| Tag | Content |
|---|
EnhancerAtlas ID | HS045-33539 | Organism | Homo sapiens | Tissue/cell | Fetal_lung | Coordinate | chr2:23892190-23893350 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr2:23892657-23892671 | CAGGCCTGGCCCCG | - | 6.24 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 23892318 | 23892426 | | chr2 | 23892400 | 23893211 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I023669 | chr2 | 23891880 | 23893663 |
| Enhancer Sequence | CAGAGTGGCA GCTGATCTTA CCGAATGGGT AGATGTTTTC TGAACGAGGG CGAAGGAATT 60
CCCTGGCAGA GGGAATAGCC TAGGTGCCAC CCTCCTCTTC CAGGCTCCCA CGCAGCCTCC 120
GTTTCCCTTC CACACAGTCC TGCCCCACAG AGTAGATAAC TGTACATGCA GAGAAGACTC 180
CCTAGGGCAG AAAGCCAGAT TGTTGCATCA CTTCTGCCCC CTGCACAGGG CCCGGCACAC 240
AGTGGGGGCT CCCTGAGTGC TGGGTACCCC GTGAGCAGCA CCCGTGGCCC GTGCTGGACA 300
CAGCCTGTTG GGGAGACTGG TCCTTCTCAG CGTTTGTGTT CACGTAGGGG ATGGTCCCCC 360
CTCTGTGTGG CTGCCCTGCC ACCCCCAGTC AGCCTCTGAG CACAGTGGCC GGTGCCCAGC 420
TCATTTAGAG CTGAGGCCCC CAGAACCCAG GGCTGCAGCC GAGTACACAG GCCTGGCCCC 480
GCCAGCGCAG GACAGCAACT CTTGGGTAAC TGTGTCCATT GGATTTGTAA AAACAGGGCC 540
GTGGTATTAT CACAGAATCT GGTAGGTTCT GCTTCCAAGA AAAACAGACT GTCAAGTTAA 600
ATACATGTGG GTAGGGACCC AAGCAGAGAG GGGTGTCAGT AAAGCCAGAA GCTCAGCTGA 660
AATGGTAGGG ACCCATGAAA AGTCCCATGC AGGGAGAATT GAGCCAGAAG GCCCCAGAGC 720
ATGGGCCGTG TGCCCAGTTA GGCCTCTCCT TCCTGCATCT GGGTTCTCAG GCGTGTAGAT 780
CGTCACGTGG AGCCCAGTGA GTGCCAGAGG CTGCACAGGG CTCTGGGAAT ATCGGGGGAG 840
GGAAAGGCGG CGGCTCCACC TACCTGAGCT CGCGGGCTAA CTGGAAGACA GGATTCAGCA 900
GGCAAAGATC ACACACCCAG GAGGAGGGAT TGGCCTGGGA CGCAGGGAGA CCAGGCACAA 960
CCTGGGGGTT GGGAGGACGG GGGTGTCAGT ACAGCCCACC TGTTGGTCCT TTCTGGGACC 1020
TCATGAGACC AGGCCGGGTG CCTCCTCACA AGCTGGGGCA CGACTGGACT CGCCGACCGG 1080
TGTGATGGGC AGGGGGGTGT GCTGGGCACC GTGCCTGCTA CACAGGGGCA CCGAAGCAGT 1140
GTTCCACCCT TGGCAGGATG 1160
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