Variant report

Variant	rs11032621
Chromosome Location	chr11:34366783-34366784
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:34366426..34367988-chr11:34371579..34373367,2	MCF-7	breast:
2	chr11:34365763..34368722-chr11:34368922..34370946,2	MCF-7	breast:
3	chr11:34351980..34355833-chr11:34364485..34369065,5	MCF-7	breast:
4	chr11:34182869..34184565-chr11:34366720..34369400,2	K562	blood:
5	chr11:34356954..34359190-chr11:34365212..34367961,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000254708	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10742313	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10742314	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10768059	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10768060	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10768061	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10768062	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10768063	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10768064	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10768065	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10768066	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10768067	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10768068	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10768069	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10836186	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10836187	1.00[ASN][1000 genomes]
rs10836189	0.96[ASN][1000 genomes]
rs10836190	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10836191	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10836194	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10836195	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10836196	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10836197	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11032617	0.83[CHB][hapmap]
rs11032618	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs11032624	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11032625	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11032627	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11032628	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11032631	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11032632	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11032634	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11032635	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12296013	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1810506	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1810507	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1883736	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1925368	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1925371	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1925372	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1925374	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1977109	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2001176	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2092485	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2145794	1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs3740795	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3740796	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3817990	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3981191	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3981192	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4140544	1.00[CEU][hapmap];0.94[CHB][hapmap];0.86[JPT][hapmap];0.84[YRI][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4993520	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6484710	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6484711	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7110380	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7124239	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs742634	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7927718	0.82[AMR][1000 genomes]
rs7929828	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs7944461	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs910088	1.00[CEU][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757435	chr11:34220504-34370236	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv2759816	chr11:34220504-34370236	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv897205	chr11:34248229-34507213	Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv897207	chr11:34253683-34621004	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
5	nsv897208	chr11:34257064-34562247	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
6	nsv897209	chr11:34309519-34548906	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh 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	19 gene(s)	inside rSNPs	diseases
7	nsv897210	chr11:34349427-34381075	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34360200-34368400	Enhancers	Liver	Liver
2	chr11:34361800-34370800	Weak transcription	GM12878-XiMat	blood
3	chr11:34362600-34366800	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr11:34362600-34370200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr11:34363000-34372400	Enhancers	Fetal Muscle Leg	muscle
6	chr11:34363200-34367200	Enhancers	Fetal Heart	heart
7	chr11:34363600-34367400	Enhancers	Osteobl	bone
8	chr11:34363600-34368800	Enhancers	NHLF	lung
9	chr11:34363800-34366800	Enhancers	NH-A	brain
10	chr11:34363800-34368400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr11:34363800-34368600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr11:34363800-34369000	Enhancers	Left Ventricle	heart
13	chr11:34364000-34366800	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr11:34364000-34366800	Weak transcription	Fetal Lung	lung
15	chr11:34364000-34366800	Enhancers	HSMM	muscle
16	chr11:34364000-34367000	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr11:34364000-34369000	Enhancers	Fetal Muscle Trunk	muscle
18	chr11:34364200-34366800	Weak transcription	Fetal Kidney	kidney
19	chr11:34364200-34367200	Weak transcription	Fetal Intestine Large	intestine
20	chr11:34364200-34376600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr11:34364400-34366800	Weak transcription	Fetal Intestine Small	intestine
22	chr11:34364400-34366800	Weak transcription	Ovary	ovary
23	chr11:34364400-34366800	Weak transcription	Small Intestine	intestine
24	chr11:34364400-34367000	Weak transcription	Rectal Smooth Muscle	rectum
25	chr11:34364400-34367000	Enhancers	Stomach Smooth Muscle	stomach
26	chr11:34364400-34371000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr11:34364600-34368600	Enhancers	HMEC	breast
28	chr11:34364800-34368400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr11:34365000-34369800	Enhancers	Brain Germinal Matrix	brain
30	chr11:34365400-34367200	Enhancers	Stomach Mucosa	stomach
31	chr11:34365400-34367400	Enhancers	Gastric	stomach
32	chr11:34365400-34367800	Enhancers	Pancreas	Pancrea
33	chr11:34365400-34372200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr11:34365600-34367600	Flanking Active TSS	Hela-S3	cervix
35	chr11:34365800-34366800	Enhancers	NHEK	skin
36	chr11:34365800-34368400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr11:34365800-34368400	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr11:34365800-34368800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr11:34366000-34367400	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr11:34366000-34367600	Enhancers	Duodenum Mucosa	Duodenum
41	chr11:34366000-34367600	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr11:34366000-34367800	Enhancers	Right Ventricle	heart
43	chr11:34366000-34368000	Enhancers	Fetal Brain Female	brain
44	chr11:34366000-34368200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr11:34366000-34368200	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr11:34366000-34368600	Flanking Active TSS	A549	lung
47	chr11:34366000-34371800	Enhancers	Right Atrium	heart
48	chr11:34366200-34367400	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr11:34366200-34367400	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr11:34366200-34367600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links