| Tag | Content |
|---|
EnhancerAtlas ID | HS113-14891 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr17:6426500-6428670 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr17:6427663-6427681 | GGAAGGAGGGATGGAAGA | + | 7.32 | | ZIC1 | MA0696.1 | chr17:6426767-6426781 | GACCTCCCGCTGTG | + | 6.6 | | ZIC3 | MA0697.1 | chr17:6426767-6426782 | GACCTCCCGCTGTGC | + | 7.03 | | ZIC4 | MA0751.1 | chr17:6426767-6426782 | GACCTCCCGCTGTGC | + | 6.55 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH17I006523 | chr17 | 6426761 | 6426950 | | GH17I006524 | chr17 | 6427941 | 6427967 |
|
Enhancer Sequence | TTTGTGAGGG CTGCCACTTG TGCAACATTG GTCATGCTTC TCCCCCTTCC ATCATTATAA 60
GAATGACCTG CTATCGAATG CACTTTGCAA ATATCATCTC ATTTAATCAT CACAGCTTTT 120
TTACTAGTCC TCCACTCTGC AGATGAAGAA ACAGAAGACC AGGGAGGTGA TGTGACTTTT 180
CCTGACCACA CAGCCATGGA GTGGCATGGC TGAAGTTCAA ACCCAGGCCT CTCTGACTCC 240
AGCACTGCAG CTTCTGCCTC TGTCCTGGAC CTCCCGCTGT GCTTCCTCGT CCCCTGCCCT 300
CCAGTGCCCT CCCAGCTCAC TCTGCCTCTT GCTCACCTGA CCGACTGCCC TTAGCTCTCA 360
CTGGGTCTGA GTCATACATT CTTTAGCAGA CAAGTGGGGA TGGGGGATGG GAAGGGGATG 420
GCCAAATGGA TGGTACAAAT CCATATTTGT CTTTTCAAGG CTACAAGCAC TATTGTGGGG 480
CAGGACCTAG AATCCATGAC CCCTTCTAGG CCCCCTCTGG GGTTCTTGGG ATGAAGGAAA 540
GAGCAGCAAA GGACCCACTG GCAGATACAT GGCTATGACG ACTGGTAAGT TGTCTCTGGA 600
TTGCCCTTGG GGGCCAGAGT CAGAGCCCCC CCTTCTCGTG GATGGGACAG TGGTACAGGG 660
TGCCTTTCCT TTCAGACTCA TGGTTCCTTG AGCCTGACTT TGTTGGGGCC CAGAACTGTG 720
CCAAGCCTTA GTCCAGTCCG GGAGGTGAAG CCCTGGACTG GGAATCAGAA GACCAGGAAT 780
CTGAGCCTGA TGTTGCCACC AGCTTGGGGG ACTTTGGGCA AGACGTGGCT CCTCTGAGCC 840
TGGGTTCTTT GTTGGTTAGA TGGGATGACC ACACCAGGCC TGCCCATTTC TCAGGATGAG 900
TGCTTTGGCA AAAGGAGAGC TCTGAACCAA GGAGGCAAGG ATGGGGATGA GAAAAGGAAC 960
AGGAACAGGG CAAGATGGTC ACTACCAAGG CAGCCGTTCC CGTGGGCTGG GCCAGGACCA 1020
TCTCACTGAA TGCCTCCTGA GAGCATGGCC TTGCCCACTC GGCAACTCTG GGCCAGAGCA 1080
CGACTGCGAA TGACAGGAGC AATAGAGGAA GGAGAAGAGA AGATGAAGAA GAAATAAAGT 1140
AGGAGGAGTG GTATGTGGGG TGGGGAAGGA GGGATGGAAG AAACCAACTT GAGGGTAACA 1200
GGTACAGAGG TTAGCACCCT GCATCCCAGA TGTGGGTCTA GCCCTGGCTC TGCTTCTCAC 1260
TCCATTGTAA CATTAATCAA ATACAGCCCT CAGCTGAAGA TCTCTGAGCT CAGTTTCCCA 1320
TATGTGAGCT CAGATTTTAC GACATCTTCA GCCACGTTGT CCGTTTGAAT TTTAAAGCCT 1380
TGCCCCATTG CTTCACTGTC AGGAGCCCTT CCTGGATCCC CTCTCCTGCC TCCTGAAAGT 1440
CATGCCTCTC CCTTCTGAGC TAACACCCTC AGCTTAAGCC TGATCCACAT ATCTTGACTT 1500
ATACGTGTCA CACATCACAA GACAGAGGCC TCAGATGAAT CACCTTTGGT TGCTCCTGCC 1560
AAGCACTTAT ACACAGTAGG TGCTCAATGA GCCTGTTAGT GATGAACAAT AGCCAAACAG 1620
ATGGATAGAT GGATGCCAAA AAGAATCAGC CTGCTTTGTA GGCTGATCAA ACTCCTGGTC 1680
AAAACTCTTC TCCATAGAAA GCCTCCTGGA TTAATCCCCA GCCATATACT CCTTCTTCAA 1740
CAACTCCACC AAAGGAAATC CTGATTCTCA CTGCTGTCCT TCTCTCTCCC CTTAGACCTC 1800
AGCTCCTGTC CTGCTCAAAG GCTCCTCCAA CTGTCACCCT CCTTATTCAG CAGATTCCAA 1860
TACCAAAGAC CTGGCAGTCC AAGGAGCTTG GACCCAGGCA CCTGCCATTA ACCACCCGTG 1920
CCACTGGGGT AGTCATTCTG TGGACAAAGG AAGCTCTGTT GAAGTAGGCT GGAGCTTTTA 1980
TGCCACAGAA AACCCCACAG AAGTCCCCAT GAGAGTTCCT GTAAGTGGCA AAATTCAGGG 2040
ATGCTATGAA GGAGGAACCA AGGCAGATAG ACTCTTCACA GAAGGCCCAA GCCCCAGCCC 2100
CAGTCACCAG CCCTACAGCC CCCCCTGCAA CACACCTATG TGCACATCCT GGTCATGAGA 2160
GAAGCAGAGT 2170
|
