Variant report

Variant	nsv591294
Chromosome Location	chr3:112091220-112208750
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1291)
CpG islands
(count:427)
Chromatin interactive
region (count:10)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1291 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:112136351-112136756	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr3:112208326-112210333	GM12878	blood:	n/a	n/a
3	ATF2	chr3:112191977-112192593	GM12878	blood:	n/a	n/a
4	ATF2	chr3:112181801-112183834	GM12878	blood:	n/a	n/a
5	ATF2	chr3:112174716-112175428	GM12878	blood:	n/a	n/a
6	ATF2	chr3:112182945-112183787	GM12878	blood:	n/a	n/a
7	ATF2	chr3:112125881-112127134	GM12878	blood:	n/a	n/a
8	ATF2	chr3:112181963-112182703	GM12878	blood:	n/a	n/a
9	ATF2	chr3:112178323-112180365	GM12878	blood:	n/a	n/a
10	ATF2	chr3:112201412-112201996	GM12878	blood:	n/a	n/a
11	ATF2	chr3:112202984-112203674	GM12878	blood:	n/a	n/a
12	ATF2	chr3:112178586-112180203	GM12878	blood:	n/a	n/a
13	ATF2	chr3:112208191-112210297	GM12878	blood:	n/a	n/a
14	ATF2	chr3:112174606-112175451	GM12878	blood:	n/a	n/a
15	ATF2	chr3:112126396-112127097	GM12878	blood:	n/a	n/a
16	ATF2	chr3:112135258-112135975	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr3:112109999-112110295	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr3:112208739-112209174	GM12878	blood:	n/a	n/a
19	BATF	chr3:112180623-112180947	GM12878	blood:	n/a	chr3:112180796-112180807
20	BATF	chr3:112183210-112183468	GM12878	blood:	n/a	n/a
21	BATF	chr3:112179396-112179832	GM12878	blood:	n/a	chr3:112179585-112179594
22	BATF	chr3:112178649-112178996	GM12878	blood:	n/a	n/a
23	BATF	chr3:112125953-112126291	GM12878	blood:	n/a	n/a
24	BATF	chr3:112125920-112126324	GM12878	blood:	n/a	n/a
25	BATF	chr3:112183149-112183504	GM12878	blood:	n/a	n/a
26	BATF	chr3:112179289-112179926	GM12878	blood:	n/a	chr3:112179889-112179899 chr3:112179585-112179594
27	BATF	chr3:112126731-112127049	GM12878	blood:	n/a	n/a
28	BCL11A	chr3:112126457-112127059	GM12878	blood:	n/a	n/a
29	BCL11A	chr3:112192183-112192464	GM12878	blood:	n/a	n/a
30	BCL11A	chr3:112125982-112126312	GM12878	blood:	n/a	n/a
31	BCL11A	chr3:112178672-112178956	GM12878	blood:	n/a	n/a
32	BCL11A	chr3:112179330-112179886	GM12878	blood:	n/a	chr3:112179524-112179533
33	BCL11A	chr3:112124731-112124980	GM12878	blood:	n/a	n/a
34	BCL11A	chr3:112125955-112126331	GM12878	blood:	n/a	n/a
35	BCL11A	chr3:112179271-112179712	GM12878	blood:	n/a	chr3:112179524-112179533
36	BCL11A	chr3:112183088-112183485	GM12878	blood:	n/a	n/a
37	BCL3	chr3:112132440-112132881	GM12878	blood:	n/a	n/a
38	BCL3	chr3:112181977-112182583	GM12878	blood:	n/a	n/a
39	BCL3	chr3:112208660-112209498	GM12878	blood:	n/a	n/a
40	BCL3	chr3:112192167-112192475	GM12878	blood:	n/a	n/a
41	BCL3	chr3:112096538-112096914	GM12878	blood:	n/a	n/a
42	BCL3	chr3:112126018-112126314	GM12878	blood:	n/a	n/a
43	BCL3	chr3:112178509-112180324	GM12878	blood:	n/a	chr3:112179524-112179533
44	BCL3	chr3:112179382-112180021	GM12878	blood:	n/a	chr3:112179524-112179533
45	BCL3	chr3:112126377-112127030	GM12878	blood:	n/a	n/a
46	BCL3	chr3:112183082-112183515	GM12878	blood:	n/a	n/a
47	BCL3	chr3:112208669-112209195	GM12878	blood:	n/a	n/a
48	BCL3	chr3:112100567-112100977	GM12878	blood:	n/a	n/a
49	BCL3	chr3:112174642-112175427	GM12878	blood:	n/a	n/a
50	BCLAF1	chr3:112156431-112156826	GM12878	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:112135991-112136041	HEEpiC	esophagus:	n/a
2	chr3:112117797-112117847	H1-hESC	embryonic stem cell:	embryo
3	chr3:112184271-112184321	PFSK-1	brain:	n/a
4	chr3:112096801-112096851	HepG2	liver:	n/a
5	chr3:112113161-112113211	LNCaP	prostate:	n/a
6	chr3:112135991-112136041	AG04449	skin:	fetal
7	chr3:112113161-112113211	HRCEpiC	kidney:	n/a
8	chr3:112184271-112184321	Hela-S3	cervix:	n/a
9	chr3:112109797-112109847	GM12891	blood:	n/a
10	chr3:112184271-112184321	Hepatocyte	liver:	n/a
11	chr3:112117797-112117847	HCT-116	colon:	n/a
12	chr3:112184271-112184321	HPAEpiC	pulmonary alveolar:	n/a
13	chr3:112109797-112109847	U87	brain:	n/a
14	chr3:112143970-112144020	HIPEpiC	eye:	n/a
15	chr3:112135991-112136041	SK-N-SH	brain:	n/a
16	chr3:112113161-112113211	H1-hESC	embryonic stem cell:	embryo
17	chr3:112184271-112184321	AG04450	lung:	fetal
18	chr3:112113161-112113211	HCM	heart:	n/a
19	chr3:112135991-112136041	NH-A	brain:	n/a
20	chr3:112096801-112096851	AG09309	skin:	n/a
21	chr3:112143970-112144020	NB4	blood:	n/a
22	chr3:112113161-112113211	AG09309	skin:	n/a
23	chr3:112117797-112117847	SKMC	muscle:	n/a
24	chr3:112117797-112117847	MCF10A-Er-Src	breast:	n/a
25	chr3:112117797-112117847	HepG2	liver:	n/a
26	chr3:112143970-112144020	AoSMC	blood vessel:	n/a
27	chr3:112113161-112113211	NH-A	brain:	n/a
28	chr3:112135991-112136041	HMEC	breast:	n/a
29	chr3:112184271-112184321	LNCaP	prostate:	n/a
30	chr3:112135991-112136041	PANC-1	pancreas:	n/a
31	chr3:112135991-112136041	CMK	blood:	n/a
32	chr3:112135991-112136041	Jurkat	blood:	n/a
33	chr3:112184271-112184321	NT2-D1	testis:	n/a
34	chr3:112143970-112144020	HRE	kidney:	n/a
35	chr3:112135991-112136041	HL-60	blood:	n/a
36	chr3:112117797-112117847	T-47D	breast:	n/a
37	chr3:112117797-112117847	AG09319	gingival:	n/a
38	chr3:112135991-112136041	LNCaP	prostate:	n/a
39	chr3:112109797-112109847	NHDF-neo	bronchial:	n/a
40	chr3:112113161-112113211	IMR90	lung:	fetal
41	chr3:112143970-112144020	RPTEC	kidney:	n/a
42	chr3:112113161-112113211	HEK293	kidney:	embryo
43	chr3:112184271-112184321	HAEpiC	amniotic membrane:	n/a
44	chr3:112117797-112117847	ProgFib	skin:	n/a
45	chr3:112117797-112117847	NT2-D1	testis:	n/a
46	chr3:112113161-112113211	Hela-S3	cervix:	n/a
47	chr3:112113161-112113211	GM12878	blood:	n/a
48	chr3:112135991-112136041	U87	brain:	n/a
49	chr3:112096801-112096851	PANC-1	pancreas:	n/a
50	chr3:112109797-112109847	Hepatocyte	liver:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:112012262..112013019-chr3:112156556..112157096,2	MCF-7	breast:
2	chr3:112045532..112046934-chr3:112156222..112157470,7	MCF-7	breast:
3	chr17:58220578..58221151-chr3:112183496..112184268,2	MCF-7	breast:
4	chr3:112046007..112046874-chr3:112156015..112156737,3	MCF-7	breast:
5	chr3:111832694..111835578-chr3:112096846..112099201,2	MCF-7	breast:
6	chr3:112052345..112054034-chr3:112155349..112157049,2	MCF-7	breast:
7	chr3:112090607..112092226-chr3:112097134..112099677,2	MCF-7	breast:
8	chr3:112189206..112190998-chr3:112191867..112193876,2	K562	blood:
9	chr3:111830414..111830964-chr3:112156344..112156927,2	MCF-7	breast:
10	chr3:112090607..112092226-chr3:112097134..112099677,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATG3-3	chr3:112188819-112189300	NONHSAT091180
2	lnc-BTLA-4	chr3:112148802-112149477	NONHSAT091178
3	lnc-BTLA-1	chr3:112127921-112127951	NONHSAT091167
4	lnc-BTLA-4	chr3:112178630-112179297	NONHSAT091178
5	lnc-BTLA-1	chr3:112099217-112099448	NONHSAT091176
6	lnc-BTLA-4	chr3:112130091-112130571	NONHSAT091178
7	lnc-ATG3-3	chr3:112184773-112185230	NONHSAT091179
8	lnc-BTLA-1	chr3:112100753-112100776	NONHSAT091168
9	lnc-ATG3-3	chr3:112188605-112188651	NONHSAT091179
10	lnc-BTLA-1	chr3:112127921-112127994	NONHSAT091172
11	lnc-BTLA-1	chr3:112099250-112099670	NONHSAT091173
12	lnc-BTLA-1	chr3:112127921-112127981	ENSG00000243081
13	lnc-BTLA-1	chr3:112123200-112123225	NONHSAT091170
14	lnc-BTLA-1	chr3:112127921-112128049	NONHSAT091169
15	lnc-BTLA-1	chr3:112099250-112099448	NONHSAT091168
16	lnc-BTLA-1	chr3:112100753-112100780	NONHSAT091174
17	lnc-BTLA-1	chr3:112099250-112099448	NONHSAT091174
18	lnc-BTLA-4	chr3:112179309-112179627	NONHSAT091178
19	lnc-ATG3-3	chr3:112188819-112188869	NONHSAT091179
20	lnc-ATG3-3	chr3:112188603-112188651	NONHSAT091180
21	lnc-BTLA-1	chr3:112100753-112100776	NONHSAT091176
22	lnc-BTLA-1	chr3:112115494-112116995	ENSG00000243081
23	lnc-BTLA-1	chr3:112099250-112099448	NONHSAT091172

No data

Variant related genes	Relation type
ENSG00000243081	TF binding region
BTLA	TF binding region
ENSG00000243081	CpG island
BTLA	CpG island
ENSG00000186265	chromatin interactions

Extended variants
information (count: 4312 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:4312 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1996722	chr3:112091220-112091221	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577588732	chr3:112091246-112091247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188759372	chr3:112091274-112091275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540540410	chr3:112091304-112091305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368589301	chr3:112091343-112091344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560798068	chr3:112091349-112091350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114815567	chr3:112091366-112091367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116540544	chr3:112091379-112091380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs60112764	chr3:112091460-112091461	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs368037939	chr3:112091483-112091484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs539675970	chr3:112091492-112091493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs13080716	chr3:112091526-112091527	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs573227289	chr3:112091529-112091530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116379211	chr3:112091597-112091598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs145667913	chr3:112091622-112091623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs151076138	chr3:112091675-112091676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552068978	chr3:112091687-112091688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564073987	chr3:112091694-112091695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs140289253	chr3:112091695-112091696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7641311	chr3:112091696-112091697	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs192192415	chr3:112091699-112091700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528939616	chr3:112091778-112091779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs7653398	chr3:112091794-112091795	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs150359711	chr3:112091830-112091831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183863105	chr3:112091890-112091891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368856743	chr3:112091903-112091904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs62265775	chr3:112091905-112091906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546826173	chr3:112091906-112091907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560415877	chr3:112091907-112091908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs71134829	chr3:112091921-112091922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138075597	chr3:112091955-112091956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571193500	chr3:112091988-112091989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533704121	chr3:112091995-112091996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546846882	chr3:112092048-112092049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs372120549	chr3:112092070-112092071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs28657378	chr3:112092075-112092076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372136463	chr3:112092077-112092078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142377316	chr3:112092078-112092079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs57875322	chr3:112092079-112092080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs9832869	chr3:112092080-112092081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10712895	chr3:112092085-112092086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189990093	chr3:112092092-112092093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7611568	chr3:112092138-112092139	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs537876970	chr3:112092148-112092149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs180794591	chr3:112092161-112092162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs577825353	chr3:112092174-112092175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs114258291	chr3:112092244-112092245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs117503372	chr3:112092251-112092252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573825107	chr3:112092253-112092254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556684146	chr3:112092274-112092275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Breast cancer	22522925	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1732 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112069200-112095400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr3:112077200-112094200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr3:112077600-112107200	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr3:112080000-112096000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr3:112081200-112092800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr3:112081400-112091600	Weak transcription	Primary T cells from cord blood	blood
7	chr3:112082200-112096000	Weak transcription	Fetal Stomach	stomach
8	chr3:112082600-112094600	Weak transcription	Brain Anterior Caudate	brain
9	chr3:112083400-112092200	Weak transcription	Primary B cells from cord blood	blood
10	chr3:112083800-112092200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr3:112084000-112094800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr3:112084200-112092600	Weak transcription	Fetal Kidney	kidney
13	chr3:112084400-112091600	Weak transcription	Placenta	Placenta
14	chr3:112084600-112093200	Weak transcription	Fetal Lung	lung
15	chr3:112084800-112096000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr3:112084800-112096800	Weak transcription	Fetal Muscle Leg	muscle
17	chr3:112085000-112095600	Weak transcription	Thymus	Thymus
18	chr3:112085400-112096000	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr3:112085600-112095400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr3:112085600-112096000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr3:112085800-112091400	Weak transcription	Primary B cells from peripheral blood	blood
22	chr3:112085800-112091400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr3:112085800-112091400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr3:112085800-112092200	Weak transcription	Primary hematopoietic stem cells	blood
25	chr3:112085800-112096400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr3:112085800-112096600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr3:112085800-112101400	Weak transcription	Aorta	Aorta
28	chr3:112086000-112095000	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr3:112086000-112095600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr3:112086200-112091400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr3:112086200-112092200	Weak transcription	Fetal Thymus	thymus
32	chr3:112087600-112096400	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr3:112088200-112092800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr3:112088400-112091400	Weak transcription	Adipose Nuclei	Adipose
35	chr3:112090400-112092600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr3:112090600-112093000	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr3:112090600-112093600	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr3:112090800-112091600	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr3:112091200-112092800	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr3:112091400-112091600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr3:112091400-112091600	Enhancers	Primary B cells from peripheral blood	blood
42	chr3:112091400-112091600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr3:112091400-112091600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr3:112091400-112093200	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr3:112091400-112098400	Enhancers	Adipose Nuclei	Adipose
46	chr3:112091600-112092000	Weak transcription	Primary B cells from peripheral blood	blood
47	chr3:112091600-112092000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr3:112091600-112092000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr3:112091600-112092400	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr3:112091600-112092600	Enhancers	Primary T cells from cord blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links