Tag | Content |
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EnhancerAtlas ID | HS098-14566 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:112007110-112009190 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr12:112008864-112008875 | TTAATCCTCTT | - | 6.14 | Crx | MA0467.1 | chr12:112009056-112009067 | AAGGGGATTAG | + | 6.32 | Nkx3-2 | MA0122.3 | chr12:112007168-112007181 | ATTAAGTGTTTAA | - | 6.19 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 112007759 | 112007843 | chr12 | 112007223 | 112007484 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I111569 | chr12 | 112007197 | 112009194 |
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Enhancer Sequence | TGGAAATTAA GTAATATTCC ATACAGATCG CATAGCTTAA AACAGTGCCT GGTATGTTAT 60 TAAGTGTTTA ATAACTGCTA GCTAATATAA TTATTTCCTC ATATTCCAGC ATACACTAGA 120 GTAGTAAAGG AGAAAAAAAA GGCCAGTCGC AGTGGCCCAC ACCTGCAATC CCAGCACTCT 180 GGGAGGCCAA GGTGAGTCCA GGAATTTGAG ACCAGCCTGG ACAACATGGC GAAATCTCGT 240 CTCTACAGAA AGTTTTAAAA ATTAGGCAGG TGTGGTGGCT CATGCCTACA GTTCCAGTTA 300 CTTGGGAGCT GAGGTGGGAG GATCACTTAA GCCCAGGAAG TCGAGGCTGC AGTGAGCCAG 360 GATCATGCCA CTGGACTCCA GCCTGAGTGA CAGAGCGAGA CCCTGTCTTA AAACACCACC 420 ACCACCACCA CACTCTTCAT ATGAAGTTTT ACCCCTTCAG TGCCTTTACC CCTTGAGTCC 480 CTCTAGAGAA AGGGATAAAA GGCTTGGTCA TGAAGCCATG AACAACTAGA TCCAACCTAG 540 ACACACCAAA AAATCCAAAC AACTCAGGTA GAAAAGGATC TTAGGGCTCT AGTCCCATGC 600 TGTCCAAGAG AACTTTGTAC AATGATGAAG ATGTCCTATG TCATGCTGTC CAATATTGCA 660 GCCATTAGGC ACATGTGGCA GCTAAGCACT TGAAATACGA TTAGTATGGC TGAGGAACTG 720 AAATATTTAA ATTTTAATCA ACATAATTTT AAATTTAAAG AACCATGTGT GGAAGTAGCC 780 ACAATACTGG ACAGTGCCCA TTCCCATCTT CTCGAGTTCT CCAGACAGTA AGCCACCCCC 840 TTCCACGGCA TTCATATCAC CTCTGACTTA TGCACCAAGA ATGCTTCCTG ACAGGAAACT 900 CAAGTCTCTC CCAACGATCT ACCCGTTGCT CATAAACTTA TCCCTTTCTG GAGGCCACAA 960 AACAATTGTA TTCCCCTTCA AAAGACTATC AGTGGAGGAG AGGGGAGTAT AGCTGAAACA 1020 ACGTTGGCCA TTTACTGATA ACTGCTAAAG CTGAGTGACA GGTACATAAG ATTCATCCAG 1080 CTGTTCTCTT TCTAAATACG TTGAAATTTT ACATTTTAAA AACCTTATTA GCGTTTACTT 1140 TAAGCTCATT TCATTTTCTA ACTGAAACAT ATTCTTCCAA ATGTGTTTCC TTACTTTCAG 1200 TGAGGACCCC CTCCAATTCT TCTATCACAC TGTGAACCAA ATTTTTTCTA CATACACCAT 1260 GTGTATAGCA ATCCCTGTAC TTTAGCACAA ACTCTTCCCG CCTGGAACTT CCTCCTCTCT 1320 TCATGGCCTT ACTGAAAACT GCTTATCTTC CTTGAAGATC CATCTCAACT CTCATTATTT 1380 TGAAGCCCTT TTTCTTCACT GCCCACCCAT GGCAGTCCCC TCCCAGTGCT ACCAATTTAA 1440 ACTATCTGCA TGCCTGCCTT CTCTACTACA CTGGGTAACC TGGAAGCAGA GATAATGTTT 1500 CATTCATCTT TGTCTCTGTC CTAGTCTGAC AGCATCAAAT GTGTAATGAA TTAATGAATA 1560 TACAAACTTA ATGAAACGCT AAACTGTAGC CATTCATACT GTACTACCCC AAGCCCATCA 1620 ATACCACTTT TCAACCTTAA CTTGCTGGTG TAGTTTCTAC TGGTTTCCAA ACATGCTAAT 1680 AAGAACAGCT AAAAGTTACT GAGCACTTAT TACTTGCCAG GCATTGCTTT AAGCGTGTTA 1740 CATGTTTAAT TCATTTAATC CTCTTCCATC CCCTTTTTAC AGGGGAAGAA ACTTAAGCAT 1800 AAGTGAAAAT AACTTGCCTT ACATCACGAA GTATGAAGGA GCAGGGATGC GAATACTAAT 1860 TGTAAAGTCC CTGCTCCTGT GTACAACAAG GAAGACAAAT CATAATCTCA AATGCAAGCT 1920 TCAAATCCCA AAATTCAGAT TTGGGAAAGG GGATTAGGAT GCCAAATAGG AATACTGACC 1980 TGTAAAAAGA AAAAGTAACT TTAGGCATTC TCCACAAAAC AGTGTGAGGG AAAATGGTAA 2040 TCTTTTTATT CTTGTAATTT ATAGTAAGCT ACTACTGAAT 2080
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