Tag | Content |
---|
EnhancerAtlas ID | HS064-09001 | Organism | Homo sapiens | Tissue/cell | GM18507 | Coordinate | chr2:228275290-228277620 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REL | MA0101.1 | chr2:228276332-228276342 | GGGGATTTCC | + | 6.02 |
| | 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 |
GH02I227410 | chr2 | 228275655 | 228277190 |
| Enhancer Sequence | GGGCTCAAAG CATCCTCCCA TGTCAGCCTC CAGAGTAGCT GGCACTACGG GCACATGCCT 60 TGCTTTGCTC TTTAATTTTT TTTTTCTTTT TTTTTTGAGA TGGTCTCTTG CTCTGTCACC 120 CAGGCTGGAG TGCAGTGGCA CAATCTCAGC TCACTGCAAC CTCTGCTTCC CAGGCTCAAG 180 CGATTCTCCT GCTTCAGCCT CCTGAATAGT TGGGATTACA GGCATGTGCC ACCACACTTG 240 GCTAATTTTT GTATTTTTAG TAGAGACGGG GTTTCACCAC ATTGGGCAGG CTGGTCTCGA 300 ACTCCTGACC TCAGGTGATC CACTCGCCTT GGCCTCCCAA AGTGCTGAGA TTATAGGTGT 360 GAGCCACCGT GCCTGGCCAG CTCTTTAAAT CTTAACGTAG TAACACCGTT ACTAATTTCT 420 CAGCTGCTTT TCTGAGTTTA ACAATTTCTG ACTGAATGCT TTATTTATAG GTTGACAATT 480 CTCAGTACCC CTAGTCAGCC AAATGTGTCT CTCTCCACAA CAGAGACTCA CCTTCTCGTG 540 GCTGCAAGCT GTGCAGCTGA AGAGGGATTC TGGAGAAAGA AGGGGAATCC TTTTGTTTGG 600 GTCTATTAAT GCTACGCAAT GTGCCTGGGT TCTTGGAGGG AGACATATCC CATTCTTCCT 660 TATTCCCTCC CATTGACTAT ACAGGAGAAA CTGTATGGAG CTTACTTCAG AAAAACTATT 720 AAGTCCCAAA GATGTGAAGT GTTTTGAATT TTATTCAAGT CCAACCTTGC AGGGCAACAA 780 CTCAACACAG CCATTCCTGC TCTTTCAGGA GAAGCCACAA GTGTGGGAAG ACAGGCAGCT 840 AAGTCTAGGG CACAGACAAA TTAGTCATAC TGTCTGCTTA GATCCTGAGG GCCTGCGAAA 900 CCCTCAAGGT TTCCTGGTGT CATCTTAAGG TGCTAGTTAT TCCATTCTGG CTGCCTTTTG 960 ATTCATTTGG TTTTCTGCCC ACAGGCAAGC AGAGGCGAAA CCAACCTGCC AACTCTTACC 1020 TCAAACCCAT TGAGAGAGAC CTGGGGATTT CCTAGGGTTT TATTTTTACC TATTGCTCCC 1080 CAAACAGAAG TTCCATTACA CAGAAGCATT TCTTTTTTTC TTTTTCTTTT CTCTTTTTCT 1140 TTGAGACGGA GTCTTGCTCT GTCACCCAGG CTGTCATGCA GTGGCACCAT CTTGGCTCAC 1200 TGCAATATCT GCCTCCCGGG TTCAAGAGAT TCTCAAGCCT CATCCTCTCG AGTAGCTGGG 1260 ATTACAGGTG TGTGCCACCA CATCCAGCTA ATTTTGTATT TTTAGTAGAG ACGGGGTTTT 1320 GCCATCTTGG CCAGTCTGGT CTCGAACTCC TGACTTCAAG TGATCTGCCC GCCTCAGCCT 1380 CCCAGAGTGC TGGGATTACA GGCATGAGCC ACCGCGCCCG GCCACACAGA AGCATTTCTC 1440 AGTGCCTAAT CTAGTTTGCA TATCAACTAT TATGGAATAA AGAAACCAAC AAGACCTTGC 1500 ATTGCACTCC CTGGGTGGGA TGACATATGC CTATCAAGGC CAGAGCCTCC TGAAACCCAT 1560 CTCTTATTTC TGTTGGCACT GCTCCCACCC AGACAGAAAT GAGTTAGAGT GAGGCATTCT 1620 CCCTAGTAAC CACGGGAAGT AGGATTTCTC CCTGCAGAGG AGCAAAGGAA TAGAGGAATG 1680 AATATCTTTG ACTCCTACTC CTGTTCACCT TATGGGAGTC TTCTCTGATC CCCACAGCTA 1740 AAACACCGTC ACTTCTACCC CATTCATCTT TATGCTCTTA TCTGGCTTTA TCTTTCCTGT 1800 CTTTTCCCCC ACCAACACTT ACCTCCCCCC TGCCCTAGAA TGTGAGCCCC CTGAGCGCAG 1860 GATCTGTCTG ATTCATTTAC TGCTGTATCC TCAGTGCCCG AAACAGTATC TGTCCCATTT 1920 CTGAGTGCAC AAAAAAAAAA TCTGTTAAAC AAATAGGGGA CCTCTACTAT TGCCAGGCAC 1980 TGTGTCAGAC CCTGTGCATA CACTATACAT GTGACACAGG TAGGTGTTAG TGGCATCATT 2040 CTACAGATGA AGAACCCAGG GAGTAACAAA GGAGGTGACA TAACTTCCTC AAGGTCACAC 2100 ACTTAGTAAA TAGTTGAGCA TTTACTGCCT CTAGAGGGTC TATCCTCTAG AACTTGATCC 2160 CTTTTGTCAA ATGCAAGAGC TAAAGAATTG TCGAGTAGAG TGTGTTTCAT TCTTGAAACC 2220 ATCTCAGTTT TCTACCTAGG TAGAATTTAG GAAAACAGAA GGGATGGCAA ATATATATAT 2280 ATATAAAAAC AGAGGAAACC TTCTTGAGGG TTACAACTTA AACAAGCACA 2330
|
| |
|
|
|