| Tag | Content |
|---|
EnhancerAtlas ID | HS017-02649 | Organism | Homo sapiens | Tissue/cell | CD14+_monocyte | Coordinate | chr1:200328740-200330170 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-3 | MA0672.1 | chr1:200328902-200328912 | ACCACTTGAA | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 200328941 | 200329384 | | chr1 | 200329509 | 200329993 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I200359 | chr1 | 200328729 | 200329728 |
| Enhancer Sequence | TAAATAAAAG AATGGAAGTA TTTTAGCTAC AGCAATGTCA CTCAAATCTT TGAAATCCTT 60
GAAAGTCATA GCCCCAAATC ACGTTGTAAT CTATCCTTAT GTTCAGCCAG GCACAGTGGT 120
GTGCAACTGT AATCCCACAC CCTTTGAGGC TGAGGTGGGA GGACCACTTG AAGTTCCAGG 180
CTGTAGTGTA CTATGATCAC ACCTGTGAAC AGCCACTGCA CTCCAGCCTG GGCAACATGG 240
TAAGACCCTA TCTCTAAAGA GTGTGTGTGT CTGTGTGTGT GTGTGTGTGT GTGTGTGTGT 300
GTGTGTTTAG GTCTCCCTTC AAGTATGTTG AAAGCGAACA GCCAGACTCA TCTGACTTGT 360
AAAAGGAAGT GTCACTGGCC CTGAGTCATT CACATTCTCC TACATGCATT ATATTTGAAA 420
TTGGACCTAG GTTTGGGTCC CGGAGGTTTT TTTTTACCTT CCCAAACACA CCATAGGAAG 480
ATGATGGAAG TGCAAGAGGT GTGCATTTTC CCTGTTCTCT AAGGGATCCA TTTGAGAAAA 540
GTGTGTATAT ATGGACAGTG AATATCTGAA AATTGCTTCC CTCCCTCAGA ACCACTGATT 600
CTATTTGCAG CCACGTGACT CTCAAATCTA GCTCATCTCT TACTAAGACC CTGACCCTGC 660
AGCCTGAAGC ACACTGCTTC ATCAGCCCTC AGGCCCCTCA ATAGGTCTCA CATTGAGCTA 720
ATCTTCCCCA AATAGATCTC CCTTACTAGC AGGCACCCTC ATGCACTCTG TTCACCACAC 780
TGCTGCCAGA TCAACATCCT ACACAAGCAA ATCCTGTCAA GTTGCTCCTC CACTTGAACT 840
CCTTCACTGG TGCCCAGAAT CTACCTTAAC CCTTTGCAGG TAAAGCACCT CATCTGAGAA 900
ACAGTGAAGT CAGGTCCTCT ATGGGGAAAT GACACATGCT CTCAGGCTGA CCCTCTGAGA 960
CCTGGTTAAG AAGTGCCAGA CCTCAAGGAG ACAGGACAGG TTAGTGGTTA AAAGGATGGA 1020
CTCTGGAATG GAACTACCTG GGTTAAAGGC AGTTTACTCA CTGATAACTT TGACCCCCTG 1080
AGCCCATTTC TTCATCTGCA GAGGATAATA CTACTATCTT TCTTAAAGGG TAGGTGTAAA 1140
GATTAAGTGA GATAATGTAT GTAATTTGCT TAGCACAGTG CTTGACACAT GCTAGAATAA 1200
TAAGTTAGAA TAATACGTCA ATGAGTCTTA GCTGCCATCA ACTTCCTCAT AATTATCAAG 1260
AAATTAACTC CCAAAGTCTT CCATTGAAGG TCCAAGTCCC TTACATGTCA AAGAAGCCCA 1320
TCTTGCAGCC TCTACTCTAC TCTTCCCCAT ACCACACCAC TTACTATCTT CCCCGTCCCT 1380
CTCCCAGATC AGGCTTTTGT ACCTCTGAGT CTGGGTACCC ACCCTTCCCC 1430
|
| |
|
|
|
