| Tag | Content |
|---|
EnhancerAtlas ID | HS182-00096 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:7530600-7532820 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr1:7532701-7532712 | GACAGCTGCTG | + | 6.14 | | Tcf12 | MA0521.1 | chr1:7532701-7532712 | GACAGCTGCTG | + | 6.02 | | ZIC3 | MA0697.1 | chr1:7532183-7532198 | AGGCAGCGGGGGGTC | - | 6.09 | | ZIC4 | MA0751.1 | chr1:7532183-7532198 | AGGCAGCGGGGGGTC | - | 6.13 | | ZNF263 | MA0528.1 | chr1:7531906-7531927 | CCTTTCTCCTGGTCCTCCACC | - | 6.09 | | ZNF263 | MA0528.1 | chr1:7530737-7530758 | GGAGGAAGGAAAGGAAGAAGT | + | 6.33 | | ZNF263 | MA0528.1 | chr1:7530726-7530747 | GGAGGAAAGAGGGAGGAAGGA | + | 6.36 | | ZNF263 | MA0528.1 | chr1:7530734-7530755 | GAGGGAGGAAGGAAAGGAAGA | + | 7.83 |
|
| | 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 |
| GH01I007468 | chr1 | 7528671 | 7533504 |
|
Enhancer Sequence | TCAGATGCCA GCCCCGAGCC AGCCTGGTCC TCTGAATGCA GGAGGCACTA GGAAAGGGAG 60
TGATGGGCTG GCCATGCTCT CTCAGCCCCC TGCAGGGGGT GAGCCTTCTA GAAAGGTAAG 120
GGCATTGGAG GAAAGAGGGA GGAAGGAAAG GAAGAAGTGC TTCTGGAAAA AGGAGACTTT 180
CTCCAAGGAA TAGCACCCAC TGCCCCACCT TTGTAGCCTC AGTTCAGTGG CCGCCTCCTG 240
CCGGCCCACT GTGAACTCGC TCCTGCCCTC TGAGATGCTC CAGCTGATGT CACCCAAGGC 300
CACTTAGCAC TTAGTGGGCA CGTCTGCCTA TGTTGGCCTC GATTTTCCTC TCCAACTAGT 360
CAGCTCCCAA GGGAGAGACA TGAATTCCTG TCTCCCCTGA GTGCCCAGCC CAGAGCCACA 420
GCCACCACAG GGCAGGAGCC AGCATTTGGG AGAGCCATGT TCTGCTGTGG TGACGTATCC 480
ACCCCGGGGC GGGAATGAGC AGGCCTCGCA GACTCGGGGC CTGGAGCTCA GGATTGGTGC 540
CAAGATTTAC AGAGAAGGGC CTGAGTTGAC GTGGCACGTA AGCTTCTGAG TCATCGGGCT 600
TTCAGGGGAG GGTGCTACCT CTCTGTCTGT GTCTGTCTGT CTGTCTTTCA GGCTCTCTGT 660
CTCTCTCTGC GTCTCTCTCT GTCATGTTCT CCCTCCCCAT CTCTCCATTG CTGACAAATA 720
TTCTATTAGG CTATGAGCGA GGAGACGGGC AGGGAGCCTC TCACAGGCAG GGCACTAGAG 780
CCCATGTGGC CCATAGGCTC ATAAAGCCAT TGGCATGACC AGTAACCACC ATGTGAGGTC 840
ACCAGGACAG CTGGGGAGGG ACCAGATGAC CTGAGCTCAG CCCACTCCAG CTGGGCAGGG 900
CCAGAGCCAT GACCTGGAAG AGGCCACCTC TTCCCCTCTG CTGGTGGCAC CCATCCTCAG 960
CATTGCTGGG GGCTCTGTGT CACAGCTGAC AGGGCCTTCA GGCTCCCCTG AGCCTACCCA 1020
GTGCATTTTC TAGAAGGATT TCTGAGACCC AGCGAGAGCA GGGCCAGGCC CAGGTCACCC 1080
AGTGGGTCAG GGGAGGAGCA GGCAGTGCTC CGTTCTCCCG ATGCCTTGGC CTCTGCCCCT 1140
ACCGCCTGAT GTGGGTGTCA CTGCAGCCGC AGGACCCTGA GCCTCGTGAG GTAGAGGAGG 1200
CATGAAGGGG TGAGCTGGAC AGAGCGGTCC CTCCTGTTTG GGATTTTCTG ATGGTTTCGA 1260
GGGGTAGGCA GCAGAGGTTC AGGGCCCCCT GACCTCCTCA TGTGCCCCTT TCTCCTGGTC 1320
CTCCACCTTC CGTCCTTCTC TGCATTCTCC GCCTGCCCCC GCAGGGGACC AGGCCCCCAT 1380
TCCAGGCCAG ACTTCCCTGC AGATTCTGTA TGGCTCATTT GGAAACTATT TCTGCTTCTA 1440
ATGAGTGTTT TCCTTTGTGC CCTTGTCCTC TAAAATGCTT AATGACTGCT TTCCGTGCTC 1500
GAGTGAAGCG GGGGTGTGTC CCCGCATGGC TGCCATTGCC AGGCCGGAGC TGTTTGGCTG 1560
CCAAGCCCGG CTTGCTTGGG TGGAGGCAGC GGGGGGTCCT TCCTGGCCCA CGCTGGCAGC 1620
ACAGACCAAG CCTGTGGGGG CAAGAGCACG GCTGCGGGGA GACGAGGACC CTGGGGCCTT 1680
AGGAGACCAC AGGACAGGGT GGCAGTGCAG GTCGGGGCTC CCACATCACT GGAACAGGCA 1740
GATCTTTGAG CCTGAGTTCT AGGAGTTGAG CTCCTTGGGG GACTCTGGAT TCAGAGTCTG 1800
AGGAGCTGGA TTCCAGCTCT GCCTGGACCT ACCTGAGCAC CAGGAGCGGT GACCATGCCA 1860
CTGGACACCT CTGGTGCTGA CTCCTGGCTG GGCAGTGAGC CTCCACCACG CACCACACTT 1920
CACCTGGGAG AAAACAGCCT CCGAGAAGCT CCACAGTTGC TCAGTCAATA GGGGGCAACC 1980
ATCGCTGCCC TCCGCTGCCT CCCCTGGGGG CACCACCATC ACCCCTGTTT ATAGATGAGG 2040
CATTTGAGAA TCAGAGAGAT TGGGCACCTT GTAGCAGATC ACGGAAGTGG CCAGAAAGTG 2100
GGACAGCTGC TGGGCCCTCA GCCTGGATGC TGTCTGCTTG CTGCCCCCAC ATGAGCCTTT 2160
GCCAGCCCTG GGTCCCCCTA GAAGTAGTGG GTGCAGGGCA CAGGGGTGCC ATCACCCCCT 2220
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