| Tag | Content |
|---|
EnhancerAtlas ID | HS062-03673 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr12:31787970-31791170 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:31789756-31789775 | TGGTGCCCCCTGGTGGCCA | - | 10.35 | | EWSR1-FLI1 | MA0149.1 | chr12:31790329-31790347 | ATTTCTTTCCTTCCCTCC | - | 6.26 | | EWSR1-FLI1 | MA0149.1 | chr12:31790345-31790363 | CCCTCCTTCCTCTCTTTC | - | 6.35 | | EWSR1-FLI1 | MA0149.1 | chr12:31790333-31790351 | CTTTCCTTCCCTCCCTCC | - | 7.62 | | EWSR1-FLI1 | MA0149.1 | chr12:31790337-31790355 | CCTTCCCTCCCTCCTTCC | - | 8.15 | | Foxd3 | MA0041.1 | chr12:31789199-31789211 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr12:31789203-31789215 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr12:31789207-31789219 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr12:31789211-31789223 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr12:31789226-31789238 | AAACAAACAAAC | - | 6.32 | | IRF1 | MA0050.2 | chr12:31790364-31790385 | TTTTTCTTTCTCTTTCTTTCT | + | 7.15 | | Nr2f6(var.2) | MA0728.1 | chr12:31788846-31788861 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr12:31790616-31790631 | TGAACTTCTGACCTC | - | 6.38 | | PLAG1 | MA0163.1 | chr12:31790975-31790989 | GAGGCCGAAGGGGG | + | 6.33 | | RARA | MA0729.1 | chr12:31790613-31790631 | TCTTGAACTTCTGACCTC | - | 6.88 | | REL | MA0101.1 | chr12:31790260-31790270 | GGGGATTTCC | + | 6.02 | | Stat6 | MA0520.1 | chr12:31790269-31790284 | CATTTCCAGAGAATT | + | 6.87 | | ZNF263 | MA0528.1 | chr12:31790336-31790357 | TCCTTCCCTCCCTCCTTCCTC | - | 6.36 | | ZNF263 | MA0528.1 | chr12:31790337-31790358 | CCTTCCCTCCCTCCTTCCTCT | - | 6.89 | | ZNF263 | MA0528.1 | chr12:31790333-31790354 | CTTTCCTTCCCTCCCTCCTTC | - | 8.28 |
|
| | 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 |
| GH12I031636 | chr12 | 31789088 | 31790203 |
|
Enhancer Sequence | TCTTTCTTTT TTTGAAAAAC AAAAAACAAA AAAACAAAGT CTTGCTGTCG CCTAGGCTGG 60
AGTGCAACGG CACAATCTTG GCTCACTTCA ACCTCTGCCT CCCAGGTTCA AGCGATTCTC 120
CTGCCTCAGC CTCCCGAGTA GCTGGGATTA CAGGCTTCGT GCCACCCCGC CTGGCTGATT 180
TTTGTATTTT TAGTAGAGAT GGGGCTTCAC CATGTTGGCC AGGCTGGTCT CAAACTCCTA 240
ACCTCAGGTG ATCCACCCAC CTCGGCCTCC CAAAGTGCTG GGATTACAGG CATGAGCCAC 300
CATGCCCAGC CTTTTAAATT TATTTTAAAA ATAAACGTAT TTCTTACAGT TCTGGAGGTT 360
TGAAAGTCCA CAGCTGTTGG GCTGCATCTG GTGAGGGCCT TCTTACCGCA GCATAACATG 420
ACAGAGAGCA TGACAGGGCA AGAGGCCATT TTCTTGTCTG AGAGTTTGAT TTAGTCTAGA 480
ATCTGACCCC ATCTTGACAT AAACACCACT GGCTCAGATA AATATTAAGT GCAACAGTTT 540
ACCTAATTTA GTTATTTATT TGTATTCTTT TATTTTTATT TTATTTATTG AGAGGGGTTT 600
TGTCATGTTG CCCATGCTGG TCTTGAACTC CTGGACTCAA GCGATCCTCT CACTTTGGCC 660
TCCCAAAGTG CTGCGATCAT AGGCTTGAAC TACCGCGTCC AGCTAGTTTA TCTAATTTAA 720
AGACATCAAA ATCTAAAGTC AGATTCTTAC TTAGATTTGG TGTTTCAGAT TTCAAAGAGA 780
TGAGATGTCA CCAGATAAAA ACTACTAGGT GGTAACCAGG CGTGGTGGCT CACGCCGTAA 840
TCCCAGCACT TTGGGAGGCT GAGGCGGGCG GATCACGAGG TCAGGAGTTC AAGACCAGCC 900
TGGCCAACAT GGTGAAACCC CGTCTGTACT AAAAATACAA AAAAAATAGC TGGGCATGGT 960
GGCAGGCACC TGTAATCCCA GCTACTCGGG AGGCTGAGGC AGGAGAATCA TTTGAACCCA 1020
GTAGGTAGAG ATTGTAGTCA GACGAGATCT CACCATTGCA CCCCAGCCTG GGCGACAGGG 1080
TGAGACTCTA TCTCAAAAAA AAAAAAAACA AAAAACGACC AGGTGGCTCA CGCCTGTAAT 1140
CCCAGCACTT CGAGAGGCCA AGGTGGACCG ATTGCTTGAG CTCAGAAGTT CAAGATCAGC 1200
CTGGGCTACA TAGTGAAACC CTGTCTCTAA AACAAACAAA CAAACAAACA AACAAAAAAC 1260
AAACAAACAA AGCTTAGCTG GGCGTGATGG CGCATGCCTT TAGCCCCAGC TACTCAAGAG 1320
GCTGAGGAGG GAGGATCACT TGAGCCTGGG AGGCAGAGGC TGCAGTGAGC TATGATCGTG 1380
CCACTGTACC CCAGCCTGGG TGAGAGAGTC CCTATCTCAA AAAAATAAAA CCAAAAAACT 1440
ACTGGGGCCA CGTCAGAACT GAAAGAGTTC TGCAGGCCCT TCAGAGAAAG GAGAAGTGAG 1500
AGTCAATTAA CCTCAAGATT ACATTTAAAA GCATTTTCCT CTTTAGTATA GAGGTGTGTT 1560
AAAAAAAAAA AAAGCATTTA TACGAGGTAT GTGAGGTATG TTAGTGAAAC AGCAAAAACC 1620
TAATTATATC CTAAATAACT GGCACGCTCT AGGTTACAAA TAGCAATTTG TAAAAGACCC 1680
ATTGAATGAA CACATTAAAC AGCAGGTTGC TTATTCCTTC TCAAACCGCA CTAAAAAATT 1740
CCTCTCTCGC ATGTGTAGGT CCCAGAGCCA GACAGTTATG AGATGATGGT GCCCCCTGGT 1800
GGCCAATGTG GGGAGCCACC CGGCCAGGCG TGCTTCCTGG CTTTGTGCCA GCCATGCCTT 1860
TATTCTTTGG TTGGTTGGTT GGTTGGTTGG TTAGTTGGTT GGTTGGTTGG CTGGTTGAGA 1920
CAGAGTCTTG CTCTGTCGCC CAGGCTGGAG TGCAGTGGCG ATTTCGGCTC ACTGCAACCT 1980
CCGTCTCCGA GGTTCAAGCA ATTCTCCTGC CTCAGCCTCC GGAGTAGGTA GGACTACAGG 2040
CGCCCACCAT CAAGCCCGGC TAATTTTTGT ATTTTTGGTA GAGACGAGGT TTCACCATAT 2100
TGGCCAGGCT GGTCTTGAAC TCCAGACTTC AAGTGATCCA CCCGCCTCTG CCTCCCAAAG 2160
TGCTGGGATT ACAGGCATGG GCCACCGTGC CCGGCCAGAC CATGCCTTTA CTTTTGCACA 2220
TATGCACAGT ATTTCTGAAA ATCAAGTGAA AAAGTTGGAT TTATATACTC TATGTGAGTT 2280
TACATGTTAT GGGGATTTCC ATTTCCAGAG AATTAAAATG GATAATCAAA TGTTTAATTT 2340
CATTTCACAA TTTTCAAATA TTTCTTTCCT TCCCTCCCTC CTTCCTCTCT TTCTTTTTTC 2400
TTTCTCTTTC TTTCTTTCTT TCTTCTCTTC CTTTTTTTTT TTTCTTAGAC AGAGTCTCAC 2460
TCTGTCGCCC CAGCTGGAGC TCAGTGGTGC AATCTCGGCT CACTGCAACC TCTGCCTCTC 2520
AGGTTCAAGT GATTCTCCTG CCTCAGCCTC CTGAATAGCT GGGACTACAG GCCTGTGCCA 2580
CCATGCCCAG CTAATTTTTG TATTTTTAGT AGAGACAGGG TTTCACTATG TTGGCCAGGC 2640
TGGTCTTGAA CTTCTGACCT CAGGTGATCC ACCCATCTCA GCCTCCCAGA GTGCTAGGAT 2700
TACAGGCGTG AGCCACTGTG CCGGGGCAGC AGGCCTTTCT TGACTGCAGA TTTTCTAATA 2760
CATGAAAACA GCCACCAATT GCAAAAATAT ATTAATTTTC GACAGGTACA AAAGGCACTT 2820
TGTGAATATC AGTATGCAGT TGGGTACACT TATCCGGAAT TAAACCTGTC TCTCCTGGAG 2880
CTACATGCCA CAGGCATCTC ACACAGGGGC CGCTGTTCTG GAACACTCCT GTGAGCCAAT 2940
AAAGGATCAA CAGCTTCTCT TCAGGCCAGG CGCAGTGGCT CACACCTGTA ATCCCAGCAC 3000
TTTGGGAGGC CGAAGGGGGC GGATCACCTG AGGTTAGGAA TTAGAGACCA ACCTGGCCAA 3060
CATGGTGAAA CCCTGTCTCT ACTAAAAATA CAAAAATTAG CCAGGTGTGG TGGCGGGCGC 3120
CTGTAATCCC AGCTACTCAG GAAGCTGAGG CAGGAGAATC ACTTGAACCT GGGAGGCGGA 3180
GGTTGCAGTG AGCTGAGATC 3200
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