| Tag | Content |
|---|
EnhancerAtlas ID | HS098-27450 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr19:18130770-18133530 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MITF | MA0620.2 | chr19:18133079-18133097 | TGTGGTCATGTGACCACA | + | 6.44 | | MITF | MA0620.2 | chr19:18133079-18133097 | TGTGGTCATGTGACCACA | - | 6.44 | | 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: 21 | 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_55387 | chr19:18132966-18133608 | 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: 5 | Chromosome | Start | End |
| chr19 | 18131787 | 18132922 | | chr19 | 18133045 | 18133309 | | chr19 | 18131991 | 18132570 | | chr19 | 18131070 | 18131394 | | chr19 | 18130949 | 18131445 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I018019 | chr19 | 18130584 | 18136229 |
|
Enhancer Sequence | TCTGATGGGG GTGGAGGTGT CATCCCTTGC ACTTGCTCCC AAGACCTCCT AGAGTCAGAC 60
GTGTCCCCCA TGCAGAGTCA AATGCTAGGT CTCTATCTCT CAGTGTCTCT GTCTGTTTCA 120
TTCTGACTCT CACCATCTTT TCTTTCCCAT CTCTGTCTCT CTCTCAATAT CTGTCTTGCT 180
TACTGTCTCT GTCTCTGTCT CTCAGTCTTA TTGCCTCTGT ACTTCTGTCT CTTTCTCCCT 240
GTCTCTGTCT CCCTCTGCCT CTGATTCTCT CACTATCTCT CTTGGCTACC ATCTCTCTGT 300
CTCTTTGGGT CCCTGACTCT CTCACCATCT CTGCCTCCTG CCCTGGCCCG GCCAGCTGGG 360
GGACAAGGGG TGACAAGCAG TCAGGGCGCC CGCTGCTTGT TTTCCCACCC ACGCTGGCAG 420
GGAGCCCAGC CCAGCCGGGC CACTGTTCAG GAATCCTCCA GCCTCCCCGC TCCAGCCACC 480
AGGCGCGGCC ACCGCCAGCC TCTCCTCCCA GCACATTCTG TCCCAAGCAA AGAGCGCCAG 540
AGATGGGGTG GGGGTGGGGG TGGGAGGGGG ACGCATTCCT GCTGAGCTCC AGTTACAGGA 600
CAGCTTGTCC TGGTGGCCCC ACCAGCACAA CCTCCTGATG GCTCCCCATC CTGCTGTGGG 660
GTTAGACCTT CCTGAATGAA GCCAAAGCCC CTCTGCCAGT TCGTGCCCAC CTCAGGGCCT 720
TTGCACCAGC CATACCTTCC ACCTGGCACT CTGTCTCCCT AGATCTCCCC AAGACCTCCT 780
CCGCCTGCAC ATCTGAGACC TCACATCACC TTCTCAGCAA GTCCCCTCTG TCCCTAGGCC 840
CGGGCACCCC AAATTCCCCT CCTGCTGCCC CAGTGCATTT AATTTCCTGG TCCTCCCCAT 900
GTCCCTGGGG TTACATATTC ACTTGTTTGT TGATGTGGTG TCTATTACAC CAGGTCCCCA 960
CTGTGTCCCA GCACCCTGAA CACACAGTAG GTGGCTTAGT GAAGGTTTTT ACAATTGACA 1020
TCTATTCCTC CCAAAGCTCA GCCCGCCCAG GCTCATCCAT GTGGATCCAC AGTTCTGACC 1080
ACCCCACCTC TGCCTCACCC TGCCTCCGCC ACCCCTGCAC CCTAATGCAG CAGGATTTCC 1140
CAAGCCCCCC TGCCTTGGCC CAGGGAGTTA TCTCCACCAG ATCCACCTTT CTGAGCGAGG 1200
AGCTGGGTGC ATTGAGGGGC AGGGGCGGCT GGAGTTCAGA TGCACCTTTT GAGCGAGGGG 1260
CTGGGCCTCT CTGTCGCTGG GCTCCAGGCA CAGGGCAGTC ATGATGTACA CACACACGTG 1320
CAAACACACA CGCACACACA TAAGCCTGTC AGCAACATAG AAACACCAGC CAGTGAACTC 1380
GGGCACAAGC AGCCGGGCAC AGAGTGTTCA CCAGGTGCTC ACATGTGGAG TACCCCAACT 1440
CCTAGGAGGA TGCGGTTATG GCCTGGATCC TACAGGTGGG GCCCAGACAT GGGCTTTGAA 1500
CCCACGCCAG GGTATGCACA AACCTATCCA AACACACGCG TGTCTGCCCT AGCTTCCCTC 1560
ACCCGGGAGT CACCCCCCCA CCCCCCACCT TGTTTTTGAT GTTCAGGAAA GTCCCCAGAA 1620
AGCACTGGGC CCGGGCAAGG GGCCAGGAGG AAATGGTGAC TCAGCCGGTG GCCATCAGTG 1680
CCTGCCACGC TGGGCTGGGT GGACTGCGCG GCCCGATCTG GGAGGATCCA CAGAAAACAA 1740
CAATAAAAGA TGAGGGCGTG GGTGCGGGGT AAAAAGGACT CAGCCCAAGA ATGATCAGAG 1800
AGGGGATGGA TCCCCCTGTG CTCCAACACT TCAACCCTGC TGGGCCTGAT TGACAAGTGG 1860
GGAAACTGAG ACACAGGGAA CAAGTGACTT CGCCAAGGCC CACCAGCCAA GATGGTACAG 1920
GCAAGGGGAT CCCTAAGTCC TTAACACAGG GGTCTGGAGG AATGTCTACC TGCCCTGCCC 1980
TTTTTTTTTT TTTTTTTTTT GGAGACAGGG TCTCACTCTG TCCGTCAGGC TGGAATGCAG 2040
TGGCATGATC TCAGCTGACT GCAATCTCCG CCTCCTGCCT CAGCCTCCCA AGTAGCTGGG 2100
ATTACCGGCG CCTGTCCCTA TGCCCAGGTA ATTTTTGTAT TTTTAGTAGA GATGGGGTTT 2160
CACCATGTTG GCCAGGCTGG TCTCAAACTC CTGACCTCAG GTGATCTGCC CACCTCGGCC 2220
TGCCAAAGTG CTGGGATTAC AGGCGTGAGC CACAGTGCCC GGCTCCCTGC CCCACTTTCT 2280
GAGACCCAGA TCCACTTCCT GGTTTCCTGT GTGGTCATGT GACCACACTT GGCCAATTGG 2340
AGCCTTTTGT TATCACAGGC ACAGGGATTG GGTCAGGGCT GGGCACGTGA TCCTGCCTGA 2400
GCCAATCATG CTACGAGTTT GGAGACTCCC TGGAAGAAGG CCTAGAAGTA AGGAAAACCA 2460
TCTTGGACGC ATGATGATGG CAGTGGATCA GAGTCCCAAG GACACTGGTG AAGATCAGAG 2520
CAGGACTCAC ACAACCTCAG ATCCCTGTGG AGTCAGGGTG GAACCAGAGG GAAGGCTGAA 2580
GGCTGGAGGG TCCTGAGAGG CCTTGCAGAA AGAGAGGACA TTGGAGCTGG GGCTTTGATG 2640
GATGAAGAGG AACTAGGGAA AGGCATTTCA AGCAGAGGGA ACAGCCTGTG CAACCACAGC 2700
AGGCAGGTGG GAGCTAGGCG TGTCCTCAGC CACCCCAGTG GCCCCATGGG GCTGGAGCAT 2760
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