| Tag | Content |
|---|
EnhancerAtlas ID | HS037-27160 | Organism | Homo sapiens | Tissue/cell | ESC | Coordinate | chr4:9692550-9694050 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA13 | MA0650.2 | chr4:9693915-9693926 | GCCAATAAAAC | + | 6.14 | | KLF5 | MA0599.1 | chr4:9693307-9693317 | GCCCCGCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr4:9693586-9693596 | GCCCCGCCCC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 9692600 | 9693454 | | chr4 | 9693473 | 9693800 |
| Enhancer Sequence | TTGTTTTCCA CTCTGTCCCC AAGTCTATAT CACCACCACC GCTAATCCCA CCCCGCAGGA 60
GCTAACTCCT CCTTCCTGTC CCTGCAAGAT CAAAACTCCT CCTGGAAGCC CCGCTAGCTC 120
TGTCTGCTCA CCTTCATGGC AGATATCGCT ATTGTACTTT TATATTCATT TGTATCATAA 180
GTACTTCAAT GTCCACTTCT TCCACGAGCC CCTGAGACCC TGGAGGGTCT GGACCACACC 240
TAGTTTTTCT CACTGTTACA TCTGCCTTGC CAGGCGCATG GTAGGCGCTT AGTAAGTATT 300
TGGTGAACGA ATGGCTTGTT TGGTGACAGT CCAAAGGCTG GAGGACAGAG GGAAAGCTCC 360
CTCCTGTCGG GCCCCAGACG GGTGGCGCTG ATGGAGAGGC GGCTGGGATA AGGCCTCCAG 420
GACCGAAGCG CGCACCCATA AGGCCCCTGC CAAAAAGACC TTCCTGAAGG CGGAGGAACT 480
GCGAGAGTGT CTACTTTGGC CCAAGGCCTG ACTCGACGAT CCCAGGGACC CTTGCCCTAA 540
CCGGCCCCGC CTCCCGGGCC CCAAACCCGT ACTCGGCCCC GCCCAAAGCT CCGGCTCCTA 600
GGGCCCGCCC CTGGCCCCGC CTCGGCCGAC CATGGCCTTG CTCCTGGGCC TGCCTCAAAC 660
CCTCCGCAGG TAACGCCTCC CGAACGTGAG CCACACTCCG ATTCCCTCCT CAAACCCCTC 720
CCCGTTTCCC ACACCCTGGA CCCCTCGCTC CGTCTCGGCC CCGCCCCAAG CCCAGCTCCG 780
TCTCGGCCCC TGAGCCCAGC CCCGACCCAC CTCCCAGTCC CTGGGTTCCT CCCGACACCG 840
GCGCCTCCCT AAGCTCCGCC TCCCAGGGCC CGAGCAGCGC CTGGCCATAC CCCCATGGCC 900
CGCCTCCTGA GCGTAGCCCG CAGCCCAGAC TCGGACCCGC CTCCCGGACC CTGGGCCCCT 960
CCCCACGTCG GCCCTCCCTA AGCTCTGCCT CCCAGAGTCC GAGCACCGCC TGGTCATGTG 1020
CTACGACATA GTCAACGCCC CGCCCCGGCC CCGCCTCCTG AGCCCTTCTC TGTGCTATTG 1080
TTTTCTTCTT AATAAAATGG GGGATATAAT GATAGCTACC TCTTAGGGTT GTTGTCAGAG 1140
TTGAGTACAA AAGCCTGTGG ATCAGTGCCT GGCTCATGGT AAATGCATGT CGGTGTTAGC 1200
TACTGTTTTT ATTCGGTCTG AAAATGTTTA ATAAATGCCT TTCGTGAGCC CGGCACCATG 1260
GATCAGCAGT ACCCATGACA GATGAGGCTC TGCTTGCATG GGAGAGCCAG AGAACAAACA 1320
AATAAATGAA TAAACAAGAA AAGACCAGAT GAGAGTAGCT TTAAAGCCAA TAAAACAGGG 1380
AAATGGTGAA TGGAGTAACT GGGGAGAAGA GTCACCAAAG TCGGGGAATC AGGGAAGCCT 1440
TCCCCAAAGA GGTGGCATTT GAACTGGGGC CTGAGTGGTG AAGCAGCTAG CCATGGGAAG 1500
|
| |
|
|
|
