Variant report

Variant	esv1828436
Chromosome Location	chr1:212577765-212591863
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:598)
CpG islands
(count:1037)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:598 , 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	chr1:212588171-212588364	HepG2	liver:	n/a	n/a
2	ATF2	chr1:212588062-212588986	GM12878	blood:	n/a	n/a
3	ATF2	chr1:212588177-212588616	GM12878	blood:	n/a	n/a
4	ATF3	chr1:212588087-212588554	GM12878	blood:	n/a	n/a
5	ATF3	chr1:212588085-212588462	K562	blood:	n/a	n/a
6	BATF	chr1:212588236-212588657	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:212588185-212588607	GM12878	blood:	n/a	chr1:212588411-212588420 chr1:212588261-212588274
8	BCL11A	chr1:212588242-212588543	GM12878	blood:	n/a	chr1:212588411-212588420 chr1:212588261-212588274
9	BCLAF1	chr1:212587937-212588751	GM12878	blood:	n/a	chr1:212588411-212588420 chr1:212587983-212587992 chr1:212588261-212588274
10	BCLAF1	chr1:212587946-212588696	GM12878	blood:	n/a	chr1:212588411-212588420 chr1:212587983-212587992 chr1:212588261-212588274
11	BHLHE40	chr1:212588084-212588543	HepG2	liver:	n/a	chr1:212588255-212588271
12	BHLHE40	chr1:212587368-212587545	K562	blood:	n/a	chr1:212587415-212587431
13	BHLHE40	chr1:212588036-212589170	K562	blood:	n/a	chr1:212588255-212588271
14	BHLHE40	chr1:212588069-212589066	GM12878	blood:	n/a	chr1:212588255-212588271
15	BRCA1	chr1:212588145-212588322	HepG2	liver:	n/a	n/a
16	BRCA1	chr1:212588159-212588216	GM12878	blood:	n/a	n/a
17	CBX3	chr1:212588110-212588539	K562	blood:	n/a	n/a
18	CBX3	chr1:212587056-212587806	K562	blood:	n/a	n/a
19	CBX3	chr1:212587912-212589221	K562	blood:	n/a	n/a
20	CCNT2	chr1:212587629-212588458	K562	blood:	n/a	n/a
21	CEBPB	chr1:212588325-212588411	K562	blood:	n/a	n/a
22	CEBPB	chr1:212588000-212589247	GM12878	blood:	n/a	n/a
23	CEBPD	chr1:212587977-212588350	HepG2	liver:	n/a	n/a
24	CHD1	chr1:212587648-212587828	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr1:212587999-212588986	GM12878	blood:	n/a	n/a
26	CHD2	chr1:212587991-212588609	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr1:212588043-212589141	GM12878	blood:	n/a	n/a
28	CHD2	chr1:212587536-212587709	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr1:212587625-212587691	HepG2	liver:	n/a	n/a
30	CHD2	chr1:212585639-212585908	GM12878	blood:	n/a	n/a
31	CHD2	chr1:212587406-212587692	GM12878	blood:	n/a	n/a
32	CHD2	chr1:212588060-212588510	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr1:212588119-212588392	HepG2	liver:	n/a	n/a
34	CHD2	chr1:212588076-212588606	K562	blood:	n/a	n/a
35	CREB1	chr1:212587968-212588510	A549	lung:	n/a	n/a
36	CTCF	chr1:212588100-212588250	GM12866	blood:	n/a	n/a
37	CTCF	chr1:212588380-212588530	A549	lung:	n/a	n/a
38	CTCF	chr1:212588260-212588410	GM12873	blood:	n/a	n/a
39	CTCF	chr1:212588300-212588450	K562	blood:	n/a	n/a
40	CTCF	chr1:212588300-212588450	HCT-116	colon:	n/a	n/a
41	CTCF	chr1:212587780-212587930	A549	lung:	n/a	chr1:212587781-212587789
42	CTCF	chr1:212588240-212588390	GM12869	blood:	n/a	n/a
43	CTCF	chr1:212588280-212588430	HCFaa	heart:	n/a	n/a
44	CTCF	chr1:212588280-212588430	HPF	lung:	n/a	n/a
45	CTCF	chr1:212588240-212588390	GM12864	blood:	n/a	n/a
46	CTCF	chr1:212588180-212588330	GM12874	blood:	n/a	n/a
47	CTCF	chr1:212588360-212588510	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr1:212587620-212587770	GM12874	blood:	n/a	n/a
49	CTCF	chr1:212588260-212588410	HEK293	kidney:	n/a	n/a
50	CTCF	chr1:212588440-212588590	GM12875	blood:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:212587798-212587848	GM12892	blood:	n/a
2	chr1:212586894-212586944	U87	brain:	n/a
3	chr1:212588580-212588630	HMEC	breast:	n/a
4	chr1:212584335-212584385	HPAEpiC	pulmonary alveolar:	n/a
5	chr1:212587798-212587848	HCT-116	colon:	n/a
6	chr1:212589072-212589122	T-47D	breast:	n/a
7	chr1:212584335-212584385	NB4	blood:	n/a
8	chr1:212584335-212584385	SK-N-SH	brain:	n/a
9	chr1:212588407-212588457	NT2-D1	testis:	n/a
10	chr1:212586894-212586944	HRCEpiC	kidney:	n/a
11	chr1:212588117-212588167	A549	lung:	n/a
12	chr1:212588350-212588400	U87	brain:	n/a
13	chr1:212588536-212588586	PrEC	prostate:	n/a
14	chr1:212591689-212591739	HRPEpiC	eye:	n/a
15	chr1:212587951-212588001	HRCEpiC	kidney:	n/a
16	chr1:212587188-212587238	PFSK-1	brain:	n/a
17	chr1:212587803-212587853	GM12892	blood:	n/a
18	chr1:212588395-212588445	Caco-2	colon:	n/a
19	chr1:212588848-212588898	HRCEpiC	kidney:	n/a
20	chr1:212586894-212586944	GM12891	blood:	n/a
21	chr1:212587803-212587853	SK-N-MC	brain:	n/a
22	chr1:212588580-212588630	SK-N-SH_RA	brain:	n/a
23	chr1:212588397-212588447	SAEC	small airway:	n/a
24	chr1:212588848-212588898	HepG2	liver:	n/a
25	chr1:212587798-212587848	NHDF-neo	bronchial:	n/a
26	chr1:212588397-212588447	Caco-2	colon:	n/a
27	chr1:212588848-212588898	HCF	heart:	n/a
28	chr1:212586894-212586944	SK-N-SH	brain:	n/a
29	chr1:212588580-212588630	GM12891	blood:	n/a
30	chr1:212588407-212588457	GM19239	blood:	n/a
31	chr1:212584335-212584385	ECC-1	luminal epithelium:	n/a
32	chr1:212588117-212588167	AG10803	skin:	n/a
33	chr1:212587803-212587853	SAEC	small airway:	n/a
34	chr1:212587951-212588001	ProgFib	skin:	n/a
35	chr1:212588350-212588400	MCF10A-Er-Src	breast:	n/a
36	chr1:212584335-212584385	PANC-1	pancreas:	n/a
37	chr1:212588580-212588630	SK-N-SH	brain:	n/a
38	chr1:212587188-212587238	HCF	heart:	n/a
39	chr1:212589072-212589122	HCF	heart:	n/a
40	chr1:212584335-212584385	MCF-7	breast:	n/a
41	chr1:212589072-212589122	HEEpiC	esophagus:	n/a
42	chr1:212589072-212589122	HRPEpiC	eye:	n/a
43	chr1:212588117-212588167	GM12878	blood:	n/a
44	chr1:212587798-212587848	HCF	heart:	n/a
45	chr1:212588117-212588167	H1-hESC	embryonic stem cell:	embryo
46	chr1:212586894-212586944	HEEpiC	esophagus:	n/a
47	chr1:212588397-212588447	U87	brain:	n/a
48	chr1:212584335-212584385	AG09319	gingival:	n/a
49	chr1:212588350-212588400	HCF	heart:	n/a
50	chr1:212587676-212587726	AG09309	skin:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:212588338..212589858-chr1:212645243..212647080,2	K562	blood:
2	chr1:212550848..212553114-chr1:212586010..212588532,2	MCF-7	breast:
3	chr1:212578826..212581261-chr1:212604877..212607699,2	K562	blood:
4	chr1:212585974..212594847-chr1:212598812..212609579,19	K562	blood:
5	chr1:212587912..212590110-chr1:212604889..212609190,4	K562	blood:
6	chr1:212589362..212592084-chr1:212630605..212632407,2	K562	blood:
7	chr1:212577419..212579979-chr1:212586021..212589542,6	K562	blood:
8	chr1:212458597..212460542-chr1:212586367..212588357,2	MCF-7	breast:
9	chr1:212586222..212588940-chr1:212781343..212783037,2	K562	blood:
10	chr1:212526286..212528256-chr1:212589016..212590996,2	K562	blood:
11	chr1:212549233..212551182-chr1:212586836..212589324,2	K562	blood:
12	chr1:212577333..212581219-chr1:212586593..212589230,4	MCF-7	breast:
13	chr1:212586060..212592297-chr1:212603893..212609565,9	MCF-7	breast:
14	chr1:212588056..212590074-chr1:212779163..212783567,3	K562	blood:
15	chr1:212587143..212589756-chr1:212965630..212967810,2	K562	blood:
16	chr1:212570221..212572169-chr1:212580241..212582437,2	K562	blood:
17	chr1:212586665..212588349-chr1:212964322..212966191,2	MCF-7	breast:
18	chr1:212581574..212584496-chr1:212586803..212589409,2	MCF-7	breast:
19	chr1:212569599..212572522-chr1:212576653..212579387,2	K562	blood:
20	chr1:212577272..212579979-chr1:212586236..212589542,6	K562	blood:
21	chr1:212591382..212593654-chr1:212604322..212606198,2	K562	blood:
22	chr1:212457988..212460167-chr1:212585002..212587734,2	MCF-7	breast:
23	chr1:212581574..212584496-chr1:212586803..212589409,2	MCF-7	breast:

No data

Variant related genes	Relation type
TMEM206	TF binding region
TMEM206	CpG island
ENSG00000066027	chromatin interactions
ENSG00000065600	chromatin interactions
ENSG00000117691	chromatin interactions
ENSG00000162772	chromatin interactions
ENSG00000117697	chromatin interactions
ENSG00000203705	chromatin interactions

Extended variants
information (count: 530 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535716756	chr1:212577789-212577790	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs17018985	chr1:212577790-212577791	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs571873408	chr1:212577887-212577888	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs188543708	chr1:212577925-212577926	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs558578690	chr1:212578002-212578003	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs547795519	chr1:212578047-212578048	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs529825625	chr1:212578063-212578064	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs576833317	chr1:212578064-212578065	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs544318605	chr1:212578083-212578084	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs537892972	chr1:212578147-212578148	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs181671551	chr1:212578151-212578152	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs150374431	chr1:212578155-212578156	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs542496388	chr1:212578172-212578173	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs376506884	chr1:212578187-212578188	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs186212856	chr1:212578227-212578228	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs189936862	chr1:212578230-212578231	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs552305250	chr1:212578244-212578245	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs137957031	chr1:212578273-212578274	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs531425817	chr1:212578287-212578288	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs372200716	chr1:212578301-212578302	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs376525173	chr1:212578311-212578312	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs182570715	chr1:212578316-212578317	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs368908959	chr1:212578332-212578333	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs553619973	chr1:212578334-212578335	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs76027393	chr1:212578425-212578426	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs114105808	chr1:212578476-212578477	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs557516941	chr1:212578531-212578532	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs187180309	chr1:212578532-212578533	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs544673062	chr1:212578549-212578550	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs552722088	chr1:212578573-212578574	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs377700215	chr1:212578594-212578595	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs566271756	chr1:212578599-212578600	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs143424171	chr1:212578603-212578604	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs74138137	chr1:212578631-212578632	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs542562563	chr1:212578637-212578638	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs77783387	chr1:212578640-212578641	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs148623674	chr1:212578652-212578653	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs369926169	chr1:212578657-212578658	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs527898116	chr1:212578660-212578661	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs546460332	chr1:212578672-212578673	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs74138138	chr1:212578689-212578690	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs531339896	chr1:212578700-212578701	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs6540739	chr1:212578708-212578709	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs191033617	chr1:212578728-212578729	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs528832175	chr1:212578768-212578769	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182066859	chr1:212578772-212578773	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs376781540	chr1:212578802-212578803	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs537149227	chr1:212578831-212578832	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs111587679	chr1:212578880-212578881	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs539342222	chr1:212578896-212578897	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Breast cancer	21364760	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
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1004 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212526800-212582800	Weak transcription	Fetal Brain Male	brain
2	chr1:212528400-212583000	Weak transcription	Fetal Kidney	kidney
3	chr1:212553200-212578400	Weak transcription	K562	blood
4	chr1:212556800-212587600	Weak transcription	Small Intestine	intestine
5	chr1:212558600-212578800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr1:212558600-212580000	Weak transcription	Left Ventricle	heart
7	chr1:212560200-212578400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr1:212560400-212580200	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr1:212560600-212578200	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr1:212560600-212578800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr1:212560600-212580200	Weak transcription	HSMMtube	muscle
12	chr1:212560600-212582000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr1:212560600-212582000	Weak transcription	Gastric	stomach
14	chr1:212561000-212578000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr1:212561000-212579800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr1:212561000-212579800	Weak transcription	Stomach Smooth Muscle	stomach
17	chr1:212561000-212580000	Weak transcription	Brain Hippocampus Middle	brain
18	chr1:212561000-212582400	Weak transcription	Aorta	Aorta
19	chr1:212562000-212578400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr1:212564200-212578800	Weak transcription	Esophagus	oesophagus
21	chr1:212564600-212577800	Weak transcription	Spleen	Spleen
22	chr1:212564600-212578600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr1:212564600-212579800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr1:212569600-212582600	Weak transcription	Ovary	ovary
25	chr1:212570400-212578800	Weak transcription	Fetal Stomach	stomach
26	chr1:212570600-212577800	Weak transcription	Fetal Muscle Trunk	muscle
27	chr1:212570600-212578400	Weak transcription	HepG2	liver
28	chr1:212570600-212582000	Weak transcription	Duodenum Mucosa	Duodenum
29	chr1:212570800-212580000	Weak transcription	Fetal Lung	lung
30	chr1:212571000-212578600	Weak transcription	Brain Anterior Caudate	brain
31	chr1:212571000-212586200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr1:212571200-212578400	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr1:212571200-212580000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr1:212571400-212577800	Weak transcription	Primary T cells fromperipheralblood	blood
35	chr1:212571400-212580000	Weak transcription	NH-A	brain
36	chr1:212571600-212578800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr1:212571800-212578600	Weak transcription	Fetal Brain Female	brain
38	chr1:212571800-212579800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr1:212572000-212577800	Weak transcription	Fetal Muscle Leg	muscle
40	chr1:212572000-212578400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr1:212572000-212579800	Weak transcription	Brain Germinal Matrix	brain
42	chr1:212572200-212578400	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr1:212572600-212582000	Weak transcription	Rectal Smooth Muscle	rectum
44	chr1:212572600-212585000	Strong transcription	Dnd41	blood
45	chr1:212572800-212585600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:212573000-212578600	Weak transcription	Primary B cells from cord blood	blood
47	chr1:212573000-212579800	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr1:212573200-212580000	Weak transcription	Fetal Intestine Small	intestine
49	chr1:212573400-212580400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:212573400-212582200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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