| Tag | Content |
|---|
EnhancerAtlas ID | HS060-11350 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr15:58876990-58878810 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr15:58878717-58878732 | AAGGTCAGGAGTTCA | + | 6.04 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr15 | 58877012 | 58877986 | | chr15 | 58877000 | 58878733 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH15I058585 | chr15 | 58877361 | 58878624 |
| Enhancer Sequence | TCTGTACTGA GGGTTCTGCT TGTAATTCTC CCTGGCTACT GGACTCCATT AGGAATCTTC 60
TTTTCCTTTG TTTGATCACT GGGGCTCTGT TCCAGATACT GAGGTACCTT AAGAGACAGC 120
ATTCGCAGCC TGATAGAAGG AACAGCAGTA TCAGCCTCCC AGGCTCAAGC TTAGCAGCAT 180
GTGGGTTGCC AGTCCTCTGG CAAGGGACTT GAAGGAAGCC TCTCTGCCCC CTTTCTAGTC 240
TCCTCACCTC TCTCAGACAC CTTCATAGCA GTGAAGGCAA CTCAACCCAT CTGGTCAGCT 300
CTTCAAGAAG CAGGGAGACC CACACATTCA CGAGGACCTT GCCCCGGATC CCCTCCTTAG 360
GCTTATGATA TGGTTCCCAG GCAGGAAGAC AATCTTGCCC CAGCTCTCTG ACAGGATTCT 420
GCTGTGGCCC GAAGCCTCAT TCACATCCCA GGCCTTATCT TCCCCCGGCA AGCCCCAGCA 480
GCTGCTTTTC TCAGGAGAGG CAAATGGGTT AAACTGCAAG TAGAAAAAAG TTCAAGCTGC 540
TATCATTCCA GAACCCCCAG TTCCTCATGT CTCGGAACTT CTTGATGTCT TTATTTTTGC 600
ATTCTAAAGT GCTTAATAAA CATCACTGAA TACATGCTAC CACCCCTACC TCAAATCCTG 660
TCTGGTGCAG GTTCAATCAA TCATGATGCC TTTGGAAGCT AACTCAAACT GGCTTAAATA 720
AAGAGGGTTT TTTGTTTGGT TGGTTTTGTT TTGTTTTTAA ATCTCACACA AAAGGAAGTT 780
CCAAGGTAGA GTGGGGCCTC AGGAAGAGCT GACTGGGCTG CTTGGTAATG TTATGAAGAT 840
GCAGTGTTTT TCCTTCTCTC TGCTCCACCA TCCTTGATGT TGGCTTCATC CTCAGGCTGT 900
TACCAAGTTG CCCACTGCAA CTGCAGGCAG CTCACTCAGG CATGGTAACA TCCAGAGAAG 960
GAACAGTAGA CATCATGCGG GAGACAGCCC TCTTATCTCA CTGGCCAAAA TTAGGTGACA 1020
TGACCATTCC TAAACTTGGC AAGGGTAATG AGATTAACCA CAGACCAAGG ACCCTAACCA 1080
CATGTCTGTT AGAGGAGAAG ATACTTAAAA TCAGGGGACA CCTGCTCGCA AGCTAAATGT 1140
TCCAGTTCAG TAAGCAGTTT TTCACATGAA AACCAGAACA GTTGACATTC GAGTGTTCAC 1200
CATATGCAAG GTGCCTTACA TACATTCTCC TTTAATCCAC ATCATAGTCC CCTGAGGTGG 1260
CTAAAACTAT TATCCCTGTT TCACAGATGA GGTACCTACA GCTTAGCTTT TACAAGGTCA 1320
CACGGCTAAT GGACCATCAT TTCCCTCTTT ATAGATTCTG TGTCCATGAA TGCAGCCTAC 1380
CATTGCAGTC AGCAACAGAA AATGTCCTTT ACATATTAAC TCCCTTGGAC CCCATGTGAG 1440
AGCTATAATT AGGTATTGTA CTTTAAGACA CTGTCTTTTC ATGTTATGGA GCTTGGTAAC 1500
CAGCTATAAG TGCAAATCAT TCATGGCAGA CCACTAGCTG TGCCCTCCCT GCTGCCGCTG 1560
AGACTGTGCA GAGGCATGTG GCTATGCTGT GGAGTTTCAC CTTTGATTAT ACAACATGCC 1620
CAGGAATCCT TTTTATAAAA CAAGCCTTAA GATCTTAATA TGGGGCCGGG CACAGTGTCT 1680
CACGCCTGTA ATCCCAGCAC TTTGGAAGGC CCAGGCAGGT GGATCACAAG GTCAGGAGTT 1740
CAAGACCAGC CTGGCCAAGA TAGTGAAACC CCCGTCTCTA CTAAAAATAC AAAAATTAGC 1800
CGGGCATGGT GGTGCAGGCC 1820
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