| Tag | Content |
|---|
EnhancerAtlas ID | HS050-70014 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:116388760-116390130 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr9:116389468-116389489 | CTCTCCTGCATCTTCTCCTCC | - | 6.25 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_00715 | chr9:116388544-116390694 | Adipose_Nuclei | | SE_01545 | chr9:116388856-116390144 | Aorta | | SE_29700 | chr9:116388511-116390414 | Fetal_Muscle | | SE_42114 | chr9:116388909-116389996 | Lung | | SE_55765 | chr9:116381308-116390127 | u87 | | SE_67932 | chr9:116381308-116390127 | u87 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I113626 | chr9 | 116388820 | 116390199 |
|
Enhancer Sequence | ACGTTATGCA GTTTTAAACT TCAGATTTTT GAAATGAAAT TGTATTAGTT ATCTTGAATG 60
TTCGATGTTG TGTTTCTCAA ACATGTGTTG GCCTACTGGA TTTCTAAGTT TCTGGCTCTT 120
TCTTTTGCAA ATGATTTTTC CTCTCATGTC ACAGATTCAA CAAATATTCA TGCTGGAATG 180
GGATGCAGAA GTCACCTACT TTCAGAGATG GGGAAACTGA GACCCAGAGA GGGCACAGCC 240
TTTTCTCGGG GGCCTCCAGT GACTCAGAGT CAAATCTGTG CTTCTTGGCT CCTGGATCTC 300
TGAGCTGCAC CCACTGGACC CCTATGCCAA CCCCAGCACC CCTGTTCTCC ATGGCGGCCC 360
CGCCCTGAGG ATTTCCTATG CCTTTCTACA GAGCTTTCTC CTTCTCCTAG ATCCCTTTTC 420
TGCAAAACGA GGCTGGGGAG TTCTGAGCCA AGCCCAGGCC CACGTGCCTG GAACCAGAGA 480
CAGCGTAAGG AGCAGACACT GCCAGGTCAC TTGCAGCAGA CTCCAGGAGG AAATGAGGGA 540
AACAGAACCT CAGCCGTAGC CTAGCCAGGG CTCTCAGAGC CTAGAAAGCT CTTAGGAGAA 600
GTGGAGAGTT GTTCAGATCC AGGCTAATTT GTCATCTCCA GCCCTTCTCT GGTGATCAGC 660
TTGCCTCTTC CTCTACCTGC CCCTATAGGT AGAGGAAGCT TGCCCTTCCT CTCCTGCATC 720
TTCTCCTCCC CTTTCTGTCA CATGCCTTCT GCTTCTTGAG GCCTCTGCCT CATTGTAGTT 780
TCTCTTGCTG TCCAGTTCCG GTGAGCTCAT GGCTTCTGTA GCCCAGTTTC TCTTTGCTTC 840
CCTTTGTGAA TCTTTCCTGC TTCGACTCTC ACTCCCAACT TCTTAACTTA CACTCAATGC 900
TCCCAGAGGG AGGACTTGAT TGGTTTGGAA GTCCCCCACC AGGACAGGCC AAGGATTAAG 960
TGAGTTCTTA TATGAGGTCT CTGATTCCCT AACTCCAGCT AGGTGTTCAA TTATTCAGTT 1020
CAATTCTGAC ACCAACTCCA GGAGTTAGTG CAGACCCCAA GGTTTAGGGC TCAGCCCCAC 1080
AGGGCTGTCC CCCTTTAGCC ACCAGTCACA CACAAGTCCA GGGACCATCT GTACATCTGA 1140
CTGCCTGGCT CTGAATTTCA GGGTTCCCAT AACCTCCCCT TCTAGTTAGA TCATTCACTA 1200
GAACAATTCA CAAAACTCAG CAAGTGCTTT ACTTACTATT ACCAGTGGAT TATAAAGGAT 1260
ACTACTCAAG AACAGACTCA TGGAAGAGAT GCAGGGAACA AAACATGGGG GATTTGCACA 1320
AAGCTTCCAC GCCCTCCCAG CGAGTCCCTG TGTTCACCAG CCCTGAAGCT 1370
|
