| Tag | Content |
|---|
EnhancerAtlas ID | HS018-13611 | Organism | Homo sapiens | Tissue/cell | CD19+ | Coordinate | chr2:228275130-228277540 | 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 | TCTGCCCTCT GCCTGTGTTG GAGCTGCTAA ATTGTAAGAA TTTGTAAGTT GGTAAAATAC 60
TTCTAAAAAC CCTCAGCTCC ATAAATATTT TTAAATTTAA ATTTAATTTT GTTTTAGAGA 120
TAGGGTCTTG CTATATTGCC CAGGCTGGTC TCAAACTCTT GGGCTCAAAG CATCCTCCCA 180
TGTCAGCCTC CAGAGTAGCT GGCACTACGG GCACATGCCT TGCTTTGCTC TTTAATTTTT 240
TTTTTCTTTT TTTTTTGAGA TGGTCTCTTG CTCTGTCACC CAGGCTGGAG TGCAGTGGCA 300
CAATCTCAGC TCACTGCAAC CTCTGCTTCC CAGGCTCAAG CGATTCTCCT GCTTCAGCCT 360
CCTGAATAGT TGGGATTACA GGCATGTGCC ACCACACTTG GCTAATTTTT GTATTTTTAG 420
TAGAGACGGG GTTTCACCAC ATTGGGCAGG CTGGTCTCGA ACTCCTGACC TCAGGTGATC 480
CACTCGCCTT GGCCTCCCAA AGTGCTGAGA TTATAGGTGT GAGCCACCGT GCCTGGCCAG 540
CTCTTTAAAT CTTAACGTAG TAACACCGTT ACTAATTTCT CAGCTGCTTT TCTGAGTTTA 600
ACAATTTCTG ACTGAATGCT TTATTTATAG GTTGACAATT CTCAGTACCC CTAGTCAGCC 660
AAATGTGTCT CTCTCCACAA CAGAGACTCA CCTTCTCGTG GCTGCAAGCT GTGCAGCTGA 720
AGAGGGATTC TGGAGAAAGA AGGGGAATCC TTTTGTTTGG GTCTATTAAT GCTACGCAAT 780
GTGCCTGGGT TCTTGGAGGG AGACATATCC CATTCTTCCT TATTCCCTCC CATTGACTAT 840
ACAGGAGAAA CTGTATGGAG CTTACTTCAG AAAAACTATT AAGTCCCAAA GATGTGAAGT 900
GTTTTGAATT TTATTCAAGT CCAACCTTGC AGGGCAACAA CTCAACACAG CCATTCCTGC 960
TCTTTCAGGA GAAGCCACAA GTGTGGGAAG ACAGGCAGCT AAGTCTAGGG CACAGACAAA 1020
TTAGTCATAC TGTCTGCTTA GATCCTGAGG GCCTGCGAAA CCCTCAAGGT TTCCTGGTGT 1080
CATCTTAAGG TGCTAGTTAT TCCATTCTGG CTGCCTTTTG ATTCATTTGG TTTTCTGCCC 1140
ACAGGCAAGC AGAGGCGAAA CCAACCTGCC AACTCTTACC TCAAACCCAT TGAGAGAGAC 1200
CTGGGGATTT CCTAGGGTTT TATTTTTACC TATTGCTCCC CAAACAGAAG TTCCATTACA 1260
CAGAAGCATT TCTTTTTTTC TTTTTCTTTT CTCTTTTTCT TTGAGACGGA GTCTTGCTCT 1320
GTCACCCAGG CTGTCATGCA GTGGCACCAT CTTGGCTCAC TGCAATATCT GCCTCCCGGG 1380
TTCAAGAGAT TCTCAAGCCT CATCCTCTCG AGTAGCTGGG ATTACAGGTG TGTGCCACCA 1440
CATCCAGCTA ATTTTGTATT TTTAGTAGAG ACGGGGTTTT GCCATCTTGG CCAGTCTGGT 1500
CTCGAACTCC TGACTTCAAG TGATCTGCCC GCCTCAGCCT CCCAGAGTGC TGGGATTACA 1560
GGCATGAGCC ACCGCGCCCG GCCACACAGA AGCATTTCTC AGTGCCTAAT CTAGTTTGCA 1620
TATCAACTAT TATGGAATAA AGAAACCAAC AAGACCTTGC ATTGCACTCC CTGGGTGGGA 1680
TGACATATGC CTATCAAGGC CAGAGCCTCC TGAAACCCAT CTCTTATTTC TGTTGGCACT 1740
GCTCCCACCC AGACAGAAAT GAGTTAGAGT GAGGCATTCT CCCTAGTAAC CACGGGAAGT 1800
AGGATTTCTC CCTGCAGAGG AGCAAAGGAA TAGAGGAATG AATATCTTTG ACTCCTACTC 1860
CTGTTCACCT TATGGGAGTC TTCTCTGATC CCCACAGCTA AAACACCGTC ACTTCTACCC 1920
CATTCATCTT TATGCTCTTA TCTGGCTTTA TCTTTCCTGT CTTTTCCCCC ACCAACACTT 1980
ACCTCCCCCC TGCCCTAGAA TGTGAGCCCC CTGAGCGCAG GATCTGTCTG ATTCATTTAC 2040
TGCTGTATCC TCAGTGCCCG AAACAGTATC TGTCCCATTT CTGAGTGCAC AAAAAAAAAA 2100
TCTGTTAAAC AAATAGGGGA CCTCTACTAT TGCCAGGCAC TGTGTCAGAC CCTGTGCATA 2160
CACTATACAT GTGACACAGG TAGGTGTTAG TGGCATCATT CTACAGATGA AGAACCCAGG 2220
GAGTAACAAA GGAGGTGACA TAACTTCCTC AAGGTCACAC ACTTAGTAAA TAGTTGAGCA 2280
TTTACTGCCT CTAGAGGGTC TATCCTCTAG AACTTGATCC CTTTTGTCAA ATGCAAGAGC 2340
TAAAGAATTG TCGAGTAGAG TGTGTTTCAT TCTTGAAACC ATCTCAGTTT TCTACCTAGG 2400
TAGAATTTAG 2410
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