| Tag | Content |
|---|
EnhancerAtlas ID | HS073-12956 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr7:24767880-24769310 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr7:24768684-24768702 | GGAAAGAGAAAGGAAAAA | + | 6.48 | | Lhx3 | MA0135.1 | chr7:24768935-24768948 | AACTAATTAATTT | - | 6.29 | | Lhx3 | MA0135.1 | chr7:24768741-24768754 | TAATTAATTAACT | + | 6.64 | | mix-a | MA0621.1 | chr7:24768936-24768947 | ACTAATTAATT | - | 6.62 |
|
| | 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 |
| GH07I024728 | chr7 | 24768249 | 24768984 |
|
Enhancer Sequence | AAGAGAACTT GAGCTGCCAG GACAGATGGC GGCTGCCACA GGGGCCCACA GAGCCACCGA 60
ACTGACCTTC TGCCGTTAAC CATTCAGTCA ACCGGGACGC ACCCTCTTCG AGATGTTTTC 120
TTATGTGAGA TAATAACAAA TGTTCTTTGC AACCAGACAC CCTAACTGGT ATATGAAGTG 180
ACCATCATCC TTATTTCAGA AAGCAACAAG AAGCACGAAG AACTCAGAAG CCAAGGGGCT 240
GGGTGAGAAT GCAGCTCAGC ACCATCCACC CTCGAAGCTC TGCGCCCATC TGCCTCTCCC 300
TCCTGAACCT TCCTGGGCCC TGCATACAGA AGGCGCTTAA TGCATGCTTG ATTGTTAAAG 360
AACTGGCAGT CTTTCTGCTC CATCCCATGA GAGCTTCCCA GAGTCAGGAA GTGGATCCTC 420
TTGGAAACGA AAGCAGCCGC CCACTGTCTC CCCCGCAGGT ACTAGCAGTC CCCATTTCAA 480
CCACGTTTCA TAACAGAAAC TTCCCACACA TCAGAGATGC TCAGCCCACA GCCGGGGGCA 540
GGAAATCTCT AGAAACCTCA ACTCCTGTGC CCTGGGCCTC CACTTCCAAC ACAGTGAGAT 600
AAGCCCTGCT CTTTCTCTCT CTGTCACTTG GCTGTAATGT AGATGACTTC AGGATTGTAA 660
AATGCTGGGA AAATCAAAAT TGGGGCAGAA TGCTCACTGC ACATTGTTGC CAAAGTGACC 720
AAGTCACCCG CAGACTGTGG CTGCTCCGCC TCTGTCCACA TTATAGTCTC TAATACCTTA 780
TCTTACTCAC ATACGACGAC CCCTGGAAAG AGAAAGGAAA AAATGACTGA GAACCTGTAG 840
ATGTTCAGCC CTTTAGACGA GTAATTAATT AACTGCAACC AGTGGATGAA ATGCAGCAAG 900
CCTGGAAGAT GATAAACCAA ACGCAGCTGA TGCCCAGAAG TGACTTCACG CCAAAGCCCT 960
TGGAACATGT GTCTGTTTCC AAGCTCTGTG CATAGAAGTT GGATCGGAAA AATCATGTGT 1020
TTAGTGAACT TGGTTTTAAA TCCTGAATCT AGGCAAACTA ATTAATTTCC ACATTCAGGC 1080
TCCTCAGTTG TAGAATAAAG ATAAACCAAT TATCCTTTCA AGCAAACTGG GCTCAGTGTG 1140
CCAAAGGCAC TGCGCCAGAC CCCACAACAA AGGAGGCAGG GCGTTCCAGG AGGGAAACGG 1200
ACACAGACGC AGGCAACTTC CGACACACTT GACCCTACGG CGTGGTTAGT ATGCCACCAG 1260
GGGTGATGTG GCTCCTGAAG GAAGTGGGGT CTAACCTAAG GAATACTGAG GAATTGGCTG 1320
GGTGACACAG GAGAAGTGAG TCTGTGTGTG TCCTTCATGC CTCTGTGCAG ACAGGAGGAG 1380
TGAACATCAG ACAAGGACTG GAGGTAGAAG GAGCCTGGAG TATTAATCCC 1430
|
