Variant report

Variant	esv3420124
Chromosome Location	chr2:67439048-67443246
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:67442430-67442736	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr2:67442440-67442590	GM12870	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
3	CTCF	chr2:67442540-67442690	NB4	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
4	CTCF	chr2:67442480-67442663	K562	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
5	CTCF	chr2:67442474-67442687	ProgFib	skin:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
6	CTCF	chr2:67442500-67442650	HPAF	blood vessel:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
7	CTCF	chr2:67442500-67442647	H1-hESC	embryonic stem cell:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
8	CTCF	chr2:67442485-67442669	GM19240	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
9	CTCF	chr2:67442500-67442650	HPF	lung:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
10	CTCF	chr2:67442278-67443123	SK-N-SH	brain:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
11	CTCF	chr2:67442500-67442650	AG04449	skin:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
12	CTCF	chr2:67442480-67442630	AoAF	blood vessel:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
13	CTCF	chr2:67442520-67442670	AG09309	skin:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
14	CTCF	chr2:67442453-67442712	NHEK	skin:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
15	CTCF	chr2:67442452-67442698	MCF-7	breast:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
16	CTCF	chr2:67442520-67442670	HCM	heart:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
17	CTCF	chr2:67442520-67442670	RPTEC	kidney:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
18	CTCF	chr2:67442480-67442630	HRE	kidney:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
19	CTCF	chr2:67442500-67442650	BJ	skin:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
20	CTCF	chr2:67442478-67442678	GM19238	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
21	CTCF	chr2:67442540-67442690	Hela-S3	cervix:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
22	CTCF	chr2:67442520-67442670	AG10803	skin:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
23	CTCF	chr2:67442640-67442790	HAc	cerebellar:	n/a	n/a
24	CTCF	chr2:67442440-67442590	HEK293	kidney:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
25	CTCF	chr2:67442349-67442718	HepG2	liver:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
26	CTCF	chr2:67442314-67442864	MCF-7	breast:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
27	CTCF	chr2:67442500-67442650	GM12865	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
28	CTCF	chr2:67442480-67442630	HEEpiC	esophagus:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
29	CTCF	chr2:67442460-67442610	NHLF	lung:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
30	CTCF	chr2:67442450-67442705	MCF-7	breast:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
31	CTCF	chr2:67442500-67442650	SAEC	small airway:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
32	CTCF	chr2:67442520-67442670	HEK293	kidney:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
33	CTCF	chr2:67442500-67442650	WERI-Rb-1	eye:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
34	CTCF	chr2:67442480-67442630	GM12866	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
35	CTCF	chr2:67442540-67442627	GM10248	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
36	CTCF	chr2:67442506-67442649	GM12891	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
37	CTCF	chr2:67442560-67442710	NHDF-neo	bronchial:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
38	CTCF	chr2:67442480-67442630	GM12872	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
39	CTCF	chr2:67442482-67442663	GM12878	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
40	CTCF	chr2:67442540-67442690	HMEC	breast:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
41	CTCF	chr2:67442480-67442630	NHEK	skin:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
42	CTCF	chr2:67442500-67442650	HEEpiC	esophagus:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
43	CTCF	chr2:67442457-67442654	A549	lung:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
44	CTCF	chr2:67442520-67442670	GM12872	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
45	CTCF	chr2:67442489-67442663	GM12892	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
46	CTCF	chr2:67442550-67442598	GM10266	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
47	CTCF	chr2:67442480-67442630	GM12873	blood:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
48	CTCF	chr2:67442497-67442671	A549	lung:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
49	CTCF	chr2:67442457-67442731	HUVEC	blood vessel:	n/a	chr2:67442567-67442585 chr2:67442573-67442582
50	CTCF	chr2:67442500-67442650	HMF	breast:	n/a	chr2:67442567-67442585 chr2:67442573-67442582

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:67443148-67443198	Hela-S3	cervix:	n/a
2	chr2:67442559-67442609	SK-N-MC	brain:	n/a
3	chr2:67442559-67442609	MCF-7	breast:	n/a
4	chr2:67443148-67443198	AG09319	gingival:	n/a
5	chr2:67442559-67442609	T-47D	breast:	n/a
6	chr2:67442562-67442612	PANC-1	pancreas:	n/a
7	chr2:67442562-67442612	A549	lung:	n/a
8	chr2:67442562-67442612	HCT-116	colon:	n/a
9	chr2:67442562-67442612	SK-N-MC	brain:	n/a
10	chr2:67443148-67443198	U87	brain:	n/a
11	chr2:67443148-67443198	K562	blood:	n/a
12	chr2:67442559-67442609	BE2_C	brain:	n/a
13	chr2:67443148-67443198	GM12878	blood:	n/a
14	chr2:67443148-67443198	H1-hESC	embryonic stem cell:	embryo
15	chr2:67443148-67443198	ovcar-3	ovarian:	n/a
16	chr2:67443148-67443198	GM12892	blood:	n/a
17	chr2:67442559-67442609	GM12891	blood:	n/a
18	chr2:67442559-67442609	HCT-116	colon:	n/a
19	chr2:67442559-67442609	HCPEpiC	choroid plexus:	n/a
20	chr2:67442562-67442612	MCF10A-Er-Src	breast:	n/a
21	chr2:67442559-67442609	K562	blood:	n/a
22	chr2:67442562-67442612	ECC-1	luminal epithelium:	n/a
23	chr2:67442562-67442612	HRE	kidney:	n/a
24	chr2:67442562-67442612	GM19239	blood:	n/a
25	chr2:67443148-67443198	HRPEpiC	eye:	n/a
26	chr2:67443148-67443198	HCT-116	colon:	n/a
27	chr2:67442559-67442609	Hepatocyte	liver:	n/a
28	chr2:67442559-67442609	Caco-2	colon:	n/a
29	chr2:67442559-67442609	RPTEC	kidney:	n/a
30	chr2:67442562-67442612	HRCEpiC	kidney:	n/a
31	chr2:67443148-67443198	NHBE	bronchial:	n/a
32	chr2:67443148-67443198	HAEpiC	amniotic membrane:	n/a
33	chr2:67442562-67442612	MCF-7	breast:	n/a
34	chr2:67442562-67442612	HCM	heart:	n/a
35	chr2:67442559-67442609	Jurkat	blood:	n/a
36	chr2:67442559-67442609	HCM	heart:	n/a
37	chr2:67442559-67442609	HL-60	blood:	n/a
38	chr2:67442562-67442612	GM06990	blood:	n/a
39	chr2:67442562-67442612	NHDF-neo	bronchial:	n/a
40	chr2:67442559-67442609	ProgFib	skin:	n/a
41	chr2:67443148-67443198	PFSK-1	brain:	n/a
42	chr2:67442559-67442609	HIPEpiC	eye:	n/a
43	chr2:67442559-67442609	AG04450	lung:	fetal
44	chr2:67443148-67443198	GM06990	blood:	n/a
45	chr2:67442562-67442612	H1-hESC	embryonic stem cell:	embryo
46	chr2:67442562-67442612	K562	blood:	n/a
47	chr2:67443148-67443198	ProgFib	skin:	n/a
48	chr2:67442559-67442609	SKMC	muscle:	n/a
49	chr2:67442559-67442609	NH-A	brain:	n/a
50	chr2:67443148-67443198	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:67442796..67445118-chr2:67455798..67458502,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C1D-3	chr2:67442360-67442409	XLOC_002142
2	lnc-C1D-3	chr2:67440771-67440848	XLOC_002142
3	lnc-ETAA1-3	chr2:67440540-67440627	ENSG00000230906
4	lnc-C1D-3	chr2:67442360-67442451	XLOC_002142
5	lnc-C1D-3	chr2:67440771-67440900	XLOC_002142
6	lnc-C1D-3	chr2:67442360-67442466	XLOC_002142

Variant related genes	Relation type
ENSG00000230906	TF binding region
ENSG00000236780	TF binding region
ENSG00000230906	CpG island
ENSG00000236780	CpG island

Extended variants
information (count: 189 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:189 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369097254	chr2:67439061-67439062	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs13432015	chr2:67439067-67439068	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs540647792	chr2:67439094-67439095	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs186884480	chr2:67439128-67439129	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs112131966	chr2:67439139-67439140	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs191641416	chr2:67439222-67439223	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs184313395	chr2:67439224-67439225	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs143048337	chr2:67439265-67439266	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs370865631	chr2:67439303-67439304	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs549461690	chr2:67439323-67439324	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs566195784	chr2:67439364-67439365	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs534985769	chr2:67439367-67439368	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs558209020	chr2:67439439-67439440	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs190228487	chr2:67439440-67439441	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs539390403	chr2:67439452-67439453	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs556319171	chr2:67439472-67439473	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs548005521	chr2:67439550-67439551	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs192958226	chr2:67439586-67439587	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs541631898	chr2:67439587-67439588	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs561617579	chr2:67439599-67439600	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs571838400	chr2:67439631-67439632	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs113879824	chr2:67439678-67439679	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs540609630	chr2:67439706-67439707	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs563966829	chr2:67439732-67439733	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs578196499	chr2:67439812-67439813	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs543713020	chr2:67439903-67439904	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs201809766	chr2:67439912-67439913	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs151141562	chr2:67439938-67439939	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs140628770	chr2:67439951-67439952	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs549617445	chr2:67439982-67439983	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs145905037	chr2:67439992-67439993	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs370425977	chr2:67439999-67440000	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs551740148	chr2:67440016-67440017	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs571597927	chr2:67440056-67440057	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs368924021	chr2:67440060-67440061	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs549767018	chr2:67440066-67440067	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs372375114	chr2:67440168-67440169	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs562250674	chr2:67440189-67440190	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs569948331	chr2:67440197-67440198	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs535250852	chr2:67440223-67440224	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs555177744	chr2:67440235-67440236	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs560339390	chr2:67440248-67440249	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs138464572	chr2:67440313-67440314	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs142961979	chr2:67440347-67440348	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs557839807	chr2:67440355-67440356	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs577527551	chr2:67440390-67440391	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs543424825	chr2:67440441-67440442	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs563802838	chr2:67440490-67440491	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs574411911	chr2:67440549-67440550	Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
50	rs145088357	chr2:67440562-67440563	Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Colorectal cancer	16272173	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67435200-67442200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr2:67436400-67440400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr2:67437800-67440400	Weak transcription	Colon Smooth Muscle	Colon
4	chr2:67438800-67440400	Weak transcription	Fetal Stomach	stomach
5	chr2:67439000-67439200	Weak transcription	Pancreas	Pancrea
6	chr2:67439000-67439400	Enhancers	Fetal Kidney	kidney
7	chr2:67439000-67440600	Enhancers	Fetal Lung	lung
8	chr2:67439200-67439600	Active TSS	Pancreas	Pancrea
9	chr2:67439400-67441000	Weak transcription	Fetal Kidney	kidney
10	chr2:67439400-67442600	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr2:67439600-67440400	Weak transcription	Pancreas	Pancrea
12	chr2:67440200-67440600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr2:67440400-67440600	Active TSS	Fetal Stomach	stomach
14	chr2:67440400-67440800	Active TSS	Colon Smooth Muscle	Colon
15	chr2:67440400-67440800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
16	chr2:67440400-67442600	Active TSS	Pancreas	Pancrea
17	chr2:67440600-67440800	Enhancers	H1 Cell Line	embryonic stem cell
18	chr2:67440600-67441000	Flanking Active TSS	Fetal Stomach	stomach
19	chr2:67440600-67441000	Active TSS	Rectal Smooth Muscle	rectum
20	chr2:67440600-67441200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr2:67440600-67441400	Flanking Active TSS	Fetal Lung	lung
22	chr2:67440600-67442200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr2:67440800-67441000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr2:67440800-67441000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:67440800-67441000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
26	chr2:67440800-67441000	Bivalent Enhancer	Fetal Brain Male	brain
27	chr2:67440800-67441200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr2:67440800-67442000	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr2:67440800-67442000	Enhancers	Colon Smooth Muscle	Colon
30	chr2:67440800-67444400	Enhancers	Stomach Mucosa	stomach
31	chr2:67441000-67441200	ZNF genes & repeats	Fetal Kidney	kidney
32	chr2:67441000-67441400	Enhancers	Fetal Stomach	stomach
33	chr2:67441000-67441800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr2:67441000-67442000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr2:67441000-67442200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr2:67441000-67444200	Enhancers	Rectal Smooth Muscle	rectum
37	chr2:67441200-67441600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr2:67441400-67441600	Flanking Active TSS	Fetal Stomach	stomach
39	chr2:67441400-67445000	Enhancers	Fetal Lung	lung
40	chr2:67441600-67442000	Enhancers	Fetal Stomach	stomach
41	chr2:67441600-67442400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr2:67441600-67444400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr2:67441800-67442200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr2:67442000-67442400	Enhancers	H1 Cell Line	embryonic stem cell
45	chr2:67442000-67442400	Flanking Active TSS	Colon Smooth Muscle	Colon
46	chr2:67442000-67442400	Flanking Active TSS	Fetal Stomach	stomach
47	chr2:67442000-67442800	Enhancers	H9 Cell Line	embryonic stem cell
48	chr2:67442000-67442800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr2:67442000-67443000	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr2:67442000-67443800	Enhancers	Fetal Kidney	kidney

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