Tag | Content |
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EnhancerAtlas ID | HS040-24581 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr22:43566960-43567820 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:43567172-43567190 | ACTTCCTTTCTTCCTTCC | - | 8.12 |
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| 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
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