| Tag | Content |
|---|
EnhancerAtlas ID | HS003-30329 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr20:62301740-62303900 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr20:62303680-62303690 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr20:62303680-62303690 | GGCACGTGCC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr20:62303455-62303470 | TGAACTCCTGACCTC | - | 6.22 | | Zfx | MA0146.2 | chr20:62303478-62303492 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAGATGGGTG GAATGGCCAG TTAACCACTG GGAGAGCATC CGGACAGACG TTTCACCAAG 60
GTGGATGGAA TGACCAGTTG AGCACATGGA AAGTCGCCCA GCATCTCCAG TCATAGGAGA 120
AGGCAGATTA AAGCCACGGG GAGCCGACAC TGTGGTCCCA CTGGCATGGC TGAAATTCAG 180
AAGCCCTGAG TGTGGCATGA GGATGTGGAA CAGCTGGATC TCATCCATCG CTGTGAAGTT 240
GTGTAGCCAC TCCACAAACG TGTGGCAAAC AGCCGAGCCG GGAGAAGGGA AGACGTGTTC 300
AAAGATTCAT ATGTGGCCAG GCTCAGTGGC TCACGCCTGT AATCCCAGAA CTTTAGGGGC 360
CAAGGCTGGG GGATCGCTTA AGCCCAGGAG TTTGAGACCA GCCTAGGCAA CATAGGGAGA 420
CCCCATCTCA AAAAAAAAAA AAAAGAAAAA AGAAAAGACT TCAGTGTGCA GGTTTACCAG 480
AGTTTTGTTT GCAGTTGCCA AAACTGGGAA GCAGCCCGCG TGAGCCCATC CACAGGTGAA 540
TGGACAGACC GTGGTACCCG AACACTAACA GCAGCCACGG GCGTGGACTG TGGTCACACA 600
GCAGCAGGGA GCCGATGAGT CTCGGACATG CTAACCCAGA GAGGCCCATT GAGGAGGACC 660
TACTGTTTTT TGTGTTTTTG TTTTTTGTTT TGAAATGGAG TCTCGCTCTG TGGTGCAGGC 720
TGGAGTGCAG TGGTGTGGTC TTGGCTCACT GCAGCTTCCG CCTCTTGGGT TCAAACAGTT 780
CTCCTGCCTC AGCCTTCCGA GTAGCTGGGA CTACAGGCAC CCGCCACCAC ACCCGGCTAA 840
TTTTTGTATT TTCAGTAGAG ACGGCAGTTC GCCATGTTGG CCAGGCTGGT CCCAAACTCC 900
TGACCTTGTC ATCCACTCAC TTTGGCCTCC CAAAGTGCTG AGGTTGCAGG CATGAACCAC 960
CGCACCCGGC TGGACCTACT GTTTTATTCC ATTTATGTGA CACTCTATTA ATAGAAAAGG 1020
CAGGGGTGGG GCTGGTGGTT ATATGGTGCA CATAACTGCC AGAACTCAGT ACACTTAAAA 1080
TGAACATCTT AATGTGTGAA ATTTTTTTTT TTGAGACGGG GTCTTGCTCT GTCACCCAGG 1140
CTAGAGTGCA GTGGTGCGAT CTCCACTCAC TGCAAGCTCT GCCTCCTGGG TTCACGCCAT 1200
TCTCCTGCCT CAGCCTCCCG AGTAGCTGGG ACTACAGGCG CCCGCCACCA CGCCTGGCTA 1260
ATTTTTTTTT TTTTTTTGTA TTTTTAGTAG AGACGGGGTT TCACAGTGTT CGCCAGGCTG 1320
GTCTCGATCT CCTGACCTCG TGATCCGCCT GCCTCGGCCT CCGAAAGTGC TGGGCTTGCA 1380
GGCGTGAGCC ACCATGCCCG GCCAATGTGT GAAAATTTAA AAGTACCAAA GCTGGACCCC 1440
ACCCCAGATT GCTCCCATGA CACTCTGTGG GTGGGACCTG GGAGTTGGGT TTTGTTTTGT 1500
TTTGTTTTGT TTTTGAGATG AAGTCTCACT CTGTCGCCTA GGCTGGAGTG CAGTGACACA 1560
ATCTCGGCTC ACATTAACCT CTGCCTCCCA GATGAAAGCG ATTCTCCTGC CTCAGCCTTC 1620
TGAGTAGCTG GGATTACAGG CACACACCAC CACCCCCTGC TAATTTTTGT ATTTTTAGTA 1680
GAGACGGGGT TTTACCATGT TGGCCAGGCT GGTCTTGAAC TCCTGACCTC GTGATCCGCC 1740
CGCCTCGGCC TCCCAAAGTG CTGGGATTAC AGGCGTGAGC CACCGCGCCT GGCTGGGAGT 1800
TGGGTTTGTA AATCTCCCTG AGTGGGGCTG GGGCAGGGAA CTGCTGGGTC TGGGTCTTCC 1860
TGGCTCCTCT GGTCTGTGGC TTCCTGACTG CGGTGGCCGG GGGCTCCCAG GGCATCGTGG 1920
CCGTCTGTCT TGCTGAGCGT GGCACGTGCC TTTCCATGCT GTGGAGGAGC GTCTCCCGGT 1980
ATGGCGAACT GCTGGTTAGG GTGGGGCGGT GTTGCCAGGT CATCCAGGTC TGGCCTCTGC 2040
TCTCGACATC GCCGGCGCTG TTGCTCATCT GCGCTTGTGA TGTTCGATGC CTGCTGCACA 2100
TGTCTTGGCT TCCCTCTTTC CCGGCCTCTG TGAGCTCCAG CGCTGCGTCC CTTCTCTTCC 2160
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