| Tag | Content |
|---|
EnhancerAtlas ID | HS187-06367 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:121197500-121200150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr12:121199598-121199613 | TTCTATTTTTAACAC | - | 6.54 |
|
| | 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 |
| GH12I120759 | chr12 | 121197296 | 121201020 |
|
Enhancer Sequence | GAACGCCTAC ACTCAACAGG GGAGGGCTGC GGGAAGTGCC AGGAGGCACA AGCGAAGGAG 60
GAAAGGTGGG GCCGGGGCTC CTGGCCAGAT GGTGGTCTTG GGGAGGGTGG CACTGCATTC 120
TACCCGCCGT CAAGCCGGCA AGGCCACGAC TCATCCGTGC GATGCTTCGT CATCTTAGTT 180
CCTCCCTGCA CTAGCAAGCG CTCAGCCTCT TTCTCTGAAA TTGGTTTCCG CCTTCCCCAG 240
GGAGCTGTCA CAGGATATGT TACTATCTGC CTGGGGATAA AAACCCCATC AAGGCACGAC 300
AGCAACCGCA GGTGTGAGGA AATTCAATCT CTAATGGCAA AGGCTCAAAC ACAAAAGCTA 360
GAAGCTCACG TGGTGGCTAC ACTCCAGCAG CTCCAGGTGG GCAGAGTGAA AGGTGGCAGT 420
AGCAGGCTGA CAGGTGGTCC GCCTGGAGAG AGGCTCTCTG GTGAGACAGA GCAACTGGTG 480
TCGGGATCCC GGGGCTGGAT CGCTTGTCTT CAGACATTTG GTTGAATGCA GTGACCATCG 540
TGCTGTCCCC CTCCGTCTCT GTCCTGTGGA CACCCACTTC CTGTCTCCCA TTCCTCACAA 600
GCGCAGGCCT GCTGCCCACT GCCTGGCGGC TTCCCCACTC CCAGTCTCTC AAGTCTTGCT 660
TCCTCTGCCT AACTGGTTCC CATTCCTGTC ATCTTTGGAT CTGGTGAGAA TCCCAGGACT 720
CCATGGGGGC TGGAGACAGC TCGTGGGCTT AGCTATTTTG GAACCTTCAG AGCCTCTGTT 780
CGCCTGCAGA CAGGTGGCGT GTTTTACAGG TTCTACTCAA CAGGAAGAAG ATGTCTTGGA 840
ACTTAAGAGA AAAACTGGTT AGGCAGACTC CAAATGAAAG GAACCAGAAG CGAAGCGGAG 900
TCTGCCGCAT GAATTCTTAA GACCTCAGGT TATCTAGGAA ATCTACCGCA CGCTAAAGTG 960
CTCCTCCGTA AGTGCTGCAG TTAGAATCTT CACAGCCTCC CTGCAGGATG TTTGTATCAA 1020
GCACCTGCTA ACCACTGGCT CCGTGCGGTA AGACTTCTGA AACCTGTAGT GACGAAAGAT 1080
CATTGCGCTT GGGGCTGTAG GCTTTCGCTT GTCTTCAGAC ATTTGGTTGA ATGCAGGCCT 1140
GTGTCCACCA GGAGCACTGG GCTTCTCCTA CACCAACTTG CTTCTCAGCC TTCTCTTCAT 1200
TGGCACATCC CGTCCAGTGA TACAGGATCC CCAGCCCAAG CCTCTGCTAT TTACAGCAAG 1260
GCCCAGAGTT ACGGAGAGAA GGCTGTGGAT TCTACTCTTG AACGCACTGT GGCATCCCTG 1320
CGTGACCTTG TGTGGGAATG GCTGCCACAC CCCCTCCCCA CAAGCCAAGC ATGCTAAAGC 1380
AAGCCCTGCA CAGACCGCAG GAGTAGGGGG TCAGGATGTC TGGTTTTGTT CACTGGGGGG 1440
CCCAGTGCCT CAAGCTTCAC TGAAACATGA CTGATTGCCT CTAACGGACA GGAAAGGGCT 1500
CTGGATTTCA AGGGAAAGGC TGAGGAGGAA ACAGATGATG GCTGGAGCGG GAAGAATTTT 1560
GTGATGGGAG AGTCTCTGCG CATGAGACAG TTGGAATCTG AACCTGCAGA AATTTGAGTT 1620
TAGAGTTTTG CAGATAGAAA GCACCCTATA CATTGCAGGG AATAGGAATA ATTTCTGGAT 1680
TAAAAAGTCT TACCTGGTTT ATCCCTTCCA ATAAGAGGAA GAAGCTTGAG TTGGATGACT 1740
CGATCTGCAG TGCTTCAGCT GACACGTGTT AGCAGCCATT GTCCTAGAAA TGATTTCACT 1800
GTTGGAAACT GCTGAAGAAA TGTGATTCGG TGAAGTGGGG GAGGCTGTCC TGGCCACTGT 1860
GCACTGAAGA CCAGAAAGAG ACCGAGATGG CTTCCTTCTG AGCCTGTACC GCTGACATAG 1920
CTCTGTAGAG AAGGGGGTTG TATAAATGAT GTCCCTAAGG CATGTACTCC CATGTATAGA 1980
CACGAGTGCT GCATTCCCAG GCTCTGACGT AAACGCTAGG CTTTACAAAA CAGAAACGTA 2040
CACACAACAT GGGATCTGGT GAGCAGTAAC GTGAGAGCTG CTAAGCAGAC ACAGCAGGTT 2100
CTATTTTTAA CACTTGATTG GCAAAATGGA ACTCCCTTCC CCTCCACCCT CACAGAGAAC 2160
GAGTACTTTT GTTTTTCTTG TGGGTGACCT AACTTACCTG TTTACCCAAG GCCTGTGAGC 2220
CTGCTACAAA AGTAATTCAG ACAGTAGCTT AGTCCCAAGC CACCGAACCG TTCCTATGCG 2280
GGGAGCTGTC ACTGTCACAT TCAGAAAGCG TATGCACTGT AATAACAGCA ATGGAACACA 2340
CTAGGCTTTG GACAGACTTT ACTGTCATAT CTTCATTAGC TCAAACTAGA AAAAAGAGTT 2400
ATTAAAAAGC GGGAGTTCTA GTAACACACA GTCTCTTTGT GAGGAAAAAG GACTTCAGAT 2460
CAGTGAGGAA GGAATCTGCT GAAATTTCAT GAGCATGCCA TGCCTAATGC AGCAGACTTC 2520
CTAGAAAACC CCTAAACCAT GGTATTTGAG AAAACAGAAT AAGAGGCGGA CCTAAGTGTA 2580
TCAGGCAGCG GGGAGCAAAC GAGCACTGGA AGGGAAGTCT AATGTGTGCT TTAACTGCAG 2640
CCACCCACTC 2650
|
