| Tag | Content |
|---|
EnhancerAtlas ID | HS080-15987 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr18:43339200-43341030 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIL3 | MA0025.1 | chr18:43339260-43339271 | ATGTTACATAA | - | 6.32 | | NFYA | MA0060.3 | chr18:43340629-43340640 | TCTGATTGGTC | - | 6.14 | | PHOX2A | MA0713.1 | chr18:43341009-43341020 | TAATTGAATTA | - | 6.14 | | Phox2b | MA0681.1 | chr18:43341009-43341020 | TAATTGAATTA | - | 6.14 | | TBX20 | MA0689.1 | chr18:43339591-43339602 | GAGGTGTGAAG | + | 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 |
| GH18I045759 | chr18 | 43339620 | 43341042 |
|
Enhancer Sequence | TTGTCTGTTA ATCTTATGTA AAAGTGCAGA TTCCTTGCAT TTCCCCTGTC CCATGTGGCC 60
ATGTTACATA AAAATGCAGA TTCACTGAGC TAGACAAAGA CATGAATATT TTCTCCCTAC 120
CCACCTCTTG CATGAAAATT GTGTACTTCT CACTATCCTG CCCTTTCCTC TTTAAATCTG 180
GAGCCCTCAA AATCATCTTC AGAGAAAAGC ATAGACCTGT CGCCCAGATG TGCATCCTTA 240
ACTTTGGCAA ATAAACCTCC TAAAATGATT GAGACTTGTC TCATCATTTT TCTCTATTGA 300
CATAATGGGC CCTCCTACAT AAAAGCCACT GCACATTCAG AAAATTCAGA GTACCCTGGA 360
GGCTGGAGTA GATGAGGATG GCTTCCTGGA GGAGGTGTGA AGGTGTGACT CTGGCCTCAT 420
TCTGACACAT TCCCTCCCTG GCTCACCTAG ACTTGGCTTT AGGAGCTCAT CTGGGCTCCC 480
CCTGGACTCC CAACCACGCC CTTTCCAGAA CCACTTCTAG AGACCAAGGA AATGATGCTC 540
TTACCAAGGG GCCATGTTGT GGTGGGGCCT AAGATTCATA GTTCAGGCAG TGTATAGAGA 600
AGGTGGCCAG AGCAGAAGGG AGTGGCCATG GCACAGAATC TATTTTCTTT AAATGCTCAA 660
AGCTTACATA TGTCAAGTCA GCCTATAATA GCCATCTCTT CCCATTTTGA TCCCACCCCA 720
CCTTGACACA GCCAAGGCAA TGTCATGGCA TTTCTCTTAA TCACCCTCAT GGTCTGCTGT 780
GTGCTTACTC CTTTTCAACT GTAAGGATGA CCTAGAAATA TATAACCATA TTTTATATAA 840
ATACAGAACT GCCTAAAGAA GCAGCTAATA TTGTGATTCC CCTGGCCCTG CCCCCACCAC 900
TTCCTGCCTC CAACTCCCCA CCCACCATGT GAGGAAAGCT TATGCTTCTC TTCCTTTCTC 960
CTGGGGACCT CCTTTCACTG CCACACCAGT CCCACTTGTC CCACCTCTGC CCTACACATT 1020
CCTCATGGAC AGCGCCCATC ACCTGCCGCT CTGCCCCTCA CTGCCAATCA CAGGGCCCTG 1080
CAAGCTCCAA GCCACACGGC CAATGGTAGC CTAAGGACCC CCTTCCTGCA CACCTCGAAT 1140
TGACCACCAC TGTCTGCTCA TCCTAGGAAC CTCCAAATTC AGGCCCTTTC AACCCTCAGG 1200
ACTCCAGATT ATTCTTCCCT ATACCCACAT CTAGGACTGA CCCACTGCTG ATTCACACCA 1260
GTGCAGACAT TCAAATTATT AAAATATTCA GTTCTTTTGC ACACTTTGTG GTAAGTAGCC 1320
ACTGCCCTGA GCCCTGTCAC TTGAGTCTCT CTATGACCTT CAGGAATTTC TCCACAATCC 1380
AGCAACTAAA GGGTTAACAC AAAGCACAGC TGTGAGTTCC AGCAATCGTT CTGATTGGTC 1440
AGTCCCCTTG CCTTACCAGG TGATTAAGGT TTTAAATTTC ACTGTGGCAC CACACGGCAG 1500
ATAAATTTTG TATGCCTAAT GCTGGTTGTA ATTTAATGCA AATAATCATT TCTTTTGAGG 1560
CTGCAAGATG GGGTCTAAGG ACTCTGGACT CAGCGTGAGG TGCATGAGGG CATGCAAACA 1620
CCTGGCATCA GGATCGTGCA GTCACACCCA CATCAAGCCA ACATCTGCAT AATGCAACTG 1680
AGAAGCAGCA AAGCTGGTCC CCTAAGATGC CTTCACCAGC AGCCCACCAC GGAGCCCAAC 1740
ATTTCTCCAC TCATTCCCTG AATTTTCAGT GAGAGAAGCA ACACAATAAG ATCTCAGATA 1800
GCAACATCCT AATTGAATTA GTTTTACCTG 1830
|
