| Tag | Content |
|---|
EnhancerAtlas ID | HS187-12789 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:8452340-8453660 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr2:8452983-8452993 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr2:8452983-8452993 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr2:8452983-8452993 | AATGGAAAAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_20349 | chr2:8448174-8458311 | CD56 |
|
| | 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 |
| GH02I008312 | chr2 | 8452320 | 8454331 |
|
Enhancer Sequence | GTCCTCCCAG CCCCACCTCC TGCTCTCTAC ATTCACAGGA CCCCAGGACT CCCCTGCCCC 60
AGATGTCTGG AAGTCCCTTC TCTCATTCTT TATGAGAGGC AAGCTCCTGC CTGTCCTTTC 120
AGATCTTCAC TTAGATTTGA CTTCCCCTGG GAGATACTGG TTGGCCCCTG AGATCAGAGG 180
TGGTGCCTCC TCTGTGTGCT GGTGGGGTCC TGGGCTCTAG CCACAGAAGC ACCTGTCAGC 240
TACATGTTGG TGAGATGGTT TTATGGCACC TGGCTCAGCG CGGGCCCTGA TGCAGACAGT 300
CCAGGTGTGA CCCCTGGCTC TGCCATTCAC TGGCTTTGTG TCCTCTGAAA AGCCACGTCA 360
CACCCCTAAG CCTCTTTCTT TCCCTGTAGA ATGAGGACAG CAGCAGCCTC TCCCTCCTCC 420
CTCGGAGGGT TATTTTGAGC CTTGAATGAT TTCATGTGGA TTGAGTGCCT TGAACATGGG 480
TGTATTGTCA GTGTTAAATA CGAGTTAACT AATACCTGTT TTGTCTCCTG TGTTTGCCCC 540
ATGCCTGATC CCCATGCCGG TGGAGGCTGT TTCCATCTTT TGTCTGTGGT CTCCATAAAT 600
GCAGCCAGTG TTGAACACCC AGTAGAGGAT CAGGCACTGC TGAAATGGAA AATTCAGAGA 660
ATGAGTGGCC CATGGAAGGC AGAAGACGTG GGCCCGCCTG CTGAGGGAGA GCAGGTGAGG 720
AGGCCAGAAA CCTATTCCTC ACAGTTTTGG AGGTTGGAAG TCCAAAGTCA AAGTCCAGCA 780
GGTTTGGTTT CTGGTGACGG CCACCCGCTG GCTATGTCTC CACATGGCCA GAAATGTGCA 840
CCTAAACTGA GAGGCAGGGA GCTCTCTGCT ATCTCTTCTT GTAAAGACAC AAATCCGATT 900
AAGTCAAGGC CCCACCCTTA TGACTCATTT AACCTTAATT ACTTCCTTAG AGGCCCCATC 960
TCCAAATACA GCCACACAGG CGGTTAGGGC TTTAGCATAG GAATTGCAGA GACACAGACA 1020
TTCAGTCCAT AGCAACCCTC CTGCCCTAGA CCCCCTGGCT CTGTATACAG AGAGAACAAC 1080
ACTGTCCTCC CCACATTCTC TGGTGTGAAG AGGTGAAAGG GAAAATCATT TCATCAGCAC 1140
TCCACCTAAG CCAGCTGCTC TAGCCACGGC TGCTAATGAC CAGCTAAGCG TGTCCATTGC 1200
TTCTGGAGCC TGAGAATTTG GTTTTTTTGT TTTTTTTTTA ACAGGGGACC TTATTAGCTG 1260
CTAACTGCTG AGATGAGAAA TTGTGGTCAG ACCATTCAGG TGCTCAGCCT TTCAGCTGAA 1320
|
