| Tag | Content |
|---|
EnhancerAtlas ID | HS017-18919 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr2:128319900-128321720 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr2:128321228-128321243 | TGAACTTTGCCCTCT | - | 7.53 | | Hnf4a | MA0114.3 | chr2:128321226-128321242 | AGTGAACTTTGCCCTC | - | 6.65 | | NR2C2 | MA0504.1 | chr2:128321228-128321243 | TGAACTTTGCCCTCT | - | 6.16 | | Nr2f6(var.2) | MA0728.1 | chr2:128320281-128320296 | TGAACTCCTGACCTT | - | 6.04 | | ZNF263 | MA0528.1 | chr2:128321583-128321604 | AGGGGAGGAGAGGAAAGGAGA | + | 6.68 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 128320587 | 128320796 | | chr2 | 128320572 | 128321000 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I127562 | chr2 | 128320376 | 128322106 |
|
Enhancer Sequence | AGTCTCTGTC AGCAAAGCTG GAGTGCAGTG GCACGATCAC AATTCACTGC AACCTCCACC 60
TCTCAGATTC AAGCAATTAT CCTGCATCAG CCTCCTGATT AGCTGGGATT ACAGGCGCCC 120
ACCACCACGC CCAGCTAATT TTTGTGGGGT TTTATTGTTT TTTTTTTTTT TTTTTTTTTT 180
TGAGACGGAG TCTTGCACTG TTGCCCATGC TGTTGTGCAG TGGCATGATC TCGGTCACTG 240
CAACCTCTGC CTCCCGGGTT CAAGCAATTC TCCTGCGTCA GCCTCCCATG TAGCTGGGAC 300
TACAGGTGCT TGCCACCACA CCCGGCTAAT TTTTGTATTT TTAGTAGAGA TGGGGTTTCA 360
CTATGTTGGC CAGGCTGGTC TTGAACTCCT GACCTTGTGA TCTGCCCGCC TCAGCCTCCC 420
AAAGTGCTGG GATTCCAGGC ATGAGCCACC ACACCCAGCC AATTTTTGCA TTTTTTTAGT 480
AGAGGCAGGG TTTCTCCATG TTGGCCAGGC TGGTCTCAAA CTCCTGGCCT GTCTTGGCCT 540
CCCAAAGTGC TGGGATTACA GGTGTGAACC ACCACATCCA GCCCCTAATT CTAATTTTTT 600
AACAAATTCT ATATCATTTT GCTCACTTTT CTCCTTCCTA CCTTTTATGA TTCTTCCCAT 660
GTTTTTATAA TCAGGGTATG TTCTCCTGCT GTTTCCAATT TTGCTTTCAT TCTGGTCTGC 720
ATTTCTTTCA TTTCCTCAAT TTTTTCATTC GGCTCTGCCA ACTCATGTCT CATCCTTTTT 780
CTCAGTTGTC CCCCATCTAA TTCCTGGGCT CTTTTGCCTC TGACCTACTC TTTGGTCAGT 840
TTTTGTAAAT TATGGTGAAA TACTTGGTCA CAACTTCCTA CTGCTCTGTG GCAGTTATTT 900
CTCTTTTGCT GAGTATTATT TGCTCCTTTC CTCCTCTTGG GTTTCAGTAC CTCCGAACAC 960
AGAACTGTGC TGGTTCCTTT TGGATTACTT CTCTTCAGAT GGGGTGAGCT TTCTTGGATT 1020
AGAAGGAGGT TCATGAGGTG TCAATGCCAC AGTGCAGGCT AGCAGAAATC TCACATGTGA 1080
ATTTTTAGTA GTGGCTTCTC CCACCCAATA GATCTGGGTA CTGCAGAGCT TTTCACAGGG 1140
CAAGACTTCT CTTTTCCCAC CCCACAGAGA GACTGCTTCC TGCAAATATG GAAGACCTGC 1200
AAATATGGTG TTTCCTAGAA CCAAGACAGG CCAGGCAAGC TCCGCCTGCC ACCTTGTGCC 1260
CTTGCTCCTA CTGCTGCAGC AAGACATGCT GCTTTTGCAT GCCAGGATGG GCTCCTGCCT 1320
TGGAGAAGTG AACTTTGCCC TCTCTTTCTG GAACCTACAG CTGGGGCCAC CTTTTCAGCT 1380
TCCTCCTGCG TCTTCTAGTG CTCGTTTCTG TTTCTCATCC TCCTATTGCT TGTGGGTGAT 1440
TTCTGAGAGG ATGCAACTCT TGCTACCGTC ATCAAGCTTG AGAAGCACTT TCTCTCTTAA 1500
CCACTCAGCC ACACCACCTT CCTAAATAGT AGCCAAGTTT CTTTTTCATT ATGAGAGGTG 1560
CTGTGGTGAG ACCAGAGCTC CTGTTCTTGT CAGCTTATTG TCCCAGACAA GACAAAGACA 1620
TGGAGAGAAG CTGTACAGGC GCTTGGTACC TGCCCAGTGA GCAGGGAGAA AGAGAGATGG 1680
GAGAGGGGAG GAGAGGAAAG GAGAGACAAG CTCCAGCCAC CTTGGGAGCT CTGGGCTGGA 1740
AGGCATAGCC CCGAAGAGAA GTAAGTATCC AGCAGGGAGG GGAAGAGAGA GCGGGGATCA 1800
CACCACTGTC TTCTGTCTGC 1820
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