Variant report

Variant	nsv971974
Chromosome Location	chr11:4009259-4018790
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:212)
CpG islands
(count:183)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:212 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:4018493-4018509	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:4018503-4018689	K562	blood:	n/a	n/a
3	ATF1	chr11:4015334-4015605	K562	blood:	n/a	n/a
4	ATF1	chr11:4017147-4017633	K562	blood:	n/a	n/a
5	ATF3	chr11:4017133-4017469	K562	blood:	n/a	n/a
6	ATF3	chr11:4015238-4015656	K562	blood:	n/a	n/a
7	BACH1	chr11:4010526-4010886	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr11:4015276-4015561	GM12878	blood:	n/a	chr11:4015481-4015492
9	BATF	chr11:4015318-4015646	GM12878	blood:	n/a	chr11:4015481-4015492
10	BCL11A	chr11:4011135-4011351	GM12878	blood:	n/a	n/a
11	BCLAF1	chr11:4015256-4015586	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:4011331-4011497	GM12878	blood:	n/a	n/a
13	BHLHE40	chr11:4017224-4017840	K562	blood:	n/a	n/a
14	BHLHE40	chr11:4015305-4015613	K562	blood:	n/a	n/a
15	CBX3	chr11:4017002-4017600	K562	blood:	n/a	n/a
16	CBX3	chr11:4015161-4015679	K562	blood:	n/a	n/a
17	CBX3	chr11:4015131-4015728	HCT-116	colon:	n/a	n/a
18	CBX3	chr11:4015231-4015739	K562	blood:	n/a	n/a
19	CCNT2	chr11:4017200-4017497	K562	blood:	n/a	n/a
20	CEBPB	chr11:4010901-4011116	A549	lung:	n/a	n/a
21	CEBPB	chr11:4010882-4011046	K562	blood:	n/a	n/a
22	CEBPB	chr11:4010874-4011119	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr11:4010872-4011155	IMR90	lung:	n/a	n/a
24	CHD2	chr11:4011188-4011329	GM12878	blood:	n/a	n/a
25	CTCF	chr11:4018460-4018610	HEK293	kidney:	n/a	n/a
26	CTCF	chr11:4018400-4018550	RPTEC	kidney:	n/a	n/a
27	CTCF	chr11:4018460-4018610	HVMF	connective:	n/a	n/a
28	CTCF	chr11:4018460-4018610	Caco-2	colon:	n/a	n/a
29	CTCF	chr11:4018460-4018610	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr11:4018499-4018608	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr11:4018480-4018630	GM12873	blood:	n/a	n/a
32	CTCF	chr11:4018320-4018470	HCM	heart:	n/a	n/a
33	CTCF	chr11:4018430-4018747	K562	blood:	n/a	n/a
34	CTCF	chr11:4018460-4018610	HPF	lung:	n/a	n/a
35	CTCF	chr11:4012508-4012560	Fibrobl	skin:	n/a	n/a
36	CTCF	chr11:4018480-4018630	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr11:4018460-4018610	HMF	breast:	n/a	n/a
38	CTCF	chr11:4018480-4018630	NHEK	skin:	n/a	n/a
39	CTCF	chr11:4018420-4018570	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr11:4018520-4018670	GM12874	blood:	n/a	n/a
41	CTCF	chr11:4018460-4018610	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr11:4018460-4018610	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr11:4018440-4018590	MCF-7	breast:	n/a	n/a
44	CTCF	chr11:4010618-4010770	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr11:4018480-4018630	AG04450	lung:	n/a	n/a
46	CTCF	chr11:4018520-4018670	K562	blood:	n/a	n/a
47	CTCF	chr11:4018440-4018590	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr11:4018420-4018570	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr11:4018468-4018632	MCF-7	breast:	n/a	n/a
50	CTCF	chr11:4018480-4018630	MCF-7	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4010625-4010675	HepG2	liver:	n/a
2	chr11:4010737-4010787	HAEpiC	amniotic membrane:	n/a
3	chr11:4010737-4010787	BE2_C	brain:	n/a
4	chr11:4010625-4010675	GM06990	blood:	n/a
5	chr11:4010737-4010787	ProgFib	skin:	n/a
6	chr11:4010752-4010802	HNPCEpiC	eye:	n/a
7	chr11:4010625-4010675	NH-A	brain:	n/a
8	chr11:4010737-4010787	GM06990	blood:	n/a
9	chr11:4010625-4010675	ProgFib	skin:	n/a
10	chr11:4010737-4010787	K562	blood:	n/a
11	chr11:4010752-4010802	HUVEC	blood vessel:	n/a
12	chr11:4010752-4010802	HRCEpiC	kidney:	n/a
13	chr11:4010752-4010802	BJ	skin:	n/a
14	chr11:4010737-4010787	GM12891	blood:	n/a
15	chr11:4010752-4010802	GM12878	blood:	n/a
16	chr11:4010737-4010787	NB4	blood:	n/a
17	chr11:4010625-4010675	IMR90	lung:	fetal
18	chr11:4010752-4010802	AoSMC	blood vessel:	n/a
19	chr11:4010752-4010802	AG04449	skin:	fetal
20	chr11:4010625-4010675	HRE	kidney:	n/a
21	chr11:4010737-4010787	U87	brain:	n/a
22	chr11:4010737-4010787	LNCaP	prostate:	n/a
23	chr11:4010737-4010787	HIPEpiC	eye:	n/a
24	chr11:4010752-4010802	HCF	heart:	n/a
25	chr11:4010737-4010787	A549	lung:	n/a
26	chr11:4010625-4010675	GM12878	blood:	n/a
27	chr11:4010625-4010675	SAEC	small airway:	n/a
28	chr11:4010737-4010787	NHDF-neo	bronchial:	n/a
29	chr11:4010625-4010675	AG04449	skin:	fetal
30	chr11:4010752-4010802	NT2-D1	testis:	n/a
31	chr11:4010737-4010787	IMR90	lung:	fetal
32	chr11:4010625-4010675	RPTEC	kidney:	n/a
33	chr11:4010625-4010675	HCPEpiC	choroid plexus:	n/a
34	chr11:4010737-4010787	HEEpiC	esophagus:	n/a
35	chr11:4010752-4010802	PANC-1	pancreas:	n/a
36	chr11:4010752-4010802	T-47D	breast:	n/a
37	chr11:4010625-4010675	HCM	heart:	n/a
38	chr11:4010752-4010802	HEK293	kidney:	embryo
39	chr11:4010737-4010787	AG04450	lung:	fetal
40	chr11:4010737-4010787	MCF-7	breast:	n/a
41	chr11:4010752-4010802	HRPEpiC	eye:	n/a
42	chr11:4010752-4010802	GM19239	blood:	n/a
43	chr11:4010625-4010675	BE2_C	brain:	n/a
44	chr11:4010752-4010802	HCPEpiC	choroid plexus:	n/a
45	chr11:4010625-4010675	SKMC	muscle:	n/a
46	chr11:4010752-4010802	HRE	kidney:	n/a
47	chr11:4010752-4010802	AG10803	skin:	n/a
48	chr11:4010625-4010675	CMK	blood:	n/a
49	chr11:4010752-4010802	ovcar-3	ovarian:	n/a
50	chr11:4010752-4010802	IMR90	lung:	fetal

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:3861767..3864262-chr11:4018054..4019726,2	MCF-7	breast:
2	chr11:3929305..3931209-chr11:4016785..4019728,2	K562	blood:
3	chr11:3861620..3863293-chr11:4016277..4018859,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000224555	TF binding region
STIM1	TF binding region
ENSG00000224555	CpG island
STIM1	CpG island
ENSG00000177105	chromatin interactions

Extended variants
information (count: 348 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140265057	chr11:4009402-4009403	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537949271	chr11:4009427-4009428	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571800259	chr11:4009436-4009437	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144176174	chr11:4009437-4009438	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78189848	chr11:4009477-4009478	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs578153216	chr11:4009481-4009482	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs117167113	chr11:4009510-4009511	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs560867449	chr11:4009518-4009519	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs370944537	chr11:4009540-4009541	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs571930168	chr11:4009543-4009544	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs542610372	chr11:4009544-4009545	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs560889488	chr11:4009558-4009559	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs11030517	chr11:4009580-4009581	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs543552423	chr11:4009605-4009606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564924608	chr11:4009654-4009655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532385671	chr11:4009659-4009660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs72482767	chr11:4009718-4009719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566001184	chr11:4009779-4009780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs56176149	chr11:4009860-4009861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529956156	chr11:4009915-4009916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548915816	chr11:4009938-4009939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114121696	chr11:4009957-4009958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs61897205	chr11:4009959-4009960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372194848	chr11:4010035-4010036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556592557	chr11:4010044-4010045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556662582	chr11:4010071-4010072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs56362566	chr11:4010079-4010080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74051582	chr11:4010086-4010087	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs139546951	chr11:4010106-4010107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554087410	chr11:4010148-4010149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs180731361	chr11:4010177-4010178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543347248	chr11:4010195-4010196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs564622566	chr11:4010225-4010226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs117692082	chr11:4010232-4010233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs576148428	chr11:4010259-4010260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543541805	chr11:4010335-4010336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565021850	chr11:4010375-4010376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs56091961	chr11:4010409-4010410	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs545811168	chr11:4010477-4010478	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs200245571	chr11:4010479-4010480	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs541188831	chr11:4010491-4010492	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs553721104	chr11:4010507-4010508	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs7928545	chr11:4010529-4010530	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs183830191	chr11:4010540-4010541	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs189280633	chr11:4010542-4010543	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs199635536	chr11:4010549-4010550	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs567316473	chr11:4010563-4010564	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs531623194	chr11:4010590-4010591	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs549991115	chr11:4010645-4010646	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs571679316	chr11:4010657-4010658	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Neuroblastoma	18923524	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:3984000-4010400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr11:3987000-4010400	Weak transcription	Fetal Intestine Small	intestine
3	chr11:3989400-4010600	Weak transcription	Spleen	Spleen
4	chr11:3989400-4031000	Weak transcription	Aorta	Aorta
5	chr11:3994400-4016600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:4000600-4010800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr11:4001400-4011800	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr11:4002600-4009600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr11:4003000-4010600	Weak transcription	Esophagus	oesophagus
10	chr11:4003200-4016600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:4004400-4009400	Enhancers	Psoas Muscle	Psoas
12	chr11:4004400-4009600	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr11:4004600-4010600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr11:4004800-4010000	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr11:4005000-4010200	Weak transcription	Dnd41	blood
16	chr11:4005400-4011800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr11:4005800-4010800	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr11:4006000-4009400	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr11:4006200-4010400	Weak transcription	Brain Anterior Caudate	brain
20	chr11:4006200-4013800	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr11:4006400-4016600	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr11:4006600-4009400	Enhancers	Liver	Liver
23	chr11:4006800-4022600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr11:4007000-4010400	Weak transcription	Fetal Muscle Leg	muscle
25	chr11:4007000-4010600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr11:4007000-4010600	Weak transcription	Fetal Thymus	thymus
27	chr11:4007000-4010600	Weak transcription	Left Ventricle	heart
28	chr11:4007000-4010800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr11:4007000-4011200	Weak transcription	K562	blood
30	chr11:4007000-4012600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr11:4007200-4010400	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr11:4007200-4010400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr11:4007200-4010400	Weak transcription	Thymus	Thymus
34	chr11:4007200-4010600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr11:4007200-4013800	Weak transcription	Primary hematopoietic stem cells	blood
36	chr11:4007200-4014000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr11:4007600-4010400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr11:4007600-4010400	Weak transcription	Fetal Brain Female	brain
39	chr11:4007600-4010400	Weak transcription	Stomach Smooth Muscle	stomach
40	chr11:4007600-4010600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr11:4007800-4010400	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr11:4007800-4015000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr11:4008000-4009600	Enhancers	HepG2	liver
44	chr11:4008400-4009400	Enhancers	Right Ventricle	heart
45	chr11:4008400-4009400	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr11:4008400-4010400	Enhancers	Fetal Lung	lung
47	chr11:4008400-4010600	Enhancers	Colon Smooth Muscle	Colon
48	chr11:4008600-4009400	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
49	chr11:4008600-4009400	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr11:4008600-4010000	Weak transcription	Fetal Brain Male	brain

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