Variant report

Variant	nsv554212
Chromosome Location	chr11:48214992-48387275
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	chr11:48356437-48356637	K562	blood:	n/a	n/a
2	ATF1	chr11:48292484-48292679	K562	blood:	n/a	n/a
3	BACH1	chr11:48356973-48356986	K562	blood:	n/a	n/a
4	BRCA1	chr11:48235490-48235559	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr11:48361931-48361935	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr11:48329323-48329679	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr11:48329320-48329744	HCT-116	colon:	n/a	n/a
8	CEBPB	chr11:48374701-48375094	Hela-S3	cervix:	n/a	chr11:48374900-48374913
9	CEBPB	chr11:48376639-48376671	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr11:48367044-48367318	HepG2	liver:	n/a	n/a
11	CEBPB	chr11:48232351-48232666	K562	blood:	n/a	chr11:48232504-48232515
12	CEBPB	chr11:48232372-48232647	Hela-S3	cervix:	n/a	chr11:48232504-48232515
13	CEBPB	chr11:48367001-48367415	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr11:48332469-48332671	HepG2	liver:	n/a	chr11:48332598-48332609
15	CEBPB	chr11:48232346-48232660	IMR90	lung:	n/a	chr11:48232504-48232515
16	CEBPB	chr11:48367014-48367428	HCT-116	colon:	n/a	n/a
17	CEBPB	chr11:48232368-48232629	A549	lung:	n/a	chr11:48232504-48232515
18	CEBPB	chr11:48232376-48232660	HepG2	liver:	n/a	chr11:48232504-48232515
19	CEBPB	chr11:48340990-48341301	A549	lung:	n/a	n/a
20	CEBPB	chr11:48367027-48367324	HCT-116	colon:	n/a	n/a
21	CEBPZ	chr11:48360331-48360376	HepG2	liver:	n/a	n/a
22	CHD2	chr11:48344566-48344658	K562	blood:	n/a	n/a
23	CHD2	chr11:48377806-48377814	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr11:48231687-48231925	MCF-7	breast:	n/a	n/a
25	CTCF	chr11:48329306-48329773	HepG2	liver:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
26	CTCF	chr11:48231680-48231830	HEK293	kidney:	n/a	n/a
27	CTCF	chr11:48231680-48231830	HepG2	liver:	n/a	n/a
28	CTCF	chr11:48329784-48329877	GM10266	blood:	n/a	n/a
29	CTCF	chr11:48329480-48329630	GM12872	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
30	CTCF	chr11:48362100-48362250	A549	lung:	n/a	n/a
31	CTCF	chr11:48329440-48329590	HAc	cerebellar:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
32	CTCF	chr11:48265836-48265927	GM10248	blood:	n/a	n/a
33	CTCF	chr11:48231720-48231870	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr11:48329391-48329589	GM12891	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
35	CTCF	chr11:48231661-48231931	MCF-7	breast:	n/a	n/a
36	CTCF	chr11:48231718-48231859	GM12891	blood:	n/a	n/a
37	CTCF	chr11:48329394-48329595	A549	lung:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
38	CTCF	chr11:48231720-48231870	BJ	skin:	n/a	n/a
39	CTCF	chr11:48231740-48231890	Caco-2	colon:	n/a	n/a
40	CTCF	chr11:48329420-48329570	SAEC	small airway:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
41	CTCF	chr11:48223852-48223893	GM13977	blood:	n/a	n/a
42	CTCF	chr11:48329460-48329610	GM12871	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
43	CTCF	chr11:48377730-48377792	A549	lung:	n/a	n/a
44	CTCF	chr11:48231660-48231810	HFF	foreskin:	n/a	n/a
45	CTCF	chr11:48231720-48231870	K562	blood:	n/a	n/a
46	CTCF	chr11:48231700-48231850	AG04450	lung:	n/a	n/a
47	CTCF	chr11:48329371-48329626	Fibrobl	skin:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
48	CTCF	chr11:48231764-48231822	GM12878	blood:	n/a	n/a
49	CTCF	chr11:48329320-48329756	HCT-116	colon:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
50	CTCF	chr11:48329406-48329641	GM20000	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48285821-48285871	GM12878	blood:	n/a
2	chr11:48326388-48326438	T-47D	breast:	n/a
3	chr11:48237353-48237403	IMR90	lung:	fetal
4	chr11:48328132-48328182	MCF10A-Er-Src	breast:	n/a
5	chr11:48238296-48238346	ECC-1	luminal epithelium:	n/a
6	chr11:48237358-48237408	HRPEpiC	eye:	n/a
7	chr11:48367974-48368024	HEK293	kidney:	embryo
8	chr11:48238296-48238346	PrEC	prostate:	n/a
9	chr11:48345815-48345865	ovcar-3	ovarian:	n/a
10	chr11:48327164-48327214	GM12878	blood:	n/a
11	chr11:48285821-48285871	NHDF-neo	bronchial:	n/a
12	chr11:48237353-48237403	H1-hESC	embryonic stem cell:	embryo
13	chr11:48328132-48328182	HRCEpiC	kidney:	n/a
14	chr11:48285821-48285871	CMK	blood:	n/a
15	chr11:48374446-48374496	SK-N-SH	brain:	n/a
16	chr11:48345815-48345865	GM12878	blood:	n/a
17	chr11:48327164-48327214	CMK	blood:	n/a
18	chr11:48266856-48266906	HL-60	blood:	n/a
19	chr11:48285821-48285871	U87	brain:	n/a
20	chr11:48238724-48238774	HPAEpiC	pulmonary alveolar:	n/a
21	chr11:48237358-48237408	T-47D	breast:	n/a
22	chr11:48266856-48266906	GM12878	blood:	n/a
23	chr11:48237353-48237403	HCF	heart:	n/a
24	chr11:48328132-48328182	HAEpiC	amniotic membrane:	n/a
25	chr11:48328132-48328182	AG04449	skin:	fetal
26	chr11:48238296-48238346	HCM	heart:	n/a
27	chr11:48266856-48266906	Hela-S3	cervix:	n/a
28	chr11:48374446-48374496	HRPEpiC	eye:	n/a
29	chr11:48327164-48327214	HL-60	blood:	n/a
30	chr11:48327164-48327214	HPAEpiC	pulmonary alveolar:	n/a
31	chr11:48326388-48326438	HEEpiC	esophagus:	n/a
32	chr11:48345361-48345411	PFSK-1	brain:	n/a
33	chr11:48328132-48328182	Hela-S3	cervix:	n/a
34	chr11:48345815-48345865	GM12892	blood:	n/a
35	chr11:48237358-48237408	GM12891	blood:	n/a
36	chr11:48238724-48238774	IMR90	lung:	fetal
37	chr11:48345815-48345865	Hepatocyte	liver:	n/a
38	chr11:48285200-48285250	GM12878	blood:	n/a
39	chr11:48374446-48374496	Jurkat	blood:	n/a
40	chr11:48374446-48374496	RPTEC	kidney:	n/a
41	chr11:48345815-48345865	SKMC	muscle:	n/a
42	chr11:48374446-48374496	CMK	blood:	n/a
43	chr11:48327164-48327214	ovcar-3	ovarian:	n/a
44	chr11:48328132-48328182	HUVEC	blood vessel:	n/a
45	chr11:48345361-48345411	Caco-2	colon:	n/a
46	chr11:48367974-48368024	HCM	heart:	n/a
47	chr11:48238296-48238346	HUVEC	blood vessel:	n/a
48	chr11:48284249-48284299	HPAEpiC	pulmonary alveolar:	n/a
49	chr11:48328132-48328182	NB4	blood:	n/a
50	chr11:48326388-48326438	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:
2	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
3	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
4	chr11:48366878..48368914-chr11:48372533..48375413,2	MCF-7	breast:
5	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
6	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:
7	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
8	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:
9	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
10	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
11	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:

Variant related genes	Relation type
OR4X2	TF binding region
OR4B2P	TF binding region
OR4X1	TF binding region
OR4C4P	TF binding region
OR4C3	TF binding region
OR4S1	TF binding region
OR4B1	TF binding region
OR4X2	CpG island
OR4B2P	CpG island
OR4X1	CpG island
OR4C4P	CpG island
OR4C3	CpG island
OR4S1	CpG island
OR4B1	CpG island
ENSG00000197161	chromatin interactions

Extended variants
information (count: 4507 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:4507 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7111194	chr11:48214992-48214993	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574591374	chr11:48215064-48215065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533845688	chr11:48215084-48215085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553938040	chr11:48215089-48215090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113070676	chr11:48215092-48215093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545854374	chr11:48215096-48215097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368254013	chr11:48215112-48215113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372968189	chr11:48215137-48215138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563193846	chr11:48215153-48215154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186323530	chr11:48215187-48215188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542518775	chr11:48215197-48215198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562105967	chr11:48215246-48215247	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs113402223	chr11:48215258-48215259	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs547460571	chr11:48215325-48215326	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs145424411	chr11:48215350-48215351	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs533155254	chr11:48215383-48215384	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs146131994	chr11:48215426-48215427	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs375624410	chr11:48215430-48215431	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs183243436	chr11:48215432-48215433	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs531474554	chr11:48215443-48215444	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs542937154	chr11:48215468-48215469	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs548486944	chr11:48215471-48215472	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs568141892	chr11:48215476-48215477	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs534014142	chr11:48215515-48215516	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs553376406	chr11:48215526-48215527	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs147202375	chr11:48215540-48215541	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs188748040	chr11:48215547-48215548	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs140499494	chr11:48215565-48215566	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs555845094	chr11:48215584-48215585	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs75735369	chr11:48215600-48215601	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs369724551	chr11:48215606-48215607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs142246125	chr11:48215622-48215623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572286456	chr11:48215638-48215639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs72905570	chr11:48215646-48215647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs565391784	chr11:48215744-48215745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564346236	chr11:48215782-48215783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192408342	chr11:48215799-48215800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543527683	chr11:48215821-48215822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563507192	chr11:48215824-48215825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373042302	chr11:48215835-48215836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183315853	chr11:48215852-48215853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs924714	chr11:48215853-48215854	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs568384391	chr11:48215862-48215863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140361487	chr11:48215891-48215892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs371541790	chr11:48215986-48215987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs145870671	chr11:48231609-48231610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs534248025	chr11:48231630-48231631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs113186361	chr11:48231653-48231654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs1503187	chr11:48231663-48231664	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs577060304	chr11:48231666-48231667	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Breast cancer	21990379	CNVD
Acute myeloid leukemia	20729466	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48214000-48215200	Enhancers	Osteobl	bone
2	chr11:48214200-48215000	Weak transcription	Left Ventricle	heart
3	chr11:48214600-48215600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr11:48215000-48215800	Enhancers	NHDF-Ad	bronchial
5	chr11:48215200-48215600	Enhancers	NHLF	lung
6	chr11:48215200-48215600	Flanking Active TSS	Osteobl	bone
7	chr11:48215200-48215800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr11:48215600-48216000	Enhancers	Osteobl	bone
9	chr11:48231600-48232000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr11:48250200-48250800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr11:48283000-48285000	Enhancers	GM12878-XiMat	blood
12	chr11:48288800-48289000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr11:48293400-48294200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
14	chr11:48293600-48294200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
15	chr11:48294000-48294400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
16	chr11:48294400-48295000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
17	chr11:48294800-48295200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
18	chr11:48295000-48295200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
19	chr11:48314000-48314400	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr11:48328000-48328400	Enhancers	Lung	lung
21	chr11:48329400-48329800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr11:48329400-48330000	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr11:48329600-48329800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
24	chr11:48329600-48329800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr11:48329600-48329800	Enhancers	Brain Angular Gyrus	brain
26	chr11:48329600-48329800	Enhancers	Brain Cingulate Gyrus	brain
27	chr11:48329600-48329800	Enhancers	Brain Hippocampus Middle	brain
28	chr11:48336400-48337600	Enhancers	Stomach Mucosa	stomach
29	chr11:48337600-48341200	Weak transcription	Stomach Mucosa	stomach
30	chr11:48341200-48342600	Enhancers	Stomach Mucosa	stomach
31	chr11:48341400-48345800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
32	chr11:48341600-48341800	Bivalent Enhancer	Left Ventricle	heart
33	chr11:48341600-48342000	Bivalent Enhancer	Right Atrium	heart
34	chr11:48341600-48342000	Enhancers	Spleen	Spleen
35	chr11:48341800-48342000	Enhancers	Left Ventricle	heart
36	chr11:48342600-48344400	Weak transcription	Stomach Mucosa	stomach
37	chr11:48344400-48344800	Enhancers	Stomach Mucosa	stomach
38	chr11:48344800-48349800	Weak transcription	Stomach Mucosa	stomach
39	chr11:48346600-48346800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr11:48346600-48347000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
41	chr11:48346600-48347400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr11:48346600-48348600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
43	chr11:48346800-48347400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr11:48348800-48350000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr11:48350000-48355600	Weak transcription	Stomach Mucosa	stomach
46	chr11:48352400-48353400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
47	chr11:48352400-48353800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
48	chr11:48353000-48359800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
49	chr11:48355200-48363800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
50	chr11:48355600-48357000	Enhancers	Stomach Mucosa	stomach

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