| Tag | Content |
|---|
EnhancerAtlas ID | HS003-00466 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr1:17612610-17614830 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:17613334-17613349 | TGGGGTCAGGGGTCA | + | 6.67 | | NR2F1 | MA0017.2 | chr1:17614474-17614487 | CACGTGACCTCTG | - | 6.04 | | Nr2f6(var.2) | MA0728.1 | chr1:17614686-17614701 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 17613600 | 17614695 | | chr1 | 17613711 | 17613962 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I017286 | chr1 | 17613436 | 17614463 |
|
Enhancer Sequence | GCACTTTCCA TAGCTGGGAA TCCCAAATGC ACATTCATCA GAGACTGTAA GGTCATTCTC 60
AGGGTATGCT CCAGTTTAGC TATTGCTGGC GGTGCGTCTG CCACACACAT GGGTCTCACT 120
GAGCTAAAGT CAACATCTTG GAAGGGCTGG TTCCTTCTGG GCTCTAGGGA AGAATCCTTT 180
TTCTTGCCTT TGCCAGCTCC TAGAGGCTGC CTACACCCCT TGGCTTCTGG GCTTTTCCTC 240
CATCTTCAAG GCCAGCAGCA TAGTAACATT TTTGTATCTT CCTCTGATGG ATTCTTCTGC 300
TTCCTTCTTC CACTTGTAAG GACCCTTGCG ATGACACTGG GCTCATCTGG ATAAGCAAGG 360
CTCACCCACC CTCTCTAGGT CAGCTGATGA GTGAACTTCA TTCAATCTGC AACCTTCATT 420
CCCTTTTACT AAGAAGGTCA TATACTCACG AGTTCTGCAG ACTCGAACGT GGAAATCTTT 480
GGAGGACCAT TTTTCTGCTG ACTACAAGCA ACCAGGCCCT GACTGCCGTT TCTGGCCTCC 540
AAGAGTGAGA CCATACCCGG TCCCCTCTGA AATCCACAGA GGCAGCAGCA GAAAGATGCA 600
GTCAATGAAC CCTCACTCTG GGACTGGTGT TCAGTTCTGG ACCCTCCGCT GGGCTGAGAT 660
CTGGGATCCC ATGGATGCAG GCTGGGTGGC TCCAAAAAGC ACTGGAAGCT GCCTCCATCA 720
GGCCTGGGGT CAGGGGTCAC CTCCGCTGGC CACTGCCTTC CCAGACAGCT GCCCATGCCA 780
CACTGCCTGG TCCCTTCCGG GGCCTGGCTC TCAGGCCTGG AAAGCCCAGG GAGACTAGGA 840
TGAGGCTTGG GTTCTCGTAG GGAAATTTCC CTTCACCCTA TTGTGGTTCC CCTAACACAG 900
TGGGCAACCT TGACCAGGCC TGAGGATAAG GGAAGATACC CAACCGACTC ACCTACTCCC 960
AGCTGGCTGC CTGAAACCCC TCGGAGTTGG ACCATCAGAT GCTGAACTCG TACTCTCTAG 1020
CTGAGCACAT AACTTGGGTG AGCCTCAGTT TCCCCCTCCA TAAAATGGGC AAAATAACTG 1080
CCGCTTCATA GAGCTTGCAT GGGGATGAAG TAGGGTAACT CACAAGATAT ACTTAGTGTC 1140
AATAGCACAG TGCATGGTGC ATAGTAAGTG CTCAGTAAAT GATGACTGCT GTTACATAAC 1200
ATCCCCCAGC CCTTCCTCAA GCATCTGCTG TGTAGAACAC TCCTAATCTC CGCGCTTTAA 1260
TAGATGACAA AGACCCTTTG AGACCCAGAG GTGAAATGAG GGAGGTAGGG ACAGGACAGC 1320
TGTCTTGGCT ACTCTCAGAT CATACCCTGC TTGTCTCAGC TGTGTAGGAC TGGCCCAGGT 1380
GGAGGCTCCT GCCTGGACAA GAAGCTGACA AGAAAGCCTG TCTTTTTTGT GGGGATTTGC 1440
AGCTCTGGGT GGCCCTGACT CATGCTTTAT TCAGAATTTG GAATAAGTAG CTGCAGGGCT 1500
TCCGCAGGCA TTGCCCAACT CTGTGGCCTC CTGCGGCTTC CAGCAGCCCA GGAAGGAGGG 1560
CCCTGGGTGA GGATGGCTGG AAAGGAATTC TGGATGGCTG GACAGAGTCC ATGGGACCTA 1620
TCACTTCCTA CAAAGTCACT GTCATCCCAA GTCCCCTCCA GCATAATGAC GGCAAGTGCA 1680
AGCATTGTGC CAGCAGGTAC TGAATGCTTC CTGAGCACCA TCTGATATAG CCCTCACAGC 1740
ATGCCAGCAG GCAGCTATTA CTATTGTTCT CACTTTATAG ACAGGGAAAC TGAGGCACAG 1800
CCACATGAAA GCGCTTGCCC TGGTCACAGA GCTATTAAGT GGGGGAAACA AATTTGAGCC 1860
TAGACACGTG ACCTCTGTAC CCAGTCACAC CAGTGGTTCT CAACCCATCT ACACATTAGA 1920
ATCACCTGGA AGGCTCTCAT GAAAACCTAG CAGGGCCAGG CCCCCACCAT CAGAGATTCT 1980
GTCTGGACAT TGGGATGTTA CACAAAGCAA CTCGGTGACT CAGGTGTGTA GCCAGGACAC 2040
AGCAACACTT TGGAAGGCCA GGCGGGCAGA CCACCTGAGG TCAGGAGTTC AAGACCAGCC 2100
TGGCCAACAT GCTGAAACCC CGTCTTTACT AAAAATACAA AAATTTGGCT GGGCGTGGTG 2160
GCTCACGCCT GTAATCCCAG CACTTTGGGA GGCCGAGGTG GGCGGATCAC GAGATCAGGA 2220
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