Tag | Content |
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EnhancerAtlas ID | HS023-22995 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr7:43847190-43848810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr7:43848478-43848493 | TGCCCCTTGACCTCT | - | 6.49 | NR2F1 | MA0017.2 | chr7:43848481-43848494 | CCCTTGACCTCTT | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 43848574 | 43848624 | chr7 | 43848090 | 43848514 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I043808 | chr7 | 43847714 | 43849035 |
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Enhancer Sequence | CTGGGTTCAA TCAGTTATCC TGCCTCAGTC TCCCAAGGAG CTGAGGATTA CAGGCGCGTG 60 CCTAATCCTG GCTAATTTTT GTAGTTTTAG TAGAGATGAG GTTTCGCCAC GTTAGCCAGC 120 CTGGTCTCGC TCGAACTCCC AACCTCAGGT AATCCACCTG CCTCGGCCTC CCAAAGTGCT 180 GGGATTAGAG GCATGAGCCA CCATGCCTGG CACCAGGTCT CTTTTCATTG TATACTAGAA 240 AATGTTGTTT GAACAGAACC CTCCGAGATG ATAGAGTCAC CGCCCTTCTG CTCTCGTGTT 300 CTCAGCTGCC CTATCTACCC TGCAGGTTGC TGCTGCTGCT GGAGCCCACG CAGGTCATGT 360 GCCACTGTGG CATTTCCTAA ACACTCCTGC CTCTGAAGGT GGCACCCCAT GCCCCAGTCA 420 CAATTCTTTC AGAGTGTCAC AGAAGGAAAG AATCCACATG TATTCCTCAG CAGTCTGTCC 480 CTCTGTCCAA TTTGAAGAAA AAAAAAGCCC TTAATCCCGC TGTACTAATG CTCCTAAGTG 540 TTGAGGGGTC CTTCAGGAGG GCCTTGTGTC TCCAGGCAAG AGTGACCACA GAGGTGCCCT 600 TTGCCCCTCA GCCCCTCTCC CTGTGGCAGC AGTGACCTGC CTGTCTGGTG AAGCTGGAAA 660 AGGGACTAAA CACATGACAC CCAGCCACCT TCTCCCTCTG AACCGACATC CTTAGGATGC 720 ACCCAAGCTT GTCCACGTGG CAGGTGACTA AAGCAGACTC TTCCTCTGCA AGTAGGTGAC 780 CTGCAGCTGT GATGAAGAAT TGAGTTACCC TAAGACAGGG CAGTTACCCT AAGACAGAGC 840 CTAAGACAGT TACCCTAAGA CAGAGCCTAA GAGTTACCCT AAGAGTTTAA GAGCCTAAGA 900 CAGAGTTACC CTAAGGTGGA GCCTAAGAGT TATCCTAAGA CAGAGTTACC CTGCAGGGAG 960 CCAAAGGCCC GCGGGACGTG ACCAACTCAG CATTCCGCTG GAGGCTATAT GATCAAACAG 1020 CGAACTGTTT ATCATGAATG CAGGATGTGG GCAAACTCAC ACTGCCTTGC CACCAAAATG 1080 TTTGCTGAGG GACATCATGC CCTGGCGCCG GGCTCCTGGA AGTTATCTAT TGAGAAATCT 1140 AGCGCCTATT GTTCACAAGC CCGCTGTGAA CCAAACGGCT GACTGACAAT TACCCGACAA 1200 CCATCCTCCC ACTTTCTTGC TGTCTCTTTC ACCTAATAAA TACAGAGGGC TGTGTAAAGC 1260 TCACGGCCCT TGTCCACTAG AGGCAAGATG CCCCTTGACC TCTTCTTCCA AATATACTCT 1320 TTTGTGTCTT GTCTTTTATT CCCACATTCG CCCCCCTTTG TTCAGTCCCC CGAGGTCCAT 1380 GCAGGTTACA AGTGGCACCC CAAACAGCAA CAGGATCGGG TGCTCTGCAT AGTGGCATCC 1440 GAACACAGGA CTTCGAGGAC ATGAATGAAG AAAGTCCGCT GGAGCAGAGG AACTGAAATT 1500 GACAAGGCGA ATGGGGACCC CGAAACGAGT CTGCCAGCAG CAGAGATAAG GTCAGTGCCC 1560 TAAAGAGGTA CTGATCAGTG CCGTAAAGAG GTACTGGGAG CAGTGCTTTA AAGAAGTACT 1620
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