Tag | Content |
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EnhancerAtlas ID | HS019-06111 | Organism | Homo sapiens | Tissue/cell | CD20+ | Coordinate | chr16:23806680-23808070 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr16:23807421-23807432 | AGGCCATAAAA | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 23807017 | 23807067 | chr16 | 23807309 | 23807369 |
| | Number: 1 | ID | Chromosome | Start | End |
GH16I023794 | chr16 | 23805761 | 23808078 |
| Enhancer Sequence | TTTCACCATG TTGGTCAGGA AGGTCTTGAA CTCCCAGCCT CAAGTGATCA GCCTGCCTCA 60 GCCTTCCAAA ATGCTGGAAT TACAGGCATG AGCCACTGCA TCTGGCCAAG ATTGATCTTT 120 TGAGATGTTT TTCAGGCTTT TACATTCTGA GTAAAGAATG GATTGACTCC CACTGAACCC 180 ATGACTCATG ATTCAATCAG TCCCGTGACC TCCACCCAGA GGCAGACTCA GTGCACGAGG 240 GCCATTTTCC GCACACCTGT GATTGCATTT CCAATCCATC AACAGGACCC ATTCCCTAAT 300 CCCCCACCCA CCAATCTATC CTTGAAAAAC CCTAACCTCC GAGCCTTTGG AGAGAATGAT 360 TTGAGTGATA ACTCCAGTTC TCCCACGTGG CCGGCCTCAC ATTAATTAAA CCCTTTCTTT 420 ACTGCAATTT CTTTACTGCA ATATCACAGT CTCAGTGAAC TGGTTTTGTT TGTGTAGTGC 480 ACAGGAAGAA CCCAACAGAT AATTATGCAT GGATACCAAA ATTGGGGGAT CTCCATTACT 540 TCTGGGCGAG AGGGGGATTT CTTGCTCCCC ACTAGGCCTC CATGGATACC TTCCTAGAAA 600 GGGCAGGAAT GGCTCCATAC TGCTTCCCAC ATGGCTTTTA CTGACATCAT GGACCAGGGG 660 TGGGGTGGGG AGATAGGAGA ATAGAGGGTT GGGGGGATAG GAAGTTGGGG GATGGGGGGG 720 TTTCTTCTCA TGACTGCTGG GAGGCCATAA AAATCCTAAC TTTCCACTAG ACCTACTATG 780 ACCCCACCCA GCAGAGAGGG AGACCTTGCT ACTGACTTGT GGAGATAAAA GGCCCAGTTC 840 CCTACCTGCC CTTCTCTGAC ACCACTTCTA GACATCTCAT TACAGCCTAG GGAGTGTGGA 900 ATTCTAGACT ATTCACTCAG CTTTGCTGCA TGGCTGTGGG TGCATTCAGT TTTTTTTTTT 960 TTTTCCTCCC CTGTGGCATT TCCTGGAGAA GAGTTATTAT CATTTAAAAG TTTTCTGTCT 1020 TGCTAGGCTG CCTCTGCCTG CTCCCTTAGC TACAGAGAAC ACTTTTGGAA GAGCATATTT 1080 ATCTGCACCT CTTGGCATTT CTGGGTTGCT GGCTTCTCCA GCTCCAAGTC TAGGCTATAT 1140 CAGGCAAAAA GAAAACCCAG AGAACTCAAC AATATGTCAT TCCTTGAGTC CCGAGGTTCT 1200 TAACTGGCCT CTCTTCTCTC TGCCTCTCAG AGCCTTTTTT TTTTTTTTGA GCGAGGGTCT 1260 CACTCTTGTT ACCCAGATTG TAGTGCAGTG GCATGATCAC AGCTCACTGC AGCCTCCTCC 1320 TCCTGGGCTC AGGTAATCCT CCCACCTCAG CCTCCAGAGT AGCTGGGACT ACAGGCGAGT 1380 GCCATCACTC 1390
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