| Tag | Content |
|---|
EnhancerAtlas ID | HS007-15328 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr7:22881870-22883190 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr7:22882227-22882245 | GGAAGGCAGGAAGTCATG | + | 6.01 | | Stat6 | MA0520.1 | chr7:22882298-22882313 | ACTTCTCTGGAAAGA | - | 6 |
|
| | 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 |
| GH07I022841 | chr7 | 22881121 | 22883941 |
|
Enhancer Sequence | CATACACCAG ATGCCATCTG GAGAGGCAAA GGGAAGGGGA GCAGAAACCC GAAAGACTAA 60
GTCTGTTACA AAAATAGACT GAACATTTAC CTCAAACGCC TGTTTAAATT ATTGAATCTG 120
AATAAATTAC TTGACTGGAC TAAAGTGTGA GACCTGCAAG GCACCTCAAG CCCTATCCAG 180
CAGAACATGG GCTCAACAGG AAGCGCAGAC CAGCAACAGA AAAATACAGA GTAACTCTGT 240
TCTCAAGCCA GCATTTGTGA CGCTGCTGCC CCAACTTGAA GACTACATTT GGCAAGGAGA 300
GGAGAAAGGA CACAGGATGG AAGCAAAAGG AACCTAAACA GGCCCTGTTG CTTTTCTGGA 360
AGGCAGGAAG TCATGTTCAC ACAGATGCTT AGGAATGTCA CGGGTTAGGA ACTGAATACA 420
CATTGTGTAC TTCTCTGGAA AGAATAAAAG GATTATTCAT TTTTCATTAT AATTTCTCTA 480
AAGCAAAAAG CATGATTTAG GAGTAGCCAT TTGTGGCATT GCCGCATTCA ATTACCCAGC 540
ACAGATCTGG ATGGGCCTGG CAGCTATTTC CAGGCTCCCA CACCACATGT GGGTCATAAA 600
TATGCGTTAA TCAAAAAGGA CAAAGCAATC AAGTGGCTTT ACGTCATTTA TTACCATTTC 660
TGTGAGGGTC AATTGTTAGT AACTGCCTGC ATGTGGCTCA GGCAGCCTGG GCTTTATATG 720
CAGAAATTAA GCAGTCACAA TTCCTACCCT CTTGAAATTT AAACTTGGCA ATGTTGATTT 780
GAACAATTAC GTAAAAAAAA AAAGGAACCA AACAAAGCTT CACCTGCAAT TATTCTCCCA 840
CACGCCCACT CCGAGATCCA GCCACAGGGA AGCTCTTTCT CATGTCCACT CAGAAATTCT 900
GTACAAGCTG TTCTCACTAC CTGGAACTCC ATCCAGATTA TAGTAGACAC TTGGAATGTG 960
GTGCTGGCTT ATACTCTTCC AGGAACTGAA AAGTGCGGGC CTTTTCCTGT AAAACAGGGA 1020
TAGGCCCACA CTGTTGGACA CCTAGCCAAT TGTTATTACT CCATGGCATC TTTTCTACAA 1080
AAGTACTCTG TTTTTATTTA GAGTGGTAAT GTGCCTAGCG TGGTGTTGTT GTTGTTGTTG 1140
TTGTTGTTGT TGTTTTGAGA CTGAGTTTCG CTCTTGTTGC CCAGACTGGA ATGCTCACTG 1200
CAACATCCGT CTCCCGGGTT CAAGCAATTC TCCTGCCTCA GCCTCCCAAG TAGCAAGGAT 1260
TACAGGTATG CGCCACCACG CCCAGCTAAT TTTTGTATTT TTGGTAGAGA CGGGGTTTCA 1320
|
