Variant report

Variant	nsv874464
Chromosome Location	chr2:85886175-85898898
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	ATF1	chr2:85890015-85890316	K562	blood:	n/a	n/a
2	ATF3	chr2:85889986-85890355	K562	blood:	n/a	n/a
3	BATF	chr2:85896696-85896947	GM12878	blood:	n/a	chr2:85896825-85896836 chr2:85896847-85896858
4	BHLHE40	chr2:85890078-85890337	K562	blood:	n/a	n/a
5	BHLHE40	chr2:85896721-85897032	GM12878	blood:	n/a	n/a
6	CBX3	chr2:85889911-85890363	K562	blood:	n/a	n/a
7	CEBPB	chr2:85890001-85890243	IMR90	lung:	n/a	n/a
8	CTCF	chr2:85893549-85893606	GM19239	blood:	n/a	n/a
9	CTCF	chr2:85897980-85898130	GM12872	blood:	n/a	n/a
10	CTCF	chr2:85890000-85890150	HUVEC	blood vessel:	n/a	n/a
11	CTCF	chr2:85892900-85893050	GM12867	blood:	n/a	n/a
12	CTCF	chr2:85896992-85897010	GM12891	blood:	n/a	chr2:85896995-85897004
13	CTCF	chr2:85890000-85890150	AG09309	skin:	n/a	n/a
14	CTCF	chr2:85896920-85897070	GM12872	blood:	n/a	chr2:85896995-85897004
15	E2F4	chr2:85890011-85890255	MCF10A-Er-Src	breast:	n/a	n/a
16	EBF1	chr2:85896683-85897030	GM12878	blood:	n/a	n/a
17	EBF1	chr2:85895885-85896003	GM12878	blood:	n/a	chr2:85895960-85895970 chr2:85895970-85895981 chr2:85895959-85895970
18	EBF1	chr2:85896704-85897049	GM12878	blood:	n/a	n/a
19	EGR1	chr2:85889960-85890192	K562	blood:	n/a	n/a
20	EGR1	chr2:85890777-85891254	ECC-1	luminal epithelium:	n/a	chr2:85890973-85890986 chr2:85890973-85890986 chr2:85890976-85890986 chr2:85890972-85890987 chr2:85890973-85890986 chr2:85890976-85890985 chr2:85890973-85890987 chr2:85890973-85890986
21	EGR1	chr2:85889937-85890286	K562	blood:	n/a	n/a
22	ELF1	chr2:85889977-85890201	K562	blood:	n/a	n/a
23	EP300	chr2:85896721-85896921	GM12878	blood:	n/a	chr2:85896877-85896891
24	EP300	chr2:85896575-85897029	GM12878	blood:	n/a	chr2:85896681-85896695 chr2:85896679-85896693 chr2:85896686-85896700 chr2:85896682-85896696 chr2:85896680-85896694 chr2:85896678-85896692 chr2:85896877-85896891
25	EP300	chr2:85896807-85896918	GM12878	blood:	n/a	chr2:85896877-85896891
26	EP300	chr2:85890073-85890263	K562	blood:	n/a	n/a
27	ESRRA	chr2:85896404-85897178	GM12878	blood:	n/a	chr2:85896856-85896874 chr2:85896729-85896745 chr2:85896855-85896865 chr2:85896856-85896872
28	FOS	chr2:85889910-85890290	MCF10A-Er-Src	breast:	n/a	chr2:85890078-85890087
29	FOS	chr2:85889916-85890310	MCF10A-Er-Src	breast:	n/a	chr2:85890078-85890087
30	FOS	chr2:85895793-85895988	MCF10A-Er-Src	breast:	n/a	chr2:85895885-85895896 chr2:85895882-85895893
31	FOS	chr2:85889905-85890334	HUVEC	blood vessel:	n/a	chr2:85890078-85890087
32	FOS	chr2:85889910-85890299	MCF10A-Er-Src	breast:	n/a	chr2:85890078-85890087
33	FOS	chr2:85889966-85890252	MCF10A-Er-Src	breast:	n/a	chr2:85890078-85890087
34	FOSL1	chr2:85889978-85890317	K562	blood:	n/a	chr2:85890078-85890087 chr2:85890168-85890179
35	FOSL1	chr2:85889966-85890398	K562	blood:	n/a	chr2:85890078-85890087 chr2:85890168-85890179
36	FOSL2	chr2:85889917-85890355	A549	lung:	n/a	chr2:85890078-85890087
37	FOSL2	chr2:85889950-85890460	SK-N-SH	brain:	n/a	chr2:85890078-85890087
38	FOSL2	chr2:85889963-85890215	A549	lung:	n/a	chr2:85890078-85890087
39	FOSL2	chr2:85889929-85890304	SK-N-SH	brain:	n/a	chr2:85890078-85890087
40	GABPA	chr2:85890096-85890359	K562	blood:	n/a	n/a
41	GATA2	chr2:85889961-85890374	HUVEC	blood vessel:	n/a	chr2:85890079-85890088 chr2:85890206-85890214 chr2:85890076-85890085
42	HCFC1	chr2:85890118-85890197	K562	blood:	n/a	n/a
43	HDAC2	chr2:85890038-85890319	K562	blood:	n/a	chr2:85890117-85890136
44	HMGN3	chr2:85890863-85891008	K562	blood:	n/a	n/a
45	IRF4	chr2:85896650-85896940	GM12878	blood:	n/a	n/a
46	JUN	chr2:85889970-85890486	K562	blood:	n/a	chr2:85890078-85890087
47	JUN	chr2:85889953-85890376	K562	blood:	n/a	chr2:85890078-85890087
48	JUN	chr2:85889950-85890313	HUVEC	blood vessel:	n/a	chr2:85890078-85890087
49	JUND	chr2:85889931-85890340	K562	blood:	n/a	chr2:85890078-85890087
50	JUND	chr2:85889993-85890263	H1-hESC	embryonic stem cell:	n/a	chr2:85890078-85890087

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:85896539-85896589	GM19239	blood:	n/a
2	chr2:85896539-85896589	GM19239	blood:	n/a
3	chr2:85896539-85896589	GM06990	blood:	n/a
4	chr2:85896494-85896544	AG04449	skin:	fetal
5	chr2:85896001-85896051	NH-A	brain:	n/a
6	chr2:85890281-85890331	HAEpiC	amniotic membrane:	n/a
7	chr2:85896001-85896051	MCF10A-Er-Src	breast:	n/a
8	chr2:85896001-85896051	GM12878	blood:	n/a
9	chr2:85896539-85896589	T-47D	breast:	n/a
10	chr2:85896539-85896589	GM12892	blood:	n/a
11	chr2:85896001-85896051	HRE	kidney:	n/a
12	chr2:85896539-85896589	PFSK-1	brain:	n/a
13	chr2:85895360-85895410	GM12891	blood:	n/a
14	chr2:85895048-85895098	HRCEpiC	kidney:	n/a
15	chr2:85895048-85895098	PFSK-1	brain:	n/a
16	chr2:85895048-85895098	K562	blood:	n/a
17	chr2:85896001-85896051	HNPCEpiC	eye:	n/a
18	chr2:85895048-85895098	HPAEpiC	pulmonary alveolar:	n/a
19	chr2:85895360-85895410	RPTEC	kidney:	n/a
20	chr2:85896001-85896051	AG10803	skin:	n/a
21	chr2:85896494-85896544	U87	brain:	n/a
22	chr2:85895048-85895098	HCPEpiC	choroid plexus:	n/a
23	chr2:85895360-85895410	HCT-116	colon:	n/a
24	chr2:85896001-85896051	GM19239	blood:	n/a
25	chr2:85895048-85895098	AG09309	skin:	n/a
26	chr2:85895048-85895098	SKMC	muscle:	n/a
27	chr2:85896539-85896589	HCM	heart:	n/a
28	chr2:85896539-85896589	SK-N-SH	brain:	n/a
29	chr2:85890281-85890331	SKMC	muscle:	n/a
30	chr2:85895048-85895098	HCM	heart:	n/a
31	chr2:85895048-85895098	GM19239	blood:	n/a
32	chr2:85895360-85895410	HUVEC	blood vessel:	n/a
33	chr2:85895360-85895410	HRPEpiC	eye:	n/a
34	chr2:85896001-85896051	HCPEpiC	choroid plexus:	n/a
35	chr2:85896001-85896051	SAEC	small airway:	n/a
36	chr2:85890281-85890331	A549	lung:	n/a
37	chr2:85890281-85890331	IMR90	lung:	fetal
38	chr2:85896494-85896544	HEEpiC	esophagus:	n/a
39	chr2:85896539-85896589	HPAEpiC	pulmonary alveolar:	n/a
40	chr2:85890281-85890331	T-47D	breast:	n/a
41	chr2:85896001-85896051	PrEC	prostate:	n/a
42	chr2:85890281-85890331	Caco-2	colon:	n/a
43	chr2:85895048-85895098	ECC-1	luminal epithelium:	n/a
44	chr2:85895360-85895410	ovcar-3	ovarian:	n/a
45	chr2:85895048-85895098	ProgFib	skin:	n/a
46	chr2:85896494-85896544	HepG2	liver:	n/a
47	chr2:85895360-85895410	AG10803	skin:	n/a
48	chr2:85890281-85890331	K562	blood:	n/a
49	chr2:85895360-85895410	HL-60	blood:	n/a
50	chr2:85895360-85895410	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:85886384..85888298-chr2:85898868..85900454,2	MCF-7	breast:
2	chr2:85889712..85892300-chr2:85895263..85898036,2	MCF-7	breast:
3	chr2:85856113..85858844-chr2:85885190..85887112,2	MCF-7	breast:
4	chr2:85879386..85881998-chr2:85891410..85893784,2	MCF-7	breast:
5	chr2:85884543..85886105-chr2:85886734..85889252,2	MCF-7	breast:
6	chr2:85880829..85882437-chr2:85885388..85887097,2	K562	blood:
7	chr2:85871308..85872948-chr2:85883878..85886209,2	K562	blood:
8	chr2:85889712..85892300-chr2:85895263..85898036,2	MCF-7	breast:
9	chr2:85886964..85889940-chr2:85892432..85895474,3	K562	blood:
10	chr2:85886384..85888298-chr2:85898868..85900454,2	MCF-7	breast:
11	chr2:85896506..85899590-chr2:85901147..85903484,4	K562	blood:
12	chr2:85883102..85885218-chr2:85885321..85888097,2	K562	blood:
13	chr2:85886996..85889867-chr2:85891019..85894482,4	MCF-7	breast:
14	chr2:85886740..85890485-chr2:85890962..85895474,8	K562	blood:
15	chr2:85886996..85889867-chr2:85891019..85894482,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C2orf68-2	chr2:85886447-85886805	NONHSAT072035
2	lnc-C2orf68-2	chr2:85888578-85888635	NONHSAT072035
3	lnc-GNLY-3	chr2:85895764-85895989	NONHSAT072038
4	lnc-C2orf68-2	chr2:85888578-85888635	NONHSAT072034
5	lnc-C2orf68-2	chr2:85890469-85890670	NONHSAT072037
6	lnc-C2orf68-2	chr2:85889337-85889402	NONHSAT072037
7	lnc-C2orf68-2	chr2:85886447-85886849	NONHSAT072034

Variant related genes	Relation type
SFTPB	TF binding region
SFTPB	CpG island
ENSG00000168878	chromatin interactions
ENSG00000168883	chromatin interactions

Extended variants
information (count: 630 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:630 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3024825	chr2:85886175-85886176	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs574947393	chr2:85886176-85886177	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs367597303	chr2:85886213-85886214	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554205820	chr2:85886221-85886222	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572397585	chr2:85886230-85886231	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144475205	chr2:85886231-85886232	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564476672	chr2:85886232-85886233	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571402858	chr2:85886270-85886271	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148430793	chr2:85886271-85886272	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185386014	chr2:85886279-85886280	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562675679	chr2:85886293-85886294	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191130863	chr2:85886307-85886308	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369576391	chr2:85886331-85886332	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs3024824	chr2:85886342-85886343	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs182975929	chr2:85886345-85886346	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs578093456	chr2:85886347-85886348	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs569810989	chr2:85886380-85886381	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545321542	chr2:85886437-85886438	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560227586	chr2:85886453-85886454	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs3024823	chr2:85886474-85886475	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs551707788	chr2:85886499-85886500	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs570119766	chr2:85886507-85886508	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs188417591	chr2:85886569-85886570	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs549483539	chr2:85886572-85886573	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs568626838	chr2:85886589-85886590	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs3024822	chr2:85886590-85886591	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs555632775	chr2:85886644-85886645	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs566196796	chr2:85886653-85886654	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs9752	chr2:85886667-85886668	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs114691084	chr2:85886669-85886670	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs1804246	chr2:85886679-85886680	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs576528370	chr2:85886691-85886692	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs543912566	chr2:85886731-85886732	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs56811788	chr2:85886740-85886741	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs369263105	chr2:85886775-85886776	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs555613505	chr2:85886780-85886781	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs77786381	chr2:85886900-85886901	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553842897	chr2:85886901-85886902	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs541703568	chr2:85886920-85886921	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs572397696	chr2:85886940-85886941	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs560296216	chr2:85886942-85886943	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs545925228	chr2:85886976-85886977	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs564220042	chr2:85886977-85886978	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs192818982	chr2:85886995-85886996	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs563707622	chr2:85887021-85887022	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs145949286	chr2:85887068-85887069	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs369624148	chr2:85887161-85887162	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182890813	chr2:85887193-85887194	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs528988665	chr2:85887244-85887245	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs556476908	chr2:85887246-85887247	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	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
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16272173	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	19115005	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:370 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:85845400-85886400	Strong transcription	Fetal Muscle Leg	muscle
2	chr2:85846000-85887000	Strong transcription	Liver	Liver
3	chr2:85846000-85887400	Strong transcription	Fetal Intestine Small	intestine
4	chr2:85846200-85889400	Strong transcription	Thymus	Thymus
5	chr2:85862000-85887200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr2:85873200-85886600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr2:85876400-85888800	Weak transcription	Fetal Heart	heart
8	chr2:85876400-85888800	Weak transcription	Right Atrium	heart
9	chr2:85876600-85895400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr2:85877000-85889000	Weak transcription	Stomach Mucosa	stomach
11	chr2:85877000-85890000	Weak transcription	Ovary	ovary
12	chr2:85877200-85888600	Weak transcription	Aorta	Aorta
13	chr2:85877200-85893200	Weak transcription	Brain Substantia Nigra	brain
14	chr2:85877800-85890200	Weak transcription	Small Intestine	intestine
15	chr2:85878200-85886400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr2:85878200-85888800	Weak transcription	Brain Anterior Caudate	brain
17	chr2:85878600-85886200	Weak transcription	Esophagus	oesophagus
18	chr2:85878800-85886600	Weak transcription	Gastric	stomach
19	chr2:85878800-85891400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr2:85879400-85888000	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr2:85879400-85889200	Weak transcription	Colonic Mucosa	Colon
22	chr2:85879400-85890200	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr2:85879400-85890200	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr2:85879600-85887000	Weak transcription	Colon Smooth Muscle	Colon
25	chr2:85879600-85889800	Weak transcription	Fetal Intestine Large	intestine
26	chr2:85879600-85894000	Weak transcription	Brain Cingulate Gyrus	brain
27	chr2:85879600-85896000	Weak transcription	GM12878-XiMat	blood
28	chr2:85879800-85888600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr2:85880000-85886400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr2:85880000-85888000	Weak transcription	Primary hematopoietic stem cells	blood
31	chr2:85880200-85887800	Weak transcription	HUVEC	blood vessel
32	chr2:85880200-85888800	Weak transcription	Brain Hippocampus Middle	brain
33	chr2:85880400-85891800	Weak transcription	HepG2	liver
34	chr2:85880600-85888800	Weak transcription	Left Ventricle	heart
35	chr2:85880600-85889400	Weak transcription	Pancreas	Pancrea
36	chr2:85880600-85889600	Weak transcription	Brain Germinal Matrix	brain
37	chr2:85880600-85890200	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr2:85880600-85890200	Weak transcription	Rectal Smooth Muscle	rectum
39	chr2:85880800-85889800	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr2:85880800-85890200	Weak transcription	K562	blood
41	chr2:85881400-85889200	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr2:85881400-85891000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr2:85881600-85888200	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr2:85881600-85888800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr2:85881600-85890200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr2:85881800-85887200	Strong transcription	Primary monocytes fromperipheralblood	blood
47	chr2:85881800-85895800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr2:85882400-85887000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr2:85882400-85887200	Strong transcription	Primary T cells from cord blood	blood
50	chr2:85882400-85887200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood

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