| Tag | Content |
|---|
EnhancerAtlas ID | HS076-26815 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr18:43340100-43341150 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| 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 |
|
| | 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 | TTCCTGCCTC CAACTCCCCA CCCACCATGT GAGGAAAGCT TATGCTTCTC TTCCTTTCTC 60
CTGGGGACCT CCTTTCACTG CCACACCAGT CCCACTTGTC CCACCTCTGC CCTACACATT 120
CCTCATGGAC AGCGCCCATC ACCTGCCGCT CTGCCCCTCA CTGCCAATCA CAGGGCCCTG 180
CAAGCTCCAA GCCACACGGC CAATGGTAGC CTAAGGACCC CCTTCCTGCA CACCTCGAAT 240
TGACCACCAC TGTCTGCTCA TCCTAGGAAC CTCCAAATTC AGGCCCTTTC AACCCTCAGG 300
ACTCCAGATT ATTCTTCCCT ATACCCACAT CTAGGACTGA CCCACTGCTG ATTCACACCA 360
GTGCAGACAT TCAAATTATT AAAATATTCA GTTCTTTTGC ACACTTTGTG GTAAGTAGCC 420
ACTGCCCTGA GCCCTGTCAC TTGAGTCTCT CTATGACCTT CAGGAATTTC TCCACAATCC 480
AGCAACTAAA GGGTTAACAC AAAGCACAGC TGTGAGTTCC AGCAATCGTT CTGATTGGTC 540
AGTCCCCTTG CCTTACCAGG TGATTAAGGT TTTAAATTTC ACTGTGGCAC CACACGGCAG 600
ATAAATTTTG TATGCCTAAT GCTGGTTGTA ATTTAATGCA AATAATCATT TCTTTTGAGG 660
CTGCAAGATG GGGTCTAAGG ACTCTGGACT CAGCGTGAGG TGCATGAGGG CATGCAAACA 720
CCTGGCATCA GGATCGTGCA GTCACACCCA CATCAAGCCA ACATCTGCAT AATGCAACTG 780
AGAAGCAGCA AAGCTGGTCC CCTAAGATGC CTTCACCAGC AGCCCACCAC GGAGCCCAAC 840
ATTTCTCCAC TCATTCCCTG AATTTTCAGT GAGAGAAGCA ACACAATAAG ATCTCAGATA 900
GCAACATCCT AATTGAATTA GTTTTACCTG GTCTCTTCCC AGTTTCTTCC TGCCTAATAG 960
CAAGAGAAAG TCCTGGCCAG TGCAGTGGCT CACGCCTGTA ATCCCAGCAC TTGAGTGCTG 1020
GGATGGATCA CTTGAGGTCA GGAGTTTGAG 1050
|
