Tag | Content |
---|
EnhancerAtlas ID | HS076-04191 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:159177270-159178630 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYB | MA0502.1 | chr1:159177797-159177812 | CTGATTGGTTCGTCC | - | 6.34 | SP2 | MA0516.2 | chr1:159178354-159178371 | CCTACCCCCGCCCCCTG | + | 6.25 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 159177600 | 159178400 | chr1 | 159178400 | 159178475 |
|
Enhancer Sequence | CATACATCTT TCCTTCCACC TTCCACACAA TACCCCAATC CCCTGGGCAC CTTTTTCCCA 60 ACCCCTGATT CTCTGGCTGC TTAATCATGA CCTTTGAGAT TTTTCTCAGT CTCTACCTAC 120 CCAAGTTTAG ATGGCTGGAA GGACAGAAAC CCCTCCTCAT CAGGGGCACA GCTTTTACCA 180 CCAAGAGCAA ATTCACCCTC TACCCAAGAG GCTACAAAAC AGTTAGTTCC TACCTCTAAC 240 CCAACTAAAG GCTGGGGAAA CTTGAGCAGA TACGTTCTAT CAGTTTGAAC CCAATTACCA 300 TCTTACCATT TTCCAAAGAT ATGCTATACC TGGTTTCTTT ACTAAAATGT TTCTGCTTGA 360 CTCTCTGGGC TTGGGAATAG TAGGCGAGTG CGGGAGAGGT GCAGAGATGA GTTAGAATAG 420 CTTAGGCAGG AGGGTGCAAA AGGCTTAGGG AATTTTCCTG GGTGGGTGCC ACGACAAGGC 480 CTCTAAATCT CCCACCTCCT GTCTCTTAGC AACCACCAGG TTAGCTCCTG ATTGGTTCGT 540 CCTCAATTGA AAGGCGGGAT TTAGGGACCG ATTGAGACGC GGGAGACATT CTGAAACAGA 600 AAGGAAGGGA GAGAAAATGA AGAGAAAGGA AATAATTTAC AAACCTAAAT TATGCTCTGG 660 TTTCCAACCA CAGTTCATGA ATGTGTTCTA GTATTTTTTC CCCCGCTTTT TTTTTTCCAG 720 GCTTCTCTCA ATATCCCCCT CCCGTCCTTG ACCACTCTTG CAATTCTACC AGATGTTGCT 780 GTCCTCCCTT ACAAGGTACT GATTTGGAAG CTGACCTAGT TGAGGGGGAG GAGAGGGCGT 840 TTTTGACTCC CTGAATCTTC CAGTGTCAAC CTGATGCAAG GGAGGCTTAA TTTAAGACCA 900 GTAGGCTTGT CTTATCTGCC CCCAACCCTG TGCCTCTGGA TAGAAATCCC TGGTCAGTCA 960 GTCCAGTTAG AGAGAACCCC AGACTCCTGG GTAATAGCTT GGCAGCTCTC ATGGCTTTCA 1020 CAAGGGAAAG GCAGCTGCAG AAGCCCGAAG CTGCTAAGAG GTTAGGGTGG GCTGGAGACA 1080 GTGCCCTACC CCCGCCCCCT GCTACATCCT CCTCATCCCC ACCCCCACCG GGATTGCTCC 1140 AGGCCTTTTG GGCTGCCCTT TCCCTGCCAT TACCTAGGCA GCACTTGGAG AGCTCCTCCT 1200 TAAGTCTAAC CCGGACCTCA GTCATTTCTT TAAAGCTTTC TTGGGGACCT GCCACCCCAT 1260 GCATTTAACC CACTGCATGC CATCAACCAC TCTAAAATTG GTCTGAGTCT GGCATCTTTT 1320 CTGCAACCCT TCAGGAATAC AAATCCTGTC TCCTTAAAGC 1360
|