Variant report

Variant	nsv592984
Chromosome Location	chr3:194990363-194991844
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:768)
CpG islands
(count:183)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:768 , 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	ARID3A	chr3:194991804-194992816	HepG2	liver:	n/a	n/a
2	ATF3	chr3:194991316-194991783	K562	blood:	n/a	n/a
3	BACH1	chr3:194991531-194991603	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr3:194991640-194992930	K562	blood:	n/a	chr3:194991896-194991909 chr3:194992411-194992420 chr3:194991873-194991886
5	BCLAF1	chr3:194991338-194991985	GM12878	blood:	n/a	chr3:194991896-194991909 chr3:194991873-194991886
6	BCLAF1	chr3:194991221-194992703	GM12878	blood:	n/a	chr3:194991896-194991909 chr3:194992411-194992420 chr3:194991873-194991886 chr3:194991263-194991276
7	BHLHE40	chr3:194991314-194992882	K562	blood:	n/a	chr3:194992401-194992417
8	BHLHE40	chr3:194991577-194993187	GM12878	blood:	n/a	chr3:194992401-194992417
9	BHLHE40	chr3:194991377-194992822	HepG2	liver:	n/a	chr3:194992401-194992417
10	BRCA1	chr3:194991686-194991875	HepG2	liver:	n/a	n/a
11	BRCA1	chr3:194991027-194991328	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr3:194991798-194991802	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr3:194991716-194991742	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr3:194990825-194992873	K562	blood:	n/a	n/a
15	CCNT2	chr3:194990575-194992714	K562	blood:	n/a	chr3:194991892-194991901
16	CEBPB	chr3:194991093-194991615	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr3:194991830-194991838	Hela-S3	cervix:	n/a	n/a
18	CEBPD	chr3:194991663-194992219	HepG2	liver:	n/a	n/a
19	CHD1	chr3:194991442-194991688	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr3:194990786-194993337	IMR90	lung:	n/a	n/a
21	CHD1	chr3:194990920-194991008	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr3:194991137-194992613	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr3:194991613-194991653	K562	blood:	n/a	n/a
24	CHD2	chr3:194991477-194991842	HepG2	liver:	n/a	n/a
25	CHD2	chr3:194991344-194992625	GM12878	blood:	n/a	n/a
26	CHD2	chr3:194991067-194992609	Hela-S3	cervix:	n/a	n/a
27	CREB1	chr3:194991546-194992583	GM12878	blood:	n/a	n/a
28	CREB1	chr3:194991515-194992515	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr3:194990914-194992860	HepG2	liver:	n/a	n/a
30	CREB1	chr3:194991517-194992609	A549	lung:	n/a	n/a
31	CTBP2	chr3:194990961-194992090	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr3:194991640-194991790	GM12865	blood:	n/a	n/a
33	CTCF	chr3:194991600-194991750	GM12873	blood:	n/a	n/a
34	CTCF	chr3:194990920-194991070	GM12873	blood:	n/a	n/a
35	CTCF	chr3:194991560-194991710	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr3:194991540-194991690	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr3:194991580-194991730	K562	blood:	n/a	n/a
38	CTCF	chr3:194991026-194991203	Gliobla	brain:	n/a	n/a
39	CTCF	chr3:194991001-194991204	A549	lung:	n/a	n/a
40	CTCF	chr3:194991372-194991807	A549	lung:	n/a	n/a
41	CTCF	chr3:194991160-194991410	HRPEpiC	eye:	n/a	chr3:194991259-194991272
42	CTCF	chr3:194991277-194991802	GM19240	blood:	n/a	n/a
43	CTCF	chr3:194991260-194991410	HMF	breast:	n/a	n/a
44	CTCF	chr3:194991040-194991190	AG04450	lung:	n/a	n/a
45	CTCF	chr3:194991466-194991804	A549	lung:	n/a	n/a
46	CTCF	chr3:194991106-194991109	LNCaP	prostate:	n/a	n/a
47	CTCF	chr3:194991494-194991871	HepG2	liver:	n/a	n/a
48	CTCF	chr3:194991580-194991730	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr3:194991413-194991771	MCF-7	breast:	n/a	n/a
50	CTCF	chr3:194991314-194991348	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:194991500-194991550	SK-N-SH_RA	brain:	n/a
2	chr3:194991685-194991735	NB4	blood:	n/a
3	chr3:194991685-194991735	HCM	heart:	n/a
4	chr3:194990988-194991038	ovcar-3	ovarian:	n/a
5	chr3:194990988-194991038	PrEC	prostate:	n/a
6	chr3:194990988-194991038	HMEC	breast:	n/a
7	chr3:194991685-194991735	GM12891	blood:	n/a
8	chr3:194990988-194991038	T-47D	breast:	n/a
9	chr3:194991500-194991550	GM12891	blood:	n/a
10	chr3:194990988-194991038	NHBE	bronchial:	n/a
11	chr3:194990988-194991038	LNCaP	prostate:	n/a
12	chr3:194991685-194991735	HRPEpiC	eye:	n/a
13	chr3:194991500-194991550	Hepatocyte	liver:	n/a
14	chr3:194991500-194991550	ProgFib	skin:	n/a
15	chr3:194990988-194991038	HPAEpiC	pulmonary alveolar:	n/a
16	chr3:194991685-194991735	GM06990	blood:	n/a
17	chr3:194991500-194991550	GM12892	blood:	n/a
18	chr3:194991500-194991550	HIPEpiC	eye:	n/a
19	chr3:194990988-194991038	GM12892	blood:	n/a
20	chr3:194991685-194991735	AoSMC	blood vessel:	n/a
21	chr3:194991500-194991550	HMEC	breast:	n/a
22	chr3:194991500-194991550	HAEpiC	amniotic membrane:	n/a
23	chr3:194991500-194991550	AG09319	gingival:	n/a
24	chr3:194990988-194991038	GM12891	blood:	n/a
25	chr3:194991500-194991550	HEEpiC	esophagus:	n/a
26	chr3:194990988-194991038	AG09319	gingival:	n/a
27	chr3:194991685-194991735	NT2-D1	testis:	n/a
28	chr3:194991685-194991735	HL-60	blood:	n/a
29	chr3:194991500-194991550	Jurkat	blood:	n/a
30	chr3:194991500-194991550	HNPCEpiC	eye:	n/a
31	chr3:194991500-194991550	AG04449	skin:	fetal
32	chr3:194991500-194991550	U87	brain:	n/a
33	chr3:194991685-194991735	U87	brain:	n/a
34	chr3:194991685-194991735	PrEC	prostate:	n/a
35	chr3:194991500-194991550	K562	blood:	n/a
36	chr3:194991685-194991735	HCF	heart:	n/a
37	chr3:194990988-194991038	HRCEpiC	kidney:	n/a
38	chr3:194991685-194991735	K562	blood:	n/a
39	chr3:194991500-194991550	SAEC	small airway:	n/a
40	chr3:194991500-194991550	H1-hESC	embryonic stem cell:	embryo
41	chr3:194991685-194991735	HMEC	breast:	n/a
42	chr3:194991500-194991550	HRE	kidney:	n/a
43	chr3:194991685-194991735	HIPEpiC	eye:	n/a
44	chr3:194990988-194991038	BE2_C	brain:	n/a
45	chr3:194991500-194991550	SKMC	muscle:	n/a
46	chr3:194991500-194991550	HepG2	liver:	n/a
47	chr3:194991500-194991550	NB4	blood:	n/a
48	chr3:194990988-194991038	HEK293	kidney:	embryo
49	chr3:194991685-194991735	HRE	kidney:	n/a
50	chr3:194991500-194991550	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:194989426..194991874-chr3:195268477..195270198,3	MCF-7	breast:
2	chr3:194990825..194992800-chr3:195162290..195164935,2	K562	blood:
3	chr3:194979343..194983092-chr3:194989595..194993137,5	K562	blood:
4	chr3:194989967..194994399-chr3:195244037..195248390,6	K562	blood:
5	chr3:194989462..194991407-chr3:195163007..195164718,2	MCF-7	breast:
6	chr3:194991198..194994178-chr3:195162096..195163902,2	K562	blood:
7	chr1:43855268..43855853-chr3:194991704..194992499,2	HCT-116	colon:
8	chr3:194990474..194992109-chr3:195269592..195271685,2	MCF-7	breast:
9	chr3:194990164..194994201-chr3:195268703..195270348,3	K562	blood:
10	chr3:194979343..194985907-chr3:194989595..194992143,7	K562	blood:
11	chr3:194990005..194994037-chr3:194997788..195001012,5	K562	blood:
12	chr3:194990545..194994377-chr3:195246139..195250306,5	K562	blood:
13	chr3:194990296..194992305-chr3:195248848..195251348,4	MCF-7	breast:
14	chr3:194991144..194993841-chr3:195162528..195164078,2	MCF-7	breast:

No data

Variant related genes	Relation type
XXYLT1	TF binding region
XXYLT1	CpG island
ENSG00000114331	chromatin interactions
ENSG00000173950	chromatin interactions
ENSG00000223711	chromatin interactions
ENSG00000198198	chromatin interactions
ENSG00000252620	chromatin interactions
ENSG00000184203	chromatin interactions
ENSG00000159479	chromatin interactions

Extended variants
information (count: 42 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:42 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs755202	chr3:194990363-194990364	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534915359	chr3:194990404-194990405	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs116288402	chr3:194990414-194990415	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs577863592	chr3:194990431-194990432	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs7626389	chr3:194990544-194990545	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs117552089	chr3:194990553-194990554	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs545981969	chr3:194990579-194990580	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs557139206	chr3:194990607-194990608	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs575676646	chr3:194990690-194990691	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs542683555	chr3:194990709-194990710	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs368795625	chr3:194990722-194990723	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs528801014	chr3:194990792-194990793	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs564364876	chr3:194990805-194990806	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs142830556	chr3:194990888-194990889	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs565142315	chr3:194990988-194990989	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs74943389	chr3:194991000-194991001	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs551472528	chr3:194991007-194991008	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs62285259	chr3:194991022-194991023	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs530608741	chr3:194991041-194991042	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs113482363	chr3:194991066-194991067	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs372383983	chr3:194991079-194991080	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs567228665	chr3:194991101-194991102	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs574022267	chr3:194991106-194991107	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs534915500	chr3:194991157-194991158	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs546886890	chr3:194991165-194991166	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs538148595	chr3:194991166-194991167	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs572464634	chr3:194991187-194991188	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs538490603	chr3:194991214-194991215	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs186432312	chr3:194991216-194991217	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs370476236	chr3:194991220-194991221	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs7640100	chr3:194991221-194991222	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs554675785	chr3:194991265-194991266	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs201594607	chr3:194991278-194991279	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs372983273	chr3:194991337-194991338	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs540548399	chr3:194991395-194991396	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs565205225	chr3:194991402-194991403	Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs74954858	chr3:194991404-194991405	Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs376126877	chr3:194991426-194991427	Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs369979304	chr3:194991556-194991557	Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs544508884	chr3:194991664-194991665	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs563097755	chr3:194991732-194991733	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs530563578	chr3:194991826-194991827	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:374 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:194981400-194990800	Weak transcription	Aorta	Aorta
2	chr3:194981600-194990600	Weak transcription	Ovary	ovary
3	chr3:194981800-194990400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr3:194981800-194990400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr3:194981800-194990400	Weak transcription	Thymus	Thymus
6	chr3:194981800-194991200	Weak transcription	Small Intestine	intestine
7	chr3:194988600-194990400	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr3:194989400-194990400	Enhancers	Brain Hippocampus Middle	brain
9	chr3:194989400-194990600	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr3:194989400-194990600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr3:194989400-194990800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr3:194989400-194990800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr3:194989400-194991000	Enhancers	Spleen	Spleen
14	chr3:194989400-194991200	Enhancers	Sigmoid Colon	Sigmoid Colon
15	chr3:194989600-194990400	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr3:194989600-194990400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr3:194989600-194990400	Enhancers	Brain Cingulate Gyrus	brain
18	chr3:194989600-194990400	Enhancers	Duodenum Mucosa	Duodenum
19	chr3:194989600-194990400	Enhancers	Duodenum Smooth Muscle	Duodenum
20	chr3:194989600-194990400	Enhancers	Fetal Heart	heart
21	chr3:194989600-194990400	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr3:194989600-194990600	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr3:194989600-194990600	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr3:194989600-194990600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr3:194989600-194990600	Enhancers	Liver	Liver
26	chr3:194989600-194990600	Enhancers	Lung	lung
27	chr3:194989600-194990600	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr3:194989600-194990800	Enhancers	Primary B cells from peripheral blood	blood
29	chr3:194989600-194990800	Enhancers	Placenta	Placenta
30	chr3:194989600-194990800	Enhancers	Right Ventricle	heart
31	chr3:194989600-194991000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr3:194989800-194990400	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr3:194989800-194990400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr3:194989800-194990400	Enhancers	Primary T cells from cord blood	blood
35	chr3:194989800-194990400	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr3:194989800-194990400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr3:194989800-194990400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr3:194989800-194990400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr3:194989800-194990400	Genic enhancers	Fetal Stomach	stomach
40	chr3:194989800-194990400	Enhancers	HMEC	breast
41	chr3:194989800-194990600	Enhancers	H1 Cell Line	embryonic stem cell
42	chr3:194989800-194990600	Enhancers	Primary T cells fromperipheralblood	blood
43	chr3:194989800-194990600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr3:194989800-194990600	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr3:194989800-194990600	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr3:194989800-194990600	Enhancers	Adipose Nuclei	Adipose
47	chr3:194989800-194990600	Enhancers	Brain Substantia Nigra	brain
48	chr3:194989800-194990600	Enhancers	Fetal Muscle Trunk	muscle
49	chr3:194989800-194990600	Enhancers	Fetal Muscle Leg	muscle
50	chr3:194989800-194990600	Enhancers	Fetal Thymus	thymus

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