| Tag | Content |
|---|
EnhancerAtlas ID | HS067-04970 | Organism | Homo sapiens | Tissue/cell | GM18522 | Coordinate | chr3:49092960-49094290 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr3:49093109-49093121 | GTTTGTTTGTTT | + | 6.32 | | REST | MA0138.2 | chr3:49094025-49094046 | AGAAGTGTCCATGGTACTTAA | - | 6.01 | | Stat6 | MA0520.1 | chr3:49094002-49094017 | CTCTTCCTGAGAAGA | + | 6.09 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TATTTTTTAA ATTTTTGTAG AGATAGGGTC TTCCTATATT GCCCAGGCTG ATCTCAAACT 60
CCTGGGCTCA AGCATTCCTC CCACCTCAGC CTCCCAGACT GCTGGGATTA CAGGCAACTG 120
CCACTGCACC CAGCACTAAT AGTTTTTTTG TTTGTTTGTT TTGAGACAAA GTCTTGCTAT 180
GTTGCCCCAG GTTGGAGTGC AGTGGCACGA TCTCAGCTCA CTGCAACCTC TGCTTCCCAG 240
GTTCAAGCAA TTCTCCTGCT TCAGCCTCCT GAGTAGGATT ACCTGGGATT ATAGGTGTGT 300
GCCACCACAC CCGGCTAATT TTTGTATTTT TAGTAGAGAC GGGGTTTCAC CATGTTGGCC 360
AAGCTGATCT CAAACTCCTG ACCTCTGGTG ACTCACCCGC CTTGGCCTCC CAAAGTACTG 420
GGGTAACATG CATGAGCCAC CGTGCCTGGC CCCTACTTTT TTCTTTTGAC AGAGTTTTGC 480
TCCTGTTGTC CAGGCTGGAA TGCAATGGCG CAATCTCAGC TCACTGCAAC CTCTGCCTCC 540
TGGGTTCAAG TGATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGGATTACA GGTACCTGCC 600
ACCATGCCCA GCTAATTTTT GTATTTTTAG TAGAGACGTG GTTTCATCAT ATTGGCCAGG 660
CTGGTCTCAA ACTCCTGACC TTGTGATCCG CCTGCCTCGG CCTCCCAAAG TGCTGGGATT 720
ACAGAAGTGC ACCACCTCGC CCGGCCGCCC CCGTAACACA AAAACTCTTG GGAGGTCCCA 780
CCACATAGAC GGCATATTCA AGCCTCCCAA TGGTGATCAC TTTTAACAGG CTCCTTATGA 840
GTTATTTTAG CTTTTCTAAT TCACCCACAC TGTGTGCCCA AAGATGAAAA ACAGAATGAA 900
CAATCTCACA GCCTCTCCAG TGATGAGTTT GTAATCTATG TGATAAACTA CAAGTGTTTT 960
GCTAAAACCA TTTACTTATG ATACAAGGAA ACAGCACTGG GACACACTTG AGGTGTCCCA 1020
TTCATCTACA CCTGTAACTT TACTCTTCCT GAGAAGAGAT TACAAAGAAG TGTCCATGGT 1080
ACTTAAACCC AAAATGTCTC CAAAACTCCA AAGCAATTCC TGGCCATCTC ATTTACCTCC 1140
AGGTACCAGG ATAAACTCTT TTTTCTGTTG CATAGCCTCA CGTGATGTTT CTCCCCCTCT 1200
TCTCCCAAAT ACTAAATACT GCATCACTGT AAGAGTAACA GCAGTAAATA AGCCAGAGGT 1260
TGCGAGGCAA GCTCTGTGCT GCACTGGGCC CTGAGGGACC AGGCTGCCTG CCCTACTGAT 1320
AAGTCTTCAC 1330
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