| Tag | Content |
|---|
EnhancerAtlas ID | HS188-10870 | Organism | Homo sapiens | Tissue/cell | Th2 | Coordinate | chr6:28393230-28394780 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr6:28394199-28394219 | GGGGAATGGTTGGTTGGTGG | - | 6.31 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGTAGCTGGG ACCACAGGTG TGTACCACCA CACCCAGCTA ATTTTTGTAT TTTTTTGTAG 60
AGACAGGGTT TTTCCATGTT GCCCAGGCTA GTCTCAAACT CCTGGGCTCA GCAATCCTCC 120
TGACTTGGCC TCTCAATGTG CTAGGATTAC AGCATGCCCA GCCAGCATGA TCCTTAAGGA 180
CTCTAGGATT TTCAGCTTAG TAAATGAGCA TTGGCTTCAA CTTCAAGTCA CCAGCTCCAT 240
TAGCTCCTAT CAAGAAAGGC AGACTGTCCT TTGAAGCCAG GCACTGACTT CTCTCTAGTT 300
ATGGAAGTCC AAGATGGTAT CTTCTTCCAA TATAAAGTGT TTCATCTACA TTAAAAATAT 360
GTTGTTTAGT ATAGCCACCT TCATCCACTA TCTTAGCTAG GTTTTCTGAA TAACTTGCTG 420
CAGTGTCTAC ACTAACATTT GCTGCTTCAC TTTGCACTGT TATGTTGTGG AGACAGCTTC 480
TTTCCTTAAA CCTCATGAAG CAACCTCTGC TAGCTTCTAA CTTTTCTTCT GCAGCTTCCT 540
CATCTCTCTC AGCCGTCACA GAATTGAAGA AAGTTAGGAC CCTGCTGTGG ATTAGGCTGT 600
GGCTTAAAGG CATGTTGTGG CTGGTTTGAT CTTCTTTCCA GATCACTCAA ACTTTCTCCG 660
TATCAGCAAT AAAGCTGTTT TGGTTTCTTA TCACTCATGT GTTCAGTGGA GTGGTTTTAC 720
TTCCTTCAAG AACTTTTCCT TTGCATTCAC AACTGGCTGT TTGGTACAAG AGGCCTAGCT 780
TTCAACCTAT CTCAGCTTTC AACATGTCTT CCTCACTAAG CTTAATCATT TCTAGCTTTT 840
AATTTAAAGA GAGAGATGTG AGACTCTTCC TTTCACGTGA ACACTGAGAG GCCACTGTAG 900
TGTTATTAAC TGGTTTCATT TCAACACTGT GTGTCTCAGG GAATAGGGAG GCCTGAGGAG 960
AGAGAAATGG GGGAATGGTT GGTTGGTGGA AGAGTCAGAA CACACACCAC ATTTATCAGT 1020
TAAGTTAGGC ATCTTATATG GGTGTGGTTA GCGGTGCCCC AAAACAATTG CAAATTACAT 1080
CAAAGATCAC TGATCACAGA TCACCATAAT AGATATAATA ATAATTTTAA ATTTTGAAAT 1140
ACTCATTTAC CAAAATGTGA CACAGAAACA CGAAGTGTGC ACATGATGTT GGAAAAATGG 1200
TGTTGACAGA CTTGCTTGAT GCAGGGTTGC CACAAACTTT CAATTTGCAG AAAACACAGT 1260
ATCTGTGAAG TGCAATAAAG CAAAGTGCAA GTAAAATGAC ATATGCCTGT ATAAGTCAAC 1320
TTCTCTGTGC CAAGAATTGT GCTAGATGAT TTCAAAAGTT TGTCTGTTTG TTTGAGACAG 1380
AGTTTTTTCT CTCATTGCCC AGGCTGGAAT GCAATGGCGC GATCTCGGCT CACTGCAGCC 1440
TCTGCCTCCC GGGTTCAAGC CTCCCAAGTA GCTGAGATTA CAGGCATGTG CCACCACACT 1500
CAGCTAATTT TGTATTTTTA GTAGAGACGG GGTTTCACCA TGTTGGTCAG 1550
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