| Tag | Content |
|---|
EnhancerAtlas ID | HS182-08565 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr16:75602520-75603980 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELF5 | MA0136.2 | chr16:75603147-75603158 | TACTTCCTGGT | - | 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 |
| GH16I075569 | chr16 | 75602990 | 75606438 |
| Enhancer Sequence | AAACTTGGTC AACTCTTTGA CATTGTAAGA GTCTATAGCT GCCTGATCCT CAAGTCTGAC 60
AAAATGACTG CGGCACAGTA AAGGGCTCTG AAGTCTCTTT ACAGACTTAT ACCTCCCTTG 120
GTAGCACTTG CTTTGACTGT CAGACTATTG TGCTGCCTGG AAGCAATCTT TGGGACTGTA 180
ACTTGTGGCC TGAATGTAGG CAGAGGCATT AGAATTCCCG TTTTCTGTGT GTTTGACAGC 240
CCAGCTTTAG TCCCCTGTGG AAAAAGGAAA GTGGATGGGC TCCGTCTAAC CTCCTGGTCA 300
GTCCTTTCCC GTTACTGAGT GGGTAGTTGT AGGCCCTGAT CCAGATTCCA GCCCCCACCT 360
CTCCCCTGAG TGTGAGTTTC TGGCCACATC TTATCTTTGT GACCCAATCT AGGTTTCATT 420
TACCACTCCC AGAAGTAATA CTTCTAAAAG TGAAGGCTCT CAGAAGCCCT GGGAACTAGC 480
CCAATGTTGT CCAAATAGGT TCCTGTTGAA AATCCTTGAA GACTCCAGAA GAGGCCTGTG 540
CCAAATTCCA GACCTTATTT CTGTTAAAGG TGGAAAGCTC TGGCCATTTT TTGGTCTGAT 600
TTCCTCTTTC CCAGTGTCCT CCACCTCTAC TTCCTGGTGT CTGATAGAAA GGCAGGGGAG 660
AAATGGAAGC TCCTTCCCTA AGGCCAGTAT TCAACCTGAG GAGACACCCC AGGGCCTGCC 720
CACTGGACGC CATTGGTCTG CCACAGCTGT AGCTCTGGAA GCTGTGGTGT TGCTTGAGGA 780
GATCTTGTCA CCCATGGGGC TCTTCTAACC TTCCTTCCCA GGCCTCTGGG CTGTGTCTTC 840
ACCAGGGGAG GAAGCCTTGG GCATCCGTGG TTACCCTGGG CTTTCCTTAA CGTGTTTGGG 900
GAGGTAATCT TCTTTCATAA CATCTGCAAC TTCTACAGAG CCTTGGTGAC TCTGTGTTTT 960
GTACTTCCTG GAGGTGTTGG CTTAGTGGGA GAAAATAAGT GACTAGGACC TATGGCATTG 1020
AGTTTATTTT CCTCAATTCT GATTCTCTGG TTCTTCTCAA AGGAAATGAA GCAGGCTTCT 1080
GGAGACCTTA AGATTACTCA GATGGCTCCA CAGTAATCTA GCAATTAAAA TGGCTACAGG 1140
TCTTATCAAC TTCCCCTCCC CCGTTATCCC TGAGATAGAA ATAGAATTGG AAATGAAAAA 1200
TGATTTTTCA GGGCAGCAGA GACTGTTTCA AGCCATTTTC TCTCCAAGTC CCATTTGCCT 1260
TTCCAGTGTG GTGAGAATCA ACCCTAAAGC AGATTACACT GGTAACTCAA GTCAGGATTT 1320
TAGGGCCGAG TAGCCAGAAA TCCAGCTCCT GACCCTTCAG GATTTAGAGT CACCAGCTAG 1380
GGCCCTTTTG CCCAGGCTGT CAGCTCTTTG GCCCCAGTTA ATGACTTATC ACCCTACACT 1440
TAATGCAACT GTTTATTTTG 1460
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