| Tag | Content |
|---|
EnhancerAtlas ID | HS082-14118 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr16:89366420-89369760 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr16:89368902-89368916 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_03739 | chr16:89366651-89367430 | Brain_Angular_Gyrus | | SE_03739 | chr16:89367645-89368766 | Brain_Angular_Gyrus | | SE_03739 | chr16:89368862-89371198 | Brain_Angular_Gyrus | | SE_05634 | chr16:89366409-89371397 | Brain_Cingulate_Gyrus | | SE_06286 | chr16:89366315-89371534 | Brain_Hippocampus_Middle | | SE_07656 | chr16:89366682-89371118 | Brain_Hippocampus_Middle_150 | | SE_08034 | chr16:89366655-89371582 | Brain_Inferior_Temporal_Lobe | | SE_26651 | chr16:89366466-89368754 | Esophagus | | SE_31628 | chr16:89366395-89368824 | Gastric | | SE_38261 | chr16:89366643-89369095 | HUVEC | | SE_40947 | chr16:89362874-89370826 | Left_Ventricle | | SE_41566 | chr16:89366569-89367663 | LNCaP | | SE_41566 | chr16:89367797-89368670 | LNCaP | | SE_41566 | chr16:89369200-89371305 | LNCaP | | SE_42507 | chr16:89364304-89368792 | Lung | | SE_42507 | chr16:89368933-89370447 | Lung | | SE_44388 | chr16:89366530-89368810 | NHDF-Ad | | SE_44388 | chr16:89368819-89369879 | NHDF-Ad | | SE_44901 | chr16:89366325-89369626 | NHLF | | SE_46181 | chr16:89366634-89369933 | Osteoblasts | | SE_47239 | chr16:89367229-89368562 | Panc1 | | SE_47239 | chr16:89368744-89369760 | Panc1 | | SE_49098 | chr16:89366397-89368791 | Right_Atrium | | SE_50942 | chr16:89367617-89368791 | Sigmoid_Colon | | SE_65322 | chr16:89366455-89369020 | Pancreatic_islets | | SE_65322 | chr16:89369163-89370422 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I089297 | chr16 | 89363825 | 89370598 |
|
Enhancer Sequence | TGCCCTGTGT GGGATGCGTG GGGTCTGTGC CCTGTGTGAG GTGCCTGCCC TGTGTGGGGT 60
GCGTGGGGTC TGTGCCCTGT GTGGGGTGCC TGCCCTGTGT GGGGTGCGTG CGGTCTGTGC 120
CCTGTGTGGG GTGCCTGCCC TGTGTGGGGT GCGTGGGGTC TGTGCCCTGT GTGGGGTGCC 180
TGCCCTGTGT GGGGTGTGTG GGGTCTGTGC CCTGTGTGGG GTGCCTGACC TGTGTGGGGT 240
GCGTGGGGTC TGCTACACGC TTGGTGAGAA ACTGCATCAG GGCTTCCCGC CGTGTGTTGC 300
TAACATCCCC ACACACGTGA GTGCCTTGGG ACCCTCGTCA ACACACTGAG CTGAGGCCAC 360
TGGTCCACGG CACACTGCAG TGCACATGCC CTTCCTGGCC AGAGGCTCCC AGGGGCGCCA 420
TGCTCTCCAG GCACCTGCCC CGCCTGCGAG CACAGCCTGG CCCCTGCTGC ACTCTGCTCT 480
CTCTGCCCGC TCGGGTCCAC TGCAGCTGAG CGGGTGGGAG AAGCCTCTTC AACTTCACAC 540
ACTTGTCGCC TCTAGCACTG GGCAAGGTCT GGCATTCAGA GTTCCAAGAA GTCCCACAGA 600
TACCAGTGGC TAAGTCTGTC TTCCCTCCAG GAATGGGGAA GCAGGAGCCG TCAGAACAGC 660
CGTCTCCTAT CTGAGGCACC AGGAACAAAC ATGACGTCAG GAAAAGACTG AAGGTGCCAA 720
GCACCTAACG CTGAAGGAAC CAGCATGTGC CTGGCAGCAC TGCAGAGAGC ACACCCCAGG 780
CACCAGAGAC CAGGGTGTCA TTCACAGGTC AAAGCAAAAT AAGAAAATCA TAATTTTTCC 840
CCTTGTTCCA AAGAAACATC CACGTGCAGA GGGCAGGCAG CTTCGGCCCA TGGCGCTCCT 900
GACGAGGGCT CCCTCGTGGC TGCCCCAGGA CAAGCAGGAC CCCGGCGGTC CTAGGCAGGG 960
AGAAGCGAGA CTCAGGGTCA CAGACGAAGG CGCAGGAGAA ACAGCGGGGC AGGAGGCTCC 1020
CCAGAACCCC AGGGAGGCCA GGCAATGATG CACAGCAACC TCAAAAACAT TCGCTGGTTG 1080
ACTGATTATT TATTTATCTA TTTTATTTTT TATGGACAGG GTCTCACTCT GTCGCCCAGG 1140
CTGGAGGGCA GTGGCGCAAT CACGGCTCAC TGCAGCCTTG ACCTCCTAGC CTCAAGGGAT 1200
CCTCCCGCCA AAGTGCTGGA AGGGTGAAGG GTGTGAGCCA CTGTGCCTGG CTACTTTTAG 1260
ATTTTTTAAG TTTTGGGAAA CCTTACACAT ATAAAAAAGT AGACAAAGTA GTATCATTTG 1320
AAGCAAATCC CAGATATCAT ATAATTTAAT ATGAATGCTT TCAGTGATAA GGCTTTTTAA 1380
ACTGAGACCA CCCTTGAGGT GGTAGAGGAC AGACTTCAAA AGCAGATACA AGAGGCCCCG 1440
GGCAGACAGG GCAGGCAGAG CAGGGCAGGC AAGATGGGCT AGAAGTCCCA GGGCAAGCTG 1500
GTCTGAGAGG GCTCGGTGGG CAGAGCTGTC TTGGGGCCGG GACATGGCAG GTGCCTTCCC 1560
ACTCCTTGCT GCACCCACAG CCCTTACAGA GGCCTGGTCC TAGGACGGGC TCTTGCCCAG 1620
CGCTCTGGAA GACACAGAGG TGATGCTGTC ACATGCTCAC GTCTGCCTGG ACAGCCTCCA 1680
GGCTGCTGTG CAGGGACCAC GCGGATGCAC AGCCTCGGGG ACTGCTTTAA ACTGGGCTGA 1740
TTCACAACAG ACAGAATCAC ATTGTTCTTG GCAGGCGGCC CCCAGCCCTG ACTAAGCACC 1800
GCAGAGGCCA CATCTCCATG GCACTGGACC GCGGGCAGGG CCGACTCAAC CCTGCATCTG 1860
GGAGGCGGGA AGCCATCCCC ACAGCAACAT GGAGGTCTCT GAGGGAGACG TGCCAGCCTC 1920
TGCCACTTGG ACACAGCCAA GGCATCCGGC ACGGTGGTGA CCCTGCATCC CTCCCACCAT 1980
AGCAAGGGGC ACCCACACCC CTCCAGAGAG GCCTGACTGC TGGGGACCAG AGAAGAGTCT 2040
CTTGTCTGTC ACGTGTCAGT TAACCCTGCA CCAATGTTTC TCTTCTCATC CCTGCTGGTG 2100
TGCGCCTCTC CCTCCACCCC ACTCATTTCT GAGCAAGAAC GGCTCCTCTG GGGGAAGGAG 2160
GGGACGCGGC GTGTGTGAGA GCCACAGCGC CCAGCAGCCT CCCGGCCCAG GGTGGGGCTG 2220
AACGCACTGG AGTTGGACTC GCTACTATTT ATTTATTTAG AGACGGAGTC TTGCTCTGTT 2280
GCCAGGCTGG AGTGCAATGG CGCAATCTTG GCTCACTGCA ACCTCCACCT ATTGGGTTCA 2340
CGCAATTCTC CTGCCTCAGC CTCCCGAGTA GCTGGGATTA CAGGCACCCG CCGCCACACC 2400
TGGCTAATTT TTGTATTTTT AGTAGCGACA GGGTTTCTTC ATGTTGGTCA GGCTGGTCTC 2460
GAACTCCTGA CCTTGTGATC TGCCCGCCTC GGCCTCCCAA AGTACTGGGA TTACAGCCGT 2520
GAGCCACCGC GCCTGGCTGT GGACTTGCTA CTTTAAGAGG GTCCTGGTTA AAATGCAAGC 2580
TTCTAGGATA AGCAACGCTC CACACTCATA CATCAGAACA ATCTTCCTAG GAAATCTAGT 2640
TTTGCAACAT TAAACAAGAA GTTATTAAAA TTGGCCCCGA AAGGGTGATA AACACAGGAG 2700
GACAAATACT ACGTTTCTTA GGTCTTTTTG TTACAATCCT TGCCTGGAAA ATTCTATTTT 2760
CAAAATGTTC TTTACTGTTT TCCCACCTCA CAGGGATTCT CACCTACCCT GTCCTCACCT 2820
AGGCCTGCCC CTCACAGAGT AAGGACATGG TGTTCAACAC GCAGTTCCAG GAGCACCCAG 2880
GGCTGTGGCA GAAAATATCC CAGAGACCCA CAGAGAGCGA GAATGGCCTC AGTGGGCCAG 2940
CACGGCTGGC ACCACGCAGG CGCTAACCAT CAACAGACAG ACCCCGGAAG CTTCTGACAA 3000
CACAACAGGG CCCTGGGTGA GAGCTTCTCT GCACCATGAT GAAACGGCCA CCACAAAGAG 3060
ACCTGAGCAG CCAGATGGGG TGGGCACCAG GTAGCCCTGG GAACGCCACC TTACCAAGTG 3120
GGATCATTCT CCCAGGAAGC AGAAGCAGAT GCTTGTCTCA TTAACCCTTT CAGCAACACC 3180
TCCAGAGACA TCACAGAAAC ACCTCAAAGG TCTGAGGCCA ACTCCCGCAT GGCCACTGTG 3240
CAAAGAGCTA ACAGCTACGT ATCAACATGA CGGCCTTCTA CAACCAAAAC CAGCATGGGG 3300
ACCAAAGACG GCAAACACAG GGTTTCAGGC CTGGACTGAC 3340
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