Variant report

Variant	nsv869936
Chromosome Location	chr1:246778181-246811161
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:376)
CpG islands
(count:732)
Chromatin interactive
region (count:17)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:376 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:246803049-246803274	K562	blood:	n/a	n/a
2	ATF2	chr1:246792236-246792998	GM12878	blood:	n/a	n/a
3	ATF2	chr1:246792272-246792758	GM12878	blood:	n/a	n/a
4	BATF	chr1:246793347-246793611	GM12878	blood:	n/a	n/a
5	BATF	chr1:246793253-246793608	GM12878	blood:	n/a	n/a
6	BATF	chr1:246792329-246792692	GM12878	blood:	n/a	n/a
7	BATF	chr1:246792324-246792693	GM12878	blood:	n/a	n/a
8	BCLAF1	chr1:246792278-246792798	GM12878	blood:	n/a	n/a
9	CBX3	chr1:246810392-246810814	K562	blood:	n/a	n/a
10	CEBPB	chr1:246796251-246796522	MCF-7	breast:	n/a	chr1:246796412-246796425 chr1:246796414-246796425 chr1:246796412-246796425 chr1:246796412-246796423
11	CEBPB	chr1:246810167-246810722	H1-hESC	embryonic stem cell:	n/a	chr1:246810302-246810319 chr1:246810304-246810315
12	CEBPB	chr1:246794845-246795163	IMR90	lung:	n/a	n/a
13	CEBPB	chr1:246810191-246810440	HepG2	liver:	n/a	chr1:246810302-246810319 chr1:246810304-246810315
14	CEBPB	chr1:246796265-246796569	HepG2	liver:	n/a	chr1:246796412-246796425 chr1:246796414-246796425 chr1:246796412-246796425 chr1:246796412-246796423
15	CEBPB	chr1:246796344-246796480	H1-hESC	embryonic stem cell:	n/a	chr1:246796412-246796425 chr1:246796414-246796425 chr1:246796412-246796425 chr1:246796412-246796423
16	CEBPB	chr1:246796228-246796590	MCF-7	breast:	n/a	chr1:246796412-246796425 chr1:246796414-246796425 chr1:246796412-246796425 chr1:246796412-246796423
17	CEBPB	chr1:246779032-246779201	K562	blood:	n/a	n/a
18	CEBPB	chr1:246796270-246796547	A549	lung:	n/a	chr1:246796412-246796425 chr1:246796414-246796425 chr1:246796412-246796425 chr1:246796412-246796423
19	CEBPB	chr1:246810151-246810454	K562	blood:	n/a	chr1:246810302-246810319 chr1:246810304-246810315
20	CEBPB	chr1:246810187-246810481	IMR90	lung:	n/a	chr1:246810302-246810319 chr1:246810304-246810315
21	CEBPB	chr1:246795940-246796613	IMR90	lung:	n/a	chr1:246796412-246796425 chr1:246796414-246796425 chr1:246796412-246796425 chr1:246796412-246796423
22	CEBPB	chr1:246796267-246796556	K562	blood:	n/a	chr1:246796412-246796425 chr1:246796414-246796425 chr1:246796412-246796425 chr1:246796412-246796423
23	CHD2	chr1:246802297-246802351	HepG2	liver:	n/a	n/a
24	CTCF	chr1:246810440-246810590	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr1:246807980-246808130	GM12864	blood:	n/a	n/a
26	CTCF	chr1:246810499-246810655	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr1:246810328-246810823	MCF-7	breast:	n/a	n/a
28	CTCF	chr1:246810480-246810630	NHLF	lung:	n/a	n/a
29	CTCF	chr1:246810400-246810550	WI-38	lung:	n/a	n/a
30	CTCF	chr1:246810520-246810670	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr1:246810500-246810650	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr1:246810520-246810670	HPF	lung:	n/a	n/a
33	CTCF	chr1:246810338-246810766	K562	blood:	n/a	n/a
34	CTCF	chr1:246810460-246810610	GM06990	blood:	n/a	n/a
35	CTCF	chr1:246810500-246810650	HCFaa	heart:	n/a	n/a
36	CTCF	chr1:246810520-246810670	A549	lung:	n/a	n/a
37	CTCF	chr1:246810500-246810650	AG09309	skin:	n/a	n/a
38	CTCF	chr1:246810514-246810649	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr1:246810600-246810750	NB4	blood:	n/a	n/a
40	CTCF	chr1:246810500-246810650	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr1:246810500-246810650	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr1:246810476-246810696	K562	blood:	n/a	n/a
43	CTCF	chr1:246810540-246810690	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr1:246810446-246810778	A549	lung:	n/a	n/a
45	CTCF	chr1:246810500-246810650	MCF-7	breast:	n/a	n/a
46	CTCF	chr1:246810427-246810790	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr1:246810458-246810727	MCF-7	breast:	n/a	n/a
48	CTCF	chr1:246810305-246810918	SK-N-SH	brain:	n/a	n/a
49	CTCF	chr1:246810460-246810610	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr1:246810440-246810590	SAEC	small airway:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246783166-246783216	NHDF-neo	bronchial:	n/a
2	chr1:246785611-246785661	GM12878	blood:	n/a
3	chr1:246799336-246799386	HUVEC	blood vessel:	n/a
4	chr1:246783518-246783568	AG09309	skin:	n/a
5	chr1:246783198-246783248	AG04450	lung:	fetal
6	chr1:246795610-246795660	HCPEpiC	choroid plexus:	n/a
7	chr1:246795610-246795660	HepG2	liver:	n/a
8	chr1:246785611-246785661	BJ	skin:	n/a
9	chr1:246783198-246783248	GM12891	blood:	n/a
10	chr1:246798258-246798308	AG09319	gingival:	n/a
11	chr1:246795610-246795660	MCF-7	breast:	n/a
12	chr1:246787626-246787676	HRPEpiC	eye:	n/a
13	chr1:246810637-246810687	HNPCEpiC	eye:	n/a
14	chr1:246781432-246781482	LNCaP	prostate:	n/a
15	chr1:246798258-246798308	HCPEpiC	choroid plexus:	n/a
16	chr1:246798258-246798308	AG04450	lung:	fetal
17	chr1:246787626-246787676	U87	brain:	n/a
18	chr1:246783518-246783568	HMEC	breast:	n/a
19	chr1:246795610-246795660	T-47D	breast:	n/a
20	chr1:246783166-246783216	HCT-116	colon:	n/a
21	chr1:246799336-246799386	SAEC	small airway:	n/a
22	chr1:246783518-246783568	HCT-116	colon:	n/a
23	chr1:246783166-246783216	SK-N-MC	brain:	n/a
24	chr1:246799336-246799386	PrEC	prostate:	n/a
25	chr1:246795610-246795660	HNPCEpiC	eye:	n/a
26	chr1:246783198-246783248	SK-N-MC	brain:	n/a
27	chr1:246783518-246783568	NB4	blood:	n/a
28	chr1:246810637-246810687	Hela-S3	cervix:	n/a
29	chr1:246783518-246783568	GM06990	blood:	n/a
30	chr1:246783904-246783954	HUVEC	blood vessel:	n/a
31	chr1:246783518-246783568	T-47D	breast:	n/a
32	chr1:246810637-246810687	HCF	heart:	n/a
33	chr1:246783904-246783954	PANC-1	pancreas:	n/a
34	chr1:246798258-246798308	Caco-2	colon:	n/a
35	chr1:246787626-246787676	SAEC	small airway:	n/a
36	chr1:246810637-246810687	SKMC	muscle:	n/a
37	chr1:246798258-246798308	NHDF-neo	bronchial:	n/a
38	chr1:246781432-246781482	A549	lung:	n/a
39	chr1:246810637-246810687	Jurkat	blood:	n/a
40	chr1:246783166-246783216	T-47D	breast:	n/a
41	chr1:246783166-246783216	BJ	skin:	n/a
42	chr1:246783166-246783216	GM19239	blood:	n/a
43	chr1:246783518-246783568	AG04449	skin:	fetal
44	chr1:246810637-246810687	SK-N-SH_RA	brain:	n/a
45	chr1:246785611-246785661	HRPEpiC	eye:	n/a
46	chr1:246799336-246799386	SKMC	muscle:	n/a
47	chr1:246785611-246785661	BE2_C	brain:	n/a
48	chr1:246783198-246783248	LNCaP	prostate:	n/a
49	chr1:246787626-246787676	HUVEC	blood vessel:	n/a
50	chr1:246783198-246783248	HCT-116	colon:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:246784949..246787437-chr1:246795091..246797673,2	K562	blood:
2	chr1:246779828..246782694-chr1:246783827..246786516,2	K562	blood:
3	chr1:246784360..246786280-chr1:246789850..246792060,3	K562	blood:
4	chr1:246802416..246804121-chr1:246807056..246809856,2	K562	blood:
5	chr1:246792973..246795440-chr1:246887335..246889540,2	K562	blood:
6	chr1:246803588..246807692-chr1:246815416..246819511,4	K562	blood:
7	chr1:246784360..246786280-chr1:246789850..246792060,3	K562	blood:
8	chr1:246775147..246776815-chr1:246778943..246781797,2	K562	blood:
9	chr1:246779828..246782694-chr1:246783827..246786516,2	K562	blood:
10	chr1:246785700..246787934-chr1:246794155..246796121,2	MCF-7	breast:
11	chr1:246809490..246812170-chr1:246921388..246923239,2	MCF-7	breast:
12	chr1:246810760..246814409-chr1:246816683..246820922,4	K562	blood:
13	chr1:246790522..246793411-chr1:246794361..246797146,2	K562	blood:
14	chr1:246810150..246810952-chr1:246916713..246917868,5	MCF-7	breast:
15	chr1:246802416..246804121-chr1:246807056..246809856,2	K562	blood:
16	chr1:246801219..246803848-chr1:246819940..246821442,2	MCF-7	breast:
17	chr1:246805689..246809236-chr1:246811706..246814341,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TFB2M-4	chr1:246795692-246795780	NONHSAT010713
2	lnc-TFB2M-4	chr1:246795553-246795685	NONHSAT010713

No data

Variant related genes	Relation type
ENSG00000228955	TF binding region
ENSG00000228955	CpG island
ENSG00000143653	chromatin interactions
ENSG00000228955	chromatin interactions

Extended variants
information (count: 1467 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561366216	chr1:246778193-246778194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs561415361	chr1:246778244-246778245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530211466	chr1:246778366-246778367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546779526	chr1:246778413-246778414	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146225652	chr1:246778415-246778416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532384713	chr1:246778470-246778471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs199887489	chr1:246778472-246778473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553560086	chr1:246778480-246778481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112264077	chr1:246778482-246778483	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139155308	chr1:246778501-246778502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537783711	chr1:246778508-246778509	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548356154	chr1:246778509-246778510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143989906	chr1:246778517-246778518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533845187	chr1:246778523-246778524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150500760	chr1:246778530-246778531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576881088	chr1:246778531-246778532	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181553392	chr1:246778538-246778539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556231174	chr1:246778559-246778560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575886461	chr1:246778564-246778565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544627508	chr1:246778604-246778605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571918743	chr1:246778668-246778669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561488817	chr1:246778704-246778705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574941189	chr1:246778720-246778721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540685121	chr1:246778729-246778730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139455462	chr1:246778772-246778773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373308967	chr1:246778773-246778774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552136760	chr1:246778942-246778943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376613573	chr1:246778975-246778976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371349760	chr1:246779025-246779026	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546739403	chr1:246779062-246779063	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186034234	chr1:246779120-246779121	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191362502	chr1:246779121-246779122	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571621771	chr1:246779122-246779123	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570547017	chr1:246779128-246779129	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559404201	chr1:246779181-246779182	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149752840	chr1:246779281-246779282	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556194428	chr1:246779287-246779288	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145621847	chr1:246779319-246779320	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs532377941	chr1:246779327-246779328	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183117223	chr1:246779368-246779369	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141379014	chr1:246779389-246779390	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs116010938	chr1:246779390-246779391	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs145196159	chr1:246779482-246779483	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560347320	chr1:246779591-246779592	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569183916	chr1:246779668-246779669	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576917199	chr1:246779688-246779689	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs116461256	chr1:246779726-246779727	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562854593	chr1:246779757-246779758	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542467121	chr1:246779786-246779787	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs542080363	chr1:246779797-246779798	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Oral cancer	21386901	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1286 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246739000-246806200	Weak transcription	Aorta	Aorta
2	chr1:246755400-246832800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr1:246764200-246784200	Weak transcription	Thymus	Thymus
4	chr1:246765800-246779600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr1:246766200-246784200	Weak transcription	Dnd41	blood
6	chr1:246771400-246784600	Weak transcription	Fetal Stomach	stomach
7	chr1:246772200-246795600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr1:246772400-246784600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr1:246772600-246779600	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr1:246772600-246780000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr1:246772600-246784000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr1:246772600-246784000	Weak transcription	Liver	Liver
13	chr1:246772600-246784000	Weak transcription	GM12878-XiMat	blood
14	chr1:246772600-246784800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr1:246772600-246784800	Weak transcription	Fetal Muscle Trunk	muscle
16	chr1:246772600-246790600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr1:246772600-246795600	Weak transcription	HepG2	liver
18	chr1:246772800-246783800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr1:246772800-246783800	Weak transcription	Fetal Intestine Small	intestine
20	chr1:246772800-246784000	Weak transcription	Duodenum Mucosa	Duodenum
21	chr1:246772800-246784000	Weak transcription	Spleen	Spleen
22	chr1:246772800-246789200	Weak transcription	Ovary	ovary
23	chr1:246773000-246779200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr1:246773000-246782600	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr1:246773000-246784800	Weak transcription	Fetal Muscle Leg	muscle
26	chr1:246773000-246784800	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr1:246773000-246790200	Weak transcription	Small Intestine	intestine
28	chr1:246773000-246790200	Weak transcription	HSMM	muscle
29	chr1:246773000-246792400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr1:246773200-246780600	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr1:246773200-246782200	Weak transcription	Primary hematopoietic stem cells	blood
32	chr1:246773200-246799000	Weak transcription	Fetal Lung	lung
33	chr1:246773400-246780200	Weak transcription	Primary B cells from cord blood	blood
34	chr1:246773400-246784400	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr1:246773400-246785000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr1:246773600-246795400	Weak transcription	Placenta	Placenta
37	chr1:246773800-246780200	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr1:246773800-246784600	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr1:246773800-246795800	Weak transcription	Hela-S3	cervix
40	chr1:246774000-246792600	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr1:246774200-246780200	Weak transcription	NHDF-Ad	bronchial
42	chr1:246774200-246781000	Weak transcription	Primary T cells from cord blood	blood
43	chr1:246774400-246778200	Weak transcription	Primary B cells from peripheral blood	blood
44	chr1:246774400-246779600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr1:246774400-246780600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr1:246774400-246785600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr1:246774600-246779000	Weak transcription	Left Ventricle	heart
48	chr1:246774600-246779200	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr1:246774600-246779600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr1:246774600-246780200	Weak transcription	Osteobl	bone

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