Tag | Content |
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EnhancerAtlas ID | HS023-14436 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr2:85517700-85519120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:85518164-85518182 | CCTTCCTTCCCTTTGTCC | - | 6.03 | IRF1 | MA0050.2 | chr2:85518678-85518699 | TTTTAGTTTTGGTTTTGGTTT | + | 6.08 | IRF1 | MA0050.2 | chr2:85518672-85518693 | TTTTGGTTTTAGTTTTGGTTT | + | 6.36 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr2 | 85518484 | 85518852 | chr2 | 85519050 | 85519090 | chr2 | 85518425 | 85519000 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I085290 | chr2 | 85518008 | 85519123 |
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Enhancer Sequence | TCAAGATATA GAACAGTTCT CCTAGTCAGC TTAGCTTGGT ATGAAAAGTA AAAATAAAAA 60 AGATATAGGA CAGTTCTGTG TTAGGGTTCT CCAGGGAAAC AGAACCAAGG TGATGTATGT 120 ATATATAGCG AGTGAGTGAG TGAGTGTGAA TGTGTAGAGG GAGAAAGATT TAAGAGGGTA 180 AGCTGGCAGG CTGGAGACTG GCAGGGAAGA GTTACAGTCT AAGTCTAAAG GCAGTCTGCT 240 AGCAGAGTTC TATTCAATTT AATGCTCAAG AATAATCCTC TTTGGCACCA TTCATTCTCT 300 GTCCTTCCAG CCCACCAGGA TGGGAGCTGG GAGCTGTGCC CCTGAGGCCC TGGGCGGCAG 360 CCACACCTTG TGAATCCCCT CTTGGGGTCA TTCTTCCCTC TTCTTGAAAG ATAACAAATG 420 TTTGCAGCCA CATCACTGTA GCCCATTCTG TAGAAGTCTG ACAGCCTTCC TTCCCTTTGT 480 CCTGTCTTTG TCCATTTTAA TCCAAAAGGG CAGTATTTCT GCTGAGGTGG TTGGTTGAAT 540 CCATGCTTCA CAGCCCCAGT CTCATTATCT GATCGTCCAG CCACACCATT GGTGTTCTCT 600 TAGGAACACA CCTTCTCATT TTTTTGCAAT GAGGCTAGGC TGAGAATTTT CTAAATTTTC 660 AAGTTCTGGT TCCTTTTTGC TTAACAATAA TTTACTTCTC ACATTTTACT ACAAGCAGTA 720 AGGAGAAACC AAGCCACACC TTCAGCACTT TGCTTAGAAA TAACTTGTGC TGAATATCTA 780 AATTCATCAC TCACAAGTTC TACCTTTCAC AAAACACTAC AAAATAACTC AGCCATGTTT 840 CTTCCCACTT TGTAACAAGA ATCGCCTTTC CACTAGTTCC AATAACATGT TCCCCATTTC 900 CATCTGAAGC CTCACCGGAA GCACCTTTAA CATCCATATT TTTGGGGTTT TGTTTTTGTG 960 TGTATGTGTT TGTTTTGGTT TTAGTTTTGG TTTTGGTTTT GGTTTTGGTT TTGGTTTTAG 1020 GACGGAGTTT CACTCTTGTC ACCCAAGCAG GAGTGCAATG GCACATGATC TCAGCTCACT 1080 GCAACCTCCA CCTCCTGGGT TCAAGAGATT CTCCTGTCTC AGCCTCCCGG ATTTTGGTTT 1140 TTTGTGCTTT GTTGAGAGAC AGGATCTCAC TCTGTCACCT AGGCTGTAGT GCAGTGGCAT 1200 GATCATAGCT CACTGCAGCC TAAACTCAAG CATTCCTCCC TCCTCAGCCT CCCAAGTAGC 1260 TAGGACTACA GGTGTGCACC ACCACATCCA GCTATTTTTA TTATTTGTTG TAGAGATGGG 1320 GTTCCACTAT ATGGCCCAAG CTGGTCTTGA CCTCCCAGGC TCAAGTGATC CTTCTGTCTC 1380 AGCCTCCCAA AGTGCTGAGT TTACTGGTCA TATGTATTTT 1420
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