Variant report

Variant	nsv469394
Chromosome Location	chr2:7197199-7230988
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:396)
CpG islands
(count:306)
Chromatin interactive
region (count:10)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:396 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:7212261-7212278	K562	blood:	n/a	n/a
2	BACH1	chr2:7215726-7215854	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr2:7197996-7198587	GM12878	blood:	n/a	n/a
4	BHLHE40	chr2:7211525-7211674	K562	blood:	n/a	n/a
5	CEBPB	chr2:7212082-7212470	HepG2	liver:	n/a	chr2:7212267-7212278
6	CEBPB	chr2:7212062-7212448	K562	blood:	n/a	chr2:7212267-7212278
7	CEBPB	chr2:7220853-7221050	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr2:7218117-7218581	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:7215974-7216305	K562	blood:	n/a	chr2:7216140-7216151
10	CEBPB	chr2:7220761-7221088	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:7215957-7216306	HepG2	liver:	n/a	chr2:7216140-7216151
12	CEBPB	chr2:7224046-7224342	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr2:7215990-7216312	IMR90	lung:	n/a	chr2:7216140-7216151
14	CEBPB	chr2:7212075-7212395	K562	blood:	n/a	chr2:7212267-7212278
15	CEBPB	chr2:7212111-7212456	HepG2	liver:	n/a	chr2:7212267-7212278
16	CEBPB	chr2:7220790-7221071	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:7220799-7221052	A549	lung:	n/a	n/a
18	CEBPB	chr2:7218198-7218246	A549	lung:	n/a	n/a
19	CEBPB	chr2:7212156-7212373	HepG2	liver:	n/a	chr2:7212267-7212278
20	CEBPB	chr2:7212056-7212368	K562	blood:	n/a	chr2:7212267-7212278
21	CEBPB	chr2:7215955-7216323	A549	lung:	n/a	chr2:7216140-7216151
22	CHD2	chr2:7198240-7198495	GM12878	blood:	n/a	n/a
23	CHD2	chr2:7224040-7224178	HepG2	liver:	n/a	n/a
24	CTCF	chr2:7224120-7224270	GM12870	blood:	n/a	n/a
25	CTCF	chr2:7224110-7224249	MCF-7	breast:	n/a	n/a
26	CTCF	chr2:7224120-7224270	HCM	heart:	n/a	n/a
27	CTCF	chr2:7224049-7224321	A549	lung:	n/a	n/a
28	CTCF	chr2:7224100-7224250	HRE	kidney:	n/a	n/a
29	CTCF	chr2:7224160-7224310	HL-60	blood:	n/a	n/a
30	CTCF	chr2:7224120-7224270	AG04449	skin:	n/a	n/a
31	CTCF	chr2:7224000-7224290	WI-38	lung:	n/a	n/a
32	CTCF	chr2:7223980-7224398	A549	lung:	n/a	n/a
33	CTCF	chr2:7224100-7224250	HVMF	connective:	n/a	n/a
34	CTCF	chr2:7224100-7224250	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr2:7224080-7224230	HCT-116	colon:	n/a	n/a
36	CTCF	chr2:7224120-7224270	AG09309	skin:	n/a	n/a
37	CTCF	chr2:7224160-7224310	SAEC	small airway:	n/a	n/a
38	CTCF	chr2:7224140-7224290	GM12874	blood:	n/a	n/a
39	CTCF	chr2:7224120-7224270	GM12868	blood:	n/a	n/a
40	CTCF	chr2:7224120-7224270	GM12872	blood:	n/a	n/a
41	CTCF	chr2:7223968-7224322	K562	blood:	n/a	n/a
42	CTCF	chr2:7224160-7224310	HAc	cerebellar:	n/a	n/a
43	CTCF	chr2:7224140-7224290	NB4	blood:	n/a	n/a
44	CTCF	chr2:7224079-7224340	HepG2	liver:	n/a	n/a
45	CTCF	chr2:7224120-7224270	GM12875	blood:	n/a	n/a
46	CTCF	chr2:7224140-7224290	GM12872	blood:	n/a	n/a
47	CTCF	chr2:7224140-7224290	GM12865	blood:	n/a	n/a
48	CTCF	chr2:7224160-7224310	GM12874	blood:	n/a	n/a
49	CTCF	chr2:7223938-7224431	HepG2	liver:	n/a	n/a
50	CTCF	chr2:7226040-7226190	AG04450	lung:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:7230143-7230193	LNCaP	prostate:	n/a
2	chr2:7230143-7230193	LNCaP	prostate:	n/a
3	chr2:7229912-7229962	ECC-1	luminal epithelium:	n/a
4	chr2:7229912-7229962	ProgFib	skin:	n/a
5	chr2:7230143-7230193	SAEC	small airway:	n/a
6	chr2:7229807-7229857	IMR90	lung:	fetal
7	chr2:7230120-7230170	HCT-116	colon:	n/a
8	chr2:7229807-7229857	GM06990	blood:	n/a
9	chr2:7230143-7230193	AoSMC	blood vessel:	n/a
10	chr2:7229724-7229774	GM12878	blood:	n/a
11	chr2:7229912-7229962	SAEC	small airway:	n/a
12	chr2:7229912-7229962	NB4	blood:	n/a
13	chr2:7229912-7229962	Hepatocyte	liver:	n/a
14	chr2:7230120-7230170	A549	lung:	n/a
15	chr2:7229724-7229774	CMK	blood:	n/a
16	chr2:7229724-7229774	ovcar-3	ovarian:	n/a
17	chr2:7229724-7229774	SK-N-MC	brain:	n/a
18	chr2:7229807-7229857	MCF-7	breast:	n/a
19	chr2:7230120-7230170	HCPEpiC	choroid plexus:	n/a
20	chr2:7230120-7230170	NHBE	bronchial:	n/a
21	chr2:7230143-7230193	HIPEpiC	eye:	n/a
22	chr2:7230120-7230170	BJ	skin:	n/a
23	chr2:7230120-7230170	U87	brain:	n/a
24	chr2:7229807-7229857	HEK293	kidney:	embryo
25	chr2:7230120-7230170	AG09309	skin:	n/a
26	chr2:7229807-7229857	Caco-2	colon:	n/a
27	chr2:7230143-7230193	HRPEpiC	eye:	n/a
28	chr2:7229724-7229774	HRCEpiC	kidney:	n/a
29	chr2:7229724-7229774	HAEpiC	amniotic membrane:	n/a
30	chr2:7229912-7229962	HCPEpiC	choroid plexus:	n/a
31	chr2:7230120-7230170	PFSK-1	brain:	n/a
32	chr2:7229807-7229857	HIPEpiC	eye:	n/a
33	chr2:7230120-7230170	GM19239	blood:	n/a
34	chr2:7230120-7230170	AG09319	gingival:	n/a
35	chr2:7229912-7229962	NT2-D1	testis:	n/a
36	chr2:7229724-7229774	GM12892	blood:	n/a
37	chr2:7229912-7229962	T-47D	breast:	n/a
38	chr2:7229807-7229857	HRE	kidney:	n/a
39	chr2:7230143-7230193	ProgFib	skin:	n/a
40	chr2:7230120-7230170	PANC-1	pancreas:	n/a
41	chr2:7229724-7229774	T-47D	breast:	n/a
42	chr2:7229912-7229962	HRCEpiC	kidney:	n/a
43	chr2:7229912-7229962	BE2_C	brain:	n/a
44	chr2:7229724-7229774	HRPEpiC	eye:	n/a
45	chr2:7230143-7230193	HUVEC	blood vessel:	n/a
46	chr2:7229724-7229774	Caco-2	colon:	n/a
47	chr2:7229912-7229962	HEEpiC	esophagus:	n/a
48	chr2:7229807-7229857	HCPEpiC	choroid plexus:	n/a
49	chr2:7230143-7230193	HCM	heart:	n/a
50	chr2:7229724-7229774	HNPCEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:7229093..7231064-chr2:7236083..7237840,2	K562	blood:
2	chr2:7204099..7206032-chr2:7209329..7211662,2	MCF-7	breast:
3	chr2:7187222..7190356-chr2:7196185..7198623,3	K562	blood:
4	chr2:7177653..7178530-chr2:7223750..7224418,3	MCF-7	breast:
5	chr2:7204099..7206032-chr2:7209329..7211662,2	MCF-7	breast:
6	chr2:7229585..7232246-chr2:7232554..7234108,2	K562	blood:
7	chr2:7202953..7205552-chr2:7208876..7210549,3	K562	blood:
8	chr2:7177508..7178231-chr2:7223675..7224637,2	K562	blood:
9	chr2:7202953..7205552-chr2:7208876..7210549,3	K562	blood:
10	chr2:7189264..7191532-chr2:7195160..7198127,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CMPK2-6	chr2:7217013-7217177	ENSG00000223884.1
2	lnc-CMPK2-6	chr2:7217502-7217809	NONHSAT068936
3	lnc-CMPK2-6	chr2:7202419-7202543	NONHSAT068936
4	lnc-CMPK2-6	chr2:7217835-7218011	ENSG00000223884.1
5	lnc-CMPK2-6	chr2:7208194-7208400	NONHSAT068937
6	lnc-CMPK2-6	chr2:7217013-7217177	ENSG00000223884.1
7	lnc-CMPK2-6	chr2:7202858-7203045	ENSG00000223884.1
8	lnc-CMPK2-6	chr2:7202794-7203045	NONHSAT068938
9	lnc-CMPK2-6	chr2:7213272-7213485	NONHSAT068938
10	lnc-CMPK2-6	chr2:7202597-7202626	NONHSAT068938
11	lnc-CMPK2-6	chr2:7214628-7214848	NONHSAT068938
12	lnc-CMPK2-6	chr2:7214635-7214847	ENSG00000223884.1
13	lnc-CMPK2-6	chr2:7217835-7218011	ENSG00000223884.1
14	lnc-CMPK2-6	chr2:7202794-7203045	NONHSAT068937
15	lnc-CMPK2-6	chr2:7198401-7198466	NONHSAT068936
16	lnc-CMPK2-6	chr2:7217013-7217177	NONHSAT068937
17	lnc-CMPK2-6	chr2:7217835-7218023	NONHSAT068937
18	lnc-CMPK2-6	chr2:7213272-7213485	NONHSAT068937
19	lnc-CMPK2-6	chr2:7217013-7217177	NONHSAT068936
20	lnc-CMPK2-6	chr2:7202794-7203045	NONHSAT068936
21	lnc-CMPK2-6	chr2:7202001-7202543	NONHSAT068937

No data

Variant related genes	Relation type
ENSG00000223884	TF binding region
ENSG00000223884	CpG island

Extended variants
information (count: 1278 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1278 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs309278	chr2:7197199-7197200	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs17611830	chr2:7197225-7197226	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs533926269	chr2:7197239-7197240	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs309277	chr2:7197264-7197265	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs573743564	chr2:7197271-7197272	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs149780927	chr2:7197294-7197295	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs372560720	chr2:7197298-7197299	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs576700156	chr2:7197309-7197310	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs192278872	chr2:7197311-7197312	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs565186664	chr2:7197312-7197313	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs183229959	chr2:7197321-7197322	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs541189859	chr2:7197345-7197346	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs145704457	chr2:7197354-7197355	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs530183842	chr2:7197486-7197487	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs376875397	chr2:7197511-7197512	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs549938050	chr2:7197518-7197519	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs188107048	chr2:7197540-7197541	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs531551577	chr2:7197544-7197545	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs551701641	chr2:7197554-7197555	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs571524616	chr2:7197575-7197576	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs533992841	chr2:7197599-7197600	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs547587306	chr2:7197639-7197640	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs574859949	chr2:7197646-7197647	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs567276749	chr2:7197774-7197775	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs6431844	chr2:7197780-7197781	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs561212961	chr2:7197788-7197789	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs555927210	chr2:7197818-7197819	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs575987559	chr2:7197825-7197826	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs115681918	chr2:7197828-7197829	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs558834490	chr2:7197897-7197898	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs557165249	chr2:7197908-7197909	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs192632478	chr2:7197914-7197915	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs541251367	chr2:7197918-7197919	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs561125220	chr2:7197936-7197937	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs373939274	chr2:7197940-7197941	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs369093517	chr2:7197942-7197943	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs369142890	chr2:7197971-7197972	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs432588	chr2:7197989-7197990	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs372417	chr2:7197990-7197991	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs148493815	chr2:7198004-7198005	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs552567435	chr2:7198021-7198022	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs369888611	chr2:7198099-7198100	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs565199628	chr2:7198100-7198101	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs531822817	chr2:7198114-7198115	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs115908066	chr2:7198143-7198144	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs547646152	chr2:7198172-7198173	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs567446542	chr2:7198181-7198182	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs536009601	chr2:7198182-7198183	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs377058508	chr2:7198187-7198188	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs569609864	chr2:7198192-7198193	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
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
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Neuroblastoma	18923524	CNVD

Chromatin state (count:251 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:7167400-7200400	Weak transcription	Rectal Smooth Muscle	rectum
2	chr2:7172200-7197200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr2:7178400-7197600	Weak transcription	Fetal Heart	heart
4	chr2:7182000-7198000	Weak transcription	Right Ventricle	heart
5	chr2:7186600-7197600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr2:7188800-7200800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr2:7189400-7203200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:7189400-7213800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr2:7191400-7200400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr2:7194000-7200000	Enhancers	Fetal Thymus	thymus
11	chr2:7194200-7234000	Weak transcription	Pancreas	Pancrea
12	chr2:7194400-7202200	Weak transcription	Ovary	ovary
13	chr2:7194400-7210800	Weak transcription	Lung	lung
14	chr2:7194600-7198200	Weak transcription	Brain Substantia Nigra	brain
15	chr2:7194600-7201800	Weak transcription	Fetal Kidney	kidney
16	chr2:7194600-7206400	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr2:7194800-7198000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr2:7194800-7202800	Weak transcription	Brain Hippocampus Middle	brain
19	chr2:7195000-7197800	Enhancers	Primary T cells from cord blood	blood
20	chr2:7195000-7197800	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr2:7195000-7198200	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr2:7195000-7217000	Weak transcription	Fetal Muscle Leg	muscle
23	chr2:7195200-7197200	Enhancers	Dnd41	blood
24	chr2:7195200-7200200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
25	chr2:7195400-7198200	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr2:7195600-7197600	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr2:7195600-7201000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr2:7195800-7200000	Enhancers	Primary B cells from peripheral blood	blood
29	chr2:7195800-7200200	Enhancers	Primary hematopoietic stem cells	blood
30	chr2:7196000-7197200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr2:7196000-7200000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr2:7196000-7200600	Enhancers	Primary T cells fromperipheralblood	blood
33	chr2:7196200-7198000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr2:7196200-7199400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr2:7196400-7197800	Enhancers	GM12878-XiMat	blood
36	chr2:7196400-7200600	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr2:7196600-7197800	Enhancers	Primary B cells from cord blood	blood
38	chr2:7196600-7199600	Enhancers	Thymus	Thymus
39	chr2:7196600-7200400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr2:7196800-7199800	Weak transcription	Spleen	Spleen
41	chr2:7196800-7200000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr2:7196800-7200200	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr2:7196800-7202000	Weak transcription	Right Atrium	heart
44	chr2:7197000-7197600	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr2:7197200-7197400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr2:7197200-7198400	Flanking Active TSS	Dnd41	blood
47	chr2:7197200-7200000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr2:7197400-7197800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr2:7197600-7198200	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr2:7197600-7198400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood

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