| Tag | Content |
|---|
EnhancerAtlas ID | HS187-21624 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:111853690-111855100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr6:111854691-111854706 | TATGGCCTTGAGCTC | - | 6.11 | | ZNF263 | MA0528.1 | chr6:111854247-111854268 | TTCTCATTCTTCCCCTCCACC | - | 6.48 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 111854366 | 111854894 | | chr6 | 111854210 | 111855021 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I111532 | chr6 | 111854090 | 111856028 |
|
Enhancer Sequence | CAGAAGCTCT GAGCTGGAAG GATTTGATCA GGGCCTCTAC AATCTAAATC TTATTAAAGG 60
CATGAATTGT CTTTGCAACA TCCCAGTAAA GTGGTCATTC TGCACTTGTT ATACTTTTGG 120
TGTAGGGATA CTCAGTGCTT ACCAACACAG TCACCTTCAA GTTCTTGGGT TTTTTTTTTT 180
TAATTGAAGC AGGGTCTCCA TCTGTTACCC AGGCTGGAGT GCAGTGGTGC GATGATGGCT 240
CACTGCAGCC TCGAACTCCT GGACTCAAGT GATCCTCCCA CTTCAGCCTC CCTAGTAGCC 300
AGGACTAGAG GCACAAGCCA CAACACTGGT TAATTTTTGT ATTTTTTGTA GAGACAGGGC 360
TTCACCATGT TGCCCAGGCT GGTCTCAAAC TCCTGGGCTC AAGTGATCCC CCAACTTCAG 420
CCTTCCGAGT ATATATACTC AGAAGTATAT ATAGGTATAT ATGGGATTAT AGGTGTGAGC 480
CACCACACCT GGCCCTCAAG TTCTTATTTA GGGAAAATAT ATTTACCTGT AATGGTGTAA 540
TCTATATATC CATTTGGTTC TCATTCTTCC CCTCCACCCT ATACAGAATA AACATCCCTC 600
CTACAATCCT TCAGATATGT GAAGACAATC ATCATGTCAT AACTGTTCTA TAACTGAGCC 660
ATCACTAACA AAGACTTGTC TCCTAAGCCT ATCAGAGCCA GGATGTTTAT TCATCCTTGC 720
CACTCAGCAA CTGAAAGATC CTCATCTCTA GAGTAGATTG GTGGTGGTAC TTCTCAGATG 780
AAAAGCCTGT GATGTGGTTG TGTTGTGTTG ATGAGTTACT GCTGAAGACA CTAGAGCCAG 840
AGAGGAAATC CTAATCCTAG AGCCCAGGCA AGAGCCGCAG ATTTGAATTA AGTTGGTGGC 900
AGCAAAGGCA GGGACCATGA TGTTTTACCT GCACCAAAAA ACAAAACCAA GAACTTTCAA 960
TTTGTGTCAT TGACATTCAA CTGAGCCTGT AATTTTCTAG TTATGGCCTT GAGCTCCATT 1020
TTACTGGCAG CTCTGCCACT GGCCAGATGC ATACCCTTGG GCAATCCTCC TCACTGCTCC 1080
CGGGTTCCTC TCTGTTATGC AAAGGCACAT GCTGCTTTTC TGCCTAGTAA ACAACACCCC 1140
CCCTCCCCCC CCCCGCCCAC AGCTAAGATG TCATTTCTCC AGGAACCCTT TCCTAACTCC 1200
TACCCCTCAC TCCAAGACTG GCCTCTGTCT TCCGATGCAC CCAATGCTCA CCTCTATTCA 1260
CTTACTTCAT TGTATTTTAA TCACCTATTT ACTTGTCTGT CTCTACTGTA CTGGAAGTTC 1320
TTTAACACTG AGGACTCAGT CCCTAGCACT TAACTCAGTG CTTCGCATAT ACCAGAACTC 1380
AGAAAAAAAT TTGTTGAAAA AAGGAAGAAA 1410
|
