| Tag | Content |
|---|
EnhancerAtlas ID | HS182-19446 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr6:170461800-170464570 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Sox6 | MA0515.1 | chr6:170461843-170461853 | CCATTGTTTT | + | 6.02 | | Zfx | MA0146.2 | chr6:170461990-170462004 | CGCGCCCAGGCCTC | + | 6.1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 170463024 | 170463652 | | chr6 | 170462600 | 170463510 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I170147 | chr6 | 170462375 | 170464090 |
|
Enhancer Sequence | AGCCTCAAAA ACAATCGAGG GCACAGGAGA AGTCACTGGA GAGCCATTGT TTTATTTAGG 60
AAACAAACTC TGAAGCAGGC CCTGCTGCTC CCCAAAGATG TGCCCACTCC AAGGACCAGA 120
TTCTCAACAC TTCACCTCTT CCCTGACAAA CACGAAGTGA GAGTCACCCC CTCTGCCAAG 180
ACAGAGGGGT CGCGCCCAGG CCTCTGCTCC AAGCAGCAAT GTCAGGAAGG TCTGGGCTGT 240
GGCAGCTGAG GGAGAGCTCG ACACCCACTC CCTGGACACC AACCCAGACG GCAGCCAGGC 300
CTGCGGAGGC AGGGCCAGTC TTCGGGGGCA AGACGCGGCA TGGAGACTCT GCACACACTT 360
AGTCCAAAGG TTGGCTGCAG AATGTTAAGG TCCCAACAGG ACAACAGGGG CAGGTGTCGG 420
CACAGGAGGG TACCGAGCTC GGAGCAAGGC CTCAGAACTG GGACTCCAGT TTCTCTCCCG 480
GGGAAGAAAA GGAGGCGGCA CCGATCCGGA CAGATGAGGG CCAGGCAGCA GCATCCTGGC 540
ATGACCGCAG CAGGAGGGAG GAGCCAACGG TGCCACGTGG TTCCCAAATG CCAAGCATAG 600
CCTGAGAGAG GAGGAAACAG GAGAGAAGGG GAGGCCGGGG GGCCGCTTGG TGCCCAAGAT 660
TTCTCAGACG TCCCAGAGCC CTGACTCTGC TGCCAGCTTG CTTTACAGTG AGGCCAAGGA 720
AGGAGCCACG GAGGGTGTGC TGGCCCTAGG AGCAGGATTC CTGTGTGTTC ACTAAGCTTG 780
CAGCATCAAG AAGCCACCAG CCAGCATGGA CATGTGAGCG TCAGAGGGTG AGCAAGGCAA 840
CAGCCAGGAC CAGGTGGAGC CAGGGGCCCC GCAGGTGCAG CCAGGACGGA CATAGGGAGA 900
CCTTGGTCCC AACAAGGGCA GTGTCTCGAT GGCCAGGCAG GAGTGGGGAC GCTGTTGAGA 960
AATGTTCTCC ACAGCAGCTC AGGCAGCAGG AAAGACCCAG CCATCAGGTC AGCGCCGTGG 1020
TCTCCCAGCC AGCGTGCGCA TGGCTGCAAA TAGAGAAAAA CACACCAGGA GGTCACACCC 1080
AAGGTCACTG CCGATCCCAG CACAGGGAGC CCCTGGCAAG GCCATTCCTG TGCTGGGCTA 1140
AGCCAACGCT GGACTCTGAT TCAGCTGACA GCCCACAGGA GCTCCGTTTC TAGTGTTGGC 1200
AGCAACGTAT CATCGCTCCA GCTTTGACTA AAACTGAAGG TTCCGATCAG TATTGTGTTT 1260
CCAGTTAAGT ATGAAATGAA GGGCAGGGCA CAGGTCTCTG CGTGCCTCTC CCACAGCTCG 1320
TGTGGGGCTG CTGCTGTGTG TGGGGAGCGG ACGCTTCCTC CTGAGCCGAT TCAAGCCTCA 1380
GTTGTGACCA GGTGTGAAAT TTCCGAAGTT CTCATTCAGA GAACCAAGCT TTCGCTTCCA 1440
TTTACCCCCC GAGCTCGGCC CTGGACACGC CTCTAGTTTT TACACCCCTC CAGGTCCCAG 1500
GTCTCGCCCC GATGGTGCCC AGAGACTGCT GCTCTCCGCT GGTTGGGCCC TAAATCCACC 1560
CTTCAGTGTT TGGCTGGCGC TTGCTGGCTC TGCCGGCGTC TCTCCAGCCA GCAGGACAGC 1620
TCTGCCGGAA GCCCCATCCC TCCTCCTCCC CATCCTGTCC CTGAGCCGTC AGCCCTGGTG 1680
GCCGCTTTGA GGTGTGGGCG GGTTCTCCTC TCCTCCGCAG ACCCCTCTTT AGCTGCCTGT 1740
CTGGGCCAGC ACAGGATGTG GGCGCCCCGT GACACTCTCT TCTGTGCCAG CCCACTGGCC 1800
CACACTTCGA CCTCCTTCCC CACTGAGACA GCTTCTCCTG TTTATTTTTT ACCATTTTGT 1860
GGCTCCCACC AACTCCTTCT GCCTTCTACC AACACGTACC CCAGGCCCAG CCAGCTGGAG 1920
CCCGTGCTGC AACCCAGCCA GGATTCCCTT TCCTGACGCC GCGGTGCCCA TCTGCCTCCA 1980
CCGATGGATC TCACAGGCAA TGCCAGGCTT GGTTATACTT CACACAGACA ACCATAGCAC 2040
ACCTGCCTGA AATCTCTCCT GTAAATTCCT AACCAATTTG AGGCTCAGAT TTTTTTTAAT 2100
TTCCCAAGTA TCTACATATA ATAAGTCAGA AGTAGAACTA CCTAAGTATT TTTTTAAGCA 2160
GCTGAGATGT AGGAGGAGTG TGTTTGTCTA CACAAACAGA GGGACATCTT CCCCAGGTGC 2220
GTTGAGGTAG GAGGCCACCC CGCCGTGGTG CGAGTCTCTC CTGAGCTGCC CAACGGCCAC 2280
TTCTTTCCAG GCAGAGAGCA CCTGTGCACA GTCCCTATGC ATTTGCGAGA AAGAGCGAGG 2340
GGGCCGTTCT GTCACCTGCA GTCCCCCACG TGGTCTTGAG GCAGTGGACA CACCAGGTGA 2400
GCATTAGGTG GGGGAGGGGT GAAGAGCCAC TGTCCCCACC AAGACCAACA GGAATGCAGA 2460
CTGAGCTCAG GAAGCTGCTG CCTGCACATG TCTACTCATC TTTCATTTAA AAACCACGCA 2520
GGAGGGAAAA CAAAACACTC ATGGGAAGAA GCGGGACCAG GCTCCAGCCG CAAAGTCGCC 2580
CTTCATGCTT CACGCAAGAA AAAGGCCTCA GAGGGTAAGG GCAGGGCGTG GGACAACACC 2640
CACCCCACAA GCCTGCTGCC CCTTCACTGC CTGCAGTGTA CACAGAGCCT CACCCCCGAC 2700
CACAAGCCTG CCACCTGCCA CCCCTCCACT GCCTGCAGTG TAGACAGAGC CTCGCCCCCC 2760
ACCACAAGCC 2770
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