Variant report

Variant	rs11559161
Chromosome Location	chr4:77957289-77957290
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:77949158..77951993-chr4:77956100..77958962,2	MCF-7	breast:
2	chr4:77932387..77934435-chr4:77956473..77959096,2	K562	blood:
3	chr4:77952881..77954867-chr4:77957235..77958797,2	K562	blood:

Variant related genes	Relation type
ENSG00000138758	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10002443	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10003222	1.00[LWK][hapmap];1.00[MKK][hapmap]
rs10006033	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.83[JPT][hapmap];1.00[LWK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs10006616	1.00[LWK][hapmap];1.00[MKK][hapmap]
rs10017180	1.00[LWK][hapmap]
rs10031961	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10470896	0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10856952	0.90[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];0.83[JPT][hapmap]
rs12186	1.00[CHB][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];0.85[ASN][1000 genomes]
rs1472399	1.00[GIH][hapmap];1.00[TSI][hapmap]
rs16996592	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17002332	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17002334	1.00[ASW][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17002336	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17002339	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17002346	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][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];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2279711	0.80[CHB][hapmap];0.85[EUR][1000 genomes]
rs2645668	1.00[GIH][hapmap]
rs2645698	0.86[MEX][hapmap]
rs28541859	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28587298	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28626429	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28685589	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28715145	0.81[AFR][1000 genomes]
rs4076784	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4076785	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4252773	1.00[GIH][hapmap]
rs4252887	0.83[ASN][1000 genomes]
rs4252896	0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];1.00[TSI][hapmap];0.82[ASN][1000 genomes]
rs4252897	0.83[ASN][1000 genomes]
rs4252913	1.00[CHB][hapmap];0.83[JPT][hapmap];0.83[ASN][1000 genomes]
rs4252930	0.81[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs4557282	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.83[JPT][hapmap];1.00[TSI][hapmap]
rs6817626	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.83[JPT][hapmap];1.00[TSI][hapmap]
rs6824360	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7667891	0.90[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.83[JPT][hapmap];1.00[TSI][hapmap]

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:77928200-77960800	Strong transcription	Fetal Intestine Large	intestine
2	chr4:77929400-77961800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr4:77932200-77962000	Strong transcription	Fetal Brain Female	brain
4	chr4:77934000-77957400	Strong transcription	Rectal Mucosa Donor 31	rectum
5	chr4:77935800-77957800	Strong transcription	Duodenum Mucosa	Duodenum
6	chr4:77935800-77960800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr4:77936000-77957600	Strong transcription	Primary hematopoietic stem cells	blood
8	chr4:77936000-77959200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr4:77936200-77961800	Strong transcription	Skeletal Muscle Female	skeletal muscle
10	chr4:77937400-77981400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr4:77939800-77960800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
12	chr4:77942800-77961000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:77943800-77969200	Weak transcription	Stomach Mucosa	stomach
14	chr4:77944000-77957600	Strong transcription	Duodenum Smooth Muscle	Duodenum
15	chr4:77944000-77962800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr4:77944200-77961200	Strong transcription	Placenta	Placenta
17	chr4:77944200-77983200	Weak transcription	Small Intestine	intestine
18	chr4:77944400-77957400	Strong transcription	Adipose Nuclei	Adipose
19	chr4:77944400-77957600	Strong transcription	HUES48 Cell Line	embryonic stem cell
20	chr4:77944400-77959800	Strong transcription	HUES64 Cell Line	embryonic stem cell
21	chr4:77944400-77960800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr4:77944400-77965400	Weak transcription	Fetal Heart	heart
23	chr4:77945000-77960000	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr4:77945000-77960200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:77945000-77962600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:77945000-77962800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr4:77945400-77960800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr4:77945600-77958400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr4:77945600-77962600	Strong transcription	Fetal Muscle Leg	muscle
30	chr4:77946000-77965000	Weak transcription	Esophagus	oesophagus
31	chr4:77946000-77971800	Strong transcription	Fetal Muscle Trunk	muscle
32	chr4:77947800-77960800	Strong transcription	GM12878-XiMat	blood
33	chr4:77948600-77958800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr4:77948800-77965400	Weak transcription	Psoas Muscle	Psoas
35	chr4:77949600-77959000	Weak transcription	Lung	lung
36	chr4:77949600-77962000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr4:77950200-77969200	Weak transcription	Thymus	Thymus
38	chr4:77950400-77959000	Weak transcription	Pancreas	Pancrea
39	chr4:77950600-77969400	Weak transcription	Right Ventricle	heart
40	chr4:77951200-77957400	Strong transcription	Brain Inferior Temporal Lobe	brain
41	chr4:77951800-77959200	Strong transcription	HUVEC	blood vessel
42	chr4:77951800-77969400	Weak transcription	Spleen	Spleen
43	chr4:77952200-77957600	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr4:77952200-77958200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr4:77952200-77961800	Weak transcription	Fetal Intestine Small	intestine
46	chr4:77952800-77959000	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr4:77952800-77962600	Genic enhancers	NHDF-Ad	bronchial
48	chr4:77953000-77959000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr4:77953000-77960400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr4:77953000-77961800	Weak transcription	Primary B cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links