| Tag | Content |
|---|
EnhancerAtlas ID | HS098-26983 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr19:7462660-7464860 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPIC | MA0687.1 | chr19:7463669-7463683 | TGAAAGGGGAAGTA | + | 6.54 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH19I007397 | chr19 | 7462261 | 7464969 |
| Enhancer Sequence | CCCAGGCTGG TCTTGAAGTC CTGGACTCAA GCGATCCTCC CACCTCGGCC TCCCAAAGTG 60
CTAGGATTAC AGGCGTGAGC TGCCACAGCC TGTGGTTTTT GTTTTTGTTT TTTTAACTGA 120
CAGATAACAG TGTATGTATT TATCATGTGC AACGTGACAT ATTCTTGAAA AATGCAAGAG 180
GAGCGGATGT TAAGCACTTT CACCACAAAA ATGAGAGCTA TGCGAAGTGC TGCATTTGTT 240
ACTAAGCTAG ATTTAATCAT GCCACTGTGT ATATATACTT CAAAGTGTGT TTCCTTTTTC 300
TTTTTCCTTT TGTTTTTTGA GACGGTCTCG CTCTGGCGCC CAGGCTGGAG TGCAGTGGTG 360
TGATCTTGGC TCACTACAAC CTCCGCCTCC CAAGTTTAAG CAATTTCGCC TCAGCCTCCC 420
GAGTAGCTGG GATTACAGGT GTGTGCCACC ACGCCCAGCT AATTTTTTGT ATTTTTAGTA 480
GAGGCGGGGT TTCGCCATGT TGGCCAGGCT GATGTCGAAC TCCTGACCTC AGGTAATATC 540
CCCTCCTTGG CCTCCAAGAG AGCTGAGATT ACATGCATGA GCCACCACGC CCGGTCATAT 600
TTCATTTTTA AATGGCATAC CTTAGAGAAG CAGAAAAGAG ACCGGGCACC ATGGCTCACA 660
CCTGTAATCC CAACACCTTG GGAGGTCGAG GTGGGCAGAG AGGCCAGGAG TTCGAGACCA 720
GCCTGGCCAA CAGGGTGAAA CCCCATCTCT ACTAAGAAAT ACAAAAATTA GCTGGGCGTG 780
GTGGCCTGCG CCTGTAATCC CAGCTACTTG GGAGGCTGAG GCAGGAGAAT CGCTTGAACC 840
CGCAAGGCAG AGGTTGCAGT GAGCCGAGAT CACGCCATTG CACTCCAGCC TGGGCAACAG 900
AGCTAGACTC TGTCTCAAAA AAAAAAAAAA AAATAAAGAA AGAAAGAAAA GAGATTCTTT 960
GGTTCCTTCT CTCTTTCTTG CTTAAATCGA CTTGAGAATG TCCCCACTTT GAAAGGGGAA 1020
GTAGCACATA CATTGTTTCT GGCATAGCTG TAGTATAATT TTCATTCTTG TCACACAGTA 1080
GCAATTACGG CTTCAAGGCC ATTGCCCTTT GTGGGCCAGG GCCGTGGTGA CTGGCTGTGC 1140
CTCCCTGGGT GTTTACCTAG CACATGTTTA ACATAGCTCA GATCGTGTGT CAAGATCTCC 1200
CTCATTCTCA CTCATCCTGG GTCATGTTTC TATCTCTTCA AACTCTATGA CTTACAAAAC 1260
ATTTTTGCTG CCACCTCTCT GAAAATCATT TAAAAGCCCA GAGACCTTAT ATGAAGTCCA 1320
GCCAATCGCT GTTTCTTTGT TATTTGTTAG GTAAACTTTA CTTTCCCCCT GAGACGGTCA 1380
AGAACTACTG TGTTTGAAAA CCCTCTCTCT AGGTGCAAAA CAGCACCAGT GGAAGCCTCG 1440
CAGCTGCCTG GAGGAATTTT TTGAGGGGAG GATTGTGGCT GACTGGGTGA GGGAGGGAAA 1500
CTGGGTAAAA TAATGTCCTC CGAGAGCATT CGGTGACAGC AGTTGTTCTC ATTTTTGTGA 1560
TGCAAATTAA GTTGTATGTG AACTAAATTA AATTTGCTTG CTTCTCTGCT TTTGTCAGAG 1620
ATAGATTCAT AGTTTCAACT GAGTATAGAG TTCTAGTCTG ATTATGTTCA ATATGTTCAA 1680
AGCAGTAGAT ACACTAATGT TTTTTTTTCC TTCTTTTTTT TTTTTGAGAC AGAGTTTTGC 1740
TCTGTGCCCC AGCCTGGAGT GCAGTGGCGC GATCTTGGCC CACTGCAAGC TCCACCTCCG 1800
GGTTCACGCC ATTCTCCTGC CTCAGCCTAC CGAGTAGCTG GGACTACAGG TGCCTGCCAC 1860
CACGCCTGGC TAATTTTTTG TATTTTTAGT AGAGATTGGG TTTCACCGTG TTAGCCAGGA 1920
TGGTCTCGAT TTCCTGACCT CGTGATCCGC CCACTTCGCC TCCCAAAGTG CTGGGATTAC 1980
AGGCGTGAGC CACCACGCCT TTTTTTTTTT TTTTTGAGAC AGAGTTTCGC TCTTATCACC 2040
TGGGCTGGAG AGCAGTGGTA CGATCACAGC TCACTACAGC CTCGACCTCC TAGGCTCAAG 2100
CAATCCTCCC ACTTCAGCCT CCCAAGGAGC TAGGACTATA GGTGCGTACC ACCGCGCCCA 2160
ATTAATTTTT GTATTTTTGT GTGTGTGTTA GAGATAGGGT 2200
|
| |
|
|
|
