| Tag | Content |
|---|
EnhancerAtlas ID | HS095-30218 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr8:139964400-139966190 |
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 | AGAAGGAGCC AAAGTCAGCG AGCTGGCAAA AGAACAAATA GAGAGGAAAA GTGGGCAACT 60
CAACATCACA GTGAGTGATC AGAGAGTCAG GGCTGGATCC CAGCTCTTCC CCAGGCTGGA 120
ACGAGTCATC TCCCTTCATC CACAGATTAC TGAGCAGCTG AAGGAGACAC AAAGGTGTAC 180
GTGGGAAGGA GTCAGGCCTC ATGGGGATGT GTGCAGTTAA AACCCTGGGG ATGCTGAAAG 240
GAAGGACCAT ACAGAGCGGT GTGAGGGCCA AGTCTTCCAT TACCTGACAC TGGAAGCCAC 300
GTGGTTAAAA CCCTGGGGAT GCTGAAAGGA AGGACCATAC AGAGCGGTGT GAGGGCCAAG 360
TCTTCCATTA CCTGACACTG GAAGCCATGT GGTTAAAACC CTGGGGATGC TGAAAGGAAG 420
GACCATACAG AGCGGTGTGA GGGCCAAGTC TTCCATTACC TGACACTGGA AGCCACGTGG 480
TTAAAACCCT GGGGATGCTG AAAGGAAGGA CCATACAGAG CGGTGTGAGG GCCAAGTCTT 540
CCATTACCTG ACACTGGAAG CCACGTGGTT AAAACCCTGG GGATGCTGAA AGGAAGGACC 600
ATACAGAGCG GTGTGAGGGC CAAGTCTTCC ATTACCTGAC ACTGGAAGCC ACGTGGTTAA 660
AACCCTGGGG ATGCTGAAAG GAAGGACCAT ACAGAGCGGT GTGAGGGCCA AGTCTTCCAT 720
TACCTGACAC TGGAAGCCAC GTGGACAATC CAGAAGATGA CTCACTTTGG CAGCCCTGAG 780
AGTTAAAAAC CAGTTTCCTT AGGCAAGACA TTAACCTCTC TATGCTGTAA TTTCACCCTT 840
TGCAAAATGG GGAAATAGCA ATGCCTCAAC AACAGGGTTA CTGTGAGGAT GAATTAGGAT 900
GACATAGGTG AGGGGCCTGG CGGGGGTGGT GAGCACACCA CAAAGGAATG CACACTGCTT 960
TGGTCATTGC TGCTGATGTC TGAAGCAGGA AAAGGTGGTC AGGGCCATCC CTCCTGCCCC 1020
ACTCAACCTT TTCTCTCCTC CCTCACCAGG GCTCTGATAG GCTCTTTCAG CTCCTGACCC 1080
TCTCCCTCTA GGATGCAGGT TCAGCCTGAG CCTGAGTCCA CTTTTCTGAG GTTGAGCAAC 1140
ACAATTAGAA TATGTGGAAA ATCTGTAAAC AGACACCAGC AAAGAGCCAG ATGCTCCCTG 1200
GAGCCAGTCC AAGAACAATT AAGCAGCCCT TTGAAGACTA ACTGAGCTGG GGGCAGTCAA 1260
GAGCTTGTCA GCTCCAGGCA GCAAGATCTC AACCTTCAGG GGCAGGGAGC ACAAACCTCT 1320
CTCCCTTCCT CTCTCTCTCT GAAAGCTAAA TAACAAAATA TCAGCCCCTC CCAAAGGCAC 1380
AGTGGTGAGA TGAGGGCCAC CAAAAGGCCT GCTTGGCAGG ACACCCTGTC AGGTTTTGGG 1440
GAGAGAAGGG CAGAACCAGT AGCCTGCAGG TCACACTTGG CCTTTAAGGT GATCATTCAT 1500
ATCATTACAG TTATTATTGC TCACATGGCA TTTTAAAAAT CTGAATTAAT TACCATCACT 1560
GAAGGATGTT GCATTTTCAC ATTCAAACTC ACATACCCAG ATTCTCTGGA GGAAGCCGTG 1620
TGTAAGGCCA CAATGAGCAC ACACGTTCCA CAAGCCACAG TGGGCTAGAG CTGAGGAGCT 1680
GCCCCTGGGA GAGTGGGTGC ATCAGAATTT GCCACAGTAA GTTCCACCCC TGTGGTTTCC 1740
CCATCCTCAC GCTGGCATTT CTGTCATTGC CTCTTTCTCA CTTTAAACAC 1790
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