Variant report

Variant	nsv521283
Chromosome Location	chr10:43866528-43871998
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:53)
CpG islands
(count:551)
Chromatin interactive
region (count:14)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:53 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr10:43866925-43867233	K562	blood:	n/a	n/a
2	CCNT2	chr10:43867032-43867212	K562	blood:	n/a	n/a
3	CEBPB	chr10:43869543-43869611	A549	lung:	n/a	n/a
4	E2F6	chr10:43866923-43867148	K562	blood:	n/a	n/a
5	EP300	chr10:43870803-43871437	MCF-7	breast:	n/a	n/a
6	FOXA2	chr10:43866690-43867040	A549	lung:	n/a	n/a
7	GATA3	chr10:43870728-43871542	MCF-7	breast:	n/a	n/a
8	GATA3	chr10:43870725-43871372	MCF-7	breast:	n/a	n/a
9	HMGN3	chr10:43867023-43867186	K562	blood:	n/a	n/a
10	HMGN3	chr10:43870233-43870245	K562	blood:	n/a	n/a
11	JUN	chr10:43866846-43867413	K562	blood:	n/a	n/a
12	JUND	chr10:43867027-43867110	K562	blood:	n/a	n/a
13	MAX	chr10:43866935-43867171	K562	blood:	n/a	chr10:43867066-43867077 chr10:43867068-43867075 chr10:43867067-43867076 chr10:43867066-43867076
14	MAX	chr10:43866939-43867235	Hela-S3	cervix:	n/a	chr10:43867066-43867077 chr10:43867068-43867075 chr10:43867067-43867076 chr10:43867066-43867076
15	MAX	chr10:43870751-43871358	MCF-7	breast:	n/a	chr10:43870913-43870922
16	MAX	chr10:43866896-43867253	K562	blood:	n/a	chr10:43867066-43867077 chr10:43867068-43867075 chr10:43867067-43867076 chr10:43867066-43867076
17	MAX	chr10:43866904-43867282	K562	blood:	n/a	chr10:43867066-43867077 chr10:43867068-43867075 chr10:43867067-43867076 chr10:43867066-43867076
18	MAZ	chr10:43866951-43867122	K562	blood:	n/a	chr10:43867066-43867077 chr10:43867068-43867075 chr10:43867067-43867076 chr10:43867066-43867076
19	MXI1	chr10:43866937-43867249	Hela-S3	cervix:	n/a	chr10:43867068-43867077 chr10:43867066-43867075
20	MXI1	chr10:43867005-43867223	K562	blood:	n/a	chr10:43867068-43867077 chr10:43867066-43867075
21	MYC	chr10:43871113-43871114	MCF-7	breast:	n/a	n/a
22	MYC	chr10:43867077-43867092	MCF-7	breast:	n/a	n/a
23	MYC	chr10:43867046-43867075	MCF-7	breast:	n/a	chr10:43867068-43867075
24	MYC	chr10:43870999-43871223	MCF-7	breast:	n/a	n/a
25	MYC	chr10:43866938-43867194	K562	blood:	n/a	chr10:43867066-43867077 chr10:43867068-43867075 chr10:43867067-43867076 chr10:43867066-43867076
26	MYC	chr10:43871131-43871244	MCF-7	breast:	n/a	n/a
27	MYC	chr10:43866923-43867298	K562	blood:	n/a	chr10:43867066-43867077 chr10:43867068-43867075 chr10:43867067-43867076 chr10:43867066-43867076
28	NR2F2	chr10:43870788-43871496	MCF-7	breast:	n/a	n/a
29	NR2F2	chr10:43870776-43871627	MCF-7	breast:	n/a	n/a
30	POLR2A	chr10:43867036-43867222	MCF-7	breast:	n/a	n/a
31	POLR2A	chr10:43870859-43871266	MCF-7	breast:	n/a	n/a
32	POLR2A	chr10:43869892-43869993	MCF-7	breast:	n/a	n/a
33	POLR2A	chr10:43869732-43869803	MCF-7	breast:	n/a	n/a
34	POLR2A	chr10:43869880-43869888	MCF-7	breast:	n/a	n/a
35	POLR2A	chr10:43869757-43869798	MCF-7	breast:	n/a	n/a
36	POLR2A	chr10:43871057-43871060	MCF-7	breast:	n/a	n/a
37	POLR2A	chr10:43871198-43871205	MCF-7	breast:	n/a	n/a
38	POLR2A	chr10:43866870-43867430	MCF-7	breast:	n/a	n/a
39	POLR2A	chr10:43870939-43871054	MCF-7	breast:	n/a	n/a
40	SIN3AK20	chr10:43866879-43867177	K562	blood:	n/a	n/a
41	TBL1XR1	chr10:43867069-43867160	K562	blood:	n/a	n/a
42	TCF7L2	chr10:43866930-43867342	Hela-S3	cervix:	n/a	n/a
43	USF1	chr10:43866952-43867263	K562	blood:	n/a	n/a
44	USF1	chr10:43868548-43868901	H1-hESC	embryonic stem cell:	n/a	n/a
45	USF1	chr10:43866914-43867182	K562	blood:	n/a	n/a
46	USF2	chr10:43866990-43867144	Hela-S3	cervix:	n/a	chr10:43867066-43867077
47	ZBTB7A	chr10:43866849-43867113	K562	blood:	n/a	n/a
48	ZBTB7A	chr10:43866848-43867076	K562	blood:	n/a	n/a
49	ZNF217	chr10:43870870-43871329	MCF-7	breast:	n/a	n/a
50	ZNF263	chr10:43869018-43869695	HEK293-T-REx	kidney:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43867064-43867114	Hela-S3	cervix:	n/a
2	chr10:43866966-43867016	AG04449	skin:	fetal
3	chr10:43867064-43867114	Hela-S3	cervix:	n/a
4	chr10:43866966-43867016	AG04449	skin:	fetal
5	chr10:43867064-43867114	HL-60	blood:	n/a
6	chr10:43867071-43867121	PrEC	prostate:	n/a
7	chr10:43867104-43867154	GM12891	blood:	n/a
8	chr10:43867064-43867114	PrEC	prostate:	n/a
9	chr10:43867041-43867091	PrEC	prostate:	n/a
10	chr10:43871590-43871640	HCPEpiC	choroid plexus:	n/a
11	chr10:43866966-43867016	HAEpiC	amniotic membrane:	n/a
12	chr10:43867155-43867205	NB4	blood:	n/a
13	chr10:43867024-43867074	NH-A	brain:	n/a
14	chr10:43867104-43867154	MCF10A-Er-Src	breast:	n/a
15	chr10:43866484-43866534	Hepatocyte	liver:	n/a
16	chr10:43867024-43867074	MCF10A-Er-Src	breast:	n/a
17	chr10:43867064-43867114	PANC-1	pancreas:	n/a
18	chr10:43867104-43867154	IMR90	lung:	fetal
19	chr10:43867071-43867121	H1-hESC	embryonic stem cell:	embryo
20	chr10:43871590-43871640	HCM	heart:	n/a
21	chr10:43867155-43867205	NH-A	brain:	n/a
22	chr10:43867071-43867121	HepG2	liver:	n/a
23	chr10:43867041-43867091	GM19239	blood:	n/a
24	chr10:43867024-43867074	T-47D	breast:	n/a
25	chr10:43867104-43867154	GM12878	blood:	n/a
26	chr10:43867064-43867114	GM12878	blood:	n/a
27	chr10:43867071-43867121	NHBE	bronchial:	n/a
28	chr10:43867041-43867091	GM12891	blood:	n/a
29	chr10:43866966-43867016	HMEC	breast:	n/a
30	chr10:43866484-43866534	NB4	blood:	n/a
31	chr10:43871590-43871640	U87	brain:	n/a
32	chr10:43866966-43867016	SAEC	small airway:	n/a
33	chr10:43866484-43866534	ProgFib	skin:	n/a
34	chr10:43867064-43867114	AoSMC	blood vessel:	n/a
35	chr10:43866484-43866534	SKMC	muscle:	n/a
36	chr10:43867104-43867154	HL-60	blood:	n/a
37	chr10:43867024-43867074	PFSK-1	brain:	n/a
38	chr10:43867064-43867114	HEEpiC	esophagus:	n/a
39	chr10:43867041-43867091	Caco-2	colon:	n/a
40	chr10:43867155-43867205	HRCEpiC	kidney:	n/a
41	chr10:43866966-43867016	HEK293	kidney:	embryo
42	chr10:43867071-43867121	HCT-116	colon:	n/a
43	chr10:43867024-43867074	HCPEpiC	choroid plexus:	n/a
44	chr10:43867071-43867121	HL-60	blood:	n/a
45	chr10:43871590-43871640	A549	lung:	n/a
46	chr10:43867041-43867091	HPAEpiC	pulmonary alveolar:	n/a
47	chr10:43867071-43867121	Jurkat	blood:	n/a
48	chr10:43871590-43871640	NHDF-neo	bronchial:	n/a
49	chr10:43867064-43867114	HAEpiC	amniotic membrane:	n/a
50	chr10:43867071-43867121	HEEpiC	esophagus:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:43632845..43635197-chr10:43871266..43873181,2	MCF-7	breast:
2	chr10:43787068..43788733-chr10:43871356..43873584,2	MCF-7	breast:
3	chr10:43871402..43874267-chr10:43884801..43886478,2	MCF-7	breast:
4	chr10:43858742..43859363-chr10:43870790..43871751,3	MCF-7	breast:
5	chr10:43871509..43873780-chr10:43874816..43877105,2	K562	blood:
6	chr10:43853521..43859723-chr10:43870896..43875408,11	MCF-7	breast:
7	chr10:43868700..43874062-chr10:43890607..43893448,6	MCF-7	breast:
8	chr10:43858596..43860755-chr10:43865023..43867031,2	K562	blood:
9	chr10:43871156..43873065-chr10:43900676..43903339,2	MCF-7	breast:
10	chr10:43870160..43871851-chr10:43949319..43951127,2	K562	blood:
11	chr10:43868968..43875759-chr10:43890269..43893335,11	MCF-7	breast:
12	chr10:43572567..43574576-chr10:43871912..43874300,2	MCF-7	breast:
13	chr10:43845581..43847759-chr10:43871473..43872986,2	MCF-7	breast:
14	chr10:43867647..43875264-chr10:43900659..43906151,11	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF487P-6	chr10:43871480-43871517	NONHSAT012958
2	lnc-ZNF487P-6	chr10:43871143-43871182	NONHSAT012958
3	lnc-ZNF487P-6	chr10:43870061-43870087	NONHSAT012958
4	lnc-ZNF487P-6	chr10:43869917-43869950	NONHSAT012958
5	lnc-ZNF487P-6	chr10:43871595-43871783	NONHSAT012958

No data

Variant related genes	Relation type
FXYD4	TF binding region
FXYD4	CpG island
ENSG00000169826	chromatin interactions
ENSG00000169813	chromatin interactions
ENSG00000273008	chromatin interactions

Extended variants
information (count: 258 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4245604	chr10:43866528-43866529	Weak transcription Enhancers	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570061099	chr10:43866577-43866578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537238795	chr10:43866587-43866588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549564404	chr10:43866627-43866628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568018753	chr10:43866641-43866642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535559694	chr10:43866665-43866666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553457379	chr10:43866671-43866672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571993083	chr10:43866674-43866675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540156455	chr10:43866680-43866681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567563854	chr10:43866694-43866695	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs558084289	chr10:43866722-43866723	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs576411497	chr10:43866770-43866771	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs543593014	chr10:43866771-43866772	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs561939094	chr10:43866772-43866773	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs574014723	chr10:43866775-43866776	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs374754063	chr10:43866784-43866785	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs541498893	chr10:43866793-43866794	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs139164503	chr10:43866841-43866842	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs112765416	chr10:43866864-43866865	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs533151524	chr10:43866876-43866877	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs191901866	chr10:43866878-43866879	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs12765756	chr10:43866907-43866908	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs12763612	chr10:43866908-43866909	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs61486460	chr10:43866909-43866910	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs61366158	chr10:43866935-43866936	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs398013320	chr10:43866936-43866937	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs74135733	chr10:43866940-43866941	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs536094754	chr10:43866972-43866973	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs184912016	chr10:43867041-43867042	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs549284008	chr10:43867063-43867064	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs74135734	chr10:43867072-43867073	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs188181439	chr10:43867096-43867097	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs547448737	chr10:43867104-43867105	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs386743183	chr10:43867139-43867140	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs76580596	chr10:43867141-43867142	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs557787650	chr10:43867142-43867143	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs569935724	chr10:43867174-43867175	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs77745107	chr10:43867185-43867186	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs193175070	chr10:43867288-43867289	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs77859478	chr10:43867363-43867364	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs10899794	chr10:43867364-43867365	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs577469630	chr10:43867429-43867430	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs540915319	chr10:43867449-43867450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs115860535	chr10:43867485-43867486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs200884560	chr10:43867493-43867494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs74380045	chr10:43867494-43867495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs398013321	chr10:43867506-43867507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs185418152	chr10:43867570-43867571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540148127	chr10:43867610-43867611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560060314	chr10:43867664-43867665	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43858600-43891000	Weak transcription	Right Atrium	heart
2	chr10:43861200-43872400	Weak transcription	Fetal Intestine Small	intestine
3	chr10:43866400-43867000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:43866400-43870400	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr10:43867000-43867200	Enhancers	Fetal Muscle Trunk	muscle
6	chr10:43867000-43867200	Enhancers	Hela-S3	cervix
7	chr10:43867000-43867200	Enhancers	K562	blood
8	chr10:43867000-43867400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr10:43867000-43867400	Enhancers	Placenta	Placenta
10	chr10:43867000-43867400	Enhancers	Stomach Mucosa	stomach
11	chr10:43867000-43868000	Enhancers	Brain Hippocampus Middle	brain
12	chr10:43867000-43868800	Enhancers	Brain Substantia Nigra	brain
13	chr10:43867200-43867400	Enhancers	Gastric	stomach
14	chr10:43867200-43867400	Flanking Active TSS	K562	blood
15	chr10:43867200-43868200	Weak transcription	Fetal Muscle Trunk	muscle
16	chr10:43867200-43870200	Enhancers	Brain Cingulate Gyrus	brain
17	chr10:43867200-43876200	Weak transcription	Hela-S3	cervix
18	chr10:43867400-43868400	Weak transcription	Gastric	stomach
19	chr10:43867400-43868600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr10:43867600-43867800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr10:43867600-43868000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr10:43867600-43868400	Enhancers	Brain Angular Gyrus	brain
23	chr10:43867800-43868000	Enhancers	Brain Anterior Caudate	brain
24	chr10:43867800-43868600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr10:43868000-43868200	Flanking Active TSS	Brain Hippocampus Middle	brain
26	chr10:43868000-43868200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr10:43868000-43868400	Flanking Active TSS	Brain Anterior Caudate	brain
28	chr10:43868000-43869000	Enhancers	HSMMtube	muscle
29	chr10:43868000-43869200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr10:43868000-43869600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr10:43868000-43870200	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr10:43868200-43868400	Enhancers	Brain Hippocampus Middle	brain
33	chr10:43868200-43868600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr10:43868200-43868800	Enhancers	Fetal Muscle Trunk	muscle
35	chr10:43868200-43869000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr10:43868200-43869200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr10:43868200-43869200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr10:43868200-43869200	Enhancers	Left Ventricle	heart
39	chr10:43868200-43869200	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr10:43868200-43869400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr10:43868200-43869400	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr10:43868200-43869600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr10:43868200-43870000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr10:43868200-43873400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr10:43868400-43868600	Flanking Active TSS	Brain Angular Gyrus	brain
46	chr10:43868400-43868600	Flanking Active TSS	Brain Hippocampus Middle	brain
47	chr10:43868400-43868600	Enhancers	Fetal Muscle Leg	muscle
48	chr10:43868400-43868800	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr10:43868400-43868800	Enhancers	Right Ventricle	heart
50	chr10:43868400-43869000	Enhancers	Gastric	stomach

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