| Tag | Content |
|---|
EnhancerAtlas ID | HS064-12476 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr5:150113710-150115170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr5:150114749-150114768 | AAGCGCCACCTCCTGGCTG | - | 6 | | MEF2C | MA0497.1 | chr5:150113994-150114009 | AATATAAAAATAGAA | + | 6.58 | | Nfe2l2 | MA0150.2 | chr5:150114450-150114465 | CAGTATGACACAGCA | + | 6.64 | | SPIC | MA0687.1 | chr5:150114219-150114233 | GTAAAGGGGAAGTA | + | 6.14 |
|
| | 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 |
| GH05I150734 | chr5 | 150113563 | 150115346 |
|
Enhancer Sequence | CAGACAGACA GAACAACATG TGGAGACTCA CACTGTGAAT TTTTATTCCA AGAACTACTG 60
CAGGAACATA CTAGGAAAAC TGAAAGAATT CACAGACCCT TTAAAAGAAG TGGCTTGCTG 120
CTGCAAAATC CATGAGACAG CAGAAAATCT GTGAGTGCCC ATGTGTAAGA GGGGGAAAAT 180
CCACCTTCAA ACACACATCC TCACTGGAGA ACCTAAAAAT CCAGATCATG GGAGAAAAAT 240
TTAACCTTAC CTAGTGCTGA AACAAAATTT AGAGAGCCGA GTGAAATATA AAAATAGAAG 300
AAGCAACAGC GGGAAGAGCC CTGTAGGCAC TCCCGGTTCC CAGTGAAGCC CAGGGAAGTC 360
ATTTCTGACT TTAATCTCAC AGGGGTCCTT GGGGAGTGCT GCCAGTGGAA CTGAGGAAGG 420
ACCACTTGGA GACAGAAACT TCCAGGTGAA CTTTGTAATA ACTTTGACGG AGAGCAAATT 480
TTCCTGGGCA CAATCAAGAT GGGGAAGGCG TAAAGGGGAA GTACAGATAT GAGCACATAA 540
GCCACAGCAG TCGGGAAGGG GCGGAGTCCA AAAGGCTAGC TTGCTTTTTC AGCAAGTAGG 600
CTTGTAGCCT GGGCCAAAAT CTTGGCCCTG CAAACCCCAT GCTGTTGGTG GGGCATGGTG 660
GGAGTGAGAC TGGCCTTGCT GGCTGCATGG GAGCTGGGTG AAGCCTGTCA CTGCTGGCTT 720
TCCCCTACTT CCCTGGCCAC CAGTATGACA CAGCAGAGGC AGCCATAATC CCCCTGGGAA 780
CATAACTCCA TTGGCCTGAG AACCACACAA CTGTCCTTCA CAGCAGCTGC AGCAAACCCT 840
GCCCAAGGAG ATTCTGAGCT CAGATATGCC CCCACCTGAT GGTCTTTCTC TACCTGCCCT 900
GGTAGCCCAA GACAAAAGAC TGTAAACTCT TGGGAGCTTT ATGGCCCCAC TGATCACCTG 960
GGAAACCCAA ATACTTATCC AGGCAACCTT AGGGCAAGCT TGTATCCCCA CCACACTACT 1020
GCAGCTGATG CTTTCTTGAA AGCGCCACCT CCTGGCTGGA GGCCAACCAA CTCATTATAG 1080
CAACTCATAA AAGAACAACC CTGCCCTCAA AAGGAGAAAA CAACAGCTAA TTCCACCACC 1140
TGTGACATCC TGGCTAACCA GAGGTCCTGA GTCTGTCCAC GTGACAATTC ACTGCTAGCA 1200
CAACCAGCAT TAAAGAAAAC TAGCATACGA AACCAAACTA CAACCAAGGA CCCTCACAGA 1260
GTCCACTTCA CTCTCCTGCT ATCTCCACCA GAGCAGGTGC TGGTATCCAC AACTGAGAGA 1320
CCTGAAGACG GACTGCATCA CTGGACTCTT TGCAGACACT CCCCAGTACC AGCTCGGAGA 1380
CTGATAGCTC TGGCCGGGTG GCTAGACCCA GAGCAGCAAT AACAATAATT GCAGTCCAGC 1440
TCTCAGGAAG CCACAGGGGG 1460
|
