Tag | Content |
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EnhancerAtlas ID | HS136-18568 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr7:111171740-111173180 |
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) |
IRF1 | MA0050.2 | chr7:111173120-111173141 | AAAGAAAAAGTAAAAATAAAT | - | 6.13 | IRF1 | MA0050.2 | chr7:111172659-111172680 | AAATGGAAAGAGAAAGTCACA | - | 7.04 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH07I111531 | chr7 | 111172015 | 111172332 |
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Enhancer Sequence | AAGCATAACT GCTATCATTA AGTAGAAGCT AAAGGCAACG TGAATTTTAA GCTAACAATG 60 TGAGGACTTA AATATGTATA TAAATGAAAC AGACCAGCTA CTTATCCATA ACCCAAGCAA 120 AGCAATTAGA GGATACTTTT CACCATAAGT CCATTTTTTC TTGAAGTAAT AATACAGTGG 180 GTTAGTAAAA GGATATATTA CCAGCATCAG GAATACTTAC TGAATAGCTA AGAAGAAAAT 240 ACTGCATTAT TTGGCATTTG GGCTGTGTTC AAAATTGGCT TTAAAAAAAT TAAGAAGGCC 300 TATAAATGGA AAAAGCACTC TTTTTAGAAA AAAAAAATCT CAAGAACCTT TCAAAAATCA 360 AAACTTAGAA GAAGTGAGAT AGGGGAAATA AGAAAAAGGT AGTAACACTC AGAACCTAAA 420 AAAAGAAGGG TACAAAATAT TAGAAAGTGG GCATTAGGCA ATAACATGAG TAATGGAAAA 480 GTATCACTAG AAACCATGTG ACAGCCAGTT TCCAAAGCAC GGTCATCCAA GTACCAAGCT 540 TTGCTGTTCC TTATCTACTT TGCTACCTCA CATTTTTTCC TACTATCTGA CACTGCTTCA 600 TATTCACTTC TCTTACACTG CAGCCCTACT TCGGTCTTAT TTTAGAATGG TACAAGGGTC 660 TTATTAGGGC TCAACAATAA GCGGAATTGA AAAACTTTTT TAAAGAACAT GGTTTCTGGG 720 TCTCATGAAA ATCCTATCCT GATCCCTACT CTTCATGCCT CAAATATATT GCTATCTATA 780 CTAGAATGCA AATGCCTTTA CTAGAATGCC ATATCAACTC AAGTCATACT TACAACATGG 840 CTTTTCCTTT GATCAGGGTT GGGAGTAAGG AGTAGGAAGG CTTCTCAAAA GAATCAGGCC 900 ACTAGACCCC AAGGGACAAA AATGGAAAGA GAAAGTCACA AAAAAGTAGG ACTGAAAAAT 960 ACAATTTAAC CAGCAAACTT ATAGCTAGCC CAGGGACTAT TACTACTCTT TACAAAATGA 1020 TAAATACAAA AAAATTAGAA ACACAGGCTC CCCCATCAGG AAAGCACATT AAGGCTCCAA 1080 TTAGTCTGTC AAAAATAAAA TCTATTCAGA CTATGGCTTG AAGATTTGGA AAGGTGCCCA 1140 CAGCCCATGT ATGGCAGCTG CAAGTCCATG GGGAGTTCAA ACAGCAACAG TGCAGAGTCA 1200 GTACTGAAGA TGCAAGCCAG AGGAAAAGAT TTATGCAATT TAAGGTGAAA GCAACAGAAA 1260 TAAACTCCCT TGGAATGAGT GCTTATGGTC CTTTTAGCTT ATAAGTGCAA GTGTACCCAC 1320 AAACATGCAT GCACACTTGC TGAAATGGCA ACAAAGGCCA AGTTAGCAGC ATATGTTAAA 1380 AAAGAAAAAG TAAAAATAAA TATATAAATA AATAGAACAG CCAAGAGGCC AGAGTATAAA 1440
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