| Tag | Content |
|---|
EnhancerAtlas ID | HS139-26412 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr19:18569660-18572380 |
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 | CCCTGGGCTC AAGCGATCCT CTGATCTCAG CCTCCCAATG TGCTGGGATT CCAGCCACCA 60
CACCTGGCTC CTATTTCTTC CAGGCTGGAG TGCAGTGGTG TGATCAAGGT TCACTGTAGC 120
TGCAAACTCC TGGGCTCAAG CGATCCTCTT GCCTCAGTCT CCCAAGTAGG TGGGCTATAA 180
GCATGCACTA TCATACCCAG CTAATTTTTT GTATAGATAG GATCTCAGTA TTTTGCATAG 240
GCTGGTCTCG AGCTCCTGGC CTCAAGGATC CTCCCACCTC AGCCTCCCAA AGTGCTGGAA 300
ACAGGCGTGA GCCACCGCGC TGGGCTCCAC CCCATTTCTG ATCACAACTC CCAGGGAAGA 360
GTCAGCCACG GCTGGGGATG CTGGGTGAGG GGTACCTCTG GGGCCACGTC TGAGCCCACC 420
TTCCCTACAA CCAGCCTGCC TTGCTGTTGC CGGTTGACCA AAGCTAAGTT CGTCTCCCAG 480
ACTGCTAACA AAGATGGATT CAGAACGTCT GCCTTAGAGG GATCTGAGGA AGCTCCAGGT 540
CACTGCCCTG AGTGGGTGCT GCGTGCTGGC CTACAGGGCA CTCTGGTCTC CATCTTGCTG 600
CAGGCATAGC AGTCACTGTT TTCTGCTGCA TCTGACATGG CTCTGCGTCA CAGCGTATCC 660
CATGGGGAGC ATTTTTTTTT TTTTTTTGAG ATGGAGTCTC GCTCAGTTGC CCAGGCTAGA 720
GTGCAATGGC GCTATCTTGG CTCACTGCAA GCTCCGCCTC CCGGGTTCAC GCCATTCTCC 780
AGCCTCAGCC TCTGGAGTAG CTGGGACTAC AGGCACCCGC CACCACGCCC GGCTAATTTT 840
TTTGTGTGTG TATTTTTAGT AGAGATGGGG TTTCACCATG TTAGCCAGGA TGGTCTCGAT 900
CTCCTGACCT CGTAATCCAC TTGCCTCGGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG 960
CCACCGCGCC CGGCCCATGG GGAGCATTTT TAACAGTTGA GTAATATCCC ACCCCCAAAC 1020
TGCTGCCAGT TTCTCTGTAG CATAAACAGA CATTACTGTG TGCAGTTTTT TTCAGGTTGG 1080
CAACAGTTTC CTTCGACGGG ATTCCCAGAA GCCAGATTAG TAGGTCAAAG GCTGAATATT 1140
TTTATGGCTC ATGACAGGCT TTGCTAAATA TTACTCAGCC GTCAACACCC CTCCCCTTGA 1200
AGGATAGGCT TGCGGGTTTC CCTGGGGCTC AGCCAGTCCT AGAGGTGGAC ACCTTCCATC 1260
TCTGCTCTAG ATTTTTCCAC AGAGGGAGGG CCAAGCACCT TTGAGGCATG CAGTTTTGTC 1320
ACTGCCATTC CTCAGCATGT CTGAGGGCCT GTGAGGGGCT GGAAATGACC AGTCTGGGTG 1380
AGGCACATCC CCCTCCTCTT CTACAAGCCA ACAGTGTCCT GCTGACCCCC ACAGCTGCTT 1440
GGGGGGAAGC AGCTGCATAA TGAATATAGA AGCAAGAAGC AGACGAGCTG TCCAGGGGAA 1500
GTCACAGTGG CACAGGAAGG GACAATCTGC CTGCAGATGC TGGCCAGGCC TGCTCCCAGG 1560
AGGCACTGAA CCAAAGTCAC CTGGAGAAGC CAGGCACCAG CACAGACACC TCCTGGCCAG 1620
GCCAATGCAG GTCCCACATC TGATGACTCC ATCGAGCTCC CTTCAGCAAC TCCTGCTGGC 1680
ACCATGCCAG CCCTAGCCTT GGGAGCAGGA TGGGGGTGGA CGAGGGCCAG GCTGACATCC 1740
TCCCAAGGAA TGTGGAACAG GGTCCCACCA GCCGCGCACC CGAGAGGGAC GCCTATGAGG 1800
AGCTCCGTAA ACATGGAAGA ACGTCCTTTA TACAGCTGCT ATCCCGGCAT GCCACAGCAT 1860
GTGCTTTTTG CTGCAGGCAT CACCTGTGTT CCTGAGGTGC TGGATGTGAC CCCGAACATC 1920
CCACTTCCAT CATCCTAAAA GGTGCAAGAG GCTCAGCCAT GTCTCTTCCT CCACCACAGC 1980
AGCGATCCGA GGAGACCCAT CCTCAGTTCA CCTCAAGGCT GCATCTGCAT AGCCTGGCTA 2040
ATGTTCTGAA GCCAGTGCGA GTCACTCCCC TTCCCAGGGA CCCCAGGAAG CCAAGGTGGA 2100
GCCTCAGGAA CCTCCATGGG TGAGGGGGGT GGAAGGCAGT CAGGGCCATC GCACCTGCTC 2160
CAATGCCCGG GGTGTTTCTC AAGAGCAGGC TCCACTCGCC AGCACCACAT TCCAGATGGC 2220
CTAGCCTCCA ACCCCAGGGA GGGGCACTGC AGGTCACAGA TGGAAGCCTG ATGGTCTGAG 2280
ACGTGAAGCC CCTCACCCGG AGGCGCAGGT GGAGGGCGGC AGGCAGCTGA TTCACACTGA 2340
GGCCTGCCAG GCTCTGCCAG GCACGTGTAG ATTCCTTCCC CAGGCCTTGA GTCCACAAAT 2400
CGTCTGCAAC TGAAGCCTGA ATCCACTGTG CCAGGCCCCA CGGCCCGTGT GTCAGCAGAC 2460
AGTGAAGGAG GGCCTGGGCT CCATGCTGAG TCCACCTCTC AACCCTGGAC AGTCGGGGCC 2520
ATGCCCAGAA ACGCATCCAT GGCCCCCTAA GCTTGTTCTA ATCCAGGAGG CCCTGGCTCT 2580
CAGGCAGGTT CTGAACCTGT GAGAGACCCC AGGAAGGGCT CTTCCTTGCC AGTCCCAATC 2640
CCAGTCTCCA TGCTCTGGCC CATCCCACCC GCACAAGACC ATCTGCGGAG ACCACTGGTA 2700
AAGACAAGAC ATCGGGGCGG 2720
|
