| Tag | Content |
|---|
EnhancerAtlas ID | HS187-13731 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:102920650-102921940 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ONECUT3 | MA0757.1 | chr2:102920742-102920756 | TATAAATCAATAAT | + | 6.18 | | SOX10 | MA0442.2 | chr2:102921120-102921131 | AAAACAAAGGA | + | 6.32 | | Sox3 | MA0514.1 | chr2:102921120-102921130 | AAAACAAAGG | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 102920800 | 102921075 | | chr2 | 102921160 | 102921494 |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH02I102306 | chr2 | 102920800 | 102921075 | | GH02I102304 | chr2 | 102921160 | 102921494 | | GH02I102305 | chr2 | 102921511 | 102922603 |
|
Enhancer Sequence | AGACTATAAT TATCTCTGAG TATTAGGTTA TGAGAATTTT TTCATTTGTA GTATTCTATA 60
CATTTTAAAA CTTATTAACT GAGCATTACT GATATAAATC AATAATTTTT AAGTGACTTT 120
TGTGCCCTAC TACGCTGGTG CTGTGTGCTT CAGACTGAAG GGCAGTGCCT GTTAGATCTT 180
ATGTGCTACA TGTTACACAA GTACTTTGGG AAATAAGCTG TTGTTTTAAA AAATGTGTCA 240
TCAATTTCTA GAGAACTGGA CATAACTTTG AAGCAAAACA ATTTTAAGTG GATGACTAAA 300
ATCCTTCCTG AAAACGCATG CCTGTGGTCC CTGTGAAATC ACCTTTTCTC CCCCTTTCCT 360
AATCTCCTTT CCCTCCTAAA TCTAAATTTT CTTGTAATGC TTCAAAATAT CTGGACTTGA 420
TCTCAGAAGA TATTCTGTCA TGCATATTGA CAGGACTGGG TACTTTCAGC AAAACAAAGG 480
ACATCTTTAA ATTTTTACCA GCCCCAGATA GAAGTGTCTA GAGTTCTAGA TTTTAGGAGA 540
AATACAGCCA TGAAGGAAAA TGTTGACATT TATTTCAACG TTTCAACAGG AGGAAAGAAT 600
GAGAACACAA TGTACAGATC AGCCTTTCCT CTCATGTTCT TACAATGGGA GAAGGAGAGA 660
GGGTATTTGA GACACCAAAG CATGAAAGCC ATGACACAGG GAAAATACTG AGAACATAAC 720
CTACAGATCA GATTTTCCTT TTATGCTCTT ACCATGTCAT AAGGCAAAGT GCTTGTTTGA 780
GATTTCAGGG CACAAGAGCC ACTACAGCAG GAAGGCGTCG CATCATCGGA ACATTTGTGA 840
TCAAAGAGAA GACTGTCTGC ACAAAGCACG GACTGCAGCC AAGGGGTCCT TCACCCACTG 900
TTCTCACAAA TGCTTGCCTT TGCTATCACA ACTGCTATTG CCAGCTGGAC GCTGAGTGTC 960
CCCTCAGGGT TCATAGAGAT CTGTCTCCCT GAGGTCTCTT AGGTGCTGCT GCTGACCAGT 1020
AGTAACTTGG TGAAGACCCT CGATTGTGAG GACATTGTGG TGAAATGTTG CTTTCTTGAC 1080
AAAACAAATG TGTTTCCTTC TGATCCATGA ACAAAGATCT GTTGAATAAA TATTATGAGC 1140
GTGTAGAAGG GAGAGACTTT ATCTGATCAG ACTAGGGAAA GGGTGCTTTT AATATCTGTG 1200
GAACAATCTG TAAGATCGGA CGTTTCCTCT GATAACAGAA ACTCCAGAGT TACAAGAGAA 1260
ATGGCTTCCT GACATCACAG ACACTAAAAG 1290
|
