Variant report

Variant	rs10020497
Chromosome Location	chr4:103202665-103202666
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10020659	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs1045155	1.00[CEU][hapmap]
rs13434535	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28402744	1.00[AMR][1000 genomes]
rs28665758	1.00[AMR][1000 genomes]
rs57245170	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59865579	1.00[EUR][1000 genomes]
rs6826943	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6836807	1.00[CEU][hapmap]
rs7654435	1.00[CEU][hapmap]
rs7681437	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869164	chr4:102483189-103213842	Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv428447	chr4:103103730-103262107	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1008680	chr4:103153709-103206555	Strong transcription Weak transcription Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1011868	chr4:103158581-103206555	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv999012	chr4:103162076-103206555	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1014733	chr4:103174196-103206240	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1002129	chr4:103174196-103206555	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1013313	chr4:103175700-103206555	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1003825	chr4:103179197-103206555	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv998689	chr4:103179788-103206555	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:103179400-103221000	Weak transcription	K562	blood
2	chr4:103181600-103210800	Weak transcription	Liver	Liver
3	chr4:103181800-103230400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr4:103182000-103255400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr4:103183400-103210600	Weak transcription	Primary B cells from cord blood	blood
6	chr4:103184200-103220600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:103186600-103229600	Weak transcription	Pancreas	Pancrea
8	chr4:103186800-103216800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr4:103187200-103229400	Weak transcription	Fetal Thymus	thymus
10	chr4:103189000-103216800	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr4:103189200-103211200	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr4:103189200-103225400	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr4:103189400-103218600	Weak transcription	Placenta	Placenta
14	chr4:103189800-103232400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr4:103192800-103206000	Weak transcription	Colonic Mucosa	Colon
16	chr4:103193400-103203000	Weak transcription	Hela-S3	cervix
17	chr4:103193800-103209600	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr4:103195000-103205400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr4:103196200-103242400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr4:103198000-103206800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr4:103199400-103221000	Weak transcription	Ovary	ovary
22	chr4:103200800-103210400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr4:103200800-103217600	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr4:103201000-103220000	Weak transcription	GM12878-XiMat	blood
25	chr4:103201400-103203400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:103201400-103205200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr4:103201400-103206400	Strong transcription	Primary hematopoietic stem cells	blood
28	chr4:103201400-103210000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr4:103201400-103210800	Weak transcription	Dnd41	blood
30	chr4:103202400-103203600	Enhancers	Fetal Heart	heart
31	chr4:103202600-103203000	Strong transcription	Primary T cells from cord blood	blood

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