Tag | Content |
---|
EnhancerAtlas ID | HS051-01836 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr1:169012570-169015110 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROD2 | MA0668.1 | chr1:169014536-169014546 | ACCATATGGC | - | 6.02 |
| | 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 |
GH01I169043 | chr1 | 169012640 | 169014838 |
| Enhancer Sequence | TCTGTACACA AAACCCCTGT GACGTACAAT TTACCCACGT AACAAACATG CACATGTACC 60 CCCTGAACCT AAAATACAAG TTGGAAAGAA AAAAGAATAG TAGTCAGAAT AGGTCTCATT 120 AAGAAGGCAA GACTTGAGCA CAGACTTGTG GGAGGTGAGA AAATATCTGT GGGAGGGGCC 180 TCCTGAAAGA GGGAAAGGTT AAAGCCAAGA CCCTACAATG GGAGCGGGCC TGAGTGTTGA 240 GGAGTGGCTC CAGGCCAGTG TGGCTAGAGC AGCACAAAGT GTAAGGAAGA GTGGTGGGCA 300 AAAACTCAAA AAGGAAACAG CAGTCAGGAG ATGCACGGCC CTAGTGCGCA ATGTAAGGGC 360 TTTGACTTTT ACTCTCAGTG AAAACTATGA CAGGGTTTTA AGCAGAGGAA TAACATGACC 420 TGACTTATGT TTTAGAAGAA TTACTTTGAG AATAAAATTT CCAGTGGCAA GTAGAGAAGC 480 AGGCTAACCT AAGCAAAACC CACTACAGGG ATCCAGGTGG CAGATAGTGG CTGAAAGCCA 540 AATTAGAAAG AGTTTAAGAG AAAAAATGGC ACAACTAAGA GATTAGCACA GCTCTTGACT 600 ACAAAGCTGC AAACACAAAA TTCAGTGCAG GGCCTGGAGA GTGCTCATGT GAGTGAGGGG 660 CCCTGATGCT TAAGCTTTGT CAGCATCTGT GCACACCCAC CTCTGTACAA GCCAAGGCCC 720 CTGGCCTGGT CAGTTGGGTG GATGGTGAGG TGCTTACCAA GTTGGGTACC CAGGAGTAGA 780 TAAGAGTTTG CAAGCAGGAA GAAGACAGAT CATGCATTTC ACTGTGAGAT TTTTGAGATT 840 CAGAGGTCAG TGCAACATCT AAGTGAAAAT GGCCAGGCTC TTTCTGCTCC TAACAATACT 900 GCCAAGAGCT ATCAGGATGA CCTTTCTAAA AGGCACATCT GATCAAGTCA CTTTCCTGCT 960 TAAAAACCTC AGTGCTTCCC TTTGCCCATA TTCCTTTGAA AAGAAACAGT TTCTCACAGT 1020 CTAGCCCTGG CCTGTCTTTC CAACTATGTC TTCCTCCATT CCATGCCTGG CACACTGTTC 1080 CCTCTGACTT GCAACTCCCT CTGTCTACAG TGTCCTTCTC TAACTACTAA ACTCCTCCTC 1140 TCCCTACACT GCCCTGATCT AATAACTTCT GTGAAACCAC GTCCCCTCCT GCACCTTCTT 1200 CAAGGCAGGA CTAACCACTT CCTCTCTGCT GACTTAAAGC CCTCTGTACA CAGTTCCATG 1260 AAATCTGCAC CCAGAAATGC GAACCCATAA GCCTGAGAGG CAGGGTTGAC AGCGGAACAA 1320 TTATGGGTTT TAGAATTAGA TTAACCTGGG TTAAAACACA CACACTTGCT TGCTGTATAT 1380 AACTTTAAGC ATGTTATTTA ATTTCTCTAA GCTCAGCTTC TTATAAAGGT AATGCCTATT 1440 TTGTAGAATA GGTGTCAAGA TTAAATGAGA AAATTTAAGT AAATCACCCC AGATAGGACC 1500 TGGCACACAA TAGGTGTCCA AAAATTATCA TTTCCCTCCA GACCCTGTTC CTCTTGGGCA 1560 GAAAATGTGT TTAATTTATA TTCTATATGT CCCATTGTCA CTGGTCACCC AGCACATAAT 1620 AGATGCTTGA TAGACATTAA CCTGAATGAA TGGACCCTGT CTTCTCAGAA ACATTTACAT 1680 ATACGTTTTA GAAGTACATG GGTTCAGAGG TTAGGATAGA AATTCTAAAG TGGACCTTGG 1740 CATGTAAATC CCCTTGGGTC TAATATCAAA CCAATTGCTT CCCCTTGGCA GCAGCAGCAG 1800 AGCCCTTCTG TGTCTCTGGG GAGCATTCAG CCATCCAGTC TGTGAAGATT TCTCTCATTG 1860 CTCTCCAGAG CTTCCGTTAC ATCGTGCTCT TCTCACTTCC TTCTCAGCTG TGCTCCCACT 1920 CCTCAGCCTT GTTTGTTCTG TTTTCCTCCG CCATTTTTCA CCACACACCA TATGGCCTTC 1980 CCTTGCCTGC CTTAAGCTTG GAACTTCACA GCCTTCTCCA GGCTTCCCCA GGGCAACCTG 2040 GGCCCTCTGG GCCTGCTGAC CACCCCCTTT AACTAGCAGC CCTGCCCTGA TGCCTACTTT 2100 GAAACCCAGC ACTGTTCCTA AGGAGACGCA GGACACAGAG CCTTTTAGTA AATTCACTTC 2160 AGGGGCTGGT TCTGCCAGTT AACTATGAGC CTAGAGTGTT TTGAACAGGT GGTGATCTTC 2220 CAAACACAAT GTGATCGTGT GTTTAATCTT AGAATCATGA GAGGCTAGTA GGGCAGATAC 2280 AGAAAAACAC AATTTTACCT ATTTGTTTCA ACCTCCTCCA GCATCCAGTG AGGCAGCCTC 2340 CTGGTGCAGA GGATCCTTGA CAAGCTCTGG AGTCTCGTGG ACACAAGTTT GTGTCCCAGC 2400 TCTGTGTCTC CCTAGCGGTA TTGTATGTAT GCTTCTCAAG TTCTCTAAAC CTTAGTTTCT 2460 TCATTTGTGA AACTAAGATA ACAATACCTG CCACACAGAG TTATTAGTTG ATATCATGCG 2520 TTTATTTGTT ATCTAGCAAT 2540
|
| |
|
|
|