| Tag | Content |
|---|
EnhancerAtlas ID | HS003-02568 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr1:159566720-159569220 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RORA | MA0071.1 | chr1:159567589-159567599 | TGACCTTGAT | - | 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 |
| GH01I159596 | chr1 | 159566407 | 159569121 |
|
Enhancer Sequence | TTCTAAAAAG CTGCTTGGAG TTCCACTGTC ACTCTCTTTA ATCTTTGCCT ATCCAACTGG 60
TATCTCAGTG GTCTCTTAAG GCAAATTCCT TTAATTTTAG TGACACACTC ATTTCTACTC 120
GAAACATTTG CCTCATTTTC CATGATGGAC TATTTTCTAA AACACCCACA ATATTTCCTA 180
GATTCCTAGT GGCAGTTCCC TAAGTGTGCC AAAATCCCCC AGCCTGTTAG TGTTACTTGT 240
TATTTAAGCA AAATGATTCA AATCATCATT TGATACATGA TGGAAATCCC AGGCTCACTC 300
ACCAAATTTC TAGCAAATAT TGTGTGTGCT TGTAAGGGGG ATGGGAGGGC AGGAGAAGGC 360
CTTGTATTTC TTCTAGTCAT TACAAGCTAG TGGTTTTTCT TCCTCAGTCT GGAACTTACT 420
CCTTGCACAT ACCTTTTTCT GCACTGTGCC ATCATCCACT TCTCTTTACT TCCTAACTAC 480
CACCAACTGA AAATTATACA TATAAAAGCT TTAAACAAAG TCTCTTGAGG CTCTCAAGGG 540
AGTTTACATT ACAGTATAGT TCAGCAAACA ATTTTAAATC AAATAGTACA CCTCTTTATT 600
CTTAGAATTC CCTCTGCCAA AAAAGAAATC AGCTACTTTT TTTTAAATTC AAGGTCCAAC 660
TTTCTGTTGT GTTGCTGATT CTCTTCTCTC TTTTTCCAAC GACTTCCACT TCTCTCTCTA 720
GTTTACATGT CTCCAAACCT TAAGCCTCTG TTAATACTTT CACAATAAGT CAATTTTGCC 780
AACGGTTTGC CTCCCCTAGA CCATCTAGGC TGGGCCCAGA ACACCTCATC TTCACTCCCA 840
CTGAAGTGTT CCTGAAGGTC AGCTCTCACT GACCTTGATT CTGCTCCCCT ACACTGTCAC 900
CAGAAGCTAT CCACCTATGG TTCTAATTCA GTAAGTCCAA CTCTCTCACC CCCTTTTTTT 960
GTCTCAGCTG TGTGGGCTTT CCCAGGATGG CATGCAATGG GACCCCTGTG CCATGCATAT 1020
TGTAAAGGAA AATGCCTCCC TCCATGCGCT ACAAAACAGC ACATTTATGA TGGCACTTTG 1080
AAAAGATATG GGTTGTGGTG TCACATATTG ACAATTCCTT GGCCAGAGGC TTAACAGTGC 1140
CAGCAGTGCC AGAAGATTAA GAAGACAGCA AAAACAGAAA AGGGAGAAGA TGGTGAAGTA 1200
GTTATATAAC ATGAGCGAGA ATGCTCCTGA TTACAAAGCA GAGAAATTGA CTTTTTTTCT 1260
TAGTGTTTTC TATAGTCATT GCTCTATCCC TGTTCTAGAA TTCAAGTCAT GATAAGAATT 1320
TCTTCACGTT GACTTCCTGC ATTGCTTTCA GACATTGCAA TTAAAGAATG CGAAGAAAGA 1380
ACCTCACAGA GGTAACAGAG TTTGTTTTCC TGGGATTCTC CAGATTCCAC AAACATCACA 1440
TCACTCTCTT TGTGGTTTTT CTCATCCTGT ACACATTAAC TGTGGCTGGC AATGCCATCA 1500
TCATGACCAT CATCTGCATT GACCGTCACC TCCACACTCC CATGTACTTC TTCCTGAGCA 1560
TGCTGGCTAG CTCAAAGACA GTGTACACAC TGTTCATCAT TCCACAGATG CTCTCCAGCT 1620
TCGTAACCCA GACCCAGCCA ATCTCCCTAG CAGGTTGTAC CACCCAAACG TTCTTCTTTG 1680
TTACCTTGGC CATCAACAAT TGCTTCTTGC TCACAGTGAT GGGCTATGAC CACTATATGG 1740
CCATCTGCAA TCCCTTGAGA TACAGGGTCA TTACGAGCAA GAAGGTGTGT GTCCAGCTGG 1800
TGTGTGGAGC CTTTAGCATT GGCCTGGCCA TGGCAGCTGT CCAGGTAACA TCCATATTTA 1860
CCTTACCTTT TTGTCACACG GTGGTTGGTC ATTTCTTCTG TGACATCCTC CCTGTCATGA 1920
AACTCTCCTG TATTAATACC ACTATCAATG AGATAATCAA TTTTGTTGTC AGGTTATTTG 1980
TCATCCTGGT CCCCATGGGT CTGGTCTTCA TCTCCTATGT CCTCATCATC TCCACTGTCC 2040
TCAAGATTGC CTCAGCTGAG GGTTGGAAGA AGACCTTTGC CACCTGTGCC TTCCACCTCA 2100
CTGTGGTCAT TGTCCATTAT GGCTGTGCTT CCATTGCCTA CCTCATGCCC AAGTCAGAAA 2160
ACTCTATAGA ACAAGACCTC CTTCTCTCAG TGACCTAAAC CATCATCACT CCCCTGCTGA 2220
ACCCTGTTGT TTACAGCCTA AAGAACAAGG AGGTCAAGGA TGCCCTATGC AGGGCCATGG 2280
GCAGAAACAT TTCTTAATGC ATTATTCCTC TATATAAATA TACATTTAGT CATAGAAATG 2340
TGTGTCCTTA CTTACATTAA ACAACCTTAC GACTCTGTCC CATGCAGTCT ATGCTGCAAT 2400
GGGATGTGCA TGTCTTGCTT TGGTATATTT ACTACAAAAT CTTAGTCTCT GTTTCCATAT 2460
ATTTCAAAGT TTTGTCCAGG CATTTTCAAC TAGGGATGTG 2500
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