| Tag | Content |
|---|
EnhancerAtlas ID | HS034-18188 | Organism | Homo sapiens | Tissue/cell | ECC-1 | Coordinate | chr2:239832240-239833210 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Znf423 | MA0116.1 | chr2:239832951-239832966 | GGACCCCAGGGTGGA | + | 6.54 |
| | | 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 |
| GH02I238910 | chr2 | 239832221 | 239832370 |
| Enhancer Sequence | CCCCATCTCT GTTCTCATCT CTACTTCGCA GCTCAGGGCT CTGCCTGAGA GAGTCAGAAC 60
AGGTTGCAAG AATCACTATT ACTTCACTTT AAAAGGCACG AGAGAGGATG TGAGACATTT 120
TATGCTGTGC ATGTTTGTAG AAATTTCTAG AAACTACCAA CTCTAACATG GTTGCCAGTG 180
TGAACAGACC GAGGCCTGGG AGAGCAGAGG GGGCCTCAGC CCTTTCCCAG TGCCTAGTCC 240
TCTGCTGCTC CCCAGCAGCC TCAGCACAAG AGACCATTGC TGTCACACCC ACGCCCCGCT 300
CTTGATACAG AAGCGTGCCC ATTCTGTGAG CCACCCCTGC TGTCCAAAGT CCGGGCCAGC 360
CTTCCCTGCT GCTCACCCTG GGTGGTATTC CCTGCTCTCC CAAGCATGGC ATTCATTTGT 420
GCCACCACCT CCCTGCTTCT CTGAACGAGT CACCGTCTGC TCCACATGCA TCCGTGCCAT 480
GTTGACCATG AGCTCACCAG GCAGCTGGCT AAGAATGGAG CACCTGGGTG TGCAGGTTAG 540
GTTGGCATCC TGCCCAGAAA TCCCAGAAGG AACATGATCT GCCATCAAGG AGAGTCAGCC 600
TGGGTCTGGT GCAGGCGGGC ACCTCTGCAT GAGGGCAAGG GCTCTATGCC CTGCCCGCTA 660
CCTCCTTACC ATGCCAGCAC CCATGAGCAC TGGGGGCTGG GTGTTGCTTG TGGACCCCAG 720
GGTGGAGGCT TCCAGCTCTG GAGACTGAGA GTCACCAGGT CACTACCCTG AGCCACCAAA 780
CGCATGTCTC CTGGGGGACA TCTGGTACCG GGGTCTGCTG GGTGGAGCTG CCCACCAAGC 840
AGTGGACACA CAGAGCCCAC CCAGCTCCTA GACAGAGGTT CTGGAAGTAG GGGTCTCTGG 900
CAGGATGGTG GTGGCTTGCG AGCCTCATTT CCCACTCCCA CCCTGTCCCC AGGTCCACCA 960
CGGCAAGGAC 970
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