Variant report

Variant	nsv3034
Chromosome Location	chr2:173160295-173200113
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:173194742-173195206	HepG2	liver:	n/a	n/a
2	BACH1	chr2:173162282-173162550	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr2:173194776-173195095	HepG2	liver:	n/a	n/a
4	BHLHE40	chr2:173194168-173194501	HepG2	liver:	n/a	n/a
5	CEBPB	chr2:173195038-173195201	A549	lung:	n/a	chr2:173195144-173195155 chr2:173195143-173195154
6	CEBPB	chr2:173164366-173164683	A549	lung:	n/a	chr2:173164525-173164536 chr2:173164524-173164535
7	CEBPB	chr2:173164356-173164756	Hela-S3	cervix:	n/a	chr2:173164525-173164536 chr2:173164524-173164535
8	CEBPB	chr2:173164443-173164646	HepG2	liver:	n/a	chr2:173164525-173164536 chr2:173164524-173164535
9	CEBPB	chr2:173164353-173164824	MCF-7	breast:	n/a	chr2:173164525-173164536 chr2:173164807-173164818 chr2:173164524-173164535
10	CEBPB	chr2:173194837-173195301	HepG2	liver:	n/a	chr2:173195144-173195155 chr2:173195143-173195154
11	CEBPB	chr2:173164349-173164959	MCF-7	breast:	n/a	chr2:173164525-173164536 chr2:173164807-173164818 chr2:173164524-173164535
12	CEBPB	chr2:173165647-173165878	Hela-S3	cervix:	n/a	chr2:173165725-173165736
13	CEBPB	chr2:173194844-173195323	HepG2	liver:	n/a	chr2:173195144-173195155 chr2:173195143-173195154
14	CEBPB	chr2:173195014-173195205	HepG2	liver:	n/a	chr2:173195144-173195155 chr2:173195143-173195154
15	CEBPB	chr2:173164365-173164706	ECC-1	luminal epithelium:	n/a	chr2:173164525-173164536 chr2:173164524-173164535
16	CEBPB	chr2:173164347-173164770	IMR90	lung:	n/a	chr2:173164525-173164536 chr2:173164524-173164535
17	CEBPB	chr2:173164355-173164717	A549	lung:	n/a	chr2:173164525-173164536 chr2:173164524-173164535
18	CEBPB	chr2:173165632-173165844	HepG2	liver:	n/a	chr2:173165725-173165736
19	CEBPB	chr2:173194896-173195330	HepG2	liver:	n/a	chr2:173195144-173195155 chr2:173195143-173195154
20	CEBPD	chr2:173194751-173195197	HepG2	liver:	n/a	chr2:173195144-173195155
21	CHD1	chr2:173191641-173191668	GM12878	blood:	n/a	n/a
22	CHD2	chr2:173199843-173199871	HepG2	liver:	n/a	n/a
23	CHD2	chr2:173194956-173195156	HepG2	liver:	n/a	n/a
24	CTCF	chr2:173169997-173170084	MCF-7	breast:	n/a	chr2:173170059-173170077 chr2:173170054-173170075
25	CTCF	chr2:173199820-173199970	AG09309	skin:	n/a	chr2:173199936-173199945
26	CTCF	chr2:173199733-173200011	H1-hESC	embryonic stem cell:	n/a	chr2:173199936-173199945
27	CTCF	chr2:173199820-173199970	HepG2	liver:	n/a	chr2:173199936-173199945
28	CTCF	chr2:173170380-173170530	GM12866	blood:	n/a	n/a
29	CTCF	chr2:173169997-173170107	MCF-7	breast:	n/a	chr2:173170059-173170077 chr2:173170054-173170075
30	CTCF	chr2:173199916-173199946	MCF-7	breast:	n/a	chr2:173199936-173199945
31	CTCF	chr2:173194580-173194730	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr2:173173520-173173670	HMEC	breast:	n/a	n/a
33	CTCF	chr2:173199873-173199898	Fibrobl	skin:	n/a	n/a
34	CTCF	chr2:173169999-173170085	MCF-7	breast:	n/a	chr2:173170059-173170077 chr2:173170054-173170075
35	CTCF	chr2:173199838-173199968	H1-hESC	embryonic stem cell:	n/a	chr2:173199936-173199945
36	CTCF	chr2:173199840-173199990	HepG2	liver:	n/a	chr2:173199936-173199945
37	CTCF	chr2:173173580-173173730	HepG2	liver:	n/a	n/a
38	CTCF	chr2:173169972-173170093	MCF-7	breast:	n/a	chr2:173170059-173170077 chr2:173170054-173170075
39	CTCF	chr2:173178600-173178750	HepG2	liver:	n/a	chr2:173178612-173178625
40	CTCF	chr2:173174569-173174598	GM10266	blood:	n/a	n/a
41	CTCF	chr2:173199759-173199992	H1-hESC	embryonic stem cell:	n/a	chr2:173199936-173199945
42	CTCF	chr2:173188120-173188270	SAEC	small airway:	n/a	n/a
43	CTCF	chr2:173188200-173188350	SAEC	small airway:	n/a	n/a
44	CTCF	chr2:173188100-173188250	GM12872	blood:	n/a	n/a
45	CTCF	chr2:173170017-173170081	MCF-7	breast:	n/a	chr2:173170059-173170077 chr2:173170054-173170075
46	CTCF	chr2:173199840-173199990	HBMEC	blood vessel:	n/a	chr2:173199936-173199945
47	E2F4	chr2:173163213-173163379	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr2:173161237-173161437	MCF10A-Er-Src	breast:	n/a	n/a
49	EGR1	chr2:173185901-173186116	GM12878	blood:	n/a	n/a
50	EP300	chr2:173194707-173195272	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:173189711-173189761	HEEpiC	esophagus:	n/a
2	chr2:173161382-173161432	HepG2	liver:	n/a
3	chr2:173161382-173161432	SKMC	muscle:	n/a
4	chr2:173189711-173189761	AoSMC	blood vessel:	n/a
5	chr2:173161382-173161432	HRE	kidney:	n/a
6	chr2:173189711-173189761	NHBE	bronchial:	n/a
7	chr2:173189711-173189761	PFSK-1	brain:	n/a
8	chr2:173161382-173161432	AG10803	skin:	n/a
9	chr2:173161382-173161432	NHBE	bronchial:	n/a
10	chr2:173189711-173189761	NHDF-neo	bronchial:	n/a
11	chr2:173189711-173189761	HL-60	blood:	n/a
12	chr2:173161382-173161432	NHDF-neo	bronchial:	n/a
13	chr2:173189711-173189761	GM12878	blood:	n/a
14	chr2:173189711-173189761	SK-N-SH	brain:	n/a
15	chr2:173161382-173161432	HMEC	breast:	n/a
16	chr2:173189711-173189761	AG04449	skin:	fetal
17	chr2:173189711-173189761	A549	lung:	n/a
18	chr2:173189711-173189761	HAEpiC	amniotic membrane:	n/a
19	chr2:173161382-173161432	GM12892	blood:	n/a
20	chr2:173189711-173189761	ECC-1	luminal epithelium:	n/a
21	chr2:173189711-173189761	NB4	blood:	n/a
22	chr2:173161382-173161432	CMK	blood:	n/a
23	chr2:173161382-173161432	HCM	heart:	n/a
24	chr2:173189711-173189761	AG04450	lung:	fetal
25	chr2:173189711-173189761	HRPEpiC	eye:	n/a
26	chr2:173161382-173161432	K562	blood:	n/a
27	chr2:173161382-173161432	HAEpiC	amniotic membrane:	n/a
28	chr2:173161382-173161432	HUVEC	blood vessel:	n/a
29	chr2:173161382-173161432	HCPEpiC	choroid plexus:	n/a
30	chr2:173189711-173189761	ProgFib	skin:	n/a
31	chr2:173161382-173161432	HCF	heart:	n/a
32	chr2:173189711-173189761	HCF	heart:	n/a
33	chr2:173189711-173189761	Hepatocyte	liver:	n/a
34	chr2:173189711-173189761	K562	blood:	n/a
35	chr2:173161382-173161432	Caco-2	colon:	n/a
36	chr2:173189711-173189761	RPTEC	kidney:	n/a
37	chr2:173189711-173189761	GM12892	blood:	n/a
38	chr2:173189711-173189761	SK-N-SH_RA	brain:	n/a
39	chr2:173161382-173161432	T-47D	breast:	n/a
40	chr2:173161382-173161432	HL-60	blood:	n/a
41	chr2:173189711-173189761	HIPEpiC	eye:	n/a
42	chr2:173161382-173161432	AG09319	gingival:	n/a
43	chr2:173189711-173189761	CMK	blood:	n/a
44	chr2:173189711-173189761	HNPCEpiC	eye:	n/a
45	chr2:173161382-173161432	GM06990	blood:	n/a
46	chr2:173161382-173161432	ovcar-3	ovarian:	n/a
47	chr2:173161382-173161432	ECC-1	luminal epithelium:	n/a
48	chr2:173189711-173189761	H1-hESC	embryonic stem cell:	embryo
49	chr2:173189711-173189761	Jurkat	blood:	n/a
50	chr2:173161382-173161432	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:173160107..173161108-chr6:26033351..26034011,4	Hela-S3	cervix:
2	chr2:173156581..173161480-chr2:173162847..173166156,5	MCF-7	breast:
3	chr2:173160607..173162129-chr6:26033215..26035045,5	MCF-7	breast:
4	chr2:173156581..173161480-chr2:173162847..173166156,5	MCF-7	breast:
5	chr2:173163058..173164820-chr2:173292652..173294328,2	MCF-7	breast:
6	chr2:173171784..173174881-chr2:173175432..173178185,3	K562	blood:
7	chr12:64796275..64798837-chr2:173189092..173191039,2	MCF-7	breast:
8	chr2:173175651..173178554-chr2:173291420..173293345,2	MCF-7	breast:
9	chr2:173171784..173174881-chr2:173175432..173178185,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DLX2-1	chr2:173190824-173190935	XLOC_002392
2	lnc-ITGA6-1	chr2:173188078-173188868	XLOC_001757
3	lnc-ITGA6-1	chr2:173188078-173188161	XLOC_001757
4	lnc-DLX2-1	chr2:173188078-173188864	XLOC_002392
5	lnc-ITGA6-2	chr2:173180016-173180136	NONHSAT075499
6	lnc-ITGA6-2	chr2:173188078-173188292	NONHSAT075495
7	lnc-ITGA6-2	chr2:173162925-173163071	NONHSAT075495
8	lnc-ITGA6-1	chr2:173165904-173165944	XLOC_001757
9	lnc-ITGA6-1	chr2:173188078-173188465	XLOC_001757
10	lnc-ITGA6-1	chr2:173188078-173188243	XLOC_001757
11	lnc-ITGA6-2	chr2:173188079-173188243	NONHSAT075499
12	lnc-ITGA6-1	chr2:173180015-173180136	XLOC_001757
13	lnc-ITGA6-1	chr2:173162904-173163071	XLOC_001757
14	lnc-ITGA6-1	chr2:173162942-173163071	XLOC_001757
15	lnc-ITGA6-1	chr2:173188050-173188243	XLOC_001757

Variant related genes	Relation type
ENSG00000232555	TF binding region
ENSG00000232555	CpG island
ENSG00000184575	chromatin interactions
ENSG00000091409	chromatin interactions
ENSG00000226963	chromatin interactions
ENSG00000137259	chromatin interactions
OLR1	miRNA target sites
KIAA0319L	miRNA target sites
TRANK1	miRNA target sites

Extended variants
information (count: 1450 )
Associated
traits (count: 47 )

Variant overlapped rSNPs/rCNVs (count:1450 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184788695	chr2:173160301-173160302	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs551559126	chr2:173160302-173160303	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs570176766	chr2:173160352-173160353	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs7425702	chr2:173160377-173160378	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs189493744	chr2:173160394-173160395	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs181391758	chr2:173160397-173160398	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs535383750	chr2:173160409-173160410	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs372636208	chr2:173160411-173160412	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs186071382	chr2:173160448-173160449	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs4594405	chr2:173160489-173160490	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs139635392	chr2:173160490-173160491	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs190639926	chr2:173160545-173160546	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs543604673	chr2:173160547-173160548	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs77398198	chr2:173160555-173160556	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs529574968	chr2:173160563-173160564	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs558928342	chr2:173160595-173160596	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs147630898	chr2:173160627-173160628	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs560117630	chr2:173160641-173160642	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs149043324	chr2:173160674-173160675	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs71415281	chr2:173160707-173160708	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs4429441	chr2:173160731-173160732	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs376719608	chr2:173160736-173160737	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs376806382	chr2:173160785-173160786	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs549682374	chr2:173160838-173160839	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs59649469	chr2:173160858-173160859	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs73033222	chr2:173160874-173160875	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs553632455	chr2:173160878-173160879	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs143024997	chr2:173160888-173160889	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs539055501	chr2:173160943-173160944	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs151176708	chr2:173160957-173160958	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs576026596	chr2:173161029-173161030	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543518246	chr2:173161038-173161039	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs555532670	chr2:173161096-173161097	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs563075344	chr2:173161130-173161131	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs530988255	chr2:173161183-173161184	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574260681	chr2:173161259-173161260	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs141082875	chr2:173161268-173161269	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs368014651	chr2:173161277-173161278	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs372224499	chr2:173161288-173161289	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs560078402	chr2:173161327-173161328	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs578202873	chr2:173161353-173161354	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs12624040	chr2:173161379-173161380	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs563724500	chr2:173161424-173161425	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs530876192	chr2:173161438-173161439	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs549441965	chr2:173161489-173161490	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs561074468	chr2:173161525-173161526	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs145309708	chr2:173161548-173161549	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs11674489	chr2:173161679-173161680	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs565600640	chr2:173161722-173161723	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs539724836	chr2:173161753-173161754	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:47)

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
Cancer	20164919	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
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	16573809	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Donnai-Barrow syndrome	21085971	CNVD
Breast cancer	21045282	CNVD
Limb abnormalities	22140379	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173151400-173168000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:173153600-173160800	Weak transcription	Right Atrium	heart
3	chr2:173158000-173160800	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr2:173158200-173160800	Enhancers	Pancreas	Pancrea
5	chr2:173158600-173161000	Enhancers	Stomach Mucosa	stomach
6	chr2:173159200-173160600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:173159200-173160600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr2:173159200-173160600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr2:173159200-173160600	Weak transcription	NHEK	skin
10	chr2:173159200-173160800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr2:173159200-173162200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr2:173159200-173162200	Weak transcription	Ovary	ovary
13	chr2:173159200-173164400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr2:173159200-173164600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr2:173159400-173160600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr2:173159400-173160600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr2:173159400-173161400	Weak transcription	Osteobl	bone
18	chr2:173159400-173164200	Weak transcription	HMEC	breast
19	chr2:173160400-173160800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
20	chr2:173160400-173160800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr2:173160400-173161000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr2:173160400-173161000	Enhancers	Right Ventricle	heart
23	chr2:173160400-173161800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
24	chr2:173160400-173162400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
25	chr2:173160400-173162600	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr2:173160400-173162800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
27	chr2:173160600-173160800	Enhancers	Esophagus	oesophagus
28	chr2:173160600-173161000	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
29	chr2:173160600-173161000	Bivalent Enhancer	Fetal Heart	heart
30	chr2:173160600-173161200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
31	chr2:173160600-173161400	Enhancers	Left Ventricle	heart
32	chr2:173160600-173161600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr2:173160600-173161800	Enhancers	NHEK	skin
34	chr2:173160600-173162000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr2:173160600-173162200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
36	chr2:173160600-173162200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr2:173160600-173162400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr2:173160600-173162600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
39	chr2:173160600-173162600	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr2:173160600-173162600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr2:173160600-173163200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
42	chr2:173160800-173161000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
43	chr2:173160800-173161000	Enhancers	Psoas Muscle	Psoas
44	chr2:173160800-173161200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr2:173160800-173161400	Enhancers	Right Atrium	heart
46	chr2:173160800-173161600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr2:173161000-173161200	Enhancers	H9 Cell Line	embryonic stem cell
48	chr2:173161000-173162400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr2:173161000-173163200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
50	chr2:173161200-173172600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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