| Tag | Content |
|---|
EnhancerAtlas ID | HS108-34849 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr6:44423950-44426200 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr6:44424175-44424194 | CAGTGCCATCTGGTGGTTA | - | 7.68 | | EWSR1-FLI1 | MA0149.1 | chr6:44426083-44426101 | CCCTCCTTGCTTCCTACC | - | 7.01 | | FOS | MA0476.1 | chr6:44424609-44424620 | AATGAGTCACC | - | 6.02 | | TCF3 | MA0522.2 | chr6:44424972-44424982 | AGCAGGTGTT | - | 6.02 |
|
| | 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 |
| GH06I044456 | chr6 | 44423939 | 44424947 |
|
Enhancer Sequence | AATAAAATAA AATAAATAAA ATAAAATAAA ATAAAATAAA ATAAAATAAA ATAAAATAAA 60
ATAAAATAAA ATAAAATAAA ATAAAATAAA AGTGACATGC CTGTATGGTT GGTTAAGGAA 120
GTGGTGGGAC ATCTCTTCCA AATTCCACCC ATCTCCTCTC TGTCCAGGCC CTCTTGGGGT 180
GTGGTCCTAA ACTCTGGAGC CAGCTGGCCC AGCCCACCGC GGCTCCAGTG CCATCTGGTG 240
GTTAAACAGA GGAATGGCTT TTAACCGAGG GACCAAGAAC TGGGTTAAGA TTTTTTGACC 300
TTCAAATCCG AGAAGCAGAA CATGTTCATT CTCAACTGTC ATCACTATTT TTAAGCAAAC 360
TTGCTTTTTT AAAAAAAAAT TTATTTTGAA CTAGATGAAT TCCAAAACAA TACCGGGTCT 420
TAAAAACCCT AGCAGATTAT GAAACAAAAG CAATGCTTTT GCTTGATGAC AAAACCATAG 480
CAAATAAGTG CAGGGAAAAA CCTAAACTAA ACCAATGCTC TTTGAAAAAC AGAGGTTCAT 540
TCGACCTGGG ATTTAAGCCT CCCGAAAACA GACTGAGCGT GTAGGGTGGG GCTCACCGTA 600
TTTACTGCTG AAGCCTGAGC GTCCAGCCCT AGTGGGGGCT CCAGGGGTGT GGAGGAGGCA 660
ATGAGTCACC GGGACGTGAC TTTAAAGTGC CACGTCTTTG GAGCTGATTA CTGGGATTGT 720
TTTGAATGCC TCCAGCAGTG CTCGGAAGAC TAACCTGTAG GCAGGGCCCG TAATGGGTTT 780
GGAGAAAAGA GAGACGGAGG CAGGAAGACC GTGAGAAGTT ATTGCAGGAG TCTGCGAGCA 840
GATGATGAGA GTGGGGTAAT GGAGAAGGAA GCGGGGTGTA TTCAAGAGCT TTGGGGAGGC 900
AGAGTGGAAG GTGTTGGTGC CTGGATATGT CTCTGATGGA CAATGATGAT ACCTCTGACA 960
GAAGGGCATG AGAAACTGAT TTTGGAGAAA AGATGAAAGG TTTGCTATTA GTAGAAATGT 1020
CAAGCAGGTG TTGGAAAATA TGGATCTGGA GGTTAAGAGG GAGGTTGTTT TTGGAGACTG 1080
ATCTGTACAT AGAACAAACA TTGTAGGTAT CTCTAATTCT AATGGCTTGT GTTGAGTAAT 1140
CATCTGACAT ACTAGGGATG AGGTTAAACC CGCCTGTTCC TTGTCTGATA TGATCCTCAC 1200
AAAACAGAAG TGTCAGTACT CGATTGTCTT CCTCTTATAG ATGGAGATCA AGTTTGAAAG 1260
GGCAAATTCC ACCCATTTCC TTCCTACCAA AGACTAAATT AAGTAAGAGA GAGGAGGAAA 1320
CAAGAAGAAA GAAACAGATG AAAAATCAAC ATGGTTACTG ATAAAAGCAG ATAGGGCTTA 1380
GATTCATGCT AGCAGTGGCT TCCTAGAGCG CCCACCACCG TTGGGCCTCA GAGCTGCCCC 1440
TTATGGGCCA GGGTGAATTT GCAGAGTGGA CTCCTTCACC CAGACTGATG CCTCATTCTG 1500
GTCTAGGACG AGAAGAAAAG GAGAAAGAGG CCTGGGACTC TTGGCTTTTG GCTGTCACCC 1560
GCCAGTCTGG TTACTCCTAC GTCTCTAGGC AGGAGGCCAG GAGAGTTTAG GGAAAACCCC 1620
TCTCTTAGAA AGCAGAGGAA TGGAGAAGGA GTGTTCCCCA TGCCTTCCCA ATACAATTCA 1680
GTAACTTGCA GAGGGCACAC ATGATTGCCG ACGCTGCATT CAGAAGACAG ACAAGATGCG 1740
ATTCCTGGTT CAGAGGAACT AGGTCTGCTC CGCAGGTGGG GAGGGGAGGT CAGGTGTGGC 1800
AACATGGTGA CAATATCATG TAGCAGGTTG TAAAACAGAG CTAAGAGTCA TGGGCCATGG 1860
AACACAGGCG GGAGCTGCAG CCTGGACTGG GCAGGTGGTG CATGTGGGGT TGCGTTTGTT 1920
GTTCTAAAGG GCAGATGGGC TTTTACCAGC AGAAGAGGAG AGAAGCTCAT TTAGGTTGAG 1980
GCATGAGTAA AGGGATGGCG ATGTGAACAG CCACTGTGGG TTCCCTAGGG TGGATAGGGC 2040
AGGGAGAAGT TCAGGATTTC AGGGCTGGAC TTGACGCTCA TCATTCGTTT CGGCCTCATA 2100
GTATGTACAG TCTCTTGGTA CGTTTGTGGA ATCCCCTCCT TGCTTCCTAC CATAGAAGCT 2160
GAAAACTTGC TCTCCTCGTC TTCCTGGCAG TGAAAGCTCC CCAGTCAGGT GCTGCTGGAC 2220
TTTGGCTCAG GAACCAGGGA TGCACAGGAG 2250
|
