| Tag | Content |
|---|
EnhancerAtlas ID | HS023-22613 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr6:170266950-170269910 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr6:170268974-170268987 | TATTAATTAATTA | - | 6.25 | | Lhx3 | MA0135.1 | chr6:170268977-170268990 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr6:170268981-170268994 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr6:170268985-170268998 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr6:170268989-170269002 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr6:170268993-170269006 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr6:170268978-170268991 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr6:170268982-170268995 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr6:170268986-170268999 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr6:170268990-170269003 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr6:170268994-170269007 | AATTAATTAATTT | - | 6.92 | | NKX2-3 | MA0672.1 | chr6:170267674-170267684 | TTCAAGTGGT | - | 6.02 | | POU6F1 | MA0628.1 | chr6:170268975-170268985 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr6:170268979-170268989 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr6:170268983-170268993 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr6:170268987-170268997 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr6:170268991-170269001 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr6:170268995-170269005 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr6:170268975-170268985 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr6:170268979-170268989 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr6:170268983-170268993 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr6:170268987-170268997 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr6:170268991-170269001 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr6:170268995-170269005 | ATTAATTAAT | - | 6.02 |
|
| | 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 |
| GH06I169868 | chr6 | 170268218 | 170269370 |
|
Enhancer Sequence | TGAGCTAGGT GCTGTGCTGG GTACACGAAG CTACCTTCTT CCTGAGCTAG GTGCTGTGCT 60
GGGTACATGA AGCTGCCTTC TTCCGGTGCT AGGTGGTTTG CTGAGTAAAT GTAGGTACCC 120
TTTGTGTGAC AGGTGTTGTG CTTAGTAAAT GAAGGCGTCT ACCATGTGTT AGGTCCTGAG 180
CTGGGTAAAT GAAGGCAGCC TCTAATAGCT CAGACCTGTG CTGGGTAAAC GGTGATAGCT 240
TCCCCGTGCC AGGTCCTGTG CTGGGTAAAT GAAGGCAGCC TCCAATAGCT CGGACCTGTG 300
CTTGGTAAAT GGTGATAGCT TGCATGCACC AGGTCCTGGG CTGGGTGAAT GAAGGCAGCC 360
TCCAATAGCT AGGTCCTGTG CTCGGTAAAT AGCTTCCCTG TGCCAGGTCT TGTGCTGGGT 420
AAATGAAGGT AGCTTCCATG TGGTAGGTGC TGCGCTGCGT AAGTGAAGGT GCCTTCCACG 480
TGCTCGGTCC TGTGCTGGGC ACTTGAAAGT GTCTCCCACT CGCGAGGTGG TTTGCTTAGT 540
AAATGAAGGC CCCTTCCACG TGCTGAGGAA ATGACACTGC CTTCCACGTG CTGGGGAAAT 600
GAATGGTACC TTTTATGTTT TCAGCCCTGG GCCAATTGTA TTCAAATATT CCGTTTTCAT 660
CTTTTTAGCA ACCATGGAAG AATACAAGTA TTTCCATTTT ATATGCAAGG ACGATGAGAC 720
CAACTTCAAG TGGTGAAGTT GGTACAGATT CCTCTTCTAT CAGGCCTGTG AGGTTTTGTG 780
TGAAACCCTC ATGCTTTATA CACAGGTTTT GCTGTCCTGT GGTTGTCCAT CAGGTTCTGG 840
GAATTCTGAG CTGGAATGAG GCACTCCAGT AGCGTCTTCC CAAGGGTAGA CCACACAGCA 900
CACGAAGCCC ACCAAGCCTG CACCGCCCAC ACAGCACGGC CCCTCGCTGC AGACCTGCTG 960
CCCTTGTGGG TTTAGGCCTG GTGCTCCCCT CTCACAGGGC CGTGCCTCAG ACCCCACATC 1020
CGCGCTGCAA CCTGGAATGC ACCTGCCGCA TGGTGTGAGA GGCGTTTTGT GGGAGACGCC 1080
CAGGGCAGTA CCTGCACTGG AAAATACTCA GTGGCTACTG GGCCATGCTG AGGGGCCTTT 1140
AGGACATGGA GCTGGAGCTG TGGAGGGCTG GGTTTTGGTC CCATTTGACT CTCCCCCATG 1200
CCTCATCCTG AAGTTCTTTA ATCTTGGTCT GATGTTTAAA GTTGGGACAG CCCCTCCTGT 1260
GACCTCGGAG GGTTCTGGCA ACCAGGTGAG CTGGTGTGTG TGTGGGAACA GCATGGAGCT 1320
CTGTGAAATA TCAGGCGTCT TCCCCGCCAT GGGGCATCGT GGTCAGTGTG TTGTAGGGTC 1380
AGTTGACCAC TTGGACACCT GGTTATGACC ATTTCAGCCT CTTTTGGAAA CATTCTGCTT 1440
TTATTCCCAT TGGCAAACAA ACTTGCTCAG AGGTTTTATG TGACAAGCTA CAGGCAGCGC 1500
TGGAGTGTGG TGTGCCAGCA TGAGAGGGTG TGAGCAGGGG GCACGTTTTC TCTGGAATCG 1560
TGCATTATAG GAATAAATCA TGTGTGTGTT TGCACCTTCT CACCCCTATG TGAAGATGAA 1620
ACTTTAGTGC TTGAGGTTAA AAAGTGTCCT CATGAAGGAG TCTGGCTCTT TCCGCCCTGG 1680
TCTAGAAAAC AGTTTCCCGT GAAGGACCAG GGACTACAGA TTTCCGGCTT CGGGGCCCTA 1740
CGGCCTCCAC CCCCGCCATG CAGCTCTGCA GCTGTAGCCT GAAAGCAGCT GCAGCTGCCG 1800
CGCGTAAGGG GTGGCTCTGG GCAGGAAACC ACGTGCGAAC CGCCCCACGG CAGGGTGCGT 1860
CCCACAGAAG GAGCAGTGTG TTCCGTCCCG CTGCACGGCC TGCGAGGGAT TTCCATGGTG 1920
AGGGTGAATC ACGAGGGCTT CTTGTGGCCT GGTCTGTCTT ACCTGCCTCT CCTTCATGCA 1980
GGCTATTTTT TTTTTAAGCA AGGAAAGAAT AACTTTATTG TAAGTATTAA TTAATTAATT 2040
AATTAATTAA TTAATTTATT TATTTTTGAG ACAGAGTCTC CCTCTGTCGC CAGACTGGAG 2100
TGCAGTGGTG GGATCTTGGC TCGCTGCAAC CTCCACCTCC CGGGTTCAAG CAATTCTCCT 2160
GCTTCAGCCT CCCGAGCAGC TGGGACTACA GGTGTGTGCC ACCACGCCCA GCTAATTTTT 2220
GTATTTTTAG TAGAGATGGG GTTTCACCAT GTTGGCCAGG ATGGTCTCGA TATCTTGACC 2280
TTGTGATCCC CCCCTTGGCT TCCCAAAGTG TTGGGATTAC AGGTGTGAGC TATGCGCCCG 2340
GCCTATAAGC ATTTATAAGC ATTTATCTCC AACTCCAAGG TTGCCATATT CAGTGATATA 2400
AACATTGGTT CTGGATGGTG GAAAATGTTA TGGCTGTGGG ATAAATTTAT TATTAAATTT 2460
ATTCAGACCA GAGGGAAGGT GAAGCCCATG TCTCCTCGCT CTTCCCCACG GGAAACGGAG 2520
GGGGGCTGCC CGGGAAGCTC CATGGACATC TTCCTGGGGC CCTGGAGAGG CACGGCTGGC 2580
GGGAGGCAGT CACTTCCAGG CTGTGGTGTG ACCCAAGATA TTAACACAGG CCCCGTGTGA 2640
GGCTCAGCTG TCTACCCAGG CAGTGGAAAA GGATTTTTCA ACAGAGACGC CGCAGACATG 2700
GGGCTTTAAA AGATTTCAAG TCTCGGATGG GTGTGGTGGC TCATGCCTAT AATTCCAGCA 2760
CTGTGGGATG CCAAGGCGGG TGGATCACAA AGTCAGGAGT TTGAGACCAG CCTGGCCAGT 2820
ATGGTGAAAC CCTGTCTCTA CTAAAAATAC AAAAATTAGC CAGGCATGGT GGCGGGCGCC 2880
TGTAGTCCCA GTTACTCGGG AGGCTGAGGC AGGAGAATGG CTCGAACCCC GGAGGCAGAG 2940
CTTGCAGTCA ACCGAGAATG 2960
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