| Tag | Content |
|---|
EnhancerAtlas ID | HS017-30386 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr7:73967460-73968960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPIB | MA0081.2 | chr7:73968154-73968166 | CACTTCCCCTTT | - | 6.07 | | Znf423 | MA0116.1 | chr7:73968365-73968380 | GGACCCCAGGGGTGC | + | 7.8 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I074553 | chr7 | 73967930 | 73968530 |
|
Enhancer Sequence | CCTGGCCTTT TGTGGGTTTT TTTTGAGACA GAGTCTCACT CCAGGCTGGA GTACAGTGGT 60
GCTGTCTCGG CTCACTGTAG CCTCCACCTT CCAGGTTTAA ACGATTCTCC TGCCTCAGCC 120
TCCCGAGTAA CTGGGATTAC AGGCGTGAGC CACCATGCCT GGCCATGAGC ATTTGTTTTA 180
AGAGACAAGT CTTTCTTTAG CCCAGGCTGG AGTGTAGTGG CACAATCATA ACTCACTGCA 240
GCCTTAAACT CCTGGGCTCA AGCAATCCTG CTTCAGCCTC CTGAGTAGCT GGGACTGCAG 300
GGGCACGCCA CCACACCTGG CTAATTTTTA CATTTTTTGT AGAGAAGGGG TCTCGCTATG 360
TTGCCCAAGC TGGTCTCCAA CTCCTGGGCT CAAAGCGATG CCCCTGCCTC AGCCTCCCAA 420
AGTGCTGGGA TTACAGGTTG AGCCACCATG CCCAGCCTTG AGCACTTTTT AAAGTCACGA 480
TGGCTTTCTC CACCTGTCAT TTGGAAAGGG AGACAGGTCA GTGCAGTGGC CGACGGGAGA 540
GGCCGTCTGG TGGGTTTGAG GCCAGCTCCT CCTGTTACTC CCTGTGGCCT TGGCAGCCGG 600
CTGTGCTATT TAAGGGGAAG CACTGTCGCT ACTCTGGCCT GGGACTCAGG GGCTCTGCCC 660
AGCTTCTGCC TCTCTAAGTT TACTGCTGGG AAGTCACTTC CCCTTTCAGA ACCTGAGTTC 720
TCCCATAAAG AGGAGGGGCC TAAATGCAGT CCGAAGCCTT TTCTAGCTCC TGAGACTGTG 780
GTTCAAGGCA GGGCTATGCT TCCCCTCCCA GCCCTGGCCC CGTGACCCCA GCTCTGTGCC 840
TGGCACTGTA CAGAAGCCTA AGAGATGCCC ACCGCCAGAG CGGGCACCAA ATCCTCATCT 900
ACTGGGGACC CCAGGGGTGC CCTCCCTGAG AGTTTGGCCT TTGGGCTCAC TCCCAGGCAG 960
AGACTCCTCG GAGTTGCTGC TTGATTACCC CTGTGACAGA GAGCTCATTA CCTCTCCAGG 1020
CCCATTACCT CTCCAGAGAG CTCATTACCT CTCTGCTCCA TGGCCTACCC TGCCATCCCC 1080
CGACAGCCCC CTTCTGGCCA GCATGATTTT CCCAGTGTCC TCTACCCACC ACAAACCCCA 1140
GCCCCACAAC AGGCTTGCTC TAACAGGACA AGTTGTGCTG AAGATGGGGC CTTCAGAAGC 1200
AGTGCTGTAT GACAAAGAAG GTTGACTCAT GTCTGGACAG GGCTTTCTGG AGTCTGTGGA 1260
GCTAAAGACA TTAGCATAAT ACAGAGCTGG GCTTGGTCAC TGGTGCTTCC GACTGCAGTA 1320
ACACAGCAGC TCTCAGACGT GAGCCGTAGA TCTCAGACCT TTCCAGAAGC TTGGAGTTCT 1380
TGCTTCGTAG TGGGCCCCGA CTGTTTCTAC TCTTTTCTTT CATTTTGAGA CGGAGTCTTA 1440
CTCTGTCACC CAGGCTGGAG TGCAGTGGTG CTATCTCAGT TCACTGCAAC CTCTGCCTCC 1500
|
