| Tag | Content |
|---|
EnhancerAtlas ID | HS042-01184 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr1:34150050-34152340 | 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 | chr1:34150119-34150133 | AAGAAATGACTCAG | + | 6.64 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCTCCCTTCT TCCTTCCCCC TCCACGAAGC CAGACAACCG TAGCTTCAAC CCGAACCACA 60
TTTGCGCATA AGAAATGACT CAGTTCTTTT GAATATAACC AGGATCCCTC AACAGTGCTC 120
CTAGGCTCCT CCCTGGCTTC CCAGCCAATT TATCCTCTGC ACTGCTGCCA CAGATCTTCC 180
TGAAGTCCTC ATATCCCCCC TAGACAATGA GCTCTTCCAG AAGCAGCTGT GTACATTCAT 240
ATCTTCCTCC CTTTCACATG CCTGGGAGGG CCTCACCTCC ACCCTGCATG GTGAGCTCCT 300
ACTGTTCTTT AAAGTGCAGC TGGAAAGGTG CTTCCTCCCT GTAGTCCACC CCCAACTGCC 360
ATACAGAATT ATGATCTGTC CTCGCAGACA CTTTTCTATT GTGTTTCGTG CATACTTCCA 420
CTATAGCATT CATCACATTA TCTTAGAATC TATAGCAGAA ACTGTGGGTT GGATGATCTG 480
TGCTTCATTT CCAAACCTCT CATCTCTCTA CTATTGAGGC TCTAAAAGCA AAGCAAAATT 540
GATTTCCCAC TTTTTCCCTG CCAGGCATGG CAAGTTCTGA CTAATGAGAT GTAGGACAGT 600
ATCTCTAAGG ATAGTGGTTC TTCCCAAATA CACAAGCAAA CTTTCATCAG GAGAGAGCTC 660
CGTGCCCTTT CCTCTTCCCT CTTCTTTTAG ACTGGAACAC AGACATAATG TCTGGAGCTG 720
CGGCAGCCAA CTAGGTAGCC ACGAGGATGA AAGCCTCAGG ATGGCAGACC AAGAAGGAAG 780
GTTATGGCTT CCTGAGCAGC GGTACCAAGT CTGGATGGGA CCTTCAGATT CTTGTTCCAG 840
GAGAAAAATG AACCCCCATC TGTTGAAGCC AGCTTTAGTC CGTTTTTCTA TTTTCATTCC 900
TAACTGATAT AATTTCTGTC TATAATACTG AGACCTTCAA GGGGAAAAGC TGTTTCTTAT 960
TTATATTTAT ACCCCCGTGC CTGGCAGAAT GCCCAGCACT GAGTAAATGC TCCAAGTTTT 1020
TAAATTGAAC TGAATGTTGT TACTGTCTTT AAAGTGTTCC AACAGCTCCT TATTATACTG 1080
AGAAATCCAT TCAGAGTTCT TGTCTTGGCC TTCAGTGTGT AAAGACTCCT CCTTACCCAC 1140
ACAGCCTTAT TTGCCCACAT GCACGCAGCT CCAGCCACGT CAAGTGAGTG CCCTTTCGTG 1200
GCCAGATCCT GTATTTTCCC CTATGTTCAT ACCTTTGCTC TCTTACCCCT AGCTGGAAAG 1260
ATTGCCTCTA CAGTCCCAGG CAGAACTCCT CTCTCTCTTC TCTGTTACTG AACTCCGTCA 1320
CTTGGCTTGC ACTTATAGCA TCTATTTTAT CTTGGAGGTA CCTGTCTGTT TGACTATTTC 1380
CCCACTAGAA TGTGAACTCT TGGCAGACAA GGCCTGGCCT TGGTCTGGAC TTTGTGTTTC 1440
CGACTGCACA GCATCACACA GTCTCTGGCA CAGAGCAGGT AATCATTGCA TATTTTGTTA 1500
GATGGAATCA GACCACAGCC TGAATGGCAG ATGGGAAAGA GCAAAGACTG ACATTAGACG 1560
GAACATGTTC CAATCCCACA TTACTGGGTA ATTGTCAGAT CTCAAGGAAG GTCATTCATT 1620
CTTTCTGGGC CTCGATGATC TCATCTATAA AATGGGGACA GTAATAACTG ATTCAGAACC 1680
TGGTGTGCTA TAGGTATTTG ATGAATGTTT TAGAGGGGCA GAACCAAGAG CAAAGGGCTT 1740
TCCCTCCCTT TCTTTTCCAG TTTTCATCTG AGCTCGCCCA CTGATTATTA AAAACAAAAC 1800
AAAACAAAAC CCTCCAGCTC AACACCAGAA GCTGAGAAGA GTTTCCACTC CTATAGGATG 1860
AAACTTCTGT GTTCTATGTA CTGATGACAC AGGCAAGGGT GACAGGGAGG GAGCAGCTCA 1920
TGGGTCTGCC CTCCTGCTGT CAGCTGCCAG GCCTGGATGG AGTGCATTGG CTCATCCACC 1980
CCATTCTTGG CACTTAGGAA GAAGCACTTG CCAGATGCTG TAGGTATTAC CAGGGTTCAA 2040
GGAAAGGGGC TGCCTTCCAT TCCACTCTTG TCACACACAT CCAGGCAGGA CCCATTTTCC 2100
AGCTTGGACC ACACCCAAGG GTAAGCCTGA CTGTAGATTC CTGCAGCCAA CTACTTTGCC 2160
TCTTGGGCAC TCCTGGGAAG GGACCATCCT TGCCCAGCTT GCTGGAGCAA ACCTGGCTAC 2220
AGATCCCTCT GGTCACCCTC AGTGCTGGAT CAGGGCTGAA GCAGGGTAGG GAGATGCATC 2280
TGCAAGCCTT 2290
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