| Tag | Content |
|---|
EnhancerAtlas ID | HS187-10101 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:16170560-16171990 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr17:16170695-16170716 | GGTGGAGGAAGTGGATGGGAA | + | 6.49 | | ZNF263 | MA0528.1 | chr17:16170653-16170674 | AGAGGCGGAAGAGGTGGAGGA | + | 6.64 | | ZNF263 | MA0528.1 | chr17:16170665-16170686 | GGTGGAGGAAGTGGATGGGGA | + | 6.96 | | ZNF263 | MA0528.1 | chr17:16170683-16170704 | GGAGGCGGAAGAGGTGGAGGA | + | 7.5 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr17 | 16171181 | 16171830 | | chr17 | 16170735 | 16170820 | | chr17 | 16170837 | 16170924 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I016267 | chr17 | 16170516 | 16172323 |
|
Enhancer Sequence | TATTTACTAT TCATGAAGTG GAAATGGATC ATCATGAAGG TCTTCATCCC TGTCTTCACA 60
TTGAGTAGGC TATCTTGCTG TCTCAGGGGT GGCAGAGGCG GAAGAGGTGG AGGAAGTGGA 120
TGGGGAGGCG GAAGAGGTGG AGGAAGTGGA TGGGAAGGCG GGAGAGGCAG GCACACTTGG 180
TGTAACTTTT GTTGAAAAAA TATCTTTGTA TAAGTGGACC CACGCAGTTC AAACGTGTTG 240
TTCAAGGGTC AACTGTGGTC ATATTGTCGG GGTTCTTTAG CCATTAGGTC TCAGAAATTA 300
GCCTGAATTT AGCCAGACAT AGTAGCACAC GCCTATAGTT CCAGCTGCTT GAGAGGCTGA 360
GGCGGGAAGA TCACTTGAAC CCAGACTGCA GTGGGCTATG ATGGTGTCAC TGCACTCCAG 420
CCTGGGTAAC ACAGTGAGAC TCCATATCAA AAAAAAGAAA AAAAGAAAAA AAAAAGAAAA 480
GGAAAGAAAT TAACCCGAAT TTGTGGTTTC TAACTTGGCA ATTAGTCTTT CTTTGACCCC 540
AAGTTTAGAC TCAATATCTT CACTAAGAGC CAGCCCAGGG GGTGCAACTT GGAGCACCAG 600
AATGTTTGTG TAATACTAGC CATGGTAAAG AAGGTGTCCC AGGCTCTCCT GGTGGAGGCA 660
GGCTCTGCTC TACTTAACTC TACTCCAGGC AAGAGCAGAC AAAGAGCAGA CTCTTTAGAC 720
TGGTAAGCAG AACAGACTCG TCCCTCAAGG AGCTCCCAGA CCAGGGAGGG GAGGAGACTG 780
TAAATATTCA CCATGCCGTG GTAACAGCAG AGATGGAGCA CAAGGGGAAG TTCAGAGAAA 840
GATCTCAGAA GAGAGGTACT TTGTCTAACC TGAGATTTAG GGAAAGTTCT CCTGAAGATG 900
ATGACTGGTC TACATGACCT GAGCCGAGAT GGGAATGAGT TGAAAGGTAG GCTTGTGAAG 960
AAGCAGGAGA AGAGCATTAT AGATAGAAAA CTCAAAGGCA TCAGAGGCCC CAAGCTGCAT 1020
GCTATGATAT TGGGATAATA GTAGTACAAA CATAGTGCAA GACAGTGGTG TAAAGTGAGA 1080
TATTTGCTTC TGAGCCATTT CCCTTCTGTT GCCACTTCCT CTTCCTCTTT TAAGTGAAAC 1140
ATTACTAGCA GCCTAATAAT TATCATAGCT GACATATATT AGGTGTTTTT TGTTTTGTTT 1200
TGTTTGTTTT GTTTTTCTTG AGATGAAGTC TCGCTCTTGT TGCCCAGACT GGACTGCAAT 1260
GGTGCCATCT TGGTTCACTG CAACCTCTGC CCCCTGGGTT CAAGCGATTC TCCTACCTTA 1320
GCCTCCTGAG TAGCTGGGAT TACAGGCGCC TGCCACCATG CCTGACTAGT TTTTTGTATT 1380
TTTAGTAGAG ATGGGGTTTC ACCATGTTGG CCAGGCTGGT CTCGAACTCC 1430
|
