| Tag | Content |
|---|
EnhancerAtlas ID | HS062-06990 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr17:37400020-37401560 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:37401167-37401186 | CCCTGCCCCCTGGTGGCCA | - | 7.81 | | RREB1 | MA0073.1 | chr17:37400258-37400278 | TGGAGGTGTGTGTGTTGGGG | - | 6.86 | | ZNF263 | MA0528.1 | chr17:37400523-37400544 | TCCTCCTCCTGCTGCTCCTCC | - | 8.06 | | ZNF263 | MA0528.1 | chr17:37400520-37400541 | CCCTCCTCCTCCTGCTGCTCC | - | 8.09 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH17I039244 | chr17 | 37401081 | 37401270 | | GH17I039245 | chr17 | 37401361 | 37401510 |
|
Enhancer Sequence | GGCGGAGGTT GCGGTGAGCT GAGATCGCGC CACTGCACTC TAACCTGCAC AACGGAGCGA 60
GACTGCAGCT CAAAAAAAAA AAAAAAAAAA AAAAGAAAAG AAAGGAGCCT GAGGCTTTCC 120
TCATCATCCT CCTGCAGCAC AAAGGAGCGG AAACTGAAAA TGGACCGTGA GAAGATGGAG 180
AAACAGCCCC TGCATGAGAG GGACAAGTAT CAGACCGCCT GCGAGAGCAC TGTCTTCTTG 240
GAGGTGTGTG TGTTGGGGCG AGAGCAGGAG GGGAGAGTTG GAGAAAAGAT CCTCACGGTA 300
CAGATGGGGA AATGGAGGCC TCCAGGGCTC TGACTGCTGC AAGCCCATCA CAGCCCCCTG 360
GGGACTCCAC CACTTCCTGC AAAGGACACT CTCTGCCCTG TCTGTGGTTG TTGAAGCTTC 420
CAGGAGCTGA CGCCCTCCAG GCTGCCTGTC CTACGCGGGC CATCGCCACC TCCTTCCTTG 480
TGTGCTCCCT CTGCCTGGCC CCCTCCTCCT CCTGCTGCTC CTCCTGGCCA GCTCCTCCAA 540
GGCCCTTCCT CACTGCCCCA GGCCCGCCGG GTGGTTAACT TCTTCCTTCC TGTGGAAACC 600
CAGTCCACTT GTCAGGCCCC TGGTCAGCTC TTAATATACA GGTGGAGAGA AGGGAGCAAT 660
GACCAGCCTT GCTGTGTGTT TGCCTGCAGT GTTCGCCATG GCCGGAGTCC CCTGCAAGGC 720
CCCGGCCACC TCTCAGCTCT CTGGCTCTGA CCTCTCCCCA CTCCTGCAGG CTCTTGTCCC 780
CAGAAAGGTG AGGCAGGATG AGCACCTCCT GTCAGCCCTT TGGGGTGAGA GTGAAGAAAA 840
GAGCTCCCAG CCCAGGCATG GAGCAAAGGG CAGGGCTGGG GATTGGTGGG GAATTTGTGG 900
GGTGAGGACA GGAGCAAGCT CTGTGTCCCA GGGCAGGCCT GGAGGAAGGG TGTTGGTGGA 960
GGGAGACTGG CTGTAATGCT CCGCAGAGTT CTTGAACCTT TGCTCCTCCT CATAGGCTCT 1020
GTTCCTCACC ACCATTCGCT CTGGATACCT TGGGGTGTAG CCCAGTTGAG GTGAGCCTTC 1080
CCCTTCCCAC TCTCCACTGT CCCAAAGCCT TCTCCGCAGC TTCATCTCAA GCTCCAGAAT 1140
GGAGTGGCCC TGCCCCCTGG TGGCCAGATG TGATATGGCC ATAGATTGTA ACTTACCTGA 1200
TAAGACTGGG CAGGAAGAGC CTCCCTTCTC AGACTTGGGA CCTCCCAAGG GAGGGGCTGT 1260
TTCCCTTTCT TGTTCTGTCC CTGGGTCCTG GTATTACCTG GACCATCCAT TTTATACCTC 1320
AGGATCTGAA CCAAAAAGCC CCCATCTCAG AGACACAGCA ATGGTTGCAT CAGCACTGGT 1380
TCTCCAGCTA CTGCCGGATG CTGGCCAACT TCACTGGTGA GGCTAGTGTC TGGCAGGAGC 1440
CAGACCTGTA GGGGACTGAG AGTGGGTGGG ACACACAGGC AGGAAGCCTG TCTCTGTCCT 1500
GGCTTGTTGT GGGCCCTTCA ACTAACATTT ACTGGGGACT 1540
|
