| Tag | Content |
|---|
EnhancerAtlas ID | HS040-18165 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr19:18130650-18132980 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:18130678-18130693 | TGAACTTCTGACCTC | - | 6.38 | | RARA | MA0729.1 | chr19:18130675-18130693 | TCTTGAACTTCTGACCTC | - | 6.88 | | RREB1 | MA0073.1 | chr19:18132340-18132360 | CACCCCCCCACCCCCCACCT | + | 6.22 | | RREB1 | MA0073.1 | chr19:18131314-18131334 | GGGGTGGGGGTGGGGGTGGG | - | 6.27 | | RREB1 | MA0073.1 | chr19:18131320-18131340 | GGGGTGGGGGTGGGAGGGGG | - | 7.19 |
|
| | Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
| SE_03528 | chr19:18130671-18131169 | Brain_Angular_Gyrus | | SE_03528 | chr19:18131311-18133631 | Brain_Angular_Gyrus | | SE_04156 | chr19:18130327-18135495 | Brain_Anterior_Caudate | | SE_05027 | chr19:18129368-18135719 | Brain_Cingulate_Gyrus | | SE_05917 | chr19:18129420-18135750 | Brain_Hippocampus_Middle | | SE_07191 | chr19:18123490-18135726 | Brain_Hippocampus_Middle_150 | | SE_08048 | chr19:18129556-18135507 | Brain_Inferior_Temporal_Lobe | | SE_11531 | chr19:18130225-18136150 | CD20 | | SE_17546 | chr19:18130687-18135928 | CD4p_CD25-_CD45RAp_Naive | | SE_32095 | chr19:18130664-18133651 | Gastric | | SE_33722 | chr19:18132360-18135625 | H2171 | | SE_41200 | chr19:18130424-18135677 | Left_Ventricle | | SE_42935 | chr19:18130491-18135643 | Lung | | SE_48098 | chr19:18117499-18135641 | Psoas_Muscle | | SE_48877 | chr19:18130441-18133652 | Right_Atrium | | SE_50498 | chr19:18130482-18133715 | Sigmoid_Colon | | SE_51440 | chr19:18125584-18135837 | Skeletal_Muscle | | SE_55387 | chr19:18131327-18132959 | Thymus | | SE_61722 | chr19:18124231-18170119 | Toledo | | SE_65475 | chr19:18130282-18133763 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr19 | 18131787 | 18132922 | | chr19 | 18131991 | 18132570 | | chr19 | 18131070 | 18131394 | | chr19 | 18130949 | 18131445 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I018019 | chr19 | 18130584 | 18136229 |
|
Enhancer Sequence | GGTTTCACCA TGTTGCCCAG GCTGGTCTTG AACTTCTGAC CTCAGGTGAT CTGCCCATCT 60
TGGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCA TGCCCAGCTC AGATGAAGAT 120
TCTGATGGGG GTGGAGGTGT CATCCCTTGC ACTTGCTCCC AAGACCTCCT AGAGTCAGAC 180
GTGTCCCCCA TGCAGAGTCA AATGCTAGGT CTCTATCTCT CAGTGTCTCT GTCTGTTTCA 240
TTCTGACTCT CACCATCTTT TCTTTCCCAT CTCTGTCTCT CTCTCAATAT CTGTCTTGCT 300
TACTGTCTCT GTCTCTGTCT CTCAGTCTTA TTGCCTCTGT ACTTCTGTCT CTTTCTCCCT 360
GTCTCTGTCT CCCTCTGCCT CTGATTCTCT CACTATCTCT CTTGGCTACC ATCTCTCTGT 420
CTCTTTGGGT CCCTGACTCT CTCACCATCT CTGCCTCCTG CCCTGGCCCG GCCAGCTGGG 480
GGACAAGGGG TGACAAGCAG TCAGGGCGCC CGCTGCTTGT TTTCCCACCC ACGCTGGCAG 540
GGAGCCCAGC CCAGCCGGGC CACTGTTCAG GAATCCTCCA GCCTCCCCGC TCCAGCCACC 600
AGGCGCGGCC ACCGCCAGCC TCTCCTCCCA GCACATTCTG TCCCAAGCAA AGAGCGCCAG 660
AGATGGGGTG GGGGTGGGGG TGGGAGGGGG ACGCATTCCT GCTGAGCTCC AGTTACAGGA 720
CAGCTTGTCC TGGTGGCCCC ACCAGCACAA CCTCCTGATG GCTCCCCATC CTGCTGTGGG 780
GTTAGACCTT CCTGAATGAA GCCAAAGCCC CTCTGCCAGT TCGTGCCCAC CTCAGGGCCT 840
TTGCACCAGC CATACCTTCC ACCTGGCACT CTGTCTCCCT AGATCTCCCC AAGACCTCCT 900
CCGCCTGCAC ATCTGAGACC TCACATCACC TTCTCAGCAA GTCCCCTCTG TCCCTAGGCC 960
CGGGCACCCC AAATTCCCCT CCTGCTGCCC CAGTGCATTT AATTTCCTGG TCCTCCCCAT 1020
GTCCCTGGGG TTACATATTC ACTTGTTTGT TGATGTGGTG TCTATTACAC CAGGTCCCCA 1080
CTGTGTCCCA GCACCCTGAA CACACAGTAG GTGGCTTAGT GAAGGTTTTT ACAATTGACA 1140
TCTATTCCTC CCAAAGCTCA GCCCGCCCAG GCTCATCCAT GTGGATCCAC AGTTCTGACC 1200
ACCCCACCTC TGCCTCACCC TGCCTCCGCC ACCCCTGCAC CCTAATGCAG CAGGATTTCC 1260
CAAGCCCCCC TGCCTTGGCC CAGGGAGTTA TCTCCACCAG ATCCACCTTT CTGAGCGAGG 1320
AGCTGGGTGC ATTGAGGGGC AGGGGCGGCT GGAGTTCAGA TGCACCTTTT GAGCGAGGGG 1380
CTGGGCCTCT CTGTCGCTGG GCTCCAGGCA CAGGGCAGTC ATGATGTACA CACACACGTG 1440
CAAACACACA CGCACACACA TAAGCCTGTC AGCAACATAG AAACACCAGC CAGTGAACTC 1500
GGGCACAAGC AGCCGGGCAC AGAGTGTTCA CCAGGTGCTC ACATGTGGAG TACCCCAACT 1560
CCTAGGAGGA TGCGGTTATG GCCTGGATCC TACAGGTGGG GCCCAGACAT GGGCTTTGAA 1620
CCCACGCCAG GGTATGCACA AACCTATCCA AACACACGCG TGTCTGCCCT AGCTTCCCTC 1680
ACCCGGGAGT CACCCCCCCA CCCCCCACCT TGTTTTTGAT GTTCAGGAAA GTCCCCAGAA 1740
AGCACTGGGC CCGGGCAAGG GGCCAGGAGG AAATGGTGAC TCAGCCGGTG GCCATCAGTG 1800
CCTGCCACGC TGGGCTGGGT GGACTGCGCG GCCCGATCTG GGAGGATCCA CAGAAAACAA 1860
CAATAAAAGA TGAGGGCGTG GGTGCGGGGT AAAAAGGACT CAGCCCAAGA ATGATCAGAG 1920
AGGGGATGGA TCCCCCTGTG CTCCAACACT TCAACCCTGC TGGGCCTGAT TGACAAGTGG 1980
GGAAACTGAG ACACAGGGAA CAAGTGACTT CGCCAAGGCC CACCAGCCAA GATGGTACAG 2040
GCAAGGGGAT CCCTAAGTCC TTAACACAGG GGTCTGGAGG AATGTCTACC TGCCCTGCCC 2100
TTTTTTTTTT TTTTTTTTTT GGAGACAGGG TCTCACTCTG TCCGTCAGGC TGGAATGCAG 2160
TGGCATGATC TCAGCTGACT GCAATCTCCG CCTCCTGCCT CAGCCTCCCA AGTAGCTGGG 2220
ATTACCGGCG CCTGTCCCTA TGCCCAGGTA ATTTTTGTAT TTTTAGTAGA GATGGGGTTT 2280
CACCATGTTG GCCAGGCTGG TCTCAAACTC CTGACCTCAG GTGATCTGCC 2330
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