Variant report

Variant	nsv522890
Chromosome Location	chr16:81341363-81348396
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:584)
CpG islands
(count:366)
Chromatin interactive
region (count:19)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:81347348-81347586	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:81348206-81348646	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:81348317-81348570	K562	blood:	n/a	n/a
4	ATF1	chr16:81348165-81348721	K562	blood:	n/a	n/a
5	ATF2	chr16:81348069-81348765	GM12878	blood:	n/a	n/a
6	ATF2	chr16:81348169-81348653	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr16:81348272-81348597	GM12878	blood:	n/a	n/a
8	ATF2	chr16:81347185-81347717	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr16:81347128-81347709	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr16:81348205-81348659	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr16:81348162-81348800	HepG2	liver:	n/a	n/a
12	ATF3	chr16:81348298-81348721	K562	blood:	n/a	n/a
13	ATF3	chr16:81348098-81348638	A549	lung:	n/a	n/a
14	ATF3	chr16:81348262-81348719	HepG2	liver:	n/a	n/a
15	ATF3	chr16:81348192-81348673	GM12878	blood:	n/a	n/a
16	ATF3	chr16:81348252-81348859	K562	blood:	n/a	n/a
17	ATF3	chr16:81348133-81348587	A549	lung:	n/a	n/a
18	ATF3	chr16:81348343-81348553	GM12878	blood:	n/a	n/a
19	ATF3	chr16:81348242-81348655	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr16:81347131-81347730	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr16:81343730-81344024	K562	blood:	n/a	n/a
22	BACH1	chr16:81348245-81348589	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCLAF1	chr16:81348101-81348654	GM12878	blood:	n/a	chr16:81348469-81348478
24	BCLAF1	chr16:81348174-81348754	GM12878	blood:	n/a	chr16:81348469-81348478
25	BHLHE40	chr16:81348192-81348730	GM12878	blood:	n/a	n/a
26	BHLHE40	chr16:81347968-81348770	K562	blood:	n/a	n/a
27	BRCA1	chr16:81348245-81348717	HepG2	liver:	n/a	n/a
28	BRCA1	chr16:81348126-81348668	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr16:81348192-81348720	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr16:81348058-81348912	K562	blood:	n/a	n/a
31	CCNT2	chr16:81348052-81349528	K562	blood:	n/a	n/a
32	CEBPB	chr16:81346884-81346991	H1-hESC	embryonic stem cell:	n/a	chr16:81346889-81346900
33	CEBPB	chr16:81347329-81347705	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr16:81346871-81347036	HepG2	liver:	n/a	chr16:81346889-81346900
35	CEBPB	chr16:81348277-81348734	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr16:81348347-81348544	K562	blood:	n/a	n/a
37	CEBPB	chr16:81346866-81347001	IMR90	lung:	n/a	chr16:81346889-81346900
38	CEBPB	chr16:81346810-81347068	K562	blood:	n/a	chr16:81346889-81346900
39	CEBPD	chr16:81348166-81348776	K562	blood:	n/a	n/a
40	CEBPD	chr16:81348322-81348637	HepG2	liver:	n/a	n/a
41	CEBPD	chr16:81348237-81348700	HepG2	liver:	n/a	n/a
42	CHD1	chr16:81347036-81348799	H1-hESC	embryonic stem cell:	n/a	chr16:81348543-81348550
43	CHD2	chr16:81348063-81348676	H1-hESC	embryonic stem cell:	n/a	chr16:81348543-81348550
44	CHD2	chr16:81347112-81347649	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr16:81348166-81348726	K562	blood:	n/a	chr16:81348543-81348550
46	CHD2	chr16:81348148-81348801	GM12878	blood:	n/a	chr16:81348543-81348550
47	CHD2	chr16:81347397-81347849	HepG2	liver:	n/a	n/a
48	CHD2	chr16:81348070-81348884	HepG2	liver:	n/a	chr16:81348543-81348550
49	CHD2	chr16:81348126-81348934	Hela-S3	cervix:	n/a	chr16:81348543-81348550
50	CREB1	chr16:81348007-81349147	K562	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:81348378-81348428	HEEpiC	esophagus:	n/a
2	chr16:81348309-81348359	HCF	heart:	n/a
3	chr16:81347858-81347908	HRPEpiC	eye:	n/a
4	chr16:81345203-81345253	AG09319	gingival:	n/a
5	chr16:81348378-81348428	HCM	heart:	n/a
6	chr16:81348309-81348359	MCF10A-Er-Src	breast:	n/a
7	chr16:81347551-81347601	ECC-1	luminal epithelium:	n/a
8	chr16:81347858-81347908	PFSK-1	brain:	n/a
9	chr16:81347858-81347908	SAEC	small airway:	n/a
10	chr16:81348309-81348359	PFSK-1	brain:	n/a
11	chr16:81348378-81348428	HPAEpiC	pulmonary alveolar:	n/a
12	chr16:81345203-81345253	A549	lung:	n/a
13	chr16:81347551-81347601	PrEC	prostate:	n/a
14	chr16:81348309-81348359	AoSMC	blood vessel:	n/a
15	chr16:81348378-81348428	AG04450	lung:	fetal
16	chr16:81347551-81347601	Caco-2	colon:	n/a
17	chr16:81348372-81348422	NHDF-neo	bronchial:	n/a
18	chr16:81348309-81348359	ECC-1	luminal epithelium:	n/a
19	chr16:81348309-81348359	SAEC	small airway:	n/a
20	chr16:81348309-81348359	HL-60	blood:	n/a
21	chr16:81347551-81347601	GM12878	blood:	n/a
22	chr16:81347858-81347908	H1-hESC	embryonic stem cell:	embryo
23	chr16:81348372-81348422	IMR90	lung:	fetal
24	chr16:81345203-81345253	PANC-1	pancreas:	n/a
25	chr16:81347551-81347601	PANC-1	pancreas:	n/a
26	chr16:81348372-81348422	AG09309	skin:	n/a
27	chr16:81345203-81345253	K562	blood:	n/a
28	chr16:81348372-81348422	AG10803	skin:	n/a
29	chr16:81347551-81347601	AG04449	skin:	fetal
30	chr16:81348378-81348428	HMEC	breast:	n/a
31	chr16:81347858-81347908	K562	blood:	n/a
32	chr16:81348378-81348428	PrEC	prostate:	n/a
33	chr16:81347551-81347601	HMEC	breast:	n/a
34	chr16:81348309-81348359	Hepatocyte	liver:	n/a
35	chr16:81348372-81348422	HCF	heart:	n/a
36	chr16:81348372-81348422	HEEpiC	esophagus:	n/a
37	chr16:81345203-81345253	BJ	skin:	n/a
38	chr16:81347858-81347908	GM12891	blood:	n/a
39	chr16:81348378-81348428	MCF-7	breast:	n/a
40	chr16:81347858-81347908	SK-N-SH	brain:	n/a
41	chr16:81348309-81348359	A549	lung:	n/a
42	chr16:81345203-81345253	HL-60	blood:	n/a
43	chr16:81345203-81345253	GM12891	blood:	n/a
44	chr16:81348372-81348422	NH-A	brain:	n/a
45	chr16:81348372-81348422	GM12892	blood:	n/a
46	chr16:81348309-81348359	K562	blood:	n/a
47	chr16:81348378-81348428	HCT-116	colon:	n/a
48	chr16:81345203-81345253	GM19239	blood:	n/a
49	chr16:81347551-81347601	MCF10A-Er-Src	breast:	n/a
50	chr16:81345203-81345253	NB4	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:81333746..81337567-chr16:81339565..81345155,7	MCF-7	breast:
2	chr16:81110316..81112473-chr16:81346981..81348533,2	MCF-7	breast:
3	chr16:81327875..81329613-chr16:81342269..81343952,2	MCF-7	breast:
4	chr16:81344126..81345083-chr20:46230975..46231590,2	MCF-7	breast:
5	chr16:81338249..81340093-chr16:81341953..81343949,3	MCF-7	breast:
6	chr16:81109518..81111024-chr16:81347327..81349963,2	K562	blood:
7	chr16:81323548..81326494-chr16:81339686..81342459,2	MCF-7	breast:
8	chr16:81038258..81040784-chr16:81347032..81349945,2	K562	blood:
9	chr16:81347950..81350114-chr16:81397372..81401433,3	MCF-7	breast:
10	chr16:81329156..81330738-chr16:81339607..81341635,2	MCF-7	breast:
11	chr11:62622890..62623673-chr16:81347895..81348866,2	Hela-S3	cervix:
12	chr16:81343775..81345598-chr16:81381932..81384912,2	MCF-7	breast:
13	chr14:77499398..77500222-chr16:81347841..81348390,2	Hela-S3	cervix:
14	chr16:81348181..81349165-chr7:152132447..152133006,2	Hela-S3	cervix:
15	chr16:81339016..81342551-chr16:81382542..81385730,3	MCF-7	breast:
16	chr16:81038653..81041025-chr16:81346635..81349129,2	MCF-7	breast:
17	chr16:81320082..81322198-chr16:81342184..81344102,2	MCF-7	breast:
18	chr16:81347539..81350872-chr16:81478035..81482618,4	MCF-7	breast:
19	chr16:81313477..81315803-chr16:81339537..81342117,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GCSH-1	chr16:81345111-81348378	NONHSAT143942
2	lnc-GCSH-1	chr16:81344336-81347028	ENSG00000260495.1
3	lnc-GAN-2	chr16:81346284-81346800	NONHSAT143940
4	lnc-GAN-2	chr16:81343952-81346073	NONHSAT143940
5	lnc-GCSH-3	chr16:81343613-81343839	NONHSAT143939

No data

Variant related genes	Relation type
GAN	TF binding region
ENSG00000260495	TF binding region
GAN	CpG island
ENSG00000260495	CpG island
ENSG00000255717	chromatin interactions
ENSG00000166451	chromatin interactions
ENSG00000245059	chromatin interactions
ENSG00000153815	chromatin interactions
ENSG00000168003	chromatin interactions
ENSG00000055609	chromatin interactions
ENSG00000103121	chromatin interactions
ENSG00000261609	chromatin interactions
ENSG00000166455	chromatin interactions

Extended variants
information (count: 286 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9889027	chr16:81341363-81341364	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74955335	chr16:81341364-81341365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186416470	chr16:81341383-81341384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535836923	chr16:81341384-81341385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190905788	chr16:81341393-81341394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547794280	chr16:81341394-81341395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112353403	chr16:81341414-81341415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145179323	chr16:81341432-81341433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558847211	chr16:81341434-81341435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs180967294	chr16:81341468-81341469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534858202	chr16:81341475-81341476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547983638	chr16:81341481-81341482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554295675	chr16:81341515-81341516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs56118809	chr16:81341544-81341545	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs185202088	chr16:81341581-81341582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536308898	chr16:81341602-81341603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576644844	chr16:81341610-81341611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543746212	chr16:81341643-81341644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs138963513	chr16:81341681-81341682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532565038	chr16:81341724-81341725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs117345002	chr16:81341739-81341740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558984060	chr16:81341742-81341743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529759352	chr16:81341754-81341755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548133756	chr16:81341779-81341780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569534041	chr16:81341791-81341792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537078180	chr16:81341808-81341809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552181660	chr16:81341866-81341867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570798213	chr16:81341888-81341889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191043111	chr16:81341889-81341890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532759153	chr16:81341954-81341955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183245298	chr16:81342009-81342010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs117561421	chr16:81342011-81342012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572546029	chr16:81342030-81342031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552327223	chr16:81342035-81342036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141545142	chr16:81342088-81342089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73585615	chr16:81342113-81342114	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs576339958	chr16:81342202-81342203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543846303	chr16:81342306-81342307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538678177	chr16:81342316-81342317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150418948	chr16:81342327-81342328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187659284	chr16:81342353-81342354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138221041	chr16:81342355-81342356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559535325	chr16:81342411-81342412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs530263327	chr16:81342438-81342439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs374099022	chr16:81342541-81342542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191840846	chr16:81342566-81342567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183119522	chr16:81342585-81342586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530412888	chr16:81342601-81342602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377667945	chr16:81342639-81342640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570710400	chr16:81342651-81342652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Neuroblastoma	18923524	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Obesity	20622171	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD

Chromatin state (count:529 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81309200-81345200	Weak transcription	Brain Hippocampus Middle	brain
2	chr16:81328000-81347000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr16:81328200-81347000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr16:81328600-81347000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr16:81328800-81344800	Weak transcription	Fetal Intestine Small	intestine
6	chr16:81328800-81345200	Weak transcription	Fetal Intestine Large	intestine
7	chr16:81330600-81344800	Weak transcription	Esophagus	oesophagus
8	chr16:81330600-81347200	Weak transcription	Gastric	stomach
9	chr16:81331600-81344800	Weak transcription	Ovary	ovary
10	chr16:81331600-81347000	Weak transcription	Right Ventricle	heart
11	chr16:81331800-81346400	Weak transcription	Brain Anterior Caudate	brain
12	chr16:81332000-81345400	Weak transcription	Thymus	Thymus
13	chr16:81332200-81346400	Weak transcription	Fetal Stomach	stomach
14	chr16:81332400-81344600	Weak transcription	Brain Angular Gyrus	brain
15	chr16:81332400-81346400	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr16:81333200-81346400	Weak transcription	Brain Germinal Matrix	brain
17	chr16:81334400-81346600	Weak transcription	Colon Smooth Muscle	Colon
18	chr16:81334600-81347200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr16:81335400-81343600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr16:81335600-81346400	Weak transcription	Primary T cells from cord blood	blood
21	chr16:81337000-81344800	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr16:81337600-81347000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr16:81338000-81346400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr16:81338200-81346600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr16:81338400-81347000	Weak transcription	Spleen	Spleen
26	chr16:81338400-81347200	Weak transcription	Primary B cells from cord blood	blood
27	chr16:81338400-81347400	Weak transcription	Aorta	Aorta
28	chr16:81338600-81346600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr16:81338600-81347400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr16:81338800-81346600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr16:81339200-81344800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr16:81339600-81346600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr16:81340000-81346400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr16:81340600-81345000	Weak transcription	Primary hematopoietic stem cells	blood
35	chr16:81340600-81346400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr16:81340800-81341600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr16:81340800-81347000	Weak transcription	Fetal Muscle Leg	muscle
38	chr16:81341200-81342000	Enhancers	Fetal Lung	lung
39	chr16:81341600-81346400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr16:81341800-81342000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr16:81342000-81346400	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr16:81342000-81347000	Weak transcription	Fetal Lung	lung
43	chr16:81342200-81346400	Weak transcription	Primary B cells from peripheral blood	blood
44	chr16:81342200-81346400	Weak transcription	Small Intestine	intestine
45	chr16:81342200-81346600	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr16:81342200-81346800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr16:81342400-81342600	Enhancers	Brain Cingulate Gyrus	brain
48	chr16:81342600-81346600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr16:81343200-81345200	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr16:81343200-81345200	Weak transcription	Fetal Muscle Trunk	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links