Variant report

Variant	rs16837063
Chromosome Location	chr1:155815572-155815573
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:155813223..155816752-chr1:155827638..155829227,3	K562	blood:
2	chr1:155815137..155817015-chr1:156023954..156025530,2	K562	blood:

Variant related genes	Relation type
ENSG00000116580	Chromatin interaction
ENSG00000116586	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1094462	1.00[CEU][hapmap];1.00[TSI][hapmap];0.80[EUR][1000 genomes]
rs11803678	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.80[EUR][1000 genomes]
rs13374129	0.91[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13376121	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13376235	0.98[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1624846	0.80[EUR][1000 genomes]
rs16837037	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs17370773	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs1749415	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs1749421	0.80[EUR][1000 genomes]
rs2363012	1.00[EUR][1000 genomes]
rs2477541	0.80[EUR][1000 genomes]
rs2686255	0.80[EUR][1000 genomes]
rs28574887	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs35044707	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs41264969	0.85[AFR][1000 genomes]
rs4612618	0.80[EUR][1000 genomes]
rs4933	1.00[ASW][hapmap];1.00[CEU][hapmap];0.87[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs4971065	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4971106	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs552778	1.00[CEU][hapmap];1.00[TSI][hapmap]
rs56758819	0.91[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs59706606	0.80[EUR][1000 genomes]
rs59791187	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs598176	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs621181	0.85[CEU][hapmap];1.00[TSI][hapmap]
rs682020	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.80[EUR][1000 genomes]
rs73001021	0.80[EUR][1000 genomes]
rs7525057	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs7530726	1.00[EUR][1000 genomes]
rs7535158	0.83[AFR][1000 genomes]
rs822016	0.80[EUR][1000 genomes]
rs822018	0.80[EUR][1000 genomes]
rs822019	1.00[CEU][hapmap];1.00[TSI][hapmap];0.80[EUR][1000 genomes]
rs822020	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.80[EUR][1000 genomes]
rs822022	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.80[EUR][1000 genomes]
rs822482	1.00[EUR][1000 genomes]
rs822495	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs822497	1.00[CEU][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs822499	1.00[EUR][1000 genomes]
rs822500	0.97[EUR][1000 genomes]
rs822523	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33869	chr1:155223283-155917961	Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases
2	esv3423892	chr1:155664084-155901487	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv1003170	chr1:155762204-155836564	Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv916198	chr1:155804210-156403997	Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	428 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155783600-155823000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:155787600-155822000	Weak transcription	Esophagus	oesophagus
3	chr1:155789600-155822000	Weak transcription	Fetal Brain Male	brain
4	chr1:155792200-155822000	Weak transcription	Pancreas	Pancrea
5	chr1:155792200-155826000	Weak transcription	Stomach Mucosa	stomach
6	chr1:155792400-155826600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:155792600-155822800	Weak transcription	Rectal Smooth Muscle	rectum
8	chr1:155793400-155820200	Weak transcription	Brain Cingulate Gyrus	brain
9	chr1:155795200-155817800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr1:155796800-155821200	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr1:155796800-155822800	Weak transcription	Small Intestine	intestine
12	chr1:155798000-155822000	Weak transcription	Aorta	Aorta
13	chr1:155803800-155826000	Weak transcription	Right Atrium	heart
14	chr1:155804600-155821600	Weak transcription	NHDF-Ad	bronchial
15	chr1:155805600-155816800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:155807400-155816800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:155808000-155826000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr1:155810000-155825200	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr1:155810400-155818400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:155810400-155825400	Strong transcription	Fetal Stomach	stomach
21	chr1:155810600-155825400	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr1:155810800-155817800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr1:155811000-155818200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr1:155811400-155817600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:155811400-155825000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr1:155811800-155818000	Strong transcription	Fetal Intestine Large	intestine
27	chr1:155812200-155815800	Strong transcription	Primary B cells from cord blood	blood
28	chr1:155812400-155825400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr1:155812600-155816200	Strong transcription	H9 Cell Line	embryonic stem cell
30	chr1:155812600-155817600	Strong transcription	Fetal Brain Female	brain
31	chr1:155812600-155818200	Strong transcription	Fetal Muscle Trunk	muscle
32	chr1:155812800-155816000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:155812800-155817000	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr1:155812800-155818400	Strong transcription	NHEK	skin
35	chr1:155812800-155819000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:155812800-155825400	Strong transcription	Fetal Thymus	thymus
37	chr1:155813000-155815600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
38	chr1:155813000-155815800	Strong transcription	Placenta	Placenta
39	chr1:155813000-155816000	Strong transcription	Hela-S3	cervix
40	chr1:155813000-155817800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr1:155813000-155818400	Strong transcription	Duodenum Mucosa	Duodenum
42	chr1:155813000-155818600	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chr1:155813000-155825400	Strong transcription	Thymus	Thymus
44	chr1:155813200-155816000	Strong transcription	A549	lung
45	chr1:155813200-155818400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
46	chr1:155813200-155818800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:155813200-155826200	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr1:155813400-155816000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr1:155813400-155817800	Strong transcription	Sigmoid Colon	Sigmoid Colon
50	chr1:155813400-155817800	Strong transcription	Dnd41	blood

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