| Tag | Content |
|---|
EnhancerAtlas ID | HS187-00671 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr1:40131910-40134110 | 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 | chr1:40133817-40133837 | GGGTTGGTGGTGGAGTGGGG | - | 6.63 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 40132600 | 40133600 | | chr1 | 40133600 | 40133926 |
| Enhancer Sequence | GCAGAGGTAT GGGAGAAGGG GTTGTCACTC AGATGACTGC CCCTGAGGCA GGCTCACATG 60
TGTGAGTCTC CCTGGGTAGT GAGGACATGG AGAAGACCCA GACCCAGTCT CTACCTAAAG 120
AGGCCCAGCC TTGAGCAGAT GTGGACTTAG GTCAGGACCC CATCTATGAC GGACCCAGAT 180
GGGGGTTGAG AGAGGTGCTG GCTCCCTTGC TGGAAGCACA ATCTGATGGA GGGAGGGCCA 240
TGCCCTTGGG AGTTTGCAAT CTAGCCAGGC ATCTGGACAC AAGAAAAAAA TGAAGCCAAT 300
GTATGTGGCC AACGTGTGAC TGATGCTGGA GATGATCTCA GTTGGTTTCC ATTGTAAAAT 360
AAGAGCTGCA TGCCCTTAGG AAGAAATGAT GCCCATAAAT ATGACAATTT ATATAAAAAA 420
TGTATCTGCA ACCCAGATCT GTCTCCTGAG CTCCAGATTC ATACATCCAT CTAACTGCCC 480
CAGTTGACTA ACAGCCTCTC AAAGTTAACA TTCCCAAGGC TGAATTCCCA TCACCTTCTC 540
CCCTCCCAAA CCTGATCCCT TCTCCCTGTA ACTCATAGCA AGGCTTAGAA CCACTATCCA 600
CTCATTACTG AAGCAGAAGC TGGGAAGTCA GCCTCAACTC CCTTCCTCAT CAATCGATTA 660
CCGAAATGAG TCAACTCTAC TAGAATCCAC CCACTTCTTT CGTTCAGGCC ATCATCATCT 720
GTCACATTCT CTAATCTGTC ATTCATGCTG CTGTCAGGGG ATTTTTCTAA AGTTCAGATC 780
TGACCACAGC CCCCCTCTTT AGTGGTGCAC ACTATTCTCA GAATATGGCT GGCAGCCTCT 840
AGTGTGGAAA TAGAAAGCCC TTCACAACAG ACCCCTACTT CTCTTTCCAT TCCCCTCTTC 900
CAATCCCCTA GCTTTGCCCC ACCTGGGCTT TCTCACATCA GGTCATACTT TCCCCCTCTT 960
TTTTTTTTTT TTTTTTTTCT GAGATGGAGT TTCACTCTTG TTGCCCAGGC TGGAGTGCAG 1020
TGGTGTGATC TCAGCTCACT GCAACCTCCA CCTCTCAGGT TCGAGCAATT GTCCTGCCTC 1080
AGCCTCCCAA GTAGCTGGGA CTATAGGTAC CCGCCACCCC AGACAGCAGC TGGACCTTTA 1140
TAGTCCCTAG GGAGGATCAG AATATGAGTG CCCAAGGGAT TTACAGATAC CCAGAGAATC 1200
CCACCACATC TCTGTGTCCT GAGCAGTCCT GGGGTCCTGA TTCCCACTTT ACAAATTAAA 1260
AATGAGGGGC TCAAATTGAG GTCAAGGCTC ATAAATGCAC CTTGCATTCT TGCCTCTCCT 1320
GATCATCCGT GGGTCATGTA CTCAACCCCA TTTCTTCTTC CTGGGGTCAG TCCTGGGCTC 1380
CAATCAGTTG ACAACATTGA GTGGTTACCA TCTGAGAGAC ACCGTGGTGG ACATGGCAGG 1440
AAACAACACA AGTGTGATCC CTGTCCCCAT GGAGCTCATG ATCCAACCCC AAGACAGAGG 1500
CCAATGCCAT CTTTTAAAAG AGCAATGTCC AATGGAACTT TCTATGATAA TGGAAATATT 1560
CCATAATCTG TGCTCTCCCT GTGGCTGTGG AACAATTTGA AATGTGACTA ATGAGACTGA 1620
GGAGCTGAAT TTTAGATTTT ACTTCATTTA AATGAACTTA AACAGCTATA CGTGGCTAGT 1680
GGTAAATGCA GCTTTAGAAC CTTATAATAG GAGTGGAAGA CAAAAGAGTT CCCCAAGGTC 1740
ATGTGGTAGA CCTCAGTTTG CATTTGACTT TTAACCCCAA CCAAGATGGT GTATGTGGCC 1800
AGCAAGGTCT GCATAAGGCA GTGGCAGGAC AGGTGCTTCT TCTTGGAGGT TCAACCCAAA 1860
TACCTTTCTC AGTTGCTGAC TACCACCATG TGTGTGTCCT AAGGGTGGGG TTGGTGGTGG 1920
AGTGGGGAGA CCCACTCTCA TAAACCCTGG AAGCCTGGAG GCCTTTGGAA CAGGAGCTGA 1980
GCTTGCTCCA CCCACTGGGC TTACTGCCCC AGGGACAGGG CCATCACCCC TCTAAGGACA 2040
GAGAGTCAGC TGCCCTCCCA GCCCCATTAG GCAGGTTCCC AAGCCTGCCA CTCCAACCCT 2100
GGCAGCCAGC TAAGGTCTCG CTCCTCACTT TCTGTCCCAC AGTCCCTGCC AGACTGCCAA 2160
GTCCTGGGCT CCCTCTGGCT GAGCTACCCA GACAGACCCC 2200
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