| Tag | Content |
|---|
EnhancerAtlas ID | HS026-17085 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr2:26835540-26837890 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxq1 | MA0040.1 | chr2:26837008-26837019 | TATTGTTTATT | + | 6.62 | | MEF2C | MA0497.1 | chr2:26837020-26837035 | TTCTATTTTTAAACA | - | 6.11 |
|
| | 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 |
| GH02I026612 | chr2 | 26834999 | 26840329 |
|
Enhancer Sequence | CAGAGAGCAG GAGCAGCTGG CCAAGCGAGG CACTGCATAT GCACAGAAGG AAGCTGTCCT 60
CAATCCACAA GAGCCCTGCC AGCTGCTCCC CGTGACGACT TTCCTGAAGG TGGGGTGGCT 120
TAAGCCCTGG GGCAGTTTAC AGAGTATGGG ACAAGGGGGA GGTTCTGCAT CAACAGGGGC 180
CAGGGCAGTA GGTGCTCCAA TCATCTCCAG AGATAACTTA TCTCCCATCT CTGGGTTTTC 240
TGCCACCTGA GAAGTGACGT CTTGGTCACT GGCCTTTGCC TCCATTCCCC TAGATGCTGG 300
GTGGGTCTGC TGGGAGCACT TCCCTCTGGC ATTTGGCCTT GGGCAGAAAG AGAGAGAAGG 360
AGGATCCTTT CCCCAAGGCC TAGGGGACTT TCAGCAGATG CAAGGGCATT CATCATCTCT 420
CCTCCTCATC TCAGCTTCAG CTTTCTAGGA GAGTGGGTTT TTCCCACCGG AGCCTGATCC 480
CCCAGCTTAT GCCTGGAGGC CTCCAGCACC TGGAGCTTGC TTTCTCTCGA CTGAGCCTCC 540
TCTCTCTGTT AGGAAATTTC CTCCCTAGGA CCAACAGAAG GGGCCCCAAG GTCACTTTTC 600
CCATCCACCT TAGCAGTACC CTTGGGGCCA AATCTAATTC CTCCTCCACC CACCAGCAAG 660
GATGTAAAGA ACGTATGTCT TCCCAAGTCT TTCTGCAGGT GGAGCACCCC AGTTTCTTAG 720
CCACCTTCCC TCTAAGCCCC TGGTGTGAGG CTGGAGCTTA CACATAAAGA CTCCCCAGGT 780
GGTCCTGCCA CTCAGAGGGC ACAGCCATGC CCTCCCTCCA CAGGCAGCTT CTGGGAATGC 840
TGCCTGCAAT CCCCCTCCCT TTCCTGGAGT ATTTTAGCAT TTCACCTCCA TTCTGTCATC 900
CAGTCTTCGT AAAAACCCTC TGAAGTAGGC AGGGCTGCTA TCATTGGATT CATTTTTCAG 960
ATGGGGAAAG CTGAGGTTAT ACACAAACTG CAGTTCAACT CCAGGGCTTT TGGTGACAAG 1020
CCTGAAGAGC CCAGGAGACT TTAGGGTTTG CATCCTGGAG TTGTATCCGG TGCCTGGCAC 1080
ACAGAAGGGG CCTGGGCTCT TGTGAGGGGC TGGGGCCAGA GCTAAGAGGA GAAGGAATGT 1140
CCTCAACAGG TCTCTCTGTA GTCGGGCCTG TGCGGGGCCT GTCCTGCCTC TCTGCACCTG 1200
GGTGAATGTG TCCCCGCATC TCAGCTGTCC CAGCTGTGAA GAGCAGAGGC CGCTGACACC 1260
GGCAGGCAGG TGGCTGAATG CCTCCTCTGA CACTAGCCAT TCGGGCTGCT GGGAAGCCCT 1320
CCAAAGCTGC AGGGCGTCTC CTCCCTGTGG AGGCAGCAGC AGGCCCAGGG CCTGCAGAGG 1380
GTCAAAAACC CTGGGAACAG AGCCCCGGCC AGCTTGGCCA GCACCTCATT AGGAGGCCCG 1440
AAGAGGGGAG GGGGTACTTC AGGAACGATA TTGTTTATTT TTCTATTTTT AAACAAGTCT 1500
GAGGTCTCTG GGGCACAAAT GAAGTTATCA GAAAAGACAT GAGTGGAATA AAGCCTCAAG 1560
CCAGCAGGCA GAGAGGGGCC CTTGGGACCA GGACTCTTGA AAAGCTGAAA TGGAGTTTGT 1620
TTATCTTGTA CTCTGGGAGT GCCGGACTGT GGCCGAGGGA CTGGATGAGC ATGTCCCCAG 1680
GCCCACCGGC CCCTTCCCCA GGCCCTCATC TGCCTGTCCC TTGGTGTCAC TGGGGAATTC 1740
AGGCACGAGC AATACTTTTT AAATGATCCC ATTAGCGTGT CATTTGCACT AGAGGGAGGA 1800
GGCTCCTCCT CTGGAAAGGA GCCTGGACTC ACTTCTCACC TCAGACACAT GAACAGTTTT 1860
CCCAGGAGGC AGAGTCTGGC AGAGTCGGTG CACCACAGGG CGCCCAGTTC CGGCTGGTCA 1920
CTGGCTGGTC CTGCCACCTC AGGCAACCCC TCCATCTCCC GAGCCTCCAT TTACTCATCT 1980
GCCAAGTGGG GCTGATTATT CCCGTCTTGA CTCACATGCA CCCCTCACAG GGAGAAGCAC 2040
ATGAGATGCT GTGTGTGCAG AGTGTCCTCA GAGAAGGGCT GAGCCACAGA ATCCTTACAT 2100
GACCCTGCAA AGGGGGCTCG CCATGCCCAA GTTCAAGGTA AGGAAGCTGA GGCTCCGGGA 2160
AGTGGAGCAA CTTGCCCGGA AGCCTGAACT CCTTCCATTT GCTAAACTGC CTCTCCAATG 2220
CTGCACGTCA AGGATAATGC GCCCTGCTCT TGGGAGCTTT GAGAGAAGTC ACGAATCATT 2280
GACAGAACCA ATTAGAGGCC TGAGTGGGTT TGACTGGATG AGAAAATCTT CCCAGGAAGT 2340
GAGAAACGTG 2350
|
