| Tag | Content |
|---|
EnhancerAtlas ID | HS023-10013 | Organism | Homo sapiens | Tissue/cell | CD8+ | Coordinate | chr16:89907150-89908580 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr16:89907602-89907623 | AAAAGGAAAAAGAAACTCAGG | - | 6.31 |
| | | 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 |
| GH16I089841 | chr16 | 89907781 | 89907930 |
| Enhancer Sequence | CTCCTGCCTC AGCCTCCCGA GTAGCTGGGA CTACAGGTGC CCGCCACCAC GCCCAGCTTA 60
TTTTTTTGTA TTTTTTAGTA GAGACGGGGT TTCACCGTGT TAGCCAGGAT GGTCTCGATC 120
TCCTGACCTC ATGATCCGCC TGCCTCGGCC TCCCAAAGTG CTGGGATTAC AGGCGTGAGC 180
CACCGCGCCC AGCTGAAACC TGTCATCTTT TACAAGCACA CACAGGATTG TTTCAAAGAA 240
GACTCCCTAG CATCTTTGTT CTAGTCATTT GTTATTTTAC ACAAAAGAAA TCTGAGTCAG 300
GTGCAGTAGC TCACACCTGT ACTCCCAGCA CTTTGGGAGG CTGAGGCGGG AGGATCGCTT 360
GAGCCCAGGA AGTCATGGCT GCAGTGAGCC ATGATTACAC CACTGCACTC CAGCCTGGGT 420
GACAGAGCAA CACCTTGTTT CAAAAAAAAA AAAAAAGGAA AAAGAAACTC AGGTGGCTTT 480
TCTTCTCTCA TTGAGGCTGT GCTTCCCTGC AGGGAGAAAT AGGCTCTTAA CTCTTAGTGG 540
TGGATGGAAA CGAGGGGTCC TGGTTCTGCC TCCCACCTTA GCATGGCACT AATAGACTTG 600
ATGAGAATCT GGGGTCCTTA CTGCCTCCGT CTGCTCTACC CTGGAGAGAA TTTTTTAGAT 660
AAGCAAAAGG TGGTTTGCAT AACCCCATGT GGCCACGTTG GTGACGTGGT TGTGGTAGCT 720
CTGTGGCCAC GTTGGTGACG TGGTTGTGGT AGCTCTGTAT GCACTTATAC CTGGGTGTTC 780
GGCTGGGTTG CTTGCTGTGG TCTGGCCATG CTCGGTGGCC CAGCTGCCCC ATTTATTAGG 840
GGTATGGTCT TGGGTAAGTT TCTCAACCTG CCTGAGCCTC GATTTCCTCA TCTGTAACGA 900
GGAAATTATG GCACCAACCT TTATGGGATG GCTGCGCAGA TAGAGGCCAC GGTAAATAAT 960
TTTTTTTTTT TTGAGATGGA GTTTTGCTTT TGTTACCCAG GCTGGAGTGC AGTGGCACGA 1020
TCTCGGCTCA CCGCAACCTC CACCTCCCAG GTTCAAGCCG TTCTCTTGCC TCAGCCTCCC 1080
AAGTAGCTGG GATTACAGGC GTGTTCCTCC CGAGTAGCTG GGATTACAGG CATGCGCCAC 1140
CATGCCCGGC TAATTTTGTA TTTTTAGGAG AGGTGGGGTT TCTCCCTGTT GGTCAGGCTG 1200
GTCTCCAACT CCTGACCTCA GGTGATCCGC CTACCTCAGC CTCCCAAAGT GCTGGGATTA 1260
CAGGCGTGAG CCACCGCACC CCACAGTAAA TAATTTTTTA ACATCTAGTT TTATAACATC 1320
TGAGTTTTAT AACATCCTGG GCTCGGGCTC TGACTGCAAA GGCCTCTGTC GGCCCCCAAG 1380
TCTCCCCCAG ATAATCTCTC ATCTCAGAAC CCAGAGACAC CCCAAGTCTT 1430
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