Variant report

Variant	nsv8662
Chromosome Location	chr10:52416662-52461079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:798)
CpG islands
(count:488)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:52420013-52420185	K562	blood:	n/a	n/a
2	BHLHE40	chr10:52419850-52420189	GM12878	blood:	n/a	n/a
3	BHLHE40	chr10:52428723-52428857	K562	blood:	n/a	n/a
4	BHLHE40	chr10:52419755-52420219	K562	blood:	n/a	n/a
5	CBX3	chr10:52419780-52420233	K562	blood:	n/a	n/a
6	CBX3	chr10:52419802-52420221	K562	blood:	n/a	n/a
7	CBX3	chr10:52428609-52429004	K562	blood:	n/a	n/a
8	CBX3	chr10:52457565-52457966	K562	blood:	n/a	n/a
9	CEBPB	chr10:52428806-52428914	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr10:52425983-52426195	K562	blood:	n/a	n/a
11	CEBPB	chr10:52419975-52420135	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr10:52419994-52420182	IMR90	lung:	n/a	n/a
13	CEBPB	chr10:52419895-52420206	K562	blood:	n/a	n/a
14	CEBPB	chr10:52419926-52420201	A549	lung:	n/a	n/a
15	CEBPB	chr10:52419900-52420194	HepG2	liver:	n/a	n/a
16	CHD2	chr10:52419835-52420206	GM12878	blood:	n/a	n/a
17	CHD2	chr10:52434377-52434505	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr10:52420022-52420103	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr10:52420008-52420023	K562	blood:	n/a	n/a
20	CHD2	chr10:52419892-52419904	HepG2	liver:	n/a	n/a
21	CREB1	chr10:52419803-52420310	A549	lung:	n/a	n/a
22	CTCF	chr10:52428558-52429057	K562	blood:	n/a	chr10:52428839-52428852 chr10:52428837-52428855
23	CTCF	chr10:52419939-52420235	GM12891	blood:	n/a	n/a
24	CTCF	chr10:52457862-52457899	GM10248	blood:	n/a	n/a
25	CTCF	chr10:52427240-52427390	GM06990	blood:	n/a	chr10:52427368-52427389 chr10:52427319-52427328
26	CTCF	chr10:52419953-52420228	MCF-7	breast:	n/a	n/a
27	CTCF	chr10:52443025-52443317	K562	blood:	n/a	n/a
28	CTCF	chr10:52428786-52428899	LNCaP	prostate:	n/a	chr10:52428839-52428852 chr10:52428837-52428855
29	CTCF	chr10:52419918-52420274	GM19239	blood:	n/a	n/a
30	CTCF	chr10:52420020-52420170	SAEC	small airway:	n/a	n/a
31	CTCF	chr10:52419973-52420174	GM10248	blood:	n/a	n/a
32	CTCF	chr10:52420120-52420270	GM12869	blood:	n/a	n/a
33	CTCF	chr10:52450426-52450450	GM20000	blood:	n/a	n/a
34	CTCF	chr10:52427260-52427410	GM06990	blood:	n/a	chr10:52427368-52427389 chr10:52427319-52427328 chr10:52427373-52427391
35	CTCF	chr10:52419900-52420050	HCFaa	heart:	n/a	n/a
36	CTCF	chr10:52443100-52443250	K562	blood:	n/a	n/a
37	CTCF	chr10:52428844-52428891	GM20000	blood:	n/a	n/a
38	CTCF	chr10:52457686-52457916	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr10:52420120-52420270	MCF-7	breast:	n/a	n/a
40	CTCF	chr10:52428655-52428919	H1-hESC	embryonic stem cell:	n/a	chr10:52428839-52428852 chr10:52428837-52428855
41	CTCF	chr10:52439021-52439335	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr10:52419977-52420186	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr10:52457702-52457812	MCF-7	breast:	n/a	n/a
44	CTCF	chr10:52428797-52428883	ProgFib	skin:	n/a	chr10:52428839-52428852 chr10:52428837-52428855
45	CTCF	chr10:52438980-52439130	GM12873	blood:	n/a	n/a
46	CTCF	chr10:52419960-52420110	NHLF	lung:	n/a	n/a
47	CTCF	chr10:52419902-52420268	T-47D	breast:	n/a	n/a
48	CTCF	chr10:52419956-52420206	GM13976	blood:	n/a	n/a
49	CTCF	chr10:52457701-52457795	GM10248	blood:	n/a	n/a
50	CTCF	chr10:52419766-52420375	A549	lung:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:52419357-52419407	T-47D	breast:	n/a
2	chr10:52434778-52434828	AG09309	skin:	n/a
3	chr10:52420019-52420069	GM12892	blood:	n/a
4	chr10:52434647-52434697	HEEpiC	esophagus:	n/a
5	chr10:52434552-52434602	MCF-7	breast:	n/a
6	chr10:52434647-52434697	AG09319	gingival:	n/a
7	chr10:52431183-52431233	HAEpiC	amniotic membrane:	n/a
8	chr10:52431183-52431233	LNCaP	prostate:	n/a
9	chr10:52420019-52420069	Caco-2	colon:	n/a
10	chr10:52433577-52433627	BJ	skin:	n/a
11	chr10:52433577-52433627	MCF10A-Er-Src	breast:	n/a
12	chr10:52419357-52419407	IMR90	lung:	fetal
13	chr10:52433577-52433627	U87	brain:	n/a
14	chr10:52431183-52431233	BE2_C	brain:	n/a
15	chr10:52419357-52419407	MCF-7	breast:	n/a
16	chr10:52434647-52434697	HCF	heart:	n/a
17	chr10:52420019-52420069	NHDF-neo	bronchial:	n/a
18	chr10:52434647-52434697	MCF-7	breast:	n/a
19	chr10:52431183-52431233	SKMC	muscle:	n/a
20	chr10:52434778-52434828	AG10803	skin:	n/a
21	chr10:52434647-52434697	SK-N-SH	brain:	n/a
22	chr10:52419357-52419407	Hela-S3	cervix:	n/a
23	chr10:52431183-52431233	T-47D	breast:	n/a
24	chr10:52434552-52434602	NH-A	brain:	n/a
25	chr10:52434778-52434828	SAEC	small airway:	n/a
26	chr10:52436125-52436175	HCPEpiC	choroid plexus:	n/a
27	chr10:52434552-52434602	AG10803	skin:	n/a
28	chr10:52436125-52436175	HMEC	breast:	n/a
29	chr10:52419357-52419407	PFSK-1	brain:	n/a
30	chr10:52434647-52434697	Hela-S3	cervix:	n/a
31	chr10:52431183-52431233	ProgFib	skin:	n/a
32	chr10:52434647-52434697	H1-hESC	embryonic stem cell:	embryo
33	chr10:52434778-52434828	AG09319	gingival:	n/a
34	chr10:52434552-52434602	BJ	skin:	n/a
35	chr10:52434778-52434828	HNPCEpiC	eye:	n/a
36	chr10:52434552-52434602	IMR90	lung:	fetal
37	chr10:52433577-52433627	LNCaP	prostate:	n/a
38	chr10:52434552-52434602	RPTEC	kidney:	n/a
39	chr10:52419357-52419407	Hepatocyte	liver:	n/a
40	chr10:52434552-52434602	AG04450	lung:	fetal
41	chr10:52434778-52434828	IMR90	lung:	fetal
42	chr10:52434647-52434697	AG10803	skin:	n/a
43	chr10:52434647-52434697	HPAEpiC	pulmonary alveolar:	n/a
44	chr10:52434552-52434602	Jurkat	blood:	n/a
45	chr10:52436125-52436175	HNPCEpiC	eye:	n/a
46	chr10:52436125-52436175	IMR90	lung:	fetal
47	chr10:52420019-52420069	GM19239	blood:	n/a
48	chr10:52434778-52434828	GM06990	blood:	n/a
49	chr10:52434552-52434602	AG09309	skin:	n/a
50	chr10:52419357-52419407	HCF	heart:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:52419903..52420416-chr10:81444547..81445060,2	MCF-7	breast:
2	chr10:52381243..52386496-chr10:52418227..52421959,6	MCF-7	breast:
3	chr10:52414539..52416441-chr10:52417401..52419945,2	MCF-7	breast:
4	chr10:52419698..52420201-chr10:81445043..81445551,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASAH2B-5	chr10:52455352-52455741	NONHSAT013397

No data

Variant related genes	Relation type
NUTM2HP	TF binding region
ENSG00000231345	TF binding region
ENSG00000226168	TF binding region
NUTM2HP	CpG island
ENSG00000231345	CpG island
ENSG00000226168	CpG island
ENSG00000226200	chromatin interactions
ENSG00000231345	chromatin interactions
ENSG00000224886	chromatin interactions
ENSG00000198964	chromatin interactions

Extended variants
information (count: 2102 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2102 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528150609	chr10:52416672-52416673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs368943401	chr10:52416718-52416719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs117882748	chr10:52416744-52416745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373285395	chr10:52416791-52416792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376325043	chr10:52416797-52416798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370362810	chr10:52416798-52416799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376151275	chr10:52416815-52416816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369465676	chr10:52416817-52416818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561060571	chr10:52416834-52416835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529913686	chr10:52416981-52416982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183645271	chr10:52417012-52417013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546457980	chr10:52417020-52417021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376344100	chr10:52417043-52417044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560133419	chr10:52417104-52417105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532334396	chr10:52417126-52417127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541259215	chr10:52417134-52417135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187402131	chr10:52417164-52417165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569333111	chr10:52417166-52417167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374088305	chr10:52417316-52417317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548748186	chr10:52417341-52417342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12358348	chr10:52417386-52417387	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs79754918	chr10:52417432-52417433	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs554465166	chr10:52417486-52417487	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs35378422	chr10:52417514-52417515	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs11816953	chr10:52417543-52417544	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs192259048	chr10:52417559-52417560	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs58499848	chr10:52417570-52417571	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs570436865	chr10:52417571-52417572	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs12248669	chr10:52417597-52417598	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs3011718	chr10:52417601-52417602	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs112442302	chr10:52417622-52417623	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs200665991	chr10:52417634-52417635	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs544101720	chr10:52417645-52417646	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs554362071	chr10:52417661-52417662	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184320293	chr10:52417663-52417664	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs555731860	chr10:52417696-52417697	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs376427429	chr10:52417701-52417702	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs540149769	chr10:52417730-52417731	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs187101156	chr10:52417775-52417776	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs140683897	chr10:52417796-52417797	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs546171560	chr10:52417850-52417851	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs562877617	chr10:52417868-52417869	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs531811353	chr10:52417910-52417911	Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs548365491	chr10:52417922-52417923	Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568687074	chr10:52417929-52417930	Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs527840402	chr10:52417930-52417931	Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs548155237	chr10:52417937-52417938	Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs571148393	chr10:52417952-52417953	Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs574428534	chr10:52417956-52417957	Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs538288301	chr10:52417987-52417988	Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
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
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
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Ollier disease	21235737	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD

Chromatin state (count:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52411200-52419200	Weak transcription	Fetal Intestine Small	intestine
2	chr10:52413600-52419200	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr10:52413600-52419600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr10:52413600-52419600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr10:52413800-52418400	Weak transcription	Fetal Thymus	thymus
6	chr10:52413800-52418600	Weak transcription	Fetal Intestine Large	intestine
7	chr10:52413800-52419200	Weak transcription	Thymus	Thymus
8	chr10:52414000-52419000	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr10:52414000-52419200	Weak transcription	Primary B cells from cord blood	blood
10	chr10:52414000-52419600	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr10:52414000-52419600	Weak transcription	Primary T cells from cord blood	blood
12	chr10:52414000-52419800	Weak transcription	HUVEC	blood vessel
13	chr10:52414200-52419200	Weak transcription	Primary B cells from peripheral blood	blood
14	chr10:52414400-52419200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr10:52414400-52419600	Weak transcription	Placenta	Placenta
16	chr10:52414600-52418000	Weak transcription	GM12878-XiMat	blood
17	chr10:52414600-52419600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr10:52414800-52417600	Weak transcription	K562	blood
19	chr10:52416400-52418000	Weak transcription	Fetal Stomach	stomach
20	chr10:52417400-52419000	Weak transcription	Right Atrium	heart
21	chr10:52417400-52419400	Weak transcription	Stomach Smooth Muscle	stomach
22	chr10:52417600-52418800	Weak transcription	Liver	Liver
23	chr10:52417600-52420200	Active TSS	K562	blood
24	chr10:52418000-52418200	Enhancers	Pancreas	Pancrea
25	chr10:52418000-52418200	Flanking Active TSS	GM12878-XiMat	blood
26	chr10:52418000-52418800	Strong transcription	Fetal Stomach	stomach
27	chr10:52418200-52418400	Enhancers	GM12878-XiMat	blood
28	chr10:52418200-52419600	Weak transcription	Pancreas	Pancrea
29	chr10:52418400-52418600	Enhancers	Fetal Thymus	thymus
30	chr10:52418400-52418600	Flanking Active TSS	GM12878-XiMat	blood
31	chr10:52418400-52418800	Enhancers	Hela-S3	cervix
32	chr10:52418600-52419000	Active TSS	GM12878-XiMat	blood
33	chr10:52418600-52419200	Weak transcription	Fetal Thymus	thymus
34	chr10:52418600-52419400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr10:52418600-52419400	Enhancers	Fetal Intestine Large	intestine
36	chr10:52418800-52419400	Enhancers	Liver	Liver
37	chr10:52418800-52419400	Weak transcription	Fetal Stomach	stomach
38	chr10:52418800-52419400	Enhancers	Stomach Mucosa	stomach
39	chr10:52419000-52419200	Active TSS	HepG2	liver
40	chr10:52419000-52419600	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr10:52419000-52419600	Flanking Active TSS	GM12878-XiMat	blood
42	chr10:52419000-52420000	Strong transcription	Right Atrium	heart
43	chr10:52419000-52420400	Active TSS	Hela-S3	cervix
44	chr10:52419200-52419400	Enhancers	Primary B cells from peripheral blood	blood
45	chr10:52419200-52419400	Enhancers	Primary T cells fromperipheralblood	blood
46	chr10:52419200-52419400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr10:52419200-52419400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr10:52419200-52419400	Active TSS	Fetal Thymus	thymus
49	chr10:52419200-52419400	Enhancers	Thymus	Thymus
50	chr10:52419200-52419600	Enhancers	Primary B cells from cord blood	blood

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