| Tag | Content |
|---|
EnhancerAtlas ID | HS050-17470 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr12:121197540-121200310 |
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 | AGGAGGCACA AGCGAAGGAG GAAAGGTGGG GCCGGGGCTC CTGGCCAGAT GGTGGTCTTG 60
GGGAGGGTGG CACTGCATTC TACCCGCCGT CAAGCCGGCA AGGCCACGAC TCATCCGTGC 120
GATGCTTCGT CATCTTAGTT CCTCCCTGCA CTAGCAAGCG CTCAGCCTCT TTCTCTGAAA 180
TTGGTTTCCG CCTTCCCCAG GGAGCTGTCA CAGGATATGT TACTATCTGC CTGGGGATAA 240
AAACCCCATC AAGGCACGAC AGCAACCGCA GGTGTGAGGA AATTCAATCT CTAATGGCAA 300
AGGCTCAAAC ACAAAAGCTA GAAGCTCACG TGGTGGCTAC ACTCCAGCAG CTCCAGGTGG 360
GCAGAGTGAA AGGTGGCAGT AGCAGGCTGA CAGGTGGTCC GCCTGGAGAG AGGCTCTCTG 420
GTGAGACAGA GCAACTGGTG TCGGGATCCC GGGGCTGGAT CGCTTGTCTT CAGACATTTG 480
GTTGAATGCA GTGACCATCG TGCTGTCCCC CTCCGTCTCT GTCCTGTGGA CACCCACTTC 540
CTGTCTCCCA TTCCTCACAA GCGCAGGCCT GCTGCCCACT GCCTGGCGGC TTCCCCACTC 600
CCAGTCTCTC AAGTCTTGCT TCCTCTGCCT AACTGGTTCC CATTCCTGTC ATCTTTGGAT 660
CTGGTGAGAA TCCCAGGACT CCATGGGGGC TGGAGACAGC TCGTGGGCTT AGCTATTTTG 720
GAACCTTCAG AGCCTCTGTT CGCCTGCAGA CAGGTGGCGT GTTTTACAGG TTCTACTCAA 780
CAGGAAGAAG ATGTCTTGGA ACTTAAGAGA AAAACTGGTT AGGCAGACTC CAAATGAAAG 840
GAACCAGAAG CGAAGCGGAG TCTGCCGCAT GAATTCTTAA GACCTCAGGT TATCTAGGAA 900
ATCTACCGCA CGCTAAAGTG CTCCTCCGTA AGTGCTGCAG TTAGAATCTT CACAGCCTCC 960
CTGCAGGATG TTTGTATCAA GCACCTGCTA ACCACTGGCT CCGTGCGGTA AGACTTCTGA 1020
AACCTGTAGT GACGAAAGAT CATTGCGCTT GGGGCTGTAG GCTTTCGCTT GTCTTCAGAC 1080
ATTTGGTTGA ATGCAGGCCT GTGTCCACCA GGAGCACTGG GCTTCTCCTA CACCAACTTG 1140
CTTCTCAGCC TTCTCTTCAT TGGCACATCC CGTCCAGTGA TACAGGATCC CCAGCCCAAG 1200
CCTCTGCTAT TTACAGCAAG GCCCAGAGTT ACGGAGAGAA GGCTGTGGAT TCTACTCTTG 1260
AACGCACTGT GGCATCCCTG CGTGACCTTG TGTGGGAATG GCTGCCACAC CCCCTCCCCA 1320
CAAGCCAAGC ATGCTAAAGC AAGCCCTGCA CAGACCGCAG GAGTAGGGGG TCAGGATGTC 1380
TGGTTTTGTT CACTGGGGGG CCCAGTGCCT CAAGCTTCAC TGAAACATGA CTGATTGCCT 1440
CTAACGGACA GGAAAGGGCT CTGGATTTCA AGGGAAAGGC TGAGGAGGAA ACAGATGATG 1500
GCTGGAGCGG GAAGAATTTT GTGATGGGAG AGTCTCTGCG CATGAGACAG TTGGAATCTG 1560
AACCTGCAGA AATTTGAGTT TAGAGTTTTG CAGATAGAAA GCACCCTATA CATTGCAGGG 1620
AATAGGAATA ATTTCTGGAT TAAAAAGTCT TACCTGGTTT ATCCCTTCCA ATAAGAGGAA 1680
GAAGCTTGAG TTGGATGACT CGATCTGCAG TGCTTCAGCT GACACGTGTT AGCAGCCATT 1740
GTCCTAGAAA TGATTTCACT GTTGGAAACT GCTGAAGAAA TGTGATTCGG TGAAGTGGGG 1800
GAGGCTGTCC TGGCCACTGT GCACTGAAGA CCAGAAAGAG ACCGAGATGG CTTCCTTCTG 1860
AGCCTGTACC GCTGACATAG CTCTGTAGAG AAGGGGGTTG TATAAATGAT GTCCCTAAGG 1920
CATGTACTCC CATGTATAGA CACGAGTGCT GCATTCCCAG GCTCTGACGT AAACGCTAGG 1980
CTTTACAAAA CAGAAACGTA CACACAACAT GGGATCTGGT GAGCAGTAAC GTGAGAGCTG 2040
CTAAGCAGAC ACAGCAGGTT CTATTTTTAA CACTTGATTG GCAAAATGGA ACTCCCTTCC 2100
CCTCCACCCT CACAGAGAAC GAGTACTTTT GTTTTTCTTG TGGGTGACCT AACTTACCTG 2160
TTTACCCAAG GCCTGTGAGC CTGCTACAAA AGTAATTCAG ACAGTAGCTT AGTCCCAAGC 2220
CACCGAACCG TTCCTATGCG GGGAGCTGTC ACTGTCACAT TCAGAAAGCG TATGCACTGT 2280
AATAACAGCA ATGGAACACA CTAGGCTTTG GACAGACTTT ACTGTCATAT CTTCATTAGC 2340
TCAAACTAGA AAAAAGAGTT ATTAAAAAGC GGGAGTTCTA GTAACACACA GTCTCTTTGT 2400
GAGGAAAAAG GACTTCAGAT CAGTGAGGAA GGAATCTGCT GAAATTTCAT GAGCATGCCA 2460
TGCCTAATGC AGCAGACTTC CTAGAAAACC CCTAAACCAT GGTATTTGAG AAAACAGAAT 2520
AAGAGGCGGA CCTAAGTGTA TCAGGCAGCG GGGAGCAAAC GAGCACTGGA AGGGAAGTCT 2580
AATGTGTGCT TTAACTGCAG CCACCCACTC AACCCTCCGA GACGAGTAGA GTATTTGCTG 2640
TTTCTCTGCC AAAGTTTTAA GGGAGTGTTT TAAGGGCTTT GAAGATTAGC AACTGGAATC 2700
CAGGGTGCAT TCACAGCCCT GTGTGGGTAT TTCCCCCCAA AACCTGCACA GAAGTGAGAA 2760
TGACAAAATA 2770
|
