Tag | Content |
---|
EnhancerAtlas ID | HS047-19530 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:102842940-102845350 |
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 | chr2:102843224-102843242 | AGAAGGGAGGAAGGGAAG | + | 6.05 | EWSR1-FLI1 | MA0149.1 | chr2:102843104-102843122 | GGGAGGGAGGAAAGAAAG | + | 6.23 | EWSR1-FLI1 | MA0149.1 | chr2:102843228-102843246 | GGGAGGAAGGGAAGAAAG | + | 6.25 | EWSR1-FLI1 | MA0149.1 | chr2:102843127-102843145 | GAGAGGGAGGAAGGAAAG | + | 6.42 | EWSR1-FLI1 | MA0149.1 | chr2:102843232-102843250 | GGAAGGGAAGAAAGAAGG | + | 6.62 | EWSR1-FLI1 | MA0149.1 | chr2:102843236-102843254 | GGGAAGAAAGAAGGAAGG | + | 6.72 | EWSR1-FLI1 | MA0149.1 | chr2:102843081-102843099 | TAGAGGAAGGAAGGAAGG | + | 6.84 | EWSR1-FLI1 | MA0149.1 | chr2:102843077-102843095 | GGAATAGAGGAAGGAAGG | + | 7.01 | EWSR1-FLI1 | MA0149.1 | chr2:102843085-102843103 | GGAAGGAAGGAAGGAGAC | + | 7.67 | ZNF263 | MA0528.1 | chr2:102843245-102843266 | GAAGGAAGGGAAGAAAAAAGA | + | 6.06 | ZNF263 | MA0528.1 | chr2:102843141-102843162 | AAAGGAGAGAGGGAGGGAAAA | + | 6.09 | ZNF263 | MA0528.1 | chr2:102843090-102843111 | GAAGGAAGGAGACAGGGAGGG | + | 6.17 | ZNF263 | MA0528.1 | chr2:102843216-102843237 | GATGGAGGAGAAGGGAGGAAG | + | 6.25 | ZNF263 | MA0528.1 | chr2:102843106-102843127 | GAGGGAGGAAAGAAAGAGAGA | + | 6.3 | ZNF263 | MA0528.1 | chr2:102843226-102843247 | AAGGGAGGAAGGGAAGAAAGA | + | 6.64 | ZNF263 | MA0528.1 | chr2:102843713-102843734 | AGAGCAGGAAAGGGAGGGAAA | + | 6.65 | ZNF263 | MA0528.1 | chr2:102843094-102843115 | GAAGGAGACAGGGAGGGAGGA | + | 6.7 | ZNF263 | MA0528.1 | chr2:102843132-102843153 | GGAGGAAGGAAAGGAGAGAGG | + | 6.94 | ZNF263 | MA0528.1 | chr2:102843229-102843250 | GGAGGAAGGGAAGAAAGAAGG | + | 7.06 | ZNF263 | MA0528.1 | chr2:102843219-102843240 | GGAGGAGAAGGGAGGAAGGGA | + | 7.12 | ZNF263 | MA0528.1 | chr2:102843222-102843243 | GGAGAAGGGAGGAAGGGAAGA | + | 7.12 | ZNF263 | MA0528.1 | chr2:102843129-102843150 | GAGGGAGGAAGGAAAGGAGAG | + | 7.51 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr2 | 102843334 | 102845009 | chr2 | 102844840 | 102845062 | chr2 | 102844003 | 102844653 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I102226 | chr2 | 102842670 | 102846324 |
|
Enhancer Sequence | GGTGCCTGAA GGGATTTAAG TCTTCAACTC TCAGATATGG AGAGAGATCA AACCAAGTTT 60 GAATGTGACT TCTCCACTTA CTCCCTATGT AAACTTAGAA AGATGTTTAA CTTTCTTCTA 120 TTTCTCAGCT ATAGAAAGGA ATAGAGGAAG GAAGGAAGGA GACAGGGAGG GAGGAAAGAA 180 AGAGAGAGAG AGGGAGGAAG GAAAGGAGAG AGGGAGGGAA AACGGAGGGA AGAAGGGAGT 240 TTCGTAGAAA AGAAACTAAA GAAAGCAGGG GAGAGAGATG GAGGAGAAGG GAGGAAGGGA 300 AGAAAGAAGG AAGGGAAGAA AAAAGAAAGA AACAAAGAAA GGGACAGTGA TTAAATCCTG 360 CTTTTTGACA GTGGGAATAA CTGAGTTGAA GTACAGGGAA GCATTCAGCG GGGCCTGGGC 420 CACAGGGCGG CCTCTATTGC TTGTCTGGAG GTCAAAACAA ATCCCCAACA CCACAGCTGT 480 GGGTTTTAGT CTGTGGGCCT ATGTCCTGCC AGTGCTGTTT GGCATAGAAA TGCCTCAGTG 540 TGATCCTGAC TCTCTGAGAG CCTGGCATTT CCCACCATGG TGCTTGTGAC TATGCTACTT 600 TTGTTTTGTT TTGTTTTGTT TTGTCTTAGA ACAGATACAA TCTATTAAGG CCTTGCAAAA 660 GTAATAAATC TGCTCTAAAG TCCCCTAATT AGATGAAAAA AGAAGCCTGG TGCAGCTGAT 720 CTGTGTGGAG ATGCACGACT TTATACCTTT TAAGTCCAGA GGCCTGAGTG ACAAGAGCAG 780 GAAAGGGAGG GAAACTGGTT GTCTGAGAAC GTTTTATGGG CCAGCTAAAA CATAAAAGAG 840 GTCACTGGCA TCAAGTGCTT GCTTTGCACA TAAAATACAC AGTACGGTTG TTGCCCACAT 900 GTTTGATAAA ACGTGGCTAT TCACTAACTT GGATTTTTTC CAAATTAAAT TTCTGAATTC 960 AGAATTAGCA ACCCTGAGCA ATGTAGAAAG CGATAAACTC CTTTTTAATG ACAAAAGTCA 1020 TCTGAACCTT AAGTGTCCAG TGCAACCTGA AGTGCTGCTA GTACTGTGGA TAGTCCGACT 1080 GGGCATGGGG AGGGGGTCTC TGGTTTTGGC TCTGGCATCT GCAGAGGCCG CCCCGTCTAA 1140 GCACACCCAT GACTGCTCTC TCCTGCTTGC GTCTTTGAGA AGAAGACAGT TCAGTCCCCC 1200 ACCACTGATT GTTTTCTGAC ACAGAGTTGA GTGGTTCAGT TGCTTTCTAC TTTTTGACTA 1260 ACAGAAGCCT GCGTCACTTT ACGTATTCTT CCTGGAAGCT CAGGCCCCAT GGTGTGTCTC 1320 TCTCACTGTC TCTCTCTCTC ACTGACTCTG TCAGTGACTC TCTCACTGAG TCATTGCGAC 1380 TCCCAGGAGC GTGACTATAG CTGTGACTTA TGGGTGTTGT GCAGTGTGTG GGGAAGCTGC 1440 TAGTGAGGTC GAGTTTAGCA GGAAGAGAAA ACAGGAATAG TGACTCACAC GGAGTAGTGG 1500 GGGCTGGGCA GATGAGAGAG TTAGGCAGCC CCGCCCTCTG CTGAGACTGG GACGCAGCCC 1560 AGATTCTGCA ACAGTGGGCA GAGGATTTGG CGATGGAGGC TAACAGGCAG CCAGGGGTCC 1620 TTTTTTTCTT TATTTTTATT TTGCTTAATT CAGAAAAGTA TGTGTGCATT TTGTGATGAA 1680 ATTCTCTACA GCTCTGTCTA CGAGAACTGC CCTGTAATAT CTCTGTGTGT TGGCTTTAAC 1740 AGTGAGCTAC TGATGAGATT CTGAGATTAG TCCCAGATCT TGTTTATGTC CTTGTTCCCC 1800 TTGAGGATAT TTTCTGAGTT AAATCAGGAA ATACCGATTA ATGGATGAAA ATGAGAAAGA 1860 GAGAAATAAT GTCCTTCGTA GGATAAGTCA TTTACCCTGA CTAGGTTAGC TAAGCTGTAT 1920 CACTCAATTA ATAATTAGGT GTGCATGACT CACCATTTTA GAAGGAGCCA TTGACAGCCC 1980 TAGCTGAAGT CAGCAAGTTC TGTATCTTCT CTAGCAAGCC ACTGGAGCTT TACAAATTCT 2040 CCTGGCAGGG GTGCATGTGT GTACGAGGAT GGAAGGGTCT GTGCACGGAT CTCCTAGAGA 2100 GATTTGAAAA TGCCTCGCCT TACTCCAGAT AGGTCTTTGG AGAATGTGCA TGTAGGATAG 2160 AATGGCTAAA ACGAAGACAA GCCAAACAGT TAGAGTGATC AAAGGGAAAC CAAGGGGACA 2220 ATGGGAAAAC AAGTCGGGGT AGAGTTAATG ACACCTTTAA CAATTATTAA AGGTGAATTT 2280 GCTTTTCAAG CTAAAGCAAA GGCAATGACA AGATCCACTG TGTGCCATTC ACAACAACCT 2340 TTCAGATTTT CATGAGAGAA CATGGCTTTT TCTGAGACTA ATTTCCAAAG GCAGATTTTT 2400 TTTCCCCCAC 2410
|