| Tag | Content |
|---|
EnhancerAtlas ID | HS180-22825 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr18:47164500-47166780 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr18:47166459-47166480 | GGAAGAGGGAGGAGGAGGAGA | + | 6.41 | | ZNF263 | MA0528.1 | chr18:47166436-47166457 | AGATGAGGAGGGTGAGGGAGG | + | 6.5 | | ZNF263 | MA0528.1 | chr18:47166463-47166484 | GAGGGAGGAGGAGGAGAATGA | + | 7.11 | | ZNF263 | MA0528.1 | chr18:47166466-47166487 | GGAGGAGGAGGAGAATGATGG | + | 7.6 |
|
| | 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 |
| GH18I049638 | chr18 | 47164738 | 47167005 |
|
Enhancer Sequence | TTACCTGTCA GGCATTATTC CTTGTGGGTA TTACTTCAAG TAATTCTTAC AAGAGTGTTG 60
TAAGTTTTAT ATTGTTATTA TTTATTTTCT ACAGAAGAAT TGGAAAGCAG TGCTCAGGGC 120
CTCTAGGAGT TGACCTGAGG CTGTTAAGTG AGATCTATTT ACAGGACTTG TGGCTAATAG 180
GAGTTTAGAA ACTTCTTTTG GGCTCTACAC AGCCTGACTG TCAAAGGTGT ATTTTTCACT 240
GTCCAAAGTC TGAAAGTCAG GCTCTGTTGA AGGACATGCT TGTGACATCA AGTGGGAAAC 300
AATGGTGGTC ATTCTTGGGG GCAGAGTGGT GTTGAGAAAG GAGCTCCGAA TTGGAAGTCC 360
AAAATCTGAG AAACAAGTGT GGGACAGCCC TTAGCATCTG TTCCACACTC TGCTCCTGAT 420
GGCTGTCGGG AGCCTTATCT CAGTCCAGGC TTCCCTACCA GAGGGATTTG TGACCTGGGC 480
AAGTCCTTTT ATCTTTTAGG CAATTGTCCA GCACTTCCTC CCTGCCTCTA GACCAATGGA 540
AACTGAATTT CTAGGAGGAG TCCACGTCTA TGTTTTTAAA AGTCCCCAGG AGATTCTAGT 600
GCTCACAGGG TTGAGAACCA ATGGAAAGGG GAGGAATCTG GAGGCCTCGA GTGCTGAGAT 660
GGGAAGGGAA CCCCCAAGGA AATCTCAGGG AAGACAGGGG AAGGCTTCAG GGGATACAGG 720
CTGACTGCAC CCAGTTGTAA TTATGCCCTG GGTAGGGACT GGGTTGGGGA TGGGGATACC 780
ACACTTTGTA GCAGGAAAGA ACATTCCCAG AGACTTGTCA TGGACCTCTG CGACCTGGCA 840
CGCCTCCCAA GCCTACCTTC TTTGCCCTGC TCCCCAGCTG CACCCAGTTC TCAGCTGGGC 900
CCCCCAGTGG GAGGCCTGGG CAGGCCTCAC CATCTGCTAG AAGCCTCCCT GCGTGTAGGC 960
CCTGCTGGTC TTCCTGGAGG CTGACCTCCC CTGCAGGCGT TGGGACCATT TAGTGTGACA 1020
CCTTATCCTT GGTATTACCC ACATTCTAAT TGTCCTATCC ACCTGTATCT GTCTCTTGTG 1080
TGTTTTTTTT GTCCTTGAGA TCTGGGACAG AGTCCTGCAG TGCAAACAGC ATGGGCCTTG 1140
GAGGCCCCCA CACCTGCACG TGCATTGTCA CTTATTAGCA GTGTCACTTT CAGCAAATGA 1200
TTAACCAAAG CCTCCTGCCC TCATCCTTAA AATGGGAACA ATGCTGTCTT CCTTTGAGGT 1260
TGTTGTGAAG ATAACACGAA GCAATGTACA TAATGTCCTT GGCACACAGT AGGTGATCGA 1320
TACATACATG TTGATTAACC AAGCATTTGG ATAATCATTG CCGTAATTAT AACCAACATT 1380
GGGGAACATT TTGCCTGTCT TTTCACAGAA TAAACCTGTG AGTTTTTATT AGTCTTGTTT 1440
TGTACACATG GGAAACGGGG TTCAGATAAA TTAGAAGGAC TCAAGGCACA CTACGCAGGA 1500
GATGCAGGAC TGGGGGTGCA CCCAGTTCTT ATCCCCTCAG ATCCTCTGCC TTCTCTACCC 1560
TATTGCTCCC TGGGTGGACA TGATAGGTGT AGGGTCAGCT GTCGCTGCTT TGGCTCTGTG 1620
AGAGCACCAC CTGTGGTTCC CAGCTCCCCA CCTGGTCCTT CCAGCAGAAC TCAAGCTTGG 1680
GAAGCTTGGC CAGTGCGCAC AGCTGCAGGG GGCATGGGGA AGGGCCCTGT CATGTTTGCC 1740
GCAGCCTCTG GTCATGTTCT GATGTTTTCT GCTGTGTTAT GGATGCACGC CACTCCTGTT 1800
CACGTCGCTG AGCAGGGATG GGGCACTGTA AGCCCTTTCC TTCTCGGTGC TATCCAAGCC 1860
TCACATCTGA GCTGCCAGCG TGGTTTGAAT CATCACGTTT TTAGTGACGG TGCTGTTCTC 1920
TTAAAGGCAA GGGTGGAGAT GAGGAGGGTG AGGGAGGCTG GAAGAGGGAG GAGGAGGAGA 1980
ATGATGGTGT TGGGGCCTTT CTGGAAAGGA ACTGAGGAAA CAGGAACCTC CTGTTCTTCT 2040
GCTCCGGCTG GCCCAAGGCC ACCGTGATGA GAGGCTGATG AGATCCAACT CTGAGTCAGC 2100
AGAACCCAGA AAGGTCCCTG TGGGTCCCCT GCTGACTCAC CATGCCCCTT CCTCACAGGC 2160
TCTGACCAGC AGTGCATGGA GTGGCCAAGC TGCAGTGTCC AGGCCGGGTC CTGACTTCCT 2220
GGGCCATGGG GAGGAAGCTG AGGAATTGAA GGACACTCAG GATTCACTGA AGGGGCTTCC 2280
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