| Tag | Content |
|---|
EnhancerAtlas ID | HS064-00645 | Organism | Homo sapiens | Tissue/cell | GM18507 | Coordinate | chr1:84736750-84738360 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZBTB18 | MA0698.1 | chr1:84737643-84737656 | ACACATCTGGAAG | - | 6.16 |
| | | 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 |
| GH01I084270 | chr1 | 84736235 | 84739462 |
| Enhancer Sequence | GGGAGGCTCC AGTAGTCATG CAGGCAAGAA GTGGTAGTGG TCCCACCTTC ATTGCAACAG 60
TGGAGGTGGG ACAAGTGGTG GAACTCAGAA CACATTTCAA AGGTGGAGCC AACAGGGTCT 120
CCTGACTGAC TGAATAGATC ATGAGAGGAA GTGGGGTGTT GAGAATGAAG CCAGTGGGAA 180
AAAACATTAT GAAGCGTTTC TCAGGTTTTA ATCACTTGGT CACAACATTT AAATTTTCCA 240
AGCCCATATA TACTTCTCTG CAAAATGCAG AGGCAAGAAC GTGCCAGGTC TGTTCCAGGA 300
AGGACAAGGA AGCCAGCATA GTTGCAGAGG AGCAAGCAAG GAGCAAAGTG GTAGGAGACA 360
GGGTCAGAAA GGTGATGGGA AGGTGTTTAT AAAGGGATTA TGTTGCTCTT TCTACAAATT 420
CAGAGTATAC AGGGGATAAT GAGTAAAGTC ACCCACAAAC GAAGCCTGTG CCACTGGGCT 480
GTGGTTAAGA ACTCAGCCTC AGACTCTTCC GGGTCATGTA AAAGATAAAC AAACCCAGAT 540
GTTAGTTAAA ACAGTGAAAA CTGATTTTGT TCAGTAGCTA CCGACAACAA GGGAAAGGGC 600
TGAGCTCCAT TCAGATTTGC ACAGAGGTGA CTGGGTGTTT TTAAAGGAGA ATGAGAGAGT 660
AGGAGAGGCG TGAGCGGAGG CTCAGTGGAA TCAGGGAAGT GAAAAATTAC AAAAGGTTGG 720
TCAATGCAAA TACAGTTAAG CCAACTGTGA ATGCTTGCTG GCAGTTATTG AAGTTAGGCT 780
GCTATCCTCC CACAGAGACT GAGACAGAGG CCCTAACCTT CCTGAGGATT ATATTTCAAA 840
GGAATGGCTT TCAAGTCCTT GAGAAAGACA CTCCTGAGTT GCAGGAGATG CATACACATC 900
TGGAAGGGAC AGAGGAAAGA TTCACAATTG TCAGCCCTTT TTAGTAAATG CTGCAAGAAA 960
GGGAGGTTAG GGACTGAACT CTTCCGGAGA GGAACTCAAA AAGTGTTTGA GTCTTCCCAG 1020
AGACAAGGCT CAGGCTGCTA AAAGCCATGC TAAAGTATGG CTAAGTCTCT CAAGAGAGGG 1080
TGAATAACGT GTTTGTGCCC AGAGTTTTTG CAGTTCTCAG CCAAAATGAT CCATTTCTAT 1140
GGGGGTTTTT TCTTCTTTTT ATTTCAAAAA TTCAGTTTAA CTAATATATA TTGAAAACAT 1200
AGACAATTTG TAAAACAGAG TCTTTTGATT TGCTCCAAAA TGAGAAAGTT GTACAGAGGT 1260
AAATCTGCTG TGAAAGTAAT AAAGCTTAAG CTTTAGAATC CTCATTTTTA CAGACCTCTT 1320
CTGAGGGCCT TTGTACTTAA TTTTATATTC ATACATTGAT TTTTTTTTCC TTAAAGAGGC 1380
TATGTCCAAG TTAGATAAGC CTTAAGACCA ACACAACCCC CTACTTAGGA AAAGCTTTCC 1440
ACCTTAGACC TAGCCTAGGA ATAAAAACAA CTGACGGGTA AAAGTAGGGG AGAGGCTGGG 1500
ACACACCTGT CTGTTAAGCA TTCCTGGCCA GGGCCTGTCA TTTACATAGC AGGAAAAGCA 1560
GCCAACACCT ACCCAGCTGC TGCTCTTTAG AAAGGTGAAG TTAAACAAAG 1610
|
| |
|
|
|
