Variant report

Variant	rs9991157
Chromosome Location	chr4:102175511-102175512
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10004830	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10015480	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10019627	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10027301	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17030915	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17030959	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17030989	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28379119	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28421266	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28464050	1.00[EUR][1000 genomes]
rs28491829	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28534411	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28542998	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28553282	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28614035	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28638143	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28640942	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28675750	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28723066	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs58084948	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs58598913	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs58898502	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6811228	1.00[EUR][1000 genomes]
rs72919782	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72919785	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9998913	0.84[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931418	chr4:101500167-102443207	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv999741	chr4:102009017-102454115	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
3	nsv537199	chr4:102009017-102454115	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1004766	chr4:102009017-102713765	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
5	nsv537200	chr4:102009017-102713765	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
6	nsv1011351	chr4:102056024-102450302	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:102157800-102179600	Weak transcription	Primary B cells from cord blood	blood
2	chr4:102159200-102179800	Weak transcription	Psoas Muscle	Psoas
3	chr4:102161000-102177400	Weak transcription	Primary B cells from peripheral blood	blood
4	chr4:102161000-102177400	Weak transcription	Colon Smooth Muscle	Colon
5	chr4:102166200-102177400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr4:102166200-102179400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:102170200-102176000	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr4:102173200-102175600	Weak transcription	HUVEC	blood vessel
9	chr4:102173200-102179400	Weak transcription	Primary hematopoietic stem cells	blood
10	chr4:102173400-102177200	Weak transcription	Brain Hippocampus Middle	brain
11	chr4:102173800-102175800	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr4:102174000-102181200	Weak transcription	Brain Anterior Caudate	brain
13	chr4:102174200-102177000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:102174200-102177200	Weak transcription	Brain Cingulate Gyrus	brain
15	chr4:102174200-102177400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr4:102174200-102177400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr4:102174200-102177600	Weak transcription	Small Intestine	intestine
18	chr4:102174200-102178800	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr4:102174200-102179400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr4:102174200-102179600	Weak transcription	Duodenum Mucosa	Duodenum
21	chr4:102174200-102179800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr4:102174200-102180000	Weak transcription	Left Ventricle	heart
23	chr4:102174200-102181000	Weak transcription	Adipose Nuclei	Adipose
24	chr4:102174200-102186000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr4:102174400-102175600	Weak transcription	Fetal Heart	heart
26	chr4:102174400-102176000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr4:102174400-102176000	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr4:102174400-102177400	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr4:102174400-102177400	Weak transcription	HepG2	liver
30	chr4:102174400-102180000	Weak transcription	NHDF-Ad	bronchial
31	chr4:102174400-102180600	Weak transcription	NHLF	lung
32	chr4:102174400-102185800	Weak transcription	HMEC	breast
33	chr4:102174600-102175800	Weak transcription	Fetal Lung	lung
34	chr4:102174600-102175800	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr4:102174600-102177200	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr4:102174600-102177200	Weak transcription	A549	lung
37	chr4:102174600-102179800	Weak transcription	Ovary	ovary
38	chr4:102175000-102177000	Weak transcription	Stomach Mucosa	stomach
39	chr4:102175000-102177600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr4:102175200-102180000	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr4:102175400-102179800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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