Variant report

Variant	esv2751839
Chromosome Location	chr2:188035947-188141690
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:446)
CpG islands
(count:123)
Chromatin interactive
region (count:16)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:188082673-188083042	K562	blood:	n/a	chr2:188082805-188082821 chr2:188082806-188082822
2	ATF2	chr2:188128538-188128835	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr2:188075532-188075733	K562	blood:	n/a	n/a
4	BATF	chr2:188092264-188092475	GM12878	blood:	n/a	n/a
5	BCL11A	chr2:188089782-188090028	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr2:188107016-188107020	IMR90	lung:	n/a	n/a
7	CEBPB	chr2:188075474-188075737	K562	blood:	n/a	chr2:188075578-188075589
8	CEBPB	chr2:188061256-188061303	K562	blood:	n/a	n/a
9	CEBPB	chr2:188092236-188092364	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:188075525-188075712	K562	blood:	n/a	chr2:188075578-188075589
11	CEBPB	chr2:188128072-188128355	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:188075456-188075728	HepG2	liver:	n/a	chr2:188075578-188075589
13	CEBPB	chr2:188128014-188128379	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr2:188064188-188064450	K562	blood:	n/a	chr2:188064300-188064311 chr2:188064301-188064312
15	CEBPB	chr2:188064139-188064438	HepG2	liver:	n/a	chr2:188064300-188064311 chr2:188064301-188064312
16	CEBPB	chr2:188075435-188075790	HepG2	liver:	n/a	chr2:188075578-188075589
17	CEBPB	chr2:188092236-188092435	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr2:188075457-188075812	Hela-S3	cervix:	n/a	chr2:188075578-188075589
19	CHD2	chr2:188089735-188090140	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr2:188073313-188073360	HepG2	liver:	n/a	n/a
21	CREB1	chr2:188089728-188090143	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr2:188039420-188039570	GM12868	blood:	n/a	n/a
23	CTCF	chr2:188039400-188039550	HPAF	blood vessel:	n/a	n/a
24	CTCF	chr2:188039460-188039610	HCT-116	colon:	n/a	n/a
25	CTCF	chr2:188136750-188136786	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr2:188039389-188039615	GM12878	blood:	n/a	n/a
27	CTCF	chr2:188039420-188039570	AG09319	gingival:	n/a	n/a
28	CTCF	chr2:188073260-188073410	HepG2	liver:	n/a	n/a
29	CTCF	chr2:188039440-188039590	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr2:188039460-188039610	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr2:188039400-188039550	GM12873	blood:	n/a	n/a
32	CTCF	chr2:188039400-188039550	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr2:188039181-188039207	K562	blood:	n/a	n/a
34	CTCF	chr2:188039244-188039633	K562	blood:	n/a	n/a
35	CTCF	chr2:188039480-188039630	GM12871	blood:	n/a	n/a
36	CTCF	chr2:188039377-188039621	HepG2	liver:	n/a	n/a
37	CTCF	chr2:188039340-188039490	A549	lung:	n/a	n/a
38	CTCF	chr2:188039320-188039470	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr2:188039388-188039643	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr2:188039420-188039570	HPF	lung:	n/a	n/a
41	CTCF	chr2:188039460-188039610	AG04450	lung:	n/a	n/a
42	CTCF	chr2:188070449-188070488	GM20000	blood:	n/a	n/a
43	CTCF	chr2:188073360-188073510	GM12867	blood:	n/a	n/a
44	CTCF	chr2:188039420-188039570	HMF	breast:	n/a	n/a
45	CTCF	chr2:188039440-188039590	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr2:188039409-188039545	GM12892	blood:	n/a	n/a
47	CTCF	chr2:188136700-188136850	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr2:188039416-188039563	GM13977	blood:	n/a	n/a
49	CTCF	chr2:188125440-188125474	Lung_OC	lung:	n/a	n/a
50	CTCF	chr2:188039401-188039616	Gliobla	brain:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:188093537-188093587	AG09319	gingival:	n/a
2	chr2:188093537-188093587	AG09319	gingival:	n/a
3	chr2:188093537-188093587	GM12892	blood:	n/a
4	chr2:188128809-188128859	MCF-7	breast:	n/a
5	chr2:188093537-188093587	Caco-2	colon:	n/a
6	chr2:188093537-188093587	AG10803	skin:	n/a
7	chr2:188128809-188128859	K562	blood:	n/a
8	chr2:188128809-188128859	HCT-116	colon:	n/a
9	chr2:188128809-188128859	CMK	blood:	n/a
10	chr2:188093537-188093587	Jurkat	blood:	n/a
11	chr2:188128809-188128859	PrEC	prostate:	n/a
12	chr2:188128809-188128859	U87	brain:	n/a
13	chr2:188093537-188093587	SK-N-SH	brain:	n/a
14	chr2:188128809-188128859	LNCaP	prostate:	n/a
15	chr2:188128809-188128859	NT2-D1	testis:	n/a
16	chr2:188093537-188093587	PFSK-1	brain:	n/a
17	chr2:188093537-188093587	SAEC	small airway:	n/a
18	chr2:188128809-188128859	HCF	heart:	n/a
19	chr2:188128809-188128859	HNPCEpiC	eye:	n/a
20	chr2:188093537-188093587	AoSMC	blood vessel:	n/a
21	chr2:188093537-188093587	HEEpiC	esophagus:	n/a
22	chr2:188128809-188128859	NB4	blood:	n/a
23	chr2:188128809-188128859	AG09319	gingival:	n/a
24	chr2:188093537-188093587	SK-N-SH_RA	brain:	n/a
25	chr2:188128809-188128859	ProgFib	skin:	n/a
26	chr2:188093537-188093587	ProgFib	skin:	n/a
27	chr2:188128809-188128859	SKMC	muscle:	n/a
28	chr2:188093537-188093587	BE2_C	brain:	n/a
29	chr2:188128809-188128859	HAEpiC	amniotic membrane:	n/a
30	chr2:188128809-188128859	AG04449	skin:	fetal
31	chr2:188093537-188093587	ovcar-3	ovarian:	n/a
32	chr2:188093537-188093587	CMK	blood:	n/a
33	chr2:188128809-188128859	GM12891	blood:	n/a
34	chr2:188093537-188093587	U87	brain:	n/a
35	chr2:188093537-188093587	HIPEpiC	eye:	n/a
36	chr2:188128809-188128859	AoSMC	blood vessel:	n/a
37	chr2:188093537-188093587	NHBE	bronchial:	n/a
38	chr2:188093537-188093587	HNPCEpiC	eye:	n/a
39	chr2:188093537-188093587	GM06990	blood:	n/a
40	chr2:188128809-188128859	SK-N-SH_RA	brain:	n/a
41	chr2:188128809-188128859	GM06990	blood:	n/a
42	chr2:188093537-188093587	HCF	heart:	n/a
43	chr2:188093537-188093587	AG04449	skin:	fetal
44	chr2:188128809-188128859	BJ	skin:	n/a
45	chr2:188128809-188128859	IMR90	lung:	fetal
46	chr2:188128809-188128859	H1-hESC	embryonic stem cell:	embryo
47	chr2:188128809-188128859	PANC-1	pancreas:	n/a
48	chr2:188093537-188093587	HPAEpiC	pulmonary alveolar:	n/a
49	chr2:188093537-188093587	HCPEpiC	choroid plexus:	n/a
50	chr2:188128809-188128859	HepG2	liver:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:188115424..188118005-chr2:188119188..188121188,2	MCF-7	breast:
2	chr2:188110055..188111838-chr2:188114697..188116780,2	K562	blood:
3	chr2:188118124..188120319-chr2:188121977..188123485,2	MCF-7	breast:
4	chr2:188081497..188084400-chr2:188085542..188087074,2	K562	blood:
5	chr2:188049075..188051640-chr2:188058153..188060182,2	K562	blood:
6	chr2:188081497..188084400-chr2:188085542..188087074,2	K562	blood:
7	chr2:188118124..188120319-chr2:188121977..188123485,2	MCF-7	breast:
8	chr2:188082290..188085324-chr2:188088101..188090494,3	K562	blood:
9	chr2:188110055..188111838-chr2:188114697..188116780,2	K562	blood:
10	chr2:188108987..188110844-chr2:188112727..188114579,2	K562	blood:
11	chr2:188082290..188085324-chr2:188088101..188090494,3	K562	blood:
12	chr2:188049075..188051640-chr2:188058153..188060182,2	K562	blood:
13	chr2:188088219..188089827-chr2:188091606..188093417,2	K562	blood:
14	chr2:188088219..188089827-chr2:188091606..188093417,2	K562	blood:
15	chr2:188115424..188118005-chr2:188119188..188121188,2	MCF-7	breast:
16	chr2:188108987..188110844-chr2:188112727..188114579,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM171B-1	chr2:188042973-188043244	NONHSAT076011
2	lnc-FAM171B-1	chr2:188056562-188056658	NONHSAT076011
3	lnc-FAM171B-1	chr2:188060089-188060574	NONHSAT076011

No data

Variant related genes	Relation type
RNU6-989P	TF binding region
RNU6-989P	CpG island

Extended variants
information (count: 1498 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1498 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10931275	chr2:188035947-188035948	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs191288093	chr2:188035970-188035971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185444144	chr2:188035977-188035978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540155256	chr2:188036006-188036007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6738913	chr2:188036021-188036022	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs73049450	chr2:188036076-188036077	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs540435346	chr2:188036081-188036082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529981043	chr2:188036151-188036152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190695711	chr2:188036195-188036196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148008960	chr2:188036244-188036245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs6739126	chr2:188036252-188036253	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs562934383	chr2:188036260-188036261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530692941	chr2:188036293-188036294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182255183	chr2:188036404-188036405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555744720	chr2:188036418-188036419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs62172500	chr2:188036460-188036461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368098597	chr2:188036517-188036518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141623639	chr2:188036544-188036545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111810409	chr2:188036549-188036550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568031926	chr2:188036555-188036556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529021875	chr2:188036579-188036580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544647221	chr2:188036595-188036596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560161333	chr2:188036597-188036598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs115525360	chr2:188036617-188036618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147151929	chr2:188036624-188036625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186880597	chr2:188036628-188036629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566823764	chr2:188036630-188036631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544436194	chr2:188036690-188036691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs527694772	chr2:188036696-188036697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552593785	chr2:188036726-188036727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534096971	chr2:188036728-188036729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555942086	chr2:188036741-188036742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140584150	chr2:188036770-188036771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs58151847	chr2:188036812-188036813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556278794	chr2:188036815-188036816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577930042	chr2:188036876-188036877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571002128	chr2:188036881-188036882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376098336	chr2:188036889-188036890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35516605	chr2:188036918-188036919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545424886	chr2:188036930-188036931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189264086	chr2:188036939-188036940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531816311	chr2:188036943-188036944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144550101	chr2:188036949-188036950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs7591971	chr2:188036991-188036992	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs181250119	chr2:188037037-188037038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147435296	chr2:188037040-188037041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564829999	chr2:188037058-188037059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185747665	chr2:188037071-188037072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532718442	chr2:188037073-188037074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372555395	chr2:188037079-188037080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
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
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188033600-188036800	Enhancers	GM12878-XiMat	blood
2	chr2:188035000-188037200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr2:188035200-188036800	Weak transcription	Ovary	ovary
4	chr2:188036000-188036200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr2:188036400-188036800	Enhancers	Stomach Mucosa	stomach
6	chr2:188042000-188042400	Active TSS	Spleen	Spleen
7	chr2:188052200-188054600	Enhancers	HUVEC	blood vessel
8	chr2:188052200-188055600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:188052400-188053000	Enhancers	Muscle Satellite Cultured Cells	--
10	chr2:188052600-188052800	Enhancers	Stomach Mucosa	stomach
11	chr2:188052800-188053400	Weak transcription	Stomach Mucosa	stomach
12	chr2:188053000-188053400	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr2:188053200-188055000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:188053400-188054200	Enhancers	Muscle Satellite Cultured Cells	--
15	chr2:188053400-188054200	Enhancers	Stomach Mucosa	stomach
16	chr2:188053600-188053800	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr2:188053600-188054200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr2:188053600-188054400	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr2:188053800-188054000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
20	chr2:188053800-188054200	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr2:188054000-188054200	Active TSS	Rectal Mucosa Donor 31	rectum
22	chr2:188054000-188054600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr2:188054200-188054600	Weak transcription	Stomach Mucosa	stomach
24	chr2:188054600-188055400	Enhancers	Stomach Mucosa	stomach
25	chr2:188062400-188063600	Enhancers	HUVEC	blood vessel
26	chr2:188070200-188071400	Enhancers	HUVEC	blood vessel
27	chr2:188070400-188071200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr2:188070600-188071200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr2:188070800-188071000	Enhancers	Adipose Nuclei	Adipose
30	chr2:188070800-188071200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr2:188072400-188073400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr2:188072800-188073400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr2:188074600-188074800	Enhancers	Fetal Intestine Small	intestine
34	chr2:188074800-188075000	Weak transcription	Fetal Intestine Small	intestine
35	chr2:188075000-188075600	ZNF genes & repeats	Fetal Intestine Small	intestine
36	chr2:188075200-188075400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr2:188075200-188075800	Enhancers	Fetal Intestine Large	intestine
38	chr2:188079400-188080200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr2:188080000-188081200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr2:188080000-188082000	Enhancers	HSMMtube	muscle
41	chr2:188080200-188080400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr2:188080200-188080600	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr2:188080200-188080600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr2:188080200-188080600	Enhancers	HSMM	muscle
45	chr2:188080200-188080800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr2:188080200-188081000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr2:188080400-188080800	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr2:188080400-188080800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr2:188080400-188080800	Enhancers	Muscle Satellite Cultured Cells	--
50	chr2:188080400-188080800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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