| Tag | Content |
|---|
EnhancerAtlas ID | HS048-02737 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:171327470-171329720 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:171327550-171327565 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 171327867 | 171328318 | | chr1 | 171329196 | 171329291 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I171358 | chr1 | 171327705 | 171329424 |
|
Enhancer Sequence | ATTAATTAAG AACCTGGGCC AGGTGTGGTG ACTCACACCT GTAATCCCAG CACTTTGGGA 60
GGCTGAGGCA GGAGGATCAC GAGGTCAGGA GTTCAAGACA AGCCTGGTCA AGATGGTGAA 120
ACCCTCTCTC TACTAAAAAT ACAAAAATTA GCTGGGCTTG GTGGCAGCCA CCTATAGTTC 180
CAGCTACTCA GGAGGCTGAG GCAGAGAATT GCTTGAAGCC GGGGGGTGGA GGTTGCAATG 240
AGCTGAGATC AAGCCACTGC ACTCCAGCCT GGGTGACAGA GTGAGACTCC ATCTCAAAAA 300
ACTAATTTGT ATGAGAGGTC AGTTAGGTAT GCATGCAAGT CACCTAAGAA AGCAGGCAAA 360
GATAAGCCTT CATATTCTTG AGACTTTTCA AATGTCTCAT CTGACACTGC AGAATTCTTT 420
CTGGCATTTT TGCAATTTCA ACCATTTAGC ATTAGTATGA GCGAAGTTTG ACCAGCAGGC 480
CATATGCTAC CAACCAAAGC TTGCAATGCA GCTTAGAATT TAATTTCAGG AATCCTTTAA 540
TCCTAATAAT GGAGAAATTG AGATTCACTT AGGTAAACTC AGCCTAGACC TAATTTGACC 600
CTTGACAGTC AATGATTTCT AATTAGGTCT TGCAGACAGG GAAGGACCAA TCAAGTGCAG 660
CAGGCTGAAC TGCTGTGTGT ACAGTTTATG GCAAGGAGTA ATTGGAAAAT CCAGTCTGAG 720
CCTGTACTTG GGCCTTTATA AGGGGTCATG GTTCAAGCTG AAGCCGACAG TTTCTCTCAG 780
AGCAGCAGCT ATGAGTCTTG CACCTCCCTG GTTGAGAATG AAACACAGTT CCCAAGAACA 840
ATTCGTAATC CCATTACATT TTAAAAATAT AATTAAAGGG AATCTTGGTG GGTGGGTGGC 900
AAGATGACAG AGTAGGAACA GCTCCGGTCT GCAGTTCCCA GTGAGATCAA CGAATAAGGT 960
GGGTGATTTC TGCATTTCCA ACTGAGGTAC CCGGCTCATC TCATTGGGAG TGGTTATACA 1020
GTGGGTGCAG CCCACGGAGG GTGAGCCAAA GCATGGTGGG GCATCACCTC ACCCGGGAAG 1080
CACAAGGGGT CAGGGAACTC CCTCCCTTAG CCAAGGGAAG CCATGAGGGA CTGTGCCGTG 1140
AGGAATGGTG CACTTTGGCC GAGACACTAC ACTTTTCCCA CAGTGTTCAC AATCCGCAGA 1200
CCAGGAGATT CCCTCAGGTG CCTACGCCAC CAGGGCCCTG GGTTTCAAGC ACAAAACTGG 1260
GCGGCCATTT GGGCAGACAC CAAGCTAGCT GCAGGAGGTT TTTTTTTTTT TTTTTTTCAT 1320
ACCCCAGTGG AGCCTGGAAT GCCGGCAAGA CAGAGCCATT CACTCCCCTG GAAAGGAGGC 1380
TGAAGCCAGG GAGCCCAGTG GTCTAGCTCA GCGGATCCCA CCCCCATGGA GCCCAGCAAG 1440
CTAAGATCCA CTGGCTTGAA ATTCTCGCTG CCAGCACAGC AGTCTGAAGT AGACCTGGGA 1500
CTCTTGAGCT TGGTGAGGGG AGGGGTGTCT GCCATTACTG AGGCTTGAGT AGGCAGTTCT 1560
TCCCTCAGAG TGTAAATAAA GCCACCAGGA AGTTTGAACT TGCAGGAGCC CACCGCAGCT 1620
TGGAAAGCCG CTGTAGCCAC CCTGCCTCTT GAGATTCCTC CTCTCTGGGC AGGGCCTCTC 1680
TGAAAGAAAA GCAGCAGCCC CAGTCAGGGG CTTGTAGATA AAACTCCCAT CTCCCTGGGA 1740
CAGAGTGCAT GGGGGAAGGG GCAGCTGTGG GCACAGCTTC AGCAGACTTA AACATTCTTG 1800
CCCGCCAGCT CTGAAGAGGG CAGTGGATCT CCCAGAACAG TGCTCAAGCT CTGCTAAGGG 1860
ACAGACAAAG TCCTCAAGTG GGTCCCTGAC CCCCATGCCT CCTGACTGGG AGACACCTCC 1920
CAGCAGTGGT CAACGGACAC CTCATACATG AGAGCTCCAG CTGGCATCTG GCGGGTGCCC 1980
TCTGGGACGA AGCTTCCAGA GGAAAGAACA GGCAGCAATC TTTACTGTTC TGCACCCTCT 2040
GCTGGTGATA TCCAGGCAAA CAGCGTCTTC AGTGGACCTC CAGCAAATTC CAACAGACCT 2100
GCAGCAGAGG GGCCTGACTG TTAGAAGGAA AACTAACAAA CAGAAAGGAA TAGCATCAAC 2160
ATCAACAAAA AGGATGTCCA CACAGAAACC CCATCTGAAG GTCACCAACA TCAAAGACCA 2220
AGGGTAGATA AATCCACAAA GTGAGGAAAA 2250
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