| Tag | Content |
|---|
EnhancerAtlas ID | HS040-18453 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr19:39187730-39190280 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
| | Number of super-enhancer constituents: 40 | ID | Coordinate | Tissue/cell |
| SE_00865 | chr19:39188085-39193891 | Adrenal_Gland | | SE_01543 | chr19:39181993-39190228 | Aorta | | SE_03166 | chr19:39185728-39189384 | Brain_Angular_Gyrus | | SE_03903 | chr19:39185394-39193508 | Brain_Anterior_Caudate | | SE_04868 | chr19:39185423-39189876 | Brain_Cingulate_Gyrus | | SE_05805 | chr19:39182078-39206004 | Brain_Hippocampus_Middle | | SE_06803 | chr19:39186740-39189302 | Brain_Hippocampus_Middle_150 | | SE_07777 | chr19:39185584-39193917 | Brain_Inferior_Temporal_Lobe | | SE_09404 | chr19:39182333-39191485 | CD14 | | SE_14624 | chr19:39188044-39189097 | CD4_Memory_Primary_7pool | | SE_20249 | chr19:39181278-39188425 | CD56 | | SE_23062 | chr19:39186752-39190129 | Colon_Crypt_1 | | SE_23732 | chr19:39188124-39189025 | Colon_Crypt_2 | | SE_23732 | chr19:39189683-39190017 | Colon_Crypt_2 | | SE_24739 | chr19:39187116-39190124 | Colon_Crypt_3 | | SE_25779 | chr19:39180965-39189795 | Duodenum_Smooth_Muscle | | SE_26525 | chr19:39180697-39193852 | Esophagus | | SE_27614 | chr19:39180632-39201469 | Fetal_Intestine | | SE_28533 | chr19:39164445-39201888 | Fetal_Intestine_Large | | SE_29583 | chr19:39188832-39190235 | Fetal_Muscle | | SE_31384 | chr19:39189487-39190222 | Gastric | | SE_34299 | chr19:39187789-39188976 | HCT-116 | | SE_34299 | chr19:39189288-39190196 | HCT-116 | | SE_35812 | chr19:39168616-39191950 | HMEC | | SE_40594 | chr19:39180727-39193965 | Left_Ventricle | | SE_41601 | chr19:39188166-39189312 | LNCaP | | SE_41601 | chr19:39189496-39190167 | LNCaP | | SE_42097 | chr19:39180674-39193834 | Lung | | SE_44161 | chr19:39186536-39189303 | NHDF-Ad | | SE_45660 | chr19:39188825-39189523 | Osteoblasts | | SE_47114 | chr19:39164477-39226374 | Panc1 | | SE_48555 | chr19:39185073-39190229 | Right_Atrium | | SE_50056 | chr19:39182445-39193963 | Sigmoid_Colon | | SE_52339 | chr19:39180899-39193971 | Small_Intestine | | SE_53291 | chr19:39181227-39190272 | Spleen | | SE_54534 | chr19:39180651-39189737 | Stomach_Smooth_Muscle | | SE_56725 | chr19:39185122-39189741 | VACO_400 | | SE_64225 | chr19:39186925-39190261 | NHEK | | SE_65266 | chr19:39188604-39190006 | Pancreatic_islets | | SE_68725 | chr19:39186614-39190205 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr19 | 39187733 | 39187838 | | chr19 | 39188765 | 39190091 | | chr19 | 39187913 | 39188715 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I038673 | chr19 | 39164536 | 39206516 |
|
Enhancer Sequence | ACCTGTGTGA TGCCCAAGCC AGAGCTCTTG TTTACTACCC AGAGAAGATG AGCACAGGTG 60
GGATGTACGT ATGGAGGGCG GGTAGGGCAG CAGCCCCTCT GAGGACAGGT GGCCAGAACC 120
CAAGCGGCGA GGTTTGTTCA CAGCCTCCAC AGGGTGGGGT GGGGCCATCC GCAGAGGGTC 180
TCCTGCCATC CCATTTTCCC TGCATACCAG TGGGTGGTCT GAGAGCCTTT GCAGAGAAGA 240
GACTGGATCT CAGCACGTGC TTATGTGCGT GTGTACATGC ACACACATGC GTGTGATTCA 300
TCTGGCTCTT ACTTTATGCC AAGGAGCCTG TCACATGCTT TAAATGTATT TTCCCTAGTT 360
TAATTCTTAG AGCACACTGC AGGAGGTAGA TTCTGATAAA TCCATCTTAC AGGGAAGGAA 420
ACAGACTTAA GTAGGTAAAG TCACTTGGTT GAAAACATGG AATGAGTAAG CCAAGGGGCA 480
GGTATTCAAA CCCAAACCCA GGTCTGTGCC CCTGCAGAGC CTGCAGGAGC AGCCCACACA 540
GGCCAAGGCT GTGAGGGGTG CTGTTTGCAC GCGTGCGTGG CCCTCCCTGC AGCCCAGGTG 600
CCTAGGTCTG GGCCTGGCAA CACCAGAGCA CGGGGCCTTG CCCTCGGGGA ACAGCCCTCT 660
TTTGTCCTCA GGCTGTGGGA TGTGTCTTGG CTACTTTGCT GCCCAGCAGT GCCTGCTCTC 720
AGGCACATGT GAGAGTAGAG GCCTAGCATC CGTGGCCACT TCCTTCCCAG CCCATTTGCT 780
GCTGCCCTTT GCTCTGCAGG GCTGCTGGGC TCCTGGGCTC CACGCCTGCT TGCTGCCTGC 840
CATCAAGGCT GGCAGTGCTC TGGGGCTGTA AAGGTGCAGG CGCCGTACTT CCCAACCCCT 900
GGAGCTCGCA CATGGTAGGA GAGAAAGCTC ATGTGCATGC AACATCCAAT AAGACTAAAA 960
GTGACTGGGG GTTGCTACGG GAGAGGTGCT GAGGGTGGGC CGGGGACAGA GCAGGCACAC 1020
TGTGGAGGGG GTGGGCAGGA CTCCTGAGAC CAGGGCAGGG AGGGAGGAGA TGCTGGGAGG 1080
CACAGGGCCA TCCAGAGAGC TGCCACTTCC TGAGCATTGC CATGCACGCT GCAGGCATGG 1140
CCATCTTGAG TCCTCACACT GCCCGTGGCC TAGGTGGGGT CTTCATCCCC ACGTTGCAGA 1200
GGAGGAAATG GAAGTTAGGA AGGTTAGGTG ACGTGCCCAC ATGAGTGGTG TAAGCATGGT 1260
TCCCGCCCTG GGCTCTCTGA ATTCAGTATT GTATGGGGGA GGCTGGGAAG GTGAGTTAGT 1320
ACTCTCCGCA GTGAGAACCT GCCTTGGCTC CCCTCCCCTC AAGGAGTTCA TAGCCGTGGG 1380
AGGGAGGGAG ACAAGAACTG TTGGAGACAA GAACTGTTAG AGACCAGAGA GCAAGGGCGT 1440
GATGTGGTCT GCAGGGAGGA GGCTGTCTGA GGCAGAACCG GGTCAGGGAG GCCATGGTGC 1500
GGGTACCCTC CAGGCACGGC ATTTGGCCTG ACTTTTGAGG GGTGCCCAGG GTTGGCTACA 1560
TGGCGGGGCG GAGGTATCTT TAGTGGGGGA ACAGCGTTGT GCCACCAGGA GGGGTCTCTG 1620
TCTCCCAGGT AGAGGAATTC TCCATGGTGA GAGGTGGTGG TGGGGGATGG TCTAGCTGTC 1680
CACTCTTGCC CCCTTTCGGA TTTGGAAGGA AGCCCCATGC TGGGTCCACA CTGGTATGGC 1740
GTATTAATTA GGCAGCTGCT TTGTCTGGGA GGGGGCTTTG TGTCGAGTCT CCCTGAATGA 1800
GCAGGGCTGG CGACAGTTGT CAAAACACAT GGTGCTTGGT CAGAGCCCCC GTAGAAGCCC 1860
CTTGTCCTCC GCATGGCCTC CGCCTGCACC CGGGGCGTGG AATGTGCTCT TGTGTGTCCC 1920
TGGCTGTCTG CTTGCTTCTA CACTGGCCCC TGCAGATGGA GGGGGTGGGG TACAGGGGTT 1980
CCTATAAGAA GCAGACACTT GGGGTTTTTC CCAGGTCCTG TTGCAGGAGG GTGCGTGGGC 2040
TGGTTTCCCT GAAGGCGCCT GGGCGTGTTG GTGTTAACTG ATCTGAGATC TTCTGTGGCC 2100
CTGATGTCTA TGAGCATGCC CCAGCTTGCA GGGGGCTGAG TAGCCGGGCA CCACCAGGAG 2160
GCTGCGTGCC CTGTGCTTGG GTGTACCCAT GCCCTGTCAG CATCGTTGGT CTGTTAGGGT 2220
CAGGGACTTC GGCTTCTTGT TTAGTACCCT CCATCCCTTC CAGTTGATCA TCAGAAACAT 2280
TCTCCTTAGA TGCGGCTGCC TGACCCCGGT GAGGGGGCCT GCCTCCCACT TGCCTTCCAG 2340
CCTCCTCTAA GCTGCACTGA GTCTTAAAAA TAGGAAGGAT AGGGCTGGGT GTGGTGGCTC 2400
ACGCCTGTAA TCCCAGCAGT TTGGGAGACC GAGGCGGGTA GATCACTTGA GGCCAGGAGT 2460
TCAAGACCAG CCTGGCCAAC ATGGTAAAAC CCCATCTCTA CTAAAAAGAC AAAAATTAGA 2520
TGGGCATGTT GGCATACACC CGTAGTCCCA 2550
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