Tag | Content |
---|
EnhancerAtlas ID | HS108-10468 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr12:112007240-112009080 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 |
|
| 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 |
GH12I111569 | chr12 | 112007197 | 112009194 |
|
Enhancer Sequence | AGAAAAAAAA GGCCAGTCGC AGTGGCCCAC ACCTGCAATC CCAGCACTCT GGGAGGCCAA 60 GGTGAGTCCA GGAATTTGAG ACCAGCCTGG ACAACATGGC GAAATCTCGT CTCTACAGAA 120 AGTTTTAAAA ATTAGGCAGG TGTGGTGGCT CATGCCTACA GTTCCAGTTA CTTGGGAGCT 180 GAGGTGGGAG GATCACTTAA GCCCAGGAAG TCGAGGCTGC AGTGAGCCAG GATCATGCCA 240 CTGGACTCCA GCCTGAGTGA CAGAGCGAGA CCCTGTCTTA AAACACCACC ACCACCACCA 300 CACTCTTCAT ATGAAGTTTT ACCCCTTCAG TGCCTTTACC CCTTGAGTCC CTCTAGAGAA 360 AGGGATAAAA GGCTTGGTCA TGAAGCCATG AACAACTAGA TCCAACCTAG ACACACCAAA 420 AAATCCAAAC AACTCAGGTA GAAAAGGATC TTAGGGCTCT AGTCCCATGC TGTCCAAGAG 480 AACTTTGTAC AATGATGAAG ATGTCCTATG TCATGCTGTC CAATATTGCA GCCATTAGGC 540 ACATGTGGCA GCTAAGCACT TGAAATACGA TTAGTATGGC TGAGGAACTG AAATATTTAA 600 ATTTTAATCA ACATAATTTT AAATTTAAAG AACCATGTGT GGAAGTAGCC ACAATACTGG 660 ACAGTGCCCA TTCCCATCTT CTCGAGTTCT CCAGACAGTA AGCCACCCCC TTCCACGGCA 720 TTCATATCAC CTCTGACTTA TGCACCAAGA ATGCTTCCTG ACAGGAAACT CAAGTCTCTC 780 CCAACGATCT ACCCGTTGCT CATAAACTTA TCCCTTTCTG GAGGCCACAA AACAATTGTA 840 TTCCCCTTCA AAAGACTATC AGTGGAGGAG AGGGGAGTAT AGCTGAAACA ACGTTGGCCA 900 TTTACTGATA ACTGCTAAAG CTGAGTGACA GGTACATAAG ATTCATCCAG CTGTTCTCTT 960 TCTAAATACG TTGAAATTTT ACATTTTAAA AACCTTATTA GCGTTTACTT TAAGCTCATT 1020 TCATTTTCTA ACTGAAACAT ATTCTTCCAA ATGTGTTTCC TTACTTTCAG TGAGGACCCC 1080 CTCCAATTCT TCTATCACAC TGTGAACCAA ATTTTTTCTA CATACACCAT GTGTATAGCA 1140 ATCCCTGTAC TTTAGCACAA ACTCTTCCCG CCTGGAACTT CCTCCTCTCT TCATGGCCTT 1200 ACTGAAAACT GCTTATCTTC CTTGAAGATC CATCTCAACT CTCATTATTT TGAAGCCCTT 1260 TTTCTTCACT GCCCACCCAT GGCAGTCCCC TCCCAGTGCT ACCAATTTAA ACTATCTGCA 1320 TGCCTGCCTT CTCTACTACA CTGGGTAACC TGGAAGCAGA GATAATGTTT CATTCATCTT 1380 TGTCTCTGTC CTAGTCTGAC AGCATCAAAT GTGTAATGAA TTAATGAATA TACAAACTTA 1440 ATGAAACGCT AAACTGTAGC CATTCATACT GTACTACCCC AAGCCCATCA ATACCACTTT 1500 TCAACCTTAA CTTGCTGGTG TAGTTTCTAC TGGTTTCCAA ACATGCTAAT AAGAACAGCT 1560 AAAAGTTACT GAGCACTTAT TACTTGCCAG GCATTGCTTT AAGCGTGTTA CATGTTTAAT 1620 TCATTTAATC CTCTTCCATC CCCTTTTTAC AGGGGAAGAA ACTTAAGCAT AAGTGAAAAT 1680 AACTTGCCTT ACATCACGAA GTATGAAGGA GCAGGGATGC GAATACTAAT TGTAAAGTCC 1740 CTGCTCCTGT GTACAACAAG GAAGACAAAT CATAATCTCA AATGCAAGCT TCAAATCCCA 1800 AAATTCAGAT TTGGGAAAGG GGATTAGGAT GCCAAATAGG 1840
|