Tag | Content |
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EnhancerAtlas ID | HS022-08381 |
Organism | Homo sapiens |
Tissue/cell | CD4+ |
Coordinate | chr2:113756000-113757660 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr2:113756570-113756580 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr2:113756570-113756580 | GGCACGTGCC | - | 6.02 | ZNF263 | MA0528.1 | chr2:113756745-113756766 | GAAGGAGGAGTGGGTAGGAAG | + | 6.44 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | CTCACCCAGA TGAATAAACA GAACTAGGAA CTTTGGAAGA ACTGTATGCC CATCCTCTAT 60 TCTATCCTCT TCTCTTCCTC CCCACAGATG TAATTGTCAT CCTAAATTTG ATGGTAACTA 120 TTCTCTTAAA TTTTGTTATA GTTTTACCAT CTATGTATAT GCCCCTAAAA TAGATATTGT 180 TTATGCTTTA AACTTTATAT AAATGAAATA ATACTGTATG TATTCTTTTA CATCTTGCTT 240 ATTCACATTC TTGGGATTCA TGGTGATATG TCATGTCAGT TTGGGTGCTT TGATGAGAAG 300 ATGTTAAGAG ATTTAATGGG AGACATGCCT GAAGGCCAAA AAAGAGGGAT CAGGAGTAGG 360 TAGGGAGAGC ATTCAGACTG TGAGGCAGGA CTGACACCAA TGATAGAAAA GAGAGAAGGA 420 AAGGCCAGGT GCGGTGGCTC ACACCTATAA TCTCAGCACT TTGGGAGGCC AAGGCAGGCA 480 GATCACTTGA GGTCAGGAGT TCGAGACCAG CCTGGCCAAC ACAGTGAAAC CCCACCTCTA 540 CTAAAAATAC AAAAATTAGC CAGCCATGGT GGCACGTGCC TATAGTCCCA GCTACTTGGG 600 AGTCTGAGGA AGGAGAATCA CTGGAACCCA GGTGGAAGAG GCTGCAGTGA GCCGAGATCA 660 TGCTACTGCA CTCCAGCCTG GGCAACAGAG CATCTTGAGA CTCTGTCAAA AAAAAAAAAA 720 AAAAAGAGAG AGAGAGAGAG AGAAGGAAGG AGGAGTGGGT AGGAAGAGCG TCAGACTGCA 780 GTGCACCTGT GAAGCTCTGA GAAAGTCTCA ACCTGGCACA TTGGGGAGCC CTAGAGCAAA 840 ACTTGGCTGC AGAGGCATTC CACATCAGTA GGAAAGACTG CCATCACTGG CTGGGAGCAG 900 CCCAAGAAAA GAGTGTTCTT GGCAGGAGCA CTGCCATGAA TCCAAAATTG CAGCAGCTGA 960 GGTTGTCTTC CAACTGTTCT CCTTGTAACA GGTTCTTTTA AAGGGAAGTC TGAGAGTCAC 1020 ACCTCCATGC TCACAATCCA CTCTTGTGCT GCATGGACCC CATCCTCTAC GTATGTTTGG 1080 GAGCAGATCA TCCATGCCTC CCATGGGTGT CTACCTGAAG GGAAACTTAG CAGAGGAATG 1140 TTAGTGAATG GACTACAGCA CCCATTTCTA TAGTTGGGCC AACAGTTTGT TCTCATCATC 1200 TTTTTTCTCC GCTGTCTATT CTAAATTTCC TTTACCCTCA ACTAATAGCT TGGCAGGTCT 1260 TAGTGGCTTT CCTGGGGATG TGATCAAATC CCTCACTCTG GCAGTCATGT ACTTCTTGAG 1320 CTGGGGTTAC TGCATGTCTA TTCACATTTA GTTATTCAAG GGAATACCAA GAGGTGTCCA 1380 AATGGATCAC TTGGGTTCCA CAAATATTAC ACACATATAC CTCCCTATCT TCATATGTAA 1440 AAGCAGCTAT ACCTCCTCTT ACATATACTG CTGGATGGCA GCCCATCCTT CCAAAGTATT 1500 ACCACTTACA TGGTGTTCCA GGTATACCTC CAGGAGGCCA TTCAATGCTC CAACAGGTTG 1560 CTACTTTTGG GTTGACCAAT GAGTCCAGGG AAGTAGTGGA GCAGGCTTAT ACTGACTTTG 1620 CAGGGTCAAT TACTACATTT TCAGGATTTT CTGTGTCGGT 1660
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