| Tag | Content |
|---|
EnhancerAtlas ID | HS188-10026 | Organism | Homo sapiens | Tissue/cell | Th2 | Coordinate | chr4:185424670-185426200 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Spz1 | MA0111.1 | chr4:185425289-185425300 | AGGGTTACAGC | + | 6.14 |
| | | 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 |
| GH04I184503 | chr4 | 185424750 | 185425961 |
| Enhancer Sequence | AATTCTCCCG CCTTAGACTT TGGAGTAGCT GGGACTACAA GAGTGCACCT TCACGCCCAG 60
CTAATTTTTC ATTTATTTTA TTTTTTACAC ATGGGGTCTC GCTTTGTTAC CCAGGCTGGT 120
CTCAAATTCC TGGCTTCAAG CAGTCCCCCC ACTTTGGCCT CCCACTGGGA TTATAGGCAC 180
GAACCACCAT GCTATATGGA ACTTTTGAAT TGGGGTTTAG AAGAAAATGC AGTAAGTTCT 240
GAGAGACTGA GGATGATGCT TGGCCAAAGG GCTGGTTTGA ACATGAAATG TATCTCTATT 300
AATGCCCGTG TGAGGGCCCA GAGGTGCCTT GGCCCTGGAG TCAGGAGATG TGGGTCCCAG 360
GCAGTGCTCT GACATGCCCT AGCTGAGCAG AGCTGCTCTC TGGGAGCCAG TTTTCTGCTT 420
GGTAAAATTA GGACAATATG CTCTATCTTT CGGGTTGGGG AGGGTGGTGC GAGGAGCAGA 480
AATAATGCGT GGAAAGCAAT CTGCACCGTG CCTTGCAGGA GAGGAAGCTG CTGTTCCTGT 540
TTGCATGTGC CAGGCCAGTT ACTGTAGAGA TGTACGCTTC ATTAAAACAC CGTCATCTTC 600
ACCAGGCTGC AGAGATACCA GGGTTACAGC ACAGCTGAGA TGAGGAGCTG ACTGATCCTG 660
TTGGGAGGAC CTGGAGATGA TTCATGGTAA GAGCACTACA GGAAGAGAGA GAAGCATCTG 720
CTTCCTCGAG TGCCAGGGTG GCAGAGAGGC CACCGGAAGT CTTCACTTGG CTGAAGACTT 780
GCAGTGAGTC TGGGGTTTAA TTCAGAGGAT TGAGAGAAGG CCAGCACCAT GGGAATTGTT 840
CAGCATGGGG GTCCAGGGCC AACAGAGAGA ATTCTGATTG TATTCAAGAA GAAAGGCGAA 900
ACTCGGAGCT AGGATAGCTG AGCTGAGCAG GAGGTCAGAG AAGTAGGAGT AGCATGCAGA 960
AAGTGGGCCA GCAGCCGGGA GAGGCCTGCG AGGTGGGATG TGCACACGGC TGATGCTGGA 1020
CACCTGGAGC CAGGGCGTGA CGGGGGCACT GGCTGACTGC CCAGGGCCCA TGCCTTATCC 1080
CCCGCCCCCA CCCACCACGC CTGCCCACAC TTTTCTGTGT GGGTCCTCAC CCAGCCTGGC 1140
CACGCTCCAG TGGCATCCGC AGCTCTGCTC TTTTCCTCAC CCACAAAGAG CACAACAAAG 1200
AGGGCAGCAA GGTTAGGCCA GGTGAGAGGC CACTCACCCT GGCCAGCAAG TATGGGTGAG 1260
GCAGGACATG CCAGGCCCCT GGCAATCCAG AAGTCCCCTT GGAAGAGATG GAAGACGCAA 1320
TTCCATCCAG CAAGAACCAA CCCTCTTGCC CACTTACCAA TCCCATTCTC TCCACGTAGC 1380
CCTCCAAAGC AACTCCCCGA GCATCTTCAA AGCCGGAGGC CTGGAAGTGA TGAGAGGCCA 1440
ACATGCGCTC TAATGAGATA CAGCCCTGGG TTCCACTTCA TCTCCTTGAG ACTCCAGCTT 1500
TTGCTTGCTC TCTCCATGTC CACCTTCCCT 1530
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