Variant report

Variant	nsv819317
Chromosome Location	chr7:127963051-127964156
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:7 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:127963233-127963871	IMR90	lung:	n/a	n/a
2	FOSL2	chr7:127963972-127964572	SK-N-SH	brain:	n/a	chr7:127964285-127964297
3	NFIC	chr7:127964063-127964786	SK-N-SH	brain:	n/a	n/a
4	POLR2A	chr7:127963668-127963752	K562	blood:	n/a	n/a
5	POLR2A	chr7:127963595-127963644	Hela-S3	cervix:	n/a	n/a
6	POLR2A	chr7:127963592-127963939	K562	blood:	n/a	n/a
7	RAD21	chr7:127962094-127963613	SK-N-SH	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:127963545-127963595	K562	blood:	n/a
2	chr7:127963545-127963595	PrEC	prostate:	n/a
3	chr7:127963545-127963595	SK-N-MC	brain:	n/a
4	chr7:127963545-127963595	NB4	blood:	n/a
5	chr7:127963545-127963595	GM12891	blood:	n/a
6	chr7:127963545-127963595	SKMC	muscle:	n/a
7	chr7:127963545-127963595	HEK293	kidney:	embryo
8	chr7:127963545-127963595	T-47D	breast:	n/a
9	chr7:127963545-127963595	SAEC	small airway:	n/a
10	chr7:127963545-127963595	H1-hESC	embryonic stem cell:	embryo
11	chr7:127963545-127963595	BE2_C	brain:	n/a
12	chr7:127963545-127963595	AoSMC	blood vessel:	n/a
13	chr7:127963545-127963595	GM06990	blood:	n/a
14	chr7:127963545-127963595	ProgFib	skin:	n/a
15	chr7:127963545-127963595	AG09319	gingival:	n/a
16	chr7:127963545-127963595	HRE	kidney:	n/a
17	chr7:127963545-127963595	NHDF-neo	bronchial:	n/a
18	chr7:127963545-127963595	AG10803	skin:	n/a
19	chr7:127963545-127963595	IMR90	lung:	fetal
20	chr7:127963545-127963595	BJ	skin:	n/a
21	chr7:127963545-127963595	HNPCEpiC	eye:	n/a
22	chr7:127963545-127963595	HEEpiC	esophagus:	n/a
23	chr7:127963545-127963595	ovcar-3	ovarian:	n/a
24	chr7:127963545-127963595	HL-60	blood:	n/a
25	chr7:127963545-127963595	Jurkat	blood:	n/a
26	chr7:127963545-127963595	NT2-D1	testis:	n/a
27	chr7:127963545-127963595	NHBE	bronchial:	n/a
28	chr7:127963545-127963595	ECC-1	luminal epithelium:	n/a
29	chr7:127963545-127963595	AG09309	skin:	n/a
30	chr7:127963545-127963595	HPAEpiC	pulmonary alveolar:	n/a
31	chr7:127963545-127963595	HMEC	breast:	n/a
32	chr7:127963545-127963595	HCF	heart:	n/a
33	chr7:127963545-127963595	HUVEC	blood vessel:	n/a
34	chr7:127963545-127963595	GM12878	blood:	n/a
35	chr7:127963545-127963595	A549	lung:	n/a
36	chr7:127963545-127963595	HCM	heart:	n/a
37	chr7:127963545-127963595	AG04449	skin:	fetal
38	chr7:127963545-127963595	GM19239	blood:	n/a
39	chr7:127963545-127963595	HCT-116	colon:	n/a
40	chr7:127963545-127963595	HIPEpiC	eye:	n/a
41	chr7:127963545-127963595	MCF-7	breast:	n/a
42	chr7:127963545-127963595	GM12892	blood:	n/a
43	chr7:127963545-127963595	Hepatocyte	liver:	n/a
44	chr7:127963545-127963595	HCPEpiC	choroid plexus:	n/a
45	chr7:127963545-127963595	MCF10A-Er-Src	breast:	n/a
46	chr7:127963545-127963595	HepG2	liver:	n/a
47	chr7:127963545-127963595	HRCEpiC	kidney:	n/a
48	chr7:127963545-127963595	NH-A	brain:	n/a
49	chr7:127963545-127963595	AG04450	lung:	fetal
50	chr7:127963545-127963595	SK-N-SH	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:127948906..127951419-chr7:127962953..127965286,2	K562	blood:
2	chr7:127963796..127966771-chr7:127971446..127974012,2	MCF-7	breast:

No data

Variant related genes	Relation type
RBM28	TF binding region
RBM28	CpG island

Extended variants
information (count: 63 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:63 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564979476	chr7:127963052-127963053	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs147287548	chr7:127963092-127963093	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs547365091	chr7:127963121-127963122	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs565540664	chr7:127963154-127963155	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs181281081	chr7:127963183-127963184	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs536903897	chr7:127963185-127963186	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs548912863	chr7:127963189-127963190	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs186395136	chr7:127963193-127963194	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs7809696	chr7:127963194-127963195	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs558919467	chr7:127963201-127963202	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs115810240	chr7:127963260-127963261	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs563857133	chr7:127963284-127963285	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs190836156	chr7:127963313-127963314	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs10263305	chr7:127963341-127963342	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs142428009	chr7:127963346-127963347	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs78195887	chr7:127963368-127963369	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs150901789	chr7:127963412-127963413	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs575968037	chr7:127963426-127963427	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs139429239	chr7:127963428-127963429	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs564982268	chr7:127963434-127963435	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs532183691	chr7:127963461-127963462	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs550990421	chr7:127963481-127963482	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs149978338	chr7:127963482-127963483	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs113268614	chr7:127963498-127963499	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs17152005	chr7:127963515-127963516	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs369440306	chr7:127963526-127963527	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs199990732	chr7:127963545-127963546	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs562845415	chr7:127963552-127963553	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs73230652	chr7:127963553-127963554	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs202220784	chr7:127963565-127963566	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs374475965	chr7:127963581-127963582	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs145972885	chr7:127963582-127963583	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs552732537	chr7:127963596-127963597	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs138703329	chr7:127963597-127963598	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs535083625	chr7:127963603-127963604	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs553213737	chr7:127963614-127963615	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs145208220	chr7:127963629-127963630	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs535443818	chr7:127963641-127963642	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs201297674	chr7:127963666-127963667	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs201127355	chr7:127963672-127963673	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs575929386	chr7:127963723-127963724	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs141281797	chr7:127963740-127963741	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs557026861	chr7:127963749-127963750	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs188002477	chr7:127963769-127963770	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs191025394	chr7:127963770-127963771	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs541090546	chr7:127963776-127963777	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs183178211	chr7:127963875-127963876	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs527252656	chr7:127963890-127963891	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs28618998	chr7:127963904-127963905	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs541835788	chr7:127963909-127963910	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:167 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127939600-127982200	Weak transcription	Stomach Mucosa	stomach
2	chr7:127940000-127980800	Strong transcription	Fetal Muscle Trunk	muscle
3	chr7:127940400-127980000	Strong transcription	Stomach Smooth Muscle	stomach
4	chr7:127940600-127980000	Strong transcription	Liver	Liver
5	chr7:127940800-127963800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr7:127940800-127971400	Strong transcription	Fetal Brain Female	brain
7	chr7:127941400-127963400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr7:127941600-127979600	Strong transcription	Sigmoid Colon	Sigmoid Colon
9	chr7:127941600-127980000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr7:127942000-127980400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr7:127942000-127980600	Strong transcription	Fetal Muscle Leg	muscle
12	chr7:127942600-127979600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:127943000-127964800	Strong transcription	Cortex derived primary cultured neurospheres	brain
14	chr7:127943000-127969000	Strong transcription	Primary B cells from cord blood	blood
15	chr7:127943000-127979800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:127943000-127979800	Strong transcription	Fetal Intestine Large	intestine
17	chr7:127943000-127981200	Strong transcription	Dnd41	blood
18	chr7:127943000-127982000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr7:127943200-127980400	Strong transcription	Duodenum Mucosa	Duodenum
20	chr7:127943200-127981600	Strong transcription	HUES48 Cell Line	embryonic stem cell
21	chr7:127943400-127979400	Strong transcription	Duodenum Smooth Muscle	Duodenum
22	chr7:127943400-127979800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr7:127943400-127980000	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr7:127943400-127980000	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr7:127943400-127980000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
26	chr7:127943400-127981400	Strong transcription	Primary B cells from peripheral blood	blood
27	chr7:127943400-127981600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
28	chr7:127944400-127965800	Strong transcription	Rectal Mucosa Donor 31	rectum
29	chr7:127944400-127971600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr7:127944400-127980000	Strong transcription	H1 Cell Line	embryonic stem cell
31	chr7:127944400-127980000	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr7:127944400-127980200	Strong transcription	Placenta	Placenta
33	chr7:127944400-127980600	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr7:127945200-127980000	Strong transcription	GM12878-XiMat	blood
35	chr7:127945400-127979200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr7:127945600-127967400	Strong transcription	Brain Substantia Nigra	brain
37	chr7:127945600-127971600	Strong transcription	NHEK	skin
38	chr7:127945600-127979400	Strong transcription	Brain Germinal Matrix	brain
39	chr7:127945800-127963400	Strong transcription	Brain Anterior Caudate	brain
40	chr7:127945800-127967200	Strong transcription	Rectal Smooth Muscle	rectum
41	chr7:127946000-127969400	Strong transcription	HUVEC	blood vessel
42	chr7:127948000-127963400	Strong transcription	Skeletal Muscle Male	skeletal muscle
43	chr7:127949200-127963200	Strong transcription	Skeletal Muscle Female	skeletal muscle
44	chr7:127949600-127978800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr7:127949600-127980000	Strong transcription	Primary monocytes fromperipheralblood	blood
46	chr7:127949800-127965000	Strong transcription	NH-A	brain
47	chr7:127949800-127969000	Strong transcription	Brain Angular Gyrus	brain
48	chr7:127949800-127969200	Strong transcription	A549	lung
49	chr7:127950000-127966000	Strong transcription	H9 Cell Line	embryonic stem cell
50	chr7:127950000-127969000	Strong transcription	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links