Variant report

Variant	nsv997782
Chromosome Location	chr1:71628776-71668906
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	CEBPB	chr1:71655590-71655695	IMR90	lung:	n/a	n/a
2	CTCF	chr1:71662520-71662670	HMEC	breast:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
3	CTCF	chr1:71636720-71636870	HEK293	kidney:	n/a	n/a
4	CTCF	chr1:71662480-71662630	SK-N-SH_RA	brain:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
5	CTCF	chr1:71662520-71662670	HRPEpiC	eye:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
6	CTCF	chr1:71662520-71662670	GM06990	blood:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
7	CTCF	chr1:71662520-71662670	BJ	skin:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
8	CTCF	chr1:71662480-71662630	HPF	lung:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
9	CTCF	chr1:71662460-71662610	AG09319	gingival:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
10	CTCF	chr1:71662525-71662591	MCF-7	breast:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
11	CTCF	chr1:71636740-71636878	MCF-7	breast:	n/a	n/a
12	CTCF	chr1:71636700-71636850	NHDF-neo	bronchial:	n/a	n/a
13	CTCF	chr1:71636760-71636910	AG09319	gingival:	n/a	n/a
14	CTCF	chr1:71636743-71636853	LNCaP	prostate:	n/a	n/a
15	CTCF	chr1:71662440-71662590	AG04450	lung:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
16	CTCF	chr1:71662450-71662687	HUVEC	blood vessel:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
17	CTCF	chr1:71636760-71636910	HEK293	kidney:	n/a	n/a
18	CTCF	chr1:71662540-71662690	GM06990	blood:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
19	CTCF	chr1:71662459-71662700	Medullo	brain:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
20	CTCF	chr1:71662440-71662590	HFF	foreskin:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
21	CTCF	chr1:71636681-71636881	GM12878	blood:	n/a	n/a
22	CTCF	chr1:71662540-71662690	AG09309	skin:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
23	CTCF	chr1:71662500-71662650	HL-60	blood:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
24	CTCF	chr1:71662507-71662628	Lung_OC	lung:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
25	CTCF	chr1:71662140-71662290	HVMF	connective:	n/a	n/a
26	CTCF	chr1:71662496-71662639	Pancreas_OC	pancreas:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
27	CTCF	chr1:71662460-71662610	AG09309	skin:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
28	CTCF	chr1:71636740-71636890	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr1:71662475-71662688	H1-hESC	embryonic stem cell:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
30	CTCF	chr1:71662440-71662590	AG04449	skin:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
31	CTCF	chr1:71636640-71636790	HVMF	connective:	n/a	n/a
32	CTCF	chr1:71636640-71636790	NB4	blood:	n/a	n/a
33	CTCF	chr1:71636820-71636970	HFF	foreskin:	n/a	n/a
34	CTCF	chr1:71662400-71662550	HAc	cerebellar:	n/a	n/a
35	CTCF	chr1:71636660-71636810	HCM	heart:	n/a	n/a
36	CTCF	chr1:71636680-71636830	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr1:71662480-71662630	HCM	heart:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
38	CTCF	chr1:71662460-71662610	MCF-7	breast:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
39	CTCF	chr1:71636682-71636971	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr1:71636700-71636850	AG10803	skin:	n/a	n/a
41	CTCF	chr1:71662500-71662650	HCPEpiC	choroid plexus:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
42	CTCF	chr1:71636840-71636990	HCM	heart:	n/a	n/a
43	CTCF	chr1:71636740-71636810	GM19238	blood:	n/a	n/a
44	CTCF	chr1:71662480-71662630	HEEpiC	esophagus:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
45	CTCF	chr1:71662540-71662690	BE2_C	brain:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
46	CTCF	chr1:71662400-71662550	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr1:71662480-71662630	AG09319	gingival:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
48	CTCF	chr1:71662480-71662630	SAEC	small airway:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
49	CTCF	chr1:71662500-71662650	HPF	lung:	n/a	chr1:71662557-71662575 chr1:71662559-71662580
50	CTCF	chr1:71662420-71662570	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:71632244-71632294	U87	brain:	n/a
2	chr1:71632244-71632294	AG09319	gingival:	n/a
3	chr1:71632244-71632294	Hela-S3	cervix:	n/a
4	chr1:71632244-71632294	SK-N-SH_RA	brain:	n/a
5	chr1:71632244-71632294	SAEC	small airway:	n/a
6	chr1:71632244-71632294	ECC-1	luminal epithelium:	n/a
7	chr1:71632244-71632294	NHDF-neo	bronchial:	n/a
8	chr1:71632244-71632294	AG09309	skin:	n/a
9	chr1:71632244-71632294	GM12892	blood:	n/a
10	chr1:71632244-71632294	Caco-2	colon:	n/a
11	chr1:71632244-71632294	HCF	heart:	n/a
12	chr1:71632244-71632294	GM06990	blood:	n/a
13	chr1:71632244-71632294	CMK	blood:	n/a
14	chr1:71632244-71632294	AG04449	skin:	fetal
15	chr1:71632244-71632294	AoSMC	blood vessel:	n/a
16	chr1:71632244-71632294	HRPEpiC	eye:	n/a
17	chr1:71632244-71632294	GM12878	blood:	n/a
18	chr1:71632244-71632294	LNCaP	prostate:	n/a
19	chr1:71632244-71632294	HNPCEpiC	eye:	n/a
20	chr1:71632244-71632294	A549	lung:	n/a
21	chr1:71632244-71632294	NH-A	brain:	n/a
22	chr1:71632244-71632294	HAEpiC	amniotic membrane:	n/a
23	chr1:71632244-71632294	SK-N-SH	brain:	n/a
24	chr1:71632244-71632294	HCPEpiC	choroid plexus:	n/a
25	chr1:71632244-71632294	HRCEpiC	kidney:	n/a
26	chr1:71632244-71632294	GM12891	blood:	n/a
27	chr1:71632244-71632294	HIPEpiC	eye:	n/a
28	chr1:71632244-71632294	ProgFib	skin:	n/a
29	chr1:71632244-71632294	IMR90	lung:	fetal
30	chr1:71632244-71632294	NT2-D1	testis:	n/a
31	chr1:71632244-71632294	HMEC	breast:	n/a
32	chr1:71632244-71632294	NHBE	bronchial:	n/a
33	chr1:71632244-71632294	AG04450	lung:	fetal
34	chr1:71632244-71632294	MCF-7	breast:	n/a
35	chr1:71632244-71632294	RPTEC	kidney:	n/a
36	chr1:71632244-71632294	BJ	skin:	n/a
37	chr1:71632244-71632294	PFSK-1	brain:	n/a
38	chr1:71632244-71632294	SKMC	muscle:	n/a
39	chr1:71632244-71632294	Hepatocyte	liver:	n/a
40	chr1:71632244-71632294	HEK293	kidney:	embryo
41	chr1:71632244-71632294	SK-N-MC	brain:	n/a
42	chr1:71632244-71632294	H1-hESC	embryonic stem cell:	embryo
43	chr1:71632244-71632294	HUVEC	blood vessel:	n/a
44	chr1:71632244-71632294	HCT-116	colon:	n/a
45	chr1:71632244-71632294	PANC-1	pancreas:	n/a
46	chr1:71632244-71632294	GM19239	blood:	n/a
47	chr1:71632244-71632294	ovcar-3	ovarian:	n/a
48	chr1:71632244-71632294	HCM	heart:	n/a
49	chr1:71632244-71632294	K562	blood:	n/a
50	chr1:71632244-71632294	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:71662113..71662902-chr1:72053492..72054309,2	MCF-7	breast:
2	chr1:71654729..71657445-chr1:71668068..71670402,2	K562	blood:
3	chr1:71650900..71653329-chr1:71661783..71664278,2	K562	blood:
4	chr1:71662232..71663221-chr1:71987100..71987819,3	MCF-7	breast:
5	chr1:71662550..71665187-chr1:71831887..71834481,2	K562	blood:
6	chr1:71650900..71653329-chr1:71661783..71664278,2	K562	blood:
7	chr1:71654729..71657445-chr1:71668068..71670402,2	K562	blood:
8	chr1:71662166..71663092-chr1:71987067..71987944,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTH-6	chr1:71668701-71668776	ENSG00000229956
2	lnc-CTH-6	chr1:71667771-71667814	ENSG00000229956.5
3	lnc-CTH-6	chr1:71659386-71659411	NONHSAT003893
4	lnc-CTH-6	chr1:71668031-71668105	ENSG00000229956.5
5	lnc-CTH-6	chr1:71664550-71664674	ENSG00000229956.5
6	lnc-CTH-6	chr1:71668701-71668776	ENSG00000229956.5
7	lnc-CTH-6	chr1:71668031-71668105	ENSG00000229956.5
8	lnc-CTH-6	chr1:71650030-71650254	ENSG00000229956.5
9	lnc-CTH-6	chr1:71667718-71667814	ENSG00000229956
10	lnc-CTH-6	chr1:71667718-71667814	ENSG00000229956.5

Variant related genes	Relation type
ZRANB2-AS2	TF binding region
ZRANB2-AS2	CpG island
ENSG00000226324	chromatin interactions
SSFA2	miRNA target sites
ZFYVE16	miRNA target sites

Extended variants
information (count: 823 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:823 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13376594	chr1:71628776-71628777	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557933377	chr1:71628826-71628827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs578044408	chr1:71628843-71628844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74087220	chr1:71628859-71628860	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs144144423	chr1:71628937-71628938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs193226173	chr1:71628943-71628944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543310438	chr1:71629006-71629007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182586650	chr1:71629010-71629011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567753717	chr1:71629020-71629021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531894386	chr1:71629051-71629052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545134633	chr1:71629068-71629069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148682451	chr1:71629109-71629110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186637376	chr1:71629113-71629114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536527497	chr1:71629126-71629127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527376892	chr1:71629127-71629128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547104593	chr1:71629128-71629129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368176641	chr1:71629161-71629162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554864881	chr1:71629169-71629170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371681745	chr1:71629177-71629178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34781062	chr1:71629197-71629198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs28498931	chr1:71629200-71629201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112091862	chr1:71629221-71629222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549634503	chr1:71629247-71629248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534529518	chr1:71629289-71629290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569514731	chr1:71629290-71629291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375932404	chr1:71629365-71629366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538489599	chr1:71629378-71629379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558716584	chr1:71629421-71629422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571680523	chr1:71629430-71629431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534285454	chr1:71629448-71629449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576546282	chr1:71629453-71629454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs386632283	chr1:71629464-71629465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574056600	chr1:71629526-71629527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147452576	chr1:71629595-71629596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556855179	chr1:71629619-71629620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576800186	chr1:71629657-71629658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545323671	chr1:71629670-71629671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559151193	chr1:71629690-71629691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565454065	chr1:71629735-71629736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140008312	chr1:71629738-71629739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145444059	chr1:71629748-71629749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35335061	chr1:71629787-71629788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191918286	chr1:71629788-71629789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529593757	chr1:71629822-71629823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549671314	chr1:71629881-71629882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547936486	chr1:71629910-71629911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs78431802	chr1:71629927-71629928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77383519	chr1:71629934-71629935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552124013	chr1:71629967-71629968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577835620	chr1:71630065-71630066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
body mass index	19812545	CNVD
Obesity	20935630	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71625400-71637800	Weak transcription	Pancreas	Pancrea
2	chr1:71630200-71631000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr1:71631000-71632200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:71631600-71632800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr1:71631600-71633400	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr1:71631800-71632800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr1:71631800-71632800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr1:71631800-71632800	Enhancers	Fetal Lung	lung
9	chr1:71631800-71633000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr1:71631800-71633000	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr1:71632200-71632800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr1:71632200-71633000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:71632200-71633600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:71632400-71632800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr1:71632800-71634800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr1:71633000-71633600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:71633600-71633800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:71633800-71635800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:71635800-71636000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr1:71636200-71638600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:71637200-71639400	Weak transcription	Ovary	ovary
22	chr1:71637800-71638000	Enhancers	Pancreas	Pancrea
23	chr1:71643000-71644000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr1:71643000-71644200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr1:71643200-71643400	Enhancers	H9 Cell Line	embryonic stem cell
26	chr1:71643200-71643400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr1:71643200-71644000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr1:71643200-71644000	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr1:71644000-71644200	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr1:71644000-71644200	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr1:71644800-71647000	Enhancers	Fetal Intestine Large	intestine
32	chr1:71645000-71646200	Enhancers	Fetal Intestine Small	intestine
33	chr1:71645400-71646200	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr1:71645400-71646200	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr1:71655200-71655600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
36	chr1:71658600-71659000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:71658600-71659200	Enhancers	Ovary	ovary
38	chr1:71658800-71659200	Enhancers	Colon Smooth Muscle	Colon
39	chr1:71658800-71659200	Enhancers	Left Ventricle	heart
40	chr1:71659000-71659400	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr1:71659000-71659400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr1:71659000-71663000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:71659200-71660000	Weak transcription	Ovary	ovary
44	chr1:71659400-71663000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr1:71660000-71660200	Enhancers	Ovary	ovary
46	chr1:71663000-71663400	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr1:71663000-71663600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:71665600-71672400	Weak transcription	Pancreas	Pancrea
49	chr1:71666000-71666800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr1:71666800-71667400	Enhancers	Brain Hippocampus Middle	brain

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