| Tag | Content |
|---|
EnhancerAtlas ID | HS116-13441 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr16:30551200-30552230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr16:30552052-30552073 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | | Nr2f6(var.2) | MA0728.1 | chr16:30552159-30552174 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_13828 | chr16:30550463-30551314 | CD34_Primary_RO01536 | | SE_24884 | chr16:30550514-30551551 | Colon_Crypt_3 | | SE_27951 | chr16:30550005-30555441 | Fetal_Intestine | | SE_28916 | chr16:30550050-30551893 | Fetal_Intestine_Large | | SE_28916 | chr16:30551903-30555588 | Fetal_Intestine_Large | | SE_31772 | chr16:30550213-30551563 | Gastric | | SE_31772 | chr16:30551937-30554596 | Gastric |
|
| | 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 |
| GH16I030538 | chr16 | 30550052 | 30555393 |
|
Enhancer Sequence | TGGGTACCCC TGGGAGCCAC CCTCATCCCC CACCCCCAGA CAGTGCTGGC CAACTGAGGA 60
GCTCACCAGG CAGTGACATT CCCACACACC TCAAGGCCAA CCAGAGGAGC CACCATCAAC 120
TACACAGGCA GCTGTTCCAG GGCCTGGGGG CCTGGAGACA GAAAGGTGAA CTTTCTTCAT 180
CCTAAATTTG AATTCACACA CTGCCACTGA ATGGGCCGAT TCATAGCACA GCCTGACTGT 240
AGTCCCATGG GATGTCACCA GTCAAATTAA GTGCTGGGCG CGGTGCCTCA CGCCTGTAAT 300
CCCAGCACTT TGGGAGGCCA AGGAGGGCAG ATCACCTGAG ATCAGGAGTT CAAGAGCAGC 360
CTGACCAACA TGGTGAAACC CCATCTCTAC AAAAAATACA AAAATTAGCT GGGTGTGGTG 420
GCACATGCCT GCAATCCCAG CTACTCCAGA GGCTGAGGAA GGAGAATGGT GCGAACCCGG 480
AAGGCGGAGG TTGCAGTGAG CCGAGATCAC ACCACTGCAC CCGAGCCTTG GTGACAGAGT 540
GAGACTCTAT CTTTAAAAAA AAAAAAAGGC CGGGCACAGT GGCTCACACC TGTAATCTCA 600
GCACTTTGGG AGGCTGAGGC GGGCCGATCA ACTGAGGTCG GGAGTTTGAG ACCAGCCTGA 660
CCAACATGGA GAAACCCCAT CTCTACTAAA AATACAAAAT TAGCCAGTCG TGGTGGCGCA 720
TGCCTGTAAT CCCAGCTACT CAGGAGGCTG AGGCAGGAGA ATCACTTGAA CCCGGGAGGC 780
AGAGGTTGCG GTGAGCCAAG ATCGCACCAT TGCACTCTAG CCTCGGCAAC AAGAGCAAAA 840
CGCCATCTCA AAAAAAAAAA AAAGAAAGAA AGAAAGAAAA GAAGCCCAGT CTCGGTCAGG 900
TGTGGTGCCT CACACCTGTA ACCCCAGCAC TTTGTGAGCC TGACGGGGGC AGATCACTTG 960
AGGTCAGGAG TTCATTACCA GCCTGGCCAA CATGGTGAAA CCCCGTCTCT ACTAAAAAAC 1020
AATTAAAAAT 1030
|
