| Tag | Content |
|---|
EnhancerAtlas ID | HS147-41457 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr8:139964290-139965900 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr8:139965151-139965165 | AGAAGATGACTCAC | + | 6.46 |
|
| | 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 |
| GH08I138952 | chr8 | 139965015 | 139966088 |
|
Enhancer Sequence | AGCAAATATT AGGGAAAACT TGTAAAATCA ATCAACTAAG CTTCCATGTT AAGAAGCTCA 60
AAAACTCAGA GCAAATTGAA TATTAAGTAA TTAAAAAACA ATGCAATTTA AGAAGGAGCC 120
AAAGTCAGCG AGCTGGCAAA AGAACAAATA GAGAGGAAAA GTGGGCAACT CAACATCACA 180
GTGAGTGATC AGAGAGTCAG GGCTGGATCC CAGCTCTTCC CCAGGCTGGA ACGAGTCATC 240
TCCCTTCATC CACAGATTAC TGAGCAGCTG AAGGAGACAC AAAGGTGTAC GTGGGAAGGA 300
GTCAGGCCTC ATGGGGATGT GTGCAGTTAA AACCCTGGGG ATGCTGAAAG GAAGGACCAT 360
ACAGAGCGGT GTGAGGGCCA AGTCTTCCAT TACCTGACAC TGGAAGCCAC GTGGTTAAAA 420
CCCTGGGGAT GCTGAAAGGA AGGACCATAC AGAGCGGTGT GAGGGCCAAG TCTTCCATTA 480
CCTGACACTG GAAGCCATGT GGTTAAAACC CTGGGGATGC TGAAAGGAAG GACCATACAG 540
AGCGGTGTGA GGGCCAAGTC TTCCATTACC TGACACTGGA AGCCACGTGG TTAAAACCCT 600
GGGGATGCTG AAAGGAAGGA CCATACAGAG CGGTGTGAGG GCCAAGTCTT CCATTACCTG 660
ACACTGGAAG CCACGTGGTT AAAACCCTGG GGATGCTGAA AGGAAGGACC ATACAGAGCG 720
GTGTGAGGGC CAAGTCTTCC ATTACCTGAC ACTGGAAGCC ACGTGGTTAA AACCCTGGGG 780
ATGCTGAAAG GAAGGACCAT ACAGAGCGGT GTGAGGGCCA AGTCTTCCAT TACCTGACAC 840
TGGAAGCCAC GTGGACAATC CAGAAGATGA CTCACTTTGG CAGCCCTGAG AGTTAAAAAC 900
CAGTTTCCTT AGGCAAGACA TTAACCTCTC TATGCTGTAA TTTCACCCTT TGCAAAATGG 960
GGAAATAGCA ATGCCTCAAC AACAGGGTTA CTGTGAGGAT GAATTAGGAT GACATAGGTG 1020
AGGGGCCTGG CGGGGGTGGT GAGCACACCA CAAAGGAATG CACACTGCTT TGGTCATTGC 1080
TGCTGATGTC TGAAGCAGGA AAAGGTGGTC AGGGCCATCC CTCCTGCCCC ACTCAACCTT 1140
TTCTCTCCTC CCTCACCAGG GCTCTGATAG GCTCTTTCAG CTCCTGACCC TCTCCCTCTA 1200
GGATGCAGGT TCAGCCTGAG CCTGAGTCCA CTTTTCTGAG GTTGAGCAAC ACAATTAGAA 1260
TATGTGGAAA ATCTGTAAAC AGACACCAGC AAAGAGCCAG ATGCTCCCTG GAGCCAGTCC 1320
AAGAACAATT AAGCAGCCCT TTGAAGACTA ACTGAGCTGG GGGCAGTCAA GAGCTTGTCA 1380
GCTCCAGGCA GCAAGATCTC AACCTTCAGG GGCAGGGAGC ACAAACCTCT CTCCCTTCCT 1440
CTCTCTCTCT GAAAGCTAAA TAACAAAATA TCAGCCCCTC CCAAAGGCAC AGTGGTGAGA 1500
TGAGGGCCAC CAAAAGGCCT GCTTGGCAGG ACACCCTGTC AGGTTTTGGG GAGAGAAGGG 1560
CAGAACCAGT AGCCTGCAGG TCACACTTGG CCTTTAAGGT GATCATTCAT 1610
|
