Variant report

Variant	nsv508691
Chromosome Location	chr1:212998319-213028392
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:205)
CpG islands
(count:366)
Chromatin interactive
region (count:15)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:205 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:213000997-213001567	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:213007402-213007600	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:213027092-213027383	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:213001177-213001236	K562	blood:	n/a	n/a
5	ATF2	chr1:213025410-213025857	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:213025373-213025890	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:212999467-212999763	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr1:213007089-213007411	GM12878	blood:	n/a	n/a
9	BATF	chr1:213007139-213007428	GM12878	blood:	n/a	n/a
10	BCL3	chr1:213026726-213027469	A549	lung:	n/a	n/a
11	BHLHE40	chr1:213001132-213001674	HepG2	liver:	n/a	n/a
12	BHLHE40	chr1:213007139-213007701	GM12878	blood:	n/a	n/a
13	CBX3	chr1:212999010-212999649	K562	blood:	n/a	n/a
14	CBX3	chr1:212999118-212999736	HCT-116	colon:	n/a	n/a
15	CBX3	chr1:213017815-213018167	K562	blood:	n/a	n/a
16	CBX3	chr1:212998889-212999749	K562	blood:	n/a	n/a
17	CBX3	chr1:213017793-213018263	K562	blood:	n/a	n/a
18	CEBPB	chr1:213005119-213005416	K562	blood:	n/a	n/a
19	CEBPB	chr1:213026879-213027123	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:213026826-213027677	A549	lung:	n/a	n/a
21	CEBPB	chr1:213005225-213005358	K562	blood:	n/a	n/a
22	CEBPB	chr1:213021044-213021335	HepG2	liver:	n/a	chr1:213021201-213021212
23	CEBPB	chr1:213026747-213027599	A549	lung:	n/a	n/a
24	CEBPB	chr1:213005224-213005365	K562	blood:	n/a	n/a
25	E2F6	chr1:212999314-212999748	H1-hESC	embryonic stem cell:	n/a	n/a
26	EBF1	chr1:213007232-213007618	GM12878	blood:	n/a	n/a
27	EGR1	chr1:213007238-213007449	GM12878	blood:	n/a	n/a
28	ELF1	chr1:213005096-213005320	K562	blood:	n/a	n/a
29	EP300	chr1:213007143-213007620	GM12878	blood:	n/a	n/a
30	EP300	chr1:213001159-213001476	HepG2	liver:	n/a	n/a
31	EP300	chr1:213017956-213018151	K562	blood:	n/a	n/a
32	EP300	chr1:213000980-213001520	HepG2	liver:	n/a	n/a
33	EP300	chr1:213007054-213007718	GM12878	blood:	n/a	n/a
34	EP300	chr1:213000920-213001660	HepG2	liver:	n/a	n/a
35	EP300	chr1:213026891-213027521	A549	lung:	n/a	n/a
36	EP300	chr1:213026776-213027521	A549	lung:	n/a	n/a
37	EP300	chr1:213001769-213002181	HepG2	liver:	n/a	n/a
38	EP300	chr1:213025420-213025772	H1-hESC	embryonic stem cell:	n/a	chr1:213025426-213025440
39	FOS	chr1:213026059-213026216	MCF10A-Er-Src	breast:	n/a	n/a
40	FOSL2	chr1:213026761-213027416	A549	lung:	n/a	n/a
41	FOSL2	chr1:213007244-213007631	A549	lung:	n/a	n/a
42	FOSL2	chr1:213026853-213027577	A549	lung:	n/a	n/a
43	FOXA1	chr1:213001061-213001694	HepG2	liver:	n/a	chr1:213001586-213001598 chr1:213001582-213001594
44	FOXA1	chr1:213007286-213007664	HepG2	liver:	n/a	n/a
45	FOXA1	chr1:213000939-213001762	HepG2	liver:	n/a	chr1:213001586-213001598 chr1:213001582-213001594
46	FOXA1	chr1:213000946-213001697	HepG2	liver:	n/a	chr1:213001586-213001598 chr1:213001582-213001594
47	FOXA1	chr1:213001098-213001728	HepG2	liver:	n/a	chr1:213001586-213001598 chr1:213001582-213001594
48	FOXA2	chr1:213001023-213001709	HepG2	liver:	n/a	chr1:213001586-213001598 chr1:213001582-213001594
49	FOXA2	chr1:213026933-213027573	A549	lung:	n/a	n/a
50	FOXA2	chr1:213001053-213001451	A549	lung:	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	chr1:213008198-213008248	PFSK-1	brain:	n/a
2	chr1:213008198-213008248	HMEC	breast:	n/a
3	chr1:213008198-213008248	SK-N-SH_RA	brain:	n/a
4	chr1:213021979-213022029	HEK293	kidney:	embryo
5	chr1:213021561-213021611	HCF	heart:	n/a
6	chr1:213021561-213021611	NH-A	brain:	n/a
7	chr1:213021561-213021611	MCF-7	breast:	n/a
8	chr1:213008198-213008248	SKMC	muscle:	n/a
9	chr1:213013952-213014002	AG09319	gingival:	n/a
10	chr1:213008198-213008248	HAEpiC	amniotic membrane:	n/a
11	chr1:213008198-213008248	RPTEC	kidney:	n/a
12	chr1:213021561-213021611	HEEpiC	esophagus:	n/a
13	chr1:213021261-213021311	T-47D	breast:	n/a
14	chr1:213020590-213020640	HPAEpiC	pulmonary alveolar:	n/a
15	chr1:213021561-213021611	NHBE	bronchial:	n/a
16	chr1:213021979-213022029	HRCEpiC	kidney:	n/a
17	chr1:213013952-213014002	GM12892	blood:	n/a
18	chr1:213020590-213020640	MCF10A-Er-Src	breast:	n/a
19	chr1:213013952-213014002	A549	lung:	n/a
20	chr1:213021979-213022029	ECC-1	luminal epithelium:	n/a
21	chr1:213021979-213022029	HCF	heart:	n/a
22	chr1:213021979-213022029	Hela-S3	cervix:	n/a
23	chr1:213021979-213022029	HUVEC	blood vessel:	n/a
24	chr1:213021261-213021311	GM19239	blood:	n/a
25	chr1:213020590-213020640	IMR90	lung:	fetal
26	chr1:213021261-213021311	GM12878	blood:	n/a
27	chr1:213008198-213008248	Hepatocyte	liver:	n/a
28	chr1:213008198-213008248	HepG2	liver:	n/a
29	chr1:213021561-213021611	CMK	blood:	n/a
30	chr1:213020590-213020640	SAEC	small airway:	n/a
31	chr1:213020590-213020640	SK-N-MC	brain:	n/a
32	chr1:213021979-213022029	IMR90	lung:	fetal
33	chr1:213013952-213014002	HIPEpiC	eye:	n/a
34	chr1:213020590-213020640	SK-N-SH_RA	brain:	n/a
35	chr1:213021561-213021611	HepG2	liver:	n/a
36	chr1:213013952-213014002	HUVEC	blood vessel:	n/a
37	chr1:213008198-213008248	MCF10A-Er-Src	breast:	n/a
38	chr1:213013952-213014002	AG10803	skin:	n/a
39	chr1:213021261-213021311	PFSK-1	brain:	n/a
40	chr1:213020590-213020640	PANC-1	pancreas:	n/a
41	chr1:213021561-213021611	HRE	kidney:	n/a
42	chr1:213008198-213008248	HRCEpiC	kidney:	n/a
43	chr1:213008198-213008248	HNPCEpiC	eye:	n/a
44	chr1:213021261-213021311	HCM	heart:	n/a
45	chr1:213021561-213021611	SK-N-SH	brain:	n/a
46	chr1:213021561-213021611	RPTEC	kidney:	n/a
47	chr1:213008198-213008248	GM19239	blood:	n/a
48	chr1:213021979-213022029	PANC-1	pancreas:	n/a
49	chr1:213013952-213014002	CMK	blood:	n/a
50	chr1:213008198-213008248	SK-N-MC	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:213025489..213028696-chr1:213029248..213033184,3	K562	blood:
2	chr1:213001465..213003584-chr1:213040615..213043476,2	MCF-7	breast:
3	chr1:212782226..212783823-chr1:212998854..213001770,2	K562	blood:
4	chr1:213025871..213028763-chr1:213030169..213033277,3	MCF-7	breast:
5	chr1:213026064..213028809-chr1:213029690..213032627,2	K562	blood:
6	chr1:213019184..213021421-chr1:213029036..213031526,2	K562	blood:
7	chr1:212984776..212986773-chr1:212997927..213000551,2	K562	blood:
8	chr1:212997378..212998898-chr17:41399483..41402356,3	K562	blood:
9	chr1:213001095..213003639-chr1:213003692..213005660,2	K562	blood:
10	chr1:213000835..213002742-chr1:213006925..213009621,2	K562	blood:
11	chr1:212782138..212783676-chr1:213005899..213008453,2	K562	blood:
12	chr1:213002092..213003822-chr1:213040039..213042148,2	K562	blood:
13	chr1:212964912..212966461-chr1:212995791..212998620,2	K562	blood:
14	chr1:213000835..213002742-chr1:213006925..213009621,2	K562	blood:
15	chr1:213001095..213003639-chr1:213003692..213005660,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C1orf227-1	chr1:213025450-213027651	ENSG00000198468.3
2	lnc-FLVCR1-1	chr1:213025477-213026496	NONHSAT009406
3	lnc-C1orf227-1	chr1:213025450-213027653	ENSG00000198468
4	lnc-TATDN3-2	chr1:212998542-212998832	NONHSAT009403

No data

Variant related genes	Relation type
C1orf227	TF binding region
ENSG00000235182	TF binding region
FLVCR1	TF binding region
C1orf227	CpG island
ENSG00000235182	CpG island
FLVCR1	CpG island
ENSG00000203705	chromatin interactions
ENSG00000117697	chromatin interactions
ENSG00000162769	chromatin interactions
ENSG00000198468	chromatin interactions
ENSG00000162772	chromatin interactions
MSL3	miRNA target sites

Extended variants
information (count: 801 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:801 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576097633	chr1:212998350-212998351	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs141133230	chr1:212998353-212998354	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs187459539	chr1:212998354-212998355	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs150724853	chr1:212998408-212998409	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs35719387	chr1:212998424-212998425	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs549923393	chr1:212998438-212998439	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs533350991	chr1:212998455-212998456	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs546869853	chr1:212998482-212998483	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs535696134	chr1:212998511-212998512	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs554020405	chr1:212998576-212998577	Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs566275817	chr1:212998631-212998632	Enhancers ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs539785761	chr1:212998678-212998679	Enhancers ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs76416882	chr1:212998691-212998692	Enhancers ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs374474669	chr1:212998701-212998702	Enhancers ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs543942504	chr1:212998739-212998740	Enhancers ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs72743920	chr1:212998811-212998812	Enhancers ZNF genes & repeats Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs551075273	chr1:212998874-212998875	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs574859418	chr1:212998875-212998876	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs3949369	chr1:212998904-212998905	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs74942074	chr1:212998924-212998925	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs11120035	chr1:212998944-212998945	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs544944760	chr1:212998945-212998946	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs368678870	chr1:212998953-212998954	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs78444357	chr1:212998976-212998977	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs530465566	chr1:212999014-212999015	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs191140145	chr1:212999049-212999050	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs183464157	chr1:212999050-212999051	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs373388860	chr1:212999063-212999064	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs116448911	chr1:212999073-212999074	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs35861002	chr1:212999164-212999165	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs374803596	chr1:212999166-212999167	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs143908593	chr1:212999184-212999185	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs146890710	chr1:212999282-212999283	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs372604709	chr1:212999293-212999294	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs558090339	chr1:212999387-212999388	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs569939342	chr1:212999398-212999399	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs188636723	chr1:212999416-212999417	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs139689406	chr1:212999430-212999431	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs574197551	chr1:212999476-212999477	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs192726597	chr1:212999480-212999481	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs184339578	chr1:212999489-212999490	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs144569248	chr1:212999512-212999513	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs138929640	chr1:212999513-212999514	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs577830502	chr1:212999521-212999522	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs544966830	chr1:212999525-212999526	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs543992402	chr1:212999527-212999528	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs188428940	chr1:212999534-212999535	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs191620721	chr1:212999535-212999536	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs542246708	chr1:212999539-212999540	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs144428644	chr1:212999540-212999541	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD

Chromatin state (count:201 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212976200-212998800	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr1:212979600-213001000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr1:212980800-213001000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr1:212988400-212998800	Weak transcription	Adipose Nuclei	Adipose
5	chr1:212988600-212998400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:212990800-212998600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:212991000-212998800	Weak transcription	Stomach Mucosa	stomach
8	chr1:212994000-212999000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr1:212996400-212998600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr1:212997000-212998600	Weak transcription	HepG2	liver
11	chr1:212997200-213000200	ZNF genes & repeats	Fetal Intestine Small	intestine
12	chr1:212997400-212999600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr1:212998600-212998800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr1:212998600-212999200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr1:212998600-212999400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr1:212998600-212999600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:212998600-212999600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr1:212998600-212999800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr1:212998600-212999800	ZNF genes & repeats	HepG2	liver
20	chr1:212998600-212999800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
21	chr1:212998800-212999800	ZNF genes & repeats	Adipose Nuclei	Adipose
22	chr1:212998800-212999800	ZNF genes & repeats	Stomach Mucosa	stomach
23	chr1:212999000-212999400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
24	chr1:212999000-212999800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr1:212999200-212999600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr1:212999400-212999600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr1:212999400-213009400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr1:212999800-213000400	Weak transcription	HepG2	liver
29	chr1:212999800-213000600	Weak transcription	Stomach Mucosa	stomach
30	chr1:212999800-213003600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr1:212999800-213005000	Weak transcription	Adipose Nuclei	Adipose
32	chr1:212999800-213005000	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr1:213000200-213000400	Weak transcription	Fetal Intestine Small	intestine
34	chr1:213000400-213000800	Enhancers	HepG2	liver
35	chr1:213000400-213002800	Enhancers	Fetal Intestine Small	intestine
36	chr1:213000600-213001000	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr1:213000600-213001800	Enhancers	Stomach Mucosa	stomach
38	chr1:213000600-213002200	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr1:213000600-213002600	Enhancers	Duodenum Mucosa	Duodenum
40	chr1:213000600-213002800	Enhancers	Fetal Intestine Large	intestine
41	chr1:213000800-213001000	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr1:213000800-213002400	Flanking Active TSS	HepG2	liver
43	chr1:213001000-213001400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr1:213001000-213001400	Enhancers	A549	lung
45	chr1:213001000-213001600	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr1:213001000-213005800	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr1:213001400-213004600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr1:213001400-213005800	Weak transcription	A549	lung
49	chr1:213001600-213002200	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr1:213001800-213008400	Weak transcription	Stomach Mucosa	stomach

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