| Tag | Content |
|---|
EnhancerAtlas ID | HS050-44493 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr22:28539590-28541090 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr22:28540135-28540146 | AGCCACACCCT | + | 6.02 | | Nr5a2 | MA0505.1 | chr22:28540997-28541012 | GAGCCCAAGGTCACC | + | 6.21 | | SRF | MA0083.3 | chr22:28539785-28539801 | AAACCATATAAGGGAA | + | 6.09 | | ZNF263 | MA0528.1 | chr22:28539962-28539983 | GAAGGAGGGAAAGAGAGTAGA | + | 6.23 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTAAATGAGG GAGAACAGAG AGCGTGAGGG AGGGGCCAAG GACAAAGATG GACTAAAAGT 60
CAGGCATGCA CTTTATGAGC ACAGCACTGC TTGTGCAATT ATTACAAACA TATTTAGAAG 120
AAAACAAAAT GCTTTTCAAG ATCACACAGA AGGTCTAAAA TGTTAAAACA GGGAAAAAGG 180
GCTCAGCAAA AGTTAAAACC ATATAAGGGA AGAAAGTTAT TTTTTCACCA GCAAAGGAAA 240
AAACTTTTCT TCCAGCGAAT CTTACAGCAC AAAAGACACT GGCCTCAATC ACCTGTTTAA 300
GTCAGGAATC TTCAAATTTT TTTACGAAGA GAAACTATTT AAAATTTTCC CAGAGCCTCG 360
ACATTATTCA GAGAAGGAGG GAAAGAGAGT AGAGAAAAAG AAGGAAAAGA GCCTAGTGGT 420
GCCAGTGGTA CCTCCAAGGC AGAAGGAAGT TTCAGTCCAA TACCAGCCAC TATTTCCTGA 480
GCCTGTACTG TGCCAGGCAC CATGCAAAAT GCTTCACATA CATCAACTCA TTTAATCCTC 540
ACAAGAGCCA CACCCTTCAT TGCTATCCTA GAGATTCTAG TCTTAATTCT ATTTTACATC 600
TTACATAACT TTCCCCAGGC CACACAGCTC ATAAATGGCA GAGCTACAAT TCAAACCAGG 660
GCCTGTCTAA TACCAAGGCT CAGGTTTTTC TGTCTCCTGG CTGCCACAGA CTCCTTCTGA 720
GAGAATCTCA GGAAGCCAAC CATGGCTTTA CCAGGCTTAA TAGTGGAAGA TGGTTTGGAA 780
AGCTATCAGG TATACCTTCA AGTTCTTTCA AAACTATAAT TGGAGATATG AGTTTCAGAA 840
ATCTGGGTTT ACCATTACAA AACAACTGGC AGTTTTCTTT CTTTGGTAAA AATGTTCTGG 900
AAAGCCAAAA TTGCTGTGCT ATGGTCATTC CTTAGCCAAG TCTGCATTTT AACATCCAAC 960
TAATTGAGAT GAGTGGAGAC ATCTGTAAGC TTATTTTAAA AAAGACAAAT CTCTCGATGT 1020
GTAATAACAG CAGTACCATT TACTGAGGGC TTGCTATGTG CTAAGCACTA CTTGTCAATT 1080
TACGTGGCAT CAAAGATTAA CAAGCTGAGA GCTAAGCACT AGGAATACAA ATGCATCAAA 1140
TGGGGAGCCC GTAGCATAGC CTCTTTGGAG GCTTACAACC TTAATGGGGA GACAGACAAG 1200
CAAGCTGACT GCTGCAGGGG AATATGCGAA GGGTGCGCCT CACCATCTGG GCACAAAGCA 1260
CTGCAAGGTG CAGAAAAGCA CTGGTTTGTA TTTGAAAAAG CTTCTTAAAG GAAGGGGTGT 1320
TTCCTCACAA CAATCCTATG AAGTTGGGAG GAACCTGATG GTCAGAAAGG TTAAGTAATG 1380
CAAAGGTACA CAGCTATGAA ATAAGTTGAG CCCAAGGTCA CCTCACTTTG AAGCCACACT 1440
TTCCATCAGT TCCTGTGGCA TCACAGAAAA ATAATCTCCT TAAATCTCTT GCCACATGAT 1500
|
