| Tag | Content |
|---|
EnhancerAtlas ID | HS060-16707 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:4117630-4120310 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr19:4119202-4119215 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr19:4119203-4119216 | AATTAATTAATTT | - | 6.92 | | POU6F1 | MA0628.1 | chr19:4119204-4119214 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr19:4119204-4119214 | ATTAATTAAT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAGAGACCCC CCAGGGTAGG GGTTAGCTAC CTAGGGAGAC TCCATCTGGC CGTTTGCTAT 60
GTGGCCGTGG TGCATCGGCC CCCAGGAGGA CACAGACTGG ATTCCTGCAC TTGAGGGGTT 120
CATGGTGTAG AAGGAAAGGA TCCATGCTGT GTACCCCCAT AGACACACCA ATGACCAGAA 180
TCCAGGGCGG CTCCCCGGGA ACTGAGGACG CTGCCTTGAT CCTGTCTCAA CAAGTCTAGC 240
AGACCTCAGG ACCTCAAGGA TAAGCTGCAG CTCAAAGGAC CCAGGAAGCC TCCGTCTTTT 300
TCTTTTCTTT TTCTTTTTTT TTTGAGACGG AGTCTCCCTC TGTTGCTCAG GCTGGAATGC 360
AGTGGCGCGA TCTCGGCTCC CTGCAACCTT GGCCTCCCGG GTTCAAGAGA TTCTCCTGCC 420
TCAGCCTCCC AAGTAGCTGA GATTACAGGC TCCCGCCACC ATGCCCGGCT AATTTTTGTA 480
TTTTCAGTAG AGACAGGGTT TCGCCATGTT GGTCAGGCTG GTCTCCAACT CCTGACATTG 540
AGTGATCCGC CTGCCTCAGC CTCTCAAAGT GCTGGGATTA TAGGCGTGAG CCATTGCACG 600
CGGCCGGGAG ACCTCCTTCC TAACGCACGA GCTCCGGACC ATGTCGGGAG GAGACGAGGA 660
AGCTGGGATC GGGTGAACGG AGCCCGGGCC AAGATGTCTG TCTTTGCAGG AGATAGAGGA 720
ACAAGCGTTC TGAGCAGCCT CAGAGCACAG AATGAGAACC AAGAGTAGAG GGCAGAAGGC 780
TCAGCACAAA AGCTGCATCA GGTAGGCACG GTGGTGCACG TTTGCAGTCC CAGCTACTTG 840
GGAGGCTGAG ACACGAGAAC TGCTTGAACC CGGGAGGGGG AGATTGCAGT GAACTGAGAT 900
CTTGCCACTG CACTCCAGCC TGGGCAGCAG AGGGAGGCTC TGTCTCAAAA CAAAACAAAC 960
CAAAAAACAA AAAAAACAAA AAATAAGCAT GACCAGCCTG GGCAACAAAG TGAGACCTAT 1020
AGCCGAGCAC AGTGGCTCAT GCCTGTAGTT CTAGTTACTC AGGAGGCTGA GCCCAGGAGG 1080
TCGAGACTGC AGTGAGCCAT GATCGTGACA ATGTACTCCA GCCTGGGTGA CAGAGCAAGA 1140
CCTTGTTTCT ACACAATAAA AAATTTCTAA CAATTTAAAC AAGCAAGTAC ATTGCACTTT 1200
ATTGGGTGAT TCAAGGAATC TTCAGAGGAA ATTTCGACAG TAAGCTATTT TCACAAATGC 1260
CTTGACTCAG AACCAGATCC TGGAGTAACA GACAACTAAG CGCAATGCAC ACAGGAACCC 1320
ATTGCTGTGC ACAAGCAATG GAATGTAAAC CATGCGCACA AATTAAAATC TTCTAGTACC 1380
CATGTTTAAA AAGAACAGGT GAACTCACTT CATTTATTTA GAGACAGGGT CCTGCTCTAC 1440
CTCCCAAGCT GGGGTGCAGC GGCACGATTA CAGCTCACTG CAGCCTCCAA CTCCTGTCCT 1500
CAAGTGATCC TCCCACCTCA GCCTTCCTAG TAGCTAGGAT CACAGGTGTG AGCCATCATG 1560
TCTGGCTCTT TTTAATTAAT TAATTTTTAT TATTATTATT ATTTTCTGAG ACAAAGTCTC 1620
ATTCTGTCGC CCAGGCTGGA GTACAGTGGT GTGATCTTGG CTCACTGCAA CCTCCACCTC 1680
ACGGGTTCAA GCAATTCTCC TGCCTCAGCC TCCGAAGTAG CTGGAATTAC AAGCACCCGC 1740
CACCACGCCC AGCTAATTTT TGTATTTTTA GTAGAGACAA GGTTTCGCCA TGTTGGTCAG 1800
GCTGCTCTTG AATTCCTGGG TTCAAGCCAC CTGCCCACCT TGGCCTCCCA AAGTGCTGGG 1860
ATTACAGACA TAAGCCACTG CACCTGGCTG AAATTAATTT TAATAACACA TTTGATTTAA 1920
CCCATCAAAA ATGTTATCAT TTTCAACGTA CAACCAGTAT GAAAAATGAA TGAATGTTTC 1980
ACACTGTTTC CGTCTTAAGC CTTTGAAATC TACAATGGCA TTATTGCGCC TATGCTCTCG 2040
TGGGTTTGGG CAATTCTTGT TTTATGTGTT GCCTGTAGCC AGGGGCTACT CAACCAGGCA 2100
GTGCAGCTTT AAATGGCTCT CTGGAAGAAC AGGCCACCTC CAGAGGTCCC AATTCAGGAA 2160
GGAGCTAAAG CCAAGGTGGA CAGCCAGAGA GGGGACTGAA GCAGGGAATG AAGGCGTGGA 2220
CTGCTCCTTC CATCTGGAAA TTTCCAATCC CAAAGTTCGA CCACTGTTCG CCTACAGCTG 2280
GAAGTGGCGT AAGCCACGGG GCACACAGGC CAGAACCGAG GCGATGGCGC TGGAGCTGGT 2340
GCTGCAAAGA GCTCGCTGGA AGGCAGGGGC CTGGGCACCG CTTCCTGGGC TGGACAAACA 2400
CCATCTCATT CCATTCTCAC CATCGTCCCC GGAGGCCCAG GCAGGAGGGA ACAGACTCAC 2460
AGGGGTGGGG GAACCTGCCC GAGGTAACAA CACCTGCCTG AGGTCAGGAC AACCCCTGCT 2520
CATCTTAGTG TCCCCCATGA GGGGAAACAG GGCCCTAGTA GGTGCTCACT GAGGAGCTGC 2580
TGAACAAGGA CCCAGAAGAA GCAGAAATGG CGAGACCCTG GGAGTGGGAC AGAAGGTAAG 2640
GAGGGGAACA TGAATGAATG AATGAATAAC ATCAATGAAT 2680
|
