| Tag | Content |
|---|
EnhancerAtlas ID | HS101-29088 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr22:43566960-43567820 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr22:43567172-43567190 | ACTTCCTTTCTTCCTTCC | - | 8.12 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23668 | chr22:43566729-43568729 | Colon_Crypt_1 | | SE_24969 | chr22:43566778-43568826 | Colon_Crypt_3 | | SE_26727 | chr22:43566596-43568785 | Esophagus | | SE_32000 | chr22:43566780-43568697 | 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 |
| GH22I043171 | chr22 | 43567110 | 43568179 |
|
Enhancer Sequence | CAGCAGCTTG AATGGTCAGG AACATACTCC TGCTGAAAAG AACCAAAGAC ATGCCTGGGA 60
ATGACAGCCA CACGTTCAGG GGTCGGGGAG CGTTGGGGCT GGCTGCATGG GGAGTCCGCG 120
GCACCTGCAA GGCTGGCGAC AGGCAGGGTG GGGTAGGTGT TCTGTGCATC TGAAACACTC 180
ATTAACCAGC CAGGCCACAG AGGCCTTCCA GGACTTCCTT TCTTCCTTCC TGTACCCAGA 240
GCTGGCCTCC TGCTTCTGTG CAGGCTGTGC CTACCTGTCC ACGTACACTG GCTGGCCAGC 300
TCTGGTTTCT CGCCCCCACC TTGGAAGGGC CTTTGTCCAG ATGCCCCTGA GCTCCAGGTG 360
CTCAGATGGT GCAGCTGCCA TTCACTGAGT GCCCACTGCA TGGGGCACCG CTCAACACTG 420
TGCACCAGGG AGGACAGGAG GTCCTAGACC CGGGCAGGGT CACGGGCCAG CAGCCAGCCG 480
GACCAGGTGG GGCCTCCCCG CCCCCGCCTG CCCTGGCACT CACAGGGTGG TCTGCTTTTC 540
CGGTTGAAGT GGTGGTGAGG AGTAAGCCCC GGCTGGGAAC ACACTGTCTC AACCTGCTGC 600
TGGACCCATC CCCCTCTGTG TCCACATTAT CTCAAACACA GCCAGTGGCC CTCTGTGCCG 660
TGGGGAGACC TACCTGAGAC AACACAGAAC CCAGCCTGGC TCATGATGGC AGCGCTAACA 720
ATCGCCTTCC ATAGCAGGAA CTCAGGAGGC GGCTCCTGGG ACTGGCCTGT GTGCCAGTCC 780
TCCTAGGAGG CAGTGTGGGC GGGGTGGGGT CGGGTGTGCC CTGGCCTCTG TGTGAACCTG 840
CTCTGCACCT CCCTCAGGCC 860
|
