| Tag | Content |
|---|
EnhancerAtlas ID | HS190-00034 | Organism | Homo sapiens | Tissue/cell | Treg_cell | Coordinate | chr1:6452130-6453310 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr1:6452272-6452287 | GAGCCCAAGGTCAGT | + | 6.17 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGTAAGGAGA GGCCCTCGAC CAGGCCAGAA GATGAGACTG AGAGTCAAGA ATCGCCATAG 60
ACCCAGGACT TGCTATATGC CCAGCCTTCC TGGAGATGTC AACATCTACA GGAAAGTAAC 120
TTGCTTCTAT TGGACTTGGC TTGAGCCCAA GGTCAGTCTG TGATGCCCAA CCCCCAAATG 180
TGAGGAACCC ACTACCAAAA CAGAAAGCAG CTCTCACTCC TGGTAGTTCA TCAAGCAGGA 240
TAGGACCGGT CGCAGGCCAC AGAGCCTGTG TGCAGTGGCT GAAAACCTAG ACTCCTTGTC 300
CTCACTTAGC TCATGCACAA ATGCCAGCCT GCTGCTTCCG ATTCTGCCGA AGAGAACTGC 360
AGAGTAACCT TCAGGCTGCC CTCCCCACCT CCTATGGGAA ATGAGCTTGT TCATGATCTC 420
CAGCCTCCAG CTTCCTCTGG GGGCCTGCAT CTATCTACTC AGTACCTGGT GGAAGAAGAG 480
GGGGTGCTCT AGAAGGACAA CCCTTTGCCT CTATTGTGTA AGATGCTTTC AGGCCCAACA 540
GACCACTGAT TCCCTTTTCT TCATAGTAAA CTGTTAGAGG TAGACAGTAT TATCTGTTCT 600
TCCTTTCAAC ACCTGCCCTC CCCCAAACCG AAGCAGTGCA CTGAAGACGG TAGCTCTGCA 660
ACCTCCTCCC ACAGGGGCAC CCACCGAGGG GCTCGCGCGG CTCTGGGCAC CTCCCCTCCA 720
CCTCTGGGGG CTTTGGTTAG CGCAGCACAA CCGCCGAGGT AATGATCCCG AATCCTCGAG 780
GAGGCTAAGC AGGACCACGG GGCTGAGGCT CCGGGATGCT CGGGCGAGGC CCGAGGCGGG 840
GCGGCCCACG GGCGCCGGTC GCCGGGCTCT GGAGCTGTGC ATTGACCTCC GCCCGCCCCG 900
TCCCTGCCTG GCTTTCTCGC CCAAACGGCC CGTGGCGCGG CCGCCGCCCT GGAGATGCGG 960
CCAGGAGGAG CCGGCTGGAG GCGGGCGGGG GCCGCCCGGC TTGTGCGGCA TCGCGAGTCG 1020
CATCCCGGCC GGGCGGGCGT CCGGGGCGGC GGCGCGGAAG GCCGTGCGGG GAATCGGCGG 1080
GCGGGGGCGG CCTCGGCGGG TGGGGACCAC AGAGCCAAGC GGGGCAGGCC TGGGGCGGTG 1140
ACCGGCGCGC CTGGCCGCTG CAGGCTGCGC GCGGGCCCTC 1180
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