| Tag | Content |
|---|
EnhancerAtlas ID | HS108-16493 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:27204190-27206350 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr17:27204448-27204459 | TCAAGGTCATA | + | 6.62 | | Esrra | MA0592.2 | chr17:27204447-27204458 | GTCAAGGTCAT | + | 6.32 | | Esrrg | MA0643.1 | chr17:27204448-27204458 | TCAAGGTCAT | + | 6.02 | | JUN(var.2) | MA0489.1 | chr17:27205377-27205391 | CTGACTCATCTCCT | - | 6.29 | | NFYB | MA0502.1 | chr17:27206176-27206191 | ATCTTAGCCAATCAG | + | 6.12 | | Nr2f6(var.2) | MA0728.1 | chr17:27205088-27205103 | TGAACTCCTGACCTT | - | 6.04 | | Zfx | MA0146.2 | chr17:27204300-27204314 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | 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 |
| GH17I028880 | chr17 | 27206121 | 27206310 |
|
Enhancer Sequence | GGATTACAGG AGCCTGCCAC CACGCCTGGC TAATTTTTGT TGTTTTAGTA GCGACAGGGT 60
TTCACCATAT TGGTCAGGCT GGTCTCAAAC TCCTGACCTC AGGTGATCCA CCCGCCTCGG 120
CCTCCCAAAG TGCTGAGATT GCAGGCATAA GCCACCATGC CTGGCTGGCC AAGACCTATT 180
GTGATGATGC AATATATCAA ATTTTTCTTT TATGGTTAGT AGTTTTTTTT TTTTTGGTCT 240
TAAGAAATCT TGCCTATGTC AAGGTCATAG AAACATTCCC TGCTTGCTCT ATGAACTTTA 300
TGTTTTGAGT TTTTACATTA GGTCTGTGAT CCACCCCAAA CTAGATTTGG GTATATGGTG 360
TGAGGTAGGG GGTTGCAATT CAATTGTTTT TTTCTTTTTT TTTTGAGACA GAGTCTCACT 420
CTGTGTGCAG TGGCATGATC TCGGCTCACT GCAACCTCTG CTGCCTGGGT TCAAGTGATT 480
CTTCTGCCTC AGCCTCCCGA GTAGCTGGGA TTACAGGTGC CTGACACTGC ACCTGGCTAA 540
TTTTTGTAGT TTTATTTTTT TGAGACGGAG TCTTGCTCTG TCACCTAGGC TGGAGTGCAG 600
TGGTGCGGAT CTCGGCTCAC TGCAAGCTCT GCCTCCTGGG TTCATGCCAT TCTCCTGCCT 660
CAGCCTCCCA AGTAGCTGGG ACTACAGGCG CCTGCCACCA TGCCTGGCTA ATTTTTTGTA 720
TTTTTAGTAG AGACAGGGTT TCACTGCATT AGCCAGGATG GTCTCGATCT CCTGACCTCG 780
TGATCTGCAC GCCTCGGCCT CCCAAAGCGC CAGGATTACA GGCGTGAGCC ACTGTGCCCA 840
GCCCATTTTT GTAGTTTTTA ATAGAGACAG GGTTTCACCA TCTTGGCCAG GCTGGTCTTG 900
AACTCCTGAC CTTGTGGTCC ACCCAACTAG GCCTCCCAAA GTGCTTGGAT TACAGGCATG 960
AACCACCACG CTCAGCTGCA ATTCAATTTT TTTCCCCAAT ACAGACCCAG TTGTTCTAGC 1020
ACCATCTGTT CCTTTCTGCC TTGAATTGTC TTGGTGCCTA GAAATACCTT TTAAGGTGTA 1080
TCAAATGATA TCACTCCTTT TTCAAAGCCT TTCAGTGGTT TCCCACCTCA GAGTAAAGAC 1140
CACAATATGC CTCATTAAGG TTCTACATGA TCTGGAAAGA TGAGATCCTG ACTCATCTCC 1200
TGATACCCTG ACTTACTCCC TTGCTCCAAA CATCCTGACC TTGCTATTCT TTCATCATGC 1260
CAGACACTCT CCTGCCTCAG GGCCTTTGGA TGGAAAACTC TTCCTTCAGA TATCTGAATG 1320
GCTCAATCCT TTACTTTCTT CAGGGCTACC TTCTTAATGA GGCCTTTTTT GGATACCCTA 1380
AAATTTCAGC GGACTCCCAC ACTTCCTATA ATTTCTTTGA CTTCTTTTCC TTATGACTTA 1440
CCATTATCTA ACATACTGTA CGTTTAATTT TTCTTGTTTC TATCTGAATG TAAGCTTGAA 1500
TGGCTGTGCA TTTATTTTGT TGACTCATTG CTCTGGCATC TAAGACAATG CTTAGTACAT 1560
TGCAAGCATT TGATAAATTC ATTAAATGAA TAAGAATATT GAGGCCCAGA AAGATGAAGT 1620
TACTCACCTA AGATTACACA GGTAATGAAC AATAAAGCTA AAATCTAAAC CTACATTGCC 1680
TTACTTCAGA GTCTAAGCTC TTAAGCCTGA GAGATGGGCT CCATTACTGA GTAGGGCTCA 1740
GTATACCGGT ACAGAGGTGC AGTGAACCTG GCAGTTTCCT CCACCTTTTC TTCTTTTTTT 1800
TTTTTAAGAG ATGGAGTCTT CCTATGTTGC CCAGGCTGGA CTCAAACTCC TGGGCTCAAG 1860
CAATTCTCTC ACCTCAGCCT CCTGAGTAGC TGGGACTACA GGCATGTGCA ACTGCACCCT 1920
GCTAGTCCCC TCCACCTTCT GCCTGTGATG GAGCCAGGTG TTCCAGGGCT GGGGTTTGGC 1980
CTAAGCATCT TAGCCAATCA GTCATGTCCA AGGCGCAACT GGGGGCAAGG CCAGTGTGCT 2040
GTTGCTCCCC AGTGGCTAGA ATGCGGAAGA ACAGGCTAAA AGCTGCCTTG AAGCTGAAGA 2100
GAGGTAGGGG ACCTGGTTGG TTCTCGGTTC GCAGTCTCTC TCCTCACAGA AGACACAATG 2160
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