| Tag | Content |
|---|
EnhancerAtlas ID | HS182-17925 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr5:142508000-142509800 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr5:142508485-142508496 | AAATCACAGCA | + | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 142508158 | 142508674 | | chr5 | 142508837 | 142509014 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH05I143128 | chr5 | 142508039 | 142514573 |
| Enhancer Sequence | TACAACTACC CAAACTACTT TCTAAATTGT TGATCCCTCT GCCAAAATGC TGATATCAAC 60
AGGACATAGG ACTTCCAACT GTCCTTAAAA AACCTCTGCA GTTACAGCCT CTGAATTTGG 120
CTTCTTAACA GTTACAATAC ATAAGCCCTG CTAAGACTTG CCTGGCTTCC ACTGTGAAGG 180
TGCTGGGTTT ATGGCTTCTC TGAGAGCACC ACGCAGTCCT CGGTCCCATT GTCTGTCATG 240
AGAAGGAGTG AGCTGTGCTC AACTGTTGTA GGTCTACTTT CCTAATGCGT CAAACAAACC 300
AATCCCACAT TACTAGGGAC CCTGGTACAT TTGTGTCTCG AGAAAATGCT CAGTCTCATT 360
TCTCGTATAA ACCTTTCTGT TTTGCTTTGT AATCCCCAGG CCTCTGCTGT TGATTTATTG 420
TCTCAGAGCT ACTTTGCAGT TGTAGACTAG GAGCTCTTCG TCATGACCTA ATTTCCCTCC 480
CATAAAAATC ACAGCACATA ATAAAGAGTA CACCACACAC ATTACAGGGA GACTCCTAAT 540
CCTTTTAAAT TGCAGGCGCA TGTGACAGAT GGGATTGAAG AAGGTCTAAA AATGTGTATG 600
TGACATGGAT AAGAACAGAT TCCACAAGTG TCAATGCTCT GCAATGTCAA GATGGGCCAG 660
AGGGGGAATC AGTGAAATTT AAATTTTGTA GACAGTGCAA GGGAATAAGA ACAGGAAATT 720
CTGTCATTGC TGTAAACAGT TAAGATCAAT GTTTTGCAAA GAACAGTAAT TATATTTACA 780
CTTATAAATT AAATCCTCAT GTCCTGACTG CAAATAATCC ATTGTTGAAT CTCCAGTTAT 840
TTCCCTTCTT GTGTGTCTCC TTTTTTATTG ACTACAGTAA TATCTTTTGA ACACTGAATG 900
TCAAACTGTA TTAGGCGTGT CAGTCCTCAC CACAGTCCTG GGACTTTTTA CAGATAAGGT 960
CTCTGAAGGT CAGAGAGTTA CATAATTTGC CCAAGGTCAC AGCGCTAGTA AGTGACTAAA 1020
ATCAGATCCG CCAGACTCCA AAACTTATGT CTTCCCATTT TGTCCTCTGT CTCTCAAATT 1080
AATAGTAGCT ATAAAGACCA CAAGTGCTTA AGACCCAGAC AGTCAAGCCA TCTAGGTCCC 1140
AGTCCAGCTG CACTCCTTAT CTATGTGACC TTGGACAAAT CAGTGAATCT CAAGGAGTCT 1200
CAGTTTTCTC ATCTCAAGAG GGCAAGAATA ATAGTACCTC CCTTACATGG TTATTGTGAG 1260
TAAAATAATC CATGTAGATA ATCCATGTAA ATAACTGAGC ATGATAAGTG CTCAAATTCT 1320
GTTTTTATTG TCATTTATAC CACCACCATC TCATGCCTAC TCTTTGCCAC ATACTGCACT 1380
GAGCATTTTA TGTGCATTGT CTTTTCAGTA GCTCTGCAAG GCAGGTATTA GATCCTTGCT 1440
TGCACAAGGG AAACAGACTC AGAAGGGTTA ATTATCTTGA CTGAGATTAC ATAGCTAGTA 1500
GGTAGCAAAG TCAGGATTTG AACCCTACTC TGTCTAGCTC CAAAGCCTGT TTGCTTTGTA 1560
CCTGTATGAT GATCTTAAGT TCCTTTCCTG TATTTGATGT GATGATATGG CAGTGATGTC 1620
AGCGTCAGTG ATGGTGAGGT CCGTGTAGCT GTAGGTGTTG CTGCCCACTG AATGAGAAGC 1680
AGAACCAAGA TCAGCCCAGG TTTGTCTGAC TGCAGAGGCC AAACCATCCC TGACCACTGT 1740
GACTTGCAGC TTAAGGCGAA ACAGTAGCTT GGTATTTATG GATCTGCTAA TTCCACTTAC 1800
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