| Tag | Content |
|---|
EnhancerAtlas ID | HS116-10272 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr13:114545820-114547520 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr13:114547025-114547037 | AGCCACGTGCTC | + | 6.04 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_24989 | chr13:114545984-114547282 | Colon_Crypt_3 | | SE_27005 | chr13:114546843-114548621 | Esophagus | | SE_32437 | chr13:114546060-114547189 | Gastric | | SE_69078 | chr13:114545967-114547601 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH13I113843 | chr13 | 114545222 | 114545860 | | GH13I113842 | chr13 | 114545968 | 114547601 |
|
Enhancer Sequence | CTTTGCCTGG AATGCCTTTC GGAAAGACCT CTGTCCCTGA GGCTGAGGGA CAGTGCCTGC 60
TCCTGCCAGG TGCCCAGCTC TTAAGCGGTC CCCAGACTCA TGCCACCTGC CCCGGGGCCT 120
CCCCCAACTC ATTTGTTTAT TTCCCTGTTG GGAATGTATT GATACCTCTA GGATGCAAGG 180
ACGGAACCAC ACCTGAGGGG TGGACAGTCA GCCGGTGCCC AGCAAATATC TGTGGAATTT 240
CCTCCACACA ACAGGGAAAG CGATGGAGAC AGAAACCTCT GCAGGCCCCC GAGGGCACCC 300
ACTTCCCTGA CCCCGTCCAC CTCCCTGACC CCCGCCCACC TCCCTGATCC CCATCCCGCA 360
AGCTGGGCCT AGGGTATCGG TGGCCTGGCT GGTCATGCCC TGGGCGCCAG CGCCTGTTCA 420
GGAGGTGAAG GGTTTATCTC AGCTTGGCCC ATGACTGCGT TGAAGGACAG GAGGGAGCGG 480
CTGTGGCTGT GGCTGGAATC TGAAGCCGGT GCGGGCGGCC AGGGCCTTTC CCTGGGTGGT 540
GACGAGCGAG GACCAGAGCC CTGTCTGCCC GAGGGAAGGG CGAGGGGACA CTCCCCGTGG 600
CGGGGGTGGG ATCCCGGTAG CCGGGGCTCA GTGACCGCTG CCTGGGCCAC CGCCTGTGGG 660
GACCTGACCT TCCTGGGGAA ACCCATGGGT CAAAGGAGCC GAGAAATCCA AGCACCAAGT 720
GGCCGCTATG GCAGGACGGG CGCGTTCGCA GTGGAGAAGC TGGGTGTGTC CGTGGGAAAG 780
GAAAGAAATG GAAGCAGAGG CTCTTCAGGG GCACCTGGGA ACGCAGCCTA CACTCTTCCC 840
AGGCCTCCTC CCTCCGTCCA CTGTGCCGCC TGGGTCCTGG GACAGCCTGA GGGCCGCAGG 900
CTCCCATGCA AGGCCCGCTG GGGGCCTGCT TGTCTGGGGC TGAATTTGGA CTTTATGGGG 960
CTATGGCTTT AATTTCACAA TGACCGATAA CCAGTGAACT GAAGCCAGGA CAGCACCGTG 1020
AGCACCAAGT CAGAGAATTT TCACGAGGGA ACCAATGAAC AGGAACAGAG TGTGAGGCTG 1080
CCCCAGCTGC ATCCTCCGGG AGGCGCCTTC CCAAGGGAGT GCAAGGCTGC CTGCTGTGGC 1140
CAGGCCACCA AAGCACCTTC TTCACCGCCA GGCATCTTTT GAGGCACGCG AACATCAGAG 1200
GCCCCAGCCA CGTGCTCTGG AGGAGAAGCT GAGAGCCCCA GGCCACAGGC AGGGCAGCCT 1260
CTGAGGGCCG GCTCAGGGAG AGTGGCCGGA GCTTCTGGCC TGGGGCAGGT GGACCCGTTA 1320
GAAACTGCAT GTGTTGCCTC TGGCACCAGC CACAGCAAGA GATTCTCTTC CTATCACACA 1380
GGGAACAAAC TCAAGGATCT TGACCTTGCC CTCCTCTCCC CAGCTGGCCG CACTTGGGGA 1440
CGCTGATGCC ACAAAGGAAA TAACCAAAAC AAGATAACTC TATTGGGCGG CGGGAACAGA 1500
AAGGAACATG TAGCAATCAC TCCTCTTCAT CCATGCAAGG AAGCGAGGCG ACGCCTTGAA 1560
AAGGACGGCC TTCTTTGCTG CAAATAGCCA GAAGTGAACT GAGCAAAGGA AGCACGGGAC 1620
GCACAGGAAG AAAAGTGCTC CAAGGGACGG ACAGGACGGT GCCGGGGTTA GGAAAGCGCA 1680
ACACTGTTCA GACACAGTCT 1700
|
