| Tag | Content |
|---|
EnhancerAtlas ID | HS104-01455 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:38029010-38030620 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:38029310-38029325 | TGAACTCCTGACCTC | - | 6.22 | | RREB1 | MA0073.1 | chr1:38029833-38029853 | CCCACCCCCACCCCCCAACA | + | 6.06 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAAATACCTT AGCATGTTTC TAACATTTAA AAGCAATCTT GTAATCTCCA GGGTGAAAGA 60
TTCTTTAGAA GTTGGCATTT TTAAATTTTT TTTCTTTTGA GACGGAGTTT TGCTCTTGTT 120
GCCCAGGCTG GAGTGCAATG GCACCATCTC AACTCATTGC AACCTCTACC TCCCGGGTTG 180
AAGTGATTCT CTTGCCTCAG CCTCCTGAGT AGCTGGGATT ACAGGCATGT GCCAGCACGC 240
CCGGCAAATT TCTGTATTTT GAATAGAGAT GGGGTTTCAC CATGTTGGCC AGGCTGGTCA 300
TGAACTCCTG ACCTCACATG ATCTGCCCAC CTTGGCCTCC CAAAGTGCTG GAATTACAGG 360
CTTGTAATAC AGGAAGTGAG CTATTTTTAT TGGCTCAAAA CTGCATTGCA AATAAAGCAG 420
CTTTGCTGTC CCCAGGATAG ACCTACCTAA AGATCTGTCC AGTATTATTT TATTGGCTAC 480
CAGAGGAACA TAGTAAATAA CTCCCAAGTG TCTTAAGCTT TACATAAAGA GGGACAGCTC 540
TCGGCTGGGT GTGGTAGCTC ACACCTGTAA TCCCAGCACT TTGGGAGGCC GAGGCAGGTG 600
GATCACATGA GGTCAGGAGT TTGAGACCAG CCTGGCCAAC GTGGTGAAAC CCATTTCTAC 660
TAAAAATACA AAAAGTAGCT GGGCGTGGTG ATGTGCATCT GTAATCCAAG CTACTCAGGA 720
GGCTGAGGCA GGAGAATCAC TTGAACCCGG GAGGTAGAGG TTGCAGTGAA CCGATATCAC 780
ACCATCACAC TCCAGCCTGG GTGACAAGAG CAAAACTCCA TTCCCCACCC CCACCCCCCA 840
ACAAAGAGGG ACAGCTCTGT ATTCACTGGC AGCATTTCTC TAATTGTGTG CCAAGTTGTC 900
TCAGTGGCTG AAAATTCACT GTTTCCCAAA CCTCTGGTCC CAGCAGAACT CCCAGGATCC 960
TAAACCAGAG AGCCAATATT TTTTTTTTTT TGAGACGGAG TCTCCCTCTG TCACCCAGGC 1020
TGGAGTGCAG TGGCACGATC TTGGCTCACT GCAAGCCCCG CCTCCCAGGT TCATGCTATT 1080
CTCCTGCCTC AGCCTCTGGA GTAGCTGGGA CTACAGACGC CTGCCACCAC GCCCAACTAA 1140
TTTTTGTATT TTTAGTAGAG ACGGGGTTTC ACCGTGTTAT CCAGGATGGT CTGGATCTCC 1200
TGACCTCACG ATCCGCCCGC CTCAGCCTCC CAAAGTGCTG GGATTACAGG AATGAGCCAC 1260
TGCGCCCGGC CAGAGAGCCA AATGTTTAAC TTAGCAGACA TATTCTGGCC TGAAACCTGA 1320
GCCATGAAAA GCCCTTACAA CAATGCATTC AATATCCTTT TCAATGCTTT ATATCATACC 1380
CGGAGCCATT ATTGTGTTGA AACCAGGACA GCTCTGGCTT CTCCTCATAT ACTAAAGACT 1440
GTATGCCAAG CTAGAAACTA GCTAATCTAG AAAATATGGA TTTGGGGATC AAGGGGAAAA 1500
AGAACCCTTG GAGTGACAGC ATGTGGATTC TTCTTCCCAG AGATTTGATC ACCTCTCAGC 1560
TATTTGTATC AGGCTGCAAG TTTCAAGTAT TAATGGAGCT TGTTTTTGTT 1610
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