Tag | Content |
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EnhancerAtlas ID | HS023-10188 | Organism | Homo sapiens | Tissue/cell | CD8+ | Coordinate | chr17:6839590-6841050 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr17:6839897-6839908 | GACCAATCAGA | + | 6.14 | NFYA | MA0060.3 | chr17:6839877-6839888 | TCTGATTGGTT | - | 6.62 |
| | 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 |
GH17I006936 | chr17 | 6839520 | 6840518 |
| Enhancer Sequence | AACAATTGGA ATAGAAGAAT GGACAGCCCA GAAACAGGCA TATATGGACA CTTCATTTTT 60 GACAGAGGTG GTGTTACCAG CTGAGGGTAG TTGTCCAGGT TCTTGGCGTT TTGAACAAAG 120 AACTGGACAA AATGGACAAA GCAAGGCAGC AAGAGCAGAG ATTTGTTTTA AATGAAAGTA 180 CACTCCACAG GGTGGGGGTG GCTCATGCAA GCAGCTCAAG ATTCTTGGTT ACAGAATTTT 240 CTGGGGTTTC AATTCCCTCT AGGAGTTTCC CATTGTCCCC CGACCAGTCT GATTGGTTGC 300 AGGAGGGGAC CAATCAGAGG TACTTTCATT TTTCAACCGC CAGGCAGAAA AAGGAGGGGC 360 AGCAACTGTC GCGCAGAAAA AGGGGGTGTT GAAGAGTAGC CTCTGATATC CAGTGAGCAT 420 GAACCGGCCT TAGGTTTCCT GCCTCCAGAC CCTATTCTCC TGCCTCATTT CCCCCCCTGA 480 GAGACAGGAT CCCCGTAAGT CTTTATGTGA GACAGAGGGA CTGATGGTCT TTTTTCTGTA 540 ACTGCGTCAC ACTGACTTGA CTGACAGTCC CTGCCTATTG GAATCACAGA ACTCTCACCC 600 TGCTCTGTCT AGTGGAGACA GGGTAGTTTC TTGATGGCCA GGGGTGGTGA ATTCATTTGG 660 AACTGGCTGG AAACCTTACT GCACAATCAT CTCCAGGCAA GAGGAAATGA ATGGTTAAAA 720 GATTTCATGG GAACTTCAGG AGGTGGACAC CTATGCTGTC AGGAATGTTT GTTATAGAAA 780 TGAATTAAAA GATTCTACTT AATTACTATG AAGGAAGTGA TTCCAACTGT TTGAAAGAAG 840 GTAATTAATC TGCAAAAAAA AAAAAAAAAA AAAAAACATG GCTACTATTA TCCAGCCTAC 900 AGTAACTATG CAACAAAAAC ACCAAGGAAC GTTGGTAGGC ATTTCTCTTT TGGCTGTCTT 960 CTAAACAGGT ACTTCAGGGC TGCCACAGGT TCACAGGTGC AGTGGCTGAT GGGAACTTCA 1020 GGTTCCAGGT CCGGGGCTTC AGGTATCACA GACTTGATCC TTGAAAGGTG TATCCAACTA 1080 TCTAATCCCA GTACTTTGAC CGCAGAAGGC GTGGCCAGTA TCACTGAAAA CGGTGCCTTC 1140 CATTGGGGTT GTAATTGTTG AGGAGGTGAC CCCTCCGTCC ATGCTTTAAC AAGCACCTTA 1200 TCTGCTGGCC TGATTTGAGG TGGCTGGTTA GCTTCCAGTA CCGGAAGCCT TTGAGTTCCA 1260 AACTTCTGTA TAAACCTGCT GACATTGTCC TAGGTTAACT AGGTATTTTA CTAAACCAGC 1320 TGTTTCTGAA TCAGTAATTA CATCATCAGT TAAGAATAGC CTTCTGTAAT CCCAGCACTT 1380 TGGGAGGCCA AGGCGGGCAG ATCACCTGAG GTTAGGAGTT CAAGACCAGC CTGACCAACG 1440 TGGAGAAACC CCATCTCTAC 1460
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