Variant report

Variant	nsv877565
Chromosome Location	chr3:143078986-143116883
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:145)
CpG islands
(count:61)
Chromatin interactive
region (count:21)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:145 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:143085532-143085796	K562	blood:	n/a	n/a
2	ATF1	chr3:143085572-143086036	K562	blood:	n/a	n/a
3	BHLHE40	chr3:143085702-143085825	K562	blood:	n/a	n/a
4	CBX3	chr3:143099970-143100368	K562	blood:	n/a	n/a
5	CEBPB	chr3:143097592-143097840	HepG2	liver:	n/a	chr3:143097712-143097723
6	CEBPB	chr3:143094498-143094735	K562	blood:	n/a	n/a
7	CEBPD	chr3:143085512-143085887	K562	blood:	n/a	n/a
8	CTCF	chr3:143085640-143085790	NB4	blood:	n/a	chr3:143085748-143085756
9	CTCF	chr3:143079200-143079350	HMEC	breast:	n/a	n/a
10	CTCF	chr3:143100176-143100217	Spleen_OC	spleen:	n/a	n/a
11	CTCF	chr3:143085660-143085815	K562	blood:	n/a	chr3:143085748-143085756
12	CTCF	chr3:143085537-143086066	K562	blood:	n/a	chr3:143085748-143085756
13	CTCF	chr3:143106778-143106874	HUVEC	blood vessel:	n/a	chr3:143106829-143106842 chr3:143106830-143106840 chr3:143106827-143106845
14	CTCF	chr3:143106740-143106890	AoAF	blood vessel:	n/a	chr3:143106829-143106842 chr3:143106830-143106840 chr3:143106827-143106845
15	CTCF	chr3:143107854-143107906	GM13976	blood:	n/a	n/a
16	CTCF	chr3:143114353-143114416	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr3:143106620-143106770	HFF-Myc	foreskin:	n/a	n/a
18	CTCF	chr3:143085660-143085810	HCPEpiC	choroid plexus:	n/a	chr3:143085748-143085756
19	CTCF	chr3:143106780-143106930	HVMF	connective:	n/a	chr3:143106829-143106842 chr3:143106830-143106840 chr3:143106827-143106845
20	CTCF	chr3:143080538-143080705	K562	blood:	n/a	n/a
21	CTCF	chr3:143085640-143085790	GM12864	blood:	n/a	chr3:143085748-143085756
22	CTCF	chr3:143085732-143085762	GM12878	blood:	n/a	chr3:143085748-143085756
23	CTCF	chr3:143106840-143106990	Caco-2	colon:	n/a	n/a
24	CTCF	chr3:143106720-143106870	K562	blood:	n/a	chr3:143106829-143106842 chr3:143106830-143106840 chr3:143106827-143106845
25	CTCF	chr3:143085640-143085790	K562	blood:	n/a	chr3:143085748-143085756
26	CTCF	chr3:143106832-143106838	K562	blood:	n/a	n/a
27	CTCF	chr3:143106700-143106850	AoAF	blood vessel:	n/a	chr3:143106829-143106842 chr3:143106830-143106840 chr3:143106827-143106845
28	CUX1	chr3:143085545-143085745	K562	blood:	n/a	n/a
29	E2F4	chr3:143079141-143079450	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr3:143080455-143080551	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr3:143087214-143087391	MCF10A-Er-Src	breast:	n/a	chr3:143087272-143087281
32	E2F4	chr3:143089994-143090035	MCF10A-Er-Src	breast:	n/a	n/a
33	EBF1	chr3:143108248-143108463	GM12878	blood:	n/a	chr3:143108387-143108397 chr3:143108387-143108396 chr3:143108385-143108396
34	EP300	chr3:143085585-143085745	K562	blood:	n/a	chr3:143085702-143085716
35	EP300	chr3:143087434-143087666	K562	blood:	n/a	n/a
36	EP300	chr3:143085328-143085850	K562	blood:	n/a	chr3:143085702-143085716
37	ESR1	chr3:143099313-143099594	ECC-1	luminal epithelium:	n/a	n/a
38	ESR1	chr3:143099270-143099593	ECC-1	luminal epithelium:	n/a	n/a
39	FAM48A	chr3:143116703-143116803	GM12878	blood:	n/a	n/a
40	FOS	chr3:143079021-143079534	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr3:143079040-143079435	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr3:143086048-143086374	MCF10A-Er-Src	breast:	n/a	chr3:143086218-143086226 chr3:143086218-143086226 chr3:143086218-143086225 chr3:143086216-143086228 chr3:143086217-143086227
43	FOS	chr3:143079004-143079495	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr3:143094532-143094856	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr3:143094528-143094889	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr3:143100563-143100775	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr3:143094528-143094813	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr3:143086156-143086219	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr3:143094582-143094715	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr3:143086064-143086264	MCF10A-Er-Src	breast:	n/a	chr3:143086218-143086226 chr3:143086218-143086226 chr3:143086218-143086225 chr3:143086216-143086228 chr3:143086217-143086227

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:143097071-143097121	HCT-116	colon:	n/a
2	chr3:143097071-143097121	GM19239	blood:	n/a
3	chr3:143097071-143097121	HPAEpiC	pulmonary alveolar:	n/a
4	chr3:143097071-143097121	SK-N-MC	brain:	n/a
5	chr3:143097071-143097121	CMK	blood:	n/a
6	chr3:143097071-143097121	MCF-7	breast:	n/a
7	chr3:143097071-143097121	BJ	skin:	n/a
8	chr3:143097071-143097121	SKMC	muscle:	n/a
9	chr3:143097071-143097121	NHBE	bronchial:	n/a
10	chr3:143097071-143097121	HAEpiC	amniotic membrane:	n/a
11	chr3:143097071-143097121	K562	blood:	n/a
12	chr3:143097071-143097121	NB4	blood:	n/a
13	chr3:143097071-143097121	HCF	heart:	n/a
14	chr3:143097071-143097121	GM12891	blood:	n/a
15	chr3:143097071-143097121	HRE	kidney:	n/a
16	chr3:143097071-143097121	SK-N-SH_RA	brain:	n/a
17	chr3:143097071-143097121	HepG2	liver:	n/a
18	chr3:143097071-143097121	HIPEpiC	eye:	n/a
19	chr3:143097071-143097121	HUVEC	blood vessel:	n/a
20	chr3:143097071-143097121	AG04449	skin:	fetal
21	chr3:143097071-143097121	HCM	heart:	n/a
22	chr3:143097071-143097121	HL-60	blood:	n/a
23	chr3:143097071-143097121	U87	brain:	n/a
24	chr3:143097071-143097121	ProgFib	skin:	n/a
25	chr3:143097071-143097121	Caco-2	colon:	n/a
26	chr3:143097071-143097121	HEEpiC	esophagus:	n/a
27	chr3:143097071-143097121	PrEC	prostate:	n/a
28	chr3:143097071-143097121	HRCEpiC	kidney:	n/a
29	chr3:143097071-143097121	HCPEpiC	choroid plexus:	n/a
30	chr3:143097071-143097121	LNCaP	prostate:	n/a
31	chr3:143097071-143097121	AG10803	skin:	n/a
32	chr3:143097071-143097121	GM12878	blood:	n/a
33	chr3:143097071-143097121	Hepatocyte	liver:	n/a
34	chr3:143097071-143097121	HMEC	breast:	n/a
35	chr3:143097071-143097121	SAEC	small airway:	n/a
36	chr3:143097071-143097121	H1-hESC	embryonic stem cell:	embryo
37	chr3:143097071-143097121	HNPCEpiC	eye:	n/a
38	chr3:143097071-143097121	ovcar-3	ovarian:	n/a
39	chr3:143097071-143097121	Jurkat	blood:	n/a
40	chr3:143097071-143097121	PANC-1	pancreas:	n/a
41	chr3:143097071-143097121	GM06990	blood:	n/a
42	chr3:143097071-143097121	RPTEC	kidney:	n/a
43	chr3:143097071-143097121	SK-N-SH	brain:	n/a
44	chr3:143097071-143097121	NH-A	brain:	n/a
45	chr3:143097071-143097121	IMR90	lung:	fetal
46	chr3:143097071-143097121	HEK293	kidney:	embryo
47	chr3:143097071-143097121	PFSK-1	brain:	n/a
48	chr3:143097071-143097121	AG09319	gingival:	n/a
49	chr3:143097071-143097121	T-47D	breast:	n/a
50	chr3:143097071-143097121	GM12892	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:143073365..143075780-chr3:143077862..143079884,2	K562	blood:
2	chr3:143083767..143087407-chr3:143088395..143091311,3	K562	blood:
3	chr3:143107077..143109366-chr3:143114729..143117403,2	K562	blood:
4	chr3:143068671..143071346-chr3:143094512..143096094,2	K562	blood:
5	chr3:143107077..143109366-chr3:143114729..143117403,2	K562	blood:
6	chr3:143079326..143082089-chr3:143083976..143087226,3	K562	blood:
7	chr3:143073351..143075780-chr3:143076251..143080121,5	K562	blood:
8	chr3:143083767..143087407-chr3:143088395..143091311,3	K562	blood:
9	chr3:143099826..143101455-chr3:143101968..143104391,2	K562	blood:
10	chr3:143094103..143096377-chr3:143119769..143122751,2	K562	blood:
11	chr3:143079326..143082089-chr3:143083976..143087226,3	K562	blood:
12	chr3:142835479..142837341-chr3:143085961..143087735,2	K562	blood:
13	chr3:143076644..143082089-chr3:143083976..143087336,5	K562	blood:
14	chr3:143081768..143084316-chr3:143087882..143089415,2	MCF-7	breast:
15	chr3:143076644..143082089-chr3:143083976..143087336,5	K562	blood:
16	chr3:143106712..143109351-chr3:143117570..143120299,2	K562	blood:
17	chr3:143089798..143091848-chr3:143094330..143096533,2	K562	blood:
18	chr3:143075166..143076875-chr3:143081187..143082787,2	K562	blood:
19	chr3:142839497..142841574-chr3:143081300..143083347,2	K562	blood:
20	chr3:143081768..143084316-chr3:143087882..143089415,2	MCF-7	breast:
21	chr3:143089798..143091848-chr3:143094330..143096533,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHST2-4	chr3:143100786-143101003	ENSG00000244493.1
2	lnc-CHST2-4	chr3:143100180-143100288	ENSG00000244493.1

No data

Variant related genes	Relation type
SLC9A9-AS2	TF binding region
SLC9A9-AS2	CpG island
ENSG00000244493	chromatin interactions

Extended variants
information (count: 1501 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1501 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1604380	chr3:143078986-143078987	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573392676	chr3:143079034-143079035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534367612	chr3:143079043-143079044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs377205900	chr3:143079047-143079048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78289198	chr3:143079210-143079211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577526277	chr3:143079216-143079217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77481965	chr3:143079234-143079235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563941814	chr3:143079237-143079238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192779295	chr3:143079241-143079242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147160124	chr3:143079244-143079245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544230105	chr3:143079314-143079315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs79002997	chr3:143079407-143079408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528581192	chr3:143079430-143079431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546728678	chr3:143079494-143079495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184910332	chr3:143079528-143079529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs148228523	chr3:143079542-143079543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141252255	chr3:143079551-143079552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189381933	chr3:143079569-143079570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536889215	chr3:143079578-143079579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs34716373	chr3:143079596-143079597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150760087	chr3:143079689-143079690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567075988	chr3:143079691-143079692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs139153513	chr3:143079758-143079759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs34043464	chr3:143079773-143079774	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs577588164	chr3:143079786-143079787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538233620	chr3:143079793-143079794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181607100	chr3:143079798-143079799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575999500	chr3:143079844-143079845	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560347563	chr3:143079845-143079846	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs114191095	chr3:143079860-143079861	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561467235	chr3:143079864-143079865	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573313079	chr3:143079874-143079875	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540745212	chr3:143079890-143079891	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs565215054	chr3:143079923-143079924	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs367962382	chr3:143079940-143079941	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs532575911	chr3:143080001-143080002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544194803	chr3:143080012-143080013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563291368	chr3:143080054-143080055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530717610	chr3:143080109-143080110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548825332	chr3:143080154-143080155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs371605462	chr3:143080172-143080173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs12489162	chr3:143080219-143080220	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs552183274	chr3:143080355-143080356	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs73144729	chr3:143080390-143080391	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs184214605	chr3:143080413-143080414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs141269450	chr3:143080457-143080458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189455710	chr3:143080459-143080460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149949041	chr3:143080466-143080467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146037708	chr3:143080476-143080477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181812572	chr3:143080535-143080536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
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
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Adrenocortical carcinoma	18281524	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:172 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143068200-143091800	Weak transcription	Lung	lung
2	chr3:143068800-143082000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr3:143069000-143080800	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr3:143069000-143081600	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr3:143069200-143080600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr3:143069800-143081200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr3:143070200-143088600	Weak transcription	Aorta	Aorta
8	chr3:143071200-143081600	Weak transcription	Fetal Lung	lung
9	chr3:143071600-143102400	Weak transcription	Esophagus	oesophagus
10	chr3:143072000-143099400	Weak transcription	Ovary	ovary
11	chr3:143072200-143081200	Weak transcription	Adipose Nuclei	Adipose
12	chr3:143072400-143081200	Weak transcription	Fetal Thymus	thymus
13	chr3:143072400-143082200	Weak transcription	Primary B cells from cord blood	blood
14	chr3:143072400-143083000	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr3:143072400-143083000	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr3:143073400-143089600	Weak transcription	Psoas Muscle	Psoas
17	chr3:143076400-143079000	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr3:143076400-143079000	Enhancers	Stomach Mucosa	stomach
19	chr3:143077000-143079400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr3:143077000-143080200	Enhancers	Dnd41	blood
21	chr3:143077400-143104800	Weak transcription	Brain Hippocampus Middle	brain
22	chr3:143077800-143079400	Enhancers	Pancreas	Pancrea
23	chr3:143078200-143081400	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr3:143078400-143079200	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr3:143078400-143081200	Weak transcription	Brain Cingulate Gyrus	brain
26	chr3:143079000-143081400	Weak transcription	Stomach Mucosa	stomach
27	chr3:143079200-143079400	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr3:143079400-143081200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr3:143079400-143081600	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr3:143079800-143080000	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
31	chr3:143080000-143081600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr3:143080200-143080400	Flanking Active TSS	Dnd41	blood
33	chr3:143080400-143080800	Enhancers	Dnd41	blood
34	chr3:143080600-143081800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr3:143080600-143083000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr3:143080800-143081600	Enhancers	K562	blood
37	chr3:143080800-143081800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr3:143080800-143082000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr3:143080800-143082200	Enhancers	NH-A	brain
40	chr3:143080800-143082800	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr3:143080800-143083000	Enhancers	Primary T cells from cord blood	blood
42	chr3:143080800-143083000	Flanking Active TSS	Dnd41	blood
43	chr3:143080800-143083200	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr3:143080800-143083600	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr3:143081000-143083200	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr3:143081200-143081400	Enhancers	Adipose Nuclei	Adipose
47	chr3:143081200-143082200	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr3:143081200-143082200	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr3:143081200-143082400	Enhancers	Fetal Thymus	thymus
50	chr3:143081200-143082800	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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