| Tag | Content |
|---|
EnhancerAtlas ID | HS069-06247 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr4:39135330-39137700 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr4:39137527-39137539 | AAACAAACAAAC | - | 6.32 |
|
| | 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 |
| GH04I039134 | chr4 | 39136289 | 39137419 |
|
Enhancer Sequence | GCATTCTAGG TCAAAAGACC TAGAAACTAT AGCTCTATAG TCAGCAAACT ACAGCCCACA 60
GGTCAACTCT GTCTGCTATT TGTTTTTATA AATAAAGTTT TATTGGAACA CAGACATGCT 120
CATTTGTTGA TGTCTGTAGC AGCTTTTGTG TTATGACAAC AAAGTTGAAT AGCTGTGACA 180
GCGACTATAT CTTTTTCTTG ACATTTACAG AAAACATTTC CAACCTGTGC ATGGGGGATC 240
ATTCTTCCGT CACCTAGAAT ATGAGGCCTC CGAGAGGATG AGAATGAGGG AAAAAACTAC 300
AAAGAAAATG GTAGCAAATA CTAGCAAAGA AAATGGTAAG CCAAGGTAAA GCTTCCAATG 360
ATAAGAAAGT AATTGAAAGA AGAGAGCATG GGGTGAAAGA CCGAGGAATG AGGGCCTGAG 420
CTCCACATGT CAGGGCCACC CTGAGAAAGT CTCTAAGAGC CTCTGAGAAA GTTTTCTCTG 480
GGTCTGAAAA CAATTAGGGA CTATCTTAGC TGTGGAGGCA CCTAAGTGAA ATTGAGTTAA 540
AAATTCATAT TTTATTAAAT TGCTTTAGAC TTGTTCATTT GATTATTTTA ACATAGGGAG 600
GTTGAGTCAA CTTGATATGT GACAGACACT GTACTAAGTA AGCATTTCAT ATGTATGTTA 660
ACTCATTTAA TTTTTACAAC AGCTGTATGA AGTAGATATG ACTATTCCCA GTTAATGATA 720
CGCAAACTAG CTAGTAAATG TCAGAGCCAA ATTTCAAAAC CAACCAGATC TGTATGACCT 780
TAGAGCCTTT TAAAAAATCT TTGCAAGATT GCTACATGGA GGTGAGTTTA AGCTGTCTAC 840
ATTACACAGG ATGATACATA CTTGATGCCA AGATACATCC TCACCACATC TGTGCTACAT 900
TTTAAGTTTT TACTTTTAGT GAGTAGAAAC AGGCTATATA ATTCTGCCTA TGGTGTGCCT 960
GAATGGATAC ACACACAGAG AGGTTTCATA AGTGCCTTTC TATTTTCTTT TTAAATATGT 1020
TCTGTGAAAG GACAAAAGAA GGGCATTTTA GAAAGGATGG CATAGTTAAT GACTTGGGTG 1080
CAGAGGGCTG TTGCTGTCAA TAAAGCAGAG AGCAGGGATG CTGAGTGGAG CAGTCATGAA 1140
TGGAAATGAG AGCATGAGCC ATTAGCAGGA AGTCATAAAC CCATTATTAG AAGTTTCATG 1200
TCATTGAAGG GAGCCAAATG CTTTACAATT CTAAGGACTA TGAATAGCCA CCTAAGGAGG 1260
ATGCGTCTGC TGCTGTGATG TATCAGACAG AGTCCAGTTG GGAGACAGAA ATCACAGGGT 1320
AATCTGAACA GGGAAGATTT TAAATAAATA ATCATGTCCC ATAACAGAGG ATTGGACTCA 1380
GAAAGGATTG GCTGGTTATC AGGATCTGAG ATTTGCTTTT GCCCTACTGG AGCTAATAAG 1440
CTGACCTGTT ATGGTTTCAT GGATGCTGGC AGAAGACATC CATGGGTTGA AGGAAAAGGA 1500
TTTTATTACT GAAGGCACAG AAAGCAGTAG GAATATCGTG TTGGGGTCAC TTCCCTGTGC 1560
CCTTCAATTC CCACAGGAAC AAGACAGAGG ATCCCAGGTG GAAATCCACG GAGCTTGGGA 1620
AATCCACTGC TTTTATAGTA AGTGGTAGGC TATCCTGCTC TTTGTCCTGG AGATTTCTCG 1680
CTGCAAACAC AACCCTGAGA AATGGCCCAG CTAATCAGTA GTGGGCGGGG ACGCTCAGAA 1740
CCCGCAGCAG AGTGCCTCTC CCCTTCCTTC TGCAATGTCT CCAGCACCCT CTACCGACAA 1800
AATTAGCACT GTGCAGACTG GCGAAGGAGA AAAAGGCTCA TGTCCACGTT GACTGAGCAG 1860
GTAATGAAGA CTGGATTTGT AGATGAGAAG CACTAATTAA AAACTGGTGT GGGCCGGGCG 1920
CGGTGGCTCA TGCCTGTAAT CCTAGCACTT TGGGAGGCCA TGGCGGGTGG ATCACCTGAA 1980
GTCAGGAGTT CGAGACCAGC CTGGCCAAGG TGGTGAAACC CTGTCTCTAC TAAAAATACA 2040
AAAATTAGCC GGACGTGTTG GTGCGCTCCT GTAATCCCAG CTACTTGGGA GGCTGAGGCA 2100
GGAGAATCAC TTGAACCTGG GGGGCAGAGG TTGCAGTAAG CCGAAATCAC ACCATTGCAC 2160
TCCAGCCTGG GCAACAAGAG CAAAACTCCA TCTCAAAAAA CAAACAAACT GGCGTATATG 2220
TTTATCAGCA GTACCAGACA CGGCCGAATT ATGATATGGT CCAAAAAGGG ACAGTGATTC 2280
AATTCATTCT AACACGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG AGATCGCCAC 2340
TATGTTCTCA GAGCTAAGGT AGCTCAAAGA 2370
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