Variant report

Variant	nsv975852
Chromosome Location	chr11:74693028-74696165
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:107)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:107 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:74694841-74694911	K562	blood:	n/a	n/a
2	ARID3A	chr11:74692994-74693351	HepG2	liver:	n/a	n/a
3	CUX1	chr11:74694535-74694893	K562	blood:	n/a	n/a
4	EP300	chr11:74694567-74694692	K562	blood:	n/a	n/a
5	FOXA1	chr11:74695128-74695440	HepG2	liver:	n/a	n/a
6	FOXA1	chr11:74695086-74695471	HepG2	liver:	n/a	n/a
7	FOXA1	chr11:74693029-74693355	HepG2	liver:	n/a	n/a
8	FOXA1	chr11:74692907-74693482	HepG2	liver:	n/a	n/a
9	FOXA1	chr11:74695051-74695578	HepG2	liver:	n/a	n/a
10	FOXA1	chr11:74695029-74695489	HepG2	liver:	n/a	n/a
11	FOXA2	chr11:74695116-74695469	HepG2	liver:	n/a	n/a
12	FOXA2	chr11:74695132-74695531	A549	lung:	n/a	n/a
13	FOXA2	chr11:74693066-74693359	HepG2	liver:	n/a	n/a
14	GATA2	chr11:74694478-74694827	HUVEC	blood vessel:	n/a	n/a
15	HNF4A	chr11:74695183-74695394	HepG2	liver:	n/a	n/a
16	JUN	chr11:74693004-74693207	HepG2	liver:	n/a	n/a
17	MAFK	chr11:74694621-74694719	K562	blood:	n/a	n/a
18	MAX	chr11:74693000-74693103	HepG2	liver:	n/a	n/a
19	NFATC1	chr11:74694631-74695063	GM12878	blood:	n/a	n/a
20	NFATC1	chr11:74694420-74694788	GM12878	blood:	n/a	n/a
21	NFATC1	chr11:74693685-74694018	GM12878	blood:	n/a	n/a
22	POLR2A	chr11:74694395-74694964	GM12878	blood:	n/a	n/a
23	POLR2A	chr11:74692981-74693221	HepG2	liver:	n/a	n/a
24	POLR2A	chr11:74694336-74694883	GM12892	blood:	n/a	n/a
25	POLR2A	chr11:74693005-74694660	PFSK-1	brain:	n/a	n/a
26	POLR2A	chr11:74694577-74694956	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr11:74694467-74694986	GM12892	blood:	n/a	n/a
28	POLR2A	chr11:74694514-74694826	GM12891	blood:	n/a	n/a
29	POLR2A	chr11:74695168-74695683	HepG2	liver:	n/a	n/a
30	POLR2A	chr11:74693956-74693995	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr11:74692920-74693171	K562	blood:	n/a	n/a
32	POLR2A	chr11:74694394-74696167	GM12878	blood:	n/a	n/a
33	POLR2A	chr11:74694961-74694997	HepG2	liver:	n/a	n/a
34	POLR2A	chr11:74693231-74693261	GM12878	blood:	n/a	n/a
35	POLR2A	chr11:74695132-74695441	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr11:74693656-74694261	GM12892	blood:	n/a	n/a
37	POLR2A	chr11:74693906-74693933	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr11:74693243-74694073	HepG2	liver:	n/a	n/a
39	POLR2A	chr11:74691723-74694340	PFSK-1	brain:	n/a	n/a
40	POLR2A	chr11:74695095-74695650	GM12878	blood:	n/a	n/a
41	POLR2A	chr11:74692787-74694099	K562	blood:	n/a	n/a
42	POLR2A	chr11:74695607-74696066	K562	blood:	n/a	n/a
43	POLR2A	chr11:74694369-74694884	K562	blood:	n/a	n/a
44	POLR2A	chr11:74695214-74696114	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr11:74693583-74694237	PANC-1	pancreas:	n/a	n/a
46	POLR2A	chr11:74691524-74696389	GM12878	blood:	n/a	n/a
47	POLR2A	chr11:74695169-74695442	K562	blood:	n/a	n/a
48	POLR2A	chr11:74694104-74694132	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr11:74693614-74694113	GM12878	blood:	n/a	n/a
50	POLR2A	chr11:74692832-74693068	HCT-116	colon:	n/a	n/a

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:74695452..74697635-chr11:74702648..74704873,2	K562	blood:
2	chr11:74692366..74695026-chr11:74708015..74709624,2	K562	blood:
3	chr11:74691371..74693128-chr19:50360262..50361984,2	MCF-7	breast:
4	chr11:74680895..74682724-chr11:74692938..74695695,2	K562	blood:
5	chr11:74668433..74670131-chr11:74694358..74696257,2	MCF-7	breast:
6	chr11:74670533..74672513-chr11:74690416..74693115,2	MCF-7	breast:
7	chr11:74659270..74662951-chr11:74693468..74696338,4	MCF-7	breast:
8	chr11:74695159..74697355-chr11:74716327..74718010,2	K562	blood:
9	chr11:74654649..74657199-chr11:74695538..74697147,2	MCF-7	breast:
10	chr11:74692434..74697441-chr11:74698257..74701616,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPCS2-1	chr11:74693547-74695088	ENSG00000249164

No data

Variant related genes	Relation type
NEU3	TF binding region
ENSG00000166435	chromatin interactions
ENSG00000118363	chromatin interactions
ENSG00000104960	chromatin interactions
ENSG00000265344	chromatin interactions
ENSG00000162139	chromatin interactions
RABGAP1	miRNA target sites

Extended variants
information (count: 126 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:126 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372586321	chr11:74693032-74693033	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs191739859	chr11:74693049-74693050	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs576000760	chr11:74693058-74693059	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs34635498	chr11:74693073-74693074	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs545707658	chr11:74693089-74693090	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs561582728	chr11:74693093-74693094	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs541530078	chr11:74693116-74693117	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs561822546	chr11:74693117-74693118	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs112887650	chr11:74693151-74693152	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs183570326	chr11:74693177-74693178	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs527640658	chr11:74693193-74693194	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs564053738	chr11:74693194-74693195	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs564719622	chr11:74693275-74693276	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs375822315	chr11:74693330-74693331	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs533648051	chr11:74693375-74693376	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374785699	chr11:74693394-74693395	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs373561839	chr11:74693396-74693397	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs188217081	chr11:74693417-74693418	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs570032282	chr11:74693458-74693459	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs535864683	chr11:74693473-74693474	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs549163327	chr11:74693485-74693486	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs192792232	chr11:74693491-74693492	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs76975576	chr11:74693499-74693500	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs553528059	chr11:74693506-74693507	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs149815276	chr11:74693549-74693550	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
26	rs114650462	chr11:74693569-74693570	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs150484578	chr11:74693592-74693593	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs372651107	chr11:74693598-74693599	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs182080281	chr11:74693605-74693606	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs577154389	chr11:74693613-74693614	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs373706762	chr11:74693673-74693674	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs543132487	chr11:74693704-74693705	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
33	rs4614477	chr11:74693745-74693746	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs4944964	chr11:74693750-74693751	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs369296203	chr11:74693754-74693755	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
36	rs186715847	chr11:74693756-74693757	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
37	rs75713564	chr11:74693764-74693765	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
38	rs192393289	chr11:74693767-74693768	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
39	rs564656589	chr11:74693792-74693793	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
40	rs533585542	chr11:74693838-74693839	Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs367612523	chr11:74693906-74693907	Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
42	rs371069576	chr11:74693914-74693915	Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
43	rs544100988	chr11:74693946-74693947	Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
44	rs201743138	chr11:74693956-74693957	Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
45	rs556789207	chr11:74694015-74694016	Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
46	rs624786	chr11:74694029-74694030	Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs548375873	chr11:74694036-74694037	Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs529232474	chr11:74694149-74694150	Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs184628149	chr11:74694186-74694187	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
50	rs565966809	chr11:74694274-74694275	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	21364760	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74661800-74699200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr11:74661800-74699400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr11:74662200-74699600	Weak transcription	Esophagus	oesophagus
4	chr11:74673400-74694400	Weak transcription	Stomach Mucosa	stomach
5	chr11:74675600-74699400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr11:74677200-74693400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr11:74677600-74693800	Strong transcription	HSMM	muscle
8	chr11:74678600-74699200	Weak transcription	Spleen	Spleen
9	chr11:74681000-74699200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr11:74681200-74699600	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr11:74684400-74693800	Weak transcription	Gastric	stomach
12	chr11:74684400-74699200	Weak transcription	Pancreas	Pancrea
13	chr11:74684800-74699200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr11:74686400-74693200	Strong transcription	Stomach Smooth Muscle	stomach
15	chr11:74686400-74693400	Weak transcription	Psoas Muscle	Psoas
16	chr11:74686400-74699400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr11:74686800-74699200	Weak transcription	Aorta	Aorta
18	chr11:74686800-74699400	Weak transcription	Fetal Brain Male	brain
19	chr11:74687200-74699200	Weak transcription	Right Ventricle	heart
20	chr11:74687600-74699600	Weak transcription	NHEK	skin
21	chr11:74687800-74699600	Weak transcription	Colon Smooth Muscle	Colon
22	chr11:74687800-74700000	Weak transcription	Fetal Heart	heart
23	chr11:74689200-74695000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr11:74689400-74699200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr11:74689400-74699200	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr11:74689400-74699200	Weak transcription	Hela-S3	cervix
27	chr11:74689400-74699200	Weak transcription	HUVEC	blood vessel
28	chr11:74689400-74699400	Weak transcription	Brain Anterior Caudate	brain
29	chr11:74689400-74699400	Weak transcription	Rectal Smooth Muscle	rectum
30	chr11:74689400-74699600	Weak transcription	Brain Hippocampus Middle	brain
31	chr11:74689600-74699000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr11:74689600-74699200	Weak transcription	Primary B cells from cord blood	blood
33	chr11:74689600-74699200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr11:74689600-74699200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr11:74689600-74699200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr11:74689600-74699200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr11:74689600-74699200	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr11:74689600-74699400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr11:74689600-74699400	Weak transcription	Brain Cingulate Gyrus	brain
40	chr11:74689600-74699400	Weak transcription	NHLF	lung
41	chr11:74689600-74699600	Weak transcription	Brain Substantia Nigra	brain
42	chr11:74689800-74699200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr11:74689800-74699200	Weak transcription	Colonic Mucosa	Colon
44	chr11:74690000-74699000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr11:74690000-74699200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr11:74690000-74699400	Weak transcription	NHDF-Ad	bronchial
47	chr11:74690200-74699200	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr11:74690200-74699200	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr11:74690200-74699200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr11:74690200-74699200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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