| Tag | Content |
|---|
EnhancerAtlas ID | HS062-02804 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr11:47661420-47663930 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr11:47661464-47661479 | AGTTAATGATTACCA | + | 6.21 | | HNF1B | MA0153.2 | chr11:47661465-47661478 | GTTAATGATTACC | + | 6.03 | | Nr2f6(var.2) | MA0728.1 | chr11:47661664-47661679 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAAACACAGG CTGTCATTAA CAGCTAATGA AGTCCATTTT ATATAGTTAA TGATTACCAT 60
GGTCTTTGTA CAATATACCC AGGATTTTTA ACACTACAGA TACTTGACAG AATGAATGCT 120
GTAGGACATA GTTTTGATTA TTGTTGTGAC TCTTAATCTG TCCTATTAAG TAACTCCTGG 180
GCTGGCGTGG TGGCTCATGC ATGTAATCCC AGCACTTTGG GAGGCCAAGG TGGGCGGATC 240
ACCTGAGGTC AGGAGTTCAA GACCAGCCTG GCCAACATGG TGAAACCCTG TCTCTACTAA 300
AAACACAAAA ATTAGCCAGG TGTGGTGGCG GACACCTGTA ATCCCAGCTA CTCAAGAGGC 360
TAAGGCAGGA CAGTCGCTTG AACCTGGGAG GCGGAGGTTG CAGTGAGCCG AGATTGTGCC 420
ATTGCATGCC AGTCTGGGTG ACAAGAGCAA AACTCCATCT CAAAAACAAC AACAAATAAA 480
TAAACAAATA ACTCCTGTCT GAGCTCCCTG AAAGTGCTAC CAAGTAACCA TTTTTATTTT 540
TATTTAGTTA GTTATTTATT TTTTGGAGAC AGAGTTTCGC TCTTGTCGCC CAGGCTGGAG 600
TGCAGTGGCA CGATCTAGGT CACTGCAACC TCCATCTCCC AGGTTTAAGC CATTCTCGTA 660
CCTCAGCCTC CTGAGTAGCT GGGATTACAG GCACCCACCA CCACACCCAG CTAATTTTTG 720
TATTTTTAGT AGAGAGGGGG TTTTGCCATG TTGGCCAGGC TAGTCTTTAA CTCCTGACCT 780
CAGGTGAACC GCCTGTTTCA GGCTCCCAAA GTGTTGGGAT TTACAGGCGT GAGCCACCGT 840
GCCCGGCCCA AGTAACTATT TTTACAACTG AGCATTTGGG AATTTCACCA AAACTCCTGG 900
GCTACTTGGC AACACATAGA TGTTGTGAAA TCAGAATTAA GAATATTCAA AGTTTTTGGG 960
GCAAGAGCTC TGAACATCAT TAGAAAACCC CGTCTCCCAG AGAAGTATTG AGTAGTGGGT 1020
TCTTTTTTGT TTTGTTTTGT TTTTTTGAGG CTGAGTTTTG CTCTGTTGCC CAGGCTGGAG 1080
TACAATGGCG CGATCTCGGC TCACTGCAAC CTTCACCTCC CGGGTTCAAG CGATTCTCCT 1140
GCCTCAGCCT CCCGACTAGC TGGGATTACG TGCACGCACC ACCACACCTG GCTATATTTT 1200
GTATTTTTAG TAGAGACGGG GTTTCACCAT GTTGGTCAGA CTGGTCTCAA ACATCGACCT 1260
CGTGATCCGC TCACCTCGGC CTCCCAAAGT GCTGGGAAGG CGTGAGCGAA CGCGCCCGGC 1320
CCCAAGGGTT CTTACTATAT ACTGCAACAT GCTGTCACCT CCGATGCTAT CTAGCCCCAA 1380
ATGTGCCAAT TCTGTTTTGG ATGTTACAGT ACATTCTAAT CAGTCTTTGT TCTAAGTACA 1440
AAGAATTTAT TTGCAATAGC CTTTAACATA TGGAATCTGA ATTCACACAG GTCTACTCAG 1500
CAAGAAATAA TTTGGATTCC CAACAACTCA AGAATAAGAA ATGGGGCCCT CTCTAGTGTC 1560
TTGCCTATTT TTTACAGAAA AGTAGACGGC GAGACAGGGG TTCTAAAAAC TGTTCCATTC 1620
CTAGGCACAG TGCATGAGGT AATTATGTCA ACTCTCAGTA AAAGCATAAA AAAAAGAATG 1680
ACCTGCCCAT TACAGGGATA TAGCAAAGGA ACTGGAAACA CTAAGTCTAT CACTTACTTG 1740
GCCTACCTGC ATGTGAATAT AAAATACCAT GTAATAATTA TTTGACAGTA GATTAGAAAC 1800
TAACTCCCAT GTTTAAACTC GCTAAAACTC AGCTTCACTA ATTTCCAGCT CTGACAAATG 1860
TGATTTTCAT TGTCAGGAGC CACATGGGCC GCTGCTGGAA AGCGCTCAAT GCATCCTTCC 1920
GAAATCTGAC AGAGCAACCC CTTCATTAAC ACTTCTGAAT GAGCTCCTTG TGTTTCTCTC 1980
AGTATCTGGT GCGAAAACCT CGGAACAGAA AAGCAGTAGT AACAGTAGCA TAAAAAGAAA 2040
AAAAAAAGGA ATAAAAAATA AAATGTTGGT TCCCACCTAA CTTCACATTT GTCTTCAACT 2100
GAGTATTTCG TGTTTTGCGT CTGAGATTTT GGGGGGAGTA GTGGTGAATG TGAATTTCGG 2160
AGGGGCGAGA GGGAGGGTTC GGAAGCCTTT GGTGGCGACC GGCCAGGATC CACCTCAGTG 2220
ACGAAGAACC AAAGTTCAGA GGATCCGCCG GGCAGGGCAG GGCCGGGTGG CGGTTGGCTA 2280
AGGGAGGAGA GGGCCTCAAC GCTGGGCGGC GAGGCGAGGG CTCGGCGAGG CCCCCAAGCG 2340
GGGCCGCGGG ACTGAGGAAG CTGTCCCTGC GGGGAGGTAA AGGGCAGCGG AGGAGCAGCA 2400
GCATCTCGGG AGAATGAAAG GCCCGCAAGG CTGAGCCGAT CCTCAGGCGC CCTGAGCAGC 2460
AGCGACCGAA CGGGGCGCCG GGCGGGGTAG GGAGCGGCGA CGCCTCATAC 2510
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