Variant report

Variant	nsv160255
Chromosome Location	chr1:224580069-224589373
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:104)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:104 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:224580298-224581002	K562	blood:	n/a	n/a
2	ATF1	chr1:224580315-224580667	K562	blood:	n/a	n/a
3	ATF3	chr1:224580246-224580777	K562	blood:	n/a	n/a
4	BCLAF1	chr1:224580181-224580760	K562	blood:	n/a	n/a
5	BCLAF1	chr1:224580147-224580849	K562	blood:	n/a	n/a
6	BHLHE40	chr1:224580260-224580639	K562	blood:	n/a	n/a
7	CBX3	chr1:224580181-224580900	K562	blood:	n/a	n/a
8	CCNT2	chr1:224580322-224581060	K562	blood:	n/a	n/a
9	CEBPB	chr1:224580295-224580630	K562	blood:	n/a	n/a
10	CEBPB	chr1:224580242-224580701	K562	blood:	n/a	n/a
11	CEBPD	chr1:224580168-224580794	K562	blood:	n/a	n/a
12	CEBPD	chr1:224580169-224580783	K562	blood:	n/a	n/a
13	CREB1	chr1:224580082-224580839	K562	blood:	n/a	n/a
14	CTCF	chr1:224586487-224586515	Spleen_OC	spleen:	n/a	n/a
15	CUX1	chr1:224580235-224581344	K562	blood:	n/a	n/a
16	E2F4	chr1:224582866-224583109	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F4	chr1:224580624-224580824	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F6	chr1:224580251-224580560	K562	blood:	n/a	n/a
19	EGR1	chr1:224580323-224580629	K562	blood:	n/a	n/a
20	EP300	chr1:224580488-224580675	GM12878	blood:	n/a	n/a
21	EP300	chr1:224580246-224580746	K562	blood:	n/a	n/a
22	EP300	chr1:224580158-224580998	K562	blood:	n/a	n/a
23	ETS1	chr1:224580386-224580714	GM12878	blood:	n/a	n/a
24	FAM48A	chr1:224585900-224585937	GM12878	blood:	n/a	n/a
25	GABPA	chr1:224580245-224580716	K562	blood:	n/a	n/a
26	GATA1	chr1:224580123-224580947	PBDE	blood:	n/a	chr1:224580487-224580504
27	GATA1	chr1:224580019-224582274	K562	blood:	n/a	chr1:224581391-224581399 chr1:224581890-224581900 chr1:224580487-224580504 chr1:224582019-224582027
28	GATA2	chr1:224580231-224580788	K562	blood:	n/a	chr1:224580487-224580504
29	GATA2	chr1:224580228-224580717	K562	blood:	n/a	chr1:224580487-224580504
30	GATA3	chr1:224583373-224583729	MCF-7	breast:	n/a	n/a
31	GATA3	chr1:224584676-224584837	SH-SY5Y	brain:	n/a	chr1:224584737-224584753 chr1:224584741-224584748 chr1:224584766-224584779 chr1:224584769-224584777 chr1:224584734-224584755 chr1:224584741-224584748 chr1:224584741-224584748 chr1:224584742-224584759
32	GATA3	chr1:224583503-224583770	SH-SY5Y	brain:	n/a	n/a
33	HDAC2	chr1:224580362-224580575	K562	blood:	n/a	n/a
34	HMGN3	chr1:224580334-224580616	K562	blood:	n/a	n/a
35	IRF1	chr1:224580325-224581520	K562	blood:	n/a	chr1:224581257-224581270 chr1:224581257-224581270 chr1:224581260-224581271
36	IRF1	chr1:224580177-224580849	K562	blood:	n/a	chr1:224580251-224580264
37	JUN	chr1:224580381-224580923	K562	blood:	n/a	n/a
38	JUND	chr1:224580280-224580783	K562	blood:	n/a	n/a
39	KAP1	chr1:224581078-224581252	K562	blood:	n/a	n/a
40	MAFK	chr1:224587319-224587362	K562	blood:	n/a	n/a
41	MAFK	chr1:224587235-224587483	HepG2	liver:	n/a	n/a
42	MAFK	chr1:224580356-224581360	K562	blood:	n/a	n/a
43	MAX	chr1:224580227-224580538	K562	blood:	n/a	n/a
44	MAX	chr1:224580328-224580566	K562	blood:	n/a	n/a
45	MXI1	chr1:224580240-224580638	K562	blood:	n/a	n/a
46	MYC	chr1:224580243-224580720	K562	blood:	n/a	n/a
47	NR2F2	chr1:224580163-224580698	K562	blood:	n/a	n/a
48	NR2F2	chr1:224580047-224580830	K562	blood:	n/a	n/a
49	PML	chr1:224580171-224580817	K562	blood:	n/a	n/a
50	PML	chr1:224580239-224580798	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:224580455-224580505	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:224580455-224580505	NH-A	brain:	n/a
3	chr1:224580455-224580505	HUVEC	blood vessel:	n/a
4	chr1:224580455-224580505	HCM	heart:	n/a
5	chr1:224580455-224580505	HCT-116	colon:	n/a
6	chr1:224580455-224580505	NHBE	bronchial:	n/a
7	chr1:224580455-224580505	HRPEpiC	eye:	n/a
8	chr1:224580455-224580505	ECC-1	luminal epithelium:	n/a
9	chr1:224580455-224580505	AG10803	skin:	n/a
10	chr1:224580455-224580505	SK-N-SH_RA	brain:	n/a
11	chr1:224580455-224580505	ovcar-3	ovarian:	n/a
12	chr1:224580455-224580505	Jurkat	blood:	n/a
13	chr1:224580455-224580505	MCF-7	breast:	n/a
14	chr1:224580455-224580505	PFSK-1	brain:	n/a
15	chr1:224580455-224580505	BE2_C	brain:	n/a
16	chr1:224580455-224580505	GM12891	blood:	n/a
17	chr1:224580455-224580505	HRCEpiC	kidney:	n/a
18	chr1:224580455-224580505	HCPEpiC	choroid plexus:	n/a
19	chr1:224580455-224580505	ProgFib	skin:	n/a
20	chr1:224580455-224580505	HNPCEpiC	eye:	n/a
21	chr1:224580455-224580505	HRE	kidney:	n/a
22	chr1:224580455-224580505	CMK	blood:	n/a
23	chr1:224580455-224580505	SKMC	muscle:	n/a
24	chr1:224580455-224580505	HEK293	kidney:	embryo
25	chr1:224580455-224580505	MCF10A-Er-Src	breast:	n/a
26	chr1:224580455-224580505	Hepatocyte	liver:	n/a
27	chr1:224580455-224580505	AG09309	skin:	n/a
28	chr1:224580455-224580505	HepG2	liver:	n/a
29	chr1:224580455-224580505	GM12892	blood:	n/a
30	chr1:224580455-224580505	AG09319	gingival:	n/a
31	chr1:224580455-224580505	LNCaP	prostate:	n/a
32	chr1:224580455-224580505	U87	brain:	n/a
33	chr1:224580455-224580505	NHDF-neo	bronchial:	n/a
34	chr1:224580455-224580505	AG04449	skin:	fetal
35	chr1:224580455-224580505	HAEpiC	amniotic membrane:	n/a
36	chr1:224580455-224580505	GM06990	blood:	n/a
37	chr1:224580455-224580505	PANC-1	pancreas:	n/a
38	chr1:224580455-224580505	PrEC	prostate:	n/a
39	chr1:224580455-224580505	BJ	skin:	n/a
40	chr1:224580455-224580505	AG04450	lung:	fetal
41	chr1:224580455-224580505	T-47D	breast:	n/a
42	chr1:224580455-224580505	AoSMC	blood vessel:	n/a
43	chr1:224580455-224580505	K562	blood:	n/a
44	chr1:224580455-224580505	Hela-S3	cervix:	n/a
45	chr1:224580455-224580505	GM12878	blood:	n/a
46	chr1:224580455-224580505	GM19239	blood:	n/a
47	chr1:224580455-224580505	H1-hESC	embryonic stem cell:	embryo
48	chr1:224580455-224580505	HIPEpiC	eye:	n/a
49	chr1:224580455-224580505	HCF	heart:	n/a
50	chr1:224580455-224580505	A549	lung:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:224589162..224592475-chr1:224593427..224596642,4	K562	blood:
2	chr1:224586518..224588836-chr1:224621196..224623489,2	MCF-7	breast:
3	chr1:224583559..224585534-chr1:224598648..224600236,2	K562	blood:
4	chr1:224577356..224581875-chr1:224621264..224626529,5	K562	blood:
5	chr1:224575943..224577760-chr1:224580442..224582845,2	K562	blood:
6	chr1:224581264..224583520-chr1:224586271..224588826,2	MCF-7	breast:
7	chr1:224585388..224587684-chr1:224620366..224622924,3	K562	blood:
8	chr1:224561356..224563352-chr1:224578652..224580931,2	K562	blood:
9	chr1:224575935..224577498-chr1:224581092..224583266,3	K562	blood:
10	chr1:224558302..224559980-chr1:224578746..224580701,2	K562	blood:
11	chr1:224562792..224564765-chr1:224585546..224588270,2	K562	blood:
12	chr1:224580375..224581963-chr1:224621518..224623187,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4742-5p	chr1:224585991-224586013	MIMAT0019872
hsa-miR-4742-3p	chr1:224585929-224585951	MIMAT0019873

No data

Variant related genes	Relation type
MIR4742	TF binding region
WDR26	TF binding region
MIR4742	CpG island
WDR26	CpG island
ENSG00000143786	chromatin interactions
ENSG00000143771	chromatin interactions
ENSG00000162923	chromatin interactions

Extended variants
information (count: 314 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12723347	chr1:224580099-224580100	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs12728016	chr1:224580105-224580106	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs547480236	chr1:224580113-224580114	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs546890841	chr1:224580133-224580134	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs567723992	chr1:224580147-224580148	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs12723535	chr1:224580196-224580197	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs186197330	chr1:224580197-224580198	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs116423439	chr1:224580199-224580200	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs147419573	chr1:224580212-224580213	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs12723679	chr1:224580226-224580227	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs568937398	chr1:224580239-224580240	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs539104872	chr1:224580251-224580252	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs72758316	chr1:224580379-224580380	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs138208698	chr1:224580381-224580382	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs6691779	chr1:224580405-224580406	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs6426119	chr1:224580417-224580418	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs538541329	chr1:224580442-224580443	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs558851570	chr1:224580456-224580457	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs12092566	chr1:224580499-224580500	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs572258821	chr1:224580546-224580547	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs190571851	chr1:224580585-224580586	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs201845991	chr1:224580604-224580605	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs202036905	chr1:224580619-224580620	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs61825764	chr1:224580622-224580623	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs560791588	chr1:224580689-224580690	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs372535661	chr1:224580759-224580760	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs544839729	chr1:224580800-224580801	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs554289811	chr1:224580815-224580816	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs527293513	chr1:224580823-224580824	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs12759275	chr1:224580880-224580881	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs143590142	chr1:224580886-224580887	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs577242334	chr1:224580932-224580933	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs111544608	chr1:224581012-224581013	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs560495916	chr1:224581020-224581021	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs527717067	chr1:224581023-224581024	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs114892403	chr1:224581052-224581053	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs562060719	chr1:224581060-224581061	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs529128504	chr1:224581065-224581066	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs543570773	chr1:224581102-224581103	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs183566237	chr1:224581106-224581107	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs144058722	chr1:224581134-224581135	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs148671264	chr1:224581234-224581235	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs551086474	chr1:224581285-224581286	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs531983380	chr1:224581335-224581336	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs533580251	chr1:224581340-224581341	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs112271613	chr1:224581355-224581356	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs567954276	chr1:224581370-224581371	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs11812007	chr1:224581376-224581377	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs116516619	chr1:224581425-224581426	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs373006606	chr1:224581479-224581480	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20808228	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224545800-224605000	Weak transcription	Aorta	Aorta
2	chr1:224547000-224593200	Weak transcription	Stomach Mucosa	stomach
3	chr1:224547400-224618600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:224555800-224581400	Weak transcription	Fetal Heart	heart
5	chr1:224556000-224591000	Weak transcription	Small Intestine	intestine
6	chr1:224563000-224593400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:224565000-224581200	Weak transcription	Right Ventricle	heart
8	chr1:224565000-224582600	Weak transcription	Esophagus	oesophagus
9	chr1:224565000-224586200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr1:224567400-224582400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr1:224571000-224594000	Strong transcription	HMEC	breast
12	chr1:224571200-224599400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr1:224571800-224593400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr1:224572000-224580600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:224572000-224594000	Strong transcription	Osteobl	bone
16	chr1:224572000-224617800	Strong transcription	Fetal Thymus	thymus
17	chr1:224572400-224601000	Strong transcription	Skeletal Muscle Female	skeletal muscle
18	chr1:224572400-224617600	Strong transcription	Placenta	Placenta
19	chr1:224572600-224582800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr1:224572600-224593600	Strong transcription	NHDF-Ad	bronchial
21	chr1:224572600-224593800	Strong transcription	Duodenum Smooth Muscle	Duodenum
22	chr1:224572600-224594000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr1:224572600-224617600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:224572600-224617600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr1:224572600-224618400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr1:224572800-224594400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr1:224573200-224593400	Strong transcription	HUVEC	blood vessel
28	chr1:224573200-224594000	Strong transcription	Muscle Satellite Cultured Cells	--
29	chr1:224573200-224594000	Strong transcription	NH-A	brain
30	chr1:224573200-224594600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
31	chr1:224573200-224618400	Strong transcription	HUES48 Cell Line	embryonic stem cell
32	chr1:224573200-224618400	Strong transcription	HUES6 Cell Line	embryonic stem cell
33	chr1:224573600-224614200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:224573600-224618200	Strong transcription	HUES64 Cell Line	embryonic stem cell
35	chr1:224573800-224615200	Strong transcription	Rectal Mucosa Donor 29	rectum
36	chr1:224574000-224589200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr1:224574000-224595800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr1:224574000-224599400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr1:224574000-224601600	Strong transcription	Primary B cells from peripheral blood	blood
40	chr1:224574000-224613600	Strong transcription	Adipose Nuclei	Adipose
41	chr1:224574200-224594400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr1:224574600-224613600	Strong transcription	Duodenum Mucosa	Duodenum
43	chr1:224575000-224580600	Strong transcription	Sigmoid Colon	Sigmoid Colon
44	chr1:224575000-224589400	Strong transcription	Brain Anterior Caudate	brain
45	chr1:224575000-224589400	Strong transcription	Left Ventricle	heart
46	chr1:224575000-224597200	Strong transcription	GM12878-XiMat	blood
47	chr1:224575000-224607600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr1:224575200-224581200	Strong transcription	A549	lung
49	chr1:224575200-224583400	Strong transcription	Primary B cells from cord blood	blood
50	chr1:224575200-224589800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood

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