Variant report

Variant	nsv3050
Chromosome Location	chr2:177713430-177760533
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:237)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:237 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr2:177737168-177737208	GM12878	blood:	n/a	n/a
2	CEBPB	chr2:177737079-177737505	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr2:177726367-177726547	A549	lung:	n/a	chr2:177726467-177726478
4	CEBPB	chr2:177726347-177726580	IMR90	lung:	n/a	chr2:177726467-177726478
5	CEBPB	chr2:177760147-177760465	HepG2	liver:	n/a	chr2:177760311-177760322 chr2:177760273-177760285
6	CEBPB	chr2:177726320-177726612	HepG2	liver:	n/a	chr2:177726467-177726478
7	CEBPB	chr2:177741798-177742127	K562	blood:	n/a	chr2:177741963-177741974
8	CTCF	chr2:177717380-177717530	HEEpiC	esophagus:	n/a	n/a
9	CTCF	chr2:177738275-177738368	Kidney_OC	kidney:	n/a	n/a
10	CTCF	chr2:177717760-177717910	RPTEC	kidney:	n/a	n/a
11	CTCF	chr2:177738253-177738414	ProgFib	skin:	n/a	n/a
12	CTCF	chr2:177717620-177717770	HCT-116	colon:	n/a	n/a
13	CTCF	chr2:177738240-177738390	AG04449	skin:	n/a	n/a
14	CTCF	chr2:177738260-177738410	HCT-116	colon:	n/a	n/a
15	CTCF	chr2:177738240-177738390	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr2:177738280-177738430	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr2:177738140-177738290	HCT-116	colon:	n/a	n/a
18	CTCF	chr2:177738200-177738350	GM12868	blood:	n/a	n/a
19	CTCF	chr2:177738220-177738370	HMF	breast:	n/a	n/a
20	CTCF	chr2:177717660-177717810	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr2:177738220-177738370	NB4	blood:	n/a	n/a
22	CTCF	chr2:177738220-177738370	GM12872	blood:	n/a	n/a
23	CTCF	chr2:177738260-177738410	AG10803	skin:	n/a	n/a
24	CTCF	chr2:177717480-177717630	MCF-7	breast:	n/a	n/a
25	CTCF	chr2:177738260-177738387	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr2:177717624-177717746	LNCaP	prostate:	n/a	n/a
27	CTCF	chr2:177738295-177738389	Gliobla	brain:	n/a	n/a
28	CTCF	chr2:177717600-177717750	HMEC	breast:	n/a	n/a
29	CTCF	chr2:177738289-177738409	MCF-7	breast:	n/a	n/a
30	CTCF	chr2:177738220-177738370	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr2:177717580-177717730	GM12871	blood:	n/a	n/a
32	CTCF	chr2:177717600-177717750	HEEpiC	esophagus:	n/a	n/a
33	CTCF	chr2:177738200-177738350	HEK293	kidney:	n/a	n/a
34	CTCF	chr2:177738277-177738306	Lung_OC	lung:	n/a	n/a
35	CTCF	chr2:177717509-177717813	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr2:177738200-177738350	GM12872	blood:	n/a	n/a
37	CTCF	chr2:177738220-177738370	AG04450	lung:	n/a	n/a
38	CTCF	chr2:177717620-177717770	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:177738318-177738367	LNCaP	prostate:	n/a	n/a
40	CTCF	chr2:177738240-177738390	BE2_C	brain:	n/a	n/a
41	CTCF	chr2:177738220-177738370	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr2:177738300-177738450	GM12872	blood:	n/a	n/a
43	CTCF	chr2:177738260-177738423	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr2:177717620-177717770	Caco-2	colon:	n/a	n/a
45	CTCF	chr2:177738298-177738395	A549	lung:	n/a	n/a
46	CTCF	chr2:177738240-177738390	HAc	cerebellar:	n/a	n/a
47	CTCF	chr2:177738237-177738434	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:177738180-177738330	GM12869	blood:	n/a	n/a
49	CTCF	chr2:177738240-177738390	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr2:177738160-177738310	HCM	heart:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:177737177-177737227	ECC-1	luminal epithelium:	n/a
2	chr2:177737177-177737227	HUVEC	blood vessel:	n/a
3	chr2:177737177-177737227	AG04450	lung:	fetal
4	chr2:177737177-177737227	U87	brain:	n/a
5	chr2:177737177-177737227	GM06990	blood:	n/a
6	chr2:177737177-177737227	SK-N-SH_RA	brain:	n/a
7	chr2:177737177-177737227	NHBE	bronchial:	n/a
8	chr2:177737177-177737227	LNCaP	prostate:	n/a
9	chr2:177737177-177737227	SK-N-SH	brain:	n/a
10	chr2:177737177-177737227	HIPEpiC	eye:	n/a
11	chr2:177737177-177737227	HRE	kidney:	n/a
12	chr2:177737177-177737227	ovcar-3	ovarian:	n/a
13	chr2:177737177-177737227	GM12878	blood:	n/a
14	chr2:177737177-177737227	HRPEpiC	eye:	n/a
15	chr2:177737177-177737227	PANC-1	pancreas:	n/a
16	chr2:177737177-177737227	HPAEpiC	pulmonary alveolar:	n/a
17	chr2:177737177-177737227	ProgFib	skin:	n/a
18	chr2:177737177-177737227	IMR90	lung:	fetal
19	chr2:177737177-177737227	GM19239	blood:	n/a
20	chr2:177737177-177737227	HCF	heart:	n/a
21	chr2:177737177-177737227	Jurkat	blood:	n/a
22	chr2:177737177-177737227	HepG2	liver:	n/a
23	chr2:177737177-177737227	AG10803	skin:	n/a
24	chr2:177737177-177737227	Caco-2	colon:	n/a
25	chr2:177737177-177737227	HMEC	breast:	n/a
26	chr2:177737177-177737227	T-47D	breast:	n/a
27	chr2:177737177-177737227	RPTEC	kidney:	n/a
28	chr2:177737177-177737227	AG09309	skin:	n/a
29	chr2:177737177-177737227	BJ	skin:	n/a
30	chr2:177737177-177737227	NH-A	brain:	n/a
31	chr2:177737177-177737227	BE2_C	brain:	n/a
32	chr2:177737177-177737227	HEEpiC	esophagus:	n/a
33	chr2:177737177-177737227	NB4	blood:	n/a
34	chr2:177737177-177737227	SAEC	small airway:	n/a
35	chr2:177737177-177737227	AG09319	gingival:	n/a
36	chr2:177737177-177737227	K562	blood:	n/a
37	chr2:177737177-177737227	H1-hESC	embryonic stem cell:	embryo
38	chr2:177737177-177737227	A549	lung:	n/a
39	chr2:177737177-177737227	SKMC	muscle:	n/a
40	chr2:177737177-177737227	HCT-116	colon:	n/a
41	chr2:177737177-177737227	NT2-D1	testis:	n/a
42	chr2:177737177-177737227	Hela-S3	cervix:	n/a
43	chr2:177737177-177737227	HL-60	blood:	n/a
44	chr2:177737177-177737227	HAEpiC	amniotic membrane:	n/a
45	chr2:177737177-177737227	Hepatocyte	liver:	n/a
46	chr2:177737177-177737227	HNPCEpiC	eye:	n/a
47	chr2:177737177-177737227	NHDF-neo	bronchial:	n/a
48	chr2:177737177-177737227	AoSMC	blood vessel:	n/a
49	chr2:177737177-177737227	HCPEpiC	choroid plexus:	n/a
50	chr2:177737177-177737227	GM12891	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:177709989..177710952-chr2:177737048..177737724,2	MCF-7	breast:
2	chr2:177755160..177757379-chr2:177776534..177778883,2	K562	blood:
3	chr2:177681843..177682647-chr2:177717606..177718164,2	MCF-7	breast:
4	chr2:177732616..177735367-chr2:177737651..177739321,2	K562	blood:
5	chr2:177706481..177708996-chr2:177712358..177714045,3	K562	blood:
6	chr2:177711466..177713806-chr2:177714846..177717263,2	MCF-7	breast:
7	chr2:177712628..177715536-chr2:177734631..177736747,2	MCF-7	breast:
8	chr2:177721738..177724544-chr2:177730328..177733547,3	MCF-7	breast:
9	chr2:177711466..177713806-chr2:177714846..177717263,2	MCF-7	breast:
10	chr2:177709383..177714584-chr2:177715247..177719528,6	K562	blood:
11	chr2:177710576..177713068-chr2:177724579..177727566,2	MCF-7	breast:
12	chr2:177708529..177710912-chr2:177735579..177738159,2	MCF-7	breast:
13	chr2:177721738..177724544-chr2:177730328..177733547,3	MCF-7	breast:
14	chr2:177732616..177735367-chr2:177737651..177739321,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NFE2L2-3	chr2:177714003-177714113	NONHSAT075684
2	lnc-NFE2L2-3	chr2:177713979-177714131	XLOC_002411
3	lnc-HNRNPA3-3	chr2:177722577-177722672	NONHSAT075687
4	lnc-HNRNPA3-3	chr2:177721242-177721356	XLOC_001768
5	lnc-HNRNPA3-3	chr2:177714313-177714347	NONHSAT075687
6	lnc-HNRNPA3-3	chr2:177721969-177722056	XLOC_001768
7	lnc-HNRNPA3-3	chr2:177714314-177714347	XLOC_001768
8	lnc-HNRNPA3-3	chr2:177721968-177722056	NONHSAT075687
9	lnc-HNRNPA3-3	chr2:177722578-177722672	XLOC_001768
10	lnc-HNRNPA3-3	chr2:177721241-177721356	NONHSAT075687

No data

Variant related genes	Relation type
ENSG00000227098	TF binding region
ENSG00000227098	CpG island
ENSG00000227098	chromatin interactions

Extended variants
information (count: 1184 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:1184 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76878882	chr2:177713441-177713442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552149954	chr2:177713601-177713602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373473994	chr2:177713609-177713610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs13026167	chr2:177713639-177713640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs13026700	chr2:177713640-177713641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571822370	chr2:177713648-177713649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4894204	chr2:177713650-177713651	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs369932862	chr2:177713710-177713711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575461810	chr2:177713736-177713737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536344669	chr2:177713737-177713738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542473626	chr2:177713767-177713768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs114494857	chr2:177713777-177713778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573297428	chr2:177713807-177713808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs4894205	chr2:177713839-177713840	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs565297221	chr2:177713847-177713848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187608695	chr2:177713852-177713853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544544671	chr2:177713857-177713858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550678737	chr2:177713866-177713867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564459771	chr2:177713871-177713872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529954481	chr2:177713874-177713875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548411875	chr2:177713884-177713885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533447457	chr2:177713887-177713888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559943805	chr2:177713903-177713904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192125214	chr2:177713910-177713911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529378355	chr2:177713912-177713913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183830954	chr2:177713936-177713937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188087203	chr2:177713964-177713965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs370410986	chr2:177713967-177713968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550910731	chr2:177713979-177713980	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs569100369	chr2:177713983-177713984	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs546716188	chr2:177714023-177714024	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs566814673	chr2:177714049-177714050	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs16864598	chr2:177714053-177714054	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs4894206	chr2:177714076-177714077	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs573221530	chr2:177714079-177714080	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs569487855	chr2:177714088-177714089	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs201898365	chr2:177714133-177714134	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs10682388	chr2:177714134-177714135	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs10692354	chr2:177714135-177714136	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs35787365	chr2:177714137-177714138	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs201082431	chr2:177714138-177714139	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs6755609	chr2:177714153-177714154	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs80212991	chr2:177714194-177714195	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs145536671	chr2:177714213-177714214	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs544507579	chr2:177714230-177714231	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs12616782	chr2:177714253-177714254	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs574784628	chr2:177714261-177714262	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs192083419	chr2:177714264-177714265	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs376079560	chr2:177714299-177714300	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs6433617	chr2:177714324-177714325	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:49)

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
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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	16573809	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	21720365	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:153 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:177710000-177716800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr2:177710600-177716000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr2:177710800-177715000	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr2:177710800-177716600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr2:177711400-177715800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr2:177711600-177713800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr2:177712200-177717200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr2:177712600-177716200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr2:177712600-177716600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr2:177712600-177717200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr2:177712600-177717200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr2:177712800-177716600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr2:177712800-177716800	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr2:177713800-177715800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr2:177715000-177715200	Enhancers	Thymus	Thymus
16	chr2:177715000-177715400	Enhancers	Primary T cells fromperipheralblood	blood
17	chr2:177715000-177715400	Enhancers	Spleen	Spleen
18	chr2:177715200-177715400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr2:177715200-177716600	Weak transcription	Thymus	Thymus
20	chr2:177715400-177716600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr2:177715400-177717600	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr2:177715600-177716000	Enhancers	Colon Smooth Muscle	Colon
23	chr2:177715600-177716800	Enhancers	Fetal Kidney	kidney
24	chr2:177715600-177717600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:177715600-177718000	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr2:177715800-177717600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr2:177715800-177722800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr2:177716000-177717400	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr2:177716000-177717400	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr2:177716000-177717800	Enhancers	Brain Germinal Matrix	brain
31	chr2:177716200-177717400	Enhancers	Fetal Brain Male	brain
32	chr2:177716200-177717600	Enhancers	Fetal Brain Female	brain
33	chr2:177716200-177718000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr2:177716200-177722400	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr2:177716400-177719000	Enhancers	Primary T cells from cord blood	blood
36	chr2:177716600-177717000	Enhancers	H9 Cell Line	embryonic stem cell
37	chr2:177716600-177717800	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr2:177716600-177717800	Enhancers	Fetal Thymus	thymus
39	chr2:177716600-177718000	Enhancers	Thymus	Thymus
40	chr2:177716600-177722200	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr2:177716600-177722600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
42	chr2:177716600-177722600	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr2:177716600-177722800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr2:177716800-177718000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr2:177716800-177718000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr2:177716800-177718200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr2:177716800-177721400	Weak transcription	Fetal Kidney	kidney
48	chr2:177717000-177717200	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr2:177717000-177717800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr2:177717000-177717800	Enhancers	Dnd41	blood

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