Variant report

Variant	nsv1044859
Chromosome Location	chr11:55900482-56121727
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	chr11:56043042-56043185	K562	blood:	n/a	n/a
2	BACH1	chr11:55919802-55920154	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr11:55917916-55917973	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr11:55937213-55937236	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr11:56000780-56000794	K562	blood:	n/a	n/a
6	CEBPB	chr11:55905952-55906317	MCF-7	breast:	n/a	n/a
7	CEBPB	chr11:55997409-55997769	K562	blood:	n/a	chr11:55997577-55997588
8	CEBPB	chr11:55997392-55997747	IMR90	lung:	n/a	chr11:55997577-55997588
9	CEBPB	chr11:55997403-55997756	HepG2	liver:	n/a	chr11:55997577-55997588
10	CEBPB	chr11:55964876-55965231	IMR90	lung:	n/a	chr11:55965053-55965066 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965054-55965065
11	CEBPB	chr11:55964899-55965188	A549	lung:	n/a	chr11:55965053-55965066 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965054-55965065
12	CEBPB	chr11:55964901-55965149	Hela-S3	cervix:	n/a	chr11:55965053-55965066 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965054-55965065
13	CEBPB	chr11:55997392-55997743	A549	lung:	n/a	chr11:55997577-55997588
14	CEBPB	chr11:55997458-55997740	H1-hESC	embryonic stem cell:	n/a	chr11:55997577-55997588
15	CEBPB	chr11:56111917-56111963	A549	lung:	n/a	n/a
16	CEBPB	chr11:55997407-55997695	Hela-S3	cervix:	n/a	chr11:55997577-55997588
17	CEBPB	chr11:55906014-55906261	A549	lung:	n/a	n/a
18	CEBPB	chr11:55921214-55921534	HepG2	liver:	n/a	chr11:55921389-55921400
19	CEBPB	chr11:56111830-56112110	HepG2	liver:	n/a	chr11:56111955-56111968 chr11:56111955-56111966 chr11:56111957-56111968 chr11:56111955-56111968 chr11:56111957-56111968 chr11:56111955-56111968
20	CEBPB	chr11:55964882-55965215	HepG2	liver:	n/a	chr11:55965053-55965066 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965054-55965065
21	CEBPB	chr11:55964893-55965195	H1-hESC	embryonic stem cell:	n/a	chr11:55965053-55965066 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965054-55965065
22	CTCF	chr11:56044797-56044900	A549	lung:	n/a	n/a
23	CTCF	chr11:55904745-55904803	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr11:56044834-56044859	HUVEC	blood vessel:	n/a	n/a
25	CTCF	chr11:56044796-56044999	GM12878	blood:	n/a	n/a
26	CTCF	chr11:55939440-55939590	GM12865	blood:	n/a	n/a
27	CTCF	chr11:55923930-55924003	GM13977	blood:	n/a	n/a
28	CTCF	chr11:56044798-56044986	IMR90	lung:	n/a	n/a
29	CTCF	chr11:56044791-56044903	GM12878	blood:	n/a	n/a
30	CTCF	chr11:56032960-56033110	Caco-2	colon:	n/a	n/a
31	CTCF	chr11:56094415-56094473	Fibrobl	skin:	n/a	n/a
32	CTCF	chr11:56120920-56121070	Caco-2	colon:	n/a	n/a
33	CTCF	chr11:56044760-56044910	HMEC	breast:	n/a	n/a
34	CTCF	chr11:56050376-56050433	GM20000	blood:	n/a	n/a
35	CTCF	chr11:56044697-56045047	A549	lung:	n/a	n/a
36	CTCF	chr11:56035842-56035886	LNCaP	prostate:	n/a	n/a
37	CTCF	chr11:56112640-56112790	GM12865	blood:	n/a	n/a
38	CTCF	chr11:56044784-56044969	A549	lung:	n/a	n/a
39	CTCF	chr11:56038545-56038609	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr11:56044731-56045088	K562	blood:	n/a	n/a
41	CTCF	chr11:56044793-56044900	GM12891	blood:	n/a	n/a
42	CTCF	chr11:56044786-56044981	A549	lung:	n/a	n/a
43	CTCF	chr11:56044757-56045045	A549	lung:	n/a	n/a
44	CTCF	chr11:56098675-56098716	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr11:56100500-56100650	GM12875	blood:	n/a	n/a
46	CTCF	chr11:56044830-56044864	ProgFib	skin:	n/a	n/a
47	CTCF	chr11:55987346-55987405	GM20000	blood:	n/a	n/a
48	CTCF	chr11:55951088-55951110	LNCaP	prostate:	n/a	n/a
49	CTCF	chr11:56064622-56064711	LNCaP	prostate:	n/a	n/a
50	CUX1	chr11:55909690-55909743	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:56058004-56058054	MCF10A-Er-Src	breast:	n/a
2	chr11:56058004-56058054	MCF10A-Er-Src	breast:	n/a
3	chr11:56112153-56112203	AG04450	lung:	fetal
4	chr11:55999683-55999733	HAEpiC	amniotic membrane:	n/a
5	chr11:56020533-56020583	CMK	blood:	n/a
6	chr11:56043514-56043564	GM12878	blood:	n/a
7	chr11:56000287-56000337	AG09319	gingival:	n/a
8	chr11:56113768-56113818	Hepatocyte	liver:	n/a
9	chr11:56085745-56085795	AG09309	skin:	n/a
10	chr11:56020533-56020583	AG09309	skin:	n/a
11	chr11:55999683-55999733	AG09319	gingival:	n/a
12	chr11:56113543-56113593	A549	lung:	n/a
13	chr11:56018532-56018582	GM12878	blood:	n/a
14	chr11:56085745-56085795	HRE	kidney:	n/a
15	chr11:56112384-56112434	BJ	skin:	n/a
16	chr11:56099798-56099848	AG09309	skin:	n/a
17	chr11:56020533-56020583	HEEpiC	esophagus:	n/a
18	chr11:56043514-56043564	HMEC	breast:	n/a
19	chr11:56113768-56113818	BJ	skin:	n/a
20	chr11:56020533-56020583	ovcar-3	ovarian:	n/a
21	chr11:56099655-56099705	HNPCEpiC	eye:	n/a
22	chr11:56112153-56112203	GM12891	blood:	n/a
23	chr11:56113768-56113818	A549	lung:	n/a
24	chr11:56086656-56086706	IMR90	lung:	fetal
25	chr11:56058004-56058054	AG10803	skin:	n/a
26	chr11:56018532-56018582	CMK	blood:	n/a
27	chr11:56099968-56100018	ProgFib	skin:	n/a
28	chr11:56099968-56100018	Hela-S3	cervix:	n/a
29	chr11:56085425-56085475	HRE	kidney:	n/a
30	chr11:55999683-55999733	AG10803	skin:	n/a
31	chr11:56112384-56112434	ovcar-3	ovarian:	n/a
32	chr11:55927697-55927747	HL-60	blood:	n/a
33	chr11:56112384-56112434	GM19239	blood:	n/a
34	chr11:55904782-55904832	Caco-2	colon:	n/a
35	chr11:56112384-56112434	GM12892	blood:	n/a
36	chr11:55905246-55905296	GM12878	blood:	n/a
37	chr11:55999683-55999733	GM12892	blood:	n/a
38	chr11:56000287-56000337	H1-hESC	embryonic stem cell:	embryo
39	chr11:56099655-56099705	Hepatocyte	liver:	n/a
40	chr11:56085425-56085475	PFSK-1	brain:	n/a
41	chr11:56113543-56113593	AG09319	gingival:	n/a
42	chr11:56018532-56018582	SK-N-SH	brain:	n/a
43	chr11:56043040-56043090	HRPEpiC	eye:	n/a
44	chr11:56086656-56086706	NHBE	bronchial:	n/a
45	chr11:56086656-56086706	HRPEpiC	eye:	n/a
46	chr11:56058004-56058054	NHBE	bronchial:	n/a
47	chr11:56020533-56020583	K562	blood:	n/a
48	chr11:56099655-56099705	LNCaP	prostate:	n/a
49	chr11:56113543-56113593	RPTEC	kidney:	n/a
50	chr11:55999683-55999733	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:55957956..55959587-chr11:55962616..55964605,2	K562	blood:
2	chr11:55861584..55863423-chr11:55907412..55909639,2	K562	blood:
3	chr11:56082649..56084354-chr11:56114300..56117003,2	K562	blood:
4	chr11:55957956..55959587-chr11:55962616..55964605,2	K562	blood:
5	chr11:56006842..56008897-chr11:56029755..56032217,2	MCF-7	breast:
6	chr11:56082649..56084354-chr11:56114300..56117003,2	K562	blood:
7	chr11:55921059..55923391-chr11:55935211..55936757,2	K562	blood:
8	chr11:55921059..55923391-chr11:55935211..55936757,2	K562	blood:
9	chr11:56006842..56008897-chr11:56029755..56032217,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR5T2-1	chr11:55972601-55973101	NONHSAT021383

Variant related genes	Relation type
OR8H1	TF binding region
OR8J3	TF binding region
OR5J2	TF binding region
OR8I1P	TF binding region
OR8J2	TF binding region
OR5J7P	TF binding region
ENSG00000213604	TF binding region
RPL5P29	TF binding region
OR5T3	TF binding region
OR8V1P	TF binding region
OR8K5	TF binding region
OR8K4P	TF binding region
OR5T2	TF binding region
OR8K3	TF binding region
FAM8A2P	TF binding region
OR8K1	TF binding region
OR8K2P	TF binding region
OR5T1	TF binding region
OR5BN1P	TF binding region
OR8H1	CpG island
OR8J3	CpG island
OR5J2	CpG island
OR8I1P	CpG island
OR8J2	CpG island
OR5J7P	CpG island
ENSG00000213604	CpG island
RPL5P29	CpG island
OR5T3	CpG island
OR8V1P	CpG island
OR8K5	CpG island
OR8K4P	CpG island
OR5T2	CpG island
OR8K3	CpG island
FAM8A2P	CpG island
OR8K1	CpG island
OR8K2P	CpG island
OR5T1	CpG island
OR5BN1P	CpG island

Extended variants
information (count: 1503 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:1503 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1947923	chr11:55904751-55904752	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs369307213	chr11:55904778-55904779	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs373232843	chr11:55904779-55904780	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs146251646	chr11:55904782-55904783	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs139290067	chr11:55904783-55904784	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs376757102	chr11:55904802-55904803	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs189377785	chr11:55904814-55904815	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs11227321	chr11:55904828-55904829	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs533978590	chr11:55904829-55904830	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs201535279	chr11:55904831-55904832	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs7936390	chr11:55904832-55904833	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs567493753	chr11:55905264-55905265	Inactive region	CpG island	2 gene(s)	Overlapped CNVs	n/a
13	rs536769141	chr11:55905962-55905963	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs2449138	chr11:55905972-55905973	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs567507645	chr11:55905978-55905979	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs538033046	chr11:55905988-55905989	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs118060806	chr11:55905993-55905994	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs115902334	chr11:55905996-55905997	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs544950178	chr11:55906044-55906045	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs553761733	chr11:55906064-55906065	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs571692122	chr11:55906070-55906071	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs376652413	chr11:55906113-55906114	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs542356716	chr11:55906126-55906127	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs142564593	chr11:55906130-55906131	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs142489321	chr11:55906138-55906139	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs191021480	chr11:55906145-55906146	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs10791829	chr11:55906156-55906157	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs532861492	chr11:55906164-55906165	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs71055574	chr11:55906170-55906171	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs398016099	chr11:55906184-55906185	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs117710887	chr11:55906244-55906245	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs374266909	chr11:55906251-55906252	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs56358425	chr11:55907472-55907473	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs183189912	chr11:55907773-55907774	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs2512932	chr11:55907816-55907817	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs575880806	chr11:55907843-55907844	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs187925270	chr11:55907856-55907857	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs575609399	chr11:55907866-55907867	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs537181214	chr11:55907881-55907882	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs192498159	chr11:55907948-55907949	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs79825887	chr11:55907987-55907988	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs78102985	chr11:55907993-55907994	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs2512931	chr11:55907996-55907997	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs188712298	chr11:55908005-55908006	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs192596783	chr11:55908027-55908028	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs571237394	chr11:55908083-55908084	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs563710948	chr11:55908105-55908106	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs116836798	chr11:55908545-55908546	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs575849186	chr11:55908556-55908557	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs545888391	chr11:55908564-55908565	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:55910400-55910800	Active TSS	Fetal Heart	heart
2	chr11:55919400-55919800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr11:55939400-55939800	Enhancers	Fetal Intestine Small	intestine
4	chr11:55939400-55940800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr11:55939400-55940800	Enhancers	Fetal Intestine Large	intestine
6	chr11:55939800-55940200	Enhancers	Brain Substantia Nigra	brain
7	chr11:56021200-56022200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:56027000-56028400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr11:56027400-56027600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr11:56028200-56028400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr11:56028200-56028600	ZNF genes & repeats	Esophagus	oesophagus
12	chr11:56028600-56029000	Weak transcription	Esophagus	oesophagus
13	chr11:56036400-56036800	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr11:56047000-56049800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:56049800-56051000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr11:56051000-56052600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:56055600-56058200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr11:56055800-56056800	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr11:56056000-56057000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr11:56056000-56057600	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr11:56056200-56057200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr11:56056400-56057600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr11:56057000-56058000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr11:56057200-56057600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr11:56057600-56058000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr11:56058000-56058200	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr11:56075200-56075600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr11:56075200-56075600	ZNF genes & repeats	Gastric	stomach
29	chr11:56094400-56094600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
30	chr11:56094600-56095800	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr11:56097200-56104800	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr11:56099400-56099800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr11:56100800-56101200	Active TSS	Brain Hippocampus Middle	brain
34	chr11:56101000-56101400	Enhancers	Brain Cingulate Gyrus	brain
35	chr11:56104400-56105400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
36	chr11:56104600-56105200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr11:56104800-56105200	Enhancers	H1 Cell Line	embryonic stem cell
38	chr11:56104800-56105400	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr11:56105000-56105200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr11:56105000-56105200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr11:56105000-56105400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
42	chr11:56105200-56105400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr11:56105200-56105400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr11:56105200-56105600	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr11:56105400-56105600	Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr11:56105400-56105600	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr11:56111800-56112400	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr11:56111800-56112600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr11:56112000-56112400	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr11:56112200-56112800	Enhancers	iPS-15b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links