Variant report

Variant	rs4916481
Chromosome Location	chr3:195908327-195908328
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:195801020..195810289-chr3:195902611..195915225,28	K562	blood:
2	chr3:195793504..195812987-chr3:195901613..195938073,113	K562	blood:
3	chr3:195903618..195905705-chr3:195906197..195908381,3	K562	blood:
4	chr3:195884789..195887031-chr3:195907240..195909901,2	K562	blood:
5	chr3:195901978..195904372-chr3:195908307..195910643,2	MCF-7	breast:
6	chr3:195795171..195797098-chr3:195906835..195910402,3	K562	blood:

Variant related genes	Relation type
ENSG00000252174	Chromatin interaction
ENSG00000072274	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs13315288	0.92[ASN][1000 genomes]
rs2015708	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28429906	0.95[ASN][1000 genomes]
rs36124256	0.90[ASN][1000 genomes]
rs3850644	0.87[ASN][1000 genomes]
rs3861957	0.89[ASN][1000 genomes]
rs3893275	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4916478	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4916483	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4916491	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4916545	0.92[ASN][1000 genomes]
rs62410535	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7374788	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9325434	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9325435	0.86[EUR][1000 genomes]
rs9812813	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9816881	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9824251	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9834661	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9847725	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9855026	0.90[ASN][1000 genomes]
rs9859292	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9859624	0.86[ASN][1000 genomes]
rs9869983	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9870228	0.85[AMR][1000 genomes]
rs9875719	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2759213	chr3:195102787-196071593	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
2	esv2757913	chr3:195379484-196071593	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
3	nsv532213	chr3:195643944-196063636	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
4	nsv997797	chr3:195658360-196212958	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
5	nsv878171	chr3:195677895-195959924	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
6	nsv1008512	chr3:195709662-195974936	Strong transcription Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
7	nsv1002584	chr3:195734933-195910772	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
8	nsv432543	chr3:195746690-196015690	Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
9	nsv532214	chr3:195762648-195916068	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
10	nsv1009105	chr3:195769609-195984388	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
11	nsv1005558	chr3:195789462-195919077	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
12	nsv536890	chr3:195789462-195919077	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
13	nsv998042	chr3:195840858-195934070	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
14	nsv1009811	chr3:195851796-196138071	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
15	nsv593070	chr3:195854279-195924203	Enhancers Genic enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
16	nsv878174	chr3:195858887-195949541	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
17	nsv461131	chr3:195858887-196072442	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
18	nsv593071	chr3:195858887-196072442	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
19	nsv1004194	chr3:195864466-195919077	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
20	nsv536891	chr3:195864466-195919077	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
21	nsv1009178	chr3:195864466-196081670	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
22	nsv536892	chr3:195864466-196081670	Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
23	nsv1003550	chr3:195885340-196159824	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
24	nsv536893	chr3:195885340-196159824	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
25	nsv878175	chr3:195907653-195973244	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195897000-195909000	Weak transcription	Spleen	Spleen
2	chr3:195901400-195911800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr3:195904400-195909400	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr3:195904800-195913600	Weak transcription	Right Atrium	heart
5	chr3:195905600-195910800	Enhancers	Primary hematopoietic stem cells	blood
6	chr3:195906800-195908400	Enhancers	Fetal Brain Female	brain
7	chr3:195907000-195910400	Weak transcription	Small Intestine	intestine
8	chr3:195907000-195910600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr3:195907000-195910800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr3:195907000-195910800	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr3:195907000-195913600	Weak transcription	Left Ventricle	heart
12	chr3:195907200-195909000	Enhancers	Primary T cells from cord blood	blood
13	chr3:195907200-195909000	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr3:195907200-195909000	Weak transcription	Stomach Mucosa	stomach
15	chr3:195907200-195909000	Enhancers	Dnd41	blood
16	chr3:195907200-195909400	Enhancers	Primary B cells from peripheral blood	blood
17	chr3:195907200-195909400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr3:195907200-195909600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr3:195907200-195909800	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr3:195907200-195909800	Weak transcription	Duodenum Mucosa	Duodenum
21	chr3:195907200-195910000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr3:195907200-195910000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr3:195907200-195910000	Weak transcription	Hela-S3	cervix
24	chr3:195907200-195910200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr3:195907200-195910200	Weak transcription	Fetal Intestine Large	intestine
26	chr3:195907200-195910400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr3:195907200-195910400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr3:195907200-195910400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr3:195907200-195910400	Weak transcription	Esophagus	oesophagus
30	chr3:195907200-195910400	Weak transcription	Fetal Intestine Small	intestine
31	chr3:195907200-195910400	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr3:195907200-195910400	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr3:195907200-195910400	Weak transcription	HMEC	breast
34	chr3:195907200-195910400	Weak transcription	HSMMtube	muscle
35	chr3:195907200-195910400	Weak transcription	NHEK	skin
36	chr3:195907200-195910800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr3:195907200-195910800	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr3:195907200-195911400	Enhancers	Primary T cells fromperipheralblood	blood
39	chr3:195907200-195913400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr3:195907200-195913400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr3:195907200-195913400	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr3:195907200-195913400	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr3:195907200-195913400	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr3:195907200-195913400	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr3:195907200-195913400	Weak transcription	Brain Anterior Caudate	brain
46	chr3:195907200-195913400	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr3:195907200-195913400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr3:195907200-195913600	Enhancers	Fetal Thymus	thymus
49	chr3:195907200-195919000	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr3:195907400-195908800	Enhancers	Primary T helper cells PMA-I stimulated	--

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