Variant report

Variant	rs1113480
Chromosome Location	chr11:48058313-48058314
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:48049637..48052585-chr11:48057175..48059884,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1039484	0.87[CEU][hapmap]
rs1039485	0.81[AFR][1000 genomes]
rs10734561	0.81[CHB][hapmap];0.84[EUR][1000 genomes]
rs10742827	0.86[GIH][hapmap];0.89[TSI][hapmap];0.84[EUR][1000 genomes]
rs10769310	0.85[EUR][1000 genomes]
rs10769312	0.87[CEU][hapmap];0.82[CHB][hapmap];0.91[CHD][hapmap]
rs10769313	0.86[CEU][hapmap];0.81[CHB][hapmap]
rs10838798	0.87[CEU][hapmap];0.82[CHB][hapmap]
rs10838800	0.87[CEU][hapmap];0.82[CHB][hapmap];0.91[CHD][hapmap]
rs10838802	0.82[CEU][hapmap];0.81[CHB][hapmap];0.89[TSI][hapmap];0.84[EUR][1000 genomes]
rs11039513	0.84[EUR][1000 genomes]
rs11039530	1.00[YRI][hapmap]
rs11039543	1.00[YRI][hapmap]
rs11601310	0.89[ASW][hapmap];0.94[CHD][hapmap];0.84[LWK][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap]
rs1472681	0.84[EUR][1000 genomes]
rs1566732	0.84[LWK][hapmap];1.00[YRI][hapmap]
rs2870080	1.00[YRI][hapmap]
rs2904315	0.87[CEU][hapmap]
rs2930196	0.88[ASN][1000 genomes]
rs34895872	0.82[AFR][1000 genomes]
rs34972471	0.87[ASN][1000 genomes]
rs4298856	0.87[CEU][hapmap];0.88[CHB][hapmap];1.00[YRI][hapmap]
rs4508163	0.86[EUR][1000 genomes]
rs4752805	0.84[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs4752894	0.84[LWK][hapmap];1.00[YRI][hapmap]
rs4752904	1.00[YRI][hapmap]
rs4752907	1.00[YRI][hapmap]
rs6485802	0.88[CHB][hapmap];0.88[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap];0.91[ASN][1000 genomes]
rs6485807	0.87[CEU][hapmap]
rs7106731	0.82[AFR][1000 genomes]
rs7114598	0.86[GIH][hapmap];0.89[TSI][hapmap];0.84[EUR][1000 genomes]
rs7130876	0.89[GIH][hapmap]
rs7395231	0.87[CEU][hapmap];0.82[CHB][hapmap]
rs7396592	0.84[EUR][1000 genomes]
rs7479361	0.87[CEU][hapmap];0.84[LWK][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap]
rs7927965	1.00[YRI][hapmap]
rs7934659	0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052397	chr11:47675470-48594256	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
2	nsv530620	chr11:47765455-48664555	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
3	nsv1036992	chr11:47794621-48666024	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv1036451	chr11:47902321-48616646	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv541037	chr11:47902321-48616646	Enhancers Strong transcription Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv1047490	chr11:47916708-48388686	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv1044266	chr11:47929586-48276132	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS 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 miRNA target site	10 gene(s)	inside rSNPs	diseases
8	nsv541038	chr11:47929586-48276132	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
9	nsv1053145	chr11:47967902-48086950	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv870381	chr11:47989434-48142648	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
11	esv3396029	chr11:47993857-48241494	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
12	nsv897327	chr11:48004369-48911660	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
13	nsv869124	chr11:48014539-48783113	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
14	nsv1051805	chr11:48016488-48378048	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
15	nsv428573	chr11:48032457-48152344	Genic enhancers Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
16	nsv897328	chr11:48043053-48901553	Strong transcription Enhancers Genic enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS 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	27 gene(s)	inside rSNPs	diseases
17	nsv897329	chr11:48052676-48319974	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48046600-48059600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr11:48047400-48073400	Weak transcription	HSMMtube	muscle
3	chr11:48047400-48073800	Weak transcription	Left Ventricle	heart
4	chr11:48049000-48058600	Genic enhancers	A549	lung
5	chr11:48050200-48068200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr11:48050800-48058600	Enhancers	Brain Anterior Caudate	brain
7	chr11:48050800-48073000	Weak transcription	Esophagus	oesophagus
8	chr11:48051600-48071200	Weak transcription	Fetal Intestine Large	intestine
9	chr11:48051600-48073800	Weak transcription	Aorta	Aorta
10	chr11:48051800-48058600	Enhancers	Primary T cells fromperipheralblood	blood
11	chr11:48052600-48060000	Enhancers	Brain Substantia Nigra	brain
12	chr11:48052800-48059200	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr11:48053200-48060000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr11:48053600-48065400	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr11:48053600-48065800	Weak transcription	Colonic Mucosa	Colon
16	chr11:48053800-48059000	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr11:48053800-48062600	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr11:48053800-48065200	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr11:48053800-48073400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr11:48054000-48059600	Weak transcription	Hela-S3	cervix
21	chr11:48054000-48062400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr11:48054400-48060000	Enhancers	Fetal Muscle Leg	muscle
23	chr11:48054400-48060000	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr11:48055000-48058600	Enhancers	Brain Angular Gyrus	brain
25	chr11:48055000-48059000	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr11:48055000-48060000	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr11:48055200-48062400	Weak transcription	Lung	lung
28	chr11:48055400-48058600	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr11:48055600-48058600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr11:48055600-48058600	Enhancers	Thymus	Thymus
31	chr11:48055600-48064800	Weak transcription	Duodenum Mucosa	Duodenum
32	chr11:48055800-48059400	Weak transcription	Gastric	stomach
33	chr11:48055800-48063800	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr11:48056200-48058400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr11:48056200-48058600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr11:48056200-48058600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr11:48056200-48058600	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr11:48056200-48058800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr11:48056200-48059000	Enhancers	Rectal Smooth Muscle	rectum
40	chr11:48056600-48058400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr11:48056800-48058600	Enhancers	Osteobl	bone
42	chr11:48056800-48058800	Enhancers	Brain Cingulate Gyrus	brain
43	chr11:48056800-48060200	Enhancers	Primary B cells from cord blood	blood
44	chr11:48056800-48064000	Weak transcription	Stomach Mucosa	stomach
45	chr11:48056800-48064800	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr11:48057000-48058600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr11:48057000-48058600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr11:48057000-48059400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr11:48057000-48059400	Weak transcription	Spleen	Spleen
50	chr11:48057000-48059600	Enhancers	GM12878-XiMat	blood

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