| Tag | Content |
|---|
EnhancerAtlas ID | HS042-00374 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr1:7531020-7533290 |
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 |
|
| | 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 | GCCACCACAG GGCAGGAGCC AGCATTTGGG AGAGCCATGT TCTGCTGTGG TGACGTATCC 60
ACCCCGGGGC GGGAATGAGC AGGCCTCGCA GACTCGGGGC CTGGAGCTCA GGATTGGTGC 120
CAAGATTTAC AGAGAAGGGC CTGAGTTGAC GTGGCACGTA AGCTTCTGAG TCATCGGGCT 180
TTCAGGGGAG GGTGCTACCT CTCTGTCTGT GTCTGTCTGT CTGTCTTTCA GGCTCTCTGT 240
CTCTCTCTGC GTCTCTCTCT GTCATGTTCT CCCTCCCCAT CTCTCCATTG CTGACAAATA 300
TTCTATTAGG CTATGAGCGA GGAGACGGGC AGGGAGCCTC TCACAGGCAG GGCACTAGAG 360
CCCATGTGGC CCATAGGCTC ATAAAGCCAT TGGCATGACC AGTAACCACC ATGTGAGGTC 420
ACCAGGACAG CTGGGGAGGG ACCAGATGAC CTGAGCTCAG CCCACTCCAG CTGGGCAGGG 480
CCAGAGCCAT GACCTGGAAG AGGCCACCTC TTCCCCTCTG CTGGTGGCAC CCATCCTCAG 540
CATTGCTGGG GGCTCTGTGT CACAGCTGAC AGGGCCTTCA GGCTCCCCTG AGCCTACCCA 600
GTGCATTTTC TAGAAGGATT TCTGAGACCC AGCGAGAGCA GGGCCAGGCC CAGGTCACCC 660
AGTGGGTCAG GGGAGGAGCA GGCAGTGCTC CGTTCTCCCG ATGCCTTGGC CTCTGCCCCT 720
ACCGCCTGAT GTGGGTGTCA CTGCAGCCGC AGGACCCTGA GCCTCGTGAG GTAGAGGAGG 780
CATGAAGGGG TGAGCTGGAC AGAGCGGTCC CTCCTGTTTG GGATTTTCTG ATGGTTTCGA 840
GGGGTAGGCA GCAGAGGTTC AGGGCCCCCT GACCTCCTCA TGTGCCCCTT TCTCCTGGTC 900
CTCCACCTTC CGTCCTTCTC TGCATTCTCC GCCTGCCCCC GCAGGGGACC AGGCCCCCAT 960
TCCAGGCCAG ACTTCCCTGC AGATTCTGTA TGGCTCATTT GGAAACTATT TCTGCTTCTA 1020
ATGAGTGTTT TCCTTTGTGC CCTTGTCCTC TAAAATGCTT AATGACTGCT TTCCGTGCTC 1080
GAGTGAAGCG GGGGTGTGTC CCCGCATGGC TGCCATTGCC AGGCCGGAGC TGTTTGGCTG 1140
CCAAGCCCGG CTTGCTTGGG TGGAGGCAGC GGGGGGTCCT TCCTGGCCCA CGCTGGCAGC 1200
ACAGACCAAG CCTGTGGGGG CAAGAGCACG GCTGCGGGGA GACGAGGACC CTGGGGCCTT 1260
AGGAGACCAC AGGACAGGGT GGCAGTGCAG GTCGGGGCTC CCACATCACT GGAACAGGCA 1320
GATCTTTGAG CCTGAGTTCT AGGAGTTGAG CTCCTTGGGG GACTCTGGAT TCAGAGTCTG 1380
AGGAGCTGGA TTCCAGCTCT GCCTGGACCT ACCTGAGCAC CAGGAGCGGT GACCATGCCA 1440
CTGGACACCT CTGGTGCTGA CTCCTGGCTG GGCAGTGAGC CTCCACCACG CACCACACTT 1500
CACCTGGGAG AAAACAGCCT CCGAGAAGCT CCACAGTTGC TCAGTCAATA GGGGGCAACC 1560
ATCGCTGCCC TCCGCTGCCT CCCCTGGGGG CACCACCATC ACCCCTGTTT ATAGATGAGG 1620
CATTTGAGAA TCAGAGAGAT TGGGCACCTT GTAGCAGATC ACGGAAGTGG CCAGAAAGTG 1680
GGACAGCTGC TGGGCCCTCA GCCTGGATGC TGTCTGCTTG CTGCCCCCAC ATGAGCCTTT 1740
GCCAGCCCTG GGTCCCCCTA GAAGTAGTGG GTGCAGGGCA CAGGGGTGCC ATCACCCCCT 1800
AGAGCAGGCA CCGTGAGACT AAGCACCACA GGCATTGTGG CCAGAACAGA GCCCAGCCAC 1860
AGCAGCCTCT GTGGCTGGTG CTGCTGAGTG GGGACTCGGG GCGGGGACAA TGCCAGTTCA 1920
CCATGGGGTT CACTCCAGGC GGTCCTGGCC CCAAAGGGCC CCCATGTCCA GGAGCGAAGT 1980
TGCCTTTACC TGGGACTCAC CACCCCCCAG GAGAGGAAGA AGATGCCTTC TCCATGGGGC 2040
TGCCTCTGGG CAGGATCCAG GCTTCCCCAC AAGGCCTGGG GCTCTGAAAC CAGGTTCACA 2100
GGGGAGAGAT GAAGCTCCAG ATCCCCAAAT CAGTGGGCCT TCCATCCCCA GAGTGGTCAG 2160
CTGCTTGTCC ACCCTGGGGC TGAGAGCAGG GTTTCCTAGG GTAGTTCCCA GAGAGGGGAG 2220
AAGGGCAAGG CTGCAGGGAG AGGCCCTAGG GGAGATGCCC CGGTTCCACT 2270
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