG TCCACCTCTC AACCCTGGAC AGTCGGGGCC ATGCCCAGAA ACGCATCCAT 2520
GGCCCCCTAA GCTTGTTCTA ATCCAGGAGG CCCTGGCTCT CAGGCAGGTT CTGAACCTGT 2580
GAGAGACCCC AGGAAGGGCT CTTCCTTGCC AGTCCCAATC CCAGTCTCCA TGCTCTGGCC 2640
CATCCCACCC GCACAAGACC ATCTGCGGAG ACCACTGGTA AAGACAAGAC ATCGGGGCGG 2700
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