Variant report

Variant	nsv875595
Chromosome Location	chr2:188573244-188690187
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:326)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:326 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:188684551-188684613	HepG2	liver:	n/a	n/a
2	ATF1	chr2:188633855-188634067	K562	blood:	n/a	n/a
3	BACH1	chr2:188689902-188690134	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:188647107-188647253	K562	blood:	n/a	n/a
5	BHLHE40	chr2:188639528-188639589	GM12878	blood:	n/a	n/a
6	CCNT2	chr2:188671617-188671704	K562	blood:	n/a	n/a
7	CEBPB	chr2:188659239-188659491	A549	lung:	n/a	n/a
8	CEBPB	chr2:188657288-188657534	HepG2	liver:	n/a	chr2:188657412-188657423
9	CEBPB	chr2:188648982-188649119	K562	blood:	n/a	chr2:188649052-188649063
10	CEBPB	chr2:188683622-188683880	HepG2	liver:	n/a	chr2:188683751-188683762
11	CEBPB	chr2:188648988-188649117	Hela-S3	cervix:	n/a	chr2:188649052-188649063
12	CEBPB	chr2:188659268-188659401	K562	blood:	n/a	n/a
13	CEBPB	chr2:188608563-188608828	HepG2	liver:	n/a	chr2:188608676-188608687
14	CEBPB	chr2:188656420-188656432	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:188608641-188608753	K562	blood:	n/a	chr2:188608676-188608687
16	CEBPB	chr2:188648876-188649229	IMR90	lung:	n/a	chr2:188649052-188649063
17	CEBPB	chr2:188626594-188626733	A549	lung:	n/a	n/a
18	CEBPB	chr2:188648886-188649231	A549	lung:	n/a	chr2:188649052-188649063
19	CEBPB	chr2:188659234-188659471	IMR90	lung:	n/a	n/a
20	CEBPB	chr2:188648874-188649234	HepG2	liver:	n/a	chr2:188649052-188649063
21	CEBPB	chr2:188608570-188608763	IMR90	lung:	n/a	chr2:188608676-188608687
22	CEBPB	chr2:188649012-188649117	H1-hESC	embryonic stem cell:	n/a	chr2:188649052-188649063
23	CEBPB	chr2:188581048-188581245	A549	lung:	n/a	n/a
24	CTCF	chr2:188648300-188648450	AG04450	lung:	n/a	n/a
25	CTCF	chr2:188648280-188648430	HAc	cerebellar:	n/a	n/a
26	CTCF	chr2:188648276-188648478	MCF-7	breast:	n/a	n/a
27	CTCF	chr2:188648302-188648395	K562	blood:	n/a	n/a
28	CTCF	chr2:188648260-188648410	HMEC	breast:	n/a	n/a
29	CTCF	chr2:188648331-188648387	GM12878	blood:	n/a	n/a
30	CTCF	chr2:188617300-188617450	HCT-116	colon:	n/a	n/a
31	CTCF	chr2:188648260-188648410	HCM	heart:	n/a	n/a
32	CTCF	chr2:188648236-188648491	K562	blood:	n/a	n/a
33	CTCF	chr2:188648300-188648450	SAEC	small airway:	n/a	n/a
34	CTCF	chr2:188648260-188648410	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr2:188618175-188618211	GM20000	blood:	n/a	n/a
36	CTCF	chr2:188648260-188648410	NHLF	lung:	n/a	n/a
37	CTCF	chr2:188617429-188617452	GM12878	blood:	n/a	n/a
38	CTCF	chr2:188648320-188648470	NHEK	skin:	n/a	n/a
39	CTCF	chr2:188648320-188648470	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr2:188648360-188648510	HCT-116	colon:	n/a	n/a
41	CTCF	chr2:188648280-188648430	A549	lung:	n/a	n/a
42	CTCF	chr2:188648290-188648417	Medullo	brain:	n/a	n/a
43	CTCF	chr2:188648212-188648481	MCF-7	breast:	n/a	n/a
44	CTCF	chr2:188648220-188648370	NHEK	skin:	n/a	n/a
45	CTCF	chr2:188648260-188648426	HepG2	liver:	n/a	n/a
46	CTCF	chr2:188648287-188648458	Gliobla	brain:	n/a	n/a
47	CTCF	chr2:188648260-188648410	AG04449	skin:	n/a	n/a
48	CTCF	chr2:188648280-188648430	HRE	kidney:	n/a	n/a
49	CTCF	chr2:188648320-188648470	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr2:188648280-188648430	HCFaa	heart:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:188689981-188690031	HUVEC	blood vessel:	n/a
2	chr2:188689981-188690031	GM19239	blood:	n/a
3	chr2:188689981-188690031	ECC-1	luminal epithelium:	n/a
4	chr2:188583082-188583132	SKMC	muscle:	n/a
5	chr2:188583082-188583132	NH-A	brain:	n/a
6	chr2:188689981-188690031	HRPEpiC	eye:	n/a
7	chr2:188583082-188583132	CMK	blood:	n/a
8	chr2:188689981-188690031	Jurkat	blood:	n/a
9	chr2:188689981-188690031	NB4	blood:	n/a
10	chr2:188689981-188690031	AG09309	skin:	n/a
11	chr2:188689981-188690031	U87	brain:	n/a
12	chr2:188689981-188690031	HepG2	liver:	n/a
13	chr2:188689981-188690031	IMR90	lung:	fetal
14	chr2:188583082-188583132	HEEpiC	esophagus:	n/a
15	chr2:188583082-188583132	IMR90	lung:	fetal
16	chr2:188689981-188690031	HRE	kidney:	n/a
17	chr2:188583082-188583132	HPAEpiC	pulmonary alveolar:	n/a
18	chr2:188583082-188583132	HAEpiC	amniotic membrane:	n/a
19	chr2:188583082-188583132	PrEC	prostate:	n/a
20	chr2:188689981-188690031	SK-N-MC	brain:	n/a
21	chr2:188689981-188690031	MCF10A-Er-Src	breast:	n/a
22	chr2:188689981-188690031	LNCaP	prostate:	n/a
23	chr2:188583082-188583132	HNPCEpiC	eye:	n/a
24	chr2:188583082-188583132	HCPEpiC	choroid plexus:	n/a
25	chr2:188583082-188583132	AG04449	skin:	fetal
26	chr2:188583082-188583132	NT2-D1	testis:	n/a
27	chr2:188583082-188583132	HCT-116	colon:	n/a
28	chr2:188583082-188583132	AG09319	gingival:	n/a
29	chr2:188583082-188583132	SAEC	small airway:	n/a
30	chr2:188583082-188583132	AG09309	skin:	n/a
31	chr2:188583082-188583132	SK-N-MC	brain:	n/a
32	chr2:188689981-188690031	AG04450	lung:	fetal
33	chr2:188583082-188583132	HIPEpiC	eye:	n/a
34	chr2:188583082-188583132	ovcar-3	ovarian:	n/a
35	chr2:188689981-188690031	HIPEpiC	eye:	n/a
36	chr2:188689981-188690031	CMK	blood:	n/a
37	chr2:188583082-188583132	T-47D	breast:	n/a
38	chr2:188583082-188583132	AoSMC	blood vessel:	n/a
39	chr2:188689981-188690031	SK-N-SH_RA	brain:	n/a
40	chr2:188689981-188690031	NH-A	brain:	n/a
41	chr2:188689981-188690031	ovcar-3	ovarian:	n/a
42	chr2:188583082-188583132	Hela-S3	cervix:	n/a
43	chr2:188689981-188690031	Hepatocyte	liver:	n/a
44	chr2:188689981-188690031	BJ	skin:	n/a
45	chr2:188689981-188690031	Hela-S3	cervix:	n/a
46	chr2:188583082-188583132	MCF10A-Er-Src	breast:	n/a
47	chr2:188689981-188690031	T-47D	breast:	n/a
48	chr2:188689981-188690031	A549	lung:	n/a
49	chr2:188583082-188583132	GM12892	blood:	n/a
50	chr2:188689981-188690031	GM12891	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:188460269..188463083-chr2:188643990..188646491,2	K562	blood:
2	chr2:188302851..188305687-chr2:188602438..188604231,2	K562	blood:
3	chr2:188591288..188593045-chr2:188603697..188606410,2	K562	blood:
4	chr2:188604449..188606812-chr2:188608184..188609837,2	K562	blood:
5	chr2:188591288..188593045-chr2:188603697..188606410,2	K562	blood:
6	chr2:188581473..188583744-chr2:188592833..188595412,2	MCF-7	breast:
7	chr2:188668614..188671113-chr2:188671408..188674313,2	K562	blood:
8	chr2:188668614..188671113-chr2:188671408..188674313,2	K562	blood:
9	chr2:188630653..188632661-chr2:188633986..188636856,2	K562	blood:
10	chr2:188601026..188603906-chr2:188607326..188609061,2	K562	blood:
11	chr2:188581473..188583744-chr2:188592833..188595412,2	MCF-7	breast:
12	chr2:188630653..188632661-chr2:188633986..188636856,2	K562	blood:
13	chr2:188634121..188636479-chr2:188637228..188640007,2	K562	blood:
14	chr2:188634121..188636479-chr2:188637228..188640007,2	K562	blood:
15	chr2:188601766..188603906-chr2:188606320..188608826,2	K562	blood:
16	chr2:188604449..188606812-chr2:188608184..188609837,2	K562	blood:
17	chr2:188523368..188524314-chr2:188579524..188580267,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DIRC1-2	chr2:188577543-188577606	ENSG00000231689

No data

Variant related genes	Relation type
ST13P2	TF binding region
ENSG00000252004	TF binding region
ST13P2	CpG island
ENSG00000252004	CpG island
ENSG00000252004	chromatin interactions

Extended variants
information (count: 2551 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:2551 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13388743	chr2:188573244-188573245	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142816398	chr2:188573304-188573305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563533250	chr2:188573314-188573315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138089749	chr2:188573421-188573422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184278620	chr2:188573436-188573437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375903905	chr2:188573462-188573463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189182126	chr2:188573469-188573470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115215495	chr2:188573547-188573548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577790398	chr2:188573550-188573551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538663765	chr2:188573564-188573565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564809392	chr2:188573570-188573571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149499531	chr2:188573618-188573619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs13391838	chr2:188573624-188573625	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs542941178	chr2:188573634-188573635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542957187	chr2:188573703-188573704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561209084	chr2:188573704-188573705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527430951	chr2:188573713-188573714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576247899	chr2:188573714-188573715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs142153195	chr2:188573718-188573719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2090751	chr2:188573740-188573741	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs565069398	chr2:188573762-188573763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182376911	chr2:188573832-188573833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs547815328	chr2:188573833-188573834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559488893	chr2:188573850-188573851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113462715	chr2:188573913-188573914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs116269445	chr2:188573982-188573983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs567537732	chr2:188574005-188574006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538065779	chr2:188574009-188574010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs143139574	chr2:188574076-188574077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571406970	chr2:188574102-188574103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186420601	chr2:188574104-188574105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190424998	chr2:188574160-188574161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs181618273	chr2:188574188-188574189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs536212660	chr2:188574189-188574190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148317519	chr2:188574243-188574244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141483599	chr2:188574256-188574257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543646406	chr2:188574277-188574278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147452806	chr2:188574300-188574301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185960775	chr2:188574312-188574313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541174916	chr2:188574351-188574352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs189985111	chr2:188574360-188574361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs528673465	chr2:188574420-188574421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139912878	chr2:188574433-188574434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112845798	chr2:188574438-188574439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542221750	chr2:188574511-188574512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545896435	chr2:188574540-188574541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561201575	chr2:188574626-188574627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531746233	chr2:188574690-188574691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550250919	chr2:188574704-188574705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571645981	chr2:188574717-188574718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

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
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	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
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
Intellectual disability	22102821	CNVD
Tetralogy of Fallot	22912587	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188566200-188586000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:188567600-188577600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr2:188570000-188575600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr2:188573400-188574400	Enhancers	HUVEC	blood vessel
5	chr2:188574200-188579800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr2:188575600-188576200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr2:188575600-188576800	Enhancers	Fetal Lung	lung
8	chr2:188575800-188576000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr2:188576000-188577800	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr2:188576200-188577600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr2:188577400-188578000	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr2:188577600-188577800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr2:188577600-188578000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr2:188577600-188578000	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr2:188577800-188578000	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr2:188577800-188578400	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr2:188578000-188579800	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr2:188578000-188580000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr2:188578400-188579400	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr2:188579400-188580000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
21	chr2:188579800-188580400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
22	chr2:188579800-188580600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr2:188580000-188580600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
24	chr2:188580000-188581000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
25	chr2:188580400-188581000	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr2:188580400-188585000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr2:188580600-188581200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr2:188580600-188582800	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr2:188580800-188581200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr2:188581000-188581600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr2:188581000-188583000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr2:188581000-188583400	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr2:188581200-188582000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr2:188581200-188582400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr2:188581600-188582000	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr2:188582000-188583000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr2:188582000-188584400	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr2:188582000-188585000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr2:188582200-188583400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr2:188582400-188582800	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr2:188582800-188583000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr2:188582800-188583400	Enhancers	H1 Cell Line	embryonic stem cell
43	chr2:188582800-188583400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:188583000-188583200	Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr2:188583000-188583400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr2:188583400-188584200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr2:188583400-188584400	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr2:188583400-188584400	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr2:188583400-188584400	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr2:188583400-188584600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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