| Tag | Content |
|---|
EnhancerAtlas ID | HS193-00351 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr1:17612580-17614760 |
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 | CTCATAGATA AGAAATGAAT CTCCGGGTTG GCACTTTCCA TAGCTGGGAA TCCCAAATGC 60
ACATTCATCA GAGACTGTAA GGTCATTCTC AGGGTATGCT CCAGTTTAGC TATTGCTGGC 120
GGTGCGTCTG CCACACACAT GGGTCTCACT GAGCTAAAGT CAACATCTTG GAAGGGCTGG 180
TTCCTTCTGG GCTCTAGGGA AGAATCCTTT TTCTTGCCTT TGCCAGCTCC TAGAGGCTGC 240
CTACACCCCT TGGCTTCTGG GCTTTTCCTC CATCTTCAAG GCCAGCAGCA TAGTAACATT 300
TTTGTATCTT CCTCTGATGG ATTCTTCTGC TTCCTTCTTC CACTTGTAAG GACCCTTGCG 360
ATGACACTGG GCTCATCTGG ATAAGCAAGG CTCACCCACC CTCTCTAGGT CAGCTGATGA 420
GTGAACTTCA TTCAATCTGC AACCTTCATT CCCTTTTACT AAGAAGGTCA TATACTCACG 480
AGTTCTGCAG ACTCGAACGT GGAAATCTTT GGAGGACCAT TTTTCTGCTG ACTACAAGCA 540
ACCAGGCCCT GACTGCCGTT TCTGGCCTCC AAGAGTGAGA CCATACCCGG TCCCCTCTGA 600
AATCCACAGA GGCAGCAGCA GAAAGATGCA GTCAATGAAC CCTCACTCTG GGACTGGTGT 660
TCAGTTCTGG ACCCTCCGCT GGGCTGAGAT CTGGGATCCC ATGGATGCAG GCTGGGTGGC 720
TCCAAAAAGC ACTGGAAGCT GCCTCCATCA GGCCTGGGGT CAGGGGTCAC CTCCGCTGGC 780
CACTGCCTTC CCAGACAGCT GCCCATGCCA CACTGCCTGG TCCCTTCCGG GGCCTGGCTC 840
TCAGGCCTGG AAAGCCCAGG GAGACTAGGA TGAGGCTTGG GTTCTCGTAG GGAAATTTCC 900
CTTCACCCTA TTGTGGTTCC CCTAACACAG TGGGCAACCT TGACCAGGCC TGAGGATAAG 960
GGAAGATACC CAACCGACTC ACCTACTCCC AGCTGGCTGC CTGAAACCCC TCGGAGTTGG 1020
ACCATCAGAT GCTGAACTCG TACTCTCTAG CTGAGCACAT AACTTGGGTG AGCCTCAGTT 1080
TCCCCCTCCA TAAAATGGGC AAAATAACTG CCGCTTCATA GAGCTTGCAT GGGGATGAAG 1140
TAGGGTAACT CACAAGATAT ACTTAGTGTC AATAGCACAG TGCATGGTGC ATAGTAAGTG 1200
CTCAGTAAAT GATGACTGCT GTTACATAAC ATCCCCCAGC CCTTCCTCAA GCATCTGCTG 1260
TGTAGAACAC TCCTAATCTC CGCGCTTTAA TAGATGACAA AGACCCTTTG AGACCCAGAG 1320
GTGAAATGAG GGAGGTAGGG ACAGGACAGC TGTCTTGGCT ACTCTCAGAT CATACCCTGC 1380
TTGTCTCAGC TGTGTAGGAC TGGCCCAGGT GGAGGCTCCT GCCTGGACAA GAAGCTGACA 1440
AGAAAGCCTG TCTTTTTTGT GGGGATTTGC AGCTCTGGGT GGCCCTGACT CATGCTTTAT 1500
TCAGAATTTG GAATAAGTAG CTGCAGGGCT TCCGCAGGCA TTGCCCAACT CTGTGGCCTC 1560
CTGCGGCTTC CAGCAGCCCA GGAAGGAGGG CCCTGGGTGA GGATGGCTGG AAAGGAATTC 1620
TGGATGGCTG GACAGAGTCC ATGGGACCTA TCACTTCCTA CAAAGTCACT GTCATCCCAA 1680
GTCCCCTCCA GCATAATGAC GGCAAGTGCA AGCATTGTGC CAGCAGGTAC TGAATGCTTC 1740
CTGAGCACCA TCTGATATAG CCCTCACAGC ATGCCAGCAG GCAGCTATTA CTATTGTTCT 1800
CACTTTATAG ACAGGGAAAC TGAGGCACAG CCACATGAAA GCGCTTGCCC TGGTCACAGA 1860
GCTATTAAGT GGGGGAAACA AATTTGAGCC TAGACACGTG ACCTCTGTAC CCAGTCACAC 1920
CAGTGGTTCT CAACCCATCT ACACATTAGA ATCACCTGGA AGGCTCTCAT GAAAACCTAG 1980
CAGGGCCAGG CCCCCACCAT CAGAGATTCT GTCTGGACAT TGGGATGTTA CACAAAGCAA 2040
CTCGGTGACT CAGGTGTGTA GCCAGGACAC AGCAACACTT TGGAAGGCCA GGCGGGCAGA 2100
CCACCTGAGG TCAGGAGTTC AAGACCAGCC TGGCCAACAT GCTGAAACCC CGTCTTTACT 2160
AAAAATACAA AAATTTGGCT 2180
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