Variant report

Variant	esv1806894
Chromosome Location	chr2:171651783-171679041
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1174)
CpG islands
(count:2136)
Chromatin interactive
region (count:26)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1174 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:171672339-171672492	K562	blood:	n/a	chr2:171672406-171672414
2	ARID3A	chr2:171669403-171669608	K562	blood:	n/a	n/a
3	ATF2	chr2:171670648-171671121	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr2:171672094-171672593	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr2:171672245-171672657	K562	blood:	n/a	n/a
6	BACH1	chr2:171678871-171679144	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr2:171672258-171672565	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr2:171676735-171676871	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:171673461-171673478	K562	blood:	n/a	n/a
10	BACH1	chr2:171673160-171673233	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCLAF1	chr2:171672186-171672566	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:171672220-171672817	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:171672229-171672838	K562	blood:	n/a	n/a
14	BHLHE40	chr2:171677545-171677612	K562	blood:	n/a	n/a
15	BHLHE40	chr2:171673040-171673653	K562	blood:	n/a	chr2:171673247-171673263
16	BHLHE40	chr2:171672221-171672496	HepG2	liver:	n/a	n/a
17	BHLHE40	chr2:171673198-171673865	GM12878	blood:	n/a	chr2:171673247-171673263
18	BRCA1	chr2:171672141-171672547	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr2:171673162-171673500	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr2:171673115-171673678	K562	blood:	n/a	n/a
21	CBX3	chr2:171677407-171677754	K562	blood:	n/a	n/a
22	CBX3	chr2:171678766-171679069	K562	blood:	n/a	n/a
23	CBX3	chr2:171672125-171672568	K562	blood:	n/a	n/a
24	CCNT2	chr2:171676799-171676806	K562	blood:	n/a	n/a
25	CCNT2	chr2:171673137-171673706	K562	blood:	n/a	n/a
26	CCNT2	chr2:171677455-171677768	K562	blood:	n/a	n/a
27	CCNT2	chr2:171672247-171672908	K562	blood:	n/a	n/a
28	CEBPB	chr2:171661343-171661591	K562	blood:	n/a	chr2:171661419-171661430
29	CEBPB	chr2:171663101-171663349	K562	blood:	n/a	chr2:171663287-171663298 chr2:171663289-171663298 chr2:171663287-171663300
30	CEBPB	chr2:171661348-171661509	HepG2	liver:	n/a	chr2:171661419-171661430
31	CEBPB	chr2:171663083-171663491	K562	blood:	n/a	chr2:171663287-171663298 chr2:171663289-171663298 chr2:171663287-171663300
32	CEBPB	chr2:171663052-171663476	K562	blood:	n/a	chr2:171663287-171663298 chr2:171663289-171663298 chr2:171663287-171663300
33	CEBPB	chr2:171665544-171665642	HepG2	liver:	n/a	chr2:171665551-171665562
34	CEBPB	chr2:171672129-171672565	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr2:171673174-171673574	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr2:171661320-171661583	HepG2	liver:	n/a	chr2:171661419-171661430
37	CEBPB	chr2:171665508-171665569	H1-hESC	embryonic stem cell:	n/a	chr2:171665551-171665562
38	CEBPD	chr2:171677356-171677830	K562	blood:	n/a	n/a
39	CHD1	chr2:171672277-171672474	GM12878	blood:	n/a	n/a
40	CHD2	chr2:171673867-171673925	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr2:171672213-171672261	K562	blood:	n/a	n/a
42	CHD2	chr2:171673226-171673605	K562	blood:	n/a	n/a
43	CHD2	chr2:171673366-171673517	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr2:171673166-171673604	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr2:171672299-171672552	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr2:171673426-171673547	HepG2	liver:	n/a	n/a
47	CHD2	chr2:171671936-171672511	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr2:171673218-171673483	GM12878	blood:	n/a	n/a
49	CHD2	chr2:171674289-171674291	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr2:171672227-171672488	GM12878	blood:	n/a	n/a

(count:2136 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:171673272-171673322	HCM	heart:	n/a
2	chr2:171673272-171673322	HCM	heart:	n/a
3	chr2:171672205-171672255	HRPEpiC	eye:	n/a
4	chr2:171678251-171678301	HUVEC	blood vessel:	n/a
5	chr2:171676925-171676975	HUVEC	blood vessel:	n/a
6	chr2:171674855-171674905	HEK293	kidney:	embryo
7	chr2:171673199-171673249	U87	brain:	n/a
8	chr2:171670379-171670429	HUVEC	blood vessel:	n/a
9	chr2:171671480-171671530	T-47D	breast:	n/a
10	chr2:171676925-171676975	IMR90	lung:	fetal
11	chr2:171669862-171669912	SK-N-SH	brain:	n/a
12	chr2:171678251-171678301	CMK	blood:	n/a
13	chr2:171670978-171671028	LNCaP	prostate:	n/a
14	chr2:171667934-171667984	ProgFib	skin:	n/a
15	chr2:171674437-171674487	HCPEpiC	choroid plexus:	n/a
16	chr2:171672694-171672744	GM12891	blood:	n/a
17	chr2:171673272-171673322	PFSK-1	brain:	n/a
18	chr2:171672899-171672949	AoSMC	blood vessel:	n/a
19	chr2:171673110-171673160	HEK293	kidney:	embryo
20	chr2:171672899-171672949	HNPCEpiC	eye:	n/a
21	chr2:171670500-171670550	HRE	kidney:	n/a
22	chr2:171673199-171673249	AG04449	skin:	fetal
23	chr2:171672205-171672255	NB4	blood:	n/a
24	chr2:171673272-171673322	ovcar-3	ovarian:	n/a
25	chr2:171676925-171676975	AG09319	gingival:	n/a
26	chr2:171670379-171670429	K562	blood:	n/a
27	chr2:171667934-171667984	SK-N-SH_RA	brain:	n/a
28	chr2:171671795-171671845	NHBE	bronchial:	n/a
29	chr2:171673272-171673322	IMR90	lung:	fetal
30	chr2:171669275-171669325	AG04449	skin:	fetal
31	chr2:171671795-171671845	HEK293	kidney:	embryo
32	chr2:171676553-171676603	AG04450	lung:	fetal
33	chr2:171671730-171671780	PFSK-1	brain:	n/a
34	chr2:171677602-171677652	HCM	heart:	n/a
35	chr2:171673207-171673257	RPTEC	kidney:	n/a
36	chr2:171676553-171676603	HAEpiC	amniotic membrane:	n/a
37	chr2:171676925-171676975	BE2_C	brain:	n/a
38	chr2:171672156-171672206	AG10803	skin:	n/a
39	chr2:171676306-171676356	HRPEpiC	eye:	n/a
40	chr2:171678251-171678301	HCT-116	colon:	n/a
41	chr2:171670795-171670845	SK-N-SH_RA	brain:	n/a
42	chr2:171670795-171670845	H1-hESC	embryonic stem cell:	embryo
43	chr2:171678954-171679004	LNCaP	prostate:	n/a
44	chr2:171677602-171677652	Hela-S3	cervix:	n/a
45	chr2:171673199-171673249	HCM	heart:	n/a
46	chr2:171669862-171669912	PANC-1	pancreas:	n/a
47	chr2:171671795-171671845	HCF	heart:	n/a
48	chr2:171678751-171678801	SKMC	muscle:	n/a
49	chr2:171672205-171672255	SK-N-MC	brain:	n/a
50	chr2:171671730-171671780	GM12892	blood:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:171671156..171674030-chr2:171674159..171676823,3	K562	blood:
2	chr2:171646997..171649171-chr2:171653953..171656426,2	K562	blood:
3	chr2:171637822..171639783-chr2:171650813..171652937,2	K562	blood:
4	chr2:171671327..171674926-chr2:171677821..171681963,4	K562	blood:
5	chr2:171669367..171672253-chr2:171672351..171673917,2	K562	blood:
6	chr2:171380154..171380707-chr2:171669167..171669696,2	K562	blood:
7	chr2:171671327..171674926-chr2:171677821..171681963,4	K562	blood:
8	chr2:171180785..171181693-chr2:171671922..171672450,2	K562	blood:
9	chr2:171639227..171641191-chr2:171653402..171655212,2	K562	blood:
10	chr2:171092620..171093414-chr2:171670841..171671812,2	MCF-7	breast:
11	chr1:210774618..210775333-chr2:171669099..171669650,2	MCF-7	breast:
12	chr2:171672266..171672902-chr2:171785238..171786136,2	MCF-7	breast:
13	chr2:171254424..171255162-chr2:171668919..171669613,2	MCF-7	breast:
14	chr2:171678939..171680621-chr2:171682789..171685918,3	MCF-7	breast:
15	chr2:171675485..171677773-chr2:171677982..171679731,3	K562	blood:
16	chr2:171234154..171234994-chr2:171671884..171672456,2	MCF-7	breast:
17	chr2:171673426..171677773-chr2:171677821..171680534,5	K562	blood:
18	chr2:171253419..171254213-chr2:171669096..171669701,2	MCF-7	breast:
19	chr2:171672408..171674860-chr2:171784778..171786781,3	MCF-7	breast:
20	chr2:171671156..171674030-chr2:171674159..171676823,3	K562	blood:
21	chr2:171664685..171667660-chr2:171785789..171787317,2	K562	blood:
22	chr2:171664350..171666185-chr2:171785817..171788559,2	K562	blood:
23	chr2:171669367..171672253-chr2:171672351..171673917,2	K562	blood:
24	chr2:171673426..171677773-chr2:171677821..171680534,5	K562	blood:
25	chr2:171672439..171674320-chr2:171784947..171786968,2	K562	blood:
26	chr2:171264048..171266072-chr2:171669517..171671938,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC007405.2.1-3	chr2:171672803-171672995	ENSG00000235934.1
2	lnc-AC007405.2.1-3	chr2:171673364-171673542	ENSG00000235934.1
3	lnc-AC007405.2.1-3	chr2:171673364-171673509	ENSG00000235934.1
4	lnc-AC007405.2.1-3	chr2:171674228-171674547	ENSG00000235934.1
5	lnc-AC007405.2.1-3	chr2:171674228-171674405	ENSG00000235934.1
6	lnc-AC007405.2.1-3	chr2:171672915-171672995	ENSG00000235934.1
7	lnc-AC007405.7.1-3	chr2:171678228-171678659	NONHSAT075433
8	lnc-AC007405.2.1-3	chr2:171673364-171673682	ENSG00000235934.1
9	lnc-AC007405.2.1-3	chr2:171672813-171672995	ENSG00000235934.1

No data

Variant related genes	Relation type
ENSG00000235934	TF binding region
GAD1	TF binding region
ENSG00000235934	CpG island
GAD1	CpG island
ENSG00000071909	chromatin interactions
ENSG00000235934	chromatin interactions
ENSG00000204334	chromatin interactions
ENSG00000115806	chromatin interactions
ENSG00000128683	chromatin interactions
ENSG00000222509	chromatin interactions

Extended variants
information (count: 1042 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:1042 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147748089	chr2:171651856-171651857	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs527924144	chr2:171651864-171651865	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs10168078	chr2:171651880-171651881	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs541807383	chr2:171651882-171651883	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs564752944	chr2:171651893-171651894	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs531919770	chr2:171651895-171651896	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs550125294	chr2:171651900-171651901	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs550862466	chr2:171651928-171651929	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs200130895	chr2:171651975-171651976	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs62168448	chr2:171652004-171652005	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs529718648	chr2:171652025-171652026	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs547916192	chr2:171652033-171652034	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs149206060	chr2:171652076-171652077	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534041418	chr2:171652083-171652084	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs552091455	chr2:171652097-171652098	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs180945322	chr2:171652103-171652104	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs570687634	chr2:171652116-171652117	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs186020320	chr2:171652252-171652253	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs190575213	chr2:171652322-171652323	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs7568115	chr2:171652365-171652366	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs535941151	chr2:171652373-171652374	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs143388478	chr2:171652384-171652385	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs12464863	chr2:171652401-171652402	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs546336446	chr2:171652503-171652504	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs564538588	chr2:171652561-171652562	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs576300393	chr2:171652578-171652579	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs151256664	chr2:171652608-171652609	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs562128987	chr2:171652653-171652654	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs564227119	chr2:171652707-171652708	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs4668318	chr2:171652747-171652748	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs4668319	chr2:171652749-171652750	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs560147844	chr2:171652757-171652758	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs36104040	chr2:171652763-171652764	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs191944820	chr2:171652774-171652775	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs552316066	chr2:171652775-171652776	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs181517247	chr2:171652795-171652796	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs538118726	chr2:171652796-171652797	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs563219542	chr2:171652797-171652798	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs140434703	chr2:171652905-171652906	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs10534608	chr2:171652921-171652922	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369136388	chr2:171652933-171652934	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs62168449	chr2:171652934-171652935	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs150504482	chr2:171652936-171652937	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs112407791	chr2:171652937-171652938	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs113121483	chr2:171652938-171652939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370083171	chr2:171652950-171652951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373654461	chr2:171652962-171652963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112413721	chr2:171652972-171652973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185818088	chr2:171653008-171653009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553887050	chr2:171653009-171653010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:45)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	16573809	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Donnai-Barrow syndrome	21085971	CNVD
Breast cancer	21045282	CNVD
Limb abnormalities	22140379	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1245 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:171629600-171658800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:171642400-171669000	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr2:171654800-171655800	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr2:171658800-171659200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr2:171659200-171668600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr2:171660600-171661200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:171663200-171664000	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr2:171665600-171665800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr2:171665800-171666200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
10	chr2:171666000-171669200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:171668600-171669600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr2:171668600-171670000	Active TSS	Brain Germinal Matrix	brain
13	chr2:171669000-171669200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:171669000-171669200	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr2:171669000-171669200	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr2:171669000-171669400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr2:171669000-171669400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
18	chr2:171669000-171669400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr2:171669000-171669400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
20	chr2:171669000-171669600	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr2:171669000-171669800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr2:171669200-171669400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr2:171669200-171669400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:171669200-171669400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr2:171669200-171669400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:171669200-171669400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
27	chr2:171669200-171669400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
28	chr2:171669200-171669400	Enhancers	Brain Anterior Caudate	brain
29	chr2:171669200-171669400	Enhancers	Colon Smooth Muscle	Colon
30	chr2:171669200-171669400	Bivalent Enhancer	Fetal Brain Male	brain
31	chr2:171669200-171669400	Bivalent Enhancer	Fetal Stomach	stomach
32	chr2:171669200-171669400	Enhancers	Gastric	stomach
33	chr2:171669200-171669400	Enhancers	Rectal Smooth Muscle	rectum
34	chr2:171669200-171669600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
35	chr2:171669200-171669600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
36	chr2:171669200-171669600	Enhancers	Brain Angular Gyrus	brain
37	chr2:171669200-171669600	Enhancers	Brain Substantia Nigra	brain
38	chr2:171669200-171670000	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
39	chr2:171669200-171670400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr2:171669200-171670400	Enhancers	K562	blood
41	chr2:171669400-171669600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:171669400-171669600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr2:171669400-171669800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr2:171669400-171669800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
45	chr2:171669400-171669800	Bivalent/Poised TSS	Fetal Brain Male	brain
46	chr2:171669400-171670000	Bivalent Enhancer	Colon Smooth Muscle	Colon
47	chr2:171669400-171670000	Weak transcription	Gastric	stomach
48	chr2:171669400-171670200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
49	chr2:171669400-171670400	Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr2:171669400-171670600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell

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