Variant report

Variant	nsv2214
Chromosome Location	chr18:14449752-14461382
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	chr18:14458091-14458453	HepG2	liver:	n/a	n/a
2	CTCF	chr18:14450218-14450363	MCF-7	breast:	n/a	chr18:14450334-14450347
3	CTCF	chr18:14458525-14458895	A549	lung:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
4	CTCF	chr18:14458486-14458977	K562	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
5	CTCF	chr18:14458056-14458161	GM19238	blood:	n/a	chr18:14458126-14458139
6	CTCF	chr18:14458600-14458750	GM12871	blood:	n/a	chr18:14458743-14458750
7	CTCF	chr18:14458680-14458830	SK-N-SH_RA	brain:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
8	CTCF	chr18:14458560-14458710	HCT-116	colon:	n/a	n/a
9	CTCF	chr18:14458680-14458830	AG09319	gingival:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
10	CTCF	chr18:14459911-14460071	MCF-7	breast:	n/a	chr18:14459995-14460013 chr18:14459998-14460011
11	CTCF	chr18:14458680-14458830	HMEC	breast:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
12	CTCF	chr18:14458578-14458911	Kidney_OC	kidney:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
13	CTCF	chr18:14459957-14460022	Gliobla	brain:	n/a	chr18:14459995-14460013 chr18:14459998-14460011
14	CTCF	chr18:14460005-14460024	GM19238	blood:	n/a	n/a
15	CTCF	chr18:14458680-14458830	GM12878	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
16	CTCF	chr18:14458645-14458867	NHEK	skin:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
17	CTCF	chr18:14458600-14458750	GM12869	blood:	n/a	chr18:14458743-14458750
18	CTCF	chr18:14459883-14460131	LNCaP	prostate:	n/a	chr18:14459995-14460013 chr18:14459998-14460011
19	CTCF	chr18:14458680-14458830	HUVEC	blood vessel:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
20	CTCF	chr18:14459229-14459320	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chr18:14450263-14450315	Fibrobl	skin:	n/a	n/a
22	CTCF	chr18:14458600-14458750	GM12864	blood:	n/a	chr18:14458743-14458750
23	CTCF	chr18:14450220-14450370	HMEC	breast:	n/a	chr18:14450334-14450347
24	CTCF	chr18:14459952-14460138	K562	blood:	n/a	chr18:14459995-14460013 chr18:14459998-14460011
25	CTCF	chr18:14458545-14458558	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr18:14457980-14458130	GM12870	blood:	n/a	n/a
27	CTCF	chr18:14458380-14458530	GM12869	blood:	n/a	n/a
28	CTCF	chr18:14458078-14458124	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr18:14458060-14458210	Caco-2	colon:	n/a	chr18:14458126-14458139
30	CTCF	chr18:14459734-14460167	SK-N-SH	brain:	n/a	chr18:14459995-14460013 chr18:14459998-14460011
31	CTCF	chr18:14458001-14458168	LNCaP	prostate:	n/a	chr18:14458126-14458139
32	CTCF	chr18:14458624-14458839	HepG2	liver:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
33	CTCF	chr18:14458658-14458829	H1-hESC	embryonic stem cell:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
34	CTCF	chr18:14458080-14458230	GM12873	blood:	n/a	chr18:14458126-14458139
35	CTCF	chr18:14457955-14458227	A549	lung:	n/a	chr18:14458126-14458139
36	CTCF	chr18:14458668-14458856	K562	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
37	CTCF	chr18:14458585-14458869	Fibrobl	skin:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
38	CTCF	chr18:14450360-14450510	HEK293	kidney:	n/a	n/a
39	CTCF	chr18:14458650-14458828	SK-N-SH_RA	brain:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
40	CTCF	chr18:14458600-14458750	GM12866	blood:	n/a	chr18:14458743-14458750
41	CTCF	chr18:14460002-14460024	NHEK	skin:	n/a	n/a
42	CTCF	chr18:14458598-14458912	A549	lung:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
43	CTCF	chr18:14458099-14458111	HepG2	liver:	n/a	n/a
44	CTCF	chr18:14458127-14458138	HepG2	liver:	n/a	n/a
45	CTCF	chr18:14458560-14458710	RPTEC	kidney:	n/a	n/a
46	CTCF	chr18:14458627-14458860	ProgFib	skin:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
47	CTCF	chr18:14458540-14458690	GM12870	blood:	n/a	n/a
48	CTCF	chr18:14458644-14458870	LNCaP	prostate:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
49	CTCF	chr18:14458638-14458842	GM13976	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
50	CTCF	chr18:14458680-14458830	HCFaa	heart:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:14458927-14458977	HAEpiC	amniotic membrane:	n/a
2	chr18:14450194-14450244	HRPEpiC	eye:	n/a
3	chr18:14455307-14455357	K562	blood:	n/a
4	chr18:14461159-14461209	T-47D	breast:	n/a
5	chr18:14455307-14455357	AG09319	gingival:	n/a
6	chr18:14455307-14455357	PANC-1	pancreas:	n/a
7	chr18:14457820-14457870	Hela-S3	cervix:	n/a
8	chr18:14457820-14457870	NT2-D1	testis:	n/a
9	chr18:14457820-14457870	PFSK-1	brain:	n/a
10	chr18:14461159-14461209	BJ	skin:	n/a
11	chr18:14459174-14459224	HRE	kidney:	n/a
12	chr18:14461159-14461209	NB4	blood:	n/a
13	chr18:14455307-14455357	ProgFib	skin:	n/a
14	chr18:14458692-14458742	T-47D	breast:	n/a
15	chr18:14458692-14458742	HMEC	breast:	n/a
16	chr18:14458927-14458977	AG09309	skin:	n/a
17	chr18:14458161-14458211	HL-60	blood:	n/a
18	chr18:14450199-14450249	A549	lung:	n/a
19	chr18:14461159-14461209	U87	brain:	n/a
20	chr18:14450199-14450249	BJ	skin:	n/a
21	chr18:14451035-14451085	HUVEC	blood vessel:	n/a
22	chr18:14458927-14458977	IMR90	lung:	fetal
23	chr18:14458692-14458742	H1-hESC	embryonic stem cell:	embryo
24	chr18:14458927-14458977	NHDF-neo	bronchial:	n/a
25	chr18:14458161-14458211	MCF10A-Er-Src	breast:	n/a
26	chr18:14450199-14450249	HAEpiC	amniotic membrane:	n/a
27	chr18:14458692-14458742	GM06990	blood:	n/a
28	chr18:14450799-14450849	Hepatocyte	liver:	n/a
29	chr18:14461159-14461209	PANC-1	pancreas:	n/a
30	chr18:14458161-14458211	HEEpiC	esophagus:	n/a
31	chr18:14458161-14458211	HCT-116	colon:	n/a
32	chr18:14458927-14458977	GM12892	blood:	n/a
33	chr18:14457820-14457870	HCPEpiC	choroid plexus:	n/a
34	chr18:14450799-14450849	T-47D	breast:	n/a
35	chr18:14458927-14458977	MCF10A-Er-Src	breast:	n/a
36	chr18:14450799-14450849	GM19239	blood:	n/a
37	chr18:14450194-14450244	K562	blood:	n/a
38	chr18:14458161-14458211	MCF-7	breast:	n/a
39	chr18:14459044-14459094	ovcar-3	ovarian:	n/a
40	chr18:14450194-14450244	NB4	blood:	n/a
41	chr18:14450799-14450849	AoSMC	blood vessel:	n/a
42	chr18:14450799-14450849	RPTEC	kidney:	n/a
43	chr18:14458927-14458977	AG09319	gingival:	n/a
44	chr18:14459044-14459094	T-47D	breast:	n/a
45	chr18:14457820-14457870	GM12878	blood:	n/a
46	chr18:14450194-14450244	Caco-2	colon:	n/a
47	chr18:14455307-14455357	SK-N-SH	brain:	n/a
48	chr18:14459174-14459224	HCPEpiC	choroid plexus:	n/a
49	chr18:14450799-14450849	GM12891	blood:	n/a
50	chr18:14450415-14450465	HNPCEpiC	eye:	n/a

Variant related genes	Relation type
LONRF2P1	TF binding region
LONRF2P1	CpG island

Extended variants
information (count: 418 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:418 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568876466	chr18:14449761-14449762	Bivalent/Poised TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs531396768	chr18:14449794-14449795	Bivalent/Poised TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs551526244	chr18:14449795-14449796	Bivalent/Poised TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs571447338	chr18:14449842-14449843	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs371838640	chr18:14449897-14449898	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs71360369	chr18:14449910-14449911	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs55937590	chr18:14449939-14449940	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs71360371	chr18:14449949-14449950	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs71360372	chr18:14450003-14450004	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs71360373	chr18:14450064-14450065	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs71360374	chr18:14450071-14450072	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs56291485	chr18:14450076-14450077	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs567599316	chr18:14450137-14450138	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs536159729	chr18:14450207-14450208	Bivalent/Poised TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs62080621	chr18:14450247-14450248	Bivalent/Poised TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs62080622	chr18:14450351-14450352	Bivalent/Poised TSS Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs191234184	chr18:14450375-14450376	Bivalent/Poised TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184199242	chr18:14450377-14450378	Bivalent/Poised TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545076561	chr18:14450387-14450388	Bivalent/Poised TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558659537	chr18:14450426-14450427	Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs62080623	chr18:14450434-14450435	Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs62080624	chr18:14450467-14450468	Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs537620302	chr18:14450495-14450496	Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs549609305	chr18:14450515-14450516	Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs561325653	chr18:14450527-14450528	Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs62080625	chr18:14450548-14450549	Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs530376159	chr18:14450601-14450602	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs543772171	chr18:14450628-14450629	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs562437169	chr18:14450650-14450651	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs535592072	chr18:14450651-14450652	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs531365400	chr18:14450780-14450781	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs551489302	chr18:14450816-14450817	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571408939	chr18:14450855-14450856	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs527493852	chr18:14450889-14450890	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs547524532	chr18:14450991-14450992	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs187032540	chr18:14451002-14451003	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs536514034	chr18:14451011-14451012	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs62080626	chr18:14451028-14451029	Weak transcription Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs193179019	chr18:14451036-14451037	Weak transcription Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs111869248	chr18:14451052-14451053	Weak transcription Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs111626226	chr18:14451058-14451059	Weak transcription Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs201139518	chr18:14451094-14451095	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs185294242	chr18:14451097-14451098	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs558622574	chr18:14451120-14451121	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs572455136	chr18:14451184-14451185	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs534815226	chr18:14451227-14451228	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs555107589	chr18:14451386-14451387	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs574953593	chr18:14451401-14451402	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs539083852	chr18:14451422-14451423	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs544109274	chr18:14451778-14451779	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:14448800-14450400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr18:14449400-14449800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
3	chr18:14449600-14451000	Active TSS	HSMM	muscle
4	chr18:14450000-14450200	Enhancers	Adipose Nuclei	Adipose
5	chr18:14450000-14450200	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr18:14450000-14450200	Flanking Active TSS	Stomach Smooth Muscle	stomach
7	chr18:14450000-14450600	Enhancers	Primary T cells fromperipheralblood	blood
8	chr18:14450000-14451000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr18:14450000-14451000	Active TSS	Brain Germinal Matrix	brain
10	chr18:14450000-14451000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
11	chr18:14450000-14451000	Active TSS	Colonic Mucosa	Colon
12	chr18:14450000-14451000	Active TSS	Colon Smooth Muscle	Colon
13	chr18:14450000-14451000	Active TSS	Fetal Brain Female	brain
14	chr18:14450000-14451200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr18:14450200-14450400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
16	chr18:14450200-14450400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr18:14450200-14450800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
18	chr18:14450200-14450800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr18:14450200-14451000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr18:14450200-14451000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr18:14450200-14451000	Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr18:14450200-14451000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr18:14450200-14451000	Active TSS	Muscle Satellite Cultured Cells	--
24	chr18:14450200-14451000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr18:14450200-14451000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr18:14450200-14451000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr18:14450200-14451000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr18:14450200-14451000	Active TSS	Adipose Nuclei	Adipose
29	chr18:14450200-14451000	Active TSS	Brain Angular Gyrus	brain
30	chr18:14450200-14451000	Active TSS	Brain Hippocampus Middle	brain
31	chr18:14450200-14451000	Active TSS	Duodenum Smooth Muscle	Duodenum
32	chr18:14450200-14451000	Active TSS	Esophagus	oesophagus
33	chr18:14450200-14451000	Active TSS	Left Ventricle	heart
34	chr18:14450200-14451000	Active TSS	Pancreas	Pancrea
35	chr18:14450200-14451000	Active TSS	Right Ventricle	heart
36	chr18:14450200-14451000	Active TSS	Skeletal Muscle Male	skeletal muscle
37	chr18:14450200-14451000	Active TSS	Skeletal Muscle Female	skeletal muscle
38	chr18:14450200-14451000	Active TSS	Stomach Smooth Muscle	stomach
39	chr18:14450200-14451200	Active TSS	HMEC	breast
40	chr18:14450200-14453400	Active TSS	Osteobl	bone
41	chr18:14450400-14450800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
42	chr18:14450400-14451000	Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr18:14450400-14451000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr18:14450400-14451000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
45	chr18:14450400-14451000	Active TSS	Primary hematopoietic stem cells	blood
46	chr18:14450400-14451000	Active TSS	Primary hematopoietic stem cells short term culture	blood
47	chr18:14450400-14451000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
48	chr18:14450400-14451000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
49	chr18:14450400-14451000	Active TSS	Primary T helper cells fromperipheralblood	blood
50	chr18:14450400-14451000	Active TSS	Primary T killer naive cells fromperipheralblood	blood

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