| Tag | Content |
|---|
EnhancerAtlas ID | HS190-07378 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr2:136806020-136808400 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU2F2 | MA0507.1 | chr2:136807496-136807509 | AACATTTGCATAT | + | 6.21 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I136048 | chr2 | 136806500 | 136806965 |
|
Enhancer Sequence | GTGCTATAGT CTCAGTTTTT CTGTATATCA GAAACTATTC TTTTTTTTTT TTTTTTTTTT 60
GAGACGGAGT CTTGCTCTGC CACCCAGGCT GGAGTGCAAT GGTGCAATCT CAGCTCACCA 120
CAACCTCTAG CTCCCAGGTT CAAGCGATTT TTCTGCCTCA GCCTCCCGAG TAGCTGGGAG 180
TACAGGCGTG TGCCACCGTG CCTGGCTAAT TTTTGTGTTT TTAGTAGAGA TGAGGTTTCA 240
CCATGTTGGC CAGGCCGGTC TTGAACTCCC AACCCCATGA TCTGCCCGCC TTGGCCTCCC 300
AAAGTGCTGG GGTTACAGGC GTGAGCCACC ACACCCGGCC TCAGAAAGTA TTCTTAAAAG 360
CAGTCTATTA TAAACAAACC AAAACCTGTC AAAAGAAGGG AGAGGTAACA GGATTGGGCA 420
GAAGAAAAAG CTGAATCACA ATGCAGGACC ATGGAAATCT CAGCTAACCC CTGGGGAGCT 480
CTGGAGAGAC TATCGTCCGA CTGTGTTTCC CACATTGAAC GGAGCTGTCT GGGCCTTTAT 540
CCTGCTGCCT CACTCCATCA CTAGGTGTGG ACTATGCCAG GAAGGCACAG TCTTGGGCAA 600
AGTGGCTCTT TCTAGCTGAG GCTGACATTG AAGAAACTGA CAGCTGAAGG CCATCTGTTG 660
GTCACACTCC TTGCAGCTGG GCAGCAAGCC CCTCCTTGAC AGAGAATCTG GGTGGCACAT 720
GTCTGTGTCC ACTACATCAG CAGTGTCTAC CTCGGTGAAT CTCTGTAGTA GACATGGAGA 780
TGTGCCACAG ATGATCTTCA GCAAGGACTT CCTGTTTCAG CTGCTGGGAG GGCAGCCATT 840
CTGATACTGG GAAGGAAGGG CCTAGGCAGG AGAGACACCA GTGAAGATGC TAGGAATTTC 900
CTATCAACCA TTGCAGCCAT CTCACAGTCA CGGGGTATCT GTGACCATGG AAACAATGCA 960
AGAATTTCCA AGAACTATGC TATGGGGTCA TAGTCTCAGG CTATTTATGA AATGCATTTA 1020
TTCTGAAATT GCATGTGCAA GTTGGTTGTT TGGAACCCTA AGTACATTTT TTTTTTCATA 1080
GAAATAGTAA GTAATAGGTT TCCTTGTAAG CCCACAAAAG ACCACAATGT ACCTGAAGTA 1140
TAGCATGATT TCAGTTTTAC CAATTGTTAT TTGTAAAACT GTGTCTTCAC AGAAAGGTAC 1200
ATTCCAGGAA GGGACACGCC TTCCACTATA GGTGGTCATG GATAGATCCA CACAGAAGGC 1260
AGCACTTTAT CTCTGCATTG CAAAAGATAA TCAAGTAAGT TAGGAGCTCT GGATTATGGT 1320
TCTGGTTTGG CTGCTTTCTT AACACTGTTA GAGTGTCTTT TTCTGTTCTG TCAAAGGATG 1380
GGGCCTAAGT AGATCATTTC TAGAGCCCCT TCTGTCTCTA GCATTCTGTA TCTCTCTAGA 1440
GCAGTCATAT AGATAATCGG AATTCAGAAA TAAAAAAACA TTTGCATATA ATAGGGCAAG 1500
AACATGGCTA AACATTCATA TTTGTCTGGG TCTTCTTCAT AGCACAGTAT TGCATAGTGA 1560
CATAATTAGT AAAACTGGGC CTCTGTGCTA AATTGAATGT GGATTCCCCT GCATAGGACA 1620
AAAGGACTCT GTGTTTCTCC AAACGACTGG GCTTTGTTAG ATCAGAACAA TGTCTTAGGG 1680
AATTGGGTGA AGAATGAAAC TTCCCCTCCC TCCAGGCCCT GCTCAAGCTT CCCCTACAGT 1740
AGAAGGCCAC TCCTCAATGC TATAGGAAAT AAAGTTCCTT GTAGTCACAC AAGGCAATTG 1800
GGAGCTGCAT GGGATCTGGG CAGACCCACT CATTTGCCCT GCCCCAGCCT GGTGACACCA 1860
TCACCACTCT TCCCTTGGGG TATCTAAGGG AGGACCTGCA TCAATGCCCT CAATGTATAG 1920
GTTTATTGTG ACCATTTGCT CAGGACAAAG GTGTGTTGGT AATTTGTGGT TGTTAATATT 1980
CACAGTAGAG TATAATTTTG AAACTCTCAT TTCCACATAT AAGCTACAAA TTAAACAATT 2040
TACCACAGTT GTTAGAAGTT TCCATATAAC GTTATTTGTA GGACAATAAT GAATAGACCA 2100
TAGCTACAGT TATCTAGGTC ACAGTCTCAA CTTTGGAATG AAATCCAAGG GTAATTCAGG 2160
TTGGTATCTT GGACTTTGCC TGAGTTGTCT AGGGAATCAG ACAGAGCTGA CATGCTTCAG 2220
AAACATGTAA CATATACTCT GCTTAAATGT ATGGCTTAAA CTCTACTGCC TGAGATCACA 2280
TGAAAATTTC ATTAATCACT GACCTGTGCC ATGTCATCGA GTCTCCTTGA GCTTAATGTG 2340
AGTCATTGAA CCTTGTTTAG CTTCAGTTCT TCATTATGAA 2380
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