Variant report

Variant	nsv1043486
Chromosome Location	chr13:48971510-48996995
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:322)
CpG islands
(count:305)
Chromatin interactive
region (count:4)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:48974495-48974932	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:48971963-48972198	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:48987140-48987798	HepG2	liver:	n/a	n/a
4	ATF2	chr13:48976685-48977143	GM12878	blood:	n/a	n/a
5	BACH1	chr13:48972984-48973002	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr13:48976672-48977012	GM12878	blood:	n/a	n/a
7	BHLHE40	chr13:48984476-48984749	HepG2	liver:	n/a	n/a
8	CEBPB	chr13:48977183-48977518	HepG2	liver:	n/a	chr13:48977347-48977356 chr13:48977346-48977357 chr13:48977345-48977358 chr13:48977347-48977356 chr13:48977347-48977356 chr13:48977347-48977356 chr13:48977345-48977356
9	CEBPB	chr13:48977223-48977475	A549	lung:	n/a	chr13:48977347-48977356 chr13:48977346-48977357 chr13:48977345-48977358 chr13:48977347-48977356 chr13:48977347-48977356 chr13:48977347-48977356 chr13:48977345-48977356
10	CEBPB	chr13:48980113-48980423	HepG2	liver:	n/a	n/a
11	CEBPB	chr13:48974888-48975322	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr13:48977229-48977461	Hela-S3	cervix:	n/a	chr13:48977347-48977356 chr13:48977346-48977357 chr13:48977345-48977358 chr13:48977347-48977356 chr13:48977347-48977356 chr13:48977347-48977356 chr13:48977345-48977356
13	CEBPB	chr13:48977159-48977542	IMR90	lung:	n/a	chr13:48977347-48977356 chr13:48977346-48977357 chr13:48977345-48977358 chr13:48977347-48977356 chr13:48977347-48977356 chr13:48977347-48977356 chr13:48977345-48977356
14	CEBPB	chr13:48980033-48980409	IMR90	lung:	n/a	n/a
15	CEBPB	chr13:48984394-48984725	HepG2	liver:	n/a	n/a
16	CEBPB	chr13:48977218-48977489	K562	blood:	n/a	chr13:48977347-48977356 chr13:48977346-48977357 chr13:48977345-48977358 chr13:48977347-48977356 chr13:48977347-48977356 chr13:48977347-48977356 chr13:48977345-48977356
17	CEBPB	chr13:48987153-48987563	HepG2	liver:	n/a	chr13:48987446-48987458
18	CHD1	chr13:48986128-48986328	GM12878	blood:	n/a	n/a
19	CREB1	chr13:48984378-48984756	HepG2	liver:	n/a	n/a
20	CREB1	chr13:48984374-48984802	HepG2	liver:	n/a	n/a
21	CREB1	chr13:48987019-48987617	HepG2	liver:	n/a	n/a
22	CREB1	chr13:48987001-48987592	HepG2	liver:	n/a	n/a
23	CTCF	chr13:48975200-48975350	GM12873	blood:	n/a	n/a
24	CTCF	chr13:48975157-48975261	GM13976	blood:	n/a	n/a
25	CTCF	chr13:48981120-48981270	GM12873	blood:	n/a	n/a
26	CTCF	chr13:48981040-48981190	HCT-116	colon:	n/a	n/a
27	CTCF	chr13:48975186-48975330	Lung_OC	lung:	n/a	n/a
28	CTCF	chr13:48975180-48975330	GM12872	blood:	n/a	n/a
29	CTCF	chr13:48975057-48975437	GM12878	blood:	n/a	n/a
30	CTCF	chr13:48975160-48975310	GM06990	blood:	n/a	n/a
31	CTCF	chr13:48975153-48975320	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr13:48975100-48975250	GM12865	blood:	n/a	n/a
33	CTCF	chr13:48975180-48975330	GM12878	blood:	n/a	n/a
34	CTCF	chr13:48975152-48975368	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr13:48995480-48995630	WI-38	lung:	n/a	n/a
36	CTCF	chr13:48981040-48981190	HepG2	liver:	n/a	n/a
37	CTCF	chr13:48975080-48975230	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr13:48975200-48975350	HCM	heart:	n/a	n/a
39	CTCF	chr13:48975162-48975309	Medullo	brain:	n/a	n/a
40	CTCF	chr13:48981120-48981270	HEK293	kidney:	n/a	n/a
41	CTCF	chr13:48981100-48981250	GM12874	blood:	n/a	n/a
42	CTCF	chr13:48980980-48981130	GM12875	blood:	n/a	n/a
43	CTCF	chr13:48981060-48981210	GM12873	blood:	n/a	n/a
44	CTCF	chr13:48975160-48975310	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr13:48981020-48981170	HVMF	connective:	n/a	n/a
46	CTCF	chr13:48975160-48975310	HVMF	connective:	n/a	n/a
47	CTCF	chr13:48980980-48981130	BE2_C	brain:	n/a	n/a
48	CTCF	chr13:48975060-48975210	HMEC	breast:	n/a	n/a
49	CTCF	chr13:48975160-48975310	HMF	breast:	n/a	n/a
50	CTCF	chr13:48981040-48981190	GM12872	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:48988353-48988403	HMEC	breast:	n/a
2	chr13:48988353-48988403	HPAEpiC	pulmonary alveolar:	n/a
3	chr13:48974707-48974757	AG10803	skin:	n/a
4	chr13:48988353-48988403	ECC-1	luminal epithelium:	n/a
5	chr13:48986124-48986174	BJ	skin:	n/a
6	chr13:48988353-48988403	NB4	blood:	n/a
7	chr13:48974707-48974757	LNCaP	prostate:	n/a
8	chr13:48974707-48974757	AG04450	lung:	fetal
9	chr13:48986124-48986174	HIPEpiC	eye:	n/a
10	chr13:48987165-48987215	SAEC	small airway:	n/a
11	chr13:48987165-48987215	HIPEpiC	eye:	n/a
12	chr13:48987165-48987215	HAEpiC	amniotic membrane:	n/a
13	chr13:48990327-48990377	HL-60	blood:	n/a
14	chr13:48990327-48990377	Hela-S3	cervix:	n/a
15	chr13:48986124-48986174	HRE	kidney:	n/a
16	chr13:48988353-48988403	HCM	heart:	n/a
17	chr13:48974707-48974757	HMEC	breast:	n/a
18	chr13:48990327-48990377	GM12892	blood:	n/a
19	chr13:48990327-48990377	HCF	heart:	n/a
20	chr13:48990327-48990377	HMEC	breast:	n/a
21	chr13:48987165-48987215	HepG2	liver:	n/a
22	chr13:48988353-48988403	AG09309	skin:	n/a
23	chr13:48986124-48986174	U87	brain:	n/a
24	chr13:48986124-48986174	HMEC	breast:	n/a
25	chr13:48974707-48974757	RPTEC	kidney:	n/a
26	chr13:48988353-48988403	LNCaP	prostate:	n/a
27	chr13:48986124-48986174	HL-60	blood:	n/a
28	chr13:48986124-48986174	SK-N-SH	brain:	n/a
29	chr13:48988353-48988403	HCF	heart:	n/a
30	chr13:48986124-48986174	GM12891	blood:	n/a
31	chr13:48986124-48986174	GM06990	blood:	n/a
32	chr13:48987165-48987215	MCF-7	breast:	n/a
33	chr13:48987165-48987215	HRPEpiC	eye:	n/a
34	chr13:48987165-48987215	AG09319	gingival:	n/a
35	chr13:48974707-48974757	SK-N-SH_RA	brain:	n/a
36	chr13:48974707-48974757	ProgFib	skin:	n/a
37	chr13:48986124-48986174	GM19239	blood:	n/a
38	chr13:48990327-48990377	PFSK-1	brain:	n/a
39	chr13:48987165-48987215	NH-A	brain:	n/a
40	chr13:48986124-48986174	AoSMC	blood vessel:	n/a
41	chr13:48974707-48974757	HPAEpiC	pulmonary alveolar:	n/a
42	chr13:48990327-48990377	HepG2	liver:	n/a
43	chr13:48986124-48986174	NHBE	bronchial:	n/a
44	chr13:48974707-48974757	Jurkat	blood:	n/a
45	chr13:48987165-48987215	PrEC	prostate:	n/a
46	chr13:48987165-48987215	SK-N-SH	brain:	n/a
47	chr13:48986124-48986174	PrEC	prostate:	n/a
48	chr13:48990327-48990377	AoSMC	blood vessel:	n/a
49	chr13:48988353-48988403	SKMC	muscle:	n/a
50	chr13:48974707-48974757	PrEC	prostate:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:48979885..48981623-chr13:48983630..48986045,2	K562	blood:
2	chr13:48992995..48995135-chr13:48999356..49001211,2	K562	blood:
3	chr13:48984068..48985636-chr13:49106032..49107936,2	K562	blood:
4	chr13:48979509..48982464-chr13:48983015..48985946,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPAR6-2	chr13:48978317-48978399	NONHSAT033712
2	lnc-LPAR6-2	chr13:48991303-48991456	NONHSAT033712
3	lnc-LPAR6-2	chr13:48996786-48996926	NONHSAT033712
4	lnc-LPAR6-2	chr13:48982760-48982903	NONHSAT033712
5	lnc-LPAR6-2	chr13:48975434-48975543	NONHSAT033712
6	lnc-LPAR6-2	chr13:48989836-48989949	NONHSAT033711
7	lnc-LPAR6-2	chr13:48978317-48978399	NONHSAT033713
8	lnc-LPAR6-2	chr13:48989836-48989952	NONHSAT033713
9	lnc-LPAR6-2	chr13:48980692-48980845	NONHSAT033710
10	lnc-LPAR6-2	chr13:48978317-48978399	NONHSAT033710
11	lnc-LPAR6-2	chr13:48989836-48989946	NONHSAT033712
12	lnc-LPAR6-2	chr13:48996783-48996926	NONHSAT033715

No data

Variant related genes	Relation type
LPAR6	TF binding region
LPAR6	CpG island
ENSG00000139679	chromatin interactions
ENSG00000136161	chromatin interactions

Extended variants
information (count: 864 )
Associated
traits (count: 130 )

Variant overlapped rSNPs/rCNVs (count:864 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548411070	chr13:48971586-48971587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs569936450	chr13:48971617-48971618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113292447	chr13:48971619-48971620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186745197	chr13:48971637-48971638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570302701	chr13:48971686-48971687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150848334	chr13:48971692-48971693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs115410483	chr13:48971786-48971787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537950364	chr13:48971808-48971809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs375565128	chr13:48971826-48971827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535621629	chr13:48971850-48971851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138290917	chr13:48971880-48971881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs575526471	chr13:48971916-48971917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34875533	chr13:48971929-48971930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs9568036	chr13:48971936-48971937	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs565383004	chr13:48972004-48972005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535352458	chr13:48972018-48972019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541458212	chr13:48972166-48972167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536781977	chr13:48972225-48972226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368582416	chr13:48972226-48972227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530356924	chr13:48972281-48972282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115899031	chr13:48972313-48972314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141604364	chr13:48972369-48972370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs563498838	chr13:48972375-48972376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149608865	chr13:48972416-48972417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2804087	chr13:48972428-48972429	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs144323284	chr13:48972434-48972435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534307045	chr13:48972460-48972461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570137791	chr13:48972492-48972493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546602218	chr13:48972553-48972554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568086676	chr13:48972566-48972567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535714573	chr13:48972590-48972591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115345200	chr13:48972605-48972606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2156910	chr13:48972611-48972612	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs574740963	chr13:48972653-48972654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs539694930	chr13:48972657-48972658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs9568037	chr13:48972703-48972704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs148799825	chr13:48972736-48972737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9595900	chr13:48972760-48972761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs76606218	chr13:48972880-48972881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs143855179	chr13:48972908-48972909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542692673	chr13:48972912-48972913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs145953979	chr13:48972947-48972948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs139809011	chr13:48973001-48973002	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369795083	chr13:48973009-48973010	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183295910	chr13:48973036-48973037	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188520545	chr13:48973062-48973063	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531000314	chr13:48973085-48973086	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2804088	chr13:48973097-48973098	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs555715195	chr13:48973149-48973150	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575670923	chr13:48973191-48973192	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:130)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Ovarian cancer	22355333	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung adenocarcinoma	21151896	CNVD
Breast cancer	21518781	CNVD
Mantle cell lymphoma	21518781	CNVD
Ovarian cancer	21518781	CNVD
Retinoblastoma	21518781	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Chronic myeloid leukemia	21384125	CNVD
Attention deficit hyperactivity disorder	22214315	CNVD
Chronic motor tic disorder	22214315	CNVD
Schizophrenia	22214315	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:1076 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:48909000-48972200	Weak transcription	NHEK	skin
2	chr13:48914800-48972000	Weak transcription	NHLF	lung
3	chr13:48916800-48985400	Weak transcription	Colonic Mucosa	Colon
4	chr13:48920200-48974400	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr13:48921600-48972000	Weak transcription	Stomach Mucosa	stomach
6	chr13:48925200-48974800	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr13:48925400-48976400	Weak transcription	Ovary	ovary
8	chr13:48926800-48972000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr13:48928200-48971800	Weak transcription	A549	lung
10	chr13:48933400-48974000	Weak transcription	Rectal Smooth Muscle	rectum
11	chr13:48934600-48984200	Weak transcription	Right Ventricle	heart
12	chr13:48936000-48974600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr13:48936400-48973200	Weak transcription	Hela-S3	cervix
14	chr13:48941800-48973200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr13:48943600-48984200	Weak transcription	Brain Angular Gyrus	brain
16	chr13:48944000-48974400	Weak transcription	Brain Anterior Caudate	brain
17	chr13:48944200-48973800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr13:48944600-48983400	Weak transcription	Psoas Muscle	Psoas
19	chr13:48945000-48972000	Weak transcription	HSMMtube	muscle
20	chr13:48945400-48974400	Weak transcription	Small Intestine	intestine
21	chr13:48949400-48972800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr13:48953800-48972000	Weak transcription	Osteobl	bone
23	chr13:48954400-48972200	Weak transcription	HUVEC	blood vessel
24	chr13:48954800-48975000	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr13:48955800-48972000	Weak transcription	HMEC	breast
26	chr13:48955800-48972000	Weak transcription	NHDF-Ad	bronchial
27	chr13:48956000-48974000	Weak transcription	Colon Smooth Muscle	Colon
28	chr13:48956200-48976600	Weak transcription	Liver	Liver
29	chr13:48959800-48972200	Weak transcription	Adipose Nuclei	Adipose
30	chr13:48961000-48972000	Weak transcription	Fetal Lung	lung
31	chr13:48964000-48974400	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr13:48965200-48974400	Weak transcription	Fetal Heart	heart
33	chr13:48966000-48971800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr13:48966200-48971600	Weak transcription	Aorta	Aorta
35	chr13:48966400-48974200	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr13:48966400-48986000	Weak transcription	Lung	lung
37	chr13:48966800-48984200	Weak transcription	Placenta	Placenta
38	chr13:48967600-48974600	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr13:48967800-48972000	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr13:48967800-48972400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr13:48968200-48972000	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr13:48968200-48972800	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr13:48968200-48976400	Weak transcription	Primary T cells fromperipheralblood	blood
44	chr13:48968400-48976600	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr13:48968800-48972400	Weak transcription	Fetal Kidney	kidney
46	chr13:48968800-48974200	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr13:48968800-48974800	Weak transcription	Primary T cells from cord blood	blood
48	chr13:48968800-48976400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr13:48968800-48977800	Weak transcription	Spleen	Spleen
50	chr13:48968800-48984200	Weak transcription	Stomach Smooth Muscle	stomach

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