Variant report

Variant	nsv873224
Chromosome Location	chr1:224746577-224794913
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	ATF1	chr1:224752911-224753149	K562	blood:	n/a	n/a
2	BCL3	chr1:224750568-224750825	GM12878	blood:	n/a	n/a
3	BCL3	chr1:224750529-224750779	GM12878	blood:	n/a	n/a
4	BRCA1	chr1:224753076-224753137	HepG2	liver:	n/a	n/a
5	CBX3	chr1:224752747-224753455	HCT-116	colon:	n/a	n/a
6	CBX3	chr1:224752690-224753428	HCT-116	colon:	n/a	n/a
7	CEBPB	chr1:224752633-224753380	HCT-116	colon:	n/a	chr1:224752954-224752965 chr1:224752822-224752833 chr1:224752822-224752833 chr1:224752822-224752835
8	CEBPB	chr1:224752799-224753185	A549	lung:	n/a	chr1:224752954-224752965 chr1:224752822-224752833 chr1:224752822-224752833 chr1:224752822-224752835
9	CEBPB	chr1:224780883-224781185	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:224752717-224753343	Hela-S3	cervix:	n/a	chr1:224752954-224752965 chr1:224752822-224752833 chr1:224752822-224752833 chr1:224752822-224752835
11	CEBPB	chr1:224752569-224753467	HCT-116	colon:	n/a	chr1:224752954-224752965 chr1:224752822-224752833 chr1:224752822-224752833 chr1:224752822-224752835
12	CEBPB	chr1:224752825-224753170	HepG2	liver:	n/a	chr1:224752954-224752965
13	CEBPB	chr1:224781737-224781826	K562	blood:	n/a	n/a
14	CEBPB	chr1:224781635-224781893	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:224752739-224753448	IMR90	lung:	n/a	chr1:224752954-224752965 chr1:224752822-224752833 chr1:224752822-224752833 chr1:224752822-224752835
16	CEBPB	chr1:224772336-224772497	A549	lung:	n/a	n/a
17	CEBPB	chr1:224752683-224753292	A549	lung:	n/a	chr1:224752954-224752965 chr1:224752822-224752833 chr1:224752822-224752833 chr1:224752822-224752835
18	CEBPB	chr1:224752772-224753349	A549	lung:	n/a	chr1:224752954-224752965 chr1:224752822-224752833 chr1:224752822-224752833 chr1:224752822-224752835
19	CEBPB	chr1:224752722-224753226	MCF-7	breast:	n/a	chr1:224752954-224752965 chr1:224752822-224752833 chr1:224752822-224752833 chr1:224752822-224752835
20	CHD2	chr1:224752841-224753284	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr1:224776460-224776610	HFF-Myc	foreskin:	n/a	chr1:224776565-224776573 chr1:224776490-224776511
22	CTCF	chr1:224782140-224782290	BE2_C	brain:	n/a	n/a
23	CTCF	chr1:224752402-224752409	NHEK	skin:	n/a	n/a
24	CTCF	chr1:224768670-224768790	K562	blood:	n/a	n/a
25	CTCF	chr1:224752415-224752434	NHEK	skin:	n/a	n/a
26	CTCF	chr1:224768629-224768872	K562	blood:	n/a	n/a
27	CTCF	chr1:224748040-224748190	HMEC	breast:	n/a	n/a
28	CTCF	chr1:224777359-224777534	GM12878	blood:	n/a	n/a
29	CTCF	chr1:224780380-224780530	GM12868	blood:	n/a	n/a
30	CTCF	chr1:224782000-224782150	NB4	blood:	n/a	n/a
31	CTCF	chr1:224782180-224782330	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr1:224768689-224768735	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr1:224782100-224782250	MCF-7	breast:	n/a	n/a
34	CTCF	chr1:224748080-224748230	HPF	lung:	n/a	n/a
35	CTCF	chr1:224752300-224752450	NB4	blood:	n/a	chr1:224752409-224752422 chr1:224752406-224752424
36	CTCF	chr1:224750380-224750530	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr1:224752660-224752810	NHLF	lung:	n/a	n/a
38	CTCF	chr1:224767340-224767490	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr1:224776800-224776950	HBMEC	blood vessel:	n/a	n/a
40	E2F4	chr1:224750655-224750914	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr1:224752653-224753160	MCF10A-Er-Src	breast:	n/a	chr1:224752728-224752737
42	E2F4	chr1:224772321-224772479	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr1:224768757-224768760	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr1:224746602-224746841	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr1:224769104-224769187	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr1:224781141-224781309	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F6	chr1:224794110-224794572	H1-hESC	embryonic stem cell:	n/a	n/a
48	E2F6	chr1:224794012-224794702	H1-hESC	embryonic stem cell:	n/a	n/a
49	EGR1	chr1:224778401-224778644	K562	blood:	n/a	chr1:224778511-224778521 chr1:224778510-224778523 chr1:224778511-224778522 chr1:224778510-224778523 chr1:224778509-224778524 chr1:224778510-224778520 chr1:224778510-224778523 chr1:224778510-224778523 chr1:224778509-224778523 chr1:224778508-224778518 chr1:224778511-224778521 chr1:224778511-224778520
50	ELK1	chr1:224752846-224753189	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:224759763-224759813	HCF	heart:	n/a
2	chr1:224776790-224776840	AoSMC	blood vessel:	n/a
3	chr1:224753137-224753187	GM19239	blood:	n/a
4	chr1:224753137-224753187	CMK	blood:	n/a
5	chr1:224776790-224776840	HRCEpiC	kidney:	n/a
6	chr1:224776790-224776840	NHDF-neo	bronchial:	n/a
7	chr1:224753137-224753187	H1-hESC	embryonic stem cell:	embryo
8	chr1:224776790-224776840	Jurkat	blood:	n/a
9	chr1:224781135-224781185	HMEC	breast:	n/a
10	chr1:224753137-224753187	HCM	heart:	n/a
11	chr1:224776790-224776840	HIPEpiC	eye:	n/a
12	chr1:224776790-224776840	HCT-116	colon:	n/a
13	chr1:224781135-224781185	GM12878	blood:	n/a
14	chr1:224759763-224759813	PANC-1	pancreas:	n/a
15	chr1:224781135-224781185	HRCEpiC	kidney:	n/a
16	chr1:224769272-224769322	Hela-S3	cervix:	n/a
17	chr1:224753137-224753187	HL-60	blood:	n/a
18	chr1:224759763-224759813	GM12878	blood:	n/a
19	chr1:224781135-224781185	NHBE	bronchial:	n/a
20	chr1:224753137-224753187	BE2_C	brain:	n/a
21	chr1:224776790-224776840	AG04449	skin:	fetal
22	chr1:224769272-224769322	HPAEpiC	pulmonary alveolar:	n/a
23	chr1:224769272-224769322	T-47D	breast:	n/a
24	chr1:224776790-224776840	NHBE	bronchial:	n/a
25	chr1:224776790-224776840	A549	lung:	n/a
26	chr1:224769272-224769322	AG04449	skin:	fetal
27	chr1:224759763-224759813	AG04450	lung:	fetal
28	chr1:224781135-224781185	AG09319	gingival:	n/a
29	chr1:224759763-224759813	ovcar-3	ovarian:	n/a
30	chr1:224759763-224759813	SK-N-SH	brain:	n/a
31	chr1:224759763-224759813	MCF10A-Er-Src	breast:	n/a
32	chr1:224769272-224769322	HCPEpiC	choroid plexus:	n/a
33	chr1:224781135-224781185	ProgFib	skin:	n/a
34	chr1:224753137-224753187	HRCEpiC	kidney:	n/a
35	chr1:224759763-224759813	Caco-2	colon:	n/a
36	chr1:224769272-224769322	Jurkat	blood:	n/a
37	chr1:224759763-224759813	GM06990	blood:	n/a
38	chr1:224759763-224759813	HCPEpiC	choroid plexus:	n/a
39	chr1:224776790-224776840	GM12891	blood:	n/a
40	chr1:224759763-224759813	HNPCEpiC	eye:	n/a
41	chr1:224753137-224753187	AG04450	lung:	fetal
42	chr1:224753137-224753187	HPAEpiC	pulmonary alveolar:	n/a
43	chr1:224769272-224769322	NH-A	brain:	n/a
44	chr1:224776790-224776840	GM12878	blood:	n/a
45	chr1:224759763-224759813	AG09319	gingival:	n/a
46	chr1:224753137-224753187	U87	brain:	n/a
47	chr1:224759763-224759813	NT2-D1	testis:	n/a
48	chr1:224769272-224769322	PrEC	prostate:	n/a
49	chr1:224776790-224776840	HAEpiC	amniotic membrane:	n/a
50	chr1:224781135-224781185	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:224783008..224785981-chr1:224788493..224791449,2	MCF-7	breast:
2	chr1:224701543..224702095-chr1:224768528..224769263,2	K562	blood:
3	chr1:224783008..224785981-chr1:224788493..224791449,2	MCF-7	breast:
4	chr1:224701148..224701914-chr1:224753158..224753989,2	MCF-7	breast:
5	chr1:224766554..224768358-chr1:224768729..224770642,2	K562	blood:
6	chr1:224760255..224762194-chr1:224803067..224805853,2	MCF-7	breast:
7	chr1:224715312..224717948-chr1:224757102..224759295,2	K562	blood:
8	chr1:224766554..224768358-chr1:224768729..224770642,2	K562	blood:
9	chr1:224772952..224775800-chr1:224777887..224779617,2	K562	blood:
10	chr1:224778814..224780539-chr1:224784357..224786736,2	K562	blood:
11	chr1:224778814..224780539-chr1:224784357..224786736,2	K562	blood:
12	chr1:224751582..224753460-chr17:58156585..58158149,2	MCF-7	breast:
13	chr1:224701239..224702203-chr1:224768211..224768996,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNIH3-2	chr1:224753901-224753966	NONHSAT009813
2	lnc-CNIH3-2	chr1:224776063-224776306	NONHSAT009816
3	lnc-WDR26-1	chr1:224789942-224793023	ucscGeneNc_uc001hqe_1
4	lnc-CNIH3-2	chr1:224774842-224775122	NONHSAT009816
5	lnc-CNIH3-2	chr1:224770866-224770969	NONHSAT009801
6	lnc-CNIH3-2	chr1:224753901-224753966	NONHSAT009815
7	lnc-CNIH3-2	chr1:224774868-224775122	NONHSAT009813
8	lnc-CNIH3-2	chr1:224776063-224776318	NONHSAT009801
9	lnc-CNIH3-2	chr1:224753901-224753966	NONHSAT009801
10	lnc-CNIH3-2	chr1:224776063-224776194	NONHSAT009813
11	lnc-CNIH3-2	chr1:224770866-224770969	NONHSAT009813
12	lnc-CNIH3-2	chr1:224770866-224770969	NONHSAT009815
13	lnc-CNIH3-2	chr1:224776063-224776257	NONHSAT009815
14	lnc-CNIH3-2	chr1:224753067-224753524	NONHSAT009815

Variant related genes	Relation type
AKR1B1P1	TF binding region
CNIH3	TF binding region
AKR1B1P1	CpG island
CNIH3	CpG island
ENSG00000143786	chromatin interactions
ENSG00000267416	chromatin interactions
ENSG00000233384	chromatin interactions

Extended variants
information (count: 1775 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1775 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17571353	chr1:224746577-224746578	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs16849590	chr1:224746608-224746609	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs536389997	chr1:224746639-224746640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138430689	chr1:224746648-224746649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576774744	chr1:224746650-224746651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544316949	chr1:224746747-224746748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186280891	chr1:224746756-224746757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs368934567	chr1:224746760-224746761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577136269	chr1:224746934-224746935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562517252	chr1:224746957-224746958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs149280708	chr1:224746958-224746959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553559982	chr1:224746981-224746982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574925115	chr1:224747009-224747010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190794886	chr1:224747014-224747015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532910206	chr1:224747045-224747046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs35628340	chr1:224747054-224747055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs530997339	chr1:224747056-224747057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545536999	chr1:224747090-224747091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546233403	chr1:224747102-224747103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564455351	chr1:224747183-224747184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73115929	chr1:224747186-224747187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs115747144	chr1:224747190-224747191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs185544720	chr1:224747219-224747220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565910086	chr1:224747237-224747238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529860532	chr1:224747247-224747248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548320807	chr1:224747249-224747250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569673735	chr1:224747286-224747287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567023727	chr1:224747289-224747290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs61825841	chr1:224747303-224747304	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs79418107	chr1:224747375-224747376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs10916639	chr1:224747445-224747446	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs535032121	chr1:224747491-224747492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182988737	chr1:224747499-224747500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs117457707	chr1:224747501-224747502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs12128745	chr1:224747578-224747579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs10916640	chr1:224747597-224747598	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs114098163	chr1:224747682-224747683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191065065	chr1:224747684-224747685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112577060	chr1:224747700-224747701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561238153	chr1:224747726-224747727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573263022	chr1:224747743-224747744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540584130	chr1:224747748-224747749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530375067	chr1:224747798-224747799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550453773	chr1:224747868-224747869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559392916	chr1:224747896-224747897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs369262436	chr1:224747908-224747909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529974546	chr1:224747951-224747952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574490171	chr1:224748009-224748010	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs183886508	chr1:224748018-224748019	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs563127735	chr1:224748045-224748046	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:350 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224740000-224762200	Weak transcription	Ovary	ovary
2	chr1:224741400-224751400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr1:224742000-224753000	Weak transcription	Pancreas	Pancrea
4	chr1:224745800-224748400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:224746000-224747800	Enhancers	HMEC	breast
6	chr1:224746000-224748600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr1:224746200-224747800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr1:224746200-224748400	Enhancers	NHDF-Ad	bronchial
9	chr1:224746200-224748400	Enhancers	NHEK	skin
10	chr1:224746400-224747000	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr1:224746400-224747200	Enhancers	Psoas Muscle	Psoas
12	chr1:224746400-224748000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:224746400-224748200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:224746400-224748600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr1:224746800-224748200	Enhancers	Muscle Satellite Cultured Cells	--
16	chr1:224747000-224747200	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr1:224747000-224751000	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr1:224747200-224751400	Weak transcription	Psoas Muscle	Psoas
19	chr1:224747200-224751600	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr1:224747600-224748200	Enhancers	Osteobl	bone
21	chr1:224747800-224748000	Weak transcription	HMEC	breast
22	chr1:224747800-224750400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:224748000-224748200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:224748000-224749800	ZNF genes & repeats	HMEC	breast
25	chr1:224748200-224748800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:224748200-224750200	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr1:224748200-224750400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:224748200-224752200	Weak transcription	Osteobl	bone
29	chr1:224748400-224748600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr1:224748400-224749400	Weak transcription	NHDF-Ad	bronchial
31	chr1:224748600-224749000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr1:224748600-224749200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr1:224748600-224749800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:224748800-224750000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:224749000-224753200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr1:224749200-224752400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr1:224749400-224753200	Enhancers	NHDF-Ad	bronchial
38	chr1:224749800-224750000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:224749800-224750000	Weak transcription	HMEC	breast
40	chr1:224750000-224750600	Enhancers	NHLF	lung
41	chr1:224750000-224753200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:224750000-224754000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:224750000-224754000	Enhancers	HMEC	breast
44	chr1:224750200-224752400	Enhancers	Muscle Satellite Cultured Cells	--
45	chr1:224750400-224750600	Enhancers	HUVEC	blood vessel
46	chr1:224750400-224750800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:224750400-224750800	Enhancers	NH-A	brain
48	chr1:224750400-224751400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr1:224750400-224754000	Enhancers	NHEK	skin
50	chr1:224750600-224752200	Weak transcription	NHLF	lung

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