| Tag | Content |
|---|
EnhancerAtlas ID | HS047-22610 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr22:30216540-30218320 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CEBPA | MA0102.3 | chr22:30217678-30217689 | ATTGCATAATA | + | 6.02 | | EWSR1-FLI1 | MA0149.1 | chr22:30216921-30216939 | GGAAAGAATAAAGGAAAG | + | 6.12 | | Gata1 | MA0035.3 | chr22:30217475-30217486 | TCCTTATCTGT | + | 6.14 | | Zfx | MA0146.2 | chr22:30216683-30216697 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_00294 | chr22:30216653-30218957 | Adipose_Nuclei | | SE_27345 | chr22:30216755-30218495 | Esophagus | | SE_31847 | chr22:30216749-30218515 | Gastric | | SE_34183 | chr22:30216878-30218402 | HCC1954 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr22 | 30218081 | 30218319 | | chr22 | 30217042 | 30217978 | | chr22 | 30216935 | 30217016 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I029820 | chr22 | 30216542 | 30218948 |
|
Enhancer Sequence | TGTAGAAATC TGGTAACTGC TTTCCTGCTT CACTATACTT TATATCCTTT CAAAATTTCT 60
TAAATTAACA CATATTATCT TTACCATTAA GAAAAAAAAA GGCTGGGCGC AGTGGCTCAC 120
CGCCTGTAAT CCCAACACTT TGGGAGGCCG AGGCGGGTGG ATCACCTGAG GTCGGGAGTT 180
CGAGACCAGC CTGATCAACG TGGAGAAACC CCATCTCTAC TAAAAATACC TGTAATCCCA 240
GCTACTTCGG AGGCTGAAGC AGGAGAATCA CTTGAACCTG GGAGGCGGAG GTTGCGGTGG 300
GCCGAGATTG CACCATTGCA CTCTAGCCTG GGCAACAAGA GCGAAACTCC ATCTCAATAC 360
ACAAAAAAAA AAAAAAAAAA AGGAAAGAAT AAAGGAAAGT GACCATTATA AGGGATAACT 420
CAGTTTTGTA ACTAGGTATT TCGAAGACTG TGTCCTACAG TCTCCAGGTG AGGAGAGCTG 480
GCAAGGGCGT CCAGGGTGAG CACCCCTCTG TGCCAGGCCC AGCTCCATGA GCTACAATTC 540
AAAGAGGAAT TCACTGGGGC GCTCCCTCTG TAACGTCCCA CAGTGCTTCT GTTTCTCTTT 600
TTTTCTTATT TTTTTGTGTG TGTGTGCGTA TAAAGAGGAA CCTCTAAAAA AAACTGCTTG 660
TTTTTGATCA AACCTTCTCC CCTCTGCCTG CTAATGGGAT CCAACGGCTA ATGTCCGTTC 720
CTTTTGCAAC CCAGAAGAGC CCTCTCTGAA CTCTGTCCCT ACCTGCTCTC AGCAACAATG 780
CAAATCATGA CATTTTTGAC ACAGTGCCAT CATCCCTGAA GCAGGGAGTT GCAGAGCAAG 840
AGCTTGAGAG TCAGGTCTAC GTTTACACAC GTCCCAGCTG GGCCACTTAT TAGTCATATC 900
CTCTCAGGCA AGTCCCCTAC ATTTTAACCT CAGTTTCCTT ATCTGTAAGT GGGGATGATG 960
ACAGCACTTA TCTCACAGGG CTGCTGTGAG GATCCAATTG ACATAACATA TGTGGAGTGC 1020
TTGGCAGAAT GCCAGGTCCC CGGAACACTC TCCAATAAAG GTTAGCTTAG TTATCACTGC 1080
TGTTCTTACA TTCGTCGCCA AAGGAAACTT CCCCATTCCT ATGTCTGATG CATGGCCAAT 1140
TGCATAATAC TAATACACTC CCAAGGCAGA ATGGTGGCTT ACACTGTAAT CTCAGCTGTT 1200
CAGGAAGCTA AAGCAGGAGG ATGACTTGAG GCCAGGAGTT CAAGACCAGC TGGAACAACA 1260
TAGTGAGACC CCATCTACTA AAAAAAATTT TTTTTTAATT CGCCAGGCAT GGTGGTGTGC 1320
ACCTGTAGTC CCAGGTACCT GGGAGGCTGA GTTGGGGGGA TAGCTTTACT CCAGGAATGT 1380
GAAGCTGCAG TGAAATATGA TTGCGCCACT GCACTCTTGC CTGAGTGACA GAGCAAGGCT 1440
TTGTCTTTTT TCTTTTTTTT TGAGATGGAG TCTTGCTCCA TCTCAAACAC TGCAACTTCT 1500
GCCTCCCAGG TTCAAGTGAT TCTCCTGAAA AAAAACAAAA ACAAAAAATT TCCAGATCCC 1560
TGGGGAACTG TCTGGTACAC AGTTTTATTT CCACCTCCCT AGGTAGTGTC ACTACCTAGT 1620
CATTTTGAGG TGACACTCAT ATATCTGTTA AGCAATTTCC CAAGACTCCC TGCCCCTATC 1680
GCCCTGAGTC CCTGGGCACT GTCAAAGCGC TGGCCTTTGC AACCTTTAGT TTGGCATGTG 1740
GGGGCCATCT TGGTGCATCC TCCCAGTCCT GCATCCTACA 1780
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