| Tag | Content |
|---|
EnhancerAtlas ID | HS040-00759 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:19716110-19719130 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:19717998-19718017 | CGTCCAGCAGAGGGCTCTG | + | 6 | | NEUROD2 | MA0668.1 | chr1:19717661-19717671 | GCCATATGGT | + | 6.02 | | TEAD1 | MA0090.2 | chr1:19717870-19717880 | CACATTCCAT | + | 6.02 | | TFAP4 | MA0691.1 | chr1:19717593-19717603 | AACAGCTGAT | + | 6.02 |
|
| | Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
| SE_01631 | chr1:19716172-19718011 | Aorta | | SE_01631 | chr1:19718069-19719052 | Aorta | | SE_04046 | chr1:19716514-19718685 | Brain_Anterior_Caudate | | SE_05077 | chr1:19716739-19718770 | Brain_Cingulate_Gyrus | | SE_05833 | chr1:19716201-19720492 | Brain_Hippocampus_Middle | | SE_18410 | chr1:19716176-19720317 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_25786 | chr1:19716549-19718828 | Duodenum_Smooth_Muscle | | SE_26537 | chr1:19716179-19720568 | Esophagus | | SE_28013 | chr1:19716841-19718501 | Fetal_Intestine | | SE_28668 | chr1:19716604-19718754 | Fetal_Intestine_Large | | SE_31164 | chr1:19716409-19719128 | Fetal_Thymus | | SE_31447 | chr1:19716397-19718506 | Gastric | | SE_42185 | chr1:19716243-19719159 | Lung | | SE_45720 | chr1:19716651-19718686 | Osteoblasts | | SE_46635 | chr1:19716568-19717616 | Ovary | | SE_46635 | chr1:19718098-19718452 | Ovary | | SE_48688 | chr1:19716506-19718426 | Right_Atrium | | SE_50058 | chr1:19716289-19720556 | Sigmoid_Colon | | SE_51211 | chr1:19716277-19718925 | Skeletal_Muscle | | SE_52345 | chr1:19716229-19719127 | Small_Intestine | | SE_54550 | chr1:19716169-19718904 | Stomach_Smooth_Muscle | | SE_65446 | chr1:19716642-19717397 | Pancreatic_islets | | SE_65446 | chr1:19717662-19720701 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 19717195 | 19718433 | | chr1 | 19716796 | 19717030 | | chr1 | 19717212 | 19718898 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I019389 | chr1 | 19716333 | 19720569 |
|
Enhancer Sequence | GGGGTTTCAC CACGTTAGCC AGGATGGTCT CTATCTCCTA ACCTCATGAT CCACCCACCT 60
CGGCCACCCA AAGTGCTAGG ATTACAGGTG TGAGCCACTG CGCCTGGCCA GGCCATGTAT 120
TTTTATTTGC TAAATCTGAC AGCCAATCCC CACTGCTCTC TTAAATCTTA CTGATCCTTC 180
AGGGCCTGGC CCAAACTCCA ACTTCTTTAT CAAGATGTCA AATTCTTCAG AATTCCTGCA 240
GTAACACTAA TATCAACTGA ATCCTAAATG CTTTGGGGAT GGCTGTTCTA ATACTGCCAA 300
TGACTTTCAC CTTACTCCTT CCTCACCACT TAGCATTTTT CATTGTGAAT TGACTCCACA 360
CCTACAGAGG CCAAGACAGG CCCTCCAGCC TCAGCGCAGC ATCACGCCCG CTGCAGCAGG 420
GATCAGTCAA TGCATGCTGA TTCCATGTAA GTGGATATTA ATCCTGTGGT CTGAGGCCAT 480
ATTACAGAAC CAGAATGAAG GCAGTGTATC TCTGTAATCT AACCAGTCCC TACACTCATC 540
TGAACCCCGG CCCCCGCCCC CTACTCATGT CGAGTGCTTA GAGCAGTGGA AGAAATCACA 600
TTAAGTGTCA CAGACCATGG GTTTGTACAG TGATTTAAAT GAAACGACAG GTCCAAACAA 660
AGCCGAGAGT TCACTTTGGG GTGCATGTGG CACTGGCTCT GTCGCCTCCA AAGCCAGGGA 720
GGGCCTCTGA GGAGGAGGAG CGGTGCTGAC ACGCGGCAGC CGGATGGTTT CTGTCTAAAC 780
CACCCATCTG AACTGCCTAA CGGCCTTGGA GGGAAGGTTC AGATAACACC AAAGGTGTCA 840
GACCAATCCA GGCTGTTGGG GGGATTTAAA CATAATTCCC AGTGACTTGG AATAATAAAC 900
ACTACACTGG TCAGGACAGT GCCTGCCGTC TTTCTGGTGG GAGTTCAGGG CTCCACCAGT 960
TCCTCTGCTG CCACAGGAGT GTGCCCACCC CAGGGAGCAG GAGCCACAAG TCCTTCACCA 1020
CCGATACTTT TGCCGGGCTC GGTGGTACCC AGGAGGCCAC TGGAAAGACG GGTGGGGAGT 1080
GGGTAAAGTG AACTAGGGCA GGGAAAAGAA AAAACCCCAG AAGGTAGAAG GTAAGGGAGA 1140
GACTAGGATG CCATTGGCAA CGGCCTCAGG TGACACCTGA ATAATAATCC GTGGAAGGAC 1200
CAGGTGATCG TAATAGCCCT GCCCTGCGTG GCAGGCACTA TGCTAGCAGC TCTCCCTGCC 1260
CTTCCCTATG ATCCTGACAA TGGCTCTTCA CACAGACACG CACTCCAGTC CTTGTTTTAA 1320
AGAAGGGGAA ACAGGGCCTT AGAGAAATAA CTTGACCGGA GCCACGCAGC TACGGGCCAA 1380
TGTCTGAGGA AGGACATGCA GTTATATACA GCACAGCTAG GTTCAAAAAG AAACTGCTTT 1440
TCCCAAACTG AACACTTTTT TTTTTTCTTA AATCATCCAA CCCAACAGCT GATCACACGA 1500
AGAGATACAA ATCAGAAGTT TCCGGCCACA AGTGAGGTTC GTGTTTGTGC CGCCATATGG 1560
TTCTACTTTG CCTCTTCCTC TTCTCCATTA GTTATTAATG TTGAAAAAAA TTGTTCAACC 1620
AGAAAAAGAA ACTTGAGATG AACCCTTAAA AAAAGCACAA AAGCCAGAGC AGCTCAGACC 1680
CACGGAGTCT AACCCACGGC GCCCTTGTCT TTAAGAAGTG CACCCTTGTA CCTCGGTTTT 1740
TTAAAAAATG GCCAAATGAA CACATTCCAT CTTTTGATCT GCCTGTTGGC CGAGAGCCCA 1800
CCACCAGCAA GATAGGAATC AAAAACAGAT TCTGCGTACT TGGGTGCACT CAGAGGAAAC 1860
TGCCACGCCA GAATGCTGCA GCTGCCGACG TCCAGCAGAG GGCTCTGTGA CAATTTGTTC 1920
CTTTTATTTT TCCAGAAGGC CCAAAACTTT CTTAAAAAGA TAAAAGAGCA TTTCAAGTGG 1980
CACATACACT CGTGTCAGAA ACAAAATATA CAGTGTGGCA TTCTGTAAAA ACACCAACCT 2040
CGAAACCGAA CAGGTTCAAA TCCTCGGTCA GTCACTTGCT GGCTGAGTGT AACCTTCCTA 2100
AGTCTCTGGA ACTGGGGGTT ACAACATCCA TGTCAAGGAG AAATTCACAC TGTTCCATAA 2160
ACCCCGAATG CCCGCTCCAG GCCCGTGTCA GGTGCAAGGG CTCAGCACGG GAAGAGATGG 2220
ACATGGGCGG CCCTGCTCTG ACAGCAAAGT CCAGCCACAG AGGCATCTCC AAGAGGCAAG 2280
GGTAGGCCAG GCATGGTGGC TCACGCCTGT AACCAGCACT TTGGGAGGCT GAGGAGGGTG 2340
GATCACTTGA GTTCAGGAGT TCAAGACCAG CCTGGCCAAT GTGGCAAAAC CCCATCTCTA 2400
CTAAAAATAT ACAAAAATTA GCCAGGTGTG GTGGTGCATG CCTATAATCC CAGCTACTCA 2460
GGAGGCCGAA GCAGGAGAAT CACTTGAATC TGGGAGATAG AGGTTGCCGT GAGCCAAGAC 2520
TGTGTCACTG CACTGTAGCC TGTGCGACAC AGAGAGACTC TGTCTCAAGG TAAAAAAAAA 2580
AAAAAAAAAA GAGGCAGGAA GCGAACCTGC AGGAGACGAC AGAAGGGGGT TGCTGTGGGG 2640
GCAAGTCAGC AGTCTAGGAG GTGGCACAGA GATGACATGT GAATAATGAC CAAGGAGCCG 2700
GCCCTCCAAG ACTGCAGGGA AAAATAACAG GGGCATCCCA AGAAGAGGGA AGAGCTGGCA 2760
TGAGGCTCTG CTGCAGAGGC CACTGAGGCA AGTGCAAGAA CAGAGAGGAG CAAAGCGCGG 2820
CTGGAGTGAG ACCCAGTGAG GCAGCACGCA GCACCTCCTG GGTCACTCCA AGTGTGAGGG 2880
CAGGCCCTGG CACACTGCTT TTCTTAAGAA TTAAAAAAAA AAAAAAAAAA AGGCCAGCTG 2940
CGGTGGCTCG CTTGAGATCA AGAGTTCGAG ACCAGCCTGG GCAACAGGGC AAGACTCCGT 3000
CCCTACTAAA ATAATAATAA 3020
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